Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84501 |
| ensemblid | ENSG00000204991.11 |
| hgncid | 30623 |
| symbol | SPIRE2 |
| name | spire type actin nucleation factor 2 |
| refseq_nuc | NM_032451.2 |
| refseq_prot | NP_115827.1 |
| ensembl_nuc | ENST00000378247.8 |
| ensembl_prot | ENSP00000367494.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89828475 |
| end | 89871319 |
| strand | + |
| ver | v1.2 |
| region | chr16:89828475-89871319 |
| region5000 | chr16:89823475-89876319 |
| regionname0 | SPIRE2_chr16_89828475_89871319 |
| regionname5000 | SPIRE2_chr16_89823475_89876319 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 714 | 292 | 89 | 65 | 84 | 15 | 37 | 66 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0002 | 0/0 | 337 | 23 | 0 | 0 | 20 | 1 | 2 | 9 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(332): Show |
chr16 | 89823475 | 89876319 |
| a0003 | 0/0 | 714 | 12 | 0 | 0 | 11 | 0 | 1 | 7 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0004 | 0/0 | 714 | 12 | 0 | 5 | 1 | 0 | 6 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0005 | 0/0 | 715 | 5 | 0 | 1 | 4 | 0 | 0 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(710): Show |
chr16 | 89823475 | 89876319 |
| a0006 | 0/0 | 336 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(331): Show |
chr16 | 89823475 | 89876319 |
| a0007 | 0/0 | 714 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MAREG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0008 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0009 | 0/0 | 714 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0010 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0011 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| a0012 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(332): Show |
chr16 | 89823475 | 89876319 |
| a0013 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(332): Show |
chr16 | 89823475 | 89876319 |
| a0014 | 0/0 | 344 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(339): Show |
chr16 | 89823475 | 89876319 |
| a0015 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | MARAG others(709): Show |
chr16 | 89823475 | 89876319 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2142 | 256 | 84 | 57 | 72 | 14 | 28 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0003 | 0/1 | 2142 | 16 | 0 | 4 | 7 | 1 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0006 | 0/0 | 2142 | 6 | 0 | 0 | 4 | 0 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0008 | 0/0 | 2142 | 4 | 2 | 2 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0009 | 0/0 | 2142 | 3 | 0 | 0 | 0 | 0 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0011 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0012 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0018 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0019 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0021 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0001c0027 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0002c0002 | 0/0 | 2237 | 23 | 0 | 0 | 20 | 1 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2232): Show |
chr16 | 89823475 | 89876319 | ||
| a0003c0004 | 0/0 | 2142 | 12 | 0 | 0 | 11 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0004c0005 | 0/0 | 2142 | 12 | 0 | 5 | 1 | 0 | 6 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0005c0007 | 0/0 | 2145 | 4 | 0 | 1 | 3 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2140): Show |
chr16 | 89823475 | 89876319 | ||
| a0005c0014 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2140): Show |
chr16 | 89823475 | 89876319 | ||
| a0006c0023 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2229): Show |
chr16 | 89823475 | 89876319 | ||
| a0006c0024 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2229): Show |
chr16 | 89823475 | 89876319 | ||
| a0007c0010 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0008c0020 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0009c0022 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0010c0017 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0011c0026 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 | ||
| a0012c0013 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2232): Show |
chr16 | 89823475 | 89876319 | ||
| a0013c0025 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2232): Show |
chr16 | 89823475 | 89876319 | ||
| a0014c0015 | 0/0 | 2191 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2186): Show |
chr16 | 89823475 | 89876319 | ||
| a0015c0016 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | ATGGC others(2137): Show |
chr16 | 89823475 | 89876319 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3268 | 217 | 65 | 47 | 64 | 14 | 26 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0002 | 0/0 | 3263 | 2 | 0 | 0 | 2 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3258): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0003 | 0/0 | 3262 | 20 | 19 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3257): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0004 | 0/0 | 3268 | 11 | 0 | 6 | 5 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0006 | 0/0 | 3268 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0007 | 0/0 | 3268 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0009 | 0/0 | 3269 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3264): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0010 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0011 | 0/0 | 3268 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0001t0015 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0003t0001 | 0/0 | 3268 | 12 | 0 | 3 | 5 | 1 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0003t0005 | 0/1 | 3268 | 3 | 0 | 0 | 2 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0003t0013 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0006t0001 | 0/0 | 3268 | 6 | 0 | 0 | 4 | 0 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0008t0001 | 0/0 | 3268 | 4 | 2 | 2 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0009t0001 | 0/0 | 3268 | 3 | 0 | 0 | 0 | 0 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0011t0001 | 0/0 | 3268 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0012t0005 | 0/0 | 3268 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0018t0012 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0019t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0021t0001 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0001c0027t0001 | 0/0 | 3268 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0002c0002t0002 | 0/0 | 3358 | 22 | 0 | 0 | 19 | 1 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3353): Show |
chr16 | 89823475 | 89876319 |
| a0002c0002t0014 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3353): Show |
chr16 | 89823475 | 89876319 |
| a0003c0004t0001 | 0/0 | 3268 | 12 | 0 | 0 | 11 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0004c0005t0001 | 0/0 | 3268 | 12 | 0 | 5 | 1 | 0 | 6 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0005c0007t0002 | 0/0 | 3266 | 4 | 0 | 1 | 3 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3261): Show |
chr16 | 89823475 | 89876319 |
| a0005c0014t0002 | 0/0 | 3266 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3261): Show |
chr16 | 89823475 | 89876319 |
| a0006c0023t0001 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3355): Show |
chr16 | 89823475 | 89876319 |
| a0006c0024t0001 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3355): Show |
chr16 | 89823475 | 89876319 |
| a0007c0010t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0007c0010t0008 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0008c0020t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0009c0022t0001 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0010c0017t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0011c0026t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| a0012c0013t0002 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3353): Show |
chr16 | 89823475 | 89876319 |
| a0013c0025t0002 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3353): Show |
chr16 | 89823475 | 89876319 |
| a0014c0015t0002 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3307): Show |
chr16 | 89823475 | 89876319 |
| a0015c0016t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | AGGCT others(3263): Show |
chr16 | 89823475 | 89876319 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0009g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0010g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0015g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0005g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0013g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0009t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0009t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0009t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0011t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0011t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0012t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0018t0012g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0019t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0021t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0027t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0014t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0006c0023t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0006c0024t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0007c0010t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0007c0010t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0008c0020t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0009c0022t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0010c0017t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0011c0026t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0012c0013t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0013c0025t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0014c0015t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0015c0016t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0104 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0258 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0348 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00408 | hp1 | a0003 | c0004 | t0001 | g0027 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00621 | hp1 | a0005 | c0014 | t0002 | g0279 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00741 | hp1 | a0004 | c0005 | t0001 | g0301 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01081 | hp1 | a0001 | c0008 | t0001 | g0013 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01099 | hp1 | a0001 | c0021 | t0001 | g0211 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0349 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01106 | hp2 | a0004 | c0005 | t0001 | g0307 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01167 | hp1 | a0004 | c0005 | t0001 | g0306 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01167 | hp2 | a0001 | c0008 | t0001 | g0012 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01169 | hp1 | a0004 | c0005 | t0001 | g0303 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01175 | hp1 | a0005 | c0007 | t0002 | g0262 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01243 | hp1 | a0001 | c0018 | t0012 | g0346 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01256 | hp1 | a0001 | c0001 | t0015 | g0125 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01884 | hp1 | a0008 | c0020 | t0001 | g0220 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01928 | hp1 | a0009 | c0022 | t0001 | g0034 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0089 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01943 | hp1 | a0001 | c0003 | t0013 | g0095 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0314 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0138 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01993 | hp1 | a0004 | c0005 | t0001 | g0302 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0315 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02015 | hp2 | a0003 | c0004 | t0001 | g0065 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02040 | hp2 | a0002 | c0002 | t0014 | g0272 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02071 | hp1 | a0004 | c0005 | t0001 | g0297 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02071 | hp2 | a0006 | c0024 | t0001 | g0153 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02074 | hp2 | a0003 | c0004 | t0001 | g0045 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02080 | hp1 | a0005 | c0007 | t0002 | g0275 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | CDX | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0330 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0137 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0340 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0145 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02451 | hp2 | a0007 | c0010 | t0008 | g0312 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02572 | hp2 | a0001 | c0008 | t0001 | g0011 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02602 | hp1 | a0004 | c0005 | t0001 | g0299 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02602 | hp2 | a0001 | c0001 | t0011 | g0091 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02698 | hp1 | a0004 | c0005 | t0001 | g0304 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0339 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02896 | hp1 | a0001 | c0011 | t0001 | g0317 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0331 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02897 | hp1 | a0001 | c0011 | t0001 | g0318 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02922 | hp2 | a0010 | c0017 | t0001 | g0172 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0022 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0338 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03139 | hp1 | a0001 | c0019 | t0001 | g0316 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03139 | hp2 | a0011 | c0026 | t0001 | g0170 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0335 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03239 | hp2 | a0001 | c0006 | t0001 | g0017 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03490 | hp2 | a0001 | c0006 | t0001 | g0020 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0280 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0281 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03669 | hp2 | a0001 | c0009 | t0001 | g0010 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03688 | hp2 | a0004 | c0005 | t0001 | g0305 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03831 | hp2 | a0001 | c0027 | t0001 | g0021 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0222 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03927 | hp2 | a0003 | c0004 | t0001 | g0064 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0117 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04115 | hp1 | a0001 | c0009 | t0001 | g0014 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04184 | hp1 | a0004 | c0005 | t0001 | g0300 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04204 | hp1 | a0001 | c0009 | t0001 | g0009 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04204 | hp2 | a0004 | c0005 | t0001 | g0298 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0178 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04228 | hp2 | a0004 | c0005 | t0001 | g0311 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18612 | hp1 | a0012 | c0013 | t0002 | g0263 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18747 | hp1 | a0003 | c0004 | t0001 | g0059 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0343 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18939 | hp2 | a0001 | c0006 | t0001 | g0019 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18943 | hp1 | a0013 | c0025 | t0002 | g0268 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18945 | hp1 | a0003 | c0004 | t0001 | g0040 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18951 | hp2 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18970 | hp1 | a0003 | c0004 | t0001 | g0056 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18977 | hp1 | a0001 | c0012 | t0005 | g0051 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0016 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18983 | hp2 | a0001 | c0003 | t0005 | g0109 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18984 | hp2 | a0005 | c0007 | t0002 | g0261 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18990 | hp1 | a0014 | c0015 | t0002 | g0277 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18995 | hp2 | a0003 | c0004 | t0001 | g0081 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18998 | hp1 | a0003 | c0004 | t0001 | g0075 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19030 | hp1 | a0015 | c0016 | t0001 | g0005 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19054 | hp1 | a0003 | c0004 | t0001 | g0041 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19057 | hp1 | a0001 | c0006 | t0001 | g0018 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19060 | hp2 | a0003 | c0004 | t0001 | g0042 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19065 | hp2 | a0001 | c0003 | t0005 | g0112 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19067 | hp2 | a0003 | c0004 | t0001 | g0046 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19070 | hp1 | a0005 | c0007 | t0002 | g0269 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0344 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0347 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | GIH | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0118 | SAS | GIH | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0323 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03471 | hp2 | a0006 | c0023 | t0001 | g0249 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0333 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA21309 | hp2 | a0007 | c0010 | t0001 | g0313 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0005 | g0285 | REF | REF | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0229 | REF | REF | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89828561 | C | A | 1 | a0007 | 2 | HG02451.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.11C>A | p.Ala4Glu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 87/3268 | 11/2145 | 4/714 | chr16 | 89828561 | |||
| chr16:89828590 | G | A | 1 | a0003 | 12 | HG00408.hp1 HG02015.hp2 HG02074.hp2 others(9): Show |
missense_variant | MODERATE | c.40G>A | p.Ala14Thr | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 116/3268 | 40/2145 | 14/714 | chr16 | 89828590 | |||
| chr16:89828705 | G | T | 1 | a0011 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.155G>T | p.Arg52Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 231/3268 | 155/2145 | 52/714 | chr16 | 89828705 | |||
| chr16:89845339 | G | A | 1 | a0012 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.262G>A | p.Val88Met | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/15 | 338/3268 | 262/2145 | 88/714 | chr16 | 89845339 | |||
| chr16:89850383 | C | T | 1 | a0013 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.368C>T | p.Pro123Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/15 | 444/3268 | 368/2145 | 123/714 | chr16 | 89850383 | |||
| chr16:89850471 | C | CGAG | 5 | a0002 a0005 a0012 others(2): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
disruptive_inframe_insertion | MODERATE | c.470_472dupAGG | p.Glu157dup | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/15 | 549/3268 | 473/2145 | 158/714 | INFO_REALIGN_3_PRIME | chr16 | 89850471 | ||
| chr16:89850607 | G | A | 1 | a0015 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.592G>A | p.Val198Met | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/15 | 668/3268 | 592/2145 | 198/714 | chr16 | 89850607 | |||
| chr16:89856144 | C | T | 1 | a0009 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1010C>T | p.Pro337Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/15 | 1086/3268 | 1010/2145 | 337/714 | chr16 | 89856144 | |||
| chr16:89859195 | C | G | 1 | a0008 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1303C>G | p.Leu435Val | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/15 | 1379/3268 | 1303/2145 | 435/714 | chr16 | 89859195 | |||
| chr16:89859283 | C | A | 1 | a0010 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1391C>A | p.Pro464Gln | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/15 | 1467/3268 | 1391/2145 | 464/714 | chr16 | 89859283 | |||
| chr16:89860743 | C | T | 1 | a0004 | 12 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(9): Show |
missense_variant | MODERATE | c.1523C>T | p.Ser508Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/15 | 1599/3268 | 1523/2145 | 508/714 | chr16 | 89860743 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89828586 | G | A | 2 | a0001c0003 a0001c0012 |
16 | HG00280.hp1 HG01928.hp2 HG01943.hp1 others(13): Show |
synonymous_variant | LOW | c.36G>A | p.Ala12Ala | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 112/3268 | 36/2145 | 12/714 | chr16 | 89828586 | |||
| chr16:89828592 | A | G | 5 | a0001c0006 a0001c0008 a0001c0009 others(2): Show |
16 | HG01081.hp1 HG01167.hp2 HG02451.hp2 others(13): Show |
synonymous_variant | LOW | c.42A>G | p.Ala14Ala | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 118/3268 | 42/2145 | 14/714 | chr16 | 89828592 | |||
| chr16:89828601 | G | C | 1 | a0001c0011 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.51G>C | p.Pro17Pro | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 127/3268 | 51/2145 | 17/714 | chr16 | 89828601 | |||
| chr16:89828655 | C | G | 1 | a0001c0012 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.105C>G | p.Leu35Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 181/3268 | 105/2145 | 35/714 | chr16 | 89828655 | |||
| chr16:89854309 | C | T | 1 | a0001c0009 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
synonymous_variant | LOW | c.669C>T | p.Asp223Asp | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 4/15 | 745/3268 | 669/2145 | 223/714 | chr16 | 89854309 | |||
| chr16:89854549 | A | G | 8 | a0002c0002 a0005c0007 a0005c0014 others(5): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
synonymous_variant | LOW | c.789A>G | p.Gln263Gln | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/15 | 865/3268 | 789/2145 | 263/714 | chr16 | 89854549 | |||
| chr16:89854585 | G | A | 1 | a0005c0014 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.825G>A | p.Gln275Gln | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/15 | 901/3268 | 825/2145 | 275/714 | chr16 | 89854585 | |||
| chr16:89856208 | G | A | 1 | a0001c0008 | 4 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(1): Show |
synonymous_variant | LOW | c.1074G>A | p.Pro358Pro | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/15 | 1150/3268 | 1074/2145 | 358/714 | chr16 | 89856208 | |||
| chr16:89858453 | C | T | 1 | a0001c0021 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.1218C>T | p.Arg406Arg | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/15 | 1294/3268 | 1218/2145 | 406/714 | chr16 | 89858453 | |||
| chr16:89859281 | C | G | 1 | a0001c0027 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.1389C>G | p.Pro463Pro | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/15 | 1465/3268 | 1389/2145 | 463/714 | chr16 | 89859281 | |||
| chr16:89860696 | G | A | 1 | a0006c0023 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1476G>A | p.Ala492Ala | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/15 | 1552/3268 | 1476/2145 | 492/714 | chr16 | 89860696 | |||
| chr16:89870104 | C | T | 1 | a0001c0019 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1977C>T | p.Tyr659Tyr | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 2053/3268 | 1977/2145 | 659/714 | chr16 | 89870104 | |||
| chr16:89870182 | G | A | 1 | a0001c0018 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.2055G>A | p.Lys685Lys | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 2131/3268 | 2055/2145 | 685/714 | chr16 | 89870182 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89870394 | C | T | 2 | a0001c0003t0005 a0001c0012t0005 |
3 | NA18977.hp1 NA18983.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*122C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 122 | chr16 | 89870394 | ||||||
| chr16:89870446 | C | T | 1 | a0001c0001t0015 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 174 | chr16 | 89870446 | ||||||
| chr16:89870508 | G | C | 1 | a0001c0001t0006 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 236 | chr16 | 89870508 | ||||||
| chr16:89870549 | C | T | 1 | a0002c0002t0014 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 277 | chr16 | 89870549 | ||||||
| chr16:89870618 | G | A | 1 | a0001c0001t0007 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 346 | chr16 | 89870618 | ||||||
| chr16:89870679 | C | T | 1 | a0001c0003t0013 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*407C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 407 | chr16 | 89870679 | ||||||
| chr16:89870762 | C | T | 1 | a0001c0018t0012 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 490 | chr16 | 89870762 | ||||||
| chr16:89870818 | G | A | 1 | a0007c0010t0008 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 546 | chr16 | 89870818 | ||||||
| chr16:89871029 | T | G | 2 | a0001c0001t0004 a0001c0001t0015 |
12 | HG01168.hp2 HG01169.hp2 HG01256.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*757T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 757 | chr16 | 89871029 | ||||||
| chr16:89871086 | G | GA | 9 | a0001c0001t0002 a0001c0001t0009 a0002c0002t0002 others(6): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*825dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 826 | INFO_REALIGN_3_PRIME | chr16 | 89871086 | |||||
| chr16:89871102 | C | T | 1 | a0001c0001t0011 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 830 | chr16 | 89871102 | ||||||
| chr16:89871118 | CTGCCCT | C | 9 | a0001c0001t0002 a0001c0001t0003 a0002c0002t0002 others(6): Show |
53 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*854_*859delGCCCTT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 854 | INFO_REALIGN_3_PRIME | chr16 | 89871118 | |||||
| chr16:89871237 | G | C | 1 | a0001c0001t0010 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*965G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 965 | chr16 | 89871237 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89828863 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244+69G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89828863 | |||||||
| chr16:89828864 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244+70G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89828864 | |||||||
| chr16:89829027 | C | T | 2 | a0003c0004t0001g0040 a0003c0004t0001g0041 |
2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.244+233C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829027 | |||||||
| chr16:89829061 | G | T | 9 | a0001c0001t0001g0345 a0001c0001t0001g0347 a0001c0001t0001g0348 others(6): Show |
9 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+267G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829061 | |||||||
| chr16:89829081 | G | C | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.244+287G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829081 | |||||||
| chr16:89829108 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0015c0016t0001g0005 |
3 | HG03486.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.244+314T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829108 | |||||||
| chr16:89829114 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.244+320G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829114 | |||||||
| chr16:89829140 | C | T | 28 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0329 others(25): Show |
28 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.244+346C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829140 | |||||||
| chr16:89829143 | T | C | 28 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0329 others(25): Show |
28 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.244+349T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829143 | |||||||
| chr16:89829184 | C | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+390C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829184 | |||||||
| chr16:89829201 | G | T | 2 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
2 | HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.244+407G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829201 | |||||||
| chr16:89829377 | C | T | 2 | a0007c0010t0001g0313 a0007c0010t0008g0312 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+583C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829377 | |||||||
| chr16:89829453 | G | A | 14 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(11): Show |
14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+659G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829453 | |||||||
| chr16:89829545 | T | C | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+751T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829545 | |||||||
| chr16:89829597 | C | G | 35 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(32): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.244+803C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829597 | |||||||
| chr16:89829649 | GGTGGGGG others(2326): Show |
G | 1 | a0001c0001t0001g0286 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.244+856_244+3188de others(1): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829649 | |||||||
| chr16:89829721 | C | G | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.244+927C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829721 | |||||||
| chr16:89829812 | T | C | 36 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(33): Show |
36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+1018T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829812 | |||||||
| chr16:89829835 | C | T | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+1041C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829835 | |||||||
| chr16:89829923 | C | A | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+1129C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829923 | |||||||
| chr16:89829924 | A | C | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+1130A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829924 | |||||||
| chr16:89829925 | T | G | 2 | a0001c0001t0001g0248 a0006c0023t0001g0249 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+1131T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829925 | |||||||
| chr16:89830015 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.244+1221A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830015 | |||||||
| chr16:89830034 | T | C | 2 | a0001c0011t0001g0317 a0001c0011t0001g0318 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.244+1240T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830034 | |||||||
| chr16:89830073 | C | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.244+1279C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830073 | |||||||
| chr16:89830105 | G | C | 2 | a0001c0001t0001g0248 a0006c0023t0001g0249 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+1311G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830105 | |||||||
| chr16:89830269 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.244+1475G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830269 | |||||||
| chr16:89830416 | C | T | 4 | a0004c0005t0001g0298 a0004c0005t0001g0299 a0004c0005t0001g0300 others(1): Show |
4 | HG02602.hp1 HG03688.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1622C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830416 | |||||||
| chr16:89830426 | G | A | 34 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+1632G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830426 | |||||||
| chr16:89830503 | A | T | 6 | a0001c0003t0001g0104 a0001c0003t0001g0111 a0001c0003t0001g0198 others(3): Show |
6 | HG00280.hp1 HG02080.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+1709A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830503 | |||||||
| chr16:89830524 | T | C | 36 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(33): Show |
36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+1730T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830524 | |||||||
| chr16:89830617 | A | G | 1 | a0002c0002t0002g0259 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.244+1823A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830617 | |||||||
| chr16:89830652 | G | A | 350 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(347): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.244+1858G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830652 | |||||||
| chr16:89830741 | C | A | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
301 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.244+1947C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830741 | |||||||
| chr16:89830744 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.244+1950T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830744 | |||||||
| chr16:89830866 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(109): Show |
113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.244+2072C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830866 | |||||||
| chr16:89830908 | C | CT | 6 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 others(3): Show |
6 | HG00323.hp1 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+2133dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | ||||||
| chr16:89830908 | C | CTT | 31 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.244+2132_244+2133d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | ||||||
| chr16:89830908 | CTT | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.244+2132_244+2133d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | ||||||
| chr16:89830908 | CTTT | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0187 a0001c0001t0001g0290 others(5): Show |
8 | HG01516.hp1 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+2131_244+2133d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | ||||||
| chr16:89830948 | T | C | 34 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+2154T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830948 | |||||||
| chr16:89830949 | G | T | 34 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+2155G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830949 | |||||||
| chr16:89830967 | C | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.244+2173C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830967 | |||||||
| chr16:89830974 | A | G | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+2180A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830974 | |||||||
| chr16:89830983 | C | T | 2 | a0007c0010t0001g0313 a0007c0010t0008g0312 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+2189C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830983 | |||||||
| chr16:89830987 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0143 a0001c0001t0001g0152 others(1): Show |
4 | HG00597.hp1 NA18971.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+2193G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830987 | |||||||
| chr16:89831036 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(109): Show |
113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.244+2242A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831036 | |||||||
| chr16:89831046 | A | T | 2 | a0007c0010t0001g0313 a0007c0010t0008g0312 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+2252A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831046 | |||||||
| chr16:89831064 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.244+2270C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831064 | |||||||
| chr16:89831066 | C | A | 15 | a0001c0001t0003g0344 a0001c0006t0001g0015 a0001c0006t0001g0016 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+2272C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831066 | |||||||
| chr16:89831071 | G | A | 15 | a0001c0001t0003g0344 a0001c0006t0001g0015 a0001c0006t0001g0016 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+2277G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831071 | |||||||
| chr16:89831111 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.244+2317G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831111 | |||||||
| chr16:89831217 | T | C | 1 | a0002c0002t0002g0256 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.244+2423T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831217 | |||||||
| chr16:89831394 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0108 |
3 | NA18949.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.244+2600T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831394 | |||||||
| chr16:89831399 | C | CT | 8 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(5): Show |
8 | HG01109.hp1 HG01123.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+2621dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89831399 | ||||||
| chr16:89831399 | CT | C | 13 | a0001c0001t0001g0038 a0001c0001t0001g0201 a0001c0001t0001g0248 others(10): Show |
13 | HG00323.hp1 HG00621.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+2621delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89831399 | ||||||
| chr16:89831482 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.244+2688T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831482 | |||||||
| chr16:89831488 | A | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.244+2694A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831488 | |||||||
| chr16:89831490 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.244+2696T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831490 | |||||||
| chr16:89831498 | C | T | 1 | a0001c0003t0001g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.244+2704C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831498 | |||||||
| chr16:89831522 | C | T | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+2728C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831522 | |||||||
| chr16:89831546 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244+2752C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831546 | |||||||
| chr16:89831556 | C | A | 5 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0003g0330 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+2762C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831556 | |||||||
| chr16:89831633 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
301 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.244+2839A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831633 | |||||||
| chr16:89831644 | A | G | 3 | a0001c0001t0001g0078 a0001c0001t0001g0133 a0006c0024t0001g0153 |
3 | HG02071.hp2 HG03927.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.244+2850A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831644 | |||||||
| chr16:89831776 | C | T | 2 | a0007c0010t0001g0313 a0007c0010t0008g0312 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+2982C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831776 | |||||||
| chr16:89831783 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
289 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.244+2989T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831783 | |||||||
| chr16:89831848 | T | A | 1 | a0001c0001t0001g0127 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.244+3054T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831848 | |||||||
| chr16:89831883 | A | G | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+3089A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831883 | |||||||
| chr16:89831922 | C | T | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(24): Show |
27 | HG01081.hp1 HG01167.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.244+3128C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831922 | |||||||
| chr16:89831965 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.244+3171C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831965 | |||||||
| chr16:89831968 | G | A | 1 | a0001c0003t0001g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.244+3174G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831968 | |||||||
| chr16:89831984 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.244+3190G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831984 | |||||||
| chr16:89832059 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.244+3265C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832059 | |||||||
| chr16:89832202 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.244+3408G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832202 | |||||||
| chr16:89832203 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.244+3409T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832203 | |||||||
| chr16:89832250 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.244+3456C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832250 | |||||||
| chr16:89832252 | C | T | 34 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+3458C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832252 | |||||||
| chr16:89832342 | A | G | 2 | a0001c0001t0001g0248 a0006c0023t0001g0249 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+3548A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832342 | |||||||
| chr16:89832356 | G | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.244+3562G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832356 | |||||||
| chr16:89832374 | A | C | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+3580A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832374 | |||||||
| chr16:89832647 | T | C | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+3853T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832647 | |||||||
| chr16:89832748 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.244+3954C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832748 | |||||||
| chr16:89832808 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.244+4014G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832808 | |||||||
| chr16:89832835 | T | G | 2 | a0001c0001t0001g0026 a0003c0004t0001g0027 |
2 | HG00408.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.244+4041T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832835 | |||||||
| chr16:89832981 | C | T | 1 | a0004c0005t0001g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.244+4187C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832981 | |||||||
| chr16:89832989 | TTTC | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.244+4198_244+4200d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89832989 | ||||||
| chr16:89832990 | TTC | T | 51 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0066 others(48): Show |
51 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.244+4198_244+4199d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89832990 | ||||||
| chr16:89832991 | TC | T | 13 | a0001c0001t0001g0181 a0001c0001t0003g0344 a0001c0006t0001g0015 others(10): Show |
13 | HG01081.hp1 HG01167.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.244+4198delC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832991 | |||||||
| chr16:89832992 | C | T | 2 | a0001c0006t0001g0017 a0001c0027t0001g0021 |
2 | HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.244+4198C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832992 | |||||||
| chr16:89833007 | G | T | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
303 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.244+4213G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833007 | |||||||
| chr16:89833060 | A | G | 2 | a0007c0010t0001g0313 a0007c0010t0008g0312 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+4266A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833060 | |||||||
| chr16:89833354 | A | C | 1 | a0001c0003t0001g0198 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.244+4560A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833354 | |||||||
| chr16:89833532 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.244+4738C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833532 | |||||||
| chr16:89833627 | A | G | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.244+4833A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833627 | |||||||
| chr16:89833671 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.244+4877C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833671 | |||||||
| chr16:89833681 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.244+4887C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833681 | |||||||
| chr16:89833763 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.244+4969G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833763 | |||||||
| chr16:89833787 | G | A | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+4993G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833787 | |||||||
| chr16:89833829 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.244+5035C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833829 | |||||||
| chr16:89833893 | A | G | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5099A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833893 | |||||||
| chr16:89833974 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.244+5180G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833974 | |||||||
| chr16:89834087 | C | T | 36 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(33): Show |
36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+5293C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834087 | |||||||
| chr16:89834088 | GCTCGCGG others(587): Show |
G | 33 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(30): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+5319_244+5912d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834088 | ||||||
| chr16:89834092 | G | A | 36 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(33): Show |
36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+5298G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834092 | |||||||
| chr16:89834092 | GCGGTTGG others(125): Show |
G | 1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.244+5357_244+5488d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834092 | ||||||
| chr16:89834094 | G | A | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+5300G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834094 | |||||||
| chr16:89834129 | C | T | 9 | a0001c0001t0003g0321 a0001c0001t0003g0323 a0001c0001t0003g0324 others(6): Show |
9 | HG01192.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+5335C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834129 | |||||||
| chr16:89834157 | C | T | 1 | a0001c0001t0007g0251 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.244+5363C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834157 | |||||||
| chr16:89834179 | CTGGATAA others(59): Show |
C | 3 | a0001c0003t0001g0093 a0001c0003t0001g0110 a0001c0003t0001g0113 |
3 | NA18970.hp2 NA19054.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.244+5423_244+5488d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834179 | ||||||
| chr16:89834280 | G | C | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+5486G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834280 | |||||||
| chr16:89834301 | T | C | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+5507T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834301 | |||||||
| chr16:89834317 | A | G | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+5523A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834317 | |||||||
| chr16:89834357 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0082 |
3 | HG02027.hp1 HG02083.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.244+5563C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834357 | |||||||
| chr16:89834358 | G | A | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+5564G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834358 | |||||||
| chr16:89834366 | G | GTCGTAGA others(59): Show |
1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.244+5648_244+5713d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834366 | ||||||
| chr16:89834366 | GTCGTAGA others(59): Show |
G | 1 | a0001c0001t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.244+5648_244+5713d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834366 | ||||||
| chr16:89834368 | CGTAGAAG others(257): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.244+5638_244+5901d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834368 | ||||||
| chr16:89834400 | A | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5606A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834400 | |||||||
| chr16:89834421 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0215 |
3 | HG00642.hp2 HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.244+5627C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834421 | |||||||
| chr16:89834432 | ATCGTAGA others(257): Show |
A | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+5828_244+6091d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834432 | ||||||
| chr16:89834460 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0139 a0001c0001t0001g0144 others(2): Show |
5 | HG01071.hp1 HG02735.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+5666G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834460 | |||||||
| chr16:89834468 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.244+5674C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834468 | |||||||
| chr16:89834488 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244+5694G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834488 | |||||||
| chr16:89834527 | T | A | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5733T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834527 | |||||||
| chr16:89834551 | T | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5757T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834551 | |||||||
| chr16:89834564 | G | A | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5770G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834564 | |||||||
| chr16:89834574 | G | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5780G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834574 | |||||||
| chr16:89834575 | C | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5781C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834575 | |||||||
| chr16:89834576 | C | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5782C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834576 | |||||||
| chr16:89834577 | C | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5783C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834577 | |||||||
| chr16:89834578 | C | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5784C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834578 | |||||||
| chr16:89834578 | CATAAGCA others(59): Show |
C | 2 | a0001c0001t0001g0146 a0001c0001t0009g0145 |
2 | HG02293.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.244+5838_244+5903d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834578 | ||||||
| chr16:89834630 | G | A | 1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.244+5836G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834630 | |||||||
| chr16:89834632 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0205 a0001c0003t0001g0117 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+5838T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834632 | |||||||
| chr16:89834698 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.244+5904C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834698 | |||||||
| chr16:89834707 | C | G | 15 | a0001c0001t0001g0337 a0001c0001t0001g0341 a0001c0001t0001g0342 others(12): Show |
15 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.244+5913C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834707 | |||||||
| chr16:89834748 | A | G | 1 | a0001c0001t0001g0351 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.244+5954A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834748 | |||||||
| chr16:89834762 | A | G | 4 | a0001c0001t0001g0351 a0002c0002t0002g0280 a0002c0002t0002g0281 others(1): Show |
4 | HG00621.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+5968A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834762 | |||||||
| chr16:89834775 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.244+5981G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834775 | |||||||
| chr16:89834788 | C | A | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+5994C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834788 | |||||||
| chr16:89834790 | A | ATGTGAAT others(59): Show |
1 | a0001c0001t0001g0329 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.244+6021_244+6086d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834790 | ||||||
| chr16:89834790 | A | G | 3 | a0002c0002t0002g0280 a0002c0002t0002g0281 a0005c0014t0002g0279 |
3 | HG00621.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.244+5996A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834790 | |||||||
| chr16:89834820 | G | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.244+6026G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834820 | |||||||
| chr16:89834830 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.244+6036C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834830 | |||||||
| chr16:89834886 | A | G | 9 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
9 | HG01256.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+6092A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834886 | |||||||
| chr16:89834910 | C | T | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+6116C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834910 | |||||||
| chr16:89834952 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG01358.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.244+6158G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834952 | |||||||
| chr16:89834954 | C | T | 1 | a0001c0008t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.244+6160C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834954 | |||||||
| chr16:89834988 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+6194G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834988 | |||||||
| chr16:89835016 | GCGGTTGG others(125): Show |
G | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+6281_244+6412d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89835016 | ||||||
| chr16:89835039 | GGATAAGC others(59): Show |
G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0319 others(1): Show |
4 | HG02965.hp1 HG03516.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+6288_244+6353d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89835039 | ||||||
| chr16:89835105 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.244+6311A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835105 | |||||||
| chr16:89835175 | AAGCATAG others(70): Show |
A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0181 others(6): Show |
11 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.244+6382_244+6458d others(79): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835175 | |||||||
| chr16:89835210 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.244+6416G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835210 | |||||||
| chr16:89835264 | G | C | 1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244+6470G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835264 | |||||||
| chr16:89835350 | C | T | 14 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(11): Show |
14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+6556C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835350 | |||||||
| chr16:89835359 | G | A | 33 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+6565G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835359 | |||||||
| chr16:89835374 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.244+6580C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835374 | |||||||
| chr16:89835821 | T | G | 1 | a0001c0001t0001g0035 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.244+7027T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835821 | |||||||
| chr16:89835828 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244+7034G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835828 | |||||||
| chr16:89836074 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
305 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.244+7280T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836074 | |||||||
| chr16:89836132 | G | A | 2 | a0007c0010t0001g0313 a0007c0010t0008g0312 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+7338G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836132 | |||||||
| chr16:89836233 | C | G | 2 | a0001c0011t0001g0317 a0001c0011t0001g0318 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.244+7439C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836233 | |||||||
| chr16:89836274 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.244+7480A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836274 | |||||||
| chr16:89836346 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.244+7552G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836346 | |||||||
| chr16:89836358 | A | C | 20 | a0001c0001t0001g0203 a0001c0001t0001g0341 a0001c0001t0001g0342 others(17): Show |
20 | HG01081.hp1 HG01167.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.244+7564A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836358 | |||||||
| chr16:89836430 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.244+7636C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836430 | |||||||
| chr16:89836456 | A | G | 1 | a0001c0003t0001g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.244+7662A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836456 | |||||||
| chr16:89836576 | C | T | 1 | a0001c0001t0003g0339 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244+7782C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836576 | |||||||
| chr16:89836777 | C | G | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+7983C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836777 | |||||||
| chr16:89836818 | G | GA | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0031 others(59): Show |
63 | HG00408.hp1 HG00408.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.244+8038dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89836818 | ||||||
| chr16:89836833 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.244+8039G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836833 | |||||||
| chr16:89836834 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.244+8040A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836834 | |||||||
| chr16:89836885 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.244+8091C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836885 | |||||||
| chr16:89836927 | G | A | 1 | a0003c0004t0001g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.244+8133G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836927 | |||||||
| chr16:89837008 | A | C | 32 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+8214A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837008 | |||||||
| chr16:89837094 | G | A | 10 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0003g0330 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-8228G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837094 | |||||||
| chr16:89837143 | C | T | 8 | a0001c0001t0001g0187 a0001c0006t0001g0015 a0001c0006t0001g0016 others(5): Show |
8 | HG02895.hp2 HG03239.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-8179C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837143 | |||||||
| chr16:89837144 | G | A | 37 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0087 others(34): Show |
37 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.245-8178G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837144 | |||||||
| chr16:89837213 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.245-8109C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837213 | |||||||
| chr16:89837247 | C | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-8075C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837247 | |||||||
| chr16:89837272 | C | T | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-8050C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837272 | |||||||
| chr16:89837320 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-8002C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837320 | |||||||
| chr16:89837415 | A | T | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.245-7907A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837415 | |||||||
| chr16:89837435 | G | A | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-7887G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837435 | |||||||
| chr16:89837582 | G | T | 2 | a0001c0011t0001g0317 a0001c0011t0001g0318 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.245-7740G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837582 | |||||||
| chr16:89837781 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-7541C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837781 | |||||||
| chr16:89837787 | A | G | 20 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(17): Show |
20 | HG01891.hp2 HG02145.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-7535A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837787 | |||||||
| chr16:89837799 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.245-7523G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837799 | |||||||
| chr16:89837889 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.245-7433C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837889 | |||||||
| chr16:89837894 | G | A | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-7428G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837894 | |||||||
| chr16:89837976 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.245-7346G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837976 | |||||||
| chr16:89838003 | T | G | 14 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(11): Show |
14 | HG01891.hp2 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.245-7319T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838003 | |||||||
| chr16:89838004 | CTTTT | C | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-7314_245-7311d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838004 | ||||||
| chr16:89838015 | T | C | 15 | a0001c0001t0003g0344 a0001c0006t0001g0015 a0001c0006t0001g0016 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-7307T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838015 | |||||||
| chr16:89838018 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
300 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.245-7304A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838018 | |||||||
| chr16:89838018 | A | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0345 a0006c0023t0001g0249 |
3 | HG01071.hp1 HG02300.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.245-7304A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838018 | |||||||
| chr16:89838094 | G | A | 2 | a0001c0011t0001g0317 a0001c0011t0001g0318 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.245-7228G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838094 | |||||||
| chr16:89838121 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.245-7201T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838121 | |||||||
| chr16:89838164 | A | AT | 8 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0204 others(5): Show |
8 | HG00140.hp1 HG00733.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-7134dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | ||||||
| chr16:89838164 | AT | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.245-7134delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | ||||||
| chr16:89838164 | ATT | A | 46 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0088 others(43): Show |
46 | HG00323.hp2 HG00733.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.245-7135_245-7134d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | ||||||
| chr16:89838164 | ATTT | A | 11 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0003g0330 others(8): Show |
11 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.245-7136_245-7134d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | ||||||
| chr16:89838271 | C | G | 13 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(10): Show |
13 | HG01891.hp2 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.245-7051C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838271 | |||||||
| chr16:89838426 | G | C | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-6896G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838426 | |||||||
| chr16:89838553 | G | A | 1 | a0003c0004t0001g0042 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.245-6769G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838553 | |||||||
| chr16:89838563 | G | A | 10 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(7): Show |
10 | HG00099.hp1 HG00735.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-6759G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838563 | |||||||
| chr16:89838707 | C | G | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-6615C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838707 | |||||||
| chr16:89838787 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-6535G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838787 | |||||||
| chr16:89838855 | G | A | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.245-6467G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838855 | |||||||
| chr16:89838928 | C | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG02451.hp2 HG02738.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-6394C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838928 | |||||||
| chr16:89839020 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.245-6302T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839020 | |||||||
| chr16:89839079 | C | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0283 |
2 | NA18982.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.245-6243C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839079 | |||||||
| chr16:89839113 | G | A | 14 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(11): Show |
14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-6209G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839113 | |||||||
| chr16:89839121 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
315 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.245-6201C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839121 | |||||||
| chr16:89839253 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-6069A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839253 | |||||||
| chr16:89839373 | C | CA | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.245-5933dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89839373 | ||||||
| chr16:89839373 | C | CAA | 38 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00438.hp1 HG00609.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.245-5934_245-5933d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89839373 | ||||||
| chr16:89839440 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.245-5882T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839440 | |||||||
| chr16:89839449 | T | A | 14 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(11): Show |
14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-5873T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839449 | |||||||
| chr16:89839451 | G | A | 2 | a0007c0010t0001g0313 a0007c0010t0008g0312 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.245-5871G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839451 | |||||||
| chr16:89839460 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.245-5862C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839460 | |||||||
| chr16:89839472 | G | C | 8 | a0001c0001t0001g0028 a0001c0001t0001g0207 a0001c0001t0001g0212 others(5): Show |
8 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-5850G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839472 | |||||||
| chr16:89839480 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG01884.hp2 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.245-5842C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839480 | |||||||
| chr16:89839517 | G | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
316 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.245-5805G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839517 | |||||||
| chr16:89839518 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.245-5804G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839518 | |||||||
| chr16:89839619 | C | T | 23 | a0001c0001t0001g0337 a0001c0001t0001g0341 a0001c0001t0001g0342 others(20): Show |
23 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.245-5703C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839619 | |||||||
| chr16:89839647 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.245-5675C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839647 | |||||||
| chr16:89839654 | C | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-5668C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839654 | |||||||
| chr16:89839691 | T | A | 1 | a0001c0003t0001g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.245-5631T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839691 | |||||||
| chr16:89839762 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.245-5560G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839762 | |||||||
| chr16:89839766 | C | T | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.245-5556C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839766 | |||||||
| chr16:89839795 | C | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-5527C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839795 | |||||||
| chr16:89839912 | CTG | C | 34 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.245-5402_245-5401d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89839912 | ||||||
| chr16:89839956 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.245-5366G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839956 | |||||||
| chr16:89840001 | T | A | 1 | a0001c0003t0013g0095 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.245-5321T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840001 | |||||||
| chr16:89840053 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.245-5269T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840053 | |||||||
| chr16:89840092 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0177 |
2 | NA18951.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.245-5230G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840092 | |||||||
| chr16:89840096 | C | A | 1 | a0002c0002t0002g0256 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.245-5226C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840096 | |||||||
| chr16:89840155 | G | A | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-5167G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840155 | |||||||
| chr16:89840159 | G | C | 1 | a0001c0001t0003g0339 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-5163G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840159 | |||||||
| chr16:89840245 | C | CT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0047 others(32): Show |
35 | HG01106.hp1 HG01106.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.245-5055dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840245 | ||||||
| chr16:89840280 | C | T | 9 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG00099.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.245-5042C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840280 | |||||||
| chr16:89840312 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-5010C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840312 | |||||||
| chr16:89840319 | G | A | 12 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(9): Show |
12 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.245-5003G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840319 | |||||||
| chr16:89840392 | G | A | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4930G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840392 | |||||||
| chr16:89840399 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.245-4923G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840399 | |||||||
| chr16:89840425 | ATTTTTAG others(381): Show |
A | 1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.245-4854_245-4467d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840425 | ||||||
| chr16:89840433 | T | C | 1 | a0001c0001t0007g0251 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.245-4889T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840433 | |||||||
| chr16:89840439 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.245-4883C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840439 | |||||||
| chr16:89840456 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02965.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.245-4866A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840456 | |||||||
| chr16:89840468 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0097 a0001c0001t0001g0236 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-4854T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840468 | |||||||
| chr16:89840484 | T | C | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-4838T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840484 | |||||||
| chr16:89840486 | G | T | 144 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.245-4836G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840486 | |||||||
| chr16:89840490 | C | T | 1 | a0001c0001t0003g0335 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-4832C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840490 | |||||||
| chr16:89840523 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-4799C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840523 | |||||||
| chr16:89840528 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-4794A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840528 | |||||||
| chr16:89840529 | T | A | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4793T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840529 | |||||||
| chr16:89840594 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.245-4728C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840594 | |||||||
| chr16:89840599 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.245-4723G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840599 | |||||||
| chr16:89840636 | AT | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.245-4667delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840636 | ||||||
| chr16:89840636 | ATT | A | 10 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0157 others(7): Show |
10 | HG01167.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-4668_245-4667d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840636 | ||||||
| chr16:89840638 | T | A | 1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.245-4684T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840638 | |||||||
| chr16:89840646 | T | G | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.245-4676T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840646 | |||||||
| chr16:89840660 | T | C | 1 | a0012c0013t0002g0263 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.245-4662T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840660 | |||||||
| chr16:89840674 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-4648C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840674 | |||||||
| chr16:89840721 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.245-4601C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840721 | |||||||
| chr16:89840756 | C | T | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4566C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840756 | |||||||
| chr16:89840785 | G | A | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-4537G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840785 | |||||||
| chr16:89840797 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.245-4525A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840797 | |||||||
| chr16:89840839 | G | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-4483G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840839 | |||||||
| chr16:89840935 | C | G | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.245-4387C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840935 | |||||||
| chr16:89841048 | G | C | 1 | a0001c0008t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.245-4274G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841048 | |||||||
| chr16:89841085 | G | T | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4237G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841085 | |||||||
| chr16:89841112 | A | T | 1 | a0001c0027t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.245-4210A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841112 | |||||||
| chr16:89841118 | T | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
271 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.245-4204T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841118 | |||||||
| chr16:89841120 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.245-4202G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841120 | |||||||
| chr16:89841183 | C | CA | 9 | a0001c0001t0001g0096 a0001c0001t0001g0148 a0001c0001t0001g0159 others(6): Show |
9 | HG01175.hp2 HG01891.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-4124dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89841183 | ||||||
| chr16:89841273 | C | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0144 a0001c0001t0001g0210 |
3 | HG03942.hp1 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.245-4049C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841273 | |||||||
| chr16:89841408 | A | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG02717.hp2 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.245-3914A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841408 | |||||||
| chr16:89841481 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.245-3841C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841481 | |||||||
| chr16:89841539 | G | A | 30 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(27): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.245-3783G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841539 | |||||||
| chr16:89841595 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
206 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.245-3727G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841595 | |||||||
| chr16:89841677 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.245-3645C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841677 | |||||||
| chr16:89841701 | A | AT | 16 | a0001c0001t0001g0047 a0001c0001t0001g0092 a0001c0001t0001g0139 others(13): Show |
16 | HG00099.hp2 HG00733.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.245-3608dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89841701 | ||||||
| chr16:89841842 | C | T | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-3480C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841842 | |||||||
| chr16:89842026 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.245-3296C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842026 | |||||||
| chr16:89842145 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.245-3177C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842145 | |||||||
| chr16:89842182 | A | C | 4 | a0001c0003t0001g0089 a0001c0003t0001g0137 a0001c0003t0001g0138 others(1): Show |
4 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-3140A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842182 | |||||||
| chr16:89842205 | G | T | 1 | a0001c0001t0001g0320 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245-3117G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842205 | |||||||
| chr16:89842208 | A | AT | 38 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(35): Show |
38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.245-3092dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-3101_245-3092d others(12): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(5): Show |
15 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0097 others(12): Show |
15 | HG00673.hp1 HG01192.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-3103_245-3092d others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(6): Show |
28 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0086 others(25): Show |
28 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.245-3104_245-3092d others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(7): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0029 others(43): Show |
48 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.245-3105_245-3092d others(16): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(8): Show |
64 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(61): Show |
65 | HG00438.hp1 HG00609.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.245-3106_245-3092d others(17): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(9): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(38): Show |
41 | HG00408.hp1 HG00673.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.245-3107_245-3092d others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(10): Show |
4 | a0001c0001t0004g0076 a0001c0003t0001g0089 a0001c0003t0001g0138 others(1): Show |
4 | HG01928.hp2 HG01952.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-3108_245-3092d others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | HG03579.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.245-3109_245-3092d others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0136 a0001c0001t0004g0083 |
2 | HG01993.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.245-3110_245-3092d others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842208 | AT | A | 10 | a0001c0001t0001g0347 a0001c0006t0001g0015 a0001c0006t0001g0016 others(7): Show |
10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-3092delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | ||||||
| chr16:89842229 | T | TTTTTTTT others(2): Show |
18 | a0001c0001t0001g0342 a0001c0001t0003g0321 a0001c0001t0003g0322 others(15): Show |
18 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.245-3092_245-3091i others(11): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842229 | ||||||
| chr16:89842236 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
231 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.245-3086G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842236 | |||||||
| chr16:89842258 | G | C | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-3064G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842258 | |||||||
| chr16:89842598 | A | G | 2 | a0003c0004t0001g0046 a0003c0004t0001g0075 |
2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.245-2724A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842598 | |||||||
| chr16:89842615 | T | C | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-2707T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842615 | |||||||
| chr16:89842631 | TGTGGG | T | 4 | a0001c0008t0001g0011 a0001c0008t0001g0012 a0001c0008t0001g0013 others(1): Show |
4 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-2690_245-2686d others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842631 | |||||||
| chr16:89842636 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0205 a0001c0001t0001g0236 |
3 | HG02559.hp2 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.245-2686G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842636 | |||||||
| chr16:89842780 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.245-2542G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842780 | |||||||
| chr16:89842845 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-2477C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842845 | |||||||
| chr16:89842875 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.245-2447G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842875 | |||||||
| chr16:89842963 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2359T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842963 | |||||||
| chr16:89842993 | T | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.245-2329T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842993 | |||||||
| chr16:89843021 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(44): Show |
48 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.245-2301A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843021 | |||||||
| chr16:89843068 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-2254C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843068 | |||||||
| chr16:89843111 | G | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-2211G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843111 | |||||||
| chr16:89843238 | C | A | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.245-2084C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843238 | |||||||
| chr16:89843261 | T | C | 9 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(6): Show |
9 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-2061T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843261 | |||||||
| chr16:89843294 | ACGGGAAG others(5): Show |
A | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2026_245-2015d others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843294 | ||||||
| chr16:89843302 | T | C | 1 | a0003c0004t0001g0081 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.245-2020T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843302 | |||||||
| chr16:89843308 | A | C | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2014A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843308 | |||||||
| chr16:89843311 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2011C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843311 | |||||||
| chr16:89843314 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2008C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843314 | |||||||
| chr16:89843317 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2005C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843317 | |||||||
| chr16:89843318 | A | C | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2004A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843318 | |||||||
| chr16:89843320 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2002C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843320 | |||||||
| chr16:89843329 | C | T | 32 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-1993C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843329 | |||||||
| chr16:89843419 | C | T | 2 | a0001c0001t0004g0071 a0001c0001t0004g0083 |
2 | NA18995.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.245-1903C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843419 | |||||||
| chr16:89843533 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.245-1789G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843533 | |||||||
| chr16:89843644 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.245-1678T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843644 | |||||||
| chr16:89843660 | C | A | 32 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-1662C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843660 | |||||||
| chr16:89843669 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.245-1644_245-1643i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843669 | ||||||
| chr16:89843673 | TTTTTTTT others(5): Show |
T | 6 | a0001c0006t0001g0015 a0001c0006t0001g0017 a0001c0006t0001g0018 others(3): Show |
6 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-1643_245-1632d others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843673 | ||||||
| chr16:89843674 | TTTTTTTG others(4): Show |
T | 1 | a0001c0001t0003g0331 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.245-1642_245-1632d others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843674 | ||||||
| chr16:89843675 | TTTTTTG | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.245-1643_245-1638d others(8): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843675 | ||||||
| chr16:89843676 | TTTTTG | T | 20 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-1642_245-1638d others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843676 | ||||||
| chr16:89843677 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0205 a0001c0001t0001g0228 others(1): Show |
4 | HG01978.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1645T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843677 | |||||||
| chr16:89843677 | TTTTG | T | 15 | a0002c0002t0002g0252 a0002c0002t0002g0253 a0002c0002t0002g0256 others(12): Show |
15 | HG00609.hp1 HG00621.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.245-1637_245-1634d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843677 | ||||||
| chr16:89843678 | TTTG | T | 7 | a0002c0002t0002g0250 a0002c0002t0002g0254 a0002c0002t0002g0264 others(4): Show |
7 | HG00438.hp2 HG00597.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-1641_245-1639d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843678 | ||||||
| chr16:89843679 | T | G | 3 | a0001c0006t0001g0016 a0001c0006t0001g0019 a0001c0009t0001g0014 |
3 | HG04115.hp1 NA18939.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.245-1643T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843679 | |||||||
| chr16:89843680 | T | G | 1 | a0001c0001t0001g0294 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.245-1642T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843680 | |||||||
| chr16:89843680 | TGTTTG | T | 4 | a0002c0002t0002g0259 a0002c0002t0002g0266 a0002c0002t0002g0280 others(1): Show |
4 | HG02165.hp1 HG03491.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-1641_245-1637d others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843680 | |||||||
| chr16:89843680 | TGTTTGTT others(4): Show |
T | 1 | a0001c0009t0001g0014 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.245-1641_245-1631d others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843680 | |||||||
| chr16:89843681 | G | T | 6 | a0001c0001t0001g0048 a0001c0006t0001g0019 a0001c0019t0001g0316 others(3): Show |
6 | HG02080.hp1 HG03139.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-1641G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843681 | |||||||
| chr16:89843682 | T | G | 2 | a0001c0001t0001g0146 a0001c0003t0001g0089 |
2 | HG01928.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.245-1640T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843682 | |||||||
| chr16:89843685 | G | T | 30 | a0001c0006t0001g0016 a0001c0006t0001g0019 a0001c0019t0001g0316 others(27): Show |
30 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.245-1637G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843685 | |||||||
| chr16:89843686 | T | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.245-1636T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843686 | |||||||
| chr16:89843687 | TTTTG | T | 10 | a0001c0001t0001g0039 a0001c0001t0001g0098 a0001c0001t0001g0134 others(7): Show |
10 | HG00099.hp2 HG01167.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-1631_245-1628d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843687 | ||||||
| chr16:89843688 | TTTG | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(160): Show |
164 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.245-1631_245-1629d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843688 | ||||||
| chr16:89843689 | TTG | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.245-1631_245-1630d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843689 | ||||||
| chr16:89843690 | T | TTTTTTTT others(281): Show |
1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-1632_245-1631i others(290): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843690 | |||||||
| chr16:89843690 | T | TTTTTTTT others(283): Show |
1 | a0001c0006t0001g0019 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.245-1632_245-1631i others(292): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843690 | |||||||
| chr16:89843690 | TG | T | 4 | a0001c0001t0001g0029 a0001c0003t0001g0093 a0001c0003t0001g0198 others(1): Show |
4 | HG02080.hp2 HG02647.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1631delG | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843690 | |||||||
| chr16:89843691 | G | C | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-1631G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843691 | |||||||
| chr16:89843691 | G | T | 34 | a0001c0001t0001g0146 a0001c0003t0001g0089 a0002c0002t0002g0250 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.245-1631G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843691 | |||||||
| chr16:89843692 | T | C | 1 | a0001c0006t0001g0019 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.245-1630T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843692 | |||||||
| chr16:89843692 | T | TTTTTTTT others(285): Show |
1 | a0001c0006t0001g0016 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.245-1625_245-1624i others(294): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843692 | ||||||
| chr16:89843693 | T | TGAGACAG others(272): Show |
1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-1629_245-1628i others(281): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843693 | |||||||
| chr16:89843697 | TG | T | 4 | a0001c0006t0001g0015 a0001c0006t0001g0017 a0001c0006t0001g0018 others(1): Show |
4 | HG03239.hp2 HG03831.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1624delG | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843697 | |||||||
| chr16:89843698 | G | GAGACAGA others(279): Show |
1 | a0001c0001t0001g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.245-1624_245-1623i others(288): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843698 | |||||||
| chr16:89843698 | G | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.245-1624G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843698 | |||||||
| chr16:89843698 | GTTT | G | 20 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-1607_245-1605d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843698 | ||||||
| chr16:89843701 | T | G | 1 | a0001c0001t0003g0335 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-1621T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843701 | |||||||
| chr16:89843705 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.245-1617T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843705 | |||||||
| chr16:89843724 | GA | G | 5 | a0001c0001t0001g0048 a0001c0006t0001g0016 a0001c0006t0001g0019 others(2): Show |
5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1597delA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843724 | |||||||
| chr16:89843732 | C | T | 5 | a0001c0001t0001g0048 a0001c0006t0001g0016 a0001c0006t0001g0019 others(2): Show |
5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1590C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843732 | |||||||
| chr16:89843734 | T | C | 2 | a0001c0001t0001g0048 a0001c0019t0001g0316 |
2 | HG03139.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.245-1588T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843734 | |||||||
| chr16:89843742 | C | A | 5 | a0001c0001t0001g0048 a0001c0006t0001g0016 a0001c0006t0001g0019 others(2): Show |
5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1580C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843742 | |||||||
| chr16:89843750 | A | C | 5 | a0001c0001t0001g0048 a0001c0006t0001g0016 a0001c0006t0001g0019 others(2): Show |
5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1572A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843750 | |||||||
| chr16:89843752 | T | C | 5 | a0001c0001t0001g0048 a0001c0006t0001g0016 a0001c0006t0001g0019 others(2): Show |
5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1570T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843752 | |||||||
| chr16:89843758 | G | T | 5 | a0001c0001t0001g0048 a0001c0006t0001g0016 a0001c0006t0001g0019 others(2): Show |
5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1564G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843758 | |||||||
| chr16:89843760 | C | CATGATCT others(296): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.245-1562_245-1561i others(305): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843760 | |||||||
| chr16:89843760 | C | CGTGATCT others(612): Show |
1 | a0001c0001t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(621): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(298): Show |
1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(307): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(289): Show |
1 | a0001c0001t0001g0347 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(298): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(297): Show |
22 | a0001c0001t0001g0038 a0001c0001t0001g0057 a0001c0001t0001g0086 others(19): Show |
22 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(306): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(299): Show |
32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(29): Show |
32 | HG00323.hp2 HG00733.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(308): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(300): Show |
2 | a0001c0001t0001g0345 a0001c0012t0005g0051 |
2 | HG02300.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(309): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(301): Show |
1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(310): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(294): Show |
2 | a0001c0001t0001g0342 a0001c0001t0003g0343 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(303): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(295): Show |
11 | a0001c0001t0001g0217 a0001c0001t0003g0322 a0001c0001t0003g0323 others(8): Show |
11 | HG00099.hp2 HG01192.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(304): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(295): Show |
1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(304): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(296): Show |
34 | a0001c0001t0003g0321 a0001c0001t0003g0326 a0001c0001t0003g0327 others(31): Show |
34 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(305): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(296): Show |
6 | a0001c0006t0001g0017 a0001c0006t0001g0018 a0001c0009t0001g0009 others(3): Show |
6 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(305): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(297): Show |
5 | a0001c0001t0003g0336 a0002c0002t0002g0274 a0002c0002t0002g0278 others(2): Show |
5 | HG00438.hp2 HG02040.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(306): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(298): Show |
1 | a0001c0001t0003g0338 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(307): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(639): Show |
1 | a0001c0001t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(648): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(638): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0237 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(647): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(635): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0239 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(644): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(636): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0240 |
2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(645): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(634): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0241 |
2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(643): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(635): Show |
1 | a0001c0001t0001g0238 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(644): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(632): Show |
1 | a0001c0001t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(641): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(630): Show |
1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(639): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(629): Show |
1 | a0001c0008t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(638): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(628): Show |
1 | a0001c0001t0001g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(637): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(626): Show |
4 | a0001c0008t0001g0012 a0001c0008t0001g0022 a0001c0011t0001g0317 others(1): Show |
4 | HG01167.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(635): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(639): Show |
1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(648): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(616): Show |
1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(625): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(613): Show |
1 | a0001c0001t0001g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(622): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(611): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0242 |
2 | HG00140.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(620): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(612): Show |
20 | a0001c0001t0001g0028 a0001c0001t0001g0203 a0001c0001t0001g0207 others(17): Show |
20 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(621): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(613): Show |
4 | a0001c0001t0001g0206 a0001c0001t0001g0232 a0001c0001t0001g0245 others(1): Show |
4 | HG00741.hp2 HG01175.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(622): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | CGTGATCT others(612): Show |
5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(621): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | ||||||
| chr16:89843760 | C | T | 5 | a0001c0001t0001g0048 a0001c0006t0001g0016 a0001c0006t0001g0019 others(2): Show |
5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1562C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843760 | |||||||
| chr16:89843818 | G | A | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-1504G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843818 | |||||||
| chr16:89843822 | C | G | 32 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-1500C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843822 | |||||||
| chr16:89843842 | T | G | 36 | a0001c0001t0002g0282 a0001c0001t0007g0251 a0001c0019t0001g0316 others(33): Show |
36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.245-1480T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843842 | |||||||
| chr16:89843948 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245-1374G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843948 | |||||||
| chr16:89844000 | C | CT | 6 | a0001c0001t0001g0044 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03041.hp2 HG03225.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-1309dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89844000 | ||||||
| chr16:89844027 | ACT | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0133 a0006c0024t0001g0153 |
3 | HG02071.hp2 HG03927.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.245-1292_245-1291d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89844027 | ||||||
| chr16:89844073 | G | A | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1249G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844073 | |||||||
| chr16:89844080 | C | A | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1242C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844080 | |||||||
| chr16:89844081 | A | G | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1241A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844081 | |||||||
| chr16:89844083 | C | T | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1239C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844083 | |||||||
| chr16:89844085 | T | G | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1237T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844085 | |||||||
| chr16:89844087 | C | G | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1235C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844087 | |||||||
| chr16:89844090 | G | T | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1232G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844090 | |||||||
| chr16:89844128 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.245-1194C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844128 | |||||||
| chr16:89844155 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.245-1167T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844155 | |||||||
| chr16:89844280 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.245-1042C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844280 | |||||||
| chr16:89844309 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.245-1013C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844309 | |||||||
| chr16:89844425 | C | T | 28 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(25): Show |
28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.245-897C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844425 | |||||||
| chr16:89844429 | G | T | 1 | a0001c0001t0003g0335 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-893G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844429 | |||||||
| chr16:89844432 | T | A | 1 | a0004c0005t0001g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.245-890T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844432 | |||||||
| chr16:89844473 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.245-849C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844473 | |||||||
| chr16:89844532 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.245-790G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844532 | |||||||
| chr16:89844539 | C | T | 23 | a0001c0001t0001g0217 a0001c0001t0001g0337 a0001c0001t0001g0342 others(20): Show |
23 | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-783C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844539 | |||||||
| chr16:89844692 | C | T | 1 | a0001c0003t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.245-630C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844692 | |||||||
| chr16:89844718 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.245-604G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844718 | |||||||
| chr16:89844764 | G | T | 3 | a0001c0008t0001g0011 a0001c0008t0001g0012 a0001c0008t0001g0022 |
3 | HG01167.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.245-558G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844764 | |||||||
| chr16:89844832 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.245-490C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844832 | |||||||
| chr16:89844840 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.245-482C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844840 | |||||||
| chr16:89845103 | G | A | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG02257.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245-219G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845103 | |||||||
| chr16:89845217 | A | G | 1 | a0001c0003t0001g0113 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.245-105A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845217 | |||||||
| chr16:89845220 | G | T | 1 | a0011c0026t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.245-102G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845220 | |||||||
| chr16:89845273 | G | C | 28 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(25): Show |
28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.245-49G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845273 | |||||||
| chr16:89845446 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.288+81T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845446 | |||||||
| chr16:89845592 | C | T | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.288+227C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845592 | |||||||
| chr16:89845640 | G | A | 13 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0004c0005t0001g0298 others(10): Show |
13 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.288+275G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845640 | |||||||
| chr16:89845655 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
232 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.288+290T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845655 | |||||||
| chr16:89845873 | G | C | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.288+508G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845873 | |||||||
| chr16:89845918 | A | G | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.288+553A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845918 | |||||||
| chr16:89845991 | G | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
206 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.288+626G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845991 | |||||||
| chr16:89846047 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.288+682C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846047 | |||||||
| chr16:89846049 | A | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
229 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.288+684A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846049 | |||||||
| chr16:89846054 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
226 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.288+689G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846054 | |||||||
| chr16:89846057 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288+692C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846057 | |||||||
| chr16:89846058 | G | A | 10 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(7): Show |
10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+693G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846058 | |||||||
| chr16:89846099 | G | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.288+734G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846099 | |||||||
| chr16:89846312 | C | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.288+947C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846312 | |||||||
| chr16:89846328 | C | CT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.288+974dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846328 | ||||||
| chr16:89846416 | C | T | 2 | a0001c0001t0003g0339 a0001c0001t0003g0344 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.288+1051C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846416 | |||||||
| chr16:89846429 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.288+1064G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846429 | |||||||
| chr16:89846499 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+1134C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846499 | |||||||
| chr16:89846517 | GT | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.288+1161delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846517 | ||||||
| chr16:89846600 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(105): Show |
109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.288+1235G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846600 | |||||||
| chr16:89846756 | C | T | 41 | a0001c0001t0004g0071 a0001c0001t0004g0083 a0001c0001t0004g0115 others(38): Show |
41 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.288+1391C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846756 | |||||||
| chr16:89846810 | C | CT | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.288+1462dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846810 | ||||||
| chr16:89846871 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.288+1506C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846871 | |||||||
| chr16:89846880 | C | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.288+1515C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846880 | |||||||
| chr16:89846930 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.288+1565G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846930 | |||||||
| chr16:89846964 | C | T | 1 | a0001c0003t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.288+1599C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846964 | |||||||
| chr16:89846973 | GATTA | G | 10 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(7): Show |
10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+1612_288+1615d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846973 | ||||||
| chr16:89847023 | C | T | 2 | a0001c0006t0001g0018 a0001c0006t0001g0019 |
2 | NA18939.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.288+1658C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847023 | |||||||
| chr16:89847252 | C | G | 1 | a0001c0001t0001g0039 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.288+1887C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847252 | |||||||
| chr16:89847318 | G | A | 10 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(7): Show |
10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+1953G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847318 | |||||||
| chr16:89847327 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.288+1962C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847327 | |||||||
| chr16:89847385 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.288+2020C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847385 | |||||||
| chr16:89847392 | C | G | 1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.288+2027C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847392 | |||||||
| chr16:89847402 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.288+2037G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847402 | |||||||
| chr16:89847408 | G | A | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.288+2043G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847408 | |||||||
| chr16:89847466 | A | T | 10 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(7): Show |
10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+2101A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847466 | |||||||
| chr16:89847588 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.288+2223A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847588 | |||||||
| chr16:89847839 | T | G | 2 | a0001c0001t0001g0337 a0001c0001t0003g0322 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.289-2465T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847839 | |||||||
| chr16:89847886 | C | T | 1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.289-2418C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847886 | |||||||
| chr16:89847943 | G | A | 2 | a0001c0001t0003g0339 a0001c0001t0003g0344 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.289-2361G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847943 | |||||||
| chr16:89848013 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-2291G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848013 | |||||||
| chr16:89848017 | C | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.289-2287C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848017 | |||||||
| chr16:89848059 | G | A | 1 | a0001c0001t0004g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.289-2245G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848059 | |||||||
| chr16:89848085 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289-2219C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848085 | |||||||
| chr16:89848100 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.289-2204C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848100 | |||||||
| chr16:89848186 | G | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02738.hp1 HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.289-2118G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848186 | |||||||
| chr16:89848225 | T | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.289-2079T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848225 | |||||||
| chr16:89848397 | A | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.289-1907A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848397 | |||||||
| chr16:89848438 | TGGCGTTT others(37): Show |
T | 3 | a0001c0001t0001g0216 a0001c0011t0001g0317 a0001c0011t0001g0318 |
3 | HG01081.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.289-1822_289-1779d others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848438 | ||||||
| chr16:89848486 | GTTTCTGC others(81): Show |
G | 31 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(28): Show |
31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.289-1778_289-1691d others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848486 | ||||||
| chr16:89848526 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.289-1778T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848526 | |||||||
| chr16:89848545 | A | T | 1 | a0001c0003t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.289-1759A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848545 | |||||||
| chr16:89848571 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.289-1733A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848571 | |||||||
| chr16:89848634 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0108 |
3 | NA18949.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.289-1670T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848634 | |||||||
| chr16:89848659 | G | A | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.289-1645G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848659 | |||||||
| chr16:89848738 | GCCTTCTG others(37): Show |
G | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.289-1522_289-1479d others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848738 | ||||||
| chr16:89848781 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.289-1523G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848781 | |||||||
| chr16:89848822 | C | T | 1 | a0003c0004t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.289-1482C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848822 | |||||||
| chr16:89848835 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.289-1469G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848835 | |||||||
| chr16:89848878 | CGGCGTTT others(125): Show |
C | 32 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.289-1406_289-1275d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848878 | ||||||
| chr16:89848906 | G | GTTCCAGG others(301): Show |
1 | a0004c0005t0001g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.289-1380_289-1379i others(310): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848906 | ||||||
| chr16:89848906 | G | GTTCCAGG others(301): Show |
1 | a0004c0005t0001g0305 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.289-1363_289-1362i others(310): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848906 | ||||||
| chr16:89848906 | G | GTTCCAGG others(37): Show |
27 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(24): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.289-1363_289-1362i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848906 | ||||||
| chr16:89848942 | C | T | 2 | a0003c0004t0001g0040 a0003c0004t0001g0041 |
2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.289-1362C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848942 | |||||||
| chr16:89848947 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289-1357C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848947 | |||||||
| chr16:89849010 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.289-1294T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849010 | |||||||
| chr16:89849088 | G | A | 1 | a0003c0004t0001g0081 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.289-1216G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849088 | |||||||
| chr16:89849158 | A | G | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289-1146A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849158 | |||||||
| chr16:89849408 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.289-896G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849408 | |||||||
| chr16:89849424 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.289-880G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849424 | |||||||
| chr16:89849429 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.289-875A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849429 | |||||||
| chr16:89849786 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.289-518G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849786 | |||||||
| chr16:89849828 | G | A | 29 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(26): Show |
29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.289-476G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849828 | |||||||
| chr16:89849844 | C | CT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0019t0001g0316 others(32): Show |
36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.289-449dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89849844 | ||||||
| chr16:89849844 | CT | C | 7 | a0001c0001t0001g0171 a0001c0001t0001g0194 a0001c0001t0001g0208 others(4): Show |
7 | HG00741.hp2 HG01256.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-449delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89849844 | ||||||
| chr16:89849873 | TG | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0090 a0001c0001t0001g0123 others(3): Show |
6 | HG01993.hp2 HG02148.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-430delG | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849873 | |||||||
| chr16:89849983 | G | A | 136 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0039 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.289-321G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849983 | |||||||
| chr16:89850192 | C | A | 32 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.289-112C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89850192 | |||||||
| chr16:89850276 | G | A | 2 | a0002c0002t0002g0280 a0002c0002t0002g0281 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.289-28G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89850276 | |||||||
| chr16:89850300 | G | A | 1 | a0001c0001t0003g0332 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.289-4G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89850300 | |||||||
| chr16:89850722 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.645+62G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850722 | |||||||
| chr16:89850749 | C | T | 1 | a0001c0008t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.645+89C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850749 | |||||||
| chr16:89850824 | G | GTT | 28 | a0002c0002t0002g0252 a0002c0002t0002g0253 a0002c0002t0002g0254 others(25): Show |
28 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.645+165_645+166dup others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89850824 | ||||||
| chr16:89850824 | G | GTTT | 3 | a0002c0002t0002g0250 a0002c0002t0002g0255 a0002c0002t0002g0267 |
3 | HG02083.hp1 NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.645+166_645+167ins others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89850824 | ||||||
| chr16:89850827 | G | T | 59 | a0001c0001t0001g0217 a0001c0001t0001g0337 a0001c0001t0001g0342 others(56): Show |
59 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.645+167G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850827 | |||||||
| chr16:89850832 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.645+172T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850832 | |||||||
| chr16:89850835 | G | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0206 a0001c0001t0001g0217 others(56): Show |
59 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.645+175G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850835 | |||||||
| chr16:89850850 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.645+190T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850850 | |||||||
| chr16:89850867 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.645+207A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850867 | |||||||
| chr16:89850967 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.645+307G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850967 | |||||||
| chr16:89850988 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0010c0017t0001g0172 |
3 | HG02145.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.645+328C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850988 | |||||||
| chr16:89850990 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.645+330C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850990 | |||||||
| chr16:89851021 | A | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.645+361A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851021 | |||||||
| chr16:89851064 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.645+404A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851064 | |||||||
| chr16:89851072 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.645+412C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851072 | |||||||
| chr16:89851098 | G | A | 1 | a0001c0001t0001g0341 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.645+438G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851098 | |||||||
| chr16:89851129 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.645+469T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851129 | |||||||
| chr16:89851215 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.645+555G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851215 | |||||||
| chr16:89851322 | A | G | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.645+662A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851322 | |||||||
| chr16:89851340 | C | T | 26 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(23): Show |
26 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.645+680C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851340 | |||||||
| chr16:89851367 | C | T | 32 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.645+707C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851367 | |||||||
| chr16:89851396 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+736C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851396 | |||||||
| chr16:89851470 | G | A | 1 | a0001c0001t0004g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.645+810G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851470 | |||||||
| chr16:89851519 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.645+859C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851519 | |||||||
| chr16:89851557 | G | A | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.645+897G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851557 | |||||||
| chr16:89851764 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.645+1104C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851764 | |||||||
| chr16:89851949 | C | G | 9 | a0001c0001t0001g0135 a0001c0001t0001g0160 a0001c0001t0001g0161 others(6): Show |
9 | HG02451.hp1 HG02976.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+1289C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851949 | |||||||
| chr16:89852013 | T | TCTCCCCC others(32): Show |
6 | a0001c0001t0001g0146 a0001c0001t0001g0152 a0001c0001t0001g0243 others(3): Show |
6 | HG00597.hp1 HG00733.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+1361_645+1399d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852013 | ||||||
| chr16:89852015 | T | TC | 7 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0179 others(4): Show |
7 | HG01106.hp2 HG01175.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.645+1361dupC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852015 | ||||||
| chr16:89852026 | CCCAGATC others(32): Show |
C | 1 | a0001c0001t0001g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.645+1400_645+1438d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852026 | ||||||
| chr16:89852036 | CTGGCCCA others(71): Show |
C | 1 | a0001c0003t0001g0198 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.645+1400_645+1477d others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852036 | ||||||
| chr16:89852036 | CTGGCCCA others(149): Show |
C | 1 | a0001c0001t0001g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.645+1400_645+1555d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852036 | ||||||
| chr16:89852037 | TGGCCCAT others(31): Show |
T | 1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1378_645+1415d others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852037 | |||||||
| chr16:89852060 | A | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(187): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.645+1400A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852060 | |||||||
| chr16:89852060 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1400A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852060 | |||||||
| chr16:89852061 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.645+1401A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852061 | |||||||
| chr16:89852065 | G | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(189): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.645+1405G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852065 | |||||||
| chr16:89852069 | G | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1409G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852069 | |||||||
| chr16:89852072 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1412C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852072 | |||||||
| chr16:89852075 | C | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1415C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852075 | |||||||
| chr16:89852075 | C | CTGGCCCA others(149): Show |
1 | a0001c0001t0001g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.645+1443_645+1444i others(158): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852075 | ||||||
| chr16:89852075 | CTGGCCCA others(32): Show |
C | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.645+1444_645+1482d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852075 | ||||||
| chr16:89852076 | T | TGGCCCAT others(504): Show |
1 | a0001c0001t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.645+1438_645+1439i others(513): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852076 | ||||||
| chr16:89852089 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1429A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852089 | |||||||
| chr16:89852095 | C | CCCCAACC others(71): Show |
1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.645+1438_645+1439i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852095 | ||||||
| chr16:89852095 | C | T | 1 | a0005c0014t0002g0279 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.645+1435C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852095 | |||||||
| chr16:89852098 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1438C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852098 | |||||||
| chr16:89852099 | C | A | 79 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0039 others(76): Show |
79 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.645+1439C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852099 | |||||||
| chr16:89852102 | C | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1442C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852102 | |||||||
| chr16:89852104 | A | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(116): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.645+1444A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852104 | |||||||
| chr16:89852104 | A | G | 69 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0039 others(66): Show |
69 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.645+1444A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852104 | |||||||
| chr16:89852107 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1447A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852107 | |||||||
| chr16:89852114 | A | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(176): Show |
180 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.645+1454A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852114 | |||||||
| chr16:89852115 | T | TGGCCCAT others(32): Show |
1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.645+1473_645+1474i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852115 | ||||||
| chr16:89852121 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1461A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852121 | |||||||
| chr16:89852128 | A | ATCCTCTC others(1596): Show |
1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.645+1473_645+1474i others(1605): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852128 | ||||||
| chr16:89852128 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1468A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852128 | |||||||
| chr16:89852134 | C | T | 10 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(7): Show |
10 | HG00735.hp2 HG01109.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.645+1474C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852134 | |||||||
| chr16:89852134 | CCCCCACC others(32): Show |
C | 1 | a0001c0003t0001g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.645+1483_645+1521d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852134 | ||||||
| chr16:89852137 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1477C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852137 | |||||||
| chr16:89852138 | C | A | 2 | a0001c0001t0001g0174 a0010c0017t0001g0172 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.645+1478C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852138 | |||||||
| chr16:89852138 | C | T | 30 | a0001c0019t0001g0316 a0002c0002t0002g0250 a0002c0002t0002g0252 others(27): Show |
30 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.645+1478C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852138 | |||||||
| chr16:89852143 | C | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(79): Show |
83 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.645+1483C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852143 | |||||||
| chr16:89852143 | C | CCCAGATC others(71): Show |
1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.645+1512_645+1513i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852143 | ||||||
| chr16:89852143 | C | G | 3 | a0001c0001t0001g0174 a0001c0006t0001g0015 a0010c0017t0001g0172 |
3 | HG02922.hp2 HG03471.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.645+1483C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852143 | |||||||
| chr16:89852146 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1486A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852146 | |||||||
| chr16:89852150 | CCCATGGC others(188): Show |
C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0176 a0001c0001t0001g0329 |
3 | HG01192.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.645+1513_645+1707d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852150 | ||||||
| chr16:89852153 | A | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(106): Show |
109 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.645+1493A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852153 | |||||||
| chr16:89852156 | G | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1496G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852156 | |||||||
| chr16:89852157 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1497C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852157 | |||||||
| chr16:89852160 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1500A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852160 | |||||||
| chr16:89852167 | A | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1507A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852167 | |||||||
| chr16:89852167 | ATCCTCTC others(701): Show |
A | 10 | a0001c0001t0001g0135 a0001c0001t0001g0159 a0001c0001t0001g0161 others(7): Show |
10 | HG01891.hp2 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.645+1513_646-1406d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852167 | ||||||
| chr16:89852172 | CTCCCCAC others(148): Show |
C | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1513_645+1667d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852172 | |||||||
| chr16:89852173 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(195): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.645+1513T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852173 | |||||||
| chr16:89852177 | C | A | 1 | a0001c0003t0001g0198 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.645+1517C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852177 | |||||||
| chr16:89852182 | A | ACCAGATC others(343): Show |
1 | a0001c0001t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.645+1555_645+1556i others(352): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852182 | ||||||
| chr16:89852182 | A | ACCAGATC others(109): Show |
3 | a0001c0008t0001g0011 a0001c0008t0001g0012 a0001c0008t0001g0022 |
3 | HG01167.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.645+1563_645+1564i others(118): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852182 | ||||||
| chr16:89852182 | A | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(87): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.645+1522A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852182 | |||||||
| chr16:89852182 | A | G | 1 | a0001c0003t0001g0198 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.645+1522A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852182 | |||||||
| chr16:89852189 | C | CCCATGGC others(927): Show |
1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.645+1555_645+1556i others(936): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852189 | ||||||
| chr16:89852189 | C | T | 2 | a0001c0001t0001g0217 a0005c0014t0002g0279 |
2 | HG00099.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.645+1529C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852189 | |||||||
| chr16:89852189 | CCCATGGC others(149): Show |
C | 1 | a0004c0005t0001g0301 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.645+1600_645+1755d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852189 | ||||||
| chr16:89852192 | A | ATGGCCCA others(266): Show |
1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.645+1563_645+1564i others(275): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852192 | ||||||
| chr16:89852192 | A | ATGGCCCA others(110): Show |
3 | a0001c0001t0003g0321 a0001c0001t0003g0325 a0001c0001t0003g0336 |
3 | HG02145.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.645+1551_645+1552i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852192 | ||||||
| chr16:89852192 | A | C | 25 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0140 others(22): Show |
25 | HG00597.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.645+1532A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852192 | |||||||
| chr16:89852210 | TC | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0028 others(40): Show |
43 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.645+1556delC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852210 | ||||||
| chr16:89852212 | C | CCCCACCC others(226): Show |
1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.645+1555_645+1556i others(235): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852212 | ||||||
| chr16:89852212 | C | CCCCACCC others(31): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.645+1555_645+1556i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852212 | ||||||
| chr16:89852212 | C | T | 21 | a0001c0001t0001g0097 a0001c0001t0001g0248 a0001c0001t0001g0337 others(18): Show |
21 | HG01109.hp2 HG01192.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.645+1552C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852212 | |||||||
| chr16:89852214 | C | T | 2 | a0001c0001t0001g0184 a0015c0016t0001g0005 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.645+1554C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852214 | |||||||
| chr16:89852216 | C | A | 2 | a0001c0001t0001g0243 a0003c0004t0001g0045 |
2 | HG00733.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.645+1556C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852216 | |||||||
| chr16:89852216 | C | T | 2 | a0002c0002t0002g0256 a0002c0002t0002g0259 |
2 | HG02165.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.645+1556C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852216 | |||||||
| chr16:89852221 | C | A | 9 | a0001c0001t0001g0097 a0001c0001t0001g0209 a0001c0001t0001g0217 others(6): Show |
9 | HG00099.hp2 HG00621.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+1561C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852221 | |||||||
| chr16:89852221 | C | CCCAGATC others(32): Show |
1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.645+1570_645+1571i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852221 | ||||||
| chr16:89852221 | C | G | 2 | a0001c0001t0001g0243 a0003c0004t0001g0045 |
2 | HG00733.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.645+1561C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852221 | |||||||
| chr16:89852222 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.645+1562C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852222 | |||||||
| chr16:89852224 | A | AGATCCCC others(463): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0181 others(2): Show |
7 | HG01243.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.645+1570_645+1571i others(472): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852224 | ||||||
| chr16:89852224 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0203 a0015c0016t0001g0005 |
3 | HG01884.hp2 HG03688.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.645+1564A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852224 | |||||||
| chr16:89852225 | G | T | 3 | a0001c0001t0003g0321 a0001c0001t0003g0325 a0001c0001t0003g0336 |
3 | HG02145.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.645+1565G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852225 | |||||||
| chr16:89852228 | C | CCCATGGC others(32): Show |
2 | a0002c0002t0002g0258 a0002c0002t0002g0260 |
2 | HG00323.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.645+1590_645+1591i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852228 | ||||||
| chr16:89852228 | C | T | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.645+1568C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852228 | |||||||
| chr16:89852231 | A | ATGGCCCA others(188): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.645+1599_645+1600i others(197): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852231 | ||||||
| chr16:89852231 | A | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0024 others(113): Show |
117 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.645+1571A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852231 | |||||||
| chr16:89852232 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.645+1572T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852232 | |||||||
| chr16:89852238 | A | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG02622.hp2 HG03927.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1578A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852238 | |||||||
| chr16:89852245 | A | G | 1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645+1585A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852245 | |||||||
| chr16:89852251 | C | T | 36 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0160 others(33): Show |
36 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.645+1591C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852251 | |||||||
| chr16:89852251 | CCCCCACC others(32): Show |
C | 1 | a0004c0005t0001g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.645+1630_645+1668d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852251 | ||||||
| chr16:89852251 | CCCCCACC others(188): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.645+1630_646-1802d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852251 | ||||||
| chr16:89852253 | C | T | 30 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(27): Show |
30 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.645+1593C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852253 | |||||||
| chr16:89852255 | C | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0057 others(29): Show |
34 | HG01071.hp1 HG01106.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.645+1595C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852255 | |||||||
| chr16:89852255 | C | CACCCCCC others(32): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0283 |
2 | HG01934.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.645+1599_645+1600i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852255 | ||||||
| chr16:89852255 | C | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.645+1595C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852255 | |||||||
| chr16:89852260 | A | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.645+1600A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852260 | |||||||
| chr16:89852260 | A | G | 27 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0088 others(24): Show |
27 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.645+1600A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852260 | |||||||
| chr16:89852262 | C | T | 1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645+1602C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852262 | |||||||
| chr16:89852263 | A | AGATCCCA others(149): Show |
1 | a0001c0001t0003g0335 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(158): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852263 | ||||||
| chr16:89852263 | A | G | 36 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(33): Show |
36 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.645+1603A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852263 | |||||||
| chr16:89852267 | C | T | 25 | a0001c0001t0001g0079 a0001c0019t0001g0316 a0002c0002t0002g0250 others(22): Show |
25 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.645+1607C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852267 | |||||||
| chr16:89852267 | CCCATGGC others(71): Show |
C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0070 others(6): Show |
9 | HG01891.hp1 HG03017.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+1630_645+1707d others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852267 | ||||||
| chr16:89852270 | A | ATGGCCCA others(385): Show |
1 | a0001c0001t0001g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.645+1629_645+1630i others(394): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852270 | ||||||
| chr16:89852270 | A | ATGGCCCA others(32): Show |
1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.645+1629_645+1630i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852270 | ||||||
| chr16:89852270 | A | ATGGCCCG others(71): Show |
1 | a0001c0001t0001g0243 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.645+1616_645+1617i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852270 | ||||||
| chr16:89852270 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.645+1610A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852270 | |||||||
| chr16:89852271 | T | TGGCCCAT others(500): Show |
1 | a0001c0001t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(509): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852271 | ||||||
| chr16:89852271 | T | TGGCCCAT others(306): Show |
1 | a0001c0001t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(315): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852271 | ||||||
| chr16:89852277 | A | ATCTTCCA others(506): Show |
1 | a0001c0001t0001g0347 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(515): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852277 | ||||||
| chr16:89852284 | A | G | 4 | a0001c0001t0001g0351 a0003c0004t0001g0027 a0003c0004t0001g0056 others(1): Show |
4 | HG00408.hp1 HG03669.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1624A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852284 | |||||||
| chr16:89852289 | C | CCCCCCAC others(419): Show |
1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.645+1629_645+1630i others(428): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852289 | |||||||
| chr16:89852290 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.645+1630T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852290 | |||||||
| chr16:89852292 | C | CCCACCCC others(773): Show |
1 | a0001c0009t0001g0014 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.645+1638_645+1639i others(782): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | ||||||
| chr16:89852292 | C | CCCACCCC others(891): Show |
1 | a0001c0009t0001g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.645+1638_645+1639i others(900): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | ||||||
| chr16:89852292 | C | CCCACCCC others(500): Show |
1 | a0001c0009t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.645+1638_645+1639i others(509): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | ||||||
| chr16:89852292 | C | T | 13 | a0001c0001t0001g0097 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
13 | HG00099.hp1 HG01109.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1632C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852292 | |||||||
| chr16:89852292 | CCCACCCA others(305): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.645+1639_646-1676d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | ||||||
| chr16:89852293 | C | CCACCCCC others(113): Show |
1 | a0001c0001t0001g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.645+1638_645+1639i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852293 | ||||||
| chr16:89852294 | C | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(84): Show |
87 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.645+1634C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852294 | |||||||
| chr16:89852294 | C | T | 1 | a0002c0002t0002g0257 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.645+1634C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852294 | |||||||
| chr16:89852299 | A | ACCAGATC others(1163): Show |
1 | a0001c0011t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.645+1681_645+1682i others(1172): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852299 | ||||||
| chr16:89852299 | A | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0032 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.645+1639A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852299 | |||||||
| chr16:89852299 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.645+1639A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852299 | |||||||
| chr16:89852299 | ACCAGATC others(188): Show |
A | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.645+1671_646-1761d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852299 | ||||||
| chr16:89852301 | C | T | 8 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(5): Show |
8 | HG00408.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.645+1641C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852301 | |||||||
| chr16:89852302 | A | AGATCCCA others(112): Show |
3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG02717.hp2 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.645+1672_645+1673i others(121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852302 | ||||||
| chr16:89852302 | A | AGATCCCA others(110): Show |
3 | a0001c0001t0003g0321 a0001c0001t0003g0325 a0001c0001t0003g0336 |
3 | HG02145.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.645+1681_645+1682i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852302 | ||||||
| chr16:89852302 | A | G | 23 | a0001c0001t0001g0097 a0001c0001t0001g0166 a0001c0001t0001g0169 others(20): Show |
23 | HG00099.hp1 HG00408.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.645+1642A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852302 | |||||||
| chr16:89852303 | G | T | 1 | a0005c0014t0002g0279 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.645+1643G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852303 | |||||||
| chr16:89852306 | C | T | 1 | a0005c0014t0002g0279 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.645+1646C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852306 | |||||||
| chr16:89852309 | A | ATGGCCCA others(149): Show |
2 | a0002c0002t0002g0256 a0002c0002t0002g0259 |
2 | HG02165.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.645+1681_645+1682i others(158): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852309 | ||||||
| chr16:89852309 | A | C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(133): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.645+1649A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852309 | |||||||
| chr16:89852310 | T | C | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.645+1650T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852310 | |||||||
| chr16:89852310 | T | TGGCCCAT others(811): Show |
1 | a0001c0001t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.645+1675_645+1676i others(820): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852310 | ||||||
| chr16:89852312 | G | GCCCATCT others(8): Show |
1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.645+1656_645+1670d others(17): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852312 | ||||||
| chr16:89852313 | C | CCCGTCTT others(73): Show |
1 | a0001c0003t0005g0109 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.645+1655_645+1656i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852313 | ||||||
| chr16:89852316 | A | G | 20 | a0001c0001t0001g0092 a0001c0001t0001g0139 a0001c0001t0001g0144 others(17): Show |
20 | HG01071.hp1 HG01099.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.645+1656A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852316 | |||||||
| chr16:89852323 | A | G | 14 | a0001c0001t0001g0097 a0001c0001t0001g0166 a0001c0001t0001g0169 others(11): Show |
14 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.645+1663A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852323 | |||||||
| chr16:89852326 | C | T | 1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1666C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852326 | |||||||
| chr16:89852327 | T | C | 1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1667T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852327 | |||||||
| chr16:89852328 | C | CCCCCCAC others(421): Show |
1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.645+1681_645+1682i others(430): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852328 | ||||||
| chr16:89852329 | C | T | 14 | a0001c0001t0001g0097 a0001c0001t0001g0185 a0001c0001t0001g0186 others(11): Show |
14 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+1669C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852329 | |||||||
| chr16:89852330 | C | CT | 6 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0171 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+1670_645+1671i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852330 | |||||||
| chr16:89852330 | C | CTCTCACC others(554): Show |
1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645+1670_645+1671i others(563): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852330 | |||||||
| chr16:89852330 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1670C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852330 | |||||||
| chr16:89852331 | C | T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0086 others(7): Show |
10 | HG01516.hp2 HG02683.hp2 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+1671C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852331 | |||||||
| chr16:89852332 | C | A | 1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1672C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852332 | |||||||
| chr16:89852332 | C | T | 8 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0171 others(5): Show |
8 | HG02622.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.645+1672C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852332 | |||||||
| chr16:89852333 | C | A | 43 | a0001c0001t0001g0092 a0001c0001t0001g0139 a0001c0001t0001g0144 others(40): Show |
43 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.645+1673C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852333 | |||||||
| chr16:89852338 | C | A | 85 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.645+1678C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852338 | |||||||
| chr16:89852338 | C | CCCAGATC others(1240): Show |
1 | a0001c0001t0001g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.645+1681_645+1682i others(1249): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852338 | ||||||
| chr16:89852338 | C | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0139 a0001c0001t0001g0144 others(10): Show |
13 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+1678C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852338 | |||||||
| chr16:89852340 | C | T | 11 | a0001c0001t0001g0097 a0001c0001t0001g0185 a0001c0001t0001g0186 others(8): Show |
11 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.645+1680C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852340 | |||||||
| chr16:89852341 | A | G | 30 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0086 others(27): Show |
30 | HG01081.hp1 HG01516.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.645+1681A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852341 | |||||||
| chr16:89852342 | T | C | 2 | a0001c0001t0001g0169 a0007c0010t0001g0313 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.645+1682T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852342 | |||||||
| chr16:89852342 | T | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(286): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.645+1682T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852342 | |||||||
| chr16:89852345 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(287): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.645+1685T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852345 | |||||||
| chr16:89852348 | A | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
158 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.645+1688A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852348 | |||||||
| chr16:89852349 | T | C | 2 | a0001c0001t0001g0217 a0001c0008t0001g0013 |
2 | HG00099.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.645+1689T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852349 | |||||||
| chr16:89852352 | C | CCCGTCTT others(73): Show |
2 | a0001c0001t0001g0296 a0004c0005t0001g0302 |
2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.645+1694_645+1695i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852352 | ||||||
| chr16:89852352 | C | CCCGTCTT others(193): Show |
3 | a0004c0005t0001g0303 a0004c0005t0001g0304 a0004c0005t0001g0306 |
3 | HG01167.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.645+1694_645+1695i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852352 | ||||||
| chr16:89852352 | C | CCCGTCTT others(393): Show |
1 | a0001c0001t0001g0352 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.645+1694_645+1695i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852352 | ||||||
| chr16:89852355 | A | G | 32 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.645+1695A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852355 | |||||||
| chr16:89852358 | T | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1698T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852358 | |||||||
| chr16:89852362 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.645+1702A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852362 | |||||||
| chr16:89852365 | C | T | 4 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1705C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852365 | |||||||
| chr16:89852367 | C | CT | 4 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1707_645+1708i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852367 | |||||||
| chr16:89852368 | C | CCCCCACC others(1163): Show |
1 | a0001c0011t0001g0318 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(1172): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852368 | ||||||
| chr16:89852368 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(21): Show |
26 | HG00621.hp1 HG01243.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.645+1708C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852368 | |||||||
| chr16:89852369 | C | CT | 26 | a0001c0001t0001g0169 a0001c0001t0001g0291 a0001c0001t0001g0294 others(23): Show |
26 | HG00280.hp1 HG00408.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.645+1709_645+1710i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | |||||||
| chr16:89852369 | C | CTCTCACC others(114): Show |
4 | a0001c0001t0001g0287 a0001c0001t0001g0293 a0001c0001t0001g0350 others(1): Show |
4 | HG00733.hp1 HG00735.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1709_645+1710i others(123): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | |||||||
| chr16:89852369 | C | CTCTCACC others(234): Show |
2 | a0001c0001t0010g0349 a0004c0005t0001g0311 |
2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.645+1709_645+1710i others(243): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | |||||||
| chr16:89852369 | C | CTCTCACC others(354): Show |
1 | a0001c0001t0001g0348 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.645+1709_645+1710i others(363): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | |||||||
| chr16:89852369 | C | T | 4 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1709C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | |||||||
| chr16:89852370 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0100 others(16): Show |
20 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.645+1710C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852370 | |||||||
| chr16:89852371 | C | CAACCCCC others(193): Show |
1 | a0001c0001t0001g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.645+1711_645+1712i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852371 | |||||||
| chr16:89852371 | C | T | 37 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0171 others(34): Show |
37 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.645+1711C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852371 | |||||||
| chr16:89852372 | C | A | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(20): Show |
23 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.645+1712C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852372 | |||||||
| chr16:89852377 | C | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0092 a0001c0001t0001g0097 others(9): Show |
12 | HG00733.hp2 HG01081.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.645+1717C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852377 | |||||||
| chr16:89852377 | C | CCCAGATC others(32): Show |
1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.645+1755_645+1756i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCAGATC others(32): Show |
1 | a0001c0001t0001g0063 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.645+1746_645+1747i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCAGATC others(32): Show |
3 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0146 |
3 | HG01934.hp2 HG02083.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.645+1726_645+1727i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCAGATC others(422): Show |
1 | a0001c0001t0001g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.645+1726_645+1727i others(431): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(2271): Show |
1 | a0001c0001t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(2280): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(2428): Show |
1 | a0001c0001t0001g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(2437): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(2428): Show |
1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(2437): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(501): Show |
1 | a0001c0021t0001g0211 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(510): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(267): Show |
3 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00642.hp2 HG00735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.645+1720_645+1721i others(276): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(267): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(276): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(306): Show |
6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+1720_645+1721i others(315): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(618): Show |
1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(627): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(306): Show |
1 | a0001c0001t0006g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(315): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(384): Show |
4 | a0001c0001t0001g0204 a0001c0001t0001g0219 a0001c0001t0001g0223 others(1): Show |
4 | HG01070.hp1 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1720_645+1721i others(393): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(345): Show |
1 | a0001c0001t0001g0235 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(354): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(307): Show |
1 | a0001c0001t0001g0215 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(316): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | CCCATATT others(307): Show |
1 | a0001c0001t0001g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(316): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | ||||||
| chr16:89852377 | C | G | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.645+1717C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852377 | |||||||
| chr16:89852379 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(13): Show |
18 | HG01243.hp2 HG01516.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.645+1719C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852379 | |||||||
| chr16:89852380 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.645+1720A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852380 | |||||||
| chr16:89852381 | G | C | 2 | a0001c0001t0010g0349 a0004c0005t0001g0311 |
2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.645+1721G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852381 | |||||||
| chr16:89852381 | G | GATCCCAT others(233): Show |
1 | a0001c0001t0001g0294 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.645+1733_645+1734i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852381 | ||||||
| chr16:89852381 | G | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(53): Show |
56 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.645+1721G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852381 | |||||||
| chr16:89852384 | C | CCCATGGC others(228): Show |
1 | a0001c0001t0003g0323 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.645+1746_645+1747i others(237): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852384 | ||||||
| chr16:89852384 | C | CCCATGGC others(227): Show |
5 | a0001c0001t0003g0322 a0001c0001t0003g0326 a0001c0001t0003g0327 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.645+1746_645+1747i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852384 | ||||||
| chr16:89852384 | C | CCCATGGC others(227): Show |
1 | a0001c0001t0003g0324 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.645+1746_645+1747i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852384 | ||||||
| chr16:89852384 | C | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(54): Show |
57 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.645+1724C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852384 | |||||||
| chr16:89852387 | A | ATGGCCCA others(32): Show |
1 | a0001c0001t0004g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.645+1750_645+1751i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852387 | ||||||
| chr16:89852387 | A | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0024 others(81): Show |
85 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.645+1727A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852387 | |||||||
| chr16:89852390 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1730G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852390 | |||||||
| chr16:89852391 | C | CCCGTCAT others(33): Show |
7 | a0001c0001t0001g0291 a0001c0001t0001g0341 a0001c0001t0001g0353 others(4): Show |
7 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.645+1733_645+1734i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852391 | ||||||
| chr16:89852391 | C | CCCGTCTT others(73): Show |
3 | a0001c0001t0001g0289 a0001c0001t0001g0295 a0001c0001t0001g0308 |
3 | HG01109.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.645+1733_645+1734i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852391 | ||||||
| chr16:89852391 | C | CCCGTCTT others(193): Show |
1 | a0001c0003t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.645+1733_645+1734i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852391 | ||||||
| chr16:89852391 | C | T | 4 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1731C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852391 | |||||||
| chr16:89852394 | A | G | 39 | a0001c0001t0001g0097 a0001c0001t0001g0169 a0001c0001t0001g0175 others(36): Show |
39 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.645+1734A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852394 | |||||||
| chr16:89852397 | T | A | 4 | a0001c0001t0001g0345 a0003c0004t0001g0027 a0003c0004t0001g0056 others(1): Show |
4 | HG00408.hp1 HG02300.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1737T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852397 | |||||||
| chr16:89852401 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0100 others(51): Show |
55 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.645+1741A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852401 | |||||||
| chr16:89852404 | C | T | 12 | a0001c0001t0001g0169 a0001c0001t0001g0345 a0001c0001t0001g0350 others(9): Show |
12 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+1744C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852404 | |||||||
| chr16:89852406 | C | CT | 13 | a0001c0001t0001g0169 a0001c0001t0001g0345 a0001c0001t0001g0350 others(10): Show |
13 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+1746_645+1747i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852406 | |||||||
| chr16:89852407 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0097 others(23): Show |
27 | HG00621.hp2 HG00673.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.645+1747C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852407 | |||||||
| chr16:89852408 | C | CT | 40 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0174 others(37): Show |
40 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.645+1748_645+1749i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852408 | |||||||
| chr16:89852408 | C | T | 12 | a0001c0001t0001g0169 a0001c0001t0001g0345 a0001c0001t0001g0350 others(9): Show |
12 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+1748C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852408 | |||||||
| chr16:89852409 | C | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0069 others(12): Show |
15 | HG00741.hp1 HG01891.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.645+1749C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852409 | |||||||
| chr16:89852410 | C | T | 52 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0171 others(49): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.645+1750C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852410 | |||||||
| chr16:89852411 | C | A | 23 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0086 others(20): Show |
23 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.645+1751C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852411 | |||||||
| chr16:89852411 | C | CACCCGCC others(71): Show |
1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.645+1755_645+1756i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852411 | ||||||
| chr16:89852416 | C | A | 25 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(22): Show |
25 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.645+1756C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852416 | |||||||
| chr16:89852416 | C | CCCAGATC others(781): Show |
1 | a0003c0004t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(790): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852416 | ||||||
| chr16:89852416 | C | G | 13 | a0001c0001t0001g0088 a0001c0001t0001g0139 a0001c0001t0001g0140 others(10): Show |
13 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+1756C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852416 | |||||||
| chr16:89852417 | C | G | 1 | a0003c0004t0001g0045 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.645+1757C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852417 | |||||||
| chr16:89852418 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0100 others(14): Show |
18 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.645+1758C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852418 | |||||||
| chr16:89852419 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0039 others(98): Show |
102 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.645+1759A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852419 | |||||||
| chr16:89852419 | AGATCCCA others(149): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.645+1766_646-1705d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852419 | ||||||
| chr16:89852420 | G | C | 3 | a0001c0001t0001g0287 a0001c0001t0001g0293 a0001c0003t0001g0117 |
3 | HG00735.hp2 HG01123.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.645+1760G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852420 | |||||||
| chr16:89852420 | G | GATCCCCT others(193): Show |
1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.645+1765_645+1766i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852420 | ||||||
| chr16:89852420 | G | T | 1 | a0002c0002t0002g0258 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.645+1760G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852420 | |||||||
| chr16:89852423 | C | T | 7 | a0002c0002t0002g0256 a0002c0002t0002g0257 a0002c0002t0002g0258 others(4): Show |
7 | HG00323.hp1 HG02015.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.645+1763C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852423 | |||||||
| chr16:89852426 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
132 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.645+1766A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852426 | |||||||
| chr16:89852429 | G | A | 14 | a0001c0001t0001g0169 a0001c0001t0001g0319 a0001c0001t0001g0320 others(11): Show |
14 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+1769G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852429 | |||||||
| chr16:89852430 | C | T | 14 | a0001c0001t0001g0169 a0001c0001t0001g0319 a0001c0001t0001g0320 others(11): Show |
14 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+1770C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852430 | |||||||
| chr16:89852433 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.645+1773A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852433 | |||||||
| chr16:89852433 | A | G | 47 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0097 others(44): Show |
47 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.645+1773A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852433 | |||||||
| chr16:89852436 | T | A | 8 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(5): Show |
8 | HG00099.hp1 HG01993.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.645+1776T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852436 | |||||||
| chr16:89852440 | A | ATCCTCCC others(32): Show |
1 | a0001c0001t0001g0194 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852440 | ||||||
| chr16:89852440 | A | ATCCTCTC others(1593): Show |
1 | a0001c0001t0001g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.646-1783_646-1782i others(1602): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852440 | ||||||
| chr16:89852440 | A | G | 56 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0039 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.645+1780A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852440 | |||||||
| chr16:89852441 | T | TCCTCCCT others(33): Show |
1 | a0001c0001t0001g0179 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852441 | ||||||
| chr16:89852443 | C | T | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(10): Show |
13 | HG00099.hp1 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1783C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852443 | |||||||
| chr16:89852444 | T | TCCCTCTC others(351): Show |
1 | a0001c0001t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(360): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852444 | ||||||
| chr16:89852444 | T | TCCCTCTC others(391): Show |
2 | a0001c0001t0001g0098 a0001c0003t0001g0178 |
2 | HG01516.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.645+1785_645+1786i others(400): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852444 | ||||||
| chr16:89852445 | CTCCCCAC others(106): Show |
C | 2 | a0003c0004t0001g0027 a0003c0004t0001g0059 |
2 | HG00408.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.645+1786_646-1728d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852445 | |||||||
| chr16:89852446 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.645+1786T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852446 | |||||||
| chr16:89852447 | C | CT | 56 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0106 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.645+1787_645+1788i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852447 | |||||||
| chr16:89852448 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(76): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.645+1788C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852448 | |||||||
| chr16:89852449 | C | CTCT | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0003t0001g0178 |
3 | HG01516.hp2 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.645+1789_645+1790i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852449 | |||||||
| chr16:89852449 | C | T | 56 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0106 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.645+1789C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852449 | |||||||
| chr16:89852450 | C | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0100 others(18): Show |
22 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.645+1790C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852450 | |||||||
| chr16:89852455 | A | ACCAGATC others(71): Show |
1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | ||||||
| chr16:89852455 | A | ACCAGATC others(346): Show |
1 | a0001c0001t0001g0216 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.646-1783_646-1782i others(355): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | ||||||
| chr16:89852455 | A | ACCAGATC others(189): Show |
1 | a0001c0001t0001g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(198): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | ||||||
| chr16:89852455 | A | ACCAGATC others(423): Show |
1 | a0001c0001t0001g0208 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(432): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | ||||||
| chr16:89852455 | A | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.645+1795A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852455 | |||||||
| chr16:89852455 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.645+1795A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852455 | |||||||
| chr16:89852457 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0069 others(9): Show |
12 | HG01256.hp2 HG01891.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+1797C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852457 | |||||||
| chr16:89852458 | A | G | 151 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(148): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.645+1798A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852458 | |||||||
| chr16:89852459 | G | C | 10 | a0001c0001t0001g0098 a0001c0001t0001g0166 a0001c0001t0001g0171 others(7): Show |
10 | HG01099.hp2 HG01516.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+1799G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852459 | |||||||
| chr16:89852459 | G | T | 2 | a0005c0007t0002g0261 a0005c0007t0002g0262 |
2 | HG01175.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.645+1799G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852459 | |||||||
| chr16:89852462 | C | CCCATGGC others(227): Show |
1 | a0001c0001t0003g0331 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.646-1802_646-1801i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852462 | ||||||
| chr16:89852462 | C | T | 22 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(19): Show |
22 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.645+1802C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852462 | |||||||
| chr16:89852465 | A | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.645+1805A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852465 | |||||||
| chr16:89852466 | T | C | 2 | a0005c0014t0002g0279 a0014c0015t0002g0277 |
2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.645+1806T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852466 | |||||||
| chr16:89852468 | G | A | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(10): Show |
13 | HG00099.hp1 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1808G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852468 | |||||||
| chr16:89852469 | C | CCCGTCAT others(33): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0106 a0001c0001t0001g0143 |
3 | HG03491.hp1 NA18993.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.645+1811_645+1812i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | ||||||
| chr16:89852469 | C | CCCGTCAT others(153): Show |
1 | a0001c0001t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.645+1811_645+1812i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | ||||||
| chr16:89852469 | C | CCCGTCTT others(73): Show |
6 | a0001c0003t0001g0089 a0001c0003t0001g0110 a0001c0003t0001g0113 others(3): Show |
6 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.645+1811_645+1812i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | ||||||
| chr16:89852469 | C | CCCGTCTT others(193): Show |
3 | a0001c0001t0001g0050 a0001c0001t0001g0100 a0001c0001t0007g0251 |
3 | HG02027.hp2 NA18960.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.645+1811_645+1812i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | ||||||
| chr16:89852469 | C | CCCGTCTT others(353): Show |
1 | a0001c0001t0001g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.645+1811_645+1812i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | ||||||
| chr16:89852469 | C | CCCGTCTT others(433): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0108 |
2 | NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.645+1811_645+1812i others(442): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | ||||||
| chr16:89852469 | C | T | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(10): Show |
13 | HG00099.hp1 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1809C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852469 | |||||||
| chr16:89852472 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0098 others(51): Show |
55 | HG00280.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.645+1812A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852472 | |||||||
| chr16:89852475 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0288 |
2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.646-1811T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852475 | |||||||
| chr16:89852479 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.646-1807A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852479 | |||||||
| chr16:89852482 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0288 a0001c0001t0001g0319 others(6): Show |
9 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1804C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852482 | |||||||
| chr16:89852484 | C | CT | 9 | a0001c0001t0001g0026 a0001c0001t0001g0288 a0001c0001t0001g0319 others(6): Show |
9 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1802_646-1801i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852484 | |||||||
| chr16:89852485 | C | CCCCCACC others(812): Show |
3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG02257.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.646-1783_646-1782i others(821): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852485 | ||||||
| chr16:89852485 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(76): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.646-1801C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852485 | |||||||
| chr16:89852486 | C | CT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0055 others(60): Show |
64 | HG00099.hp1 HG00323.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.646-1800_646-1799i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | |||||||
| chr16:89852486 | C | CTCTCACC others(74): Show |
1 | a0001c0001t0001g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.646-1800_646-1799i others(83): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | |||||||
| chr16:89852486 | C | CTCTCACC others(194): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0154 |
2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.646-1800_646-1799i others(203): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | |||||||
| chr16:89852486 | C | CTCTCACC others(234): Show |
1 | a0003c0004t0001g0045 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.646-1800_646-1799i others(243): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | |||||||
| chr16:89852486 | C | CTCTCACC others(354): Show |
1 | a0001c0001t0002g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.646-1800_646-1799i others(363): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | |||||||
| chr16:89852486 | C | T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0288 a0001c0001t0001g0319 others(7): Show |
10 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-1800C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | |||||||
| chr16:89852487 | C | T | 9 | a0001c0001t0001g0049 a0001c0001t0001g0079 a0001c0001t0001g0097 others(6): Show |
9 | HG00408.hp2 HG02622.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1799C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852487 | |||||||
| chr16:89852488 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0050 others(75): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.646-1798C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852488 | |||||||
| chr16:89852489 | C | A | 16 | a0001c0001t0001g0024 a0001c0001t0001g0069 a0001c0001t0001g0147 others(13): Show |
16 | HG00741.hp1 HG01175.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-1797C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852489 | |||||||
| chr16:89852489 | C | CACCCCCC others(773): Show |
1 | a0001c0001t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.646-1783_646-1782i others(782): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852489 | ||||||
| chr16:89852489 | C | CACCCCCC others(1202): Show |
1 | a0001c0001t0001g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(1211): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852489 | ||||||
| chr16:89852494 | C | A | 23 | a0001c0001t0001g0243 a0001c0001t0001g0286 a0001c0001t0001g0329 others(20): Show |
23 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.646-1792C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852494 | |||||||
| chr16:89852495 | C | G | 2 | a0003c0004t0001g0046 a0003c0004t0001g0075 |
2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.646-1791C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852495 | |||||||
| chr16:89852496 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(74): Show |
77 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.646-1790C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852496 | |||||||
| chr16:89852497 | A | ATATTCCA others(578): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.646-1789_646-1788i others(587): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852497 | |||||||
| chr16:89852497 | A | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(164): Show |
168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.646-1789A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852497 | |||||||
| chr16:89852498 | G | C | 23 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0174 others(20): Show |
23 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.646-1788G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852498 | |||||||
| chr16:89852498 | G | T | 2 | a0005c0014t0002g0279 a0014c0015t0002g0277 |
2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.646-1788G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852498 | |||||||
| chr16:89852501 | C | T | 2 | a0005c0014t0002g0279 a0014c0015t0002g0277 |
2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.646-1785C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852501 | |||||||
| chr16:89852504 | A | ATGGCCCA others(71): Show |
1 | a0001c0001t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-1763_646-1762i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852504 | ||||||
| chr16:89852504 | A | ATGGCCCA others(711): Show |
1 | a0001c0008t0001g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.646-1763_646-1762i others(720): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852504 | ||||||
| chr16:89852504 | A | C | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.646-1782A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852504 | |||||||
| chr16:89852505 | T | C | 5 | a0001c0001t0001g0337 a0002c0002t0002g0256 a0002c0002t0002g0259 others(2): Show |
5 | HG01109.hp2 HG02080.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1781T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852505 | |||||||
| chr16:89852507 | G | A | 10 | a0001c0001t0001g0026 a0001c0001t0001g0166 a0001c0001t0001g0288 others(7): Show |
10 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-1779G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852507 | |||||||
| chr16:89852508 | C | CCCGTCAT others(33): Show |
1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.646-1776_646-1775i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852508 | ||||||
| chr16:89852508 | C | CCCGTCTT others(73): Show |
1 | a0001c0001t0001g0351 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.646-1776_646-1775i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852508 | ||||||
| chr16:89852508 | C | T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0166 a0001c0001t0001g0288 others(7): Show |
10 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-1778C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852508 | |||||||
| chr16:89852511 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0050 others(76): Show |
80 | HG00099.hp1 HG00323.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.646-1775A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852511 | |||||||
| chr16:89852514 | T | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
6 | NA18949.hp1 NA18951.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1772T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852514 | |||||||
| chr16:89852517 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0171 |
2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.646-1769C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852517 | |||||||
| chr16:89852518 | A | ATCCTCCC others(384): Show |
1 | a0001c0001t0001g0225 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.646-1759_646-1758i others(393): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852518 | ||||||
| chr16:89852518 | A | ATCCTCCC others(384): Show |
1 | a0001c0001t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.646-1759_646-1758i others(393): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852518 | ||||||
| chr16:89852518 | A | ATCCTCTC others(71): Show |
4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG00642.hp1 HG01123.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1763_646-1762i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852518 | ||||||
| chr16:89852518 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0050 others(82): Show |
86 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.646-1768A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852518 | |||||||
| chr16:89852521 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0345 a0001c0006t0001g0015 others(1): Show |
5 | HG02300.hp2 NA18951.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1765C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852521 | |||||||
| chr16:89852524 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0079 others(14): Show |
18 | HG01081.hp1 HG01175.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.646-1762C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852524 | |||||||
| chr16:89852526 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(136): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.646-1760T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852526 | |||||||
| chr16:89852526 | T | TCTCACCC others(825): Show |
2 | a0001c0008t0001g0012 a0001c0008t0001g0022 |
2 | HG01167.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.646-1759_646-1758i others(834): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852526 | ||||||
| chr16:89852526 | T | TCTCACCC others(666): Show |
1 | a0001c0008t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.646-1759_646-1758i others(675): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852526 | ||||||
| chr16:89852527 | C | CCACCCCC others(1032): Show |
1 | a0001c0001t0001g0342 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1041): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | ||||||
| chr16:89852527 | C | CCACCCCC others(832): Show |
1 | a0001c0001t0003g0343 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(841): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | ||||||
| chr16:89852527 | C | CCACCCCC others(1152): Show |
1 | a0001c0001t0003g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1161): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | ||||||
| chr16:89852527 | C | CCACCCCC others(1192): Show |
1 | a0001c0001t0003g0334 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1201): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | ||||||
| chr16:89852527 | C | CCACCCCC others(1112): Show |
1 | a0001c0001t0003g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | ||||||
| chr16:89852527 | C | CCACCCCC others(1112): Show |
1 | a0001c0001t0003g0340 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | ||||||
| chr16:89852527 | C | CT | 89 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(86): Show |
90 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.646-1759_646-1758i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852527 | |||||||
| chr16:89852527 | C | CTCACCCC others(891): Show |
3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.646-1759_646-1758i others(900): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852527 | |||||||
| chr16:89852527 | C | CTCACCCC others(874): Show |
1 | a0001c0001t0003g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.646-1759_646-1758i others(883): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852527 | |||||||
| chr16:89852527 | CCACCCCC others(70): Show |
C | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.646-1757_646-1681d others(79): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | ||||||
| chr16:89852528 | C | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(80): Show |
83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.646-1758C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852528 | |||||||
| chr16:89852528 | C | CACCCCCC others(227): Show |
1 | a0002c0002t0002g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | ||||||
| chr16:89852528 | C | CACCCCCC others(71): Show |
13 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0255 others(10): Show |
13 | HG00438.hp2 HG00597.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.646-1751_646-1750i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | ||||||
| chr16:89852528 | C | CACCCCCC others(188): Show |
1 | a0013c0025t0002g0268 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(197): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | ||||||
| chr16:89852528 | C | CACCCCCC others(266): Show |
1 | a0002c0002t0002g0257 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(275): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | ||||||
| chr16:89852528 | C | CACCCCCC others(32): Show |
5 | a0002c0002t0002g0256 a0002c0002t0002g0259 a0002c0002t0002g0260 others(2): Show |
5 | HG02015.hp1 HG02080.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1751_646-1750i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | ||||||
| chr16:89852528 | C | CACCCCCC others(72): Show |
1 | a0002c0002t0014g0272 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(81): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | ||||||
| chr16:89852533 | C | A | 2 | a0002c0002t0002g0280 a0002c0002t0002g0281 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.646-1753C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852533 | |||||||
| chr16:89852533 | C | CCCATATT others(539): Show |
1 | a0001c0001t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(548): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852533 | ||||||
| chr16:89852535 | C | T | 9 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0124 others(6): Show |
9 | HG01175.hp1 HG02148.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1751C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852535 | |||||||
| chr16:89852536 | G | A | 135 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(132): Show |
135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.646-1750G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852536 | |||||||
| chr16:89852537 | G | C | 19 | a0001c0001t0001g0050 a0001c0001t0001g0100 a0001c0001t0001g0106 others(16): Show |
19 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.646-1749G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852537 | |||||||
| chr16:89852537 | G | T | 2 | a0001c0001t0003g0333 a0001c0001t0003g0339 |
2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.646-1749G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852537 | |||||||
| chr16:89852540 | C | CCCATGGC others(232): Show |
1 | a0001c0006t0001g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-1744_646-1743i others(241): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852540 | ||||||
| chr16:89852540 | C | T | 2 | a0001c0001t0003g0333 a0001c0001t0003g0339 |
2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.646-1746C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852540 | |||||||
| chr16:89852542 | C | T | 12 | a0001c0001t0001g0337 a0001c0001t0003g0321 a0001c0001t0003g0322 others(9): Show |
12 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.646-1744C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852542 | |||||||
| chr16:89852543 | C | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(115): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.646-1743C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852543 | |||||||
| chr16:89852543 | C | CTGGCCCA others(32): Show |
1 | a0001c0009t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.646-1730_646-1729i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852543 | ||||||
| chr16:89852544 | T | C | 1 | a0002c0002t0002g0278 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.646-1742T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852544 | |||||||
| chr16:89852546 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0345 a0001c0006t0001g0015 others(1): Show |
5 | HG02300.hp2 NA18951.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1740G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852546 | |||||||
| chr16:89852547 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0345 a0001c0006t0001g0015 others(1): Show |
5 | HG02300.hp2 NA18951.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1739C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852547 | |||||||
| chr16:89852550 | A | G | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(171): Show |
174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.646-1736A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852550 | |||||||
| chr16:89852553 | T | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0069 a0001c0001t0001g0147 others(10): Show |
13 | HG00741.hp1 HG01891.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.646-1733T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852553 | |||||||
| chr16:89852557 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0030 others(64): Show |
68 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.646-1729G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852557 | |||||||
| chr16:89852557 | GTCCTCTC others(32): Show |
G | 1 | a0004c0005t0001g0307 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.646-1723_646-1685d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852557 | ||||||
| chr16:89852560 | C | T | 29 | a0001c0001t0001g0024 a0001c0001t0001g0069 a0001c0001t0001g0143 others(26): Show |
29 | HG00741.hp1 HG01099.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.646-1726C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852560 | |||||||
| chr16:89852561 | T | TCCCTCTC others(76): Show |
1 | a0003c0004t0001g0042 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(85): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(71): Show |
1 | a0001c0001t0001g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(71): Show |
44 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(41): Show |
44 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.646-1724_646-1723i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(111): Show |
2 | a0001c0001t0001g0074 a0001c0001t0004g0076 |
2 | NA18947.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.646-1724_646-1723i others(120): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(312): Show |
1 | a0001c0001t0001g0066 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(321): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(151): Show |
1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(160): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(311): Show |
2 | a0003c0004t0001g0046 a0003c0004t0001g0075 |
2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.646-1724_646-1723i others(320): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(551): Show |
1 | a0001c0001t0001g0082 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(560): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(191): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0001g0130 others(2): Show |
5 | HG01256.hp1 HG02572.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1724_646-1723i others(200): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(471): Show |
1 | a0001c0001t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(480): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(871): Show |
1 | a0001c0001t0001g0309 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(880): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(871): Show |
1 | a0001c0001t0001g0310 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(880): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(110): Show |
1 | a0001c0001t0001g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852561 | T | TCCCTCTC others(71): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0077 a0001c0001t0001g0288 others(1): Show |
4 | HG00673.hp1 HG03017.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1724_646-1723i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | ||||||
| chr16:89852563 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0025 others(107): Show |
111 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.646-1723T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852563 | |||||||
| chr16:89852563 | T | TCCCCACC others(71): Show |
1 | a0001c0009t0001g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.646-1713_646-1712i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852563 | ||||||
| chr16:89852564 | C | CT | 102 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(99): Show |
103 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.646-1722_646-1721i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852564 | |||||||
| chr16:89852564 | C | CTCTCACC others(34): Show |
4 | a0001c0001t0001g0069 a0001c0001t0001g0147 a0001c0001t0001g0171 others(1): Show |
4 | HG02135.hp1 HG02970.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1722_646-1721i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852564 | |||||||
| chr16:89852565 | C | T | 7 | a0001c0001t0001g0160 a0001c0001t0001g0245 a0001c0006t0001g0015 others(4): Show |
7 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-1721C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852565 | |||||||
| chr16:89852566 | C | CCACCCCC others(1193): Show |
1 | a0001c0001t0003g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.646-1713_646-1712i others(1202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852566 | ||||||
| chr16:89852566 | C | CCACCCCC others(233): Show |
1 | a0001c0001t0003g0339 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.646-1713_646-1712i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852566 | ||||||
| chr16:89852566 | C | CTCT | 65 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(62): Show |
65 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.646-1720_646-1719i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852566 | |||||||
| chr16:89852566 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(103): Show |
107 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.646-1720C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852566 | |||||||
| chr16:89852567 | C | A | 10 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0290 others(7): Show |
10 | HG01175.hp1 HG02622.hp2 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-1719C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852567 | |||||||
| chr16:89852568 | A | C | 2 | a0001c0006t0001g0015 a0003c0004t0001g0042 |
2 | NA18951.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.646-1718A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852568 | |||||||
| chr16:89852572 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0206 a0001c0001t0001g0287 |
3 | HG01123.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.646-1714C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852572 | |||||||
| chr16:89852574 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.646-1712T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852574 | |||||||
| chr16:89852574 | T | TGGATCCC others(507): Show |
1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.646-1705_646-1704i others(516): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852574 | ||||||
| chr16:89852575 | G | A | 34 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0066 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.646-1711G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852575 | |||||||
| chr16:89852575 | G | GGATCCCC others(32): Show |
4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG00642.hp1 HG01123.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1683_646-1682i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852575 | ||||||
| chr16:89852576 | G | C | 30 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0092 others(27): Show |
30 | HG00280.hp1 HG00733.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.646-1710G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852576 | |||||||
| chr16:89852576 | G | T | 3 | a0001c0001t0003g0331 a0002c0002t0002g0253 a0002c0002t0002g0278 |
3 | HG00609.hp1 HG02896.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.646-1710G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852576 | |||||||
| chr16:89852579 | C | T | 3 | a0001c0001t0003g0331 a0002c0002t0002g0253 a0002c0002t0002g0278 |
3 | HG00609.hp1 HG02896.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.646-1707C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852579 | |||||||
| chr16:89852582 | C | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
276 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.646-1704C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852582 | |||||||
| chr16:89852583 | T | C | 1 | a0001c0006t0001g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-1703T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852583 | |||||||
| chr16:89852583 | T | TGGCCCAT others(351): Show |
1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646-1691_646-1690i others(360): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852583 | ||||||
| chr16:89852585 | G | A | 25 | a0001c0001t0001g0024 a0001c0001t0001g0143 a0001c0001t0001g0158 others(22): Show |
25 | HG00741.hp1 HG01099.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.646-1701G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852585 | |||||||
| chr16:89852586 | C | CCCGTCAT others(33): Show |
7 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(4): Show |
7 | HG02738.hp1 HG03654.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1698_646-1697i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852586 | ||||||
| chr16:89852586 | C | CCCGTCTT others(73): Show |
1 | a0001c0001t0001g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.646-1698_646-1697i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852586 | ||||||
| chr16:89852586 | C | CCCGTCTT others(393): Show |
1 | a0001c0001t0001g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.646-1698_646-1697i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852586 | ||||||
| chr16:89852586 | C | T | 25 | a0001c0001t0001g0024 a0001c0001t0001g0143 a0001c0001t0001g0158 others(22): Show |
25 | HG00741.hp1 HG01099.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.646-1700C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852586 | |||||||
| chr16:89852589 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.646-1697A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852589 | |||||||
| chr16:89852592 | T | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0134 others(3): Show |
6 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1694T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852592 | |||||||
| chr16:89852596 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(149): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.646-1690A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852596 | |||||||
| chr16:89852599 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0134 others(2): Show |
5 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1687C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852599 | |||||||
| chr16:89852602 | C | T | 9 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0134 others(6): Show |
9 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1684C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852602 | |||||||
| chr16:89852604 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0030 others(101): Show |
106 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.646-1682T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852604 | |||||||
| chr16:89852604 | T | TCCACCCC others(32): Show |
1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.646-1673_646-1672i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852604 | ||||||
| chr16:89852605 | C | CAACCCCC others(713): Show |
1 | a0002c0002t0002g0258 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.646-1681_646-1680i others(722): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | |||||||
| chr16:89852605 | C | CT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(183): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.646-1681_646-1680i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | |||||||
| chr16:89852605 | C | CTCACCCC others(674): Show |
2 | a0005c0007t0002g0261 a0005c0007t0002g0262 |
2 | HG01175.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.646-1681_646-1680i others(683): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | |||||||
| chr16:89852605 | C | CTCACCCC others(114): Show |
1 | a0001c0006t0001g0016 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.646-1681_646-1680i others(123): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | |||||||
| chr16:89852605 | C | CTCACCCC others(274): Show |
1 | a0009c0022t0001g0034 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.646-1681_646-1680i others(283): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | |||||||
| chr16:89852605 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.646-1681C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | |||||||
| chr16:89852606 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0031 others(87): Show |
92 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.646-1680C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852606 | |||||||
| chr16:89852606 | C | CACCCCCC others(32): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.646-1673_646-1672i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852606 | ||||||
| chr16:89852613 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0173 a0001c0001t0001g0245 others(1): Show |
4 | HG02015.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1673C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852613 | |||||||
| chr16:89852614 | A | AGATCCCA others(151): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.646-1666_646-1665i others(160): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852614 | ||||||
| chr16:89852614 | A | ATATTCCA others(1113): Show |
1 | a0001c0001t0003g0331 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.646-1672_646-1671i others(1122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852614 | |||||||
| chr16:89852614 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(191): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.646-1672A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852614 | |||||||
| chr16:89852615 | G | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(89): Show |
93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.646-1671G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852615 | |||||||
| chr16:89852615 | G | GATCCCAT others(1146): Show |
1 | a0002c0002t0002g0253 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.646-1666_646-1665i others(1155): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852615 | ||||||
| chr16:89852618 | C | CCCATGGC others(383): Show |
1 | a0001c0009t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.646-1666_646-1665i others(392): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852618 | ||||||
| chr16:89852621 | C | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.646-1665C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852621 | |||||||
| chr16:89852621 | C | CTGGCCCA others(507): Show |
2 | a0002c0002t0002g0280 a0002c0002t0002g0281 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.646-1659_646-1658i others(516): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCA others(32): Show |
1 | a0001c0009t0001g0014 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.646-1659_646-1658i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCG others(234): Show |
1 | a0002c0002t0002g0278 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.646-1633_646-1632i others(243): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCG others(232): Show |
1 | a0005c0007t0002g0275 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(241): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCG others(233): Show |
3 | a0002c0002t0002g0256 a0002c0002t0002g0260 a0002c0002t0002g0267 |
3 | HG02015.hp1 NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.646-1623_646-1622i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCG others(913): Show |
1 | a0002c0002t0002g0259 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(922): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCG others(73): Show |
1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.646-1619_646-1618i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCG others(113): Show |
1 | a0001c0001t0001g0219 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852621 | C | CTGGCCCG others(112): Show |
1 | a0001c0001t0001g0286 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.646-1646_646-1645i others(121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | ||||||
| chr16:89852624 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0134 others(2): Show |
5 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1662G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852624 | |||||||
| chr16:89852625 | C | CCCATCTT others(424): Show |
1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-1659_646-1658i others(433): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852625 | ||||||
| chr16:89852625 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0134 others(2): Show |
5 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1661C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852625 | |||||||
| chr16:89852628 | G | A | 20 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0134 others(17): Show |
20 | HG00741.hp2 HG01074.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.646-1658G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852628 | |||||||
| chr16:89852628 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.646-1658G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852628 | |||||||
| chr16:89852631 | T | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0175 others(3): Show |
6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1655T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852631 | |||||||
| chr16:89852635 | G | A | 19 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0134 others(16): Show |
19 | HG00741.hp2 HG01074.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.646-1651G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852635 | |||||||
| chr16:89852637 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0150 |
2 | HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.646-1649C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852637 | |||||||
| chr16:89852638 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0175 others(3): Show |
6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1648C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852638 | |||||||
| chr16:89852641 | C | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0175 others(4): Show |
7 | HG01106.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1645C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852641 | |||||||
| chr16:89852644 | C | CCACCCCC others(70): Show |
1 | a0001c0001t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.646-1642_646-1641i others(79): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852644 | |||||||
| chr16:89852644 | CT | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0001c0001t0001g0225 others(1): Show |
4 | HG01074.hp1 HG01261.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1641delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852644 | |||||||
| chr16:89852645 | T | C | 2 | a0001c0001t0001g0232 a0001c0009t0001g0010 |
2 | HG00741.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.646-1641T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852645 | |||||||
| chr16:89852645 | T | TCACCCCC others(32): Show |
1 | a0001c0001t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.646-1634_646-1633i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852645 | ||||||
| chr16:89852654 | G | A | 9 | a0001c0001t0001g0066 a0001c0001t0001g0160 a0001c0001t0001g0225 others(6): Show |
9 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.646-1632G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852654 | |||||||
| chr16:89852654 | G | GCATCCCA others(833): Show |
1 | a0001c0001t0001g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646-1632_646-1631i others(842): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852654 | |||||||
| chr16:89852655 | G | C | 40 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0052 others(37): Show |
40 | HG00735.hp2 HG01099.hp2 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.646-1631G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852655 | |||||||
| chr16:89852655 | G | GATCCCAT others(593): Show |
2 | a0002c0002t0002g0276 a0012c0013t0002g0263 |
2 | HG02074.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.646-1623_646-1622i others(602): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852655 | G | GATCCCAT others(753): Show |
1 | a0002c0002t0002g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.646-1623_646-1622i others(762): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852655 | G | GATCCCAT others(830): Show |
1 | a0002c0002t0002g0264 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.646-1623_646-1622i others(839): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852655 | G | GATCCCAT others(633): Show |
1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(642): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852655 | G | GATCCCAT others(634): Show |
1 | a0002c0002t0002g0255 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(643): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852655 | G | GATCCCAT others(633): Show |
11 | a0002c0002t0002g0252 a0002c0002t0002g0254 a0002c0002t0002g0257 others(8): Show |
11 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-1623_646-1622i others(642): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852655 | G | GATCCCAT others(673): Show |
1 | a0013c0025t0002g0268 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(682): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852655 | G | GATCCCAT others(673): Show |
1 | a0002c0002t0002g0266 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(682): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | ||||||
| chr16:89852661 | A | C | 6 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0001c0001t0001g0225 others(3): Show |
6 | HG00741.hp2 HG01074.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1625A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852661 | |||||||
| chr16:89852664 | G | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0175 others(3): Show |
6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1622G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852664 | |||||||
| chr16:89852665 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0175 others(3): Show |
6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1621C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852665 | |||||||
| chr16:89852665 | CCCGTCAT others(33): Show |
C | 8 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0070 others(5): Show |
8 | HG00408.hp2 HG00741.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-1615_646-1576d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852665 | ||||||
| chr16:89852668 | G | A | 8 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0175 others(5): Show |
8 | HG01106.hp2 HG01261.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.646-1618G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852668 | |||||||
| chr16:89852671 | A | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(219): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.646-1615A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852671 | |||||||
| chr16:89852673 | C | A | 7 | a0002c0002t0002g0256 a0002c0002t0002g0260 a0002c0002t0002g0267 others(4): Show |
7 | HG02015.hp1 HG02080.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1613C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852673 | |||||||
| chr16:89852675 | G | A | 7 | a0001c0001t0001g0079 a0001c0001t0001g0097 a0001c0001t0001g0175 others(4): Show |
7 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1611G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852675 | |||||||
| chr16:89852678 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(190): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.646-1608T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852678 | |||||||
| chr16:89852681 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(188): Show |
192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.646-1605T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852681 | |||||||
| chr16:89852683 | T | C | 2 | a0001c0001t0001g0206 a0001c0009t0001g0010 |
2 | HG01261.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.646-1603T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852683 | |||||||
| chr16:89852684 | C | CCACCCCC others(31): Show |
1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.646-1602_646-1601i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852684 | |||||||
| chr16:89852685 | T | C | 2 | a0001c0001t0001g0206 a0001c0009t0001g0010 |
2 | HG01261.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.646-1601T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852685 | |||||||
| chr16:89852694 | G | A | 7 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0096 others(4): Show |
7 | HG00621.hp2 HG01256.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-1592G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852694 | |||||||
| chr16:89852694 | G | C | 1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.646-1592G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852694 | |||||||
| chr16:89852695 | G | C | 49 | a0001c0001t0001g0050 a0001c0001t0001g0074 a0001c0001t0001g0092 others(46): Show |
49 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.646-1591G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852695 | |||||||
| chr16:89852695 | G | T | 1 | a0001c0009t0001g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.646-1591G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852695 | |||||||
| chr16:89852696 | A | C | 1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.646-1590A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852696 | |||||||
| chr16:89852697 | T | A | 1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.646-1589T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852697 | |||||||
| chr16:89852698 | C | T | 2 | a0001c0006t0001g0015 a0001c0009t0001g0010 |
2 | HG03669.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.646-1588C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852698 | |||||||
| chr16:89852701 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.646-1585A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852701 | |||||||
| chr16:89852703 | G | GGCCCGTC others(230): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.646-1583_646-1582i others(239): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | |||||||
| chr16:89852703 | G | GGCCCGTC others(270): Show |
1 | a0001c0001t0001g0031 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.646-1583_646-1582i others(279): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | |||||||
| chr16:89852703 | G | GGCCCGTC others(310): Show |
1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.646-1583_646-1582i others(319): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | |||||||
| chr16:89852703 | G | GGCCCGTC others(110): Show |
1 | a0001c0001t0001g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.646-1583_646-1582i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | |||||||
| chr16:89852704 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(188): Show |
192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.646-1582A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852704 | |||||||
| chr16:89852705 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(188): Show |
192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.646-1581T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852705 | |||||||
| chr16:89852705 | T | TCCATCTT others(153): Show |
1 | a0001c0001t0001g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(994): Show |
1 | a0001c0001t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1003): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(33): Show |
19 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0131 others(16): Show |
19 | HG00597.hp1 HG00733.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.646-1579_646-1578i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(553): Show |
1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(562): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(74): Show |
1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(83): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(73): Show |
6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0289 others(3): Show |
6 | HG01109.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1579_646-1578i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(313): Show |
1 | a0001c0001t0001g0351 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(711): Show |
1 | a0001c0027t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(720): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(153): Show |
1 | a0001c0001t0001g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(113): Show |
4 | a0004c0005t0001g0298 a0004c0005t0001g0299 a0004c0005t0001g0300 others(1): Show |
4 | HG02602.hp1 HG03688.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1579_646-1578i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(233): Show |
1 | a0001c0001t0001g0139 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(274): Show |
1 | a0001c0001t0001g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(283): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(153): Show |
1 | a0001c0001t0001g0067 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(193): Show |
1 | a0001c0001t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(473): Show |
1 | a0001c0001t0001g0194 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(353): Show |
1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(433): Show |
1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(442): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(473): Show |
1 | a0001c0003t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(73): Show |
1 | a0004c0005t0001g0304 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(393): Show |
1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(353): Show |
1 | a0001c0001t0003g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1434): Show |
1 | a0001c0001t0003g0325 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1443): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1313): Show |
2 | a0001c0001t0003g0321 a0001c0001t0003g0336 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.646-1579_646-1578i others(1322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1793): Show |
1 | a0001c0001t0003g0338 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1802): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1153): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1313): Show |
1 | a0001c0001t0003g0327 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1953): Show |
1 | a0001c0001t0003g0328 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1962): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1193): Show |
2 | a0001c0001t0003g0322 a0001c0001t0003g0323 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.646-1579_646-1578i others(1202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(953): Show |
1 | a0001c0001t0003g0335 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(962): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1233): Show |
1 | a0001c0001t0003g0324 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(393): Show |
1 | a0002c0002t0002g0278 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(433): Show |
1 | a0005c0007t0002g0275 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(442): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(273): Show |
1 | a0001c0001t0004g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(282): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(993): Show |
1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1002): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1073): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0183 |
3 | HG02109.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.646-1579_646-1578i others(1082): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(913): Show |
1 | a0001c0001t0001g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(922): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1073): Show |
1 | a0001c0001t0001g0181 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1082): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(1073): Show |
1 | a0001c0001t0001g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1082): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCATCTT others(233): Show |
1 | a0001c0001t0001g0286 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCGTCTT others(33): Show |
1 | a0001c0001t0001g0246 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.646-1471_646-1432d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCGTCTT others(73): Show |
1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.646-1511_646-1432d others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TCCGTCTT others(113): Show |
1 | a0001c0001t0001g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.646-1551_646-1432d others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | T | TGGC | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1581_646-1580i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852705 | |||||||
| chr16:89852705 | TCCGTCTT others(33): Show |
T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.646-1471_646-1432d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852705 | TCCGTCTT others(73): Show |
T | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.646-1511_646-1432d others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | ||||||
| chr16:89852708 | G | A | 21 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0088 others(18): Show |
21 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.646-1578G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852708 | |||||||
| chr16:89852711 | T | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0225 a0001c0001t0001g0230 others(5): Show |
8 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-1575T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852711 | |||||||
| chr16:89852714 | C | T | 23 | a0001c0001t0001g0082 a0002c0002t0002g0252 a0002c0002t0002g0254 others(20): Show |
23 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.646-1572C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852714 | |||||||
| chr16:89852715 | G | A | 20 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0088 others(17): Show |
20 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.646-1571G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852715 | |||||||
| chr16:89852718 | C | T | 6 | a0001c0001t0001g0160 a0001c0001t0001g0225 a0001c0001t0001g0230 others(3): Show |
6 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1568C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852718 | |||||||
| chr16:89852721 | C | T | 6 | a0001c0001t0001g0160 a0001c0001t0001g0225 a0001c0001t0001g0230 others(3): Show |
6 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1565C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852721 | |||||||
| chr16:89852734 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0043 others(16): Show |
21 | HG00408.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.646-1552G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852734 | |||||||
| chr16:89852735 | G | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(154): Show |
158 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.646-1551G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852735 | |||||||
| chr16:89852735 | G | GATCCCAT others(152): Show |
1 | a0001c0001t0001g0044 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.646-1512_646-1511i others(161): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852735 | ||||||
| chr16:89852735 | G | GATCCCAT others(353): Show |
2 | a0002c0002t0002g0280 a0002c0002t0002g0281 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.646-1474_646-1473i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852735 | ||||||
| chr16:89852735 | G | GATCCCAT others(473): Show |
1 | a0002c0002t0002g0260 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.646-1474_646-1473i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852735 | ||||||
| chr16:89852741 | A | ATGGCCCA others(32): Show |
1 | a0001c0001t0001g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.646-1539_646-1538i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852741 | ||||||
| chr16:89852744 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0225 a0007c0010t0008g0312 |
3 | HG01074.hp1 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.646-1542G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852744 | |||||||
| chr16:89852745 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0225 a0007c0010t0008g0312 |
3 | HG01074.hp1 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.646-1541C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852745 | |||||||
| chr16:89852748 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.646-1538G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852748 | |||||||
| chr16:89852748 | G | GTCTTCCG others(153): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0242 |
2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.646-1419_646-1418i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852748 | ||||||
| chr16:89852748 | GTCTTCCG others(113): Show |
G | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.646-1471_646-1352d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852748 | ||||||
| chr16:89852751 | T | A | 2 | a0001c0001t0001g0206 a0001c0001t0002g0282 |
2 | HG00673.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.646-1535T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852751 | |||||||
| chr16:89852755 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.646-1531G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852755 | |||||||
| chr16:89852758 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0353 a0003c0004t0001g0059 |
3 | HG01261.hp1 HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.646-1528C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852758 | |||||||
| chr16:89852761 | C | CCTCTCAC others(33): Show |
1 | a0001c0001t0001g0082 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.646-1516_646-1515i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852761 | ||||||
| chr16:89852761 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0353 a0003c0004t0001g0059 |
3 | HG01261.hp1 HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.646-1525C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852761 | |||||||
| chr16:89852774 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0030 others(13): Show |
16 | HG00099.hp2 HG00621.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-1512G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852774 | |||||||
| chr16:89852775 | G | C | 69 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0052 others(66): Show |
69 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.646-1511G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852775 | |||||||
| chr16:89852775 | G | GATCCCAT others(591): Show |
1 | a0001c0001t0001g0347 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.646-1489_646-1488i others(600): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852775 | ||||||
| chr16:89852784 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0353 |
2 | HG01261.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.646-1502G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852784 | |||||||
| chr16:89852785 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0353 |
2 | HG01261.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.646-1501C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852785 | |||||||
| chr16:89852788 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0353 |
2 | HG02293.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.646-1498G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852788 | |||||||
| chr16:89852788 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.646-1498G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852788 | |||||||
| chr16:89852788 | GTCTTCCG others(73): Show |
G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0001g0080 others(1): Show |
4 | HG00408.hp2 NA19005.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1418_646-1339d others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852788 | ||||||
| chr16:89852791 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.646-1495T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852791 | |||||||
| chr16:89852794 | C | CGTCCTCC others(353): Show |
1 | a0002c0002t0002g0256 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.646-1474_646-1473i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852794 | ||||||
| chr16:89852795 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0353 a0007c0010t0001g0313 |
3 | HG02293.hp2 HG03017.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.646-1491G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852795 | |||||||
| chr16:89852798 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0345 |
2 | HG01192.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.646-1488C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852798 | |||||||
| chr16:89852801 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0345 |
2 | HG01192.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.646-1485C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852801 | |||||||
| chr16:89852814 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.646-1472G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | |||||||
| chr16:89852814 | G | GCATCCCA others(73): Show |
1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.646-1472_646-1471i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | |||||||
| chr16:89852814 | G | GCATCCCA others(273): Show |
1 | a0001c0001t0001g0348 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.646-1472_646-1471i others(282): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | |||||||
| chr16:89852814 | G | GCATCCCA others(193): Show |
1 | a0010c0017t0001g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.646-1472_646-1471i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | |||||||
| chr16:89852814 | G | GGATCCCA others(553): Show |
1 | a0001c0001t0001g0345 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.646-1463_646-1462i others(562): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852814 | ||||||
| chr16:89852815 | G | C | 64 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0050 others(61): Show |
64 | HG00597.hp1 HG00733.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.646-1471G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852815 | |||||||
| chr16:89852821 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.646-1465A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852821 | |||||||
| chr16:89852824 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0003g0326 |
2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.646-1462G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852824 | |||||||
| chr16:89852825 | C | CCCGTCTT others(33): Show |
1 | a0002c0002t0002g0267 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.646-1451_646-1450i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852825 | ||||||
| chr16:89852825 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0003g0326 |
2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.646-1461C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852825 | |||||||
| chr16:89852828 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.646-1458G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852828 | |||||||
| chr16:89852828 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.646-1458G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852828 | |||||||
| chr16:89852828 | GTCTTCCG others(33): Show |
G | 1 | a0001c0001t0001g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.646-1431_646-1392d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852828 | ||||||
| chr16:89852835 | G | A | 3 | a0001c0001t0001g0050 a0001c0019t0001g0316 a0007c0010t0001g0313 |
3 | HG03139.hp1 NA19007.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.646-1451G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852835 | |||||||
| chr16:89852837 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.646-1449C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852837 | |||||||
| chr16:89852847 | A | ACCCCCCG others(314): Show |
1 | a0001c0006t0001g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-1432_646-1431i others(323): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852847 | ||||||
| chr16:89852851 | C | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-1435C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852851 | |||||||
| chr16:89852853 | C | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-1433C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852853 | |||||||
| chr16:89852853 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.646-1433C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852853 | |||||||
| chr16:89852854 | G | A | 30 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0086 others(27): Show |
30 | HG00280.hp1 HG00621.hp2 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.646-1432G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852854 | |||||||
| chr16:89852854 | G | GGATCCCA others(33): Show |
1 | a0001c0001t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.646-1432_646-1431i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852854 | |||||||
| chr16:89852854 | G | GGATCCCA others(153): Show |
1 | a0001c0001t0001g0039 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.646-1432_646-1431i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852854 | |||||||
| chr16:89852855 | C | CATCCCAT others(353): Show |
1 | a0001c0001t0001g0350 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.646-1419_646-1418i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | ||||||
| chr16:89852855 | C | CATCCCAT others(33): Show |
1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.646-1419_646-1418i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | ||||||
| chr16:89852855 | C | CATCCCAT others(473): Show |
1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.646-1419_646-1418i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | ||||||
| chr16:89852855 | C | CATCCCAT others(33): Show |
1 | a0001c0001t0001g0353 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.646-1419_646-1418i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | ||||||
| chr16:89852855 | C | CATCCCAT others(73): Show |
7 | a0001c0001t0001g0097 a0001c0001t0001g0152 a0001c0001t0001g0283 others(4): Show |
7 | HG00597.hp1 HG01106.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1419_646-1418i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | ||||||
| chr16:89852855 | C | CATCCCAT others(113): Show |
11 | a0001c0001t0001g0057 a0001c0001t0001g0063 a0001c0001t0001g0079 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-1419_646-1418i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | ||||||
| chr16:89852855 | C | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.646-1431C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852855 | |||||||
| chr16:89852861 | A | ATGGCCCG others(33): Show |
5 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0294 others(2): Show |
5 | HG01109.hp1 HG01123.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1419_646-1418i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852861 | ||||||
| chr16:89852861 | A | ATGGCCCG others(193): Show |
1 | a0001c0001t0001g0291 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.646-1419_646-1418i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852861 | ||||||
| chr16:89852861 | A | ATGGCCCG others(753): Show |
1 | a0001c0001t0001g0341 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.646-1419_646-1418i others(762): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852861 | ||||||
| chr16:89852861 | A | C | 1 | a0001c0001t0001g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.646-1425A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852861 | |||||||
| chr16:89852868 | C | A | 9 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(6): Show |
9 | HG01109.hp1 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1418C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852868 | |||||||
| chr16:89852868 | C | CTCTTCCG others(113): Show |
6 | a0001c0001t0001g0201 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
6 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1332_646-1331i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852868 | ||||||
| chr16:89852868 | C | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.646-1418C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852868 | |||||||
| chr16:89852868 | C | TTCTTCCG others(113): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.646-1418delCinsTTC others(118): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852868 | |||||||
| chr16:89852875 | G | A | 1 | a0001c0001t0003g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.646-1411G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852875 | |||||||
| chr16:89852875 | G | GTCCTCCC others(193): Show |
1 | a0009c0022t0001g0034 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.646-1396_646-1395i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852875 | ||||||
| chr16:89852891 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0284 |
2 | HG03209.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.646-1395C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852891 | |||||||
| chr16:89852893 | C | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0284 |
2 | HG03209.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.646-1393C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852893 | |||||||
| chr16:89852893 | C | CAGATCCC others(33): Show |
4 | a0001c0003t0001g0089 a0001c0003t0001g0137 a0001c0003t0001g0138 others(1): Show |
4 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1393_646-1392i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852893 | |||||||
| chr16:89852894 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0134 a0001c0001t0001g0284 |
3 | HG03209.hp2 HG04199.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.646-1392G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852894 | |||||||
| chr16:89852895 | G | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0092 others(46): Show |
51 | HG00099.hp1 HG00741.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.646-1391G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852895 | |||||||
| chr16:89852895 | G | GATCCCAT others(113): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG02698.hp2 HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.646-1353_646-1352i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | ||||||
| chr16:89852895 | G | GATCCCAT others(153): Show |
2 | a0001c0006t0001g0019 a0001c0006t0001g0020 |
2 | HG03490.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.646-1353_646-1352i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | ||||||
| chr16:89852895 | G | GATCCCAT others(33): Show |
2 | a0001c0001t0001g0218 a0001c0001t0001g0243 |
2 | HG00733.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.646-1371_646-1332d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | ||||||
| chr16:89852895 | G | GATCCCAT others(73): Show |
1 | a0001c0001t0001g0156 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | ||||||
| chr16:89852895 | G | GATCCCAT others(313): Show |
2 | a0004c0005t0001g0303 a0004c0005t0001g0306 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.646-1352_646-1351i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | ||||||
| chr16:89852895 | G | GATCCCAT others(113): Show |
1 | a0001c0001t0001g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | ||||||
| chr16:89852895 | G | GATCCCAT others(313): Show |
1 | a0001c0001t0001g0130 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.646-1356_646-1355i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | ||||||
| chr16:89852908 | G | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG01074.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.646-1378G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852908 | |||||||
| chr16:89852908 | G | GTCTTCCA others(33): Show |
1 | a0001c0001t0001g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.646-1372_646-1371i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852908 | ||||||
| chr16:89852908 | G | GTCTTCCA others(353): Show |
3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0235 |
3 | HG01123.hp1 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.646-1372_646-1371i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852908 | ||||||
| chr16:89852908 | G | GTCTTCCA others(273): Show |
1 | a0001c0001t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-1372_646-1371i others(282): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852908 | ||||||
| chr16:89852915 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0292 a0004c0005t0001g0301 |
3 | HG00099.hp1 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.646-1371G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852915 | |||||||
| chr16:89852915 | G | GTCCTCCC others(713): Show |
1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(722): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852915 | ||||||
| chr16:89852921 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.646-1365C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852921 | |||||||
| chr16:89852931 | C | T | 2 | a0001c0001t0001g0043 a0009c0022t0001g0034 |
2 | HG01928.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.646-1355C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852931 | |||||||
| chr16:89852933 | C | A | 2 | a0001c0001t0001g0043 a0009c0022t0001g0034 |
2 | HG01928.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.646-1353C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852933 | |||||||
| chr16:89852934 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0179 a0009c0022t0001g0034 |
3 | HG01928.hp1 NA19067.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.646-1352G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852934 | |||||||
| chr16:89852934 | G | GGATCCCA others(313): Show |
1 | a0001c0001t0001g0107 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852934 | |||||||
| chr16:89852935 | C | CATCCCAT others(113): Show |
1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-1332_646-1331i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | ||||||
| chr16:89852935 | C | CATCCCAT others(33): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0171 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.646-1332_646-1331i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | ||||||
| chr16:89852935 | C | CATCCCAT others(73): Show |
1 | a0001c0001t0001g0101 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.646-1332_646-1331i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | ||||||
| chr16:89852935 | C | CATCCCAT others(233): Show |
1 | a0002c0002t0002g0267 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.646-1333_646-1332i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | ||||||
| chr16:89852935 | C | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
174 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.646-1351C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852935 | |||||||
| chr16:89852944 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.646-1342G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852944 | |||||||
| chr16:89852948 | G | GTCTTCCG others(153): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0154 |
2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.646-1332_646-1331i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852948 | ||||||
| chr16:89852948 | G | GTCTTCCG others(73): Show |
1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.646-1332_646-1331i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852948 | ||||||
| chr16:89852955 | A | ATCCTCCC others(33): Show |
18 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0290 others(15): Show |
18 | HG00735.hp2 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.646-1312_646-1311i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | ||||||
| chr16:89852955 | A | ATCCTCCC others(113): Show |
1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.646-1312_646-1311i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | ||||||
| chr16:89852955 | A | ATCCTCCC others(153): Show |
1 | a0001c0001t0010g0349 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.646-1312_646-1311i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | ||||||
| chr16:89852955 | A | ATCCTCCC others(73): Show |
1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.646-1292_646-1291i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | ||||||
| chr16:89852955 | A | ATCCTCCC others(1673): Show |
1 | a0001c0001t0003g0339 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.646-1316_646-1315i others(1682): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | ||||||
| chr16:89852955 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.646-1331A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852955 | |||||||
| chr16:89852967 | A | ACCCCCCG others(118): Show |
1 | a0001c0001t0001g0179 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.646-1307_646-1306i others(127): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852967 | ||||||
| chr16:89852971 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0208 |
2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.646-1315C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852971 | |||||||
| chr16:89852973 | C | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0208 |
2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.646-1313C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852973 | |||||||
| chr16:89852974 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0208 a0006c0023t0001g0249 |
3 | HG01256.hp2 HG01346.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.646-1312G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852974 | |||||||
| chr16:89852974 | GGATCCCA others(33): Show |
G | 1 | a0008c0020t0001g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.646-1298_646-1259d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852974 | ||||||
| chr16:89852975 | G | C | 1 | a0001c0001t0003g0340 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.646-1311G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852975 | |||||||
| chr16:89852995 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
257 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.646-1291A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852995 | |||||||
| chr16:89853028 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0176 a0001c0001t0001g0283 |
3 | HG00673.hp2 HG01192.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.646-1258A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853028 | |||||||
| chr16:89853081 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-1205C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853081 | |||||||
| chr16:89853310 | ACTTT | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.646-971_646-968del others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89853310 | ||||||
| chr16:89853476 | C | T | 12 | a0001c0001t0003g0321 a0001c0001t0003g0322 a0001c0001t0003g0323 others(9): Show |
12 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.646-810C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853476 | |||||||
| chr16:89853602 | C | T | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646-684C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853602 | |||||||
| chr16:89853617 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.646-669C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853617 | |||||||
| chr16:89853679 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.646-607C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853679 | |||||||
| chr16:89853705 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.646-581G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853705 | |||||||
| chr16:89853738 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.646-548G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853738 | |||||||
| chr16:89853794 | G | A | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.646-492G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853794 | |||||||
| chr16:89853911 | C | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-375C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853911 | |||||||
| chr16:89853975 | C | A | 33 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.646-311C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853975 | |||||||
| chr16:89853991 | C | A | 3 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 |
3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.646-295C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853991 | |||||||
| chr16:89854089 | C | T | 39 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0050 others(36): Show |
39 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.646-197C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89854089 | |||||||
| chr16:89854105 | T | G | 1 | a0001c0001t0003g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.646-181T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89854105 | |||||||
| chr16:89854195 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.646-91C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89854195 | |||||||
| chr16:89854405 | C | T | 1 | a0003c0004t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.726+39C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 4/14 | chr16 | 89854405 | |||||||
| chr16:89854649 | A | ATGGTGAG others(39): Show |
1 | a0014c0015t0002g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.891+12_891+57dupAG others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854649 | ||||||
| chr16:89854649 | A | ATGGTGAG others(85): Show |
1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.891+57_891+58insAG others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854649 | ||||||
| chr16:89854649 | A | ATGGTGAG others(85): Show |
26 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 others(23): Show |
26 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.891+59_891+60insCC others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854649 | ||||||
| chr16:89854663 | A | G | 2 | a0001c0019t0001g0316 a0007c0010t0001g0313 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.891+12A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854663 | |||||||
| chr16:89854665 | A | ACGCAGAG others(39): Show |
2 | a0005c0007t0002g0269 a0005c0014t0002g0279 |
2 | HG00621.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.891+59_891+60insCC others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854665 | ||||||
| chr16:89854665 | A | C | 2 | a0001c0019t0001g0316 a0007c0010t0001g0313 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.891+14A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854665 | |||||||
| chr16:89854670 | GA | G | 3 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 |
3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.891+20delA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854670 | |||||||
| chr16:89854674 | GGCAGCCT others(39): Show |
G | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.891+36_891+81delCA others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854674 | ||||||
| chr16:89854695 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.891+44G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854695 | |||||||
| chr16:89854709 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0177 a0001c0009t0001g0009 others(2): Show |
5 | HG03669.hp2 HG04115.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+58G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854709 | |||||||
| chr16:89854711 | A | ACGCAGAG others(85): Show |
1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.891+66_891+67insGG others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854711 | ||||||
| chr16:89854711 | A | C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(53): Show |
56 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.891+60A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854711 | |||||||
| chr16:89854718 | T | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(56): Show |
59 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.891+67T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854718 | |||||||
| chr16:89854720 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(56): Show |
59 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.891+69A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854720 | |||||||
| chr16:89854735 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.891+84G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854735 | |||||||
| chr16:89854939 | A | AT | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.891+298dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854939 | ||||||
| chr16:89855001 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.891+350C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855001 | |||||||
| chr16:89855004 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.891+353C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855004 | |||||||
| chr16:89855042 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.891+391G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855042 | |||||||
| chr16:89855123 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.891+472A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855123 | |||||||
| chr16:89855150 | C | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0224 |
2 | HG01074.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.892-450C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855150 | |||||||
| chr16:89855180 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.892-420T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855180 | |||||||
| chr16:89855185 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.892-415A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855185 | |||||||
| chr16:89855222 | G | A | 1 | a0001c0001t0003g0335 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.892-378G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855222 | |||||||
| chr16:89855257 | C | G | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.892-343C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855257 | |||||||
| chr16:89855387 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892-213C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855387 | |||||||
| chr16:89855412 | C | A | 11 | a0001c0001t0003g0321 a0001c0001t0003g0322 a0001c0001t0003g0323 others(8): Show |
11 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.892-188C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855412 | |||||||
| chr16:89855585 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.892-15C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855585 | |||||||
| chr16:89855810 | C | T | 1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.978+124C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855810 | |||||||
| chr16:89855824 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.978+138C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855824 | |||||||
| chr16:89855856 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0004g0151 |
3 | NA18974.hp1 NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.978+170C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855856 | |||||||
| chr16:89855973 | G | T | 2 | a0004c0005t0001g0303 a0004c0005t0001g0306 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.979-140G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855973 | |||||||
| chr16:89855990 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.979-123G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855990 | |||||||
| chr16:89856018 | A | G | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.979-95A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89856018 | |||||||
| chr16:89856057 | CGCTTCCC others(13): Show |
C | 3 | a0001c0001t0001g0063 a0001c0019t0001g0316 a0007c0010t0001g0313 |
3 | HG03139.hp1 NA18954.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.979-37_979-18delCT others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 89856057 | ||||||
| chr16:89856077 | T | C | 40 | a0001c0001t0001g0345 a0001c0001t0001g0348 a0001c0001t0001g0350 others(37): Show |
40 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-36T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89856077 | |||||||
| chr16:89856319 | A | C | 2 | a0001c0001t0001g0174 a0010c0017t0001g0172 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1102+83A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856319 | |||||||
| chr16:89856327 | G | A | 16 | a0001c0001t0001g0092 a0001c0001t0001g0101 a0001c0001t0001g0139 others(13): Show |
16 | HG00733.hp2 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1102+91G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856327 | |||||||
| chr16:89856340 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1102+104C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856340 | |||||||
| chr16:89856459 | G | C | 1 | a0001c0003t0001g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1102+223G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856459 | |||||||
| chr16:89856508 | G | A | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1102+272G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856508 | |||||||
| chr16:89856530 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1102+294C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856530 | |||||||
| chr16:89856538 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1102+302G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856538 | |||||||
| chr16:89856547 | T | G | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1102+311T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856547 | |||||||
| chr16:89856551 | G | T | 33 | a0001c0001t0002g0036 a0002c0002t0002g0250 a0002c0002t0002g0252 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1102+315G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856551 | |||||||
| chr16:89856611 | AT | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0055 others(15): Show |
18 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1102+395delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89856611 | ||||||
| chr16:89856611 | ATT | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1102+394_1102+395d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89856611 | ||||||
| chr16:89856611 | ATTT | A | 13 | a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0001g0086 others(10): Show |
13 | HG02083.hp1 HG02083.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+393_1102+395d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89856611 | ||||||
| chr16:89856718 | C | T | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1102+482C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856718 | |||||||
| chr16:89856822 | A | C | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1102+586A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856822 | |||||||
| chr16:89856985 | G | A | 2 | a0004c0005t0001g0298 a0004c0005t0001g0305 |
2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1102+749G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856985 | |||||||
| chr16:89856993 | G | A | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0018t0012g0346 |
3 | HG01243.hp1 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1102+757G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856993 | |||||||
| chr16:89857004 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
302 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1102+768C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857004 | |||||||
| chr16:89857065 | C | CA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0055 others(41): Show |
44 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1102+844dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857065 | ||||||
| chr16:89857136 | C | CT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1102+918dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857136 | ||||||
| chr16:89857136 | CT | C | 28 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0337 others(25): Show |
28 | HG00099.hp2 HG01081.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1102+918delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857136 | ||||||
| chr16:89857177 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0011t0001g0317 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+941C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857177 | |||||||
| chr16:89857351 | G | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1103-987G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857351 | |||||||
| chr16:89857396 | G | A | 4 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 others(1): Show |
4 | HG02451.hp2 HG03669.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-942G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857396 | |||||||
| chr16:89857427 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1103-911T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857427 | |||||||
| chr16:89857498 | C | T | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1103-840C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857498 | |||||||
| chr16:89857552 | T | A | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1103-786T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857552 | |||||||
| chr16:89857558 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1103-780G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857558 | |||||||
| chr16:89857601 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1103-737G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857601 | |||||||
| chr16:89857603 | C | T | 1 | a0001c0027t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1103-735C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857603 | |||||||
| chr16:89857609 | T | G | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1103-729T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857609 | |||||||
| chr16:89857620 | G | T | 1 | a0001c0001t0003g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1103-718G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857620 | |||||||
| chr16:89857624 | G | A | 2 | a0001c0003t0001g0110 a0001c0003t0001g0113 |
2 | NA18970.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1103-714G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857624 | |||||||
| chr16:89857714 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1103-624G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857714 | |||||||
| chr16:89857720 | G | A | 1 | a0003c0004t0001g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1103-618G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857720 | |||||||
| chr16:89857793 | C | T | 1 | a0001c0021t0001g0211 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1103-545C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857793 | |||||||
| chr16:89857849 | C | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0218 a0001c0001t0001g0234 others(1): Show |
4 | HG00733.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-489C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857849 | |||||||
| chr16:89857850 | G | A | 3 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 |
3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1103-488G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857850 | |||||||
| chr16:89857881 | C | CT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1103-438dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857881 | ||||||
| chr16:89857881 | CT | C | 7 | a0001c0001t0001g0202 a0001c0001t0001g0217 a0001c0001t0001g0219 others(4): Show |
7 | HG00099.hp2 HG01070.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1103-438delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857881 | ||||||
| chr16:89857883 | T | TC | 16 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0165 others(13): Show |
16 | HG00099.hp1 HG00735.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1103-455_1103-454i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857883 | |||||||
| chr16:89857884 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0225 |
2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1103-454T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857884 | |||||||
| chr16:89857916 | T | C | 3 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 |
3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1103-422T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857916 | |||||||
| chr16:89857951 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1103-387C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857951 | |||||||
| chr16:89857994 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1103-344T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857994 | |||||||
| chr16:89858007 | C | T | 13 | a0001c0001t0001g0101 a0001c0001t0001g0139 a0001c0001t0001g0155 others(10): Show |
13 | HG00733.hp2 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1103-331C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858007 | |||||||
| chr16:89858038 | A | G | 20 | a0001c0001t0001g0135 a0001c0001t0001g0159 a0001c0001t0001g0160 others(17): Show |
20 | HG01891.hp2 HG02145.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1103-300A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858038 | |||||||
| chr16:89858121 | G | A | 21 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(18): Show |
21 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1103-217G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858121 | |||||||
| chr16:89858128 | A | G | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1103-210A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858128 | |||||||
| chr16:89858134 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1103-204C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858134 | |||||||
| chr16:89858136 | T | C | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1103-202T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858136 | |||||||
| chr16:89858162 | G | A | 2 | a0001c0011t0001g0317 a0001c0011t0001g0318 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1103-176G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858162 | |||||||
| chr16:89858542 | G | A | 3 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 |
3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1272+35G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858542 | |||||||
| chr16:89858609 | G | C | 3 | a0001c0009t0001g0009 a0001c0009t0001g0010 a0001c0009t0001g0014 |
3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1272+102G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858609 | |||||||
| chr16:89858711 | C | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+204C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858711 | |||||||
| chr16:89858762 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1272+255C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858762 | |||||||
| chr16:89858846 | C | T | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1273-319C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858846 | |||||||
| chr16:89859148 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1273-17G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89859148 | |||||||
| chr16:89859500 | C | T | 1 | a0001c0003t0001g0111 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1462+146C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859500 | |||||||
| chr16:89859689 | G | T | 1 | a0008c0020t0001g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1462+335G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859689 | |||||||
| chr16:89859697 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1462+343G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859697 | |||||||
| chr16:89859766 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1462+412G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859766 | |||||||
| chr16:89859785 | G | A | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1462+431G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859785 | |||||||
| chr16:89859986 | G | A | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1462+632G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859986 | |||||||
| chr16:89859995 | G | C | 1 | a0004c0005t0001g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1462+641G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859995 | |||||||
| chr16:89860046 | C | A | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1463-637C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860046 | |||||||
| chr16:89860110 | T | G | 1 | a0003c0004t0001g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1463-573T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860110 | |||||||
| chr16:89860185 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1463-498C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860185 | |||||||
| chr16:89860214 | C | T | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1463-469C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860214 | |||||||
| chr16:89860311 | T | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1463-372T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860311 | |||||||
| chr16:89860331 | T | C | 1 | a0008c0020t0001g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1463-352T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860331 | |||||||
| chr16:89860365 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1463-318C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860365 | |||||||
| chr16:89860413 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0337 a0001c0001t0001g0342 others(11): Show |
14 | HG01109.hp2 HG01192.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1463-270G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860413 | |||||||
| chr16:89860462 | C | T | 34 | a0001c0001t0001g0025 a0001c0001t0001g0189 a0001c0001t0001g0191 others(31): Show |
34 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1463-221C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860462 | |||||||
| chr16:89860810 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1575+15G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860810 | |||||||
| chr16:89860857 | C | T | 34 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0002c0002t0002g0250 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1575+62C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860857 | |||||||
| chr16:89860908 | G | A | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1575+113G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860908 | |||||||
| chr16:89860917 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1575+122G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860917 | |||||||
| chr16:89860920 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0097 |
3 | HG02622.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1575+125C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860920 | |||||||
| chr16:89860926 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1575+131G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860926 | |||||||
| chr16:89860926 | G | T | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1575+131G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860926 | |||||||
| chr16:89860945 | T | TC | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1575+150_1575+151i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860945 | |||||||
| chr16:89860949 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0295 a0001c0001t0001g0308 |
3 | HG01109.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1575+154G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860949 | |||||||
| chr16:89860974 | G | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0329 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1575+179G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860974 | |||||||
| chr16:89861117 | G | C | 1 | a0005c0007t0002g0275 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1575+322G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861117 | |||||||
| chr16:89861387 | G | A | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1575+592G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861387 | |||||||
| chr16:89861499 | C | G | 1 | a0001c0001t0004g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1575+704C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861499 | |||||||
| chr16:89861528 | G | A | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1575+733G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861528 | |||||||
| chr16:89861595 | CAAAT | C | 4 | a0001c0008t0001g0011 a0001c0008t0001g0012 a0001c0008t0001g0013 others(1): Show |
4 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+802_1575+805d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89861595 | ||||||
| chr16:89861705 | C | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0171 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1575+910C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861705 | |||||||
| chr16:89861716 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1575+921C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861716 | |||||||
| chr16:89861730 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1575+935C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861730 | |||||||
| chr16:89861834 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1575+1039C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861834 | |||||||
| chr16:89861905 | T | C | 1 | a0001c0001t0004g0083 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1575+1110T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861905 | |||||||
| chr16:89862003 | C | CT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0175 others(24): Show |
27 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1575+1225dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89862003 | ||||||
| chr16:89862054 | A | G | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1575+1259A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862054 | |||||||
| chr16:89862090 | G | A | 33 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1575+1295G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862090 | |||||||
| chr16:89862104 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1575+1309T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862104 | |||||||
| chr16:89862153 | A | G | 1 | a0001c0008t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-1323A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862153 | |||||||
| chr16:89862158 | C | A | 2 | a0003c0004t0001g0046 a0003c0004t0001g0075 |
2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1576-1318C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862158 | |||||||
| chr16:89862159 | G | A | 1 | a0001c0008t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-1317G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862159 | |||||||
| chr16:89862161 | A | G | 1 | a0001c0008t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-1315A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862161 | |||||||
| chr16:89862193 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1576-1283C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862193 | |||||||
| chr16:89862315 | T | C | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1576-1161T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862315 | |||||||
| chr16:89862327 | C | T | 1 | a0002c0002t0002g0274 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1576-1149C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862327 | |||||||
| chr16:89862374 | GAC | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1576-1098_1576-109 others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89862374 | ||||||
| chr16:89862446 | G | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1576-1030G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862446 | |||||||
| chr16:89862610 | C | G | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-866C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862610 | |||||||
| chr16:89862807 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1576-669C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862807 | |||||||
| chr16:89863054 | G | A | 1 | a0007c0010t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1576-422G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863054 | |||||||
| chr16:89863168 | A | G | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-308A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863168 | |||||||
| chr16:89863173 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1576-303G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863173 | |||||||
| chr16:89863321 | GGATGGCT others(9): Show |
G | 1 | a0001c0001t0001g0156 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1576-139_1576-124d others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89863321 | ||||||
| chr16:89863355 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0011t0001g0317 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-121G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863355 | |||||||
| chr16:89863434 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1576-42G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863434 | |||||||
| chr16:89863449 | G | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0171 |
3 | HG02622.hp1 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1576-27G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863449 | |||||||
| chr16:89863627 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1710+17G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863627 | |||||||
| chr16:89863668 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1710+58G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863668 | |||||||
| chr16:89863679 | T | A | 56 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0002g0036 others(53): Show |
56 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1710+69T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863679 | |||||||
| chr16:89863721 | G | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1711-73G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863721 | |||||||
| chr16:89863731 | G | C | 23 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(20): Show |
23 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1711-63G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863731 | |||||||
| chr16:89863734 | C | T | 1 | a0001c0003t0001g0198 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1711-60C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863734 | |||||||
| chr16:89863917 | G | A | 21 | a0001c0001t0002g0282 a0002c0002t0002g0250 a0002c0002t0002g0252 others(18): Show |
21 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1778+56G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89863917 | |||||||
| chr16:89864006 | G | A | 33 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1778+145G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864006 | |||||||
| chr16:89864018 | A | G | 56 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0002g0036 others(53): Show |
56 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1778+157A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864018 | |||||||
| chr16:89864173 | C | A | 1 | a0001c0019t0001g0316 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1778+312C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864173 | |||||||
| chr16:89864248 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1778+387A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864248 | |||||||
| chr16:89864329 | C | T | 1 | a0001c0001t0006g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1778+468C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864329 | |||||||
| chr16:89864331 | C | G | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1778+470C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864331 | |||||||
| chr16:89864332 | C | T | 1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1778+471C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864332 | |||||||
| chr16:89864382 | T | A | 1 | a0001c0003t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1778+521T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864382 | |||||||
| chr16:89864509 | G | A | 1 | a0004c0005t0001g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1778+648G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864509 | |||||||
| chr16:89864593 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1778+732C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864593 | |||||||
| chr16:89864599 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1778+738T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864599 | |||||||
| chr16:89864733 | T | G | 1 | a0001c0003t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1778+872T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864733 | |||||||
| chr16:89864735 | A | T | 1 | a0015c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1778+874A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864735 | |||||||
| chr16:89864831 | TCAACAAA others(9): Show |
T | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1778+973_1778+988d others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89864831 | ||||||
| chr16:89864995 | CT | C | 32 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0002c0002t0002g0252 others(29): Show |
32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1778+1141delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89864995 | ||||||
| chr16:89865002 | T | C | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1778+1141T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865002 | |||||||
| chr16:89865004 | C | CT | 55 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0039 others(52): Show |
55 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.1778+1163dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865004 | ||||||
| chr16:89865004 | C | T | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1778+1143C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865004 | |||||||
| chr16:89865004 | CT | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0063 a0001c0001t0001g0079 others(6): Show |
9 | HG01070.hp2 HG01099.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1778+1163delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865004 | ||||||
| chr16:89865063 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0296 |
2 | HG00735.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1778+1202G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865063 | |||||||
| chr16:89865069 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1778+1208C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865069 | |||||||
| chr16:89865078 | C | G | 9 | a0001c0001t0001g0342 a0001c0001t0003g0330 a0001c0001t0003g0331 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1778+1217C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865078 | |||||||
| chr16:89865093 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1778+1232G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865093 | |||||||
| chr16:89865098 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1778+1237C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865098 | |||||||
| chr16:89865106 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1778+1245C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865106 | |||||||
| chr16:89865130 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0329 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1778+1269C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865130 | |||||||
| chr16:89865357 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1778+1496G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865357 | |||||||
| chr16:89865566 | C | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(321): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.1778+1705C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865566 | |||||||
| chr16:89865638 | G | A | 8 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1778+1777G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865638 | |||||||
| chr16:89865735 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1778+1874A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865735 | |||||||
| chr16:89865965 | C | CA | 78 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0038 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1778+2126dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | ||||||
| chr16:89865965 | C | CAA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0024 others(39): Show |
44 | HG00642.hp1 HG00733.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.1778+2125_1778+212 others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | ||||||
| chr16:89865965 | C | CAAA | 7 | a0001c0001t0001g0155 a0001c0001t0001g0175 a0001c0001t0001g0188 others(4): Show |
7 | HG01123.hp1 HG01934.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1778+2124_1778+212 others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | ||||||
| chr16:89865965 | CA | C | 55 | a0001c0001t0001g0114 a0001c0001t0001g0179 a0001c0001t0001g0213 others(52): Show |
55 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1778+2126delA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | ||||||
| chr16:89866112 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1779-2077G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866112 | |||||||
| chr16:89866168 | T | C | 6 | a0001c0003t0001g0104 a0001c0003t0001g0111 a0001c0003t0005g0109 others(3): Show |
6 | HG00280.hp1 NA18970.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1779-2021T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866168 | |||||||
| chr16:89866308 | T | C | 11 | a0001c0001t0001g0176 a0001c0001t0001g0217 a0001c0006t0001g0015 others(8): Show |
11 | HG00099.hp2 HG01192.hp1 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.1779-1881T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866308 | |||||||
| chr16:89866492 | C | G | 1 | a0001c0001t0015g0125 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1779-1697C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866492 | |||||||
| chr16:89866523 | C | G | 33 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1779-1666C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866523 | |||||||
| chr16:89866586 | C | T | 22 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0003g0321 others(19): Show |
22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1779-1603C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866586 | |||||||
| chr16:89866599 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1779-1590A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866599 | |||||||
| chr16:89866599 | A | T | 2 | a0002c0002t0002g0250 a0002c0002t0002g0271 |
2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1779-1590A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866599 | |||||||
| chr16:89866599 | AT | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1779-1577delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89866599 | ||||||
| chr16:89866672 | A | G | 1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1779-1517A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866672 | |||||||
| chr16:89866898 | C | T | 33 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1779-1291C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866898 | |||||||
| chr16:89866916 | T | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1779-1273T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866916 | |||||||
| chr16:89867012 | A | G | 55 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0002g0036 others(52): Show |
55 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1779-1177A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867012 | |||||||
| chr16:89867093 | CTT | C | 8 | a0001c0006t0001g0015 a0001c0006t0001g0016 a0001c0006t0001g0017 others(5): Show |
8 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.1779-1094_1779-109 others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89867093 | ||||||
| chr16:89867101 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1779-1088G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867101 | |||||||
| chr16:89867124 | G | T | 1 | a0004c0005t0001g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1779-1065G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867124 | |||||||
| chr16:89867160 | T | C | 3 | a0001c0019t0001g0316 a0007c0010t0001g0313 a0007c0010t0008g0312 |
3 | HG02451.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1779-1029T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867160 | |||||||
| chr16:89867194 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0205 a0001c0001t0001g0236 |
3 | HG02559.hp2 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1779-995C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867194 | |||||||
| chr16:89867213 | C | T | 6 | a0001c0001t0001g0101 a0001c0001t0001g0139 a0001c0001t0001g0155 others(3): Show |
6 | HG00733.hp2 HG01071.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1779-976C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867213 | |||||||
| chr16:89867264 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1779-925C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867264 | |||||||
| chr16:89867304 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1779-885C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867304 | |||||||
| chr16:89867306 | GC | G | 34 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0050 others(31): Show |
34 | HG00280.hp1 HG00597.hp1 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.1779-882delC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867306 | |||||||
| chr16:89867369 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02738.hp1 HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1779-820A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867369 | |||||||
| chr16:89867421 | G | T | 2 | a0001c0019t0001g0316 a0007c0010t0001g0313 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1779-768G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867421 | |||||||
| chr16:89867443 | G | A | 33 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0050 others(30): Show |
33 | HG00280.hp1 HG00597.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1779-746G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867443 | |||||||
| chr16:89867451 | G | A | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1779-738G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867451 | |||||||
| chr16:89867587 | A | AT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0024 others(113): Show |
118 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1779-587dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89867587 | ||||||
| chr16:89867646 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1779-543G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867646 | |||||||
| chr16:89867841 | T | A | 1 | a0001c0003t0001g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1779-348T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867841 | |||||||
| chr16:89868115 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1779-74C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89868115 | |||||||
| chr16:89868122 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1779-67C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89868122 | |||||||
| chr16:89868346 | C | T | 1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1806+130C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868346 | |||||||
| chr16:89868391 | G | C | 2 | a0003c0004t0001g0046 a0003c0004t0001g0075 |
2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1806+175G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868391 | |||||||
| chr16:89868425 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1806+209C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868425 | |||||||
| chr16:89868437 | C | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0234 a0001c0001t0001g0243 |
3 | HG00733.hp2 HG01106.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1806+221C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868437 | |||||||
| chr16:89868478 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1806+262A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868478 | |||||||
| chr16:89868681 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1806+465C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868681 | |||||||
| chr16:89868891 | C | T | 2 | a0001c0001t0001g0174 a0001c0019t0001g0316 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1806+675C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868891 | |||||||
| chr16:89869032 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1807-535A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869032 | |||||||
| chr16:89869045 | A | AACATATA others(19): Show |
1 | a0002c0002t0002g0264 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1807-521_1807-520i others(28): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869045 | ||||||
| chr16:89869045 | A | ACAT | 3 | a0002c0002t0014g0272 a0005c0007t0002g0261 a0005c0014t0002g0279 |
3 | HG00621.hp1 HG02040.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(6): Show |
1 | a0002c0002t0002g0274 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1807-522_1807-521i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(10): Show |
1 | a0014c0015t0002g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1807-522_1807-521i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(12): Show |
8 | a0001c0001t0002g0282 a0002c0002t0002g0252 a0002c0002t0002g0260 others(5): Show |
8 | HG00673.hp1 HG02015.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-522_1807-521i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(14): Show |
2 | a0002c0002t0002g0255 a0002c0002t0002g0271 |
2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(16): Show |
4 | a0002c0002t0002g0250 a0002c0002t0002g0259 a0002c0002t0002g0266 others(1): Show |
4 | HG02165.hp1 NA18943.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-522_1807-521i others(25): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(18): Show |
2 | a0002c0002t0002g0257 a0002c0002t0002g0276 |
2 | HG02074.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(20): Show |
1 | a0002c0002t0002g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1807-522_1807-521i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(24): Show |
2 | a0002c0002t0002g0258 a0002c0002t0002g0278 |
2 | HG00323.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(26): Show |
3 | a0001c0001t0002g0036 a0002c0002t0002g0253 a0005c0007t0002g0275 |
3 | HG00609.hp1 HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869045 | A | ACATATAT others(30): Show |
2 | a0002c0002t0002g0256 a0005c0007t0002g0262 |
2 | HG01175.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | |||||||
| chr16:89869047 | A | AACATATA others(25): Show |
1 | a0001c0001t0003g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1807-519_1807-518i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869047 | ||||||
| chr16:89869047 | A | T | 33 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0002c0002t0002g0250 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1807-520A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869047 | |||||||
| chr16:89869049 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1807-518_1807-517i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869049 | |||||||
| chr16:89869049 | A | ATATATAT others(20): Show |
1 | a0001c0006t0001g0015 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1807-518_1807-517i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869049 | |||||||
| chr16:89869049 | A | T | 34 | a0001c0001t0002g0036 a0001c0001t0002g0282 a0001c0001t0003g0326 others(31): Show |
34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1807-518A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869049 | |||||||
| chr16:89869051 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0099 a0007c0010t0001g0313 |
2 | HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1807-516_1807-515i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869051 | |||||||
| chr16:89869051 | A | ATATATAT others(18): Show |
1 | a0010c0017t0001g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1807-516_1807-515i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869051 | |||||||
| chr16:89869051 | A | T | 36 | a0001c0001t0001g0233 a0001c0001t0002g0036 a0001c0001t0002g0282 others(33): Show |
36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1807-516A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869051 | |||||||
| chr16:89869053 | A | AAAAAAAA others(46): Show |
1 | a0001c0009t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(55): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0147 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(39): Show |
1 | a0001c0001t0010g0349 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(48): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(49): Show |
1 | a0001c0001t0001g0124 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(58): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0238 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0001g0123 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(32): Show |
1 | a0001c0001t0001g0047 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(34): Show |
2 | a0001c0001t0009g0145 a0003c0004t0001g0027 |
2 | HG00408.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0080 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(29): Show |
1 | a0003c0004t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(18): Show |
1 | a0003c0004t0001g0045 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(26): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0128 |
2 | HG01261.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0069 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(32): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0157 |
2 | HG02300.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(40): Show |
2 | a0001c0001t0001g0096 a0001c0001t0001g0350 |
2 | HG00733.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(49): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(11): Show |
1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0141 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(27): Show |
1 | a0001c0001t0011g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(33): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0084 |
3 | NA19000.hp2 NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0120 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(10): Show |
1 | a0006c0023t0001g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0001g0039 a0001c0001t0001g0152 a0001c0001t0001g0196 |
3 | HG00597.hp1 NA18522.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0119 |
4 | HG02615.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(24): Show |
1 | a0011c0026t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(28): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0142 |
2 | NA18612.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(34): Show |
1 | a0001c0001t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(36): Show |
1 | a0001c0001t0001g0130 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(45): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0235 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(11): Show |
7 | a0001c0001t0001g0055 a0001c0001t0001g0140 a0001c0001t0001g0186 others(4): Show |
7 | HG01928.hp2 HG01952.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(13): Show |
4 | a0001c0001t0001g0154 a0001c0001t0001g0353 a0001c0003t0001g0117 others(1): Show |
4 | HG02293.hp2 HG03942.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(17): Show |
1 | a0003c0004t0001g0046 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(28): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0043 |
2 | NA19000.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(25): Show |
4 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0127 others(1): Show |
4 | NA18979.hp2 NA18982.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(27): Show |
5 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0068 others(2): Show |
5 | HG02027.hp1 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0030 a0003c0004t0001g0059 |
2 | HG01358.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(33): Show |
1 | a0001c0001t0004g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0136 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(41): Show |
1 | a0001c0001t0001g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(50): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(4): Show |
3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG00642.hp1 HG01074.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(17): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(10): Show |
10 | a0001c0001t0001g0158 a0001c0001t0001g0185 a0001c0001t0001g0286 others(7): Show |
10 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(12): Show |
7 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0237 others(4): Show |
7 | HG00323.hp2 HG01891.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(14): Show |
2 | a0001c0003t0005g0109 a0001c0003t0005g0112 |
2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0050 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(31): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(26): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0146 a0003c0004t0001g0065 |
3 | HG02015.hp2 NA18940.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(28): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0094 a0001c0001t0004g0072 |
3 | HG00673.hp2 NA18971.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(30): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(32): Show |
3 | a0001c0001t0001g0121 a0001c0001t0001g0217 a0001c0001t0004g0151 |
3 | HG00099.hp2 HG02165.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(34): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0223 |
2 | HG01168.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(40): Show |
1 | a0008c0020t0001g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(49): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0228 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(12): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(11): Show |
7 | a0001c0001t0001g0155 a0001c0001t0001g0234 a0001c0001t0001g0288 others(4): Show |
7 | HG01106.hp1 HG02148.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(13): Show |
9 | a0001c0001t0001g0097 a0001c0001t0001g0187 a0001c0001t0001g0188 others(6): Show |
9 | HG02071.hp1 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0135 a0001c0001t0001g0292 a0001c0001t0001g0296 |
3 | HG00099.hp1 HG01978.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(25): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0194 |
2 | HG01256.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(27): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
2 | HG01255.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(29): Show |
3 | a0001c0001t0001g0179 a0001c0001t0001g0224 a0003c0004t0001g0064 |
3 | HG01074.hp2 HG03927.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(31): Show |
5 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0073 others(2): Show |
5 | NA18945.hp1 NA18945.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(33): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0114 others(1): Show |
4 | NA18943.hp2 NA19060.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAA others(35): Show |
1 | a0001c0009t0001g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAC others(24): Show |
1 | a0001c0001t0003g0323 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAC others(28): Show |
1 | a0001c0001t0003g0343 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAC others(34): Show |
1 | a0001c0001t0003g0338 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAC others(38): Show |
1 | a0001c0001t0003g0335 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(4): Show |
1 | a0003c0004t0001g0081 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(10): Show |
1 | a0001c0001t0001g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(12): Show |
6 | a0001c0001t0001g0182 a0001c0001t0001g0192 a0001c0001t0001g0287 others(3): Show |
6 | HG00280.hp1 HG01123.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(14): Show |
3 | a0001c0001t0001g0180 a0001c0001t0001g0189 a0001c0003t0001g0111 |
3 | HG02258.hp2 HG02970.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(16): Show |
1 | a0001c0001t0001g0101 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(25): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(24): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0283 |
2 | NA18951.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(28): Show |
2 | a0001c0001t0004g0132 a0001c0001t0015g0125 |
2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(34): Show |
1 | a0009c0022t0001g0034 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAAAT others(38): Show |
1 | a0001c0001t0001g0219 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAACA others(7): Show |
1 | a0001c0001t0003g0324 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(16): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAACA others(25): Show |
1 | a0001c0001t0003g0322 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAACA others(27): Show |
1 | a0001c0001t0003g0325 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAACA others(31): Show |
1 | a0001c0001t0003g0327 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAACA others(37): Show |
2 | a0001c0001t0003g0328 a0001c0001t0003g0336 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(5): Show |
1 | a0007c0010t0008g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(11): Show |
10 | a0001c0001t0001g0026 a0001c0001t0001g0139 a0001c0001t0001g0143 others(7): Show |
10 | HG00733.hp2 HG01071.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(13): Show |
7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0103 others(4): Show |
7 | HG00408.hp2 HG01884.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(15): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0174 |
2 | HG02027.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(24): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(21): Show |
1 | a0001c0001t0001g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(25): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0006c0024t0001g0153 |
3 | HG02071.hp2 HG03927.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(27): Show |
4 | a0001c0001t0001g0122 a0001c0001t0001g0310 a0001c0001t0004g0115 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(29): Show |
1 | a0001c0001t0004g0126 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(31): Show |
1 | a0001c0001t0001g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(33): Show |
1 | a0001c0001t0001g0035 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(35): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0195 |
2 | HG00438.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(39): Show |
1 | a0001c0001t0001g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(48): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAAATA others(51): Show |
1 | a0001c0001t0001g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(60): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAACAT others(30): Show |
1 | a0001c0001t0003g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(10): Show |
2 | a0004c0005t0001g0298 a0004c0005t0001g0305 |
2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(12): Show |
2 | a0001c0001t0001g0308 a0001c0001t0001g0320 |
2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(14): Show |
1 | a0001c0001t0001g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(16): Show |
3 | a0001c0001t0001g0171 a0001c0001t0001g0291 a0001c0001t0001g0293 |
3 | HG00735.hp2 HG01358.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(25): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(22): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0190 |
3 | HG02976.hp2 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(31): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(26): Show |
3 | a0001c0001t0001g0177 a0001c0001t0004g0116 a0001c0027t0001g0021 |
3 | HG01169.hp2 HG03831.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(28): Show |
1 | a0001c0001t0001g0309 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAAATAT others(32): Show |
1 | a0001c0003t0001g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAACAAA others(37): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0031 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(7): Show |
1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(16): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(9): Show |
1 | a0004c0005t0001g0299 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(11): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0183 |
2 | HG01516.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(15): Show |
2 | a0001c0001t0001g0175 a0001c0019t0001g0316 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(24): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(17): Show |
1 | a0001c0001t0001g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(21): Show |
1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAAATATA others(23): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0168 |
2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAACAAAC others(37): Show |
1 | a0001c0001t0003g0340 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAACAAAC others(30): Show |
1 | a0001c0001t0003g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAACAAAC others(32): Show |
1 | a0001c0001t0003g0339 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAACAAAC others(34): Show |
1 | a0001c0001t0003g0334 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAACAAAC others(36): Show |
2 | a0001c0001t0001g0342 a0001c0001t0003g0330 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(45): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAACAAAC others(38): Show |
1 | a0001c0001t0003g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAACAAAC others(32): Show |
2 | a0001c0001t0003g0331 a0001c0001t0003g0332 |
2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0181 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAATATAT others(14): Show |
1 | a0001c0012t0005g0051 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAATATAT others(18): Show |
1 | a0001c0001t0001g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAATATAT others(20): Show |
1 | a0001c0001t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(31): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAATATAT others(28): Show |
1 | a0001c0001t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AAATATAT others(34): Show |
1 | a0001c0001t0004g0314 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1807-511_1807-492d others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0053 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1807-513_1807-492d others(24): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | ||||||
| chr16:89869053 | A | ATATATAT others(4): Show |
1 | a0004c0005t0001g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1807-514_1807-513i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | |||||||
| chr16:89869053 | A | ATATATAT others(14): Show |
1 | a0001c0006t0001g0016 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1807-514_1807-513i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | |||||||
| chr16:89869053 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1807-514_1807-513i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | |||||||
| chr16:89869053 | A | ATATATAT others(24): Show |
1 | a0001c0006t0001g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1807-514_1807-513i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | |||||||
| chr16:89869053 | A | T | 45 | a0001c0001t0001g0099 a0001c0001t0001g0214 a0001c0001t0001g0221 others(42): Show |
45 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1807-514A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | |||||||
| chr16:89869054 | AT | A | 3 | a0001c0001t0001g0239 a0001c0008t0001g0011 a0001c0011t0001g0318 |
3 | HG02572.hp2 HG02647.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1807-512delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869054 | |||||||
| chr16:89869055 | T | A | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01081.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-512T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869055 | |||||||
| chr16:89869057 | T | A | 7 | a0001c0001t0001g0006 a0001c0008t0001g0011 a0001c0008t0001g0012 others(4): Show |
7 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-510T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869057 | |||||||
| chr16:89869059 | T | A | 5 | a0001c0001t0001g0006 a0001c0008t0001g0011 a0001c0008t0001g0012 others(2): Show |
5 | HG01167.hp2 HG02572.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1807-508T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869059 | |||||||
| chr16:89869072 | A | ATATATAT others(23): Show |
1 | a0001c0006t0001g0019 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | ||||||
| chr16:89869072 | A | ATATATAT others(21): Show |
1 | a0001c0006t0001g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | ||||||
| chr16:89869072 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1807-492_1807-491i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | ||||||
| chr16:89869072 | A | ATATATAT others(11): Show |
1 | a0001c0003t0001g0198 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | ||||||
| chr16:89869072 | A | ATATATAT others(18): Show |
1 | a0001c0009t0001g0014 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1807-492_1807-491i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | ||||||
| chr16:89869072 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | ||||||
| chr16:89869072 | A | ATGTATG | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1807-494_1807-493i others(8): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | ||||||
| chr16:89869072 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0024 others(116): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1807-495A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869072 | |||||||
| chr16:89869239 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1807-328G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869239 | |||||||
| chr16:89869302 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1807-265G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869302 | |||||||
| chr16:89869725 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1922+43G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869725 | |||||||
| chr16:89869745 | G | A | 1 | a0004c0005t0001g0298 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1922+63G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869745 | |||||||
| chr16:89869746 | C | G | 1 | a0001c0001t0003g0343 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1922+64C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869746 | |||||||
| chr16:89869817 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1922+135G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869817 | |||||||
| chr16:89869959 | G | A | 1 | a0001c0001t0003g0338 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1923-91G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869959 |