Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54849 |
| ensemblid | ENSG00000140995.17 |
| hgncid | 25969 |
| symbol | DEF8 |
| name | differentially expressed in FDCP 8 homolog |
| refseq_nuc | NM_001242818.2 |
| refseq_prot | NP_001229747.1 |
| ensembl_nuc | ENST00000563594.6 |
| ensembl_prot | ENSP00000458019.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89948755 |
| end | 89968060 |
| strand | + |
| ver | v1.2 |
| region | chr16:89948755-89968060 |
| region5000 | chr16:89943755-89973060 |
| regionname0 | DEF8_chr16_89948755_89968060 |
| regionname5000 | DEF8_chr16_89943755_89973060 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 451 | 377 | 88 | 74 | 148 | 18 | 47 | 118 | DEF8_chr16_89943755_89973060 | DEF8 | MEYDE others(446): Show |
chr16 | 89943755 | 89973060 |
| a0002 | 0/0 | 451 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | MEYDE others(446): Show |
chr16 | 89943755 | 89973060 |
| a0003 | 0/0 | 451 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | MEYDE others(446): Show |
chr16 | 89943755 | 89973060 |
| a0004 | 0/0 | 268 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | MEYDE others(263): Show |
chr16 | 89943755 | 89973060 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1353 | 328 | 50 | 70 | 148 | 17 | 41 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0001c0002 | 0/0 | 1353 | 40 | 30 | 3 | 0 | 1 | 6 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0001c0003 | 0/0 | 1353 | 7 | 6 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0001c0008 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0001c0009 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0002c0004 | 0/0 | 1353 | 7 | 7 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0002c0005 | 0/0 | 1353 | 5 | 5 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0003c0006 | 0/0 | 1353 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1348): Show |
chr16 | 89943755 | 89973060 | ||
| a0004c0007 | 0/0 | 1363 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | ATGGA others(1358): Show |
chr16 | 89943755 | 89973060 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3620 | 257 | 42 | 54 | 117 | 12 | 31 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0002 | 0/0 | 3620 | 30 | 0 | 1 | 29 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0003 | 0/0 | 3620 | 14 | 0 | 6 | 0 | 0 | 8 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0004 | 1/0 | 3620 | 10 | 1 | 4 | 0 | 4 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0010 | 0/0 | 3620 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0013 | 0/0 | 3620 | 3 | 0 | 2 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0015 | 0/0 | 3620 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0016 | 0/0 | 3620 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0018 | 0/0 | 3620 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0019 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0020 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0021 | 0/0 | 3620 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0023 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0001t0027 | 0/0 | 3620 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0001 | 0/0 | 3620 | 4 | 3 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0005 | 0/0 | 3620 | 8 | 1 | 1 | 0 | 0 | 6 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0006 | 0/0 | 3620 | 8 | 8 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0007 | 0/0 | 3620 | 6 | 5 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0011 | 0/0 | 3620 | 4 | 3 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0012 | 0/0 | 3620 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0014 | 0/0 | 3620 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0017 | 0/0 | 3620 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0024 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0025 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0002t0026 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0003t0007 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0003t0008 | 0/0 | 3620 | 6 | 5 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0008t0005 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0001c0009t0022 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0002c0004t0001 | 0/0 | 3620 | 7 | 7 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0002c0005t0009 | 0/0 | 3620 | 5 | 5 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0003c0006t0001 | 0/0 | 3620 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3615): Show |
chr16 | 89943755 | 89973060 |
| a0004c0007t0005 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | GTAGC others(3625): Show |
chr16 | 89943755 | 89973060 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 54 | 0 | 17 | 34 | 1 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0002 | 0/0 | 26 | 0 | 8 | 11 | 3 | 4 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0004 | 0/1 | 15 | 0 | 0 | 14 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0005 | 0/0 | 12 | 1 | 7 | 0 | 3 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0006 | 0/0 | 5 | 3 | 0 | 1 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0003 | 0/0 | 18 | 0 | 1 | 17 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0004g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0004g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0010g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0013g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0013g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0015g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0016g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0016g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0018g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0020g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0021g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0023g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0001t0027g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0005g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0005g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0007g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0007g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0011g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0017g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0017g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0024g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0025g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0002t0026g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0003t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0003t0008g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0003t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0003t0008g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0003t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0003t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0008t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0001c0009t0022g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0002c0004t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0002c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0002c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0002c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0002c0005t0009g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0002c0005t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0002c0005t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0003c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0003c0006t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| a0004c0007t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0013 | g0037 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00099 | hp2 | a0001 | c0002 | t0011 | g0188 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0151 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00639 | hp1 | a0001 | c0002 | t0005 | g0044 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00733 | hp2 | a0001 | c0001 | t0027 | g0051 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01069 | hp2 | a0001 | c0001 | t0015 | g0023 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01071 | hp1 | a0001 | c0001 | t0015 | g0023 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01081 | hp2 | a0001 | c0003 | t0008 | g0162 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01109 | hp2 | a0001 | c0002 | t0007 | g0029 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0120 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01358 | hp1 | a0001 | c0001 | t0013 | g0037 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01433 | hp2 | a0001 | c0001 | t0013 | g0010 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01884 | hp1 | a0001 | c0008 | t0005 | g0159 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01891 | hp2 | a0001 | c0003 | t0008 | g0039 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02015 | hp2 | a0001 | c0001 | t0016 | g0178 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02055 | hp1 | a0001 | c0003 | t0007 | g0191 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02055 | hp2 | a0002 | c0005 | t0009 | g0196 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02145 | hp1 | a0001 | c0001 | t0019 | g0083 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02145 | hp2 | a0002 | c0005 | t0009 | g0170 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0193 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0182 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02258 | hp2 | a0001 | c0002 | t0007 | g0024 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0043 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02280 | hp2 | a0001 | c0002 | t0007 | g0024 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02451 | hp1 | a0001 | c0002 | t0006 | g0075 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02451 | hp2 | a0002 | c0005 | t0009 | g0022 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02602 | hp1 | a0001 | c0002 | t0005 | g0016 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02717 | hp2 | a0001 | c0002 | t0012 | g0073 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02723 | hp1 | a0001 | c0002 | t0026 | g0200 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02738 | hp2 | a0001 | c0002 | t0005 | g0186 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0139 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02818 | hp1 | a0001 | c0002 | t0011 | g0057 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02886 | hp1 | a0002 | c0004 | t0001 | g0015 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02886 | hp2 | a0002 | c0004 | t0001 | g0194 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02895 | hp2 | a0002 | c0004 | t0001 | g0015 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0183 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02897 | hp2 | a0002 | c0004 | t0001 | g0015 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02965 | hp1 | a0001 | c0002 | t0017 | g0052 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0044 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02970 | hp1 | a0001 | c0009 | t0022 | g0197 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02976 | hp1 | a0002 | c0005 | t0009 | g0022 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02976 | hp2 | a0001 | c0002 | t0007 | g0029 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03041 | hp2 | a0001 | c0002 | t0012 | g0072 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03139 | hp1 | a0001 | c0001 | t0023 | g0166 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0143 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0064 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0070 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0015 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03225 | hp2 | a0001 | c0002 | t0006 | g0047 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0062 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03453 | hp1 | a0001 | c0002 | t0007 | g0085 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03486 | hp1 | a0001 | c0002 | t0007 | g0056 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03486 | hp2 | a0001 | c0003 | t0008 | g0190 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03490 | hp1 | a0004 | c0007 | t0005 | g0046 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03516 | hp1 | a0001 | c0002 | t0017 | g0053 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03579 | hp2 | a0001 | c0002 | t0024 | g0160 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03688 | hp1 | a0001 | c0002 | t0005 | g0016 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03927 | hp1 | a0001 | c0001 | t0018 | g0187 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04184 | hp1 | a0001 | c0002 | t0005 | g0185 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04184 | hp2 | a0001 | c0002 | t0005 | g0045 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04204 | hp2 | a0001 | c0002 | t0005 | g0016 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18906 | hp1 | a0001 | c0002 | t0011 | g0161 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18906 | hp2 | a0001 | c0002 | t0012 | g0071 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18973 | hp1 | a0003 | c0006 | t0001 | g0019 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18973 | hp2 | a0003 | c0006 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19030 | hp1 | a0001 | c0002 | t0014 | g0149 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19043 | hp1 | a0001 | c0002 | t0006 | g0144 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19043 | hp2 | a0001 | c0003 | t0008 | g0173 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19087 | hp1 | a0001 | c0001 | t0016 | g0164 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19240 | hp1 | a0002 | c0005 | t0009 | g0022 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA19240 | hp2 | a0001 | c0002 | t0011 | g0058 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20129 | hp1 | a0001 | c0003 | t0008 | g0146 | AFR | ASW | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0076 | AFR | ASW | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | GIH | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02109 | hp1 | a0001 | c0002 | t0025 | g0074 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02109 | hp2 | a0002 | c0004 | t0001 | g0195 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0043 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03471 | hp1 | a0001 | c0003 | t0008 | g0039 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG03471 | hp2 | a0001 | c0002 | t0006 | g0077 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA21309 | hp1 | a0001 | c0002 | t0014 | g0150 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0004 | REF | REF | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0004 | REF | REF | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89954337 | C | G | 1 | a0002 | 12 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
missense_variant | MODERATE | c.85C>G | p.Gln29Glu | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/13 | 252/3620 | 85/1356 | 29/451 | chr16 | 89954337 | |||
| chr16:89961847 | G | GACTTTGA others(3): Show |
1 | a0004 | 1 | HG03490.hp1 | frameshift_variant&stop_gained | HIGH | c.791_800dupACTTTGAG others(2): Show |
p.Arg268fs | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 8/13 | 968/3620 | 801/1356 | 267/451 | INFO_REALIGN_3_PRIME | chr16 | 89961847 | ||
| chr16:89962072 | C | T | 1 | a0003 | 2 | NA18973.hp1 NA18973.hp2 |
missense_variant | MODERATE | c.868C>T | p.Arg290Trp | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/13 | 1035/3620 | 868/1356 | 290/451 | chr16 | 89962072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89957577 | C | T | 1 | a0001c0009 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.289C>T | p.Leu97Leu | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/13 | 456/3620 | 289/1356 | 97/451 | chr16 | 89957577 | |||
| chr16:89957654 | G | A | 1 | a0001c0003 | 7 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
synonymous_variant | LOW | c.366G>A | p.Glu122Glu | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/13 | 533/3620 | 366/1356 | 122/451 | chr16 | 89957654 | |||
| chr16:89963395 | G | A | 1 | a0001c0008 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.954G>A | p.Pro318Pro | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/13 | 1121/3620 | 954/1356 | 318/451 | chr16 | 89963395 | |||
| chr16:89965888 | T | G | 5 | a0001c0002 a0001c0003 a0001c0008 others(2): Show |
54 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(51): Show |
synonymous_variant | LOW | c.1281T>G | p.Thr427Thr | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1448/3620 | 1281/1356 | 427/451 | chr16 | 89965888 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89948768 | C | G | 1 | a0001c0001t0027 | 1 | HG00733.hp2 | 5_prime_UTR_variant | MODIFIER | c.-154C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/13 | 5485 | chr16 | 89948768 | ||||||
| chr16:89948793 | A | G | 3 | a0001c0001t0002 a0001c0001t0016 a0001c0002t0017 |
34 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-129A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/13 | 5460 | chr16 | 89948793 | ||||||
| chr16:89966025 | G | C | 1 | a0001c0002t0014 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*62G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 62 | chr16 | 89966025 | ||||||
| chr16:89966038 | C | T | 1 | a0001c0003t0008 | 6 | HG01081.hp2 HG01891.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*75C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 75 | chr16 | 89966038 | ||||||
| chr16:89966047 | C | T | 1 | a0001c0001t0013 | 3 | HG00099.hp1 HG01358.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*84C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 84 | chr16 | 89966047 | ||||||
| chr16:89966147 | C | T | 12 | a0001c0002t0005 a0001c0002t0006 a0001c0002t0007 others(9): Show |
43 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*184C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 184 | chr16 | 89966147 | ||||||
| chr16:89966149 | G | T | 15 | a0001c0002t0005 a0001c0002t0006 a0001c0002t0007 others(12): Show |
50 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*186G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 186 | chr16 | 89966149 | ||||||
| chr16:89966285 | C | T | 2 | a0001c0002t0011 a0001c0002t0017 |
6 | HG00099.hp2 HG02818.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 322 | chr16 | 89966285 | ||||||
| chr16:89966328 | C | A | 1 | a0001c0001t0018 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 365 | chr16 | 89966328 | ||||||
| chr16:89966368 | A | G | 3 | a0001c0002t0011 a0001c0002t0017 a0001c0002t0024 |
7 | HG00099.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 405 | chr16 | 89966368 | ||||||
| chr16:89966433 | G | A | 1 | a0001c0001t0010 | 4 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*470G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 470 | chr16 | 89966433 | ||||||
| chr16:89966454 | G | T | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(26): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
3_prime_UTR_variant | MODIFIER | c.*491G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 491 | chr16 | 89966454 | ||||||
| chr16:89966634 | C | T | 1 | a0001c0002t0026 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 671 | chr16 | 89966634 | ||||||
| chr16:89966825 | C | T | 3 | a0001c0002t0011 a0001c0002t0017 a0001c0002t0024 |
7 | HG00099.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*862C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 862 | chr16 | 89966825 | ||||||
| chr16:89966847 | C | G | 11 | a0001c0002t0005 a0001c0002t0006 a0001c0002t0007 others(8): Show |
40 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*884C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 884 | chr16 | 89966847 | ||||||
| chr16:89967030 | G | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(22): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*1067G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1067 | chr16 | 89967030 | ||||||
| chr16:89967038 | G | A | 1 | a0001c0001t0015 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1075G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1075 | chr16 | 89967038 | ||||||
| chr16:89967112 | G | A | 1 | a0001c0001t0019 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1149G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1149 | chr16 | 89967112 | ||||||
| chr16:89967113 | G | A | 1 | a0001c0002t0006 | 8 | HG02451.hp1 HG03139.hp2 HG03195.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1150G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1150 | chr16 | 89967113 | ||||||
| chr16:89967422 | C | G | 12 | a0001c0002t0005 a0001c0002t0006 a0001c0002t0007 others(9): Show |
41 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1459C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1459 | chr16 | 89967422 | ||||||
| chr16:89967500 | G | T | 1 | a0001c0001t0021 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1537G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1537 | chr16 | 89967500 | ||||||
| chr16:89967502 | C | A | 13 | a0001c0002t0005 a0001c0002t0006 a0001c0002t0007 others(10): Show |
46 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1539C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1539 | chr16 | 89967502 | ||||||
| chr16:89967640 | C | G | 1 | a0001c0001t0023 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1677 | chr16 | 89967640 | ||||||
| chr16:89967709 | A | G | 4 | a0001c0001t0002 a0001c0002t0011 a0001c0002t0017 others(1): Show |
37 | HG00099.hp2 HG00438.hp2 HG01175.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1746A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1746 | chr16 | 89967709 | ||||||
| chr16:89967970 | G | C | 3 | a0001c0001t0010 a0001c0001t0020 a0001c0009t0022 |
6 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2007G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 2007 | chr16 | 89967970 | ||||||
| chr16:89968050 | T | C | 3 | a0001c0002t0007 a0001c0002t0026 a0001c0003t0007 |
8 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2087T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 2087 | chr16 | 89968050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89948824 | GCGGGGCC others(143): Show |
G | 8 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(5): Show |
9 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+25_-108+174de others(1): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948824 | ||||||
| chr16:89948824 | GCGGGGCC others(188): Show |
G | 2 | a0001c0002t0017g0052 a0001c0002t0017g0053 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-108+25_-108+219de others(1): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948824 | ||||||
| chr16:89948839 | T | A | 33 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0059 others(30): Show |
44 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-108+25T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948839 | |||||||
| chr16:89948839 | T | TCGGGGCC others(8): Show |
1 | a0001c0001t0001g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-108+61_-108+75dup others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | ||||||
| chr16:89948839 | TCGGGGCC others(8): Show |
T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(11): Show |
26 | HG01433.hp2 HG02896.hp1 HG02897.hp1 others(23): Show |
intron_variant | MODIFIER | c.-108+61_-108+75del others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | ||||||
| chr16:89948839 | TCGGGGCC others(23): Show |
T | 8 | a0001c0001t0001g0060 a0001c0002t0006g0064 a0001c0002t0007g0024 others(5): Show |
9 | HG02258.hp2 HG02280.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+46_-108+75del others(30): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | ||||||
| chr16:89948839 | TCGGGGCC others(38): Show |
T | 1 | a0001c0001t0001g0005 | 5 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108+31_-108+75del others(45): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | ||||||
| chr16:89948839 | TCGGGGCC others(68): Show |
T | 5 | a0001c0001t0001g0158 a0001c0002t0011g0161 a0001c0002t0024g0160 others(2): Show |
5 | HG01081.hp2 HG01884.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108+46_-108+120de others(76): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | ||||||
| chr16:89948850 | G | GGGGACGG others(98): Show |
1 | a0001c0001t0001g0147 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-108+76_-108+180du others(106): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | ||||||
| chr16:89948850 | G | GGGGTCGG others(8): Show |
1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+39_-108+40ins others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | ||||||
| chr16:89948850 | GGGGACGG others(53): Show |
G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0163 a0001c0001t0016g0164 |
6 | HG00438.hp2 HG02083.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108+61_-108+120de others(61): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | ||||||
| chr16:89948850 | GGGGACGG others(98): Show |
G | 1 | a0001c0001t0003g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-108+76_-108+180de others(1): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | ||||||
| chr16:89948854 | A | T | 30 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0059 others(27): Show |
41 | HG00140.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-108+40A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948854 | |||||||
| chr16:89948860 | C | T | 11 | a0001c0001t0001g0099 a0001c0002t0007g0085 a0001c0002t0011g0188 others(8): Show |
16 | HG00099.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-108+46C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948860 | |||||||
| chr16:89948861 | C | T | 30 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0059 others(27): Show |
41 | HG00140.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-108+47C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948861 | |||||||
| chr16:89948864 | C | G | 31 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0059 others(28): Show |
42 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-108+50C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948864 | |||||||
| chr16:89948865 | G | A | 31 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0059 others(28): Show |
42 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-108+51G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948865 | |||||||
| chr16:89948865 | G | GGGGACGG others(53): Show |
1 | a0001c0001t0003g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-108+75_-108+76ins others(60): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | ||||||
| chr16:89948865 | G | GGGGACGG others(143): Show |
1 | a0001c0001t0001g0017 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-108+121_-108+270d others(152): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | ||||||
| chr16:89948865 | G | GGGGACGG others(23): Show |
1 | a0001c0001t0001g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-108+60_-108+61ins others(30): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | ||||||
| chr16:89948865 | G | GGGGTCGG others(8): Show |
1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-108+54_-108+55ins others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | ||||||
| chr16:89948865 | GGGGACGG others(38): Show |
G | 3 | a0001c0001t0001g0002 a0001c0003t0008g0039 a0001c0003t0008g0146 |
4 | HG01261.hp1 HG01358.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108+85_-108+129de others(46): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | ||||||
| chr16:89948870 | C | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0154 a0001c0001t0001g0156 others(3): Show |
7 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108+56C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948870 | |||||||
| chr16:89948874 | G | T | 3 | a0001c0001t0001g0201 a0001c0002t0005g0044 a0001c0002t0026g0200 |
4 | HG00639.hp1 HG02723.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108+60G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948874 | |||||||
| chr16:89948875 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0040 others(44): Show |
76 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-108+61C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948875 | |||||||
| chr16:89948876 | C | T | 7 | a0001c0002t0007g0085 a0002c0004t0001g0015 a0002c0004t0001g0193 others(4): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108+62C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948876 | |||||||
| chr16:89948876 | CGGCGGGG others(23): Show |
C | 1 | a0001c0002t0006g0075 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-108+65_-108+94del others(30): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948876 | ||||||
| chr16:89948879 | C | G | 25 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(22): Show |
32 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+65C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948879 | |||||||
| chr16:89948880 | G | A | 25 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(22): Show |
32 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+66G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948880 | |||||||
| chr16:89948880 | GGGGACGG others(68): Show |
G | 1 | a0001c0001t0001g0001 | 2 | NA18998.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-108+76_-108+150de others(76): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948880 | ||||||
| chr16:89948884 | A | T | 9 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0001t0002g0176 others(6): Show |
25 | HG01175.hp2 HG02015.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-108+70A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948884 | |||||||
| chr16:89948889 | G | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-108+75G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948889 | |||||||
| chr16:89948890 | T | C | 26 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0192 others(23): Show |
48 | HG00639.hp1 HG00741.hp1 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.-108+76T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948890 | |||||||
| chr16:89948890 | TCGGCGGG others(98): Show |
T | 1 | a0001c0002t0005g0016 | 3 | HG02602.hp1 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-108+130_-108+234d others(2): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948890 | ||||||
| chr16:89948891 | C | T | 15 | a0001c0001t0001g0192 a0001c0001t0001g0201 a0001c0001t0002g0003 others(12): Show |
32 | HG00639.hp1 HG01175.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+77C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948891 | |||||||
| chr16:89948894 | C | G | 15 | a0001c0001t0001g0192 a0001c0001t0001g0201 a0001c0001t0002g0003 others(12): Show |
32 | HG00639.hp1 HG01175.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+80C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948894 | |||||||
| chr16:89948895 | G | A | 15 | a0001c0001t0001g0192 a0001c0001t0001g0201 a0001c0001t0002g0003 others(12): Show |
32 | HG00639.hp1 HG01175.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+81G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948895 | |||||||
| chr16:89948895 | GGGGTCGG others(8): Show |
G | 1 | a0001c0002t0007g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-108+85_-108+99del others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948895 | ||||||
| chr16:89948899 | T | A | 50 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0060 others(47): Show |
75 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(72): Show |
intron_variant | MODIFIER | c.-108+85T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948899 | |||||||
| chr16:89948899 | TCGGGGCT others(38): Show |
T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0004g0120 |
5 | HG01256.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108+121_-108+165d others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948899 | ||||||
| chr16:89948905 | C | T | 24 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(21): Show |
31 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-108+91C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948905 | |||||||
| chr16:89948906 | T | C | 39 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(36): Show |
63 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-108+92T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948906 | |||||||
| chr16:89948909 | G | C | 39 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(36): Show |
63 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-108+95G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948909 | |||||||
| chr16:89948910 | A | AGGGACGG others(8): Show |
1 | a0001c0001t0002g0003 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-108+106_-108+120d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948910 | ||||||
| chr16:89948910 | A | G | 39 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(36): Show |
63 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-108+96A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948910 | |||||||
| chr16:89948910 | AGGGACGG others(53): Show |
A | 2 | a0001c0002t0005g0185 a0001c0002t0005g0186 |
2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-108+121_-108+180d others(62): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948910 | ||||||
| chr16:89948910 | AGGGACGG others(68): Show |
A | 5 | a0001c0001t0003g0021 a0001c0001t0003g0041 a0001c0001t0004g0012 others(2): Show |
11 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.-108+115_-108+189d others(77): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948910 | ||||||
| chr16:89948914 | A | T | 18 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(15): Show |
20 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-108+100A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948914 | |||||||
| chr16:89948914 | ACGGGGCC others(188): Show |
A | 1 | a0001c0001t0001g0040 | 2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-108+121_-107-288d others(2): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948914 | ||||||
| chr16:89948920 | C | T | 2 | a0001c0001t0003g0054 a0001c0002t0006g0075 |
2 | HG00741.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-108+106C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948920 | |||||||
| chr16:89948920 | CCGGCGGG others(8): Show |
C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0189 |
2 | HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-108+121_-108+135d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948920 | ||||||
| chr16:89948921 | C | T | 25 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(22): Show |
33 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-108+107C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948921 | |||||||
| chr16:89948924 | C | G | 25 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(22): Show |
33 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-108+110C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948924 | |||||||
| chr16:89948925 | G | A | 25 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(22): Show |
33 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-108+111G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948925 | |||||||
| chr16:89948929 | A | T | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+115A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948929 | |||||||
| chr16:89948933 | G | A | 2 | a0001c0001t0001g0158 a0001c0008t0005g0159 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-108+119G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948933 | |||||||
| chr16:89948935 | T | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0059 others(45): Show |
61 | HG00099.hp2 HG00639.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.-108+121T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948935 | |||||||
| chr16:89948935 | TCGGCGGG others(128): Show |
T | 1 | a0001c0002t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-108+137_-108+271d others(2): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948935 | ||||||
| chr16:89948936 | C | T | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+122C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948936 | |||||||
| chr16:89948939 | C | G | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+125C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948939 | |||||||
| chr16:89948940 | G | A | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+126G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948940 | |||||||
| chr16:89948940 | GGGGACGG others(8): Show |
G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0063 others(1): Show |
7 | HG00733.hp1 HG01891.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108+137_-108+151d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948940 | ||||||
| chr16:89948941 | G | GGGTCGGG others(158): Show |
1 | a0001c0001t0023g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-108+129_-108+130i others(167): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948941 | ||||||
| chr16:89948944 | A | ACGGGGCC others(38): Show |
1 | a0001c0001t0001g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-108+136_-108+137i others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948944 | ||||||
| chr16:89948944 | A | ACGGGGCT others(98): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0094 |
4 | HG01928.hp2 HG02148.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108+187_-108+291d others(107): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948944 | ||||||
| chr16:89948944 | A | T | 42 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0060 others(39): Show |
65 | HG00438.hp2 HG00741.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.-108+130A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948944 | |||||||
| chr16:89948949 | G | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
9 | HG01192.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+135G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948949 | |||||||
| chr16:89948950 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0167 a0001c0001t0001g0168 others(4): Show |
10 | HG00099.hp2 HG01192.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108+136C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948950 | |||||||
| chr16:89948951 | T | C | 20 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0097 others(17): Show |
29 | HG00099.hp2 HG01192.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.-108+137T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948951 | |||||||
| chr16:89948954 | G | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0097 a0001c0001t0001g0167 others(11): Show |
22 | HG01192.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108+140G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948954 | |||||||
| chr16:89948955 | A | AGGGACGG others(8): Show |
1 | a0001c0002t0007g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-108+175_-108+189d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948955 | ||||||
| chr16:89948955 | A | AGGGACGG others(23): Show |
1 | a0001c0001t0019g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-108+165_-108+166i others(32): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948955 | ||||||
| chr16:89948955 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0097 a0001c0001t0001g0167 others(11): Show |
22 | HG01192.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108+141A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948955 | |||||||
| chr16:89948955 | AGGGACGG others(8): Show |
A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(23): Show |
57 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-108+175_-108+189d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948955 | ||||||
| chr16:89948959 | A | T | 7 | a0001c0001t0003g0152 a0002c0004t0001g0015 a0002c0004t0001g0193 others(4): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108+145A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948959 | |||||||
| chr16:89948965 | C | T | 20 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(17): Show |
23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-108+151C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948965 | |||||||
| chr16:89948966 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0167 others(6): Show |
13 | HG01192.hp1 HG02145.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-108+152C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948966 | |||||||
| chr16:89948966 | CGGCGGGG others(83): Show |
C | 5 | a0001c0001t0001g0060 a0001c0002t0007g0024 a0001c0002t0007g0056 others(2): Show |
6 | HG02258.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108+155_-108+244d others(92): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948966 | ||||||
| chr16:89948969 | C | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0026 others(27): Show |
37 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.-108+155C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948969 | |||||||
| chr16:89948970 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0026 others(27): Show |
37 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.-108+156G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948970 | |||||||
| chr16:89948970 | G | GGGGACGG others(38): Show |
1 | a0001c0001t0001g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-108+181_-108+225d others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948970 | ||||||
| chr16:89948970 | G | GGGGACGG others(83): Show |
1 | a0001c0001t0001g0172 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-108+180_-108+181i others(92): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948970 | ||||||
| chr16:89948970 | G | GGGGACGG others(23): Show |
1 | a0001c0001t0001g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-108+165_-108+166i others(32): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948970 | ||||||
| chr16:89948974 | A | T | 2 | a0001c0001t0003g0054 a0001c0001t0023g0166 |
2 | HG00741.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-108+160A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948974 | |||||||
| chr16:89948980 | C | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0198 others(13): Show |
22 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108+166C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948980 | |||||||
| chr16:89948980 | CCGGCGGG others(53): Show |
C | 1 | a0001c0001t0018g0187 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-108+175_-108+234d others(62): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948980 | ||||||
| chr16:89948989 | A | ACGGGGCC others(8): Show |
1 | a0001c0001t0003g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-108+186_-108+187i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948989 | ||||||
| chr16:89948989 | A | T | 30 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0199 others(27): Show |
54 | HG00099.hp2 HG00639.hp1 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.-108+175A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948989 | |||||||
| chr16:89948989 | ACGGGGCC others(8): Show |
A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0189 |
2 | HG02080.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-108+182_-108+196d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948989 | ||||||
| chr16:89948995 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0158 a0001c0001t0001g0165 others(16): Show |
25 | HG00438.hp2 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-108+181C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948995 | |||||||
| chr16:89948996 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-108+182C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948996 | |||||||
| chr16:89948996 | C | T | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+182C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948996 | |||||||
| chr16:89948999 | C | G | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+185C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948999 | |||||||
| chr16:89949000 | G | A | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+186G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949000 | |||||||
| chr16:89949004 | T | A | 18 | a0001c0001t0001g0055 a0001c0001t0001g0192 a0001c0001t0001g0198 others(15): Show |
24 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-108+190T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949004 | |||||||
| chr16:89949004 | TCGGGGCT others(68): Show |
T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0001t0002g0176 others(9): Show |
30 | HG01175.hp2 HG02015.hp1 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.-108+197_-108+271d others(77): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949004 | ||||||
| chr16:89949010 | C | T | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+196C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949010 | |||||||
| chr16:89949011 | T | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0167 a0001c0001t0001g0168 others(21): Show |
33 | HG00099.hp2 HG00639.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.-108+197T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949011 | |||||||
| chr16:89949014 | G | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0167 a0001c0001t0001g0168 others(20): Show |
32 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-108+200G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949014 | |||||||
| chr16:89949015 | A | AGGGACGG others(8): Show |
2 | a0001c0001t0001g0007 a0001c0003t0008g0162 |
4 | HG01081.hp2 HG01891.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108+211_-108+225d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949015 | ||||||
| chr16:89949015 | A | AGGGACGG others(173): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0154 a0001c0001t0001g0156 |
4 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108+225_-108+226i others(182): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949015 | ||||||
| chr16:89949015 | A | G | 23 | a0001c0001t0001g0014 a0001c0001t0001g0167 a0001c0001t0001g0168 others(20): Show |
32 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-108+201A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949015 | |||||||
| chr16:89949015 | AGGGACGG others(53): Show |
A | 1 | a0001c0003t0008g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-108+226_-108+285d others(62): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949015 | ||||||
| chr16:89949025 | C | T | 14 | a0001c0001t0003g0021 a0001c0001t0003g0041 a0001c0001t0003g0048 others(11): Show |
21 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-108+211C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949025 | |||||||
| chr16:89949027 | G | A | 3 | a0001c0001t0001g0192 a0001c0003t0007g0191 a0001c0003t0008g0190 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-108+213G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949027 | |||||||
| chr16:89949030 | G | GGGGTCGG others(8): Show |
1 | a0001c0001t0001g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-108+219_-108+220i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949030 | ||||||
| chr16:89949030 | GGGGACGG others(23): Show |
G | 8 | a0001c0001t0001g0158 a0001c0001t0020g0139 a0001c0002t0006g0143 others(5): Show |
8 | HG01884.hp1 HG02809.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108+226_-108+255d others(32): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949030 | ||||||
| chr16:89949034 | A | T | 22 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(19): Show |
25 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-108+220A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949034 | |||||||
| chr16:89949040 | T | C | 44 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0042 others(41): Show |
59 | HG00438.hp2 HG00639.hp1 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.-108+226T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949040 | |||||||
| chr16:89949041 | C | T | 8 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
9 | HG00639.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+227C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949041 | |||||||
| chr16:89949044 | C | G | 8 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
9 | HG00639.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+230C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949044 | |||||||
| chr16:89949045 | G | A | 8 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
9 | HG00639.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+231G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949045 | |||||||
| chr16:89949049 | T | A | 12 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0199 others(9): Show |
16 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-108+235T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949049 | |||||||
| chr16:89949049 | TCGGGGCT others(8): Show |
T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0133 others(9): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-108+242_-108+256d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949049 | ||||||
| chr16:89949056 | T | C | 15 | a0001c0001t0001g0059 a0001c0001t0001g0192 a0001c0001t0001g0198 others(12): Show |
19 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108+242T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949056 | |||||||
| chr16:89949059 | G | C | 15 | a0001c0001t0001g0059 a0001c0001t0001g0192 a0001c0001t0001g0198 others(12): Show |
19 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108+245G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949059 | |||||||
| chr16:89949060 | A | AGGGACGG others(9): Show |
1 | a0001c0001t0001g0154 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-108+249_-108+264d others(18): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949060 | ||||||
| chr16:89949060 | A | G | 15 | a0001c0001t0001g0059 a0001c0001t0001g0192 a0001c0001t0001g0198 others(12): Show |
19 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108+246A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949060 | |||||||
| chr16:89949060 | AGGGACGG others(8): Show |
A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0119 others(5): Show |
9 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+277_-108+291d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949060 | ||||||
| chr16:89949064 | A | ACGGGGCC others(113): Show |
1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+264_-108+265i others(122): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949064 | ||||||
| chr16:89949064 | A | T | 10 | a0001c0001t0001g0059 a0001c0001t0001g0201 a0001c0001t0002g0013 others(7): Show |
13 | HG00438.hp2 HG02083.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-108+250A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949064 | |||||||
| chr16:89949064 | ACGGGGCC others(38): Show |
A | 1 | a0001c0001t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-108+272_-107-287d others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949064 | ||||||
| chr16:89949079 | A | ACGGGGCC others(8): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0201 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-108+276_-108+277i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949079 | ||||||
| chr16:89949079 | A | ACGGGGCC others(8): Show |
20 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0060 others(17): Show |
30 | HG01192.hp1 HG02055.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-108+279_-108+280i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949079 | ||||||
| chr16:89949079 | A | T | 53 | a0001c0001t0001g0026 a0001c0001t0001g0133 a0001c0001t0001g0154 others(50): Show |
68 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-108+265A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949079 | |||||||
| chr16:89949100 | C | T | 2 | a0001c0002t0017g0052 a0001c0002t0017g0053 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-108+286C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949100 | |||||||
| chr16:89949106 | A | G | 3 | a0001c0002t0017g0052 a0001c0002t0017g0053 a0001c0003t0008g0173 |
3 | HG02965.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-108+292A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949106 | |||||||
| chr16:89949109 | T | A | 3 | a0001c0002t0017g0052 a0001c0002t0017g0053 a0001c0003t0008g0173 |
3 | HG02965.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-108+295T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949109 | |||||||
| chr16:89949162 | C | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0154 others(17): Show |
25 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-107-255C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949162 | |||||||
| chr16:89949171 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0002t0007g0024 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-107-246G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949171 | |||||||
| chr16:89949357 | C | T | 14 | a0001c0001t0001g0040 a0001c0001t0001g0153 a0001c0001t0003g0021 others(11): Show |
22 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-107-60C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949357 | |||||||
| chr16:89949388 | C | T | 2 | a0001c0002t0014g0149 a0001c0002t0014g0150 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-107-29C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949388 | |||||||
| chr16:89949552 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0003g0061 a0001c0001t0021g0062 |
4 | HG00323.hp1 HG01099.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+39G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949552 | |||||||
| chr16:89949737 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11+224G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949737 | |||||||
| chr16:89949820 | C | G | 14 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0002g0003 others(11): Show |
34 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+307C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949820 | |||||||
| chr16:89949913 | G | C | 4 | a0001c0001t0001g0158 a0001c0002t0011g0161 a0001c0002t0024g0160 others(1): Show |
4 | HG01884.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+400G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949913 | |||||||
| chr16:89949915 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-11+402C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949915 | |||||||
| chr16:89949929 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-11+416A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949929 | |||||||
| chr16:89949998 | C | T | 3 | a0001c0003t0008g0039 a0001c0003t0008g0146 a0001c0009t0022g0197 |
4 | HG01891.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+485C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949998 | |||||||
| chr16:89950007 | G | C | 1 | a0001c0001t0002g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+494G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950007 | |||||||
| chr16:89950016 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-11+503C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950016 | |||||||
| chr16:89950217 | C | G | 9 | a0001c0003t0008g0039 a0001c0003t0008g0146 a0001c0009t0022g0197 others(6): Show |
15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+704C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950217 | |||||||
| chr16:89950303 | C | G | 2 | a0001c0002t0006g0143 a0001c0002t0006g0144 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-11+790C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950303 | |||||||
| chr16:89950390 | A | AT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0138 a0001c0001t0001g0140 others(3): Show |
7 | HG02809.hp2 HG03540.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+893dupT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89950390 | ||||||
| chr16:89950390 | AT | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(51): Show |
88 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-11+893delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89950390 | ||||||
| chr16:89950481 | C | T | 1 | a0001c0002t0006g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-11+968C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950481 | |||||||
| chr16:89950574 | C | T | 12 | a0001c0001t0003g0137 a0001c0002t0006g0047 a0001c0002t0006g0070 others(9): Show |
12 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+1061C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950574 | |||||||
| chr16:89950578 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-11+1065C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950578 | |||||||
| chr16:89950786 | CCT | C | 31 | a0001c0001t0001g0040 a0001c0001t0003g0021 a0001c0001t0003g0041 others(28): Show |
41 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-11+1274_-11+1275d others(4): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950786 | |||||||
| chr16:89950791 | G | C | 1 | a0001c0002t0006g0070 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+1278G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950791 | |||||||
| chr16:89950792 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11+1279C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950792 | |||||||
| chr16:89951039 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-11+1526G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951039 | |||||||
| chr16:89951073 | T | C | 1 | a0001c0002t0007g0029 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-11+1560T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951073 | |||||||
| chr16:89951260 | CT | C | 6 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0138 others(3): Show |
6 | HG01081.hp2 HG02896.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+1759delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89951260 | ||||||
| chr16:89951261 | T | C | 1 | a0001c0001t0001g0009 | 4 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1748T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951261 | |||||||
| chr16:89951305 | G | A | 1 | a0001c0002t0006g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-11+1792G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951305 | |||||||
| chr16:89951403 | C | G | 1 | a0001c0001t0021g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-11+1890C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951403 | |||||||
| chr16:89951425 | G | T | 1 | a0002c0005t0009g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11+1912G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951425 | |||||||
| chr16:89951434 | G | A | 28 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0003g0021 others(25): Show |
37 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-11+1921G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951434 | |||||||
| chr16:89951481 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-11+1968G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951481 | |||||||
| chr16:89951503 | C | A | 3 | a0001c0001t0001g0192 a0001c0003t0007g0191 a0001c0003t0008g0190 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-11+1990C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951503 | |||||||
| chr16:89951550 | G | A | 34 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0080 others(31): Show |
45 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11+2037G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951550 | |||||||
| chr16:89951569 | G | A | 2 | a0001c0003t0008g0162 a0001c0003t0008g0173 |
2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-11+2056G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951569 | |||||||
| chr16:89951577 | C | A | 26 | a0001c0001t0001g0040 a0001c0001t0003g0021 a0001c0001t0003g0041 others(23): Show |
34 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+2064C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951577 | |||||||
| chr16:89951577 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+2064C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951577 | |||||||
| chr16:89951603 | G | A | 3 | a0002c0004t0001g0015 a0002c0004t0001g0193 a0002c0004t0001g0194 |
6 | HG02257.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+2090G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951603 | |||||||
| chr16:89951664 | C | T | 29 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0133 others(26): Show |
37 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-11+2151C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951664 | |||||||
| chr16:89951682 | T | C | 1 | a0001c0001t0001g0005 | 12 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+2169T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951682 | |||||||
| chr16:89951778 | T | C | 13 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0002g0003 others(10): Show |
33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11+2265T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951778 | |||||||
| chr16:89951782 | G | C | 1 | a0001c0001t0002g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+2269G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951782 | |||||||
| chr16:89951827 | C | CACACACA others(17): Show |
2 | a0001c0002t0017g0052 a0001c0002t0017g0053 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+2324_-11+2347d others(26): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89951827 | ||||||
| chr16:89951874 | A | G | 1 | a0001c0001t0023g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-11+2361A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951874 | |||||||
| chr16:89951879 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-10-2364A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951879 | |||||||
| chr16:89951880 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-10-2363G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951880 | |||||||
| chr16:89951881 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-10-2362A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951881 | |||||||
| chr16:89951881 | AT | A | 37 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0080 others(34): Show |
48 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10-2348delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89951881 | ||||||
| chr16:89951981 | T | C | 39 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0040 others(36): Show |
51 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-2262T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951981 | |||||||
| chr16:89952014 | G | A | 36 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0080 others(33): Show |
47 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.-10-2229G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952014 | |||||||
| chr16:89952035 | A | G | 35 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0080 others(32): Show |
46 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.-10-2208A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952035 | |||||||
| chr16:89952065 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-10-2178G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952065 | |||||||
| chr16:89952068 | A | G | 39 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0080 others(36): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.-10-2175A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952068 | |||||||
| chr16:89952077 | A | C | 7 | a0001c0001t0016g0164 a0002c0004t0001g0015 a0002c0004t0001g0193 others(4): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-2166A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952077 | |||||||
| chr16:89952078 | T | C | 7 | a0001c0001t0016g0164 a0002c0004t0001g0015 a0002c0004t0001g0193 others(4): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-2165T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952078 | |||||||
| chr16:89952086 | C | T | 7 | a0001c0002t0006g0076 a0002c0004t0001g0015 a0002c0004t0001g0193 others(4): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-2157C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952086 | |||||||
| chr16:89952088 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-10-2155A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952088 | |||||||
| chr16:89952096 | T | C | 101 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0026 others(98): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-10-2147T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952096 | |||||||
| chr16:89952217 | A | C | 37 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0080 others(34): Show |
48 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10-2026A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952217 | |||||||
| chr16:89952228 | C | T | 6 | a0002c0004t0001g0015 a0002c0004t0001g0193 a0002c0004t0001g0194 others(3): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-2015C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952228 | |||||||
| chr16:89952449 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-10-1794C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952449 | |||||||
| chr16:89952580 | G | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0133 others(19): Show |
27 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10-1663G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952580 | |||||||
| chr16:89952653 | C | T | 6 | a0001c0001t0001g0080 a0001c0002t0005g0016 a0001c0002t0005g0045 others(3): Show |
8 | HG02602.hp1 HG02738.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-1590C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952653 | |||||||
| chr16:89952676 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-10-1567T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952676 | |||||||
| chr16:89952786 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-1457C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952786 | |||||||
| chr16:89952818 | C | T | 1 | a0001c0002t0006g0075 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-10-1425C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952818 | |||||||
| chr16:89952857 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-10-1386A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952857 | |||||||
| chr16:89952990 | C | T | 31 | a0001c0001t0001g0080 a0001c0001t0003g0021 a0001c0001t0003g0041 others(28): Show |
40 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-10-1253C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952990 | |||||||
| chr16:89953236 | C | G | 1 | a0001c0001t0002g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-10-1007C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953236 | |||||||
| chr16:89953254 | C | A | 1 | a0001c0001t0001g0087 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-10-989C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953254 | |||||||
| chr16:89953271 | C | T | 2 | a0001c0002t0017g0052 a0001c0002t0017g0053 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-972C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953271 | |||||||
| chr16:89953275 | T | C | 3 | a0001c0001t0004g0012 a0001c0001t0004g0069 a0001c0001t0004g0151 |
6 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-968T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953275 | |||||||
| chr16:89953825 | T | C | 4 | a0001c0002t0007g0029 a0001c0002t0011g0161 a0001c0002t0011g0188 others(1): Show |
5 | HG00099.hp2 HG01109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-418T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953825 | |||||||
| chr16:89953933 | T | C | 61 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(58): Show |
98 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-10-310T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953933 | |||||||
| chr16:89953938 | A | C | 65 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(62): Show |
102 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-10-305A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953938 | |||||||
| chr16:89953948 | T | C | 1 | a0001c0001t0001g0030 | 2 | NA18939.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-10-295T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953948 | |||||||
| chr16:89953958 | G | T | 1 | a0001c0001t0002g0163 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-10-285G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953958 | |||||||
| chr16:89953998 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-10-245G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953998 | |||||||
| chr16:89954389 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.124+13G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954389 | |||||||
| chr16:89954392 | A | C | 2 | a0001c0002t0011g0161 a0001c0002t0024g0160 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.124+16A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954392 | |||||||
| chr16:89954453 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(156): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.124+77C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954453 | |||||||
| chr16:89954656 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.124+280C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954656 | |||||||
| chr16:89954701 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0133 others(8): Show |
14 | HG01192.hp1 HG02615.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.124+325G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954701 | |||||||
| chr16:89954730 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.124+354T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954730 | |||||||
| chr16:89954886 | A | G | 16 | a0001c0001t0001g0165 a0001c0001t0001g0192 a0001c0001t0003g0137 others(13): Show |
17 | HG01243.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.125-283A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954886 | |||||||
| chr16:89955059 | T | G | 3 | a0001c0001t0004g0012 a0001c0001t0004g0069 a0001c0001t0004g0151 |
6 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-110T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955059 | |||||||
| chr16:89955111 | G | C | 2 | a0001c0002t0012g0071 a0001c0002t0012g0072 |
2 | HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.125-58G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955111 | |||||||
| chr16:89955140 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.125-29G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955140 | |||||||
| chr16:89955157 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-12G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955157 | |||||||
| chr16:89955161 | T | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0167 others(15): Show |
42 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.125-8T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955161 | |||||||
| chr16:89955277 | A | G | 20 | a0001c0001t0001g0081 a0001c0001t0001g0192 a0001c0001t0002g0003 others(17): Show |
41 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.222+11A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955277 | |||||||
| chr16:89955303 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.222+37G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955303 | |||||||
| chr16:89955355 | G | T | 1 | a0001c0008t0005g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.222+89G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955355 | |||||||
| chr16:89955452 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.222+186C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955452 | |||||||
| chr16:89955485 | C | T | 2 | a0001c0002t0011g0161 a0001c0002t0024g0160 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.222+219C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955485 | |||||||
| chr16:89955517 | T | C | 2 | a0001c0002t0011g0161 a0001c0002t0024g0160 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.222+251T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955517 | |||||||
| chr16:89955629 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+363G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955629 | |||||||
| chr16:89955663 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.222+397T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955663 | |||||||
| chr16:89955715 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.222+449C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955715 | |||||||
| chr16:89955729 | T | C | 13 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(10): Show |
33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+463T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955729 | |||||||
| chr16:89955778 | T | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0174 |
2 | HG01192.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.222+512T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955778 | |||||||
| chr16:89955779 | A | T | 2 | a0001c0001t0019g0083 a0002c0005t0009g0196 |
2 | HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.222+513A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955779 | |||||||
| chr16:89955795 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.222+529G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955795 | |||||||
| chr16:89955799 | G | A | 7 | a0001c0001t0001g0060 a0001c0002t0007g0024 a0001c0002t0007g0056 others(4): Show |
8 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+533G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955799 | |||||||
| chr16:89955825 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+559C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955825 | |||||||
| chr16:89955828 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.222+562T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955828 | |||||||
| chr16:89955838 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+572T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955838 | |||||||
| chr16:89955839 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+573G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955839 | |||||||
| chr16:89955848 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+582G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955848 | |||||||
| chr16:89955861 | A | G | 13 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(10): Show |
33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+595A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955861 | |||||||
| chr16:89955888 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0010g0043 a0001c0001t0010g0182 others(1): Show |
5 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+622C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955888 | |||||||
| chr16:89956076 | G | GA | 49 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0109 others(46): Show |
77 | HG00099.hp2 HG00438.hp2 HG01081.hp2 others(74): Show |
intron_variant | MODIFIER | c.222+819dupA | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 89956076 | ||||||
| chr16:89956094 | A | G | 1 | a0001c0008t0005g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.222+828A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956094 | |||||||
| chr16:89956116 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.222+850A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956116 | |||||||
| chr16:89956195 | C | T | 12 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(9): Show |
32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.222+929C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956195 | |||||||
| chr16:89956228 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222+962G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956228 | |||||||
| chr16:89956283 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.222+1017C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956283 | |||||||
| chr16:89956285 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.222+1019T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956285 | |||||||
| chr16:89956330 | C | T | 12 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(9): Show |
32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.222+1064C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956330 | |||||||
| chr16:89956374 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.222+1108C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956374 | |||||||
| chr16:89956375 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0135 others(1): Show |
5 | HG00733.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+1109G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956375 | |||||||
| chr16:89956489 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.223-1022T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956489 | |||||||
| chr16:89956534 | C | T | 6 | a0001c0001t0001g0060 a0001c0002t0007g0024 a0001c0002t0007g0085 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-977C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956534 | |||||||
| chr16:89956544 | C | T | 1 | a0001c0001t0019g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.223-967C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956544 | |||||||
| chr16:89956566 | C | T | 1 | a0001c0001t0001g0020 | 3 | HG03927.hp2 NA18977.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.223-945C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956566 | |||||||
| chr16:89956679 | A | AT | 41 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0105 others(38): Show |
52 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.223-822dupT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 89956679 | ||||||
| chr16:89956766 | C | A | 1 | a0001c0009t0022g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.223-745C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956766 | |||||||
| chr16:89956864 | A | G | 15 | a0001c0001t0001g0092 a0001c0001t0003g0021 a0001c0001t0003g0041 others(12): Show |
22 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.223-647A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956864 | |||||||
| chr16:89956959 | C | G | 1 | a0001c0009t0022g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.223-552C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956959 | |||||||
| chr16:89956961 | C | G | 5 | a0001c0002t0011g0161 a0001c0002t0011g0188 a0001c0002t0017g0052 others(2): Show |
5 | HG00099.hp2 HG02965.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-550C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956961 | |||||||
| chr16:89956997 | C | A | 18 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(15): Show |
41 | HG00438.hp2 HG00639.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.223-514C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956997 | |||||||
| chr16:89957031 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.223-480C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957031 | |||||||
| chr16:89957061 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.223-450G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957061 | |||||||
| chr16:89957112 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.223-399C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957112 | |||||||
| chr16:89957236 | AAGGAAGT others(26): Show |
A | 1 | a0004c0007t0005g0046 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.223-273_223-241del others(33): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 89957236 | ||||||
| chr16:89957284 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.223-227G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957284 | |||||||
| chr16:89957417 | C | T | 2 | a0001c0002t0014g0149 a0001c0002t0014g0150 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.223-94C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957417 | |||||||
| chr16:89957440 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18970.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.223-71C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957440 | |||||||
| chr16:89957493 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(42): Show |
114 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.223-18C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957493 | |||||||
| chr16:89957683 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.372+23G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957683 | |||||||
| chr16:89957778 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.372+118A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957778 | |||||||
| chr16:89957794 | G | A | 38 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0109 others(35): Show |
60 | HG00099.hp2 HG00438.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.372+134G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957794 | |||||||
| chr16:89957798 | A | G | 60 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0109 others(57): Show |
92 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.372+138A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957798 | |||||||
| chr16:89957820 | C | T | 12 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(9): Show |
32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.372+160C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957820 | |||||||
| chr16:89958005 | C | T | 12 | a0001c0001t0003g0021 a0001c0001t0003g0049 a0001c0001t0003g0050 others(9): Show |
18 | HG00140.hp2 HG00733.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.372+345C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958005 | |||||||
| chr16:89958025 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.372+365G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958025 | |||||||
| chr16:89958039 | T | C | 12 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(9): Show |
32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.372+379T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958039 | |||||||
| chr16:89958248 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.372+588C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958248 | |||||||
| chr16:89958255 | T | G | 7 | a0001c0001t0001g0060 a0001c0002t0007g0024 a0001c0002t0007g0056 others(4): Show |
8 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+595T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958255 | |||||||
| chr16:89958306 | C | G | 11 | a0001c0002t0011g0161 a0001c0002t0011g0188 a0001c0002t0017g0052 others(8): Show |
12 | HG00099.hp2 HG01081.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.372+646C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958306 | |||||||
| chr16:89958317 | G | A | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.372+657G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958317 | |||||||
| chr16:89958439 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.373-575G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958439 | |||||||
| chr16:89958458 | C | T | 12 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(9): Show |
32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.373-556C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958458 | |||||||
| chr16:89958491 | T | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0081 a0001c0001t0002g0003 others(16): Show |
40 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.373-523T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958491 | |||||||
| chr16:89958492 | A | G | 19 | a0001c0001t0001g0060 a0001c0001t0001g0081 a0001c0001t0002g0003 others(16): Show |
40 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.373-522A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958492 | |||||||
| chr16:89958506 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.373-508A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958506 | |||||||
| chr16:89958558 | A | C | 1 | a0001c0001t0019g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.373-456A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958558 | |||||||
| chr16:89958562 | C | G | 24 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0002t0006g0047 others(21): Show |
26 | HG00099.hp2 HG01081.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.373-452C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958562 | |||||||
| chr16:89958713 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.373-301G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958713 | |||||||
| chr16:89958717 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.373-297G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958717 | |||||||
| chr16:89958727 | C | T | 13 | a0001c0001t0001g0081 a0001c0001t0001g0174 a0001c0001t0002g0003 others(10): Show |
33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.373-287C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958727 | |||||||
| chr16:89958881 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.373-133A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958881 | |||||||
| chr16:89958912 | C | T | 28 | a0001c0001t0001g0060 a0001c0001t0001g0081 a0001c0001t0002g0003 others(25): Show |
52 | HG00438.hp2 HG00639.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.373-102C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958912 | |||||||
| chr16:89959213 | G | A | 1 | a0001c0001t0010g0043 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.514+58G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959213 | |||||||
| chr16:89959232 | G | C | 26 | a0001c0001t0001g0060 a0001c0001t0001g0081 a0001c0001t0002g0003 others(23): Show |
50 | HG00438.hp2 HG00639.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.514+77G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959232 | |||||||
| chr16:89959411 | G | T | 3 | a0001c0003t0008g0162 a0001c0003t0008g0173 a0001c0003t0008g0190 |
3 | HG01081.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.514+256G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959411 | |||||||
| chr16:89959524 | T | G | 1 | a0001c0001t0019g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.514+369T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959524 | |||||||
| chr16:89959531 | A | G | 1 | a0001c0001t0001g0034 | 2 | NA18942.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.514+376A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959531 | |||||||
| chr16:89959533 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.514+378C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959533 | |||||||
| chr16:89959544 | G | T | 1 | a0001c0001t0003g0041 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.514+389G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959544 | |||||||
| chr16:89959597 | C | A | 13 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(10): Show |
33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.514+442C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959597 | |||||||
| chr16:89959641 | C | G | 13 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(10): Show |
33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.514+486C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959641 | |||||||
| chr16:89959662 | T | A | 7 | a0001c0002t0005g0016 a0001c0002t0005g0044 a0001c0002t0005g0045 others(4): Show |
10 | HG00639.hp1 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+507T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959662 | |||||||
| chr16:89959688 | G | A | 8 | a0001c0001t0001g0060 a0001c0002t0007g0024 a0001c0002t0007g0056 others(5): Show |
9 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+533G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959688 | |||||||
| chr16:89959698 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.514+543C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959698 | |||||||
| chr16:89959744 | A | G | 69 | a0001c0001t0001g0026 a0001c0001t0001g0060 a0001c0001t0001g0081 others(66): Show |
102 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.514+589A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959744 | |||||||
| chr16:89959760 | G | C | 7 | a0001c0002t0005g0016 a0001c0002t0005g0044 a0001c0002t0005g0045 others(4): Show |
10 | HG00639.hp1 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+605G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959760 | |||||||
| chr16:89959796 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.514+641C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959796 | |||||||
| chr16:89959804 | C | T | 1 | a0002c0004t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.514+649C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959804 | |||||||
| chr16:89959934 | G | A | 2 | a0001c0002t0017g0052 a0001c0002t0017g0053 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.514+779G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959934 | |||||||
| chr16:89959946 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.514+791G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959946 | |||||||
| chr16:89959964 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0133 others(11): Show |
20 | HG01192.hp1 HG02257.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.514+809C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959964 | |||||||
| chr16:89960006 | G | A | 1 | a0001c0002t0011g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.514+851G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960006 | |||||||
| chr16:89960080 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.515-851G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960080 | |||||||
| chr16:89960081 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.515-850C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960081 | |||||||
| chr16:89960104 | T | C | 66 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0109 others(63): Show |
97 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.515-827T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960104 | |||||||
| chr16:89960349 | T | G | 1 | a0001c0001t0023g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.515-582T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960349 | |||||||
| chr16:89960367 | A | G | 12 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0013 others(9): Show |
32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.515-564A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960367 | |||||||
| chr16:89960502 | C | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0100 others(2): Show |
6 | HG00733.hp1 HG01346.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-429C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960502 | |||||||
| chr16:89960571 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
122 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.515-360T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960571 | |||||||
| chr16:89960600 | C | T | 1 | a0001c0001t0023g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.515-331C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960600 | |||||||
| chr16:89960638 | G | T | 2 | a0001c0001t0003g0102 a0001c0001t0003g0152 |
2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.515-293G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960638 | |||||||
| chr16:89960792 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0100 others(2): Show |
6 | HG00733.hp1 HG01346.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-139C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960792 | |||||||
| chr16:89960861 | C | T | 4 | a0001c0001t0001g0192 a0002c0005t0009g0022 a0002c0005t0009g0170 others(1): Show |
6 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-70C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960861 | |||||||
| chr16:89961218 | A | T | 70 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0109 others(67): Show |
103 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.679+123A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961218 | |||||||
| chr16:89961274 | G | A | 1 | a0001c0001t0021g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.679+179G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961274 | |||||||
| chr16:89961297 | C | T | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp1 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+202C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961297 | |||||||
| chr16:89961398 | C | T | 1 | a0001c0001t0001g0009 | 4 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+303C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961398 | |||||||
| chr16:89961414 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0133 others(11): Show |
21 | HG00639.hp1 HG01192.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.679+319A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961414 | |||||||
| chr16:89961430 | G | A | 34 | a0001c0001t0001g0026 a0001c0001t0003g0021 a0001c0001t0003g0041 others(31): Show |
40 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.680-307G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961430 | |||||||
| chr16:89961476 | C | G | 6 | a0001c0002t0005g0016 a0001c0002t0005g0045 a0001c0002t0005g0185 others(3): Show |
8 | HG01884.hp1 HG02602.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-261C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961476 | |||||||
| chr16:89961536 | G | T | 30 | a0001c0001t0001g0026 a0001c0001t0001g0192 a0001c0001t0003g0021 others(27): Show |
38 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.680-201G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961536 | |||||||
| chr16:89961640 | C | T | 1 | a0001c0001t0019g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.680-97C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961640 | |||||||
| chr16:89961645 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.680-92G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961645 | |||||||
| chr16:89961674 | G | A | 2 | a0001c0002t0011g0161 a0001c0002t0024g0160 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.680-63G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961674 | |||||||
| chr16:89961698 | T | G | 43 | a0001c0001t0001g0026 a0001c0001t0001g0192 a0001c0001t0003g0021 others(40): Show |
52 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.680-39T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961698 | |||||||
| chr16:89961715 | C | T | 3 | a0001c0001t0010g0043 a0001c0001t0010g0182 a0001c0001t0010g0183 |
4 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-22C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961715 | |||||||
| chr16:89961996 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0189 |
3 | HG02738.hp1 HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.808-16C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 8/12 | chr16 | 89961996 | |||||||
| chr16:89962181 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.921+56G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962181 | |||||||
| chr16:89962268 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.921+143C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962268 | |||||||
| chr16:89962363 | T | C | 9 | a0001c0001t0001g0158 a0001c0002t0011g0161 a0001c0002t0011g0188 others(6): Show |
10 | HG00099.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.921+238T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962363 | |||||||
| chr16:89962387 | C | T | 6 | a0001c0002t0005g0016 a0001c0002t0005g0045 a0001c0002t0005g0185 others(3): Show |
8 | HG01884.hp1 HG02602.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+262C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962387 | |||||||
| chr16:89962581 | G | T | 1 | a0001c0001t0001g0017 | 3 | NA18945.hp2 NA19064.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.921+456G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962581 | |||||||
| chr16:89962697 | G | C | 11 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0163 others(8): Show |
31 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.921+572G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962697 | |||||||
| chr16:89962841 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.922-522G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962841 | |||||||
| chr16:89962994 | G | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0063 others(10): Show |
18 | HG00733.hp1 HG00733.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.922-369G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962994 | |||||||
| chr16:89962997 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.922-366C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962997 | |||||||
| chr16:89963009 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
77 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.922-354G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963009 | |||||||
| chr16:89963030 | G | A | 1 | a0001c0002t0005g0045 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.922-333G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963030 | |||||||
| chr16:89963089 | G | A | 1 | a0001c0001t0001g0030 | 2 | NA18939.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.922-274G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963089 | |||||||
| chr16:89963157 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.922-206G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963157 | |||||||
| chr16:89963172 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.922-191C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963172 | |||||||
| chr16:89963252 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0013g0010 a0001c0001t0013g0037 |
6 | HG00099.hp1 HG01074.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.922-111C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963252 | |||||||
| chr16:89963305 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.922-58A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963305 | |||||||
| chr16:89963342 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.922-21C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963342 | |||||||
| chr16:89963460 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1002+17G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963460 | |||||||
| chr16:89963491 | T | C | 6 | a0001c0002t0007g0024 a0001c0002t0007g0029 a0001c0002t0007g0056 others(3): Show |
8 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1002+48T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963491 | |||||||
| chr16:89963521 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1002+78C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963521 | |||||||
| chr16:89963522 | G | A | 15 | a0001c0001t0001g0192 a0001c0002t0007g0024 a0001c0002t0007g0029 others(12): Show |
20 | HG01081.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1002+79G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963522 | |||||||
| chr16:89963640 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1002+197C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963640 | |||||||
| chr16:89963655 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1002+212T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963655 | |||||||
| chr16:89963810 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1003-360C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963810 | |||||||
| chr16:89963878 | G | C | 3 | a0001c0001t0010g0043 a0001c0001t0010g0182 a0001c0001t0010g0183 |
4 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-292G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963878 | |||||||
| chr16:89963947 | T | C | 89 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
131 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1003-223T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963947 | |||||||
| chr16:89964012 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1003-158G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89964012 | |||||||
| chr16:89964066 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1003-104G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89964066 | |||||||
| chr16:89964122 | G | C | 10 | a0001c0002t0014g0149 a0001c0002t0014g0150 a0001c0003t0008g0039 others(7): Show |
13 | HG01081.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1003-48G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89964122 | |||||||
| chr16:89964362 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1143+52A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964362 | |||||||
| chr16:89964365 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1143+55G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964365 | |||||||
| chr16:89964409 | G | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0189 |
3 | HG02738.hp1 HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1144-57G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964409 | |||||||
| chr16:89964449 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1144-17C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964449 | |||||||
| chr16:89964595 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1253+20C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964595 | |||||||
| chr16:89964738 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1253+163T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964738 | |||||||
| chr16:89964814 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0125 |
2 | NA18939.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1253+239C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964814 | |||||||
| chr16:89964819 | C | A | 1 | a0001c0001t0002g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1253+244C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964819 | |||||||
| chr16:89964848 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1253+273C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964848 | |||||||
| chr16:89964954 | T | G | 3 | a0002c0005t0009g0022 a0002c0005t0009g0170 a0002c0005t0009g0196 |
5 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253+379T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964954 | |||||||
| chr16:89964964 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0138 a0003c0006t0001g0019 |
4 | NA18951.hp1 NA18968.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253+389G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964964 | |||||||
| chr16:89964986 | AT | A | 8 | a0001c0002t0007g0024 a0001c0002t0007g0029 a0001c0002t0007g0056 others(5): Show |
10 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1253+417delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr16 | 89964986 | ||||||
| chr16:89964994 | A | C | 8 | a0001c0002t0007g0024 a0001c0002t0007g0029 a0001c0002t0007g0056 others(5): Show |
10 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1253+419A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964994 | |||||||
| chr16:89965011 | G | A | 11 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0163 others(8): Show |
31 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.1253+436G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965011 | |||||||
| chr16:89965019 | T | A | 11 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0163 others(8): Show |
31 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.1253+444T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965019 | |||||||
| chr16:89965072 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1253+497C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965072 | |||||||
| chr16:89965320 | T | C | 1 | a0001c0009t0022g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1254-541T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965320 | |||||||
| chr16:89965357 | A | G | 1 | a0001c0002t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1254-504A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965357 | |||||||
| chr16:89965408 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1254-453A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965408 | |||||||
| chr16:89965640 | T | C | 50 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0088 others(47): Show |
63 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1254-221T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965640 | |||||||
| chr16:89965687 | C | T | 1 | a0001c0002t0025g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1254-174C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965687 | |||||||
| chr16:89965709 | G | A | 1 | a0001c0002t0024g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1254-152G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965709 | |||||||
| chr16:89965741 | T | C | 47 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0079 others(44): Show |
58 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.1254-120T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965741 | |||||||
| chr16:89965758 | G | C | 1 | a0001c0001t0001g0026 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1254-103G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965758 | |||||||
| chr16:89965824 | T | C | 37 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0002t0005g0016 others(34): Show |
45 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1254-37T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965824 | |||||||
| chr16:89965847 | C | G | 44 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0002t0005g0016 others(41): Show |
52 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1254-14C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965847 |