Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8796 |
| ensemblid | ENSG00000136155.17 |
| hgncid | 10573 |
| symbol | SCEL |
| name | sciellin |
| refseq_nuc | NM_144777.3 |
| refseq_prot | NP_659001.2 |
| ensembl_nuc | ENST00000349847.4 |
| ensembl_prot | ENSP00000302579.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 77535706 |
| end | 77645263 |
| strand | + |
| ver | v1.2 |
| region | chr13:77535706-77645263 |
| region5000 | chr13:77530706-77650263 |
| regionname0 | SCEL_chr13_77535706_77645263 |
| regionname5000 | SCEL_chr13_77530706_77650263 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 688 | 159 | 43 | 36 | 54 | 9 | 15 | 43 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0002 | 0/0 | 688 | 95 | 8 | 12 | 69 | 1 | 5 | 49 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0003 | 0/0 | 688 | 88 | 28 | 14 | 39 | 1 | 6 | 33 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0004 | 0/0 | 688 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0005 | 0/0 | 688 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0006 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0007 | 0/0 | 688 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0008 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(668): Show |
chr13 | 77530706 | 77650263 |
| a0009 | 0/0 | 688 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0010 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0011 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0012 | 0/0 | 688 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0013 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| a0014 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | MSNVT others(683): Show |
chr13 | 77530706 | 77650263 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 2064 | 94 | 16 | 26 | 31 | 6 | 14 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0001c0004 | 0/0 | 2064 | 60 | 24 | 10 | 22 | 3 | 1 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0001c0007 | 1/0 | 2064 | 3 | 2 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0001c0012 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0001c0016 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0002c0001 | 0/0 | 2064 | 94 | 8 | 12 | 68 | 1 | 5 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0002c0014 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0003c0003 | 0/0 | 2064 | 67 | 10 | 11 | 39 | 1 | 6 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0003c0005 | 0/0 | 2064 | 14 | 11 | 3 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0003c0006 | 0/0 | 2064 | 7 | 7 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0004c0008 | 0/0 | 2064 | 2 | 0 | 0 | 1 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0004c0015 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0005c0009 | 0/0 | 2064 | 2 | 0 | 2 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0006c0019 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0007c0018 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0008c0013 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2014): Show |
chr13 | 77530706 | 77650263 | ||
| a0009c0010 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0010c0017 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0011c0020 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0012c0011 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0013c0022 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 | ||
| a0014c0021 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | ATGTC others(2059): Show |
chr13 | 77530706 | 77650263 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/1 | 3194 | 94 | 16 | 26 | 31 | 6 | 14 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0001c0004t0001 | 0/0 | 3190 | 33 | 18 | 6 | 9 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0001c0004t0002 | 0/0 | 3194 | 26 | 5 | 4 | 13 | 3 | 1 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0001c0004t0005 | 0/0 | 3190 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0001c0007t0002 | 1/0 | 3194 | 3 | 2 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0001c0012t0002 | 0/0 | 3194 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0001c0016t0001 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0002c0001t0001 | 0/0 | 3190 | 89 | 7 | 12 | 64 | 1 | 5 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0002c0001t0002 | 0/0 | 3194 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0002c0001t0003 | 0/0 | 3190 | 3 | 0 | 0 | 3 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0002c0001t0007 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0002c0014t0002 | 0/0 | 3194 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0003c0003t0001 | 0/0 | 3190 | 65 | 10 | 11 | 37 | 1 | 6 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0003c0003t0004 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0003c0003t0006 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0003c0005t0002 | 0/0 | 3194 | 14 | 11 | 3 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0003c0006t0002 | 0/0 | 3194 | 7 | 7 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0004c0008t0001 | 0/0 | 3190 | 2 | 0 | 0 | 1 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0004c0015t0001 | 0/0 | 3190 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0005c0009t0002 | 0/0 | 3194 | 2 | 0 | 2 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0006c0019t0001 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0007c0018t0001 | 0/0 | 3190 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0008c0013t0002 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3144): Show |
chr13 | 77530706 | 77650263 |
| a0009c0010t0002 | 0/0 | 3194 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0010c0017t0001 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0011c0020t0001 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0012c0011t0002 | 0/0 | 3194 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3189): Show |
chr13 | 77530706 | 77650263 |
| a0013c0022t0001 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| a0014c0021t0001 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | AGGTA others(3185): Show |
chr13 | 77530706 | 77650263 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0004t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0007t0002g0329 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0007t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0007t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0012t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0001c0016t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0002c0014t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0003t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0005t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0006t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0006t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0006t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0006t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0006t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0006t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0003c0006t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0004c0008t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0004c0008t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0004c0015t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0005c0009t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0005c0009t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0006c0019t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0007c0018t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0008c0013t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0009c0010t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0010c0017t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0011c0020t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0012c0011t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0013c0022t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| a0014c0021t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0209 | EUR | GBR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0263 | EUR | GBR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00408 | hp1 | a0006 | c0019 | t0001 | g0085 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0171 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00438 | hp2 | a0001 | c0004 | t0002 | g0127 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00544 | hp1 | a0002 | c0001 | t0003 | g0299 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0252 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0187 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00597 | hp1 | a0001 | c0004 | t0002 | g0119 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0309 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00621 | hp2 | a0002 | c0001 | t0003 | g0297 | EAS | CHS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0142 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00733 | hp1 | a0001 | c0004 | t0002 | g0111 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0339 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00735 | hp2 | a0003 | c0005 | t0002 | g0044 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0264 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0114 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01071 | hp1 | a0001 | c0004 | t0002 | g0113 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0281 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0077 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0327 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0287 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0082 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0278 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01243 | hp1 | a0003 | c0005 | t0002 | g0018 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0277 | AMR | PUR | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01256 | hp1 | a0005 | c0009 | t0002 | g0211 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0270 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01258 | hp1 | a0005 | c0009 | t0002 | g0210 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01258 | hp2 | a0001 | c0004 | t0001 | g0243 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0245 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0266 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0140 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0222 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0275 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01496 | hp1 | a0003 | c0005 | t0002 | g0041 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0139 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01515 | hp1 | a0001 | c0004 | t0002 | g0118 | EUR | IBS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01515 | hp2 | a0007 | c0018 | t0001 | g0069 | EUR | IBS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0074 | EUR | IBS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01517 | hp1 | a0001 | c0004 | t0002 | g0109 | EUR | IBS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0072 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0328 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01891 | hp1 | a0003 | c0005 | t0002 | g0042 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0343 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0235 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0189 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0191 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0062 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01981 | hp1 | a0001 | c0004 | t0001 | g0326 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0313 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0196 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02015 | hp2 | a0001 | c0004 | t0002 | g0124 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0078 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0163 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0247 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0320 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0312 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0316 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0188 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0159 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02083 | hp1 | a0003 | c0003 | t0001 | g0173 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0186 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0233 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | CDX | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0168 | EAS | CDX | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | CDX | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0193 | EAS | CDX | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0267 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0227 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0176 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0302 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0300 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0244 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0234 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PEL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0335 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0166 | EAS | KHV | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0259 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0324 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02615 | hp1 | a0003 | c0005 | t0002 | g0052 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02615 | hp2 | a0001 | c0004 | t0002 | g0321 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02622 | hp1 | a0003 | c0005 | t0002 | g0047 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0261 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0285 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02630 | hp2 | a0001 | c0007 | t0002 | g0330 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02647 | hp1 | a0003 | c0006 | t0002 | g0012 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0334 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0154 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0103 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0340 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02717 | hp2 | a0002 | c0001 | t0001 | g0262 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02723 | hp1 | a0003 | c0005 | t0002 | g0016 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0286 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02735 | hp1 | a0004 | c0008 | t0001 | g0053 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0228 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0260 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0204 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02818 | hp2 | a0003 | c0005 | t0002 | g0280 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0063 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0135 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0205 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02896 | hp1 | a0003 | c0006 | t0002 | g0010 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0323 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0134 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0325 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0107 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02970 | hp1 | a0002 | c0001 | t0001 | g0322 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02970 | hp2 | a0003 | c0006 | t0002 | g0274 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0288 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0337 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0138 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0148 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03041 | hp1 | a0003 | c0006 | t0002 | g0011 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03041 | hp2 | a0001 | c0004 | t0002 | g0289 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03098 | hp2 | a0003 | c0005 | t0002 | g0061 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0065 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03130 | hp2 | a0002 | c0001 | t0002 | g0268 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0201 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03139 | hp2 | a0004 | c0015 | t0001 | g0019 | AFR | ESN | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03209 | hp1 | a0003 | c0006 | t0002 | g0347 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03225 | hp1 | a0001 | c0004 | t0002 | g0290 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03453 | hp2 | a0003 | c0005 | t0002 | g0273 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03486 | hp1 | a0003 | c0005 | t0002 | g0049 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0336 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0276 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0338 | AFR | GWD | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03579 | hp2 | a0003 | c0005 | t0002 | g0040 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0137 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0161 | SAS | PJL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03688 | hp1 | a0009 | c0010 | t0002 | g0232 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0094 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0265 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0150 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0116 | SAS | BEB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0093 | SAS | BEB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0081 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0147 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0027 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0279 | SAS | STU | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18522 | hp1 | a0003 | c0005 | t0002 | g0043 | AFR | YRI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18522 | hp2 | a0003 | c0006 | t0002 | g0344 | AFR | YRI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | CHB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18612 | hp2 | a0001 | c0004 | t0002 | g0225 | EAS | CHB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | CHB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0296 | EAS | CHB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18906 | hp1 | a0003 | c0005 | t0002 | g0017 | AFR | YRI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | YRI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0314 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0146 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18941 | hp1 | a0001 | c0004 | t0001 | g0283 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0169 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18944 | hp2 | a0001 | c0004 | t0001 | g0284 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18948 | hp1 | a0001 | c0016 | t0001 | g0218 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18952 | hp2 | a0002 | c0014 | t0002 | g0153 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18954 | hp2 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18956 | hp1 | a0010 | c0017 | t0001 | g0249 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18956 | hp2 | a0001 | c0004 | t0002 | g0122 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0076 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18961 | hp1 | a0002 | c0001 | t0001 | g0308 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18962 | hp2 | a0002 | c0001 | t0001 | g0304 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0318 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0251 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18967 | hp1 | a0002 | c0001 | t0001 | g0319 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18967 | hp2 | a0003 | c0003 | t0001 | g0291 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0269 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0238 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0307 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0236 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0095 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0108 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18975 | hp1 | a0001 | c0004 | t0002 | g0123 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0096 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18981 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18986 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18987 | hp1 | a0002 | c0001 | t0007 | g0157 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18987 | hp2 | a0001 | c0004 | t0001 | g0246 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18989 | hp1 | a0001 | c0004 | t0002 | g0256 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0272 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0315 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0100 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18997 | hp1 | a0002 | c0001 | t0001 | g0190 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18997 | hp2 | a0002 | c0001 | t0001 | g0305 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18998 | hp1 | a0001 | c0004 | t0002 | g0088 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0317 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0311 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0162 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19001 | hp2 | a0003 | c0003 | t0004 | g0056 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19002 | hp1 | a0001 | c0004 | t0002 | g0120 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19002 | hp2 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19007 | hp1 | a0001 | c0004 | t0002 | g0101 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19007 | hp2 | a0011 | c0020 | t0001 | g0180 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0181 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0133 | AFR | LWK | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19030 | hp2 | a0012 | c0011 | t0002 | g0346 | AFR | LWK | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19054 | hp1 | a0003 | c0003 | t0001 | g0055 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19055 | hp1 | a0001 | c0004 | t0001 | g0089 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19055 | hp2 | a0001 | c0004 | t0002 | g0129 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0306 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0237 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19062 | hp2 | a0002 | c0001 | t0003 | g0132 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19064 | hp1 | a0003 | c0003 | t0006 | g0106 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19064 | hp2 | a0001 | c0004 | t0002 | g0125 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19065 | hp1 | a0013 | c0022 | t0001 | g0298 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0282 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0271 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19070 | hp2 | a0004 | c0008 | t0001 | g0102 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19075 | hp1 | a0002 | c0001 | t0001 | g0149 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19076 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19076 | hp2 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0141 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0194 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19083 | hp1 | a0014 | c0021 | t0001 | g0172 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19085 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0310 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0152 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19089 | hp2 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19240 | hp1 | a0003 | c0006 | t0002 | g0345 | AFR | YRI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0206 | AFR | YRI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0341 | AFR | ASW | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | ASW | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0110 | EUR | TSI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0292 | EUR | TSI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | TSI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0241 | EUR | TSI | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | GIH | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20905 | hp2 | a0001 | c0004 | t0002 | g0121 | SAS | GIH | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0303 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | CLM | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02109 | hp1 | a0008 | c0013 | t0002 | g0200 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02109 | hp2 | a0001 | c0012 | t0002 | g0333 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0332 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG02559 | hp2 | a0001 | c0007 | t0002 | g0331 | AFR | ACB | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0050 | AFR | MSL | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA18955 | hp2 | a0001 | c0004 | t0002 | g0128 | EAS | JPT | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20300 | hp1 | a0001 | c0004 | t0005 | g0342 | AFR | USA | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA20300 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | USA | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA21309 | hp1 | a0001 | c0004 | t0002 | g0126 | AFR | LWK | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | LWK | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0036 | REF | REF | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| homoSapiens | grch38p0 | a0001 | c0007 | t0002 | g0329 | REF | REF | SCEL_chr13_77530706_77650263 | SCEL | chr13 | 77530706 | 77650263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77555907 | C | T | 1 | a0013 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.32C>T | p.Pro11Leu | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 2/33 | 170/3194 | 32/2067 | 11/688 | chr13 | 77555907 | |||
| chr13:77556617 | G | A | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.65G>A | p.Gly22Glu | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/33 | 203/3194 | 65/2067 | 22/688 | chr13 | 77556617 | |||
| chr13:77569381 | G | A | 1 | a0012 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.409G>A | p.Gly137Ser | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/33 | 547/3194 | 409/2067 | 137/688 | chr13 | 77569381 | |||
| chr13:77572138 | C | T | 1 | a0014 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.494C>T | p.Pro165Leu | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/33 | 632/3194 | 494/2067 | 165/688 | chr13 | 77572138 | |||
| chr13:77572168 | C | T | 1 | a0005 | 2 | HG01256.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.524C>T | p.Ser175Leu | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/33 | 662/3194 | 524/2067 | 175/688 | chr13 | 77572168 | |||
| chr13:77591459 | A | G | 1 | a0011 | 1 | NA19007.hp2 | missense_variant&splice_region_variant | MODERATE | c.691A>G | p.Arg231Gly | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/33 | 829/3194 | 691/2067 | 231/688 | chr13 | 77591459 | |||
| chr13:77597135 | TGTATGAA others(908): Show |
T | 1 | a0008 | 1 | HG02109.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.753-409_797+461del | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/33 | chr13 | 77597135 | |||||||
| chr13:77602697 | A | C | 1 | a0006 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.1021A>C | p.Asn341His | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 17/33 | 1159/3194 | 1021/2067 | 341/688 | chr13 | 77602697 | |||
| chr13:77604415 | G | A | 6 | a0002 a0004 a0008 others(3): Show |
102 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
missense_variant&splice_region_variant | MODERATE | c.1157G>A | p.Arg386Lys | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/33 | 1295/3194 | 1157/2067 | 386/688 | chr13 | 77604415 | |||
| chr13:77613943 | A | G | 5 | a0003 a0004 a0006 others(2): Show |
94 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
missense_variant | MODERATE | c.1439A>G | p.Lys480Arg | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/33 | 1577/3194 | 1439/2067 | 480/688 | chr13 | 77613943 | |||
| chr13:77618018 | A | G | 1 | a0007 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1586A>G | p.Asn529Ser | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/33 | 1724/3194 | 1586/2067 | 529/688 | chr13 | 77618018 | |||
| chr13:77634384 | A | G | 1 | a0010 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.1697A>G | p.Asn566Ser | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/33 | 1835/3194 | 1697/2067 | 566/688 | chr13 | 77634384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77572166 | C | T | 20 | a0001c0002 a0001c0004 a0001c0016 others(17): Show |
351 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(348): Show |
synonymous_variant | LOW | c.522C>T | p.Ser174Ser | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/33 | 660/3194 | 522/2067 | 174/688 | chr13 | 77572166 | |||
| chr13:77634442 | G | T | 1 | a0010c0017 | 1 | NA18956.hp1 | synonymous_variant | LOW | c.1755G>T | p.Val585Val | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/33 | 1893/3194 | 1755/2067 | 585/688 | chr13 | 77634442 | |||
| chr13:77642738 | A | G | 7 | a0001c0002 a0001c0012 a0002c0014 others(4): Show |
106 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(103): Show |
synonymous_variant | LOW | c.1980A>G | p.Leu660Leu | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/33 | 2118/3194 | 1980/2067 | 660/688 | chr13 | 77642738 | |||
| chr13:77642780 | C | T | 5 | a0001c0016 a0003c0003 a0004c0008 others(2): Show |
72 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
synonymous_variant | LOW | c.2022C>T | p.His674His | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/33 | 2160/3194 | 2022/2067 | 674/688 | chr13 | 77642780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77644305 | A | G | 1 | a0002c0001t0007 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 33/33 | 31 | chr13 | 77644305 | ||||||
| chr13:77644370 | T | C | 1 | a0003c0003t0004 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 33/33 | 96 | chr13 | 77644370 | ||||||
| chr13:77644629 | C | G | 1 | a0003c0003t0006 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*355C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 33/33 | 355 | chr13 | 77644629 | ||||||
| chr13:77644835 | T | C | 1 | a0001c0004t0005 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 33/33 | 561 | chr13 | 77644835 | ||||||
| chr13:77644967 | A | G | 1 | a0002c0001t0003 | 3 | HG00544.hp1 HG00621.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 33/33 | 693 | chr13 | 77644967 | ||||||
| chr13:77645088 | ATTTG | A | 17 | a0001c0004t0001 a0001c0004t0005 a0001c0016t0001 others(14): Show |
204 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*817_*820delTGTT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 33/33 | 817 | INFO_REALIGN_3_PRIME | chr13 | 77645088 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77536041 | T | C | 3 | a0003c0006t0002g0010 a0003c0006t0002g0011 a0003c0006t0002g0012 |
3 | HG02647.hp1 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-20+217T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77536041 | |||||||
| chr13:77536867 | A | C | 17 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+1043A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77536867 | |||||||
| chr13:77536939 | G | A | 39 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(36): Show |
39 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.-20+1115G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77536939 | |||||||
| chr13:77537139 | T | A | 100 | a0001c0002t0002g0002 a0001c0002t0002g0059 a0001c0002t0002g0064 others(97): Show |
102 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.-20+1315T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537139 | |||||||
| chr13:77537342 | G | A | 341 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(338): Show |
350 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.-20+1518G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537342 | |||||||
| chr13:77537437 | G | A | 3 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 |
3 | HG00642.hp2 HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-20+1613G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537437 | |||||||
| chr13:77537521 | C | T | 1 | a0002c0001t0001g0328 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+1697C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537521 | |||||||
| chr13:77537669 | C | T | 26 | a0001c0002t0002g0112 a0001c0002t0002g0116 a0001c0002t0002g0117 others(23): Show |
26 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-20+1845C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537669 | |||||||
| chr13:77537823 | T | C | 1 | a0001c0002t0002g0013 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-20+1999T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537823 | |||||||
| chr13:77537829 | A | G | 1 | a0001c0004t0001g0327 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-20+2005A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537829 | |||||||
| chr13:77537990 | G | C | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-20+2166G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77537990 | |||||||
| chr13:77538002 | T | C | 165 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(162): Show |
168 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.-20+2178T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538002 | |||||||
| chr13:77538073 | A | G | 9 | a0001c0004t0005g0342 a0002c0001t0001g0343 a0003c0006t0002g0010 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+2249A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538073 | |||||||
| chr13:77538115 | C | CT | 5 | a0001c0002t0002g0002 a0001c0002t0002g0293 a0001c0002t0002g0294 others(2): Show |
6 | HG00642.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+2311dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77538115 | ||||||
| chr13:77538115 | CT | C | 92 | a0001c0002t0002g0059 a0001c0002t0002g0138 a0001c0002t0002g0150 others(89): Show |
95 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-20+2311delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77538115 | ||||||
| chr13:77538115 | CTT | C | 41 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(38): Show |
41 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20+2310_-20+2311d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77538115 | ||||||
| chr13:77538202 | C | T | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-20+2378C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538202 | |||||||
| chr13:77538220 | G | A | 1 | a0001c0002t0002g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-20+2396G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538220 | |||||||
| chr13:77538277 | C | T | 2 | a0001c0002t0002g0292 a0001c0004t0001g0133 |
2 | NA19030.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-20+2453C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538277 | |||||||
| chr13:77538278 | G | A | 1 | a0003c0005t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-20+2454G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538278 | |||||||
| chr13:77538488 | A | AT | 10 | a0001c0004t0001g0009 a0001c0004t0001g0320 a0001c0004t0001g0323 others(7): Show |
11 | HG01099.hp2 HG01981.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+2671dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77538488 | ||||||
| chr13:77538505 | T | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(71): Show |
77 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.-20+2681T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538505 | |||||||
| chr13:77538887 | A | G | 1 | a0003c0005t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-20+3063A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538887 | |||||||
| chr13:77538908 | A | G | 17 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+3084A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538908 | |||||||
| chr13:77538925 | A | G | 2 | a0002c0001t0001g0193 a0002c0001t0001g0194 |
2 | HG02165.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-20+3101A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77538925 | |||||||
| chr13:77539089 | A | G | 131 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(128): Show |
134 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.-20+3265A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539089 | |||||||
| chr13:77539208 | G | A | 1 | a0002c0001t0001g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-20+3384G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539208 | |||||||
| chr13:77539242 | C | T | 28 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(25): Show |
31 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+3418C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539242 | |||||||
| chr13:77539606 | C | T | 48 | a0001c0002t0002g0059 a0001c0002t0002g0070 a0001c0002t0002g0087 others(45): Show |
49 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.-20+3782C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539606 | |||||||
| chr13:77539629 | C | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(2): Show |
6 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+3805C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539629 | |||||||
| chr13:77539710 | A | G | 17 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+3886A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539710 | |||||||
| chr13:77539735 | A | C | 342 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(339): Show |
351 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.-20+3911A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539735 | |||||||
| chr13:77539781 | G | A | 1 | a0002c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-20+3957G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539781 | |||||||
| chr13:77539792 | C | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(2): Show |
6 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+3968C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539792 | |||||||
| chr13:77539965 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(71): Show |
77 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.-20+4141C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539965 | |||||||
| chr13:77539982 | C | A | 84 | a0001c0002t0002g0150 a0001c0002t0002g0175 a0001c0002t0002g0176 others(81): Show |
84 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-20+4158C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77539982 | |||||||
| chr13:77540222 | T | G | 5 | a0002c0001t0001g0141 a0002c0001t0001g0143 a0002c0001t0001g0144 others(2): Show |
5 | HG00639.hp2 HG01346.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+4398T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77540222 | |||||||
| chr13:77540343 | G | A | 1 | a0003c0005t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-20+4519G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77540343 | |||||||
| chr13:77540365 | T | G | 341 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(338): Show |
350 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.-20+4541T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77540365 | |||||||
| chr13:77540765 | G | C | 17 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+4941G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77540765 | |||||||
| chr13:77540824 | T | C | 2 | a0002c0001t0001g0145 a0002c0001t0001g0146 |
2 | NA18939.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-20+5000T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77540824 | |||||||
| chr13:77541210 | T | C | 80 | a0001c0002t0002g0150 a0001c0002t0002g0175 a0001c0002t0002g0176 others(77): Show |
80 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-20+5386T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541210 | |||||||
| chr13:77541477 | C | T | 39 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(36): Show |
39 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.-20+5653C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541477 | |||||||
| chr13:77541495 | AT | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0320 a0001c0004t0001g0323 others(3): Show |
7 | HG01099.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+5672delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541495 | |||||||
| chr13:77541787 | T | G | 39 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(36): Show |
39 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.-20+5963T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541787 | |||||||
| chr13:77541881 | A | G | 1 | a0003c0003t0006g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-20+6057A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541881 | |||||||
| chr13:77541889 | C | T | 17 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+6065C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541889 | |||||||
| chr13:77541913 | G | T | 1 | a0001c0002t0002g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-20+6089G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541913 | |||||||
| chr13:77541929 | T | G | 17 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+6105T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77541929 | |||||||
| chr13:77542129 | G | A | 54 | a0001c0002t0002g0337 a0001c0004t0001g0009 a0001c0004t0001g0320 others(51): Show |
58 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.-20+6305G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542129 | |||||||
| chr13:77542136 | T | A | 26 | a0001c0002t0002g0112 a0001c0002t0002g0116 a0001c0002t0002g0117 others(23): Show |
26 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-20+6312T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542136 | |||||||
| chr13:77542178 | G | A | 4 | a0001c0002t0002g0281 a0001c0004t0001g0282 a0001c0004t0001g0283 others(1): Show |
4 | HG01081.hp1 NA18941.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+6354G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542178 | |||||||
| chr13:77542213 | C | G | 1 | a0003c0003t0001g0060 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-20+6389C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542213 | |||||||
| chr13:77542285 | C | T | 1 | a0001c0004t0001g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20+6461C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542285 | |||||||
| chr13:77542334 | G | A | 3 | a0003c0005t0002g0016 a0003c0005t0002g0017 a0003c0005t0002g0018 |
3 | HG01243.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-20+6510G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542334 | |||||||
| chr13:77542399 | C | CAACA | 56 | a0001c0002t0002g0002 a0001c0002t0002g0059 a0001c0002t0002g0064 others(53): Show |
58 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-20+6595_-20+6598d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77542399 | ||||||
| chr13:77542443 | A | G | 1 | a0003c0003t0001g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+6619A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542443 | |||||||
| chr13:77542450 | T | G | 1 | a0001c0002t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-20+6626T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542450 | |||||||
| chr13:77542601 | C | A | 1 | a0002c0001t0003g0297 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-20+6777C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542601 | |||||||
| chr13:77542683 | G | T | 2 | a0002c0001t0001g0145 a0002c0001t0001g0146 |
2 | NA18939.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-20+6859G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542683 | |||||||
| chr13:77542797 | A | G | 1 | a0002c0001t0001g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-20+6973A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542797 | |||||||
| chr13:77542873 | T | C | 9 | a0001c0004t0001g0009 a0001c0004t0001g0320 a0001c0004t0001g0323 others(6): Show |
10 | HG01099.hp2 HG01981.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+7049T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542873 | |||||||
| chr13:77542963 | C | T | 1 | a0002c0001t0001g0322 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-20+7139C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542963 | |||||||
| chr13:77542978 | T | C | 1 | a0001c0004t0001g0326 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-20+7154T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77542978 | |||||||
| chr13:77543082 | C | CT | 35 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0104 others(32): Show |
35 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.-20+7277dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77543082 | ||||||
| chr13:77543082 | C | CTT | 32 | a0001c0002t0002g0112 a0001c0002t0002g0116 a0001c0002t0002g0117 others(29): Show |
32 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-20+7276_-20+7277d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77543082 | ||||||
| chr13:77543082 | C | T | 1 | a0001c0004t0001g0326 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-20+7258C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543082 | |||||||
| chr13:77543083 | T | TC | 16 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(13): Show |
16 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+7259_-20+7260i others(3): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543083 | |||||||
| chr13:77543084 | T | C | 1 | a0003c0006t0002g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-20+7260T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543084 | |||||||
| chr13:77543115 | G | A | 1 | a0001c0002t0002g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-20+7291G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543115 | |||||||
| chr13:77543116 | C | A | 1 | a0001c0002t0002g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-20+7292C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543116 | |||||||
| chr13:77543118 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-20+7294C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543118 | |||||||
| chr13:77543240 | C | T | 2 | a0001c0004t0002g0321 a0002c0001t0001g0322 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-20+7416C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543240 | |||||||
| chr13:77543300 | G | C | 57 | a0001c0002t0002g0002 a0001c0002t0002g0059 a0001c0002t0002g0064 others(54): Show |
59 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.-20+7476G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543300 | |||||||
| chr13:77543326 | G | A | 1 | a0001c0002t0002g0260 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20+7502G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543326 | |||||||
| chr13:77543375 | G | A | 80 | a0001c0002t0002g0150 a0001c0002t0002g0175 a0001c0002t0002g0176 others(77): Show |
80 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-20+7551G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543375 | |||||||
| chr13:77543505 | A | C | 1 | a0002c0001t0001g0316 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20+7681A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543505 | |||||||
| chr13:77543537 | C | A | 4 | a0001c0002t0002g0281 a0001c0004t0001g0282 a0001c0004t0001g0283 others(1): Show |
4 | HG01081.hp1 NA18941.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7713C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543537 | |||||||
| chr13:77543828 | C | T | 1 | a0003c0003t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-20+8004C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77543828 | |||||||
| chr13:77544348 | C | T | 3 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0002c0001t0001g0328 |
3 | HG01884.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-20+8524C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544348 | |||||||
| chr13:77544366 | G | T | 1 | a0003c0003t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-20+8542G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544366 | |||||||
| chr13:77544372 | G | A | 3 | a0001c0002t0002g0020 a0001c0004t0002g0021 a0004c0015t0001g0019 |
3 | HG02451.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-20+8548G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544372 | |||||||
| chr13:77544696 | G | T | 1 | a0001c0002t0002g0257 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-20+8872G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544696 | |||||||
| chr13:77544728 | C | T | 1 | a0003c0005t0002g0280 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-20+8904C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544728 | |||||||
| chr13:77544796 | T | C | 1 | a0007c0018t0001g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-20+8972T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544796 | |||||||
| chr13:77544799 | A | G | 1 | a0001c0004t0002g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-20+8975A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544799 | |||||||
| chr13:77544915 | A | T | 1 | a0003c0003t0001g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-20+9091A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544915 | |||||||
| chr13:77544958 | A | G | 1 | a0002c0001t0001g0328 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+9134A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77544958 | |||||||
| chr13:77545011 | T | C | 1 | a0001c0002t0002g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-20+9187T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545011 | |||||||
| chr13:77545203 | G | C | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-20+9379G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545203 | |||||||
| chr13:77545382 | C | T | 25 | a0001c0002t0002g0112 a0001c0002t0002g0116 a0001c0002t0002g0117 others(22): Show |
25 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20+9558C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545382 | |||||||
| chr13:77545405 | T | C | 2 | a0003c0003t0001g0001 a0003c0003t0001g0071 |
3 | NA18983.hp2 NA19056.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-20+9581T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545405 | |||||||
| chr13:77545462 | G | A | 1 | a0003c0003t0001g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-20+9638G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545462 | |||||||
| chr13:77545597 | T | C | 1 | a0003c0003t0001g0334 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-20+9773T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545597 | |||||||
| chr13:77545696 | T | G | 341 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(338): Show |
350 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.-20+9872T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545696 | |||||||
| chr13:77545717 | T | C | 1 | a0003c0003t0001g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-20+9893T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545717 | |||||||
| chr13:77545750 | C | T | 17 | a0001c0002t0002g0337 a0001c0004t0001g0335 a0001c0004t0005g0342 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+9926C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545750 | |||||||
| chr13:77545828 | G | A | 1 | a0003c0003t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-20+10004G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545828 | |||||||
| chr13:77545909 | G | A | 341 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(338): Show |
350 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.-19-9948G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545909 | |||||||
| chr13:77545976 | C | T | 26 | a0001c0002t0002g0112 a0001c0002t0002g0116 a0001c0002t0002g0117 others(23): Show |
26 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19-9881C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77545976 | |||||||
| chr13:77546001 | C | T | 2 | a0001c0004t0002g0321 a0002c0001t0001g0322 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-19-9856C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546001 | |||||||
| chr13:77546025 | T | C | 1 | a0002c0001t0001g0322 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-19-9832T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546025 | |||||||
| chr13:77546107 | C | T | 1 | a0004c0008t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-19-9750C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546107 | |||||||
| chr13:77546135 | G | A | 5 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0002c0001t0001g0259 others(2): Show |
5 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-9722G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546135 | |||||||
| chr13:77546646 | A | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(2): Show |
6 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-9211A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546646 | |||||||
| chr13:77546683 | CA | C | 48 | a0001c0002t0002g0059 a0001c0002t0002g0070 a0001c0002t0002g0087 others(45): Show |
49 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.-19-9161delA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77546683 | ||||||
| chr13:77546814 | C | T | 1 | a0001c0002t0002g0068 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-19-9043C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546814 | |||||||
| chr13:77546843 | C | T | 1 | a0001c0004t0002g0256 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-19-9014C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546843 | |||||||
| chr13:77546915 | G | C | 1 | a0003c0003t0001g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-19-8942G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546915 | |||||||
| chr13:77546916 | C | G | 1 | a0003c0003t0001g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-19-8941C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546916 | |||||||
| chr13:77546957 | A | G | 26 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(23): Show |
29 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-19-8900A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77546957 | |||||||
| chr13:77547195 | C | A | 159 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(156): Show |
165 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.-19-8662C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77547195 | |||||||
| chr13:77547263 | G | A | 28 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(25): Show |
31 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-8594G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77547263 | |||||||
| chr13:77547265 | G | A | 122 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(119): Show |
124 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.-19-8592G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77547265 | |||||||
| chr13:77547391 | A | G | 10 | a0001c0002t0002g0255 a0001c0004t0001g0009 a0001c0004t0001g0320 others(7): Show |
11 | HG01099.hp2 HG01981.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-8466A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77547391 | |||||||
| chr13:77547561 | A | G | 122 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(119): Show |
124 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.-19-8296A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77547561 | |||||||
| chr13:77547601 | G | A | 7 | a0001c0002t0002g0285 a0001c0004t0001g0287 a0001c0004t0001g0288 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-8256G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77547601 | |||||||
| chr13:77548118 | A | G | 1 | a0003c0005t0002g0049 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19-7739A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77548118 | |||||||
| chr13:77548264 | C | T | 2 | a0001c0002t0002g0253 a0001c0002t0002g0254 |
2 | HG00558.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-19-7593C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77548264 | |||||||
| chr13:77548447 | C | T | 6 | a0001c0004t0001g0287 a0001c0004t0001g0288 a0001c0004t0002g0289 others(3): Show |
6 | HG01109.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-7410C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77548447 | |||||||
| chr13:77548967 | G | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(2): Show |
6 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-6890G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77548967 | |||||||
| chr13:77549114 | T | C | 1 | a0002c0001t0003g0299 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-19-6743T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549114 | |||||||
| chr13:77549214 | C | G | 56 | a0001c0002t0002g0002 a0001c0002t0002g0059 a0001c0002t0002g0064 others(53): Show |
58 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-19-6643C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549214 | |||||||
| chr13:77549218 | C | T | 56 | a0001c0002t0002g0002 a0001c0002t0002g0059 a0001c0002t0002g0064 others(53): Show |
58 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-19-6639C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549218 | |||||||
| chr13:77549393 | A | C | 86 | a0001c0002t0002g0002 a0001c0002t0002g0059 a0001c0002t0002g0064 others(83): Show |
88 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-19-6464A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549393 | |||||||
| chr13:77549587 | T | C | 1 | a0003c0005t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19-6270T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549587 | |||||||
| chr13:77549663 | C | T | 22 | a0001c0002t0002g0005 a0001c0002t0002g0198 a0001c0002t0002g0241 others(19): Show |
23 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-19-6194C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549663 | |||||||
| chr13:77549808 | G | A | 1 | a0001c0004t0001g0326 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-19-6049G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549808 | |||||||
| chr13:77549878 | C | T | 1 | a0001c0002t0002g0192 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-19-5979C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549878 | |||||||
| chr13:77549884 | G | A | 1 | a0001c0004t0002g0111 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-19-5973G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77549884 | |||||||
| chr13:77550008 | G | GT | 28 | a0001c0002t0002g0116 a0001c0002t0002g0117 a0001c0002t0002g0130 others(25): Show |
28 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19-5833dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77550008 | ||||||
| chr13:77550008 | GT | G | 52 | a0001c0002t0002g0059 a0001c0002t0002g0070 a0001c0002t0002g0087 others(49): Show |
53 | HG00408.hp1 HG00544.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.-19-5833delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77550008 | ||||||
| chr13:77550293 | C | T | 56 | a0001c0002t0002g0059 a0001c0002t0002g0070 a0001c0002t0002g0087 others(53): Show |
57 | HG00408.hp1 HG00544.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.-19-5564C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77550293 | |||||||
| chr13:77550387 | AAT | A | 213 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.-19-5445_-19-5444d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77550387 | ||||||
| chr13:77550387 | AATAT | A | 98 | a0001c0002t0002g0046 a0001c0002t0002g0059 a0001c0002t0002g0070 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19-5447_-19-5444d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77550387 | ||||||
| chr13:77550392 | A | G | 29 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(26): Show |
29 | HG00642.hp2 HG01081.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-19-5465A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77550392 | |||||||
| chr13:77550394 | A | G | 187 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.-19-5463A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77550394 | |||||||
| chr13:77550396 | A | G | 99 | a0001c0002t0002g0005 a0001c0002t0002g0046 a0001c0002t0002g0059 others(96): Show |
104 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19-5461A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77550396 | |||||||
| chr13:77550463 | C | T | 1 | a0001c0002t0002g0037 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-19-5394C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77550463 | |||||||
| chr13:77550532 | C | G | 2 | a0001c0002t0002g0231 a0009c0010t0002g0232 |
2 | HG00733.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-19-5325C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77550532 | |||||||
| chr13:77550547 | A | C | 80 | a0001c0002t0002g0013 a0001c0002t0002g0015 a0001c0002t0002g0028 others(77): Show |
80 | HG00544.hp1 HG00544.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.-19-5310A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77550547 | |||||||
| chr13:77551100 | C | T | 1 | a0001c0002t0002g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-4757C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551100 | |||||||
| chr13:77551121 | G | A | 2 | a0001c0004t0002g0113 a0001c0004t0002g0114 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-19-4736G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551121 | |||||||
| chr13:77551158 | C | G | 19 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19-4699C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551158 | |||||||
| chr13:77551241 | T | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.-19-4616T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551241 | |||||||
| chr13:77551266 | C | T | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-19-4591C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551266 | |||||||
| chr13:77551277 | C | T | 1 | a0014c0021t0001g0172 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-19-4580C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551277 | |||||||
| chr13:77551396 | A | C | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-4461A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551396 | |||||||
| chr13:77551513 | T | A | 1 | a0003c0005t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19-4344T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551513 | |||||||
| chr13:77551566 | C | T | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(98): Show |
104 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-4291C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551566 | |||||||
| chr13:77551610 | G | A | 1 | a0002c0001t0003g0299 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-19-4247G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551610 | |||||||
| chr13:77551680 | G | T | 1 | a0001c0004t0002g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-19-4177G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551680 | |||||||
| chr13:77551935 | A | C | 14 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-3922A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551935 | |||||||
| chr13:77551963 | C | T | 3 | a0001c0002t0002g0285 a0001c0004t0005g0342 a0002c0001t0001g0171 |
3 | HG00438.hp1 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-19-3894C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77551963 | |||||||
| chr13:77552143 | C | T | 9 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(6): Show |
10 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-3714C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552143 | |||||||
| chr13:77552144 | G | A | 33 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(30): Show |
33 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19-3713G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552144 | |||||||
| chr13:77552304 | C | A | 1 | a0001c0002t0002g0294 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-19-3553C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552304 | |||||||
| chr13:77552306 | C | G | 1 | a0001c0002t0002g0294 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-19-3551C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552306 | |||||||
| chr13:77552450 | A | G | 3 | a0001c0002t0002g0285 a0001c0004t0005g0342 a0002c0001t0001g0272 |
3 | HG02630.hp1 NA18989.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-19-3407A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552450 | |||||||
| chr13:77552451 | G | A | 3 | a0001c0002t0002g0285 a0001c0004t0005g0342 a0002c0001t0001g0272 |
3 | HG02630.hp1 NA18989.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-19-3406G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552451 | |||||||
| chr13:77552563 | T | G | 3 | a0001c0004t0001g0326 a0001c0004t0001g0335 a0001c0004t0002g0289 |
3 | HG01981.hp1 HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-3294T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552563 | |||||||
| chr13:77552688 | G | C | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-3169G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552688 | |||||||
| chr13:77552926 | T | A | 16 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-2931T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552926 | |||||||
| chr13:77552926 | T | C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-2931T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552926 | |||||||
| chr13:77552970 | T | A | 1 | a0001c0002t0002g0203 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-19-2887T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552970 | |||||||
| chr13:77552996 | T | C | 6 | a0003c0003t0001g0103 a0003c0003t0001g0199 a0003c0003t0001g0275 others(3): Show |
6 | HG01168.hp2 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-2861T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77552996 | |||||||
| chr13:77553024 | T | C | 3 | a0002c0001t0003g0132 a0002c0001t0003g0297 a0002c0001t0003g0299 |
3 | HG00544.hp1 HG00621.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-19-2833T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553024 | |||||||
| chr13:77553151 | C | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19-2706C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553151 | |||||||
| chr13:77553191 | C | T | 1 | a0002c0001t0001g0144 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-19-2666C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553191 | |||||||
| chr13:77553351 | A | G | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(98): Show |
104 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-2506A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553351 | |||||||
| chr13:77553437 | G | GA | 63 | a0001c0002t0002g0070 a0002c0001t0001g0073 a0003c0003t0001g0001 others(60): Show |
64 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-19-2411dupA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77553437 | ||||||
| chr13:77553479 | G | C | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19-2378G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553479 | |||||||
| chr13:77553505 | G | A | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.-19-2352G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553505 | |||||||
| chr13:77553634 | C | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(35): Show |
42 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-19-2223C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553634 | |||||||
| chr13:77553634 | C | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2223C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553634 | |||||||
| chr13:77553635 | G | A | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19-2222G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553635 | |||||||
| chr13:77553693 | G | A | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(98): Show |
104 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-2164G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553693 | |||||||
| chr13:77553731 | G | A | 2 | a0001c0004t0001g0201 a0001c0004t0001g0227 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-19-2126G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553731 | |||||||
| chr13:77553847 | G | A | 342 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(339): Show |
351 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.-19-2010G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553847 | |||||||
| chr13:77553856 | A | G | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-19-2001A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553856 | |||||||
| chr13:77553894 | G | A | 3 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 |
3 | HG00642.hp2 HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-19-1963G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77553894 | |||||||
| chr13:77554254 | T | C | 1 | a0001c0002t0002g0203 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-19-1603T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77554254 | |||||||
| chr13:77554257 | C | T | 1 | a0001c0002t0002g0091 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-19-1600C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77554257 | |||||||
| chr13:77554471 | C | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-1386C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77554471 | |||||||
| chr13:77554475 | G | A | 68 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(65): Show |
68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19-1382G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77554475 | |||||||
| chr13:77554608 | C | T | 8 | a0003c0003t0001g0174 a0003c0003t0001g0236 a0003c0003t0001g0237 others(5): Show |
8 | NA18953.hp1 NA18967.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-1249C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77554608 | |||||||
| chr13:77554677 | C | T | 1 | a0003c0003t0001g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-19-1180C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77554677 | |||||||
| chr13:77555134 | C | T | 2 | a0001c0004t0001g0065 a0001c0004t0001g0107 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-19-723C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77555134 | |||||||
| chr13:77555188 | A | G | 1 | a0003c0003t0001g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-19-669A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77555188 | |||||||
| chr13:77555264 | A | G | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19-593A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77555264 | |||||||
| chr13:77555635 | A | G | 2 | a0001c0002t0002g0035 a0001c0002t0002g0051 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-19-222A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | chr13 | 77555635 | |||||||
| chr13:77555673 | A | AAAAC | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-180_-19-177dup others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr13 | 77555673 | ||||||
| chr13:77555967 | A | G | 1 | a0001c0004t0002g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.43+49A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 2/32 | chr13 | 77555967 | |||||||
| chr13:77556074 | T | C | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.43+156T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 2/32 | chr13 | 77556074 | |||||||
| chr13:77556075 | C | T | 1 | a0001c0002t0002g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.43+157C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 2/32 | chr13 | 77556075 | |||||||
| chr13:77556323 | T | C | 1 | a0002c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.44-273T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 2/32 | chr13 | 77556323 | |||||||
| chr13:77556948 | A | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.161+235A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77556948 | |||||||
| chr13:77557071 | T | A | 1 | a0003c0003t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161+358T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77557071 | |||||||
| chr13:77557374 | C | T | 1 | a0001c0002t0002g0004 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.161+661C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77557374 | |||||||
| chr13:77557623 | C | T | 1 | a0002c0001t0001g0314 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.161+910C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77557623 | |||||||
| chr13:77557624 | A | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.161+911A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77557624 | |||||||
| chr13:77557631 | G | A | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.161+918G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77557631 | |||||||
| chr13:77557772 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+1059C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77557772 | |||||||
| chr13:77557954 | A | G | 1 | a0002c0001t0003g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.161+1241A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77557954 | |||||||
| chr13:77558016 | A | G | 220 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(217): Show |
227 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(224): Show |
intron_variant | MODIFIER | c.161+1303A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558016 | |||||||
| chr13:77558156 | C | T | 3 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0003c0003t0001g0235 |
3 | HG01928.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.161+1443C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558156 | |||||||
| chr13:77558421 | C | T | 14 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.162-1383C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558421 | |||||||
| chr13:77558535 | C | G | 1 | a0003c0003t0001g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.162-1269C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558535 | |||||||
| chr13:77558535 | C | T | 1 | a0001c0002t0002g0230 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.162-1269C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558535 | |||||||
| chr13:77558765 | G | A | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.162-1039G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558765 | |||||||
| chr13:77558773 | G | A | 1 | a0001c0002t0002g0013 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162-1031G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558773 | |||||||
| chr13:77558819 | C | CA | 98 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(95): Show |
101 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.162-964dupA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr13 | 77558819 | ||||||
| chr13:77558819 | CA | C | 68 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(65): Show |
69 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.162-964delA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr13 | 77558819 | ||||||
| chr13:77558819 | CAAA | C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.162-966_162-964del others(3): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr13 | 77558819 | ||||||
| chr13:77558941 | C | T | 16 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.162-863C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77558941 | |||||||
| chr13:77559065 | G | A | 1 | a0002c0001t0001g0147 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.162-739G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559065 | |||||||
| chr13:77559190 | C | G | 1 | a0001c0002t0002g0257 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-614C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559190 | |||||||
| chr13:77559296 | C | G | 1 | a0002c0001t0001g0182 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.162-508C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559296 | |||||||
| chr13:77559298 | G | A | 14 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.162-506G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559298 | |||||||
| chr13:77559302 | A | T | 10 | a0003c0003t0001g0001 a0003c0003t0001g0039 a0003c0003t0001g0071 others(7): Show |
11 | NA18954.hp1 NA18959.hp2 NA18968.hp2 others(8): Show |
intron_variant | MODIFIER | c.162-502A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559302 | |||||||
| chr13:77559389 | C | A | 1 | a0002c0001t0001g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.162-415C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559389 | |||||||
| chr13:77559401 | A | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.162-403A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559401 | |||||||
| chr13:77559422 | G | T | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-382G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559422 | |||||||
| chr13:77559510 | A | AAACAC | 55 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0002g0204 others(52): Show |
58 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.162-258_162-254dup others(5): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr13 | 77559510 | ||||||
| chr13:77559510 | A | AAACACAA others(3): Show |
13 | a0001c0002t0002g0116 a0001c0002t0002g0241 a0001c0004t0001g0009 others(10): Show |
14 | HG00735.hp1 HG01099.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.162-263_162-254dup others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr13 | 77559510 | ||||||
| chr13:77559510 | AAACAC | A | 35 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(32): Show |
36 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.162-258_162-254del others(5): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr13 | 77559510 | ||||||
| chr13:77559510 | AAACACAA others(3): Show |
A | 74 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(71): Show |
74 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.162-263_162-254del others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr13 | 77559510 | ||||||
| chr13:77559726 | C | T | 1 | a0001c0004t0001g0320 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-78C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 3/32 | chr13 | 77559726 | |||||||
| chr13:77559901 | C | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+38C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77559901 | |||||||
| chr13:77559951 | C | T | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.221+88C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77559951 | |||||||
| chr13:77560048 | C | G | 1 | a0002c0001t0001g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.221+185C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560048 | |||||||
| chr13:77560265 | T | TA | 251 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.221+421dupA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr13 | 77560265 | ||||||
| chr13:77560265 | T | TAAA | 28 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(25): Show |
31 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.221+419_221+421dup others(3): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr13 | 77560265 | ||||||
| chr13:77560333 | G | C | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+470G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560333 | |||||||
| chr13:77560418 | C | T | 2 | a0001c0002t0002g0223 a0001c0004t0001g0227 |
2 | HG02071.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.221+555C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560418 | |||||||
| chr13:77560419 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.221+556G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560419 | |||||||
| chr13:77560486 | A | G | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.221+623A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560486 | |||||||
| chr13:77560540 | C | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.221+677C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560540 | |||||||
| chr13:77560700 | A | G | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(98): Show |
104 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.221+837A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560700 | |||||||
| chr13:77560865 | G | A | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.221+1002G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560865 | |||||||
| chr13:77560873 | T | C | 8 | a0003c0003t0001g0077 a0003c0003t0001g0082 a0003c0003t0001g0140 others(5): Show |
8 | HG00639.hp2 HG01099.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+1010T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560873 | |||||||
| chr13:77560894 | G | T | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.221+1031G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560894 | |||||||
| chr13:77560900 | C | T | 94 | a0001c0002t0002g0070 a0001c0002t0002g0104 a0003c0003t0001g0001 others(91): Show |
95 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.221+1037C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77560900 | |||||||
| chr13:77560960 | T | TTGTGACC others(317): Show |
1 | a0003c0003t0001g0340 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.221+1110_221+1111i others(326): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr13 | 77560960 | ||||||
| chr13:77560960 | T | TTGTGACC others(318): Show |
4 | a0003c0003t0001g0334 a0003c0003t0001g0338 a0003c0003t0001g0339 others(1): Show |
4 | HG00735.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+1110_221+1111i others(327): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr13 | 77560960 | ||||||
| chr13:77561037 | A | G | 1 | a0003c0003t0001g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.221+1174A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561037 | |||||||
| chr13:77561253 | A | G | 1 | a0003c0003t0001g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.221+1390A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561253 | |||||||
| chr13:77561255 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.221+1392G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561255 | |||||||
| chr13:77561335 | A | G | 3 | a0002c0001t0001g0259 a0002c0001t0001g0261 a0002c0001t0001g0262 |
3 | HG02572.hp1 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.221+1472A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561335 | |||||||
| chr13:77561388 | T | TATAA | 3 | a0003c0003t0001g0174 a0003c0003t0001g0236 a0003c0003t0001g0291 |
3 | NA18967.hp2 NA18971.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.221+1526_221+1529d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr13 | 77561388 | ||||||
| chr13:77561467 | T | G | 77 | a0001c0002t0002g0070 a0001c0002t0002g0104 a0003c0003t0001g0001 others(74): Show |
78 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.221+1604T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561467 | |||||||
| chr13:77561600 | G | C | 1 | a0001c0004t0002g0290 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.221+1737G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561600 | |||||||
| chr13:77561701 | C | T | 1 | a0002c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.221+1838C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561701 | |||||||
| chr13:77561851 | A | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.222-1980A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561851 | |||||||
| chr13:77561975 | C | T | 61 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(58): Show |
62 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.222-1856C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77561975 | |||||||
| chr13:77562026 | T | C | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(104): Show |
111 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.222-1805T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562026 | |||||||
| chr13:77562130 | A | G | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.222-1701A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562130 | |||||||
| chr13:77562167 | C | G | 1 | a0003c0003t0001g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.222-1664C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562167 | |||||||
| chr13:77562206 | T | C | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.222-1625T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562206 | |||||||
| chr13:77562247 | C | T | 1 | a0002c0001t0001g0190 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.222-1584C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562247 | |||||||
| chr13:77562257 | G | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.222-1574G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562257 | |||||||
| chr13:77562316 | C | T | 1 | a0002c0001t0001g0151 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.222-1515C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562316 | |||||||
| chr13:77562420 | T | C | 19 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.222-1411T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562420 | |||||||
| chr13:77562544 | G | A | 17 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-1287G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562544 | |||||||
| chr13:77562636 | T | C | 1 | a0012c0011t0002g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.222-1195T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562636 | |||||||
| chr13:77562704 | T | G | 193 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(190): Show |
197 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.222-1127T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562704 | |||||||
| chr13:77562849 | C | G | 1 | a0002c0001t0001g0313 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.222-982C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562849 | |||||||
| chr13:77562949 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.222-882A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77562949 | |||||||
| chr13:77563225 | C | T | 1 | a0004c0008t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.222-606C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77563225 | |||||||
| chr13:77563229 | CCTTT | C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.222-599_222-596del others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr13 | 77563229 | ||||||
| chr13:77563268 | C | T | 2 | a0001c0004t0001g0326 a0001c0004t0001g0335 |
2 | HG01981.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.222-563C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77563268 | |||||||
| chr13:77563796 | G | T | 4 | a0001c0004t0001g0243 a0001c0004t0001g0244 a0001c0004t0001g0245 others(1): Show |
4 | HG01258.hp2 HG01261.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-35G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | chr13 | 77563796 | |||||||
| chr13:77563797 | A | AT | 52 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(49): Show |
53 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.222-21dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr13 | 77563797 | ||||||
| chr13:77564062 | C | G | 94 | a0001c0002t0002g0070 a0001c0002t0002g0104 a0003c0003t0001g0001 others(91): Show |
95 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.290+163C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564062 | |||||||
| chr13:77564117 | T | A | 1 | a0001c0004t0001g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290+218T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564117 | |||||||
| chr13:77564191 | G | GT | 50 | a0001c0002t0002g0031 a0001c0002t0002g0067 a0001c0002t0002g0094 others(47): Show |
50 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.290+309dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr13 | 77564191 | ||||||
| chr13:77564191 | GT | G | 34 | a0001c0002t0002g0020 a0001c0002t0002g0045 a0001c0002t0002g0285 others(31): Show |
37 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.290+309delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr13 | 77564191 | ||||||
| chr13:77564300 | G | A | 1 | a0001c0002t0002g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.290+401G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564300 | |||||||
| chr13:77564421 | G | T | 1 | a0003c0005t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.290+522G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564421 | |||||||
| chr13:77564531 | A | T | 19 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.290+632A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564531 | |||||||
| chr13:77564796 | T | C | 1 | a0003c0003t0001g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.290+897T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564796 | |||||||
| chr13:77564819 | G | A | 1 | a0003c0003t0001g0276 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.290+920G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564819 | |||||||
| chr13:77564938 | A | G | 99 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(96): Show |
102 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.290+1039A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77564938 | |||||||
| chr13:77565097 | A | G | 1 | a0001c0002t0002g0222 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.290+1198A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77565097 | |||||||
| chr13:77565148 | C | T | 4 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0252 others(1): Show |
4 | HG00544.hp2 NA18956.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+1249C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77565148 | |||||||
| chr13:77565341 | A | G | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.290+1442A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77565341 | |||||||
| chr13:77565784 | G | A | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.290+1885G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77565784 | |||||||
| chr13:77565786 | CAT | C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.290+1889_290+1890d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr13 | 77565786 | ||||||
| chr13:77565912 | C | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.291-1768C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77565912 | |||||||
| chr13:77566157 | G | T | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.291-1523G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77566157 | |||||||
| chr13:77566461 | T | TGATAACC others(1911): Show |
26 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(23): Show |
29 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.291-1206_291-1205i others(1920): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr13 | 77566461 | ||||||
| chr13:77566461 | T | TGATAACC others(1911): Show |
1 | a0002c0001t0001g0311 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.291-1206_291-1205i others(1920): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr13 | 77566461 | ||||||
| chr13:77566633 | C | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-1047C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77566633 | |||||||
| chr13:77566641 | C | G | 5 | a0003c0003t0001g0334 a0003c0003t0001g0338 a0003c0003t0001g0339 others(2): Show |
5 | HG00735.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-1039C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77566641 | |||||||
| chr13:77566720 | T | G | 2 | a0001c0004t0001g0201 a0001c0004t0001g0227 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.291-960T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77566720 | |||||||
| chr13:77566757 | C | T | 1 | a0001c0004t0002g0127 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.291-923C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77566757 | |||||||
| chr13:77567130 | C | T | 1 | a0001c0002t0002g0150 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.291-550C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567130 | |||||||
| chr13:77567154 | A | G | 94 | a0001c0002t0002g0070 a0001c0002t0002g0104 a0003c0003t0001g0001 others(91): Show |
95 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.291-526A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567154 | |||||||
| chr13:77567166 | A | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.291-514A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567166 | |||||||
| chr13:77567193 | C | T | 7 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(4): Show |
8 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-487C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567193 | |||||||
| chr13:77567314 | C | T | 1 | a0002c0001t0001g0322 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.291-366C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567314 | |||||||
| chr13:77567315 | G | A | 94 | a0001c0002t0002g0070 a0001c0002t0002g0104 a0003c0003t0001g0001 others(91): Show |
95 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.291-365G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567315 | |||||||
| chr13:77567343 | G | A | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.291-337G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567343 | |||||||
| chr13:77567634 | A | G | 1 | a0003c0003t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.291-46A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 5/32 | chr13 | 77567634 | |||||||
| chr13:77567944 | C | G | 1 | a0001c0004t0001g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.359+196C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 6/32 | chr13 | 77567944 | |||||||
| chr13:77568070 | G | A | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.360-225G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 6/32 | chr13 | 77568070 | |||||||
| chr13:77568109 | T | C | 1 | a0001c0004t0001g0089 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.360-186T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 6/32 | chr13 | 77568109 | |||||||
| chr13:77568377 | C | T | 1 | a0003c0005t0002g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.398+44C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568377 | |||||||
| chr13:77568460 | A | T | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.398+127A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568460 | |||||||
| chr13:77568470 | A | G | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.398+137A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568470 | |||||||
| chr13:77568472 | C | A | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.398+139C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568472 | |||||||
| chr13:77568473 | A | G | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.398+140A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568473 | |||||||
| chr13:77568475 | A | G | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.398+142A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568475 | |||||||
| chr13:77568476 | A | T | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.398+143A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568476 | |||||||
| chr13:77568518 | GA | G | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.398+193delA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr13 | 77568518 | ||||||
| chr13:77568605 | C | T | 4 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0002g0248 others(1): Show |
4 | HG00741.hp1 HG01070.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+272C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568605 | |||||||
| chr13:77568751 | C | T | 3 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 |
3 | HG00642.hp2 HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.398+418C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77568751 | |||||||
| chr13:77569023 | A | G | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.399-348A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77569023 | |||||||
| chr13:77569054 | A | G | 1 | a0001c0002t0002g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.399-317A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77569054 | |||||||
| chr13:77569092 | G | A | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.399-279G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77569092 | |||||||
| chr13:77569136 | A | G | 11 | a0002c0001t0001g0115 a0002c0001t0001g0136 a0002c0001t0001g0163 others(8): Show |
11 | HG00597.hp2 HG02027.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.399-235A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77569136 | |||||||
| chr13:77569190 | G | T | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.399-181G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 7/32 | chr13 | 77569190 | |||||||
| chr13:77569525 | T | C | 1 | a0003c0003t0001g0079 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.479+74T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77569525 | |||||||
| chr13:77569621 | C | G | 1 | a0001c0002t0002g0117 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.479+170C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77569621 | |||||||
| chr13:77569699 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.479+248A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77569699 | |||||||
| chr13:77569973 | G | A | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.479+522G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77569973 | |||||||
| chr13:77570421 | C | T | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.479+970C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77570421 | |||||||
| chr13:77570581 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.479+1130C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77570581 | |||||||
| chr13:77570657 | T | C | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+1206T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77570657 | |||||||
| chr13:77570876 | T | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.480-1248T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77570876 | |||||||
| chr13:77570993 | A | G | 14 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.480-1131A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77570993 | |||||||
| chr13:77571055 | C | T | 2 | a0001c0004t0002g0113 a0001c0004t0002g0114 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.480-1069C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571055 | |||||||
| chr13:77571170 | C | T | 1 | a0003c0003t0001g0275 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.480-954C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571170 | |||||||
| chr13:77571304 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.480-820G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571304 | |||||||
| chr13:77571339 | C | T | 1 | a0002c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.480-785C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571339 | |||||||
| chr13:77571378 | CA | C | 233 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(230): Show |
240 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.480-729delA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571378 | ||||||
| chr13:77571378 | CAA | C | 75 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(72): Show |
76 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.480-730_480-729del others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571378 | ||||||
| chr13:77571395 | A | T | 1 | a0002c0001t0001g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.480-729A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571395 | |||||||
| chr13:77571397 | T | A | 1 | a0002c0001t0001g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.480-727T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571397 | |||||||
| chr13:77571515 | C | A | 77 | a0001c0002t0002g0070 a0001c0002t0002g0104 a0003c0003t0001g0001 others(74): Show |
78 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.480-609C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571515 | |||||||
| chr13:77571636 | C | T | 1 | a0002c0001t0001g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.480-488C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571636 | |||||||
| chr13:77571653 | C | T | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.480-471C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571653 | |||||||
| chr13:77571659 | G | A | 321 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(318): Show |
330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.480-465G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571659 | |||||||
| chr13:77571660 | G | C | 1 | a0002c0001t0001g0006 | 2 | NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.480-464G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571660 | |||||||
| chr13:77571712 | C | CAT | 191 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.480-394_480-393dup others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571712 | ||||||
| chr13:77571712 | C | CATAT | 10 | a0001c0004t0002g0139 a0002c0001t0001g0262 a0002c0001t0001g0270 others(7): Show |
10 | HG01243.hp1 HG01256.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-396_480-393dup others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571712 | ||||||
| chr13:77571712 | C | CATATAT | 4 | a0003c0003t0001g0334 a0003c0003t0001g0338 a0003c0003t0001g0340 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-398_480-393dup others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571712 | ||||||
| chr13:77571712 | C | CATATATA others(1): Show |
14 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(11): Show |
17 | HG00544.hp1 HG00735.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.480-400_480-393dup others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571712 | ||||||
| chr13:77571712 | C | CATATATA others(3): Show |
13 | a0002c0001t0001g0304 a0002c0001t0001g0305 a0002c0001t0001g0306 others(10): Show |
13 | HG00621.hp1 HG00621.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.480-402_480-393dup others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571712 | ||||||
| chr13:77571712 | C | CATATATA others(5): Show |
2 | a0002c0001t0001g0318 a0002c0001t0001g0319 |
2 | NA18964.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.480-404_480-393dup others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr13 | 77571712 | ||||||
| chr13:77571728 | T | G | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-396T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571728 | |||||||
| chr13:77571730 | T | G | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-394T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571730 | |||||||
| chr13:77571856 | G | A | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.480-268G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571856 | |||||||
| chr13:77571944 | G | A | 1 | a0002c0001t0003g0299 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.480-180G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 8/32 | chr13 | 77571944 | |||||||
| chr13:77572300 | G | T | 1 | a0003c0003t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.545+111G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77572300 | |||||||
| chr13:77572519 | T | C | 1 | a0001c0002t0002g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.545+330T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77572519 | |||||||
| chr13:77572696 | C | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.545+507C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77572696 | |||||||
| chr13:77572941 | C | T | 1 | a0001c0002t0002g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.545+752C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77572941 | |||||||
| chr13:77572992 | G | T | 11 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(8): Show |
12 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.545+803G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77572992 | |||||||
| chr13:77573330 | A | G | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.545+1141A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573330 | |||||||
| chr13:77573380 | A | T | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.545+1191A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573380 | |||||||
| chr13:77573428 | C | T | 1 | a0003c0003t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.545+1239C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573428 | |||||||
| chr13:77573546 | A | G | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.545+1357A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573546 | |||||||
| chr13:77573590 | G | A | 107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(104): Show |
111 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.545+1401G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573590 | |||||||
| chr13:77573598 | AC | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.545+1410delC | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573598 | |||||||
| chr13:77573601 | C | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.545+1412C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573601 | |||||||
| chr13:77573613 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.545+1424G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573613 | |||||||
| chr13:77573638 | C | CATCT | 27 | a0001c0002t0002g0064 a0001c0002t0002g0138 a0001c0002t0002g0175 others(24): Show |
27 | HG00099.hp2 HG00741.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.545+1490_545+1493d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77573638 | ||||||
| chr13:77573638 | C | CATCTATC others(1): Show |
3 | a0001c0002t0002g0104 a0001c0004t0001g0108 a0002c0001t0001g0322 |
3 | HG02970.hp1 HG03225.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.545+1486_545+1493d others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77573638 | ||||||
| chr13:77573638 | CATCT | C | 119 | a0001c0002t0002g0004 a0001c0002t0002g0014 a0001c0002t0002g0025 others(116): Show |
121 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.545+1490_545+1493d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77573638 | ||||||
| chr13:77573638 | CATCTATC others(1): Show |
C | 29 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0223 others(26): Show |
29 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.545+1486_545+1493d others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77573638 | ||||||
| chr13:77573638 | CATCTATC others(5): Show |
C | 6 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(3): Show |
6 | HG02015.hp2 HG02257.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+1482_545+1493d others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77573638 | ||||||
| chr13:77573638 | CATCTATC others(9): Show |
C | 2 | a0001c0004t0002g0125 a0002c0001t0001g0184 |
2 | NA19064.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.545+1478_545+1493d others(18): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77573638 | ||||||
| chr13:77573697 | T | A | 3 | a0003c0003t0001g0095 a0003c0003t0001g0096 a0003c0003t0001g0097 |
3 | NA18973.hp2 NA18980.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.545+1508T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573697 | |||||||
| chr13:77573767 | C | T | 1 | a0001c0002t0002g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.545+1578C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573767 | |||||||
| chr13:77573871 | G | T | 1 | a0001c0004t0001g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.545+1682G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573871 | |||||||
| chr13:77573915 | C | T | 1 | a0003c0005t0002g0280 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.545+1726C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77573915 | |||||||
| chr13:77574144 | A | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.545+1955A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77574144 | |||||||
| chr13:77574145 | A | G | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.545+1956A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77574145 | |||||||
| chr13:77574306 | T | C | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.545+2117T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77574306 | |||||||
| chr13:77574577 | G | A | 17 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.545+2388G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77574577 | |||||||
| chr13:77574651 | T | C | 1 | a0003c0003t0001g0095 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.545+2462T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77574651 | |||||||
| chr13:77574877 | C | G | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.545+2688C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77574877 | |||||||
| chr13:77574892 | A | G | 9 | a0003c0005t0002g0016 a0003c0005t0002g0017 a0003c0005t0002g0018 others(6): Show |
9 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.545+2703A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77574892 | |||||||
| chr13:77575253 | CT | C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.545+3075delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77575253 | ||||||
| chr13:77575345 | T | G | 1 | a0001c0002t0002g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.545+3156T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77575345 | |||||||
| chr13:77575549 | A | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.545+3360A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77575549 | |||||||
| chr13:77575553 | A | G | 19 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.545+3364A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77575553 | |||||||
| chr13:77575994 | G | A | 76 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(73): Show |
77 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.545+3805G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77575994 | |||||||
| chr13:77576102 | T | C | 1 | a0001c0002t0002g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.545+3913T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77576102 | |||||||
| chr13:77576124 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+3935G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77576124 | |||||||
| chr13:77576316 | T | TCCC | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.545+4129_545+4130i others(5): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77576316 | ||||||
| chr13:77576370 | T | C | 1 | a0001c0002t0002g0205 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.545+4181T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77576370 | |||||||
| chr13:77576452 | CT | C | 14 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.545+4264delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77576452 | |||||||
| chr13:77576616 | A | C | 2 | a0001c0002t0002g0002 a0001c0002t0002g0064 |
3 | HG01175.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.545+4427A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77576616 | |||||||
| chr13:77576676 | C | T | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02818.hp1 HG02895.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+4487C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77576676 | |||||||
| chr13:77577149 | G | A | 1 | a0001c0002t0002g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.545+4960G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77577149 | |||||||
| chr13:77577373 | G | A | 193 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(190): Show |
197 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.545+5184G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77577373 | |||||||
| chr13:77577592 | G | A | 1 | a0003c0003t0001g0233 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.545+5403G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77577592 | |||||||
| chr13:77577758 | A | G | 1 | a0001c0002t0002g0028 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.545+5569A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77577758 | |||||||
| chr13:77577854 | T | C | 1 | a0003c0003t0001g0340 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.545+5665T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77577854 | |||||||
| chr13:77577973 | C | T | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+5784C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77577973 | |||||||
| chr13:77578206 | C | T | 1 | a0001c0002t0002g0004 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.545+6017C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578206 | |||||||
| chr13:77578279 | C | G | 1 | a0002c0001t0001g0191 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.545+6090C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578279 | |||||||
| chr13:77578322 | C | T | 1 | a0001c0004t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.545+6133C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578322 | |||||||
| chr13:77578371 | G | A | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02818.hp1 HG02895.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+6182G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578371 | |||||||
| chr13:77578393 | T | C | 17 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.545+6204T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578393 | |||||||
| chr13:77578690 | G | A | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.545+6501G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578690 | |||||||
| chr13:77578731 | T | C | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+6542T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578731 | |||||||
| chr13:77578811 | T | C | 1 | a0013c0022t0001g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.545+6622T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578811 | |||||||
| chr13:77578989 | T | C | 1 | a0003c0005t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.545+6800T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77578989 | |||||||
| chr13:77579075 | G | C | 1 | a0002c0001t0001g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.545+6886G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77579075 | |||||||
| chr13:77579093 | C | T | 29 | a0001c0002t0002g0025 a0001c0002t0002g0026 a0002c0001t0001g0006 others(26): Show |
32 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.545+6904C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77579093 | |||||||
| chr13:77579440 | T | C | 1 | a0001c0002t0002g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.545+7251T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77579440 | |||||||
| chr13:77579479 | A | T | 1 | a0003c0003t0001g0095 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.545+7290A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77579479 | |||||||
| chr13:77579723 | G | A | 61 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(58): Show |
62 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.545+7534G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77579723 | |||||||
| chr13:77579821 | G | A | 2 | a0001c0002t0002g0093 a0009c0010t0002g0232 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.545+7632G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77579821 | |||||||
| chr13:77579899 | G | A | 1 | a0001c0004t0001g0024 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.545+7710G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77579899 | |||||||
| chr13:77580168 | C | G | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.545+7979C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77580168 | |||||||
| chr13:77580180 | A | T | 14 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.545+7991A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77580180 | |||||||
| chr13:77580283 | T | G | 2 | a0002c0001t0001g0145 a0002c0001t0001g0146 |
2 | NA18939.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.545+8094T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77580283 | |||||||
| chr13:77580526 | T | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.545+8337T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77580526 | |||||||
| chr13:77580546 | A | T | 77 | a0001c0002t0002g0070 a0001c0002t0002g0104 a0003c0003t0001g0001 others(74): Show |
78 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.545+8357A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77580546 | |||||||
| chr13:77581292 | A | G | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.546-7852A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581292 | |||||||
| chr13:77581408 | A | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.546-7736A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581408 | |||||||
| chr13:77581486 | C | A | 1 | a0002c0001t0001g0265 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.546-7658C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581486 | |||||||
| chr13:77581538 | G | A | 1 | a0002c0001t0001g0190 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.546-7606G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581538 | |||||||
| chr13:77581584 | C | G | 1 | a0001c0002t0002g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.546-7560C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581584 | |||||||
| chr13:77581735 | G | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.546-7409G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581735 | |||||||
| chr13:77581773 | A | G | 1 | a0003c0003t0001g0057 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.546-7371A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581773 | |||||||
| chr13:77581912 | G | A | 93 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(90): Show |
94 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.546-7232G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77581912 | |||||||
| chr13:77582354 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.546-6790G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582354 | |||||||
| chr13:77582373 | C | T | 71 | a0001c0012t0002g0333 a0002c0001t0001g0062 a0002c0001t0001g0073 others(68): Show |
71 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.546-6771C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582373 | |||||||
| chr13:77582429 | T | A | 1 | a0003c0006t0002g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.546-6715T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582429 | |||||||
| chr13:77582512 | A | G | 1 | a0001c0002t0002g0030 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.546-6632A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582512 | |||||||
| chr13:77582689 | C | T | 1 | a0002c0001t0002g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.546-6455C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582689 | |||||||
| chr13:77582820 | TTC | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.546-6322_546-6321d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr13 | 77582820 | ||||||
| chr13:77582822 | C | T | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.546-6322C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582822 | |||||||
| chr13:77582858 | C | G | 1 | a0003c0003t0001g0252 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.546-6286C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582858 | |||||||
| chr13:77582862 | T | C | 1 | a0003c0003t0001g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.546-6282T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582862 | |||||||
| chr13:77582920 | C | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.546-6224C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77582920 | |||||||
| chr13:77583113 | A | G | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-6031A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583113 | |||||||
| chr13:77583215 | A | G | 2 | a0002c0001t0001g0149 a0002c0014t0002g0153 |
2 | NA18952.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.546-5929A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583215 | |||||||
| chr13:77583325 | C | A | 3 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 |
3 | HG02886.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.546-5819C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583325 | |||||||
| chr13:77583452 | G | A | 2 | a0001c0004t0001g0326 a0001c0004t0001g0335 |
2 | HG01981.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.546-5692G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583452 | |||||||
| chr13:77583475 | T | C | 2 | a0002c0001t0001g0259 a0002c0001t0001g0262 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.546-5669T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583475 | |||||||
| chr13:77583602 | G | T | 2 | a0001c0002t0002g0197 a0001c0002t0002g0292 |
2 | HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.546-5542G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583602 | |||||||
| chr13:77583703 | C | A | 1 | a0001c0004t0002g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.546-5441C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583703 | |||||||
| chr13:77583977 | C | T | 1 | a0001c0002t0002g0068 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.546-5167C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583977 | |||||||
| chr13:77583978 | G | A | 1 | a0003c0006t0002g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.546-5166G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77583978 | |||||||
| chr13:77584044 | T | C | 1 | a0001c0002t0002g0230 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.546-5100T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77584044 | |||||||
| chr13:77584807 | A | G | 10 | a0001c0002t0002g0203 a0001c0002t0002g0213 a0001c0002t0002g0214 others(7): Show |
10 | HG02165.hp1 NA18747.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-4337A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77584807 | |||||||
| chr13:77584894 | T | G | 1 | a0002c0014t0002g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.546-4250T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77584894 | |||||||
| chr13:77585479 | C | G | 8 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(5): Show |
9 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.546-3665C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77585479 | |||||||
| chr13:77585489 | A | G | 195 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(192): Show |
199 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(196): Show |
intron_variant | MODIFIER | c.546-3655A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77585489 | |||||||
| chr13:77585523 | T | C | 325 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(322): Show |
334 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.546-3621T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77585523 | |||||||
| chr13:77585528 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-3616G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77585528 | |||||||
| chr13:77585738 | T | C | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-3406T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77585738 | |||||||
| chr13:77585965 | G | T | 1 | a0002c0001t0001g0146 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.546-3179G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77585965 | |||||||
| chr13:77585966 | G | A | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.546-3178G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77585966 | |||||||
| chr13:77586132 | C | T | 1 | a0003c0005t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.546-3012C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586132 | |||||||
| chr13:77586133 | G | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.546-3011G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586133 | |||||||
| chr13:77586170 | G | T | 20 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(17): Show |
20 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.546-2974G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586170 | |||||||
| chr13:77586213 | C | T | 66 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(63): Show |
69 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.546-2931C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586213 | |||||||
| chr13:77586228 | G | T | 1 | a0001c0004t0001g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.546-2916G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586228 | |||||||
| chr13:77586234 | T | C | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-2910T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586234 | |||||||
| chr13:77586428 | A | G | 1 | a0014c0021t0001g0172 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.546-2716A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586428 | |||||||
| chr13:77586701 | A | T | 1 | a0003c0003t0001g0339 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546-2443A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586701 | |||||||
| chr13:77586792 | T | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-2352T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586792 | |||||||
| chr13:77586864 | G | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.546-2280G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586864 | |||||||
| chr13:77586897 | T | TG | 5 | a0002c0001t0001g0008 a0002c0001t0001g0300 a0002c0001t0001g0302 others(2): Show |
6 | HG01123.hp1 HG01255.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.546-2247_546-2246i others(3): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586897 | |||||||
| chr13:77586904 | G | A | 1 | a0001c0002t0002g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.546-2240G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77586904 | |||||||
| chr13:77587289 | C | T | 1 | a0002c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.546-1855C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587289 | |||||||
| chr13:77587306 | C | T | 8 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(5): Show |
9 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.546-1838C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587306 | |||||||
| chr13:77587362 | A | G | 1 | a0001c0002t0002g0117 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.546-1782A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587362 | |||||||
| chr13:77587412 | T | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.546-1732T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587412 | |||||||
| chr13:77587440 | A | T | 1 | a0002c0001t0001g0311 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.546-1704A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587440 | |||||||
| chr13:77587455 | C | T | 11 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(8): Show |
12 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.546-1689C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587455 | |||||||
| chr13:77587523 | C | T | 1 | a0003c0003t0001g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.546-1621C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587523 | |||||||
| chr13:77587553 | G | A | 1 | a0014c0021t0001g0172 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.546-1591G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587553 | |||||||
| chr13:77587645 | C | T | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.546-1499C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587645 | |||||||
| chr13:77587935 | G | A | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-1209G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77587935 | |||||||
| chr13:77588013 | A | T | 1 | a0001c0002t0002g0219 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.546-1131A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588013 | |||||||
| chr13:77588058 | T | C | 1 | a0001c0002t0002g0213 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.546-1086T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588058 | |||||||
| chr13:77588111 | A | G | 63 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.546-1033A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588111 | |||||||
| chr13:77588197 | T | C | 61 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(58): Show |
62 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.546-947T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588197 | |||||||
| chr13:77588202 | G | A | 1 | a0002c0001t0001g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.546-942G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588202 | |||||||
| chr13:77588269 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.546-875A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588269 | |||||||
| chr13:77588365 | A | G | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.546-779A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588365 | |||||||
| chr13:77588377 | A | G | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.546-767A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588377 | |||||||
| chr13:77588391 | C | T | 2 | a0001c0002t0002g0253 a0001c0002t0002g0254 |
2 | HG00558.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.546-753C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588391 | |||||||
| chr13:77588407 | C | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-737C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588407 | |||||||
| chr13:77588564 | C | G | 17 | a0001c0002t0002g0116 a0001c0002t0002g0197 a0001c0002t0002g0198 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.546-580C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588564 | |||||||
| chr13:77588576 | T | C | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-568T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588576 | |||||||
| chr13:77588578 | T | C | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-566T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588578 | |||||||
| chr13:77588681 | G | A | 2 | a0002c0001t0001g0186 a0002c0001t0001g0317 |
2 | HG02083.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.546-463G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588681 | |||||||
| chr13:77588796 | A | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-348A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588796 | |||||||
| chr13:77588809 | C | T | 100 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(97): Show |
103 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.546-335C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588809 | |||||||
| chr13:77588940 | A | G | 5 | a0002c0001t0001g0008 a0002c0001t0001g0300 a0002c0001t0001g0302 others(2): Show |
6 | HG01123.hp1 HG01255.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.546-204A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588940 | |||||||
| chr13:77588954 | C | T | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.546-190C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77588954 | |||||||
| chr13:77589007 | C | A | 1 | a0002c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.546-137C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77589007 | |||||||
| chr13:77589108 | C | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.546-36C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77589108 | |||||||
| chr13:77589125 | G | A | 1 | a0003c0003t0001g0238 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.546-19G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 9/32 | chr13 | 77589125 | |||||||
| chr13:77589312 | A | G | 1 | a0003c0003t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.626+88A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589312 | |||||||
| chr13:77589339 | A | C | 5 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0002g0241 others(2): Show |
5 | HG00741.hp1 HG01070.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+115A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589339 | |||||||
| chr13:77589555 | C | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.626+331C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589555 | |||||||
| chr13:77589617 | T | C | 193 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(190): Show |
197 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.626+393T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589617 | |||||||
| chr13:77589652 | C | T | 14 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+428C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589652 | |||||||
| chr13:77589666 | C | T | 1 | a0003c0003t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.626+442C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589666 | |||||||
| chr13:77589782 | A | G | 108 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(105): Show |
111 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.626+558A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589782 | |||||||
| chr13:77589800 | C | G | 2 | a0001c0004t0001g0326 a0001c0004t0001g0335 |
2 | HG01981.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.626+576C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589800 | |||||||
| chr13:77589893 | T | C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.626+669T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77589893 | |||||||
| chr13:77590127 | A | C | 1 | a0002c0001t0001g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.626+903A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590127 | |||||||
| chr13:77590217 | C | T | 321 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(318): Show |
330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.626+993C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590217 | |||||||
| chr13:77590317 | T | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.627-1078T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590317 | |||||||
| chr13:77590355 | T | A | 20 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(17): Show |
20 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.627-1040T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590355 | |||||||
| chr13:77590688 | A | G | 110 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(107): Show |
113 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.627-707A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590688 | |||||||
| chr13:77590692 | T | A | 1 | a0003c0003t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.627-703T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590692 | |||||||
| chr13:77590787 | A | G | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-608A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590787 | |||||||
| chr13:77590877 | A | C | 1 | a0001c0002t0002g0257 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.627-518A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77590877 | |||||||
| chr13:77591077 | G | A | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.627-318G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77591077 | |||||||
| chr13:77591119 | T | C | 85 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(82): Show |
86 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.627-276T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77591119 | |||||||
| chr13:77591322 | T | G | 14 | a0003c0003t0001g0072 a0003c0003t0001g0334 a0003c0003t0001g0336 others(11): Show |
14 | HG00735.hp1 HG01884.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.627-73T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 10/32 | chr13 | 77591322 | |||||||
| chr13:77591500 | TG | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.692+41delG | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77591500 | |||||||
| chr13:77591502 | A | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.692+42A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77591502 | |||||||
| chr13:77591590 | T | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.692+130T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77591590 | |||||||
| chr13:77592009 | T | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.692+549T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592009 | |||||||
| chr13:77592063 | A | G | 8 | a0001c0002t0002g0025 a0001c0002t0002g0026 a0001c0002t0002g0087 others(5): Show |
8 | NA18953.hp2 NA18962.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.692+603A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592063 | |||||||
| chr13:77592183 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.692+723G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592183 | |||||||
| chr13:77592218 | C | T | 9 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(6): Show |
10 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.692+758C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592218 | |||||||
| chr13:77592219 | A | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.692+759A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592219 | |||||||
| chr13:77592226 | G | A | 2 | a0001c0002t0002g0022 a0001c0002t0002g0023 |
2 | NA18971.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.692+766G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592226 | |||||||
| chr13:77592331 | G | T | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.692+871G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592331 | |||||||
| chr13:77592517 | A | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.693-997A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592517 | |||||||
| chr13:77592534 | T | G | 1 | a0003c0003t0001g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.693-980T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592534 | |||||||
| chr13:77592543 | TTTC | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-955_693-953del others(3): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77592543 | ||||||
| chr13:77592562 | C | CT | 92 | a0001c0002t0002g0070 a0001c0002t0002g0091 a0001c0012t0002g0333 others(89): Show |
93 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.693-936dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77592562 | ||||||
| chr13:77592562 | CT | C | 22 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(19): Show |
23 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.693-936delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77592562 | ||||||
| chr13:77592699 | C | T | 193 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(190): Show |
197 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.693-815C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592699 | |||||||
| chr13:77592700 | G | A | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.693-814G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592700 | |||||||
| chr13:77592896 | A | G | 1 | a0002c0001t0001g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.693-618A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77592896 | |||||||
| chr13:77593126 | T | C | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.693-388T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593126 | |||||||
| chr13:77593254 | AG | A | 4 | a0001c0002t0002g0064 a0001c0004t0001g0320 a0001c0004t0001g0326 others(1): Show |
4 | HG01175.hp2 HG01981.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-256delG | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593254 | ||||||
| chr13:77593257 | G | GA | 6 | a0001c0002t0002g0002 a0001c0002t0002g0066 a0001c0002t0002g0067 others(3): Show |
7 | HG01167.hp1 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-257_693-256ins others(1): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593257 | |||||||
| chr13:77593257 | G | GAGT | 3 | a0001c0002t0002g0337 a0001c0004t0001g0063 a0001c0004t0001g0133 |
3 | HG02886.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.693-257_693-256ins others(3): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593257 | |||||||
| chr13:77593259 | A | AGTGTGT | 9 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0111 others(6): Show |
9 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.693-222_693-217dup others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593259 | ||||||
| chr13:77593259 | A | AGTGTGTG others(3): Show |
6 | a0001c0004t0002g0110 a0001c0004t0002g0113 a0001c0004t0002g0114 others(3): Show |
6 | HG00597.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.693-226_693-217dup others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593259 | ||||||
| chr13:77593259 | A | AGTGTGTG others(5): Show |
2 | a0001c0004t0002g0128 a0001c0004t0002g0225 |
2 | NA18612.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.693-228_693-217dup others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593259 | ||||||
| chr13:77593259 | A | T | 10 | a0001c0002t0002g0002 a0001c0002t0002g0066 a0001c0002t0002g0067 others(7): Show |
11 | HG01167.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.693-255A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593259 | |||||||
| chr13:77593259 | AGT | A | 77 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(74): Show |
80 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.693-218_693-217del others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593259 | ||||||
| chr13:77593259 | AGTGT | A | 11 | a0001c0002t0002g0020 a0001c0002t0002g0030 a0001c0002t0002g0045 others(8): Show |
11 | HG02451.hp1 NA18747.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.693-220_693-217del others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593259 | ||||||
| chr13:77593259 | AGTGTGTG others(15): Show |
A | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.693-238_693-217del others(22): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593259 | ||||||
| chr13:77593293 | T | C | 3 | a0001c0002t0002g0130 a0001c0002t0002g0192 a0008c0013t0002g0200 |
3 | HG02109.hp1 HG02148.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.693-221T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593293 | |||||||
| chr13:77593293 | T | TGCGCGCG others(3): Show |
3 | a0002c0001t0003g0132 a0002c0001t0003g0297 a0002c0001t0003g0299 |
3 | HG00544.hp1 HG00621.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.693-220_693-219ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593293 | ||||||
| chr13:77593295 | T | C | 95 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(92): Show |
97 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.693-219T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593295 | |||||||
| chr13:77593295 | T | TGCGCGC | 5 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(2): Show |
6 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-218_693-217ins others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGCGC | 3 | a0002c0001t0001g0162 a0002c0001t0001g0264 a0002c0001t0001g0267 |
3 | HG00741.hp2 HG02257.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.693-217_693-216ins others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGCGCG others(1): Show |
4 | a0001c0004t0002g0321 a0003c0003t0001g0226 a0003c0003t0001g0336 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGCGCG others(3): Show |
7 | a0002c0001t0001g0322 a0003c0003t0001g0057 a0003c0003t0001g0058 others(4): Show |
7 | HG02970.hp1 NA18951.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGCGCG others(5): Show |
6 | a0003c0003t0001g0077 a0003c0003t0001g0140 a0003c0003t0001g0142 others(3): Show |
6 | HG00639.hp2 HG01099.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGCG others(1): Show |
25 | a0001c0002t0002g0285 a0001c0004t0005g0342 a0002c0001t0001g0062 others(22): Show |
25 | HG00408.hp2 HG00735.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGCG others(3): Show |
12 | a0002c0001t0001g0073 a0002c0001t0001g0164 a0002c0001t0001g0261 others(9): Show |
12 | HG00735.hp1 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGCG others(5): Show |
2 | a0003c0003t0001g0027 a0003c0003t0001g0060 |
2 | HG04204.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.693-217_693-216ins others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGCG others(7): Show |
2 | a0003c0003t0001g0082 a0007c0018t0001g0069 |
2 | HG01109.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.693-217_693-216ins others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(3): Show |
29 | a0002c0001t0001g0075 a0002c0001t0001g0076 a0002c0001t0001g0115 others(26): Show |
29 | HG00597.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(5): Show |
6 | a0003c0003t0001g0072 a0003c0006t0002g0010 a0003c0006t0002g0011 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(7): Show |
27 | a0003c0003t0001g0039 a0003c0003t0001g0054 a0003c0003t0001g0071 others(24): Show |
27 | HG00408.hp1 HG00544.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(5): Show |
12 | a0002c0001t0001g0136 a0002c0001t0001g0147 a0002c0001t0001g0159 others(9): Show |
12 | HG00099.hp2 HG00558.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(7): Show |
6 | a0003c0003t0001g0074 a0003c0003t0001g0103 a0003c0003t0001g0199 others(3): Show |
6 | HG01168.hp2 HG01433.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(9): Show |
10 | a0003c0003t0001g0001 a0003c0003t0001g0055 a0003c0003t0001g0079 others(7): Show |
11 | HG02523.hp1 HG02723.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(16): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(7): Show |
9 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0002c0001t0001g0141 others(6): Show |
9 | HG00438.hp1 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.693-217_693-216ins others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(9): Show |
1 | a0003c0003t0001g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.693-217_693-216ins others(16): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593295 | T | TGTGTGTG others(11): Show |
1 | a0003c0003t0001g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.693-217_693-216ins others(18): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593295 | ||||||
| chr13:77593296 | G | C | 6 | a0001c0002t0002g0130 a0001c0002t0002g0192 a0002c0001t0001g0315 others(3): Show |
6 | HG00544.hp1 HG00621.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.693-218G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593296 | |||||||
| chr13:77593296 | G | GCGCGCGC others(3): Show |
20 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(17): Show |
23 | HG00621.hp1 HG01123.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.693-218_693-217ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593296 | |||||||
| chr13:77593296 | G | GTGCGCGC others(5): Show |
1 | a0002c0001t0001g0313 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.693-217_693-216ins others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593296 | ||||||
| chr13:77593296 | G | GTGTGCGC others(3): Show |
1 | a0011c0020t0001g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.693-217_693-216ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593296 | ||||||
| chr13:77593296 | G | GTGTGTGC others(5): Show |
1 | a0003c0005t0002g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.693-217_693-216ins others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593296 | ||||||
| chr13:77593296 | G | GTGTGTGT others(13): Show |
2 | a0002c0001t0001g0305 a0002c0001t0001g0318 |
2 | NA18964.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.693-217_693-216ins others(20): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593296 | ||||||
| chr13:77593297 | T | C | 1 | a0001c0002t0002g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.693-217T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593297 | |||||||
| chr13:77593298 | C | G | 54 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(51): Show |
58 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.693-216C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593298 | |||||||
| chr13:77593300 | G | C | 4 | a0001c0002t0002g0104 a0001c0004t0001g0287 a0001c0004t0001g0288 others(1): Show |
4 | HG01109.hp1 HG02818.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.693-214G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593300 | |||||||
| chr13:77593300 | G | GCGCGCGC others(3): Show |
4 | a0001c0002t0002g0066 a0001c0002t0002g0068 a0001c0004t0001g0134 others(1): Show |
4 | HG01167.hp1 HG02258.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.693-214_693-213ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593300 | |||||||
| chr13:77593300 | G | GCGCGCGT others(1): Show |
11 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0067 others(8): Show |
12 | HG01175.hp2 HG01516.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.693-214_693-213ins others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593300 | |||||||
| chr13:77593300 | G | GCGCGTC | 5 | a0001c0002t0002g0337 a0001c0004t0001g0063 a0001c0004t0001g0065 others(2): Show |
5 | HG02055.hp2 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.693-214_693-213ins others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593300 | |||||||
| chr13:77593300 | G | GTGCGCGC others(3): Show |
1 | a0001c0004t0001g0284 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.693-212_693-211ins others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr13 | 77593300 | ||||||
| chr13:77593354 | G | A | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.693-160G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593354 | |||||||
| chr13:77593390 | C | T | 1 | a0001c0002t0002g0230 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.693-124C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593390 | |||||||
| chr13:77593400 | C | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.693-114C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 11/32 | chr13 | 77593400 | |||||||
| chr13:77593646 | A | G | 1 | a0001c0004t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.752+73A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77593646 | |||||||
| chr13:77593771 | C | T | 10 | a0001c0002t0002g0203 a0001c0002t0002g0213 a0001c0002t0002g0214 others(7): Show |
10 | HG02165.hp1 NA18747.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.752+198C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77593771 | |||||||
| chr13:77593867 | C | T | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.752+294C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77593867 | |||||||
| chr13:77594012 | TCCTTCC | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.752+450_752+455del others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77594012 | ||||||
| chr13:77594084 | G | A | 1 | a0001c0002t0002g0091 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.752+511G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594084 | |||||||
| chr13:77594203 | T | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.752+630T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594203 | |||||||
| chr13:77594227 | A | G | 1 | a0001c0002t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.752+654A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594227 | |||||||
| chr13:77594347 | C | T | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.752+774C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594347 | |||||||
| chr13:77594450 | C | G | 1 | a0003c0003t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.752+877C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594450 | |||||||
| chr13:77594460 | C | T | 5 | a0003c0003t0001g0334 a0003c0006t0002g0010 a0003c0006t0002g0011 others(2): Show |
5 | HG02647.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.752+887C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594460 | |||||||
| chr13:77594482 | G | A | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.752+909G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594482 | |||||||
| chr13:77594527 | A | G | 20 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(17): Show |
20 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.752+954A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594527 | |||||||
| chr13:77594584 | G | C | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.752+1011G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594584 | |||||||
| chr13:77594648 | A | G | 13 | a0003c0003t0001g0334 a0003c0003t0001g0336 a0003c0003t0001g0338 others(10): Show |
13 | HG00735.hp1 HG02647.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.752+1075A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594648 | |||||||
| chr13:77594690 | A | G | 1 | a0002c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.752+1117A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594690 | |||||||
| chr13:77594698 | A | T | 2 | a0001c0002t0002g0093 a0009c0010t0002g0232 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.752+1125A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594698 | |||||||
| chr13:77594719 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.752+1146G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594719 | |||||||
| chr13:77594845 | G | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.752+1272G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77594845 | |||||||
| chr13:77595222 | A | C | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.752+1649A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77595222 | |||||||
| chr13:77595266 | G | A | 1 | a0013c0022t0001g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.752+1693G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77595266 | |||||||
| chr13:77595495 | G | T | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.752+1922G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77595495 | |||||||
| chr13:77595658 | T | C | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.753-1887T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77595658 | |||||||
| chr13:77595765 | TTTG | T | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.753-1771_753-1769d others(5): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77595765 | ||||||
| chr13:77595836 | C | T | 1 | a0002c0001t0001g0328 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.753-1709C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77595836 | |||||||
| chr13:77595974 | ATC | A | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.753-1563_753-1562d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77595974 | ||||||
| chr13:77595980 | C | T | 100 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(97): Show |
103 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.753-1565C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77595980 | |||||||
| chr13:77596136 | C | G | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.753-1409C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596136 | |||||||
| chr13:77596144 | C | A | 1 | a0001c0002t0002g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.753-1401C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596144 | |||||||
| chr13:77596145 | A | C | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.753-1400A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596145 | |||||||
| chr13:77596202 | G | T | 1 | a0001c0002t0002g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.753-1343G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596202 | |||||||
| chr13:77596221 | T | C | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.753-1324T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596221 | |||||||
| chr13:77596270 | T | G | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.753-1275T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596270 | |||||||
| chr13:77596342 | A | AG | 65 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(62): Show |
68 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.753-1203_753-1202i others(3): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596342 | |||||||
| chr13:77596373 | A | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.753-1172A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596373 | |||||||
| chr13:77596377 | A | C | 1 | a0001c0002t0002g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.753-1168A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77596377 | |||||||
| chr13:77596688 | G | GGT | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0031 others(98): Show |
106 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.753-823_753-822dup others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77596688 | ||||||
| chr13:77596688 | G | GGTGT | 40 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0025 others(37): Show |
43 | HG00099.hp2 HG00438.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.753-825_753-822dup others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77596688 | ||||||
| chr13:77596688 | G | GGTGTGT | 4 | a0001c0002t0002g0242 a0001c0002t0002g0337 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02080.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.753-827_753-822dup others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77596688 | ||||||
| chr13:77596688 | G | GGTGTGTG others(3): Show |
1 | a0001c0004t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.753-831_753-822dup others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77596688 | ||||||
| chr13:77596688 | GGT | G | 12 | a0002c0001t0001g0264 a0002c0001t0001g0267 a0002c0001t0002g0268 others(9): Show |
12 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.753-823_753-822del others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77596688 | ||||||
| chr13:77596688 | GGTGT | G | 87 | a0001c0002t0002g0020 a0001c0002t0002g0045 a0001c0002t0002g0070 others(84): Show |
88 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.753-825_753-822del others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr13 | 77596688 | ||||||
| chr13:77597109 | A | G | 100 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(97): Show |
103 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.753-436A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77597109 | |||||||
| chr13:77597165 | G | A | 1 | a0001c0004t0001g0320 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.753-380G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77597165 | |||||||
| chr13:77597301 | G | A | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.753-244G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 12/32 | chr13 | 77597301 | |||||||
| chr13:77597640 | T | C | 1 | a0001c0002t0002g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.797+51T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77597640 | |||||||
| chr13:77597643 | T | C | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.797+54T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77597643 | |||||||
| chr13:77597657 | C | T | 2 | a0005c0009t0002g0210 a0005c0009t0002g0211 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.797+68C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77597657 | |||||||
| chr13:77597808 | C | T | 2 | a0002c0001t0001g0162 a0003c0003t0001g0074 |
2 | HG01516.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.797+219C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77597808 | |||||||
| chr13:77597939 | T | C | 1 | a0003c0003t0001g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.797+350T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77597939 | |||||||
| chr13:77598032 | A | G | 34 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(31): Show |
34 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.797+443A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598032 | |||||||
| chr13:77598052 | C | A | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.797+463C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598052 | |||||||
| chr13:77598053 | C | A | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.797+464C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598053 | |||||||
| chr13:77598271 | T | A | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.797+682T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598271 | |||||||
| chr13:77598272 | G | A | 1 | a0001c0004t0002g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.797+683G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598272 | |||||||
| chr13:77598326 | G | C | 2 | a0003c0005t0002g0273 a0003c0005t0002g0280 |
2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.797+737G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598326 | |||||||
| chr13:77598359 | A | G | 2 | a0001c0004t0001g0326 a0001c0004t0001g0335 |
2 | HG01981.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.797+770A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598359 | |||||||
| chr13:77598569 | T | C | 1 | a0002c0001t0001g0179 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.798-760T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598569 | |||||||
| chr13:77598649 | C | A | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.798-680C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598649 | |||||||
| chr13:77598695 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.798-634G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598695 | |||||||
| chr13:77598745 | C | A | 1 | a0002c0001t0001g0152 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.798-584C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77598745 | |||||||
| chr13:77599011 | C | T | 1 | a0002c0014t0002g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.798-318C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77599011 | |||||||
| chr13:77599194 | A | G | 4 | a0002c0001t0001g0158 a0002c0001t0001g0160 a0002c0001t0001g0171 others(1): Show |
4 | HG00438.hp1 HG02165.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.798-135A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77599194 | |||||||
| chr13:77599239 | T | A | 10 | a0001c0002t0002g0203 a0001c0002t0002g0213 a0001c0002t0002g0214 others(7): Show |
10 | HG02165.hp1 NA18747.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.798-90T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 13/32 | chr13 | 77599239 | |||||||
| chr13:77599770 | C | A | 17 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.917+22C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77599770 | |||||||
| chr13:77599932 | G | A | 1 | a0001c0004t0001g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.917+184G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77599932 | |||||||
| chr13:77599991 | C | G | 4 | a0002c0001t0001g0136 a0002c0001t0001g0163 a0002c0001t0001g0167 others(1): Show |
4 | HG00597.hp2 HG02040.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.917+243C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77599991 | |||||||
| chr13:77600248 | C | G | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.917+500C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77600248 | |||||||
| chr13:77600268 | T | A | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.917+520T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77600268 | |||||||
| chr13:77600277 | C | T | 93 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(90): Show |
94 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.917+529C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77600277 | |||||||
| chr13:77600809 | T | G | 1 | a0002c0001t0001g0267 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.917+1061T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77600809 | |||||||
| chr13:77601114 | C | CT | 91 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(88): Show |
92 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.918-936dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr13 | 77601114 | ||||||
| chr13:77601114 | CTT | C | 100 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(97): Show |
102 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.918-937_918-936del others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr13 | 77601114 | ||||||
| chr13:77601116 | T | C | 1 | a0002c0001t0001g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.918-949T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77601116 | |||||||
| chr13:77601235 | G | A | 1 | a0001c0007t0002g0331 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.918-830G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77601235 | |||||||
| chr13:77601335 | C | T | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.918-730C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77601335 | |||||||
| chr13:77601645 | A | T | 1 | a0001c0002t0002g0222 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.918-420A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77601645 | |||||||
| chr13:77601661 | A | G | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.918-404A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77601661 | |||||||
| chr13:77601837 | T | A | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.918-228T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77601837 | |||||||
| chr13:77601989 | C | T | 1 | a0002c0001t0001g0147 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.918-76C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 15/32 | chr13 | 77601989 | |||||||
| chr13:77602429 | G | A | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.978-225G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 16/32 | chr13 | 77602429 | |||||||
| chr13:77602531 | C | A | 17 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.978-123C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 16/32 | chr13 | 77602531 | |||||||
| chr13:77602856 | A | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1037+143A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 17/32 | chr13 | 77602856 | |||||||
| chr13:77602864 | C | T | 58 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(55): Show |
59 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.1037+151C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 17/32 | chr13 | 77602864 | |||||||
| chr13:77602947 | T | A | 203 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(200): Show |
208 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1038-129T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 17/32 | chr13 | 77602947 | |||||||
| chr13:77603467 | G | A | 93 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(90): Show |
94 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1097+332G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77603467 | |||||||
| chr13:77603477 | T | C | 1 | a0001c0002t0002g0253 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1097+342T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77603477 | |||||||
| chr13:77603502 | C | A | 1 | a0003c0006t0002g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1097+367C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77603502 | |||||||
| chr13:77603537 | C | T | 100 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(97): Show |
103 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1097+402C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77603537 | |||||||
| chr13:77603563 | G | C | 1 | a0003c0003t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1097+428G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77603563 | |||||||
| chr13:77603566 | T | C | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1097+431T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77603566 | |||||||
| chr13:77603711 | C | T | 14 | a0001c0004t0002g0021 a0001c0004t0002g0111 a0001c0004t0002g0119 others(11): Show |
14 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1097+576C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77603711 | |||||||
| chr13:77604018 | A | G | 1 | a0003c0003t0001g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1098-338A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77604018 | |||||||
| chr13:77604028 | AT | A | 343 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(340): Show |
352 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.1098-326delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr13 | 77604028 | ||||||
| chr13:77604040 | A | G | 108 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(105): Show |
112 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1098-316A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77604040 | |||||||
| chr13:77604229 | G | C | 1 | a0001c0002t0002g0013 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1098-127G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77604229 | |||||||
| chr13:77604316 | C | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1098-40C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77604316 | |||||||
| chr13:77604346 | T | G | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1098-10T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 18/32 | chr13 | 77604346 | |||||||
| chr13:77604437 | C | T | 2 | a0001c0004t0002g0122 a0001c0004t0002g0256 |
2 | NA18956.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1157+22C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77604437 | |||||||
| chr13:77604482 | T | C | 3 | a0001c0004t0001g0089 a0001c0004t0001g0108 a0001c0004t0001g0131 |
3 | NA18954.hp2 NA18974.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1157+67T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77604482 | |||||||
| chr13:77604786 | T | C | 2 | a0001c0002t0002g0214 a0001c0002t0002g0293 |
2 | NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1157+371T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77604786 | |||||||
| chr13:77604824 | A | C | 1 | a0001c0002t0002g0230 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1157+409A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77604824 | |||||||
| chr13:77604893 | G | A | 2 | a0001c0002t0002g0022 a0001c0002t0002g0023 |
2 | NA18971.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1157+478G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77604893 | |||||||
| chr13:77604938 | G | A | 70 | a0002c0001t0001g0062 a0002c0001t0001g0073 a0002c0001t0001g0075 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1157+523G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77604938 | |||||||
| chr13:77604947 | T | G | 1 | a0002c0001t0001g0302 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1157+532T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77604947 | |||||||
| chr13:77605117 | C | A | 1 | a0003c0005t0002g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1157+702C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605117 | |||||||
| chr13:77605132 | T | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1157+717T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605132 | |||||||
| chr13:77605143 | A | G | 1 | a0001c0002t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1157+728A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605143 | |||||||
| chr13:77605228 | CAT | C | 76 | a0001c0002t0002g0070 a0003c0003t0001g0001 a0003c0003t0001g0027 others(73): Show |
77 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1157+814_1157+815d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605228 | |||||||
| chr13:77605298 | C | T | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1157+883C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605298 | |||||||
| chr13:77605517 | A | G | 1 | a0002c0001t0001g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1157+1102A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605517 | |||||||
| chr13:77605571 | T | C | 8 | a0003c0003t0001g0077 a0003c0003t0001g0082 a0003c0003t0001g0140 others(5): Show |
8 | HG00639.hp2 HG01099.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+1156T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605571 | |||||||
| chr13:77605575 | G | A | 3 | a0001c0002t0002g0208 a0001c0002t0002g0228 a0001c0002t0002g0229 |
3 | HG01346.hp1 HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1157+1160G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605575 | |||||||
| chr13:77605763 | T | C | 60 | a0003c0003t0001g0001 a0003c0003t0001g0027 a0003c0003t0001g0039 others(57): Show |
61 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1157+1348T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605763 | |||||||
| chr13:77605778 | G | A | 1 | a0001c0002t0002g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1157+1363G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605778 | |||||||
| chr13:77605947 | A | G | 5 | a0001c0002t0002g0094 a0001c0002t0002g0138 a0001c0002t0002g0212 others(2): Show |
5 | HG01071.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+1532A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77605947 | |||||||
| chr13:77606089 | T | G | 1 | a0003c0003t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1157+1674T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77606089 | |||||||
| chr13:77606325 | G | C | 1 | a0001c0002t0002g0176 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1158-1731G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77606325 | |||||||
| chr13:77606561 | A | C | 1 | a0001c0004t0001g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1158-1495A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77606561 | |||||||
| chr13:77606636 | C | T | 66 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(63): Show |
69 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1158-1420C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77606636 | |||||||
| chr13:77606847 | C | A | 1 | a0001c0002t0002g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1158-1209C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77606847 | |||||||
| chr13:77606914 | C | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158-1142C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77606914 | |||||||
| chr13:77607019 | C | T | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1158-1037C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607019 | |||||||
| chr13:77607172 | A | G | 1 | a0003c0003t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1158-884A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607172 | |||||||
| chr13:77607175 | A | T | 5 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(2): Show |
6 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158-881A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607175 | |||||||
| chr13:77607325 | G | A | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1158-731G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607325 | |||||||
| chr13:77607360 | C | T | 1 | a0003c0003t0001g0080 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1158-696C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607360 | |||||||
| chr13:77607659 | A | G | 1 | a0003c0003t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1158-397A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607659 | |||||||
| chr13:77607660 | T | C | 1 | a0003c0003t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1158-396T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607660 | |||||||
| chr13:77607709 | G | A | 2 | a0003c0005t0002g0273 a0003c0005t0002g0280 |
2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1158-347G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 19/32 | chr13 | 77607709 | |||||||
| chr13:77608211 | A | G | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1217+96A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608211 | |||||||
| chr13:77608327 | C | T | 75 | a0003c0003t0001g0001 a0003c0003t0001g0027 a0003c0003t0001g0039 others(72): Show |
76 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1217+212C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608327 | |||||||
| chr13:77608338 | G | A | 2 | a0001c0002t0002g0093 a0009c0010t0002g0232 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1217+223G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608338 | |||||||
| chr13:77608354 | C | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+239C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608354 | |||||||
| chr13:77608375 | G | A | 3 | a0003c0003t0001g0338 a0003c0003t0001g0341 a0008c0013t0002g0200 |
3 | HG02109.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1217+260G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608375 | |||||||
| chr13:77608381 | C | G | 2 | a0001c0004t0001g0326 a0001c0004t0001g0335 |
2 | HG01981.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1217+266C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608381 | |||||||
| chr13:77608421 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+306G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608421 | |||||||
| chr13:77608579 | G | A | 1 | a0001c0002t0002g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1217+464G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608579 | |||||||
| chr13:77608740 | A | C | 92 | a0003c0003t0001g0001 a0003c0003t0001g0027 a0003c0003t0001g0039 others(89): Show |
93 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.1218-318A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608740 | |||||||
| chr13:77608754 | G | A | 1 | a0001c0002t0002g0202 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1218-304G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608754 | |||||||
| chr13:77608765 | T | C | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1218-293T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608765 | |||||||
| chr13:77608766 | G | A | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218-292G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608766 | |||||||
| chr13:77608952 | A | C | 100 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(97): Show |
103 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1218-106A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77608952 | |||||||
| chr13:77609032 | G | C | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1218-26G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 20/32 | chr13 | 77609032 | |||||||
| chr13:77609211 | A | G | 1 | a0001c0004t0001g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1277+94A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 21/32 | chr13 | 77609211 | |||||||
| chr13:77609722 | A | G | 73 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0002g0122 others(70): Show |
73 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1278-325A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 21/32 | chr13 | 77609722 | |||||||
| chr13:77609853 | A | T | 1 | a0001c0002t0002g0203 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1278-194A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 21/32 | chr13 | 77609853 | |||||||
| chr13:77609963 | A | G | 1 | a0002c0001t0001g0317 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1278-84A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 21/32 | chr13 | 77609963 | |||||||
| chr13:77610134 | C | T | 1 | a0001c0002t0002g0231 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1337+28C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610134 | |||||||
| chr13:77610140 | T | C | 1 | a0001c0002t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1337+34T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610140 | |||||||
| chr13:77610148 | T | C | 2 | a0001c0002t0002g0093 a0009c0010t0002g0232 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1337+42T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610148 | |||||||
| chr13:77610262 | C | G | 2 | a0001c0002t0002g0033 a0001c0002t0002g0112 |
2 | HG01978.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1337+156C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610262 | |||||||
| chr13:77610311 | G | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1337+205G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610311 | |||||||
| chr13:77610322 | G | A | 72 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0002c0001t0001g0062 others(69): Show |
72 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1337+216G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610322 | |||||||
| chr13:77610447 | G | A | 1 | a0001c0002t0002g0004 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1337+341G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610447 | |||||||
| chr13:77610449 | CA | C | 308 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(305): Show |
317 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.1337+362delA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77610449 | ||||||
| chr13:77610449 | CAA | C | 6 | a0001c0002t0002g0026 a0001c0002t0002g0285 a0001c0004t0001g0089 others(3): Show |
6 | HG01168.hp2 HG01884.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1337+361_1337+362d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77610449 | ||||||
| chr13:77610522 | C | T | 1 | a0001c0004t0001g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1337+416C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610522 | |||||||
| chr13:77610545 | T | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1337+439T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610545 | |||||||
| chr13:77610700 | A | ATT | 10 | a0002c0001t0001g0075 a0002c0001t0001g0076 a0002c0001t0001g0141 others(7): Show |
10 | HG01928.hp2 HG01934.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.1337+596_1337+597d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77610700 | ||||||
| chr13:77610830 | A | C | 1 | a0001c0004t0002g0021 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1337+724A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610830 | |||||||
| chr13:77610944 | C | T | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1337+838C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610944 | |||||||
| chr13:77610988 | A | T | 1 | a0011c0020t0001g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1337+882A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77610988 | |||||||
| chr13:77611075 | T | C | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1337+969T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611075 | |||||||
| chr13:77611253 | G | A | 1 | a0002c0001t0002g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1337+1147G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611253 | |||||||
| chr13:77611265 | C | G | 1 | a0001c0016t0001g0218 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1337+1159C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611265 | |||||||
| chr13:77611300 | G | A | 13 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(10): Show |
16 | HG00544.hp1 HG00621.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1337+1194G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611300 | |||||||
| chr13:77611378 | T | C | 52 | a0003c0003t0001g0001 a0003c0003t0001g0027 a0003c0003t0001g0039 others(49): Show |
53 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1337+1272T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611378 | |||||||
| chr13:77611707 | C | T | 1 | a0003c0003t0001g0057 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1338-1184C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611707 | |||||||
| chr13:77611708 | T | A | 1 | a0003c0003t0001g0057 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1338-1183T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611708 | |||||||
| chr13:77611735 | C | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1338-1156C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611735 | |||||||
| chr13:77611830 | C | T | 2 | a0001c0002t0002g0002 a0001c0002t0002g0064 |
3 | HG01175.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1338-1061C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611830 | |||||||
| chr13:77611895 | A | C | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1338-996A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77611895 | |||||||
| chr13:77612054 | G | A | 1 | a0001c0004t0001g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1338-837G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612054 | |||||||
| chr13:77612450 | T | C | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1338-441T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612450 | |||||||
| chr13:77612456 | CT | C | 35 | a0001c0002t0002g0023 a0001c0002t0002g0029 a0001c0004t0001g0324 others(32): Show |
38 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1338-406delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77612456 | ||||||
| chr13:77612456 | CTT | C | 95 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(92): Show |
96 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1338-407_1338-406d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77612456 | ||||||
| chr13:77612456 | CTTT | C | 36 | a0001c0002t0002g0020 a0001c0002t0002g0033 a0001c0002t0002g0045 others(33): Show |
36 | HG00558.hp2 HG00741.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1338-408_1338-406d others(5): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77612456 | ||||||
| chr13:77612456 | CTTTT | C | 35 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(32): Show |
38 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1338-409_1338-406d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77612456 | ||||||
| chr13:77612456 | CTTTTTTT others(2): Show |
C | 11 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(8): Show |
12 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1338-414_1338-406d others(11): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77612456 | ||||||
| chr13:77612456 | CTTTTTTT others(3): Show |
C | 103 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0201 others(100): Show |
104 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1338-415_1338-406d others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77612456 | ||||||
| chr13:77612456 | CTTTTTTT others(4): Show |
C | 1 | a0003c0003t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1338-416_1338-406d others(13): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr13 | 77612456 | ||||||
| chr13:77612468 | T | C | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1338-423T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612468 | |||||||
| chr13:77612470 | T | C | 91 | a0003c0003t0001g0001 a0003c0003t0001g0027 a0003c0003t0001g0039 others(88): Show |
92 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1338-421T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612470 | |||||||
| chr13:77612471 | T | C | 1 | a0003c0003t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1338-420T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612471 | |||||||
| chr13:77612474 | T | C | 1 | a0003c0003t0001g0238 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1338-417T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612474 | |||||||
| chr13:77612567 | C | G | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1338-324C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612567 | |||||||
| chr13:77612567 | C | T | 1 | a0002c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1338-324C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612567 | |||||||
| chr13:77612571 | T | C | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1338-320T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612571 | |||||||
| chr13:77612572 | G | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1338-319G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612572 | |||||||
| chr13:77612575 | T | C | 1 | a0001c0004t0001g0243 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1338-316T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612575 | |||||||
| chr13:77612705 | T | C | 20 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0110 others(17): Show |
20 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1338-186T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612705 | |||||||
| chr13:77612804 | G | A | 14 | a0003c0003t0001g0072 a0003c0003t0001g0334 a0003c0003t0001g0336 others(11): Show |
14 | HG00735.hp1 HG01884.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1338-87G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612804 | |||||||
| chr13:77612852 | T | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1338-39T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 22/32 | chr13 | 77612852 | |||||||
| chr13:77612951 | T | C | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1388+10T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77612951 | |||||||
| chr13:77613089 | TTCTG | T | 8 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(5): Show |
9 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1388+152_1388+155d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr13 | 77613089 | ||||||
| chr13:77613193 | G | T | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1388+252G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613193 | |||||||
| chr13:77613213 | T | C | 8 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0029 others(5): Show |
8 | NA18946.hp2 NA18955.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1388+272T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613213 | |||||||
| chr13:77613275 | G | A | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1388+334G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613275 | |||||||
| chr13:77613322 | G | A | 1 | a0013c0022t0001g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1388+381G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613322 | |||||||
| chr13:77613361 | G | T | 1 | a0003c0005t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1388+420G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613361 | |||||||
| chr13:77613452 | A | G | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1389-441A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613452 | |||||||
| chr13:77613671 | T | C | 1 | a0001c0004t0001g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1389-222T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613671 | |||||||
| chr13:77613711 | A | G | 327 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(324): Show |
336 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.1389-182A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613711 | |||||||
| chr13:77613766 | A | T | 2 | a0001c0004t0001g0326 a0001c0004t0001g0335 |
2 | HG01981.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1389-127A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 23/32 | chr13 | 77613766 | |||||||
| chr13:77613974 | T | A | 1 | a0001c0002t0002g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1451+19T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77613974 | |||||||
| chr13:77613990 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1451+35G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77613990 | |||||||
| chr13:77614119 | G | A | 99 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(96): Show |
102 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1451+164G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77614119 | |||||||
| chr13:77614530 | G | A | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1451+575G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77614530 | |||||||
| chr13:77614705 | C | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0220 |
3 | HG02258.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1451+750C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77614705 | |||||||
| chr13:77615376 | G | A | 1 | a0003c0005t0002g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1451+1421G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77615376 | |||||||
| chr13:77615395 | G | A | 1 | a0003c0003t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1451+1440G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77615395 | |||||||
| chr13:77615406 | A | T | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1451+1451A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77615406 | |||||||
| chr13:77615870 | A | G | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1452-1729A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77615870 | |||||||
| chr13:77615998 | GTC | G | 33 | a0001c0002t0002g0005 a0001c0002t0002g0064 a0001c0002t0002g0066 others(30): Show |
34 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1452-1595_1452-159 others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77615998 | ||||||
| chr13:77616002 | C | CTG | 19 | a0001c0002t0002g0093 a0001c0002t0002g0177 a0001c0002t0002g0229 others(16): Show |
19 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1452-1596_1452-159 others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616002 | C | CTGTG | 14 | a0001c0002t0002g0230 a0001c0004t0001g0245 a0001c0004t0001g0288 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1452-1596_1452-159 others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616002 | CTCTG | C | 85 | a0001c0002t0002g0020 a0001c0002t0002g0045 a0001c0002t0002g0067 others(82): Show |
86 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1452-1595_1452-159 others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616002 | CTCTGTG | C | 7 | a0002c0001t0001g0263 a0002c0001t0001g0266 a0002c0001t0001g0270 others(4): Show |
7 | HG00099.hp2 HG01256.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1452-1595_1452-159 others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616002 | CTCTGTGT others(1): Show |
C | 3 | a0002c0001t0001g0144 a0002c0001t0001g0264 a0002c0001t0001g0267 |
3 | HG00741.hp2 HG02257.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1452-1595_1452-158 others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616002 | CTCTGTGT others(3): Show |
C | 1 | a0001c0004t0001g0024 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1452-1595_1452-158 others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616002 | CTCTGTGT others(7): Show |
C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1452-1595_1452-158 others(18): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616002 | CTCTGTGT others(9): Show |
C | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1452-1595_1452-158 others(20): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616002 | ||||||
| chr13:77616004 | C | CTG | 5 | a0001c0004t0002g0119 a0001c0004t0002g0120 a0001c0004t0002g0122 others(2): Show |
5 | HG00597.hp1 HG02015.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.1452-1554_1452-155 others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616004 | ||||||
| chr13:77616004 | C | CTGTGTGT others(5): Show |
1 | a0001c0004t0002g0290 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1452-1564_1452-155 others(16): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616004 | ||||||
| chr13:77616004 | C | G | 133 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(130): Show |
137 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1452-1595C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616004 | |||||||
| chr13:77616004 | CTG | C | 8 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0032 others(5): Show |
8 | HG01934.hp1 HG02738.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1452-1554_1452-155 others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616004 | ||||||
| chr13:77616004 | CTGTG | C | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(16): Show |
19 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1452-1556_1452-155 others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616004 | ||||||
| chr13:77616009 | T | A | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1452-1590T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616009 | |||||||
| chr13:77616011 | T | A | 1 | a0002c0001t0001g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1452-1588T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616011 | |||||||
| chr13:77616013 | T | A | 62 | a0001c0004t0001g0038 a0002c0001t0001g0062 a0002c0001t0001g0073 others(59): Show |
62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1452-1586T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616013 | |||||||
| chr13:77616015 | T | A | 4 | a0002c0001t0001g0263 a0002c0001t0001g0266 a0002c0001t0001g0270 others(1): Show |
4 | HG00099.hp2 HG01256.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452-1584T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616015 | |||||||
| chr13:77616017 | T | A | 3 | a0002c0001t0001g0144 a0002c0001t0001g0264 a0002c0001t0001g0267 |
3 | HG00741.hp2 HG02257.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1452-1582T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616017 | |||||||
| chr13:77616019 | T | A | 1 | a0001c0004t0001g0024 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1452-1580T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616019 | |||||||
| chr13:77616034 | GTGTGTGT others(4): Show |
G | 1 | a0002c0001t0001g0310 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1452-1564_1452-155 others(15): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616034 | |||||||
| chr13:77616062 | C | T | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1452-1537C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616062 | |||||||
| chr13:77616485 | A | G | 16 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0003c0003t0001g0226 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1452-1114A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616485 | |||||||
| chr13:77616504 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1452-1095A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616504 | |||||||
| chr13:77616715 | C | T | 72 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0002c0001t0001g0062 others(69): Show |
72 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1452-884C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616715 | |||||||
| chr13:77616742 | CT | C | 237 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(234): Show |
240 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.1452-840delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616742 | ||||||
| chr13:77616742 | CTT | C | 21 | a0001c0002t0002g0206 a0001c0002t0002g0230 a0001c0004t0001g0201 others(18): Show |
21 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1452-841_1452-840d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr13 | 77616742 | ||||||
| chr13:77616794 | A | G | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452-805A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616794 | |||||||
| chr13:77616818 | A | G | 1 | a0002c0001t0001g0315 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1452-781A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77616818 | |||||||
| chr13:77617091 | T | G | 1 | a0001c0004t0001g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1452-508T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77617091 | |||||||
| chr13:77617200 | G | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1452-399G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77617200 | |||||||
| chr13:77617267 | T | C | 1 | a0003c0003t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1452-332T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 24/32 | chr13 | 77617267 | |||||||
| chr13:77617689 | G | T | 344 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(341): Show |
353 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.1511+31G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 25/32 | chr13 | 77617689 | |||||||
| chr13:77617772 | A | G | 1 | a0003c0003t0001g0275 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1512-31A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 25/32 | chr13 | 77617772 | |||||||
| chr13:77617956 | C | CA | 6 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(3): Show |
7 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572-44dupA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr13 | 77617956 | ||||||
| chr13:77618067 | G | T | 2 | a0001c0002t0002g0285 a0001c0004t0005g0342 |
2 | HG02630.hp1 NA20300.hp1 |
splice_region_variant&intron_variant | LOW | c.1628+7G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618067 | |||||||
| chr13:77618072 | T | C | 191 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0005 others(188): Show |
195 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.1628+12T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618072 | |||||||
| chr13:77618189 | C | A | 1 | a0002c0001t0001g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1628+129C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618189 | |||||||
| chr13:77618357 | A | T | 4 | a0001c0004t0001g0243 a0001c0004t0001g0244 a0001c0004t0001g0245 others(1): Show |
4 | HG01258.hp2 HG01261.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1628+297A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618357 | |||||||
| chr13:77618492 | TTTC | T | 11 | a0002c0001t0001g0115 a0002c0001t0001g0136 a0002c0001t0001g0163 others(8): Show |
11 | HG00597.hp2 HG02027.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1628+438_1628+440d others(5): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77618492 | ||||||
| chr13:77618546 | T | C | 23 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(20): Show |
24 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628+486T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618546 | |||||||
| chr13:77618650 | A | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(2): Show |
6 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628+590A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618650 | |||||||
| chr13:77618699 | C | T | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1628+639C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618699 | |||||||
| chr13:77618743 | C | A | 323 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(320): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1628+683C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77618743 | |||||||
| chr13:77618763 | GA | G | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1628+709delA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77618763 | ||||||
| chr13:77619088 | A | T | 1 | a0001c0002t0002g0248 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1628+1028A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619088 | |||||||
| chr13:77619124 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1628+1064G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619124 | |||||||
| chr13:77619469 | G | C | 2 | a0001c0002t0002g0093 a0009c0010t0002g0232 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1628+1409G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619469 | |||||||
| chr13:77619632 | C | T | 1 | a0001c0004t0002g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1628+1572C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619632 | |||||||
| chr13:77619811 | T | G | 1 | a0003c0005t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1628+1751T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619811 | |||||||
| chr13:77619841 | T | A | 3 | a0001c0002t0002g0215 a0001c0002t0002g0216 a0001c0002t0002g0219 |
3 | NA19001.hp1 NA19075.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1628+1781T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619841 | |||||||
| chr13:77619895 | T | C | 6 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0301 others(3): Show |
8 | HG00544.hp1 HG00621.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.1628+1835T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619895 | |||||||
| chr13:77619939 | GT | G | 8 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(5): Show |
9 | HG01099.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1628+1885delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77619939 | ||||||
| chr13:77619959 | T | C | 1 | a0003c0003t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1628+1899T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77619959 | |||||||
| chr13:77620030 | C | G | 343 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(340): Show |
352 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.1628+1970C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620030 | |||||||
| chr13:77620054 | A | T | 4 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0002g0248 others(1): Show |
4 | HG00741.hp1 HG01070.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628+1994A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620054 | |||||||
| chr13:77620132 | C | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1628+2072C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620132 | |||||||
| chr13:77620198 | A | G | 2 | a0001c0004t0002g0113 a0001c0004t0002g0114 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1628+2138A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620198 | |||||||
| chr13:77620274 | C | T | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1628+2214C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620274 | |||||||
| chr13:77620398 | C | T | 1 | a0002c0001t0001g0145 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1628+2338C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620398 | |||||||
| chr13:77620449 | C | T | 5 | a0001c0004t0001g0201 a0001c0004t0001g0227 a0001c0004t0001g0282 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1628+2389C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620449 | |||||||
| chr13:77620606 | G | A | 72 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0002c0001t0001g0062 others(69): Show |
72 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1628+2546G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620606 | |||||||
| chr13:77620611 | A | G | 33 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(30): Show |
33 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.1628+2551A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620611 | |||||||
| chr13:77620698 | T | A | 1 | a0002c0001t0001g0319 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1628+2638T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620698 | |||||||
| chr13:77620737 | T | C | 1 | a0002c0001t0001g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1628+2677T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620737 | |||||||
| chr13:77620800 | G | GA | 313 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.1628+2749dupA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77620800 | ||||||
| chr13:77620866 | T | C | 1 | a0003c0006t0002g0344 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1628+2806T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620866 | |||||||
| chr13:77620937 | C | T | 16 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0003c0005t0002g0016 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1628+2877C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77620937 | |||||||
| chr13:77621152 | C | T | 2 | a0003c0003t0001g0096 a0003c0003t0001g0097 |
2 | NA18980.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1628+3092C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621152 | |||||||
| chr13:77621153 | A | G | 100 | a0001c0002t0002g0117 a0001c0004t0001g0009 a0001c0004t0001g0323 others(97): Show |
102 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1628+3093A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621153 | |||||||
| chr13:77621278 | A | G | 11 | a0001c0002t0002g0002 a0001c0002t0002g0064 a0001c0002t0002g0066 others(8): Show |
12 | HG01167.hp1 HG01175.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1628+3218A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621278 | |||||||
| chr13:77621319 | T | A | 2 | a0003c0006t0002g0274 a0003c0006t0002g0345 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1628+3259T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621319 | |||||||
| chr13:77621399 | G | T | 198 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(195): Show |
206 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(203): Show |
intron_variant | MODIFIER | c.1628+3339G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621399 | |||||||
| chr13:77621530 | C | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1628+3470C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621530 | |||||||
| chr13:77621665 | A | G | 29 | a0001c0004t0001g0009 a0001c0004t0001g0201 a0001c0004t0001g0227 others(26): Show |
30 | HG00735.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1628+3605A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621665 | |||||||
| chr13:77621925 | A | C | 71 | a0001c0004t0001g0089 a0001c0004t0001g0108 a0001c0004t0001g0131 others(68): Show |
71 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1628+3865A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77621925 | |||||||
| chr13:77622155 | C | G | 72 | a0001c0016t0001g0218 a0003c0003t0001g0001 a0003c0003t0001g0027 others(69): Show |
73 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1628+4095C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77622155 | |||||||
| chr13:77622156 | G | A | 31 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(28): Show |
31 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1628+4096G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77622156 | |||||||
| chr13:77622768 | G | A | 2 | a0001c0004t0001g0326 a0001c0004t0001g0335 |
2 | HG01981.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1628+4708G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77622768 | |||||||
| chr13:77622866 | AAAAC | A | 6 | a0003c0003t0001g0103 a0003c0003t0001g0199 a0003c0003t0001g0275 others(3): Show |
6 | HG01168.hp2 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628+4814_1628+481 others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77622866 | ||||||
| chr13:77622925 | T | C | 1 | a0001c0002t0002g0004 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1628+4865T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77622925 | |||||||
| chr13:77623112 | C | G | 1 | a0004c0015t0001g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1629-4835C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77623112 | |||||||
| chr13:77623138 | A | G | 10 | a0001c0004t0001g0009 a0001c0004t0001g0201 a0001c0004t0001g0227 others(7): Show |
11 | HG01099.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1629-4809A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77623138 | |||||||
| chr13:77623466 | G | A | 22 | a0001c0004t0001g0009 a0001c0004t0001g0063 a0001c0004t0001g0065 others(19): Show |
23 | HG01099.hp2 HG01109.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1629-4481G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77623466 | |||||||
| chr13:77623498 | T | A | 1 | a0003c0003t0001g0233 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1629-4449T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77623498 | |||||||
| chr13:77623941 | A | G | 77 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1629-4006A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77623941 | |||||||
| chr13:77624017 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0220 |
3 | HG02258.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1629-3930C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624017 | |||||||
| chr13:77624039 | G | C | 2 | a0001c0002t0002g0020 a0001c0002t0002g0045 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1629-3908G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624039 | |||||||
| chr13:77624100 | C | CT | 33 | a0001c0002t0002g0031 a0001c0002t0002g0064 a0001c0002t0002g0222 others(30): Show |
36 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1629-3825dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77624100 | ||||||
| chr13:77624100 | CT | C | 12 | a0001c0002t0002g0051 a0001c0002t0002g0130 a0001c0002t0002g0215 others(9): Show |
12 | HG01167.hp2 HG01256.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1629-3825delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77624100 | ||||||
| chr13:77624100 | CTT | C | 22 | a0001c0004t0001g0063 a0001c0004t0001g0065 a0001c0004t0001g0107 others(19): Show |
22 | HG00735.hp2 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1629-3826_1629-382 others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77624100 | ||||||
| chr13:77624100 | CTTT | C | 71 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(68): Show |
71 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1629-3827_1629-382 others(7): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77624100 | ||||||
| chr13:77624369 | G | C | 1 | a0003c0003t0001g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1629-3578G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624369 | |||||||
| chr13:77624654 | A | G | 1 | a0004c0015t0001g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1629-3293A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624654 | |||||||
| chr13:77624714 | G | C | 102 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(99): Show |
106 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1629-3233G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624714 | |||||||
| chr13:77624801 | C | A | 77 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1629-3146C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624801 | |||||||
| chr13:77624925 | A | G | 1 | a0001c0002t0002g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1629-3022A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624925 | |||||||
| chr13:77624947 | C | A | 1 | a0003c0003t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1629-3000C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77624947 | |||||||
| chr13:77625036 | A | G | 102 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(99): Show |
106 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1629-2911A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77625036 | |||||||
| chr13:77625052 | G | A | 300 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(297): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.1629-2895G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77625052 | |||||||
| chr13:77625095 | T | C | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1629-2852T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77625095 | |||||||
| chr13:77625182 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1629-2765C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77625182 | |||||||
| chr13:77625562 | T | A | 343 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(340): Show |
352 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.1629-2385T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77625562 | |||||||
| chr13:77626030 | T | G | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1629-1917T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626030 | |||||||
| chr13:77626074 | A | G | 1 | a0001c0004t0001g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1629-1873A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626074 | |||||||
| chr13:77626108 | C | T | 104 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(101): Show |
108 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1629-1839C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626108 | |||||||
| chr13:77626306 | C | G | 1 | a0008c0013t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1629-1641C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626306 | |||||||
| chr13:77626428 | G | A | 1 | a0002c0001t0001g0152 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1629-1519G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626428 | |||||||
| chr13:77626617 | A | G | 77 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1629-1330A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626617 | |||||||
| chr13:77626641 | C | T | 1 | a0001c0002t0002g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1629-1306C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626641 | |||||||
| chr13:77626727 | C | T | 66 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(63): Show |
70 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1629-1220C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626727 | |||||||
| chr13:77626878 | T | G | 1 | a0003c0003t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1629-1069T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626878 | |||||||
| chr13:77626901 | A | G | 72 | a0001c0016t0001g0218 a0003c0003t0001g0001 a0003c0003t0001g0027 others(69): Show |
73 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1629-1046A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626901 | |||||||
| chr13:77626961 | C | A | 319 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1629-986C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77626961 | |||||||
| chr13:77627605 | C | T | 1 | a0002c0001t0001g0178 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629-342C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77627605 | |||||||
| chr13:77627625 | GTACATCT others(4): Show |
G | 1 | a0003c0003t0001g0054 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1629-315_1629-305d others(13): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr13 | 77627625 | ||||||
| chr13:77627744 | T | A | 1 | a0002c0001t0001g0178 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1629-203T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77627744 | |||||||
| chr13:77627902 | A | G | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1629-45A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77627902 | |||||||
| chr13:77627933 | A | T | 1 | a0003c0003t0001g0060 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1629-14A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 27/32 | chr13 | 77627933 | |||||||
| chr13:77628132 | G | A | 1 | a0002c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1691+123G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628132 | |||||||
| chr13:77628170 | G | GTATA | 16 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0002g0289 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1691+179_1691+182d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | G | GTATATA | 4 | a0001c0004t0001g0287 a0001c0004t0001g0288 a0001c0004t0002g0321 others(1): Show |
4 | HG01109.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1691+177_1691+182d others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | G | GTGTA | 69 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(66): Show |
69 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1691+162_1691+163i others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | G | GTGTATA | 9 | a0001c0004t0001g0332 a0002c0001t0001g0164 a0002c0001t0001g0165 others(6): Show |
9 | HG00544.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1691+162_1691+163i others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | G | GTGTATAT others(1): Show |
25 | a0001c0004t0001g0063 a0001c0004t0001g0065 a0001c0004t0001g0107 others(22): Show |
27 | HG00621.hp1 HG01123.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1691+162_1691+163i others(10): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | G | GTGTATAT others(3): Show |
9 | a0001c0004t0001g0282 a0001c0004t0001g0284 a0001c0004t0001g0320 others(6): Show |
10 | HG00621.hp2 HG02055.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1691+162_1691+163i others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | G | GTGTATAT others(5): Show |
7 | a0001c0004t0001g0009 a0001c0004t0001g0283 a0001c0004t0001g0323 others(4): Show |
8 | HG01099.hp2 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1691+162_1691+163i others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | G | GTGTATAT others(7): Show |
2 | a0001c0004t0001g0201 a0001c0004t0001g0227 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1691+162_1691+163i others(16): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628170 | GTA | G | 87 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(84): Show |
91 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1691+181_1691+182d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628170 | ||||||
| chr13:77628172 | A | G | 1 | a0001c0004t0002g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1691+163A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628172 | |||||||
| chr13:77628177 | T | TAC | 72 | a0001c0016t0001g0218 a0003c0003t0001g0001 a0003c0003t0001g0027 others(69): Show |
73 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1691+169_1691+170i others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77628177 | ||||||
| chr13:77628192 | C | A | 77 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1691+183C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628192 | |||||||
| chr13:77628729 | T | C | 1 | a0004c0008t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1691+720T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628729 | |||||||
| chr13:77628732 | T | C | 301 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(298): Show |
310 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.1691+723T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628732 | |||||||
| chr13:77628748 | G | A | 1 | a0003c0003t0001g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1691+739G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628748 | |||||||
| chr13:77628773 | G | A | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1691+764G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628773 | |||||||
| chr13:77628906 | A | G | 1 | a0001c0002t0002g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1691+897A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628906 | |||||||
| chr13:77628908 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1691+899G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77628908 | |||||||
| chr13:77629022 | T | C | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1691+1013T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77629022 | |||||||
| chr13:77629044 | T | G | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1691+1035T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77629044 | |||||||
| chr13:77629273 | G | A | 343 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(340): Show |
352 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.1691+1264G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77629273 | |||||||
| chr13:77629360 | C | T | 1 | a0003c0005t0002g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1691+1351C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77629360 | |||||||
| chr13:77629378 | A | AT | 199 | a0001c0004t0001g0009 a0001c0004t0001g0024 a0001c0004t0001g0038 others(196): Show |
204 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1691+1378dupT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77629378 | ||||||
| chr13:77629936 | T | A | 1 | a0002c0001t0001g0343 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1691+1927T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77629936 | |||||||
| chr13:77629939 | T | A | 1 | a0002c0001t0001g0343 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1691+1930T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77629939 | |||||||
| chr13:77630301 | C | G | 1 | a0001c0004t0002g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1691+2292C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77630301 | |||||||
| chr13:77630367 | C | A | 301 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(298): Show |
310 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.1691+2358C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77630367 | |||||||
| chr13:77630443 | T | C | 3 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0002c0014t0002g0153 |
3 | NA18952.hp2 NA18971.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1691+2434T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77630443 | |||||||
| chr13:77631020 | T | C | 319 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1691+3011T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631020 | |||||||
| chr13:77631097 | G | A | 14 | a0002c0001t0002g0268 a0003c0005t0002g0016 a0003c0005t0002g0017 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1691+3088G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631097 | |||||||
| chr13:77631277 | A | G | 1 | a0001c0004t0002g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1692-3102A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631277 | |||||||
| chr13:77631389 | G | T | 1 | a0002c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1692-2990G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631389 | |||||||
| chr13:77631462 | C | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1692-2917C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631462 | |||||||
| chr13:77631529 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1692-2850G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631529 | |||||||
| chr13:77631586 | T | C | 1 | a0002c0001t0001g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1692-2793T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631586 | |||||||
| chr13:77631587 | T | C | 319 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1692-2792T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631587 | |||||||
| chr13:77631676 | A | C | 4 | a0001c0004t0001g0089 a0001c0004t0001g0108 a0001c0004t0001g0131 others(1): Show |
4 | NA18954.hp2 NA18974.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1692-2703A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631676 | |||||||
| chr13:77631681 | GA | G | 14 | a0002c0001t0002g0268 a0003c0005t0002g0016 a0003c0005t0002g0017 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1692-2697delA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631681 | |||||||
| chr13:77631786 | T | C | 2 | a0001c0002t0002g0253 a0001c0002t0002g0254 |
2 | HG00558.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1692-2593T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77631786 | |||||||
| chr13:77632057 | T | C | 1 | a0001c0002t0002g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1692-2322T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632057 | |||||||
| chr13:77632100 | C | T | 1 | a0001c0004t0005g0342 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1692-2279C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632100 | |||||||
| chr13:77632186 | G | T | 1 | a0002c0001t0001g0162 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1692-2193G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632186 | |||||||
| chr13:77632227 | CTTATCTC others(51): Show |
C | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1692-2151_1692-209 others(62): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632227 | |||||||
| chr13:77632259 | G | A | 5 | a0001c0002t0002g0092 a0001c0002t0002g0175 a0001c0002t0002g0176 others(2): Show |
5 | HG00639.hp1 HG01952.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1692-2120G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632259 | |||||||
| chr13:77632275 | C | T | 18 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0001c0004t0002g0321 others(15): Show |
18 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1692-2104C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632275 | |||||||
| chr13:77632289 | A | G | 1 | a0001c0002t0002g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1692-2090A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632289 | |||||||
| chr13:77632334 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0220 |
3 | HG02258.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1692-2045G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632334 | |||||||
| chr13:77632385 | C | A | 1 | a0003c0006t0002g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1692-1994C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632385 | |||||||
| chr13:77632394 | G | C | 5 | a0001c0002t0002g0092 a0001c0002t0002g0175 a0001c0002t0002g0176 others(2): Show |
5 | HG00639.hp1 HG01952.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1692-1985G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632394 | |||||||
| chr13:77632509 | T | G | 343 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(340): Show |
352 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.1692-1870T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632509 | |||||||
| chr13:77632542 | C | T | 1 | a0013c0022t0001g0298 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1692-1837C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632542 | |||||||
| chr13:77632758 | G | A | 319 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1692-1621G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77632758 | |||||||
| chr13:77633012 | G | C | 1 | a0002c0001t0001g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1692-1367G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633012 | |||||||
| chr13:77633197 | G | A | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1692-1182G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633197 | |||||||
| chr13:77633198 | A | G | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1692-1181A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633198 | |||||||
| chr13:77633304 | C | T | 1 | a0001c0004t0002g0122 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1692-1075C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633304 | |||||||
| chr13:77633430 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1692-949G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633430 | |||||||
| chr13:77633437 | C | T | 26 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(23): Show |
26 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1692-942C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633437 | |||||||
| chr13:77633442 | C | CA | 8 | a0001c0002t0002g0023 a0001c0002t0002g0030 a0001c0002t0002g0031 others(5): Show |
8 | HG01978.hp2 HG02071.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1692-913dupA | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(2): Show |
30 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0243 others(27): Show |
30 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1692-921_1692-913d others(11): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(3): Show |
24 | a0001c0004t0001g0089 a0001c0004t0001g0108 a0001c0004t0001g0131 others(21): Show |
24 | HG00438.hp1 HG00597.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1692-922_1692-913d others(12): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(4): Show |
15 | a0001c0004t0001g0246 a0001c0004t0002g0122 a0002c0001t0001g0076 others(12): Show |
15 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1692-923_1692-913d others(13): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(5): Show |
18 | a0002c0001t0001g0075 a0002c0001t0001g0152 a0002c0001t0001g0194 others(15): Show |
18 | HG00544.hp2 HG01099.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1692-924_1692-913d others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(6): Show |
34 | a0002c0001t0001g0115 a0002c0001t0001g0161 a0002c0001t0001g0189 others(31): Show |
34 | HG00408.hp1 HG01433.hp2 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.1692-925_1692-913d others(15): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(7): Show |
16 | a0001c0016t0001g0218 a0002c0001t0001g0156 a0003c0003t0001g0055 others(13): Show |
16 | HG00639.hp2 HG01109.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1692-926_1692-913d others(16): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(8): Show |
3 | a0003c0003t0001g0097 a0003c0003t0001g0137 a0003c0003t0001g0291 |
3 | HG03669.hp1 NA18967.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1692-927_1692-913d others(17): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(9): Show |
3 | a0003c0003t0001g0083 a0003c0003t0001g0286 a0003c0003t0004g0056 |
3 | HG02723.hp2 NA18954.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1692-928_1692-913d others(18): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(12): Show |
6 | a0001c0004t0002g0088 a0001c0004t0002g0123 a0001c0004t0002g0124 others(3): Show |
6 | HG02015.hp2 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1692-931_1692-913d others(21): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(13): Show |
6 | a0001c0004t0002g0021 a0001c0004t0002g0101 a0001c0004t0002g0120 others(3): Show |
6 | HG00438.hp2 NA18955.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.1692-932_1692-913d others(22): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(14): Show |
1 | a0001c0004t0002g0125 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1692-933_1692-913d others(23): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(15): Show |
4 | a0001c0004t0002g0114 a0001c0004t0002g0121 a0003c0003t0001g0001 others(1): Show |
5 | HG01070.hp1 HG02615.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1692-934_1692-913d others(24): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(16): Show |
6 | a0001c0004t0002g0113 a0001c0004t0002g0126 a0001c0004t0002g0139 others(3): Show |
6 | HG00735.hp2 HG01071.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1692-935_1692-913d others(25): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(17): Show |
8 | a0001c0004t0002g0111 a0001c0004t0002g0119 a0002c0001t0001g0008 others(5): Show |
9 | HG00597.hp1 HG00733.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692-936_1692-913d others(26): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(18): Show |
13 | a0001c0004t0002g0256 a0002c0001t0001g0296 a0002c0001t0001g0301 others(10): Show |
13 | HG00621.hp1 HG01243.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1692-913_1692-912i others(27): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(19): Show |
8 | a0001c0004t0002g0109 a0001c0004t0002g0118 a0002c0001t0001g0303 others(5): Show |
8 | HG00621.hp2 HG01123.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1692-913_1692-912i others(28): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(20): Show |
3 | a0002c0001t0001g0006 a0002c0001t0003g0299 a0003c0005t0002g0042 |
4 | HG00544.hp1 HG01891.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1692-913_1692-912i others(29): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(21): Show |
2 | a0003c0005t0002g0043 a0003c0005t0002g0049 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1692-913_1692-912i others(30): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(23): Show |
1 | a0002c0001t0001g0007 | 2 | NA19066.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1692-913_1692-912i others(32): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(24): Show |
2 | a0002c0001t0001g0300 a0002c0001t0001g0312 |
2 | HG02071.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1692-913_1692-912i others(33): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(28): Show |
1 | a0003c0005t0002g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1692-913_1692-912i others(37): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | C | CAAAAAAA others(35): Show |
1 | a0003c0005t0002g0280 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1692-913_1692-912i others(44): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | CAAAA | C | 9 | a0001c0004t0001g0009 a0001c0004t0001g0201 a0001c0004t0001g0282 others(6): Show |
10 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1692-916_1692-913d others(6): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | CAAAAA | C | 12 | a0001c0004t0001g0063 a0001c0004t0001g0065 a0001c0004t0001g0107 others(9): Show |
12 | HG01109.hp1 HG01981.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1692-917_1692-913d others(7): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633442 | CAAAAAA | C | 6 | a0002c0001t0001g0178 a0003c0003t0001g0334 a0003c0003t0001g0338 others(3): Show |
6 | HG00735.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1692-918_1692-913d others(8): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633442 | ||||||
| chr13:77633467 | G | A | 1 | a0003c0005t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1692-912G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633467 | |||||||
| chr13:77633565 | G | A | 17 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0002c0001t0002g0268 others(14): Show |
17 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1692-814G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633565 | |||||||
| chr13:77633587 | C | G | 5 | a0002c0001t0001g0062 a0002c0001t0001g0264 a0002c0001t0001g0267 others(2): Show |
5 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1692-792C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633587 | |||||||
| chr13:77633592 | G | A | 72 | a0001c0016t0001g0218 a0003c0003t0001g0001 a0003c0003t0001g0027 others(69): Show |
73 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1692-787G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633592 | |||||||
| chr13:77633596 | GATGCCCA others(5): Show |
G | 1 | a0001c0004t0002g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1692-779_1692-768d others(14): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr13 | 77633596 | ||||||
| chr13:77633620 | A | C | 1 | a0002c0001t0001g0006 | 2 | NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1692-759A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633620 | |||||||
| chr13:77633717 | A | T | 1 | a0001c0004t0005g0342 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1692-662A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633717 | |||||||
| chr13:77633764 | T | C | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1692-615T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633764 | |||||||
| chr13:77633767 | C | T | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1692-612C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633767 | |||||||
| chr13:77633768 | T | C | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1692-611T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633768 | |||||||
| chr13:77633876 | T | C | 342 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(339): Show |
351 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.1692-503T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633876 | |||||||
| chr13:77633884 | C | T | 1 | a0003c0003t0001g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1692-495C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633884 | |||||||
| chr13:77633913 | T | A | 1 | a0001c0002t0002g0260 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1692-466T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633913 | |||||||
| chr13:77633920 | G | A | 1 | a0001c0002t0002g0253 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1692-459G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 28/32 | chr13 | 77633920 | |||||||
| chr13:77634540 | G | A | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1763+90G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77634540 | |||||||
| chr13:77634561 | G | A | 2 | a0001c0004t0002g0122 a0001c0004t0002g0256 |
2 | NA18956.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1763+111G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77634561 | |||||||
| chr13:77634601 | A | G | 1 | a0001c0004t0005g0342 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1763+151A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77634601 | |||||||
| chr13:77634700 | G | T | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1763+250G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77634700 | |||||||
| chr13:77634735 | A | G | 102 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(99): Show |
106 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1763+285A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77634735 | |||||||
| chr13:77634849 | T | G | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1763+399T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77634849 | |||||||
| chr13:77634895 | T | A | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1763+445T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77634895 | |||||||
| chr13:77635088 | G | A | 1 | a0001c0002t0002g0281 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1763+638G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77635088 | |||||||
| chr13:77635440 | C | G | 1 | a0003c0005t0002g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1763+990C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77635440 | |||||||
| chr13:77635613 | A | T | 9 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0029 others(6): Show |
9 | NA18946.hp2 NA18952.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.1763+1163A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77635613 | |||||||
| chr13:77635927 | A | T | 77 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1764-1193A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77635927 | |||||||
| chr13:77636063 | G | A | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1764-1057G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636063 | |||||||
| chr13:77636176 | T | C | 301 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(298): Show |
310 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.1764-944T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636176 | |||||||
| chr13:77636201 | C | T | 22 | a0001c0004t0001g0009 a0001c0004t0001g0063 a0001c0004t0001g0065 others(19): Show |
23 | HG01099.hp2 HG01109.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1764-919C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636201 | |||||||
| chr13:77636232 | A | G | 5 | a0003c0003t0001g0334 a0003c0003t0001g0338 a0003c0003t0001g0339 others(2): Show |
5 | HG00735.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1764-888A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636232 | |||||||
| chr13:77636279 | A | C | 8 | a0001c0004t0001g0063 a0001c0004t0001g0065 a0001c0004t0001g0107 others(5): Show |
8 | HG01981.hp1 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1764-841A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636279 | |||||||
| chr13:77636305 | T | C | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1764-815T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636305 | |||||||
| chr13:77636572 | T | C | 2 | a0002c0001t0002g0268 a0003c0005t0002g0052 |
2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1764-548T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636572 | |||||||
| chr13:77636620 | T | C | 1 | a0001c0002t0002g0033 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1764-500T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636620 | |||||||
| chr13:77636669 | A | G | 22 | a0001c0004t0001g0009 a0001c0004t0001g0063 a0001c0004t0001g0065 others(19): Show |
23 | HG01099.hp2 HG01109.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1764-451A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636669 | |||||||
| chr13:77636672 | T | C | 1 | a0001c0002t0002g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1764-448T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636672 | |||||||
| chr13:77636780 | G | A | 1 | a0001c0004t0005g0342 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1764-340G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636780 | |||||||
| chr13:77636893 | G | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1764-227G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636893 | |||||||
| chr13:77636979 | A | G | 10 | a0001c0004t0001g0009 a0001c0004t0001g0201 a0001c0004t0001g0227 others(7): Show |
11 | HG01099.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1764-141A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77636979 | |||||||
| chr13:77637093 | T | G | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1764-27T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 29/32 | chr13 | 77637093 | |||||||
| chr13:77637239 | G | GAC | 78 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(75): Show |
78 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1838+57_1838+58dup others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637239 | ||||||
| chr13:77637251 | C | CAT | 9 | a0001c0004t0001g0009 a0001c0004t0001g0201 a0001c0004t0001g0282 others(6): Show |
10 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1838+73_1838+74dup others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637251 | ||||||
| chr13:77637251 | CAT | C | 117 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(114): Show |
121 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.1838+73_1838+74del others(2): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637251 | ||||||
| chr13:77637253 | T | C | 31 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0001c0004t0002g0321 others(28): Show |
34 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1838+59T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637253 | |||||||
| chr13:77637255 | T | C | 42 | a0001c0002t0002g0258 a0002c0001t0001g0006 a0002c0001t0001g0007 others(39): Show |
45 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1838+61T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637255 | |||||||
| chr13:77637267 | T | C | 174 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(171): Show |
179 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.1838+73T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637267 | |||||||
| chr13:77637287 | C | CACATATA others(13): Show |
1 | a0001c0002t0002g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1838+123_1838+142d others(22): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637287 | ||||||
| chr13:77637287 | CACATATA others(13): Show |
C | 15 | a0001c0004t0002g0021 a0001c0004t0002g0109 a0001c0004t0002g0111 others(12): Show |
15 | HG00733.hp1 HG01515.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1838+123_1838+142d others(22): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637287 | ||||||
| chr13:77637289 | CATATATA others(12): Show |
C | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1838+96_1838+114de others(20): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637289 | |||||||
| chr13:77637301 | TATATATA others(31): Show |
T | 1 | a0001c0004t0005g0342 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1838+123_1838+160d others(40): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637301 | ||||||
| chr13:77637309 | C | G | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1838+115C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637309 | |||||||
| chr13:77637309 | CAT | C | 66 | a0001c0002t0002g0094 a0001c0002t0002g0138 a0001c0002t0002g0212 others(63): Show |
67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1838+123_1838+124d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637309 | ||||||
| chr13:77637311 | T | TATATAAA others(9): Show |
1 | a0003c0003t0001g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1838+122_1838+123i others(18): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637311 | ||||||
| chr13:77637321 | T | C | 68 | a0001c0002t0002g0094 a0001c0002t0002g0138 a0001c0002t0002g0212 others(65): Show |
69 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1838+127T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637321 | |||||||
| chr13:77637321 | T | TATATATA others(11): Show |
24 | a0001c0004t0001g0065 a0001c0004t0001g0107 a0001c0004t0001g0133 others(21): Show |
24 | HG00735.hp2 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1838+181_1838+198d others(20): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637321 | ||||||
| chr13:77637321 | T | TATATATA others(29): Show |
1 | a0001c0004t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1838+163_1838+198d others(38): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637321 | ||||||
| chr13:77637339 | CAT | C | 5 | a0001c0002t0002g0094 a0001c0002t0002g0138 a0001c0002t0002g0212 others(2): Show |
5 | HG01071.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+151_1838+152d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637339 | ||||||
| chr13:77637341 | T | TATATACA others(9): Show |
97 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(94): Show |
101 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1838+153_1838+168d others(18): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637341 | ||||||
| chr13:77637371 | T | TAAACATA others(11): Show |
1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1838+188_1838+189i others(20): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637371 | ||||||
| chr13:77637393 | T | C | 5 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0001c0004t0002g0321 others(2): Show |
5 | HG02615.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1838+199T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637393 | |||||||
| chr13:77637413 | A | AAT | 4 | a0001c0004t0001g0134 a0001c0004t0001g0135 a0001c0004t0001g0287 others(1): Show |
4 | HG01109.hp1 HG02109.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838+236_1838+237d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637413 | ||||||
| chr13:77637413 | A | T | 5 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0001c0004t0002g0321 others(2): Show |
5 | HG02615.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1838+219A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637413 | |||||||
| chr13:77637413 | AAT | A | 291 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(288): Show |
299 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.1838+236_1838+237d others(4): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637413 | ||||||
| chr13:77637415 | T | TATACATA others(9): Show |
5 | a0001c0004t0002g0289 a0001c0004t0002g0290 a0001c0004t0002g0321 others(2): Show |
5 | HG02615.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1838+224_1838+225i others(18): Show |
SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr13 | 77637415 | ||||||
| chr13:77637423 | T | A | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1838+229T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637423 | |||||||
| chr13:77637423 | T | C | 29 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(26): Show |
29 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1838+229T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637423 | |||||||
| chr13:77637480 | C | T | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1838+286C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637480 | |||||||
| chr13:77637481 | A | G | 2 | a0002c0001t0001g0075 a0002c0001t0001g0076 |
2 | NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1838+287A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637481 | |||||||
| chr13:77637494 | G | A | 1 | a0002c0001t0001g0311 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1838+300G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637494 | |||||||
| chr13:77637498 | G | C | 17 | a0001c0004t0002g0021 a0001c0004t0002g0088 a0001c0004t0002g0101 others(14): Show |
17 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.1838+304G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637498 | |||||||
| chr13:77637550 | A | C | 301 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(298): Show |
310 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.1838+356A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637550 | |||||||
| chr13:77637967 | G | T | 1 | a0001c0002t0002g0117 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1838+773G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77637967 | |||||||
| chr13:77638112 | T | A | 1 | a0003c0003t0001g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1838+918T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638112 | |||||||
| chr13:77638171 | T | A | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1838+977T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638171 | |||||||
| chr13:77638659 | C | A | 2 | a0003c0006t0002g0010 a0003c0006t0002g0011 |
2 | HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1838+1465C>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638659 | |||||||
| chr13:77638659 | C | T | 1 | a0001c0002t0002g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1838+1465C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638659 | |||||||
| chr13:77638763 | C | T | 13 | a0002c0001t0001g0304 a0002c0001t0001g0305 a0002c0001t0001g0306 others(10): Show |
13 | HG00621.hp1 HG02071.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1838+1569C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638763 | |||||||
| chr13:77638881 | C | T | 1 | a0001c0004t0002g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1838+1687C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638881 | |||||||
| chr13:77638883 | A | C | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1838+1689A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638883 | |||||||
| chr13:77638892 | A | G | 5 | a0003c0003t0001g0334 a0003c0003t0001g0338 a0003c0003t0001g0339 others(2): Show |
5 | HG00735.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+1698A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638892 | |||||||
| chr13:77638933 | G | A | 301 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(298): Show |
310 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.1838+1739G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77638933 | |||||||
| chr13:77639032 | C | G | 319 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1839-1644C>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77639032 | |||||||
| chr13:77639194 | T | A | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1839-1482T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77639194 | |||||||
| chr13:77639516 | C | T | 1 | a0002c0001t0001g0266 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1839-1160C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77639516 | |||||||
| chr13:77639880 | A | T | 8 | a0001c0002t0002g0285 a0003c0006t0002g0010 a0003c0006t0002g0011 others(5): Show |
8 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1839-796A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77639880 | |||||||
| chr13:77639911 | G | A | 102 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(99): Show |
106 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1839-765G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77639911 | |||||||
| chr13:77639940 | C | T | 122 | a0001c0004t0001g0009 a0001c0004t0001g0063 a0001c0004t0001g0065 others(119): Show |
127 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1839-736C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77639940 | |||||||
| chr13:77640105 | C | T | 4 | a0003c0003t0001g0095 a0003c0003t0001g0096 a0003c0003t0001g0097 others(1): Show |
4 | NA18973.hp2 NA18980.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839-571C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77640105 | |||||||
| chr13:77640122 | T | G | 1 | a0010c0017t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1839-554T>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77640122 | |||||||
| chr13:77640303 | G | A | 1 | a0014c0021t0001g0172 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1839-373G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77640303 | |||||||
| chr13:77640441 | G | A | 6 | a0002c0001t0001g0304 a0002c0001t0001g0306 a0002c0001t0001g0307 others(3): Show |
6 | HG02071.hp1 HG02074.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1839-235G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 30/32 | chr13 | 77640441 | |||||||
| chr13:77640960 | G | C | 1 | a0001c0002t0002g0202 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1947+176G>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77640960 | |||||||
| chr13:77641120 | A | C | 77 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1947+336A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641120 | |||||||
| chr13:77641222 | T | C | 22 | a0001c0004t0001g0009 a0001c0004t0001g0063 a0001c0004t0001g0065 others(19): Show |
23 | HG01099.hp2 HG01109.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1947+438T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641222 | |||||||
| chr13:77641316 | A | T | 1 | a0001c0002t0002g0013 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1947+532A>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641316 | |||||||
| chr13:77641317 | G | A | 1 | a0001c0004t0002g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1947+533G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641317 | |||||||
| chr13:77641365 | C | T | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1947+581C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641365 | |||||||
| chr13:77641576 | T | C | 2 | a0001c0002t0002g0195 a0001c0002t0002g0223 |
2 | HG02071.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1947+792T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641576 | |||||||
| chr13:77641636 | G | T | 1 | a0002c0001t0001g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1947+852G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641636 | |||||||
| chr13:77641673 | A | C | 1 | a0003c0003t0001g0080 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1947+889A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641673 | |||||||
| chr13:77641843 | C | T | 2 | a0001c0004t0001g0134 a0001c0004t0001g0135 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1948-863C>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641843 | |||||||
| chr13:77641888 | G | T | 342 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(339): Show |
351 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.1948-818G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641888 | |||||||
| chr13:77641946 | T | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1948-760T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641946 | |||||||
| chr13:77641986 | T | A | 71 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(68): Show |
75 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1948-720T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77641986 | |||||||
| chr13:77642005 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1948-701A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77642005 | |||||||
| chr13:77642582 | G | A | 2 | a0001c0004t0001g0287 a0001c0004t0001g0288 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1948-124G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 31/32 | chr13 | 77642582 | |||||||
| chr13:77642946 | A | G | 1 | a0002c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2050+138A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77642946 | |||||||
| chr13:77643369 | A | G | 4 | a0001c0004t0001g0009 a0001c0004t0001g0323 a0001c0004t0001g0324 others(1): Show |
5 | HG01099.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2050+561A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77643369 | |||||||
| chr13:77643556 | G | A | 77 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0089 others(74): Show |
77 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2051-702G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77643556 | |||||||
| chr13:77643779 | AT | A | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2051-477delT | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr13 | 77643779 | ||||||
| chr13:77643949 | T | A | 1 | a0003c0003t0001g0295 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2051-309T>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77643949 | |||||||
| chr13:77644045 | A | G | 1 | a0001c0004t0005g0342 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2051-213A>G | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77644045 | |||||||
| chr13:77644097 | T | C | 2 | a0001c0004t0002g0289 a0001c0004t0002g0290 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2051-161T>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77644097 | |||||||
| chr13:77644135 | A | C | 1 | a0001c0012t0002g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2051-123A>C | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77644135 | |||||||
| chr13:77644174 | G | A | 1 | a0001c0004t0001g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2051-84G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77644174 | |||||||
| chr13:77644205 | G | A | 2 | a0003c0003t0001g0055 a0003c0003t0004g0056 |
2 | NA19001.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2051-53G>A | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77644205 | |||||||
| chr13:77644210 | G | T | 27 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0008 others(24): Show |
30 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2051-48G>T | SCEL | ENSG00000136155.17 | transcript | ENST00000349847.4 | protein_coding | 32/32 | chr13 | 77644210 |