Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9092 |
| ensemblid | ENSG00000175467.15 |
| hgncid | 10538 |
| symbol | SART1 |
| name | spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP |
| refseq_nuc | NM_005146.5 |
| refseq_prot | NP_005137.1 |
| ensembl_nuc | ENST00000312397.10 |
| ensembl_prot | ENSP00000310448.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 65961734 |
| end | 65980137 |
| strand | + |
| ver | v1.2 |
| region | chr11:65961734-65980137 |
| region5000 | chr11:65956734-65985137 |
| regionname0 | SART1_chr11_65961734_65980137 |
| regionname5000 | SART1_chr11_65956734_65985137 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 800 | 220 | 86 | 30 | 70 | 7 | 25 | 48 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0002 | 0/0 | 800 | 151 | 5 | 38 | 87 | 5 | 16 | 61 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0003 | 0/0 | 800 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0004 | 0/0 | 800 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0005 | 0/0 | 800 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0006 | 0/0 | 800 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0007 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0008 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0009 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0010 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| a0011 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | MGSSK others(795): Show |
chr11 | 65956734 | 65985137 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 2400 | 111 | 24 | 23 | 31 | 7 | 25 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0003 | 1/0 | 2400 | 46 | 26 | 3 | 16 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0004 | 0/0 | 2400 | 29 | 6 | 1 | 22 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0005 | 0/0 | 2400 | 24 | 22 | 2 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0006 | 0/0 | 2400 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0007 | 0/0 | 2400 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0016 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0017 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0019 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0001c0021 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0002c0001 | 0/0 | 2400 | 149 | 5 | 37 | 86 | 5 | 16 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0002c0011 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0002c0012 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0003c0008 | 0/0 | 2400 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0004c0009 | 0/0 | 2400 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0005c0010 | 0/0 | 2400 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0006c0022 | 0/0 | 2400 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0007c0014 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0008c0018 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0009c0020 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0010c0013 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 | ||
| a0011c0015 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | ATGGG others(2395): Show |
chr11 | 65956734 | 65985137 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 3557 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0002t0002 | 0/0 | 3557 | 49 | 22 | 9 | 3 | 3 | 12 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0002t0003 | 0/1 | 3557 | 54 | 1 | 12 | 26 | 4 | 10 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0002t0008 | 0/0 | 3557 | 2 | 1 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0002t0009 | 0/0 | 3557 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0002t0011 | 0/0 | 3557 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0002t0012 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0002t0013 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0003t0002 | 0/0 | 3557 | 23 | 6 | 1 | 16 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0003t0003 | 0/0 | 3557 | 8 | 7 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0003t0004 | 0/0 | 3556 | 8 | 7 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3551): Show |
chr11 | 65956734 | 65985137 |
| a0001c0003t0005 | 1/0 | 3557 | 5 | 4 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0003t0010 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3551): Show |
chr11 | 65956734 | 65985137 |
| a0001c0003t0015 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0004t0002 | 0/0 | 3557 | 23 | 1 | 1 | 21 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0004t0006 | 0/0 | 3557 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0004t0007 | 0/0 | 3557 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0004t0014 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0005t0001 | 0/0 | 3557 | 16 | 15 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0005t0002 | 0/0 | 3557 | 8 | 7 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0006t0001 | 0/0 | 3557 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0007t0002 | 0/0 | 3557 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0016t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0017t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0019t0002 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0001c0021t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0002c0001t0001 | 0/0 | 3557 | 146 | 5 | 37 | 84 | 5 | 15 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0002c0001t0016 | 0/0 | 3557 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0002c0001t0017 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0002c0001t0018 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0002c0011t0001 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0002c0012t0001 | 0/0 | 3557 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0003c0008t0002 | 0/0 | 3557 | 3 | 0 | 0 | 3 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0004c0009t0001 | 0/0 | 3557 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0005c0010t0003 | 0/0 | 3557 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0006c0022t0001 | 0/0 | 3557 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0007c0014t0001 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0008c0018t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0009c0020t0002 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0010c0013t0001 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| a0011c0015t0002 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | CGTTG others(3552): Show |
chr11 | 65956734 | 65985137 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0006 | 0/0 | 7 | 3 | 1 | 0 | 2 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0001 | 0/0 | 14 | 0 | 3 | 9 | 1 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0003g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0009g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0011g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0012g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0002t0013g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0004g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0005g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0003t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0004t0014g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0005t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0006t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0006t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0007t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0007t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0016t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0017t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0019t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0001c0021t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0002 | 0/0 | 11 | 0 | 2 | 7 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0003 | 0/0 | 10 | 0 | 3 | 5 | 0 | 2 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0004 | 0/0 | 9 | 1 | 2 | 3 | 0 | 3 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0016g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0017g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0001t0018g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0011t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0002c0012t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0003c0008t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0003c0008t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0003c0008t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0004c0009t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0004c0009t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0005c0010t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0005c0010t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0006c0022t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0007c0014t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0008c0018t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0009c0020t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0010c0013t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| a0011c0015t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0118 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0077 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0078 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | GBR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0185 | EUR | FIN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | FIN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0149 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0247 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0249 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0143 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0095 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0251 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0128 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00673 | hp1 | a0001 | c0004 | t0014 | g0053 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | CHS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0135 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0030 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0009 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0027 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0027 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0227 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01099 | hp2 | a0001 | c0002 | t0011 | g0193 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01106 | hp1 | a0001 | c0005 | t0002 | g0042 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0166 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0112 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0146 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0202 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01169 | hp2 | a0002 | c0001 | t0001 | g0145 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0225 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0157 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0013 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0063 | AMR | PUR | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01255 | hp1 | a0002 | c0012 | t0001 | g0003 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0140 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0195 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0156 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0075 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0200 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01496 | hp2 | a0001 | c0002 | t0008 | g0171 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0006 | EUR | IBS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0006 | EUR | IBS | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01884 | hp1 | a0001 | c0003 | t0010 | g0232 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01891 | hp1 | a0001 | c0007 | t0002 | g0018 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0073 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01934 | hp1 | a0001 | c0005 | t0001 | g0010 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0074 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0114 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0076 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0111 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0115 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0108 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02027 | hp2 | a0001 | c0002 | t0013 | g0035 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0031 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02055 | hp2 | a0001 | c0004 | t0006 | g0045 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02056 | hp2 | a0001 | c0003 | t0002 | g0017 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02074 | hp2 | a0001 | c0004 | t0002 | g0020 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02080 | hp1 | a0001 | c0004 | t0002 | g0005 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02080 | hp2 | a0001 | c0004 | t0002 | g0044 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0218 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02129 | hp2 | a0001 | c0004 | t0002 | g0005 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02135 | hp2 | a0002 | c0001 | t0018 | g0119 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0065 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02155 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02155 | hp2 | a0001 | c0004 | t0002 | g0019 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | CDX | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0147 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02257 | hp2 | a0001 | c0004 | t0007 | g0068 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02258 | hp1 | a0001 | c0003 | t0004 | g0175 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02258 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02273 | hp1 | a0002 | c0001 | t0001 | g0100 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02273 | hp2 | a0001 | c0004 | t0002 | g0021 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0022 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0164 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0245 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02293 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0223 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0160 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0229 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0124 | EAS | KHV | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0064 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0188 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0003 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0236 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0187 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0261 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0023 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0163 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0226 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0222 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0191 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02717 | hp1 | a0001 | c0005 | t0002 | g0264 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0158 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02735 | hp1 | a0006 | c0022 | t0001 | g0004 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02738 | hp1 | a0002 | c0001 | t0016 | g0133 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0150 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02809 | hp1 | a0001 | c0005 | t0002 | g0262 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0110 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0023 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02895 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02895 | hp2 | a0002 | c0001 | t0001 | g0126 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02922 | hp2 | a0001 | c0005 | t0002 | g0265 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02970 | hp1 | a0001 | c0005 | t0002 | g0041 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02970 | hp2 | a0001 | c0004 | t0006 | g0047 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02976 | hp1 | a0001 | c0003 | t0005 | g0243 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02976 | hp2 | a0001 | c0017 | t0002 | g0165 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03017 | hp2 | a0001 | c0002 | t0009 | g0224 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03041 | hp1 | a0001 | c0003 | t0015 | g0022 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0203 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0113 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0031 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03130 | hp2 | a0001 | c0007 | t0002 | g0048 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0235 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0060 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0180 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03225 | hp1 | a0001 | c0003 | t0004 | g0174 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0039 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03453 | hp1 | a0007 | c0014 | t0001 | g0161 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0241 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0168 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0198 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0142 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0059 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | ESN | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03540 | hp1 | a0001 | c0005 | t0002 | g0041 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0162 | AFR | GWD | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03579 | hp2 | a0001 | c0003 | t0005 | g0242 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0182 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0032 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0079 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0086 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0189 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0016 | SAS | PJL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0116 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0219 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0132 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0210 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0080 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0206 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0003 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | BEB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0194 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0173 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0197 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | STU | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18522 | hp1 | a0001 | c0004 | t0007 | g0069 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0237 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0255 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0030 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | CHB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18906 | hp2 | a0001 | c0007 | t0002 | g0018 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18944 | hp1 | a0001 | c0004 | t0002 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18945 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0248 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18947 | hp2 | a0001 | c0019 | t0002 | g0017 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18948 | hp1 | a0002 | c0001 | t0001 | g0148 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18948 | hp2 | a0001 | c0003 | t0002 | g0259 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18949 | hp1 | a0001 | c0004 | t0002 | g0058 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18949 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18950 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18950 | hp2 | a0003 | c0008 | t0002 | g0050 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18954 | hp2 | a0010 | c0013 | t0001 | g0125 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18960 | hp1 | a0004 | c0009 | t0001 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18960 | hp2 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18961 | hp1 | a0001 | c0003 | t0002 | g0253 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18967 | hp1 | a0002 | c0001 | t0001 | g0129 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0097 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18969 | hp2 | a0001 | c0004 | t0002 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18971 | hp2 | a0005 | c0010 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18973 | hp2 | a0001 | c0004 | t0002 | g0043 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18974 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18975 | hp1 | a0001 | c0004 | t0002 | g0054 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0153 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18980 | hp2 | a0001 | c0004 | t0002 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18984 | hp1 | a0001 | c0004 | t0002 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18984 | hp2 | a0003 | c0008 | t0002 | g0052 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0101 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18985 | hp2 | a0001 | c0004 | t0002 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0254 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18986 | hp2 | a0011 | c0015 | t0002 | g0021 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18988 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18989 | hp2 | a0003 | c0008 | t0002 | g0051 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18992 | hp1 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18992 | hp2 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18999 | hp1 | a0002 | c0011 | t0001 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18999 | hp2 | a0001 | c0004 | t0002 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19001 | hp1 | a0001 | c0004 | t0002 | g0020 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19001 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0081 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19003 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19004 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19005 | hp1 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0257 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19009 | hp2 | a0001 | c0004 | t0002 | g0005 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0152 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19030 | hp1 | a0001 | c0004 | t0002 | g0057 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19030 | hp2 | a0001 | c0005 | t0002 | g0263 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0233 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19057 | hp1 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19060 | hp1 | a0001 | c0004 | t0002 | g0055 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19066 | hp2 | a0004 | c0009 | t0001 | g0011 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19070 | hp2 | a0001 | c0002 | t0012 | g0006 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19075 | hp1 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19075 | hp2 | a0001 | c0004 | t0002 | g0056 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19077 | hp2 | a0002 | c0001 | t0017 | g0159 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0204 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19081 | hp2 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19084 | hp1 | a0001 | c0004 | t0002 | g0049 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0258 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19086 | hp2 | a0002 | c0001 | t0001 | g0083 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0221 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19088 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19089 | hp1 | a0005 | c0010 | t0003 | g0216 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19089 | hp2 | a0001 | c0004 | t0002 | g0070 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0250 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19240 | hp1 | a0001 | c0003 | t0004 | g0177 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0067 | AFR | YRI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20129 | hp1 | a0001 | c0021 | t0002 | g0006 | AFR | ASW | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20129 | hp2 | a0001 | c0016 | t0002 | g0066 | AFR | ASW | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0121 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0123 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0001 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0032 | EUR | TSI | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0144 | SAS | GIH | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0039 | SAS | GIH | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0141 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0061 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0209 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02486 | hp2 | a0001 | c0004 | t0006 | g0046 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | ACB | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03471 | hp1 | a0008 | c0018 | t0002 | g0234 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG03471 | hp2 | a0009 | c0020 | t0002 | g0179 | AFR | MSL | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG06807 | hp1 | a0001 | c0002 | t0008 | g0176 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18955 | hp1 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA18955 | hp2 | a0001 | c0003 | t0002 | g0252 | EAS | JPT | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20300 | hp1 | a0001 | c0003 | t0005 | g0240 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0167 | AFR | USA | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0062 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| NA21309 | hp2 | a0001 | c0005 | t0002 | g0266 | AFR | LWK | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0260 | REF | REF | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0005 | g0246 | REF | REF | SART1_chr11_65956734_65985137 | SART1 | chr11 | 65956734 | 65985137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65962042 | C | G | 1 | a0006 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.262C>G | p.Pro88Ala | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/20 | 309/3557 | 262/2403 | 88/800 | chr11 | 65962042 | |||
| chr11:65966214 | C | T | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.977C>T | p.Ala326Val | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 8/20 | 1024/3557 | 977/2403 | 326/800 | chr11 | 65966214 | |||
| chr11:65966521 | C | T | 1 | a0003 | 3 | NA18950.hp2 NA18984.hp2 NA18989.hp2 |
missense_variant | MODERATE | c.1153C>T | p.Arg385Trp | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/20 | 1200/3557 | 1153/2403 | 385/800 | chr11 | 65966521 | |||
| chr11:65967490 | C | T | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1333C>T | p.Arg445Cys | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1380/3557 | 1333/2403 | 445/800 | chr11 | 65967490 | |||
| chr11:65967542 | C | T | 1 | a0010 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1385C>T | p.Pro462Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1432/3557 | 1385/2403 | 462/800 | chr11 | 65967542 | |||
| chr11:65967557 | G | T | 1 | a0008 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1400G>T | p.Arg467Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1447/3557 | 1400/2403 | 467/800 | chr11 | 65967557 | |||
| chr11:65967703 | G | C | 4 | a0002 a0004 a0006 others(1): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
missense_variant | MODERATE | c.1454G>C | p.Gly485Ala | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1501/3557 | 1454/2403 | 485/800 | chr11 | 65967703 | |||
| chr11:65967735 | G | A | 1 | a0011 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.1486G>A | p.Glu496Lys | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1533/3557 | 1486/2403 | 496/800 | chr11 | 65967735 | |||
| chr11:65967781 | A | G | 1 | a0005 | 2 | NA18971.hp2 NA19089.hp1 |
missense_variant | MODERATE | c.1532A>G | p.Gln511Arg | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1579/3557 | 1532/2403 | 511/800 | chr11 | 65967781 | |||
| chr11:65976671 | G | A | 1 | a0004 | 2 | NA18960.hp1 NA19066.hp2 |
missense_variant | MODERATE | c.1762G>A | p.Glu588Lys | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/20 | 1809/3557 | 1762/2403 | 588/800 | chr11 | 65976671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65965180 | G | A | 9 | a0001c0005 a0001c0006 a0002c0001 others(6): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
synonymous_variant | LOW | c.516G>A | p.Ala172Ala | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/20 | 563/3557 | 516/2403 | 172/800 | chr11 | 65965180 | |||
| chr11:65965922 | C | T | 3 | a0001c0002 a0001c0021 a0005c0010 |
113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
synonymous_variant | LOW | c.774C>T | p.Thr258Thr | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 7/20 | 821/3557 | 774/2403 | 258/800 | chr11 | 65965922 | |||
| chr11:65967348 | C | T | 1 | a0001c0019 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.1278C>T | p.Leu426Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 10/20 | 1325/3557 | 1278/2403 | 426/800 | chr11 | 65967348 | |||
| chr11:65967543 | G | A | 1 | a0001c0021 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1386G>A | p.Pro462Pro | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 11/20 | 1433/3557 | 1386/2403 | 462/800 | chr11 | 65967543 | |||
| chr11:65967746 | G | A | 2 | a0001c0006 a0001c0007 |
6 | HG01109.hp2 HG01891.hp1 HG02809.hp2 others(3): Show |
synonymous_variant | LOW | c.1497G>A | p.Leu499Leu | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/20 | 1544/3557 | 1497/2403 | 499/800 | chr11 | 65967746 | |||
| chr11:65976481 | C | T | 1 | a0002c0012 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.1659C>T | p.Phe553Phe | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 13/20 | 1706/3557 | 1659/2403 | 553/800 | chr11 | 65976481 | |||
| chr11:65977061 | T | C | 1 | a0001c0016 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1905T>C | p.Asn635Asn | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/20 | 1952/3557 | 1905/2403 | 635/800 | chr11 | 65977061 | |||
| chr11:65978665 | G | T | 5 | a0001c0004 a0001c0007 a0001c0016 others(2): Show |
37 | HG00673.hp1 HG01891.hp1 HG02055.hp2 others(34): Show |
synonymous_variant | LOW | c.2238G>T | p.Arg746Arg | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/20 | 2285/3557 | 2238/2403 | 746/800 | chr11 | 65978665 | |||
| chr11:65978816 | C | T | 1 | a0002c0011 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.2286C>T | p.Ser762Ser | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/20 | 2333/3557 | 2286/2403 | 762/800 | chr11 | 65978816 | |||
| chr11:65978819 | C | T | 1 | a0001c0017 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2289C>T | p.Asp763Asp | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/20 | 2336/3557 | 2289/2403 | 763/800 | chr11 | 65978819 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65979182 | A | G | 13 | a0001c0002t0001 a0001c0005t0001 a0001c0006t0001 others(10): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*152A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 152 | chr11 | 65979182 | ||||||
| chr11:65979274 | C | T | 1 | a0001c0002t0008 | 2 | HG01496.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*244C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 244 | chr11 | 65979274 | ||||||
| chr11:65979331 | G | T | 1 | a0001c0004t0007 | 2 | HG02257.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*301G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 301 | chr11 | 65979331 | ||||||
| chr11:65979346 | C | T | 1 | a0001c0003t0015 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 316 | chr11 | 65979346 | ||||||
| chr11:65979347 | G | C | 2 | a0001c0002t0009 a0001c0004t0007 |
3 | HG02257.hp2 HG03017.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*317G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 317 | chr11 | 65979347 | ||||||
| chr11:65979451 | C | T | 1 | a0002c0001t0018 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 421 | chr11 | 65979451 | ||||||
| chr11:65979515 | T | C | 1 | a0001c0003t0010 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 485 | chr11 | 65979515 | ||||||
| chr11:65979586 | G | A | 5 | a0001c0002t0003 a0001c0002t0009 a0001c0003t0003 others(2): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*556G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 556 | chr11 | 65979586 | ||||||
| chr11:65979609 | A | G | 1 | a0001c0004t0006 | 3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*579A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 579 | chr11 | 65979609 | ||||||
| chr11:65979614 | C | T | 1 | a0001c0004t0014 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 584 | chr11 | 65979614 | ||||||
| chr11:65979723 | T | C | 40 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(37): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
3_prime_UTR_variant | MODIFIER | c.*693T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 693 | chr11 | 65979723 | ||||||
| chr11:65979782 | T | C | 1 | a0001c0002t0011 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 752 | chr11 | 65979782 | ||||||
| chr11:65979872 | G | A | 1 | a0002c0001t0016 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 842 | chr11 | 65979872 | ||||||
| chr11:65979986 | G | A | 1 | a0002c0001t0017 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*956G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 956 | chr11 | 65979986 | ||||||
| chr11:65980002 | A | G | 1 | a0001c0002t0013 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 972 | chr11 | 65980002 | ||||||
| chr11:65980035 | C | T | 1 | a0001c0002t0012 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 1005 | chr11 | 65980035 | ||||||
| chr11:65980110 | CA | C | 2 | a0001c0003t0004 a0001c0003t0010 |
9 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1088delA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 20/20 | 1088 | INFO_REALIGN_3_PRIME | chr11 | 65980110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65962204 | G | A | 1 | a0001c0005t0002g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.313+111G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962204 | |||||||
| chr11:65962206 | T | C | 36 | a0001c0003t0002g0067 a0001c0003t0003g0022 a0001c0003t0003g0059 others(33): Show |
47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.313+113T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962206 | |||||||
| chr11:65962209 | T | C | 36 | a0001c0003t0002g0067 a0001c0003t0003g0022 a0001c0003t0003g0059 others(33): Show |
47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.313+116T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962209 | |||||||
| chr11:65962381 | C | T | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313+288C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962381 | |||||||
| chr11:65962396 | G | A | 1 | a0001c0005t0001g0023 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.313+303G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962396 | |||||||
| chr11:65962507 | G | T | 6 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.313+414G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962507 | |||||||
| chr11:65962531 | C | A | 108 | a0001c0006t0001g0110 a0001c0006t0001g0112 a0001c0006t0001g0113 others(105): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.313+438C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962531 | |||||||
| chr11:65962532 | A | T | 108 | a0001c0006t0001g0110 a0001c0006t0001g0112 a0001c0006t0001g0113 others(105): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.313+439A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962532 | |||||||
| chr11:65962617 | G | A | 1 | a0001c0004t0002g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+524G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962617 | |||||||
| chr11:65962746 | G | A | 124 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0023 others(121): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.313+653G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962746 | |||||||
| chr11:65962767 | T | C | 5 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+674T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962767 | |||||||
| chr11:65962986 | G | T | 1 | a0001c0004t0002g0070 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.313+893G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65962986 | |||||||
| chr11:65963105 | T | C | 1 | a0002c0001t0001g0071 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.314-969T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963105 | |||||||
| chr11:65963385 | G | T | 5 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-689G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963385 | |||||||
| chr11:65963444 | G | A | 5 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-630G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963444 | |||||||
| chr11:65963469 | G | T | 1 | a0001c0003t0004g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.314-605G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963469 | |||||||
| chr11:65963474 | T | G | 160 | a0001c0003t0002g0067 a0001c0003t0003g0022 a0001c0003t0003g0059 others(157): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.314-600T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963474 | |||||||
| chr11:65963482 | G | T | 72 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(69): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.314-592G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963482 | |||||||
| chr11:65963483 | T | G | 2 | a0001c0002t0002g0170 a0001c0002t0008g0171 |
2 | HG01496.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.314-591T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963483 | |||||||
| chr11:65963544 | C | T | 1 | a0001c0005t0002g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.314-530C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963544 | |||||||
| chr11:65963885 | G | A | 2 | a0001c0005t0001g0012 a0001c0005t0001g0160 |
4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-189G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963885 | |||||||
| chr11:65963902 | C | T | 1 | a0002c0001t0017g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.314-172C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 1/19 | chr11 | 65963902 | |||||||
| chr11:65964153 | T | C | 1 | a0002c0001t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.371+22T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964153 | |||||||
| chr11:65964387 | G | T | 2 | a0001c0005t0001g0163 a0001c0005t0001g0164 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.372-128G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964387 | |||||||
| chr11:65964470 | C | A | 1 | a0001c0004t0002g0044 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.372-45C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964470 | |||||||
| chr11:65964486 | C | G | 1 | a0002c0001t0001g0158 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.372-29C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 2/19 | chr11 | 65964486 | |||||||
| chr11:65964598 | G | T | 1 | a0001c0005t0002g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.427+28G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964598 | |||||||
| chr11:65964615 | T | C | 3 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 |
3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.427+45T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964615 | |||||||
| chr11:65964710 | C | T | 1 | a0002c0001t0001g0157 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.427+140C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964710 | |||||||
| chr11:65964812 | G | C | 1 | a0001c0007t0002g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.427+242G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964812 | |||||||
| chr11:65964843 | C | T | 1 | a0002c0001t0001g0156 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.428-249C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65964843 | |||||||
| chr11:65965022 | G | A | 1 | a0001c0002t0002g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.428-70G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65965022 | |||||||
| chr11:65965059 | G | A | 1 | a0002c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.428-33G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 3/19 | chr11 | 65965059 | |||||||
| chr11:65965297 | G | C | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555-45G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965297 | |||||||
| chr11:65965299 | G | T | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555-43G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965299 | |||||||
| chr11:65965319 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.555-23G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965319 | |||||||
| chr11:65965329 | T | C | 166 | a0001c0002t0008g0176 a0001c0003t0002g0067 a0001c0003t0003g0022 others(163): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.555-13T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 4/19 | chr11 | 65965329 | |||||||
| chr11:65965510 | C | T | 1 | a0001c0003t0002g0259 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.660+63C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965510 | |||||||
| chr11:65965537 | G | A | 1 | a0001c0002t0002g0178 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.660+90G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965537 | |||||||
| chr11:65965629 | T | C | 1 | a0001c0017t0002g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.661-73T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965629 | |||||||
| chr11:65965679 | G | A | 1 | a0009c0020t0002g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.661-23G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 5/19 | chr11 | 65965679 | |||||||
| chr11:65965818 | G | A | 144 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(141): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.738+39G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 6/19 | chr11 | 65965818 | |||||||
| chr11:65965829 | G | A | 1 | a0001c0002t0002g0180 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738+50G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 6/19 | chr11 | 65965829 | |||||||
| chr11:65965868 | T | A | 1 | a0002c0001t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.739-19T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 6/19 | chr11 | 65965868 | |||||||
| chr11:65965994 | G | A | 4 | a0002c0001t0001g0075 a0002c0001t0001g0076 a0002c0001t0001g0077 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01361.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.838+8G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 7/19 | chr11 | 65965994 | |||||||
| chr11:65966072 | C | T | 2 | a0001c0003t0004g0013 a0001c0003t0004g0177 |
4 | HG01243.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.839-4C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 7/19 | chr11 | 65966072 | |||||||
| chr11:65966667 | G | A | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1188+111G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966667 | |||||||
| chr11:65966762 | C | G | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1188+206C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966762 | |||||||
| chr11:65966838 | C | T | 2 | a0001c0004t0007g0068 a0001c0004t0007g0069 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1188+282C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966838 | |||||||
| chr11:65966966 | C | T | 7 | a0001c0003t0002g0067 a0001c0004t0006g0045 a0001c0004t0006g0046 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-293C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966966 | |||||||
| chr11:65966972 | G | A | 5 | a0001c0003t0002g0067 a0001c0004t0006g0045 a0001c0004t0006g0046 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-287G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966972 | |||||||
| chr11:65966994 | G | A | 1 | a0002c0001t0001g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1189-265G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65966994 | |||||||
| chr11:65967068 | C | T | 165 | a0001c0003t0002g0067 a0001c0003t0002g0166 a0001c0003t0002g0167 others(162): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1189-191C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65967068 | |||||||
| chr11:65967074 | C | T | 15 | a0001c0003t0002g0017 a0001c0003t0002g0247 a0001c0003t0002g0248 others(12): Show |
16 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-185C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 9/19 | chr11 | 65967074 | |||||||
| chr11:65967413 | T | C | 5 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1313+30T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 10/19 | chr11 | 65967413 | |||||||
| chr11:65967912 | A | C | 1 | a0002c0001t0001g0155 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1572+91A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65967912 | |||||||
| chr11:65967949 | GT | G | 255 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(252): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1572+146delT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65967949 | ||||||
| chr11:65967988 | C | T | 1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+167C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65967988 | |||||||
| chr11:65968095 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1572+274G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968095 | |||||||
| chr11:65968150 | A | G | 2 | a0002c0001t0001g0077 a0002c0001t0001g0078 |
2 | HG00099.hp2 HG00140.hp1 |
intron_variant | MODIFIER | c.1572+329A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968150 | |||||||
| chr11:65968201 | G | A | 108 | a0001c0006t0001g0110 a0001c0006t0001g0112 a0001c0006t0001g0113 others(105): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1572+380G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968201 | |||||||
| chr11:65968391 | T | C | 20 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(17): Show |
31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+570T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968391 | |||||||
| chr11:65968403 | T | C | 272 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(269): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1572+582T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968403 | |||||||
| chr11:65968640 | C | T | 3 | a0001c0004t0007g0068 a0001c0004t0007g0069 a0001c0005t0001g0164 |
3 | HG02257.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1572+819C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968640 | |||||||
| chr11:65968641 | G | A | 1 | a0001c0004t0002g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1572+820G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968641 | |||||||
| chr11:65968651 | G | A | 2 | a0001c0007t0002g0018 a0001c0007t0002g0048 |
3 | HG01891.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1572+830G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968651 | |||||||
| chr11:65968702 | G | A | 1 | a0001c0003t0005g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1572+881G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968702 | |||||||
| chr11:65968737 | G | T | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+916G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968737 | |||||||
| chr11:65968776 | G | A | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+955G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968776 | |||||||
| chr11:65968860 | G | A | 1 | a0001c0003t0002g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1572+1039G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968860 | |||||||
| chr11:65968980 | T | G | 1 | a0001c0002t0002g0032 | 2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1572+1159T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968980 | |||||||
| chr11:65968981 | C | G | 1 | a0002c0001t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1572+1160C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65968981 | |||||||
| chr11:65969132 | C | T | 3 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 |
3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+1311C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969132 | |||||||
| chr11:65969269 | C | A | 1 | a0002c0001t0001g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1572+1448C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969269 | |||||||
| chr11:65969323 | C | T | 2 | a0001c0002t0003g0238 a0001c0002t0003g0239 |
2 | HG02040.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1572+1502C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969323 | |||||||
| chr11:65969388 | A | T | 1 | a0002c0001t0001g0149 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1572+1567A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969388 | |||||||
| chr11:65969548 | C | T | 1 | a0001c0004t0002g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1572+1727C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969548 | |||||||
| chr11:65969611 | C | T | 1 | a0002c0001t0001g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1572+1790C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969611 | |||||||
| chr11:65969662 | G | A | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+1841G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969662 | |||||||
| chr11:65969662 | G | GCCTCCAC others(10): Show |
1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+1842_1572+185 others(21): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65969662 | ||||||
| chr11:65969755 | G | T | 1 | a0002c0001t0001g0154 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1572+1934G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969755 | |||||||
| chr11:65969846 | C | T | 8 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0023 others(5): Show |
16 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+2025C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969846 | |||||||
| chr11:65969884 | A | G | 1 | a0001c0003t0004g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1572+2063A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65969884 | |||||||
| chr11:65970017 | C | T | 1 | a0001c0002t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1572+2196C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970017 | |||||||
| chr11:65970160 | C | T | 6 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+2339C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970160 | |||||||
| chr11:65970266 | C | T | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+2445C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970266 | |||||||
| chr11:65970321 | G | A | 1 | a0002c0001t0001g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1572+2500G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970321 | |||||||
| chr11:65970344 | A | C | 36 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(33): Show |
47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+2523A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970344 | |||||||
| chr11:65970346 | T | A | 1 | a0001c0002t0013g0035 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1572+2525T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970346 | |||||||
| chr11:65970368 | A | G | 3 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 |
3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+2547A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970368 | |||||||
| chr11:65970396 | T | G | 5 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+2575T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970396 | |||||||
| chr11:65970428 | G | A | 20 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(17): Show |
31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+2607G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970428 | |||||||
| chr11:65970444 | C | T | 7 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(4): Show |
8 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+2623C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970444 | |||||||
| chr11:65970470 | C | T | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+2649C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970470 | |||||||
| chr11:65970497 | A | G | 1 | a0001c0003t0005g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1572+2676A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970497 | |||||||
| chr11:65970523 | G | A | 7 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(4): Show |
8 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+2702G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970523 | |||||||
| chr11:65970567 | GCTGTGGG others(22): Show |
G | 1 | a0001c0002t0002g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1572+2747_1572+277 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970567 | |||||||
| chr11:65970624 | GT | G | 144 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(141): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1572+2808delT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970624 | ||||||
| chr11:65970663 | G | A | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0023 others(12): Show |
24 | HG01106.hp1 HG01934.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1572+2842G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970663 | |||||||
| chr11:65970667 | T | C | 251 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(248): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1572+2846T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970667 | |||||||
| chr11:65970728 | A | C | 7 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+2907A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970728 | |||||||
| chr11:65970777 | A | AATTCATG others(84): Show |
4 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(1): Show |
4 | HG01109.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+2975_1572+306 others(95): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970777 | ||||||
| chr11:65970794 | G | GGGAGGGG others(83): Show |
1 | a0001c0002t0003g0230 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1572+2995_1572+308 others(94): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970794 | ||||||
| chr11:65970794 | GGGAGGGG others(112): Show |
G | 4 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0263 others(1): Show |
4 | HG01106.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3085_1572+320 others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970794 | ||||||
| chr11:65970827 | G | GGGGGATG others(86): Show |
2 | a0002c0001t0001g0003 a0002c0001t0001g0004 |
2 | NA18974.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1572+3030_1572+303 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970827 | ||||||
| chr11:65970845 | T | TGAGCTGC others(25): Show |
45 | a0001c0006t0001g0110 a0001c0006t0001g0112 a0001c0006t0001g0113 others(42): Show |
59 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1572+3030_1572+303 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970845 | ||||||
| chr11:65970847 | A | AGCT | 60 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(57): Show |
94 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1572+3028_1572+303 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | ||||||
| chr11:65970847 | A | AGCTGAGG others(54): Show |
3 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 |
3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+3059_1572+306 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | ||||||
| chr11:65970847 | A | AGCTGCTG others(711): Show |
1 | a0002c0001t0001g0140 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1572+3030_1572+303 others(722): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | ||||||
| chr11:65970847 | A | AGCTGCTG others(801): Show |
2 | a0002c0001t0001g0141 a0002c0001t0001g0142 |
2 | HG01123.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1572+3030_1572+303 others(812): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970847 | ||||||
| chr11:65970874 | T | G | 60 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(57): Show |
94 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1572+3053T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970874 | |||||||
| chr11:65970879 | T | TGAGGAGG others(51): Show |
3 | a0002c0001t0001g0145 a0002c0001t0001g0146 a0002c0001t0001g0147 |
3 | HG01168.hp1 HG01169.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1572+3059_1572+306 others(62): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | ||||||
| chr11:65970879 | T | TGAGGAGG others(80): Show |
55 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(52): Show |
89 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1572+3059_1572+306 others(91): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | ||||||
| chr11:65970879 | T | TGAGGAGG others(167): Show |
1 | a0002c0001t0001g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1572+3059_1572+306 others(178): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | ||||||
| chr11:65970879 | T | TGAGGAGG others(232): Show |
1 | a0002c0001t0001g0132 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1572+3059_1572+306 others(243): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | ||||||
| chr11:65970879 | T | TGCTGAGG others(54): Show |
9 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1572+3084_1572+308 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970879 | ||||||
| chr11:65970888 | G | A | 48 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 others(45): Show |
62 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1572+3067G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970888 | |||||||
| chr11:65970895 | G | GGTGGGAT others(25): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3084_1572+308 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970895 | ||||||
| chr11:65970895 | G | T | 3 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 |
3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+3074G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970895 | |||||||
| chr11:65970904 | C | CATG | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3084_1572+308 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970904 | ||||||
| chr11:65970906 | G | T | 150 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(147): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1572+3085G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970906 | |||||||
| chr11:65970908 | A | AGCT | 6 | a0001c0003t0003g0065 a0001c0016t0002g0066 a0002c0001t0001g0138 others(3): Show |
6 | HG01123.hp1 HG01257.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3089_1572+309 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970908 | ||||||
| chr11:65970908 | A | AGCTGCTG others(57): Show |
1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3091_1572+309 others(68): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970908 | ||||||
| chr11:65970908 | A | T | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3087A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970908 | |||||||
| chr11:65970911 | TGAGGAGG others(19): Show |
T | 20 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(17): Show |
31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+3092_1572+311 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970911 | ||||||
| chr11:65970917 | G | A | 2 | a0001c0004t0007g0068 a0001c0016t0002g0066 |
2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1572+3096G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970917 | |||||||
| chr11:65970922 | A | G | 4 | a0001c0002t0002g0228 a0001c0002t0002g0229 a0001c0005t0002g0041 others(1): Show |
5 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3101A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970922 | |||||||
| chr11:65970924 | G | T | 2 | a0001c0004t0007g0068 a0001c0016t0002g0066 |
2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1572+3103G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970924 | |||||||
| chr11:65970935 | T | G | 4 | a0001c0002t0002g0228 a0001c0002t0002g0229 a0001c0005t0002g0041 others(1): Show |
5 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3114T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970935 | |||||||
| chr11:65970935 | T | TGAGCTGA others(86): Show |
4 | a0001c0002t0003g0016 a0001c0002t0003g0225 a0001c0002t0003g0226 others(1): Show |
6 | HG00140.hp2 HG00280.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3149_1572+315 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970935 | ||||||
| chr11:65970946 | G | A | 21 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(18): Show |
32 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+3125G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970946 | |||||||
| chr11:65970953 | G | T | 20 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(17): Show |
31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1572+3132G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65970953 | |||||||
| chr11:65970964 | T | TGAGCTGA others(22): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3171_1572+317 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970964 | ||||||
| chr11:65970966 | A | AGCT | 8 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(5): Show |
8 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+3147_1572+314 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | ||||||
| chr11:65970966 | A | AGCTGAGG others(25): Show |
1 | a0001c0002t0002g0170 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1572+3176_1572+320 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | ||||||
| chr11:65970966 | A | AGCTGAGG others(179): Show |
5 | a0002c0001t0001g0024 a0002c0001t0001g0082 a0002c0001t0001g0083 others(2): Show |
6 | NA18983.hp2 NA19004.hp1 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3178_1572+317 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | ||||||
| chr11:65970966 | A | AGCTGAGG others(298): Show |
2 | a0001c0005t0001g0012 a0001c0005t0001g0160 |
4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3178_1572+317 others(309): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | ||||||
| chr11:65970966 | A | AGCTGCTG others(455): Show |
1 | a0001c0017t0002g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3149_1572+315 others(466): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | ||||||
| chr11:65970966 | A | AGCTGCTG others(60): Show |
1 | a0001c0003t0003g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1572+3149_1572+315 others(71): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970966 | ||||||
| chr11:65970993 | TGAGCTGC others(57): Show |
T | 1 | a0003c0008t0002g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1572+3179_1572+324 others(68): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970993 | ||||||
| chr11:65970995 | AGCT | A | 7 | a0001c0005t0001g0010 a0001c0005t0001g0023 a0001c0005t0001g0031 others(4): Show |
13 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1572+3179_1572+318 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970995 | ||||||
| chr11:65970995 | AGCTGCTG others(208): Show |
A | 19 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(16): Show |
30 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.1572+3179_1572+339 others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970995 | ||||||
| chr11:65970998 | T | TGAGGAGG others(19): Show |
1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3178_1572+317 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970998 | ||||||
| chr11:65970998 | T | TGCTGAGG others(458): Show |
1 | a0001c0002t0003g0204 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1572+3207_1572+320 others(469): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65970998 | ||||||
| chr11:65971007 | G | A | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3186G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971007 | |||||||
| chr11:65971014 | G | T | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3193G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971014 | |||||||
| chr11:65971028 | G | GCTGAGGA others(19): Show |
1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3207_1572+320 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971028 | |||||||
| chr11:65971029 | G | C | 87 | a0001c0002t0002g0033 a0001c0002t0002g0228 a0001c0002t0002g0229 others(84): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1572+3208G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971029 | |||||||
| chr11:65971030 | T | A | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+3209T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971030 | |||||||
| chr11:65971044 | G | A | 27 | a0001c0002t0002g0033 a0001c0002t0002g0228 a0001c0002t0002g0229 others(24): Show |
38 | HG00140.hp2 HG00280.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1572+3223G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971044 | |||||||
| chr11:65971044 | G | GTGGTGGG others(89): Show |
2 | a0002c0001t0001g0085 a0002c0001t0001g0086 |
2 | HG02015.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1572+3235_1572+323 others(100): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971044 | ||||||
| chr11:65971056 | A | G | 4 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3235A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971056 | |||||||
| chr11:65971057 | G | GGAGCTGA others(22): Show |
1 | a0002c0001t0001g0111 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1572+3272_1572+330 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | ||||||
| chr11:65971057 | G | GGAGCTGA others(80): Show |
1 | a0001c0003t0002g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1572+3277_1572+327 others(91): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | ||||||
| chr11:65971057 | G | GGAGCTGA others(420): Show |
2 | a0001c0003t0002g0166 a0001c0003t0002g0168 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1572+3277_1572+327 others(431): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | ||||||
| chr11:65971057 | G | GGAGCTGA others(51): Show |
1 | a0001c0017t0002g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3280_1572+328 others(62): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971057 | ||||||
| chr11:65971057 | G | T | 82 | a0001c0002t0002g0033 a0001c0002t0002g0228 a0001c0002t0002g0229 others(79): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1572+3236G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971057 | |||||||
| chr11:65971058 | G | A | 2 | a0002c0001t0001g0085 a0002c0001t0001g0086 |
2 | HG02015.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1572+3237G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971058 | |||||||
| chr11:65971059 | A | AGCT | 70 | a0001c0002t0002g0229 a0001c0002t0003g0016 a0001c0002t0003g0225 others(67): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1572+3240_1572+324 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | ||||||
| chr11:65971059 | A | AGCTGAGG others(618): Show |
3 | a0002c0001t0001g0095 a0002c0001t0001g0096 a0002c0001t0001g0097 |
3 | HG00621.hp1 NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(629): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | ||||||
| chr11:65971059 | A | AGCTGCTG others(179): Show |
1 | a0001c0002t0002g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1572+3242_1572+324 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | ||||||
| chr11:65971059 | A | AGCTGCTG others(243): Show |
1 | a0001c0002t0003g0239 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1572+3242_1572+324 others(254): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971059 | ||||||
| chr11:65971059 | A | T | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3238A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971059 | |||||||
| chr11:65971068 | G | GGGGGATG others(25): Show |
6 | a0001c0005t0001g0010 a0001c0005t0001g0023 a0001c0005t0001g0031 others(3): Show |
12 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1572+3271_1572+327 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971068 | ||||||
| chr11:65971073 | A | ATGGTGGG others(391): Show |
1 | a0001c0003t0002g0167 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1572+3277_1572+327 others(402): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971073 | ||||||
| chr11:65971073 | A | G | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3252A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971073 | |||||||
| chr11:65971073 | ATGG | A | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3256_1572+325 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971073 | ||||||
| chr11:65971085 | A | G | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3264A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971085 | |||||||
| chr11:65971086 | T | G | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3265T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971086 | |||||||
| chr11:65971088 | A | AGCT | 72 | a0001c0002t0002g0228 a0001c0002t0002g0229 a0001c0002t0003g0016 others(69): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1572+3269_1572+327 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971088 | A | AGCTGAGG others(301): Show |
1 | a0002c0001t0001g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(312): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971088 | A | AGCTGAGG others(182): Show |
1 | a0002c0001t0001g0088 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(193): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971088 | A | AGCTGAGG others(182): Show |
6 | a0002c0001t0001g0025 a0002c0001t0001g0089 a0002c0001t0001g0090 others(3): Show |
7 | HG02074.hp1 HG02132.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(193): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971088 | A | AGCTGAGG others(400): Show |
1 | a0002c0001t0001g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(411): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971088 | A | AGCTGAGG others(461): Show |
3 | a0002c0001t0001g0026 a0002c0001t0001g0093 a0002c0001t0001g0094 |
4 | HG00609.hp2 NA18980.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(472): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971088 | A | AGCTGCTG others(28): Show |
1 | a0001c0005t0001g0164 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1572+3271_1572+327 others(39): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971088 | A | AGCTGCTG others(60): Show |
2 | a0001c0005t0001g0012 a0001c0005t0001g0160 |
4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3271_1572+327 others(71): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971088 | ||||||
| chr11:65971113 | CATG | C | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3294_1572+329 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971113 | ||||||
| chr11:65971119 | C | A | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3298C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971119 | |||||||
| chr11:65971120 | T | A | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3299T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971120 | |||||||
| chr11:65971120 | T | TGAGGAGG others(891): Show |
1 | a0002c0001t0001g0109 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(902): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | ||||||
| chr11:65971120 | T | TGAGGAGG others(641): Show |
1 | a0002c0001t0001g0103 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(652): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | ||||||
| chr11:65971120 | T | TGAGGAGG others(614): Show |
1 | a0002c0001t0001g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(625): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | ||||||
| chr11:65971120 | T | TGAGGAGG others(615): Show |
18 | a0002c0001t0001g0007 a0002c0001t0001g0008 a0002c0001t0001g0074 others(15): Show |
28 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1572+3300_1572+330 others(626): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | ||||||
| chr11:65971120 | T | TGAGGAGG others(647): Show |
1 | a0002c0001t0001g0008 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1572+3300_1572+330 others(658): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | ||||||
| chr11:65971120 | TGCTGAGG others(51): Show |
T | 3 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0265 |
3 | HG01106.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1572+3317_1572+337 others(62): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971120 | ||||||
| chr11:65971134 | A | ATGG | 208 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(205): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1572+3314_1572+331 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | ||||||
| chr11:65971134 | A | ATGGTGGG others(307): Show |
1 | a0001c0002t0003g0218 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1572+3316_1572+331 others(318): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | ||||||
| chr11:65971134 | A | ATGGTGGG others(490): Show |
2 | a0001c0002t0003g0188 a0001c0002t0003g0189 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1572+3316_1572+331 others(501): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | ||||||
| chr11:65971134 | A | ATGGTGGG others(679): Show |
2 | a0001c0002t0002g0037 a0001c0002t0002g0203 |
3 | HG02559.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1572+3316_1572+331 others(690): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971134 | ||||||
| chr11:65971134 | A | G | 1 | a0001c0002t0009g0224 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1572+3313A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971134 | |||||||
| chr11:65971144 | T | G | 1 | a0001c0002t0003g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572+3323T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971144 | |||||||
| chr11:65971146 | AGCT | A | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3330_1572+333 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971146 | ||||||
| chr11:65971149 | T | TGAGGAGG others(1010): Show |
1 | a0001c0002t0003g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572+3329_1572+333 others(1021): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971149 | ||||||
| chr11:65971149 | TGCTGAGG others(22): Show |
T | 1 | a0001c0005t0002g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3355_1572+338 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971149 | ||||||
| chr11:65971174 | C | CATG | 58 | a0001c0002t0002g0037 a0001c0002t0002g0180 a0001c0002t0002g0203 others(55): Show |
73 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1572+3354_1572+335 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | ||||||
| chr11:65971174 | C | CATGAGCT others(336): Show |
1 | a0001c0003t0002g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1572+3354_1572+335 others(347): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | ||||||
| chr11:65971174 | C | CATGAGCT others(592): Show |
1 | a0002c0001t0001g0111 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1572+3354_1572+335 others(603): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | ||||||
| chr11:65971174 | C | CATGAGCT others(589): Show |
2 | a0001c0006t0001g0112 a0001c0006t0001g0113 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1572+3354_1572+335 others(600): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971174 | ||||||
| chr11:65971175 | A | AT | 68 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(65): Show |
98 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1572+3354_1572+335 others(5): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971175 | |||||||
| chr11:65971176 | G | GGAGCTGA others(22): Show |
1 | a0001c0005t0001g0164 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1572+3355_1572+335 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971176 | |||||||
| chr11:65971176 | G | T | 8 | a0001c0002t0003g0182 a0001c0005t0001g0010 a0001c0005t0001g0023 others(5): Show |
14 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1572+3355G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971176 | |||||||
| chr11:65971176 | GAAGCTGA others(22): Show |
G | 1 | a0003c0008t0002g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+338 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971176 | |||||||
| chr11:65971177 | A | AAGCTGAG others(949): Show |
1 | a0009c0020t0002g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1572+3383_1572+338 others(960): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(22): Show |
31 | a0002c0001t0001g0002 a0002c0001t0001g0011 a0002c0001t0001g0025 others(28): Show |
47 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+3362_1572+339 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(4080): Show |
1 | a0001c0003t0002g0247 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(4091): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(2857): Show |
1 | a0001c0003t0002g0248 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(2868): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(2921): Show |
2 | a0001c0003t0002g0249 a0001c0003t0002g0259 |
2 | HG00597.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(2932): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(2922): Show |
1 | a0001c0003t0002g0250 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(2933): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1553): Show |
1 | a0001c0003t0002g0251 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1564): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(2407): Show |
4 | a0001c0003t0002g0017 a0001c0003t0002g0231 a0001c0003t0002g0258 others(1): Show |
5 | HG02056.hp2 NA18947.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(2418): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1524): Show |
2 | a0001c0003t0002g0252 a0001c0003t0002g0253 |
2 | NA18955.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(1535): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1495): Show |
1 | a0001c0003t0002g0254 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1506): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(3357): Show |
1 | a0001c0003t0002g0255 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(3368): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(2081): Show |
1 | a0001c0003t0004g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(2092): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1525): Show |
1 | a0001c0003t0010g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1536): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1798): Show |
1 | a0001c0003t0005g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1809): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1557): Show |
2 | a0001c0003t0005g0240 a0001c0003t0005g0242 |
2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(1568): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1711): Show |
1 | a0001c0003t0005g0243 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1722): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1557): Show |
2 | a0001c0003t0004g0013 a0001c0003t0004g0177 |
4 | HG01243.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(1568): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(673): Show |
1 | a0001c0002t0003g0225 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(684): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1980): Show |
1 | a0001c0003t0002g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1991): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(2407): Show |
2 | a0001c0003t0002g0235 a0008c0018t0002g0234 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(2418): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(1274): Show |
1 | a0001c0002t0002g0229 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1285): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AAGCTGAG others(644): Show |
4 | a0001c0002t0003g0016 a0001c0002t0003g0226 a0001c0002t0003g0227 others(1): Show |
6 | HG00140.hp2 HG00280.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(655): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971177 | ||||||
| chr11:65971177 | A | AGCTGCTG others(1334): Show |
1 | a0001c0002t0002g0033 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1345): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(53): Show |
1 | a0002c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(64): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1316): Show |
1 | a0001c0003t0004g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1327): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(736): Show |
1 | a0001c0002t0002g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(951): Show |
1 | a0001c0002t0003g0034 | 2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(962): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(736): Show |
1 | a0001c0003t0002g0067 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(736): Show |
1 | a0001c0002t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1410): Show |
2 | a0001c0002t0003g0184 a0001c0002t0003g0185 |
2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1421): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(85): Show |
1 | a0001c0003t0003g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(96): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(736): Show |
1 | a0001c0002t0008g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(747): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(768): Show |
1 | a0001c0002t0003g0186 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(779): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(765): Show |
1 | a0001c0002t0002g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(776): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1230): Show |
1 | a0001c0002t0008g0171 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1241): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(704): Show |
4 | a0001c0002t0002g0173 a0001c0002t0002g0199 a0001c0002t0002g0200 others(1): Show |
4 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(715): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1427): Show |
4 | a0001c0002t0002g0035 a0001c0002t0002g0172 a0001c0002t0002g0190 others(1): Show |
4 | HG00558.hp2 HG02027.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1438): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1305): Show |
2 | a0001c0002t0002g0191 a0001c0002t0002g0192 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1316): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1398): Show |
12 | a0001c0002t0002g0006 a0001c0002t0002g0032 a0001c0002t0002g0036 others(9): Show |
20 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(1409): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1398): Show |
1 | a0001c0002t0002g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1409): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(829): Show |
1 | a0001c0002t0003g0202 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(840): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(768): Show |
18 | a0001c0002t0001g0038 a0001c0002t0002g0014 a0001c0002t0002g0170 others(15): Show |
36 | HG01123.hp2 HG01169.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(779): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(925): Show |
1 | a0001c0002t0003g0213 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(936): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(769): Show |
1 | a0005c0010t0003g0216 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(780): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1366): Show |
1 | a0001c0002t0002g0217 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1377): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1395): Show |
1 | a0001c0002t0002g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1406): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(800): Show |
2 | a0001c0002t0003g0219 a0001c0002t0003g0245 |
2 | HG02293.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(811): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(364): Show |
1 | a0001c0002t0002g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(375): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(864): Show |
1 | a0001c0002t0009g0224 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(875): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(646): Show |
1 | a0001c0002t0003g0221 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(657): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGCTGCTG others(1552): Show |
1 | a0001c0002t0002g0222 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1572+3356_1572+335 others(1563): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | AGGTGCTG others(518): Show |
2 | a0001c0002t0003g0015 a0001c0002t0003g0223 |
4 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3356_1572+335 others(529): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | C | 62 | a0001c0002t0002g0037 a0001c0002t0002g0180 a0001c0002t0002g0203 others(59): Show |
77 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1572+3356A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971177 | A | G | 13 | a0001c0002t0003g0182 a0001c0003t0002g0166 a0001c0003t0002g0167 others(10): Show |
19 | HG00099.hp2 HG01109.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1572+3356A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971177 | |||||||
| chr11:65971178 | A | AGCTGAGG others(54): Show |
27 | a0002c0001t0001g0003 a0002c0001t0001g0004 a0002c0001t0001g0009 others(24): Show |
48 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971178 | ||||||
| chr11:65971178 | A | AGCTGAGG others(86): Show |
2 | a0001c0003t0004g0175 a0001c0003t0004g0261 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971178 | ||||||
| chr11:65971178 | A | AGCTGAGG others(179): Show |
2 | a0002c0001t0001g0141 a0002c0001t0001g0142 |
2 | HG01123.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971178 | ||||||
| chr11:65971178 | A | T | 62 | a0001c0002t0002g0037 a0001c0002t0002g0180 a0001c0002t0002g0203 others(59): Show |
77 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1572+3357A>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971178 | |||||||
| chr11:65971192 | A | G | 1 | a0001c0006t0001g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1572+3371A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971192 | |||||||
| chr11:65971195 | G | GTGGGATT others(83): Show |
2 | a0001c0005t0001g0012 a0001c0005t0001g0160 |
4 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(94): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | ||||||
| chr11:65971195 | G | GTGGGATT others(147): Show |
4 | a0002c0001t0001g0087 a0002c0001t0001g0088 a0002c0001t0001g0140 others(1): Show |
4 | HG00673.hp2 HG01257.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(158): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | ||||||
| chr11:65971195 | G | GTGGGATT others(272): Show |
6 | a0001c0005t0001g0010 a0001c0005t0001g0023 a0001c0005t0001g0031 others(3): Show |
12 | HG01934.hp1 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(283): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | ||||||
| chr11:65971195 | G | GTGGGATT others(22): Show |
7 | a0002c0001t0001g0024 a0002c0001t0001g0082 a0002c0001t0001g0083 others(4): Show |
8 | HG02015.hp1 HG03704.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+3378_1572+340 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971195 | ||||||
| chr11:65971205 | T | G | 27 | a0001c0006t0001g0112 a0001c0006t0001g0113 a0002c0001t0001g0007 others(24): Show |
38 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1572+3384T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971205 | |||||||
| chr11:65971205 | T | TGAGCTGA others(804): Show |
1 | a0002c0001t0001g0147 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(815): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971205 | ||||||
| chr11:65971207 | AGCT | A | 3 | a0001c0002t0002g0228 a0002c0001t0001g0081 a0002c0001t0001g0114 |
3 | HG01978.hp1 HG06807.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1572+3391_1572+339 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971207 | ||||||
| chr11:65971210 | T | TGAGGAGG others(455): Show |
1 | a0001c0002t0003g0218 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(466): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | ||||||
| chr11:65971210 | T | TGAGGAGG others(1878): Show |
1 | a0001c0003t0002g0256 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1889): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | ||||||
| chr11:65971210 | T | TGAGGAGG others(1422): Show |
1 | a0001c0003t0002g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(1433): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | ||||||
| chr11:65971210 | T | TGAGGAGG others(208): Show |
1 | a0002c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1572+3390_1572+339 others(219): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | ||||||
| chr11:65971210 | T | TGAGGAGG others(144): Show |
3 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 |
3 | HG01109.hp1 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1572+3390_1572+339 others(155): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971210 | ||||||
| chr11:65971224 | A | G | 3 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 |
3 | HG01109.hp1 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1572+3403A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971224 | |||||||
| chr11:65971237 | T | G | 24 | a0001c0003t0002g0169 a0001c0003t0003g0022 a0001c0003t0003g0060 others(21): Show |
32 | HG01243.hp2 HG01934.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1572+3416T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971237 | |||||||
| chr11:65971238 | G | A | 10 | a0001c0003t0004g0175 a0001c0003t0004g0261 a0001c0005t0001g0010 others(7): Show |
18 | HG01934.hp1 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1572+3417G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971238 | |||||||
| chr11:65971239 | A | AGCT | 83 | a0001c0002t0003g0188 a0001c0002t0003g0189 a0001c0005t0001g0164 others(80): Show |
122 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1572+3420_1572+342 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971239 | ||||||
| chr11:65971239 | A | AGCTGCTG others(769): Show |
3 | a0001c0002t0002g0180 a0001c0002t0002g0214 a0001c0002t0002g0215 |
3 | HG02647.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1572+3422_1572+342 others(780): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971239 | ||||||
| chr11:65971242 | TGAGGAGG others(19): Show |
T | 3 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0265 |
3 | HG01106.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1572+3423_1572+344 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971242 | ||||||
| chr11:65971253 | A | G | 1 | a0001c0017t0002g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3432A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971253 | |||||||
| chr11:65971266 | T | G | 1 | a0001c0005t0002g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3445T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971266 | |||||||
| chr11:65971267 | G | A | 1 | a0001c0005t0002g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3446G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971267 | |||||||
| chr11:65971268 | A | AGCT | 87 | a0001c0002t0002g0228 a0001c0003t0003g0059 a0001c0004t0002g0005 others(84): Show |
125 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1572+3449_1572+345 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | ||||||
| chr11:65971268 | A | AGCTGAGG others(89): Show |
10 | a0001c0003t0003g0022 a0001c0003t0003g0060 a0001c0003t0003g0061 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1572+3505_1572+350 others(100): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | ||||||
| chr11:65971268 | A | AGCTGAGG others(243): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(254): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | ||||||
| chr11:65971268 | A | AGCTGCTG others(153): Show |
3 | a0002c0001t0001g0002 a0002c0001t0001g0028 a0010c0013t0001g0125 |
7 | HG00423.hp1 HG00544.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+3451_1572+345 others(164): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | ||||||
| chr11:65971268 | A | AGCTGCTG others(153): Show |
14 | a0002c0001t0001g0002 a0002c0001t0001g0028 a0002c0001t0001g0029 others(11): Show |
20 | HG00738.hp2 HG01257.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1572+3451_1572+345 others(164): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | ||||||
| chr11:65971268 | AGCTGAGG others(57): Show |
A | 1 | a0001c0005t0002g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572+3481_1572+354 others(68): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971268 | ||||||
| chr11:65971275 | G | T | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1572+3454G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971275 | |||||||
| chr11:65971282 | ATGG | A | 30 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0265 others(27): Show |
51 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1572+3465_1572+346 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971282 | ||||||
| chr11:65971300 | T | TGAGGAGG others(19): Show |
1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3480_1572+348 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971300 | ||||||
| chr11:65971314 | ATGG | A | 17 | a0002c0001t0001g0011 a0002c0001t0001g0025 a0002c0001t0001g0027 others(14): Show |
20 | HG00099.hp1 HG00438.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1572+3497_1572+349 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971314 | ||||||
| chr11:65971317 | G | GTGGGATT others(22): Show |
1 | a0002c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971317 | ||||||
| chr11:65971327 | G | GAAGCTGA others(208): Show |
1 | a0001c0006t0001g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1572+3506_1572+350 others(219): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | |||||||
| chr11:65971327 | G | T | 140 | a0001c0002t0002g0228 a0001c0003t0002g0166 a0001c0003t0002g0167 others(137): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1572+3506G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | |||||||
| chr11:65971327 | G | TGAGCTGC others(1898): Show |
1 | a0001c0003t0004g0175 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(1909): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | |||||||
| chr11:65971327 | G | TGAGCTGC others(1403): Show |
1 | a0001c0003t0004g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1572+3505_1572+350 others(1414): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971327 | |||||||
| chr11:65971328 | G | A | 3 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0265 |
3 | HG01106.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1572+3507G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971328 | |||||||
| chr11:65971329 | AGCT | A | 22 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(19): Show |
35 | HG00423.hp1 HG00544.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572+3513_1572+351 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971329 | ||||||
| chr11:65971332 | T | TGCTGAGG others(647): Show |
1 | a0002c0001t0001g0026 | 2 | NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1572+3537_1572+353 others(658): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971332 | T | TGCTGAGG others(461): Show |
1 | a0002c0001t0001g0093 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1572+3537_1572+353 others(472): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971332 | T | TGCTGAGG others(22): Show |
10 | a0002c0001t0001g0024 a0002c0001t0001g0030 a0002c0001t0001g0081 others(7): Show |
11 | HG00597.hp2 HG00738.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1572+3545_1572+357 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971332 | T | TGCTGAGG others(118): Show |
2 | a0002c0001t0001g0003 a0002c0001t0001g0130 |
2 | HG02083.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1572+3544_1572+354 others(129): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971332 | T | TGCTGAGG others(86): Show |
1 | a0002c0001t0001g0030 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1572+3544_1572+354 others(97): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971332 | T | TGCTGAGG others(118): Show |
7 | a0001c0006t0001g0110 a0002c0001t0001g0003 a0002c0001t0001g0128 others(4): Show |
15 | HG00609.hp1 HG00639.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1572+3544_1572+354 others(129): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971332 | TGCTGAGG others(22): Show |
T | 1 | a0001c0016t0002g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+3545_1572+357 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971332 | TGCTGAGG others(147): Show |
T | 1 | a0003c0008t0002g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1572+3574_1572+372 others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971332 | ||||||
| chr11:65971346 | A | G | 29 | a0001c0006t0001g0112 a0001c0006t0001g0113 a0002c0001t0001g0007 others(26): Show |
40 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1572+3525A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971346 | |||||||
| chr11:65971359 | T | G | 1 | a0001c0003t0003g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1572+3538T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971359 | |||||||
| chr11:65971361 | A | AGCT | 85 | a0001c0002t0002g0228 a0001c0003t0002g0166 a0001c0003t0002g0167 others(82): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1572+3542_1572+354 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971361 | ||||||
| chr11:65971368 | G | A | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+3547G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971368 | |||||||
| chr11:65971369 | A | G | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+3548A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971369 | |||||||
| chr11:65971370 | G | A | 1 | a0001c0004t0002g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1572+3549G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971370 | |||||||
| chr11:65971375 | A | G | 5 | a0001c0003t0004g0013 a0001c0003t0004g0174 a0001c0003t0004g0175 others(2): Show |
7 | HG01243.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+3554A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971375 | |||||||
| chr11:65971388 | T | G | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3567T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971388 | |||||||
| chr11:65971388 | T | TGAGCTGA others(144): Show |
1 | a0001c0002t0003g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1572+3573_1572+357 others(155): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971388 | ||||||
| chr11:65971390 | AGCT | A | 10 | a0001c0003t0003g0065 a0001c0005t0001g0010 a0001c0005t0001g0012 others(7): Show |
18 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1572+3574_1572+357 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971390 | ||||||
| chr11:65971393 | T | TGAGGAGG others(173): Show |
1 | a0001c0002t0003g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3573_1572+357 others(184): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGAGGAGG others(115): Show |
5 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572+3573_1572+357 others(126): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(22): Show |
1 | a0001c0002t0003g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1572+3577_1572+360 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(963): Show |
2 | a0001c0002t0002g0199 a0001c0002t0002g0200 |
2 | HG00642.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1572+3605_1572+360 others(974): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(960): Show |
1 | a0001c0002t0002g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1572+3605_1572+360 others(971): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(960): Show |
1 | a0001c0002t0002g0201 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1572+3605_1572+360 others(971): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(266): Show |
1 | a0001c0002t0003g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(277): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(266): Show |
1 | a0001c0002t0002g0170 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(277): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(266): Show |
70 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(67): Show |
103 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(277): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971393 | T | TGCTGAGG others(1358): Show |
1 | a0001c0002t0002g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(1369): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971393 | ||||||
| chr11:65971425 | T | TGAGGAGG others(19): Show |
1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3605_1572+360 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | ||||||
| chr11:65971425 | T | TGAGGAGG others(388): Show |
4 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(1): Show |
4 | HG01109.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3605_1572+360 others(399): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | ||||||
| chr11:65971425 | T | TGCTGAGG others(205): Show |
1 | a0001c0017t0002g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1572+3621_1572+362 others(216): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | ||||||
| chr11:65971425 | T | TGCTGAGG others(234): Show |
2 | a0001c0002t0002g0183 a0001c0002t0011g0193 |
2 | HG01099.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(245): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971425 | ||||||
| chr11:65971452 | T | G | 42 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0263 others(39): Show |
66 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1572+3631T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971452 | |||||||
| chr11:65971452 | T | TGAGCTGA others(115): Show |
1 | a0002c0001t0001g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(126): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971452 | ||||||
| chr11:65971457 | T | TGAGGAGG others(234): Show |
1 | a0002c0001t0001g0132 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1572+3637_1572+363 others(245): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGAGGAGG others(144): Show |
16 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0073 others(13): Show |
28 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(155): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGAGGAGG others(115): Show |
2 | a0002c0001t0001g0072 a0002c0001t0001g0139 |
2 | NA18954.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1572+3637_1572+363 others(126): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGCTGAGG others(519): Show |
1 | a0002c0001t0001g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(530): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGCTGAGG others(517): Show |
1 | a0002c0001t0001g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(528): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGCTGAGG others(1019): Show |
1 | a0002c0001t0001g0100 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(1030): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGCTGAGG others(426): Show |
1 | a0002c0001t0001g0147 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(437): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGCTGAGG others(519): Show |
13 | a0001c0006t0001g0112 a0002c0001t0001g0007 a0002c0001t0001g0075 others(10): Show |
19 | HG00099.hp2 HG01070.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1572+3662_1572+366 others(530): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGCTGAGG others(54): Show |
1 | a0002c0001t0001g0082 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1572+3662_1572+366 others(65): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | T | TGCTGAGG others(22): Show |
1 | a0001c0002t0002g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1572+3728_1572+375 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971457 | TGCTGAGG others(22): Show |
T | 19 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(16): Show |
30 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.1572+3728_1572+375 others(33): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971457 | ||||||
| chr11:65971471 | A | G | 1 | a0002c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1572+3650A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971471 | |||||||
| chr11:65971484 | T | G | 26 | a0001c0004t0007g0069 a0001c0005t0001g0010 a0001c0005t0001g0012 others(23): Show |
40 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1572+3663T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971484 | |||||||
| chr11:65971485 | G | A | 11 | a0001c0006t0001g0113 a0002c0001t0001g0008 a0002c0001t0001g0074 others(8): Show |
16 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3664G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971485 | |||||||
| chr11:65971486 | A | AGCT | 20 | a0001c0002t0002g0183 a0001c0002t0011g0193 a0001c0003t0002g0166 others(17): Show |
21 | HG00673.hp2 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1572+3667_1572+366 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | ||||||
| chr11:65971486 | A | AGCTGCTG others(60): Show |
8 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0023 others(5): Show |
16 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3669_1572+367 others(71): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | ||||||
| chr11:65971486 | A | AGCTGCTG others(371): Show |
6 | a0001c0003t0003g0022 a0001c0003t0003g0060 a0001c0003t0003g0061 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1572+3669_1572+367 others(382): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | ||||||
| chr11:65971486 | A | AGCTGCTG others(403): Show |
1 | a0001c0003t0003g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1572+3669_1572+367 others(414): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | ||||||
| chr11:65971486 | A | AGCTGCTG others(563): Show |
1 | a0001c0003t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1572+3669_1572+367 others(574): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971486 | ||||||
| chr11:65971513 | T | G | 36 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(33): Show |
47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+3692T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971513 | |||||||
| chr11:65971513 | T | TGAGCTGA others(949): Show |
1 | a0001c0004t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1572+3727_1572+372 others(960): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971513 | ||||||
| chr11:65971515 | A | AGCT | 40 | a0001c0003t0002g0256 a0001c0003t0002g0257 a0001c0006t0001g0112 others(37): Show |
58 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1572+3696_1572+369 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971515 | ||||||
| chr11:65971515 | A | AGCTGAGG others(25): Show |
4 | a0002c0001t0001g0085 a0002c0001t0001g0122 a0002c0001t0001g0141 others(1): Show |
4 | HG01123.hp1 HG02015.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3696_1572+372 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971515 | ||||||
| chr11:65971515 | A | AGCTGAGG others(179): Show |
11 | a0002c0001t0001g0011 a0002c0001t0001g0027 a0002c0001t0001g0071 others(8): Show |
13 | HG00099.hp1 HG00438.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1572+3727_1572+372 others(190): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971515 | ||||||
| chr11:65971529 | ATGG | A | 8 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0023 others(5): Show |
16 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3712_1572+371 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971529 | ||||||
| chr11:65971542 | T | G | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3721T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971542 | |||||||
| chr11:65971544 | A | AGCT | 57 | a0001c0003t0002g0256 a0001c0003t0002g0257 a0001c0005t0002g0042 others(54): Show |
87 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1572+3725_1572+372 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971544 | ||||||
| chr11:65971550 | GGAGGGGG others(25): Show |
G | 4 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0263 others(1): Show |
4 | HG01106.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+3750_1572+378 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971550 | ||||||
| chr11:65971552 | A | G | 1 | a0002c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1572+3731A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971552 | |||||||
| chr11:65971571 | T | G | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+3750T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971571 | |||||||
| chr11:65971571 | T | TGAGCTGC others(25): Show |
1 | a0001c0002t0003g0039 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(36): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971571 | ||||||
| chr11:65971573 | AGCT | A | 52 | a0001c0005t0002g0266 a0001c0006t0001g0112 a0002c0001t0001g0004 others(49): Show |
71 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1572+3757_1572+375 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971573 | ||||||
| chr11:65971576 | T | TGAGGAGG others(19): Show |
32 | a0001c0006t0001g0110 a0002c0001t0001g0002 a0002c0001t0001g0003 others(29): Show |
56 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1572+3756_1572+375 others(30): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | ||||||
| chr11:65971576 | T | TGAGGAGG others(1074): Show |
1 | a0002c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1572+3756_1572+375 others(1085): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | ||||||
| chr11:65971576 | T | TGCTGAGG others(173): Show |
2 | a0002c0001t0001g0114 a0002c0001t0001g0143 |
2 | HG00597.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(184): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | ||||||
| chr11:65971576 | T | TGCTGAGG others(920): Show |
1 | a0002c0001t0001g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1572+3760_1572+376 others(931): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | ||||||
| chr11:65971576 | T | TGCTGAGG others(516): Show |
11 | a0001c0006t0001g0113 a0002c0001t0001g0008 a0002c0001t0001g0074 others(8): Show |
16 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(527): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | ||||||
| chr11:65971576 | T | TGCTGAGG others(798): Show |
3 | a0002c0001t0001g0087 a0002c0001t0001g0088 a0002c0001t0001g0155 |
3 | HG00673.hp2 HG02056.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1572+3760_1572+376 others(809): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971576 | ||||||
| chr11:65971582 | A | G | 268 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(265): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1572+3761A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971582 | |||||||
| chr11:65971595 | G | A | 1 | a0001c0004t0014g0053 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1572+3774G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971595 | |||||||
| chr11:65971603 | G | T | 2 | a0001c0003t0002g0256 a0001c0003t0002g0257 |
2 | NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1572+3782G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971603 | |||||||
| chr11:65971635 | G | T | 7 | a0001c0003t0002g0256 a0001c0003t0002g0257 a0002c0001t0001g0025 others(4): Show |
8 | HG02074.hp1 HG02132.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+3814G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971635 | |||||||
| chr11:65971637 | A | AGCTGAGG others(452): Show |
2 | a0001c0003t0002g0256 a0001c0003t0002g0257 |
2 | NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1572+3840_1572+384 others(463): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971637 | ||||||
| chr11:65971637 | A | AGCTGAGG others(182): Show |
5 | a0002c0001t0001g0025 a0002c0001t0001g0089 a0002c0001t0001g0090 others(2): Show |
6 | HG02074.hp1 HG02132.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+3840_1572+384 others(193): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65971637 | ||||||
| chr11:65971678 | G | A | 1 | a0001c0003t0003g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1572+3857G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971678 | |||||||
| chr11:65971876 | A | G | 1 | a0001c0002t0002g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1572+4055A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971876 | |||||||
| chr11:65971887 | A | G | 36 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(33): Show |
47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+4066A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971887 | |||||||
| chr11:65971910 | G | C | 36 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(33): Show |
47 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1572+4089G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65971910 | |||||||
| chr11:65972078 | T | G | 164 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(161): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1572+4257T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972078 | |||||||
| chr11:65972464 | T | C | 1 | a0001c0004t0002g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1573-3931T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972464 | |||||||
| chr11:65972586 | T | C | 35 | a0001c0003t0003g0022 a0001c0003t0003g0059 a0001c0003t0003g0060 others(32): Show |
46 | HG00673.hp1 HG01243.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.1573-3809T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972586 | |||||||
| chr11:65972661 | G | A | 1 | a0002c0001t0016g0133 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1573-3734G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972661 | |||||||
| chr11:65972785 | C | CA | 7 | a0001c0002t0002g0195 a0001c0002t0002g0244 a0001c0002t0003g0204 others(4): Show |
7 | HG00597.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573-3595dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65972785 | ||||||
| chr11:65972801 | C | A | 1 | a0001c0003t0002g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1573-3594C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972801 | |||||||
| chr11:65972844 | C | T | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1573-3551C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972844 | |||||||
| chr11:65972863 | G | A | 246 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(243): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1573-3532G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972863 | |||||||
| chr11:65972873 | A | G | 1 | a0001c0004t0002g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1573-3522A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972873 | |||||||
| chr11:65972893 | C | T | 1 | a0001c0003t0004g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1573-3502C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972893 | |||||||
| chr11:65972897 | C | T | 1 | a0002c0001t0001g0027 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1573-3498C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972897 | |||||||
| chr11:65972899 | C | T | 117 | a0001c0002t0002g0033 a0001c0005t0001g0010 a0001c0005t0001g0012 others(114): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1573-3496C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972899 | |||||||
| chr11:65972900 | G | C | 1 | a0001c0004t0002g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1573-3495G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972900 | |||||||
| chr11:65972901 | A | G | 9 | a0001c0002t0002g0033 a0001c0002t0002g0183 a0001c0002t0003g0212 others(6): Show |
11 | HG01069.hp2 HG01071.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1573-3494A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972901 | |||||||
| chr11:65972905 | C | T | 1 | a0001c0004t0006g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1573-3490C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972905 | |||||||
| chr11:65972909 | C | T | 3 | a0001c0004t0007g0068 a0001c0004t0007g0069 a0001c0005t0001g0164 |
3 | HG02257.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1573-3486C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972909 | |||||||
| chr11:65972943 | G | A | 2 | a0001c0004t0006g0045 a0001c0004t0006g0046 |
2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1573-3452G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972943 | |||||||
| chr11:65972946 | C | A | 1 | a0001c0002t0003g0205 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1573-3449C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972946 | |||||||
| chr11:65972969 | G | A | 1 | a0002c0001t0001g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1573-3426G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972969 | |||||||
| chr11:65972997 | T | C | 42 | a0001c0002t0001g0038 a0001c0002t0002g0206 a0001c0002t0003g0001 others(39): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1573-3398T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65972997 | |||||||
| chr11:65973099 | A | G | 1 | a0001c0005t0002g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1573-3296A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973099 | |||||||
| chr11:65973131 | A | G | 275 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(272): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1573-3264A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973131 | |||||||
| chr11:65973148 | T | A | 1 | a0001c0003t0003g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1573-3247T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973148 | |||||||
| chr11:65973173 | C | CA | 4 | a0001c0002t0003g0245 a0001c0003t0002g0252 a0002c0001t0001g0024 others(1): Show |
5 | HG02293.hp1 NA18955.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1573-3213dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65973173 | ||||||
| chr11:65973391 | A | G | 2 | a0001c0003t0002g0256 a0001c0003t0002g0257 |
2 | NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1573-3004A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973391 | |||||||
| chr11:65973463 | A | G | 1 | a0002c0001t0001g0108 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1573-2932A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973463 | |||||||
| chr11:65973520 | C | T | 6 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573-2875C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973520 | |||||||
| chr11:65973615 | G | A | 41 | a0001c0002t0002g0006 a0001c0002t0002g0014 a0001c0002t0002g0032 others(38): Show |
52 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1573-2780G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973615 | |||||||
| chr11:65973690 | C | T | 1 | a0002c0001t0017g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1573-2705C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65973690 | |||||||
| chr11:65974091 | G | A | 1 | a0001c0002t0002g0196 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1573-2304G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974091 | |||||||
| chr11:65974159 | G | A | 2 | a0001c0002t0002g0199 a0001c0002t0002g0200 |
2 | HG00642.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1573-2236G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974159 | |||||||
| chr11:65974198 | T | TA | 50 | a0001c0002t0002g0006 a0001c0002t0002g0014 a0001c0002t0002g0032 others(47): Show |
63 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1573-2171dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974198 | ||||||
| chr11:65974198 | TA | T | 143 | a0001c0002t0001g0038 a0001c0002t0003g0001 a0001c0002t0003g0015 others(140): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1573-2171delA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974198 | ||||||
| chr11:65974198 | TAA | T | 19 | a0001c0002t0003g0227 a0001c0003t0002g0233 a0001c0004t0002g0005 others(16): Show |
30 | HG00673.hp1 HG01099.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1573-2172_1573-217 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974198 | ||||||
| chr11:65974225 | T | G | 1 | a0002c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1573-2170T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974225 | |||||||
| chr11:65974299 | G | A | 117 | a0001c0002t0001g0038 a0001c0005t0001g0010 a0001c0005t0001g0012 others(114): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1573-2096G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974299 | |||||||
| chr11:65974346 | C | T | 2 | a0002c0001t0001g0120 a0002c0001t0001g0137 |
2 | NA18944.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1573-2049C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974346 | |||||||
| chr11:65974371 | C | CA | 50 | a0001c0002t0002g0190 a0001c0002t0002g0197 a0001c0002t0002g0199 others(47): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1573-2004dupA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | ||||||
| chr11:65974371 | C | CAA | 105 | a0001c0002t0001g0038 a0001c0002t0002g0206 a0001c0002t0003g0184 others(102): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1573-2005_1573-200 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | ||||||
| chr11:65974371 | C | CAAA | 16 | a0001c0002t0003g0219 a0001c0005t0001g0162 a0001c0006t0001g0113 others(13): Show |
21 | HG00423.hp1 HG01069.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1573-2006_1573-200 others(7): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | ||||||
| chr11:65974371 | CA | C | 8 | a0001c0002t0002g0037 a0001c0002t0002g0203 a0001c0004t0002g0019 others(5): Show |
10 | HG02055.hp2 HG02155.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1573-2004delA | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | ||||||
| chr11:65974371 | CAA | C | 21 | a0001c0004t0002g0005 a0001c0004t0002g0020 a0001c0004t0002g0021 others(18): Show |
31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573-2005_1573-200 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65974371 | ||||||
| chr11:65974392 | C | A | 123 | a0001c0002t0001g0038 a0001c0005t0001g0010 a0001c0005t0001g0012 others(120): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1573-2003C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974392 | |||||||
| chr11:65974395 | T | C | 1 | a0001c0003t0003g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1573-2000T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974395 | |||||||
| chr11:65974402 | C | A | 1 | a0001c0004t0007g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1573-1993C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974402 | |||||||
| chr11:65974462 | C | T | 1 | a0001c0003t0002g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1573-1933C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974462 | |||||||
| chr11:65974633 | C | T | 1 | a0001c0002t0003g0202 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1573-1762C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974633 | |||||||
| chr11:65974713 | C | T | 2 | a0001c0002t0002g0236 a0001c0003t0002g0067 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1573-1682C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974713 | |||||||
| chr11:65974772 | A | G | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1573-1623A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974772 | |||||||
| chr11:65974812 | A | G | 73 | a0001c0002t0002g0206 a0001c0002t0003g0001 a0001c0002t0003g0015 others(70): Show |
104 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1573-1583A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974812 | |||||||
| chr11:65974851 | C | T | 1 | a0002c0001t0001g0103 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1573-1544C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974851 | |||||||
| chr11:65974852 | G | A | 4 | a0001c0005t0002g0042 a0001c0005t0002g0262 a0001c0005t0002g0263 others(1): Show |
4 | HG01106.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573-1543G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974852 | |||||||
| chr11:65974900 | C | T | 1 | a0001c0003t0005g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1573-1495C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974900 | |||||||
| chr11:65974901 | G | C | 1 | a0001c0003t0004g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1573-1494G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974901 | |||||||
| chr11:65974911 | G | C | 3 | a0001c0002t0002g0195 a0001c0002t0002g0201 a0001c0002t0002g0244 |
3 | HG00642.hp1 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1573-1484G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974911 | |||||||
| chr11:65974946 | A | C | 3 | a0003c0008t0002g0050 a0003c0008t0002g0051 a0003c0008t0002g0052 |
3 | NA18950.hp2 NA18984.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1573-1449A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974946 | |||||||
| chr11:65974955 | C | G | 273 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(270): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1573-1440C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65974955 | |||||||
| chr11:65975061 | GACAA | G | 2 | a0002c0001t0001g0026 a0002c0001t0001g0098 |
3 | NA18961.hp2 NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1573-1320_1573-131 others(8): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975061 | ||||||
| chr11:65975065 | A | G | 1 | a0001c0003t0010g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1573-1330A>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975065 | |||||||
| chr11:65975101 | C | CT | 41 | a0001c0002t0002g0180 a0001c0002t0002g0192 a0001c0002t0002g0214 others(38): Show |
59 | HG00673.hp1 HG01106.hp1 HG01433.hp2 others(56): Show |
intron_variant | MODIFIER | c.1573-1275dupT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975101 | ||||||
| chr11:65975101 | C | CTT | 5 | a0001c0004t0002g0020 a0001c0004t0002g0055 a0001c0004t0002g0070 others(2): Show |
6 | HG02074.hp2 HG02647.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1573-1276_1573-127 others(6): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975101 | ||||||
| chr11:65975367 | T | C | 124 | a0001c0002t0001g0038 a0001c0005t0001g0010 a0001c0005t0001g0012 others(121): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1573-1028T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975367 | |||||||
| chr11:65975410 | A | AT | 184 | a0001c0002t0001g0038 a0001c0002t0002g0006 a0001c0002t0002g0014 others(181): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1573-965dupT | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975410 | ||||||
| chr11:65975410 | A | ATT | 10 | a0001c0002t0002g0192 a0001c0002t0002g0203 a0001c0003t0002g0166 others(7): Show |
10 | HG01109.hp1 HG03098.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.1573-966_1573-965d others(4): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975410 | ||||||
| chr11:65975430 | T | C | 1 | a0003c0008t0002g0051 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1573-965T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975430 | |||||||
| chr11:65975430 | T | TC | 23 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(20): Show |
34 | HG00673.hp1 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1573-964dupC | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 65975430 | ||||||
| chr11:65975462 | T | C | 119 | a0001c0002t0001g0038 a0001c0002t0003g0209 a0001c0005t0001g0010 others(116): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1573-933T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975462 | |||||||
| chr11:65975632 | C | T | 6 | a0002c0001t0001g0026 a0002c0001t0001g0088 a0002c0001t0001g0093 others(3): Show |
7 | HG00673.hp2 HG02027.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573-763C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975632 | |||||||
| chr11:65975652 | C | T | 1 | a0002c0001t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1573-743C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975652 | |||||||
| chr11:65975809 | T | C | 1 | a0001c0002t0003g0225 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1573-586T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65975809 | |||||||
| chr11:65976039 | G | A | 26 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(23): Show |
37 | HG00673.hp1 HG01891.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1573-356G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976039 | |||||||
| chr11:65976040 | G | A | 20 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(17): Show |
31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573-355G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976040 | |||||||
| chr11:65976049 | G | A | 5 | a0001c0003t0002g0166 a0001c0003t0002g0167 a0001c0003t0002g0168 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1573-346G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976049 | |||||||
| chr11:65976260 | A | C | 1 | a0001c0003t0003g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1573-135A>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976260 | |||||||
| chr11:65976278 | C | A | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1573-117C>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976278 | |||||||
| chr11:65976280 | T | G | 1 | a0002c0001t0001g0130 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1573-115T>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976280 | |||||||
| chr11:65976308 | C | T | 2 | a0001c0003t0004g0013 a0001c0003t0004g0177 |
4 | HG01243.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573-87C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | chr11 | 65976308 | |||||||
| chr11:65976633 | G | C | 1 | a0001c0002t0002g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1747-23G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 13/19 | chr11 | 65976633 | |||||||
| chr11:65976776 | G | A | 44 | a0001c0002t0002g0006 a0001c0002t0002g0014 a0001c0002t0002g0032 others(41): Show |
56 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1857+10G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976776 | |||||||
| chr11:65976780 | C | T | 1 | a0002c0001t0001g0101 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1857+14C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976780 | |||||||
| chr11:65976794 | C | T | 42 | a0002c0001t0001g0007 a0002c0001t0001g0008 a0002c0001t0001g0025 others(39): Show |
55 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1857+28C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976794 | |||||||
| chr11:65976804 | T | C | 202 | a0001c0002t0001g0038 a0001c0002t0002g0206 a0001c0002t0003g0001 others(199): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1857+38T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976804 | |||||||
| chr11:65976832 | C | T | 20 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(17): Show |
31 | HG00673.hp1 HG01891.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1857+66C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976832 | |||||||
| chr11:65976950 | C | T | 125 | a0001c0002t0001g0038 a0001c0005t0001g0010 a0001c0005t0001g0012 others(122): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1858-64C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 14/19 | chr11 | 65976950 | |||||||
| chr11:65977126 | C | T | 46 | a0001c0002t0002g0206 a0001c0002t0003g0001 a0001c0002t0003g0015 others(43): Show |
66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1945+25C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977126 | |||||||
| chr11:65977165 | C | T | 1 | a0001c0002t0003g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1945+64C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977165 | |||||||
| chr11:65977266 | G | A | 1 | a0001c0002t0003g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1945+165G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977266 | |||||||
| chr11:65977414 | C | T | 1 | a0002c0001t0001g0109 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1946-149C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977414 | |||||||
| chr11:65977550 | C | T | 1 | a0001c0003t0003g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1946-13C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 15/19 | chr11 | 65977550 | |||||||
| chr11:65977760 | C | T | 17 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(14): Show |
27 | HG00673.hp1 HG02074.hp2 HG02080.hp1 others(24): Show |
splice_region_variant&intron_variant | LOW | c.2037-4C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 16/19 | chr11 | 65977760 | |||||||
| chr11:65977922 | G | A | 9 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0023 others(6): Show |
17 | HG01934.hp1 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2172+23G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65977922 | |||||||
| chr11:65977932 | C | G | 7 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(4): Show |
8 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2172+33C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65977932 | |||||||
| chr11:65977955 | AGGGCCAT others(10): Show |
A | 1 | a0002c0001t0001g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2172+74_2172+90del others(17): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr11 | 65977955 | ||||||
| chr11:65978017 | T | C | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2172+118T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978017 | |||||||
| chr11:65978145 | G | A | 1 | a0010c0013t0001g0125 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2172+246G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978145 | |||||||
| chr11:65978283 | T | A | 6 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2173-317T>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978283 | |||||||
| chr11:65978305 | T | TCCAGCC | 16 | a0001c0004t0002g0005 a0001c0004t0002g0019 a0001c0004t0002g0020 others(13): Show |
26 | HG00673.hp1 HG02074.hp2 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.2173-295_2173-294i others(8): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978305 | |||||||
| chr11:65978390 | C | T | 1 | a0001c0005t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2173-210C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978390 | |||||||
| chr11:65978415 | C | T | 1 | a0001c0002t0003g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2173-185C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978415 | |||||||
| chr11:65978417 | G | A | 4 | a0001c0003t0003g0059 a0001c0003t0003g0061 a0001c0003t0003g0062 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2173-183G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978417 | |||||||
| chr11:65978418 | G | A | 1 | a0001c0002t0003g0039 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2173-182G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978418 | |||||||
| chr11:65978460 | T | C | 7 | a0002c0001t0001g0029 a0002c0001t0001g0081 a0002c0001t0001g0117 others(4): Show |
8 | HG00423.hp2 HG02523.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.2173-140T>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978460 | |||||||
| chr11:65978467 | C | G | 1 | a0001c0003t0004g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2173-133C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978467 | |||||||
| chr11:65978514 | C | T | 18 | a0001c0003t0002g0017 a0001c0003t0002g0231 a0001c0003t0002g0233 others(15): Show |
19 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.2173-86C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978514 | |||||||
| chr11:65978552 | C | T | 5 | a0001c0005t0002g0041 a0001c0005t0002g0042 a0001c0005t0002g0262 others(2): Show |
6 | HG01106.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2173-48C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 17/19 | chr11 | 65978552 | |||||||
| chr11:65978713 | G | T | 1 | a0001c0005t0002g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2262+24G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/19 | chr11 | 65978713 | |||||||
| chr11:65978742 | C | T | 2 | a0001c0004t0007g0068 a0001c0004t0007g0069 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2263-51C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/19 | chr11 | 65978742 | |||||||
| chr11:65978782 | C | T | 1 | a0002c0001t0001g0127 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2263-11C>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 18/19 | chr11 | 65978782 | |||||||
| chr11:65978937 | G | C | 2 | a0001c0002t0002g0236 a0001c0003t0002g0067 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2384+23G>C | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978937 | |||||||
| chr11:65978985 | G | A | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2385-27G>A | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978985 | |||||||
| chr11:65978987 | C | G | 3 | a0001c0004t0006g0045 a0001c0004t0006g0046 a0001c0004t0006g0047 |
3 | HG02055.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2385-25C>G | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978987 | |||||||
| chr11:65978992 | G | T | 2 | a0001c0005t0002g0041 a0001c0005t0002g0264 |
3 | HG02717.hp1 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2385-20G>T | SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 19/19 | chr11 | 65978992 |