Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3059 |
| ensemblid | ENSG00000180353.11 |
| hgncid | 4844 |
| symbol | HCLS1 |
| name | hematopoietic cell-specific Lyn substrate 1 |
| refseq_nuc | NM_005335.6 |
| refseq_prot | NP_005326.3 |
| ensembl_nuc | ENST00000314583.8 |
| ensembl_prot | ENSP00000320176.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 121631399 |
| end | 121660903 |
| strand | - |
| ver | v1.2 |
| region | chr3:121631399-121660903 |
| region5000 | chr3:121626399-121665903 |
| regionname0 | HCLS1_chr3_121631399_121660903 |
| regionname5000 | HCLS1_chr3_121626399_121665903 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 486 | 113 | 29 | 16 | 55 | 0 | 13 | 43 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0002 | 0/0 | 486 | 106 | 36 | 19 | 31 | 4 | 16 | 25 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0003 | 0/0 | 490 | 100 | 7 | 15 | 66 | 5 | 7 | 45 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(485): Show |
chr3 | 121626399 | 121665903 |
| a0004 | 0/0 | 486 | 50 | 13 | 14 | 18 | 2 | 3 | 16 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0005 | 0/1 | 486 | 5 | 0 | 0 | 0 | 2 | 2 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0006 | 1/0 | 486 | 3 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0007 | 0/0 | 486 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0008 | 0/0 | 490 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(485): Show |
chr3 | 121626399 | 121665903 |
| a0009 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0010 | 0/0 | 490 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(485): Show |
chr3 | 121626399 | 121665903 |
| a0011 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0012 | 0/0 | 490 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(485): Show |
chr3 | 121626399 | 121665903 |
| a0013 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(481): Show |
chr3 | 121626399 | 121665903 |
| a0014 | 0/0 | 490 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | MWKSV others(485): Show |
chr3 | 121626399 | 121665903 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1458 | 102 | 23 | 15 | 51 | 0 | 13 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0001c0007 | 0/0 | 1458 | 5 | 4 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0001c0012 | 0/0 | 1458 | 3 | 0 | 0 | 3 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0001c0014 | 0/0 | 1458 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0001c0018 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0002c0001 | 0/0 | 1458 | 102 | 36 | 19 | 27 | 4 | 16 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0002c0008 | 0/0 | 1458 | 4 | 0 | 0 | 4 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0003c0003 | 0/0 | 1470 | 97 | 4 | 15 | 66 | 5 | 7 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1465): Show |
chr3 | 121626399 | 121665903 | ||
| a0003c0013 | 0/0 | 1470 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1465): Show |
chr3 | 121626399 | 121665903 | ||
| a0003c0017 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1465): Show |
chr3 | 121626399 | 121665903 | ||
| a0004c0004 | 0/0 | 1458 | 40 | 10 | 9 | 18 | 1 | 2 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0004c0005 | 0/0 | 1458 | 10 | 3 | 5 | 0 | 1 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0005c0006 | 0/1 | 1458 | 5 | 0 | 0 | 0 | 2 | 2 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0006c0011 | 1/0 | 1458 | 3 | 1 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0007c0009 | 0/0 | 1458 | 4 | 3 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0008c0010 | 0/0 | 1470 | 3 | 3 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1465): Show |
chr3 | 121626399 | 121665903 | ||
| a0009c0020 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0010c0015 | 0/0 | 1470 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1465): Show |
chr3 | 121626399 | 121665903 | ||
| a0011c0021 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0012c0019 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1465): Show |
chr3 | 121626399 | 121665903 | ||
| a0013c0022 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1453): Show |
chr3 | 121626399 | 121665903 | ||
| a0014c0016 | 0/0 | 1470 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ATGTG others(1465): Show |
chr3 | 121626399 | 121665903 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003 | 0/0 | 1994 | 63 | 8 | 13 | 36 | 0 | 6 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0002t0005 | 0/0 | 1994 | 34 | 13 | 2 | 12 | 0 | 7 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0002t0007 | 0/0 | 1994 | 3 | 0 | 0 | 3 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0002t0010 | 0/0 | 1994 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0007t0003 | 0/0 | 1994 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0007t0004 | 0/0 | 1994 | 4 | 4 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0012t0003 | 0/0 | 1994 | 3 | 0 | 0 | 3 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0014t0008 | 0/0 | 1994 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0001c0018t0003 | 0/0 | 1994 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0002c0001t0001 | 0/0 | 1992 | 100 | 36 | 19 | 25 | 4 | 16 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1987): Show |
chr3 | 121626399 | 121665903 |
| a0002c0001t0009 | 0/0 | 1992 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1987): Show |
chr3 | 121626399 | 121665903 |
| a0002c0008t0001 | 0/0 | 1992 | 4 | 0 | 0 | 4 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1987): Show |
chr3 | 121626399 | 121665903 |
| a0003c0003t0002 | 0/0 | 2006 | 97 | 4 | 15 | 66 | 5 | 7 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| a0003c0013t0002 | 0/0 | 2006 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| a0003c0013t0011 | 0/0 | 2006 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| a0003c0017t0002 | 0/0 | 2006 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| a0004c0004t0004 | 0/0 | 1994 | 40 | 10 | 9 | 18 | 1 | 2 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0004c0005t0004 | 0/0 | 1994 | 10 | 3 | 5 | 0 | 1 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0005c0006t0004 | 0/1 | 1994 | 5 | 0 | 0 | 0 | 2 | 2 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0006c0011t0001 | 1/0 | 1992 | 3 | 1 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1987): Show |
chr3 | 121626399 | 121665903 |
| a0007c0009t0006 | 0/0 | 1994 | 4 | 3 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0008c0010t0002 | 0/0 | 2006 | 3 | 3 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| a0009c0020t0001 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1987): Show |
chr3 | 121626399 | 121665903 |
| a0010c0015t0002 | 0/0 | 2006 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| a0011c0021t0003 | 0/0 | 1994 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0012c0019t0002 | 0/0 | 2006 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| a0013c0022t0003 | 0/0 | 1994 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(1989): Show |
chr3 | 121626399 | 121665903 |
| a0014c0016t0002 | 0/0 | 2006 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | ACTCC others(2001): Show |
chr3 | 121626399 | 121665903 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003g0001 | 0/0 | 14 | 3 | 2 | 9 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0008 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0009 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0007g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0002t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0007t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0007t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0007t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0007t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0007t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0012t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0012t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0014t0008g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0001c0018t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0003 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0005 | 0/0 | 8 | 1 | 4 | 1 | 0 | 2 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0001t0009g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0008t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0002c0008t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0004 | 0/0 | 8 | 1 | 2 | 2 | 3 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0013t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0013t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0003c0017t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0021 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0004t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0004c0005t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0005c0006t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0005c0006t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0005c0006t0004g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0005c0006t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0005c0006t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0006c0011t0001g0051 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0006c0011t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0007c0009t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0007c0009t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0007c0009t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0007c0009t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0008c0010t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0008c0010t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0009c0020t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0010c0015t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0011c0021t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0012c0019t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0013c0022t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| a0014c0016t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0005 | c0006 | t0004 | g0194 | EUR | GBR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0093 | EUR | GBR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00280 | hp1 | a0003 | c0003 | t0002 | g0096 | EUR | FIN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00280 | hp2 | a0004 | c0005 | t0004 | g0190 | EUR | FIN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0220 | EUR | FIN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00323 | hp2 | a0005 | c0006 | t0004 | g0195 | EUR | FIN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0156 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00423 | hp1 | a0003 | c0003 | t0002 | g0175 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00423 | hp2 | a0001 | c0002 | t0005 | g0257 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00438 | hp1 | a0003 | c0003 | t0002 | g0024 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0059 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00597 | hp2 | a0003 | c0003 | t0002 | g0173 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00621 | hp1 | a0003 | c0003 | t0002 | g0152 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00621 | hp2 | a0003 | c0003 | t0002 | g0060 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0052 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00642 | hp1 | a0002 | c0001 | t0001 | g0218 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0091 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0115 | EAS | CHS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00733 | hp1 | a0004 | c0004 | t0004 | g0075 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0114 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00735 | hp1 | a0006 | c0011 | t0001 | g0051 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0061 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00738 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0111 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00741 | hp1 | a0003 | c0003 | t0002 | g0024 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0137 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01069 | hp1 | a0004 | c0004 | t0004 | g0010 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01069 | hp2 | a0003 | c0003 | t0002 | g0017 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01071 | hp2 | a0004 | c0004 | t0004 | g0010 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01074 | hp1 | a0007 | c0009 | t0006 | g0065 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0214 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0015 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0247 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0033 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01106 | hp2 | a0003 | c0003 | t0002 | g0092 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0260 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0233 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01168 | hp2 | a0004 | c0004 | t0004 | g0069 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01169 | hp1 | a0004 | c0004 | t0004 | g0070 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01169 | hp2 | a0001 | c0007 | t0003 | g0098 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01192 | hp2 | a0003 | c0003 | t0002 | g0063 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0033 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0197 | AMR | PUR | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01255 | hp1 | a0004 | c0004 | t0004 | g0022 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0196 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0008 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01256 | hp2 | a0004 | c0005 | t0004 | g0014 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0136 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01257 | hp2 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01258 | hp2 | a0004 | c0005 | t0004 | g0014 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01261 | hp1 | a0004 | c0004 | t0004 | g0022 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01261 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01361 | hp1 | a0004 | c0005 | t0004 | g0186 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0101 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0057 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01433 | hp2 | a0003 | c0003 | t0002 | g0090 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01496 | hp2 | a0004 | c0004 | t0004 | g0020 | AMR | CLM | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01515 | hp1 | a0003 | c0003 | t0002 | g0004 | EUR | IBS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0043 | EUR | IBS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0240 | EUR | IBS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0004 | EUR | IBS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01517 | hp1 | a0003 | c0003 | t0002 | g0004 | EUR | IBS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0043 | EUR | IBS | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0009 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01884 | hp2 | a0003 | c0003 | t0002 | g0039 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01891 | hp1 | a0002 | c0001 | t0001 | g0232 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01891 | hp2 | a0001 | c0007 | t0004 | g0105 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01943 | hp2 | a0003 | c0003 | t0002 | g0062 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0144 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0169 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02027 | hp1 | a0009 | c0020 | t0001 | g0236 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0038 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0123 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0048 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02055 | hp2 | a0004 | c0005 | t0004 | g0187 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02056 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02056 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02071 | hp1 | a0003 | c0003 | t0002 | g0165 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02071 | hp2 | a0003 | c0003 | t0002 | g0146 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0180 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0099 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02083 | hp1 | a0004 | c0004 | t0004 | g0071 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02129 | hp1 | a0003 | c0003 | t0002 | g0154 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02129 | hp2 | a0003 | c0003 | t0002 | g0042 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0206 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02132 | hp2 | a0003 | c0003 | t0002 | g0038 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0176 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0216 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0275 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02148 | hp1 | a0004 | c0005 | t0004 | g0189 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0053 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02257 | hp2 | a0001 | c0014 | t0008 | g0018 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0267 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02258 | hp2 | a0004 | c0004 | t0004 | g0023 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0056 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0210 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02300 | hp1 | a0004 | c0005 | t0004 | g0014 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02300 | hp2 | a0004 | c0004 | t0004 | g0019 | AMR | PEL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0134 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0271 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02523 | hp1 | a0004 | c0004 | t0004 | g0088 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02523 | hp2 | a0001 | c0002 | t0005 | g0252 | EAS | KHV | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02572 | hp1 | a0004 | c0004 | t0004 | g0086 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0245 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0217 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02602 | hp2 | a0001 | c0002 | t0005 | g0008 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02615 | hp1 | a0003 | c0013 | t0002 | g0139 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02615 | hp2 | a0001 | c0002 | t0005 | g0274 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02622 | hp1 | a0008 | c0010 | t0002 | g0138 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02622 | hp2 | a0007 | c0009 | t0006 | g0066 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0246 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02630 | hp2 | a0004 | c0004 | t0004 | g0010 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02647 | hp1 | a0002 | c0001 | t0001 | g0044 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0133 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02683 | hp1 | a0002 | c0001 | t0001 | g0047 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02683 | hp2 | a0003 | c0003 | t0002 | g0100 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0054 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02698 | hp2 | a0005 | c0006 | t0004 | g0192 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0009 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02717 | hp2 | a0002 | c0001 | t0001 | g0053 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02723 | hp1 | a0004 | c0004 | t0004 | g0021 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0215 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02735 | hp1 | a0001 | c0002 | t0005 | g0255 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0219 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02738 | hp1 | a0001 | c0002 | t0005 | g0269 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02738 | hp2 | a0004 | c0005 | t0004 | g0188 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0276 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02809 | hp2 | a0002 | c0001 | t0001 | g0005 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0239 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0270 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0231 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02895 | hp2 | a0002 | c0001 | t0001 | g0226 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02897 | hp2 | a0002 | c0001 | t0001 | g0211 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02922 | hp1 | a0007 | c0009 | t0006 | g0064 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0225 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02965 | hp1 | a0001 | c0002 | t0010 | g0126 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0055 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02970 | hp1 | a0008 | c0010 | t0002 | g0034 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0110 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02976 | hp1 | a0004 | c0004 | t0004 | g0083 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0221 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0132 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03041 | hp2 | a0001 | c0007 | t0004 | g0104 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03098 | hp1 | a0004 | c0004 | t0004 | g0084 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03098 | hp2 | a0003 | c0013 | t0011 | g0141 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03139 | hp1 | a0001 | c0007 | t0004 | g0103 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0055 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03195 | hp1 | a0002 | c0001 | t0001 | g0049 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03195 | hp2 | a0002 | c0001 | t0001 | g0248 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03209 | hp1 | a0006 | c0011 | t0001 | g0212 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03225 | hp1 | a0007 | c0009 | t0006 | g0067 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03225 | hp2 | a0001 | c0007 | t0004 | g0106 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0124 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03239 | hp2 | a0010 | c0015 | t0002 | g0170 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03453 | hp1 | a0008 | c0010 | t0002 | g0034 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0229 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0277 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03486 | hp2 | a0004 | c0005 | t0004 | g0185 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0244 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03490 | hp2 | a0003 | c0003 | t0002 | g0094 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0054 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03491 | hp2 | a0003 | c0003 | t0002 | g0102 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0256 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03516 | hp2 | a0003 | c0003 | t0002 | g0157 | AFR | ESN | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03540 | hp1 | a0002 | c0001 | t0001 | g0204 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0208 | AFR | GWD | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03579 | hp1 | a0003 | c0003 | t0002 | g0039 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0272 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0058 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03654 | hp2 | a0001 | c0002 | t0005 | g0009 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0047 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03669 | hp2 | a0001 | c0002 | t0005 | g0008 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03688 | hp1 | a0004 | c0004 | t0004 | g0077 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0228 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03704 | hp1 | a0001 | c0002 | t0005 | g0008 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0179 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03710 | hp1 | a0003 | c0003 | t0002 | g0017 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0125 | SAS | PJL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03834 | hp1 | a0003 | c0003 | t0002 | g0155 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03834 | hp2 | a0005 | c0006 | t0004 | g0184 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0242 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0207 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0178 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0118 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0243 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04115 | hp2 | a0002 | c0001 | t0001 | g0230 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04184 | hp1 | a0001 | c0002 | t0005 | g0259 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04184 | hp2 | a0004 | c0004 | t0004 | g0079 | SAS | BEB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0241 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0109 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0279 | SAS | STU | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18522 | hp1 | a0004 | c0004 | t0004 | g0085 | AFR | YRI | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18522 | hp2 | a0002 | c0001 | t0001 | g0044 | AFR | YRI | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18612 | hp1 | a0001 | c0002 | t0005 | g0253 | EAS | CHB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | CHB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18747 | hp1 | a0003 | c0003 | t0002 | g0037 | EAS | CHB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18747 | hp2 | a0003 | c0003 | t0002 | g0168 | EAS | CHB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0238 | AFR | YRI | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18906 | hp2 | a0004 | c0004 | t0004 | g0019 | AFR | YRI | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18941 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18943 | hp1 | a0003 | c0003 | t0002 | g0148 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18944 | hp1 | a0003 | c0003 | t0002 | g0143 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18945 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18949 | hp1 | a0001 | c0012 | t0003 | g0120 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18952 | hp1 | a0001 | c0002 | t0007 | g0030 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18952 | hp2 | a0004 | c0004 | t0004 | g0080 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18954 | hp1 | a0004 | c0004 | t0004 | g0021 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18954 | hp2 | a0003 | c0003 | t0002 | g0164 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18956 | hp1 | a0002 | c0008 | t0001 | g0046 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18956 | hp2 | a0011 | c0021 | t0003 | g0119 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18959 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18960 | hp1 | a0003 | c0003 | t0002 | g0161 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18962 | hp1 | a0003 | c0003 | t0002 | g0041 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18963 | hp1 | a0003 | c0003 | t0002 | g0035 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18963 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18964 | hp1 | a0003 | c0003 | t0002 | g0035 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0222 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18966 | hp2 | a0001 | c0002 | t0005 | g0266 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18969 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18970 | hp1 | a0004 | c0004 | t0004 | g0076 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18970 | hp2 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0040 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18974 | hp2 | a0002 | c0001 | t0001 | g0209 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0167 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18978 | hp1 | a0003 | c0003 | t0002 | g0150 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18978 | hp2 | a0004 | c0004 | t0004 | g0073 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18979 | hp1 | a0003 | c0003 | t0002 | g0041 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0151 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18983 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18984 | hp2 | a0001 | c0002 | t0005 | g0131 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18990 | hp2 | a0004 | c0004 | t0004 | g0068 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18992 | hp1 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18992 | hp2 | a0001 | c0002 | t0005 | g0264 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18993 | hp1 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18994 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18994 | hp2 | a0002 | c0001 | t0009 | g0045 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18997 | hp1 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18997 | hp2 | a0004 | c0004 | t0004 | g0078 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18999 | hp1 | a0004 | c0004 | t0004 | g0087 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19001 | hp1 | a0002 | c0001 | t0001 | g0202 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19001 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19002 | hp1 | a0004 | c0004 | t0004 | g0006 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19002 | hp2 | a0003 | c0003 | t0002 | g0037 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19004 | hp2 | a0012 | c0019 | t0002 | g0160 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19005 | hp1 | a0001 | c0002 | t0005 | g0261 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19005 | hp2 | a0001 | c0012 | t0003 | g0027 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19009 | hp1 | a0004 | c0004 | t0004 | g0072 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0116 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19012 | hp1 | a0004 | c0004 | t0004 | g0089 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19012 | hp2 | a0003 | c0003 | t0002 | g0145 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0278 | AFR | LWK | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0048 | AFR | LWK | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19043 | hp1 | a0002 | c0001 | t0001 | g0249 | AFR | LWK | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19043 | hp2 | a0001 | c0002 | t0005 | g0056 | AFR | LWK | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19054 | hp1 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19055 | hp1 | a0003 | c0003 | t0002 | g0174 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19055 | hp2 | a0001 | c0012 | t0003 | g0027 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19056 | hp1 | a0001 | c0002 | t0005 | g0009 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0166 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19057 | hp1 | a0004 | c0004 | t0004 | g0081 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19057 | hp2 | a0003 | c0003 | t0002 | g0171 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0181 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19060 | hp1 | a0001 | c0002 | t0007 | g0121 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19060 | hp2 | a0001 | c0018 | t0003 | g0159 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19062 | hp1 | a0002 | c0008 | t0001 | g0199 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19062 | hp2 | a0003 | c0003 | t0002 | g0172 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19063 | hp1 | a0002 | c0008 | t0001 | g0198 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19064 | hp1 | a0004 | c0004 | t0004 | g0006 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19066 | hp1 | a0004 | c0004 | t0004 | g0250 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19066 | hp2 | a0001 | c0002 | t0005 | g0258 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19067 | hp1 | a0003 | c0003 | t0002 | g0149 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19067 | hp2 | a0002 | c0001 | t0009 | g0045 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19070 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19070 | hp2 | a0002 | c0008 | t0001 | g0046 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19072 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19072 | hp2 | a0013 | c0022 | t0003 | g0130 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0182 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19080 | hp1 | a0001 | c0002 | t0007 | g0030 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19080 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19082 | hp1 | a0003 | c0003 | t0002 | g0147 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19082 | hp2 | a0001 | c0002 | t0005 | g0262 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19083 | hp1 | a0001 | c0002 | t0005 | g0263 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19083 | hp2 | a0003 | c0003 | t0002 | g0095 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0112 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0183 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19085 | hp1 | a0001 | c0002 | t0005 | g0254 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19085 | hp2 | a0003 | c0003 | t0002 | g0163 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19086 | hp1 | a0004 | c0004 | t0004 | g0006 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19087 | hp1 | a0003 | c0003 | t0002 | g0162 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0113 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0040 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19089 | hp1 | a0004 | c0004 | t0004 | g0082 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA20805 | hp1 | a0014 | c0016 | t0002 | g0097 | EUR | TSI | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA20805 | hp2 | a0004 | c0004 | t0004 | g0020 | EUR | TSI | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | GIH | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0128 | SAS | GIH | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0273 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02109 | hp2 | a0003 | c0017 | t0002 | g0140 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02486 | hp1 | a0001 | c0014 | t0008 | g0018 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0213 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0049 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG02559 | hp2 | a0004 | c0004 | t0004 | g0023 | AFR | ACB | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG03471 | hp2 | a0002 | c0001 | t0001 | g0052 | AFR | MSL | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG06807 | hp1 | a0004 | c0005 | t0004 | g0191 | AFR | USA | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0227 | AFR | USA | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18955 | hp1 | a0003 | c0003 | t0002 | g0042 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA18955 | hp2 | a0004 | c0004 | t0004 | g0006 | EAS | JPT | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0234 | AFR | USA | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA20300 | hp2 | a0001 | c0002 | t0005 | g0268 | AFR | USA | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA21309 | hp1 | a0004 | c0004 | t0004 | g0074 | AFR | LWK | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| NA21309 | hp2 | a0003 | c0003 | t0002 | g0004 | AFR | LWK | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| homoSapiens | chm13v2 | a0005 | c0006 | t0004 | g0193 | REF | REF | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| homoSapiens | grch38p0 | a0006 | c0011 | t0001 | g0051 | REF | REF | HCLS1_chr3_121626399_121665903 | HCLS1 | chr3 | 121626399 | 121665903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:121631907 | C | T | 1 | a0011 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.1400G>A | p.Arg467Gln | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 1484/1992 | 1400/1461 | 467/486 | chr3 | 121631907 | |||
| chr3:121632119 | C | G | 13 | a0001 a0002 a0003 others(10): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
missense_variant | MODERATE | c.1306G>C | p.Val436Leu | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 13/14 | 1390/1992 | 1306/1461 | 436/486 | chr3 | 121632119 | |||
| chr3:121632410 | C | T | 1 | a0005 | 4 | HG00140.hp1 HG00323.hp2 HG02698.hp2 others(1): Show |
missense_variant | MODERATE | c.1162G>A | p.Glu388Lys | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 12/14 | 1246/1992 | 1162/1461 | 388/486 | chr3 | 121632410 | |||
| chr3:121632468 | G | GGGCTCAG others(5): Show |
5 | a0003 a0008 a0010 others(2): Show |
106 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
disruptive_inframe_insertion | MODERATE | c.1092_1103dupTGAGCC others(6): Show |
p.Pro368_Glu369insGl others(10): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 12/14 | 1187/1992 | 1103/1461 | 368/486 | chr3 | 121632468 | |||
| chr3:121632491 | C | T | 2 | a0004 a0005 |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
missense_variant | MODERATE | c.1081G>A | p.Glu361Lys | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 12/14 | 1165/1992 | 1081/1461 | 361/486 | chr3 | 121632491 | |||
| chr3:121634245 | C | T | 1 | a0013 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.865G>A | p.Ala289Thr | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/14 | 949/1992 | 865/1461 | 289/486 | chr3 | 121634245 | |||
| chr3:121634263 | T | A | 1 | a0007 | 4 | HG01074.hp1 HG02622.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.847A>T | p.Ile283Leu | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/14 | 931/1992 | 847/1461 | 283/486 | chr3 | 121634263 | |||
| chr3:121634391 | G | A | 1 | a0012 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.719C>T | p.Ala240Val | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/14 | 803/1992 | 719/1461 | 240/486 | chr3 | 121634391 | |||
| chr3:121634407 | T | C | 11 | a0001 a0003 a0004 others(8): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
missense_variant | MODERATE | c.703A>G | p.Thr235Ala | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/14 | 787/1992 | 703/1461 | 235/486 | chr3 | 121634407 | |||
| chr3:121637215 | C | T | 1 | a0014 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.496G>A | p.Asp166Asn | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/14 | 580/1992 | 496/1461 | 166/486 | chr3 | 121637215 | |||
| chr3:121637233 | G | A | 1 | a0009 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.478C>T | p.Arg160Trp | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/14 | 562/1992 | 478/1461 | 160/486 | chr3 | 121637233 | |||
| chr3:121642972 | C | T | 1 | a0010 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.409G>A | p.Gly137Ser | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/14 | 493/1992 | 409/1461 | 137/486 | chr3 | 121642972 | |||
| chr3:121657294 | C | T | 1 | a0008 | 3 | HG02622.hp1 HG02970.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.143G>A | p.Arg48His | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/14 | 227/1992 | 143/1461 | 48/486 | chr3 | 121657294 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:121631864 | A | G | 1 | a0002c0008 | 4 | NA18956.hp1 NA19062.hp1 NA19063.hp1 others(1): Show |
synonymous_variant | LOW | c.1443T>C | p.Tyr481Tyr | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 1527/1992 | 1443/1461 | 481/486 | chr3 | 121631864 | |||
| chr3:121631921 | G | A | 2 | a0003c0017 a0008c0010 |
4 | HG02109.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.1386C>T | p.Asp462Asp | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 1470/1992 | 1386/1461 | 462/486 | chr3 | 121631921 | |||
| chr3:121632120 | A | G | 1 | a0001c0012 | 3 | NA18949.hp1 NA19005.hp2 NA19055.hp2 |
synonymous_variant | LOW | c.1305T>C | p.Ala435Ala | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 13/14 | 1389/1992 | 1305/1461 | 435/486 | chr3 | 121632120 | |||
| chr3:121634246 | T | C | 1 | a0013c0022 | 1 | NA19072.hp2 | synonymous_variant | LOW | c.864A>G | p.Pro288Pro | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/14 | 948/1992 | 864/1461 | 288/486 | chr3 | 121634246 | |||
| chr3:121635736 | G | A | 5 | a0001c0018 a0003c0003 a0010c0015 others(2): Show |
101 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
splice_region_variant&synonymous_variant | LOW | c.690C>T | p.Ala230Ala | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/14 | 774/1992 | 690/1461 | 230/486 | chr3 | 121635736 | |||
| chr3:121642940 | G | A | 4 | a0001c0002 a0001c0012 a0011c0021 others(1): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
synonymous_variant | LOW | c.441C>T | p.His147His | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/14 | 525/1992 | 441/1461 | 147/486 | chr3 | 121642940 | |||
| chr3:121644833 | C | T | 2 | a0004c0005 a0005c0006 |
14 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
synonymous_variant | LOW | c.384G>A | p.Arg128Arg | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/14 | 468/1992 | 384/1461 | 128/486 | chr3 | 121644833 | |||
| chr3:121658309 | G | A | 2 | a0001c0014 a0007c0009 |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.39C>T | p.Ser13Ser | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/14 | 123/1992 | 39/1461 | 13/486 | chr3 | 121658309 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:121631457 | T | TCA | 23 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0007 others(20): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*387_*388dupTG | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 388 | chr3 | 121631457 | ||||||
| chr3:121631600 | G | A | 1 | a0003c0013t0011 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 246 | chr3 | 121631600 | ||||||
| chr3:121631604 | A | C | 1 | a0001c0002t0005 | 34 | HG00423.hp2 HG01109.hp1 HG01256.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*242T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 242 | chr3 | 121631604 | ||||||
| chr3:121631611 | A | G | 1 | a0001c0002t0007 | 3 | NA18952.hp1 NA19060.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*235T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 235 | chr3 | 121631611 | ||||||
| chr3:121631726 | A | G | 8 | a0003c0003t0002 a0003c0013t0002 a0003c0013t0011 others(5): Show |
106 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*120T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 120 | chr3 | 121631726 | ||||||
| chr3:121631731 | G | A | 1 | a0001c0014t0008 | 2 | HG02257.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 115 | chr3 | 121631731 | ||||||
| chr3:121631736 | C | T | 13 | a0001c0007t0004 a0001c0014t0008 a0003c0003t0002 others(10): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 110 | chr3 | 121631736 | ||||||
| chr3:121631746 | C | A | 9 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0007 others(6): Show |
109 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*100G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 100 | chr3 | 121631746 | ||||||
| chr3:121631769 | G | T | 9 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0007 others(6): Show |
109 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 77 | chr3 | 121631769 | ||||||
| chr3:121631773 | G | A | 1 | a0002c0001t0009 | 2 | NA18994.hp2 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*73C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 73 | chr3 | 121631773 | ||||||
| chr3:121631808 | C | A | 1 | a0001c0002t0010 | 2 | HG02965.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*38G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 14/14 | 38 | chr3 | 121631808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:121632283 | C | T | 1 | a0002c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1240+49G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 12/13 | chr3 | 121632283 | |||||||
| chr3:121632633 | T | C | 155 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(152): Show |
221 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1009-70A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 11/13 | chr3 | 121632633 | |||||||
| chr3:121632679 | T | G | 1 | a0001c0002t0003g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1009-116A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 11/13 | chr3 | 121632679 | |||||||
| chr3:121632795 | A | G | 1 | a0003c0003t0002g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1009-232T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 11/13 | chr3 | 121632795 | |||||||
| chr3:121632903 | A | C | 196 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(193): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1008+164T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 11/13 | chr3 | 121632903 | |||||||
| chr3:121633023 | G | C | 1 | a0001c0014t0008g0018 | 2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1008+44C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 11/13 | chr3 | 121633023 | |||||||
| chr3:121633174 | G | A | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.904-3C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633174 | |||||||
| chr3:121633209 | C | T | 2 | a0002c0001t0001g0277 a0002c0001t0001g0278 |
2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.904-38G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633209 | |||||||
| chr3:121633221 | C | CT | 26 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0056 others(23): Show |
33 | HG00423.hp2 HG01109.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.904-51dupA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633221 | |||||||
| chr3:121633317 | G | A | 1 | a0003c0013t0011g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.904-146C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633317 | |||||||
| chr3:121633365 | G | A | 1 | a0001c0002t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.904-194C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633365 | |||||||
| chr3:121633477 | C | T | 4 | a0003c0013t0002g0139 a0003c0017t0002g0140 a0008c0010t0002g0034 others(1): Show |
5 | HG02109.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-306G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633477 | |||||||
| chr3:121633504 | G | A | 1 | a0002c0001t0001g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.904-333C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633504 | |||||||
| chr3:121633521 | C | T | 1 | a0002c0001t0001g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.904-350G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633521 | |||||||
| chr3:121633539 | T | TTTTATTT others(32): Show |
1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.904-369_904-368ins others(39): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633539 | |||||||
| chr3:121633597 | G | A | 1 | a0004c0004t0004g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.904-426C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633597 | |||||||
| chr3:121633672 | G | T | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.904-501C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633672 | |||||||
| chr3:121633743 | T | A | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.903+464A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633743 | |||||||
| chr3:121633759 | A | G | 1 | a0003c0013t0011g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.903+448T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633759 | |||||||
| chr3:121633898 | G | C | 46 | a0001c0007t0004g0103 a0001c0007t0004g0104 a0001c0007t0004g0105 others(43): Show |
58 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.903+309C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633898 | |||||||
| chr3:121633918 | G | C | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.903+289C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633918 | |||||||
| chr3:121633919 | C | T | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.903+288G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633919 | |||||||
| chr3:121633920 | T | A | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.903+287A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121633920 | |||||||
| chr3:121634008 | T | G | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.903+199A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121634008 | |||||||
| chr3:121634086 | A | C | 2 | a0002c0001t0001g0216 a0002c0001t0001g0227 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.903+121T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 10/13 | chr3 | 121634086 | |||||||
| chr3:121634444 | G | A | 44 | a0001c0007t0004g0105 a0001c0007t0004g0106 a0004c0004t0004g0006 others(41): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.692-26C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634444 | |||||||
| chr3:121634481 | A | C | 74 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(71): Show |
108 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.692-63T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634481 | |||||||
| chr3:121634520 | G | A | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.692-102C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634520 | |||||||
| chr3:121634521 | A | G | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.692-103T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634521 | |||||||
| chr3:121634700 | T | G | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.692-282A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634700 | |||||||
| chr3:121634710 | C | A | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.692-292G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634710 | |||||||
| chr3:121634722 | C | T | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.692-304G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634722 | |||||||
| chr3:121634764 | T | A | 1 | a0002c0001t0001g0233 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.692-346A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634764 | |||||||
| chr3:121634844 | C | A | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.692-426G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634844 | |||||||
| chr3:121634862 | G | A | 1 | a0003c0003t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.692-444C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634862 | |||||||
| chr3:121634892 | A | G | 6 | a0001c0002t0005g0056 a0001c0002t0005g0256 a0001c0002t0005g0267 others(3): Show |
7 | HG02258.hp1 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.692-474T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634892 | |||||||
| chr3:121634900 | G | T | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.692-482C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634900 | |||||||
| chr3:121634914 | G | A | 1 | a0002c0001t0001g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.692-496C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121634914 | |||||||
| chr3:121635041 | T | C | 201 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(198): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.692-623A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635041 | |||||||
| chr3:121635070 | T | G | 5 | a0004c0004t0004g0023 a0004c0004t0004g0083 a0004c0004t0004g0084 others(2): Show |
6 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-652A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635070 | |||||||
| chr3:121635088 | C | A | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.691+647G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635088 | |||||||
| chr3:121635148 | T | C | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.691+587A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635148 | |||||||
| chr3:121635149 | C | T | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.691+586G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635149 | |||||||
| chr3:121635233 | C | T | 1 | a0002c0001t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.691+502G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635233 | |||||||
| chr3:121635237 | T | C | 1 | a0002c0001t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.691+498A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TCTCTCTC others(6): Show |
1 | a0002c0001t0001g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.691+497_691+498ins others(13): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TCTCTCTC others(8): Show |
1 | a0002c0001t0001g0207 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.691+497_691+498ins others(15): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTC | 24 | a0001c0002t0003g0109 a0001c0002t0003g0110 a0001c0002t0003g0114 others(21): Show |
33 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.691+496_691+497dup others(2): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTC | 17 | a0001c0002t0003g0026 a0001c0002t0003g0111 a0001c0002t0003g0118 others(14): Show |
19 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.691+494_691+497dup others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTC | 12 | a0002c0001t0001g0044 a0002c0001t0001g0048 a0002c0001t0001g0197 others(9): Show |
12 | HG01168.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.691+492_691+497dup others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(1): Show |
9 | a0002c0001t0001g0044 a0002c0001t0001g0057 a0002c0001t0001g0208 others(6): Show |
9 | HG00642.hp1 HG01099.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.691+490_691+497dup others(8): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(3): Show |
4 | a0002c0001t0001g0005 a0002c0001t0001g0016 a0002c0001t0001g0054 others(1): Show |
4 | HG03491.hp1 HG04204.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+488_691+497dup others(10): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(5): Show |
10 | a0002c0001t0001g0005 a0002c0001t0001g0016 a0002c0001t0001g0054 others(7): Show |
11 | HG00673.hp1 HG02040.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.691+486_691+497dup others(12): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(7): Show |
8 | a0002c0001t0001g0005 a0002c0001t0001g0058 a0002c0001t0001g0201 others(5): Show |
9 | HG01192.hp1 HG02602.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.691+484_691+497dup others(14): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(9): Show |
3 | a0002c0001t0001g0206 a0002c0001t0009g0045 a0002c0008t0001g0046 |
5 | HG02132.hp1 NA18956.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.691+482_691+497dup others(16): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(11): Show |
1 | a0002c0001t0001g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.691+480_691+497dup others(18): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(13): Show |
1 | a0002c0001t0001g0047 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.691+478_691+497dup others(20): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | T | TTCTCTCT others(17): Show |
1 | a0002c0001t0001g0047 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.691+474_691+497dup others(24): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | TTC | T | 38 | a0001c0002t0003g0001 a0001c0002t0003g0125 a0001c0002t0003g0133 others(35): Show |
53 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.691+496_691+497del others(2): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | TTCTC | T | 51 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(48): Show |
74 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.691+494_691+497del others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | TTCTCTC | T | 46 | a0001c0018t0003g0159 a0002c0001t0001g0203 a0003c0003t0002g0002 others(43): Show |
59 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.691+492_691+497del others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | TTCTCTCT others(1): Show |
T | 5 | a0001c0002t0003g0012 a0001c0002t0003g0113 a0001c0002t0003g0128 others(2): Show |
5 | HG01109.hp2 HG02135.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.691+490_691+497del others(8): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | TTCTCTCT others(3): Show |
T | 1 | a0002c0001t0001g0251 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.691+488_691+497del others(10): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | TTCTCTCT others(5): Show |
T | 1 | a0004c0004t0004g0082 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.691+486_691+497del others(12): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635237 | TTCTCTCT others(7): Show |
T | 41 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0019 others(38): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.691+484_691+497del others(14): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635237 | |||||||
| chr3:121635239 | C | T | 1 | a0001c0002t0005g0131 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.691+496G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635239 | |||||||
| chr3:121635274 | T | TCTCTCTC others(3): Show |
1 | a0002c0001t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.691+460_691+461ins others(10): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635274 | |||||||
| chr3:121635334 | G | A | 1 | a0002c0001t0001g0205 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.691+401C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635334 | |||||||
| chr3:121635356 | C | T | 1 | a0001c0002t0003g0125 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.691+379G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635356 | |||||||
| chr3:121635409 | C | T | 1 | a0001c0002t0005g0253 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.691+326G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635409 | |||||||
| chr3:121635534 | A | T | 201 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(198): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.691+201T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 9/13 | chr3 | 121635534 | |||||||
| chr3:121636035 | A | G | 1 | a0004c0005t0004g0190 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.622-231T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636035 | |||||||
| chr3:121636078 | T | C | 196 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(193): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.622-274A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636078 | |||||||
| chr3:121636124 | G | T | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.621+310C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636124 | |||||||
| chr3:121636255 | C | A | 196 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(193): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.621+179G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636255 | |||||||
| chr3:121636261 | T | C | 1 | a0003c0003t0002g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.621+173A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636261 | |||||||
| chr3:121636303 | G | A | 5 | a0001c0002t0005g0254 a0001c0002t0005g0261 a0001c0002t0005g0262 others(2): Show |
5 | NA18992.hp2 NA19005.hp1 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+131C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636303 | |||||||
| chr3:121636386 | C | T | 2 | a0002c0001t0001g0215 a0002c0001t0001g0226 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.621+48G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636386 | |||||||
| chr3:121636414 | T | C | 1 | a0001c0002t0005g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.621+20A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636414 | |||||||
| chr3:121636423 | C | T | 1 | a0001c0002t0003g0129 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.621+11G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 8/13 | chr3 | 121636423 | |||||||
| chr3:121636645 | A | G | 2 | a0003c0003t0002g0091 a0003c0003t0002g0096 |
2 | HG00280.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.566-156T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/13 | chr3 | 121636645 | |||||||
| chr3:121636680 | A | C | 1 | a0003c0003t0002g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.566-191T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/13 | chr3 | 121636680 | |||||||
| chr3:121636786 | G | T | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.566-297C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/13 | chr3 | 121636786 | |||||||
| chr3:121636875 | C | T | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.565+271G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/13 | chr3 | 121636875 | |||||||
| chr3:121636876 | T | C | 201 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(198): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.565+270A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/13 | chr3 | 121636876 | |||||||
| chr3:121637072 | G | A | 2 | a0003c0003t0002g0154 a0004c0005t0004g0189 |
2 | HG02129.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.565+74C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 7/13 | chr3 | 121637072 | |||||||
| chr3:121637266 | A | G | 1 | a0004c0005t0004g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.455-10T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637266 | |||||||
| chr3:121637391 | G | A | 1 | a0002c0001t0001g0200 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.455-135C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637391 | |||||||
| chr3:121637521 | A | C | 196 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(193): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.455-265T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637521 | |||||||
| chr3:121637547 | G | GA | 25 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0056 others(22): Show |
32 | HG00423.hp2 HG01109.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.455-292dupT | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637547 | |||||||
| chr3:121637596 | A | T | 1 | a0002c0001t0001g0242 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.455-340T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637596 | |||||||
| chr3:121637716 | C | T | 1 | a0003c0003t0002g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.455-460G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637716 | |||||||
| chr3:121637809 | G | A | 42 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0019 others(39): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.455-553C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637809 | |||||||
| chr3:121637863 | G | T | 2 | a0001c0002t0003g0128 a0001c0014t0008g0018 |
3 | HG02257.hp2 HG02486.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.455-607C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637863 | |||||||
| chr3:121637872 | G | A | 74 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(71): Show |
108 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.455-616C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637872 | |||||||
| chr3:121637885 | A | G | 74 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(71): Show |
108 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.455-629T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637885 | |||||||
| chr3:121637922 | C | A | 1 | a0001c0002t0003g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.455-666G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121637922 | |||||||
| chr3:121638039 | A | C | 3 | a0003c0017t0002g0140 a0008c0010t0002g0034 a0008c0010t0002g0138 |
4 | HG02109.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-783T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121638039 | |||||||
| chr3:121638059 | ACCCAAGG others(19): Show |
A | 1 | a0013c0022t0003g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.455-829_455-804del others(26): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121638059 | |||||||
| chr3:121638240 | A | T | 1 | a0003c0003t0002g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.455-984T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121638240 | |||||||
| chr3:121638655 | A | G | 1 | a0007c0009t0006g0066 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.455-1399T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121638655 | |||||||
| chr3:121638774 | T | C | 1 | a0004c0004t0004g0022 | 2 | HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.455-1518A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121638774 | |||||||
| chr3:121638779 | G | C | 42 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0019 others(39): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.455-1523C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121638779 | |||||||
| chr3:121639010 | AAC | A | 57 | a0001c0007t0004g0105 a0001c0007t0004g0106 a0003c0003t0002g0038 others(54): Show |
72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.455-1756_455-1755d others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639010 | |||||||
| chr3:121639010 | AACACACA others(9): Show |
A | 1 | a0003c0013t0011g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.455-1770_455-1755d others(18): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639010 | |||||||
| chr3:121639017 | ACACACAC others(1): Show |
A | 5 | a0001c0002t0005g0254 a0001c0002t0005g0261 a0001c0002t0005g0262 others(2): Show |
5 | NA18992.hp2 NA19005.hp1 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-1769_455-1762d others(10): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639017 | |||||||
| chr3:121639019 | A | ACACG | 5 | a0001c0007t0004g0103 a0001c0007t0004g0104 a0003c0003t0002g0002 others(2): Show |
6 | HG03041.hp2 HG03139.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-1764_455-1763i others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639019 | |||||||
| chr3:121639019 | ACACACG | A | 86 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(83): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.455-1769_455-1764d others(8): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639019 | |||||||
| chr3:121639021 | ACACG | A | 6 | a0001c0002t0005g0275 a0003c0003t0002g0171 a0003c0017t0002g0140 others(3): Show |
7 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.455-1769_455-1766d others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639021 | |||||||
| chr3:121639023 | A | G | 37 | a0001c0018t0003g0159 a0003c0003t0002g0002 a0003c0003t0002g0013 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(47): Show |
intron_variant | MODIFIER | c.455-1767T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639023 | |||||||
| chr3:121639025 | G | A | 41 | a0001c0007t0004g0103 a0001c0007t0004g0104 a0001c0018t0003g0159 others(38): Show |
57 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(54): Show |
intron_variant | MODIFIER | c.455-1769C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639025 | |||||||
| chr3:121639025 | G | GCA | 4 | a0002c0001t0001g0003 a0002c0001t0001g0052 a0002c0001t0001g0207 others(1): Show |
4 | HG00639.hp1 HG00639.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-1771_455-1770d others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639025 | |||||||
| chr3:121639025 | GCA | G | 6 | a0002c0001t0001g0218 a0002c0008t0001g0199 a0007c0009t0006g0064 others(3): Show |
6 | HG00642.hp1 HG01074.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-1771_455-1770d others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639025 | |||||||
| chr3:121639027 | A | G | 10 | a0001c0002t0005g0270 a0001c0002t0005g0275 a0002c0001t0001g0197 others(7): Show |
11 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.455-1771T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639027 | |||||||
| chr3:121639029 | A | G | 88 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(85): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.455-1773T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639029 | |||||||
| chr3:121639031 | A | G | 5 | a0001c0002t0005g0254 a0001c0002t0005g0261 a0001c0002t0005g0262 others(2): Show |
5 | NA18992.hp2 NA19005.hp1 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-1775T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639031 | |||||||
| chr3:121639039 | A | G | 1 | a0003c0013t0011g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.455-1783T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639039 | |||||||
| chr3:121639058 | A | C | 1 | a0003c0003t0002g0158 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.455-1802T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639058 | |||||||
| chr3:121639168 | A | T | 1 | a0003c0003t0002g0095 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.455-1912T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639168 | |||||||
| chr3:121639230 | A | C | 5 | a0004c0004t0004g0023 a0004c0004t0004g0083 a0004c0004t0004g0084 others(2): Show |
6 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-1974T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639230 | |||||||
| chr3:121639259 | T | C | 1 | a0002c0001t0001g0242 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.455-2003A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639259 | |||||||
| chr3:121639289 | T | C | 1 | a0002c0001t0001g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.455-2033A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639289 | |||||||
| chr3:121639407 | T | G | 1 | a0003c0003t0002g0150 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.455-2151A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639407 | |||||||
| chr3:121639521 | AT | A | 113 | a0001c0007t0004g0103 a0001c0007t0004g0104 a0001c0007t0004g0105 others(110): Show |
155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.455-2266delA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639521 | |||||||
| chr3:121639523 | T | TTA | 4 | a0003c0003t0002g0100 a0003c0003t0002g0157 a0003c0013t0002g0139 others(1): Show |
4 | HG02615.hp1 HG02683.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-2268_455-2267i others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639523 | |||||||
| chr3:121639525 | T | A | 5 | a0003c0017t0002g0140 a0005c0006t0004g0184 a0005c0006t0004g0194 others(2): Show |
6 | HG00140.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-2269A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639525 | |||||||
| chr3:121639526 | A | T | 9 | a0003c0003t0002g0100 a0003c0003t0002g0157 a0003c0013t0002g0139 others(6): Show |
10 | HG00140.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.455-2270T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639526 | |||||||
| chr3:121639527 | T | TTTG | 3 | a0001c0002t0005g0056 a0001c0002t0005g0272 a0001c0014t0008g0018 |
5 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-2272_455-2271i others(5): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639527 | |||||||
| chr3:121639530 | T | G | 10 | a0001c0002t0005g0056 a0001c0002t0005g0272 a0001c0014t0008g0018 others(7): Show |
12 | HG01074.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-2274A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639530 | |||||||
| chr3:121639530 | T | TTGTTG | 2 | a0008c0010t0002g0034 a0008c0010t0002g0138 |
3 | HG02622.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.455-2275_455-2274i others(7): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639530 | |||||||
| chr3:121639530 | T | TTTG | 69 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(66): Show |
102 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.455-2277_455-2275d others(5): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639530 | |||||||
| chr3:121639530 | T | TTTGTTG | 4 | a0001c0002t0003g0124 a0001c0002t0005g0266 a0001c0002t0010g0126 others(1): Show |
4 | HG02965.hp1 HG03041.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-2280_455-2275d others(8): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639530 | |||||||
| chr3:121639533 | G | T | 34 | a0001c0007t0004g0104 a0001c0007t0004g0105 a0001c0007t0004g0106 others(31): Show |
43 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.455-2277C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639533 | |||||||
| chr3:121639536 | G | T | 2 | a0004c0004t0004g0085 a0004c0005t0004g0191 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.455-2280C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639536 | |||||||
| chr3:121639539 | G | T | 1 | a0004c0005t0004g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.455-2283C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639539 | |||||||
| chr3:121639601 | T | C | 76 | a0001c0018t0003g0159 a0003c0003t0002g0002 a0003c0003t0002g0004 others(73): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.455-2345A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639601 | |||||||
| chr3:121639823 | C | T | 1 | a0001c0002t0003g0115 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.455-2567G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639823 | |||||||
| chr3:121639849 | C | T | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-2593G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639849 | |||||||
| chr3:121639850 | T | C | 201 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(198): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.455-2594A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639850 | |||||||
| chr3:121639902 | CA | C | 2 | a0004c0004t0004g0020 a0004c0004t0004g0077 |
3 | HG01496.hp2 HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.455-2647delT | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639902 | |||||||
| chr3:121639971 | G | A | 1 | a0001c0002t0005g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455-2715C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121639971 | |||||||
| chr3:121640468 | G | A | 1 | a0002c0008t0001g0199 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.454+2459C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640468 | |||||||
| chr3:121640587 | T | C | 4 | a0001c0002t0003g0031 a0001c0002t0003g0112 a0001c0002t0003g0127 others(1): Show |
5 | NA18968.hp1 NA19009.hp2 NA19084.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+2340A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640587 | |||||||
| chr3:121640619 | C | G | 2 | a0001c0002t0003g0117 a0011c0021t0003g0119 |
2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.454+2308G>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640619 | |||||||
| chr3:121640702 | A | G | 2 | a0003c0003t0002g0039 a0003c0003t0002g0157 |
3 | HG01884.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.454+2225T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640702 | |||||||
| chr3:121640715 | A | T | 1 | a0001c0002t0005g0253 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.454+2212T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640715 | |||||||
| chr3:121640778 | A | C | 1 | a0002c0001t0001g0223 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.454+2149T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640778 | |||||||
| chr3:121640782 | AAGGGG | A | 126 | a0001c0007t0004g0103 a0001c0007t0004g0104 a0001c0014t0008g0018 others(123): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.454+2140_454+2144d others(7): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640782 | |||||||
| chr3:121640782 | AAGGGGAG others(3): Show |
A | 74 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(71): Show |
108 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.454+2135_454+2144d others(12): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640782 | |||||||
| chr3:121640787 | G | A | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.454+2140C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640787 | |||||||
| chr3:121640812 | G | C | 1 | a0003c0003t0002g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.454+2115C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640812 | |||||||
| chr3:121640817 | C | G | 1 | a0003c0003t0002g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.454+2110G>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640817 | |||||||
| chr3:121640827 | G | A | 1 | a0003c0003t0002g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.454+2100C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640827 | |||||||
| chr3:121640828 | A | G | 1 | a0003c0003t0002g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.454+2099T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640828 | |||||||
| chr3:121640835 | G | A | 1 | a0001c0002t0003g0025 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.454+2092C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640835 | |||||||
| chr3:121640837 | GAGGGC | G | 76 | a0001c0018t0003g0159 a0003c0003t0002g0002 a0003c0003t0002g0004 others(73): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.454+2085_454+2089d others(7): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640837 | |||||||
| chr3:121640837 | GAGGGCAG others(13): Show |
G | 2 | a0002c0001t0001g0057 a0002c0001t0001g0231 |
2 | HG01433.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.454+2070_454+2089d others(22): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640837 | |||||||
| chr3:121640874 | G | A | 1 | a0003c0003t0002g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.454+2053C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121640874 | |||||||
| chr3:121641006 | A | G | 1 | a0003c0003t0002g0092 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.454+1921T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641006 | |||||||
| chr3:121641206 | A | T | 1 | a0002c0001t0001g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.454+1721T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641206 | |||||||
| chr3:121641266 | G | GAGAT | 2 | a0003c0003t0002g0039 a0003c0003t0002g0157 |
3 | HG01884.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.454+1657_454+1660d others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641266 | |||||||
| chr3:121641327 | A | C | 1 | a0001c0002t0003g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.454+1600T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641327 | |||||||
| chr3:121641380 | T | C | 12 | a0004c0005t0004g0014 a0004c0005t0004g0185 a0004c0005t0004g0186 others(9): Show |
14 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.454+1547A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641380 | |||||||
| chr3:121641495 | T | A | 1 | a0001c0002t0003g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.454+1432A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641495 | |||||||
| chr3:121641573 | A | G | 2 | a0003c0003t0002g0093 a0003c0003t0002g0102 |
2 | HG00140.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.454+1354T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641573 | |||||||
| chr3:121641594 | GAAC | G | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+1330_454+1332d others(5): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641594 | |||||||
| chr3:121641626 | G | T | 1 | a0004c0004t0004g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.454+1301C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641626 | |||||||
| chr3:121641807 | C | A | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.454+1120G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641807 | |||||||
| chr3:121641808 | G | T | 2 | a0002c0001t0001g0210 a0002c0001t0001g0225 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.454+1119C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641808 | |||||||
| chr3:121641874 | G | A | 128 | a0001c0007t0003g0098 a0001c0007t0004g0103 a0001c0007t0004g0104 others(125): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.454+1053C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641874 | |||||||
| chr3:121641926 | A | G | 1 | a0004c0004t0004g0075 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.454+1001T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641926 | |||||||
| chr3:121641970 | C | T | 2 | a0002c0001t0001g0277 a0002c0001t0001g0278 |
2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.454+957G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121641970 | |||||||
| chr3:121642045 | A | C | 72 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0003c0003t0002g0002 others(69): Show |
102 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.454+882T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642045 | |||||||
| chr3:121642071 | C | A | 2 | a0003c0003t0002g0148 a0003c0003t0002g0167 |
2 | NA18943.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.454+856G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642071 | |||||||
| chr3:121642079 | C | CA | 105 | a0001c0002t0003g0109 a0001c0002t0003g0116 a0001c0002t0003g0127 others(102): Show |
148 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.454+847dupT | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642079 | |||||||
| chr3:121642079 | C | CAA | 20 | a0001c0014t0008g0018 a0002c0001t0001g0203 a0002c0001t0001g0232 others(17): Show |
23 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.454+846_454+847dup others(2): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642079 | |||||||
| chr3:121642092 | A | C | 3 | a0003c0017t0002g0140 a0008c0010t0002g0034 a0008c0010t0002g0138 |
4 | HG02109.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+835T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642092 | |||||||
| chr3:121642103 | A | T | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.454+824T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642103 | |||||||
| chr3:121642211 | G | A | 2 | a0003c0003t0002g0148 a0003c0003t0002g0167 |
2 | NA18943.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.454+716C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642211 | |||||||
| chr3:121642251 | A | T | 1 | a0004c0004t0004g0087 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.454+676T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642251 | |||||||
| chr3:121642263 | T | C | 2 | a0002c0001t0001g0277 a0002c0001t0001g0278 |
2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.454+664A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642263 | |||||||
| chr3:121642303 | C | CA | 107 | a0001c0002t0003g0129 a0001c0002t0003g0265 a0001c0002t0005g0008 others(104): Show |
144 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.454+623dupT | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642303 | |||||||
| chr3:121642303 | C | CAA | 53 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(50): Show |
81 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.454+622_454+623dup others(2): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642303 | |||||||
| chr3:121642303 | CA | C | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+623delT | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642303 | |||||||
| chr3:121642397 | A | T | 6 | a0002c0001t0001g0048 a0002c0001t0001g0049 a0002c0001t0001g0211 others(3): Show |
8 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+530T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642397 | |||||||
| chr3:121642498 | G | A | 77 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0003c0003t0002g0002 others(74): Show |
108 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.454+429C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642498 | |||||||
| chr3:121642713 | C | A | 3 | a0003c0017t0002g0140 a0008c0010t0002g0034 a0008c0010t0002g0138 |
4 | HG02109.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+214G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642713 | |||||||
| chr3:121642747 | G | T | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+180C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642747 | |||||||
| chr3:121642799 | G | A | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.454+128C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 6/13 | chr3 | 121642799 | |||||||
| chr3:121643180 | T | G | 1 | a0002c0001t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.400-199A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121643180 | |||||||
| chr3:121643560 | A | T | 42 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0019 others(39): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.400-579T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121643560 | |||||||
| chr3:121643792 | T | C | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.400-811A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121643792 | |||||||
| chr3:121643862 | G | C | 2 | a0003c0003t0002g0149 a0003c0003t0002g0161 |
2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.400-881C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121643862 | |||||||
| chr3:121643980 | G | A | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.399+838C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121643980 | |||||||
| chr3:121644103 | C | A | 1 | a0001c0014t0008g0018 | 2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.399+715G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644103 | |||||||
| chr3:121644116 | G | T | 1 | a0002c0001t0001g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.399+702C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644116 | |||||||
| chr3:121644181 | TGAGTTCA others(38): Show |
T | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.399+592_399+636del others(45): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644181 | |||||||
| chr3:121644539 | G | A | 5 | a0004c0004t0004g0023 a0004c0004t0004g0083 a0004c0004t0004g0084 others(2): Show |
6 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+279C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644539 | |||||||
| chr3:121644547 | T | C | 1 | a0001c0002t0003g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.399+271A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644547 | |||||||
| chr3:121644556 | G | C | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.399+262C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644556 | |||||||
| chr3:121644711 | A | G | 1 | a0001c0002t0005g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.399+107T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644711 | |||||||
| chr3:121644802 | G | C | 2 | a0003c0003t0002g0061 a0003c0003t0002g0062 |
2 | HG00735.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.399+16C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 5/13 | chr3 | 121644802 | |||||||
| chr3:121645084 | C | T | 1 | a0002c0001t0001g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.289-156G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645084 | |||||||
| chr3:121645095 | T | C | 1 | a0007c0009t0006g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.289-167A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645095 | |||||||
| chr3:121645161 | C | G | 1 | a0003c0003t0002g0093 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.289-233G>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645161 | |||||||
| chr3:121645243 | A | G | 1 | a0001c0002t0003g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.289-315T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645243 | |||||||
| chr3:121645326 | A | T | 14 | a0002c0001t0001g0003 a0002c0001t0001g0015 a0002c0001t0001g0050 others(11): Show |
26 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-398T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645326 | |||||||
| chr3:121645389 | A | G | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.289-461T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645389 | |||||||
| chr3:121645404 | A | T | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.289-476T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645404 | |||||||
| chr3:121645489 | G | C | 4 | a0007c0009t0006g0064 a0007c0009t0006g0065 a0007c0009t0006g0066 others(1): Show |
4 | HG01074.hp1 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-561C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645489 | |||||||
| chr3:121645597 | A | G | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.289-669T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645597 | |||||||
| chr3:121645640 | T | C | 202 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(199): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.289-712A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645640 | |||||||
| chr3:121645777 | C | T | 44 | a0001c0007t0004g0105 a0001c0007t0004g0106 a0004c0004t0004g0006 others(41): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.289-849G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645777 | |||||||
| chr3:121645828 | A | C | 1 | a0003c0003t0002g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.289-900T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645828 | |||||||
| chr3:121645933 | C | T | 44 | a0001c0007t0004g0105 a0001c0007t0004g0106 a0004c0004t0004g0006 others(41): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.289-1005G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121645933 | |||||||
| chr3:121646151 | T | TATATA | 216 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(213): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.288+1163_288+1167d others(7): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646151 | |||||||
| chr3:121646214 | TTATATAT others(12): Show |
T | 1 | a0002c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.288+1086_288+1104d others(21): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646214 | |||||||
| chr3:121646272 | T | C | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.288+1047A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646272 | |||||||
| chr3:121646287 | A | G | 2 | a0003c0003t0002g0150 a0003c0003t0002g0163 |
2 | NA18978.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.288+1032T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646287 | |||||||
| chr3:121646348 | AATAT | A | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+967_288+970del others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646348 | |||||||
| chr3:121646356 | AC | A | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+962delG | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646356 | |||||||
| chr3:121646364 | T | G | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+955A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646364 | |||||||
| chr3:121646365 | TAC | T | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+952_288+953del others(2): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646365 | |||||||
| chr3:121646371 | TTATTACT others(8): Show |
T | 14 | a0002c0001t0001g0003 a0002c0001t0001g0015 a0002c0001t0001g0050 others(11): Show |
26 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.288+933_288+947del others(15): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646371 | |||||||
| chr3:121646372 | T | A | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+947A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646372 | |||||||
| chr3:121646377 | CTATGTAA others(1): Show |
C | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+934_288+941del others(8): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646377 | |||||||
| chr3:121646388 | ATTACTAT | A | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+924_288+930del others(7): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646388 | |||||||
| chr3:121646401 | A | ATATTACT others(6): Show |
1 | a0001c0002t0005g0261 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.288+917_288+918ins others(13): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646401 | |||||||
| chr3:121646414 | A | T | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+905T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646414 | |||||||
| chr3:121646415 | TA | T | 14 | a0002c0001t0001g0003 a0002c0001t0001g0015 a0002c0001t0001g0050 others(11): Show |
26 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.288+903delT | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646415 | |||||||
| chr3:121646447 | T | TTATATAT others(27): Show |
1 | a0003c0003t0002g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.288+838_288+871dup others(34): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646447 | |||||||
| chr3:121646482 | G | T | 15 | a0003c0003t0002g0013 a0003c0003t0002g0037 a0003c0003t0002g0038 others(12): Show |
20 | HG00408.hp2 HG00621.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.288+837C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646482 | |||||||
| chr3:121646484 | T | C | 1 | a0001c0002t0003g0128 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.288+835A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646484 | |||||||
| chr3:121646508 | T | C | 1 | a0002c0001t0001g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.288+811A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646508 | |||||||
| chr3:121646535 | A | C | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.288+784T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646535 | |||||||
| chr3:121646564 | A | G | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+755T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646564 | |||||||
| chr3:121646566 | T | A | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+753A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646566 | |||||||
| chr3:121646567 | T | A | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+752A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646567 | |||||||
| chr3:121646568 | A | T | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+751T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646568 | |||||||
| chr3:121646569 | T | A | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+750A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646569 | |||||||
| chr3:121646570 | T | A | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+749A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646570 | |||||||
| chr3:121646572 | C | T | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+747G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646572 | |||||||
| chr3:121646597 | T | C | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288+722A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646597 | |||||||
| chr3:121646609 | C | T | 1 | a0002c0001t0001g0222 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.288+710G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646609 | |||||||
| chr3:121646644 | A | C | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.288+675T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646644 | |||||||
| chr3:121646672 | T | A | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.288+647A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646672 | |||||||
| chr3:121646684 | T | A | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.288+635A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646684 | |||||||
| chr3:121646688 | AAATAT | A | 28 | a0001c0002t0003g0265 a0001c0002t0005g0008 a0001c0002t0005g0009 others(25): Show |
35 | HG00423.hp2 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.288+626_288+630del others(5): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646688 | |||||||
| chr3:121646718 | A | C | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.288+601T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646718 | |||||||
| chr3:121646868 | A | G | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.288+451T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646868 | |||||||
| chr3:121646985 | A | T | 154 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(151): Show |
220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.288+334T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646985 | |||||||
| chr3:121646986 | T | A | 154 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(151): Show |
220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.288+333A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646986 | |||||||
| chr3:121646987 | T | A | 1 | a0003c0003t0002g0162 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.288+332A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646987 | |||||||
| chr3:121646989 | T | A | 2 | a0001c0007t0004g0104 a0005c0006t0004g0195 |
2 | HG00323.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.288+330A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646989 | |||||||
| chr3:121646991 | T | A | 78 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(75): Show |
113 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.288+328A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121646991 | |||||||
| chr3:121647082 | C | T | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+237G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121647082 | |||||||
| chr3:121647106 | TGA | T | 9 | a0001c0002t0003g0025 a0001c0002t0003g0026 a0001c0002t0003g0033 others(6): Show |
12 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.288+211_288+212del others(2): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121647106 | |||||||
| chr3:121647139 | G | A | 44 | a0001c0007t0004g0105 a0001c0007t0004g0106 a0004c0004t0004g0006 others(41): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.288+180C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121647139 | |||||||
| chr3:121647148 | A | G | 2 | a0001c0002t0003g0029 a0001c0002t0003g0123 |
3 | HG02040.hp1 NA18990.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.288+171T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121647148 | |||||||
| chr3:121647254 | T | C | 2 | a0003c0003t0002g0150 a0003c0003t0002g0163 |
2 | NA18978.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.288+65A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121647254 | |||||||
| chr3:121647260 | C | T | 1 | a0002c0001t0001g0055 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.288+59G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121647260 | |||||||
| chr3:121647276 | C | T | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.288+43G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 4/13 | chr3 | 121647276 | |||||||
| chr3:121647530 | A | G | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.159-82T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121647530 | |||||||
| chr3:121647634 | A | G | 1 | a0001c0002t0003g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159-186T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121647634 | |||||||
| chr3:121647639 | C | G | 1 | a0001c0002t0003g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.159-191G>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121647639 | |||||||
| chr3:121647744 | T | G | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-296A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121647744 | |||||||
| chr3:121647790 | T | A | 2 | a0002c0001t0001g0277 a0002c0001t0001g0278 |
2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.159-342A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121647790 | |||||||
| chr3:121647931 | A | T | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-483T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121647931 | |||||||
| chr3:121648338 | A | C | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-890T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121648338 | |||||||
| chr3:121648524 | G | T | 1 | a0002c0001t0001g0204 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159-1076C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121648524 | |||||||
| chr3:121648600 | G | A | 2 | a0002c0001t0001g0233 a0002c0001t0001g0241 |
2 | HG01168.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.159-1152C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121648600 | |||||||
| chr3:121648611 | A | T | 1 | a0002c0001t0001g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.159-1163T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121648611 | |||||||
| chr3:121648747 | G | A | 1 | a0002c0001t0001g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159-1299C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121648747 | |||||||
| chr3:121648768 | G | T | 1 | a0002c0001t0001g0241 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.159-1320C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121648768 | |||||||
| chr3:121649022 | A | G | 3 | a0002c0008t0001g0046 a0002c0008t0001g0198 a0002c0008t0001g0199 |
4 | NA18956.hp1 NA19062.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-1574T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649022 | |||||||
| chr3:121649028 | A | T | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-1580T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649028 | |||||||
| chr3:121649051 | T | C | 1 | a0002c0001t0001g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159-1603A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649051 | |||||||
| chr3:121649137 | A | C | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-1689T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649137 | |||||||
| chr3:121649233 | T | TTTA | 3 | a0005c0006t0004g0184 a0005c0006t0004g0194 a0005c0006t0004g0195 |
3 | HG00140.hp1 HG00323.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.159-1788_159-1786d others(5): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649233 | |||||||
| chr3:121649252 | T | A | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-1804A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649252 | |||||||
| chr3:121649258 | C | A | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-1810G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649258 | |||||||
| chr3:121649329 | G | A | 3 | a0001c0002t0005g0261 a0001c0002t0005g0262 a0001c0002t0005g0263 |
3 | NA19005.hp1 NA19082.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.159-1881C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649329 | |||||||
| chr3:121649536 | A | G | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.159-2088T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649536 | |||||||
| chr3:121649844 | GTGTT | G | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-2400_159-2397d others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649844 | |||||||
| chr3:121649953 | A | C | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-2505T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121649953 | |||||||
| chr3:121650025 | A | G | 6 | a0002c0001t0001g0048 a0002c0001t0001g0049 a0002c0001t0001g0211 others(3): Show |
8 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-2577T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650025 | |||||||
| chr3:121650142 | C | G | 1 | a0002c0001t0001g0048 | 2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.159-2694G>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650142 | |||||||
| chr3:121650186 | G | T | 1 | a0003c0003t0002g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.159-2738C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650186 | |||||||
| chr3:121650239 | T | A | 1 | a0001c0007t0004g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.159-2791A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650239 | |||||||
| chr3:121650244 | C | T | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.159-2796G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650244 | |||||||
| chr3:121650360 | A | C | 37 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0019 others(34): Show |
48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.159-2912T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650360 | |||||||
| chr3:121650373 | CT | C | 33 | a0001c0002t0003g0117 a0001c0002t0003g0265 a0001c0002t0005g0008 others(30): Show |
41 | HG00423.hp2 HG01074.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.159-2926delA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650373 | |||||||
| chr3:121650506 | T | C | 1 | a0002c0001t0001g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159-3058A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650506 | |||||||
| chr3:121650557 | A | T | 1 | a0002c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-3109T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650557 | |||||||
| chr3:121650714 | A | G | 1 | a0004c0005t0004g0190 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.159-3266T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650714 | |||||||
| chr3:121650762 | C | T | 1 | a0001c0007t0004g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.159-3314G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650762 | |||||||
| chr3:121650867 | G | C | 9 | a0002c0001t0001g0016 a0002c0001t0001g0200 a0002c0001t0001g0201 others(6): Show |
13 | HG00673.hp1 NA18956.hp1 NA18963.hp2 others(10): Show |
intron_variant | MODIFIER | c.159-3419C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650867 | |||||||
| chr3:121650909 | G | A | 1 | a0002c0001t0001g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.159-3461C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650909 | |||||||
| chr3:121650951 | T | C | 1 | a0001c0007t0004g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.159-3503A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650951 | |||||||
| chr3:121650964 | C | T | 1 | a0002c0001t0001g0047 | 2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.159-3516G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121650964 | |||||||
| chr3:121651009 | G | A | 7 | a0001c0007t0004g0103 a0001c0007t0004g0104 a0001c0014t0008g0018 others(4): Show |
8 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-3561C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121651009 | |||||||
| chr3:121651545 | T | C | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-4097A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121651545 | |||||||
| chr3:121651608 | T | G | 44 | a0001c0007t0004g0105 a0001c0007t0004g0106 a0004c0004t0004g0006 others(41): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.159-4160A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121651608 | |||||||
| chr3:121651834 | G | A | 1 | a0002c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.159-4386C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121651834 | |||||||
| chr3:121651903 | G | A | 1 | a0001c0007t0004g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.159-4455C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121651903 | |||||||
| chr3:121652095 | G | T | 1 | a0003c0003t0002g0041 | 2 | NA18962.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.159-4647C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652095 | |||||||
| chr3:121652110 | C | T | 2 | a0004c0004t0004g0010 a0004c0004t0004g0074 |
4 | HG01069.hp1 HG01071.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-4662G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652110 | |||||||
| chr3:121652216 | T | C | 202 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(199): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.159-4768A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652216 | |||||||
| chr3:121652608 | C | T | 1 | a0003c0003t0002g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.158+4671G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652608 | |||||||
| chr3:121652655 | G | A | 1 | a0002c0001t0001g0055 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.158+4624C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652655 | |||||||
| chr3:121652856 | T | C | 1 | a0001c0002t0005g0264 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.158+4423A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652856 | |||||||
| chr3:121652884 | G | A | 5 | a0003c0003t0002g0041 a0003c0003t0002g0153 a0003c0003t0002g0164 others(2): Show |
6 | HG02071.hp1 NA18954.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+4395C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652884 | |||||||
| chr3:121652900 | T | C | 1 | a0001c0007t0004g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.158+4379A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652900 | |||||||
| chr3:121652916 | A | T | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158+4363T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652916 | |||||||
| chr3:121652988 | C | T | 1 | a0001c0002t0003g0122 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.158+4291G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121652988 | |||||||
| chr3:121653001 | C | T | 11 | a0001c0002t0005g0008 a0001c0002t0005g0252 a0001c0002t0005g0253 others(8): Show |
14 | HG00423.hp2 HG01109.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.158+4278G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653001 | |||||||
| chr3:121653084 | C | T | 3 | a0001c0007t0004g0105 a0001c0007t0004g0106 a0002c0001t0001g0202 |
3 | HG01891.hp2 HG03225.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.158+4195G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653084 | |||||||
| chr3:121653195 | C | T | 2 | a0001c0002t0005g0253 a0001c0002t0005g0257 |
2 | HG00423.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.158+4084G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653195 | |||||||
| chr3:121653351 | G | A | 3 | a0002c0001t0001g0235 a0002c0001t0001g0237 a0009c0020t0001g0236 |
3 | HG02027.hp1 HG02074.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.158+3928C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653351 | |||||||
| chr3:121653666 | C | T | 42 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0019 others(39): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.158+3613G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653666 | |||||||
| chr3:121653728 | C | T | 1 | a0001c0002t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.158+3551G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653728 | |||||||
| chr3:121653776 | A | G | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.158+3503T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653776 | |||||||
| chr3:121653787 | A | G | 2 | a0002c0001t0001g0201 a0002c0001t0009g0045 |
3 | NA18994.hp2 NA19054.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.158+3492T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653787 | |||||||
| chr3:121653882 | G | A | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158+3397C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121653882 | |||||||
| chr3:121654028 | A | G | 202 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(199): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.158+3251T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654028 | |||||||
| chr3:121654032 | T | A | 1 | a0003c0003t0002g0177 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.158+3247A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654032 | |||||||
| chr3:121654183 | G | A | 1 | a0003c0003t0002g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.158+3096C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654183 | |||||||
| chr3:121654211 | T | C | 73 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(70): Show |
103 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.158+3068A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654211 | |||||||
| chr3:121654264 | T | C | 202 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(199): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.158+3015A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654264 | |||||||
| chr3:121654446 | A | T | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158+2833T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654446 | |||||||
| chr3:121654524 | T | G | 1 | a0001c0007t0004g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.158+2755A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654524 | |||||||
| chr3:121654770 | T | C | 1 | a0002c0001t0001g0237 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+2509A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654770 | |||||||
| chr3:121654838 | C | T | 2 | a0003c0003t0002g0037 a0003c0003t0002g0154 |
3 | HG02129.hp1 NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.158+2441G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121654838 | |||||||
| chr3:121655030 | A | G | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+2249T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655030 | |||||||
| chr3:121655098 | G | A | 1 | a0003c0003t0002g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.158+2181C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655098 | |||||||
| chr3:121655439 | T | C | 2 | a0001c0007t0004g0105 a0001c0007t0004g0106 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.158+1840A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655439 | |||||||
| chr3:121655462 | C | CT | 32 | a0002c0001t0001g0196 a0002c0001t0001g0197 a0002c0001t0001g0200 others(29): Show |
33 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.158+1816dupA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655462 | |||||||
| chr3:121655462 | C | CTTTTT | 20 | a0004c0004t0004g0020 a0004c0004t0004g0021 a0004c0004t0004g0022 others(17): Show |
23 | HG00733.hp1 HG01168.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.158+1812_158+1816d others(7): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655462 | |||||||
| chr3:121655462 | C | CTTTTTT | 16 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0023 others(13): Show |
22 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.158+1811_158+1816d others(8): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655462 | |||||||
| chr3:121655462 | C | CTTTTTTT | 5 | a0004c0004t0004g0019 a0004c0004t0004g0071 a0004c0005t0004g0014 others(2): Show |
8 | HG01256.hp2 HG01258.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.158+1810_158+1816d others(9): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655462 | |||||||
| chr3:121655462 | CT | C | 20 | a0001c0002t0003g0012 a0001c0002t0003g0109 a0001c0002t0003g0110 others(17): Show |
23 | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.158+1816delA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655462 | |||||||
| chr3:121655462 | CTT | C | 58 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0025 others(55): Show |
89 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.158+1815_158+1816d others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655462 | |||||||
| chr3:121655497 | C | T | 1 | a0003c0003t0002g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.158+1782G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655497 | |||||||
| chr3:121655514 | G | A | 73 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(70): Show |
103 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.158+1765C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655514 | |||||||
| chr3:121655670 | G | C | 1 | a0001c0002t0003g0025 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.158+1609C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655670 | |||||||
| chr3:121655680 | G | GT | 12 | a0001c0007t0004g0103 a0002c0001t0001g0210 a0002c0001t0001g0211 others(9): Show |
12 | HG00642.hp2 HG01192.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.158+1598dupA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655680 | |||||||
| chr3:121655680 | G | GTT | 8 | a0001c0002t0003g0026 a0001c0002t0003g0118 a0001c0002t0003g0129 others(5): Show |
9 | HG01099.hp2 HG02148.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+1597_158+1598d others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655680 | |||||||
| chr3:121655680 | G | GTTT | 54 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(51): Show |
84 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.158+1596_158+1598d others(5): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655680 | |||||||
| chr3:121655680 | G | GTTTT | 11 | a0001c0002t0003g0028 a0001c0002t0003g0033 a0001c0002t0003g0110 others(8): Show |
14 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.158+1595_158+1598d others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655680 | |||||||
| chr3:121655680 | GT | G | 46 | a0001c0014t0008g0018 a0003c0003t0002g0100 a0003c0003t0002g0167 others(43): Show |
59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.158+1598delA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655680 | |||||||
| chr3:121655687 | T | C | 4 | a0003c0003t0002g0174 a0003c0003t0002g0175 a0003c0003t0002g0176 others(1): Show |
4 | HG00423.hp1 HG02135.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+1592A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655687 | |||||||
| chr3:121655700 | G | T | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158+1579C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655700 | |||||||
| chr3:121655790 | G | A | 1 | a0001c0002t0005g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.158+1489C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655790 | |||||||
| chr3:121655823 | C | CATTT | 121 | a0001c0002t0003g0007 a0001c0002t0003g0025 a0001c0002t0003g0026 others(118): Show |
169 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.158+1452_158+1455d others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655823 | |||||||
| chr3:121655823 | C | CATTTATT others(1): Show |
11 | a0001c0002t0003g0109 a0002c0001t0001g0044 a0003c0003t0002g0035 others(8): Show |
13 | HG00735.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.158+1448_158+1455d others(10): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655823 | |||||||
| chr3:121655823 | CATTT | C | 18 | a0001c0002t0005g0131 a0001c0002t0010g0132 a0001c0007t0004g0104 others(15): Show |
18 | HG00423.hp1 HG00597.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.158+1452_158+1455d others(6): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655823 | |||||||
| chr3:121655823 | CATTTATT others(1): Show |
C | 7 | a0001c0002t0003g0134 a0002c0001t0001g0241 a0003c0003t0002g0178 others(4): Show |
8 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+1448_158+1455d others(10): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655823 | |||||||
| chr3:121655823 | CATTTATT others(5): Show |
C | 2 | a0002c0001t0001g0244 a0003c0003t0002g0180 |
2 | HG02074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.158+1444_158+1455d others(14): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655823 | |||||||
| chr3:121655880 | G | A | 2 | a0003c0003t0002g0181 a0003c0003t0002g0182 |
2 | NA19058.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.158+1399C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121655880 | |||||||
| chr3:121656005 | C | T | 2 | a0003c0003t0002g0144 a0003c0003t0002g0145 |
2 | HG01952.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.158+1274G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656005 | |||||||
| chr3:121656096 | C | T | 3 | a0001c0002t0003g0059 a0001c0002t0003g0107 a0001c0002t0003g0108 |
3 | HG00408.hp1 HG00438.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.158+1183G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656096 | |||||||
| chr3:121656100 | C | T | 1 | a0001c0014t0008g0018 | 2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.158+1179G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656100 | |||||||
| chr3:121656297 | G | T | 78 | a0001c0007t0003g0098 a0001c0018t0003g0159 a0002c0001t0001g0251 others(75): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.158+982C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656297 | |||||||
| chr3:121656372 | T | A | 3 | a0001c0002t0003g0032 a0001c0002t0003g0133 a0001c0002t0003g0134 |
4 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+907A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656372 | |||||||
| chr3:121656392 | C | A | 3 | a0001c0002t0003g0032 a0001c0002t0003g0133 a0001c0002t0003g0134 |
4 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+887G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656392 | |||||||
| chr3:121656476 | G | C | 1 | a0001c0002t0003g0135 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.158+803C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656476 | |||||||
| chr3:121656569 | T | TTTTG | 72 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(69): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.158+706_158+709dup others(4): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656569 | |||||||
| chr3:121656899 | T | C | 3 | a0001c0002t0003g0033 a0001c0002t0003g0136 a0001c0002t0003g0137 |
4 | HG00741.hp2 HG01106.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+380A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656899 | |||||||
| chr3:121656955 | T | G | 73 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(70): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158+324A>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656955 | |||||||
| chr3:121656992 | G | A | 3 | a0004c0004t0004g0087 a0004c0004t0004g0088 a0004c0004t0004g0089 |
3 | HG02523.hp1 NA18999.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.158+287C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121656992 | |||||||
| chr3:121657259 | C | T | 1 | a0004c0004t0004g0068 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.158+20G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 3/13 | chr3 | 121657259 | |||||||
| chr3:121657369 | G | A | 1 | a0001c0002t0005g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.85-17C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/13 | chr3 | 121657369 | |||||||
| chr3:121657660 | A | T | 42 | a0004c0004t0004g0006 a0004c0004t0004g0010 a0004c0004t0004g0019 others(39): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.85-308T>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/13 | chr3 | 121657660 | |||||||
| chr3:121657790 | G | A | 5 | a0003c0013t0002g0139 a0003c0013t0011g0141 a0003c0017t0002g0140 others(2): Show |
6 | HG02109.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-438C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/13 | chr3 | 121657790 | |||||||
| chr3:121657837 | C | A | 1 | a0001c0002t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.84+427G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/13 | chr3 | 121657837 | |||||||
| chr3:121657880 | G | A | 2 | a0002c0001t0001g0242 a0002c0001t0001g0243 |
2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.84+384C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/13 | chr3 | 121657880 | |||||||
| chr3:121658016 | G | A | 202 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(199): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.84+248C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/13 | chr3 | 121658016 | |||||||
| chr3:121658144 | G | A | 1 | a0002c0001t0001g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.84+120C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 2/13 | chr3 | 121658144 | |||||||
| chr3:121658449 | C | A | 1 | a0003c0003t0002g0183 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1-102G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121658449 | |||||||
| chr3:121658451 | A | AT | 5 | a0001c0014t0008g0018 a0007c0009t0006g0064 a0007c0009t0006g0065 others(2): Show |
6 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-105dupA | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121658451 | |||||||
| chr3:121658680 | C | G | 1 | a0003c0003t0002g0143 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1-333G>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121658680 | |||||||
| chr3:121658727 | A | G | 4 | a0003c0003t0002g0017 a0003c0003t0002g0061 a0003c0003t0002g0062 others(1): Show |
5 | HG00735.hp2 HG01069.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-380T>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121658727 | |||||||
| chr3:121658735 | C | A | 4 | a0002c0001t0001g0245 a0002c0001t0001g0246 a0002c0001t0001g0247 others(1): Show |
4 | HG01099.hp1 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-388G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121658735 | |||||||
| chr3:121659003 | G | T | 1 | a0002c0001t0001g0043 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1-656C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659003 | |||||||
| chr3:121659020 | T | A | 53 | a0001c0018t0003g0159 a0002c0001t0001g0251 a0003c0003t0002g0002 others(50): Show |
72 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1-673A>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659020 | |||||||
| chr3:121659058 | C | A | 12 | a0004c0005t0004g0014 a0004c0005t0004g0185 a0004c0005t0004g0186 others(9): Show |
14 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.1-711G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659058 | |||||||
| chr3:121659350 | G | C | 1 | a0003c0003t0002g0042 | 2 | HG02129.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1-1003C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659350 | |||||||
| chr3:121659352 | C | G | 1 | a0003c0003t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1-1005G>C | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659352 | |||||||
| chr3:121659404 | C | A | 1 | a0002c0001t0001g0249 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1-1057G>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659404 | |||||||
| chr3:121659440 | C | T | 202 | a0001c0002t0003g0001 a0001c0002t0003g0007 a0001c0002t0003g0012 others(199): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1-1093G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659440 | |||||||
| chr3:121659547 | T | C | 1 | a0004c0004t0004g0250 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1-1200A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659547 | |||||||
| chr3:121659763 | GCAA | G | 27 | a0001c0002t0003g0265 a0001c0002t0005g0008 a0001c0002t0005g0009 others(24): Show |
34 | HG00423.hp2 HG01109.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1+1054_-1+1056del others(3): Show |
HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659763 | |||||||
| chr3:121659801 | G | C | 1 | a0002c0001t0001g0251 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-1+1019C>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659801 | |||||||
| chr3:121659970 | A | C | 1 | a0001c0002t0003g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-1+850T>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121659970 | |||||||
| chr3:121660080 | G | A | 27 | a0001c0002t0003g0265 a0001c0002t0005g0008 a0001c0002t0005g0009 others(24): Show |
34 | HG00423.hp2 HG01109.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1+740C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121660080 | |||||||
| chr3:121660322 | G | A | 3 | a0002c0001t0001g0276 a0002c0001t0001g0277 a0002c0001t0001g0278 |
3 | HG02809.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+498C>T | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121660322 | |||||||
| chr3:121660488 | T | C | 1 | a0001c0002t0003g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-1+332A>G | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121660488 | |||||||
| chr3:121660762 | G | T | 1 | a0002c0001t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1+58C>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121660762 | |||||||
| chr3:121660799 | C | T | 1 | a0002c0001t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-1+21G>A | HCLS1 | ENSG00000180353.11 | transcript | ENST00000314583.8 | protein_coding | 1/13 | chr3 | 121660799 |