Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 114823 |
| ensemblid | ENSG00000167615.18 |
| hgncid | 15500 |
| symbol | LENG8 |
| name | leukocyte receptor cluster member 8 |
| refseq_nuc | NM_052925.4 |
| refseq_prot | NP_443157.1 |
| ensembl_nuc | ENST00000326764.10 |
| ensembl_prot | ENSP00000318374.5 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 54449199 |
| end | 54462016 |
| strand | + |
| ver | v1.2 |
| region | chr19:54449199-54462016 |
| region5000 | chr19:54444199-54467016 |
| regionname0 | LENG8_chr19_54449199_54462016 |
| regionname5000 | LENG8_chr19_54444199_54467016 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 800 | 395 | 94 | 66 | 177 | 14 | 43 | 136 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0002 | 0/0 | 800 | 15 | 1 | 7 | 2 | 0 | 5 | 2 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0003 | 0/0 | 800 | 8 | 0 | 2 | 6 | 0 | 0 | 3 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0004 | 0/0 | 800 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0005 | 0/0 | 800 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0006 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0007 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0008 | 0/0 | 800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0009 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0010 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0011 | 0/0 | 800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| a0012 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | MAANV others(795): Show |
chr19 | 54444199 | 54467016 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2400 | 202 | 64 | 38 | 72 | 7 | 21 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0002 | 0/1 | 2400 | 178 | 22 | 28 | 101 | 7 | 19 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0005 | 0/0 | 2400 | 7 | 6 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0008 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0011 | 0/0 | 2400 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0015 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0017 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0018 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0019 | 0/0 | 2400 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0001c0020 | 0/0 | 2400 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0002c0003 | 0/0 | 2400 | 15 | 1 | 7 | 2 | 0 | 5 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0003c0004 | 0/0 | 2400 | 8 | 0 | 2 | 6 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0004c0006 | 0/0 | 2400 | 3 | 0 | 0 | 3 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0004c0009 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0005c0007 | 0/0 | 2400 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0006c0010 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0007c0022 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0008c0016 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0009c0012 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0010c0013 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0011c0021 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 | ||
| a0012c0014 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | ATGGC others(2395): Show |
chr19 | 54444199 | 54467016 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3658 | 165 | 43 | 30 | 67 | 6 | 19 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0003 | 0/0 | 3658 | 14 | 12 | 1 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0005 | 0/0 | 3658 | 4 | 0 | 1 | 3 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0006 | 0/0 | 3658 | 2 | 0 | 1 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0007 | 0/0 | 3658 | 5 | 5 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0008 | 0/0 | 3658 | 4 | 0 | 3 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0009 | 0/0 | 3658 | 2 | 0 | 1 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0014 | 0/0 | 3658 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0015 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0016 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0017 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0018 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0001t0020 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0002t0001 | 0/0 | 3658 | 19 | 14 | 2 | 0 | 0 | 3 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0002t0002 | 0/0 | 3658 | 142 | 8 | 26 | 86 | 6 | 16 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0002t0004 | 0/0 | 3658 | 10 | 0 | 0 | 10 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0002t0011 | 0/0 | 3658 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0002t0012 | 0/0 | 3658 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0002t0013 | 0/1 | 3658 | 2 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0002t0019 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0005t0005 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0005t0006 | 0/0 | 3658 | 6 | 6 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0008t0001 | 0/0 | 3658 | 2 | 2 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0011t0001 | 0/0 | 3658 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0015t0004 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0017t0002 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0018t0002 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0019t0001 | 0/0 | 3658 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0001c0020t0001 | 0/0 | 3658 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0002c0003t0001 | 0/0 | 3658 | 15 | 1 | 7 | 2 | 0 | 5 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0003c0004t0001 | 0/0 | 3658 | 3 | 0 | 0 | 3 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0003c0004t0005 | 0/0 | 3658 | 3 | 0 | 0 | 3 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0003c0004t0010 | 0/0 | 3658 | 2 | 0 | 2 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0004c0006t0001 | 0/0 | 3658 | 3 | 0 | 0 | 3 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0004c0009t0001 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0005c0007t0002 | 0/0 | 3658 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0006c0010t0001 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0007c0022t0002 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0008c0016t0002 | 0/0 | 3658 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0009c0012t0001 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0010c0013t0001 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0011c0021t0003 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| a0012c0014t0001 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | CGTCG others(3653): Show |
chr19 | 54444199 | 54467016 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 33 | 0 | 7 | 15 | 1 | 10 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0004 | 0/0 | 17 | 3 | 6 | 5 | 0 | 3 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0006 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0008 | 0/0 | 8 | 1 | 1 | 5 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0007g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0008g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0009g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0014g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0015g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0016g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0001t0020g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0031 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0001 | 0/0 | 42 | 1 | 8 | 25 | 2 | 6 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0003 | 0/0 | 34 | 0 | 7 | 25 | 0 | 2 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0009 | 0/0 | 8 | 0 | 5 | 0 | 2 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0017 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0029 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0011g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0012g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0013g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0013g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0002t0019g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0005t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0005t0006g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0005t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0005t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0005t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0008t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0008t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0011t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0015t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0017t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0018t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0019t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0001c0020t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0002c0003t0001g0007 | 0/0 | 11 | 0 | 5 | 1 | 0 | 5 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0002c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0003c0004t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0003c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0003c0004t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0003c0004t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0003c0004t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0003c0004t0010g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0004c0006t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0004c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0004c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0004c0009t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0005c0007t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0005c0007t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0006c0010t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0007c0022t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0008c0016t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0009c0012t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0010c0013t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0011c0021t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| a0012c0014t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | GBR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00140 | hp2 | a0001 | c0002 | t0013 | g0001 | EUR | GBR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | FIN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0123 | EUR | FIN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00408 | hp1 | a0003 | c0004 | t0005 | g0025 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00423 | hp2 | a0001 | c0002 | t0019 | g0001 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00438 | hp1 | a0005 | c0007 | t0002 | g0014 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00544 | hp1 | a0003 | c0004 | t0001 | g0044 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00558 | hp1 | a0006 | c0010 | t0001 | g0005 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00609 | hp1 | a0004 | c0009 | t0001 | g0005 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00621 | hp1 | a0007 | c0022 | t0002 | g0130 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00735 | hp1 | a0008 | c0016 | t0002 | g0001 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0126 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0117 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0029 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01192 | hp1 | a0001 | c0001 | t0014 | g0004 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01257 | hp2 | a0002 | c0003 | t0001 | g0115 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01258 | hp2 | a0003 | c0004 | t0010 | g0025 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0151 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01433 | hp2 | a0003 | c0004 | t0010 | g0025 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0147 | EUR | IBS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01884 | hp1 | a0001 | c0005 | t0006 | g0106 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0067 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0034 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0083 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02056 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02132 | hp1 | a0003 | c0004 | t0001 | g0044 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02145 | hp2 | a0001 | c0005 | t0006 | g0027 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0043 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02280 | hp1 | a0009 | c0012 | t0001 | g0040 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02602 | hp1 | a0001 | c0011 | t0001 | g0041 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02622 | hp2 | a0001 | c0008 | t0001 | g0110 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0134 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02630 | hp2 | a0010 | c0013 | t0001 | g0010 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02647 | hp2 | a0011 | c0021 | t0003 | g0026 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0007 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02738 | hp1 | a0001 | c0020 | t0001 | g0094 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02895 | hp2 | a0001 | c0005 | t0006 | g0107 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0104 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02897 | hp1 | a0001 | c0005 | t0006 | g0027 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03017 | hp1 | a0001 | c0019 | t0001 | g0112 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0111 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03041 | hp2 | a0001 | c0005 | t0006 | g0027 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03130 | hp1 | a0001 | c0005 | t0006 | g0105 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0118 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0140 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0124 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0007 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0128 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0007 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0007 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0022 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0007 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | STU | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18522 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | YRI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | YRI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18612 | hp2 | a0001 | c0018 | t0002 | g0001 | EAS | CHB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | CHB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | YRI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0102 | AFR | YRI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18954 | hp1 | a0001 | c0002 | t0012 | g0028 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18959 | hp2 | a0012 | c0014 | t0001 | g0023 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0022 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18963 | hp2 | a0005 | c0007 | t0002 | g0120 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18966 | hp2 | a0004 | c0006 | t0001 | g0023 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18967 | hp2 | a0003 | c0004 | t0005 | g0093 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18977 | hp1 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18983 | hp1 | a0004 | c0006 | t0001 | g0081 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18989 | hp2 | a0001 | c0002 | t0004 | g0132 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18998 | hp2 | a0001 | c0002 | t0012 | g0028 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19010 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19011 | hp1 | a0001 | c0002 | t0011 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19012 | hp1 | a0001 | c0005 | t0005 | g0021 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | LWK | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19057 | hp2 | a0001 | c0002 | t0004 | g0125 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19065 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19065 | hp2 | a0001 | c0017 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19081 | hp2 | a0001 | c0002 | t0011 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19085 | hp1 | a0001 | c0015 | t0004 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19090 | hp2 | a0003 | c0004 | t0005 | g0097 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | YRI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | ASW | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0034 | EUR | TSI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | GIH | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18955 | hp1 | a0004 | c0006 | t0001 | g0021 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA18955 | hp2 | a0003 | c0004 | t0001 | g0096 | EAS | JPT | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | USA | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | LWK | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0082 | AFR | LWK | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0013 | g0141 | REF | REF | LENG8_chr19_54444199_54467016 | LENG8 | chr19 | 54444199 | 54467016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:54451290 | A | G | 4 | a0001 a0005 a0007 others(1): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
splice_region_variant | LOW | c.-55A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 2/16 | chr19 | 54451290 | |||||||
| chr19:54452692 | G | C | 2 | a0004 a0006 |
5 | HG00558.hp1 HG00609.hp1 NA18955.hp1 others(2): Show |
missense_variant | MODERATE | c.255G>C | p.Gln85His | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/16 | 422/3658 | 255/2403 | 85/800 | chr19 | 54452692 | |||
| chr19:54454545 | G | T | 1 | a0007 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.542G>T | p.Ser181Ile | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/16 | 709/3658 | 542/2403 | 181/800 | chr19 | 54454545 | |||
| chr19:54454550 | C | T | 1 | a0011 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.547C>T | p.Pro183Ser | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/16 | 714/3658 | 547/2403 | 183/800 | chr19 | 54454550 | |||
| chr19:54454959 | G | T | 1 | a0012 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.688G>T | p.Gly230Trp | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 7/16 | 855/3658 | 688/2403 | 230/800 | chr19 | 54454959 | |||
| chr19:54455378 | G | C | 1 | a0003 | 8 | HG00408.hp1 HG00544.hp1 HG01258.hp2 others(5): Show |
missense_variant | MODERATE | c.836G>C | p.Arg279Pro | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/16 | 1003/3658 | 836/2403 | 279/800 | chr19 | 54455378 | |||
| chr19:54456092 | C | T | 1 | a0006 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1151C>T | p.Thr384Met | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 9/16 | 1318/3658 | 1151/2403 | 384/800 | chr19 | 54456092 | |||
| chr19:54456434 | C | T | 1 | a0008 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.1414C>T | p.Arg472Trp | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/16 | 1581/3658 | 1414/2403 | 472/800 | chr19 | 54456434 | |||
| chr19:54456758 | G | A | 1 | a0005 | 2 | HG00438.hp1 NA18963.hp2 |
missense_variant | MODERATE | c.1568G>A | p.Arg523His | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/16 | 1735/3658 | 1568/2403 | 523/800 | chr19 | 54456758 | |||
| chr19:54456859 | A | G | 1 | a0002 | 15 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(12): Show |
missense_variant | MODERATE | c.1669A>G | p.Ile557Val | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/16 | 1836/3658 | 1669/2403 | 557/800 | chr19 | 54456859 | |||
| chr19:54457792 | A | C | 1 | a0010 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1777A>C | p.Lys593Gln | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 12/16 | 1944/3658 | 1777/2403 | 593/800 | chr19 | 54457792 | |||
| chr19:54460821 | G | A | 1 | a0009 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.2296G>A | p.Glu766Lys | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 2463/3658 | 2296/2403 | 766/800 | chr19 | 54460821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:54454597 | C | T | 1 | a0001c0020 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.594C>T | p.Pro198Pro | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/16 | 761/3658 | 594/2403 | 198/800 | chr19 | 54454597 | |||
| chr19:54454681 | A | G | 10 | a0001c0002 a0001c0008 a0001c0015 others(7): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
splice_region_variant&synonymous_variant | LOW | c.678A>G | p.Lys226Lys | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/16 | 845/3658 | 678/2403 | 226/800 | chr19 | 54454681 | |||
| chr19:54455400 | G | C | 9 | a0001c0002 a0001c0005 a0001c0008 others(6): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
synonymous_variant | LOW | c.858G>C | p.Pro286Pro | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/16 | 1025/3658 | 858/2403 | 286/800 | chr19 | 54455400 | |||
| chr19:54455523 | C | T | 1 | a0001c0008 | 2 | HG02622.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.981C>T | p.Asp327Asp | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/16 | 1148/3658 | 981/2403 | 327/800 | chr19 | 54455523 | |||
| chr19:54456174 | C | T | 1 | a0001c0018 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.1233C>T | p.Asn411Asn | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 9/16 | 1400/3658 | 1233/2403 | 411/800 | chr19 | 54456174 | |||
| chr19:54456406 | C | T | 1 | a0001c0017 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.1386C>T | p.Gly462Gly | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/16 | 1553/3658 | 1386/2403 | 462/800 | chr19 | 54456406 | |||
| chr19:54456900 | G | A | 1 | a0001c0011 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1710G>A | p.Pro570Pro | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/16 | 1877/3658 | 1710/2403 | 570/800 | chr19 | 54456900 | |||
| chr19:54457773 | C | T | 1 | a0001c0015 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.1758C>T | p.Val586Val | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 12/16 | 1925/3658 | 1758/2403 | 586/800 | chr19 | 54457773 | |||
| chr19:54457990 | C | T | 1 | a0001c0019 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.1890C>T | p.Ile630Ile | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 13/16 | 2057/3658 | 1890/2403 | 630/800 | chr19 | 54457990 | |||
| chr19:54460826 | C | T | 1 | a0004c0009 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.2301C>T | p.Ala767Ala | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 2468/3658 | 2301/2403 | 767/800 | chr19 | 54460826 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:54449258 | G | A | 1 | a0001c0001t0014 | 1 | HG01192.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/16 | 2087 | chr19 | 54449258 | ||||||
| chr19:54449282 | C | T | 3 | a0001c0001t0003 a0001c0001t0020 a0011c0021t0003 |
16 | HG00733.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/16 | 2063 | chr19 | 54449282 | ||||||
| chr19:54449304 | C | T | 1 | a0001c0002t0019 | 1 | HG00423.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-62C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/16 | chr19 | 54449304 | |||||||
| chr19:54461173 | A | G | 1 | a0001c0001t0018 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 245 | chr19 | 54461173 | ||||||
| chr19:54461189 | T | C | 1 | a0001c0002t0011 | 2 | NA19011.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*261T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 261 | chr19 | 54461189 | ||||||
| chr19:54461198 | G | A | 1 | a0001c0001t0015 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*270G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 270 | chr19 | 54461198 | ||||||
| chr19:54461221 | C | T | 1 | a0001c0001t0017 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*293C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 293 | chr19 | 54461221 | ||||||
| chr19:54461321 | C | T | 1 | a0001c0001t0008 | 4 | HG01975.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*393C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 393 | chr19 | 54461321 | ||||||
| chr19:54461395 | C | T | 1 | a0001c0002t0013 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*467C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 467 | chr19 | 54461395 | ||||||
| chr19:54461453 | A | T | 1 | a0001c0002t0012 | 2 | NA18954.hp1 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*525A>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 525 | chr19 | 54461453 | ||||||
| chr19:54461473 | G | T | 1 | a0001c0001t0016 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 545 | chr19 | 54461473 | ||||||
| chr19:54461539 | A | T | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0020 others(2): Show |
24 | HG00733.hp1 HG01496.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*611A>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 611 | chr19 | 54461539 | ||||||
| chr19:54461547 | C | T | 2 | a0001c0001t0007 a0003c0004t0010 |
7 | HG01258.hp2 HG01433.hp2 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*619C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 619 | chr19 | 54461547 | ||||||
| chr19:54461580 | C | T | 1 | a0001c0001t0020 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*652C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 652 | chr19 | 54461580 | ||||||
| chr19:54461630 | T | C | 1 | a0001c0001t0009 | 2 | HG01433.hp1 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*702T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 702 | chr19 | 54461630 | ||||||
| chr19:54461738 | T | C | 8 | a0001c0001t0005 a0001c0002t0004 a0001c0002t0011 others(5): Show |
25 | HG00408.hp1 HG00597.hp2 HG01074.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*810T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 16/16 | 810 | chr19 | 54461738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:54449325 | A | G | 91 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0052 others(88): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-56+15A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449325 | |||||||
| chr19:54449340 | C | T | 1 | a0001c0001t0015g0104 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-56+30C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449340 | |||||||
| chr19:54449380 | C | G | 10 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0045 others(7): Show |
16 | HG00733.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-56+70C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449380 | |||||||
| chr19:54449406 | G | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0108 a0001c0005t0006g0027 others(3): Show |
9 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56+96G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449406 | |||||||
| chr19:54449423 | G | A | 1 | a0001c0001t0008g0034 | 2 | HG01981.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-56+113G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449423 | |||||||
| chr19:54449524 | A | C | 91 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0052 others(88): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-56+214A>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449524 | |||||||
| chr19:54449534 | C | T | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0031 others(8): Show |
19 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-56+224C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449534 | |||||||
| chr19:54449541 | T | A | 1 | a0001c0001t0001g0035 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-56+231T>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449541 | |||||||
| chr19:54449569 | C | T | 8 | a0001c0002t0002g0095 a0001c0020t0001g0094 a0003c0004t0001g0044 others(5): Show |
10 | HG00408.hp1 HG00544.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56+259C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449569 | |||||||
| chr19:54449695 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 |
13 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56+385C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449695 | |||||||
| chr19:54449741 | C | A | 1 | a0001c0002t0002g0109 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-56+431C>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449741 | |||||||
| chr19:54449768 | G | T | 1 | a0001c0002t0002g0155 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-56+458G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449768 | |||||||
| chr19:54449803 | C | T | 75 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0121 others(72): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.-56+493C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449803 | |||||||
| chr19:54449836 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0090 |
4 | HG01891.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56+526C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449836 | |||||||
| chr19:54449840 | C | T | 3 | a0003c0004t0001g0044 a0003c0004t0001g0096 a0003c0004t0005g0097 |
4 | HG00544.hp1 HG02132.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56+530C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449840 | |||||||
| chr19:54449889 | C | T | 5 | a0002c0003t0001g0007 a0002c0003t0001g0115 a0002c0003t0001g0116 others(2): Show |
15 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56+579C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449889 | |||||||
| chr19:54449957 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
19 | HG00408.hp1 HG00544.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-56+647C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449957 | |||||||
| chr19:54449996 | G | A | 85 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0113 others(82): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-56+686G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54449996 | |||||||
| chr19:54450045 | C | T | 76 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0121 others(73): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-56+735C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450045 | |||||||
| chr19:54450077 | T | C | 1 | a0001c0002t0002g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-56+767T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450077 | |||||||
| chr19:54450103 | A | G | 1 | a0001c0002t0002g0154 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-56+793A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450103 | |||||||
| chr19:54450138 | T | A | 3 | a0001c0002t0002g0014 a0005c0007t0002g0014 a0005c0007t0002g0120 |
5 | HG00438.hp1 HG00609.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56+828T>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450138 | |||||||
| chr19:54450191 | C | A | 122 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(119): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-56+881C>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450191 | |||||||
| chr19:54450211 | C | T | 2 | a0002c0003t0001g0117 a0002c0003t0001g0118 |
2 | HG01070.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-56+901C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450211 | |||||||
| chr19:54450273 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-56+963C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450273 | |||||||
| chr19:54450380 | A | G | 76 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0031 others(73): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-55-910A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450380 | |||||||
| chr19:54450494 | C | T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(33): Show |
65 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-55-796C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450494 | |||||||
| chr19:54450525 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-55-765C>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450525 | |||||||
| chr19:54450584 | G | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(12): Show |
34 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-55-706G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450584 | |||||||
| chr19:54450614 | C | T | 76 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0031 others(73): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-55-676C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450614 | |||||||
| chr19:54450618 | C | CT | 16 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
22 | HG00733.hp1 HG01981.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-55-651dupT | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 54450618 | ||||||
| chr19:54450618 | CT | C | 71 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0036 others(68): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-55-651delT | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 54450618 | ||||||
| chr19:54450618 | CTT | C | 12 | a0001c0002t0001g0156 a0001c0002t0002g0015 a0001c0002t0002g0047 others(9): Show |
16 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.-55-652_-55-651del others(2): Show |
LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 54450618 | ||||||
| chr19:54450626 | T | TA | 1 | a0001c0001t0001g0018 | 3 | HG03195.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-55-664_-55-663ins others(1): Show |
LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450626 | |||||||
| chr19:54450639 | T | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
18 | HG00408.hp1 HG00544.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-55-651T>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450639 | |||||||
| chr19:54450703 | C | T | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0031 others(11): Show |
22 | HG01255.hp2 HG01346.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-55-587C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450703 | |||||||
| chr19:54450707 | G | A | 78 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0018 others(75): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-55-583G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450707 | |||||||
| chr19:54450792 | G | C | 5 | a0002c0003t0001g0007 a0002c0003t0001g0115 a0002c0003t0001g0116 others(2): Show |
15 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-55-498G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450792 | |||||||
| chr19:54450819 | C | A | 1 | a0001c0001t0003g0100 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-55-471C>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450819 | |||||||
| chr19:54450848 | G | A | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-55-442G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450848 | |||||||
| chr19:54450876 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-55-414T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450876 | |||||||
| chr19:54450909 | C | T | 3 | a0001c0001t0003g0026 a0001c0002t0002g0145 a0011c0021t0003g0026 |
4 | HG02451.hp1 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-55-381C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450909 | |||||||
| chr19:54450954 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0019 others(10): Show |
30 | HG00639.hp1 HG01243.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.-55-336G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54450954 | |||||||
| chr19:54451017 | C | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0018 others(13): Show |
35 | HG00639.hp1 HG01243.hp1 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.-55-273C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451017 | |||||||
| chr19:54451026 | C | T | 77 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0031 others(74): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-55-264C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451026 | |||||||
| chr19:54451060 | C | T | 1 | a0001c0002t0002g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-55-230C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451060 | |||||||
| chr19:54451122 | C | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0019 others(10): Show |
30 | HG00639.hp1 HG01243.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.-55-168C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451122 | |||||||
| chr19:54451148 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-55-142C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451148 | |||||||
| chr19:54451196 | C | T | 1 | a0001c0001t0015g0104 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-55-94C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451196 | |||||||
| chr19:54451197 | G | A | 63 | a0001c0002t0001g0143 a0001c0002t0002g0001 a0001c0002t0002g0003 others(60): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-55-93G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451197 | |||||||
| chr19:54451286 | A | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0019 others(12): Show |
34 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.-55-4A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 1/15 | chr19 | 54451286 | |||||||
| chr19:54451402 | T | C | 118 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(115): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.38+20T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 2/15 | chr19 | 54451402 | |||||||
| chr19:54451506 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.38+124G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 2/15 | chr19 | 54451506 | |||||||
| chr19:54451517 | G | A | 85 | a0001c0001t0001g0121 a0001c0001t0008g0034 a0001c0001t0008g0067 others(82): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.38+135G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 2/15 | chr19 | 54451517 | |||||||
| chr19:54451609 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0108 a0001c0005t0006g0027 others(3): Show |
9 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.38+227C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 2/15 | chr19 | 54451609 | |||||||
| chr19:54452090 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0108 a0001c0005t0006g0027 others(3): Show |
9 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.39-3C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 2/15 | chr19 | 54452090 | |||||||
| chr19:54452281 | A | G | 1 | a0001c0019t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.213+14A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 3/15 | chr19 | 54452281 | |||||||
| chr19:54452375 | G | A | 86 | a0001c0001t0001g0046 a0001c0001t0001g0108 a0001c0002t0001g0031 others(83): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.213+108G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 3/15 | chr19 | 54452375 | |||||||
| chr19:54452414 | A | C | 1 | a0001c0002t0002g0047 | 2 | NA19005.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.213+147A>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 3/15 | chr19 | 54452414 | |||||||
| chr19:54452606 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.214-45T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 3/15 | chr19 | 54452606 | |||||||
| chr19:54452635 | G | T | 1 | a0001c0001t0007g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214-16G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 3/15 | chr19 | 54452635 | |||||||
| chr19:54452636 | C | CCT | 149 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(146): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.214-12_214-11dupCT | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 54452636 | ||||||
| chr19:54452641 | G | C | 1 | a0001c0001t0003g0045 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.214-10G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 3/15 | chr19 | 54452641 | |||||||
| chr19:54452840 | T | C | 82 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(79): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.315+88T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54452840 | |||||||
| chr19:54452840 | T | G | 1 | a0001c0002t0002g0152 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.315+88T>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54452840 | |||||||
| chr19:54452841 | G | A | 6 | a0001c0019t0001g0112 a0002c0003t0001g0007 a0002c0003t0001g0115 others(3): Show |
16 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.315+89G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54452841 | |||||||
| chr19:54452912 | C | T | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.315+160C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54452912 | |||||||
| chr19:54453055 | G | C | 6 | a0001c0019t0001g0112 a0002c0003t0001g0007 a0002c0003t0001g0115 others(3): Show |
16 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.315+303G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54453055 | |||||||
| chr19:54453056 | C | T | 6 | a0001c0019t0001g0112 a0002c0003t0001g0007 a0002c0003t0001g0115 others(3): Show |
16 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.315+304C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54453056 | |||||||
| chr19:54453130 | CTGAT | C | 5 | a0002c0003t0001g0007 a0002c0003t0001g0115 a0002c0003t0001g0116 others(2): Show |
15 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.315+382_315+385del others(4): Show |
LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 54453130 | ||||||
| chr19:54453234 | T | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0108 a0001c0005t0006g0027 others(3): Show |
9 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-312T>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54453234 | |||||||
| chr19:54453389 | T | C | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.316-157T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54453389 | |||||||
| chr19:54453429 | A | G | 83 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(80): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.316-117A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54453429 | |||||||
| chr19:54453438 | A | AGGGGTGA others(11): Show |
1 | a0001c0001t0001g0018 | 3 | HG03195.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.316-107_316-90dupG others(17): Show |
LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 54453438 | ||||||
| chr19:54453458 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG03195.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.316-88G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 4/15 | chr19 | 54453458 | |||||||
| chr19:54453683 | C | T | 9 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(6): Show |
15 | HG01255.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.426+27C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54453683 | |||||||
| chr19:54453792 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.426+136G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54453792 | |||||||
| chr19:54453859 | T | C | 1 | a0001c0002t0002g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.426+203T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54453859 | |||||||
| chr19:54453915 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0003c0004t0001g0044 others(6): Show |
15 | HG00408.hp1 HG00544.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.426+259G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54453915 | |||||||
| chr19:54453946 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.426+290A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54453946 | |||||||
| chr19:54454023 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.426+367C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54454023 | |||||||
| chr19:54454030 | C | T | 4 | a0001c0002t0002g0009 a0001c0002t0002g0127 a0001c0002t0002g0139 others(1): Show |
11 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.426+374C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54454030 | |||||||
| chr19:54454243 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.427-187A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54454243 | |||||||
| chr19:54454329 | T | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.427-101T>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54454329 | |||||||
| chr19:54454348 | T | C | 74 | a0001c0001t0001g0068 a0001c0002t0001g0087 a0001c0002t0001g0143 others(71): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.427-82T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54454348 | |||||||
| chr19:54454417 | C | G | 1 | a0001c0001t0001g0065 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.427-13C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 5/15 | chr19 | 54454417 | |||||||
| chr19:54454710 | C | G | 72 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(69): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.679+28C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/15 | chr19 | 54454710 | |||||||
| chr19:54454714 | C | T | 1 | a0004c0006t0001g0081 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.679+32C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/15 | chr19 | 54454714 | |||||||
| chr19:54454715 | G | A | 1 | a0003c0004t0005g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.679+33G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/15 | chr19 | 54454715 | |||||||
| chr19:54454728 | T | C | 148 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(145): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.679+46T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/15 | chr19 | 54454728 | |||||||
| chr19:54454838 | G | A | 3 | a0001c0001t0001g0113 a0001c0008t0001g0110 a0001c0008t0001g0111 |
3 | HG02622.hp2 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-113G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 6/15 | chr19 | 54454838 | |||||||
| chr19:54455220 | T | G | 1 | a0001c0002t0002g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.821+128T>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 7/15 | chr19 | 54455220 | |||||||
| chr19:54455259 | A | G | 3 | a0001c0002t0001g0032 a0001c0002t0001g0156 a0001c0002t0001g0158 |
5 | HG02572.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.822-105A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 7/15 | chr19 | 54455259 | |||||||
| chr19:54455279 | G | T | 1 | a0001c0002t0002g0138 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.822-85G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 7/15 | chr19 | 54455279 | |||||||
| chr19:54455325 | G | A | 1 | a0001c0001t0001g0013 | 4 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.822-39G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 7/15 | chr19 | 54455325 | |||||||
| chr19:54455579 | TG | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0108 a0001c0002t0001g0158 |
4 | HG02257.hp2 HG02258.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+17delG | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr19 | 54455579 | ||||||
| chr19:54455606 | T | C | 1 | a0001c0001t0003g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1025+39T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455606 | |||||||
| chr19:54455683 | T | C | 83 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(80): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1025+116T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455683 | |||||||
| chr19:54455730 | G | A | 4 | a0001c0002t0002g0009 a0001c0002t0002g0127 a0001c0002t0002g0139 others(1): Show |
11 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1025+163G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455730 | |||||||
| chr19:54455736 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1025+169G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455736 | |||||||
| chr19:54455803 | C | T | 8 | a0001c0008t0001g0110 a0001c0008t0001g0111 a0001c0019t0001g0112 others(5): Show |
18 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1026-164C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455803 | |||||||
| chr19:54455818 | C | T | 13 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(10): Show |
29 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1026-149C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455818 | |||||||
| chr19:54455850 | C | T | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1026-117C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455850 | |||||||
| chr19:54455931 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1026-36C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 8/15 | chr19 | 54455931 | |||||||
| chr19:54456249 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0023 others(12): Show |
27 | HG00558.hp1 HG00609.hp1 HG02074.hp2 others(24): Show |
splice_region_variant&intron_variant | LOW | c.1304+4C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 9/15 | chr19 | 54456249 | |||||||
| chr19:54456321 | G | A | 4 | a0001c0005t0006g0027 a0001c0005t0006g0105 a0001c0005t0006g0106 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1305-4G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 9/15 | chr19 | 54456321 | |||||||
| chr19:54456485 | C | T | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1445+20C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456485 | |||||||
| chr19:54456504 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0016g0043 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1445+39G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456504 | |||||||
| chr19:54456556 | G | A | 4 | a0001c0005t0006g0027 a0001c0005t0006g0105 a0001c0005t0006g0106 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1446-80G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456556 | |||||||
| chr19:54456567 | G | A | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1446-69G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456567 | |||||||
| chr19:54456588 | G | T | 1 | a0001c0001t0007g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1446-48G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456588 | |||||||
| chr19:54456607 | C | T | 1 | a0001c0002t0002g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1446-29C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456607 | |||||||
| chr19:54456609 | C | T | 1 | a0001c0002t0002g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1446-27C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456609 | |||||||
| chr19:54456624 | A | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0076 others(10): Show |
19 | HG00408.hp1 HG00544.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1446-12A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 10/15 | chr19 | 54456624 | |||||||
| chr19:54456958 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1731+37C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54456958 | |||||||
| chr19:54456982 | C | A | 1 | a0001c0001t0007g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1731+61C>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54456982 | |||||||
| chr19:54456994 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1731+73G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54456994 | |||||||
| chr19:54457011 | C | T | 4 | a0001c0005t0006g0027 a0001c0005t0006g0105 a0001c0005t0006g0106 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1731+90C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457011 | |||||||
| chr19:54457066 | A | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(104): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1731+145A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457066 | |||||||
| chr19:54457088 | G | A | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1731+167G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457088 | |||||||
| chr19:54457135 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1731+214C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457135 | |||||||
| chr19:54457206 | G | C | 2 | a0001c0002t0002g0129 a0007c0022t0002g0130 |
2 | HG00621.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1731+285G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457206 | |||||||
| chr19:54457220 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0108 |
3 | HG02257.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1731+299G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457220 | |||||||
| chr19:54457222 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1731+301G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457222 | |||||||
| chr19:54457233 | T | C | 82 | a0001c0001t0001g0073 a0001c0002t0001g0031 a0001c0002t0001g0032 others(79): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1731+312T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457233 | |||||||
| chr19:54457396 | A | T | 1 | a0001c0002t0002g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1732-351A>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457396 | |||||||
| chr19:54457402 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0018 others(14): Show |
38 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.1732-345G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457402 | |||||||
| chr19:54457409 | T | G | 1 | a0001c0002t0002g0122 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1732-338T>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457409 | |||||||
| chr19:54457434 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1732-313G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457434 | |||||||
| chr19:54457482 | A | G | 9 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(6): Show |
15 | HG01255.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-265A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457482 | |||||||
| chr19:54457540 | C | T | 1 | a0001c0002t0002g0016 | 4 | HG02083.hp2 HG04184.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-207C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457540 | |||||||
| chr19:54457738 | C | T | 9 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(6): Show |
15 | HG01255.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-9C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 11/15 | chr19 | 54457738 | |||||||
| chr19:54457860 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01257.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1833+12G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 12/15 | chr19 | 54457860 | |||||||
| chr19:54457896 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(13): Show |
35 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1834-38C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 12/15 | chr19 | 54457896 | |||||||
| chr19:54458568 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG03195.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2240+47C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458568 | |||||||
| chr19:54458569 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0038 others(1): Show |
8 | NA18970.hp2 NA18981.hp1 NA18987.hp1 others(5): Show |
intron_variant | MODIFIER | c.2240+48G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458569 | |||||||
| chr19:54458618 | C | A | 1 | a0001c0001t0001g0062 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2240+97C>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458618 | |||||||
| chr19:54458749 | C | G | 1 | a0001c0001t0001g0018 | 3 | HG03195.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2240+228C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458749 | |||||||
| chr19:54458794 | T | C | 1 | a0001c0019t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2240+273T>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458794 | |||||||
| chr19:54458811 | C | G | 1 | a0001c0002t0002g0015 | 4 | NA18981.hp2 NA18997.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2240+290C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458811 | |||||||
| chr19:54458824 | C | T | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2240+303C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458824 | |||||||
| chr19:54458888 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0017g0012 |
6 | HG01243.hp1 HG02004.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2240+367C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54458888 | |||||||
| chr19:54459080 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2240+559G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459080 | |||||||
| chr19:54459130 | A | G | 1 | a0001c0005t0006g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2240+609A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459130 | |||||||
| chr19:54459165 | G | A | 1 | a0001c0005t0006g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2240+644G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459165 | |||||||
| chr19:54459190 | C | G | 75 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(72): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2240+669C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459190 | |||||||
| chr19:54459380 | C | G | 1 | a0001c0001t0001g0018 | 3 | HG03195.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2240+859C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459380 | |||||||
| chr19:54459429 | ATGGTCAC others(105): Show |
A | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2240+933_2240+1044 others(3): Show |
LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 54459429 | ||||||
| chr19:54459434 | C | T | 1 | a0001c0019t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2240+913C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459434 | |||||||
| chr19:54459446 | G | T | 1 | a0001c0001t0001g0051 | 2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2240+925G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459446 | |||||||
| chr19:54459454 | TGCCTGGC others(105): Show |
T | 1 | a0001c0002t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2240+1010_2240+112 others(4): Show |
LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 54459454 | ||||||
| chr19:54459500 | A | G | 1 | a0002c0003t0001g0007 | 3 | HG02698.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2240+979A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459500 | |||||||
| chr19:54459502 | G | C | 1 | a0001c0002t0002g0014 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2240+981G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459502 | |||||||
| chr19:54459532 | C | T | 75 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(72): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2240+1011C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459532 | |||||||
| chr19:54459556 | G | A | 2 | a0001c0008t0001g0110 a0001c0008t0001g0111 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2240+1035G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459556 | |||||||
| chr19:54459597 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2240+1076A>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459597 | |||||||
| chr19:54459718 | G | T | 1 | a0001c0001t0001g0035 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2241-1048G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459718 | |||||||
| chr19:54459798 | G | C | 1 | a0001c0002t0002g0109 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2241-968G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459798 | |||||||
| chr19:54459847 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0019 others(12): Show |
34 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.2241-919G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459847 | |||||||
| chr19:54459855 | G | T | 1 | a0001c0002t0002g0134 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2241-911G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459855 | |||||||
| chr19:54459936 | G | A | 1 | a0003c0004t0001g0044 | 2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2241-830G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54459936 | |||||||
| chr19:54460010 | G | A | 1 | a0001c0002t0002g0131 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2241-756G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460010 | |||||||
| chr19:54460050 | C | T | 30 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0030 others(27): Show |
68 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.2241-716C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460050 | |||||||
| chr19:54460065 | C | T | 1 | a0001c0001t0005g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2241-701C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460065 | |||||||
| chr19:54460081 | G | C | 3 | a0001c0005t0006g0027 a0001c0005t0006g0105 a0001c0005t0006g0107 |
5 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2241-685G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460081 | |||||||
| chr19:54460213 | G | A | 12 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(9): Show |
18 | HG01255.hp2 HG01346.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2241-553G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460213 | |||||||
| chr19:54460316 | G | A | 5 | a0002c0003t0001g0007 a0002c0003t0001g0115 a0002c0003t0001g0116 others(2): Show |
15 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.2241-450G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460316 | |||||||
| chr19:54460347 | C | T | 1 | a0001c0002t0002g0049 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2241-419C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460347 | |||||||
| chr19:54460367 | G | T | 1 | a0001c0002t0002g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2241-399G>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460367 | |||||||
| chr19:54460442 | G | A | 1 | a0001c0002t0002g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2241-324G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460442 | |||||||
| chr19:54460585 | A | AC | 71 | a0001c0001t0001g0024 a0001c0001t0001g0035 a0001c0001t0001g0041 others(68): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2241-173dupC | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 54460585 | ||||||
| chr19:54460585 | A | ACC | 17 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(14): Show |
28 | HG00408.hp2 HG00597.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.2241-174_2241-173d others(4): Show |
LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 54460585 | ||||||
| chr19:54460593 | C | CG | 18 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0039 others(15): Show |
20 | HG01099.hp1 HG01099.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2241-170dupG | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 54460593 | ||||||
| chr19:54460594 | G | C | 1 | a0001c0002t0002g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2241-172G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460594 | |||||||
| chr19:54460595 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
18 | HG00408.hp1 HG00544.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2241-171G>A | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460595 | |||||||
| chr19:54460596 | G | C | 5 | a0001c0002t0002g0048 a0001c0002t0002g0050 a0001c0002t0002g0139 others(2): Show |
7 | HG01978.hp2 HG02080.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241-170G>C | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460596 | |||||||
| chr19:54460597 | C | G | 1 | a0001c0002t0002g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2241-169C>G | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460597 | |||||||
| chr19:54460604 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2241-162C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460604 | |||||||
| chr19:54460609 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0045 others(8): Show |
17 | HG00733.hp1 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2241-157C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460609 | |||||||
| chr19:54460681 | C | T | 1 | a0001c0002t0004g0132 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2241-85C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460681 | |||||||
| chr19:54460726 | C | T | 1 | a0001c0002t0002g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2241-40C>T | LENG8 | ENSG00000167615.18 | transcript | ENST00000326764.10 | protein_coding | 15/15 | chr19 | 54460726 |