Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 143903 |
| ensemblid | ENSG00000204381.12 |
| hgncid | 29471 |
| symbol | LAYN |
| name | layilin |
| refseq_nuc | NM_178834.5 |
| refseq_prot | NP_849156.1 |
| ensembl_nuc | ENST00000375614.7 |
| ensembl_prot | ENSP00000364764.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 111540720 |
| end | 111561745 |
| strand | + |
| ver | v1.2 |
| region | chr11:111540720-111561745 |
| region5000 | chr11:111535720-111566745 |
| regionname0 | LAYN_chr11_111540720_111561745 |
| regionname5000 | LAYN_chr11_111535720_111566745 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 374 | 264 | 62 | 70 | 85 | 9 | 36 | 57 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0002 | 0/0 | 374 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0003 | 0/0 | 374 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0004 | 0/0 | 374 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0005 | 0/0 | 374 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0006 | 0/0 | 374 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0007 | 0/0 | 374 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0008 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| a0009 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | MRPGT others(369): Show |
chr11 | 111535720 | 111566745 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1122 | 243 | 52 | 63 | 82 | 9 | 36 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0001c0003 | 1/0 | 1122 | 13 | 8 | 4 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0001c0005 | 0/0 | 1122 | 8 | 2 | 3 | 3 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0002c0002 | 0/0 | 1122 | 14 | 13 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0003c0004 | 0/0 | 1122 | 9 | 9 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0004c0007 | 0/0 | 1122 | 3 | 2 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0005c0006 | 0/0 | 1122 | 3 | 0 | 0 | 3 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0006c0008 | 0/0 | 1122 | 2 | 2 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0007c0010 | 0/0 | 1122 | 1 | 0 | 0 | 0 | 1 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0008c0011 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 | ||
| a0009c0009 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | ATGAG others(1117): Show |
chr11 | 111535720 | 111566745 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2533 | 162 | 21 | 46 | 65 | 5 | 24 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0002 | 0/0 | 2533 | 45 | 15 | 12 | 8 | 4 | 6 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0003 | 0/0 | 2533 | 6 | 6 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0004 | 0/0 | 2536 | 4 | 4 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2531): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0005 | 0/0 | 2533 | 8 | 0 | 2 | 0 | 0 | 6 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0006 | 0/0 | 2533 | 7 | 0 | 0 | 7 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0007 | 0/0 | 2533 | 4 | 1 | 2 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0009 | 0/0 | 2533 | 2 | 2 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0010 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0011 | 0/0 | 2533 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0012 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0013 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0001t0014 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0003t0001 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0001c0003t0004 | 1/0 | 2536 | 12 | 7 | 4 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2531): Show |
chr11 | 111535720 | 111566745 |
| a0001c0005t0001 | 0/0 | 2533 | 8 | 2 | 3 | 3 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0002c0002t0002 | 0/0 | 2533 | 13 | 12 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0002c0002t0003 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0003c0004t0003 | 0/0 | 2533 | 9 | 9 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0004c0007t0002 | 0/0 | 2533 | 3 | 2 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0005c0006t0001 | 0/0 | 2533 | 3 | 0 | 0 | 3 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0006c0008t0008 | 0/0 | 2533 | 2 | 2 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0007c0010t0002 | 0/0 | 2533 | 1 | 0 | 0 | 0 | 1 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0008c0011t0001 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| a0009c0009t0002 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | GTGCG others(2528): Show |
chr11 | 111535720 | 111566745 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 0 | 10 | 18 | 1 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 3 | 5 | 0 | 4 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 0 | 9 | 1 | 2 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0002 | 0/0 | 12 | 4 | 1 | 2 | 3 | 2 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0039 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0006g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0007g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0011g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0003t0004g0006 | 1/0 | 6 | 2 | 3 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0003t0004g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0003t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0003t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0005t0001g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0001c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0002g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0002g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0002c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0003c0004t0003g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0003c0004t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0003c0004t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0003c0004t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0004c0007t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0004c0007t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0004c0007t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0005c0006t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0005c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0006c0008t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0006c0008t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0007c0010t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0008c0011t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| a0009c0009t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0007 | c0010 | t0002 | g0072 | EUR | GBR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0135 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00738 | hp1 | a0001 | c0003 | t0004 | g0006 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0006 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01109 | hp2 | a0004 | c0007 | t0002 | g0125 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0059 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0008 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01496 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01884 | hp2 | a0003 | c0004 | t0003 | g0119 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01891 | hp2 | a0003 | c0004 | t0003 | g0007 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01952 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0070 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02055 | hp2 | a0008 | c0011 | t0001 | g0103 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02280 | hp1 | a0003 | c0004 | t0003 | g0007 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02647 | hp1 | a0009 | c0009 | t0002 | g0055 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02809 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02818 | hp2 | a0004 | c0007 | t0002 | g0038 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0049 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02922 | hp1 | a0006 | c0008 | t0008 | g0068 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02922 | hp2 | a0001 | c0003 | t0004 | g0060 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0050 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02970 | hp2 | a0003 | c0004 | t0003 | g0007 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02976 | hp1 | a0003 | c0004 | t0003 | g0007 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0136 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0052 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0051 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03486 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0062 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0137 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0073 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18522 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | YRI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18522 | hp2 | a0004 | c0007 | t0002 | g0002 | AFR | YRI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18950 | hp2 | a0005 | c0006 | t0001 | g0146 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18952 | hp2 | a0005 | c0006 | t0001 | g0011 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18965 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18974 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18982 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18988 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18990 | hp2 | a0005 | c0006 | t0001 | g0011 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | LWK | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | LWK | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19240 | hp1 | a0003 | c0004 | t0003 | g0007 | AFR | YRI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | YRI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | TSI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0123 | SAS | GIH | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01123 | hp1 | a0001 | c0003 | t0004 | g0006 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG01123 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02486 | hp2 | a0003 | c0004 | t0003 | g0007 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| HG06807 | hp2 | a0003 | c0004 | t0003 | g0118 | AFR | USA | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | USA | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA20300 | hp2 | a0003 | c0004 | t0003 | g0120 | AFR | USA | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA21309 | hp1 | a0006 | c0008 | t0008 | g0069 | AFR | LWK | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | LWK | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0093 | REF | REF | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0006 | REF | REF | LAYN_chr11_111535720_111566745 | LAYN | chr11 | 111535720 | 111566745 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111540883 | G | A | 2 | a0002 a0006 |
16 | HG01952.hp2 HG02572.hp2 HG02723.hp1 others(13): Show |
missense_variant | MODERATE | c.40G>A | p.Val14Met | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/7 | 164/2536 | 40/1125 | 14/374 | chr11 | 111540883 | |||
| chr11:111543938 | G | A | 1 | a0009 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.101G>A | p.Arg34Gln | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/7 | 225/2536 | 101/1125 | 34/374 | chr11 | 111543938 | |||
| chr11:111544009 | G | A | 1 | a0003 | 9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
missense_variant | MODERATE | c.172G>A | p.Glu58Lys | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/7 | 296/2536 | 172/1125 | 58/374 | chr11 | 111544009 | |||
| chr11:111549674 | A | G | 1 | a0006 | 2 | HG02922.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.440A>G | p.His147Arg | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/7 | 564/2536 | 440/1125 | 147/374 | chr11 | 111549674 | |||
| chr11:111549715 | T | C | 1 | a0005 | 3 | NA18950.hp2 NA18952.hp2 NA18990.hp2 |
missense_variant | MODERATE | c.481T>C | p.Phe161Leu | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/7 | 605/2536 | 481/1125 | 161/374 | chr11 | 111549715 | |||
| chr11:111560265 | C | T | 1 | a0008 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.932C>T | p.Ser311Leu | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 1056/2536 | 932/1125 | 311/374 | chr11 | 111560265 | |||
| chr11:111560325 | C | T | 1 | a0004 | 3 | HG01109.hp2 HG02818.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.992C>T | p.Ser331Leu | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 1116/2536 | 992/1125 | 331/374 | chr11 | 111560325 | |||
| chr11:111560352 | G | A | 1 | a0007 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1019G>A | p.Ser340Asn | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 1143/2536 | 1019/1125 | 340/374 | chr11 | 111560352 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111549639 | A | G | 10 | a0001c0001 a0001c0005 a0002c0002 others(7): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
synonymous_variant | LOW | c.405A>G | p.Pro135Pro | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/7 | 529/2536 | 405/1125 | 135/374 | chr11 | 111549639 | |||
| chr11:111560299 | C | T | 1 | a0001c0005 | 8 | HG01123.hp2 HG01496.hp1 HG01952.hp1 others(5): Show |
synonymous_variant | LOW | c.966C>T | p.Asp322Asp | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 1090/2536 | 966/1125 | 322/374 | chr11 | 111560299 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111540810 | G | T | 1 | a0001c0001t0009 | 2 | HG02886.hp1 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-34G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/7 | 34 | chr11 | 111540810 | ||||||
| chr11:111540821 | G | A | 1 | a0001c0001t0010 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/7 | 23 | chr11 | 111540821 | ||||||
| chr11:111560611 | C | A | 1 | a0001c0001t0011 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*153C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 153 | chr11 | 111560611 | ||||||
| chr11:111560868 | G | T | 1 | a0001c0001t0014 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 410 | chr11 | 111560868 | ||||||
| chr11:111560869 | C | T | 1 | a0001c0001t0014 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 411 | chr11 | 111560869 | ||||||
| chr11:111560889 | C | T | 8 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0011 others(5): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*431C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 431 | chr11 | 111560889 | ||||||
| chr11:111560908 | T | G | 1 | a0006c0008t0008 | 2 | HG02922.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*450T>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 450 | chr11 | 111560908 | ||||||
| chr11:111560931 | GAAT | G | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(20): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*479_*481delTAA | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 479 | INFO_REALIGN_3_PRIME | chr11 | 111560931 | |||||
| chr11:111560965 | G | A | 1 | a0001c0001t0006 | 7 | HG00597.hp2 NA18944.hp1 NA18963.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*507G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 507 | chr11 | 111560965 | ||||||
| chr11:111561064 | A | G | 1 | a0001c0001t0013 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*606A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 606 | chr11 | 111561064 | ||||||
| chr11:111561158 | C | G | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(3): Show |
23 | HG00733.hp1 HG01099.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*700C>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 700 | chr11 | 111561158 | ||||||
| chr11:111561436 | G | T | 9 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(6): Show |
191 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*978G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 978 | chr11 | 111561436 | ||||||
| chr11:111561518 | T | C | 1 | a0001c0001t0007 | 4 | HG00733.hp1 HG01099.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1060T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 1060 | chr11 | 111561518 | ||||||
| chr11:111561601 | T | C | 1 | a0001c0001t0009 | 2 | HG02886.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1143T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 1143 | chr11 | 111561601 | ||||||
| chr11:111561706 | A | G | 1 | a0001c0001t0012 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1248A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 7/7 | 1248 | chr11 | 111561706 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111540950 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.85+22G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111540950 | |||||||
| chr11:111541005 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.85+77G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541005 | |||||||
| chr11:111541031 | C | T | 1 | a0005c0006t0001g0146 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.85+103C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541031 | |||||||
| chr11:111541218 | G | A | 7 | a0001c0001t0004g0021 a0001c0001t0007g0018 a0001c0001t0009g0048 others(4): Show |
10 | HG00733.hp1 HG01099.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.85+290G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541218 | |||||||
| chr11:111541263 | A | T | 1 | a0001c0001t0004g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+335A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541263 | |||||||
| chr11:111541295 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.85+367C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541295 | |||||||
| chr11:111541333 | C | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.85+405C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541333 | |||||||
| chr11:111541389 | G | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.85+461G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541389 | |||||||
| chr11:111541594 | C | CTCTGGCT | 5 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0056 others(2): Show |
5 | HG02647.hp1 HG02886.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+677_85+683dupGG others(5): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr11 | 111541594 | ||||||
| chr11:111541658 | C | A | 1 | a0001c0001t0007g0018 | 3 | HG00733.hp1 HG01099.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.85+730C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541658 | |||||||
| chr11:111541683 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0011g0008 |
6 | HG01361.hp1 HG01496.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+755G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541683 | |||||||
| chr11:111541952 | C | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0042 others(5): Show |
16 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.85+1024C>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541952 | |||||||
| chr11:111541969 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.85+1041G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541969 | |||||||
| chr11:111541980 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.85+1052C>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111541980 | |||||||
| chr11:111542220 | T | C | 12 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0002g0014 others(9): Show |
18 | HG01952.hp2 HG02572.hp2 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.85+1292T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542220 | |||||||
| chr11:111542236 | G | C | 1 | a0001c0001t0012g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.85+1308G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542236 | |||||||
| chr11:111542319 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.85+1391G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542319 | |||||||
| chr11:111542325 | C | G | 4 | a0001c0001t0004g0021 a0001c0001t0012g0050 a0001c0005t0001g0051 others(1): Show |
5 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+1397C>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542325 | |||||||
| chr11:111542373 | G | C | 1 | a0001c0001t0007g0018 | 3 | HG00733.hp1 HG01099.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.85+1445G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542373 | |||||||
| chr11:111542554 | AT | A | 14 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0009g0048 others(11): Show |
20 | HG01952.hp2 HG02572.hp2 HG02723.hp1 others(17): Show |
intron_variant | MODIFIER | c.86-1367delT | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr11 | 111542554 | ||||||
| chr11:111542662 | G | A | 1 | a0002c0002t0003g0062 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.86-1261G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542662 | |||||||
| chr11:111542677 | G | T | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.86-1246G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542677 | |||||||
| chr11:111542686 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0140 |
5 | HG00733.hp2 HG02148.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-1237C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542686 | |||||||
| chr11:111542718 | G | A | 2 | a0001c0001t0009g0048 a0001c0001t0009g0049 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.86-1205G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542718 | |||||||
| chr11:111542730 | C | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.86-1193C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542730 | |||||||
| chr11:111542740 | C | T | 37 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0138 others(34): Show |
57 | HG00140.hp2 HG00558.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.86-1183C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542740 | |||||||
| chr11:111542971 | T | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.86-952T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111542971 | |||||||
| chr11:111543186 | G | C | 12 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0002g0014 others(9): Show |
18 | HG01952.hp2 HG02572.hp2 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-737G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111543186 | |||||||
| chr11:111543365 | T | A | 1 | a0001c0001t0001g0042 | 2 | HG00544.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.86-558T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111543365 | |||||||
| chr11:111543402 | C | G | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.86-521C>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111543402 | |||||||
| chr11:111543752 | T | G | 1 | a0001c0001t0001g0022 | 2 | HG00140.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.86-171T>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 1/6 | chr11 | 111543752 | |||||||
| chr11:111544486 | G | T | 6 | a0001c0001t0004g0021 a0001c0001t0012g0050 a0003c0004t0003g0007 others(3): Show |
12 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+266G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544486 | |||||||
| chr11:111544573 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.383+353C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544573 | |||||||
| chr11:111544666 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.383+446A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544666 | |||||||
| chr11:111544669 | G | A | 1 | a0001c0001t0010g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.383+449G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544669 | |||||||
| chr11:111544710 | T | C | 7 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0009g0048 others(4): Show |
7 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+490T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544710 | |||||||
| chr11:111544820 | G | A | 4 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 others(1): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+600G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544820 | |||||||
| chr11:111544898 | A | T | 2 | a0002c0002t0002g0063 a0002c0002t0002g0064 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.383+678A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544898 | |||||||
| chr11:111544905 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.383+685G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544905 | |||||||
| chr11:111544928 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.383+708G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111544928 | |||||||
| chr11:111545014 | C | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.383+794C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545014 | |||||||
| chr11:111545019 | A | G | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.383+799A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545019 | |||||||
| chr11:111545023 | A | G | 1 | a0001c0001t0004g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383+803A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545023 | |||||||
| chr11:111545055 | A | AAT | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(45): Show |
82 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.383+854_383+855dup others(2): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 111545055 | ||||||
| chr11:111545055 | A | AATAT | 6 | a0001c0001t0002g0053 a0001c0001t0002g0121 a0001c0001t0002g0122 others(3): Show |
7 | HG03490.hp1 HG03492.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+852_383+855dup others(4): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 111545055 | ||||||
| chr11:111545055 | A | AATATAT | 3 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 |
8 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+850_383+855dup others(6): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 111545055 | ||||||
| chr11:111545055 | A | AATATATA others(5): Show |
1 | a0001c0001t0004g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383+844_383+855dup others(12): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 111545055 | ||||||
| chr11:111545055 | AAT | A | 11 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0004g0021 others(8): Show |
14 | HG00733.hp1 HG01099.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.383+854_383+855del others(2): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 111545055 | ||||||
| chr11:111545072 | A | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.383+852A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545072 | |||||||
| chr11:111545074 | A | T | 3 | a0001c0001t0001g0115 a0001c0001t0003g0046 a0001c0001t0003g0047 |
3 | HG03130.hp2 NA18951.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.383+854A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545074 | |||||||
| chr11:111545076 | T | A | 40 | a0001c0001t0001g0040 a0001c0001t0002g0002 a0001c0001t0002g0016 others(37): Show |
61 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.383+856T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545076 | |||||||
| chr11:111545079 | T | C | 2 | a0001c0001t0009g0048 a0001c0001t0009g0049 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.383+859T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545079 | |||||||
| chr11:111545097 | G | A | 40 | a0001c0001t0001g0040 a0001c0001t0002g0002 a0001c0001t0002g0016 others(37): Show |
61 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.383+877G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545097 | |||||||
| chr11:111545271 | A | G | 19 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0111 others(16): Show |
27 | HG00733.hp1 HG01099.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.383+1051A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545271 | |||||||
| chr11:111545315 | T | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0075 others(4): Show |
15 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.383+1095T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545315 | |||||||
| chr11:111545330 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.383+1110C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545330 | |||||||
| chr11:111545364 | G | T | 1 | a0001c0001t0004g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383+1144G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545364 | |||||||
| chr11:111545411 | C | T | 2 | a0006c0008t0008g0068 a0006c0008t0008g0069 |
2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.383+1191C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545411 | |||||||
| chr11:111545449 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0035 others(2): Show |
15 | HG00597.hp2 HG00733.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.383+1229A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545449 | |||||||
| chr11:111545553 | C | T | 2 | a0001c0001t0004g0021 a0001c0001t0012g0050 |
3 | HG02280.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.383+1333C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545553 | |||||||
| chr11:111545620 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.383+1400C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545620 | |||||||
| chr11:111545665 | C | A | 5 | a0001c0001t0012g0050 a0003c0004t0003g0007 a0003c0004t0003g0118 others(2): Show |
10 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.383+1445C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545665 | |||||||
| chr11:111545848 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.383+1628G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545848 | |||||||
| chr11:111545907 | T | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.383+1687T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111545907 | |||||||
| chr11:111546088 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.383+1868G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546088 | |||||||
| chr11:111546236 | A | G | 1 | a0001c0001t0004g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383+2016A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546236 | |||||||
| chr11:111546266 | A | G | 2 | a0001c0001t0009g0048 a0001c0001t0009g0049 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.383+2046A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546266 | |||||||
| chr11:111546287 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.383+2067T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546287 | |||||||
| chr11:111546457 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.383+2237C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546457 | |||||||
| chr11:111546500 | C | A | 2 | a0002c0002t0002g0063 a0002c0002t0002g0064 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.383+2280C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546500 | |||||||
| chr11:111546602 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.383+2382A>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546602 | |||||||
| chr11:111546698 | G | A | 1 | a0002c0002t0002g0014 | 4 | HG02809.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+2478G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546698 | |||||||
| chr11:111546849 | G | T | 1 | a0001c0001t0001g0034 | 2 | HG00621.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.383+2629G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546849 | |||||||
| chr11:111546853 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.383+2633G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546853 | |||||||
| chr11:111546959 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0140 |
5 | HG00733.hp2 HG02148.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-2659A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546959 | |||||||
| chr11:111546977 | T | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.384-2641T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111546977 | |||||||
| chr11:111547054 | A | G | 41 | a0001c0001t0001g0040 a0001c0001t0002g0002 a0001c0001t0002g0016 others(38): Show |
62 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.384-2564A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547054 | |||||||
| chr11:111547061 | T | C | 6 | a0001c0001t0004g0021 a0001c0001t0012g0050 a0003c0004t0003g0007 others(3): Show |
12 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.384-2557T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547061 | |||||||
| chr11:111547314 | G | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.384-2304G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547314 | |||||||
| chr11:111547336 | A | G | 1 | a0001c0005t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384-2282A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547336 | |||||||
| chr11:111547431 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0107 |
3 | HG00609.hp2 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.384-2187C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547431 | |||||||
| chr11:111547458 | C | T | 5 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0002g0063 others(2): Show |
5 | HG02572.hp2 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-2160C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547458 | |||||||
| chr11:111547681 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.384-1937A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547681 | |||||||
| chr11:111547695 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.384-1923G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547695 | |||||||
| chr11:111547842 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0139 others(1): Show |
4 | HG01261.hp1 HG02055.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-1776C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111547842 | |||||||
| chr11:111548330 | C | T | 4 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0113 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-1288C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111548330 | |||||||
| chr11:111548780 | C | T | 5 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0002g0063 others(2): Show |
5 | HG02572.hp2 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-838C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111548780 | |||||||
| chr11:111548879 | C | A | 2 | a0001c0001t0009g0048 a0001c0001t0009g0049 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.384-739C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111548879 | |||||||
| chr11:111548973 | C | A | 4 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 others(1): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.384-645C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111548973 | |||||||
| chr11:111549065 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0102 |
2 | NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.384-553A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111549065 | |||||||
| chr11:111549518 | T | A | 1 | a0001c0001t0002g0121 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.384-100T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111549518 | |||||||
| chr11:111549580 | T | A | 1 | a0001c0001t0001g0043 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.384-38T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 2/6 | chr11 | 111549580 | |||||||
| chr11:111549982 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.541+207A>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111549982 | |||||||
| chr11:111550051 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.541+276G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550051 | |||||||
| chr11:111550100 | C | T | 5 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0002g0063 others(2): Show |
5 | HG02572.hp2 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+325C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550100 | |||||||
| chr11:111550211 | T | C | 61 | a0001c0001t0001g0040 a0001c0001t0001g0116 a0001c0001t0002g0002 others(58): Show |
89 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.541+436T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550211 | |||||||
| chr11:111550365 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.541+590C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550365 | |||||||
| chr11:111550480 | A | G | 2 | a0001c0001t0004g0021 a0001c0001t0012g0050 |
3 | HG02280.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.541+705A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550480 | |||||||
| chr11:111550668 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.541+893G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550668 | |||||||
| chr11:111550962 | C | A | 1 | a0001c0001t0002g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.541+1187C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550962 | |||||||
| chr11:111550985 | T | C | 1 | a0004c0007t0002g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.541+1210T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111550985 | |||||||
| chr11:111551023 | G | A | 1 | a0001c0001t0004g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.541+1248G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551023 | |||||||
| chr11:111551144 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.541+1369G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551144 | |||||||
| chr11:111551181 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0081 a0001c0001t0001g0100 others(1): Show |
5 | HG00140.hp1 HG01256.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.541+1406A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551181 | |||||||
| chr11:111551297 | C | A | 4 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 others(1): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.541+1522C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551297 | |||||||
| chr11:111551492 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.541+1717C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551492 | |||||||
| chr11:111551552 | G | A | 2 | a0006c0008t0008g0068 a0006c0008t0008g0069 |
2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.541+1777G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551552 | |||||||
| chr11:111551757 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.541+1982G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551757 | |||||||
| chr11:111551883 | C | A | 1 | a0001c0001t0003g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.541+2108C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111551883 | |||||||
| chr11:111552004 | ATG | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.541+2239_541+2240d others(4): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111552004 | ||||||
| chr11:111552012 | G | GTA | 6 | a0001c0001t0001g0085 a0001c0001t0003g0047 a0003c0004t0003g0007 others(3): Show |
11 | HG01884.hp2 HG01891.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.541+2238_541+2239i others(4): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111552012 | ||||||
| chr11:111552012 | GTGTA | G | 3 | a0001c0001t0001g0043 a0002c0002t0002g0063 a0002c0002t0002g0064 |
4 | HG00639.hp1 HG01074.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2239_541+2242d others(6): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111552012 | ||||||
| chr11:111552012 | GTGTATA | G | 4 | a0001c0001t0003g0141 a0001c0001t0009g0048 a0001c0001t0009g0049 others(1): Show |
4 | HG02886.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2239_541+2244d others(8): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111552012 | ||||||
| chr11:111552014 | G | A | 23 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0081 others(20): Show |
38 | HG00140.hp1 HG00733.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.541+2239G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552014 | |||||||
| chr11:111552014 | GTA | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0105 a0001c0001t0004g0079 |
4 | HG01261.hp1 HG03139.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2257_541+2258d others(4): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111552014 | ||||||
| chr11:111552057 | C | T | 4 | a0001c0001t0003g0141 a0001c0001t0009g0048 a0001c0001t0009g0049 others(1): Show |
4 | HG02886.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2282C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552057 | |||||||
| chr11:111552078 | T | TAGAA | 4 | a0001c0001t0003g0141 a0001c0001t0009g0048 a0001c0001t0009g0049 others(1): Show |
4 | HG02886.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2306_541+2307i others(6): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111552078 | ||||||
| chr11:111552153 | A | C | 6 | a0001c0001t0005g0036 a0001c0001t0005g0073 a0001c0001t0005g0123 others(3): Show |
7 | HG00639.hp2 HG03017.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+2378A>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552153 | |||||||
| chr11:111552214 | T | TA | 3 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0120 |
8 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.542-2340dupA | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111552214 | ||||||
| chr11:111552224 | A | T | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.542-2337A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552224 | |||||||
| chr11:111552395 | G | A | 2 | a0001c0001t0009g0048 a0001c0001t0009g0049 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.542-2166G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552395 | |||||||
| chr11:111552433 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.542-2128G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552433 | |||||||
| chr11:111552561 | G | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.542-2000G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552561 | |||||||
| chr11:111552980 | A | G | 1 | a0002c0002t0003g0062 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-1581A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552980 | |||||||
| chr11:111552992 | C | T | 1 | a0001c0001t0002g0019 | 3 | HG01069.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.542-1569C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111552992 | |||||||
| chr11:111553069 | C | T | 3 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0113 |
3 | HG02486.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.542-1492C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553069 | |||||||
| chr11:111553150 | G | A | 7 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0113 others(4): Show |
12 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-1411G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553150 | |||||||
| chr11:111553222 | G | T | 1 | a0001c0001t0001g0031 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.542-1339G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553222 | |||||||
| chr11:111553244 | A | AAAAT | 3 | a0001c0001t0003g0141 a0001c0001t0009g0048 a0001c0001t0009g0049 |
3 | HG02886.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.542-1297_542-1294d others(6): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553244 | ||||||
| chr11:111553311 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.542-1250T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553311 | |||||||
| chr11:111553380 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0082 others(3): Show |
8 | HG00423.hp1 HG00609.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.542-1181G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553380 | |||||||
| chr11:111553429 | C | T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0114 |
4 | HG00733.hp1 HG01099.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-1132C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553429 | |||||||
| chr11:111553486 | G | T | 2 | a0002c0002t0002g0063 a0002c0002t0002g0064 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.542-1075G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553486 | |||||||
| chr11:111553551 | G | A | 4 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 others(1): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.542-1010G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553551 | |||||||
| chr11:111553620 | T | TA | 62 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0081 others(59): Show |
94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.542-926dupA | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553620 | ||||||
| chr11:111553620 | TA | T | 8 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0007g0018 others(5): Show |
10 | HG00733.hp1 HG01099.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.542-926delA | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553620 | ||||||
| chr11:111553633 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.542-928A>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553633 | |||||||
| chr11:111553693 | A | G | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.542-868A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553693 | |||||||
| chr11:111553715 | T | TAC | 22 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0020 others(19): Show |
40 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.542-809_542-808dup others(2): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553715 | T | TACAC | 20 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0041 others(17): Show |
36 | HG00558.hp2 HG00597.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.542-811_542-808dup others(4): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553715 | T | TACACAC | 30 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0025 others(27): Show |
54 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.542-813_542-808dup others(6): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553715 | T | TACACACA others(1): Show |
6 | a0001c0001t0001g0091 a0001c0001t0002g0023 a0001c0001t0002g0053 others(3): Show |
7 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-815_542-808dup others(8): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553715 | T | TACACACA others(3): Show |
5 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0127 others(2): Show |
5 | HG02647.hp1 HG02886.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-817_542-808dup others(10): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553715 | T | TACACACA others(7): Show |
1 | a0001c0001t0002g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.542-821_542-808dup others(14): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553715 | TAC | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0138 others(8): Show |
15 | HG00423.hp1 HG01934.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.542-809_542-808del others(2): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553715 | TACACACA others(9): Show |
T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0114 |
4 | HG00733.hp1 HG01099.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-823_542-808del others(16): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 111553715 | ||||||
| chr11:111553754 | T | A | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.542-807T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553754 | |||||||
| chr11:111553755 | T | C | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.542-806T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553755 | |||||||
| chr11:111553757 | T | C | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.542-804T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553757 | |||||||
| chr11:111553983 | T | C | 1 | a0001c0001t0001g0035 | 2 | NA18977.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.542-578T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553983 | |||||||
| chr11:111553991 | A | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.542-570A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111553991 | |||||||
| chr11:111554207 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.542-354T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111554207 | |||||||
| chr11:111554323 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.542-238T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111554323 | |||||||
| chr11:111554331 | A | G | 4 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 others(1): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.542-230A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111554331 | |||||||
| chr11:111554350 | AG | A | 6 | a0001c0001t0010g0070 a0002c0002t0002g0014 a0002c0002t0002g0015 others(3): Show |
12 | HG01952.hp2 HG02055.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-210delG | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111554350 | |||||||
| chr11:111554356 | A | G | 9 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0141 others(6): Show |
11 | HG00733.hp1 HG01099.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.542-205A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111554356 | |||||||
| chr11:111554380 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.542-181C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111554380 | |||||||
| chr11:111554523 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.542-38T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 3/6 | chr11 | 111554523 | |||||||
| chr11:111554668 | T | C | 1 | a0001c0001t0005g0036 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.574+75T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 4/6 | chr11 | 111554668 | |||||||
| chr11:111554780 | T | A | 4 | a0001c0001t0003g0141 a0001c0001t0009g0048 a0001c0001t0009g0049 others(1): Show |
4 | HG02886.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+187T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 4/6 | chr11 | 111554780 | |||||||
| chr11:111554933 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.575-274C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 4/6 | chr11 | 111554933 | |||||||
| chr11:111555155 | T | G | 1 | a0001c0001t0002g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.575-52T>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 4/6 | chr11 | 111555155 | |||||||
| chr11:111555386 | C | G | 2 | a0002c0002t0002g0015 a0002c0002t0002g0067 |
5 | HG01952.hp2 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.658+96C>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111555386 | |||||||
| chr11:111555425 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.658+135G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111555425 | |||||||
| chr11:111555691 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.658+401T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111555691 | |||||||
| chr11:111555886 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.658+596G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111555886 | |||||||
| chr11:111555932 | G | A | 4 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 others(1): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.658+642G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111555932 | |||||||
| chr11:111555973 | G | T | 1 | a0001c0001t0002g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.658+683G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111555973 | |||||||
| chr11:111556013 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.658+723G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556013 | |||||||
| chr11:111556075 | A | G | 1 | a0003c0004t0003g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.658+785A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556075 | |||||||
| chr11:111556137 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.658+847C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556137 | |||||||
| chr11:111556225 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.658+935C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556225 | |||||||
| chr11:111556234 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0002g0129 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.658+944G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556234 | |||||||
| chr11:111556281 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.658+991G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556281 | |||||||
| chr11:111556296 | C | T | 1 | a0001c0003t0004g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.658+1006C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556296 | |||||||
| chr11:111556453 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.659-1088A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556453 | |||||||
| chr11:111556528 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.659-1013T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556528 | |||||||
| chr11:111556538 | G | T | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.659-1003G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556538 | |||||||
| chr11:111556546 | T | A | 1 | a0001c0003t0004g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.659-995T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556546 | |||||||
| chr11:111556577 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.659-964C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556577 | |||||||
| chr11:111556765 | C | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.659-776C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556765 | |||||||
| chr11:111556815 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.659-726C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556815 | |||||||
| chr11:111556939 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.659-602A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111556939 | |||||||
| chr11:111557127 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.659-414G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111557127 | |||||||
| chr11:111557290 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.659-251G>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111557290 | |||||||
| chr11:111557300 | C | T | 1 | a0001c0001t0001g0030 | 2 | NA18942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.659-241C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111557300 | |||||||
| chr11:111557370 | C | T | 4 | a0003c0004t0003g0007 a0003c0004t0003g0118 a0003c0004t0003g0119 others(1): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.659-171C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111557370 | |||||||
| chr11:111557460 | C | G | 1 | a0001c0001t0001g0043 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.659-81C>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 5/6 | chr11 | 111557460 | |||||||
| chr11:111557785 | T | C | 6 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0141 others(3): Show |
8 | HG00733.hp1 HG01099.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.761+142T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111557785 | |||||||
| chr11:111557935 | C | A | 1 | a0001c0001t0009g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.761+292C>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111557935 | |||||||
| chr11:111558190 | G | A | 3 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0003g0062 |
3 | HG02886.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.761+547G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558190 | |||||||
| chr11:111558220 | A | T | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.761+577A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558220 | |||||||
| chr11:111558390 | T | A | 1 | a0001c0001t0002g0130 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.761+747T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558390 | |||||||
| chr11:111558417 | G | A | 16 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0111 others(13): Show |
23 | HG00733.hp1 HG01099.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.761+774G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558417 | |||||||
| chr11:111558449 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.761+806A>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558449 | |||||||
| chr11:111558479 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.761+836G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558479 | |||||||
| chr11:111558483 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.761+840G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558483 | |||||||
| chr11:111558725 | A | T | 3 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0003g0062 |
3 | HG02886.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.761+1082A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558725 | |||||||
| chr11:111558777 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.761+1134T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558777 | |||||||
| chr11:111558777 | T | TA | 5 | a0001c0001t0002g0037 a0001c0001t0002g0057 a0001c0001t0009g0048 others(2): Show |
6 | HG02572.hp1 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.761+1141dupA | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 111558777 | ||||||
| chr11:111558777 | T | TAA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.761+1140_761+1141d others(4): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 111558777 | ||||||
| chr11:111558779 | AAAAAATA others(3): Show |
A | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.761+1138_761+1147d others(12): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 111558779 | ||||||
| chr11:111558781 | A | AATAT | 1 | a0002c0002t0002g0014 | 4 | HG02809.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+1139_761+1140i others(6): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 111558781 | ||||||
| chr11:111558783 | A | AAT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0080 a0001c0001t0002g0128 others(5): Show |
11 | HG01952.hp2 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.761+1159_761+1160d others(4): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 111558783 | ||||||
| chr11:111558783 | A | T | 1 | a0002c0002t0002g0014 | 4 | HG02809.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+1140A>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558783 | |||||||
| chr11:111558785 | T | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
122 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.761+1142T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558785 | |||||||
| chr11:111558787 | T | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(5): Show |
13 | HG00609.hp2 HG00741.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.761+1144T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558787 | |||||||
| chr11:111558849 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0012g0050 |
3 | HG02970.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.761+1206G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111558849 | |||||||
| chr11:111559005 | C | T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0114 |
4 | HG00733.hp1 HG01099.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.762-1090C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559005 | |||||||
| chr11:111559050 | T | G | 1 | a0009c0009t0002g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.762-1045T>G | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559050 | |||||||
| chr11:111559411 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.762-684G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559411 | |||||||
| chr11:111559454 | ATTATTTT others(3): Show |
A | 1 | a0007c0010t0002g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.762-623_762-614del others(10): Show |
LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 111559454 | ||||||
| chr11:111559491 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.762-604G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559491 | |||||||
| chr11:111559522 | C | T | 3 | a0001c0001t0009g0048 a0001c0001t0009g0049 a0002c0002t0003g0062 |
3 | HG02886.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.762-573C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559522 | |||||||
| chr11:111559564 | T | C | 1 | a0001c0001t0001g0044 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.762-531T>C | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559564 | |||||||
| chr11:111559601 | G | A | 2 | a0001c0001t0009g0048 a0001c0001t0009g0049 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.762-494G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559601 | |||||||
| chr11:111559647 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.762-448C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559647 | |||||||
| chr11:111559667 | C | T | 1 | a0002c0002t0003g0062 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.762-428C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559667 | |||||||
| chr11:111559682 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.762-413C>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559682 | |||||||
| chr11:111559726 | T | A | 1 | a0001c0001t0002g0037 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.762-369T>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559726 | |||||||
| chr11:111559782 | G | T | 1 | a0001c0001t0003g0112 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.762-313G>T | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559782 | |||||||
| chr11:111559848 | G | A | 2 | a0002c0002t0002g0063 a0002c0002t0002g0064 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.762-247G>A | LAYN | ENSG00000204381.12 | transcript | ENST00000375614.7 | protein_coding | 6/6 | chr11 | 111559848 |