Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4060 |
| ensemblid | ENSG00000139329.5 |
| hgncid | 6724 |
| symbol | LUM |
| name | lumican |
| refseq_nuc | NM_002345.4 |
| refseq_prot | NP_002336.1 |
| ensembl_nuc | ENST00000266718.5 |
| ensembl_prot | ENSP00000266718.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 91102629 |
| end | 91111494 |
| strand | - |
| ver | v1.2 |
| region | chr12:91102629-91111494 |
| region5000 | chr12:91097629-91116494 |
| regionname0 | LUM_chr12_91102629_91111494 |
| regionname5000 | LUM_chr12_91097629_91116494 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 338 | 379 | 95 | 61 | 173 | 12 | 36 | 133 | LUM_chr12_91097629_91116494 | LUM | MSLSA others(333): Show |
chr12 | 91097629 | 91116494 |
| a0002 | 0/0 | 338 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LUM_chr12_91097629_91116494 | LUM | MSLSA others(333): Show |
chr12 | 91097629 | 91116494 |
| a0003 | 0/0 | 338 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | MSLSA others(333): Show |
chr12 | 91097629 | 91116494 |
| a0004 | 0/0 | 338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | MSLSA others(333): Show |
chr12 | 91097629 | 91116494 |
| a0005 | 0/0 | 338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | MSLSA others(333): Show |
chr12 | 91097629 | 91116494 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1014 | 317 | 91 | 58 | 123 | 12 | 31 | LUM_chr12_91097629_91116494 | LUM | ATGAG others(1009): Show |
chr12 | 91097629 | 91116494 | ||
| a0001c0002 | 0/0 | 1014 | 60 | 4 | 3 | 48 | 0 | 5 | LUM_chr12_91097629_91116494 | LUM | ATGAG others(1009): Show |
chr12 | 91097629 | 91116494 | ||
| a0001c0003 | 0/0 | 1014 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | ATGAG others(1009): Show |
chr12 | 91097629 | 91116494 | ||
| a0002c0004 | 0/0 | 1014 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | ATGAG others(1009): Show |
chr12 | 91097629 | 91116494 | ||
| a0003c0006 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | ATGAG others(1009): Show |
chr12 | 91097629 | 91116494 | ||
| a0004c0005 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | ATGAG others(1009): Show |
chr12 | 91097629 | 91116494 | ||
| a0005c0007 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | ATGAG others(1009): Show |
chr12 | 91097629 | 91116494 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2671 | 257 | 62 | 53 | 105 | 8 | 28 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0002 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0003 | 0/0 | 2671 | 12 | 11 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0004 | 0/0 | 2671 | 11 | 0 | 0 | 11 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0005 | 1/0 | 2671 | 8 | 6 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0006 | 0/0 | 2671 | 7 | 0 | 2 | 0 | 3 | 2 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0007 | 0/0 | 2671 | 6 | 5 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0008 | 0/0 | 2671 | 2 | 0 | 0 | 0 | 1 | 1 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0009 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0011 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0012 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0013 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0014 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0015 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0016 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0017 | 0/0 | 2645 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2640): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0018 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0019 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0020 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0021 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0001t0022 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0002t0001 | 0/0 | 2671 | 3 | 3 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0002t0002 | 0/0 | 2671 | 56 | 1 | 2 | 48 | 0 | 5 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0002t0010 | 0/0 | 2671 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0001c0003t0001 | 0/0 | 2671 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0002c0004t0002 | 0/0 | 2671 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0003c0006t0001 | 0/0 | 2671 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0004c0005t0001 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| a0005c0007t0001 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | AGTTC others(2666): Show |
chr12 | 91097629 | 91116494 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 38 | 0 | 9 | 20 | 1 | 8 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0002 | 0/0 | 18 | 4 | 5 | 5 | 1 | 3 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0003 | 0/0 | 14 | 2 | 3 | 8 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0004 | 0/0 | 14 | 1 | 3 | 8 | 1 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0008 | 0/0 | 8 | 2 | 3 | 2 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0009 | 0/0 | 7 | 4 | 0 | 2 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0012 | 0/0 | 6 | 1 | 0 | 3 | 2 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0014 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0018 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0004g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0005g0013 | 1/0 | 6 | 4 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0006g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0007g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0008g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0009g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0012g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0013g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0014g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0015g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0016g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0018g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0019g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0020g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0021g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0001t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0006 | 0/0 | 11 | 1 | 0 | 10 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0007 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0010 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0022 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0002t0010g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0001c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0002c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0002c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0003c0006t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0004c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| a0005c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0113 | EUR | GBR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00438 | hp1 | a0001 | c0001 | t0018 | g0102 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01106 | hp1 | a0003 | c0006 | t0001 | g0079 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01256 | hp2 | a0001 | c0002 | t0010 | g0068 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0146 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0145 | EUR | IBS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0046 | EUR | IBS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CDX | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | CDX | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02280 | hp1 | a0001 | c0001 | t0021 | g0149 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0165 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02723 | hp1 | a0001 | c0001 | t0019 | g0154 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0104 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03209 | hp1 | a0004 | c0005 | t0001 | g0125 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0130 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0086 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0144 | SAS | PJL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0019 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0093 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0056 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | YRI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18612 | hp1 | a0001 | c0001 | t0012 | g0099 | EAS | CHB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18943 | hp2 | a0005 | c0007 | t0001 | g0101 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18957 | hp1 | a0001 | c0001 | t0014 | g0100 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18962 | hp2 | a0001 | c0001 | t0009 | g0098 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18975 | hp1 | a0002 | c0004 | t0002 | g0071 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18987 | hp1 | a0001 | c0001 | t0022 | g0179 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19004 | hp1 | a0002 | c0004 | t0002 | g0070 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19012 | hp1 | a0001 | c0001 | t0011 | g0117 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | LWK | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | LWK | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19059 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19059 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19089 | hp2 | a0001 | c0001 | t0016 | g0106 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20129 | hp1 | a0001 | c0001 | t0020 | g0137 | AFR | ASW | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ASW | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0143 | EUR | TSI | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | USA | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | USA | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | LWK | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0155 | REF | REF | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0013 | REF | REF | LUM_chr12_91097629_91116494 | LUM | chr12 | 91097629 | 91116494 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91104239 | G | A | 1 | a0005 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.943C>T | p.Arg315Cys | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1061/2671 | 943/1017 | 315/338 | chr12 | 91104239 | |||
| chr12:91108384 | A | G | 1 | a0003 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.596T>C | p.Leu199Pro | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/3 | 714/2671 | 596/1017 | 199/338 | chr12 | 91108384 | |||
| chr12:91108589 | A | T | 1 | a0004 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.391T>A | p.Ser131Thr | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/3 | 509/2671 | 391/1017 | 131/338 | chr12 | 91108589 | |||
| chr12:91108624 | T | C | 1 | a0002 | 2 | NA18975.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.356A>G | p.Lys119Arg | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/3 | 474/2671 | 356/1017 | 119/338 | chr12 | 91108624 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91108131 | G | A | 1 | a0001c0003 | 2 | HG02080.hp1 NA18982.hp2 |
synonymous_variant | LOW | c.849C>T | p.Val283Val | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/3 | 967/2671 | 849/1017 | 283/338 | chr12 | 91108131 | |||
| chr12:91108473 | A | G | 2 | a0001c0002 a0002c0004 |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
synonymous_variant | LOW | c.507T>C | p.Asn169Asn | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/3 | 625/2671 | 507/1017 | 169/338 | chr12 | 91108473 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91102633 | T | A | 1 | a0001c0002t0010 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1532A>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1532 | chr12 | 91102633 | ||||||
| chr12:91102777 | C | A | 1 | a0001c0001t0016 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1388G>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1388 | chr12 | 91102777 | ||||||
| chr12:91102781 | C | T | 1 | a0001c0001t0015 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1384G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1384 | chr12 | 91102781 | ||||||
| chr12:91102822 | C | T | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
375 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*1343G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1343 | chr12 | 91102822 | ||||||
| chr12:91102862 | A | G | 1 | a0001c0001t0014 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1303T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1303 | chr12 | 91102862 | ||||||
| chr12:91102864 | GTGGTGTG others(19): Show |
G | 1 | a0001c0001t0017 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275_*1300delAAGG others(22): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1275 | chr12 | 91102864 | ||||||
| chr12:91102984 | C | T | 2 | a0001c0001t0003 a0001c0001t0013 |
13 | HG01167.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1181G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1181 | chr12 | 91102984 | ||||||
| chr12:91102987 | A | G | 1 | a0001c0001t0003 | 12 | HG01167.hp1 HG02109.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1178T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1178 | chr12 | 91102987 | ||||||
| chr12:91103047 | T | G | 1 | a0001c0001t0006 | 7 | HG01261.hp1 HG01361.hp2 HG01516.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1118A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1118 | chr12 | 91103047 | ||||||
| chr12:91103100 | C | T | 1 | a0001c0001t0012 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1065G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 1065 | chr12 | 91103100 | ||||||
| chr12:91103243 | A | G | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0010 others(1): Show |
60 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*922T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 922 | chr12 | 91103243 | ||||||
| chr12:91103263 | G | T | 1 | a0001c0001t0004 | 11 | HG00544.hp2 HG02015.hp1 HG02523.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*902C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 902 | chr12 | 91103263 | ||||||
| chr12:91103276 | T | C | 1 | a0001c0001t0018 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*889A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 889 | chr12 | 91103276 | ||||||
| chr12:91103471 | C | A | 1 | a0001c0001t0019 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*694G>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 694 | chr12 | 91103471 | ||||||
| chr12:91103495 | T | G | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0010 others(1): Show |
60 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*670A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 670 | chr12 | 91103495 | ||||||
| chr12:91103511 | A | G | 1 | a0001c0001t0007 | 6 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*654T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 654 | chr12 | 91103511 | ||||||
| chr12:91103516 | A | G | 1 | a0001c0001t0006 | 7 | HG01261.hp1 HG01361.hp2 HG01516.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*649T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 649 | chr12 | 91103516 | ||||||
| chr12:91103540 | C | T | 1 | a0001c0001t0006 | 7 | HG01261.hp1 HG01361.hp2 HG01516.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 625 | chr12 | 91103540 | ||||||
| chr12:91103595 | T | C | 1 | a0001c0001t0008 | 2 | HG00099.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*570A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 570 | chr12 | 91103595 | ||||||
| chr12:91103703 | C | T | 1 | a0001c0001t0011 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*462G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 462 | chr12 | 91103703 | ||||||
| chr12:91103708 | A | G | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0010 others(1): Show |
60 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*457T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 457 | chr12 | 91103708 | ||||||
| chr12:91103865 | A | G | 1 | a0001c0001t0009 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*300T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 300 | chr12 | 91103865 | ||||||
| chr12:91103909 | T | C | 1 | a0001c0001t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*256A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 256 | chr12 | 91103909 | ||||||
| chr12:91104007 | T | G | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02280.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*158A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 3/3 | 158 | chr12 | 91104007 | ||||||
| chr12:91111437 | G | C | 1 | a0001c0001t0022 | 1 | NA18987.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61C>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/3 | chr12 | 91111437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91104397 | T | G | 1 | a0001c0001t0007g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.863-78A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104397 | |||||||
| chr12:91104402 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.863-83A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104402 | |||||||
| chr12:91104422 | C | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(14): Show |
30 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.863-103G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104422 | |||||||
| chr12:91104517 | A | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0109 |
3 | HG02572.hp2 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.863-198T>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104517 | |||||||
| chr12:91104522 | T | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(30): Show |
49 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.863-203A>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104522 | |||||||
| chr12:91104695 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.863-376T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104695 | |||||||
| chr12:91104889 | C | T | 2 | a0001c0002t0002g0065 a0001c0002t0002g0067 |
2 | NA18962.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.863-570G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104889 | |||||||
| chr12:91104909 | A | G | 26 | a0001c0001t0002g0074 a0001c0002t0002g0006 a0001c0002t0002g0007 others(23): Show |
60 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.863-590T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91104909 | |||||||
| chr12:91105093 | TTAACAAA others(10): Show |
T | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.863-791_863-775del others(17): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105093 | |||||||
| chr12:91105235 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.863-916A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105235 | |||||||
| chr12:91105258 | G | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
302 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.863-939C>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105258 | |||||||
| chr12:91105590 | T | C | 28 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(25): Show |
44 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.863-1271A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105590 | |||||||
| chr12:91105687 | T | C | 7 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0050 others(4): Show |
11 | HG02257.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.863-1368A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105687 | |||||||
| chr12:91105709 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.863-1390A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105709 | |||||||
| chr12:91105755 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
376 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.863-1436C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105755 | |||||||
| chr12:91105760 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0028 others(10): Show |
30 | HG00733.hp1 HG01993.hp2 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.863-1441G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105760 | |||||||
| chr12:91105864 | G | A | 5 | a0001c0001t0007g0033 a0001c0001t0007g0072 a0001c0001t0007g0073 others(2): Show |
6 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.863-1545C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105864 | |||||||
| chr12:91105933 | T | C | 1 | a0001c0001t0007g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.863-1614A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105933 | |||||||
| chr12:91105996 | C | T | 2 | a0001c0001t0008g0086 a0001c0001t0008g0113 |
2 | HG00099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.863-1677G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91105996 | |||||||
| chr12:91106081 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
5 | HG01928.hp2 HG01934.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.863-1762G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106081 | |||||||
| chr12:91106120 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
277 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.863-1801G>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106120 | |||||||
| chr12:91106225 | A | T | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.862+1893T>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106225 | |||||||
| chr12:91106334 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.862+1784C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106334 | |||||||
| chr12:91106649 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.862+1469C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106649 | |||||||
| chr12:91106679 | T | G | 1 | a0001c0002t0002g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.862+1439A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106679 | |||||||
| chr12:91106690 | T | TAA | 12 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): Show |
19 | HG01074.hp1 HG01074.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.862+1426_862+1427d others(4): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.862+1425_862+1427d others(5): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAAA | 28 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0040 others(25): Show |
40 | HG00438.hp1 HG00544.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.862+1424_862+1427d others(6): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAAAA | 17 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(14): Show |
32 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.862+1423_862+1427d others(7): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAAAAAA others(7): Show |
2 | a0001c0001t0007g0033 a0001c0001t0007g0072 |
3 | HG01192.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.862+1414_862+1427d others(16): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAAAAAA others(9): Show |
1 | a0001c0001t0007g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.862+1412_862+1427d others(18): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0002g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.862+1411_862+1427d others(19): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0007g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.862+1408_862+1427d others(22): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | T | TAAAAAAA others(17): Show |
1 | a0001c0001t0021g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.862+1427_862+1428i others(26): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106690 | TA | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
14 | HG02055.hp1 HG02257.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.862+1427delT | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106690 | |||||||
| chr12:91106692 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.862+1425_862+1426i others(31): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106692 | |||||||
| chr12:91106711 | A | AAAAAAAA others(1): Show |
11 | a0001c0002t0002g0015 a0001c0002t0002g0019 a0001c0002t0002g0020 others(8): Show |
20 | HG00438.hp2 HG00597.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.862+1406_862+1407i others(10): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106711 | |||||||
| chr12:91106711 | A | AAAAAAAC | 11 | a0001c0002t0001g0032 a0001c0002t0002g0006 a0001c0002t0002g0007 others(8): Show |
37 | HG00408.hp2 HG01255.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.862+1406_862+1407i others(9): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106711 | |||||||
| chr12:91106711 | A | C | 1 | a0001c0002t0002g0066 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.862+1407T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106711 | |||||||
| chr12:91106729 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.862+1389A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106729 | |||||||
| chr12:91106943 | A | G | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.862+1175T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106943 | |||||||
| chr12:91106984 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0169 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.862+1134A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91106984 | |||||||
| chr12:91107015 | C | T | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.862+1103G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107015 | |||||||
| chr12:91107083 | T | C | 1 | a0001c0002t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.862+1035A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107083 | |||||||
| chr12:91107124 | C | T | 5 | a0001c0001t0002g0074 a0001c0001t0007g0033 a0001c0001t0007g0072 others(2): Show |
6 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.862+994G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107124 | |||||||
| chr12:91107131 | G | A | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.862+987C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107131 | |||||||
| chr12:91107137 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0171 a0001c0001t0001g0172 |
4 | HG01928.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+981G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107137 | |||||||
| chr12:91107151 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0171 a0001c0001t0001g0172 |
4 | HG01928.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+967T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107151 | |||||||
| chr12:91107155 | G | A | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
60 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.862+963C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107155 | |||||||
| chr12:91107176 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.862+942G>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107176 | |||||||
| chr12:91107176 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0004g0095 |
2 | HG00544.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.862+942G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107176 | |||||||
| chr12:91107184 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.862+934T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107184 | |||||||
| chr12:91107191 | AGG | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0119 |
3 | HG03831.hp2 NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.862+925_862+926del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107191 | |||||||
| chr12:91107192 | G | C | 5 | a0001c0002t0002g0007 a0001c0002t0002g0015 a0001c0002t0002g0021 others(2): Show |
6 | HG01255.hp1 HG01358.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+926C>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107192 | |||||||
| chr12:91107199 | A | AAAAG | 18 | a0001c0001t0001g0120 a0001c0001t0021g0149 a0001c0002t0001g0032 others(15): Show |
43 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.862+915_862+918dup others(4): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107199 | |||||||
| chr12:91107199 | A | AAAAGAAA others(1): Show |
28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0017 others(25): Show |
56 | HG00099.hp2 HG00735.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.862+911_862+918dup others(8): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107199 | |||||||
| chr12:91107199 | A | AAAAGAAA others(5): Show |
6 | a0001c0001t0001g0048 a0001c0001t0003g0126 a0001c0001t0003g0127 others(3): Show |
7 | HG01167.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.862+907_862+918dup others(12): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107199 | |||||||
| chr12:91107199 | A | AAG | 3 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0119 |
3 | HG03831.hp2 NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.862+918_862+919ins others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107199 | |||||||
| chr12:91107199 | AAAAGAAA others(33): Show |
A | 1 | a0001c0001t0001g0170 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.862+879_862+918del others(40): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107199 | |||||||
| chr12:91107202 | AGAAAGAA others(29): Show |
A | 3 | a0001c0001t0002g0074 a0001c0001t0007g0072 a0001c0001t0007g0073 |
3 | HG02258.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.862+880_862+915del others(36): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107202 | |||||||
| chr12:91107210 | AGAAAGAG others(21): Show |
A | 1 | a0001c0001t0007g0033 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.862+880_862+907del others(28): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107210 | |||||||
| chr12:91107212 | AAAGAGAG others(4): Show |
A | 4 | a0001c0002t0002g0010 a0001c0002t0002g0019 a0001c0002t0002g0056 others(1): Show |
11 | HG02040.hp2 HG02071.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.862+895_862+905del others(11): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107212 | |||||||
| chr12:91107214 | AGAGAGAA others(17): Show |
A | 2 | a0001c0001t0007g0033 a0001c0001t0007g0075 |
2 | HG01192.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.862+880_862+903del others(24): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107214 | |||||||
| chr12:91107216 | AGAGAAAG | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(39): Show |
124 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.862+895_862+901del others(7): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107216 | |||||||
| chr12:91107217 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(62): Show |
120 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.862+901C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107217 | |||||||
| chr12:91107220 | AAAG | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
60 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.862+895_862+897del others(3): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107220 | |||||||
| chr12:91107221 | A | G | 3 | a0001c0001t0001g0167 a0001c0002t0002g0063 a0001c0002t0002g0065 |
3 | HG00609.hp1 HG02135.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.862+897T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107221 | |||||||
| chr12:91107223 | G | GA | 10 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0050 others(7): Show |
16 | HG02055.hp1 HG02280.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.862+894dupT | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107223 | |||||||
| chr12:91107224 | A | AG | 17 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(14): Show |
38 | HG00408.hp1 HG00642.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.862+893_862+894ins others(1): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107224 | |||||||
| chr12:91107226 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0167 |
3 | HG00609.hp1 HG01975.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.862+892C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107226 | |||||||
| chr12:91107227 | A | AAAG | 3 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0001g0160 |
7 | HG01515.hp1 HG02486.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+888_862+890dup others(3): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107227 | |||||||
| chr12:91107227 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0167 |
2 | HG00609.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.862+891T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107227 | |||||||
| chr12:91107228 | A | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(43): Show |
75 | HG00597.hp1 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.862+890T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107228 | |||||||
| chr12:91107230 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.862+888C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107230 | |||||||
| chr12:91107230 | GA | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(11): Show |
30 | HG00408.hp1 HG00642.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.862+887delT | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107230 | |||||||
| chr12:91107231 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.862+887T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107231 | |||||||
| chr12:91107232 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
137 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.862+886T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107232 | |||||||
| chr12:91107236 | AAG | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(41): Show |
73 | HG00597.hp1 HG00639.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.862+880_862+881del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107236 | |||||||
| chr12:91107237 | AG | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(14): Show |
35 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.862+880delC | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107237 | |||||||
| chr12:91107238 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0017g0165 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.862+880C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107238 | |||||||
| chr12:91107238 | GGA | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0039 others(19): Show |
60 | HG00558.hp1 HG00621.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.862+878_862+879del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107238 | |||||||
| chr12:91107238 | GGAAAGA | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(21): Show |
75 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.862+874_862+879del others(6): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107238 | |||||||
| chr12:91107238 | GGAAAGAA others(3): Show |
G | 2 | a0001c0001t0001g0168 a0001c0001t0003g0044 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.862+870_862+879del others(10): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107238 | |||||||
| chr12:91107238 | GGAAAGAA others(13): Show |
G | 1 | a0001c0001t0006g0046 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.862+860_862+879del others(20): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107238 | |||||||
| chr12:91107239 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0001g0160 |
7 | HG01975.hp1 HG02486.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+879C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107239 | |||||||
| chr12:91107242 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0001g0160 |
7 | HG01975.hp1 HG02486.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+876T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107242 | |||||||
| chr12:91107244 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.862+874T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107244 | |||||||
| chr12:91107245 | A | G | 2 | a0001c0001t0007g0033 a0001c0001t0007g0075 |
2 | HG01192.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.862+873T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107245 | |||||||
| chr12:91107246 | A | AG | 15 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(12): Show |
31 | HG00408.hp1 HG00642.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.862+871dupC | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107246 | |||||||
| chr12:91107249 | A | G | 1 | a0001c0001t0007g0033 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.862+869T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107249 | |||||||
| chr12:91107250 | A | AG | 19 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(16): Show |
30 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.862+867dupC | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107250 | |||||||
| chr12:91107251 | GAAA | G | 27 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0029 others(24): Show |
45 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.862+864_862+866del others(3): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107251 | |||||||
| chr12:91107255 | GAAA | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0039 others(19): Show |
60 | HG00558.hp1 HG00621.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.862+860_862+862del others(3): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107255 | |||||||
| chr12:91107255 | GAAAGAAA others(11): Show |
G | 1 | a0001c0001t0003g0129 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.862+845_862+862del others(18): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107255 | |||||||
| chr12:91107255 | GAAAGAAA others(15): Show |
G | 3 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0131 |
3 | HG02109.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.862+841_862+862del others(22): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107255 | |||||||
| chr12:91107257 | A | G | 3 | a0001c0001t0002g0074 a0001c0001t0007g0072 a0001c0001t0007g0073 |
3 | HG02258.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.862+861T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107257 | |||||||
| chr12:91107258 | A | AGAAAGAG others(21): Show |
1 | a0001c0001t0017g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.862+859_862+860ins others(28): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107258 | |||||||
| chr12:91107259 | GAAA | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(21): Show |
75 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.862+856_862+858del others(3): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107259 | |||||||
| chr12:91107261 | AAGAAAGA others(19): Show |
A | 7 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(4): Show |
20 | HG00597.hp2 HG02056.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.862+831_862+856del others(26): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107261 | |||||||
| chr12:91107263 | GA | G | 3 | a0001c0001t0002g0074 a0001c0001t0007g0072 a0001c0001t0007g0073 |
3 | HG02258.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.862+854delT | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107263 | |||||||
| chr12:91107263 | GAAAGAA | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0171 |
5 | HG01074.hp1 HG01074.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.862+849_862+854del others(6): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107263 | |||||||
| chr12:91107263 | GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0006g0144 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.862+845_862+854del others(10): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107263 | |||||||
| chr12:91107263 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.862+841_862+854del others(14): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107263 | |||||||
| chr12:91107263 | GAAAGAAA others(10): Show |
G | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.862+838_862+854del others(17): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107263 | |||||||
| chr12:91107263 | GAAAGAAA others(11): Show |
G | 1 | a0001c0001t0001g0083 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.862+837_862+854del others(18): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107263 | |||||||
| chr12:91107263 | GAAAGAAA others(25): Show |
G | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.862+823_862+854del others(32): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107263 | |||||||
| chr12:91107265 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.862+853T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107265 | |||||||
| chr12:91107265 | AAGAAAGA others(15): Show |
A | 1 | a0001c0002t0002g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.862+831_862+852del others(22): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107265 | |||||||
| chr12:91107267 | GAA | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0112 others(4): Show |
16 | HG00735.hp2 HG01928.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.862+849_862+850del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107267 | |||||||
| chr12:91107267 | GAAAGAA | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0114 a0001c0001t0001g0120 others(2): Show |
6 | HG02080.hp2 HG02886.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.862+845_862+850del others(6): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107267 | |||||||
| chr12:91107267 | GAAAGAAA others(7): Show |
G | 2 | a0001c0001t0001g0048 a0001c0001t0006g0046 |
2 | HG01361.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.862+837_862+850del others(14): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107267 | |||||||
| chr12:91107271 | GAA | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0091 others(3): Show |
15 | HG00408.hp1 HG01109.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+845_862+846del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107271 | |||||||
| chr12:91107271 | GAAAGAA | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0076 a0001c0001t0001g0133 |
4 | HG01261.hp2 HG01433.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+841_862+846del others(6): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107271 | |||||||
| chr12:91107273 | AAGAAAGA others(7): Show |
A | 1 | a0001c0002t0002g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.862+831_862+844del others(14): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107273 | |||||||
| chr12:91107275 | GAA | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0028 others(14): Show |
38 | HG00733.hp1 HG00733.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.862+841_862+842del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107275 | |||||||
| chr12:91107277 | A | AAGAAAGA others(4): Show |
1 | a0001c0001t0001g0049 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.862+840_862+841ins others(11): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107277 | |||||||
| chr12:91107278 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.862+840T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107278 | |||||||
| chr12:91107279 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.862+839C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107279 | |||||||
| chr12:91107279 | GAAAGAAA others(29): Show |
G | 1 | a0001c0001t0005g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.862+803_862+838del others(36): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107279 | |||||||
| chr12:91107280 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.862+838T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107280 | |||||||
| chr12:91107281 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0116 |
3 | HG01884.hp1 HG02145.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.862+837T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107281 | |||||||
| chr12:91107283 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0116 |
3 | HG01884.hp1 HG02145.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.862+835C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107283 | |||||||
| chr12:91107283 | GAAAGAGA others(17): Show |
G | 1 | a0001c0001t0001g0002 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.862+811_862+834del others(24): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107283 | |||||||
| chr12:91107283 | GAAAGAGA others(25): Show |
G | 1 | a0001c0001t0005g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.862+803_862+834del others(32): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107283 | |||||||
| chr12:91107283 | GAAAGAGA others(33): Show |
G | 2 | a0001c0002t0002g0022 a0001c0002t0002g0064 |
3 | HG01255.hp1 HG01358.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.862+795_862+834del others(40): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107283 | |||||||
| chr12:91107284 | A | G | 3 | a0001c0001t0002g0074 a0001c0001t0007g0072 a0001c0001t0007g0073 |
3 | HG02258.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.862+834T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107284 | |||||||
| chr12:91107285 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(25): Show |
48 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.862+833T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107285 | |||||||
| chr12:91107285 | AAG | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(71): Show |
136 | HG00099.hp2 HG00408.hp1 HG00733.hp1 others(133): Show |
intron_variant | MODIFIER | c.862+831_862+832del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107285 | |||||||
| chr12:91107286 | A | G | 2 | a0001c0001t0001g0023 a0001c0002t0002g0065 |
2 | HG01975.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.862+832T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107286 | |||||||
| chr12:91107286 | AG | A | 3 | a0001c0001t0002g0074 a0001c0001t0007g0072 a0001c0001t0007g0073 |
3 | HG02258.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.862+831delC | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107286 | |||||||
| chr12:91107287 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(27): Show |
51 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.862+831C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107287 | G | GAA | 6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0049 others(3): Show |
8 | HG02055.hp1 HG02083.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+830_862+831ins others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107287 | G | GAAAGAAA others(21): Show |
1 | a0001c0001t0001g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.862+830_862+831ins others(28): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107287 | GAGAA | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(11): Show |
25 | HG00621.hp1 HG01346.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.862+827_862+830del others(4): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107287 | GAGAAAGA others(1): Show |
G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(9): Show |
18 | HG00642.hp2 HG02015.hp1 HG02735.hp2 others(15): Show |
intron_variant | MODIFIER | c.862+823_862+830del others(8): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107287 | GAGAAAGA others(5): Show |
G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(5): Show |
13 | HG00735.hp1 HG01981.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+819_862+830del others(12): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107287 | GAGAAAGA others(9): Show |
G | 5 | a0001c0001t0001g0001 a0001c0001t0004g0011 a0001c0001t0004g0095 others(2): Show |
11 | HG00544.hp2 HG00639.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.862+815_862+830del others(16): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107287 | GAGAAAGA others(21): Show |
G | 1 | a0001c0001t0005g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.862+803_862+830del others(28): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107287 | |||||||
| chr12:91107289 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0030 others(9): Show |
18 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.862+829C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107289 | |||||||
| chr12:91107290 | AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.862+813_862+827del others(15): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107290 | |||||||
| chr12:91107291 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0030 others(9): Show |
18 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.862+827T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107291 | |||||||
| chr12:91107297 | GAA | G | 2 | a0001c0001t0001g0156 a0001c0001t0005g0013 |
3 | HG01257.hp1 HG02074.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.862+819_862+820del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107297 | |||||||
| chr12:91107297 | GAAAGAAA others(19): Show |
G | 1 | a0001c0002t0002g0065 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.862+795_862+820del others(26): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107297 | |||||||
| chr12:91107303 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.862+815T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107303 | |||||||
| chr12:91107305 | GAA | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
9 | HG01109.hp2 HG01433.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.862+811_862+812del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107305 | |||||||
| chr12:91107306 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.862+812T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107306 | |||||||
| chr12:91107307 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.862+811T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107307 | |||||||
| chr12:91107309 | GAAAGAAA others(33): Show |
G | 4 | a0001c0002t0002g0007 a0001c0002t0002g0015 a0001c0002t0002g0057 others(1): Show |
7 | HG00408.hp2 HG01256.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.862+769_862+808del others(40): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107309 | |||||||
| chr12:91107311 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
10 | HG01109.hp2 HG01433.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.862+807T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107311 | |||||||
| chr12:91107313 | GAAAGAAA others(29): Show |
G | 5 | a0001c0002t0002g0007 a0001c0002t0002g0015 a0001c0002t0002g0066 others(2): Show |
10 | HG00609.hp2 NA18941.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.862+769_862+804del others(36): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107313 | |||||||
| chr12:91107315 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.862+803T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107315 | |||||||
| chr12:91107317 | GAA | G | 11 | a0001c0001t0003g0027 a0001c0001t0003g0043 a0001c0001t0003g0044 others(8): Show |
15 | HG01167.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.862+799_862+800del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107317 | |||||||
| chr12:91107321 | GAA | G | 16 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(13): Show |
39 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.862+795_862+796del others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107321 | |||||||
| chr12:91107332 | AGAAAGAA others(6): Show |
A | 1 | a0001c0001t0004g0121 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.862+773_862+785del others(13): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107332 | |||||||
| chr12:91107338 | A | T | 1 | a0001c0001t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.862+780T>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107338 | |||||||
| chr12:91107346 | GGAAA | G | 20 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(17): Show |
45 | HG00438.hp2 HG00597.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.862+768_862+771del others(4): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107346 | |||||||
| chr12:91107350 | A | G | 7 | a0001c0002t0002g0007 a0001c0002t0002g0015 a0001c0002t0002g0057 others(4): Show |
17 | HG00408.hp2 HG00609.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.862+768T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107350 | |||||||
| chr12:91107380 | AGAGG | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
5 | HG01928.hp2 HG01934.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.862+734_862+737del others(4): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107380 | |||||||
| chr12:91107421 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.862+697T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107421 | |||||||
| chr12:91107423 | G | A | 10 | a0001c0001t0003g0027 a0001c0001t0003g0043 a0001c0001t0003g0044 others(7): Show |
14 | HG01167.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.862+695C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107423 | |||||||
| chr12:91107448 | G | A | 1 | a0004c0005t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.862+670C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107448 | |||||||
| chr12:91107539 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0021g0149 |
3 | HG02280.hp1 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.862+579A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107539 | |||||||
| chr12:91107575 | G | A | 1 | a0001c0001t0003g0142 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.862+543C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107575 | |||||||
| chr12:91107623 | G | T | 1 | a0004c0005t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.862+495C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107623 | |||||||
| chr12:91107678 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0019g0154 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.862+440T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107678 | |||||||
| chr12:91107719 | AT | A | 32 | a0001c0001t0006g0046 a0001c0001t0006g0143 a0001c0001t0006g0144 others(29): Show |
68 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.862+398delA | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107719 | |||||||
| chr12:91107767 | G | A | 5 | a0001c0001t0002g0074 a0001c0001t0007g0033 a0001c0001t0007g0072 others(2): Show |
6 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.862+351C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107767 | |||||||
| chr12:91107792 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.862+326A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107792 | |||||||
| chr12:91107821 | T | G | 1 | a0001c0001t0003g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.862+297A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107821 | |||||||
| chr12:91107983 | A | G | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.862+135T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107983 | |||||||
| chr12:91107984 | T | C | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.862+134A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91107984 | |||||||
| chr12:91108040 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.862+78T>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91108040 | |||||||
| chr12:91108089 | A | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0080 |
3 | HG01981.hp1 NA18979.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.862+29T>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 2/2 | chr12 | 91108089 | |||||||
| chr12:91109197 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-21-197T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109197 | |||||||
| chr12:91109198 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-21-198C>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109198 | |||||||
| chr12:91109269 | C | CTT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
374 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(371): Show |
intron_variant | MODIFIER | c.-21-270_-21-269ins others(2): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109269 | |||||||
| chr12:91109444 | A | C | 9 | a0001c0001t0003g0027 a0001c0001t0003g0043 a0001c0001t0003g0044 others(6): Show |
13 | HG01167.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21-444T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109444 | |||||||
| chr12:91109447 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-21-447G>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109447 | |||||||
| chr12:91109449 | T | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.-21-449A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109449 | |||||||
| chr12:91109481 | G | T | 1 | a0001c0001t0001g0174 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-21-481C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109481 | |||||||
| chr12:91109484 | T | G | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-21-484A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109484 | |||||||
| chr12:91109550 | G | T | 1 | a0001c0002t0002g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-21-550C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109550 | |||||||
| chr12:91109582 | A | C | 1 | a0004c0005t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-21-582T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109582 | |||||||
| chr12:91109625 | A | G | 1 | a0001c0001t0001g0016 | 4 | NA18963.hp2 NA18969.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-625T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109625 | |||||||
| chr12:91109644 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
374 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(371): Show |
intron_variant | MODIFIER | c.-21-644C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109644 | |||||||
| chr12:91109825 | TACTC | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0077 |
3 | NA18972.hp2 NA19063.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-21-829_-21-826del others(4): Show |
LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109825 | |||||||
| chr12:91109830 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0021g0149 |
3 | HG02280.hp1 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-21-830T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109830 | |||||||
| chr12:91109856 | A | C | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-21-856T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109856 | |||||||
| chr12:91109941 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-21-941A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91109941 | |||||||
| chr12:91110010 | T | C | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-21-1010A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110010 | |||||||
| chr12:91110164 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-21-1164A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110164 | |||||||
| chr12:91110205 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
253 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-22+1193T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110205 | |||||||
| chr12:91110237 | T | C | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22+1161A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110237 | |||||||
| chr12:91110290 | G | C | 1 | a0001c0001t0001g0175 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-22+1108C>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110290 | |||||||
| chr12:91110300 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-22+1098C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110300 | |||||||
| chr12:91110305 | A | G | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22+1093T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110305 | |||||||
| chr12:91110306 | A | C | 1 | a0001c0002t0002g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-22+1092T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110306 | |||||||
| chr12:91110407 | C | T | 1 | a0004c0005t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-22+991G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110407 | |||||||
| chr12:91110459 | T | G | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22+939A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110459 | |||||||
| chr12:91110567 | G | A | 5 | a0001c0001t0002g0074 a0001c0001t0007g0033 a0001c0001t0007g0072 others(2): Show |
6 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+831C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110567 | |||||||
| chr12:91110628 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-22+770T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110628 | |||||||
| chr12:91110648 | T | C | 5 | a0001c0001t0002g0074 a0001c0001t0007g0033 a0001c0001t0007g0072 others(2): Show |
6 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+750A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110648 | |||||||
| chr12:91110997 | C | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
11 | HG01109.hp2 HG01433.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-22+401G>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91110997 | |||||||
| chr12:91111068 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
190 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-22+330T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111068 | |||||||
| chr12:91111071 | C | T | 5 | a0001c0001t0002g0074 a0001c0001t0007g0033 a0001c0001t0007g0072 others(2): Show |
6 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+327G>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111071 | |||||||
| chr12:91111174 | T | A | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22+224A>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111174 | |||||||
| chr12:91111205 | T | C | 1 | a0001c0001t0001g0054 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-22+193A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111205 | |||||||
| chr12:91111296 | A | G | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22+102T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111296 | |||||||
| chr12:91111301 | T | C | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+97A>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111301 | |||||||
| chr12:91111303 | G | A | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+95C>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111303 | |||||||
| chr12:91111304 | G | T | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+94C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111304 | |||||||
| chr12:91111305 | C | A | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+93G>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111305 | |||||||
| chr12:91111306 | A | C | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+92T>G | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111306 | |||||||
| chr12:91111308 | A | T | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+90T>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111308 | |||||||
| chr12:91111310 | T | G | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+88A>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111310 | |||||||
| chr12:91111313 | C | A | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+85G>T | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111313 | |||||||
| chr12:91111315 | C | G | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+83G>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111315 | |||||||
| chr12:91111317 | G | T | 1 | a0001c0002t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-22+81C>A | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111317 | |||||||
| chr12:91111364 | A | G | 27 | a0001c0002t0001g0032 a0001c0002t0001g0062 a0001c0002t0002g0006 others(24): Show |
62 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22+34T>C | LUM | ENSG00000139329.5 | transcript | ENST00000266718.5 | protein_coding | 1/2 | chr12 | 91111364 |