Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11160 |
| ensemblid | ENSG00000147475.17 |
| hgncid | 1356 |
| symbol | ERLIN2 |
| name | ER lipid raft associated 2 |
| refseq_nuc | NM_007175.8 |
| refseq_prot | NP_009106.1 |
| ensembl_nuc | ENST00000519638.3 |
| ensembl_prot | ENSP00000428112.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 37736634 |
| end | 37758422 |
| strand | + |
| ver | v1.2 |
| region | chr8:37736634-37758422 |
| region5000 | chr8:37731634-37763422 |
| regionname0 | ERLIN2_chr8_37736634_37758422 |
| regionname5000 | ERLIN2_chr8_37731634_37763422 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1017 | 214 | 59 | 56 | 73 | 6 | 20 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | ATGGC others(1012): Show |
chr8 | 37731634 | 37763422 | ||
| a0001c0002 | 0/0 | 1017 | 7 | 7 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | ATGGC others(1012): Show |
chr8 | 37731634 | 37763422 | ||
| a0001c0003 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | ATGGC others(1012): Show |
chr8 | 37731634 | 37763422 | ||
| a0001c0004 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | ATGGC others(1012): Show |
chr8 | 37731634 | 37763422 | ||
| a0001c0005 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | ATGGC others(1012): Show |
chr8 | 37731634 | 37763422 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5387 | 174 | 33 | 48 | 68 | 6 | 19 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0002 | 0/0 | 5387 | 5 | 5 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0003 | 0/0 | 5387 | 5 | 5 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0004 | 0/0 | 5387 | 3 | 3 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0005 | 0/0 | 5387 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0006 | 0/0 | 5387 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0007 | 0/0 | 5387 | 2 | 0 | 2 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0008 | 0/0 | 5387 | 2 | 0 | 0 | 2 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0009 | 0/0 | 5387 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0010 | 0/0 | 5387 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0011 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0012 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0013 | 0/0 | 5387 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0014 | 0/0 | 5387 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0015 | 0/0 | 5387 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0016 | 0/0 | 5387 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0017 | 0/0 | 5387 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0018 | 0/0 | 5387 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0019 | 0/0 | 5387 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0020 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0021 | 0/0 | 5387 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0023 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0024 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0025 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0026 | 0/0 | 5387 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0001t0028 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5369): Show |
chr8 | 37731634 | 37763422 |
| a0001c0002t0001 | 0/0 | 5387 | 7 | 7 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0003t0027 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0004t0022 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| a0001c0005t0001 | 0/0 | 5387 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | GCTCG others(5382): Show |
chr8 | 37731634 | 37763422 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 75 | 11 | 18 | 34 | 2 | 10 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0002 | 0/0 | 25 | 0 | 12 | 10 | 1 | 2 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0002g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0004g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0005g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0018g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0020g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0023g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0024g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0025g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0026g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0001t0028g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0002t0001g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0003t0027g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0004t0022g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| a0001c0005t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01175 | hp1 | a0001 | c0001 | t0013 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01192 | hp1 | a0001 | c0001 | t0014 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01258 | hp1 | a0001 | c0001 | t0018 | g0035 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01952 | hp2 | a0001 | c0001 | t0019 | g0001 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02004 | hp1 | a0001 | c0001 | t0026 | g0068 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02300 | hp1 | a0001 | c0001 | t0017 | g0001 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02451 | hp2 | a0001 | c0001 | t0025 | g0067 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | KHV | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02698 | hp1 | a0001 | c0001 | t0021 | g0001 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02922 | hp2 | a0001 | c0004 | t0022 | g0070 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02976 | hp1 | a0001 | c0001 | t0024 | g0023 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0044 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0007 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0022 | AFR | ESN | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | YRI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18747 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | CHB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18906 | hp1 | a0001 | c0003 | t0027 | g0072 | AFR | YRI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18971 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | LWK | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | LWK | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19043 | hp2 | a0001 | c0001 | t0028 | g0069 | AFR | LWK | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19055 | hp1 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19068 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | USA | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA21309 | hp1 | a0001 | c0001 | t0023 | g0071 | AFR | LWK | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ERLIN2_chr8_37731634_37763422 | ERLIN2 | chr8 | 37731634 | 37763422 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:37740380 | G | A | 1 | a0001c0003 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.123G>A | p.Leu41Leu | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/12 | 183/5387 | 123/1020 | 41/339 | chr8 | 37740380 | |||
| chr8:37744590 | C | T | 1 | a0001c0002 | 7 | HG02615.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.318C>T | p.Asn106Asn | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/12 | 378/5387 | 318/1020 | 106/339 | chr8 | 37744590 | |||
| chr8:37750410 | A | T | 1 | a0001c0005 | 1 | NA19055.hp1 | synonymous_variant | LOW | c.573A>T | p.Thr191Thr | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/12 | 633/5387 | 573/1020 | 191/339 | chr8 | 37750410 | |||
| chr8:37753526 | T | C | 1 | a0001c0004 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.816T>C | p.Asn272Asn | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 11/12 | 876/5387 | 816/1020 | 272/339 | chr8 | 37753526 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:37754189 | C | G | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0025 others(3): Show |
14 | HG02004.hp1 HG02257.hp2 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*74C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 74 | chr8 | 37754189 | ||||||
| chr8:37754690 | C | T | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(7): Show |
19 | HG02004.hp1 HG02257.hp2 HG02451.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*575C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 575 | chr8 | 37754690 | ||||||
| chr8:37755056 | G | C | 1 | a0001c0001t0002 | 5 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*941G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 941 | chr8 | 37755056 | ||||||
| chr8:37755146 | C | G | 2 | a0001c0001t0009 a0001c0001t0024 |
3 | HG02630.hp1 HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1031C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1031 | chr8 | 37755146 | ||||||
| chr8:37755212 | A | C | 1 | a0001c0001t0023 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1097A>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1097 | chr8 | 37755212 | ||||||
| chr8:37755285 | C | A | 1 | a0001c0001t0005 | 2 | HG02055.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1170C>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1170 | chr8 | 37755285 | ||||||
| chr8:37755365 | G | A | 1 | a0001c0001t0010 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1250G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1250 | chr8 | 37755365 | ||||||
| chr8:37755555 | A | C | 1 | a0001c0001t0021 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440A>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1440 | chr8 | 37755555 | ||||||
| chr8:37755562 | ACCCCCCA others(6): Show |
A | 1 | a0001c0001t0028 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1454_*1466delACCC others(9): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1454 | INFO_REALIGN_3_PRIME | chr8 | 37755562 | |||||
| chr8:37755568 | C | A | 1 | a0001c0001t0026 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1453C>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1453 | chr8 | 37755568 | ||||||
| chr8:37755569 | A | AC | 4 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(1): Show |
46 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1466dupC | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1467 | INFO_REALIGN_3_PRIME | chr8 | 37755569 | |||||
| chr8:37755569 | A | C | 1 | a0001c0001t0001 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454A>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1454 | chr8 | 37755569 | ||||||
| chr8:37755569 | AC | A | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(11): Show |
55 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1466delC | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1466 | INFO_REALIGN_3_PRIME | chr8 | 37755569 | |||||
| chr8:37755576 | C | T | 1 | a0001c0001t0020 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1461 | chr8 | 37755576 | ||||||
| chr8:37755582 | G | A | 1 | a0001c0001t0011 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1467 | chr8 | 37755582 | ||||||
| chr8:37755649 | T | G | 1 | a0001c0001t0004 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1534T>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1534 | chr8 | 37755649 | ||||||
| chr8:37755650 | T | C | 1 | a0001c0001t0004 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1535T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1535 | chr8 | 37755650 | ||||||
| chr8:37755912 | G | A | 1 | a0001c0001t0012 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1797G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1797 | chr8 | 37755912 | ||||||
| chr8:37756114 | G | A | 1 | a0001c0001t0006 | 2 | HG01884.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1999G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 1999 | chr8 | 37756114 | ||||||
| chr8:37756202 | C | G | 1 | a0001c0001t0019 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2087 | chr8 | 37756202 | ||||||
| chr8:37756327 | A | G | 1 | a0001c0001t0008 | 2 | HG02523.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2212A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2212 | chr8 | 37756327 | ||||||
| chr8:37756416 | C | G | 1 | a0001c0001t0018 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2301C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2301 | chr8 | 37756416 | ||||||
| chr8:37756648 | A | G | 1 | a0001c0001t0017 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2533A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2533 | chr8 | 37756648 | ||||||
| chr8:37756816 | T | A | 1 | a0001c0001t0013 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2701T>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2701 | chr8 | 37756816 | ||||||
| chr8:37756986 | G | A | 2 | a0001c0001t0013 a0001c0001t0014 |
2 | HG01175.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2871G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2871 | chr8 | 37756986 | ||||||
| chr8:37757020 | T | C | 1 | a0001c0001t0024 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2905T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2905 | chr8 | 37757020 | ||||||
| chr8:37757052 | G | A | 1 | a0001c0001t0015 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2937G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 2937 | chr8 | 37757052 | ||||||
| chr8:37757206 | C | T | 1 | a0001c0001t0016 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3091C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 3091 | chr8 | 37757206 | ||||||
| chr8:37757460 | A | C | 1 | a0001c0003t0027 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3345A>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 3345 | chr8 | 37757460 | ||||||
| chr8:37757660 | G | A | 1 | a0001c0003t0027 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3545G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 3545 | chr8 | 37757660 | ||||||
| chr8:37757801 | A | G | 1 | a0001c0001t0007 | 2 | HG01257.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3686A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 3686 | chr8 | 37757801 | ||||||
| chr8:37758056 | T | C | 1 | a0001c0001t0004 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3941T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 3941 | chr8 | 37758056 | ||||||
| chr8:37758302 | A | G | 4 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0026 others(1): Show |
12 | HG02004.hp1 HG02257.hp2 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4187A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 4187 | chr8 | 37758302 | ||||||
| chr8:37758346 | G | T | 1 | a0001c0001t0026 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4231G>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 12/12 | 4231 | chr8 | 37758346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:37736834 | T | A | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0024g0023 |
3 | HG02630.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-16+156T>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 1/11 | chr8 | 37736834 | |||||||
| chr8:37737050 | A | T | 3 | a0001c0001t0001g0007 a0001c0001t0011g0007 a0001c0001t0020g0007 |
4 | HG02055.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+372A>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 1/11 | chr8 | 37737050 | |||||||
| chr8:37737289 | G | A | 1 | a0001c0001t0002g0004 | 5 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+611G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 1/11 | chr8 | 37737289 | |||||||
| chr8:37737421 | T | C | 1 | a0001c0001t0009g0021 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-15-487T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 1/11 | chr8 | 37737421 | |||||||
| chr8:37738123 | A | G | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.107+94A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37738123 | |||||||
| chr8:37738225 | A | G | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.107+196A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37738225 | |||||||
| chr8:37738356 | TCCTCTGG others(18): Show |
T | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.107+376_107+400del others(25): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 37738356 | ||||||
| chr8:37739059 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.107+1030C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37739059 | |||||||
| chr8:37739205 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
6 | HG00408.hp1 NA18954.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-1160C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37739205 | |||||||
| chr8:37739812 | C | CT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0063 others(2): Show |
7 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-541dupT | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 37739812 | ||||||
| chr8:37739820 | T | G | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.108-545T>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37739820 | |||||||
| chr8:37740048 | A | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0061 a0001c0001t0001g0062 |
4 | HG01069.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-317A>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37740048 | |||||||
| chr8:37740072 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.108-293G>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37740072 | |||||||
| chr8:37740097 | GGTTCTGC others(1): Show |
G | 1 | a0001c0001t0002g0004 | 5 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-265_108-258del others(8): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 37740097 | ||||||
| chr8:37740228 | T | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108-137T>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37740228 | |||||||
| chr8:37740265 | A | G | 2 | a0001c0001t0003g0020 a0001c0001t0003g0073 |
3 | HG02615.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.108-100A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 2/11 | chr8 | 37740265 | |||||||
| chr8:37740481 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.189+35G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37740481 | |||||||
| chr8:37740598 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.189+152A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37740598 | |||||||
| chr8:37740600 | A | G | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0024g0023 |
3 | HG02630.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.189+154A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37740600 | |||||||
| chr8:37740607 | T | TAC | 7 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(4): Show |
13 | HG02004.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.189+167_189+168dup others(2): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 37740607 | ||||||
| chr8:37740840 | A | G | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.189+394A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37740840 | |||||||
| chr8:37740843 | T | G | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.189+397T>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37740843 | |||||||
| chr8:37741269 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.190-503T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37741269 | |||||||
| chr8:37741282 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.190-490A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37741282 | |||||||
| chr8:37741408 | G | T | 1 | a0001c0003t0027g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.190-364G>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37741408 | |||||||
| chr8:37741592 | C | G | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.190-180C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 3/11 | chr8 | 37741592 | |||||||
| chr8:37742065 | C | T | 3 | a0001c0001t0003g0019 a0001c0001t0026g0068 a0001c0001t0028g0069 |
4 | HG02004.hp1 HG03195.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+247C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37742065 | |||||||
| chr8:37742340 | TA | T | 12 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
15 | HG01168.hp2 HG01192.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.236+539delA | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 37742340 | ||||||
| chr8:37742340 | TAA | T | 6 | a0001c0001t0002g0004 a0001c0001t0003g0020 a0001c0001t0003g0073 others(3): Show |
11 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.236+538_236+539del others(2): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 37742340 | ||||||
| chr8:37742796 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.236+978A>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37742796 | |||||||
| chr8:37742836 | T | G | 1 | a0001c0001t0023g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.236+1018T>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37742836 | |||||||
| chr8:37743035 | G | A | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.236+1217G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743035 | |||||||
| chr8:37743139 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.237-1216C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743139 | |||||||
| chr8:37743200 | C | G | 1 | a0001c0001t0002g0004 | 5 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-1155C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743200 | |||||||
| chr8:37743342 | G | A | 1 | a0001c0001t0001g0003 | 6 | HG02145.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-1013G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743342 | |||||||
| chr8:37743517 | AT | A | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0024g0023 |
3 | HG02630.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237-836delT | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 37743517 | ||||||
| chr8:37743586 | G | C | 1 | a0001c0001t0001g0027 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.237-769G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743586 | |||||||
| chr8:37743641 | T | TAAGG | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.237-712_237-709dup others(4): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 37743641 | ||||||
| chr8:37743784 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.237-571A>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743784 | |||||||
| chr8:37743800 | A | G | 1 | a0001c0001t0002g0004 | 5 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-555A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743800 | |||||||
| chr8:37743873 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.237-482T>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743873 | |||||||
| chr8:37743880 | C | T | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.237-475C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743880 | |||||||
| chr8:37743896 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.237-459A>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743896 | |||||||
| chr8:37743899 | T | C | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.237-456T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743899 | |||||||
| chr8:37743941 | G | T | 1 | a0001c0004t0022g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237-414G>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37743941 | |||||||
| chr8:37744048 | C | T | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0024g0023 |
3 | HG02630.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237-307C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37744048 | |||||||
| chr8:37744321 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.237-34C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 4/11 | chr8 | 37744321 | |||||||
| chr8:37744476 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.298+60G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 5/11 | chr8 | 37744476 | |||||||
| chr8:37744750 | G | T | 1 | a0001c0002t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.424+54G>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37744750 | |||||||
| chr8:37744770 | G | A | 1 | a0001c0003t0027g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.424+74G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37744770 | |||||||
| chr8:37744875 | T | A | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+179T>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37744875 | |||||||
| chr8:37745405 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.424+709A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37745405 | |||||||
| chr8:37745478 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.424+782T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37745478 | |||||||
| chr8:37745801 | C | T | 1 | a0001c0001t0025g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.424+1105C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37745801 | |||||||
| chr8:37746338 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.424+1642A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37746338 | |||||||
| chr8:37746432 | A | C | 1 | a0001c0001t0001g0016 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.424+1736A>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37746432 | |||||||
| chr8:37746434 | A | T | 1 | a0001c0003t0027g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.424+1738A>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37746434 | |||||||
| chr8:37746693 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.424+1997G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37746693 | |||||||
| chr8:37746779 | GTT | G | 1 | a0001c0001t0002g0004 | 5 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2084_424+2085d others(4): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37746779 | |||||||
| chr8:37746925 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG00735.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.424+2229A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37746925 | |||||||
| chr8:37746934 | G | A | 1 | a0001c0001t0026g0068 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.424+2238G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37746934 | |||||||
| chr8:37747049 | T | G | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+2353T>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37747049 | |||||||
| chr8:37747050 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.424+2354A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37747050 | |||||||
| chr8:37747054 | AT | A | 1 | a0001c0001t0001g0008 | 3 | HG01109.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.424+2360delT | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 37747054 | ||||||
| chr8:37747128 | GA | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
223 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.425-2423delA | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 37747128 | ||||||
| chr8:37747780 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.425-1779C>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37747780 | |||||||
| chr8:37747841 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.425-1718C>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37747841 | |||||||
| chr8:37748081 | G | C | 1 | a0001c0003t0027g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.425-1478G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37748081 | |||||||
| chr8:37748215 | C | T | 8 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(5): Show |
14 | HG02004.hp1 HG02257.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.425-1344C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37748215 | |||||||
| chr8:37748258 | G | T | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.425-1301G>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37748258 | |||||||
| chr8:37748305 | G | C | 1 | a0001c0001t0023g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.425-1254G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37748305 | |||||||
| chr8:37748473 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.425-1086T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37748473 | |||||||
| chr8:37748643 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.425-916A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37748643 | |||||||
| chr8:37748804 | A | T | 1 | a0001c0001t0001g0005 | 4 | HG01928.hp2 NA18944.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-755A>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37748804 | |||||||
| chr8:37749073 | T | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0073 |
3 | HG02615.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.425-486T>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749073 | |||||||
| chr8:37749139 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.425-420T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749139 | |||||||
| chr8:37749189 | T | C | 1 | a0001c0001t0001g0016 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.425-370T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749189 | |||||||
| chr8:37749192 | C | T | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.425-367C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749192 | |||||||
| chr8:37749225 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-334G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749225 | |||||||
| chr8:37749225 | G | C | 1 | a0001c0001t0001g0034 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.425-334G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749225 | |||||||
| chr8:37749258 | T | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0073 |
3 | HG02615.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.425-301T>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749258 | |||||||
| chr8:37749272 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.425-287A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749272 | |||||||
| chr8:37749405 | C | G | 2 | a0001c0001t0003g0020 a0001c0001t0003g0073 |
3 | HG02615.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.425-154C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749405 | |||||||
| chr8:37749514 | A | G | 1 | a0001c0001t0004g0011 | 3 | HG01884.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.425-45A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 6/11 | chr8 | 37749514 | |||||||
| chr8:37749867 | C | T | 1 | a0001c0001t0001g0010 | 3 | NA19004.hp1 NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.557+15C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 8/11 | chr8 | 37749867 | |||||||
| chr8:37749917 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.557+65C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 8/11 | chr8 | 37749917 | |||||||
| chr8:37750037 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0006g0009 |
4 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+185G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 8/11 | chr8 | 37750037 | |||||||
| chr8:37750173 | T | C | 1 | a0001c0001t0025g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.558-222T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 8/11 | chr8 | 37750173 | |||||||
| chr8:37750238 | A | G | 1 | a0001c0003t0027g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.558-157A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 8/11 | chr8 | 37750238 | |||||||
| chr8:37750322 | A | T | 1 | a0001c0001t0012g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.558-73A>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 8/11 | chr8 | 37750322 | |||||||
| chr8:37750375 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0028 |
3 | NA18948.hp2 NA18952.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.558-20C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 8/11 | chr8 | 37750375 | |||||||
| chr8:37750623 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0005g0013 |
3 | HG02055.hp2 HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.649+137C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37750623 | |||||||
| chr8:37750636 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.649+150T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37750636 | |||||||
| chr8:37750652 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.649+166A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37750652 | |||||||
| chr8:37750715 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.649+229G>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37750715 | |||||||
| chr8:37750787 | G | A | 1 | a0001c0001t0028g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.649+301G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37750787 | |||||||
| chr8:37750872 | C | T | 1 | a0001c0001t0023g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.649+386C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37750872 | |||||||
| chr8:37750946 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0043 others(8): Show |
38 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.649+460C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37750946 | |||||||
| chr8:37751018 | C | G | 1 | a0001c0001t0002g0004 | 5 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.649+532C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37751018 | |||||||
| chr8:37751498 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.650-128G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37751498 | |||||||
| chr8:37751600 | C | A | 1 | a0001c0001t0018g0035 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.650-26C>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 9/11 | chr8 | 37751600 | |||||||
| chr8:37751879 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.739+164G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37751879 | |||||||
| chr8:37751897 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.739+182G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37751897 | |||||||
| chr8:37751994 | G | A | 1 | a0001c0003t0027g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.739+279G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37751994 | |||||||
| chr8:37752577 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.739+862G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37752577 | |||||||
| chr8:37752577 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.739+862G>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37752577 | |||||||
| chr8:37752607 | C | CTGAGGGC others(6): Show |
1 | a0001c0001t0026g0068 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.740-839_740-827dup others(13): Show |
ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 37752607 | ||||||
| chr8:37752730 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.740-720A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37752730 | |||||||
| chr8:37752837 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.740-613G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37752837 | |||||||
| chr8:37752988 | A | G | 14 | a0001c0001t0002g0004 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
22 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.740-462A>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37752988 | |||||||
| chr8:37753029 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.740-421T>C | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37753029 | |||||||
| chr8:37753382 | C | G | 1 | a0001c0004t0022g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.740-68C>G | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37753382 | |||||||
| chr8:37753411 | TA | T | 1 | a0001c0001t0001g0012 | 2 | HG00323.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.740-38delA | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 10/11 | chr8 | 37753411 | |||||||
| chr8:37753541 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.819+12G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 11/11 | chr8 | 37753541 | |||||||
| chr8:37753607 | C | T | 1 | a0001c0001t0023g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+78C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 11/11 | chr8 | 37753607 | |||||||
| chr8:37753639 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.819+110G>A | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 11/11 | chr8 | 37753639 | |||||||
| chr8:37753743 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0047 |
2 | HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.820-172C>T | ERLIN2 | ENSG00000147475.17 | transcript | ENST00000519638.3 | protein_coding | 11/11 | chr8 | 37753743 |