Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10455 |
| ensemblid | ENSG00000198721.13 |
| hgncid | 14601 |
| symbol | ECI2 |
| name | enoyl-CoA delta isomerase 2 |
| refseq_nuc | NM_206836.3 |
| refseq_prot | NP_996667.2 |
| ensembl_nuc | ENST00000380118.8 |
| ensembl_prot | ENSP00000369461.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 4115706 |
| end | 4135575 |
| strand | - |
| ver | v1.2 |
| region | chr6:4115706-4135575 |
| region5000 | chr6:4110706-4140575 |
| regionname0 | ECI2_chr6_4115706_4135575 |
| regionname5000 | ECI2_chr6_4110706_4140575 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 394 | 218 | 58 | 41 | 89 | 4 | 24 | 74 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0002 | 0/0 | 394 | 107 | 18 | 17 | 65 | 3 | 4 | 50 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0003 | 0/0 | 394 | 32 | 8 | 13 | 2 | 5 | 4 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0004 | 0/0 | 394 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0005 | 0/0 | 394 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0006 | 0/0 | 394 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0007 | 0/0 | 394 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0008 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0009 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| a0010 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | MAMAY others(389): Show |
chr6 | 4110706 | 4140575 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1182 | 193 | 33 | 41 | 89 | 4 | 24 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0001c0004 | 0/0 | 1182 | 11 | 11 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0001c0005 | 0/0 | 1182 | 8 | 8 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0001c0006 | 0/0 | 1182 | 5 | 5 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0001c0012 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0002c0002 | 0/0 | 1182 | 107 | 18 | 17 | 65 | 3 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0003c0003 | 0/0 | 1182 | 32 | 8 | 13 | 2 | 5 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0004c0007 | 0/0 | 1182 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0005c0008 | 0/0 | 1182 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0006c0009 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0007c0013 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0008c0014 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0009c0010 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 | ||
| a0010c0011 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | ATGGC others(1177): Show |
chr6 | 4110706 | 4140575 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1368 | 189 | 33 | 40 | 87 | 4 | 23 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0001c0001t0003 | 0/0 | 1368 | 2 | 0 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0001c0001t0004 | 0/0 | 1368 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0001c0004t0001 | 0/0 | 1368 | 11 | 11 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0001c0005t0001 | 0/0 | 1368 | 8 | 8 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0001c0006t0002 | 0/0 | 1368 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGA others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0001c0006t0005 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGA others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0001c0012t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0002c0002t0001 | 0/0 | 1368 | 107 | 18 | 17 | 65 | 3 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0003c0003t0001 | 0/0 | 1368 | 32 | 8 | 13 | 2 | 5 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0004c0007t0001 | 0/0 | 1368 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0005c0008t0001 | 0/0 | 1368 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0006c0009t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0006c0009t0002 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGA others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0007c0013t0001 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0008c0014t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0009c0010t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| a0010c0011t0001 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | AGAGC others(1363): Show |
chr6 | 4110706 | 4140575 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 72 | 2 | 19 | 41 | 4 | 5 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0003 | 0/0 | 27 | 2 | 2 | 21 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0006 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0007 | 0/0 | 9 | 5 | 2 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0010 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0004t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0004t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0005t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0006t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0006t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0006t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0001c0012t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0002 | 0/0 | 30 | 0 | 1 | 27 | 2 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0004 | 0/0 | 17 | 0 | 9 | 8 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0009 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0005 | 0/0 | 11 | 2 | 5 | 0 | 1 | 3 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0008 | 0/0 | 8 | 0 | 5 | 0 | 3 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0004c0007t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0004c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0005c0008t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0005c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0006c0009t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0006c0009t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0007c0013t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0008c0014t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0009c0010t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| a0010c0011t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | GBR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0032 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0120 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00558 | hp1 | a0005 | c0008 | t0001 | g0026 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0117 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0119 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01496 | hp2 | a0007 | c0013 | t0001 | g0106 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0005 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01993 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02004 | hp2 | a0003 | c0003 | t0001 | g0115 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02055 | hp2 | a0008 | c0014 | t0001 | g0128 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02071 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0075 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02257 | hp1 | a0001 | c0012 | t0001 | g0077 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02293 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0076 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0074 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02723 | hp2 | a0006 | c0009 | t0001 | g0068 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0079 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02965 | hp2 | a0009 | c0010 | t0001 | g0071 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02970 | hp1 | a0006 | c0009 | t0002 | g0039 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0116 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03209 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0113 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03516 | hp1 | a0001 | c0006 | t0002 | g0018 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0112 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03540 | hp2 | a0001 | c0006 | t0002 | g0041 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0073 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0027 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18906 | hp2 | a0001 | c0006 | t0002 | g0018 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18943 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18951 | hp1 | a0005 | c0008 | t0001 | g0026 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18959 | hp2 | a0004 | c0007 | t0001 | g0020 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18988 | hp1 | a0010 | c0011 | t0001 | g0050 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18999 | hp2 | a0004 | c0007 | t0001 | g0046 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19003 | hp2 | a0004 | c0007 | t0001 | g0020 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19030 | hp2 | a0001 | c0006 | t0002 | g0018 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19058 | hp2 | a0005 | c0008 | t0001 | g0042 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19085 | hp2 | a0004 | c0007 | t0001 | g0020 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA20129 | hp1 | a0001 | c0006 | t0005 | g0040 | AFR | ASW | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0008 | EUR | TSI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0095 | REF | REF | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4116028 | G | A | 6 | a0002 a0003 a0004 others(3): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
missense_variant&splice_region_variant | MODERATE | c.1031C>T | p.Ala344Val | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 1046/1368 | 1031/1185 | 344/394 | chr6 | 4116028 | |||
| chr6:4117373 | G | A | 1 | a0006 | 2 | HG02723.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.964C>T | p.Pro322Ser | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/10 | 979/1368 | 964/1185 | 322/394 | chr6 | 4117373 | |||
| chr6:4125269 | G | A | 1 | a0009 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.776C>T | p.Ala259Val | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/10 | 791/1368 | 776/1185 | 259/394 | chr6 | 4125269 | |||
| chr6:4125317 | T | C | 1 | a0010 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.728A>G | p.Asn243Ser | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/10 | 743/1368 | 728/1185 | 243/394 | chr6 | 4125317 | |||
| chr6:4126145 | C | T | 1 | a0005 | 3 | HG00558.hp1 NA18951.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.664G>A | p.Val222Ile | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/10 | 679/1368 | 664/1185 | 222/394 | chr6 | 4126145 | |||
| chr6:4126225 | T | C | 1 | a0004 | 4 | NA18959.hp2 NA18999.hp2 NA19003.hp2 others(1): Show |
missense_variant | MODERATE | c.584A>G | p.Tyr195Cys | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/10 | 599/1368 | 584/1185 | 195/394 | chr6 | 4126225 | |||
| chr6:4133621 | C | T | 1 | a0003 | 32 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(29): Show |
missense_variant | MODERATE | c.141G>A | p.Met47Ile | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/10 | 156/1368 | 141/1185 | 47/394 | chr6 | 4133621 | |||
| chr6:4133656 | T | C | 1 | a0007 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.106A>G | p.Met36Val | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/10 | 121/1368 | 106/1185 | 36/394 | chr6 | 4133656 | |||
| chr6:4135520 | G | C | 1 | a0008 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.41C>G | p.Ser14Trp | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/10 | 56/1368 | 41/1185 | 14/394 | chr6 | 4135520 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4117413 | C | T | 2 | a0001c0005 a0001c0012 |
9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
synonymous_variant | LOW | c.924G>A | p.Ala308Ala | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/10 | 939/1368 | 924/1185 | 308/394 | chr6 | 4117413 | |||
| chr6:4119258 | T | C | 3 | a0001c0004 a0001c0005 a0001c0012 |
20 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
synonymous_variant | LOW | c.813A>G | p.Pro271Pro | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/10 | 828/1368 | 813/1185 | 271/394 | chr6 | 4119258 | |||
| chr6:4125334 | A | G | 1 | a0005c0008 | 3 | HG00558.hp1 NA18951.hp1 NA19058.hp2 |
synonymous_variant | LOW | c.711T>C | p.Pro237Pro | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/10 | 726/1368 | 711/1185 | 237/394 | chr6 | 4125334 | |||
| chr6:4126146 | G | A | 2 | a0001c0006 a0006c0009 |
7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
synonymous_variant | LOW | c.663C>T | p.Ala221Ala | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/10 | 678/1368 | 663/1185 | 221/394 | chr6 | 4126146 | |||
| chr6:4133564 | G | A | 1 | a0001c0012 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.198C>T | p.Tyr66Tyr | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/10 | 213/1368 | 198/1185 | 66/394 | chr6 | 4133564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4115714 | C | T | 1 | a0001c0001t0004 | 2 | NA18955.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*160G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 160 | chr6 | 4115714 | ||||||
| chr6:4115746 | A | G | 1 | a0001c0001t0003 | 2 | HG01243.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*128T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 128 | chr6 | 4115746 | ||||||
| chr6:4115789 | A | G | 1 | a0001c0006t0005 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 85 | chr6 | 4115789 | ||||||
| chr6:4135571 | G | T | 3 | a0001c0006t0002 a0001c0006t0005 a0006c0009t0002 |
6 | HG02970.hp1 HG03516.hp1 HG03540.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-11C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/10 | 11 | chr6 | 4135571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4116032 | G | A | 10 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0031 others(7): Show |
30 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.1030-3C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116032 | |||||||
| chr6:4116071 | G | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1030-42C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116071 | |||||||
| chr6:4116106 | T | G | 32 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(29): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1030-77A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116106 | |||||||
| chr6:4116107 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1030-78A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116107 | |||||||
| chr6:4116134 | T | C | 2 | a0001c0006t0002g0041 a0001c0006t0005g0040 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1030-105A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116134 | |||||||
| chr6:4116171 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1030-142A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116171 | |||||||
| chr6:4116177 | C | A | 1 | a0002c0002t0001g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1030-148G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116177 | |||||||
| chr6:4116307 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1030-278G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116307 | |||||||
| chr6:4116351 | A | C | 1 | a0002c0002t0001g0027 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1030-322T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116351 | |||||||
| chr6:4116444 | CT | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.1030-416delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116444 | |||||||
| chr6:4116480 | G | A | 1 | a0002c0002t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1030-451C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116480 | |||||||
| chr6:4116535 | G | C | 32 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(29): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1030-506C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116535 | |||||||
| chr6:4116586 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(6): Show |
27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1030-557G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116586 | |||||||
| chr6:4116587 | G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1030-558C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116587 | |||||||
| chr6:4116588 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1030-559G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116588 | |||||||
| chr6:4116824 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1029+484C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116824 | |||||||
| chr6:4117080 | G | GC | 62 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(59): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1029+227dupG | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4117080 | |||||||
| chr6:4118161 | G | T | 1 | a0002c0002t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.886-710C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118161 | |||||||
| chr6:4118180 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(6): Show |
27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.886-729C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118180 | |||||||
| chr6:4118257 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0090 others(1): Show |
9 | HG01167.hp1 HG01175.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.886-806G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118257 | |||||||
| chr6:4118440 | T | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(54): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.885+746A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118440 | |||||||
| chr6:4118523 | T | C | 5 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(2): Show |
7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.885+663A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118523 | |||||||
| chr6:4118555 | G | A | 56 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(53): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.885+631C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118555 | |||||||
| chr6:4118695 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.885+491C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118695 | |||||||
| chr6:4118745 | C | T | 17 | a0002c0002t0001g0078 a0002c0002t0001g0084 a0002c0002t0001g0123 others(14): Show |
36 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.885+441G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118745 | |||||||
| chr6:4118750 | T | G | 25 | a0002c0002t0001g0017 a0002c0002t0001g0025 a0002c0002t0001g0038 others(22): Show |
50 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.885+436A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118750 | |||||||
| chr6:4118783 | C | T | 8 | a0002c0002t0001g0017 a0002c0002t0001g0025 a0002c0002t0001g0038 others(5): Show |
14 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.885+403G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118783 | |||||||
| chr6:4118795 | T | C | 32 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(29): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.885+391A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118795 | |||||||
| chr6:4118817 | C | T | 56 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(53): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.885+369G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118817 | |||||||
| chr6:4119282 | A | G | 84 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(81): Show |
208 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
splice_region_variant&intron_variant | LOW | c.796-7T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119282 | |||||||
| chr6:4119319 | AT | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(33): Show |
89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.796-45delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119319 | |||||||
| chr6:4119319 | ATT | A | 45 | a0001c0001t0001g0067 a0001c0012t0001g0077 a0002c0002t0001g0002 others(42): Show |
116 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.796-46_796-45delAA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119319 | |||||||
| chr6:4119409 | C | T | 1 | a0002c0002t0001g0126 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.796-134G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119409 | |||||||
| chr6:4119424 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.796-149C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119424 | |||||||
| chr6:4119430 | C | G | 1 | a0001c0001t0001g0010 | 7 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-155G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119430 | |||||||
| chr6:4119470 | G | A | 56 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(53): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.796-195C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119470 | |||||||
| chr6:4119501 | C | A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0031 others(8): Show |
31 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.796-226G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119501 | |||||||
| chr6:4119502 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.796-227C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119502 | |||||||
| chr6:4119616 | T | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0030 others(5): Show |
20 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.796-341A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119616 | |||||||
| chr6:4119654 | A | G | 1 | a0002c0002t0001g0047 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.796-379T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119654 | |||||||
| chr6:4119762 | T | C | 59 | a0001c0006t0002g0041 a0001c0006t0005g0040 a0002c0002t0001g0002 others(56): Show |
150 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.796-487A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119762 | |||||||
| chr6:4119780 | C | T | 1 | a0002c0002t0001g0025 | 3 | HG02109.hp1 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.796-505G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119780 | |||||||
| chr6:4119823 | T | A | 32 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(29): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.796-548A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119823 | |||||||
| chr6:4119824 | T | G | 3 | a0001c0004t0001g0013 a0001c0004t0001g0075 a0001c0004t0001g0076 |
7 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-549A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119824 | |||||||
| chr6:4119926 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0033 |
6 | NA18949.hp1 NA18978.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-651A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119926 | |||||||
| chr6:4119947 | A | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(54): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.796-672T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119947 | |||||||
| chr6:4120022 | T | C | 5 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(2): Show |
7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-747A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120022 | |||||||
| chr6:4120067 | T | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0125 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.796-792A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120067 | |||||||
| chr6:4120077 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.796-802A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120077 | |||||||
| chr6:4120094 | T | G | 1 | a0003c0003t0001g0117 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.796-819A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120094 | |||||||
| chr6:4120317 | C | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0070 |
3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.796-1042G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120317 | |||||||
| chr6:4120331 | A | T | 62 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(59): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.796-1056T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120331 | |||||||
| chr6:4120333 | C | G | 62 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(59): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.796-1058G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120333 | |||||||
| chr6:4120449 | G | A | 56 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(53): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.796-1174C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120449 | |||||||
| chr6:4120491 | C | T | 1 | a0001c0001t0001g0010 | 7 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1216G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120491 | |||||||
| chr6:4120506 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.796-1231G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120506 | |||||||
| chr6:4120516 | C | G | 1 | a0001c0001t0001g0010 | 7 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1241G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120516 | |||||||
| chr6:4120630 | G | A | 20 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(17): Show |
66 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.796-1355C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120630 | |||||||
| chr6:4120694 | T | C | 4 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0075 others(1): Show |
11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.796-1419A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120694 | |||||||
| chr6:4120729 | A | C | 1 | a0002c0002t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.796-1454T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120729 | |||||||
| chr6:4120764 | A | C | 2 | a0001c0006t0002g0041 a0001c0006t0005g0040 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.796-1489T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120764 | |||||||
| chr6:4121059 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.796-1784T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121059 | |||||||
| chr6:4121099 | C | T | 24 | a0002c0002t0001g0017 a0002c0002t0001g0025 a0002c0002t0001g0038 others(21): Show |
49 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.796-1824G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121099 | |||||||
| chr6:4121241 | C | T | 1 | a0002c0002t0001g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.796-1966G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121241 | |||||||
| chr6:4121325 | G | T | 1 | a0001c0001t0001g0034 | 2 | HG00423.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.796-2050C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121325 | |||||||
| chr6:4121388 | G | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0070 |
3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.796-2113C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121388 | |||||||
| chr6:4121546 | C | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0070 |
3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.796-2271G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121546 | |||||||
| chr6:4121597 | T | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(54): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.796-2322A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121597 | |||||||
| chr6:4121608 | T | C | 4 | a0001c0005t0001g0011 a0001c0005t0001g0073 a0001c0005t0001g0074 others(1): Show |
9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.796-2333A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121608 | |||||||
| chr6:4121693 | GT | G | 26 | a0001c0001t0001g0089 a0002c0002t0001g0017 a0002c0002t0001g0025 others(23): Show |
51 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.796-2419delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121693 | |||||||
| chr6:4121693 | GTT | G | 31 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(28): Show |
97 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.796-2420_796-2419d others(4): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121693 | |||||||
| chr6:4121695 | T | G | 4 | a0003c0003t0001g0008 a0003c0003t0001g0115 a0003c0003t0001g0119 others(1): Show |
11 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.796-2420A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121695 | |||||||
| chr6:4121780 | G | A | 1 | a0003c0003t0001g0121 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.796-2505C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121780 | |||||||
| chr6:4121924 | T | C | 2 | a0001c0006t0002g0018 a0003c0003t0001g0116 |
4 | HG03017.hp2 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.796-2649A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121924 | |||||||
| chr6:4122015 | C | A | 62 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(59): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.796-2740G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122015 | |||||||
| chr6:4122045 | A | G | 4 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0075 others(1): Show |
11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.796-2770T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122045 | |||||||
| chr6:4122144 | C | T | 5 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(2): Show |
7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-2869G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122144 | |||||||
| chr6:4122153 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.796-2878C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122153 | |||||||
| chr6:4122170 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.796-2895G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122170 | |||||||
| chr6:4122224 | C | CT | 60 | a0001c0001t0001g0087 a0001c0006t0002g0018 a0001c0006t0002g0041 others(57): Show |
153 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.796-2950dupA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122224 | |||||||
| chr6:4122250 | T | C | 12 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0031 others(9): Show |
32 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.796-2975A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122250 | |||||||
| chr6:4122346 | G | T | 2 | a0004c0007t0001g0020 a0004c0007t0001g0046 |
4 | NA18959.hp2 NA18999.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+2904C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122346 | |||||||
| chr6:4122352 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.795+2898A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122352 | |||||||
| chr6:4122371 | C | A | 1 | a0002c0002t0001g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.795+2879G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122371 | |||||||
| chr6:4122812 | G | A | 32 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(29): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.795+2438C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122812 | |||||||
| chr6:4122843 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.795+2407C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122843 | |||||||
| chr6:4123050 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.795+2200A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123050 | |||||||
| chr6:4123147 | T | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0070 |
3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.795+2103A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123147 | |||||||
| chr6:4123207 | C | T | 32 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(29): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.795+2043G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123207 | |||||||
| chr6:4123240 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.795+2010C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123240 | |||||||
| chr6:4123286 | C | G | 4 | a0001c0005t0001g0011 a0001c0005t0001g0073 a0001c0005t0001g0074 others(1): Show |
9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.795+1964G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123286 | |||||||
| chr6:4123308 | C | G | 4 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0075 others(1): Show |
11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.795+1942G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123308 | |||||||
| chr6:4123348 | T | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(6): Show |
27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.795+1902A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123348 | |||||||
| chr6:4123617 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.795+1633C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123617 | |||||||
| chr6:4123826 | C | T | 1 | a0002c0002t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.795+1424G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123826 | |||||||
| chr6:4123838 | A | T | 2 | a0006c0009t0001g0068 a0006c0009t0002g0039 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.795+1412T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123838 | |||||||
| chr6:4123843 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.795+1407G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123843 | |||||||
| chr6:4124031 | G | A | 32 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(29): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.795+1219C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124031 | |||||||
| chr6:4124074 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.795+1176A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124074 | |||||||
| chr6:4124173 | A | C | 1 | a0002c0002t0001g0044 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.795+1077T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124173 | |||||||
| chr6:4124203 | A | G | 4 | a0001c0005t0001g0011 a0001c0005t0001g0073 a0001c0005t0001g0074 others(1): Show |
9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.795+1047T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124203 | |||||||
| chr6:4124245 | T | G | 1 | a0001c0001t0001g0006 | 10 | HG01175.hp1 HG01975.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.795+1005A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124245 | |||||||
| chr6:4124325 | C | T | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.795+925G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124325 | |||||||
| chr6:4124354 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.795+896G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124354 | |||||||
| chr6:4124466 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.795+784C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124466 | |||||||
| chr6:4124545 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.795+705C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124545 | |||||||
| chr6:4124615 | G | A | 7 | a0002c0002t0001g0004 a0002c0002t0001g0031 a0002c0002t0001g0060 others(4): Show |
24 | HG01069.hp2 HG01070.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.795+635C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124615 | |||||||
| chr6:4124627 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.795+623C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124627 | |||||||
| chr6:4124644 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0070 |
3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.795+606C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124644 | |||||||
| chr6:4124770 | T | G | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.795+480A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124770 | |||||||
| chr6:4124772 | T | C | 1 | a0007c0013t0001g0106 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.795+478A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124772 | |||||||
| chr6:4124965 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.795+285G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124965 | |||||||
| chr6:4125085 | T | C | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.795+165A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4125085 | |||||||
| chr6:4125240 | G | A | 20 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(17): Show |
66 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.795+10C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4125240 | |||||||
| chr6:4125380 | T | G | 1 | a0002c0002t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.675-10A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125380 | |||||||
| chr6:4125421 | A | G | 57 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(54): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.675-51T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125421 | |||||||
| chr6:4125707 | A | G | 62 | a0001c0006t0002g0018 a0001c0006t0002g0041 a0001c0006t0005g0040 others(59): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.675-337T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125707 | |||||||
| chr6:4125773 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.674+362G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125773 | |||||||
| chr6:4125801 | G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.674+334C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125801 | |||||||
| chr6:4125862 | A | G | 3 | a0002c0002t0001g0019 a0002c0002t0001g0043 a0002c0002t0001g0053 |
5 | NA18955.hp1 NA18979.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+273T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125862 | |||||||
| chr6:4125863 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(80): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.674+272C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125863 | |||||||
| chr6:4126400 | A | G | 1 | a0001c0005t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.572-163T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126400 | |||||||
| chr6:4126413 | G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.572-176C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126413 | |||||||
| chr6:4126467 | A | C | 4 | a0001c0006t0002g0041 a0001c0006t0005g0040 a0006c0009t0001g0068 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-230T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126467 | |||||||
| chr6:4126501 | A | C | 1 | a0002c0002t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.572-264T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126501 | |||||||
| chr6:4126529 | C | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(80): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.572-292G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126529 | |||||||
| chr6:4126682 | G | A | 57 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(54): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.572-445C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126682 | |||||||
| chr6:4126701 | G | A | 2 | a0006c0009t0001g0068 a0006c0009t0002g0039 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.572-464C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126701 | |||||||
| chr6:4126811 | TTTAA | T | 1 | a0002c0002t0001g0012 | 5 | HG00558.hp2 NA18612.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.572-578_572-575del others(4): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126811 | |||||||
| chr6:4126966 | A | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.572-729T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126966 | |||||||
| chr6:4126979 | C | A | 2 | a0006c0009t0001g0068 a0006c0009t0002g0039 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.572-742G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126979 | |||||||
| chr6:4127019 | C | T | 57 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(54): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.571+743G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127019 | |||||||
| chr6:4127097 | T | C | 4 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0075 others(1): Show |
11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.571+665A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127097 | |||||||
| chr6:4127123 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.571+639G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127123 | |||||||
| chr6:4127124 | A | T | 1 | a0003c0003t0001g0112 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.571+638T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127124 | |||||||
| chr6:4127237 | C | T | 2 | a0001c0006t0002g0041 a0001c0006t0005g0040 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.571+525G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127237 | |||||||
| chr6:4127387 | G | A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0031 others(8): Show |
31 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.571+375C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127387 | |||||||
| chr6:4127404 | C | CT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0033 others(18): Show |
64 | HG00544.hp1 HG01167.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.571+357dupA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | |||||||
| chr6:4127404 | C | CTT | 7 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0085 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+356_571+357dup others(2): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | |||||||
| chr6:4127404 | CT | C | 27 | a0001c0001t0001g0101 a0001c0001t0003g0052 a0001c0006t0002g0018 others(24): Show |
68 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.571+357delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | |||||||
| chr6:4127404 | CTT | C | 21 | a0002c0002t0001g0004 a0002c0002t0001g0028 a0002c0002t0001g0032 others(18): Show |
58 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.571+356_571+357del others(2): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | |||||||
| chr6:4127404 | CTTTTTTT others(4): Show |
C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(6): Show |
27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.571+347_571+357del others(11): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | |||||||
| chr6:4127483 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0125 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.571+279G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127483 | |||||||
| chr6:4127496 | A | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0009 others(54): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.571+266T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127496 | |||||||
| chr6:4127546 | C | A | 2 | a0002c0002t0001g0123 a0002c0002t0001g0125 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.571+216G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127546 | |||||||
| chr6:4127841 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0003g0051 a0001c0001t0003g0052 |
3 | HG00741.hp2 HG01243.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.502-10C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4127841 | |||||||
| chr6:4127847 | A | G | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.502-16T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4127847 | |||||||
| chr6:4127892 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.502-61C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4127892 | |||||||
| chr6:4128079 | T | C | 2 | a0006c0009t0001g0068 a0006c0009t0002g0039 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-248A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128079 | |||||||
| chr6:4128209 | A | G | 2 | a0001c0006t0002g0041 a0001c0006t0005g0040 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.502-378T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128209 | |||||||
| chr6:4128506 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.502-675C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128506 | |||||||
| chr6:4128859 | A | T | 2 | a0006c0009t0001g0068 a0006c0009t0002g0039 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-1028T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128859 | |||||||
| chr6:4128886 | G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.502-1055C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128886 | |||||||
| chr6:4128971 | T | C | 1 | a0003c0003t0001g0121 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.502-1140A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128971 | |||||||
| chr6:4129066 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.502-1235A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129066 | |||||||
| chr6:4129080 | A | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0125 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.502-1249T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129080 | |||||||
| chr6:4129089 | T | TCTCCCTC others(1): Show |
7 | a0002c0002t0001g0017 a0002c0002t0001g0025 a0002c0002t0001g0038 others(4): Show |
13 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.502-1266_502-1259d others(10): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129089 | |||||||
| chr6:4129289 | T | A | 4 | a0001c0006t0002g0041 a0001c0006t0005g0040 a0006c0009t0001g0068 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+1083A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129289 | |||||||
| chr6:4129389 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.501+983G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129389 | |||||||
| chr6:4129491 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.501+881T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129491 | |||||||
| chr6:4129659 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.501+713A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129659 | |||||||
| chr6:4129685 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.501+687G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129685 | |||||||
| chr6:4129702 | G | T | 1 | a0003c0003t0001g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.501+670C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129702 | |||||||
| chr6:4129897 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.501+475C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129897 | |||||||
| chr6:4130079 | A | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
60 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.501+293T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4130079 | |||||||
| chr6:4130973 | T | C | 4 | a0001c0006t0002g0041 a0001c0006t0005g0040 a0006c0009t0001g0068 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-108A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4130973 | |||||||
| chr6:4131124 | T | TA | 28 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(25): Show |
61 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.214-260dupT | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131124 | |||||||
| chr6:4131248 | T | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
60 | HG01074.hp1 HG01099.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.214-383A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131248 | |||||||
| chr6:4131297 | G | A | 2 | a0001c0001t0001g0070 a0002c0002t0001g0069 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.214-432C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131297 | |||||||
| chr6:4131412 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214-547C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131412 | |||||||
| chr6:4131424 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.214-559T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131424 | |||||||
| chr6:4131477 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.214-612T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131477 | |||||||
| chr6:4131702 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.214-837G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131702 | |||||||
| chr6:4131724 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
28 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.214-859C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131724 | |||||||
| chr6:4131746 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
59 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.214-881C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131746 | |||||||
| chr6:4131875 | CAAAAGAA | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(56): Show |
156 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.214-1017_214-1011d others(9): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131875 | |||||||
| chr6:4131900 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.214-1035C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131900 | |||||||
| chr6:4132368 | G | C | 25 | a0001c0001t0001g0029 a0001c0001t0003g0051 a0001c0001t0003g0052 others(22): Show |
72 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.213+1181C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132368 | |||||||
| chr6:4132417 | A | G | 4 | a0001c0005t0001g0011 a0001c0005t0001g0073 a0001c0005t0001g0074 others(1): Show |
9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.213+1132T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132417 | |||||||
| chr6:4132528 | C | G | 37 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(34): Show |
89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.213+1021G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132528 | |||||||
| chr6:4132651 | T | G | 1 | a0002c0002t0001g0053 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.213+898A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132651 | |||||||
| chr6:4132752 | ATC | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0025 a0002c0002t0001g0038 others(3): Show |
12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.213+795_213+796del others(2): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132752 | |||||||
| chr6:4132766 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.213+783A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132766 | |||||||
| chr6:4132791 | G | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.213+758C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132791 | |||||||
| chr6:4132796 | G | A | 10 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0031 others(7): Show |
30 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.213+753C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132796 | |||||||
| chr6:4132825 | C | T | 1 | a0003c0003t0001g0115 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.213+724G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132825 | |||||||
| chr6:4133102 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.213+447G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133102 | |||||||
| chr6:4133188 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.213+361C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133188 | |||||||
| chr6:4133199 | G | A | 1 | a0001c0001t0001g0006 | 10 | HG01175.hp1 HG01975.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+350C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133199 | |||||||
| chr6:4133257 | T | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0125 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.213+292A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133257 | |||||||
| chr6:4133263 | G | C | 1 | a0002c0002t0001g0054 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.213+286C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133263 | |||||||
| chr6:4133313 | A | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(17): Show |
58 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.213+236T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133313 | |||||||
| chr6:4133454 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.213+95T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133454 | |||||||
| chr6:4133460 | A | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.213+89T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133460 | |||||||
| chr6:4133532 | C | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(17): Show |
58 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.213+17G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133532 | |||||||
| chr6:4133719 | T | C | 3 | a0001c0001t0001g0022 a0002c0002t0001g0072 a0009c0010t0001g0071 |
5 | HG02647.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.51-8A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133719 | |||||||
| chr6:4133797 | A | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(34): Show |
89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.51-86T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133797 | |||||||
| chr6:4133807 | AT | A | 8 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0075 others(5): Show |
20 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.51-97delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133807 | |||||||
| chr6:4133813 | G | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0033 |
6 | NA18949.hp1 NA18978.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.51-102C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133813 | |||||||
| chr6:4133863 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.51-152A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133863 | |||||||
| chr6:4134012 | A | C | 1 | a0003c0003t0001g0112 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.51-301T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134012 | |||||||
| chr6:4134197 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.51-486C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134197 | |||||||
| chr6:4134263 | G | A | 37 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(34): Show |
89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.51-552C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134263 | |||||||
| chr6:4134283 | A | G | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51-572T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134283 | |||||||
| chr6:4134347 | C | T | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.51-636G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134347 | |||||||
| chr6:4134534 | A | G | 61 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(58): Show |
159 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.51-823T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134534 | |||||||
| chr6:4134853 | T | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG03688.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.50+658A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134853 | |||||||
| chr6:4134862 | A | C | 22 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0002c0002t0001g0002 others(19): Show |
68 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.50+649T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134862 | |||||||
| chr6:4134898 | A | T | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.50+613T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134898 | |||||||
| chr6:4134991 | C | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0003c0003t0001g0005 others(8): Show |
29 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.50+520G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134991 | |||||||
| chr6:4135028 | T | C | 15 | a0001c0001t0001g0037 a0001c0001t0001g0114 a0001c0001t0001g0122 others(12): Show |
35 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.50+483A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135028 | |||||||
| chr6:4135085 | T | G | 2 | a0002c0002t0001g0123 a0002c0002t0001g0125 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.50+426A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135085 | |||||||
| chr6:4135108 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0003g0051 a0001c0001t0003g0052 others(21): Show |
71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+403G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135108 | |||||||
| chr6:4135318 | G | A | 1 | a0002c0002t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.50+193C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135318 | |||||||
| chr6:4135416 | T | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.50+95A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135416 | |||||||
| chr6:4135426 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50+85C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135426 | |||||||
| chr6:4135482 | G | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0025 a0002c0002t0001g0038 others(3): Show |
12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50+29C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135482 |