Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100129583 |
| ensemblid | ENSG00000189157.14 |
| hgncid | 34343 |
| symbol | FAM47E |
| name | family with sequence similarity 47 member E |
| refseq_nuc | NM_001136570.3 |
| refseq_prot | NP_001130042.1 |
| ensembl_nuc | ENST00000424749.7 |
| ensembl_prot | ENSP00000409423.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 76251721 |
| end | 76283783 |
| strand | + |
| ver | v1.2 |
| region | chr4:76251721-76283783 |
| region5000 | chr4:76246721-76288783 |
| regionname0 | FAM47E_chr4_76251721_76283783 |
| regionname5000 | FAM47E_chr4_76246721_76288783 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 393 | 151 | 22 | 22 | 89 | 3 | 14 | 66 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0002 | 0/0 | 393 | 131 | 19 | 28 | 66 | 4 | 14 | 58 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0003 | 0/0 | 393 | 53 | 31 | 3 | 14 | 4 | 1 | 11 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0004 | 0/1 | 393 | 42 | 13 | 11 | 8 | 1 | 8 | 8 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0005 | 0/0 | 393 | 8 | 7 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0006 | 0/0 | 393 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0007 | 0/0 | 393 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0008 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0009 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| a0010 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | MADRR others(388): Show |
chr4 | 76246721 | 76288783 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1179 | 149 | 22 | 22 | 88 | 3 | 13 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0001c0010 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0001c0012 | 0/0 | 1179 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0002c0002 | 0/0 | 1179 | 131 | 19 | 28 | 66 | 4 | 14 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0003c0003 | 0/0 | 1179 | 53 | 31 | 3 | 14 | 4 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0004c0004 | 0/0 | 1179 | 39 | 13 | 9 | 8 | 1 | 8 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0004c0006 | 0/1 | 1179 | 3 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0005c0005 | 0/0 | 1179 | 8 | 7 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0006c0008 | 0/0 | 1179 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0007c0007 | 0/0 | 1179 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0008c0009 | 0/0 | 1179 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0009c0013 | 0/0 | 1179 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 | ||
| a0010c0011 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ATGGC others(1174): Show |
chr4 | 76246721 | 76288783 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1533 | 149 | 22 | 22 | 88 | 3 | 13 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0001c0010t0001 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0001c0012t0001 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0002c0002t0001 | 0/0 | 1533 | 130 | 19 | 27 | 66 | 4 | 14 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0002c0002t0003 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0003c0003t0001 | 0/0 | 1533 | 50 | 28 | 3 | 14 | 4 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0003c0003t0002 | 0/0 | 1533 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0003c0003t0004 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0004c0004t0001 | 0/0 | 1533 | 38 | 12 | 9 | 8 | 1 | 8 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0004c0004t0002 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0004c0006t0001 | 0/1 | 1533 | 3 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0005c0005t0001 | 0/0 | 1533 | 8 | 7 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0006c0008t0001 | 0/0 | 1533 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0007c0007t0001 | 0/0 | 1533 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0008c0009t0001 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0009c0013t0001 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| a0010c0011t0001 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | ACGGT others(1528): Show |
chr4 | 76246721 | 76288783 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 19 | 0 | 7 | 7 | 1 | 4 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0003 | 0/0 | 14 | 2 | 2 | 9 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0033 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0010t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0001c0012t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0001 | 0/0 | 31 | 1 | 4 | 24 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0005 | 0/0 | 9 | 0 | 2 | 1 | 3 | 3 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0007 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0002c0002t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0009 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0024 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0003c0003t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0008 | 0/0 | 7 | 1 | 3 | 0 | 1 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0004t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0006t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0006t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0004c0006t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0005c0005t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0005c0005t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0005c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0005c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0005c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0005c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0006c0008t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0007c0007t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0007c0007t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0008c0009t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0009c0013t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| a0010c0011t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0182 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00323 | hp1 | a0004 | c0004 | t0001 | g0008 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0158 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00735 | hp2 | a0008 | c0009 | t0001 | g0005 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00738 | hp2 | a0004 | c0006 | t0001 | g0008 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00741 | hp1 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01070 | hp1 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01071 | hp2 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01109 | hp2 | a0004 | c0004 | t0001 | g0008 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0050 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01167 | hp2 | a0004 | c0004 | t0001 | g0100 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0050 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01257 | hp2 | a0004 | c0004 | t0001 | g0008 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0114 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01361 | hp2 | a0004 | c0006 | t0001 | g0118 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0049 | EUR | IBS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01928 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01934 | hp2 | a0009 | c0013 | t0001 | g0003 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01943 | hp2 | a0004 | c0004 | t0001 | g0008 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02015 | hp1 | a0001 | c0010 | t0001 | g0149 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02258 | hp1 | a0004 | c0004 | t0001 | g0028 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0068 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02572 | hp2 | a0003 | c0003 | t0002 | g0146 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0155 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0032 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0069 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02647 | hp1 | a0004 | c0004 | t0001 | g0008 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0125 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02717 | hp2 | a0004 | c0004 | t0001 | g0102 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02723 | hp1 | a0005 | c0005 | t0001 | g0052 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02735 | hp1 | a0001 | c0012 | t0001 | g0002 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02735 | hp2 | a0004 | c0004 | t0001 | g0089 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02738 | hp2 | a0005 | c0005 | t0001 | g0160 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02818 | hp1 | a0004 | c0004 | t0001 | g0028 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02895 | hp1 | a0005 | c0005 | t0001 | g0038 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02897 | hp2 | a0005 | c0005 | t0001 | g0038 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0169 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02970 | hp1 | a0005 | c0005 | t0001 | g0161 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0185 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03195 | hp1 | a0005 | c0005 | t0001 | g0097 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0159 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03209 | hp1 | a0004 | c0004 | t0001 | g0105 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0101 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03453 | hp1 | a0004 | c0004 | t0001 | g0113 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03491 | hp1 | a0004 | c0004 | t0001 | g0126 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03516 | hp1 | a0004 | c0004 | t0002 | g0094 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0093 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03654 | hp1 | a0004 | c0004 | t0001 | g0127 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0036 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03704 | hp1 | a0004 | c0004 | t0001 | g0117 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03704 | hp2 | a0004 | c0004 | t0001 | g0008 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0087 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0088 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03942 | hp2 | a0004 | c0004 | t0001 | g0008 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0036 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04184 | hp2 | a0004 | c0004 | t0001 | g0067 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0096 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18906 | hp1 | a0004 | c0004 | t0001 | g0150 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18947 | hp1 | a0004 | c0004 | t0001 | g0143 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18948 | hp1 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18962 | hp2 | a0010 | c0011 | t0001 | g0082 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18969 | hp1 | a0004 | c0004 | t0001 | g0047 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18970 | hp2 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18974 | hp1 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18985 | hp2 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18993 | hp1 | a0006 | c0008 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA18999 | hp2 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19001 | hp2 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19012 | hp1 | a0007 | c0007 | t0001 | g0070 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19030 | hp2 | a0004 | c0004 | t0001 | g0104 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0181 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19064 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19074 | hp1 | a0007 | c0007 | t0001 | g0037 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19074 | hp2 | a0004 | c0004 | t0001 | g0047 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19075 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19089 | hp1 | a0006 | c0008 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0172 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0039 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | ASW | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0049 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0157 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20905 | hp1 | a0004 | c0004 | t0001 | g0107 | SAS | GIH | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02109 | hp2 | a0004 | c0004 | t0001 | g0028 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02486 | hp1 | a0004 | c0004 | t0001 | g0103 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02486 | hp2 | a0005 | c0005 | t0001 | g0153 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0032 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA21309 | hp1 | a0003 | c0003 | t0004 | g0029 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| NA21309 | hp2 | a0005 | c0005 | t0001 | g0052 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| homoSapiens | chm13v2 | a0004 | c0006 | t0001 | g0115 | REF | REF | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0166 | REF | REF | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76251793 | T | C | 1 | a0007 | 2 | NA19012.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.47T>C | p.Val16Ala | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/8 | 73/1533 | 47/1182 | 16/393 | chr4 | 76251793 | |||
| chr4:76256200 | G | A | 1 | a0008 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.97G>A | p.Gly33Arg | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/8 | 123/1533 | 97/1182 | 33/393 | chr4 | 76256200 | |||
| chr4:76263843 | C | T | 1 | a0009 | 1 | HG01934.hp2 | missense_variant&splice_region_variant | MODERATE | c.560C>T | p.Pro187Leu | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/8 | 586/1533 | 560/1182 | 187/393 | chr4 | 76263843 | |||
| chr4:76271575 | C | T | 1 | a0006 | 2 | NA18993.hp1 NA19089.hp1 |
missense_variant | MODERATE | c.677C>T | p.Ser226Leu | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/8 | 703/1533 | 677/1182 | 226/393 | chr4 | 76271575 | |||
| chr4:76271685 | A | C | 1 | a0003 | 53 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(50): Show |
missense_variant | MODERATE | c.787A>C | p.Lys263Gln | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/8 | 813/1533 | 787/1182 | 263/393 | chr4 | 76271685 | |||
| chr4:76271715 | G | A | 4 | a0002 a0007 a0008 others(1): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
missense_variant | MODERATE | c.817G>A | p.Glu273Lys | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/8 | 843/1533 | 817/1182 | 273/393 | chr4 | 76271715 | |||
| chr4:76280334 | C | T | 6 | a0002 a0003 a0004 others(3): Show |
236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
missense_variant | MODERATE | c.1097C>T | p.Thr366Met | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/8 | 1123/1533 | 1097/1182 | 366/393 | chr4 | 76280334 | |||
| chr4:76283417 | C | T | 1 | a0005 | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
missense_variant | MODERATE | c.1141C>T | p.Arg381Cys | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 1167/1533 | 1141/1182 | 381/393 | chr4 | 76283417 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76256262 | C | T | 1 | a0004c0006 | 2 | HG00738.hp2 HG01361.hp2 |
synonymous_variant | LOW | c.159C>T | p.Asp53Asp | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/8 | 185/1533 | 159/1182 | 53/393 | chr4 | 76256262 | |||
| chr4:76256418 | G | A | 1 | a0001c0010 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.315G>A | p.Ser105Ser | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/8 | 341/1533 | 315/1182 | 105/393 | chr4 | 76256418 | |||
| chr4:76280278 | A | G | 1 | a0001c0012 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1041A>G | p.Ala347Ala | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/8 | 1067/1533 | 1041/1182 | 347/393 | chr4 | 76280278 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76283549 | T | C | 1 | a0002c0002t0003 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 91 | chr4 | 76283549 | ||||||
| chr4:76283677 | T | G | 2 | a0003c0003t0002 a0004c0004t0002 |
3 | HG02572.hp2 HG03516.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*219T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 219 | chr4 | 76283677 | ||||||
| chr4:76283720 | C | T | 1 | a0003c0003t0004 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 262 | chr4 | 76283720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76252138 | C | T | 2 | a0003c0003t0001g0024 a0003c0003t0001g0185 |
5 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+318C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252138 | |||||||
| chr4:76252146 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(142): Show |
300 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.74+326T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252146 | |||||||
| chr4:76252269 | GC | G | 10 | a0002c0002t0001g0007 a0002c0002t0001g0025 a0002c0002t0001g0034 others(7): Show |
19 | HG00609.hp2 HG01255.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+452delC | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76252269 | ||||||
| chr4:76252323 | C | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(20): Show |
56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.74+503C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252323 | |||||||
| chr4:76252528 | T | G | 1 | a0002c0002t0001g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.74+708T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252528 | |||||||
| chr4:76252586 | T | C | 10 | a0001c0001t0001g0156 a0003c0003t0001g0050 a0003c0003t0001g0051 others(7): Show |
13 | HG00597.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.74+766T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252586 | |||||||
| chr4:76252724 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.74+904A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252724 | |||||||
| chr4:76252761 | C | A | 60 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0066 others(57): Show |
133 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.74+941C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252761 | |||||||
| chr4:76252919 | T | C | 5 | a0002c0002t0001g0007 a0002c0002t0001g0034 a0002c0002t0001g0059 others(2): Show |
12 | HG01255.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.74+1099T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252919 | |||||||
| chr4:76252942 | T | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0066 others(46): Show |
119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.74+1122T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252942 | |||||||
| chr4:76252994 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.74+1174C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252994 | |||||||
| chr4:76253285 | G | GGTTGTTT others(11): Show |
57 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0066 others(54): Show |
129 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.74+1469_74+1486dup others(18): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253285 | ||||||
| chr4:76253316 | A | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(101): Show |
192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.74+1496A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253316 | |||||||
| chr4:76253329 | T | C | 1 | a0003c0003t0001g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.74+1509T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253329 | |||||||
| chr4:76253335 | C | T | 4 | a0003c0003t0001g0159 a0005c0005t0001g0052 a0005c0005t0001g0160 others(1): Show |
5 | HG02723.hp1 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+1515C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253335 | |||||||
| chr4:76253432 | A | G | 1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.74+1612A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253432 | |||||||
| chr4:76253444 | C | T | 3 | a0002c0002t0001g0022 a0002c0002t0001g0170 a0004c0004t0001g0169 |
6 | HG01175.hp1 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.74+1624C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253444 | |||||||
| chr4:76253509 | A | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0066 others(51): Show |
125 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.74+1689A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253509 | |||||||
| chr4:76253719 | A | C | 1 | a0002c0002t0001g0090 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.74+1899A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253719 | |||||||
| chr4:76253780 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.74+1960G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253780 | |||||||
| chr4:76253783 | A | C | 3 | a0002c0002t0001g0087 a0002c0002t0001g0088 a0004c0004t0001g0089 |
3 | HG02735.hp2 HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.74+1963A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253783 | |||||||
| chr4:76253796 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.74+1976C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253796 | |||||||
| chr4:76253803 | C | G | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+1983C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253803 | |||||||
| chr4:76253808 | T | TA | 71 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(68): Show |
138 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.74+2000dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253808 | ||||||
| chr4:76253808 | T | TAA | 29 | a0001c0001t0001g0108 a0002c0002t0001g0005 a0002c0002t0001g0022 others(26): Show |
52 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.74+1999_74+2000dup others(2): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253808 | ||||||
| chr4:76253808 | TA | T | 9 | a0001c0001t0001g0086 a0002c0002t0001g0084 a0002c0002t0001g0085 others(6): Show |
11 | HG02486.hp2 HG02523.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+2000delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253808 | ||||||
| chr4:76253838 | G | T | 2 | a0002c0002t0001g0022 a0002c0002t0001g0170 |
5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+2018G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253838 | |||||||
| chr4:76253849 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(105): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.74+2029G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253849 | |||||||
| chr4:76253878 | G | A | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2058G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253878 | |||||||
| chr4:76253897 | G | A | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2077G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253897 | |||||||
| chr4:76253936 | A | G | 2 | a0001c0001t0001g0151 a0004c0004t0001g0150 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.74+2116A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253936 | |||||||
| chr4:76253955 | C | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(64): Show |
134 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.74+2135C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253955 | |||||||
| chr4:76253959 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(20): Show |
56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.74+2139A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253959 | |||||||
| chr4:76253960 | G | A | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2140G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253960 | |||||||
| chr4:76253966 | T | A | 4 | a0001c0001t0001g0098 a0002c0002t0001g0053 a0003c0003t0001g0024 others(1): Show |
8 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2146T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253966 | |||||||
| chr4:76253981 | G | T | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2161G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253981 | |||||||
| chr4:76254092 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(105): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.75-2086T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254092 | |||||||
| chr4:76254110 | A | G | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-2068A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254110 | |||||||
| chr4:76254128 | GA | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(110): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.75-2034delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76254128 | ||||||
| chr4:76254144 | A | C | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-2034A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254144 | |||||||
| chr4:76254389 | A | G | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-1789A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254389 | |||||||
| chr4:76254534 | A | G | 20 | a0001c0001t0001g0108 a0002c0002t0001g0005 a0002c0002t0001g0106 others(17): Show |
39 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.75-1644A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254534 | |||||||
| chr4:76254542 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(57): Show |
124 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.75-1636G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254542 | |||||||
| chr4:76254590 | A | G | 34 | a0001c0001t0001g0108 a0002c0002t0001g0005 a0002c0002t0001g0054 others(31): Show |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.75-1588A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254590 | |||||||
| chr4:76254625 | C | T | 6 | a0003c0003t0001g0159 a0005c0005t0001g0038 a0005c0005t0001g0052 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-1553C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254625 | |||||||
| chr4:76254813 | G | A | 34 | a0001c0001t0001g0108 a0002c0002t0001g0005 a0002c0002t0001g0054 others(31): Show |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.75-1365G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254813 | |||||||
| chr4:76254888 | T | C | 1 | a0002c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.75-1290T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254888 | |||||||
| chr4:76254914 | C | G | 1 | a0001c0001t0001g0058 | 2 | NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.75-1264C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254914 | |||||||
| chr4:76254937 | C | G | 5 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0153 others(2): Show |
7 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-1241C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254937 | |||||||
| chr4:76254942 | G | A | 2 | a0002c0002t0001g0022 a0002c0002t0001g0170 |
5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-1236G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254942 | |||||||
| chr4:76255034 | G | A | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-1144G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255034 | |||||||
| chr4:76255049 | A | G | 1 | a0002c0002t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.75-1129A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255049 | |||||||
| chr4:76255050 | T | C | 1 | a0003c0003t0001g0018 | 4 | HG01884.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-1128T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255050 | |||||||
| chr4:76255128 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(80): Show |
199 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.75-1050G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255128 | |||||||
| chr4:76255136 | A | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.75-1042A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255136 | |||||||
| chr4:76255283 | C | T | 1 | a0004c0004t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75-895C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255283 | |||||||
| chr4:76255356 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.75-822C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255356 | |||||||
| chr4:76255371 | T | C | 95 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0001c0001t0001g0108 others(92): Show |
185 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.75-807T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255371 | |||||||
| chr4:76255378 | C | G | 2 | a0003c0003t0001g0024 a0003c0003t0001g0185 |
5 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-800C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255378 | |||||||
| chr4:76255399 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(130): Show |
281 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.75-779G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255399 | |||||||
| chr4:76255479 | A | G | 1 | a0004c0006t0001g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.75-699A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255479 | |||||||
| chr4:76255480 | A | G | 2 | a0003c0003t0001g0040 a0003c0003t0001g0096 |
3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.75-698A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255480 | |||||||
| chr4:76255521 | G | A | 31 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(28): Show |
77 | HG00423.hp1 HG00558.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.75-657G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255521 | |||||||
| chr4:76255547 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75-631A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255547 | |||||||
| chr4:76255592 | A | G | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.75-586A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255592 | |||||||
| chr4:76255613 | G | A | 2 | a0002c0002t0001g0022 a0002c0002t0001g0170 |
5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-565G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255613 | |||||||
| chr4:76255615 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
221 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.75-563T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255615 | |||||||
| chr4:76255633 | T | G | 2 | a0002c0002t0001g0022 a0002c0002t0001g0170 |
5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-545T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255633 | |||||||
| chr4:76255691 | C | T | 2 | a0001c0001t0001g0141 a0004c0004t0001g0117 |
2 | HG03704.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.75-487C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255691 | |||||||
| chr4:76255695 | T | C | 44 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(41): Show |
102 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.75-483T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255695 | |||||||
| chr4:76255699 | G | A | 7 | a0004c0004t0001g0107 a0005c0005t0001g0038 a0005c0005t0001g0052 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.75-479G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255699 | |||||||
| chr4:76255716 | C | T | 1 | a0004c0004t0001g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75-462C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255716 | |||||||
| chr4:76255744 | C | T | 58 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(55): Show |
125 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.75-434C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255744 | |||||||
| chr4:76255789 | CAAG | C | 1 | a0002c0002t0001g0014 | 4 | NA18951.hp2 NA19000.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-385_75-383delAA others(1): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76255789 | ||||||
| chr4:76255814 | G | A | 7 | a0002c0002t0001g0092 a0003c0003t0001g0040 a0003c0003t0001g0095 others(4): Show |
8 | HG02055.hp1 HG03195.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-364G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255814 | |||||||
| chr4:76255874 | A | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(27): Show |
74 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.75-304A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255874 | |||||||
| chr4:76255881 | A | G | 1 | a0002c0002t0001g0015 | 4 | HG01884.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-297A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255881 | |||||||
| chr4:76255887 | C | T | 1 | a0005c0005t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.75-291C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255887 | |||||||
| chr4:76255894 | A | G | 9 | a0002c0002t0001g0022 a0002c0002t0001g0092 a0002c0002t0001g0170 others(6): Show |
13 | HG01175.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.75-284A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255894 | |||||||
| chr4:76255967 | G | C | 4 | a0001c0001t0001g0066 a0002c0002t0001g0011 a0002c0002t0001g0012 others(1): Show |
12 | HG02040.hp1 NA18940.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.75-211G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255967 | |||||||
| chr4:76256078 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0140 |
3 | NA18982.hp1 NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.75-100A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76256078 | |||||||
| chr4:76256664 | A | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.420+141A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76256664 | |||||||
| chr4:76256664 | A | G | 90 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0001c0001t0001g0108 others(87): Show |
178 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.420+141A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76256664 | |||||||
| chr4:76256693 | G | A | 35 | a0001c0001t0001g0108 a0002c0002t0001g0005 a0002c0002t0001g0046 others(32): Show |
58 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.420+170G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76256693 | |||||||
| chr4:76257083 | G | A | 1 | a0003c0003t0001g0123 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.420+560G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257083 | |||||||
| chr4:76257226 | A | G | 46 | a0001c0001t0001g0156 a0002c0002t0001g0005 a0002c0002t0001g0046 others(43): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.420+703A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257226 | |||||||
| chr4:76257257 | G | C | 1 | a0004c0004t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.420+734G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257257 | |||||||
| chr4:76257461 | A | C | 3 | a0002c0002t0001g0092 a0003c0003t0001g0040 a0003c0003t0001g0096 |
4 | HG02055.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+938A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257461 | |||||||
| chr4:76257529 | C | T | 3 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0185 |
7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+1006C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257529 | |||||||
| chr4:76257674 | C | T | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+1151C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257674 | |||||||
| chr4:76257709 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.420+1186C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257709 | |||||||
| chr4:76257951 | G | A | 2 | a0003c0003t0001g0024 a0003c0003t0001g0185 |
5 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+1428G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257951 | |||||||
| chr4:76258039 | C | G | 1 | a0004c0004t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.420+1516C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258039 | |||||||
| chr4:76258339 | G | A | 1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.420+1816G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258339 | |||||||
| chr4:76258365 | G | T | 89 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(86): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.420+1842G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258365 | |||||||
| chr4:76258448 | T | C | 34 | a0002c0002t0001g0005 a0002c0002t0001g0046 a0002c0002t0001g0109 others(31): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.420+1925T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258448 | |||||||
| chr4:76258499 | A | C | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+1976A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258499 | |||||||
| chr4:76258538 | G | A | 1 | a0004c0004t0001g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.420+2015G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258538 | |||||||
| chr4:76258563 | T | C | 7 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0095 others(4): Show |
11 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+2040T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258563 | |||||||
| chr4:76258598 | T | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.420+2075T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258598 | |||||||
| chr4:76258677 | C | T | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.420+2154C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258677 | |||||||
| chr4:76258745 | C | T | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.420+2222C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258745 | |||||||
| chr4:76258832 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.420+2309T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258832 | |||||||
| chr4:76258992 | T | C | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.420+2469T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258992 | |||||||
| chr4:76259017 | A | G | 1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.420+2494A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259017 | |||||||
| chr4:76259051 | G | T | 1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.420+2528G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259051 | |||||||
| chr4:76259062 | C | T | 1 | a0004c0004t0001g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.420+2539C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259062 | |||||||
| chr4:76259408 | G | A | 3 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0185 |
7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+2885G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259408 | |||||||
| chr4:76259459 | G | A | 89 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(86): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.420+2936G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259459 | |||||||
| chr4:76259514 | C | A | 1 | a0004c0004t0001g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.420+2991C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259514 | |||||||
| chr4:76259663 | T | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(26): Show |
72 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.420+3140T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259663 | |||||||
| chr4:76259667 | C | T | 1 | a0003c0003t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.420+3144C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259667 | |||||||
| chr4:76259781 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.420+3258A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259781 | |||||||
| chr4:76259787 | A | C | 91 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0001c0001t0001g0098 others(88): Show |
178 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.420+3264A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259787 | |||||||
| chr4:76259864 | A | AGG | 3 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0185 |
7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+3342_420+3343i others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76259864 | ||||||
| chr4:76259980 | A | G | 1 | a0001c0001t0001g0031 | 3 | HG02698.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.420+3457A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259980 | |||||||
| chr4:76260170 | G | A | 89 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(86): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.421-3534G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260170 | |||||||
| chr4:76260284 | G | A | 89 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(86): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.421-3420G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260284 | |||||||
| chr4:76260383 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.421-3321A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260383 | |||||||
| chr4:76260391 | T | G | 89 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(86): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.421-3313T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260391 | |||||||
| chr4:76260549 | A | G | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-3155A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260549 | |||||||
| chr4:76260559 | TAACTC | T | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-3142_421-3138d others(7): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76260559 | ||||||
| chr4:76260602 | A | G | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-3102A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260602 | |||||||
| chr4:76260786 | A | G | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-2918A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260786 | |||||||
| chr4:76260824 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.421-2880G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260824 | |||||||
| chr4:76260830 | T | C | 2 | a0002c0002t0001g0022 a0002c0002t0001g0170 |
5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-2874T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260830 | |||||||
| chr4:76260851 | G | T | 89 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(86): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.421-2853G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260851 | |||||||
| chr4:76260859 | T | C | 38 | a0002c0002t0001g0005 a0002c0002t0001g0046 a0002c0002t0001g0109 others(35): Show |
61 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.421-2845T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260859 | |||||||
| chr4:76260880 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(127): Show |
275 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.421-2824T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260880 | |||||||
| chr4:76260983 | C | CA | 8 | a0001c0001t0001g0121 a0002c0002t0001g0022 a0002c0002t0001g0053 others(5): Show |
12 | HG01175.hp1 HG02258.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-2708dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76260983 | ||||||
| chr4:76261037 | A | C | 1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421-2667A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261037 | |||||||
| chr4:76261120 | C | T | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-2584C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261120 | |||||||
| chr4:76261256 | A | G | 47 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(44): Show |
107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-2448A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261256 | |||||||
| chr4:76261325 | A | G | 1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421-2379A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261325 | |||||||
| chr4:76261523 | G | A | 2 | a0002c0002t0001g0164 a0002c0002t0001g0174 |
2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.421-2181G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261523 | |||||||
| chr4:76261525 | C | T | 4 | a0003c0003t0001g0095 a0003c0003t0001g0159 a0003c0003t0002g0093 others(1): Show |
4 | HG03195.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-2179C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261525 | |||||||
| chr4:76261527 | T | C | 1 | a0003c0003t0001g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.421-2177T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261527 | |||||||
| chr4:76261573 | A | G | 89 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0002c0002t0001g0001 others(86): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.421-2131A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261573 | |||||||
| chr4:76261677 | G | A | 3 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0185 |
7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-2027G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261677 | |||||||
| chr4:76262147 | A | C | 37 | a0002c0002t0001g0022 a0002c0002t0001g0092 a0002c0002t0001g0164 others(34): Show |
55 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.421-1557A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262147 | |||||||
| chr4:76262148 | A | G | 7 | a0004c0004t0001g0028 a0005c0005t0001g0038 a0005c0005t0001g0052 others(4): Show |
11 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-1556A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262148 | |||||||
| chr4:76262176 | A | T | 1 | a0003c0003t0001g0051 | 2 | NA18988.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.421-1528A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262176 | |||||||
| chr4:76262251 | C | A | 1 | a0002c0002t0001g0062 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.421-1453C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262251 | |||||||
| chr4:76262267 | G | A | 1 | a0001c0001t0001g0058 | 2 | NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.421-1437G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262267 | |||||||
| chr4:76262272 | T | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.421-1432T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262272 | |||||||
| chr4:76262281 | T | C | 37 | a0002c0002t0001g0022 a0002c0002t0001g0092 a0002c0002t0001g0164 others(34): Show |
55 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.421-1423T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262281 | |||||||
| chr4:76262423 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.421-1281C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262423 | |||||||
| chr4:76262493 | A | G | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(34): Show |
92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.421-1211A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262493 | |||||||
| chr4:76262713 | A | G | 1 | a0004c0004t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.421-991A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262713 | |||||||
| chr4:76262724 | T | C | 3 | a0002c0002t0001g0092 a0003c0003t0001g0040 a0003c0003t0001g0096 |
4 | HG02055.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-980T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262724 | |||||||
| chr4:76262778 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(34): Show |
92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.421-926T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262778 | |||||||
| chr4:76262876 | C | G | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-828C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262876 | |||||||
| chr4:76262939 | T | A | 7 | a0002c0002t0001g0053 a0002c0002t0001g0091 a0003c0003t0001g0024 others(4): Show |
11 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-765T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262939 | |||||||
| chr4:76262943 | TTAAATAG others(189): Show |
T | 1 | a0005c0005t0001g0097 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.421-756_421-561del | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76262943 | ||||||
| chr4:76263031 | C | T | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.421-673C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263031 | |||||||
| chr4:76263184 | A | G | 1 | a0003c0003t0001g0050 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.421-520A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263184 | |||||||
| chr4:76263191 | T | C | 1 | a0007c0007t0001g0070 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.421-513T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263191 | |||||||
| chr4:76263242 | G | C | 96 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(93): Show |
187 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.421-462G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263242 | |||||||
| chr4:76263380 | T | G | 1 | a0001c0001t0001g0140 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.421-324T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263380 | |||||||
| chr4:76263402 | T | C | 5 | a0002c0002t0001g0022 a0002c0002t0001g0091 a0002c0002t0001g0164 others(2): Show |
8 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-302T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263402 | |||||||
| chr4:76263844 | G | A | 5 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0068 others(2): Show |
9 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
splice_donor_variant&intron_variant | HIGH | c.560+1G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263844 | |||||||
| chr4:76263844 | G | C | 2 | a0002c0002t0001g0026 a0002c0002t0001g0131 |
4 | NA18957.hp2 NA19063.hp2 NA19067.hp2 others(1): Show |
splice_donor_variant&intron_variant | HIGH | c.560+1G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263844 | |||||||
| chr4:76263898 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.560+55G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263898 | |||||||
| chr4:76263993 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.560+150C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263993 | |||||||
| chr4:76264023 | A | T | 19 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0029 others(16): Show |
37 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+180A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264023 | |||||||
| chr4:76264041 | C | T | 19 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0029 others(16): Show |
37 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+198C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264041 | |||||||
| chr4:76264056 | C | T | 3 | a0001c0001t0001g0098 a0004c0004t0001g0107 a0004c0004t0001g0169 |
3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+213C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264056 | |||||||
| chr4:76264140 | G | A | 59 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(56): Show |
131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.560+297G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264140 | |||||||
| chr4:76264206 | T | C | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.560+363T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264206 | |||||||
| chr4:76264213 | A | G | 1 | a0001c0001t0001g0021 | 4 | HG01070.hp2 HG01361.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+370A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264213 | |||||||
| chr4:76264376 | G | C | 53 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(50): Show |
121 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.560+533G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264376 | |||||||
| chr4:76264547 | G | A | 3 | a0001c0001t0001g0098 a0004c0004t0001g0107 a0004c0004t0001g0169 |
3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+704G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264547 | |||||||
| chr4:76264552 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.560+709G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264552 | |||||||
| chr4:76264726 | A | G | 30 | a0003c0003t0001g0095 a0003c0003t0002g0093 a0004c0004t0001g0008 others(27): Show |
44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.560+883A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264726 | |||||||
| chr4:76264747 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.560+904C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264747 | |||||||
| chr4:76264795 | C | T | 1 | a0003c0003t0001g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+952C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264795 | |||||||
| chr4:76264844 | C | T | 59 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(56): Show |
131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.560+1001C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264844 | |||||||
| chr4:76264947 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.560+1104G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264947 | |||||||
| chr4:76265099 | A | T | 1 | a0004c0004t0001g0016 | 4 | HG00642.hp2 HG00741.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+1256A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265099 | |||||||
| chr4:76265262 | A | C | 60 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(57): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.560+1419A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265262 | |||||||
| chr4:76265277 | C | T | 3 | a0003c0003t0001g0095 a0003c0003t0002g0093 a0004c0004t0002g0094 |
3 | HG03486.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.560+1434C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265277 | |||||||
| chr4:76265294 | G | A | 2 | a0002c0002t0001g0109 a0002c0002t0001g0110 |
2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.560+1451G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265294 | |||||||
| chr4:76265424 | A | G | 1 | a0001c0001t0001g0058 | 2 | NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.560+1581A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265424 | |||||||
| chr4:76265434 | C | T | 3 | a0001c0001t0001g0098 a0004c0004t0001g0107 a0004c0004t0001g0169 |
3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+1591C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265434 | |||||||
| chr4:76265443 | C | G | 53 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(50): Show |
122 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.560+1600C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265443 | |||||||
| chr4:76265489 | G | A | 30 | a0003c0003t0001g0095 a0003c0003t0002g0093 a0004c0004t0001g0008 others(27): Show |
44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.560+1646G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265489 | |||||||
| chr4:76265519 | T | C | 60 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(57): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.560+1676T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265519 | |||||||
| chr4:76265609 | T | TTATTCAT others(1): Show |
97 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(94): Show |
188 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.560+1767_560+1774d others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 76265609 | ||||||
| chr4:76265659 | T | C | 97 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(94): Show |
188 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.560+1816T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265659 | |||||||
| chr4:76265660 | G | A | 2 | a0003c0003t0001g0040 a0003c0003t0001g0096 |
3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.560+1817G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265660 | |||||||
| chr4:76265683 | G | A | 1 | a0002c0002t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+1840G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265683 | |||||||
| chr4:76265771 | A | C | 90 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(87): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.560+1928A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265771 | |||||||
| chr4:76265781 | C | T | 2 | a0001c0001t0001g0098 a0004c0004t0001g0107 |
2 | HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+1938C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265781 | |||||||
| chr4:76265868 | C | T | 1 | a0003c0003t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.560+2025C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265868 | |||||||
| chr4:76265879 | T | C | 90 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(87): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.560+2036T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265879 | |||||||
| chr4:76265947 | T | TA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(34): Show |
92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.560+2105dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 76265947 | ||||||
| chr4:76266070 | G | C | 6 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0068 others(3): Show |
10 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+2227G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266070 | |||||||
| chr4:76266143 | G | A | 4 | a0003c0003t0001g0095 a0003c0003t0002g0093 a0004c0004t0001g0150 others(1): Show |
4 | HG03486.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+2300G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266143 | |||||||
| chr4:76266160 | T | C | 1 | a0004c0004t0001g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.560+2317T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266160 | |||||||
| chr4:76266328 | C | T | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.561-2332C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266328 | |||||||
| chr4:76266403 | G | A | 60 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(57): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.561-2257G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266403 | |||||||
| chr4:76266473 | A | G | 97 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(94): Show |
188 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.561-2187A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266473 | |||||||
| chr4:76266517 | T | C | 1 | a0004c0004t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.561-2143T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266517 | |||||||
| chr4:76266668 | G | A | 3 | a0003c0003t0001g0040 a0003c0003t0001g0096 a0004c0004t0002g0094 |
4 | HG03516.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-1992G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266668 | |||||||
| chr4:76266726 | T | C | 2 | a0003c0003t0001g0040 a0003c0003t0001g0096 |
3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1934T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266726 | |||||||
| chr4:76266763 | C | T | 37 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0040 others(34): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-1897C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266763 | |||||||
| chr4:76266905 | A | G | 37 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0040 others(34): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-1755A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266905 | |||||||
| chr4:76266967 | T | C | 3 | a0001c0001t0001g0098 a0004c0004t0001g0107 a0004c0004t0001g0169 |
3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.561-1693T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266967 | |||||||
| chr4:76266979 | A | G | 55 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(52): Show |
124 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.561-1681A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266979 | |||||||
| chr4:76267021 | TCC | T | 37 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0040 others(34): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-1635_561-1634d others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 76267021 | ||||||
| chr4:76267087 | A | G | 60 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(57): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.561-1573A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267087 | |||||||
| chr4:76267091 | G | A | 97 | a0001c0001t0001g0066 a0002c0002t0001g0001 a0002c0002t0001g0005 others(94): Show |
188 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.561-1569G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267091 | |||||||
| chr4:76267124 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0180 |
5 | NA18945.hp2 NA18970.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-1536C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267124 | |||||||
| chr4:76267135 | G | C | 37 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0040 others(34): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-1525G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267135 | |||||||
| chr4:76267174 | T | G | 37 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0040 others(34): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-1486T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267174 | |||||||
| chr4:76267186 | A | T | 21 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0029 others(18): Show |
40 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.561-1474A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267186 | |||||||
| chr4:76267218 | T | C | 2 | a0003c0003t0001g0040 a0003c0003t0001g0096 |
3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1442T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267218 | |||||||
| chr4:76267223 | G | A | 1 | a0004c0004t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.561-1437G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267223 | |||||||
| chr4:76267251 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.561-1409T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267251 | |||||||
| chr4:76267265 | C | G | 37 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0040 others(34): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-1395C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267265 | |||||||
| chr4:76267330 | G | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0081 others(4): Show |
19 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.561-1330G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267330 | |||||||
| chr4:76267460 | T | C | 102 | a0001c0001t0001g0066 a0001c0001t0001g0147 a0001c0001t0001g0148 others(99): Show |
194 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.561-1200T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267460 | |||||||
| chr4:76267613 | A | T | 37 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0040 others(34): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-1047A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267613 | |||||||
| chr4:76267753 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561-907A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267753 | |||||||
| chr4:76268119 | G | C | 2 | a0003c0003t0001g0095 a0004c0004t0002g0094 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.561-541G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268119 | |||||||
| chr4:76268227 | A | G | 35 | a0002c0002t0001g0053 a0003c0003t0001g0024 a0003c0003t0001g0068 others(32): Show |
53 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.561-433A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268227 | |||||||
| chr4:76268265 | C | T | 34 | a0003c0003t0001g0024 a0003c0003t0001g0040 a0003c0003t0001g0068 others(31): Show |
52 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.561-395C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268265 | |||||||
| chr4:76268408 | T | A | 1 | a0002c0002t0001g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.561-252T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268408 | |||||||
| chr4:76268409 | A | T | 1 | a0002c0002t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561-251A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268409 | |||||||
| chr4:76268460 | C | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0068 a0003c0003t0001g0069 others(1): Show |
7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-200C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268460 | |||||||
| chr4:76268830 | A | G | 2 | a0003c0003t0001g0040 a0003c0003t0001g0096 |
3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.669+62A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76268830 | |||||||
| chr4:76268831 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+63T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76268831 | |||||||
| chr4:76268916 | C | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+148C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76268916 | |||||||
| chr4:76269068 | T | A | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+300T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269068 | |||||||
| chr4:76269116 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+348T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269116 | |||||||
| chr4:76269194 | G | A | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+426G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269194 | |||||||
| chr4:76269240 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.669+472C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269240 | |||||||
| chr4:76269245 | A | G | 112 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(109): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.669+477A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269245 | |||||||
| chr4:76269343 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.669+575G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269343 | |||||||
| chr4:76269496 | A | G | 30 | a0003c0003t0001g0095 a0003c0003t0002g0093 a0004c0004t0001g0008 others(27): Show |
44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.669+728A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269496 | |||||||
| chr4:76269527 | G | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(51): Show |
123 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.669+759G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269527 | |||||||
| chr4:76269580 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+812T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269580 | |||||||
| chr4:76269621 | A | ATATAT | 6 | a0002c0002t0001g0022 a0002c0002t0001g0053 a0002c0002t0001g0054 others(3): Show |
11 | HG01175.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+853_669+854ins others(5): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269621 | |||||||
| chr4:76269621 | A | ATATATAA others(2): Show |
55 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(52): Show |
124 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.669+853_669+854ins others(9): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269621 | |||||||
| chr4:76269623 | T | A | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+855T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269623 | |||||||
| chr4:76269720 | C | A | 2 | a0003c0003t0001g0040 a0003c0003t0001g0096 |
3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.669+952C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269720 | |||||||
| chr4:76269749 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+981T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269749 | |||||||
| chr4:76269779 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1011T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269779 | |||||||
| chr4:76269787 | C | CA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0027 others(100): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.669+1032dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 76269787 | ||||||
| chr4:76269787 | CA | C | 4 | a0003c0003t0001g0024 a0003c0003t0001g0068 a0003c0003t0001g0069 others(1): Show |
7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+1032delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 76269787 | ||||||
| chr4:76269850 | G | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1082G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269850 | |||||||
| chr4:76269896 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1128T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269896 | |||||||
| chr4:76269959 | T | C | 121 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(118): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.669+1191T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269959 | |||||||
| chr4:76269990 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.669+1222G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269990 | |||||||
| chr4:76270107 | A | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1339A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270107 | |||||||
| chr4:76270163 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1395T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270163 | |||||||
| chr4:76270202 | TC | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-1362delC | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 76270202 | ||||||
| chr4:76270269 | G | A | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-1299G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270269 | |||||||
| chr4:76270443 | A | G | 55 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(52): Show |
125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-1125A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270443 | |||||||
| chr4:76270564 | T | C | 1 | a0002c0002t0001g0128 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.670-1004T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270564 | |||||||
| chr4:76270768 | C | A | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-800C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270768 | |||||||
| chr4:76270799 | G | A | 28 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(25): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.670-769G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270799 | |||||||
| chr4:76270910 | T | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-658T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270910 | |||||||
| chr4:76270926 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.670-642A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270926 | |||||||
| chr4:76271039 | T | C | 1 | a0004c0004t0001g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.670-529T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271039 | |||||||
| chr4:76271235 | T | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-333T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271235 | |||||||
| chr4:76271339 | C | T | 1 | a0002c0002t0001g0036 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.670-229C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271339 | |||||||
| chr4:76271359 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.670-209C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271359 | |||||||
| chr4:76271459 | A | T | 1 | a0004c0004t0001g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.670-109A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271459 | |||||||
| chr4:76271469 | A | T | 1 | a0004c0004t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-99A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271469 | |||||||
| chr4:76271535 | G | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-33G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271535 | |||||||
| chr4:76271793 | G | A | 1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.870+25G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271793 | |||||||
| chr4:76271854 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0121 |
5 | NA18946.hp2 NA18981.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+86G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271854 | |||||||
| chr4:76271880 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.870+112C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271880 | |||||||
| chr4:76271894 | A | G | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+126A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271894 | |||||||
| chr4:76271904 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.870+136T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271904 | |||||||
| chr4:76271942 | T | G | 1 | a0002c0002t0001g0034 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.870+174T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271942 | |||||||
| chr4:76271983 | A | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+215A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271983 | |||||||
| chr4:76272055 | A | T | 20 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(17): Show |
32 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.870+287A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272055 | |||||||
| chr4:76272075 | T | C | 2 | a0003c0003t0001g0049 a0003c0003t0001g0125 |
3 | HG01516.hp2 HG02647.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.870+307T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272075 | |||||||
| chr4:76272296 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+528T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272296 | |||||||
| chr4:76272392 | T | G | 121 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(118): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.870+624T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272392 | |||||||
| chr4:76272413 | C | T | 1 | a0001c0001t0001g0020 | 4 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+645C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272413 | |||||||
| chr4:76272437 | A | G | 1 | a0003c0003t0001g0050 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.870+669A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272437 | |||||||
| chr4:76272496 | T | A | 21 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0029 others(18): Show |
40 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.870+728T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272496 | |||||||
| chr4:76272575 | T | G | 121 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(118): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.870+807T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272575 | |||||||
| chr4:76272589 | C | A | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+821C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272589 | |||||||
| chr4:76272782 | T | G | 1 | a0001c0001t0001g0033 | 3 | HG02165.hp1 HG03834.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.870+1014T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272782 | |||||||
| chr4:76272893 | A | G | 5 | a0003c0003t0001g0024 a0003c0003t0001g0068 a0003c0003t0001g0069 others(2): Show |
8 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+1125A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272893 | |||||||
| chr4:76272911 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.870+1143A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272911 | |||||||
| chr4:76272939 | G | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1171G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272939 | |||||||
| chr4:76272993 | G | T | 1 | a0001c0001t0001g0056 | 2 | HG01106.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.870+1225G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272993 | |||||||
| chr4:76273068 | A | G | 5 | a0002c0002t0001g0022 a0002c0002t0001g0053 a0002c0002t0001g0091 others(2): Show |
9 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+1300A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273068 | |||||||
| chr4:76273070 | T | C | 1 | a0001c0001t0001g0031 | 3 | HG02698.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.870+1302T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273070 | |||||||
| chr4:76273093 | G | A | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1325G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273093 | |||||||
| chr4:76273119 | T | C | 1 | a0001c0001t0001g0031 | 3 | HG02698.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.870+1351T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273119 | |||||||
| chr4:76273158 | G | C | 1 | a0003c0003t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.870+1390G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273158 | |||||||
| chr4:76273159 | G | T | 1 | a0003c0003t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.870+1391G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273159 | |||||||
| chr4:76273320 | G | A | 114 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(111): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.870+1552G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273320 | |||||||
| chr4:76273448 | GCCTT | G | 3 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0161 |
5 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.870+1684_870+1687d others(6): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76273448 | ||||||
| chr4:76273511 | T | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1743T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273511 | |||||||
| chr4:76273517 | G | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1749G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273517 | |||||||
| chr4:76273524 | C | G | 1 | a0005c0005t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.870+1756C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273524 | |||||||
| chr4:76273531 | C | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1763C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273531 | |||||||
| chr4:76273650 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.870+1882G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273650 | |||||||
| chr4:76273728 | C | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1960C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273728 | |||||||
| chr4:76273844 | G | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+2076G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273844 | |||||||
| chr4:76273856 | A | AT | 60 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(57): Show |
134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.870+2097dupT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76273856 | ||||||
| chr4:76273920 | T | C | 5 | a0002c0002t0001g0022 a0002c0002t0001g0053 a0002c0002t0001g0091 others(2): Show |
9 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+2152T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273920 | |||||||
| chr4:76273953 | G | C | 22 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(19): Show |
34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.870+2185G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273953 | |||||||
| chr4:76273957 | T | C | 27 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(24): Show |
49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.870+2189T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273957 | |||||||
| chr4:76274165 | C | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+2397C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274165 | |||||||
| chr4:76274380 | C | T | 1 | a0004c0004t0001g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.870+2612C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274380 | |||||||
| chr4:76274389 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.870+2621T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274389 | |||||||
| chr4:76274409 | C | CA | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+2650dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76274409 | ||||||
| chr4:76274579 | T | C | 65 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(62): Show |
147 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.870+2811T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274579 | |||||||
| chr4:76274837 | C | A | 1 | a0003c0003t0001g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.870+3069C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274837 | |||||||
| chr4:76274881 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+3113T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274881 | |||||||
| chr4:76274953 | C | T | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.871-3116C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274953 | |||||||
| chr4:76274990 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.871-3079C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274990 | |||||||
| chr4:76275035 | T | C | 28 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(25): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.871-3034T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275035 | |||||||
| chr4:76275067 | A | AT | 21 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(18): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.871-2996dupT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76275067 | ||||||
| chr4:76275294 | T | C | 2 | a0003c0003t0001g0041 a0003c0003t0001g0124 |
3 | NA18948.hp2 NA18954.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.871-2775T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275294 | |||||||
| chr4:76275323 | T | G | 20 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(17): Show |
32 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.871-2746T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275323 | |||||||
| chr4:76275347 | C | T | 56 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(53): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.871-2722C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275347 | |||||||
| chr4:76275426 | C | T | 2 | a0003c0003t0001g0032 a0003c0003t0002g0146 |
4 | HG02572.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2643C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275426 | |||||||
| chr4:76275519 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.871-2550A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275519 | |||||||
| chr4:76275524 | G | A | 58 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(55): Show |
95 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.871-2545G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275524 | |||||||
| chr4:76275695 | A | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.871-2374A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275695 | |||||||
| chr4:76275872 | G | T | 1 | a0002c0002t0001g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.871-2197G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275872 | |||||||
| chr4:76276029 | GACAGACA others(9): Show |
G | 32 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(29): Show |
56 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.871-2036_871-2021d others(18): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276029 | ||||||
| chr4:76276033 | G | GACACACA others(3): Show |
1 | a0004c0004t0001g0013 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.871-2033_871-2032i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276033 | ||||||
| chr4:76276033 | GACAGACA others(7): Show |
G | 3 | a0003c0003t0001g0040 a0003c0003t0001g0096 a0003c0003t0001g0172 |
4 | NA18522.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2032_871-2019d others(16): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276033 | ||||||
| chr4:76276033 | GACAGACA others(9): Show |
G | 23 | a0003c0003t0002g0093 a0004c0004t0001g0008 a0004c0004t0001g0016 others(20): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.871-2032_871-2017d others(18): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276033 | ||||||
| chr4:76276037 | G | C | 5 | a0001c0001t0001g0045 a0002c0002t0001g0062 a0002c0002t0001g0063 others(2): Show |
5 | HG00609.hp2 HG01069.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-2032G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276037 | |||||||
| chr4:76276037 | G | GAC | 4 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0108 others(1): Show |
5 | HG00642.hp1 HG01255.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-2001_871-2000d others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACAC | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(34): Show |
92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-2003_871-2000d others(6): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACACAC | 9 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0152 others(6): Show |
13 | HG01884.hp2 HG02055.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.871-2005_871-2000d others(8): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACACACA others(1): Show |
17 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0011 others(14): Show |
35 | HG00140.hp2 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.871-2007_871-2000d others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACACACA others(3): Show |
20 | a0001c0001t0001g0098 a0002c0002t0001g0001 a0002c0002t0001g0011 others(17): Show |
49 | HG00423.hp1 HG00558.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.871-2009_871-2000d others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACACACA others(5): Show |
8 | a0002c0002t0001g0014 a0002c0002t0001g0035 a0002c0002t0001g0078 others(5): Show |
9 | HG01081.hp1 HG01258.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-2011_871-2000d others(14): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACAGACA others(1): Show |
8 | a0001c0001t0001g0136 a0002c0002t0001g0005 a0002c0002t0001g0022 others(5): Show |
13 | HG00735.hp2 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.871-2029_871-2028i others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACAGACA others(3): Show |
1 | a0002c0002t0001g0072 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.871-2029_871-2028i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276037 | G | GACAGACA others(3): Show |
1 | a0002c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.871-2029_871-2028i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | ||||||
| chr4:76276070 | C | A | 56 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(53): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.871-1999C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276070 | |||||||
| chr4:76276071 | C | A | 1 | a0002c0002t0001g0064 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.871-1998C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276071 | |||||||
| chr4:76276073 | T | C | 1 | a0002c0002t0001g0064 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.871-1996T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276073 | |||||||
| chr4:76276074 | C | T | 1 | a0002c0002t0001g0064 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.871-1995C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276074 | |||||||
| chr4:76276077 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0080 |
4 | NA18939.hp2 NA18941.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-1992C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276077 | |||||||
| chr4:76276231 | T | C | 1 | a0002c0002t0001g0042 | 2 | NA18961.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.871-1838T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276231 | |||||||
| chr4:76276243 | C | T | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-1826C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276243 | |||||||
| chr4:76276244 | A | G | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-1825A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276244 | |||||||
| chr4:76276285 | GA | G | 5 | a0002c0002t0001g0022 a0002c0002t0001g0053 a0002c0002t0001g0091 others(2): Show |
9 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-1781delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276285 | ||||||
| chr4:76276355 | C | CTTTTTGT others(3): Show |
26 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(23): Show |
48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.871-1709_871-1708i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276355 | ||||||
| chr4:76276355 | C | CTTTTTGT others(4): Show |
7 | a0004c0004t0001g0150 a0005c0005t0001g0038 a0005c0005t0001g0052 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-1709_871-1708i others(13): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276355 | ||||||
| chr4:76276356 | T | TTTTTGTT others(21): Show |
1 | a0004c0004t0001g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.871-1709_871-1708i others(30): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276356 | ||||||
| chr4:76276356 | T | TTTTTGTT others(12): Show |
1 | a0004c0004t0001g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.871-1709_871-1708i others(21): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276356 | ||||||
| chr4:76276356 | T | TTTTTGTT others(21): Show |
20 | a0003c0003t0002g0093 a0004c0004t0001g0008 a0004c0004t0001g0016 others(17): Show |
32 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.871-1709_871-1708i others(30): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276356 | ||||||
| chr4:76276364 | G | GT | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-1702dupT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276364 | ||||||
| chr4:76276368 | G | GTTTGTTT others(1): Show |
57 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.871-1693_871-1686d others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276368 | ||||||
| chr4:76276368 | G | T | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-1701G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276368 | |||||||
| chr4:76276384 | A | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
321 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.871-1685A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276384 | |||||||
| chr4:76276397 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.871-1672G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276397 | |||||||
| chr4:76276411 | C | T | 1 | a0004c0004t0001g0114 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.871-1658C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276411 | |||||||
| chr4:76276434 | G | A | 2 | a0001c0001t0001g0139 a0002c0002t0001g0076 |
2 | HG00423.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.871-1635G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276434 | |||||||
| chr4:76276498 | G | A | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-1571G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276498 | |||||||
| chr4:76276518 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.871-1551A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276518 | |||||||
| chr4:76276521 | C | T | 56 | a0001c0001t0001g0098 a0003c0003t0001g0009 a0003c0003t0001g0018 others(53): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1548C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276521 | |||||||
| chr4:76276588 | CCCAA | C | 55 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(52): Show |
128 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.871-1478_871-1475d others(6): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276588 | ||||||
| chr4:76276692 | A | G | 30 | a0003c0003t0001g0095 a0003c0003t0002g0093 a0004c0004t0001g0008 others(27): Show |
44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.871-1377A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276692 | |||||||
| chr4:76276729 | G | C | 57 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.871-1340G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276729 | |||||||
| chr4:76276901 | C | T | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-1168C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276901 | |||||||
| chr4:76276913 | G | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0068 a0003c0003t0001g0069 others(1): Show |
7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-1156G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276913 | |||||||
| chr4:76277077 | T | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0078 |
3 | NA18947.hp2 NA19056.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.871-992T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277077 | |||||||
| chr4:76277210 | C | T | 20 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(17): Show |
32 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.871-859C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277210 | |||||||
| chr4:76277211 | G | A | 1 | a0003c0003t0001g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.871-858G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277211 | |||||||
| chr4:76277266 | C | T | 1 | a0001c0001t0001g0019 | 4 | HG00609.hp1 NA18952.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-803C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277266 | |||||||
| chr4:76277312 | G | A | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-757G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277312 | |||||||
| chr4:76277413 | G | A | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-656G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277413 | |||||||
| chr4:76277418 | G | A | 58 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(55): Show |
133 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.871-651G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277418 | |||||||
| chr4:76277434 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.871-635C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277434 | |||||||
| chr4:76277484 | C | T | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-585C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277484 | |||||||
| chr4:76277489 | C | G | 4 | a0003c0003t0001g0024 a0003c0003t0001g0068 a0003c0003t0001g0069 others(1): Show |
7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-580C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277489 | |||||||
| chr4:76277509 | GA | G | 1 | a0002c0002t0001g0012 | 5 | NA18946.hp1 NA18952.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-550delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76277509 | ||||||
| chr4:76277547 | T | TA | 32 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(29): Show |
56 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.871-511dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76277547 | ||||||
| chr4:76277547 | TA | T | 20 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(17): Show |
32 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.871-511delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76277547 | ||||||
| chr4:76277603 | A | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
321 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.871-466A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277603 | |||||||
| chr4:76277635 | A | G | 3 | a0002c0002t0001g0022 a0002c0002t0001g0164 a0002c0002t0001g0174 |
6 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-434A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277635 | |||||||
| chr4:76277638 | G | A | 60 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(57): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.871-431G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277638 | |||||||
| chr4:76277758 | C | T | 2 | a0003c0003t0002g0093 a0004c0004t0002g0094 |
2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.871-311C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277758 | |||||||
| chr4:76277833 | C | T | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-236C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277833 | |||||||
| chr4:76277953 | A | G | 1 | a0004c0004t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.871-116A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277953 | |||||||
| chr4:76277986 | C | T | 1 | a0002c0002t0001g0072 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.871-83C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277986 | |||||||
| chr4:76278058 | A | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(24): Show |
65 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.871-11A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76278058 | |||||||
| chr4:76278261 | C | A | 59 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(56): Show |
134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1026+37C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278261 | |||||||
| chr4:76278309 | G | A | 2 | a0003c0003t0002g0093 a0004c0004t0002g0094 |
2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1026+85G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278309 | |||||||
| chr4:76278338 | C | T | 2 | a0003c0003t0001g0096 a0003c0003t0001g0172 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1026+114C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278338 | |||||||
| chr4:76278548 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0183 |
2 | HG00544.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1026+324C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278548 | |||||||
| chr4:76278751 | A | G | 116 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(113): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1026+527A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278751 | |||||||
| chr4:76278760 | G | A | 55 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(52): Show |
91 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1026+536G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278760 | |||||||
| chr4:76278788 | C | T | 59 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(56): Show |
134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1026+564C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278788 | |||||||
| chr4:76279503 | T | C | 1 | a0002c0002t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1027-761T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279503 | |||||||
| chr4:76279646 | C | T | 59 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(56): Show |
134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1027-618C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279646 | |||||||
| chr4:76279652 | C | T | 59 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(56): Show |
134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1027-612C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279652 | |||||||
| chr4:76279664 | C | A | 2 | a0004c0004t0001g0107 a0004c0004t0001g0169 |
2 | HG02965.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1027-600C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279664 | |||||||
| chr4:76279720 | C | A | 1 | a0002c0002t0001g0059 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1027-544C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279720 | |||||||
| chr4:76279722 | A | G | 59 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(56): Show |
134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1027-542A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279722 | |||||||
| chr4:76279913 | A | T | 121 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(118): Show |
236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1027-351A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279913 | |||||||
| chr4:76279927 | T | A | 26 | a0003c0003t0001g0009 a0003c0003t0001g0018 a0003c0003t0001g0024 others(23): Show |
48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1027-337T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279927 | |||||||
| chr4:76280065 | G | C | 2 | a0002c0002t0001g0071 a0002c0002t0001g0072 |
2 | HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1027-199G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76280065 | |||||||
| chr4:76280179 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
321 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.1027-85G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76280179 | |||||||
| chr4:76280402 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1104+61C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280402 | |||||||
| chr4:76280475 | A | T | 1 | a0002c0002t0001g0110 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1104+134A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280475 | |||||||
| chr4:76280485 | C | T | 1 | a0003c0003t0001g0048 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1104+144C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280485 | |||||||
| chr4:76280497 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1104+156C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280497 | |||||||
| chr4:76280684 | C | G | 2 | a0004c0004t0001g0107 a0004c0004t0001g0169 |
2 | HG02965.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1104+343C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280684 | |||||||
| chr4:76280710 | G | A | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1104+369G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280710 | |||||||
| chr4:76280866 | T | C | 21 | a0003c0003t0002g0093 a0004c0004t0001g0008 a0004c0004t0001g0016 others(18): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1104+525T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280866 | |||||||
| chr4:76281033 | G | A | 1 | a0004c0004t0001g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1104+692G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281033 | |||||||
| chr4:76281251 | A | T | 114 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0002c0002t0001g0001 others(111): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1104+910A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281251 | |||||||
| chr4:76281322 | C | G | 1 | a0004c0004t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1104+981C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281322 | |||||||
| chr4:76281560 | A | G | 121 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(118): Show |
236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1104+1219A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281560 | |||||||
| chr4:76281609 | A | G | 122 | a0001c0001t0001g0098 a0001c0001t0001g0162 a0001c0001t0001g0163 others(119): Show |
237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1104+1268A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281609 | |||||||
| chr4:76281659 | A | G | 63 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(60): Show |
146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1104+1318A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281659 | |||||||
| chr4:76281708 | A | G | 100 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0002c0002t0001g0001 others(97): Show |
203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1104+1367A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281708 | |||||||
| chr4:76281729 | C | A | 63 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(60): Show |
146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1104+1388C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281729 | |||||||
| chr4:76281765 | G | A | 6 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1104+1424G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281765 | |||||||
| chr4:76281821 | C | T | 1 | a0002c0002t0001g0131 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1104+1480C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281821 | |||||||
| chr4:76281825 | T | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1104+1484T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281825 | |||||||
| chr4:76281888 | G | A | 30 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0002c0002t0001g0022 others(27): Show |
47 | HG00280.hp2 HG00597.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.1105-1493G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281888 | |||||||
| chr4:76281890 | C | T | 63 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0007 others(60): Show |
146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1105-1491C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281890 | |||||||
| chr4:76281961 | G | A | 2 | a0001c0001t0001g0030 a0003c0003t0001g0159 |
4 | HG02165.hp2 HG03195.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1420G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281961 | |||||||
| chr4:76281964 | G | C | 27 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0002c0002t0001g0022 others(24): Show |
44 | HG00280.hp2 HG00597.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.1105-1417G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281964 | |||||||
| chr4:76281994 | G | A | 1 | a0003c0003t0001g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1105-1387G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281994 | |||||||
| chr4:76281999 | A | G | 96 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0001g0136 others(93): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1105-1382A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281999 | |||||||
| chr4:76282037 | TAACATTT others(8): Show |
T | 1 | a0002c0002t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1105-1341_1105-132 others(19): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282037 | ||||||
| chr4:76282038 | A | AACATTTG others(16): Show |
1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1105-1319_1105-129 others(27): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282038 | ||||||
| chr4:76282038 | AACATTTG others(16): Show |
A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0027 others(46): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1105-1319_1105-129 others(27): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282038 | ||||||
| chr4:76282042 | TTTGTATG others(11): Show |
T | 1 | a0002c0002t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1105-1337_1105-132 others(22): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282042 | ||||||
| chr4:76282061 | T | A | 1 | a0002c0002t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1105-1320T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282061 | |||||||
| chr4:76282062 | ACATTTGT others(16): Show |
A | 3 | a0001c0001t0001g0142 a0005c0005t0001g0097 a0005c0005t0001g0153 |
3 | HG02486.hp2 HG03195.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1105-1318_1105-129 others(27): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282062 | |||||||
| chr4:76282085 | G | A | 5 | a0003c0003t0001g0024 a0005c0005t0001g0038 a0005c0005t0001g0052 others(2): Show |
9 | HG02622.hp2 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1105-1296G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282085 | |||||||
| chr4:76282119 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0179 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1105-1262G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282119 | |||||||
| chr4:76282123 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0179 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1105-1258A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282123 | |||||||
| chr4:76282124 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0179 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1105-1257T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282124 | |||||||
| chr4:76282260 | C | G | 68 | a0001c0001t0001g0098 a0001c0001t0001g0136 a0002c0002t0001g0001 others(65): Show |
151 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1105-1121C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282260 | |||||||
| chr4:76282458 | T | C | 5 | a0005c0005t0001g0038 a0005c0005t0001g0052 a0005c0005t0001g0097 others(2): Show |
7 | HG02486.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-923T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282458 | |||||||
| chr4:76282703 | C | T | 1 | a0002c0002t0001g0015 | 4 | HG01884.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-678C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282703 | |||||||
| chr4:76282706 | CT | C | 63 | a0001c0001t0001g0098 a0002c0002t0001g0001 a0002c0002t0001g0005 others(60): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1105-674delT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282706 | |||||||
| chr4:76282919 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1105-462A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282919 | |||||||
| chr4:76282963 | A | T | 1 | a0003c0003t0001g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1105-418A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282963 | |||||||
| chr4:76283152 | T | C | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1105-229T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283152 | |||||||
| chr4:76283245 | CAT | C | 17 | a0004c0004t0001g0008 a0004c0004t0001g0016 a0004c0004t0001g0028 others(14): Show |
28 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1105-135_1105-134d others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283245 | |||||||
| chr4:76283347 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
280 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.1105-34C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283347 | |||||||
| chr4:76283379 | A | G | 1 | a0004c0004t0001g0169 | 1 | HG02965.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1105-2A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283379 |