Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 121506 |
| ensemblid | ENSG00000139055.7 |
| hgncid | 26495 |
| symbol | ERP27 |
| name | endoplasmic reticulum protein 27 |
| refseq_nuc | NM_152321.4 |
| refseq_prot | NP_689534.1 |
| ensembl_nuc | ENST00000266397.7 |
| ensembl_prot | ENSP00000266397.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 14914039 |
| end | 14938537 |
| strand | - |
| ver | v1.2 |
| region | chr12:14914039-14938537 |
| region5000 | chr12:14909039-14943537 |
| regionname0 | ERP27_chr12_14914039_14938537 |
| regionname5000 | ERP27_chr12_14909039_14943537 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 273 | 383 | 91 | 78 | 155 | 16 | 41 | 119 | ERP27_chr12_14909039_14943537 | ERP27 | MEAAP others(268): Show |
chr12 | 14909039 | 14943537 |
| a0002 | 0/0 | 273 | 16 | 0 | 0 | 11 | 0 | 5 | 7 | ERP27_chr12_14909039_14943537 | ERP27 | MEAAP others(268): Show |
chr12 | 14909039 | 14943537 |
| a0003 | 0/0 | 273 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | MEAAP others(268): Show |
chr12 | 14909039 | 14943537 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 819 | 372 | 80 | 78 | 155 | 16 | 41 | ERP27_chr12_14909039_14943537 | ERP27 | ATGGA others(814): Show |
chr12 | 14909039 | 14943537 | ||
| a0001c0003 | 0/0 | 819 | 11 | 11 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | ATGGA others(814): Show |
chr12 | 14909039 | 14943537 | ||
| a0002c0002 | 0/0 | 819 | 15 | 0 | 0 | 10 | 0 | 5 | ERP27_chr12_14909039_14943537 | ERP27 | ATGGA others(814): Show |
chr12 | 14909039 | 14943537 | ||
| a0002c0005 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | ATGGA others(814): Show |
chr12 | 14909039 | 14943537 | ||
| a0003c0004 | 0/0 | 819 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | ATGGA others(814): Show |
chr12 | 14909039 | 14943537 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1551 | 165 | 42 | 38 | 64 | 7 | 13 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0002 | 1/0 | 1547 | 79 | 17 | 24 | 26 | 5 | 6 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1542): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0003 | 0/0 | 1553 | 73 | 0 | 6 | 48 | 1 | 18 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1548): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0004 | 0/0 | 1551 | 12 | 11 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0005 | 0/0 | 1549 | 9 | 3 | 3 | 1 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1544): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0006 | 0/0 | 1547 | 9 | 1 | 5 | 1 | 2 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1542): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0007 | 0/0 | 1553 | 7 | 0 | 0 | 7 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1548): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0008 | 0/0 | 1551 | 5 | 5 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0009 | 0/0 | 1551 | 5 | 0 | 0 | 4 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0011 | 0/0 | 1545 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1540): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0013 | 0/0 | 1509 | 2 | 0 | 0 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1504): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0014 | 0/0 | 1549 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1544): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0015 | 0/0 | 1553 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1548): Show |
chr12 | 14909039 | 14943537 |
| a0001c0001t0016 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0001c0003t0001 | 0/0 | 1551 | 8 | 8 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0001c0003t0012 | 0/0 | 1553 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1548): Show |
chr12 | 14909039 | 14943537 |
| a0002c0002t0002 | 0/0 | 1547 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1542): Show |
chr12 | 14909039 | 14943537 |
| a0002c0002t0004 | 0/0 | 1551 | 14 | 0 | 0 | 10 | 0 | 4 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0002c0005t0001 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| a0003c0004t0010 | 0/0 | 1551 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | AGGGT others(1546): Show |
chr12 | 14909039 | 14943537 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 5 | 9 | 14 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0004 | 0/0 | 7 | 2 | 2 | 0 | 2 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0011 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 2 | 1 | 2 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0002 | 0/0 | 18 | 0 | 1 | 10 | 0 | 7 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0007g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0008g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0009g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0011g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0011g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0013g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0013g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0014g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0015g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0001t0016g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0003t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0003t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0003t0012g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0001c0003t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0002c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0003c0004t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0003c0004t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| a0003c0004t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00140 | hp2 | a0001 | c0001 | t0013 | g0087 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00544 | hp2 | a0001 | c0001 | t0009 | g0220 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00597 | hp2 | a0001 | c0001 | t0016 | g0203 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0149 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0138 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0040 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01346 | hp2 | a0001 | c0001 | t0015 | g0234 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0154 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02015 | hp2 | a0002 | c0002 | t0004 | g0118 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02027 | hp2 | a0002 | c0005 | t0001 | g0129 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0240 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02083 | hp2 | a0002 | c0002 | t0004 | g0036 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02129 | hp2 | a0001 | c0001 | t0009 | g0214 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02135 | hp1 | a0001 | c0001 | t0011 | g0037 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02145 | hp1 | a0003 | c0004 | t0010 | g0056 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02165 | hp1 | a0002 | c0002 | t0004 | g0121 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02258 | hp1 | a0001 | c0003 | t0012 | g0029 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02886 | hp2 | a0003 | c0004 | t0010 | g0057 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03225 | hp2 | a0001 | c0001 | t0014 | g0245 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0017 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03490 | hp2 | a0002 | c0002 | t0004 | g0116 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03491 | hp2 | a0002 | c0002 | t0004 | g0035 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03492 | hp1 | a0002 | c0002 | t0004 | g0120 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03492 | hp2 | a0002 | c0002 | t0004 | g0035 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03579 | hp2 | a0003 | c0004 | t0010 | g0055 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0204 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0217 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04184 | hp1 | a0001 | c0001 | t0013 | g0088 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0188 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | CHB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18939 | hp2 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18945 | hp1 | a0002 | c0002 | t0004 | g0115 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18948 | hp2 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18965 | hp1 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18968 | hp2 | a0001 | c0001 | t0011 | g0123 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18978 | hp1 | a0002 | c0002 | t0004 | g0122 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18990 | hp1 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19012 | hp2 | a0002 | c0002 | t0004 | g0119 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0243 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19065 | hp1 | a0001 | c0001 | t0011 | g0037 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19066 | hp2 | a0002 | c0002 | t0004 | g0191 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19068 | hp1 | a0002 | c0002 | t0004 | g0206 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19075 | hp1 | a0002 | c0002 | t0004 | g0109 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19077 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0166 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0205 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ASW | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20129 | hp2 | a0001 | c0003 | t0012 | g0111 | AFR | ASW | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0221 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0133 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0040 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | GIH | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | GIH | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02486 | hp1 | a0001 | c0003 | t0012 | g0029 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0159 | REF | REF | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0258 | REF | REF | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14917253 | T | C | 1 | a0002 | 15 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(12): Show |
missense_variant | MODERATE | c.501A>G | p.Ile167Met | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/7 | 530/1547 | 501/822 | 167/273 | chr12 | 14917253 | |||
| chr12:14917254 | A | G | 1 | a0002 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.500T>C | p.Ile167Thr | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/7 | 529/1547 | 500/822 | 167/273 | chr12 | 14917254 | |||
| chr12:14921018 | C | T | 1 | a0003 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.364G>A | p.Glu122Lys | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/7 | 393/1547 | 364/822 | 122/273 | chr12 | 14921018 | |||
| chr12:14937993 | A | G | 1 | a0003 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.154T>C | p.Phe52Leu | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/7 | 183/1547 | 154/822 | 52/273 | chr12 | 14937993 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14917235 | T | A | 1 | a0001c0003 | 11 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
synonymous_variant | LOW | c.519A>T | p.Pro173Pro | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/7 | 548/1547 | 519/822 | 173/273 | chr12 | 14917235 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14914065 | A | G | 1 | a0001c0001t0015 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 670 | chr12 | 14914065 | ||||||
| chr12:14914092 | G | T | 1 | a0001c0001t0016 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 643 | chr12 | 14914092 | ||||||
| chr12:14914195 | C | G | 4 | a0001c0001t0004 a0001c0001t0014 a0002c0002t0004 others(1): Show |
30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*540G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 540 | chr12 | 14914195 | ||||||
| chr12:14914242 | C | T | 1 | a0001c0001t0008 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*493G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 493 | chr12 | 14914242 | ||||||
| chr12:14914257 | G | A | 1 | a0001c0003t0012 | 3 | HG02258.hp1 HG02486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*478C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 478 | chr12 | 14914257 | ||||||
| chr12:14914284 | G | C | 1 | a0003c0004t0010 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*451C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 451 | chr12 | 14914284 | ||||||
| chr12:14914469 | G | A | 4 | a0001c0001t0004 a0001c0001t0014 a0002c0002t0004 others(1): Show |
30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 266 | chr12 | 14914469 | ||||||
| chr12:14914531 | C | T | 4 | a0001c0001t0004 a0001c0001t0014 a0002c0002t0004 others(1): Show |
30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 204 | chr12 | 14914531 | ||||||
| chr12:14914558 | CTG | C | 1 | a0001c0001t0011 | 3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*175_*176delCA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 175 | chr12 | 14914558 | ||||||
| chr12:14914573 | T | C | 4 | a0001c0001t0004 a0001c0001t0014 a0002c0002t0004 others(1): Show |
30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 162 | chr12 | 14914573 | ||||||
| chr12:14914575 | T | C | 3 | a0001c0001t0004 a0002c0002t0004 a0003c0004t0010 |
29 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 160 | chr12 | 14914575 | ||||||
| chr12:14914575 | TGTGCGTG others(31): Show |
T | 1 | a0001c0001t0013 | 2 | HG00140.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*122_*159delGTGCAC others(32): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 122 | chr12 | 14914575 | ||||||
| chr12:14914577 | T | C | 2 | a0001c0001t0006 a0001c0001t0014 |
10 | HG01081.hp1 HG01106.hp1 HG01261.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*158A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 158 | chr12 | 14914577 | ||||||
| chr12:14914577 | T | TGC | 1 | a0001c0001t0005 | 9 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*156_*157dupGC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | ||||||
| chr12:14914577 | T | TGCGC | 2 | a0001c0001t0008 a0001c0001t0009 |
10 | HG00544.hp2 HG02055.hp1 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCGC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | ||||||
| chr12:14914577 | T | TGTGC | 4 | a0001c0001t0001 a0001c0001t0016 a0001c0003t0001 others(1): Show |
174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | ||||||
| chr12:14914577 | T | TGTGCGC | 1 | a0001c0001t0007 | 7 | NA18955.hp1 NA18965.hp1 NA19064.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCGCAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | ||||||
| chr12:14914577 | T | TGTGTGC | 3 | a0001c0001t0003 a0001c0001t0015 a0001c0003t0012 |
77 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCACAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | ||||||
| chr12:14914579 | C | CGT | 3 | a0001c0001t0004 a0002c0002t0004 a0003c0004t0010 |
29 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*154_*155dupAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 155 | chr12 | 14914579 | ||||||
| chr12:14914579 | C | T | 1 | a0001c0001t0014 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*156G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 156 | chr12 | 14914579 | ||||||
| chr12:14914617 | C | CAT | 4 | a0001c0001t0004 a0001c0001t0014 a0002c0002t0004 others(1): Show |
30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*117_*118insAT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 117 | chr12 | 14914617 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14914992 | CT | C | 58 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0014 others(55): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.775-211delA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14914992 | |||||||
| chr12:14915109 | T | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(16): Show |
30 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.775-327A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915109 | |||||||
| chr12:14915187 | G | A | 11 | a0001c0001t0004g0059 a0001c0001t0004g0060 a0001c0001t0004g0101 others(8): Show |
11 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.774+302C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915187 | |||||||
| chr12:14915213 | A | G | 12 | a0002c0002t0004g0035 a0002c0002t0004g0036 a0002c0002t0004g0109 others(9): Show |
14 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.774+276T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915213 | |||||||
| chr12:14915381 | C | G | 2 | a0001c0001t0004g0107 a0001c0001t0014g0245 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.774+108G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915381 | |||||||
| chr12:14915432 | G | T | 1 | a0001c0001t0003g0202 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.774+57C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915432 | |||||||
| chr12:14915483 | A | G | 1 | a0001c0001t0003g0221 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.774+6T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915483 | |||||||
| chr12:14915721 | T | C | 19 | a0001c0001t0004g0059 a0001c0001t0004g0060 a0001c0001t0004g0101 others(16): Show |
20 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.577-35A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14915721 | |||||||
| chr12:14915754 | T | C | 2 | a0001c0003t0001g0013 a0001c0003t0001g0064 |
4 | HG02451.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-68A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14915754 | |||||||
| chr12:14916008 | T | G | 5 | a0001c0003t0001g0013 a0001c0003t0001g0064 a0001c0003t0001g0243 others(2): Show |
8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-322A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916008 | |||||||
| chr12:14916029 | G | T | 19 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(16): Show |
30 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.577-343C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916029 | |||||||
| chr12:14916041 | G | C | 1 | a0001c0001t0006g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.577-355C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916041 | |||||||
| chr12:14916068 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.577-382C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916068 | |||||||
| chr12:14916324 | C | T | 1 | a0001c0001t0003g0021 | 3 | HG02698.hp2 HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.577-638G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916324 | |||||||
| chr12:14916389 | G | A | 17 | a0001c0001t0002g0238 a0001c0001t0004g0059 a0001c0001t0004g0060 others(14): Show |
17 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.577-703C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916389 | |||||||
| chr12:14916449 | G | A | 4 | a0001c0001t0001g0186 a0001c0001t0002g0092 a0001c0001t0002g0170 others(1): Show |
4 | HG00423.hp1 HG02155.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+729C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916449 | |||||||
| chr12:14916724 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.576+454C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916724 | |||||||
| chr12:14916828 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
238 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.576+350C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916828 | |||||||
| chr12:14917015 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.576+163T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14917015 | |||||||
| chr12:14917080 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.576+98C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14917080 | |||||||
| chr12:14917314 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.451-11C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917314 | |||||||
| chr12:14917380 | A | G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(16): Show |
30 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.451-77T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917380 | |||||||
| chr12:14917502 | C | G | 2 | a0001c0001t0003g0194 a0001c0001t0003g0200 |
2 | HG00597.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.451-199G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917502 | |||||||
| chr12:14917647 | T | C | 1 | a0001c0001t0003g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.451-344A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917647 | |||||||
| chr12:14917688 | G | A | 12 | a0002c0002t0004g0035 a0002c0002t0004g0036 a0002c0002t0004g0109 others(9): Show |
14 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-385C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917688 | |||||||
| chr12:14917699 | A | G | 1 | a0001c0001t0003g0181 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.451-396T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917699 | |||||||
| chr12:14917701 | C | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
276 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.451-398G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917701 | |||||||
| chr12:14917722 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.451-419A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917722 | |||||||
| chr12:14917741 | T | C | 1 | a0001c0001t0003g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.451-438A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917741 | |||||||
| chr12:14917744 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.451-441T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917744 | |||||||
| chr12:14917862 | C | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0071 a0001c0001t0002g0075 others(2): Show |
6 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-559G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917862 | |||||||
| chr12:14917876 | A | G | 3 | a0001c0001t0003g0126 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG01346.hp1 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.451-573T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917876 | |||||||
| chr12:14917931 | T | C | 11 | a0002c0002t0004g0035 a0002c0002t0004g0036 a0002c0002t0004g0109 others(8): Show |
13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-628A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917931 | |||||||
| chr12:14917961 | A | G | 1 | a0002c0002t0002g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.451-658T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917961 | |||||||
| chr12:14918016 | AC | A | 3 | a0001c0001t0001g0061 a0001c0001t0008g0008 a0001c0001t0008g0240 |
6 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-714delG | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918016 | |||||||
| chr12:14918020 | A | T | 3 | a0001c0001t0001g0061 a0001c0001t0008g0008 a0001c0001t0008g0240 |
6 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-717T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918020 | |||||||
| chr12:14918037 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.451-734A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918037 | |||||||
| chr12:14918078 | C | T | 1 | a0001c0001t0003g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.451-775G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918078 | |||||||
| chr12:14918086 | G | A | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.451-783C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918086 | |||||||
| chr12:14918161 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0145 |
3 | NA18952.hp2 NA18962.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.451-858C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918161 | |||||||
| chr12:14918308 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.451-1005C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918308 | |||||||
| chr12:14918336 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.451-1033G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918336 | |||||||
| chr12:14918520 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.451-1217C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918520 | |||||||
| chr12:14918552 | C | G | 1 | a0001c0001t0001g0224 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.451-1249G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918552 | |||||||
| chr12:14918569 | CT | C | 30 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0014 others(27): Show |
45 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.451-1267delA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918569 | |||||||
| chr12:14918678 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.451-1375T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918678 | |||||||
| chr12:14918713 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.451-1410T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918713 | |||||||
| chr12:14918799 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.451-1496C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918799 | |||||||
| chr12:14919080 | G | A | 11 | a0002c0002t0004g0035 a0002c0002t0004g0036 a0002c0002t0004g0109 others(8): Show |
13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-1777C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919080 | |||||||
| chr12:14919118 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0247 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.450+1814G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919118 | |||||||
| chr12:14919130 | A | T | 1 | a0001c0001t0002g0078 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.450+1802T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919130 | |||||||
| chr12:14919240 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.450+1692A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919240 | |||||||
| chr12:14919318 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.450+1614A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919318 | |||||||
| chr12:14919321 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.450+1611C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919321 | |||||||
| chr12:14919420 | A | C | 1 | a0001c0001t0003g0022 | 3 | HG02040.hp1 NA18953.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.450+1512T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919420 | |||||||
| chr12:14919475 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0008g0008 a0001c0001t0008g0240 |
6 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+1457G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919475 | |||||||
| chr12:14919768 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.450+1164G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919768 | |||||||
| chr12:14919816 | C | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(13): Show |
27 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.450+1116G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919816 | |||||||
| chr12:14919948 | C | CA | 17 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0048 others(14): Show |
30 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.450+983dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919948 | |||||||
| chr12:14920073 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.450+859C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920073 | |||||||
| chr12:14920098 | C | G | 1 | a0002c0002t0004g0122 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.450+834G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920098 | |||||||
| chr12:14920145 | C | T | 5 | a0001c0001t0004g0059 a0001c0001t0004g0060 a0001c0001t0004g0101 others(2): Show |
5 | HG00733.hp1 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+787G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920145 | |||||||
| chr12:14920198 | T | A | 1 | a0001c0001t0014g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.450+734A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920198 | |||||||
| chr12:14920209 | G | C | 4 | a0001c0003t0001g0013 a0001c0003t0001g0023 a0001c0003t0001g0064 others(1): Show |
8 | HG02451.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+723C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920209 | |||||||
| chr12:14920307 | C | A | 1 | a0001c0001t0002g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.450+625G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920307 | |||||||
| chr12:14920310 | T | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
322 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.450+622A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920310 | |||||||
| chr12:14920327 | G | A | 28 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0031 others(25): Show |
33 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.450+605C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920327 | |||||||
| chr12:14920376 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.450+556T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920376 | |||||||
| chr12:14920695 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
294 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.450+237G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920695 | |||||||
| chr12:14920711 | C | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
294 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.450+221G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920711 | |||||||
| chr12:14920730 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
294 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.450+202A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920730 | |||||||
| chr12:14920758 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.450+174G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920758 | |||||||
| chr12:14920897 | G | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
294 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.450+35C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920897 | |||||||
| chr12:14920922 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.450+10A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920922 | |||||||
| chr12:14921108 | C | T | 1 | a0001c0003t0001g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-60G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921108 | |||||||
| chr12:14921161 | A | G | 1 | a0001c0001t0006g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.334-113T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921161 | |||||||
| chr12:14921193 | C | A | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-145G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921193 | |||||||
| chr12:14921265 | A | G | 1 | a0001c0001t0005g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.334-217T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921265 | |||||||
| chr12:14921379 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.334-331T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921379 | |||||||
| chr12:14921396 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-348T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921396 | |||||||
| chr12:14921442 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-394C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921442 | |||||||
| chr12:14921505 | G | A | 2 | a0001c0001t0002g0169 a0001c0001t0002g0219 |
2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.334-457C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921505 | |||||||
| chr12:14921554 | C | G | 1 | a0001c0001t0001g0015 | 3 | NA18965.hp2 NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.334-506G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921554 | |||||||
| chr12:14921636 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.334-588C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921636 | |||||||
| chr12:14921723 | G | A | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-675C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921723 | |||||||
| chr12:14921748 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.334-700G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921748 | |||||||
| chr12:14921828 | C | T | 2 | a0001c0001t0004g0114 a0001c0001t0004g0241 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.334-780G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921828 | |||||||
| chr12:14922119 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.334-1071A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922119 | |||||||
| chr12:14922144 | A | T | 1 | a0001c0001t0002g0074 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.334-1096T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922144 | |||||||
| chr12:14922268 | C | T | 56 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0002g0005 others(53): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.334-1220G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922268 | |||||||
| chr12:14922299 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-1251A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922299 | |||||||
| chr12:14922496 | C | T | 19 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(16): Show |
32 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.334-1448G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922496 | |||||||
| chr12:14922641 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0174 |
6 | NA18940.hp2 NA18961.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-1593C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922641 | |||||||
| chr12:14922716 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.334-1668C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922716 | |||||||
| chr12:14922804 | G | A | 7 | a0001c0003t0001g0013 a0001c0003t0001g0023 a0001c0003t0001g0064 others(4): Show |
11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-1756C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922804 | |||||||
| chr12:14922842 | G | A | 18 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0038 others(15): Show |
22 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.334-1794C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922842 | |||||||
| chr12:14922861 | A | T | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-1813T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922861 | |||||||
| chr12:14922862 | G | A | 3 | a0001c0001t0005g0113 a0001c0001t0005g0252 a0001c0001t0006g0062 |
3 | HG01891.hp2 HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.334-1814C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922862 | |||||||
| chr12:14922920 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
243 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.334-1872G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922920 | |||||||
| chr12:14923009 | G | C | 1 | a0001c0003t0012g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.334-1961C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923009 | |||||||
| chr12:14923033 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.334-1985G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923033 | |||||||
| chr12:14923043 | C | T | 1 | a0001c0001t0006g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.334-1995G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923043 | |||||||
| chr12:14923067 | C | T | 18 | a0001c0001t0002g0134 a0001c0001t0002g0239 a0001c0001t0002g0250 others(15): Show |
18 | HG00733.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-2019G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923067 | |||||||
| chr12:14923068 | T | C | 1 | a0001c0001t0003g0009 | 4 | NA18944.hp2 NA18948.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-2020A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923068 | |||||||
| chr12:14923073 | C | CA | 25 | a0001c0001t0002g0026 a0001c0001t0002g0030 a0001c0001t0002g0076 others(22): Show |
33 | HG01123.hp2 HG02015.hp2 HG02083.hp2 others(30): Show |
intron_variant | MODIFIER | c.334-2026dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | |||||||
| chr12:14923073 | CA | C | 21 | a0001c0001t0001g0190 a0001c0001t0002g0073 a0001c0001t0002g0108 others(18): Show |
22 | HG00733.hp1 HG01168.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.334-2026delT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | |||||||
| chr12:14923073 | CAA | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
249 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.334-2027_334-2026d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | |||||||
| chr12:14923073 | CAAA | C | 18 | a0001c0001t0001g0061 a0001c0001t0001g0098 a0001c0001t0001g0100 others(15): Show |
22 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.334-2028_334-2026d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | |||||||
| chr12:14923092 | AT | A | 1 | a0001c0001t0003g0019 | 3 | HG00609.hp1 NA18967.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.334-2045delA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923092 | |||||||
| chr12:14923396 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.334-2348T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923396 | |||||||
| chr12:14923400 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334-2352T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923400 | |||||||
| chr12:14923479 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.334-2431A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923479 | |||||||
| chr12:14923484 | C | A | 1 | a0001c0001t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2436G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923484 | |||||||
| chr12:14923485 | T | A | 1 | a0001c0001t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2437A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923485 | |||||||
| chr12:14923486 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2438T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923486 | |||||||
| chr12:14923487 | T | C | 1 | a0001c0001t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2439A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923487 | |||||||
| chr12:14923487 | TAATC | T | 37 | a0001c0001t0001g0053 a0001c0001t0001g0136 a0001c0001t0001g0146 others(34): Show |
43 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.334-2443_334-2440d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923487 | |||||||
| chr12:14923488 | A | AATCT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
123 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.334-2441_334-2440i others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | |||||||
| chr12:14923488 | A | AATCTATC others(1): Show |
43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(40): Show |
55 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.334-2441_334-2440i others(10): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | |||||||
| chr12:14923488 | A | AATCTATC others(5): Show |
1 | a0001c0001t0003g0002 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.334-2441_334-2440i others(14): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | |||||||
| chr12:14923488 | A | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0250 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.334-2440T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | |||||||
| chr12:14923492 | A | AATCT | 21 | a0001c0001t0001g0089 a0001c0001t0002g0026 a0001c0001t0002g0027 others(18): Show |
25 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.334-2448_334-2445d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | |||||||
| chr12:14923492 | A | AATCTATC others(1): Show |
17 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0038 others(14): Show |
24 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.334-2452_334-2445d others(10): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | |||||||
| chr12:14923492 | A | AATCTATC others(5): Show |
1 | a0001c0001t0002g0070 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.334-2456_334-2445d others(14): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | |||||||
| chr12:14923492 | A | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
279 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.334-2444T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | |||||||
| chr12:14923495 | C | T | 1 | a0001c0001t0001g0048 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.334-2447G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923495 | |||||||
| chr12:14923496 | T | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0256 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.334-2448A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923496 | |||||||
| chr12:14923500 | T | A | 1 | a0001c0001t0002g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.334-2452A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923500 | |||||||
| chr12:14923825 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-2777G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923825 | |||||||
| chr12:14923831 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-2783A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923831 | |||||||
| chr12:14924022 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
294 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.334-2974T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924022 | |||||||
| chr12:14924081 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-3033A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924081 | |||||||
| chr12:14924088 | C | G | 1 | a0001c0001t0002g0219 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.334-3040G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924088 | |||||||
| chr12:14924196 | A | G | 12 | a0002c0002t0002g0117 a0002c0002t0004g0035 a0002c0002t0004g0036 others(9): Show |
14 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-3148T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924196 | |||||||
| chr12:14924209 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-3161T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924209 | |||||||
| chr12:14924210 | C | T | 15 | a0001c0001t0002g0134 a0001c0001t0002g0239 a0001c0001t0002g0250 others(12): Show |
15 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.334-3162G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924210 | |||||||
| chr12:14924241 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-3193T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924241 | |||||||
| chr12:14924286 | C | T | 19 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(16): Show |
33 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.334-3238G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924286 | |||||||
| chr12:14924453 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.334-3405T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924453 | |||||||
| chr12:14924469 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-3421A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924469 | |||||||
| chr12:14924555 | T | C | 2 | a0001c0001t0005g0113 a0001c0001t0006g0062 |
2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.334-3507A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924555 | |||||||
| chr12:14924593 | A | T | 56 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0002g0005 others(53): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.334-3545T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924593 | |||||||
| chr12:14924625 | G | A | 1 | a0001c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.334-3577C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924625 | |||||||
| chr12:14924687 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-3639C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924687 | |||||||
| chr12:14924730 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-3682T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924730 | |||||||
| chr12:14924755 | T | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(18): Show |
35 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.334-3707A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924755 | |||||||
| chr12:14924917 | C | T | 1 | a0001c0001t0003g0195 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.334-3869G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924917 | |||||||
| chr12:14924921 | G | A | 3 | a0001c0001t0002g0239 a0001c0001t0002g0250 a0001c0001t0014g0245 |
3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.334-3873C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924921 | |||||||
| chr12:14925068 | C | G | 7 | a0001c0003t0001g0013 a0001c0003t0001g0023 a0001c0003t0001g0064 others(4): Show |
11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-4020G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925068 | |||||||
| chr12:14925109 | C | G | 1 | a0001c0001t0004g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.334-4061G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925109 | |||||||
| chr12:14925123 | C | T | 2 | a0001c0001t0008g0008 a0001c0001t0008g0240 |
5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-4075G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925123 | |||||||
| chr12:14925399 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.334-4351C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925399 | |||||||
| chr12:14925538 | C | T | 4 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0247 others(1): Show |
4 | HG02735.hp1 HG03669.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-4490G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925538 | |||||||
| chr12:14925640 | T | C | 1 | a0001c0001t0003g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-4592A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925640 | |||||||
| chr12:14925642 | T | A | 2 | a0001c0001t0002g0239 a0001c0001t0002g0250 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.334-4594A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925642 | |||||||
| chr12:14925755 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-4707T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925755 | |||||||
| chr12:14925759 | C | T | 6 | a0001c0001t0002g0134 a0001c0001t0004g0059 a0001c0001t0004g0060 others(3): Show |
6 | HG00733.hp1 HG01891.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-4711G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925759 | |||||||
| chr12:14925795 | C | T | 3 | a0001c0001t0002g0239 a0001c0001t0002g0250 a0001c0001t0014g0245 |
3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.334-4747G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925795 | |||||||
| chr12:14925796 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0007g0166 |
2 | NA18942.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.334-4748C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925796 | |||||||
| chr12:14925826 | T | A | 11 | a0002c0002t0004g0035 a0002c0002t0004g0036 a0002c0002t0004g0109 others(8): Show |
13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.334-4778A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925826 | |||||||
| chr12:14925842 | G | C | 7 | a0001c0003t0001g0013 a0001c0003t0001g0023 a0001c0003t0001g0064 others(4): Show |
11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-4794C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925842 | |||||||
| chr12:14925848 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-4800G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925848 | |||||||
| chr12:14925946 | G | A | 11 | a0002c0002t0004g0035 a0002c0002t0004g0036 a0002c0002t0004g0109 others(8): Show |
13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.334-4898C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925946 | |||||||
| chr12:14926069 | C | CA | 19 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0038 others(16): Show |
23 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.334-5022dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926069 | |||||||
| chr12:14926256 | C | A | 1 | a0001c0001t0003g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.334-5208G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926256 | |||||||
| chr12:14926281 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.334-5233A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926281 | |||||||
| chr12:14926285 | GTATTAA | G | 3 | a0001c0001t0002g0239 a0001c0001t0002g0250 a0001c0001t0014g0245 |
3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.334-5243_334-5238d others(8): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926285 | |||||||
| chr12:14926428 | T | C | 1 | a0001c0001t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-5380A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926428 | |||||||
| chr12:14926436 | A | G | 1 | a0001c0001t0003g0044 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.334-5388T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926436 | |||||||
| chr12:14926447 | C | T | 2 | a0001c0001t0011g0037 a0001c0001t0011g0123 |
3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.334-5399G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926447 | |||||||
| chr12:14926486 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
324 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.334-5438T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926486 | |||||||
| chr12:14926517 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
278 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.334-5469G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926517 | |||||||
| chr12:14926662 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.334-5614T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926662 | |||||||
| chr12:14926693 | A | T | 1 | a0001c0001t0004g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-5645T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926693 | |||||||
| chr12:14926748 | G | A | 2 | a0001c0001t0011g0037 a0001c0001t0011g0123 |
3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.334-5700C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926748 | |||||||
| chr12:14926977 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.334-5929G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926977 | |||||||
| chr12:14926979 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0001t0001g0158 others(1): Show |
6 | HG00735.hp1 HG01255.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-5931C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926979 | |||||||
| chr12:14927024 | C | T | 1 | a0001c0001t0005g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.334-5976G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927024 | |||||||
| chr12:14927052 | G | A | 1 | a0002c0002t0004g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.334-6004C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927052 | |||||||
| chr12:14927073 | G | A | 2 | a0001c0001t0008g0008 a0001c0001t0008g0240 |
5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6025C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927073 | |||||||
| chr12:14927101 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
243 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.334-6053G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927101 | |||||||
| chr12:14927324 | C | T | 7 | a0001c0003t0001g0013 a0001c0003t0001g0023 a0001c0003t0001g0064 others(4): Show |
11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-6276G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927324 | |||||||
| chr12:14927333 | A | ATG | 2 | a0001c0003t0012g0029 a0001c0003t0012g0111 |
3 | HG02258.hp1 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.334-6287_334-6286d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927333 | |||||||
| chr12:14927347 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0046 others(22): Show |
41 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.334-6299C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927347 | |||||||
| chr12:14927349 | A | G | 57 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0002g0005 others(54): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-6301T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927349 | |||||||
| chr12:14927351 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.334-6303T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927351 | |||||||
| chr12:14927425 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-6377A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927425 | |||||||
| chr12:14927499 | GTGT | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
277 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.334-6454_334-6452d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927499 | |||||||
| chr12:14927584 | C | T | 1 | a0001c0001t0003g0137 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.334-6536G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927584 | |||||||
| chr12:14927596 | T | G | 1 | a0001c0001t0003g0181 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.334-6548A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927596 | |||||||
| chr12:14927712 | TC | T | 56 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0002g0005 others(53): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.334-6665delG | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927712 | |||||||
| chr12:14927714 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.334-6666G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927714 | |||||||
| chr12:14927744 | G | GCACA | 4 | a0002c0002t0004g0109 a0002c0002t0004g0119 a0002c0002t0004g0121 others(1): Show |
4 | HG02165.hp1 NA18978.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-6700_334-6697d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | |||||||
| chr12:14927744 | G | GCACACA | 4 | a0002c0002t0002g0117 a0002c0002t0004g0035 a0002c0002t0004g0036 others(1): Show |
6 | HG02083.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-6702_334-6697d others(8): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | |||||||
| chr12:14927744 | G | GCACACAC others(3): Show |
2 | a0002c0002t0004g0116 a0002c0002t0004g0120 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.334-6706_334-6697d others(12): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | |||||||
| chr12:14927744 | GCA | G | 58 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0127 others(55): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.334-6698_334-6697d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | |||||||
| chr12:14927744 | GCACA | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
283 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.334-6700_334-6697d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | |||||||
| chr12:14927744 | GCACACA | G | 11 | a0001c0001t0001g0052 a0001c0001t0001g0065 a0001c0001t0001g0136 others(8): Show |
12 | HG02145.hp2 HG02155.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-6702_334-6697d others(8): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | |||||||
| chr12:14928084 | A | G | 1 | a0001c0001t0003g0192 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.333+6772T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928084 | |||||||
| chr12:14928107 | C | A | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.333+6749G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928107 | |||||||
| chr12:14928272 | G | C | 1 | a0001c0001t0003g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.333+6584C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928272 | |||||||
| chr12:14928284 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
296 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.333+6572C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928284 | |||||||
| chr12:14928286 | G | A | 1 | a0001c0001t0005g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.333+6570C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928286 | |||||||
| chr12:14928355 | G | A | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+6501C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928355 | |||||||
| chr12:14928400 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.333+6456A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928400 | |||||||
| chr12:14928512 | T | C | 1 | a0001c0001t0004g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.333+6344A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928512 | |||||||
| chr12:14928540 | G | A | 1 | a0001c0003t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.333+6316C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928540 | |||||||
| chr12:14928559 | A | G | 4 | a0001c0001t0001g0061 a0001c0001t0004g0125 a0001c0001t0004g0131 others(1): Show |
4 | HG01934.hp1 HG02055.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+6297T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928559 | |||||||
| chr12:14928599 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.333+6257G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928599 | |||||||
| chr12:14928700 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.333+6156T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928700 | |||||||
| chr12:14928712 | C | T | 1 | a0001c0001t0015g0234 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.333+6144G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928712 | |||||||
| chr12:14928844 | C | T | 3 | a0001c0001t0005g0113 a0001c0001t0005g0252 a0001c0001t0006g0062 |
3 | HG01891.hp2 HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.333+6012G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928844 | |||||||
| chr12:14928936 | G | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA19006.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.333+5920C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928936 | |||||||
| chr12:14928964 | G | A | 62 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0173 others(59): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.333+5892C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928964 | |||||||
| chr12:14929056 | A | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0175 |
5 | HG00423.hp2 HG00621.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+5800T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929056 | |||||||
| chr12:14929070 | T | A | 62 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0173 others(59): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.333+5786A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929070 | |||||||
| chr12:14929140 | C | G | 1 | a0002c0002t0004g0035 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.333+5716G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929140 | |||||||
| chr12:14929143 | C | G | 5 | a0001c0001t0002g0168 a0001c0003t0001g0013 a0001c0003t0001g0023 others(2): Show |
9 | HG02451.hp2 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+5713G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929143 | |||||||
| chr12:14929162 | C | T | 1 | a0001c0001t0003g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.333+5694G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929162 | |||||||
| chr12:14929163 | G | A | 2 | a0001c0003t0001g0013 a0001c0003t0001g0064 |
4 | HG02451.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+5693C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929163 | |||||||
| chr12:14929191 | G | A | 1 | a0001c0001t0009g0220 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.333+5665C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929191 | |||||||
| chr12:14929311 | G | C | 1 | a0001c0001t0003g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.333+5545C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929311 | |||||||
| chr12:14929346 | T | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
13 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+5510A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929346 | |||||||
| chr12:14929363 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.333+5493G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929363 | |||||||
| chr12:14929448 | T | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(30): Show |
44 | HG00733.hp1 HG01109.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.333+5408A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929448 | |||||||
| chr12:14929484 | G | A | 1 | a0001c0001t0004g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.333+5372C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929484 | |||||||
| chr12:14929508 | A | G | 3 | a0001c0001t0002g0239 a0001c0001t0002g0250 a0001c0001t0014g0245 |
3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.333+5348T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929508 | |||||||
| chr12:14929566 | T | C | 2 | a0001c0001t0008g0008 a0001c0001t0008g0240 |
5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5290A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929566 | |||||||
| chr12:14929742 | A | C | 2 | a0001c0001t0006g0133 a0001c0001t0006g0154 |
2 | HG02004.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.333+5114T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929742 | |||||||
| chr12:14929861 | G | T | 2 | a0001c0001t0008g0008 a0001c0001t0008g0240 |
5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4995C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929861 | |||||||
| chr12:14929903 | G | T | 2 | a0001c0001t0007g0020 a0001c0001t0007g0187 |
4 | NA18955.hp1 NA19064.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+4953C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929903 | |||||||
| chr12:14929919 | G | C | 1 | a0002c0002t0002g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.333+4937C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929919 | |||||||
| chr12:14930082 | A | G | 1 | a0001c0001t0003g0009 | 4 | NA18944.hp2 NA18948.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+4774T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930082 | |||||||
| chr12:14930098 | G | A | 3 | a0001c0001t0002g0014 a0001c0001t0002g0096 a0001c0001t0002g0097 |
5 | HG00558.hp1 HG02071.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+4758C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930098 | |||||||
| chr12:14930140 | C | A | 1 | a0001c0001t0004g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.333+4716G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930140 | |||||||
| chr12:14930150 | A | C | 103 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(100): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.333+4706T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930150 | |||||||
| chr12:14930214 | G | A | 1 | a0001c0001t0006g0154 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.333+4642C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930214 | |||||||
| chr12:14930268 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.333+4588C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930268 | |||||||
| chr12:14930268 | G | C | 3 | a0001c0001t0005g0113 a0001c0001t0005g0252 a0001c0001t0006g0062 |
3 | HG01891.hp2 HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.333+4588C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930268 | |||||||
| chr12:14930297 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.333+4559T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930297 | |||||||
| chr12:14930485 | G | C | 3 | a0001c0001t0003g0126 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG01346.hp1 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.333+4371C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930485 | |||||||
| chr12:14930529 | A | G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(16): Show |
30 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.333+4327T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930529 | |||||||
| chr12:14930576 | A | T | 83 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0098 others(80): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.333+4280T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930576 | |||||||
| chr12:14930588 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.333+4268G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930588 | |||||||
| chr12:14930619 | T | C | 1 | a0001c0001t0014g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.333+4237A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930619 | |||||||
| chr12:14930626 | C | CTTA | 83 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0098 others(80): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.333+4227_333+4229d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930626 | |||||||
| chr12:14930651 | A | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(16): Show |
30 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.333+4205T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930651 | |||||||
| chr12:14930788 | C | T | 3 | a0001c0001t0014g0245 a0001c0003t0001g0013 a0001c0003t0001g0064 |
5 | HG02451.hp2 HG02970.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4068G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930788 | |||||||
| chr12:14930963 | T | C | 11 | a0002c0002t0002g0117 a0002c0002t0004g0035 a0002c0002t0004g0036 others(8): Show |
13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+3893A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930963 | |||||||
| chr12:14931045 | C | G | 1 | a0001c0001t0002g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333+3811G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931045 | |||||||
| chr12:14931088 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0081 a0001c0001t0001g0228 |
5 | HG01175.hp1 HG01433.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+3768C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931088 | |||||||
| chr12:14931158 | ATTTC | A | 26 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0173 others(23): Show |
41 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.333+3694_333+3697d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931158 | |||||||
| chr12:14931177 | A | G | 84 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0066 others(81): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.333+3679T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931177 | |||||||
| chr12:14931308 | A | G | 2 | a0001c0001t0011g0037 a0001c0001t0011g0123 |
3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.333+3548T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931308 | |||||||
| chr12:14931363 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.333+3493G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | |||||||
| chr12:14931363 | C | CA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
247 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.333+3492dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | |||||||
| chr12:14931363 | C | CAA | 18 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0025 others(15): Show |
29 | HG01109.hp1 HG02027.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.333+3491_333+3492d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | |||||||
| chr12:14931363 | CA | C | 57 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0066 others(54): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.333+3492delT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | |||||||
| chr12:14931747 | G | A | 1 | a0003c0004t0010g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.333+3109C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931747 | |||||||
| chr12:14931773 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0249 a0001c0001t0001g0254 others(2): Show |
7 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+3083C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931773 | |||||||
| chr12:14931833 | G | A | 2 | a0001c0001t0006g0155 a0001c0001t0006g0156 |
2 | HG01081.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.333+3023C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931833 | |||||||
| chr12:14931867 | AATT | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0110 a0001c0001t0001g0112 others(2): Show |
7 | HG02258.hp1 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+2986_333+2988d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931867 | |||||||
| chr12:14931906 | CA | C | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+2949delT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931906 | |||||||
| chr12:14931958 | C | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0110 a0001c0001t0001g0112 others(5): Show |
10 | HG02258.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+2898G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931958 | |||||||
| chr12:14932056 | A | C | 2 | a0001c0001t0005g0113 a0001c0003t0001g0243 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.333+2800T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932056 | |||||||
| chr12:14932266 | A | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0249 a0001c0001t0001g0251 others(5): Show |
10 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+2590T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932266 | |||||||
| chr12:14932331 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.333+2525C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932331 | |||||||
| chr12:14932349 | T | C | 1 | a0001c0001t0002g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.333+2507A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932349 | |||||||
| chr12:14932385 | C | T | 4 | a0001c0001t0001g0246 a0001c0001t0014g0245 a0001c0003t0001g0013 others(1): Show |
6 | HG02451.hp2 HG02897.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+2471G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932385 | |||||||
| chr12:14932422 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.333+2434A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932422 | |||||||
| chr12:14932680 | C | T | 61 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(58): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.333+2176G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932680 | |||||||
| chr12:14932717 | T | C | 1 | a0002c0002t0004g0121 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.333+2139A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932717 | |||||||
| chr12:14932871 | T | C | 1 | a0001c0001t0003g0233 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.333+1985A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932871 | |||||||
| chr12:14932942 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.333+1914G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932942 | |||||||
| chr12:14933016 | T | C | 86 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0061 others(83): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.333+1840A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933016 | |||||||
| chr12:14933020 | G | A | 1 | a0001c0001t0015g0234 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.333+1836C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933020 | |||||||
| chr12:14933073 | T | TATTC | 6 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0003t0012g0111 others(3): Show |
7 | HG02145.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+1779_333+1782d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933073 | |||||||
| chr12:14933101 | G | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0003t0012g0111 |
4 | HG02486.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+1755C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933101 | |||||||
| chr12:14933366 | G | A | 1 | a0001c0001t0003g0012 | 4 | NA18953.hp2 NA18973.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1490C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933366 | |||||||
| chr12:14933506 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.333+1350A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933506 | |||||||
| chr12:14933509 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.333+1347A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933509 | |||||||
| chr12:14933560 | A | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
9 | HG00609.hp1 NA18940.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+1296T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933560 | |||||||
| chr12:14933652 | A | C | 1 | a0001c0001t0004g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.333+1204T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933652 | |||||||
| chr12:14933984 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.333+872G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933984 | |||||||
| chr12:14934083 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.333+773G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934083 | |||||||
| chr12:14934089 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.333+767A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934089 | |||||||
| chr12:14934115 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.333+741T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934115 | |||||||
| chr12:14934192 | G | T | 1 | a0001c0001t0002g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333+664C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934192 | |||||||
| chr12:14934281 | T | C | 83 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0063 others(80): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.333+575A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934281 | |||||||
| chr12:14934339 | A | G | 22 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(19): Show |
26 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.333+517T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934339 | |||||||
| chr12:14934422 | G | A | 2 | a0001c0001t0004g0244 a0001c0003t0001g0243 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.333+434C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934422 | |||||||
| chr12:14934441 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0128 a0001c0001t0001g0130 others(1): Show |
6 | HG00621.hp1 HG02027.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+415T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934441 | |||||||
| chr12:14934518 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.333+338T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934518 | |||||||
| chr12:14934558 | A | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
5 | HG02132.hp1 HG02155.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+298T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934558 | |||||||
| chr12:14934622 | G | A | 1 | a0002c0002t0004g0122 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.333+234C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934622 | |||||||
| chr12:14934719 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.333+137T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934719 | |||||||
| chr12:14934838 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0236 |
3 | HG02976.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.333+18C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934838 | |||||||
| chr12:14935018 | C | T | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.196-25G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935018 | |||||||
| chr12:14935040 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196-47G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935040 | |||||||
| chr12:14935112 | G | GTAAC | 2 | a0001c0001t0002g0031 a0001c0001t0002g0106 |
3 | HG02622.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-123_196-120dup others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935112 | |||||||
| chr12:14935181 | G | C | 2 | a0001c0001t0001g0246 a0001c0001t0014g0245 |
2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.196-188C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935181 | |||||||
| chr12:14935201 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196-208C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935201 | |||||||
| chr12:14935225 | C | A | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196-232G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935225 | |||||||
| chr12:14935263 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0110 a0001c0001t0001g0112 others(1): Show |
5 | HG02486.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-270C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935263 | |||||||
| chr12:14935351 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.196-358T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935351 | |||||||
| chr12:14935531 | A | T | 1 | a0001c0001t0008g0008 | 4 | HG02280.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-538T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935531 | |||||||
| chr12:14935715 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.196-722A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935715 | |||||||
| chr12:14935717 | G | A | 64 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(61): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.196-724C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935717 | |||||||
| chr12:14935885 | A | C | 21 | a0001c0001t0001g0034 a0001c0001t0001g0246 a0001c0001t0004g0114 others(18): Show |
27 | HG00733.hp1 HG02015.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.196-892T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935885 | |||||||
| chr12:14935895 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.196-902A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935895 | |||||||
| chr12:14935977 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0018 others(37): Show |
55 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.196-984G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935977 | |||||||
| chr12:14936007 | T | C | 83 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0063 others(80): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.196-1014A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936007 | |||||||
| chr12:14936008 | C | A | 1 | a0001c0001t0002g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196-1015G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936008 | |||||||
| chr12:14936018 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0108 a0002c0002t0004g0109 |
4 | NA19055.hp2 NA19062.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-1025C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936018 | |||||||
| chr12:14936098 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196-1105G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936098 | |||||||
| chr12:14936295 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0014g0245 |
2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.196-1302T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936295 | |||||||
| chr12:14936331 | G | A | 1 | a0001c0001t0008g0008 | 4 | HG02280.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1338C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936331 | |||||||
| chr12:14936349 | C | G | 1 | a0001c0001t0014g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196-1356G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936349 | |||||||
| chr12:14936411 | G | C | 4 | a0001c0001t0001g0242 a0001c0001t0002g0239 a0001c0001t0004g0241 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-1418C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936411 | |||||||
| chr12:14936482 | A | C | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1470T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936482 | |||||||
| chr12:14936503 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0014g0245 |
2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.195+1449G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936503 | |||||||
| chr12:14936570 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0014g0245 |
2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.195+1382A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936570 | |||||||
| chr12:14936605 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0110 a0001c0001t0001g0112 others(1): Show |
5 | HG02486.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+1347T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936605 | |||||||
| chr12:14936621 | G | C | 1 | a0001c0001t0001g0053 | 2 | NA18940.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.195+1331C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936621 | |||||||
| chr12:14936623 | T | C | 2 | a0001c0001t0011g0037 a0001c0001t0011g0123 |
3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.195+1329A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936623 | |||||||
| chr12:14936646 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195+1306T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936646 | |||||||
| chr12:14936726 | A | G | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1226T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936726 | |||||||
| chr12:14936824 | C | T | 2 | a0001c0001t0004g0124 a0001c0001t0004g0125 |
2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.195+1128G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936824 | |||||||
| chr12:14936869 | G | T | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1083C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936869 | |||||||
| chr12:14936890 | A | G | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1062T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936890 | |||||||
| chr12:14936975 | A | G | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+977T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936975 | |||||||
| chr12:14937047 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0006g0062 |
3 | HG01934.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195+905G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937047 | |||||||
| chr12:14937080 | C | T | 2 | a0001c0001t0004g0059 a0001c0001t0004g0060 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.195+872G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937080 | |||||||
| chr12:14937156 | T | A | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+796A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937156 | |||||||
| chr12:14937412 | A | G | 64 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(61): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.195+540T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937412 | |||||||
| chr12:14937421 | A | T | 1 | a0001c0001t0001g0015 | 3 | NA18965.hp2 NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.195+531T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937421 | |||||||
| chr12:14937438 | A | C | 87 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0061 others(84): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.195+514T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937438 | |||||||
| chr12:14937460 | G | A | 3 | a0003c0004t0010g0055 a0003c0004t0010g0056 a0003c0004t0010g0057 |
3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.195+492C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937460 | |||||||
| chr12:14937658 | A | G | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+294T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937658 | |||||||
| chr12:14937828 | G | C | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+124C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937828 | |||||||
| chr12:14937835 | G | T | 1 | a0001c0001t0002g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.195+117C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937835 | |||||||
| chr12:14937903 | A | G | 66 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(63): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+49T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937903 | |||||||
| chr12:14938073 | T | C | 2 | a0001c0001t0004g0244 a0001c0003t0001g0243 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.95-21A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938073 | |||||||
| chr12:14938120 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0014g0245 |
2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.95-68A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938120 | |||||||
| chr12:14938217 | G | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG00735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.95-165C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938217 | |||||||
| chr12:14938287 | A | AT | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.94+127_94+128insA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938287 |