Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5000 |
| ensemblid | ENSG00000115947.14 |
| hgncid | 8490 |
| symbol | ORC4 |
| name | origin recognition complex subunit 4 |
| refseq_nuc | NM_181741.4 |
| refseq_prot | NP_859525.1 |
| ensembl_nuc | ENST00000392857.10 |
| ensembl_prot | ENSP00000376597.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 147930396 |
| end | 148020737 |
| strand | - |
| ver | v1.2 |
| region | chr2:147930396-148020737 |
| region5000 | chr2:147925396-148025737 |
| regionname0 | ORC4_chr2_147930396_148020737 |
| regionname5000 | ORC4_chr2_147925396_148025737 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 436 | 194 | 61 | 31 | 74 | 5 | 21 | 57 | ORC4_chr2_147925396_148025737 | ORC4 | MSSRK others(431): Show |
chr2 | 147925396 | 148025737 |
| a0002 | 0/0 | 436 | 132 | 20 | 31 | 58 | 6 | 17 | 46 | ORC4_chr2_147925396_148025737 | ORC4 | MSSRK others(431): Show |
chr2 | 147925396 | 148025737 |
| a0003 | 0/0 | 436 | 7 | 2 | 2 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | MSSRK others(431): Show |
chr2 | 147925396 | 148025737 |
| a0004 | 0/0 | 436 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | MSSRK others(431): Show |
chr2 | 147925396 | 148025737 |
| a0005 | 0/0 | 436 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | MSSRK others(431): Show |
chr2 | 147925396 | 148025737 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1308 | 192 | 59 | 31 | 74 | 5 | 21 | ORC4_chr2_147925396_148025737 | ORC4 | ATGAG others(1303): Show |
chr2 | 147925396 | 148025737 | ||
| a0001c0004 | 0/0 | 1308 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | ATGAG others(1303): Show |
chr2 | 147925396 | 148025737 | ||
| a0002c0002 | 0/0 | 1308 | 132 | 20 | 31 | 58 | 6 | 17 | ORC4_chr2_147925396_148025737 | ORC4 | ATGAG others(1303): Show |
chr2 | 147925396 | 148025737 | ||
| a0003c0003 | 0/0 | 1308 | 7 | 2 | 2 | 0 | 3 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | ATGAG others(1303): Show |
chr2 | 147925396 | 148025737 | ||
| a0004c0005 | 0/0 | 1308 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | ATGAG others(1303): Show |
chr2 | 147925396 | 148025737 | ||
| a0005c0006 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | ATGAG others(1303): Show |
chr2 | 147925396 | 148025737 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6547 | 78 | 1 | 13 | 48 | 4 | 12 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0003 | 0/1 | 6547 | 36 | 3 | 7 | 17 | 0 | 8 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0005 | 1/0 | 6547 | 13 | 6 | 5 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0006 | 0/0 | 6547 | 6 | 6 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0007 | 0/0 | 6546 | 5 | 5 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0008 | 0/0 | 6546 | 6 | 5 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0012 | 0/0 | 6549 | 4 | 1 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6544): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0014 | 0/0 | 6550 | 4 | 4 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6545): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0016 | 0/0 | 6550 | 3 | 3 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6545): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0018 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0019 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0021 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0022 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0023 | 0/0 | 6548 | 2 | 0 | 0 | 1 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6543): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0024 | 0/0 | 6547 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0026 | 0/0 | 6549 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6544): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0028 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0035 | 0/0 | 6550 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6545): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0041 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0042 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0043 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0044 | 0/0 | 6547 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0045 | 0/0 | 6547 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0046 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6543): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0047 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6543): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0048 | 0/0 | 6550 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6545): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0049 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6543): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0050 | 0/0 | 6546 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0051 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0052 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6543): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0053 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0054 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0055 | 0/0 | 6549 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6544): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0056 | 0/0 | 6550 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6545): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0057 | 0/0 | 6549 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6544): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0058 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6543): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0059 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0060 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0061 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0001t0062 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0004t0006 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0001c0004t0007 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0002 | 0/0 | 6546 | 77 | 5 | 13 | 43 | 5 | 11 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0004 | 0/0 | 6546 | 24 | 3 | 13 | 8 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0009 | 0/0 | 6547 | 5 | 1 | 1 | 1 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0010 | 0/0 | 6547 | 5 | 5 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0013 | 0/0 | 6546 | 4 | 0 | 2 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0015 | 0/0 | 6550 | 3 | 1 | 1 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6545): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0017 | 0/0 | 6546 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0025 | 0/0 | 6546 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0027 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0029 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0030 | 0/0 | 6546 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0031 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0032 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0033 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0034 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0036 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0038 | 0/0 | 6547 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0039 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0002c0002t0040 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0003c0003t0011 | 0/0 | 6547 | 5 | 2 | 2 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0003c0003t0020 | 0/0 | 6547 | 2 | 0 | 0 | 0 | 2 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0004c0005t0001 | 0/0 | 6547 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6542): Show |
chr2 | 147925396 | 148025737 |
| a0005c0006t0037 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | AGTGG others(6541): Show |
chr2 | 147925396 | 148025737 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0015 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0006g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0006g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0007g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0012g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0012g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0014g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0016g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0016g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0016g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0018g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0019g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0021g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0021g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0022g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0022g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0023g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0023g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0024g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0024g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0026g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0028g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0035g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0041g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0042g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0043g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0044g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0045g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0046g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0047g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0048g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0049g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0050g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0051g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0052g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0053g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0054g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0055g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0056g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0057g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0058g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0059g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0060g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0061g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0001t0062g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0004t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0001c0004t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0009g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0009g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0010g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0013g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0013g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0013g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0013g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0015g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0015g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0017g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0025g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0027g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0029g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0030g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0031g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0032g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0033g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0034g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0036g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0038g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0039g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0002c0002t0040g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0003c0003t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0003c0003t0011g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0003c0003t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0003c0003t0011g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0003c0003t0011g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0003c0003t0020g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0003c0003t0020g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0004c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0004c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| a0005c0006t0037g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0038 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00099 | hp2 | a0003 | c0003 | t0011 | g0301 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00140 | hp1 | a0002 | c0002 | t0015 | g0031 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0033 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0028 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00408 | hp1 | a0001 | c0001 | t0012 | g0042 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0125 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00558 | hp2 | a0002 | c0002 | t0009 | g0083 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00642 | hp1 | a0002 | c0002 | t0013 | g0023 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0225 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00673 | hp2 | a0004 | c0005 | t0001 | g0284 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00733 | hp2 | a0001 | c0001 | t0044 | g0148 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0065 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0211 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0261 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00738 | hp2 | a0002 | c0002 | t0004 | g0053 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0207 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0289 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01106 | hp1 | a0001 | c0001 | t0045 | g0176 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01109 | hp1 | a0003 | c0003 | t0011 | g0300 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0175 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01168 | hp1 | a0001 | c0001 | t0024 | g0229 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01168 | hp2 | a0003 | c0003 | t0011 | g0296 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01169 | hp1 | a0001 | c0001 | t0024 | g0230 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01175 | hp1 | a0002 | c0002 | t0004 | g0006 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01256 | hp1 | a0002 | c0002 | t0013 | g0025 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01261 | hp1 | a0001 | c0001 | t0050 | g0160 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01261 | hp2 | a0002 | c0002 | t0004 | g0060 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0206 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01516 | hp2 | a0003 | c0003 | t0020 | g0298 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0093 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01517 | hp2 | a0003 | c0003 | t0020 | g0299 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01884 | hp1 | a0002 | c0002 | t0015 | g0030 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01891 | hp1 | a0001 | c0004 | t0007 | g0150 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0221 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01928 | hp1 | a0002 | c0002 | t0004 | g0052 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01934 | hp1 | a0002 | c0002 | t0004 | g0006 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01934 | hp2 | a0002 | c0002 | t0009 | g0088 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01943 | hp1 | a0002 | c0002 | t0004 | g0136 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01975 | hp2 | a0002 | c0002 | t0004 | g0139 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01978 | hp1 | a0002 | c0002 | t0004 | g0045 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01981 | hp2 | a0002 | c0002 | t0004 | g0050 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02004 | hp1 | a0002 | c0002 | t0004 | g0047 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02055 | hp1 | a0002 | c0002 | t0033 | g0126 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02071 | hp1 | a0001 | c0001 | t0060 | g0201 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02145 | hp1 | a0001 | c0001 | t0052 | g0208 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0182 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | CDX | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0174 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02258 | hp1 | a0002 | c0002 | t0031 | g0110 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0157 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02273 | hp1 | a0002 | c0002 | t0025 | g0049 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0096 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02293 | hp1 | a0002 | c0002 | t0004 | g0099 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02300 | hp1 | a0002 | c0002 | t0004 | g0051 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02300 | hp2 | a0002 | c0002 | t0015 | g0029 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02523 | hp2 | a0002 | c0002 | t0036 | g0107 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0279 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02622 | hp1 | a0001 | c0001 | t0053 | g0286 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02622 | hp2 | a0002 | c0002 | t0010 | g0120 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0184 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02630 | hp2 | a0001 | c0001 | t0054 | g0259 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0183 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02647 | hp2 | a0001 | c0004 | t0006 | g0303 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02683 | hp1 | a0002 | c0002 | t0038 | g0124 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0021 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0154 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02738 | hp2 | a0002 | c0002 | t0013 | g0037 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02809 | hp2 | a0001 | c0001 | t0059 | g0165 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0173 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02818 | hp2 | a0001 | c0001 | t0058 | g0155 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02886 | hp1 | a0001 | c0001 | t0055 | g0170 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02886 | hp2 | a0002 | c0002 | t0010 | g0121 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02895 | hp1 | a0002 | c0002 | t0010 | g0011 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02895 | hp2 | a0002 | c0002 | t0004 | g0123 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02896 | hp2 | a0001 | c0001 | t0021 | g0218 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02897 | hp1 | a0001 | c0001 | t0021 | g0177 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02897 | hp2 | a0002 | c0002 | t0010 | g0011 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02922 | hp1 | a0001 | c0001 | t0041 | g0293 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0219 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02965 | hp2 | a0002 | c0002 | t0010 | g0119 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0220 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0168 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0134 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03098 | hp1 | a0002 | c0002 | t0009 | g0058 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03098 | hp2 | a0001 | c0001 | t0048 | g0153 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03139 | hp1 | a0002 | c0002 | t0004 | g0122 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0186 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0097 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03453 | hp1 | a0001 | c0001 | t0057 | g0185 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03453 | hp2 | a0001 | c0001 | t0022 | g0159 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03486 | hp1 | a0001 | c0001 | t0051 | g0169 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03486 | hp2 | a0001 | c0001 | t0022 | g0156 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03490 | hp2 | a0002 | c0002 | t0013 | g0138 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03516 | hp1 | a0001 | c0001 | t0026 | g0020 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0059 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03669 | hp1 | a0001 | c0001 | t0023 | g0234 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0055 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03831 | hp2 | a0002 | c0002 | t0030 | g0026 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0032 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04115 | hp1 | a0002 | c0002 | t0009 | g0063 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0108 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04204 | hp2 | a0002 | c0002 | t0009 | g0062 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18522 | hp1 | a0001 | c0001 | t0049 | g0172 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CHB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | CHB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0158 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18942 | hp2 | a0002 | c0002 | t0017 | g0007 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18944 | hp2 | a0001 | c0001 | t0061 | g0271 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18945 | hp1 | a0002 | c0002 | t0017 | g0007 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18946 | hp1 | a0001 | c0001 | t0043 | g0294 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18959 | hp1 | a0001 | c0001 | t0012 | g0040 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18968 | hp1 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18969 | hp2 | a0002 | c0002 | t0004 | g0132 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18971 | hp2 | a0002 | c0002 | t0004 | g0133 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18972 | hp2 | a0004 | c0005 | t0001 | g0269 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18974 | hp2 | a0001 | c0001 | t0012 | g0041 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18984 | hp1 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18985 | hp1 | a0002 | c0002 | t0027 | g0067 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18986 | hp1 | a0002 | c0002 | t0032 | g0113 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18987 | hp1 | a0002 | c0002 | t0004 | g0129 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18994 | hp1 | a0001 | c0001 | t0023 | g0281 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19005 | hp1 | a0001 | c0001 | t0062 | g0226 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19010 | hp1 | a0002 | c0002 | t0029 | g0140 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19030 | hp2 | a0001 | c0001 | t0035 | g0115 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19043 | hp2 | a0001 | c0001 | t0046 | g0171 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19079 | hp1 | a0001 | c0001 | t0028 | g0090 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19082 | hp2 | a0002 | c0002 | t0004 | g0127 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19087 | hp2 | a0002 | c0002 | t0004 | g0130 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19240 | hp1 | a0005 | c0006 | t0037 | g0118 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA19240 | hp2 | a0002 | c0002 | t0040 | g0142 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA20129 | hp1 | a0001 | c0001 | t0056 | g0214 | AFR | ASW | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA20129 | hp2 | a0001 | c0001 | t0047 | g0151 | AFR | ASW | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0022 | EUR | TSI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0311 | EUR | TSI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01123 | hp1 | a0002 | c0002 | t0004 | g0131 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02109 | hp1 | a0002 | c0002 | t0034 | g0117 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG02486 | hp2 | a0001 | c0001 | t0042 | g0167 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03471 | hp1 | a0002 | c0002 | t0039 | g0141 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG06807 | hp1 | a0003 | c0003 | t0011 | g0145 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA20300 | hp1 | a0001 | c0001 | t0019 | g0280 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0112 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA21309 | hp1 | a0003 | c0003 | t0011 | g0297 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0043 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0305 | REF | REF | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0216 | REF | REF | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147948209 | A | C | 1 | a0005 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.604T>G | p.Leu202Val | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/14 | 726/6547 | 604/1311 | 202/436 | chr2 | 147948209 | |||
| chr2:147958805 | T | C | 1 | a0004 | 2 | HG00673.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.287A>G | p.Gln96Arg | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/14 | 409/6547 | 287/1311 | 96/436 | chr2 | 147958805 | |||
| chr2:147958859 | T | C | 2 | a0002 a0005 |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
missense_variant | MODERATE | c.233A>G | p.Asn78Ser | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/14 | 355/6547 | 233/1311 | 78/436 | chr2 | 147958859 | |||
| chr2:147972798 | G | C | 1 | a0003 | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
missense_variant | MODERATE | c.166C>G | p.Leu56Val | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/14 | 288/6547 | 166/1311 | 56/436 | chr2 | 147972798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147938389 | T | C | 1 | a0001c0004 | 2 | HG01891.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.963A>G | p.Leu321Leu | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 12/14 | 1085/6547 | 963/1311 | 321/436 | chr2 | 147938389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147930513 | T | C | 1 | a0001c0001t0053 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4997A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4997 | chr2 | 147930513 | ||||||
| chr2:147930605 | A | G | 1 | a0002c0002t0031 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4905T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4905 | chr2 | 147930605 | ||||||
| chr2:147930614 | T | C | 1 | a0001c0001t0050 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4896A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4896 | chr2 | 147930614 | ||||||
| chr2:147930821 | G | A | 2 | a0001c0001t0054 a0002c0002t0031 |
2 | HG02258.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4689C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4689 | chr2 | 147930821 | ||||||
| chr2:147930856 | G | GT | 6 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0035 others(3): Show |
10 | HG02145.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4653dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4653 | chr2 | 147930856 | ||||||
| chr2:147930856 | GT | G | 28 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(25): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*4653delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4653 | chr2 | 147930856 | ||||||
| chr2:147930878 | T | A | 6 | a0001c0001t0018 a0001c0001t0046 a0001c0001t0048 others(3): Show |
7 | HG02257.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4632A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4632 | chr2 | 147930878 | ||||||
| chr2:147930934 | C | T | 1 | a0001c0001t0044 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4576G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4576 | chr2 | 147930934 | ||||||
| chr2:147930988 | T | C | 3 | a0002c0002t0013 a0002c0002t0015 a0002c0002t0030 |
8 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4522A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4522 | chr2 | 147930988 | ||||||
| chr2:147930989 | A | G | 2 | a0002c0002t0013 a0002c0002t0015 |
7 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4521T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4521 | chr2 | 147930989 | ||||||
| chr2:147931006 | A | AC | 5 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0022 others(2): Show |
12 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4503_*4504insG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4503 | chr2 | 147931006 | ||||||
| chr2:147931006 | A | ACC | 5 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0048 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4503_*4504insGG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4503 | chr2 | 147931006 | ||||||
| chr2:147931006 | A | C | 3 | a0002c0002t0013 a0002c0002t0015 a0002c0002t0030 |
8 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4504T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4504 | chr2 | 147931006 | ||||||
| chr2:147931007 | T | C | 17 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(14): Show |
33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4503A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4503 | chr2 | 147931007 | ||||||
| chr2:147931021 | A | C | 3 | a0002c0002t0013 a0002c0002t0015 a0002c0002t0030 |
8 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4489T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4489 | chr2 | 147931021 | ||||||
| chr2:147931077 | A | G | 3 | a0001c0001t0014 a0001c0001t0035 a0001c0001t0057 |
6 | HG02145.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4433T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4433 | chr2 | 147931077 | ||||||
| chr2:147931125 | T | C | 1 | a0001c0001t0012 | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4385A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4385 | chr2 | 147931125 | ||||||
| chr2:147931154 | A | G | 1 | a0001c0001t0062 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4356T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4356 | chr2 | 147931154 | ||||||
| chr2:147931234 | G | A | 2 | a0002c0002t0017 a0002c0002t0027 |
3 | NA18942.hp2 NA18945.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4276C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4276 | chr2 | 147931234 | ||||||
| chr2:147931520 | T | C | 1 | a0001c0001t0026 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3990A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3990 | chr2 | 147931520 | ||||||
| chr2:147931537 | A | ATGAT | 1 | a0002c0002t0015 | 3 | HG00140.hp1 HG01884.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3969_*3972dupATCA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3972 | chr2 | 147931537 | ||||||
| chr2:147931577 | A | G | 1 | a0002c0002t0029 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3933T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3933 | chr2 | 147931577 | ||||||
| chr2:147931642 | C | T | 1 | a0001c0001t0043 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3868G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3868 | chr2 | 147931642 | ||||||
| chr2:147931655 | C | T | 1 | a0002c0002t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3855G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3855 | chr2 | 147931655 | ||||||
| chr2:147931678 | G | A | 1 | a0002c0002t0032 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3832C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3832 | chr2 | 147931678 | ||||||
| chr2:147931708 | C | T | 1 | a0001c0001t0019 | 2 | HG02615.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3802G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3802 | chr2 | 147931708 | ||||||
| chr2:147931756 | A | G | 1 | a0001c0001t0056 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3754T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3754 | chr2 | 147931756 | ||||||
| chr2:147931789 | G | T | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3721C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3721 | chr2 | 147931789 | ||||||
| chr2:147931800 | T | C | 23 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0026 others(20): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*3710A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3710 | chr2 | 147931800 | ||||||
| chr2:147931896 | C | G | 28 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(25): Show |
86 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3614G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3614 | chr2 | 147931896 | ||||||
| chr2:147931917 | C | T | 1 | a0001c0001t0046 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3593 | chr2 | 147931917 | ||||||
| chr2:147931935 | T | TAA | 4 | a0001c0001t0014 a0001c0001t0035 a0001c0001t0056 others(1): Show |
7 | HG02145.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3574_*3575insTT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3574 | chr2 | 147931935 | ||||||
| chr2:147931948 | T | C | 21 | a0001c0001t0016 a0002c0002t0002 a0002c0002t0004 others(18): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*3562A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3562 | chr2 | 147931948 | ||||||
| chr2:147931950 | T | C | 1 | a0002c0002t0033 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3560A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3560 | chr2 | 147931950 | ||||||
| chr2:147931963 | T | C | 1 | a0003c0003t0020 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3547A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3547 | chr2 | 147931963 | ||||||
| chr2:147932023 | T | C | 1 | a0002c0002t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3487A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3487 | chr2 | 147932023 | ||||||
| chr2:147932035 | T | C | 1 | a0001c0001t0045 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3475A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3475 | chr2 | 147932035 | ||||||
| chr2:147932151 | T | C | 1 | a0002c0002t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3359A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3359 | chr2 | 147932151 | ||||||
| chr2:147932159 | C | T | 13 | a0001c0001t0016 a0002c0002t0002 a0002c0002t0009 others(10): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3351G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3351 | chr2 | 147932159 | ||||||
| chr2:147932189 | T | G | 1 | a0001c0001t0026 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3321A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3321 | chr2 | 147932189 | ||||||
| chr2:147932202 | A | G | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3308T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3308 | chr2 | 147932202 | ||||||
| chr2:147932282 | G | A | 1 | a0001c0001t0021 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3228C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3228 | chr2 | 147932282 | ||||||
| chr2:147932284 | T | C | 1 | a0001c0001t0021 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3226A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3226 | chr2 | 147932284 | ||||||
| chr2:147932442 | T | C | 1 | a0001c0001t0012 | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3068A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3068 | chr2 | 147932442 | ||||||
| chr2:147932486 | A | G | 23 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0026 others(20): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*3024T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3024 | chr2 | 147932486 | ||||||
| chr2:147932844 | G | A | 6 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0024 others(3): Show |
13 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2666C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2666 | chr2 | 147932844 | ||||||
| chr2:147932869 | A | ACT | 2 | a0001c0001t0012 a0001c0001t0026 |
5 | HG00408.hp1 HG03516.hp1 NA18959.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2639_*2640dupAG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2640 | chr2 | 147932869 | ||||||
| chr2:147932994 | A | T | 1 | a0001c0001t0061 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2516T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2516 | chr2 | 147932994 | ||||||
| chr2:147933026 | A | AATC | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2481_*2483dupGAT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2483 | chr2 | 147933026 | ||||||
| chr2:147933258 | G | A | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2252C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2252 | chr2 | 147933258 | ||||||
| chr2:147933261 | T | G | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2249A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2249 | chr2 | 147933261 | ||||||
| chr2:147933546 | G | C | 1 | a0001c0001t0059 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1964 | chr2 | 147933546 | ||||||
| chr2:147933588 | C | T | 1 | a0001c0001t0042 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1922 | chr2 | 147933588 | ||||||
| chr2:147933687 | A | G | 6 | a0001c0001t0003 a0001c0001t0028 a0001c0001t0043 others(3): Show |
40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1823T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1823 | chr2 | 147933687 | ||||||
| chr2:147933776 | G | A | 1 | a0001c0001t0012 | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1734C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1734 | chr2 | 147933776 | ||||||
| chr2:147933791 | A | C | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1719T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1719 | chr2 | 147933791 | ||||||
| chr2:147933866 | A | C | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1644 | chr2 | 147933866 | ||||||
| chr2:147933954 | A | C | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1556 | chr2 | 147933954 | ||||||
| chr2:147934193 | G | T | 1 | a0002c0002t0039 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1317 | chr2 | 147934193 | ||||||
| chr2:147934492 | A | C | 1 | a0001c0001t0042 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1018 | chr2 | 147934492 | ||||||
| chr2:147934558 | T | G | 1 | a0001c0001t0060 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 952 | chr2 | 147934558 | ||||||
| chr2:147934664 | A | G | 2 | a0001c0001t0012 a0001c0001t0026 |
5 | HG00408.hp1 HG03516.hp1 NA18959.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*846T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 846 | chr2 | 147934664 | ||||||
| chr2:147934828 | G | A | 1 | a0005c0006t0037 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*682C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 682 | chr2 | 147934828 | ||||||
| chr2:147935095 | C | T | 1 | a0002c0002t0025 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 415 | chr2 | 147935095 | ||||||
| chr2:147935207 | T | C | 7 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0024 others(4): Show |
87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*303A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 303 | chr2 | 147935207 | ||||||
| chr2:147935235 | A | G | 1 | a0001c0001t0041 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 275 | chr2 | 147935235 | ||||||
| chr2:148020685 | G | A | 1 | a0002c0002t0039 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/14 | 44727 | chr2 | 148020685 | ||||||
| chr2:148020698 | G | A | 1 | a0002c0002t0040 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-83C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/14 | 44740 | chr2 | 148020698 | ||||||
| chr2:148020703 | A | G | 24 | a0001c0001t0012 a0001c0001t0026 a0001c0001t0028 others(21): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
5_prime_UTR_variant | MODIFIER | c.-88T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/14 | 44745 | chr2 | 148020703 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147935712 | G | T | 2 | a0001c0001t0014g0183 a0001c0001t0014g0184 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1123-14C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147935712 | |||||||
| chr2:147935955 | A | G | 1 | a0001c0001t0008g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1123-257T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147935955 | |||||||
| chr2:147936231 | A | G | 1 | a0002c0002t0002g0009 | 2 | HG02083.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1123-533T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936231 | |||||||
| chr2:147936420 | GA | G | 5 | a0001c0001t0001g0224 a0001c0001t0001g0266 a0001c0001t0003g0198 others(2): Show |
5 | HG03139.hp1 HG03654.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-723delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936420 | |||||||
| chr2:147936430 | A | C | 1 | a0002c0002t0002g0077 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1123-732T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936430 | |||||||
| chr2:147936747 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1123-1049C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936747 | |||||||
| chr2:147936786 | C | T | 9 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1123-1088G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936786 | |||||||
| chr2:147937018 | C | CA | 101 | a0001c0001t0001g0247 a0001c0001t0001g0250 a0001c0001t0003g0187 others(98): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1122+1127dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937018 | |||||||
| chr2:147937018 | C | CAA | 13 | a0001c0001t0001g0255 a0001c0001t0008g0158 a0001c0001t0012g0040 others(10): Show |
13 | HG00408.hp1 HG00642.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1122+1126_1122+112 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937018 | |||||||
| chr2:147937018 | CA | C | 17 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0254 others(14): Show |
18 | HG00738.hp1 HG01167.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.1122+1127delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937018 | |||||||
| chr2:147937283 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1122+863G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937283 | |||||||
| chr2:147937490 | A | G | 2 | a0002c0002t0002g0111 a0002c0002t0031g0110 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1122+656T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937490 | |||||||
| chr2:147937557 | T | G | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1122+589A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937557 | |||||||
| chr2:147937563 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+583A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937563 | |||||||
| chr2:147937619 | T | C | 3 | a0002c0002t0002g0080 a0002c0002t0002g0101 a0002c0002t0002g0103 |
3 | HG00544.hp1 NA18612.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1122+527A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937619 | |||||||
| chr2:147937774 | A | G | 3 | a0002c0002t0002g0003 a0002c0002t0002g0068 a0002c0002t0002g0100 |
5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122+372T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937774 | |||||||
| chr2:147937972 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+174C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937972 | |||||||
| chr2:147938952 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+188G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 11/13 | chr2 | 147938952 | |||||||
| chr2:147938991 | C | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0246 |
2 | HG01081.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.958+149G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 11/13 | chr2 | 147938991 | |||||||
| chr2:147939533 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.850-285T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939533 | |||||||
| chr2:147939825 | C | T | 1 | a0001c0001t0045g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.850-577G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939825 | |||||||
| chr2:147939827 | C | G | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-579G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939827 | |||||||
| chr2:147939882 | A | G | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-634T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939882 | |||||||
| chr2:147939897 | G | A | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.850-649C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939897 | |||||||
| chr2:147939978 | A | C | 1 | a0001c0001t0012g0042 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.850-730T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939978 | |||||||
| chr2:147940024 | C | T | 20 | a0002c0002t0004g0006 a0002c0002t0004g0045 a0002c0002t0004g0047 others(17): Show |
21 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-776G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940024 | |||||||
| chr2:147940319 | T | C | 5 | a0001c0001t0003g0188 a0001c0001t0003g0191 a0001c0001t0003g0192 others(2): Show |
5 | HG00609.hp1 HG00673.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1071A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940319 | |||||||
| chr2:147940630 | G | GAT | 14 | a0001c0001t0014g0182 a0001c0001t0014g0183 a0001c0001t0014g0184 others(11): Show |
14 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.850-1384_850-1383d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940630 | |||||||
| chr2:147940775 | G | A | 5 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(2): Show |
5 | HG00408.hp1 HG03516.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1527C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940775 | |||||||
| chr2:147940847 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.850-1599A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940847 | |||||||
| chr2:147941185 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0290 a0001c0001t0001g0291 |
4 | HG00558.hp1 NA18981.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-1937A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941185 | |||||||
| chr2:147941241 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850-1993A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941241 | |||||||
| chr2:147941310 | T | C | 5 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0175 others(2): Show |
5 | HG01167.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-2062A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941310 | |||||||
| chr2:147941646 | A | G | 1 | a0001c0001t0023g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.849+1790T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941646 | |||||||
| chr2:147941661 | T | A | 1 | a0002c0002t0004g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.849+1775A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941661 | |||||||
| chr2:147941680 | G | A | 1 | a0002c0002t0002g0114 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.849+1756C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941680 | |||||||
| chr2:147941772 | G | GTA | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+1662_849+1663d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941772 | |||||||
| chr2:147941895 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+1541T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941895 | |||||||
| chr2:147942323 | A | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+1113T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942323 | |||||||
| chr2:147942474 | A | G | 1 | a0002c0002t0009g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.849+962T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942474 | |||||||
| chr2:147942696 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+740A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942696 | |||||||
| chr2:147942919 | A | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.849+517T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942919 | |||||||
| chr2:147942969 | G | T | 1 | a0002c0002t0002g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.849+467C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942969 | |||||||
| chr2:147943079 | G | C | 1 | a0002c0002t0002g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.849+357C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943079 | |||||||
| chr2:147943096 | T | TGAAAGTA others(3309): Show |
1 | a0002c0002t0002g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.849+339_849+340ins others(3316): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943096 | |||||||
| chr2:147943346 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+90A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943346 | |||||||
| chr2:147943376 | C | A | 21 | a0002c0002t0004g0006 a0002c0002t0004g0045 a0002c0002t0004g0047 others(18): Show |
22 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.849+60G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943376 | |||||||
| chr2:147943530 | GA | G | 168 | a0001c0001t0001g0149 a0001c0001t0001g0257 a0001c0001t0006g0012 others(165): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.763-9delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147943530 | |||||||
| chr2:147943650 | G | C | 1 | a0002c0002t0002g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.763-128C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147943650 | |||||||
| chr2:147943852 | T | C | 2 | a0002c0002t0002g0003 a0002c0002t0002g0100 |
4 | NA18952.hp2 NA18962.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-330A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147943852 | |||||||
| chr2:147944075 | G | T | 1 | a0002c0002t0009g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.763-553C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944075 | |||||||
| chr2:147944617 | A | G | 1 | a0001c0001t0019g0279 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.763-1095T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944617 | |||||||
| chr2:147944661 | T | C | 2 | a0002c0002t0004g0122 a0002c0002t0004g0123 |
2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.763-1139A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944661 | |||||||
| chr2:147944693 | CT | C | 121 | a0001c0001t0003g0147 a0001c0001t0026g0020 a0002c0002t0002g0003 others(118): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.763-1172delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944693 | |||||||
| chr2:147944697 | T | A | 5 | a0002c0002t0002g0104 a0002c0002t0002g0111 a0002c0002t0004g0122 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.763-1175A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944697 | |||||||
| chr2:147944697 | TA | T | 84 | a0001c0001t0001g0210 a0001c0001t0001g0256 a0001c0001t0003g0004 others(81): Show |
90 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.763-1176delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944697 | |||||||
| chr2:147944770 | G | A | 2 | a0001c0001t0005g0233 a0001c0001t0005g0261 |
2 | HG00738.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.763-1248C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944770 | |||||||
| chr2:147945426 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.763-1904A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945426 | |||||||
| chr2:147945430 | A | G | 128 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(125): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.763-1908T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945430 | |||||||
| chr2:147945595 | T | C | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.763-2073A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945595 | |||||||
| chr2:147945643 | A | G | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.763-2121T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945643 | |||||||
| chr2:147945647 | G | A | 1 | a0001c0001t0049g0172 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.763-2125C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945647 | |||||||
| chr2:147945741 | C | T | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.763-2219G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945741 | |||||||
| chr2:147945887 | G | C | 2 | a0001c0001t0005g0260 a0001c0001t0054g0259 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.762+2164C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945887 | |||||||
| chr2:147946293 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1758A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946293 | |||||||
| chr2:147946295 | G | GA | 35 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(32): Show |
38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.762+1755dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946295 | |||||||
| chr2:147946377 | A | G | 1 | a0001c0001t0001g0274 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.762+1674T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946377 | |||||||
| chr2:147946396 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(75): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.762+1655T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946396 | |||||||
| chr2:147947047 | C | T | 38 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(35): Show |
41 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.762+1004G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947047 | |||||||
| chr2:147947069 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.762+982G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947069 | |||||||
| chr2:147947152 | A | C | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.762+899T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947152 | |||||||
| chr2:147947164 | T | C | 3 | a0001c0001t0005g0260 a0001c0001t0054g0259 a0005c0006t0037g0118 |
3 | HG02280.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.762+887A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947164 | |||||||
| chr2:147947280 | G | A | 1 | a0001c0001t0014g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.762+771C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947280 | |||||||
| chr2:147947337 | C | A | 1 | a0001c0001t0005g0289 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.762+714G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947337 | |||||||
| chr2:147947363 | T | C | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.762+688A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947363 | |||||||
| chr2:147947410 | C | T | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.762+641G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947410 | |||||||
| chr2:147947502 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0239 |
3 | HG02071.hp2 NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.762+549T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947502 | |||||||
| chr2:147947564 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.762+487C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947564 | |||||||
| chr2:147947784 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+267G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947784 | |||||||
| chr2:147947855 | G | C | 1 | a0001c0001t0003g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.762+196C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947855 | |||||||
| chr2:147948349 | A | G | 1 | a0003c0003t0011g0296 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.589-125T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948349 | |||||||
| chr2:147948653 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.589-429G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948653 | |||||||
| chr2:147948670 | C | CT | 6 | a0001c0001t0001g0243 a0001c0001t0003g0199 a0001c0001t0003g0200 others(3): Show |
6 | HG00673.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-447dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948670 | |||||||
| chr2:147948801 | G | T | 88 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(85): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.589-577C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948801 | |||||||
| chr2:147948928 | C | T | 211 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(208): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.589-704G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948928 | |||||||
| chr2:147948995 | G | GCATATTA others(18): Show |
1 | a0001c0001t0045g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.589-796_589-772dup others(25): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948995 | |||||||
| chr2:147949005 | T | G | 1 | a0003c0003t0011g0301 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.589-781A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949005 | |||||||
| chr2:147949024 | A | G | 25 | a0002c0002t0004g0006 a0002c0002t0004g0045 a0002c0002t0004g0047 others(22): Show |
26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.589-800T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949024 | |||||||
| chr2:147949054 | T | C | 1 | a0001c0001t0056g0214 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.589-830A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949054 | |||||||
| chr2:147949197 | A | G | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-973T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949197 | |||||||
| chr2:147949463 | C | T | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.589-1239G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949463 | |||||||
| chr2:147949950 | C | G | 7 | a0001c0001t0003g0215 a0001c0001t0014g0182 a0001c0001t0014g0183 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-1726G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949950 | |||||||
| chr2:147949950 | C | T | 11 | a0002c0002t0004g0006 a0002c0002t0004g0045 a0002c0002t0004g0047 others(8): Show |
12 | HG00738.hp2 HG01175.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-1726G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949950 | |||||||
| chr2:147949968 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589-1744A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949968 | |||||||
| chr2:147950156 | A | G | 1 | a0001c0001t0008g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.589-1932T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950156 | |||||||
| chr2:147950253 | C | T | 1 | a0002c0002t0002g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.589-2029G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950253 | |||||||
| chr2:147950262 | G | T | 3 | a0001c0001t0001g0245 a0002c0002t0004g0122 a0002c0002t0004g0123 |
3 | HG02895.hp2 HG03139.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.589-2038C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950262 | |||||||
| chr2:147950397 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.588+1976T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950397 | |||||||
| chr2:147950541 | T | C | 46 | a0001c0001t0001g0248 a0001c0001t0012g0040 a0001c0001t0012g0041 others(43): Show |
48 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.588+1832A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950541 | |||||||
| chr2:147950563 | G | C | 2 | a0002c0002t0002g0111 a0002c0002t0031g0110 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.588+1810C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950563 | |||||||
| chr2:147950564 | A | G | 2 | a0001c0001t0021g0177 a0001c0001t0021g0218 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.588+1809T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950564 | |||||||
| chr2:147950764 | C | CA | 156 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(153): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.588+1608dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950764 | |||||||
| chr2:147950939 | G | A | 1 | a0003c0003t0011g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.588+1434C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950939 | |||||||
| chr2:147950943 | A | AT | 87 | a0001c0001t0060g0201 a0002c0002t0002g0003 a0002c0002t0002g0005 others(84): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.588+1429dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950943 | |||||||
| chr2:147950993 | G | A | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.588+1380C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950993 | |||||||
| chr2:147951088 | T | C | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.588+1285A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951088 | |||||||
| chr2:147951277 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.588+1096G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951277 | |||||||
| chr2:147951310 | T | G | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.588+1063A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951310 | |||||||
| chr2:147951547 | G | A | 5 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(2): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+826C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951547 | |||||||
| chr2:147951583 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.588+790A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951583 | |||||||
| chr2:147951615 | G | A | 1 | a0001c0001t0005g0289 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.588+758C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951615 | |||||||
| chr2:147951801 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 |
3 | HG00544.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.588+572G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951801 | |||||||
| chr2:147952084 | A | G | 88 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(85): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.588+289T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147952084 | |||||||
| chr2:147952201 | C | T | 1 | a0001c0001t0041g0293 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.588+172G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147952201 | |||||||
| chr2:147952722 | C | T | 5 | a0001c0001t0003g0202 a0001c0001t0003g0204 a0001c0001t0003g0307 others(2): Show |
5 | NA18943.hp1 NA18985.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-198G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147952722 | |||||||
| chr2:147952792 | T | C | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.437-268A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147952792 | |||||||
| chr2:147952941 | G | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-417C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147952941 | |||||||
| chr2:147953159 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
6 | NA18960.hp2 NA18980.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-635T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953159 | |||||||
| chr2:147953170 | TA | T | 75 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(72): Show |
79 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.437-647delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953170 | |||||||
| chr2:147953237 | A | G | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.437-713T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953237 | |||||||
| chr2:147953275 | A | G | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-751T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953275 | |||||||
| chr2:147953403 | A | G | 1 | a0002c0002t0002g0044 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.437-879T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953403 | |||||||
| chr2:147953606 | G | T | 211 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(208): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.437-1082C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953606 | |||||||
| chr2:147954015 | G | T | 4 | a0002c0002t0002g0059 a0002c0002t0002g0096 a0002c0002t0002g0097 others(1): Show |
4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1332C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954015 | |||||||
| chr2:147954122 | A | C | 1 | a0002c0002t0029g0140 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.436+1225T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954122 | |||||||
| chr2:147954512 | C | A | 21 | a0001c0001t0006g0012 a0001c0001t0008g0154 a0001c0001t0008g0157 others(18): Show |
22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.436+835G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954512 | |||||||
| chr2:147954614 | T | C | 1 | a0002c0002t0013g0138 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.436+733A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954614 | |||||||
| chr2:147954667 | A | G | 1 | a0002c0002t0002g0081 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.436+680T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954667 | |||||||
| chr2:147954844 | T | A | 1 | a0001c0001t0003g0197 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.436+503A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954844 | |||||||
| chr2:147955250 | CT | C | 23 | a0002c0002t0004g0006 a0002c0002t0004g0045 a0002c0002t0004g0047 others(20): Show |
24 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.436+96delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147955250 | |||||||
| chr2:147955547 | A | G | 1 | a0002c0002t0013g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.388-152T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955547 | |||||||
| chr2:147955689 | G | A | 4 | a0002c0002t0002g0010 a0002c0002t0002g0093 a0002c0002t0002g0094 others(1): Show |
5 | HG01123.hp2 HG01517.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-294C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955689 | |||||||
| chr2:147955899 | T | C | 1 | a0001c0001t0001g0016 | 2 | NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.388-504A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955899 | |||||||
| chr2:147955919 | C | T | 2 | a0002c0002t0002g0111 a0002c0002t0031g0110 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.388-524G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955919 | |||||||
| chr2:147955930 | T | C | 1 | a0001c0001t0041g0293 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.388-535A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955930 | |||||||
| chr2:147955983 | C | A | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388-588G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955983 | |||||||
| chr2:147955984 | C | A | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388-589G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955984 | |||||||
| chr2:147956038 | G | T | 36 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(33): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.388-643C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956038 | |||||||
| chr2:147956085 | T | C | 10 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0158 others(7): Show |
10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.388-690A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956085 | |||||||
| chr2:147956097 | A | T | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.388-702T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956097 | |||||||
| chr2:147956268 | T | C | 1 | a0002c0002t0002g0104 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.388-873A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956268 | |||||||
| chr2:147956555 | A | T | 1 | a0002c0002t0002g0101 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.388-1160T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956555 | |||||||
| chr2:147956748 | C | T | 1 | a0001c0004t0006g0303 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.388-1353G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956748 | |||||||
| chr2:147956810 | T | C | 1 | a0002c0002t0002g0105 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.388-1415A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956810 | |||||||
| chr2:147956825 | A | G | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.388-1430T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956825 | |||||||
| chr2:147956833 | A | T | 1 | a0002c0002t0002g0106 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.388-1438T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956833 | |||||||
| chr2:147957156 | T | C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | HG01256.hp2 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+1142A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957156 | |||||||
| chr2:147957348 | T | G | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.387+950A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957348 | |||||||
| chr2:147957469 | T | C | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.387+829A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957469 | |||||||
| chr2:147957677 | G | A | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.387+621C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957677 | |||||||
| chr2:147957787 | C | T | 1 | a0002c0002t0002g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.387+511G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957787 | |||||||
| chr2:147958025 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.387+273A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147958025 | |||||||
| chr2:147958219 | C | T | 1 | a0002c0002t0013g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.387+79G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147958219 | |||||||
| chr2:147958406 | G | T | 1 | a0002c0002t0002g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.302-23C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958406 | |||||||
| chr2:147958482 | T | A | 5 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(2): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-99A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958482 | |||||||
| chr2:147958530 | G | T | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.302-147C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958530 | |||||||
| chr2:147958595 | A | C | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.301+196T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958595 | |||||||
| chr2:147958877 | A | C | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.226-11T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147958877 | |||||||
| chr2:147959141 | T | G | 21 | a0002c0002t0002g0005 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.226-275A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959141 | |||||||
| chr2:147959242 | T | C | 1 | a0001c0001t0050g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.226-376A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959242 | |||||||
| chr2:147959260 | C | G | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-394G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959260 | |||||||
| chr2:147959261 | C | T | 211 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(208): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.226-395G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959261 | |||||||
| chr2:147959361 | C | CT | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.226-496dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959361 | |||||||
| chr2:147959621 | A | G | 1 | a0002c0002t0004g0048 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.226-755T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959621 | |||||||
| chr2:147959911 | G | A | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-1045C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959911 | |||||||
| chr2:147959928 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-1062A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959928 | |||||||
| chr2:147960038 | C | T | 26 | a0002c0002t0004g0006 a0002c0002t0004g0045 a0002c0002t0004g0047 others(23): Show |
27 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.226-1172G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960038 | |||||||
| chr2:147960289 | A | G | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1423T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960289 | |||||||
| chr2:147960583 | C | T | 1 | a0002c0002t0002g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.226-1717G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960583 | |||||||
| chr2:147960617 | C | CTA | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.226-1752_226-1751i others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960617 | |||||||
| chr2:147960849 | G | A | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1983C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960849 | |||||||
| chr2:147960914 | T | A | 1 | a0002c0002t0002g0089 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.226-2048A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960914 | |||||||
| chr2:147960950 | T | A | 1 | a0002c0002t0004g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.226-2084A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960950 | |||||||
| chr2:147961118 | T | C | 6 | a0002c0002t0002g0009 a0002c0002t0002g0044 a0002c0002t0002g0072 others(3): Show |
7 | HG02083.hp1 NA18948.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-2252A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961118 | |||||||
| chr2:147961351 | T | C | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.226-2485A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961351 | |||||||
| chr2:147961438 | GA | G | 165 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(162): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.226-2573delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961438 | |||||||
| chr2:147961820 | C | T | 2 | a0002c0002t0004g0122 a0002c0002t0004g0123 |
2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.226-2954G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961820 | |||||||
| chr2:147961844 | T | C | 1 | a0001c0001t0007g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-2978A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961844 | |||||||
| chr2:147962235 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.226-3369T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962235 | |||||||
| chr2:147962534 | C | T | 9 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-3668G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962534 | |||||||
| chr2:147962618 | A | G | 203 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(200): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.226-3752T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962618 | |||||||
| chr2:147962704 | C | G | 1 | a0002c0002t0002g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.226-3838G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962704 | |||||||
| chr2:147962747 | G | A | 4 | a0001c0001t0001g0255 a0002c0002t0002g0073 a0002c0002t0002g0074 others(1): Show |
4 | HG01981.hp1 NA18969.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-3881C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962747 | |||||||
| chr2:147962778 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-3912G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962778 | |||||||
| chr2:147962869 | G | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-4003C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962869 | |||||||
| chr2:147962984 | G | T | 1 | a0001c0001t0054g0259 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.226-4118C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962984 | |||||||
| chr2:147963019 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4153G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963019 | |||||||
| chr2:147963100 | C | A | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-4234G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963100 | |||||||
| chr2:147963155 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4289G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963155 | |||||||
| chr2:147963276 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4410A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963276 | |||||||
| chr2:147963362 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.226-4496C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963362 | |||||||
| chr2:147963460 | T | A | 1 | a0002c0002t0002g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.226-4594A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963460 | |||||||
| chr2:147963465 | A | G | 1 | a0002c0002t0004g0130 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.226-4599T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963465 | |||||||
| chr2:147963537 | A | G | 2 | a0001c0001t0024g0229 a0001c0001t0024g0230 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.226-4671T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963537 | |||||||
| chr2:147963734 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-4868A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963734 | |||||||
| chr2:147963888 | T | C | 1 | a0001c0001t0012g0042 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.226-5022A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963888 | |||||||
| chr2:147963897 | C | A | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.226-5031G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963897 | |||||||
| chr2:147964165 | G | A | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-5299C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964165 | |||||||
| chr2:147964254 | A | G | 3 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0225 |
3 | HG00642.hp2 HG00741.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.226-5388T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964254 | |||||||
| chr2:147964301 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.226-5435A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964301 | |||||||
| chr2:147964415 | T | A | 1 | a0001c0001t0046g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226-5549A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964415 | |||||||
| chr2:147964714 | C | T | 36 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(33): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.226-5848G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964714 | |||||||
| chr2:147964863 | C | T | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226-5997G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964863 | |||||||
| chr2:147964875 | T | C | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226-6009A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964875 | |||||||
| chr2:147964905 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-6039C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964905 | |||||||
| chr2:147964956 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.226-6090T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964956 | |||||||
| chr2:147965037 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-6171G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965037 | |||||||
| chr2:147965308 | T | C | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.226-6442A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965308 | |||||||
| chr2:147965557 | A | C | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.226-6691T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965557 | |||||||
| chr2:147965596 | A | G | 30 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(27): Show |
33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.226-6730T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965596 | |||||||
| chr2:147965757 | G | A | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226-6891C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965757 | |||||||
| chr2:147965948 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.225+6791C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965948 | |||||||
| chr2:147966049 | T | A | 1 | a0002c0002t0002g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.225+6690A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966049 | |||||||
| chr2:147966050 | A | T | 3 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 |
3 | HG00408.hp1 NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.225+6689T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966050 | |||||||
| chr2:147966071 | GAACATTA others(13): Show |
G | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225+6648_225+6667d others(22): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966071 | |||||||
| chr2:147966340 | A | G | 1 | a0001c0001t0003g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.225+6399T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966340 | |||||||
| chr2:147966343 | T | C | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+6396A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966343 | |||||||
| chr2:147966600 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.225+6139G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966600 | |||||||
| chr2:147966696 | G | A | 1 | a0002c0002t0004g0127 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.225+6043C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966696 | |||||||
| chr2:147966787 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.225+5952A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966787 | |||||||
| chr2:147966845 | G | A | 2 | a0002c0002t0002g0074 a0002c0002t0002g0089 |
2 | NA18969.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.225+5894C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966845 | |||||||
| chr2:147966988 | A | G | 36 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(33): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.225+5751T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966988 | |||||||
| chr2:147966992 | T | C | 1 | a0002c0002t0040g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.225+5747A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966992 | |||||||
| chr2:147967102 | T | C | 36 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(33): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.225+5637A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967102 | |||||||
| chr2:147967288 | C | T | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225+5451G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967288 | |||||||
| chr2:147967449 | C | T | 8 | a0001c0001t0041g0293 a0003c0003t0011g0145 a0003c0003t0011g0296 others(5): Show |
8 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+5290G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967449 | |||||||
| chr2:147967559 | G | A | 1 | a0002c0002t0032g0113 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.225+5180C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967559 | |||||||
| chr2:147967591 | G | A | 1 | a0001c0001t0045g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.225+5148C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967591 | |||||||
| chr2:147967595 | A | G | 9 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+5144T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967595 | |||||||
| chr2:147967997 | A | G | 1 | a0001c0001t0003g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.225+4742T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967997 | |||||||
| chr2:147968002 | C | T | 1 | a0001c0001t0006g0013 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.225+4737G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968002 | |||||||
| chr2:147968171 | G | C | 7 | a0001c0001t0003g0202 a0001c0001t0003g0203 a0001c0001t0003g0204 others(4): Show |
7 | NA18943.hp1 NA18948.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+4568C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968171 | |||||||
| chr2:147968376 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225+4363A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968376 | |||||||
| chr2:147968680 | T | C | 9 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+4059A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968680 | |||||||
| chr2:147969021 | T | C | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+3718A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969021 | |||||||
| chr2:147969052 | G | A | 2 | a0001c0001t0019g0279 a0001c0001t0019g0280 |
2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.225+3687C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969052 | |||||||
| chr2:147969202 | A | T | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.225+3537T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969202 | |||||||
| chr2:147969257 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.225+3482T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969257 | |||||||
| chr2:147969406 | T | A | 1 | a0001c0001t0050g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.225+3333A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969406 | |||||||
| chr2:147969457 | C | T | 211 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(208): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.225+3282G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969457 | |||||||
| chr2:147969922 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.225+2817A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969922 | |||||||
| chr2:147970154 | CAT | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+2583_225+2584d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970154 | |||||||
| chr2:147970194 | A | G | 1 | a0005c0006t0037g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.225+2545T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970194 | |||||||
| chr2:147970225 | C | T | 5 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0024g0229 others(2): Show |
5 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+2514G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970225 | |||||||
| chr2:147970293 | A | T | 1 | a0002c0002t0002g0101 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2446T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970293 | |||||||
| chr2:147970423 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+2316A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970423 | |||||||
| chr2:147970589 | T | C | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.225+2150A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970589 | |||||||
| chr2:147970593 | T | C | 1 | a0002c0002t0002g0101 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2146A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970593 | |||||||
| chr2:147970615 | C | CA | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.225+2123dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970615 | |||||||
| chr2:147970627 | A | G | 1 | a0002c0002t0002g0101 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2112T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970627 | |||||||
| chr2:147970628 | G | A | 1 | a0002c0002t0002g0101 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2111C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970628 | |||||||
| chr2:147970628 | G | GA | 7 | a0001c0001t0001g0250 a0001c0001t0003g0192 a0001c0001t0005g0178 others(4): Show |
7 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+2110dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970628 | |||||||
| chr2:147970739 | T | C | 1 | a0001c0001t0003g0196 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.225+2000A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970739 | |||||||
| chr2:147970743 | A | T | 7 | a0002c0002t0002g0070 a0002c0002t0002g0075 a0002c0002t0002g0076 others(4): Show |
7 | HG00438.hp1 NA18943.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1996T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970743 | |||||||
| chr2:147970871 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.225+1868T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970871 | |||||||
| chr2:147971272 | AAT | A | 3 | a0001c0001t0003g0215 a0001c0001t0035g0115 a0001c0001t0057g0185 |
3 | HG01243.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.225+1465_225+1466d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971272 | |||||||
| chr2:147971409 | C | T | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225+1330G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971409 | |||||||
| chr2:147971469 | A | G | 1 | a0002c0002t0004g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.225+1270T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971469 | |||||||
| chr2:147971481 | T | C | 214 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(211): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.225+1258A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971481 | |||||||
| chr2:147971528 | T | C | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.225+1211A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971528 | |||||||
| chr2:147971533 | A | G | 1 | a0002c0002t0038g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225+1206T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971533 | |||||||
| chr2:147971922 | C | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(31): Show |
37 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.225+817G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971922 | |||||||
| chr2:147971957 | G | A | 1 | a0001c0001t0003g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.225+782C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971957 | |||||||
| chr2:147971998 | A | G | 2 | a0002c0002t0002g0081 a0002c0002t0002g0082 |
2 | NA18988.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.225+741T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971998 | |||||||
| chr2:147972040 | C | A | 1 | a0002c0002t0002g0101 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+699G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972040 | |||||||
| chr2:147972041 | A | C | 1 | a0002c0002t0002g0101 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+698T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972041 | |||||||
| chr2:147972178 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.225+561A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972178 | |||||||
| chr2:147972396 | T | G | 2 | a0001c0001t0005g0235 a0001c0001t0052g0208 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.225+343A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972396 | |||||||
| chr2:147972532 | T | G | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+207A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972532 | |||||||
| chr2:147972885 | T | C | 3 | a0002c0002t0002g0003 a0002c0002t0002g0068 a0002c0002t0002g0100 |
5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-56A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147972885 | |||||||
| chr2:147973058 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.135-229A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973058 | |||||||
| chr2:147973070 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.135-241G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973070 | |||||||
| chr2:147973305 | T | C | 1 | a0002c0002t0004g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.134+143A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973305 | |||||||
| chr2:147973337 | T | C | 2 | a0002c0002t0002g0081 a0002c0002t0002g0082 |
2 | NA18988.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.134+111A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973337 | |||||||
| chr2:147973683 | T | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(304): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.58-159A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973683 | |||||||
| chr2:147973684 | G | A | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.58-160C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973684 | |||||||
| chr2:147973686 | T | TA | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.58-163dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973686 | |||||||
| chr2:147973762 | G | A | 2 | a0002c0002t0002g0093 a0002c0002t0002g0094 |
2 | HG01123.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.58-238C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973762 | |||||||
| chr2:147973823 | C | T | 1 | a0001c0001t0019g0279 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-299G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973823 | |||||||
| chr2:147973826 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58-302C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973826 | |||||||
| chr2:147974103 | T | C | 1 | a0001c0001t0056g0214 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-579A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974103 | |||||||
| chr2:147974290 | G | T | 210 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(207): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.58-766C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974290 | |||||||
| chr2:147974372 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-848C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974372 | |||||||
| chr2:147974381 | C | T | 88 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(85): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.58-857G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974381 | |||||||
| chr2:147974385 | A | G | 1 | a0002c0002t0036g0107 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58-861T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974385 | |||||||
| chr2:147974466 | C | A | 8 | a0001c0001t0003g0215 a0001c0001t0014g0182 a0001c0001t0014g0183 others(5): Show |
8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-942G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974466 | |||||||
| chr2:147974530 | G | C | 83 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(80): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.58-1006C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974530 | |||||||
| chr2:147974591 | C | T | 12 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0158 others(9): Show |
12 | HG01167.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-1067G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974591 | |||||||
| chr2:147974628 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58-1104A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974628 | |||||||
| chr2:147974807 | T | TA | 11 | a0001c0001t0001g0228 a0001c0001t0001g0240 a0001c0001t0001g0251 others(8): Show |
11 | HG00099.hp1 HG00642.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.57+1094dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974807 | |||||||
| chr2:147974807 | TA | T | 129 | a0001c0001t0001g0253 a0001c0001t0003g0004 a0001c0001t0003g0015 others(126): Show |
138 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.57+1094delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974807 | |||||||
| chr2:147974841 | T | C | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.57+1061A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974841 | |||||||
| chr2:147974866 | G | A | 25 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(22): Show |
26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.57+1036C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974866 | |||||||
| chr2:147975010 | T | A | 7 | a0001c0001t0003g0202 a0001c0001t0003g0203 a0001c0001t0003g0204 others(4): Show |
7 | NA18943.hp1 NA18948.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+892A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975010 | |||||||
| chr2:147975134 | A | G | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.57+768T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975134 | |||||||
| chr2:147975141 | G | T | 4 | a0001c0001t0001g0231 a0001c0001t0001g0238 a0001c0001t0001g0242 others(1): Show |
4 | HG00609.hp2 NA18945.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+761C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975141 | |||||||
| chr2:147975194 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+708G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975194 | |||||||
| chr2:147975215 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+687C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975215 | |||||||
| chr2:147975354 | A | G | 1 | a0002c0002t0002g0070 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.57+548T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975354 | |||||||
| chr2:147975364 | A | G | 1 | a0001c0001t0003g0204 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57+538T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975364 | |||||||
| chr2:147975426 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.57+476A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975426 | |||||||
| chr2:147975506 | GA | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(169): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.57+395delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975506 | |||||||
| chr2:147975506 | GAAA | G | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.57+393_57+395delTT others(1): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975506 | |||||||
| chr2:147975624 | T | A | 1 | a0002c0002t0009g0083 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.57+278A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975624 | |||||||
| chr2:147975750 | C | T | 1 | a0002c0002t0038g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.57+152G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975750 | |||||||
| chr2:147975784 | T | C | 25 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(22): Show |
26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.57+118A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975784 | |||||||
| chr2:147975979 | T | TA | 219 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(216): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
splice_region_variant&intron_variant | LOW | c.-17-5dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147975979 | |||||||
| chr2:147976230 | G | A | 30 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(27): Show |
33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-255C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976230 | |||||||
| chr2:147976291 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-17-316T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976291 | |||||||
| chr2:147976475 | G | T | 1 | a0002c0002t0004g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-17-500C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976475 | |||||||
| chr2:147976659 | G | C | 1 | a0001c0001t0003g0193 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-17-684C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976659 | |||||||
| chr2:147976892 | A | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0239 |
3 | HG02071.hp2 NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-17-917T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976892 | |||||||
| chr2:147976912 | TCTC | T | 36 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(33): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-17-940_-17-938del others(3): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976912 | |||||||
| chr2:147977084 | C | T | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1109G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977084 | |||||||
| chr2:147977106 | T | C | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-17-1131A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977106 | |||||||
| chr2:147977120 | T | C | 1 | a0001c0001t0003g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-17-1145A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977120 | |||||||
| chr2:147977260 | T | C | 2 | a0002c0002t0004g0122 a0002c0002t0004g0123 |
2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-1285A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977260 | |||||||
| chr2:147977324 | G | C | 2 | a0002c0002t0004g0122 a0002c0002t0004g0123 |
2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-1349C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977324 | |||||||
| chr2:147977355 | T | G | 1 | a0001c0001t0012g0042 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-17-1380A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977355 | |||||||
| chr2:147977400 | T | C | 1 | a0005c0006t0037g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-1425A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977400 | |||||||
| chr2:147977680 | T | TA | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-1706dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977680 | |||||||
| chr2:147977819 | G | C | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-17-1844C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977819 | |||||||
| chr2:147977975 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-17-2000G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977975 | |||||||
| chr2:147978012 | G | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-2037C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978012 | |||||||
| chr2:147978105 | C | T | 1 | a0002c0002t0010g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-2130G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978105 | |||||||
| chr2:147978110 | C | T | 1 | a0005c0006t0037g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-2135G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978110 | |||||||
| chr2:147978243 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2268A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978243 | |||||||
| chr2:147978434 | A | G | 18 | a0001c0001t0003g0004 a0001c0001t0003g0147 a0001c0001t0003g0188 others(15): Show |
20 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17-2459T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978434 | |||||||
| chr2:147978464 | C | T | 1 | a0001c0001t0041g0293 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-17-2489G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978464 | |||||||
| chr2:147978553 | C | T | 1 | a0001c0001t0019g0279 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-17-2578G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978553 | |||||||
| chr2:147978570 | T | C | 1 | a0002c0002t0002g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-17-2595A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978570 | |||||||
| chr2:147978586 | G | A | 3 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 |
3 | NA18988.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-17-2611C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978586 | |||||||
| chr2:147978669 | G | A | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-17-2694C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978669 | |||||||
| chr2:147978796 | C | T | 1 | a0001c0001t0061g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-17-2821G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978796 | |||||||
| chr2:147979021 | A | G | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-3046T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979021 | |||||||
| chr2:147979038 | C | T | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-3063G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979038 | |||||||
| chr2:147979481 | A | G | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-3506T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979481 | |||||||
| chr2:147979484 | A | G | 5 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0175 others(2): Show |
5 | HG01167.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-3509T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979484 | |||||||
| chr2:147979714 | T | C | 7 | a0001c0001t0001g0146 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-3739A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979714 | |||||||
| chr2:147979756 | C | T | 119 | a0001c0001t0003g0190 a0002c0002t0002g0003 a0002c0002t0002g0005 others(116): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-17-3781G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979756 | |||||||
| chr2:147979790 | TGTTCAAC others(4): Show |
T | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-3826_-17-3816d others(13): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979790 | |||||||
| chr2:147979917 | G | C | 8 | a0001c0001t0006g0013 a0001c0001t0006g0152 a0001c0001t0006g0163 others(5): Show |
10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-3942C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979917 | |||||||
| chr2:147979992 | T | C | 1 | a0002c0002t0009g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-17-4017A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979992 | |||||||
| chr2:147980044 | C | G | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-4069G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980044 | |||||||
| chr2:147980260 | T | A | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-17-4285A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980260 | |||||||
| chr2:147980449 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-4474C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980449 | |||||||
| chr2:147980616 | C | T | 1 | a0002c0002t0009g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-17-4641G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980616 | |||||||
| chr2:147980958 | A | C | 2 | a0002c0002t0002g0036 a0002c0002t0002g0039 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17-4983T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980958 | |||||||
| chr2:147980965 | C | T | 1 | a0002c0002t0010g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-4990G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980965 | |||||||
| chr2:147981251 | T | C | 1 | a0001c0001t0003g0196 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-17-5276A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981251 | |||||||
| chr2:147981504 | G | C | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-5529C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981504 | |||||||
| chr2:147981546 | T | C | 8 | a0002c0002t0002g0008 a0002c0002t0002g0055 a0002c0002t0002g0057 others(5): Show |
9 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-5571A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981546 | |||||||
| chr2:147981552 | G | T | 2 | a0002c0002t0002g0084 a0002c0002t0002g0085 |
2 | NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-17-5577C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981552 | |||||||
| chr2:147981602 | C | A | 1 | a0002c0002t0004g0052 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-5627G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981602 | |||||||
| chr2:147981681 | A | G | 2 | a0001c0004t0006g0303 a0001c0004t0007g0150 |
2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-17-5706T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981681 | |||||||
| chr2:147981824 | G | A | 165 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(162): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-17-5849C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981824 | |||||||
| chr2:147982102 | A | G | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-6127T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982102 | |||||||
| chr2:147982160 | C | A | 1 | a0002c0002t0002g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-17-6185G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982160 | |||||||
| chr2:147982254 | G | C | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-17-6279C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982254 | |||||||
| chr2:147982911 | A | G | 1 | a0002c0002t0002g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-17-6936T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982911 | |||||||
| chr2:147982912 | T | C | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-6937A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982912 | |||||||
| chr2:147982941 | C | T | 5 | a0001c0001t0005g0178 a0001c0001t0005g0211 a0001c0001t0005g0235 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-6966G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982941 | |||||||
| chr2:147983018 | C | T | 128 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(125): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-17-7043G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983018 | |||||||
| chr2:147983264 | C | T | 25 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(22): Show |
26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17-7289G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983264 | |||||||
| chr2:147983485 | G | T | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-7510C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983485 | |||||||
| chr2:147983673 | A | C | 1 | a0001c0001t0008g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17-7698T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983673 | |||||||
| chr2:147984052 | C | T | 83 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(80): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-17-8077G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984052 | |||||||
| chr2:147984091 | A | G | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-8116T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984091 | |||||||
| chr2:147984192 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-17-8217G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984192 | |||||||
| chr2:147984205 | C | T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(31): Show |
37 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.-17-8230G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984205 | |||||||
| chr2:147984409 | T | C | 124 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(121): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-17-8434A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984409 | |||||||
| chr2:147984411 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-17-8436G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984411 | |||||||
| chr2:147984543 | G | A | 7 | a0001c0001t0006g0013 a0001c0001t0006g0152 a0001c0001t0006g0163 others(4): Show |
9 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-8568C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984543 | |||||||
| chr2:147984608 | C | T | 1 | a0001c0001t0045g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-17-8633G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984608 | |||||||
| chr2:147984612 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-17-8637T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984612 | |||||||
| chr2:147984745 | C | A | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-8770G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984745 | |||||||
| chr2:147984942 | A | G | 1 | a0002c0002t0002g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-17-8967T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984942 | |||||||
| chr2:147985035 | T | G | 1 | a0001c0001t0003g0202 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-17-9060A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985035 | |||||||
| chr2:147985263 | C | G | 1 | a0001c0001t0003g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-17-9288G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985263 | |||||||
| chr2:147985266 | G | A | 8 | a0001c0001t0006g0013 a0001c0001t0006g0152 a0001c0001t0006g0163 others(5): Show |
10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-9291C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985266 | |||||||
| chr2:147985271 | A | G | 25 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(22): Show |
26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17-9296T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985271 | |||||||
| chr2:147985333 | A | G | 10 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0158 others(7): Show |
10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-9358T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985333 | |||||||
| chr2:147985387 | G | A | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-9412C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985387 | |||||||
| chr2:147986504 | G | A | 8 | a0001c0001t0003g0215 a0001c0001t0014g0182 a0001c0001t0014g0183 others(5): Show |
8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-10529C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986504 | |||||||
| chr2:147986744 | C | T | 8 | a0001c0001t0041g0293 a0003c0003t0011g0145 a0003c0003t0011g0296 others(5): Show |
8 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-10769G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986744 | |||||||
| chr2:147986790 | T | C | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-10815A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TAC | 15 | a0001c0001t0001g0213 a0001c0001t0001g0231 a0001c0001t0001g0277 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-10817_-17-1081 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACAC | 67 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(64): Show |
72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-17-10819_-17-1081 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACACAC | 28 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0215 others(25): Show |
28 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17-10821_-17-1081 others(10): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACACACA others(1): Show |
88 | a0001c0001t0006g0012 a0001c0001t0012g0040 a0001c0001t0012g0041 others(85): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-10823_-17-1081 others(12): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACACACA others(3): Show |
15 | a0001c0001t0018g0174 a0001c0004t0006g0303 a0002c0002t0002g0010 others(12): Show |
16 | HG01168.hp2 HG01943.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-10825_-17-1081 others(14): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACACACA others(5): Show |
2 | a0001c0001t0007g0161 a0001c0001t0059g0165 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-17-10827_-17-1081 others(16): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACACACA others(7): Show |
2 | a0001c0001t0007g0162 a0001c0001t0050g0160 |
2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-17-10829_-17-1081 others(18): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACACACA others(9): Show |
4 | a0001c0001t0006g0152 a0001c0001t0006g0163 a0001c0001t0007g0014 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-10831_-17-1081 others(20): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986790 | T | TACACACA others(11): Show |
1 | a0001c0001t0006g0013 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-17-10833_-17-1081 others(22): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | |||||||
| chr2:147986814 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-17-10839G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986814 | |||||||
| chr2:147987186 | T | TA | 121 | a0001c0001t0001g0237 a0002c0002t0002g0003 a0002c0002t0002g0005 others(118): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-17-11212dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987186 | |||||||
| chr2:147987273 | T | TAC | 6 | a0002c0002t0002g0084 a0002c0002t0002g0085 a0002c0002t0002g0086 others(3): Show |
6 | NA18944.hp1 NA18986.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-11300_-17-1129 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987273 | |||||||
| chr2:147987289 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-11314A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987289 | |||||||
| chr2:147987357 | G | GAT | 4 | a0002c0002t0013g0037 a0002c0002t0015g0029 a0002c0002t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01884.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-11384_-17-1138 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987357 | |||||||
| chr2:147987366 | A | ATATG | 119 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(116): Show |
128 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-17-11392_-17-1139 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987366 | |||||||
| chr2:147987366 | A | ATG | 93 | a0001c0001t0001g0306 a0001c0001t0003g0004 a0001c0001t0003g0015 others(90): Show |
99 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.-17-11393_-17-1139 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987366 | |||||||
| chr2:147987368 | G | A | 2 | a0002c0002t0002g0036 a0002c0002t0002g0039 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17-11393C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987368 | |||||||
| chr2:147987382 | G | A | 126 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(123): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-17-11407C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987382 | |||||||
| chr2:147987382 | G | GTGTA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(62): Show |
75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-17-11408_-17-1140 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987382 | |||||||
| chr2:147987384 | A | G | 17 | a0001c0001t0001g0149 a0001c0001t0001g0210 a0001c0001t0001g0236 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-17-11409T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987384 | |||||||
| chr2:147987391 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(63): Show |
76 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-17-11416A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987391 | |||||||
| chr2:147987391 | T | TACAC | 8 | a0001c0001t0001g0149 a0001c0001t0001g0210 a0001c0001t0001g0256 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-11420_-17-1141 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987391 | |||||||
| chr2:147987393 | C | T | 19 | a0001c0001t0003g0215 a0001c0001t0005g0260 a0001c0001t0006g0012 others(16): Show |
20 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17-11418G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987393 | |||||||
| chr2:147987413 | A | C | 165 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(162): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-17-11438T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987413 | |||||||
| chr2:147987682 | G | A | 1 | a0002c0002t0004g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-17-11707C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987682 | |||||||
| chr2:147987830 | G | T | 4 | a0002c0002t0002g0059 a0002c0002t0002g0096 a0002c0002t0002g0097 others(1): Show |
4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-11855C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987830 | |||||||
| chr2:147987850 | G | A | 2 | a0001c0001t0047g0151 a0001c0001t0059g0165 |
2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-17-11875C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987850 | |||||||
| chr2:147987984 | C | T | 3 | a0001c0001t0026g0020 a0002c0002t0004g0122 a0002c0002t0004g0123 |
3 | HG02895.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-17-12009G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987984 | |||||||
| chr2:147988006 | T | G | 1 | a0001c0001t0001g0258 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-17-12031A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988006 | |||||||
| chr2:147988039 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-12064G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988039 | |||||||
| chr2:147988213 | C | T | 1 | a0001c0001t0012g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-17-12238G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988213 | |||||||
| chr2:147988224 | G | A | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-12249C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988224 | |||||||
| chr2:147988291 | A | C | 1 | a0001c0001t0001g0270 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-17-12316T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988291 | |||||||
| chr2:147988362 | A | AT | 14 | a0001c0001t0001g0268 a0001c0001t0005g0225 a0001c0001t0006g0012 others(11): Show |
15 | HG00642.hp2 HG02257.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-12388dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988362 | |||||||
| chr2:147988390 | C | T | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-12415G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988390 | |||||||
| chr2:147988510 | A | G | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-12535T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988510 | |||||||
| chr2:147988516 | C | T | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-12541G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988516 | |||||||
| chr2:147988524 | A | C | 1 | a0001c0001t0003g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-17-12549T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988524 | |||||||
| chr2:147988618 | G | A | 1 | a0002c0002t0009g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-17-12643C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988618 | |||||||
| chr2:147988789 | A | C | 1 | a0002c0002t0010g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-12814T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988789 | |||||||
| chr2:147988792 | C | CA | 113 | a0001c0001t0005g0178 a0001c0001t0005g0211 a0001c0001t0005g0235 others(110): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-17-12818dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988792 | |||||||
| chr2:147988792 | C | CAA | 21 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(18): Show |
22 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-12819_-17-1281 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988792 | |||||||
| chr2:147988792 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(102): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-17-12818delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988792 | |||||||
| chr2:147988987 | T | C | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-13012A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988987 | |||||||
| chr2:147989124 | A | G | 214 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(211): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.-17-13149T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989124 | |||||||
| chr2:147989223 | G | T | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-13248C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989223 | |||||||
| chr2:147989348 | C | T | 1 | a0002c0002t0031g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-17-13373G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989348 | |||||||
| chr2:147989406 | A | T | 1 | a0001c0004t0007g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-17-13431T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989406 | |||||||
| chr2:147989531 | C | T | 1 | a0001c0001t0048g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-13556G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989531 | |||||||
| chr2:147989639 | G | A | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-13664C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989639 | |||||||
| chr2:147989709 | A | C | 3 | a0001c0001t0005g0178 a0001c0001t0005g0211 a0001c0001t0021g0177 |
3 | HG00735.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-13734T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989709 | |||||||
| chr2:147989709 | AAAC | A | 21 | a0001c0001t0006g0012 a0001c0001t0008g0154 a0001c0001t0008g0157 others(18): Show |
22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-17-13737_-17-1373 others(7): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989709 | |||||||
| chr2:147989870 | A | G | 165 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(162): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-17-13895T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989870 | |||||||
| chr2:147990284 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-14309A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990284 | |||||||
| chr2:147990333 | G | A | 8 | a0001c0001t0006g0013 a0001c0001t0006g0152 a0001c0001t0006g0163 others(5): Show |
10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-14358C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990333 | |||||||
| chr2:147990409 | G | A | 36 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(33): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-17-14434C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990409 | |||||||
| chr2:147990677 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-14702C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990677 | |||||||
| chr2:147990696 | T | C | 1 | a0002c0002t0002g0009 | 2 | HG02083.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-17-14721A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990696 | |||||||
| chr2:147990736 | T | C | 1 | a0002c0002t0013g0037 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-17-14761A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990736 | |||||||
| chr2:147990787 | AGTTAAGT others(9): Show |
A | 1 | a0002c0002t0002g0089 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-17-14828_-17-1481 others(20): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990787 | |||||||
| chr2:147990819 | A | G | 1 | a0002c0002t0002g0044 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-17-14844T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990819 | |||||||
| chr2:147991008 | A | G | 88 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(85): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-15033T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991008 | |||||||
| chr2:147991050 | C | CT | 77 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(74): Show |
82 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.-17-15076dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991050 | |||||||
| chr2:147991050 | CT | C | 123 | a0001c0001t0001g0224 a0002c0002t0002g0003 a0002c0002t0002g0005 others(120): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-17-15076delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991050 | |||||||
| chr2:147991122 | A | G | 2 | a0002c0002t0002g0055 a0002c0002t0002g0069 |
2 | HG01943.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-17-15147T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991122 | |||||||
| chr2:147991150 | C | T | 1 | a0001c0001t0012g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-17-15175G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991150 | |||||||
| chr2:147991208 | C | T | 1 | a0002c0002t0033g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-17-15233G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991208 | |||||||
| chr2:147991239 | G | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-15264C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991239 | |||||||
| chr2:147991398 | G | A | 93 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(90): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-15423C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991398 | |||||||
| chr2:147991458 | T | C | 1 | a0002c0002t0002g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-17-15483A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991458 | |||||||
| chr2:147991490 | G | A | 3 | a0002c0002t0002g0003 a0002c0002t0002g0068 a0002c0002t0002g0100 |
5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-15515C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991490 | |||||||
| chr2:147991491 | A | G | 3 | a0002c0002t0002g0003 a0002c0002t0002g0068 a0002c0002t0002g0100 |
5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-15516T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991491 | |||||||
| chr2:147991551 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-17-15576C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991551 | |||||||
| chr2:147991698 | C | T | 1 | a0001c0001t0001g0016 | 2 | NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-17-15723G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991698 | |||||||
| chr2:147991766 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-17-15791A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991766 | |||||||
| chr2:147991790 | T | C | 5 | a0001c0001t0005g0178 a0001c0001t0005g0211 a0001c0001t0005g0235 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-15815A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991790 | |||||||
| chr2:147991824 | C | T | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-17-15849G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991824 | |||||||
| chr2:147992023 | C | T | 30 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(27): Show |
33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-16048G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992023 | |||||||
| chr2:147992254 | C | T | 37 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(34): Show |
40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17-16279G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992254 | |||||||
| chr2:147992401 | T | A | 5 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(2): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-16426A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992401 | |||||||
| chr2:147992481 | G | A | 1 | a0002c0002t0004g0052 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-16506C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992481 | |||||||
| chr2:147992537 | C | T | 1 | a0001c0001t0049g0172 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17-16562G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992537 | |||||||
| chr2:147992557 | GA | G | 5 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(2): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-16583delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992557 | |||||||
| chr2:147992575 | A | G | 1 | a0002c0002t0004g0099 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-17-16600T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992575 | |||||||
| chr2:147992675 | G | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-16700C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992675 | |||||||
| chr2:147992827 | C | T | 2 | a0001c0001t0018g0174 a0001c0001t0046g0171 |
2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-17-16852G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992827 | |||||||
| chr2:147992920 | C | T | 1 | a0001c0001t0050g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-17-16945G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992920 | |||||||
| chr2:147992933 | A | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-16958T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992933 | |||||||
| chr2:147992940 | T | C | 165 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(162): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-17-16965A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992940 | |||||||
| chr2:147993014 | T | C | 1 | a0002c0002t0036g0107 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-17-17039A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993014 | |||||||
| chr2:147993018 | C | T | 1 | a0001c0001t0051g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-17-17043G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993018 | |||||||
| chr2:147993197 | C | T | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-17222G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993197 | |||||||
| chr2:147993544 | C | T | 5 | a0001c0001t0005g0178 a0001c0001t0005g0211 a0001c0001t0005g0235 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-17569G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993544 | |||||||
| chr2:147993996 | T | G | 1 | a0002c0002t0002g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-17-18021A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993996 | |||||||
| chr2:147994043 | C | T | 88 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0008 others(85): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-18068G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994043 | |||||||
| chr2:147994233 | A | T | 1 | a0001c0001t0003g0188 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-17-18258T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994233 | |||||||
| chr2:147994322 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17-18347G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994322 | |||||||
| chr2:147994862 | T | A | 1 | a0001c0001t0042g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-18887A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994862 | |||||||
| chr2:147995048 | T | G | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-19073A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995048 | |||||||
| chr2:147995118 | CTGTAAAT others(121): Show |
C | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-19271_-17-1914 others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995118 | |||||||
| chr2:147995193 | C | T | 1 | a0001c0001t0003g0015 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-17-19218G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995193 | |||||||
| chr2:147995293 | T | C | 203 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(200): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-17-19318A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995293 | |||||||
| chr2:147995295 | C | T | 1 | a0001c0001t0059g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-19320G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995295 | |||||||
| chr2:147995363 | TGTGGGGC others(46): Show |
T | 1 | a0002c0002t0027g0067 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-17-19441_-17-1938 others(57): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995363 | |||||||
| chr2:147995417 | G | A | 8 | a0001c0001t0003g0215 a0001c0001t0014g0182 a0001c0001t0014g0183 others(5): Show |
8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-19442C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995417 | |||||||
| chr2:147995451 | C | T | 5 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(2): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-19476G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995451 | |||||||
| chr2:147995581 | C | G | 1 | a0001c0001t0047g0151 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-19606G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995581 | |||||||
| chr2:147995661 | C | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-19686G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995661 | |||||||
| chr2:147995751 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17-19776C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995751 | |||||||
| chr2:147995787 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-19812G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995787 | |||||||
| chr2:147995902 | A | T | 1 | a0002c0002t0002g0032 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-17-19927T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995902 | |||||||
| chr2:147995932 | A | G | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-19957T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995932 | |||||||
| chr2:147995948 | C | T | 1 | a0002c0002t0002g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-17-19973G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995948 | |||||||
| chr2:147995999 | C | CA | 39 | a0001c0001t0001g0263 a0001c0001t0001g0283 a0001c0001t0003g0203 others(36): Show |
40 | HG00099.hp2 HG00423.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17-20025dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995999 | |||||||
| chr2:147996008 | A | T | 1 | a0001c0001t0003g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-17-20033T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996008 | |||||||
| chr2:147996059 | C | T | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-20084G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996059 | |||||||
| chr2:147996212 | G | A | 3 | a0002c0002t0002g0028 a0002c0002t0002g0036 a0002c0002t0002g0039 |
3 | HG00323.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17-20237C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996212 | |||||||
| chr2:147996239 | A | C | 5 | a0001c0001t0003g0215 a0001c0001t0014g0183 a0001c0001t0014g0184 others(2): Show |
5 | HG01243.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-20264T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996239 | |||||||
| chr2:147996245 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-17-20270T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996245 | |||||||
| chr2:147996257 | T | C | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-17-20282A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996257 | |||||||
| chr2:147996330 | T | C | 1 | a0005c0006t0037g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-20355A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996330 | |||||||
| chr2:147996400 | C | T | 1 | a0001c0001t0023g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-17-20425G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996400 | |||||||
| chr2:147996417 | A | C | 10 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0158 others(7): Show |
10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-20442T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996417 | |||||||
| chr2:147996442 | C | T | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-20467G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996442 | |||||||
| chr2:147996637 | G | A | 35 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(32): Show |
38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-20662C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996637 | |||||||
| chr2:147996898 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-17-20923T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996898 | |||||||
| chr2:147997091 | T | A | 2 | a0002c0002t0004g0122 a0002c0002t0004g0123 |
2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-21116A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997091 | |||||||
| chr2:147997164 | A | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-21189T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997164 | |||||||
| chr2:147997256 | A | G | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-21281T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997256 | |||||||
| chr2:147997293 | T | G | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-21318A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997293 | |||||||
| chr2:147997368 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-17-21393T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997368 | |||||||
| chr2:147997392 | G | A | 1 | a0002c0002t0040g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-17-21417C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997392 | |||||||
| chr2:147997450 | T | A | 22 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(19): Show |
23 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-17-21475A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997450 | |||||||
| chr2:147997541 | A | C | 2 | a0002c0002t0002g0066 a0002c0002t0002g0098 |
2 | HG00741.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-17-21566T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997541 | |||||||
| chr2:147997668 | C | T | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-21693G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997668 | |||||||
| chr2:147997689 | C | T | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-21714G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997689 | |||||||
| chr2:147997820 | G | A | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-21845C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997820 | |||||||
| chr2:147997854 | G | A | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-21879C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997854 | |||||||
| chr2:147997857 | A | G | 1 | a0002c0002t0004g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-17-21882T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997857 | |||||||
| chr2:147997999 | C | A | 1 | a0004c0005t0001g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-17-22024G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997999 | |||||||
| chr2:147998028 | C | G | 21 | a0001c0001t0006g0012 a0001c0001t0008g0154 a0001c0001t0008g0157 others(18): Show |
22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-17-22053G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998028 | |||||||
| chr2:147998099 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-17-22124A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998099 | |||||||
| chr2:147998244 | GA | G | 203 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(200): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-17-22270delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998244 | |||||||
| chr2:147998272 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-22297G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998272 | |||||||
| chr2:147998503 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(29): Show |
35 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-18+22130T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998503 | |||||||
| chr2:147998731 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+21902A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998731 | |||||||
| chr2:147998753 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+21880A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998753 | |||||||
| chr2:147998754 | A | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+21879T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998754 | |||||||
| chr2:147998929 | C | T | 1 | a0001c0001t0055g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18+21704G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998929 | |||||||
| chr2:147999055 | G | A | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-18+21578C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999055 | |||||||
| chr2:147999099 | A | T | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+21534T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999099 | |||||||
| chr2:147999575 | A | G | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+21058T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999575 | |||||||
| chr2:147999874 | G | C | 2 | a0002c0002t0002g0010 a0002c0002t0002g0108 |
3 | HG02602.hp1 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-18+20759C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999874 | |||||||
| chr2:148000077 | A | C | 1 | a0001c0001t0001g0267 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-18+20556T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000077 | |||||||
| chr2:148000145 | G | T | 1 | a0001c0001t0018g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+20488C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000145 | |||||||
| chr2:148000162 | A | G | 4 | a0002c0002t0010g0119 a0002c0002t0010g0120 a0002c0002t0010g0121 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+20471T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000162 | |||||||
| chr2:148000255 | A | G | 33 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(30): Show |
36 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-18+20378T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000255 | |||||||
| chr2:148000301 | A | G | 125 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+20332T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000301 | |||||||
| chr2:148000303 | G | C | 4 | a0002c0002t0013g0037 a0002c0002t0015g0029 a0002c0002t0015g0030 others(1): Show |
4 | HG00140.hp1 HG01884.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+20330C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000303 | |||||||
| chr2:148000334 | C | A | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+20299G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000334 | |||||||
| chr2:148000583 | C | T | 1 | a0001c0001t0021g0218 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-18+20050G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000583 | |||||||
| chr2:148000623 | T | C | 7 | a0001c0001t0003g0215 a0001c0001t0014g0182 a0001c0001t0014g0183 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+20010A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000623 | |||||||
| chr2:148000910 | A | G | 89 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(86): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-18+19723T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000910 | |||||||
| chr2:148001066 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-18+19567C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001066 | |||||||
| chr2:148001363 | G | A | 1 | a0002c0002t0015g0031 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-18+19270C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001363 | |||||||
| chr2:148001418 | G | A | 1 | a0001c0001t0008g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+19215C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001418 | |||||||
| chr2:148001581 | G | A | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+19052C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001581 | |||||||
| chr2:148001675 | T | C | 2 | a0001c0001t0005g0285 a0001c0001t0053g0286 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-18+18958A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001675 | |||||||
| chr2:148001707 | G | C | 4 | a0002c0002t0002g0010 a0002c0002t0002g0093 a0002c0002t0002g0094 others(1): Show |
5 | HG01123.hp2 HG01517.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+18926C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001707 | |||||||
| chr2:148001779 | T | C | 89 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(86): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-18+18854A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001779 | |||||||
| chr2:148002008 | A | T | 1 | a0002c0002t0002g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-18+18625T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002008 | |||||||
| chr2:148002087 | A | G | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+18546T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002087 | |||||||
| chr2:148002138 | T | C | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+18495A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002138 | |||||||
| chr2:148002144 | C | T | 30 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(27): Show |
33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-18+18489G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002144 | |||||||
| chr2:148002330 | G | A | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+18303C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002330 | |||||||
| chr2:148002347 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+18286C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002347 | |||||||
| chr2:148002710 | A | G | 1 | a0002c0002t0002g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-18+17923T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002710 | |||||||
| chr2:148002721 | A | G | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+17912T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002721 | |||||||
| chr2:148002929 | A | G | 1 | a0001c0001t0012g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+17704T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002929 | |||||||
| chr2:148003049 | A | G | 1 | a0002c0002t0033g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18+17584T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003049 | |||||||
| chr2:148003057 | C | T | 125 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+17576G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003057 | |||||||
| chr2:148003058 | C | T | 125 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+17575G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003058 | |||||||
| chr2:148003084 | A | T | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+17549T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003084 | |||||||
| chr2:148003393 | A | C | 1 | a0001c0001t0003g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-18+17240T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003393 | |||||||
| chr2:148003400 | A | G | 1 | a0005c0006t0037g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-18+17233T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003400 | |||||||
| chr2:148003523 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-18+17110G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003523 | |||||||
| chr2:148003539 | C | T | 1 | a0002c0002t0004g0125 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-18+17094G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003539 | |||||||
| chr2:148003642 | A | G | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+16991T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003642 | |||||||
| chr2:148003644 | G | A | 1 | a0002c0002t0002g0095 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-18+16989C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003644 | |||||||
| chr2:148003756 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18+16877C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003756 | |||||||
| chr2:148003842 | T | C | 2 | a0002c0002t0002g0032 a0002c0002t0002g0033 |
2 | HG00280.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-18+16791A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003842 | |||||||
| chr2:148003989 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-18+16644A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003989 | |||||||
| chr2:148004132 | A | G | 2 | a0002c0002t0009g0062 a0002c0002t0009g0063 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-18+16501T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004132 | |||||||
| chr2:148004140 | C | T | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-18+16493G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004140 | |||||||
| chr2:148004180 | C | A | 2 | a0001c0001t0001g0288 a0001c0001t0005g0289 |
2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+16453G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004180 | |||||||
| chr2:148004182 | G | A | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+16451C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004182 | |||||||
| chr2:148004294 | G | A | 4 | a0002c0002t0002g0059 a0002c0002t0002g0096 a0002c0002t0002g0097 others(1): Show |
4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+16339C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004294 | |||||||
| chr2:148004344 | G | A | 1 | a0001c0001t0003g0204 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-18+16289C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004344 | |||||||
| chr2:148004344 | G | C | 3 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0225 |
3 | HG00642.hp2 HG00741.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-18+16289C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004344 | |||||||
| chr2:148004494 | T | C | 25 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(22): Show |
26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-18+16139A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004494 | |||||||
| chr2:148004514 | G | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+16119C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004514 | |||||||
| chr2:148004548 | G | T | 1 | a0001c0001t0041g0293 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-18+16085C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004548 | |||||||
| chr2:148004722 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+15911G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004722 | |||||||
| chr2:148004879 | T | C | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+15754A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004879 | |||||||
| chr2:148004999 | G | A | 125 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+15634C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004999 | |||||||
| chr2:148005201 | A | C | 2 | a0003c0003t0020g0298 a0003c0003t0020g0299 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-18+15432T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005201 | |||||||
| chr2:148005224 | C | T | 129 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-18+15409G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005224 | |||||||
| chr2:148005354 | A | T | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+15279T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005354 | |||||||
| chr2:148005586 | C | A | 2 | a0001c0001t0001g0266 a0001c0001t0062g0226 |
2 | NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-18+15047G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005586 | |||||||
| chr2:148005656 | C | CA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(89): Show |
99 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-18+14976dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | |||||||
| chr2:148005656 | C | CAA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0180 others(38): Show |
45 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-18+14975_-18+1497 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | |||||||
| chr2:148005656 | CA | C | 12 | a0001c0001t0041g0293 a0001c0001t0043g0294 a0002c0002t0004g0139 others(9): Show |
12 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+14976delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | |||||||
| chr2:148005656 | CAAAAAAA others(4): Show |
C | 2 | a0002c0002t0002g0061 a0002c0002t0002g0109 |
2 | HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-18+14966_-18+1497 others(15): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | |||||||
| chr2:148005656 | CAAAAAAA others(6): Show |
C | 1 | a0002c0002t0004g0060 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18+14964_-18+1497 others(17): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | |||||||
| chr2:148005671 | A | C | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+14962T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005671 | |||||||
| chr2:148005676 | A | C | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18+14957T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005676 | |||||||
| chr2:148005750 | G | A | 10 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(7): Show |
11 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+14883C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005750 | |||||||
| chr2:148005788 | C | A | 1 | a0001c0004t0007g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+14845G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005788 | |||||||
| chr2:148005898 | C | T | 1 | a0001c0001t0041g0293 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-18+14735G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005898 | |||||||
| chr2:148005900 | C | A | 10 | a0001c0001t0003g0202 a0001c0001t0003g0203 a0001c0001t0003g0204 others(7): Show |
10 | NA18943.hp1 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+14733G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005900 | |||||||
| chr2:148006040 | C | A | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+14593G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006040 | |||||||
| chr2:148006041 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0205 a0001c0001t0003g0223 |
5 | HG01255.hp1 HG01358.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+14592C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006041 | |||||||
| chr2:148006075 | G | A | 1 | a0002c0002t0002g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-18+14558C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006075 | |||||||
| chr2:148006106 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+14527C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006106 | |||||||
| chr2:148006203 | C | T | 2 | a0002c0002t0002g0111 a0002c0002t0031g0110 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-18+14430G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006203 | |||||||
| chr2:148006290 | T | A | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18+14343A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006290 | |||||||
| chr2:148006310 | C | CA | 211 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(208): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-18+14322_-18+1432 others(5): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006310 | |||||||
| chr2:148006312 | C | T | 8 | a0001c0001t0003g0215 a0001c0001t0014g0182 a0001c0001t0014g0183 others(5): Show |
8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+14321G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006312 | |||||||
| chr2:148006315 | A | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(95): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-18+14318T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006315 | |||||||
| chr2:148006461 | A | G | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+14172T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006461 | |||||||
| chr2:148006476 | G | A | 35 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(32): Show |
38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-18+14157C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006476 | |||||||
| chr2:148006576 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+14057A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006576 | |||||||
| chr2:148006634 | G | A | 2 | a0003c0003t0020g0298 a0003c0003t0020g0299 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-18+13999C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006634 | |||||||
| chr2:148006644 | C | T | 1 | a0002c0002t0031g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-18+13989G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006644 | |||||||
| chr2:148006762 | C | A | 25 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(22): Show |
26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-18+13871G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006762 | |||||||
| chr2:148006784 | G | C | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+13849C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006784 | |||||||
| chr2:148006891 | C | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+13742G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006891 | |||||||
| chr2:148006892 | C | G | 5 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(2): Show |
5 | HG00408.hp1 HG03486.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+13741G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006892 | |||||||
| chr2:148006929 | T | C | 9 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+13704A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006929 | |||||||
| chr2:148006986 | T | G | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18+13647A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006986 | |||||||
| chr2:148007145 | C | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-18+13488G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007145 | |||||||
| chr2:148007321 | C | T | 125 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+13312G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007321 | |||||||
| chr2:148007525 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+13108T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007525 | |||||||
| chr2:148007655 | T | G | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+12978A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007655 | |||||||
| chr2:148007857 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+12776T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007857 | |||||||
| chr2:148007927 | C | T | 90 | a0001c0001t0028g0090 a0001c0001t0062g0226 a0002c0002t0002g0003 others(87): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-18+12706G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007927 | |||||||
| chr2:148008022 | G | A | 2 | a0002c0002t0004g0122 a0002c0002t0004g0123 |
2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-18+12611C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008022 | |||||||
| chr2:148008092 | T | C | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+12541A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008092 | |||||||
| chr2:148008150 | A | C | 4 | a0001c0001t0001g0306 a0001c0001t0005g0206 a0001c0001t0005g0207 others(1): Show |
4 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+12483T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008150 | |||||||
| chr2:148008167 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0290 a0001c0001t0001g0291 |
4 | HG00558.hp1 NA18981.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+12466A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008167 | |||||||
| chr2:148008247 | A | T | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+12386T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008247 | |||||||
| chr2:148008253 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-18+12380T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008253 | |||||||
| chr2:148008315 | A | T | 203 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(200): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-18+12318T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008315 | |||||||
| chr2:148008439 | T | G | 1 | a0002c0002t0002g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18+12194A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008439 | |||||||
| chr2:148008510 | G | C | 22 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(19): Show |
23 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+12123C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008510 | |||||||
| chr2:148008519 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+12114A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008519 | |||||||
| chr2:148008530 | G | A | 1 | a0001c0001t0003g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-18+12103C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008530 | |||||||
| chr2:148008566 | A | G | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+12067T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008566 | |||||||
| chr2:148008842 | C | T | 1 | a0002c0002t0040g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-18+11791G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008842 | |||||||
| chr2:148008906 | C | T | 125 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+11727G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008906 | |||||||
| chr2:148009018 | G | A | 1 | a0003c0003t0011g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-18+11615C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009018 | |||||||
| chr2:148009054 | G | A | 1 | a0002c0002t0004g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-18+11579C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009054 | |||||||
| chr2:148009102 | A | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+11531T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009102 | |||||||
| chr2:148009249 | A | G | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18+11384T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009249 | |||||||
| chr2:148009347 | T | C | 1 | a0001c0001t0021g0218 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-18+11286A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009347 | |||||||
| chr2:148009522 | A | G | 22 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(19): Show |
23 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+11111T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009522 | |||||||
| chr2:148009657 | G | C | 1 | a0003c0003t0011g0301 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-18+10976C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009657 | |||||||
| chr2:148009887 | C | T | 2 | a0002c0002t0004g0060 a0002c0002t0004g0112 |
2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+10746G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009887 | |||||||
| chr2:148010103 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-18+10530G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010103 | |||||||
| chr2:148010177 | T | G | 1 | a0002c0002t0039g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+10456A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010177 | |||||||
| chr2:148010252 | G | T | 52 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(49): Show |
56 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18+10381C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010252 | |||||||
| chr2:148010321 | A | T | 1 | a0002c0002t0038g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-18+10312T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010321 | |||||||
| chr2:148010401 | T | C | 1 | a0002c0002t0004g0133 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-18+10232A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010401 | |||||||
| chr2:148010478 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0018g0173 a0001c0001t0018g0174 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+10155C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010478 | |||||||
| chr2:148010545 | T | C | 1 | a0002c0002t0002g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18+10088A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010545 | |||||||
| chr2:148010598 | C | T | 1 | a0001c0001t0012g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-18+10035G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010598 | |||||||
| chr2:148010604 | A | C | 1 | a0001c0001t0003g0187 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-18+10029T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010604 | |||||||
| chr2:148010848 | C | CT | 14 | a0001c0001t0003g0181 a0001c0001t0006g0013 a0001c0001t0006g0152 others(11): Show |
15 | HG01884.hp2 HG01978.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+9784dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010848 | |||||||
| chr2:148010848 | CT | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(98): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+9784delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010848 | |||||||
| chr2:148010848 | CTTTTTT | C | 21 | a0002c0002t0004g0006 a0002c0002t0004g0047 a0002c0002t0004g0048 others(18): Show |
22 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+9779_-18+9784d others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010848 | |||||||
| chr2:148010931 | C | T | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+9702G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010931 | |||||||
| chr2:148010932 | G | C | 1 | a0001c0001t0003g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-18+9701C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010932 | |||||||
| chr2:148010978 | G | A | 3 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 |
3 | NA18988.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-18+9655C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010978 | |||||||
| chr2:148011004 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9629A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011004 | |||||||
| chr2:148011019 | G | A | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9614C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011019 | |||||||
| chr2:148011117 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-18+9516G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011117 | |||||||
| chr2:148011160 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-18+9473G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011160 | |||||||
| chr2:148011304 | T | C | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+9329A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011304 | |||||||
| chr2:148011391 | G | C | 1 | a0002c0002t0002g0114 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+9242C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011391 | |||||||
| chr2:148011415 | A | G | 1 | a0002c0002t0034g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18+9218T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011415 | |||||||
| chr2:148011446 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+9187C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011446 | |||||||
| chr2:148011711 | AACCTAAA others(4): Show |
A | 1 | a0001c0001t0035g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+8911_-18+8921d others(13): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011711 | |||||||
| chr2:148011838 | A | T | 3 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 |
3 | HG00408.hp1 NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-18+8795T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011838 | |||||||
| chr2:148011962 | GAA | G | 2 | a0001c0001t0006g0012 a0001c0001t0047g0151 |
3 | HG02723.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-18+8669_-18+8670d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011962 | |||||||
| chr2:148011996 | T | C | 8 | a0001c0001t0041g0293 a0003c0003t0011g0145 a0003c0003t0011g0296 others(5): Show |
8 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+8637A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011996 | |||||||
| chr2:148012282 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-18+8351G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012282 | |||||||
| chr2:148012485 | C | A | 131 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(128): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-18+8148G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012485 | |||||||
| chr2:148012537 | T | C | 1 | a0002c0002t0002g0116 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-18+8096A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012537 | |||||||
| chr2:148012618 | A | G | 2 | a0001c0001t0005g0178 a0001c0001t0021g0177 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+8015T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012618 | |||||||
| chr2:148012663 | T | C | 2 | a0001c0001t0003g0295 a0001c0001t0043g0294 |
2 | NA18946.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-18+7970A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012663 | |||||||
| chr2:148012705 | G | T | 95 | a0001c0001t0028g0090 a0001c0001t0035g0115 a0002c0002t0002g0003 others(92): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-18+7928C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012705 | |||||||
| chr2:148012724 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+7909A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012724 | |||||||
| chr2:148012740 | C | T | 1 | a0001c0004t0007g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+7893G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012740 | |||||||
| chr2:148012839 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7794A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012839 | |||||||
| chr2:148012897 | T | C | 7 | a0003c0003t0011g0145 a0003c0003t0011g0296 a0003c0003t0011g0297 others(4): Show |
7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+7736A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012897 | |||||||
| chr2:148013071 | A | T | 1 | a0001c0001t0045g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18+7562T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013071 | |||||||
| chr2:148013091 | C | A | 1 | a0002c0002t0002g0135 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-18+7542G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013091 | |||||||
| chr2:148013248 | TA | T | 11 | a0002c0002t0002g0046 a0002c0002t0004g0006 a0002c0002t0004g0045 others(8): Show |
12 | HG00738.hp2 HG01175.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+7384delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013248 | |||||||
| chr2:148013262 | A | T | 1 | a0002c0002t0002g0044 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-18+7371T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013262 | |||||||
| chr2:148013368 | A | G | 30 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(27): Show |
33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-18+7265T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013368 | |||||||
| chr2:148013400 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+7233T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013400 | |||||||
| chr2:148013438 | G | A | 1 | a0002c0002t0004g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-18+7195C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013438 | |||||||
| chr2:148013483 | T | C | 1 | a0001c0004t0006g0303 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+7150A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013483 | |||||||
| chr2:148013860 | C | T | 3 | a0001c0001t0003g0147 a0001c0001t0003g0304 a0001c0001t0044g0148 |
3 | HG00733.hp2 HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-18+6773G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013860 | |||||||
| chr2:148013967 | T | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6666A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013967 | |||||||
| chr2:148013998 | G | A | 1 | a0001c0001t0003g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-18+6635C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013998 | |||||||
| chr2:148014122 | T | G | 126 | a0001c0001t0028g0090 a0001c0001t0035g0115 a0002c0002t0002g0003 others(123): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-18+6511A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014122 | |||||||
| chr2:148014194 | A | G | 21 | a0002c0002t0002g0005 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+6439T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014194 | |||||||
| chr2:148014399 | T | C | 1 | a0001c0004t0006g0303 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+6234A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014399 | |||||||
| chr2:148014622 | G | A | 1 | a0001c0001t0003g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18+6011C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014622 | |||||||
| chr2:148014640 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-18+5993T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014640 | |||||||
| chr2:148014686 | C | T | 2 | a0002c0002t0002g0137 a0002c0002t0039g0141 |
2 | HG03471.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-18+5947G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014686 | |||||||
| chr2:148014691 | ATAAAAAA others(4793): Show |
A | 1 | a0002c0002t0002g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-18+1142_-18+5941d others(2): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014691 | |||||||
| chr2:148014918 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-18+5715C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014918 | |||||||
| chr2:148014927 | T | C | 1 | a0001c0004t0006g0303 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+5706A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014927 | |||||||
| chr2:148014929 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-18+5704G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014929 | |||||||
| chr2:148015087 | AC | A | 4 | a0002c0002t0010g0119 a0002c0002t0010g0120 a0002c0002t0010g0121 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+5545delG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015087 | |||||||
| chr2:148015091 | C | T | 6 | a0002c0002t0002g0084 a0002c0002t0002g0085 a0002c0002t0002g0086 others(3): Show |
6 | NA18944.hp1 NA18986.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+5542G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015091 | |||||||
| chr2:148015201 | A | C | 2 | a0001c0001t0005g0260 a0001c0001t0054g0259 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-18+5432T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015201 | |||||||
| chr2:148015307 | A | AT | 48 | a0001c0001t0001g0019 a0001c0001t0001g0149 a0001c0001t0001g0244 others(45): Show |
50 | HG00673.hp2 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+5325dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015307 | |||||||
| chr2:148015307 | AT | A | 66 | a0001c0001t0001g0277 a0001c0001t0003g0004 a0001c0001t0003g0015 others(63): Show |
68 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-18+5325delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015307 | |||||||
| chr2:148015378 | G | A | 10 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0158 others(7): Show |
10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+5255C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015378 | |||||||
| chr2:148015440 | G | C | 1 | a0001c0001t0005g0225 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-18+5193C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015440 | |||||||
| chr2:148015469 | C | T | 4 | a0002c0002t0002g0059 a0002c0002t0002g0096 a0002c0002t0002g0097 others(1): Show |
4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+5164G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015469 | |||||||
| chr2:148015549 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0290 |
2 | NA18981.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-18+5084G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015549 | |||||||
| chr2:148015556 | C | T | 1 | a0001c0001t0003g0015 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-18+5077G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015556 | |||||||
| chr2:148015674 | C | CT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0268 a0001c0001t0001g0270 others(6): Show |
9 | HG02129.hp2 HG02155.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+4958dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015674 | |||||||
| chr2:148015674 | CT | C | 37 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0152 others(34): Show |
40 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18+4958delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015674 | |||||||
| chr2:148015742 | A | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 |
3 | HG00544.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-18+4891T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015742 | |||||||
| chr2:148015826 | T | C | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+4807A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015826 | |||||||
| chr2:148015849 | A | T | 1 | a0001c0001t0035g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+4784T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015849 | |||||||
| chr2:148015868 | G | A | 4 | a0002c0002t0010g0119 a0002c0002t0010g0120 a0002c0002t0010g0121 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+4765C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015868 | |||||||
| chr2:148015976 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-18+4657A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015976 | |||||||
| chr2:148016111 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0005g0289 |
2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+4522G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016111 | |||||||
| chr2:148016134 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-18+4499G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016134 | |||||||
| chr2:148016173 | C | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0248 |
2 | HG01496.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-18+4460G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016173 | |||||||
| chr2:148016258 | G | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+4375C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016258 | |||||||
| chr2:148016301 | A | T | 2 | a0001c0001t0019g0279 a0001c0001t0019g0280 |
2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-18+4332T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016301 | |||||||
| chr2:148016457 | G | C | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+4176C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016457 | |||||||
| chr2:148016622 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0005g0289 |
2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+4011G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016622 | |||||||
| chr2:148016752 | A | G | 4 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(1): Show |
4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3881T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016752 | |||||||
| chr2:148016783 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-18+3850C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016783 | |||||||
| chr2:148016868 | A | G | 10 | a0001c0001t0008g0154 a0001c0001t0008g0157 a0001c0001t0008g0158 others(7): Show |
10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+3765T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016868 | |||||||
| chr2:148017410 | G | C | 1 | a0001c0001t0022g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18+3223C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017410 | |||||||
| chr2:148017475 | C | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0263 |
2 | NA18942.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-18+3158G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017475 | |||||||
| chr2:148017539 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18+3094C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017539 | |||||||
| chr2:148017634 | T | C | 8 | a0001c0001t0006g0013 a0001c0001t0006g0152 a0001c0001t0006g0163 others(5): Show |
10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+2999A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017634 | |||||||
| chr2:148017674 | G | A | 1 | a0002c0002t0004g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-18+2959C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017674 | |||||||
| chr2:148018009 | G | A | 6 | a0002c0002t0010g0011 a0002c0002t0010g0119 a0002c0002t0010g0120 others(3): Show |
7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+2624C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018009 | |||||||
| chr2:148018198 | C | A | 21 | a0001c0001t0006g0012 a0001c0001t0008g0154 a0001c0001t0008g0157 others(18): Show |
22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18+2435G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018198 | |||||||
| chr2:148018311 | T | C | 1 | a0001c0004t0007g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+2322A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018311 | |||||||
| chr2:148018331 | A | C | 1 | a0002c0002t0004g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-18+2302T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018331 | |||||||
| chr2:148018368 | G | A | 35 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0147 others(32): Show |
38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-18+2265C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018368 | |||||||
| chr2:148018579 | TTATTATA others(1): Show |
T | 125 | a0001c0001t0028g0090 a0001c0001t0035g0115 a0002c0002t0002g0003 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+2046_-18+2053d others(10): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018579 | |||||||
| chr2:148018619 | G | A | 2 | a0001c0001t0019g0279 a0001c0001t0019g0280 |
2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-18+2014C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018619 | |||||||
| chr2:148018712 | G | C | 3 | a0001c0001t0016g0219 a0001c0001t0016g0220 a0001c0001t0016g0221 |
3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+1921C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018712 | |||||||
| chr2:148018869 | G | A | 125 | a0001c0001t0028g0090 a0001c0001t0035g0115 a0002c0002t0002g0003 others(122): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+1764C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018869 | |||||||
| chr2:148018988 | AT | A | 3 | a0001c0001t0005g0178 a0001c0001t0005g0211 a0001c0001t0021g0177 |
3 | HG00735.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+1644delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018988 | |||||||
| chr2:148019029 | G | A | 1 | a0001c0001t0003g0004 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+1604C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019029 | |||||||
| chr2:148019052 | AT | A | 93 | a0001c0001t0028g0090 a0002c0002t0002g0003 a0002c0002t0002g0005 others(90): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-18+1580delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019052 | |||||||
| chr2:148019207 | G | A | 1 | a0001c0001t0003g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18+1426C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019207 | |||||||
| chr2:148019224 | G | T | 1 | a0002c0002t0002g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-18+1409C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019224 | |||||||
| chr2:148019290 | A | C | 130 | a0001c0001t0012g0040 a0001c0001t0012g0041 a0001c0001t0012g0042 others(127): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+1343T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019290 | |||||||
| chr2:148019388 | G | A | 1 | a0002c0002t0004g0130 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-18+1245C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019388 | |||||||
| chr2:148019509 | T | C | 1 | a0002c0002t0013g0138 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-18+1124A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019509 | |||||||
| chr2:148019625 | G | T | 1 | a0003c0003t0011g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-18+1008C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019625 | |||||||
| chr2:148019746 | T | C | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+887A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019746 | |||||||
| chr2:148019808 | T | G | 1 | a0001c0001t0001g0306 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-18+825A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019808 | |||||||
| chr2:148019816 | T | TAAATCCT others(282): Show |
1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+816_-18+817ins others(289): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019816 | |||||||
| chr2:148019999 | G | A | 3 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 |
3 | NA18988.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-18+634C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019999 | |||||||
| chr2:148020100 | C | G | 1 | a0001c0001t0026g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+533G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020100 | |||||||
| chr2:148020278 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18+355C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020278 | |||||||
| chr2:148020471 | T | C | 1 | a0002c0002t0004g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-18+162A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020471 | |||||||
| chr2:148020474 | C | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-18+159G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020474 | |||||||
| chr2:148020497 | C | A | 1 | a0002c0002t0029g0140 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-18+136G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020497 | |||||||
| chr2:148020569 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-18+64G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020569 |