Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 745 |
| ensemblid | ENSG00000124920.14 |
| hgncid | 1181 |
| symbol | MYRF |
| name | myelin regulatory factor |
| refseq_nuc | NM_001127392.3 |
| refseq_prot | NP_001120864.1 |
| ensembl_nuc | ENST00000278836.10 |
| ensembl_prot | ENSP00000278836.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 61752636 |
| end | 61788518 |
| strand | + |
| ver | v1.2 |
| region | chr11:61752636-61788518 |
| region5000 | chr11:61747636-61793518 |
| regionname0 | MYRF_chr11_61752636_61788518 |
| regionname5000 | MYRF_chr11_61747636_61793518 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1151 | 317 | 92 | 60 | 108 | 14 | 41 | 74 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0002 | 0/0 | 1151 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0003 | 0/0 | 1151 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0004 | 0/0 | 1151 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0005 | 0/0 | 1151 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0006 | 0/0 | 1151 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0007 | 0/0 | 1151 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0008 | 0/0 | 1151 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0009 | 0/0 | 1151 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| a0010 | 0/0 | 1151 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | MEVVD others(1146): Show |
chr11 | 61747636 | 61793518 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3453 | 168 | 73 | 18 | 43 | 6 | 26 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0002 | 0/0 | 3453 | 121 | 13 | 29 | 62 | 8 | 9 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0003 | 0/0 | 3453 | 15 | 1 | 12 | 0 | 0 | 2 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0006 | 0/0 | 3453 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0007 | 0/0 | 3453 | 2 | 0 | 0 | 0 | 0 | 2 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0008 | 0/0 | 3453 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0009 | 0/0 | 3453 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0010 | 0/0 | 3453 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0017 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0018 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0019 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0001c0020 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0002c0004 | 0/0 | 3453 | 4 | 0 | 4 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0003c0005 | 0/0 | 3453 | 2 | 0 | 0 | 0 | 2 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0004c0016 | 0/0 | 3453 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0005c0021 | 0/0 | 3453 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0006c0014 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0007c0012 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0008c0015 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0009c0013 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 | ||
| a0010c0011 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | ATGGA others(3448): Show |
chr11 | 61747636 | 61793518 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5940 | 163 | 70 | 18 | 42 | 6 | 25 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0001t0003 | 0/0 | 5940 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0001t0006 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0001t0007 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0001t0008 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0002t0001 | 0/0 | 5940 | 114 | 13 | 29 | 55 | 8 | 9 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0002t0002 | 0/0 | 5940 | 5 | 0 | 0 | 5 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0002t0004 | 0/0 | 5940 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0003t0001 | 0/0 | 5940 | 15 | 1 | 12 | 0 | 0 | 2 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0006t0001 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0006t0005 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0007t0001 | 0/0 | 5940 | 2 | 0 | 0 | 0 | 0 | 2 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0008t0001 | 0/0 | 5940 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0009t0001 | 0/0 | 5940 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0010t0001 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0017t0001 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0018t0001 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0019t0001 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0001c0020t0001 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0002c0004t0001 | 0/0 | 5940 | 4 | 0 | 4 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0003c0005t0001 | 0/0 | 5940 | 2 | 0 | 0 | 0 | 2 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0004c0016t0001 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0005c0021t0001 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0006c0014t0001 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0007c0012t0001 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0008c0015t0001 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0009c0013t0001 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| a0010c0011t0001 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | GTAGC others(5935): Show |
chr11 | 61747636 | 61793518 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0003 | 0/0 | 8 | 5 | 2 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0006 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0004 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0006t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0006t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0007t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0007t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0008t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0009t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0010t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0017t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0018t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0019t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0001c0020t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0002c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0002c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0002c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0002c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0003c0005t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0004c0016t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0005c0021t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0006c0014t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0007c0012t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0008c0015t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0009c0013t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| a0010c0011t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0165 | EUR | GBR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0161 | EUR | GBR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00280 | hp2 | a0003 | c0005 | t0001 | g0025 | EUR | FIN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00323 | hp2 | a0003 | c0005 | t0001 | g0025 | EUR | FIN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0063 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00597 | hp1 | a0001 | c0008 | t0001 | g0069 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0174 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | CHS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00733 | hp1 | a0002 | c0004 | t0001 | g0030 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0233 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01168 | hp2 | a0004 | c0016 | t0001 | g0150 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0057 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01433 | hp2 | a0005 | c0021 | t0001 | g0117 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0239 | EUR | IBS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0240 | EUR | IBS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0059 | EUR | IBS | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01884 | hp2 | a0001 | c0019 | t0001 | g0242 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01975 | hp2 | a0001 | c0010 | t0001 | g0146 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01981 | hp2 | a0002 | c0004 | t0001 | g0215 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01993 | hp2 | a0002 | c0004 | t0001 | g0224 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02148 | hp1 | a0002 | c0004 | t0001 | g0221 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | CDX | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02523 | hp1 | a0001 | c0002 | t0004 | g0183 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0056 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02683 | hp2 | a0006 | c0014 | t0001 | g0013 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02698 | hp2 | a0001 | c0020 | t0001 | g0236 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0035 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03098 | hp2 | a0007 | c0012 | t0001 | g0038 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03130 | hp2 | a0008 | c0015 | t0001 | g0187 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03195 | hp1 | a0001 | c0009 | t0001 | g0098 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03239 | hp1 | a0001 | c0017 | t0001 | g0175 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0083 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0164 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0140 | SAS | PJL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0206 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03831 | hp2 | a0001 | c0007 | t0001 | g0081 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04115 | hp2 | a0001 | c0007 | t0001 | g0090 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18522 | hp2 | a0001 | c0009 | t0001 | g0050 | AFR | YRI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18952 | hp2 | a0001 | c0008 | t0001 | g0060 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18986 | hp1 | a0009 | c0013 | t0001 | g0235 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19062 | hp2 | a0010 | c0011 | t0001 | g0108 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19088 | hp2 | a0001 | c0018 | t0001 | g0014 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19240 | hp1 | a0001 | c0006 | t0005 | g0135 | AFR | YRI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ASW | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0228 | EUR | TSI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0202 | EUR | TSI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0054 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | USA | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | LWK | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0115 | REF | REF | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0153 | REF | REF | MYRF_chr11_61747636_61793518 | MYRF | chr11 | 61747636 | 61793518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61769289 | G | C | 1 | a0010 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.428G>C | p.Gly143Ala | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/27 | 537/5940 | 428/3456 | 143/1151 | chr11 | 61769289 | |||
| chr11:61770340 | G | C | 1 | a0007 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.555G>C | p.Leu185Phe | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 5/27 | 664/5940 | 555/3456 | 185/1151 | chr11 | 61770340 | |||
| chr11:61770410 | G | C | 1 | a0009 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.625G>C | p.Ala209Pro | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 5/27 | 734/5940 | 625/3456 | 209/1151 | chr11 | 61770410 | |||
| chr11:61771607 | C | T | 1 | a0005 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.848C>T | p.Thr283Ile | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 6/27 | 957/5940 | 848/3456 | 283/1151 | chr11 | 61771607 | |||
| chr11:61779416 | G | A | 1 | a0002 | 4 | HG00733.hp1 HG01981.hp2 HG01993.hp2 others(1): Show |
missense_variant | MODERATE | c.2167G>A | p.Ala723Thr | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 15/27 | 2276/5940 | 2167/3456 | 723/1151 | chr11 | 61779416 | |||
| chr11:61781324 | G | A | 1 | a0003 | 2 | HG00280.hp2 HG00323.hp2 |
missense_variant | MODERATE | c.2759G>A | p.Arg920His | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 21/27 | 2868/5940 | 2759/3456 | 920/1151 | chr11 | 61781324 | |||
| chr11:61781744 | G | A | 1 | a0006 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.2936G>A | p.Gly979Asp | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/27 | 3045/5940 | 2936/3456 | 979/1151 | chr11 | 61781744 | |||
| chr11:61783507 | T | C | 1 | a0008 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.3026T>C | p.Leu1009Pro | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 23/27 | 3135/5940 | 3026/3456 | 1009/1151 | chr11 | 61783507 | |||
| chr11:61784357 | A | G | 1 | a0004 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.3272A>G | p.Gln1091Arg | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/27 | 3381/5940 | 3272/3456 | 1091/1151 | chr11 | 61784357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61752774 | G | A | 1 | a0001c0010 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.30G>A | p.Leu10Leu | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/27 | 139/5940 | 30/3456 | 10/1151 | chr11 | 61752774 | |||
| chr11:61769290 | C | T | 1 | a0010c0011 | 1 | NA19062.hp2 | synonymous_variant | LOW | c.429C>T | p.Gly143Gly | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/27 | 538/5940 | 429/3456 | 143/1151 | chr11 | 61769290 | |||
| chr11:61771548 | C | G | 1 | a0001c0003 | 15 | HG00639.hp1 HG00642.hp1 HG00741.hp1 others(12): Show |
synonymous_variant | LOW | c.789C>G | p.Pro263Pro | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 6/27 | 898/5940 | 789/3456 | 263/1151 | chr11 | 61771548 | |||
| chr11:61774120 | C | T | 1 | a0001c0020 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.1269C>T | p.Leu423Leu | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/27 | 1378/5940 | 1269/3456 | 423/1151 | chr11 | 61774120 | |||
| chr11:61777428 | C | T | 1 | a0001c0019 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.1755C>T | p.His585His | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 12/27 | 1864/5940 | 1755/3456 | 585/1151 | chr11 | 61777428 | |||
| chr11:61777788 | A | C | 1 | a0001c0009 | 2 | HG03195.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1846A>C | p.Arg616Arg | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 13/27 | 1955/5940 | 1846/3456 | 616/1151 | chr11 | 61777788 | |||
| chr11:61778387 | C | T | 1 | a0001c0018 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.1911C>T | p.Ile637Ile | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 14/27 | 2020/5940 | 1911/3456 | 637/1151 | chr11 | 61778387 | |||
| chr11:61779292 | C | T | 1 | a0001c0017 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.2043C>T | p.Ala681Ala | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 15/27 | 2152/5940 | 2043/3456 | 681/1151 | chr11 | 61779292 | |||
| chr11:61783568 | C | T | 1 | a0001c0008 | 2 | HG00597.hp1 NA18952.hp2 |
synonymous_variant | LOW | c.3087C>T | p.Thr1029Thr | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 23/27 | 3196/5940 | 3087/3456 | 1029/1151 | chr11 | 61783568 | |||
| chr11:61783884 | T | C | 10 | a0001c0002 a0001c0006 a0001c0010 others(7): Show |
134 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(131): Show |
synonymous_variant | LOW | c.3153T>C | p.Ser1051Ser | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 24/27 | 3262/5940 | 3153/3456 | 1051/1151 | chr11 | 61783884 | |||
| chr11:61784292 | C | T | 1 | a0001c0007 | 2 | HG03831.hp2 HG04115.hp2 |
synonymous_variant | LOW | c.3207C>T | p.Pro1069Pro | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/27 | 3316/5940 | 3207/3456 | 1069/1151 | chr11 | 61784292 | |||
| chr11:61786092 | C | T | 1 | a0001c0006 | 2 | HG02717.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.3405C>T | p.Leu1135Leu | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 3514/5940 | 3405/3456 | 1135/1151 | chr11 | 61786092 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61786357 | C | T | 1 | a0001c0001t0008 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 214 | chr11 | 61786357 | ||||||
| chr11:61786690 | G | C | 1 | a0001c0006t0005 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 547 | chr11 | 61786690 | ||||||
| chr11:61786868 | A | G | 1 | a0001c0002t0002 | 5 | HG00408.hp1 HG00673.hp1 NA18999.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*725A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 725 | chr11 | 61786868 | ||||||
| chr11:61787702 | G | A | 2 | a0001c0001t0003 a0001c0001t0006 |
3 | HG02258.hp2 HG03041.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1559G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 1559 | chr11 | 61787702 | ||||||
| chr11:61787866 | C | T | 1 | a0001c0001t0003 | 2 | HG03041.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1723C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 1723 | chr11 | 61787866 | ||||||
| chr11:61788321 | T | C | 1 | a0001c0002t0004 | 2 | HG00423.hp2 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2178T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 2178 | chr11 | 61788321 | ||||||
| chr11:61788491 | A | T | 1 | a0001c0001t0007 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2348A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 27/27 | 2348 | chr11 | 61788491 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61752953 | C | A | 1 | a0001c0006t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46+163C>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61752953 | |||||||
| chr11:61753068 | G | A | 1 | a0001c0002t0001g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.46+278G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753068 | |||||||
| chr11:61753141 | TG | T | 15 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.46+352delG | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753141 | |||||||
| chr11:61753196 | T | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(63): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.46+406T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753196 | |||||||
| chr11:61753210 | C | T | 1 | a0001c0002t0001g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.46+420C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753210 | |||||||
| chr11:61753553 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.46+763C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753553 | |||||||
| chr11:61753597 | C | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
8 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.46+807C>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753597 | |||||||
| chr11:61753846 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(74): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.46+1056G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753846 | |||||||
| chr11:61753974 | C | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.46+1184C>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61753974 | |||||||
| chr11:61754030 | G | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0077 others(14): Show |
21 | HG00544.hp2 HG00673.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.46+1240G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61754030 | |||||||
| chr11:61754149 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.46+1359G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61754149 | |||||||
| chr11:61754189 | A | T | 1 | a0001c0006t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46+1399A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61754189 | |||||||
| chr11:61754435 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0241 a0001c0001t0001g0243 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+1645C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61754435 | |||||||
| chr11:61754699 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46+1909G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61754699 | |||||||
| chr11:61754885 | C | G | 2 | a0001c0002t0001g0239 a0001c0002t0001g0240 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.46+2095C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61754885 | |||||||
| chr11:61755120 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.46+2330G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61755120 | |||||||
| chr11:61755219 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.46+2429G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61755219 | |||||||
| chr11:61755313 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46+2523G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61755313 | |||||||
| chr11:61755487 | G | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0077 others(14): Show |
21 | HG00544.hp2 HG00673.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.46+2697G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61755487 | |||||||
| chr11:61755586 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+2796C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61755586 | |||||||
| chr11:61755828 | GA | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.46+3039delA | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61755828 | |||||||
| chr11:61755975 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0017 others(3): Show |
7 | HG02258.hp2 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+3185G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61755975 | |||||||
| chr11:61756145 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.46+3355A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756145 | |||||||
| chr11:61756263 | C | T | 63 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0028 others(60): Show |
83 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.46+3473C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756263 | |||||||
| chr11:61756397 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0006t0005g0135 |
3 | HG02886.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.46+3607G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756397 | |||||||
| chr11:61756545 | G | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.46+3755G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756545 | |||||||
| chr11:61756639 | T | C | 21 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0077 others(18): Show |
25 | HG00544.hp2 HG00673.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.46+3849T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756639 | |||||||
| chr11:61756647 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.46+3857G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756647 | |||||||
| chr11:61756684 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.46+3894C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756684 | |||||||
| chr11:61756700 | C | T | 1 | a0008c0015t0001g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46+3910C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756700 | |||||||
| chr11:61756894 | A | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(73): Show |
100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.46+4104A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756894 | |||||||
| chr11:61756894 | A | G | 2 | a0001c0001t0001g0132 a0001c0002t0001g0186 |
2 | HG03209.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.46+4104A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61756894 | |||||||
| chr11:61757035 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(49): Show |
83 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.46+4245T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61757035 | |||||||
| chr11:61757362 | A | T | 1 | a0001c0002t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.46+4572A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61757362 | |||||||
| chr11:61757502 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.46+4712G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61757502 | |||||||
| chr11:61757548 | G | A | 9 | a0001c0001t0001g0055 a0001c0002t0001g0051 a0001c0003t0001g0004 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.46+4758G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61757548 | |||||||
| chr11:61757574 | G | T | 2 | a0001c0002t0001g0186 a0001c0002t0004g0183 |
2 | HG02523.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.46+4784G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61757574 | |||||||
| chr11:61757666 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+4876G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61757666 | |||||||
| chr11:61757975 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.46+5185C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61757975 | |||||||
| chr11:61758092 | AG | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(150): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.46+5309delG | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr11 | 61758092 | ||||||
| chr11:61758138 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.46+5348G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758138 | |||||||
| chr11:61758255 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.46+5465A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758255 | |||||||
| chr11:61758258 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(88): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.46+5468G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758258 | |||||||
| chr11:61758345 | C | T | 27 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0077 others(24): Show |
32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.46+5555C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758345 | |||||||
| chr11:61758349 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(238): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.46+5559T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758349 | |||||||
| chr11:61758450 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.46+5660C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758450 | |||||||
| chr11:61758542 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.46+5752T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758542 | |||||||
| chr11:61758578 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.46+5788G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758578 | |||||||
| chr11:61758599 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.46+5809T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758599 | |||||||
| chr11:61758760 | G | C | 1 | a0004c0016t0001g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.46+5970G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758760 | |||||||
| chr11:61758799 | T | C | 1 | a0001c0009t0001g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.46+6009T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758799 | |||||||
| chr11:61758898 | G | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.46+6108G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758898 | |||||||
| chr11:61758909 | G | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0017 others(3): Show |
7 | HG02258.hp2 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+6119G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61758909 | |||||||
| chr11:61759001 | T | C | 1 | a0001c0002t0001g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.46+6211T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759001 | |||||||
| chr11:61759074 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0130 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.46+6284G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759074 | |||||||
| chr11:61759084 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(151): Show |
219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.46+6294G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759084 | |||||||
| chr11:61759208 | A | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0241 a0001c0001t0001g0243 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.47-6417A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759208 | |||||||
| chr11:61759464 | G | A | 1 | a0001c0009t0001g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.47-6161G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759464 | |||||||
| chr11:61759503 | C | G | 1 | a0008c0015t0001g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.47-6122C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759503 | |||||||
| chr11:61759651 | C | T | 57 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0028 others(54): Show |
76 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.47-5974C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759651 | |||||||
| chr11:61759655 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.47-5970G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759655 | |||||||
| chr11:61759723 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.47-5902C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759723 | |||||||
| chr11:61759794 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(152): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.47-5831G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61759794 | |||||||
| chr11:61760038 | G | T | 1 | a0001c0002t0001g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.47-5587G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760038 | |||||||
| chr11:61760161 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.47-5464G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760161 | |||||||
| chr11:61760238 | A | T | 1 | a0001c0002t0001g0228 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.47-5387A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760238 | |||||||
| chr11:61760239 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.47-5386T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760239 | |||||||
| chr11:61760455 | C | T | 59 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0027 others(56): Show |
69 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.47-5170C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760455 | |||||||
| chr11:61760629 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.47-4996T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760629 | |||||||
| chr11:61760821 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.47-4804T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760821 | |||||||
| chr11:61760834 | C | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0033 others(40): Show |
59 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.47-4791C>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61760834 | |||||||
| chr11:61761007 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.47-4618G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761007 | |||||||
| chr11:61761081 | T | C | 1 | a0001c0006t0005g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.47-4544T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761081 | |||||||
| chr11:61761176 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.47-4449C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761176 | |||||||
| chr11:61761184 | TC | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
6 | HG01884.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-4438delC | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr11 | 61761184 | ||||||
| chr11:61761259 | T | G | 1 | a0001c0002t0001g0147 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.47-4366T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761259 | |||||||
| chr11:61761259 | T | TG | 44 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0074 others(41): Show |
52 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.47-4355dupG | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr11 | 61761259 | ||||||
| chr11:61761259 | T | TGG | 72 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(69): Show |
95 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.47-4356_47-4355dup others(2): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr11 | 61761259 | ||||||
| chr11:61761259 | T | TGGG | 25 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0001g0094 others(22): Show |
25 | HG00140.hp1 HG00597.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.47-4357_47-4355dup others(3): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr11 | 61761259 | ||||||
| chr11:61761342 | C | T | 56 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0079 others(53): Show |
65 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.47-4283C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761342 | |||||||
| chr11:61761414 | A | G | 1 | a0001c0002t0001g0216 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.47-4211A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761414 | |||||||
| chr11:61761422 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.47-4203G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761422 | |||||||
| chr11:61761438 | G | A | 2 | a0001c0002t0001g0196 a0001c0002t0001g0197 |
2 | HG01081.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.47-4187G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761438 | |||||||
| chr11:61761479 | G | A | 7 | a0001c0001t0001g0042 a0001c0002t0001g0043 a0001c0002t0001g0044 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-4146G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761479 | |||||||
| chr11:61761480 | G | A | 1 | a0008c0015t0001g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.47-4145G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761480 | |||||||
| chr11:61761795 | T | G | 59 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0027 others(56): Show |
69 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.47-3830T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761795 | |||||||
| chr11:61761978 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.47-3647A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61761978 | |||||||
| chr11:61762184 | G | C | 1 | a0001c0002t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.47-3441G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762184 | |||||||
| chr11:61762204 | G | A | 1 | a0001c0002t0002g0198 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.47-3421G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762204 | |||||||
| chr11:61762358 | A | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.47-3267A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762358 | |||||||
| chr11:61762377 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.47-3248G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762377 | |||||||
| chr11:61762391 | T | TGGGCAGC others(3): Show |
1 | a0001c0001t0006g0037 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.47-3223_47-3214dup others(10): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr11 | 61762391 | ||||||
| chr11:61762415 | C | T | 1 | a0002c0004t0001g0215 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.47-3210C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762415 | |||||||
| chr11:61762494 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
5 | HG01884.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-3131C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762494 | |||||||
| chr11:61762604 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0091 a0001c0001t0001g0241 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.47-3021G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762604 | |||||||
| chr11:61762702 | C | T | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.47-2923C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762702 | |||||||
| chr11:61762703 | C | T | 1 | a0001c0002t0001g0165 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.47-2922C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762703 | |||||||
| chr11:61762710 | C | T | 1 | a0001c0002t0001g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.47-2915C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762710 | |||||||
| chr11:61762859 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0016 others(78): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.47-2766G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762859 | |||||||
| chr11:61762923 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.47-2702C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762923 | |||||||
| chr11:61762983 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0092 others(12): Show |
17 | HG01884.hp1 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.47-2642G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61762983 | |||||||
| chr11:61763028 | A | G | 3 | a0001c0002t0001g0164 a0001c0002t0001g0166 a0001c0002t0001g0167 |
3 | HG00741.hp2 HG01167.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.47-2597A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763028 | |||||||
| chr11:61763041 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.47-2584G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763041 | |||||||
| chr11:61763134 | G | A | 1 | a0001c0006t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.47-2491G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763134 | |||||||
| chr11:61763189 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.47-2436T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763189 | |||||||
| chr11:61763229 | G | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0100 a0008c0015t0001g0187 |
4 | HG02896.hp1 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-2396G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763229 | |||||||
| chr11:61763244 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(237): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.47-2381A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763244 | |||||||
| chr11:61763282 | G | A | 1 | a0004c0016t0001g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.47-2343G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763282 | |||||||
| chr11:61763293 | T | C | 2 | a0001c0001t0001g0136 a0001c0006t0005g0135 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.47-2332T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763293 | |||||||
| chr11:61763365 | C | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(105): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.47-2260C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763365 | |||||||
| chr11:61763647 | T | G | 1 | a0001c0002t0001g0195 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.47-1978T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763647 | |||||||
| chr11:61763737 | C | T | 1 | a0001c0002t0001g0226 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.47-1888C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763737 | |||||||
| chr11:61763871 | A | C | 2 | a0001c0001t0001g0181 a0001c0009t0001g0098 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.47-1754A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763871 | |||||||
| chr11:61763955 | T | G | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.47-1670T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763955 | |||||||
| chr11:61763971 | A | G | 73 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(70): Show |
86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.47-1654A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61763971 | |||||||
| chr11:61764038 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.47-1587C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764038 | |||||||
| chr11:61764056 | C | T | 6 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(3): Show |
6 | HG01109.hp1 HG02257.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-1569C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764056 | |||||||
| chr11:61764067 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47-1558G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764067 | |||||||
| chr11:61764319 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
6 | HG01884.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-1306C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764319 | |||||||
| chr11:61764338 | A | G | 1 | a0001c0002t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.47-1287A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764338 | |||||||
| chr11:61764385 | A | T | 1 | a0001c0002t0001g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.47-1240A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764385 | |||||||
| chr11:61764417 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.47-1208A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764417 | |||||||
| chr11:61764442 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.47-1183G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764442 | |||||||
| chr11:61764514 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.47-1111G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764514 | |||||||
| chr11:61764519 | A | G | 71 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(68): Show |
84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.47-1106A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764519 | |||||||
| chr11:61764577 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0132 a0001c0001t0001g0182 others(3): Show |
7 | HG02717.hp1 HG03041.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.47-1048C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764577 | |||||||
| chr11:61764660 | C | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0084 |
4 | HG00544.hp2 HG02040.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-965C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764660 | |||||||
| chr11:61764728 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(115): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.47-897C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764728 | |||||||
| chr11:61764806 | G | A | 1 | a0001c0001t0007g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.47-819G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764806 | |||||||
| chr11:61764933 | G | A | 1 | a0001c0002t0001g0218 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.47-692G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61764933 | |||||||
| chr11:61765033 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47-592A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61765033 | |||||||
| chr11:61765301 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.47-324A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61765301 | |||||||
| chr11:61765421 | G | C | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.47-204G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61765421 | |||||||
| chr11:61765422 | C | G | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.47-203C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61765422 | |||||||
| chr11:61765500 | G | C | 1 | a0001c0009t0001g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.47-125G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 1/26 | chr11 | 61765500 | |||||||
| chr11:61765742 | C | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0212 |
2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.134+30C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 2/26 | chr11 | 61765742 | |||||||
| chr11:61766316 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.398+95T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766316 | |||||||
| chr11:61766325 | A | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(28): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.398+104A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766325 | |||||||
| chr11:61766428 | A | G | 2 | a0001c0001t0001g0181 a0001c0009t0001g0098 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.398+207A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766428 | |||||||
| chr11:61766436 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(24): Show |
38 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.398+215T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766436 | |||||||
| chr11:61766441 | A | G | 1 | a0001c0002t0001g0197 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.398+220A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766441 | |||||||
| chr11:61766461 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.398+240C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766461 | |||||||
| chr11:61766482 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0095 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.398+261G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766482 | |||||||
| chr11:61766496 | A | T | 2 | a0001c0001t0001g0181 a0001c0009t0001g0098 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.398+275A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766496 | |||||||
| chr11:61766538 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(112): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.398+317C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766538 | |||||||
| chr11:61766837 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.398+616C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766837 | |||||||
| chr11:61766856 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0132 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.398+635G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61766856 | |||||||
| chr11:61767058 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.398+837G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767058 | |||||||
| chr11:61767123 | G | A | 1 | a0001c0002t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.398+902G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767123 | |||||||
| chr11:61767400 | A | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(193): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.398+1179A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767400 | |||||||
| chr11:61767407 | G | A | 1 | a0001c0003t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.398+1186G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767407 | |||||||
| chr11:61767566 | C | G | 2 | a0001c0001t0001g0181 a0001c0009t0001g0098 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.398+1345C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767566 | |||||||
| chr11:61767623 | C | G | 1 | a0004c0016t0001g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.398+1402C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767623 | |||||||
| chr11:61767674 | A | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(24): Show |
38 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.398+1453A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767674 | |||||||
| chr11:61767703 | A | T | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.398+1482A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767703 | |||||||
| chr11:61767769 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.399-1491A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767769 | |||||||
| chr11:61767779 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.399-1481A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61767779 | |||||||
| chr11:61767813 | C | CA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
157 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.399-1425dupA | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr11 | 61767813 | ||||||
| chr11:61767813 | C | CAA | 78 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0055 others(75): Show |
96 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.399-1426_399-1425d others(4): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr11 | 61767813 | ||||||
| chr11:61767813 | C | CAAA | 11 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0092 others(8): Show |
12 | HG00408.hp1 HG00408.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.399-1427_399-1425d others(5): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr11 | 61767813 | ||||||
| chr11:61768117 | C | CA | 6 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0181 others(3): Show |
6 | HG00408.hp1 HG00408.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.399-1127dupA | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr11 | 61768117 | ||||||
| chr11:61768117 | CA | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0093 others(10): Show |
14 | HG01069.hp1 HG01168.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.399-1127delA | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr11 | 61768117 | ||||||
| chr11:61768146 | A | T | 1 | a0004c0016t0001g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.399-1114A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768146 | |||||||
| chr11:61768160 | C | T | 2 | a0001c0001t0001g0136 a0001c0006t0005g0135 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.399-1100C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768160 | |||||||
| chr11:61768220 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.399-1040G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768220 | |||||||
| chr11:61768247 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.399-1013A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768247 | |||||||
| chr11:61768504 | G | A | 5 | a0001c0002t0001g0071 a0001c0002t0001g0201 a0001c0002t0001g0213 others(2): Show |
5 | HG00733.hp2 HG02074.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.399-756G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768504 | |||||||
| chr11:61768600 | C | G | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.399-660C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768600 | |||||||
| chr11:61768846 | C | T | 3 | a0001c0002t0002g0198 a0001c0002t0002g0205 a0001c0002t0002g0222 |
3 | NA18999.hp1 NA19067.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.399-414C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768846 | |||||||
| chr11:61768917 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0125 a0001c0001t0001g0126 |
5 | HG02559.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.399-343G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768917 | |||||||
| chr11:61768958 | C | T | 42 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(39): Show |
55 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.399-302C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61768958 | |||||||
| chr11:61769037 | T | G | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.399-223T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61769037 | |||||||
| chr11:61769111 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(193): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.399-149G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61769111 | |||||||
| chr11:61769164 | G | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
6 | HG01884.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.399-96G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 3/26 | chr11 | 61769164 | |||||||
| chr11:61769371 | T | G | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.460+50T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769371 | |||||||
| chr11:61769376 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.460+55C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769376 | |||||||
| chr11:61769463 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.460+142G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769463 | |||||||
| chr11:61769526 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.460+205C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769526 | |||||||
| chr11:61769579 | C | T | 2 | a0001c0001t0001g0136 a0001c0006t0005g0135 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.460+258C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769579 | |||||||
| chr11:61769788 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0096 others(6): Show |
13 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.461-458G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769788 | |||||||
| chr11:61769910 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.461-336C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769910 | |||||||
| chr11:61769911 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.461-335G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769911 | |||||||
| chr11:61769938 | G | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0051 a0001c0002t0001g0100 others(1): Show |
5 | HG00735.hp2 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-308G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61769938 | |||||||
| chr11:61770057 | T | G | 74 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(71): Show |
89 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.461-189T>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61770057 | |||||||
| chr11:61770176 | TG | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(22): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.461-66delG | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr11 | 61770176 | ||||||
| chr11:61770218 | G | A | 5 | a0001c0002t0001g0005 a0001c0002t0001g0142 a0001c0002t0001g0145 others(2): Show |
10 | HG00735.hp1 HG01070.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.461-28G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 4/26 | chr11 | 61770218 | |||||||
| chr11:61770570 | C | A | 1 | a0010c0011t0001g0108 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.740+45C>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 5/26 | chr11 | 61770570 | |||||||
| chr11:61770929 | G | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.740+404G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 5/26 | chr11 | 61770929 | |||||||
| chr11:61771134 | A | G | 25 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(22): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.741-366A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 5/26 | chr11 | 61771134 | |||||||
| chr11:61771267 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0207 a0001c0001t0001g0220 |
3 | HG03669.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.741-233G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 5/26 | chr11 | 61771267 | |||||||
| chr11:61771458 | G | T | 1 | a0007c0012t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.741-42G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 5/26 | chr11 | 61771458 | |||||||
| chr11:61771789 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.991+39C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 6/26 | chr11 | 61771789 | |||||||
| chr11:61771811 | G | T | 4 | a0001c0001t0001g0209 a0001c0002t0001g0111 a0001c0002t0001g0204 others(1): Show |
4 | NA18956.hp1 NA18970.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-18G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 6/26 | chr11 | 61771811 | |||||||
| chr11:61771813 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.992-16C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 6/26 | chr11 | 61771813 | |||||||
| chr11:61772219 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(36): Show |
58 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1115+267G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61772219 | |||||||
| chr11:61772252 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0207 a0001c0001t0001g0220 |
3 | HG03669.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1115+300C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61772252 | |||||||
| chr11:61772269 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0185 |
2 | HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1115+317A>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61772269 | |||||||
| chr11:61772302 | C | G | 1 | a0001c0002t0001g0217 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1115+350C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61772302 | |||||||
| chr11:61772322 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1115+370A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61772322 | |||||||
| chr11:61772484 | T | C | 1 | a0001c0002t0001g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1115+532T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61772484 | |||||||
| chr11:61772979 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1116-988G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61772979 | |||||||
| chr11:61773004 | CT | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0105 others(8): Show |
14 | HG01261.hp2 HG02080.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1116-944delT | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr11 | 61773004 | ||||||
| chr11:61773004 | CTT | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1116-945_1116-944d others(4): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr11 | 61773004 | ||||||
| chr11:61773010 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1116-957T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773010 | |||||||
| chr11:61773013 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1116-954T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773013 | |||||||
| chr11:61773182 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0096 others(1): Show |
6 | HG02280.hp2 HG02451.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116-785G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773182 | |||||||
| chr11:61773240 | G | A | 1 | a0001c0002t0001g0234 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1116-727G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773240 | |||||||
| chr11:61773268 | G | A | 1 | a0001c0017t0001g0175 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1116-699G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773268 | |||||||
| chr11:61773336 | A | C | 4 | a0001c0002t0001g0024 a0001c0002t0001g0051 a0001c0002t0001g0089 others(1): Show |
5 | HG00735.hp2 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116-631A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773336 | |||||||
| chr11:61773387 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0134 a0001c0001t0001g0148 others(1): Show |
5 | HG02486.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116-580G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773387 | |||||||
| chr11:61773415 | C | T | 4 | a0001c0002t0001g0024 a0001c0002t0001g0051 a0001c0002t0001g0089 others(1): Show |
5 | HG00735.hp2 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116-552C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773415 | |||||||
| chr11:61773694 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1116-273G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773694 | |||||||
| chr11:61773840 | G | A | 5 | a0001c0001t0001g0073 a0001c0001t0001g0181 a0001c0001t0001g0241 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116-127G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773840 | |||||||
| chr11:61773855 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0123 a0001c0001t0001g0132 others(1): Show |
4 | HG01261.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-112G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773855 | |||||||
| chr11:61773911 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1116-56G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773911 | |||||||
| chr11:61773961 | C | T | 1 | a0001c0002t0001g0218 | 1 | NA18999.hp2 | splice_region_variant&intron_variant | LOW | c.1116-6C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 7/26 | chr11 | 61773961 | |||||||
| chr11:61774297 | T | C | 5 | a0001c0001t0001g0092 a0001c0001t0001g0182 a0001c0001t0003g0017 others(2): Show |
6 | HG02258.hp2 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+135T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61774297 | |||||||
| chr11:61774416 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(233): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1311+254A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61774416 | |||||||
| chr11:61774534 | G | A | 1 | a0001c0002t0001g0084 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1311+372G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61774534 | |||||||
| chr11:61774534 | GA | G | 93 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0077 others(90): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1311+384delA | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr11 | 61774534 | ||||||
| chr11:61774535 | A | G | 3 | a0001c0002t0001g0084 a0001c0002t0001g0228 a0001c0002t0001g0240 |
3 | HG01517.hp1 NA18940.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1311+373A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61774535 | |||||||
| chr11:61775250 | G | A | 1 | a0001c0001t0001g0012 | 3 | HG02723.hp1 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1312-806G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61775250 | |||||||
| chr11:61775751 | TGGG | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0152 others(4): Show |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312-301_1312-299d others(5): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr11 | 61775751 | ||||||
| chr11:61775900 | A | C | 2 | a0001c0006t0001g0035 a0001c0006t0005g0135 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1312-156A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61775900 | |||||||
| chr11:61776027 | T | C | 128 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0047 others(125): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1312-29T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61776027 | |||||||
| chr11:61776028 | G | A | 1 | a0001c0009t0001g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1312-28G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 8/26 | chr11 | 61776028 | |||||||
| chr11:61776457 | G | A | 1 | a0007c0012t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1499+25G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 10/26 | chr11 | 61776457 | |||||||
| chr11:61776489 | T | C | 110 | a0001c0001t0001g0231 a0001c0001t0007g0140 a0001c0002t0001g0002 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1499+57T>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 10/26 | chr11 | 61776489 | |||||||
| chr11:61776526 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
6 | HG02602.hp1 HG02683.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499+94C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 10/26 | chr11 | 61776526 | |||||||
| chr11:61778734 | G | GC | 3 | a0001c0001t0001g0033 a0001c0001t0001g0097 a0001c0001t0001g0136 |
4 | HG02717.hp2 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+247dupC | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr11 | 61778734 | ||||||
| chr11:61778942 | C | T | 1 | a0001c0002t0001g0032 | 2 | HG02074.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2014-321C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 14/26 | chr11 | 61778942 | |||||||
| chr11:61779120 | A | G | 92 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(89): Show |
118 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2014-143A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 14/26 | chr11 | 61779120 | |||||||
| chr11:61779228 | T | TTGGCCCA others(7): Show |
1 | a0001c0001t0001g0154 | 1 | HG02109.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.2014-16_2014-3dupC others(13): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr11 | 61779228 | ||||||
| chr11:61779228 | TTGGCCCA others(7): Show |
T | 1 | a0001c0002t0001g0196 | 1 | NA18971.hp1 | splice_region_variant&intron_variant | LOW | c.2014-16_2014-3delC others(13): Show |
MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr11 | 61779228 | ||||||
| chr11:61779596 | G | A | 10 | a0001c0002t0001g0006 a0001c0002t0001g0058 a0001c0002t0001g0061 others(7): Show |
14 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2247+26G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 16/26 | chr11 | 61779596 | |||||||
| chr11:61779765 | C | T | 86 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(83): Show |
112 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2248-77C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 16/26 | chr11 | 61779765 | |||||||
| chr11:61779772 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2248-70C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 16/26 | chr11 | 61779772 | |||||||
| chr11:61780097 | G | T | 1 | a0001c0002t0001g0208 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2337-125G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 17/26 | chr11 | 61780097 | |||||||
| chr11:61780197 | C | T | 1 | a0001c0002t0001g0029 | 2 | HG02040.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2337-25C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 17/26 | chr11 | 61780197 | |||||||
| chr11:61780479 | C | T | 7 | a0001c0001t0001g0092 a0001c0001t0001g0181 a0001c0001t0001g0241 others(4): Show |
7 | HG01515.hp1 HG01517.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2405+189C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 18/26 | chr11 | 61780479 | |||||||
| chr11:61780684 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2406-28C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 18/26 | chr11 | 61780684 | |||||||
| chr11:61780686 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0157 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2406-26C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 18/26 | chr11 | 61780686 | |||||||
| chr11:61781087 | A | G | 112 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0001c0001t0001g0067 others(109): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2572+42A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 20/26 | chr11 | 61781087 | |||||||
| chr11:61781402 | G | A | 13 | a0001c0001t0001g0055 a0001c0001t0001g0116 a0001c0001t0001g0158 others(10): Show |
19 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.2764+73G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 21/26 | chr11 | 61781402 | |||||||
| chr11:61781553 | G | A | 91 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2765-20G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 21/26 | chr11 | 61781553 | |||||||
| chr11:61781959 | G | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0152 others(4): Show |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3016+135G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/26 | chr11 | 61781959 | |||||||
| chr11:61781986 | A | G | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(84): Show |
113 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3016+162A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/26 | chr11 | 61781986 | |||||||
| chr11:61782292 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3016+468C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/26 | chr11 | 61782292 | |||||||
| chr11:61782872 | C | T | 1 | a0001c0006t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3017-626C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/26 | chr11 | 61782872 | |||||||
| chr11:61782893 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3017-605G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/26 | chr11 | 61782893 | |||||||
| chr11:61783064 | G | A | 2 | a0001c0002t0001g0044 a0001c0002t0001g0045 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3017-434G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/26 | chr11 | 61783064 | |||||||
| chr11:61783087 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3017-411G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 22/26 | chr11 | 61783087 | |||||||
| chr11:61783653 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3119+53C>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 23/26 | chr11 | 61783653 | |||||||
| chr11:61783713 | G | T | 1 | a0001c0002t0001g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3119+113G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 23/26 | chr11 | 61783713 | |||||||
| chr11:61784130 | G | C | 1 | a0001c0001t0006g0037 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3195-150G>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 24/26 | chr11 | 61784130 | |||||||
| chr11:61784455 | A | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.3300+70A>C | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61784455 | |||||||
| chr11:61784624 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0151 a0001c0001t0003g0017 others(2): Show |
6 | HG01168.hp2 HG02258.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300+239C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61784624 | |||||||
| chr11:61784636 | G | T | 1 | a0001c0002t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3300+251G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61784636 | |||||||
| chr11:61784734 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0095 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3300+349G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61784734 | |||||||
| chr11:61784824 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3300+439C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61784824 | |||||||
| chr11:61784868 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0134 a0001c0001t0001g0148 others(2): Show |
6 | HG02486.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300+483C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61784868 | |||||||
| chr11:61784882 | G | A | 13 | a0001c0002t0001g0024 a0001c0002t0001g0040 a0001c0002t0001g0043 others(10): Show |
14 | HG00735.hp2 HG01109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3300+497G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61784882 | |||||||
| chr11:61785030 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0095 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3300+645C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61785030 | |||||||
| chr11:61785189 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0095 a0001c0002t0001g0046 |
3 | HG01243.hp1 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3301-611C>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61785189 | |||||||
| chr11:61785208 | G | T | 91 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.3301-592G>T | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61785208 | |||||||
| chr11:61785221 | G | A | 2 | a0001c0001t0001g0131 a0001c0002t0002g0085 |
2 | HG00673.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3301-579G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61785221 | |||||||
| chr11:61785231 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3301-569A>G | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61785231 | |||||||
| chr11:61785729 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0223 |
4 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.3301-71G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 25/26 | chr11 | 61785729 | |||||||
| chr11:61785882 | G | A | 1 | a0001c0002t0001g0204 | 1 | NA18970.hp2 | splice_region_variant&intron_variant | LOW | c.3375+8G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 26/26 | chr11 | 61785882 | |||||||
| chr11:61785904 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3375+30G>A | MYRF | ENSG00000124920.14 | transcript | ENST00000278836.10 | protein_coding | 26/26 | chr11 | 61785904 |