Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4223 |
| ensemblid | ENSG00000106511.6 |
| hgncid | 7014 |
| symbol | MEOX2 |
| name | mesenchyme homeobox 2 |
| refseq_nuc | NM_005924.5 |
| refseq_prot | NP_005915.2 |
| ensembl_nuc | ENST00000262041.6 |
| ensembl_prot | ENSP00000262041.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 15611212 |
| end | 15686683 |
| strand | - |
| ver | v1.2 |
| region | chr7:15611212-15686683 |
| region5000 | chr7:15606212-15691683 |
| regionname0 | MEOX2_chr7_15611212_15686683 |
| regionname5000 | MEOX2_chr7_15606212_15691683 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 303 | 239 | 77 | 38 | 97 | 7 | 20 | 80 | MEOX2_chr7_15606212_15691683 | MEOX2 | MEHPL others(298): Show |
chr7 | 15606212 | 15691683 |
| a0002 | 1/1 | 304 | 103 | 12 | 27 | 35 | 8 | 19 | 28 | MEOX2_chr7_15606212_15691683 | MEOX2 | MEHPL others(299): Show |
chr7 | 15606212 | 15691683 |
| a0003 | 0/0 | 304 | 7 | 0 | 3 | 4 | 0 | 0 | 2 | MEOX2_chr7_15606212_15691683 | MEOX2 | MEHPL others(299): Show |
chr7 | 15606212 | 15691683 |
| a0004 | 0/0 | 303 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | MEHPL others(298): Show |
chr7 | 15606212 | 15691683 |
| a0005 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | MEHPL others(298): Show |
chr7 | 15606212 | 15691683 |
| a0006 | 0/0 | 304 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | MEHPL others(299): Show |
chr7 | 15606212 | 15691683 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 909 | 176 | 71 | 36 | 44 | 7 | 18 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0001c0003 | 0/0 | 909 | 57 | 3 | 2 | 52 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0001c0007 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0001c0008 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0001c0009 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0001c0010 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0001c0011 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0001c0013 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0002c0002 | 1/1 | 912 | 103 | 12 | 27 | 35 | 8 | 19 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(907): Show |
chr7 | 15606212 | 15691683 | ||
| a0003c0004 | 0/0 | 912 | 7 | 0 | 3 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(907): Show |
chr7 | 15606212 | 15691683 | ||
| a0004c0006 | 0/0 | 909 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0005c0005 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(904): Show |
chr7 | 15606212 | 15691683 | ||
| a0006c0012 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | ATGGA others(907): Show |
chr7 | 15606212 | 15691683 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2370 | 92 | 15 | 25 | 36 | 6 | 10 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0006 | 0/0 | 2370 | 12 | 6 | 1 | 2 | 1 | 2 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0007 | 0/0 | 2370 | 8 | 6 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0008 | 0/0 | 2370 | 8 | 5 | 2 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0009 | 0/0 | 2368 | 8 | 6 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2363): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0012 | 0/0 | 2371 | 6 | 4 | 0 | 1 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0013 | 0/0 | 2371 | 5 | 1 | 1 | 0 | 0 | 3 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0014 | 0/0 | 2369 | 5 | 4 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2364): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0015 | 0/0 | 2372 | 4 | 3 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2367): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0016 | 0/0 | 2372 | 4 | 4 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2367): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0018 | 0/0 | 2370 | 4 | 1 | 0 | 2 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0019 | 0/0 | 2370 | 3 | 2 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0020 | 0/0 | 2368 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2363): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0021 | 0/0 | 2368 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2363): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0023 | 0/0 | 2372 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2367): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0024 | 0/0 | 2370 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0031 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0032 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0033 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0034 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2364): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0035 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2364): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0036 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2364): Show |
chr7 | 15606212 | 15691683 |
| a0001c0001t0037 | 0/0 | 2368 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2363): Show |
chr7 | 15606212 | 15691683 |
| a0001c0003t0003 | 0/0 | 2370 | 49 | 0 | 2 | 47 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0003t0008 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0003t0017 | 0/0 | 2370 | 4 | 0 | 0 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0003t0027 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0001c0003t0030 | 0/0 | 2371 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0001c0003t0038 | 0/0 | 2368 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2363): Show |
chr7 | 15606212 | 15691683 |
| a0001c0007t0003 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0008t0007 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0009t0001 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0010t0029 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0001c0011t0001 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0001c0013t0003 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0001 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2368): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0002 | 1/0 | 2371 | 52 | 1 | 11 | 23 | 2 | 14 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0004 | 0/0 | 2371 | 19 | 4 | 6 | 5 | 1 | 3 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0005 | 0/0 | 2371 | 13 | 0 | 5 | 6 | 2 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0010 | 0/1 | 2371 | 8 | 2 | 3 | 0 | 1 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0022 | 0/0 | 2371 | 3 | 1 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0025 | 0/0 | 2371 | 2 | 0 | 0 | 0 | 2 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0026 | 0/0 | 2371 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0028 | 0/0 | 2374 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2369): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0039 | 0/0 | 2371 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0002c0002t0040 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0003c0004t0011 | 0/0 | 2371 | 7 | 0 | 3 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| a0004c0006t0001 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0005c0005t0001 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2365): Show |
chr7 | 15606212 | 15691683 |
| a0006c0012t0005 | 0/0 | 2371 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | GAAAG others(2366): Show |
chr7 | 15606212 | 15691683 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0012g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0013g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0013g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0013g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0014g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0014g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0015g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0015g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0016g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0016g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0016g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0018g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0018g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0018g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0018g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0019g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0020g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0020g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0020g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0021g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0021g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0021g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0023g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0024g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0024g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0031g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0032g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0033g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0034g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0035g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0036g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0001t0037g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0017g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0017g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0027g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0030g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0003t0038g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0007t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0008t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0009t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0010t0029g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0011t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0001c0013t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0301 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0010g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0022g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0022g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0022g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0025g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0025g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0026g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0026g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0028g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0039g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0002c0002t0040g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0003c0004t0011g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0003c0004t0011g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0003c0004t0011g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0003c0004t0011g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0003c0004t0011g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0003c0004t0011g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0003c0004t0011g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0004c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0005c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| a0006c0012t0005g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0320 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0134 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00323 | hp1 | a0004 | c0006 | t0001 | g0036 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00323 | hp2 | a0002 | c0002 | t0010 | g0306 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00408 | hp2 | a0001 | c0003 | t0003 | g0160 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00558 | hp1 | a0003 | c0004 | t0011 | g0311 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00558 | hp2 | a0001 | c0003 | t0003 | g0191 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00609 | hp1 | a0001 | c0003 | t0003 | g0156 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0289 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0300 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0226 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0221 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00673 | hp1 | a0003 | c0004 | t0011 | g0276 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0290 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00735 | hp1 | a0002 | c0002 | t0004 | g0327 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00735 | hp2 | a0002 | c0002 | t0005 | g0265 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0321 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00741 | hp1 | a0003 | c0004 | t0011 | g0314 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG00741 | hp2 | a0002 | c0002 | t0022 | g0316 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01074 | hp1 | a0001 | c0001 | t0019 | g0117 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01074 | hp2 | a0002 | c0002 | t0005 | g0263 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0072 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01099 | hp2 | a0002 | c0002 | t0005 | g0273 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0332 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01109 | hp1 | a0002 | c0002 | t0004 | g0254 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01109 | hp2 | a0002 | c0002 | t0022 | g0255 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0042 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0135 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0043 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01175 | hp2 | a0002 | c0002 | t0010 | g0303 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01192 | hp2 | a0003 | c0004 | t0011 | g0313 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0179 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0277 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0024 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01358 | hp2 | a0002 | c0002 | t0010 | g0308 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0331 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01361 | hp2 | a0002 | c0002 | t0005 | g0267 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01433 | hp2 | a0002 | c0002 | t0004 | g0322 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0282 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01515 | hp1 | a0002 | c0002 | t0004 | g0240 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01515 | hp2 | a0002 | c0002 | t0025 | g0334 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01517 | hp1 | a0002 | c0002 | t0025 | g0333 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01884 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0015 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01928 | hp1 | a0001 | c0003 | t0003 | g0127 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0330 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0304 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0338 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01943 | hp2 | a0003 | c0004 | t0011 | g0310 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01952 | hp1 | a0002 | c0002 | t0010 | g0269 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01993 | hp1 | a0001 | c0001 | t0033 | g0212 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0291 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02015 | hp1 | a0001 | c0003 | t0003 | g0155 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0110 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02055 | hp2 | a0001 | c0003 | t0008 | g0111 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02056 | hp2 | a0001 | c0001 | t0018 | g0100 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0058 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02071 | hp2 | a0001 | c0003 | t0003 | g0098 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02074 | hp2 | a0002 | c0002 | t0005 | g0264 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02129 | hp1 | a0002 | c0002 | t0005 | g0257 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0077 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0023 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02145 | hp2 | a0001 | c0001 | t0034 | g0216 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0305 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | CDX | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02258 | hp2 | a0002 | c0002 | t0022 | g0302 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02273 | hp1 | a0002 | c0002 | t0004 | g0237 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02273 | hp2 | a0001 | c0003 | t0003 | g0163 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02280 | hp1 | a0001 | c0011 | t0001 | g0210 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0219 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02572 | hp1 | a0001 | c0001 | t0021 | g0236 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0181 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0021 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02602 | hp2 | a0001 | c0009 | t0001 | g0079 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0116 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0032 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0178 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0243 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02647 | hp2 | a0001 | c0001 | t0032 | g0081 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0324 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0069 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0225 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0317 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0019 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0228 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0235 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02896 | hp1 | a0001 | c0003 | t0038 | g0233 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02897 | hp1 | a0005 | c0005 | t0001 | g0035 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02922 | hp1 | a0002 | c0002 | t0004 | g0245 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02965 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0182 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03017 | hp1 | a0001 | c0001 | t0008 | g0073 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0323 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03098 | hp1 | a0002 | c0002 | t0010 | g0246 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0214 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0230 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0231 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03195 | hp2 | a0002 | c0002 | t0040 | g0251 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03209 | hp1 | a0001 | c0001 | t0037 | g0234 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03209 | hp2 | a0001 | c0001 | t0018 | g0176 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0315 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03453 | hp1 | a0001 | c0008 | t0007 | g0177 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0013 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03486 | hp1 | a0002 | c0002 | t0026 | g0242 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03486 | hp2 | a0001 | c0001 | t0016 | g0017 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0274 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03490 | hp2 | a0002 | c0002 | t0004 | g0256 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03491 | hp1 | a0001 | c0001 | t0018 | g0076 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0319 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0275 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0318 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03516 | hp1 | a0002 | c0002 | t0026 | g0249 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0119 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0033 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03540 | hp2 | a0001 | c0001 | t0021 | g0224 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03579 | hp1 | a0001 | c0003 | t0027 | g0026 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0217 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03654 | hp1 | a0006 | c0012 | t0005 | g0339 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0325 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0172 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03831 | hp2 | a0001 | c0013 | t0003 | g0211 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0022 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0266 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0326 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03942 | hp2 | a0002 | c0002 | t0028 | g0027 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04115 | hp1 | a0002 | c0002 | t0010 | g0309 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04184 | hp1 | a0002 | c0002 | t0004 | g0307 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0328 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04204 | hp2 | a0001 | c0001 | t0012 | g0030 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04228 | hp1 | a0001 | c0001 | t0013 | g0025 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0335 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0040 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18612 | hp1 | a0001 | c0003 | t0003 | g0122 | EAS | CHB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | CHB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0253 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0229 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18939 | hp1 | a0001 | c0003 | t0003 | g0103 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18940 | hp1 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18941 | hp1 | a0001 | c0003 | t0017 | g0009 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18944 | hp1 | a0002 | c0002 | t0004 | g0295 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18944 | hp2 | a0002 | c0002 | t0005 | g0271 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18947 | hp1 | a0001 | c0001 | t0015 | g0020 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18948 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18949 | hp1 | a0001 | c0003 | t0003 | g0105 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18949 | hp2 | a0003 | c0004 | t0011 | g0239 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18950 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18954 | hp1 | a0001 | c0007 | t0003 | g0038 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18956 | hp2 | a0001 | c0003 | t0003 | g0194 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0141 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18960 | hp1 | a0001 | c0003 | t0003 | g0104 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18961 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18963 | hp2 | a0001 | c0003 | t0003 | g0106 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18964 | hp1 | a0002 | c0002 | t0004 | g0286 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18964 | hp2 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18965 | hp1 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18965 | hp2 | a0002 | c0002 | t0005 | g0260 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18968 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18969 | hp2 | a0001 | c0003 | t0003 | g0201 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18975 | hp2 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18977 | hp1 | a0001 | c0003 | t0003 | g0050 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18977 | hp2 | a0001 | c0003 | t0003 | g0118 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18978 | hp2 | a0001 | c0003 | t0017 | g0209 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18983 | hp1 | a0001 | c0001 | t0024 | g0140 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18986 | hp1 | a0002 | c0002 | t0004 | g0238 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0337 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18988 | hp2 | a0001 | c0003 | t0003 | g0199 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18990 | hp1 | a0001 | c0001 | t0018 | g0101 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18990 | hp2 | a0001 | c0003 | t0003 | g0207 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18992 | hp2 | a0001 | c0003 | t0003 | g0204 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18993 | hp1 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0096 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18998 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19000 | hp2 | a0001 | c0003 | t0030 | g0034 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19001 | hp1 | a0001 | c0003 | t0003 | g0158 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19002 | hp1 | a0002 | c0002 | t0039 | g0299 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19003 | hp1 | a0001 | c0003 | t0003 | g0097 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19004 | hp1 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19004 | hp2 | a0001 | c0001 | t0012 | g0031 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19007 | hp2 | a0002 | c0002 | t0004 | g0259 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0180 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0232 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19043 | hp1 | a0001 | c0001 | t0016 | g0016 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0244 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19056 | hp2 | a0001 | c0003 | t0003 | g0190 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19058 | hp2 | a0001 | c0003 | t0003 | g0195 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19062 | hp1 | a0001 | c0003 | t0017 | g0009 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19063 | hp2 | a0001 | c0003 | t0003 | g0193 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19065 | hp1 | a0001 | c0003 | t0003 | g0173 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19066 | hp2 | a0002 | c0002 | t0005 | g0272 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19068 | hp1 | a0003 | c0004 | t0011 | g0312 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19074 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19077 | hp2 | a0001 | c0003 | t0017 | g0205 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19083 | hp1 | a0001 | c0003 | t0003 | g0136 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19083 | hp2 | a0001 | c0001 | t0024 | g0197 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19084 | hp1 | a0002 | c0002 | t0004 | g0258 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19084 | hp2 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0102 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0153 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19089 | hp1 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19089 | hp2 | a0002 | c0002 | t0005 | g0278 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20129 | hp1 | a0002 | c0002 | t0010 | g0248 | AFR | ASW | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ASW | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20752 | hp1 | a0002 | c0002 | t0005 | g0261 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0329 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20805 | hp2 | a0002 | c0002 | t0005 | g0262 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0336 | SAS | GIH | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20905 | hp2 | a0002 | c0002 | t0004 | g0241 | SAS | GIH | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01123 | hp1 | a0002 | c0002 | t0005 | g0268 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG01123 | hp2 | a0001 | c0001 | t0014 | g0220 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0018 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0188 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0215 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG02559 | hp2 | a0001 | c0001 | t0035 | g0213 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03471 | hp1 | a0001 | c0001 | t0031 | g0029 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG06807 | hp1 | a0001 | c0001 | t0036 | g0218 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0125 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA18955 | hp2 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA20300 | hp2 | a0001 | c0001 | t0020 | g0227 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA21309 | hp1 | a0001 | c0010 | t0029 | g0028 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0010 | g0250 | REF | REF | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0301 | REF | REF | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:15612428 | T | A | 1 | a0001 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.874A>T | p.Ser292Cys | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1155/2371 | 874/915 | 292/304 | chr7 | 15612428 | |||
| chr7:15612442 | A | G | 1 | a0001 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.860T>C | p.Ile287Thr | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1141/2371 | 860/915 | 287/304 | chr7 | 15612442 | |||
| chr7:15612443 | T | G | 2 | a0001 a0003 |
66 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(63): Show |
missense_variant | MODERATE | c.859A>C | p.Ile287Leu | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1140/2371 | 859/915 | 287/304 | chr7 | 15612443 | |||
| chr7:15686064 | G | T | 1 | a0001 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.339C>A | p.Asp113Glu | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 620/2371 | 339/915 | 113/304 | chr7 | 15686064 | |||
| chr7:15686105 | G | C | 1 | a0001 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.298C>G | p.Pro100Ala | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 579/2371 | 298/915 | 100/304 | chr7 | 15686105 | |||
| chr7:15686172 | ATGG | A | 3 | a0001 a0004 a0005 |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
disruptive_inframe_deletion | MODERATE | c.228_230delCCA | p.His77del | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 511/2371 | 228/915 | 76/304 | chr7 | 15686172 | |||
| chr7:15686191 | T | C | 1 | a0006 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.212A>G | p.His71Arg | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 493/2371 | 212/915 | 71/304 | chr7 | 15686191 | |||
| chr7:15686198 | G | T | 1 | a0004 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.205C>A | p.His69Asn | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 486/2371 | 205/915 | 69/304 | chr7 | 15686198 | |||
| chr7:15686342 | G | T | 1 | a0005 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.61C>A | p.Pro21Thr | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 342/2371 | 61/915 | 21/304 | chr7 | 15686342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:15626848 | T | C | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.588A>G | p.Lys196Lys | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/3 | 869/2371 | 588/915 | 196/304 | chr7 | 15626848 | |||
| chr7:15686343 | G | A | 1 | a0001c0013 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.60C>T | p.His20His | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 341/2371 | 60/915 | 20/304 | chr7 | 15686343 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:15611372 | C | T | 1 | a0001c0001t0019 | 3 | HG01074.hp1 HG02615.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1015G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1015 | chr7 | 15611372 | ||||||
| chr7:15611505 | G | C | 1 | a0002c0002t0025 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*882C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 882 | chr7 | 15611505 | ||||||
| chr7:15611533 | G | T | 43 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(40): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*854C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 854 | chr7 | 15611533 | ||||||
| chr7:15611966 | T | C | 1 | a0002c0002t0040 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 421 | chr7 | 15611966 | ||||||
| chr7:15611973 | C | T | 1 | a0001c0003t0017 | 4 | NA18941.hp1 NA18978.hp2 NA19062.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 414 | chr7 | 15611973 | ||||||
| chr7:15611974 | C | G | 5 | a0001c0001t0018 a0001c0001t0024 a0002c0002t0005 others(2): Show |
21 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*413G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 413 | chr7 | 15611974 | ||||||
| chr7:15612067 | T | C | 7 | a0001c0003t0003 a0001c0003t0017 a0001c0003t0030 others(4): Show |
64 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*320A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 320 | chr7 | 15612067 | ||||||
| chr7:15612145 | C | T | 26 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(23): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*242G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 242 | chr7 | 15612145 | ||||||
| chr7:15612276 | A | T | 27 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(24): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*111T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 111 | chr7 | 15612276 | ||||||
| chr7:15612279 | A | G | 1 | a0001c0001t0032 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 108 | chr7 | 15612279 | ||||||
| chr7:15686408 | G | A | 1 | a0001c0001t0033 | 1 | HG01993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 6 | chr7 | 15686408 | ||||||
| chr7:15686433 | A | G | 1 | a0001c0010t0029 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 31 | chr7 | 15686433 | ||||||
| chr7:15686441 | G | A | 38 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(35): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
5_prime_UTR_variant | MODIFIER | c.-39C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 39 | chr7 | 15686441 | ||||||
| chr7:15686492 | A | AT | 4 | a0001c0001t0014 a0001c0001t0034 a0001c0001t0035 others(1): Show |
8 | HG01123.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-91dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | ||||||
| chr7:15686492 | A | ATT | 20 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(17): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
5_prime_UTR_variant | MODIFIER | c.-92_-91dupAA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | ||||||
| chr7:15686492 | A | ATTT | 7 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0031 others(4): Show |
16 | HG01261.hp1 HG02145.hp1 HG02602.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-91dupAAA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | ||||||
| chr7:15686492 | A | ATTTT | 3 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0023 |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-94_-91dupAAAA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | ||||||
| chr7:15686504 | A | C | 39 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(36): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
5_prime_UTR_variant | MODIFIER | c.-102T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 102 | chr7 | 15686504 | ||||||
| chr7:15686672 | A | G | 5 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0016 others(2): Show |
16 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-270T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 270 | chr7 | 15686672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:15612789 | A | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-178T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15612789 | |||||||
| chr7:15612852 | T | G | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.691-241A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15612852 | |||||||
| chr7:15612898 | A | G | 1 | a0002c0002t0002g0291 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.691-287T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15612898 | |||||||
| chr7:15613028 | A | T | 7 | a0001c0001t0001g0045 a0001c0001t0012g0003 a0001c0001t0012g0032 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-417T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613028 | |||||||
| chr7:15613070 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.691-459T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613070 | |||||||
| chr7:15613095 | C | G | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-484G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613095 | |||||||
| chr7:15613158 | T | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-547A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613158 | |||||||
| chr7:15613273 | G | C | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-662C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613273 | |||||||
| chr7:15613282 | C | T | 1 | a0002c0002t0010g0269 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.691-671G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613282 | |||||||
| chr7:15613285 | C | T | 1 | a0002c0002t0002g0324 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.691-674G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613285 | |||||||
| chr7:15613310 | G | T | 1 | a0001c0003t0003g0199 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.691-699C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613310 | |||||||
| chr7:15613395 | C | CA | 257 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(254): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.691-785dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613395 | |||||||
| chr7:15613429 | A | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-818T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613429 | |||||||
| chr7:15613435 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.691-824A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613435 | |||||||
| chr7:15613509 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0138 others(2): Show |
6 | HG01192.hp1 HG01256.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-898T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613509 | |||||||
| chr7:15613516 | T | C | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-905A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613516 | |||||||
| chr7:15613544 | T | C | 2 | a0001c0001t0023g0002 a0001c0001t0034g0216 |
3 | HG01884.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.691-933A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613544 | |||||||
| chr7:15613861 | T | A | 221 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.691-1250A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613861 | |||||||
| chr7:15613914 | G | A | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-1303C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613914 | |||||||
| chr7:15614022 | T | C | 1 | a0001c0001t0035g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.691-1411A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614022 | |||||||
| chr7:15614024 | A | T | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-1413T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614024 | |||||||
| chr7:15614053 | TTG | T | 15 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0093 others(12): Show |
15 | HG01106.hp1 HG01261.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.691-1444_691-1443d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614053 | |||||||
| chr7:15614054 | TG | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.691-1444delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614054 | |||||||
| chr7:15614059 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-1448G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614059 | |||||||
| chr7:15614081 | T | C | 1 | a0002c0002t0002g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.691-1470A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614081 | |||||||
| chr7:15614118 | T | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0078 others(8): Show |
12 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.691-1507A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614118 | |||||||
| chr7:15614132 | G | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.691-1521C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614132 | |||||||
| chr7:15614136 | C | G | 2 | a0002c0002t0026g0242 a0002c0002t0026g0249 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.691-1525G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614136 | |||||||
| chr7:15614148 | G | T | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-1537C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614148 | |||||||
| chr7:15614201 | A | T | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-1590T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614201 | |||||||
| chr7:15614202 | G | GATAAA | 14 | a0001c0001t0006g0134 a0001c0001t0016g0016 a0002c0002t0002g0012 others(11): Show |
15 | HG00280.hp1 HG00738.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-1596_691-1592d others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | |||||||
| chr7:15614202 | G | GATAAAAT others(3): Show |
6 | a0001c0001t0016g0015 a0002c0002t0002g0282 a0002c0002t0002g0304 others(3): Show |
6 | HG00099.hp2 HG01361.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-1601_691-1592d others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | |||||||
| chr7:15614202 | GATAAA | G | 20 | a0001c0001t0006g0059 a0001c0001t0006g0069 a0001c0001t0006g0080 others(17): Show |
20 | HG00639.hp2 HG01074.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.691-1596_691-1592d others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | |||||||
| chr7:15614202 | GATAAAAT others(3): Show |
G | 64 | a0001c0001t0006g0057 a0001c0001t0006g0061 a0001c0001t0006g0062 others(61): Show |
65 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.691-1601_691-1592d others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | |||||||
| chr7:15614202 | GATAAAAT others(8): Show |
G | 4 | a0001c0001t0008g0188 a0001c0001t0021g0235 a0001c0001t0021g0236 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1606_691-1592d others(17): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | |||||||
| chr7:15614202 | GATAAAAT others(13): Show |
G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.691-1611_691-1592d others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | |||||||
| chr7:15614202 | GATAAAAT others(18): Show |
G | 1 | a0001c0001t0007g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.691-1616_691-1592d others(27): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | |||||||
| chr7:15614240 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.691-1629T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614240 | |||||||
| chr7:15614315 | A | G | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-1704T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614315 | |||||||
| chr7:15614316 | G | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-1705C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614316 | |||||||
| chr7:15614356 | G | T | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.691-1745C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614356 | |||||||
| chr7:15614399 | G | T | 1 | a0001c0003t0003g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.691-1788C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614399 | |||||||
| chr7:15614416 | A | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-1805T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614416 | |||||||
| chr7:15614419 | G | GA | 222 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.691-1809dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614419 | |||||||
| chr7:15614495 | G | A | 3 | a0001c0001t0007g0072 a0001c0001t0023g0002 a0001c0001t0034g0216 |
4 | HG01081.hp1 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1884C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614495 | |||||||
| chr7:15614536 | C | A | 1 | a0002c0002t0004g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.691-1925G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614536 | |||||||
| chr7:15614537 | A | T | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-1926T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614537 | |||||||
| chr7:15614670 | T | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2059A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614670 | |||||||
| chr7:15614692 | T | C | 1 | a0001c0001t0020g0228 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.691-2081A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614692 | |||||||
| chr7:15614755 | G | A | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.691-2144C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614755 | |||||||
| chr7:15614794 | A | G | 1 | a0001c0003t0003g0199 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.691-2183T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614794 | |||||||
| chr7:15614804 | A | T | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-2193T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614804 | |||||||
| chr7:15614989 | T | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0078 others(8): Show |
12 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.691-2378A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614989 | |||||||
| chr7:15615031 | T | A | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 |
3 | HG02486.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.691-2420A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615031 | |||||||
| chr7:15615180 | GT | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2570delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615180 | |||||||
| chr7:15615284 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.691-2673T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615284 | |||||||
| chr7:15615364 | G | T | 1 | a0001c0001t0015g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.691-2753C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615364 | |||||||
| chr7:15615426 | T | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2815A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615426 | |||||||
| chr7:15615429 | TA | T | 209 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.691-2819delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615429 | |||||||
| chr7:15615438 | AG | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0044 others(11): Show |
15 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.691-2828delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615438 | |||||||
| chr7:15615467 | G | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2856C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615467 | |||||||
| chr7:15615510 | G | T | 5 | a0002c0002t0004g0240 a0002c0002t0004g0241 a0002c0002t0022g0255 others(2): Show |
5 | HG00741.hp2 HG01109.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-2899C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615510 | |||||||
| chr7:15615540 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2929A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615540 | |||||||
| chr7:15615568 | T | C | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-2957A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615568 | |||||||
| chr7:15615640 | G | T | 1 | a0001c0001t0035g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.691-3029C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615640 | |||||||
| chr7:15615668 | T | C | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.691-3057A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615668 | |||||||
| chr7:15615892 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-3281A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615892 | |||||||
| chr7:15615923 | T | C | 1 | a0001c0001t0034g0216 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.691-3312A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615923 | |||||||
| chr7:15616049 | T | G | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.691-3438A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616049 | |||||||
| chr7:15616228 | T | A | 1 | a0001c0003t0008g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-3617A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616228 | |||||||
| chr7:15616371 | A | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-3760T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616371 | |||||||
| chr7:15616444 | T | C | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.691-3833A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616444 | |||||||
| chr7:15616465 | A | G | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.691-3854T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616465 | |||||||
| chr7:15616477 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.691-3866C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616477 | |||||||
| chr7:15616562 | A | T | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.691-3951T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616562 | |||||||
| chr7:15616641 | C | G | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.691-4030G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616641 | |||||||
| chr7:15616680 | T | A | 18 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-4069A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616680 | |||||||
| chr7:15616765 | T | C | 6 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 others(3): Show |
7 | HG01109.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-4154A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616765 | |||||||
| chr7:15616825 | C | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4214G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616825 | |||||||
| chr7:15616851 | G | T | 2 | a0001c0003t0003g0096 a0001c0003t0003g0097 |
2 | NA18995.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.691-4240C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616851 | |||||||
| chr7:15616867 | A | G | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-4256T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616867 | |||||||
| chr7:15616908 | A | G | 18 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-4297T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616908 | |||||||
| chr7:15616937 | T | A | 7 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(4): Show |
8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-4326A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616937 | |||||||
| chr7:15616981 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4370G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616981 | |||||||
| chr7:15616984 | T | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4373A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616984 | |||||||
| chr7:15617031 | C | G | 1 | a0001c0001t0006g0069 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.691-4420G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617031 | |||||||
| chr7:15617082 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.691-4471T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617082 | |||||||
| chr7:15617103 | A | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4492T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617103 | |||||||
| chr7:15617188 | A | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4577T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617188 | |||||||
| chr7:15617337 | A | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4726T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617337 | |||||||
| chr7:15617429 | G | A | 18 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-4818C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617429 | |||||||
| chr7:15617499 | T | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-4888A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617499 | |||||||
| chr7:15617500 | G | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.691-4889C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617500 | |||||||
| chr7:15617619 | C | G | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.691-5008G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617619 | |||||||
| chr7:15617647 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.691-5036G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617647 | |||||||
| chr7:15617681 | G | T | 2 | a0001c0001t0023g0002 a0001c0001t0034g0216 |
3 | HG01884.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.691-5070C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617681 | |||||||
| chr7:15617682 | T | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.691-5071A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617682 | |||||||
| chr7:15617697 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691-5086A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617697 | |||||||
| chr7:15617734 | C | T | 18 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-5123G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617734 | |||||||
| chr7:15617803 | C | A | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.691-5192G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617803 | |||||||
| chr7:15617839 | G | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5228C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617839 | |||||||
| chr7:15617867 | T | G | 2 | a0002c0002t0001g0037 a0002c0002t0004g0322 |
2 | HG01433.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.691-5256A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617867 | |||||||
| chr7:15617874 | T | A | 1 | a0001c0001t0009g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.691-5263A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617874 | |||||||
| chr7:15617890 | T | C | 19 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(16): Show |
19 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.691-5279A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617890 | |||||||
| chr7:15617903 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.691-5292T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617903 | |||||||
| chr7:15617948 | G | C | 1 | a0001c0003t0003g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.691-5337C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617948 | |||||||
| chr7:15617970 | G | A | 1 | a0001c0003t0008g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-5359C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617970 | |||||||
| chr7:15618027 | C | G | 1 | a0001c0003t0003g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.691-5416G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618027 | |||||||
| chr7:15618038 | C | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5427G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618038 | |||||||
| chr7:15618124 | G | C | 1 | a0001c0001t0009g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.691-5513C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618124 | |||||||
| chr7:15618157 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5546A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618157 | |||||||
| chr7:15618173 | G | A | 1 | a0001c0001t0006g0152 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.691-5562C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618173 | |||||||
| chr7:15618324 | T | A | 8 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(5): Show |
9 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-5713A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618324 | |||||||
| chr7:15618350 | C | CT | 4 | a0001c0001t0006g0057 a0001c0001t0006g0061 a0001c0001t0006g0062 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-5740dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618350 | |||||||
| chr7:15618352 | T | G | 2 | a0002c0002t0004g0243 a0002c0002t0004g0244 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.691-5741A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618352 | |||||||
| chr7:15618358 | C | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5747G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618358 | |||||||
| chr7:15618395 | G | A | 1 | a0001c0003t0003g0200 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.691-5784C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618395 | |||||||
| chr7:15618488 | C | T | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-5877G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618488 | |||||||
| chr7:15618510 | C | T | 1 | a0002c0002t0002g0252 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.691-5899G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618510 | |||||||
| chr7:15618555 | T | C | 1 | a0002c0002t0002g0252 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.691-5944A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618555 | |||||||
| chr7:15618681 | T | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6070A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618681 | |||||||
| chr7:15618750 | A | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-6139T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618750 | |||||||
| chr7:15618800 | A | T | 1 | a0001c0003t0003g0098 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.691-6189T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618800 | |||||||
| chr7:15618819 | A | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6208T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618819 | |||||||
| chr7:15618896 | C | T | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-6285G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618896 | |||||||
| chr7:15618918 | G | A | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.691-6307C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618918 | |||||||
| chr7:15618943 | C | T | 336 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(333): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.691-6332G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618943 | |||||||
| chr7:15618958 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6347A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618958 | |||||||
| chr7:15618974 | A | C | 1 | a0001c0001t0015g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.691-6363T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618974 | |||||||
| chr7:15618978 | G | A | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-6367C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618978 | |||||||
| chr7:15619003 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0192 |
2 | HG02155.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.691-6392C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619003 | |||||||
| chr7:15619038 | G | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6427C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619038 | |||||||
| chr7:15619039 | T | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6428A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619039 | |||||||
| chr7:15619041 | G | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6430C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619041 | |||||||
| chr7:15619160 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6549A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619160 | |||||||
| chr7:15619175 | A | C | 3 | a0001c0001t0019g0116 a0001c0001t0019g0117 a0001c0010t0029g0028 |
3 | HG01074.hp1 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.691-6564T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619175 | |||||||
| chr7:15619197 | G | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6586C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619197 | |||||||
| chr7:15619332 | G | A | 18 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-6721C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619332 | |||||||
| chr7:15619356 | G | C | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-6745C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619356 | |||||||
| chr7:15619369 | A | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6758T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619369 | |||||||
| chr7:15619412 | A | G | 1 | a0002c0002t0004g0307 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.691-6801T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619412 | |||||||
| chr7:15619418 | A | G | 13 | a0001c0001t0007g0008 a0001c0001t0007g0072 a0001c0001t0007g0178 others(10): Show |
15 | HG01081.hp1 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.691-6807T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619418 | |||||||
| chr7:15619453 | A | C | 1 | a0001c0001t0016g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.691-6842T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619453 | |||||||
| chr7:15619455 | A | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6844T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619455 | |||||||
| chr7:15619576 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6965G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619576 | |||||||
| chr7:15619596 | G | A | 1 | a0002c0002t0004g0327 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.691-6985C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619596 | |||||||
| chr7:15619647 | T | A | 1 | a0001c0001t0015g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.691-7036A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619647 | |||||||
| chr7:15619674 | A | G | 1 | a0001c0001t0018g0176 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.691-7063T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619674 | |||||||
| chr7:15619695 | C | T | 18 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+7051G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619695 | |||||||
| chr7:15619714 | A | G | 1 | a0001c0001t0014g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690+7032T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619714 | |||||||
| chr7:15619763 | G | C | 7 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(4): Show |
8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+6983C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619763 | |||||||
| chr7:15619975 | A | G | 1 | a0002c0002t0004g0237 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.690+6771T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619975 | |||||||
| chr7:15620121 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+6625G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620121 | |||||||
| chr7:15620125 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.690+6621C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620125 | |||||||
| chr7:15620341 | A | G | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+6405T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620341 | |||||||
| chr7:15620424 | C | T | 2 | a0002c0002t0004g0243 a0002c0002t0004g0244 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+6322G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620424 | |||||||
| chr7:15620466 | G | A | 3 | a0002c0002t0002g0279 a0002c0002t0002g0280 a0002c0002t0002g0281 |
3 | NA18940.hp2 NA18955.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.690+6280C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620466 | |||||||
| chr7:15620476 | G | C | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+6270C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620476 | |||||||
| chr7:15620496 | T | G | 1 | a0001c0009t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.690+6250A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620496 | |||||||
| chr7:15620505 | G | A | 7 | a0001c0001t0014g0219 a0001c0001t0015g0018 a0001c0001t0019g0116 others(4): Show |
7 | HG01074.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+6241C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620505 | |||||||
| chr7:15620521 | C | T | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.690+6225G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620521 | |||||||
| chr7:15620555 | A | AAAC | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+6188_690+6190d others(5): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620555 | |||||||
| chr7:15620576 | A | C | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+6170T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620576 | |||||||
| chr7:15620604 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.690+6142T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620604 | |||||||
| chr7:15620719 | A | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG01071.hp2 HG01167.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+6027T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620719 | |||||||
| chr7:15620761 | T | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0044 others(14): Show |
18 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+5985A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620761 | |||||||
| chr7:15620820 | T | C | 2 | a0002c0002t0026g0242 a0002c0002t0026g0249 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.690+5926A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620820 | |||||||
| chr7:15620854 | A | G | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.690+5892T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620854 | |||||||
| chr7:15620862 | A | G | 264 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.690+5884T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620862 | |||||||
| chr7:15620939 | ACT | A | 21 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(18): Show |
21 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.690+5805_690+5806d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620939 | |||||||
| chr7:15620954 | C | G | 1 | a0001c0003t0003g0189 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.690+5792G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620954 | |||||||
| chr7:15621012 | G | A | 4 | a0001c0001t0006g0057 a0001c0001t0006g0061 a0001c0001t0006g0062 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+5734C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621012 | |||||||
| chr7:15621046 | G | C | 1 | a0001c0003t0008g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.690+5700C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621046 | |||||||
| chr7:15621121 | A | C | 1 | a0001c0003t0003g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.690+5625T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621121 | |||||||
| chr7:15621275 | C | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(101): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.690+5471G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621275 | |||||||
| chr7:15621363 | G | C | 2 | a0001c0003t0008g0111 a0001c0003t0027g0026 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+5383C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621363 | |||||||
| chr7:15621435 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.690+5311C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621435 | |||||||
| chr7:15621450 | C | G | 1 | a0002c0002t0002g0285 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.690+5296G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621450 | |||||||
| chr7:15621515 | T | C | 1 | a0002c0002t0005g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.690+5231A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621515 | |||||||
| chr7:15621608 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.690+5138C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621608 | |||||||
| chr7:15621630 | T | A | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+5116A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621630 | |||||||
| chr7:15621651 | T | C | 2 | a0001c0001t0023g0002 a0001c0001t0034g0216 |
3 | HG01884.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.690+5095A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621651 | |||||||
| chr7:15621702 | A | G | 1 | a0002c0002t0002g0285 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.690+5044T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621702 | |||||||
| chr7:15621766 | A | C | 1 | a0001c0001t0035g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.690+4980T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621766 | |||||||
| chr7:15621899 | A | C | 2 | a0002c0002t0026g0242 a0002c0002t0026g0249 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.690+4847T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621899 | |||||||
| chr7:15622053 | G | T | 1 | a0002c0002t0001g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690+4693C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622053 | |||||||
| chr7:15622135 | C | A | 1 | a0002c0002t0005g0261 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.690+4611G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622135 | |||||||
| chr7:15622144 | T | C | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.690+4602A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622144 | |||||||
| chr7:15622262 | T | C | 8 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(5): Show |
9 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.690+4484A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622262 | |||||||
| chr7:15622373 | C | G | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.690+4373G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622373 | |||||||
| chr7:15622524 | T | G | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+4222A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622524 | |||||||
| chr7:15622580 | A | C | 1 | a0001c0001t0015g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.690+4166T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622580 | |||||||
| chr7:15622696 | A | T | 194 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.690+4050T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622696 | |||||||
| chr7:15622747 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA18998.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.690+3999A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622747 | |||||||
| chr7:15622807 | C | T | 55 | a0001c0001t0009g0232 a0001c0003t0003g0001 a0001c0003t0003g0050 others(52): Show |
58 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.690+3939G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622807 | |||||||
| chr7:15622840 | T | C | 17 | a0001c0001t0001g0044 a0001c0001t0007g0008 a0001c0001t0007g0072 others(14): Show |
19 | HG01074.hp1 HG01081.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+3906A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622840 | |||||||
| chr7:15623014 | C | G | 1 | a0001c0001t0037g0234 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.690+3732G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623014 | |||||||
| chr7:15623385 | T | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+3361A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623385 | |||||||
| chr7:15623526 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+3220G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623526 | |||||||
| chr7:15623529 | C | G | 1 | a0001c0001t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.690+3217G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623529 | |||||||
| chr7:15623634 | T | A | 2 | a0002c0002t0004g0243 a0002c0002t0004g0244 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+3112A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623634 | |||||||
| chr7:15623803 | C | T | 4 | a0001c0001t0008g0188 a0001c0001t0021g0235 a0001c0001t0021g0236 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+2943G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623803 | |||||||
| chr7:15623824 | A | T | 7 | a0002c0002t0005g0261 a0002c0002t0005g0262 a0002c0002t0005g0263 others(4): Show |
7 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+2922T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623824 | |||||||
| chr7:15623828 | C | A | 2 | a0002c0002t0026g0242 a0002c0002t0026g0249 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.690+2918G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623828 | |||||||
| chr7:15623887 | A | G | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+2859T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623887 | |||||||
| chr7:15623970 | G | A | 1 | a0001c0001t0014g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.690+2776C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623970 | |||||||
| chr7:15624346 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+2400G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624346 | |||||||
| chr7:15624354 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+2392G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624354 | |||||||
| chr7:15624470 | G | A | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+2276C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624470 | |||||||
| chr7:15624541 | A | G | 1 | a0001c0001t0016g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.690+2205T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624541 | |||||||
| chr7:15624592 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.690+2154T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624592 | |||||||
| chr7:15624625 | A | G | 1 | a0001c0003t0003g0189 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.690+2121T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624625 | |||||||
| chr7:15624629 | C | G | 3 | a0001c0003t0003g0105 a0001c0003t0003g0127 a0001c0003t0003g0163 |
3 | HG01928.hp1 HG02273.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.690+2117G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624629 | |||||||
| chr7:15624735 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+2011G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624735 | |||||||
| chr7:15624823 | G | A | 1 | a0002c0002t0005g0272 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.690+1923C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624823 | |||||||
| chr7:15624946 | G | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+1800C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624946 | |||||||
| chr7:15625144 | A | G | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+1602T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625144 | |||||||
| chr7:15625181 | A | G | 2 | a0001c0001t0019g0116 a0001c0001t0019g0117 |
2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.690+1565T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625181 | |||||||
| chr7:15625240 | G | A | 2 | a0001c0001t0016g0015 a0001c0001t0016g0016 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.690+1506C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625240 | |||||||
| chr7:15625257 | A | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0056 others(3): Show |
7 | HG01243.hp1 HG01258.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+1489T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625257 | |||||||
| chr7:15625461 | C | G | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.690+1285G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625461 | |||||||
| chr7:15625465 | T | C | 20 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(17): Show |
20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+1281A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625465 | |||||||
| chr7:15625748 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.690+998C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625748 | |||||||
| chr7:15626179 | A | G | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.690+567T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626179 | |||||||
| chr7:15626242 | G | C | 1 | a0001c0003t0008g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.690+504C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626242 | |||||||
| chr7:15626354 | C | G | 1 | a0002c0002t0002g0279 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.690+392G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626354 | |||||||
| chr7:15626392 | T | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+354A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626392 | |||||||
| chr7:15626463 | C | G | 1 | a0002c0002t0026g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.690+283G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626463 | |||||||
| chr7:15626546 | A | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+200T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626546 | |||||||
| chr7:15626598 | T | G | 14 | a0001c0001t0007g0008 a0001c0001t0007g0072 a0001c0001t0007g0178 others(11): Show |
16 | HG01081.hp1 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.690+148A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626598 | |||||||
| chr7:15626605 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+141G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626605 | |||||||
| chr7:15626650 | C | CAAGAATT others(321): Show |
1 | a0002c0002t0004g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.690+95_690+96insTT others(326): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626650 | |||||||
| chr7:15626650 | C | CAAGAATT others(323): Show |
1 | a0002c0002t0001g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690+95_690+96insTT others(328): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626650 | |||||||
| chr7:15626705 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.690+41C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626705 | |||||||
| chr7:15627019 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-101C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627019 | |||||||
| chr7:15627124 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.518-206A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627124 | |||||||
| chr7:15627126 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.518-208G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627126 | |||||||
| chr7:15627153 | T | A | 1 | a0001c0001t0014g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518-235A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627153 | |||||||
| chr7:15627243 | T | C | 9 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-325A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627243 | |||||||
| chr7:15627422 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.518-504C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627422 | |||||||
| chr7:15627454 | G | C | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-536C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627454 | |||||||
| chr7:15627504 | G | T | 2 | a0001c0003t0003g0118 a0001c0003t0003g0153 |
2 | NA18977.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.518-586C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627504 | |||||||
| chr7:15627512 | A | G | 1 | a0001c0003t0003g0106 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.518-594T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627512 | |||||||
| chr7:15627522 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
7 | HG00140.hp1 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-604C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627522 | |||||||
| chr7:15627546 | A | T | 20 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(17): Show |
20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-628T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627546 | |||||||
| chr7:15627643 | G | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-725C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627643 | |||||||
| chr7:15627715 | G | A | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-797C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627715 | |||||||
| chr7:15627782 | A | T | 1 | a0001c0003t0003g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.518-864T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627782 | |||||||
| chr7:15627808 | A | AACACACA others(5): Show |
92 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(89): Show |
95 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.518-902_518-891dup others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(7): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0137 a0001c0001t0021g0224 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-904_518-891dup others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(9): Show |
12 | a0001c0001t0001g0060 a0001c0001t0007g0008 a0001c0001t0013g0022 others(9): Show |
13 | HG00735.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.518-906_518-891dup others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(11): Show |
19 | a0001c0001t0001g0055 a0001c0001t0001g0078 a0001c0001t0001g0094 others(16): Show |
19 | HG00099.hp1 HG01081.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-908_518-891dup others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(13): Show |
101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.518-891_518-890ins others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(15): Show |
15 | a0001c0001t0001g0075 a0001c0001t0001g0093 a0001c0001t0001g0099 others(12): Show |
16 | HG01243.hp1 HG01255.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.518-891_518-890ins others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(17): Show |
9 | a0001c0001t0001g0044 a0001c0001t0001g0095 a0001c0001t0001g0161 others(6): Show |
9 | HG01074.hp1 HG01081.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-891_518-890ins others(24): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(19): Show |
3 | a0001c0001t0020g0228 a0001c0001t0034g0216 a0001c0011t0001g0210 |
3 | HG02145.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.518-891_518-890ins others(26): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | AACACACA others(21): Show |
2 | a0001c0001t0015g0018 a0001c0001t0023g0002 |
3 | HG01884.hp2 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.518-891_518-890ins others(28): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627808 | A | ACACACAC others(14): Show |
2 | a0001c0001t0001g0070 a0002c0002t0004g0338 |
2 | HG01934.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.518-891_518-890ins others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | |||||||
| chr7:15627827 | G | A | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-909C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627827 | |||||||
| chr7:15627828 | T | C | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-910A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627828 | |||||||
| chr7:15627838 | A | G | 3 | a0001c0003t0003g0105 a0001c0003t0003g0127 a0001c0003t0003g0163 |
3 | HG01928.hp1 HG02273.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.518-920T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627838 | |||||||
| chr7:15627906 | A | T | 263 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(260): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.518-988T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627906 | |||||||
| chr7:15628070 | G | T | 219 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.518-1152C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628070 | |||||||
| chr7:15628204 | T | A | 1 | a0001c0001t0008g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.518-1286A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628204 | |||||||
| chr7:15628254 | T | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1336A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628254 | |||||||
| chr7:15628402 | C | A | 219 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.518-1484G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628402 | |||||||
| chr7:15628445 | C | G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1527G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628445 | |||||||
| chr7:15628467 | G | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1549C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628467 | |||||||
| chr7:15628468 | G | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0159 others(1): Show |
4 | HG02155.hp2 NA18959.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-1550C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628468 | |||||||
| chr7:15628554 | T | G | 2 | a0001c0003t0003g0118 a0001c0003t0003g0153 |
2 | NA18977.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.518-1636A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628554 | |||||||
| chr7:15628561 | G | C | 8 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-1643C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628561 | |||||||
| chr7:15628628 | C | G | 20 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(17): Show |
20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-1710G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628628 | |||||||
| chr7:15628697 | C | T | 2 | a0002c0002t0026g0242 a0002c0002t0026g0249 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.518-1779G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628697 | |||||||
| chr7:15628865 | C | A | 1 | a0002c0002t0028g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.518-1947G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628865 | |||||||
| chr7:15628901 | G | A | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1983C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628901 | |||||||
| chr7:15628957 | A | G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-2039T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628957 | |||||||
| chr7:15628990 | T | C | 1 | a0001c0001t0021g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.518-2072A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628990 | |||||||
| chr7:15629068 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.518-2150G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629068 | |||||||
| chr7:15629092 | T | C | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.518-2174A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629092 | |||||||
| chr7:15629112 | C | T | 20 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(17): Show |
20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-2194G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629112 | |||||||
| chr7:15629223 | A | T | 1 | a0002c0002t0010g0308 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.518-2305T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629223 | |||||||
| chr7:15629358 | G | C | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.518-2440C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629358 | |||||||
| chr7:15629359 | C | T | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.518-2441G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629359 | |||||||
| chr7:15629375 | A | G | 150 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.518-2457T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629375 | |||||||
| chr7:15629394 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.518-2476A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629394 | |||||||
| chr7:15629458 | A | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0162 others(1): Show |
4 | HG00140.hp2 HG01934.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-2540T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629458 | |||||||
| chr7:15629554 | A | C | 4 | a0001c0001t0006g0057 a0001c0001t0006g0061 a0001c0001t0006g0062 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-2636T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629554 | |||||||
| chr7:15629671 | G | C | 21 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(18): Show |
22 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.518-2753C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629671 | |||||||
| chr7:15629774 | CCT | C | 12 | a0001c0001t0001g0186 a0001c0001t0013g0022 a0001c0001t0013g0023 others(9): Show |
12 | HG01106.hp1 HG01261.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.518-2858_518-2857d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629774 | |||||||
| chr7:15629808 | G | A | 2 | a0002c0002t0005g0261 a0002c0002t0005g0273 |
2 | HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.518-2890C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629808 | |||||||
| chr7:15629847 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.518-2929A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629847 | |||||||
| chr7:15629982 | A | T | 1 | a0001c0001t0006g0152 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.518-3064T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629982 | |||||||
| chr7:15630031 | C | G | 1 | a0001c0003t0003g0190 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.518-3113G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630031 | |||||||
| chr7:15630033 | A | G | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.518-3115T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630033 | |||||||
| chr7:15630181 | C | A | 55 | a0001c0001t0009g0232 a0001c0003t0003g0001 a0001c0003t0003g0050 others(52): Show |
58 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-3263G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630181 | |||||||
| chr7:15630277 | C | T | 4 | a0001c0001t0008g0188 a0001c0001t0021g0235 a0001c0001t0021g0236 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-3359G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630277 | |||||||
| chr7:15630487 | C | G | 1 | a0001c0001t0023g0002 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.518-3569G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630487 | |||||||
| chr7:15630638 | T | A | 1 | a0002c0002t0010g0309 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.518-3720A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630638 | |||||||
| chr7:15631017 | G | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.518-4099C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631017 | |||||||
| chr7:15631020 | T | A | 20 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(17): Show |
20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-4102A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631020 | |||||||
| chr7:15631082 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.518-4164A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631082 | |||||||
| chr7:15631143 | C | G | 21 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(18): Show |
22 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.518-4225G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631143 | |||||||
| chr7:15631192 | C | T | 2 | a0002c0002t0002g0288 a0002c0002t0002g0290 |
2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.518-4274G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631192 | |||||||
| chr7:15631214 | T | C | 4 | a0001c0001t0008g0188 a0001c0001t0021g0235 a0001c0001t0021g0236 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-4296A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631214 | |||||||
| chr7:15631231 | C | CA | 23 | a0001c0001t0001g0048 a0001c0001t0001g0107 a0001c0001t0018g0076 others(20): Show |
23 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.518-4314dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631231 | |||||||
| chr7:15631490 | T | C | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.518-4572A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631490 | |||||||
| chr7:15631677 | C | G | 15 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(12): Show |
15 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.518-4759G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631677 | |||||||
| chr7:15631700 | C | T | 261 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.518-4782G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631700 | |||||||
| chr7:15631846 | A | C | 23 | a0001c0001t0015g0018 a0001c0001t0018g0076 a0001c0001t0018g0100 others(20): Show |
24 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.518-4928T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631846 | |||||||
| chr7:15631871 | A | G | 1 | a0001c0001t0006g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.518-4953T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631871 | |||||||
| chr7:15631906 | A | ATG | 5 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0009g0221 others(2): Show |
5 | HG00639.hp2 HG00741.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-4990_518-4989d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTG | 3 | a0001c0001t0006g0057 a0001c0001t0037g0234 a0002c0002t0022g0255 |
3 | HG01109.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.518-4992_518-4989d others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0007g0180 a0001c0001t0014g0217 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.518-4998_518-4989d others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(7): Show |
5 | a0001c0001t0007g0178 a0001c0001t0007g0179 a0001c0001t0007g0181 others(2): Show |
5 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-5002_518-4989d others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(9): Show |
60 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0114 others(57): Show |
65 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.518-5004_518-4989d others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(11): Show |
35 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp2 HG00323.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.518-5006_518-4989d others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(13): Show |
34 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(31): Show |
36 | HG00140.hp1 HG00735.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.518-5008_518-4989d others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(15): Show |
62 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0063 others(59): Show |
63 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.518-5010_518-4989d others(24): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(17): Show |
22 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0065 others(19): Show |
24 | HG00280.hp2 HG01175.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.518-5012_518-4989d others(26): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(19): Show |
19 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0145 others(16): Show |
19 | HG01123.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-5014_518-4989d others(28): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(21): Show |
13 | a0001c0001t0001g0055 a0001c0001t0001g0090 a0001c0001t0001g0112 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.518-4989_518-4988i others(30): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631906 | A | ATGTGTGT others(23): Show |
4 | a0001c0001t0035g0213 a0001c0010t0029g0028 a0002c0002t0005g0273 others(1): Show |
4 | HG01099.hp2 HG02559.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-4989_518-4988i others(32): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | |||||||
| chr7:15631932 | G | GTGTGTGT others(14): Show |
1 | a0001c0001t0001g0060 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.518-5015_518-5014i others(23): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631932 | |||||||
| chr7:15631932 | G | GTGTGTGT others(18): Show |
1 | a0001c0001t0013g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.518-5015_518-5014i others(27): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631932 | |||||||
| chr7:15631933 | G | T | 24 | a0001c0001t0007g0008 a0001c0001t0007g0072 a0001c0001t0007g0178 others(21): Show |
26 | HG01081.hp1 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.518-5015C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631933 | |||||||
| chr7:15631982 | T | C | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 |
3 | HG02486.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.518-5064A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631982 | |||||||
| chr7:15632056 | A | C | 2 | a0002c0002t0002g0282 a0002c0002t0002g0320 |
2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.518-5138T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632056 | |||||||
| chr7:15632139 | A | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.518-5221T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632139 | |||||||
| chr7:15632234 | G | A | 4 | a0001c0001t0006g0057 a0001c0001t0006g0061 a0001c0001t0006g0062 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-5316C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632234 | |||||||
| chr7:15632403 | T | C | 1 | a0002c0002t0005g0263 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.518-5485A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632403 | |||||||
| chr7:15632490 | A | C | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 |
3 | HG02486.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.518-5572T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632490 | |||||||
| chr7:15632988 | G | C | 1 | a0001c0003t0008g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.518-6070C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632988 | |||||||
| chr7:15633073 | G | T | 1 | a0001c0003t0008g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.518-6155C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633073 | |||||||
| chr7:15633187 | G | A | 1 | a0001c0003t0003g0050 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.518-6269C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633187 | |||||||
| chr7:15633282 | C | T | 55 | a0001c0001t0009g0232 a0001c0003t0003g0001 a0001c0003t0003g0050 others(52): Show |
58 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-6364G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633282 | |||||||
| chr7:15633312 | C | G | 3 | a0001c0001t0019g0116 a0001c0001t0019g0117 a0001c0010t0029g0028 |
3 | HG01074.hp1 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.518-6394G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633312 | |||||||
| chr7:15633332 | C | G | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-6414G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633332 | |||||||
| chr7:15633420 | A | G | 3 | a0002c0002t0002g0274 a0002c0002t0002g0275 a0002c0002t0002g0277 |
3 | HG01255.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.518-6502T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633420 | |||||||
| chr7:15633453 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.518-6535G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633453 | |||||||
| chr7:15633559 | C | G | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.518-6641G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633559 | |||||||
| chr7:15633642 | G | A | 19 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(16): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-6724C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633642 | |||||||
| chr7:15633696 | C | T | 67 | a0001c0001t0007g0008 a0001c0001t0007g0072 a0001c0001t0007g0178 others(64): Show |
71 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.518-6778G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633696 | |||||||
| chr7:15633741 | T | C | 1 | a0002c0002t0004g0332 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.518-6823A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633741 | |||||||
| chr7:15634022 | G | A | 56 | a0001c0001t0009g0232 a0001c0003t0003g0001 a0001c0003t0003g0050 others(53): Show |
59 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.518-7104C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634022 | |||||||
| chr7:15634240 | A | G | 1 | a0001c0001t0037g0234 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.518-7322T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634240 | |||||||
| chr7:15634314 | G | C | 16 | a0001c0001t0006g0057 a0001c0001t0006g0061 a0001c0001t0006g0062 others(13): Show |
16 | HG00639.hp1 HG00639.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.518-7396C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634314 | |||||||
| chr7:15634371 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.518-7453T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634371 | |||||||
| chr7:15634546 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.518-7628C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634546 | |||||||
| chr7:15634610 | A | G | 20 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(17): Show |
20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-7692T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634610 | |||||||
| chr7:15634748 | C | T | 8 | a0001c0001t0001g0045 a0001c0001t0012g0003 a0001c0001t0012g0032 others(5): Show |
9 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-7830G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634748 | |||||||
| chr7:15634756 | C | G | 4 | a0001c0001t0001g0044 a0001c0001t0019g0116 a0001c0001t0019g0117 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-7838G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634756 | |||||||
| chr7:15634789 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0138 |
4 | HG01192.hp1 HG01256.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-7871A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634789 | |||||||
| chr7:15635033 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0019g0116 a0001c0001t0019g0117 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-8115T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635033 | |||||||
| chr7:15635049 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.518-8131T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635049 | |||||||
| chr7:15635084 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0078 others(17): Show |
21 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.518-8166A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635084 | |||||||
| chr7:15635132 | C | T | 1 | a0001c0001t0006g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.518-8214G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635132 | |||||||
| chr7:15635205 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.518-8287C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635205 | |||||||
| chr7:15635362 | G | T | 14 | a0001c0001t0006g0175 a0001c0001t0018g0076 a0001c0001t0018g0101 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.518-8444C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635362 | |||||||
| chr7:15635407 | T | C | 1 | a0002c0002t0004g0327 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.518-8489A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635407 | |||||||
| chr7:15635672 | T | A | 18 | a0001c0001t0001g0183 a0001c0001t0007g0008 a0001c0001t0007g0072 others(15): Show |
19 | HG01081.hp1 HG01255.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-8754A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635672 | |||||||
| chr7:15635673 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.518-8755T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635673 | |||||||
| chr7:15635713 | T | TA | 30 | a0001c0001t0006g0175 a0001c0001t0009g0229 a0001c0001t0009g0230 others(27): Show |
31 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.518-8796dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635713 | |||||||
| chr7:15635924 | A | C | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-9006T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635924 | |||||||
| chr7:15635944 | G | A | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.518-9026C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635944 | |||||||
| chr7:15635968 | A | T | 1 | a0002c0002t0002g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518-9050T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635968 | |||||||
| chr7:15636010 | G | A | 269 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.518-9092C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636010 | |||||||
| chr7:15636117 | T | G | 9 | a0001c0001t0001g0183 a0001c0001t0007g0072 a0001c0001t0009g0232 others(6): Show |
9 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-9199A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636117 | |||||||
| chr7:15636285 | C | A | 2 | a0001c0003t0038g0233 a0002c0002t0026g0249 |
2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.518-9367G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636285 | |||||||
| chr7:15636394 | G | A | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.518-9476C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636394 | |||||||
| chr7:15636417 | A | C | 2 | a0001c0001t0018g0176 a0001c0001t0023g0002 |
3 | HG01884.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.518-9499T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636417 | |||||||
| chr7:15636579 | T | G | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-9661A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636579 | |||||||
| chr7:15636648 | A | G | 1 | a0001c0001t0007g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.518-9730T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636648 | |||||||
| chr7:15636789 | A | G | 9 | a0001c0001t0001g0183 a0001c0001t0007g0072 a0001c0001t0009g0232 others(6): Show |
9 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-9871T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636789 | |||||||
| chr7:15637074 | A | C | 2 | a0001c0001t0014g0219 a0001c0001t0020g0228 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.518-10156T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637074 | |||||||
| chr7:15637318 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-10400G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637318 | |||||||
| chr7:15637370 | C | T | 13 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(10): Show |
14 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.518-10452G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637370 | |||||||
| chr7:15637386 | T | C | 9 | a0001c0001t0001g0183 a0001c0001t0007g0072 a0001c0001t0009g0232 others(6): Show |
9 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-10468A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637386 | |||||||
| chr7:15637400 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.518-10482G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637400 | |||||||
| chr7:15637520 | ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0089 a0001c0001t0013g0025 |
2 | HG00621.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.518-10614_518-1060 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637520 | |||||||
| chr7:15637534 | A | G | 1 | a0002c0002t0005g0272 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.518-10616T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637534 | |||||||
| chr7:15637554 | A | G | 1 | a0001c0003t0027g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-10636T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637554 | |||||||
| chr7:15637610 | T | C | 1 | a0001c0003t0017g0205 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.518-10692A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637610 | |||||||
| chr7:15637678 | A | C | 3 | a0002c0002t0010g0306 a0002c0002t0010g0308 a0002c0002t0010g0309 |
3 | HG00323.hp2 HG01358.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.518-10760T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637678 | |||||||
| chr7:15637709 | T | C | 2 | a0002c0002t0004g0245 a0002c0002t0010g0246 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-10791A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637709 | |||||||
| chr7:15637814 | T | G | 2 | a0001c0001t0008g0042 a0001c0001t0008g0043 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.518-10896A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637814 | |||||||
| chr7:15637929 | C | G | 1 | a0004c0006t0001g0036 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.518-11011G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637929 | |||||||
| chr7:15638037 | T | A | 1 | a0002c0002t0002g0304 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.518-11119A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638037 | |||||||
| chr7:15638125 | T | C | 6 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(3): Show |
6 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.518-11207A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638125 | |||||||
| chr7:15638145 | C | A | 7 | a0001c0001t0001g0183 a0001c0001t0009g0232 a0002c0002t0002g0247 others(4): Show |
7 | HG02647.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-11227G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638145 | |||||||
| chr7:15638309 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0137 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.518-11391G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638309 | |||||||
| chr7:15638373 | C | T | 1 | a0001c0001t0009g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.518-11455G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638373 | |||||||
| chr7:15638391 | C | T | 2 | a0001c0003t0003g0154 a0001c0003t0003g0196 |
2 | NA18948.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.518-11473G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638391 | |||||||
| chr7:15638494 | ATCT | A | 6 | a0001c0001t0001g0183 a0002c0002t0002g0247 a0002c0002t0004g0243 others(3): Show |
6 | HG02647.hp1 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-11579_518-1157 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638494 | |||||||
| chr7:15638526 | A | G | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-11608T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638526 | |||||||
| chr7:15638543 | G | A | 11 | a0001c0001t0001g0044 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-11625C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638543 | |||||||
| chr7:15638753 | T | C | 1 | a0001c0001t0016g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.518-11835A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638753 | |||||||
| chr7:15638771 | G | C | 2 | a0002c0002t0002g0274 a0002c0002t0002g0275 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.518-11853C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638771 | |||||||
| chr7:15638804 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.518-11886G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638804 | |||||||
| chr7:15638870 | C | T | 114 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
119 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.518-11952G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638870 | |||||||
| chr7:15638981 | C | A | 4 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0180 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-12063G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638981 | |||||||
| chr7:15638982 | C | T | 1 | a0001c0001t0014g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.518-12064G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638982 | |||||||
| chr7:15638999 | G | A | 289 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.518-12081C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638999 | |||||||
| chr7:15639130 | C | A | 1 | a0001c0001t0014g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.518-12212G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639130 | |||||||
| chr7:15639141 | AT | A | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-12224delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639141 | |||||||
| chr7:15639188 | T | C | 1 | a0001c0001t0013g0021 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.518-12270A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639188 | |||||||
| chr7:15639289 | T | C | 3 | a0001c0001t0001g0186 a0001c0001t0015g0013 a0001c0001t0015g0014 |
3 | HG02809.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.518-12371A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639289 | |||||||
| chr7:15639502 | T | C | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-12584A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639502 | |||||||
| chr7:15639578 | CT | C | 6 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-12661delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639578 | |||||||
| chr7:15639672 | T | C | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-12754A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639672 | |||||||
| chr7:15639871 | T | C | 1 | a0002c0002t0026g0249 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.518-12953A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639871 | |||||||
| chr7:15639921 | T | A | 1 | a0002c0002t0010g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.518-13003A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639921 | |||||||
| chr7:15639986 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0137 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.518-13068C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639986 | |||||||
| chr7:15640108 | T | G | 3 | a0002c0002t0004g0253 a0002c0002t0004g0254 a0002c0002t0040g0251 |
3 | HG01109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.518-13190A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640108 | |||||||
| chr7:15640252 | G | T | 1 | a0002c0002t0002g0320 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.518-13334C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640252 | |||||||
| chr7:15640254 | T | G | 1 | a0002c0002t0002g0320 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.518-13336A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640254 | |||||||
| chr7:15640254 | T | TTG | 28 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(25): Show |
29 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.518-13338_518-1333 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640254 | |||||||
| chr7:15640254 | T | TTGTG | 3 | a0001c0001t0001g0161 a0001c0001t0015g0020 a0002c0002t0010g0306 |
3 | HG00323.hp2 HG02015.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.518-13340_518-1333 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640254 | |||||||
| chr7:15640370 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0137 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-13452A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640370 | |||||||
| chr7:15640447 | C | T | 70 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0186 others(67): Show |
73 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.518-13529G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640447 | |||||||
| chr7:15640478 | G | A | 7 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0002g0247 others(4): Show |
7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-13560C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640478 | |||||||
| chr7:15640483 | A | G | 1 | a0001c0001t0018g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.518-13565T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640483 | |||||||
| chr7:15640515 | T | C | 7 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(4): Show |
8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-13597A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640515 | |||||||
| chr7:15640642 | G | A | 1 | a0001c0003t0003g0190 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.518-13724C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640642 | |||||||
| chr7:15640825 | A | G | 7 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0002g0247 others(4): Show |
7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-13907T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640825 | |||||||
| chr7:15640833 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.518-13915T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640833 | |||||||
| chr7:15640842 | T | C | 4 | a0002c0002t0002g0304 a0002c0002t0002g0305 a0002c0002t0002g0330 others(1): Show |
4 | HG01361.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-13924A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640842 | |||||||
| chr7:15640849 | C | A | 1 | a0005c0005t0001g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.518-13931G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640849 | |||||||
| chr7:15641230 | C | A | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.518-14312G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641230 | |||||||
| chr7:15641230 | C | T | 2 | a0001c0001t0019g0116 a0001c0001t0019g0117 |
2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.518-14312G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641230 | |||||||
| chr7:15641344 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-14426G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641344 | |||||||
| chr7:15641361 | T | TTTTG | 3 | a0001c0001t0001g0121 a0001c0003t0003g0189 a0001c0007t0003g0038 |
3 | NA18942.hp1 NA18954.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.518-14447_518-1444 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641361 | |||||||
| chr7:15641361 | TTTTG | T | 12 | a0002c0002t0002g0274 a0002c0002t0002g0275 a0002c0002t0004g0332 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-14447_518-1444 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641361 | |||||||
| chr7:15641579 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0015g0013 a0001c0001t0015g0014 |
3 | HG02809.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.518-14661C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641579 | |||||||
| chr7:15641787 | A | G | 1 | a0001c0003t0003g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.518-14869T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641787 | |||||||
| chr7:15641806 | T | A | 2 | a0001c0001t0018g0100 a0002c0002t0005g0257 |
2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.518-14888A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641806 | |||||||
| chr7:15641889 | G | A | 2 | a0002c0002t0022g0302 a0002c0002t0022g0316 |
2 | HG00741.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.518-14971C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641889 | |||||||
| chr7:15641976 | T | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0078 others(20): Show |
25 | HG00099.hp1 HG00323.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.518-15058A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641976 | |||||||
| chr7:15642090 | T | C | 1 | a0001c0001t0014g0219 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.518-15172A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642090 | |||||||
| chr7:15642110 | C | T | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-15192G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642110 | |||||||
| chr7:15642165 | T | A | 1 | a0001c0003t0003g0200 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.518-15247A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642165 | |||||||
| chr7:15642244 | G | A | 1 | a0001c0008t0007g0177 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.518-15326C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642244 | |||||||
| chr7:15642279 | C | T | 1 | a0002c0002t0026g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.518-15361G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642279 | |||||||
| chr7:15642387 | T | C | 1 | a0001c0003t0027g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-15469A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642387 | |||||||
| chr7:15642413 | G | C | 2 | a0002c0002t0004g0245 a0002c0002t0010g0246 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-15495C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642413 | |||||||
| chr7:15642544 | C | T | 5 | a0003c0004t0011g0310 a0003c0004t0011g0311 a0003c0004t0011g0312 others(2): Show |
5 | HG00558.hp1 HG00741.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-15626G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642544 | |||||||
| chr7:15642546 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0131 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.518-15628T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642546 | |||||||
| chr7:15642652 | C | A | 2 | a0002c0002t0002g0274 a0002c0002t0002g0275 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.518-15734G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642652 | |||||||
| chr7:15642974 | T | C | 2 | a0002c0002t0002g0325 a0002c0002t0002g0326 |
2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.518-16056A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642974 | |||||||
| chr7:15642982 | G | A | 7 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0002g0247 others(4): Show |
7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-16064C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642982 | |||||||
| chr7:15643044 | A | G | 1 | a0001c0003t0003g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.518-16126T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643044 | |||||||
| chr7:15643193 | C | G | 7 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0002g0247 others(4): Show |
7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-16275G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643193 | |||||||
| chr7:15643264 | T | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
76 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.518-16346A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643264 | |||||||
| chr7:15643273 | G | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.518-16355C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643273 | |||||||
| chr7:15643343 | C | T | 4 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 others(1): Show |
5 | HG01123.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-16425G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643343 | |||||||
| chr7:15643493 | G | T | 2 | a0001c0001t0016g0015 a0001c0001t0016g0016 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.518-16575C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643493 | |||||||
| chr7:15643505 | T | C | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.518-16587A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643505 | |||||||
| chr7:15643508 | G | A | 1 | a0004c0006t0001g0036 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.518-16590C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643508 | |||||||
| chr7:15643619 | G | C | 2 | a0002c0002t0004g0240 a0002c0002t0004g0241 |
2 | HG01515.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.518-16701C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643619 | |||||||
| chr7:15643667 | G | T | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-16749C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643667 | |||||||
| chr7:15643751 | A | C | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-16833T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643751 | |||||||
| chr7:15644212 | A | C | 1 | a0003c0004t0011g0312 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.518-17294T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644212 | |||||||
| chr7:15644273 | C | T | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-17355G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644273 | |||||||
| chr7:15644426 | A | G | 15 | a0001c0001t0018g0076 a0001c0001t0018g0100 a0001c0001t0018g0101 others(12): Show |
16 | HG00738.hp1 HG01069.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.518-17508T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644426 | |||||||
| chr7:15644444 | C | T | 2 | a0001c0001t0016g0015 a0001c0001t0016g0016 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.518-17526G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644444 | |||||||
| chr7:15644460 | C | G | 1 | a0002c0002t0010g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.518-17542G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644460 | |||||||
| chr7:15644626 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.518-17708A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644626 | |||||||
| chr7:15644821 | A | G | 35 | a0001c0001t0006g0175 a0001c0001t0009g0229 a0001c0001t0009g0230 others(32): Show |
36 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.518-17903T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644821 | |||||||
| chr7:15644898 | C | T | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-17980G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644898 | |||||||
| chr7:15645417 | T | C | 1 | a0001c0001t0009g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.518-18499A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645417 | |||||||
| chr7:15645457 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18983.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.518-18539C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645457 | |||||||
| chr7:15645506 | T | C | 1 | a0002c0002t0022g0302 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.518-18588A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645506 | |||||||
| chr7:15645558 | A | G | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-18640T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645558 | |||||||
| chr7:15645618 | T | TA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0166 |
4 | HG02559.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-18701dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645618 | |||||||
| chr7:15645725 | A | G | 7 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0002g0247 others(4): Show |
7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-18807T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645725 | |||||||
| chr7:15645734 | T | C | 1 | a0002c0002t0002g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518-18816A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645734 | |||||||
| chr7:15645756 | C | A | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-18838G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645756 | |||||||
| chr7:15645833 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.518-18915A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645833 | |||||||
| chr7:15645946 | G | A | 7 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(4): Show |
8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-19028C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645946 | |||||||
| chr7:15645963 | A | G | 1 | a0006c0012t0005g0339 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.518-19045T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645963 | |||||||
| chr7:15645982 | C | T | 5 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0002g0247 others(2): Show |
5 | HG01081.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-19064G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645982 | |||||||
| chr7:15646002 | G | A | 30 | a0001c0001t0006g0175 a0001c0001t0009g0229 a0001c0001t0009g0230 others(27): Show |
30 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.518-19084C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646002 | |||||||
| chr7:15646075 | T | A | 1 | a0001c0003t0003g0103 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.518-19157A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646075 | |||||||
| chr7:15646126 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0078 others(12): Show |
16 | HG00099.hp1 HG00323.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.518-19208T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646126 | |||||||
| chr7:15646146 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-19228A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646146 | |||||||
| chr7:15646370 | T | A | 1 | a0001c0003t0027g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-19452A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646370 | |||||||
| chr7:15646394 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.518-19476T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646394 | |||||||
| chr7:15646452 | T | G | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.518-19534A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646452 | |||||||
| chr7:15646548 | G | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.518-19630C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646548 | |||||||
| chr7:15646892 | G | T | 3 | a0001c0001t0014g0219 a0001c0001t0020g0228 a0001c0010t0029g0028 |
3 | HG02280.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.518-19974C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646892 | |||||||
| chr7:15646956 | A | G | 7 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0002g0247 others(4): Show |
7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-20038T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646956 | |||||||
| chr7:15647283 | G | C | 34 | a0001c0001t0006g0175 a0001c0001t0009g0229 a0001c0001t0009g0230 others(31): Show |
35 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.518-20365C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647283 | |||||||
| chr7:15647417 | C | G | 2 | a0002c0002t0004g0245 a0002c0002t0010g0246 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-20499G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647417 | |||||||
| chr7:15647813 | C | G | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-20895G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647813 | |||||||
| chr7:15647872 | A | C | 1 | a0002c0002t0004g0238 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.518-20954T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647872 | |||||||
| chr7:15648375 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
89 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.518-21457A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648375 | |||||||
| chr7:15648387 | G | A | 1 | a0001c0001t0006g0152 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.518-21469C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648387 | |||||||
| chr7:15648656 | G | A | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-21738C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648656 | |||||||
| chr7:15648843 | T | C | 1 | a0001c0001t0019g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.518-21925A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648843 | |||||||
| chr7:15648855 | T | C | 1 | a0002c0002t0002g0323 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.518-21937A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648855 | |||||||
| chr7:15648887 | A | G | 2 | a0002c0002t0004g0243 a0002c0002t0026g0242 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.518-21969T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648887 | |||||||
| chr7:15649222 | A | C | 253 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.518-22304T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649222 | |||||||
| chr7:15649323 | A | C | 1 | a0001c0001t0035g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.518-22405T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649323 | |||||||
| chr7:15649350 | T | A | 3 | a0001c0001t0007g0072 a0002c0002t0004g0245 a0002c0002t0010g0246 |
3 | HG01081.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-22432A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649350 | |||||||
| chr7:15649354 | C | T | 4 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0245 others(1): Show |
4 | HG01081.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-22436G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649354 | |||||||
| chr7:15649399 | G | A | 1 | a0001c0001t0021g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.518-22481C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649399 | |||||||
| chr7:15649414 | T | C | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-22496A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649414 | |||||||
| chr7:15649454 | A | T | 1 | a0001c0001t0001g0145 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.518-22536T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649454 | |||||||
| chr7:15649472 | GT | G | 7 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(4): Show |
8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-22555delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649472 | |||||||
| chr7:15649579 | T | C | 2 | a0001c0003t0003g0096 a0001c0003t0003g0097 |
2 | NA18995.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.518-22661A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649579 | |||||||
| chr7:15649712 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.518-22794C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649712 | |||||||
| chr7:15649735 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.518-22817T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649735 | |||||||
| chr7:15649921 | A | T | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-23003T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649921 | |||||||
| chr7:15650144 | A | G | 1 | a0002c0002t0005g0261 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.518-23226T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650144 | |||||||
| chr7:15650488 | G | C | 2 | a0001c0001t0001g0045 a0001c0001t0006g0057 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.518-23570C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650488 | |||||||
| chr7:15650507 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.518-23589T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650507 | |||||||
| chr7:15650586 | T | A | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-23668A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650586 | |||||||
| chr7:15650605 | T | G | 2 | a0001c0001t0001g0075 a0001c0009t0001g0079 |
2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.518-23687A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650605 | |||||||
| chr7:15650615 | A | C | 1 | a0001c0001t0015g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.518-23697T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650615 | |||||||
| chr7:15650714 | A | G | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-23796T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650714 | |||||||
| chr7:15650731 | T | A | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.518-23813A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650731 | |||||||
| chr7:15651046 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.518-24128C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651046 | |||||||
| chr7:15651177 | G | C | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.518-24259C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651177 | |||||||
| chr7:15651287 | A | G | 2 | a0002c0002t0004g0243 a0002c0002t0026g0242 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.518-24369T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651287 | |||||||
| chr7:15651306 | T | A | 1 | a0001c0003t0003g0195 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.518-24388A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651306 | |||||||
| chr7:15651644 | C | T | 1 | a0001c0003t0003g0156 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.518-24726G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651644 | |||||||
| chr7:15651775 | AG | A | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-24858delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651775 | |||||||
| chr7:15651793 | C | T | 4 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0245 others(1): Show |
4 | HG01081.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-24875G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651793 | |||||||
| chr7:15651954 | G | A | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-25036C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651954 | |||||||
| chr7:15651975 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.518-25057A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651975 | |||||||
| chr7:15651982 | C | G | 3 | a0002c0002t0002g0323 a0002c0002t0002g0325 a0002c0002t0002g0326 |
3 | HG03017.hp2 HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.518-25064G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651982 | |||||||
| chr7:15652044 | G | C | 1 | a0001c0001t0007g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.518-25126C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652044 | |||||||
| chr7:15652182 | G | A | 3 | a0001c0001t0014g0219 a0001c0001t0020g0228 a0001c0010t0029g0028 |
3 | HG02280.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.518-25264C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652182 | |||||||
| chr7:15652259 | C | G | 1 | a0002c0002t0005g0264 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.518-25341G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652259 | |||||||
| chr7:15652294 | G | A | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-25376C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652294 | |||||||
| chr7:15652421 | T | C | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-25503A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652421 | |||||||
| chr7:15652468 | A | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
70 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.518-25550T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652468 | |||||||
| chr7:15652525 | A | G | 38 | a0001c0001t0006g0175 a0001c0001t0009g0229 a0001c0001t0009g0230 others(35): Show |
39 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.518-25607T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652525 | |||||||
| chr7:15652687 | T | G | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-25769A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652687 | |||||||
| chr7:15652711 | A | G | 1 | a0002c0002t0022g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.518-25793T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652711 | |||||||
| chr7:15652716 | G | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
7 | HG00140.hp1 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-25798C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652716 | |||||||
| chr7:15652752 | T | G | 5 | a0001c0001t0007g0072 a0002c0002t0004g0243 a0002c0002t0004g0245 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25834A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652752 | |||||||
| chr7:15652775 | G | A | 5 | a0001c0001t0007g0072 a0002c0002t0004g0243 a0002c0002t0004g0245 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25857C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652775 | |||||||
| chr7:15652830 | G | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0056 others(1): Show |
5 | HG01243.hp2 HG01258.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25912C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652830 | |||||||
| chr7:15652903 | A | G | 5 | a0001c0003t0003g0104 a0001c0003t0003g0105 a0001c0003t0003g0106 others(2): Show |
5 | NA18948.hp2 NA18949.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25985T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652903 | |||||||
| chr7:15653096 | C | T | 6 | a0001c0001t0013g0022 a0001c0001t0013g0023 a0001c0001t0013g0024 others(3): Show |
6 | HG01255.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-26178G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653096 | |||||||
| chr7:15653190 | T | C | 3 | a0001c0001t0009g0222 a0002c0002t0004g0244 a0002c0002t0010g0248 |
3 | HG02486.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.518-26272A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653190 | |||||||
| chr7:15653267 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.518-26349C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653267 | |||||||
| chr7:15653365 | A | C | 1 | a0001c0001t0007g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.518-26447T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653365 | |||||||
| chr7:15653374 | G | A | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-26456C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653374 | |||||||
| chr7:15653473 | G | A | 192 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.518-26555C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653473 | |||||||
| chr7:15653750 | T | G | 1 | a0002c0002t0004g0295 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.518-26832A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653750 | |||||||
| chr7:15653788 | C | T | 1 | a0001c0003t0003g0190 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.518-26870G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653788 | |||||||
| chr7:15653797 | T | C | 2 | a0001c0001t0020g0225 a0001c0001t0020g0227 |
2 | HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.518-26879A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653797 | |||||||
| chr7:15653851 | A | G | 1 | a0001c0001t0018g0076 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.518-26933T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653851 | |||||||
| chr7:15653986 | A | T | 2 | a0002c0002t0004g0245 a0002c0002t0010g0246 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-27068T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653986 | |||||||
| chr7:15654074 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.518-27156A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654074 | |||||||
| chr7:15654154 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-27236C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654154 | |||||||
| chr7:15654281 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.518-27363T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654281 | |||||||
| chr7:15654377 | T | C | 1 | a0001c0001t0019g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.518-27459A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654377 | |||||||
| chr7:15654468 | G | A | 3 | a0001c0001t0007g0072 a0002c0002t0004g0245 a0002c0002t0010g0246 |
3 | HG01081.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-27550C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654468 | |||||||
| chr7:15654490 | G | T | 1 | a0001c0001t0015g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.518-27572C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654490 | |||||||
| chr7:15654518 | T | C | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-27600A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654518 | |||||||
| chr7:15654640 | G | A | 1 | a0001c0003t0027g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-27722C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654640 | |||||||
| chr7:15654950 | A | T | 1 | a0001c0003t0003g0087 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.518-28032T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654950 | |||||||
| chr7:15654958 | A | T | 6 | a0002c0002t0005g0261 a0002c0002t0005g0262 a0002c0002t0005g0263 others(3): Show |
6 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.518-28040T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654958 | |||||||
| chr7:15655009 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-28091G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655009 | |||||||
| chr7:15655020 | T | A | 5 | a0001c0001t0001g0113 a0001c0001t0014g0214 a0001c0001t0014g0215 others(2): Show |
5 | HG01243.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-28102A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655020 | |||||||
| chr7:15655090 | A | C | 1 | a0001c0003t0003g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.518-28172T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655090 | |||||||
| chr7:15655130 | G | C | 2 | a0001c0001t0006g0061 a0001c0001t0006g0062 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.518-28212C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655130 | |||||||
| chr7:15655168 | G | A | 18 | a0001c0001t0001g0044 a0001c0001t0001g0187 a0001c0001t0008g0040 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-28250C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655168 | |||||||
| chr7:15655212 | T | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.518-28294A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655212 | |||||||
| chr7:15655355 | T | C | 6 | a0001c0001t0013g0022 a0001c0001t0013g0023 a0001c0001t0013g0024 others(3): Show |
6 | HG01255.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-28437A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655355 | |||||||
| chr7:15655397 | C | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-28479G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655397 | |||||||
| chr7:15655454 | C | T | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-28536G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655454 | |||||||
| chr7:15655524 | C | G | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-28606G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655524 | |||||||
| chr7:15655657 | G | A | 1 | a0001c0001t0012g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.518-28739C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655657 | |||||||
| chr7:15655793 | A | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.518-28875T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655793 | |||||||
| chr7:15655837 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
89 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.518-28919T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655837 | |||||||
| chr7:15655924 | T | A | 2 | a0001c0003t0038g0233 a0002c0002t0026g0249 |
2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.518-29006A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655924 | |||||||
| chr7:15656064 | C | T | 3 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 |
3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-29146G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656064 | |||||||
| chr7:15656097 | A | C | 1 | a0003c0004t0011g0276 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.518-29179T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656097 | |||||||
| chr7:15656099 | C | A | 2 | a0001c0001t0019g0116 a0001c0001t0019g0117 |
2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.518-29181G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656099 | |||||||
| chr7:15656291 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.518-29373C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656291 | |||||||
| chr7:15656339 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.518-29421A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656339 | |||||||
| chr7:15656370 | T | G | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-29452A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656370 | |||||||
| chr7:15656387 | G | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(74): Show |
79 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.518-29469C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656387 | |||||||
| chr7:15656437 | C | CT | 8 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0001c0001t0023g0002 others(5): Show |
9 | HG01081.hp1 HG01884.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+29448dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656437 | |||||||
| chr7:15656526 | T | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.517+29360A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656526 | |||||||
| chr7:15656612 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.517+29274A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656612 | |||||||
| chr7:15656717 | A | C | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.517+29169T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656717 | |||||||
| chr7:15656800 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.517+29086A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656800 | |||||||
| chr7:15656823 | T | C | 2 | a0001c0003t0003g0058 a0001c0003t0003g0158 |
2 | HG02071.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.517+29063A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656823 | |||||||
| chr7:15656934 | T | C | 1 | a0001c0001t0006g0135 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.517+28952A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656934 | |||||||
| chr7:15656980 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.517+28906C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656980 | |||||||
| chr7:15657051 | T | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.517+28835A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657051 | |||||||
| chr7:15657070 | G | A | 2 | a0002c0002t0004g0245 a0002c0002t0010g0246 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.517+28816C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657070 | |||||||
| chr7:15657359 | T | C | 1 | a0001c0003t0038g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.517+28527A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657359 | |||||||
| chr7:15657417 | T | A | 1 | a0001c0001t0007g0008 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.517+28469A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657417 | |||||||
| chr7:15657444 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.517+28442A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657444 | |||||||
| chr7:15657451 | T | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+28435A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657451 | |||||||
| chr7:15657953 | G | A | 1 | a0001c0003t0003g0206 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.517+27933C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657953 | |||||||
| chr7:15658021 | C | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0006g0057 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+27865G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658021 | |||||||
| chr7:15658086 | G | A | 2 | a0002c0002t0004g0243 a0002c0002t0026g0242 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+27800C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658086 | |||||||
| chr7:15658311 | A | T | 1 | a0002c0002t0002g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.517+27575T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658311 | |||||||
| chr7:15658334 | G | A | 2 | a0001c0003t0038g0233 a0002c0002t0026g0249 |
2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.517+27552C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658334 | |||||||
| chr7:15658382 | G | A | 1 | a0001c0001t0015g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517+27504C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658382 | |||||||
| chr7:15658465 | C | A | 264 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.517+27421G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658465 | |||||||
| chr7:15658553 | C | T | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.517+27333G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658553 | |||||||
| chr7:15658604 | G | A | 6 | a0001c0001t0007g0072 a0001c0001t0009g0232 a0002c0002t0004g0243 others(3): Show |
6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+27282C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658604 | |||||||
| chr7:15658620 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.517+27266G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658620 | |||||||
| chr7:15658659 | T | G | 2 | a0002c0002t0004g0243 a0002c0002t0026g0242 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+27227A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658659 | |||||||
| chr7:15658701 | G | A | 38 | a0001c0001t0006g0175 a0001c0001t0009g0229 a0001c0001t0009g0230 others(35): Show |
39 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.517+27185C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658701 | |||||||
| chr7:15658822 | C | T | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+27064G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658822 | |||||||
| chr7:15659157 | G | A | 1 | a0001c0001t0021g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517+26729C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659157 | |||||||
| chr7:15659190 | G | C | 252 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(249): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.517+26696C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659190 | |||||||
| chr7:15659382 | T | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(56): Show |
61 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.517+26504A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659382 | |||||||
| chr7:15659396 | G | A | 5 | a0001c0001t0007g0072 a0002c0002t0004g0243 a0002c0002t0004g0245 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+26490C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659396 | |||||||
| chr7:15659401 | T | G | 1 | a0002c0002t0022g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.517+26485A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659401 | |||||||
| chr7:15659411 | G | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(74): Show |
79 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.517+26475C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659411 | |||||||
| chr7:15659690 | G | A | 2 | a0001c0001t0014g0219 a0001c0001t0020g0228 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.517+26196C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659690 | |||||||
| chr7:15659758 | C | CA | 64 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0044 others(61): Show |
67 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.517+26127dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659758 | |||||||
| chr7:15659758 | CA | C | 9 | a0001c0001t0001g0046 a0001c0001t0006g0057 a0001c0001t0016g0017 others(6): Show |
9 | HG00558.hp1 HG00738.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+26127delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659758 | |||||||
| chr7:15659758 | CAAAAA | C | 11 | a0001c0001t0006g0175 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.517+26123_517+2612 others(9): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659758 | |||||||
| chr7:15660007 | A | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+25879T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660007 | |||||||
| chr7:15660025 | A | G | 5 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0007g0072 others(2): Show |
5 | HG01081.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+25861T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660025 | |||||||
| chr7:15660045 | G | A | 2 | a0002c0002t0004g0245 a0002c0002t0010g0246 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.517+25841C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660045 | |||||||
| chr7:15660113 | A | G | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+25773T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660113 | |||||||
| chr7:15660191 | C | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.517+25695G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660191 | |||||||
| chr7:15660274 | G | A | 1 | a0002c0002t0004g0256 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.517+25612C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660274 | |||||||
| chr7:15660406 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.517+25480A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660406 | |||||||
| chr7:15660565 | C | T | 1 | a0001c0001t0018g0176 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.517+25321G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660565 | |||||||
| chr7:15660649 | T | G | 1 | a0001c0001t0001g0185 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.517+25237A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660649 | |||||||
| chr7:15660691 | C | T | 1 | a0001c0001t0016g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517+25195G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660691 | |||||||
| chr7:15660816 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0006g0057 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.517+25070C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660816 | |||||||
| chr7:15660935 | C | G | 1 | a0001c0001t0007g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.517+24951G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660935 | |||||||
| chr7:15661000 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0012g0031 a0002c0002t0004g0295 |
3 | NA18944.hp1 NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.517+24886C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661000 | |||||||
| chr7:15661005 | T | G | 1 | a0001c0007t0003g0038 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.517+24881A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661005 | |||||||
| chr7:15661012 | C | CA | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(138): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.517+24873dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | |||||||
| chr7:15661012 | C | CAA | 40 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0078 others(37): Show |
40 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.517+24872_517+2487 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | |||||||
| chr7:15661012 | C | CAAA | 12 | a0001c0001t0001g0113 a0001c0001t0001g0186 a0001c0001t0012g0031 others(9): Show |
12 | HG00609.hp1 HG01243.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+24871_517+2487 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | |||||||
| chr7:15661012 | CA | C | 35 | a0001c0001t0001g0044 a0001c0001t0001g0183 a0001c0001t0001g0187 others(32): Show |
36 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.517+24873delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | |||||||
| chr7:15661012 | CAA | C | 6 | a0001c0001t0007g0008 a0001c0001t0007g0182 a0001c0001t0014g0214 others(3): Show |
7 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+24872_517+2487 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | |||||||
| chr7:15661012 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0056 |
4 | HG01258.hp2 HG01433.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+24864_517+2487 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | |||||||
| chr7:15661041 | A | G | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+24845T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661041 | |||||||
| chr7:15661042 | G | A | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+24844C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661042 | |||||||
| chr7:15661242 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.517+24644G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661242 | |||||||
| chr7:15661347 | G | A | 1 | a0004c0006t0001g0036 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.517+24539C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661347 | |||||||
| chr7:15661437 | C | T | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+24449G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661437 | |||||||
| chr7:15661467 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+24419G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661467 | |||||||
| chr7:15661511 | C | A | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+24375G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661511 | |||||||
| chr7:15661569 | A | C | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+24317T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661569 | |||||||
| chr7:15661728 | A | G | 1 | a0001c0001t0006g0152 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.517+24158T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661728 | |||||||
| chr7:15661835 | A | G | 1 | a0001c0003t0003g0208 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.517+24051T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661835 | |||||||
| chr7:15661889 | C | T | 1 | a0002c0002t0005g0263 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.517+23997G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661889 | |||||||
| chr7:15662202 | C | A | 1 | a0001c0001t0013g0024 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.517+23684G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662202 | |||||||
| chr7:15662251 | A | T | 1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.517+23635T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662251 | |||||||
| chr7:15662377 | G | A | 13 | a0001c0001t0001g0044 a0001c0001t0006g0175 a0001c0001t0008g0040 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.517+23509C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662377 | |||||||
| chr7:15662383 | A | T | 15 | a0001c0001t0001g0044 a0001c0001t0006g0175 a0001c0001t0008g0040 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+23503T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662383 | |||||||
| chr7:15662393 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+23493A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662393 | |||||||
| chr7:15662410 | C | A | 2 | a0002c0002t0002g0305 a0002c0002t0004g0295 |
2 | HG02148.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.517+23476G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662410 | |||||||
| chr7:15662416 | A | G | 1 | a0001c0003t0003g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.517+23470T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662416 | |||||||
| chr7:15662467 | T | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+23419A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662467 | |||||||
| chr7:15662479 | G | A | 1 | a0002c0002t0002g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.517+23407C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662479 | |||||||
| chr7:15662514 | A | G | 90 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(87): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+23372T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662514 | |||||||
| chr7:15662653 | A | C | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+23233T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662653 | |||||||
| chr7:15662709 | T | C | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+23177A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662709 | |||||||
| chr7:15662816 | C | T | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+23070G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662816 | |||||||
| chr7:15662985 | C | T | 1 | a0003c0004t0011g0312 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.517+22901G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662985 | |||||||
| chr7:15663005 | G | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(57): Show |
62 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.517+22881C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663005 | |||||||
| chr7:15663008 | T | C | 2 | a0001c0001t0014g0219 a0001c0001t0020g0228 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.517+22878A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663008 | |||||||
| chr7:15663098 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(86): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.517+22788G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663098 | |||||||
| chr7:15663276 | A | G | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+22610T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663276 | |||||||
| chr7:15663332 | A | C | 2 | a0002c0002t0004g0244 a0002c0002t0010g0248 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+22554T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663332 | |||||||
| chr7:15663335 | CT | C | 7 | a0001c0001t0001g0066 a0001c0001t0001g0131 a0001c0001t0014g0219 others(4): Show |
7 | HG01069.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+22550delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663335 | |||||||
| chr7:15663415 | C | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(74): Show |
79 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.517+22471G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663415 | |||||||
| chr7:15663442 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(84): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.517+22444G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663442 | |||||||
| chr7:15663507 | AT | A | 255 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.517+22378delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663507 | |||||||
| chr7:15663583 | C | G | 1 | a0002c0002t0026g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517+22303G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663583 | |||||||
| chr7:15663685 | T | G | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+22201A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663685 | |||||||
| chr7:15663756 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517+22130G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663756 | |||||||
| chr7:15663814 | G | A | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+22072C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663814 | |||||||
| chr7:15663937 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.517+21949T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663937 | |||||||
| chr7:15663942 | G | A | 1 | a0001c0001t0006g0152 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.517+21944C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663942 | |||||||
| chr7:15663944 | C | T | 2 | a0002c0002t0004g0243 a0002c0002t0026g0242 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+21942G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663944 | |||||||
| chr7:15663952 | T | C | 4 | a0001c0001t0001g0186 a0001c0001t0015g0013 a0001c0001t0015g0014 others(1): Show |
4 | HG02809.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+21934A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663952 | |||||||
| chr7:15663971 | T | G | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+21915A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663971 | |||||||
| chr7:15663982 | A | G | 4 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+21904T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663982 | |||||||
| chr7:15663994 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+21892C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663994 | |||||||
| chr7:15664190 | G | A | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+21696C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664190 | |||||||
| chr7:15664284 | T | G | 2 | a0002c0002t0004g0243 a0002c0002t0026g0242 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+21602A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664284 | |||||||
| chr7:15664305 | A | G | 1 | a0001c0001t0015g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517+21581T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664305 | |||||||
| chr7:15664316 | C | A | 9 | a0002c0002t0002g0012 a0002c0002t0002g0282 a0002c0002t0002g0291 others(6): Show |
10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+21570G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664316 | |||||||
| chr7:15664344 | A | T | 1 | a0002c0002t0010g0308 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.517+21542T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664344 | |||||||
| chr7:15664432 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.517+21454G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664432 | |||||||
| chr7:15664693 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.517+21193G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664693 | |||||||
| chr7:15665008 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+20878C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665008 | |||||||
| chr7:15665041 | T | TCA | 53 | a0001c0001t0001g0078 a0001c0001t0001g0147 a0001c0001t0001g0164 others(50): Show |
54 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.517+20843_517+2084 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | T | TCACA | 25 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0121 others(22): Show |
25 | HG00639.hp1 HG01243.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.517+20841_517+2084 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | T | TCACACA | 12 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0161 others(9): Show |
12 | HG02015.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+20839_517+2084 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | T | TCACACAC others(1): Show |
6 | a0001c0001t0001g0044 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG01074.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.517+20837_517+2084 others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | T | TCACACAC others(3): Show |
2 | a0001c0001t0008g0042 a0001c0001t0008g0043 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.517+20835_517+2084 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | TCA | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0055 others(14): Show |
18 | HG01081.hp1 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+20843_517+2084 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | TCACA | T | 9 | a0001c0001t0007g0182 a0001c0001t0012g0003 a0001c0001t0012g0032 others(6): Show |
10 | HG01099.hp2 HG02132.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+20841_517+2084 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | TCACACA | T | 6 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(3): Show |
7 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+20839_517+2084 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | TCACACAC others(1): Show |
T | 6 | a0001c0001t0012g0031 a0001c0003t0003g0098 a0001c0003t0003g0127 others(3): Show |
6 | HG01928.hp1 HG02071.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+20837_517+2084 others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | TCACACAC others(3): Show |
T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(55): Show |
60 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.517+20835_517+2084 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.517+20833_517+2084 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665041 | TCACACAC others(7): Show |
T | 4 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+20831_517+2084 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | |||||||
| chr7:15665140 | C | T | 2 | a0001c0001t0016g0015 a0001c0001t0016g0016 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.517+20746G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665140 | |||||||
| chr7:15665230 | G | T | 282 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(279): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.517+20656C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665230 | |||||||
| chr7:15665280 | T | G | 1 | a0001c0001t0006g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.517+20606A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665280 | |||||||
| chr7:15665289 | G | GA | 36 | a0001c0001t0009g0229 a0001c0001t0009g0230 a0001c0001t0009g0231 others(33): Show |
37 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.517+20596dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665289 | |||||||
| chr7:15665302 | C | G | 1 | a0001c0001t0013g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.517+20584G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665302 | |||||||
| chr7:15665376 | T | A | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+20510A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665376 | |||||||
| chr7:15665580 | T | C | 1 | a0002c0002t0002g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.517+20306A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665580 | |||||||
| chr7:15665624 | G | C | 5 | a0001c0001t0007g0072 a0002c0002t0004g0243 a0002c0002t0004g0245 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+20262C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665624 | |||||||
| chr7:15665742 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.517+20144A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665742 | |||||||
| chr7:15665917 | T | G | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19969A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665917 | |||||||
| chr7:15665918 | C | CATATATG others(31): Show |
1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19967_517+1996 others(42): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665918 | |||||||
| chr7:15665919 | C | A | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19967G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665919 | |||||||
| chr7:15665920 | C | T | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19966G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665920 | |||||||
| chr7:15665985 | G | C | 3 | a0002c0002t0002g0010 a0002c0002t0002g0266 a0002c0002t0002g0329 |
4 | HG00738.hp1 HG01069.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19901C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665985 | |||||||
| chr7:15666154 | T | A | 1 | a0002c0002t0010g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.517+19732A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666154 | |||||||
| chr7:15666233 | A | G | 3 | a0002c0002t0004g0253 a0002c0002t0004g0254 a0002c0002t0040g0251 |
3 | HG01109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.517+19653T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666233 | |||||||
| chr7:15666284 | A | G | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19602T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666284 | |||||||
| chr7:15666478 | C | G | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19408G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666478 | |||||||
| chr7:15666503 | C | G | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.517+19383G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666503 | |||||||
| chr7:15666590 | A | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0107 |
2 | NA18963.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.517+19296T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666590 | |||||||
| chr7:15666611 | G | T | 4 | a0001c0001t0006g0059 a0001c0001t0006g0080 a0001c0001t0032g0081 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19275C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666611 | |||||||
| chr7:15666620 | T | C | 1 | a0001c0003t0027g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+19266A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666620 | |||||||
| chr7:15666657 | C | G | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.517+19229G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666657 | |||||||
| chr7:15666694 | G | GT | 4 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0088 others(1): Show |
5 | HG00408.hp1 HG02056.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+19191dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666694 | |||||||
| chr7:15666751 | C | CA | 16 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0008g0073 others(13): Show |
17 | HG01175.hp2 HG01433.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.517+19134dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | |||||||
| chr7:15666751 | C | CAA | 7 | a0002c0002t0002g0285 a0002c0002t0002g0323 a0002c0002t0002g0324 others(4): Show |
7 | HG02683.hp1 HG03017.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+19133_517+1913 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | |||||||
| chr7:15666751 | C | CAAA | 7 | a0001c0001t0001g0165 a0001c0001t0014g0220 a0002c0002t0002g0329 others(4): Show |
7 | HG01074.hp2 HG01123.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+19132_517+1913 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | |||||||
| chr7:15666751 | CA | C | 12 | a0001c0001t0008g0041 a0001c0001t0018g0076 a0001c0001t0018g0100 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.517+19134delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | |||||||
| chr7:15666751 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0012g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.517+19123_517+1913 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | |||||||
| chr7:15666751 | CAAAAAAA others(7): Show |
C | 4 | a0001c0003t0003g0050 a0001c0003t0003g0102 a0001c0003t0003g0118 others(1): Show |
4 | NA18977.hp1 NA18977.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+19121_517+1913 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | |||||||
| chr7:15666765 | AAAAAAAA others(9): Show |
A | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+19105_517+1912 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666765 | |||||||
| chr7:15666766 | AAAAAAAA others(8): Show |
A | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+19105_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666766 | |||||||
| chr7:15666767 | AAAAAAAA others(9): Show |
A | 2 | a0001c0003t0003g0158 a0001c0003t0003g0193 |
2 | NA19001.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.517+19103_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666767 | |||||||
| chr7:15666767 | AAAAAAAA others(11): Show |
A | 3 | a0001c0001t0001g0045 a0001c0001t0006g0057 a0001c0001t0009g0226 |
3 | HG00639.hp1 HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.517+19101_517+1911 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666767 | |||||||
| chr7:15666768 | AAAAAAAA others(8): Show |
A | 4 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0172 others(1): Show |
4 | HG02015.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19103_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666768 | |||||||
| chr7:15666768 | AAAAAAAA others(10): Show |
A | 10 | a0001c0001t0009g0223 a0001c0001t0013g0022 a0001c0001t0013g0023 others(7): Show |
10 | HG00609.hp1 HG01255.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+19101_517+1911 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666768 | |||||||
| chr7:15666769 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0012g0003 a0001c0001t0012g0033 |
3 | HG02818.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.517+19105_517+1911 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | |||||||
| chr7:15666769 | AAAAAAAA others(7): Show |
A | 11 | a0001c0001t0001g0055 a0001c0001t0001g0145 a0001c0001t0021g0224 others(8): Show |
11 | HG01891.hp2 HG03540.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+19103_517+1911 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | |||||||
| chr7:15666769 | AAAAAAAA others(9): Show |
A | 60 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(57): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.517+19101_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | |||||||
| chr7:15666769 | AAAAAAAA others(11): Show |
A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0094 others(1): Show |
4 | HG01167.hp1 HG02602.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+19099_517+1911 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | |||||||
| chr7:15666770 | AAAAAAAA others(8): Show |
A | 10 | a0001c0001t0001g0048 a0001c0001t0001g0123 a0001c0001t0001g0126 others(7): Show |
10 | HG01884.hp1 HG04115.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+19101_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666770 | |||||||
| chr7:15666770 | AAAAAAAA others(10): Show |
A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(46): Show |
50 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.517+19099_517+1911 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666770 | |||||||
| chr7:15666771 | AAAAAAAA others(9): Show |
A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0169 a0001c0001t0012g0030 others(1): Show |
4 | HG00323.hp1 HG03239.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+19099_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666771 | |||||||
| chr7:15666771 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.517+19097_517+1911 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666771 | |||||||
| chr7:15666772 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0108 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517+19099_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666772 | |||||||
| chr7:15666772 | AAAAAAAA others(10): Show |
A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0109 a0001c0001t0001g0113 others(1): Show |
4 | HG01243.hp1 HG02056.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19097_517+1911 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666772 | |||||||
| chr7:15666773 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.517+19097_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666773 | |||||||
| chr7:15666774 | AAAAAAAT others(4): Show |
A | 1 | a0001c0003t0003g0141 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.517+19101_517+1911 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666774 | |||||||
| chr7:15666777 | A | T | 8 | a0001c0001t0007g0179 a0001c0001t0018g0076 a0001c0001t0018g0101 others(5): Show |
9 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+19109T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666777 | |||||||
| chr7:15666779 | A | AAAAAAAA others(6): Show |
1 | a0002c0002t0026g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517+19106_517+1910 others(17): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | |||||||
| chr7:15666779 | A | AAAAAAAA others(8): Show |
1 | a0002c0002t0004g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517+19106_517+1910 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | |||||||
| chr7:15666779 | A | AT | 3 | a0003c0004t0011g0311 a0003c0004t0011g0312 a0003c0004t0011g0314 |
3 | HG00558.hp1 HG00741.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.517+19106_517+1910 others(5): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | |||||||
| chr7:15666779 | A | ATATATAT | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0034g0216 |
3 | HG02145.hp2 HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.517+19106_517+1910 others(11): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | |||||||
| chr7:15666779 | A | ATATATAT others(4): Show |
1 | a0001c0001t0014g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.517+19106_517+1910 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | |||||||
| chr7:15666779 | A | T | 25 | a0001c0001t0001g0187 a0001c0001t0007g0008 a0001c0001t0007g0178 others(22): Show |
27 | HG00738.hp1 HG01069.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.517+19107T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | |||||||
| chr7:15666779 | AATAT | A | 7 | a0001c0001t0001g0039 a0001c0001t0006g0175 a0001c0001t0008g0042 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+19103_517+1910 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | |||||||
| chr7:15666780 | AT | A | 12 | a0001c0001t0001g0192 a0001c0001t0006g0082 a0001c0001t0009g0230 others(9): Show |
12 | HG01361.hp1 HG01928.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+19105delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666780 | |||||||
| chr7:15666780 | ATAT | A | 8 | a0001c0001t0001g0007 a0001c0001t0006g0059 a0001c0001t0006g0080 others(5): Show |
9 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+19103_517+1910 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666780 | |||||||
| chr7:15666781 | T | A | 57 | a0001c0001t0001g0078 a0001c0001t0001g0161 a0001c0001t0001g0165 others(54): Show |
59 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.517+19105A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666781 | |||||||
| chr7:15666783 | T | A | 18 | a0001c0001t0001g0166 a0001c0001t0006g0082 a0001c0001t0006g0152 others(15): Show |
19 | HG00621.hp1 HG02647.hp2 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.517+19103A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666783 | |||||||
| chr7:15666785 | T | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0166 others(4): Show |
8 | HG02559.hp1 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.517+19101A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666785 | |||||||
| chr7:15666787 | T | A | 2 | a0001c0001t0006g0175 a0001c0001t0018g0176 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.517+19099A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666787 | |||||||
| chr7:15666962 | A | T | 1 | a0001c0001t0014g0219 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.517+18924T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666962 | |||||||
| chr7:15667010 | G | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(79): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.517+18876C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667010 | |||||||
| chr7:15667135 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.517+18751G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667135 | |||||||
| chr7:15667142 | T | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+18744A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667142 | |||||||
| chr7:15667145 | G | T | 1 | a0002c0002t0002g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.517+18741C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667145 | |||||||
| chr7:15667242 | G | A | 35 | a0001c0001t0009g0229 a0001c0001t0009g0230 a0001c0001t0009g0231 others(32): Show |
36 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+18644C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667242 | |||||||
| chr7:15667289 | C | CAAAAAA | 70 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.517+18591_517+1859 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA | 15 | a0001c0001t0001g0126 a0001c0001t0001g0132 a0001c0001t0001g0146 others(12): Show |
15 | HG01346.hp2 HG01934.hp2 HG03098.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+18590_517+1859 others(11): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(2): Show |
6 | HG01255.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.517+18589_517+1859 others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0039 a0001c0001t0006g0057 a0001c0001t0007g0072 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+18588_517+1859 others(13): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(3): Show |
17 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0078 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+18587_517+1859 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(4): Show |
19 | a0001c0001t0001g0045 a0001c0001t0001g0167 a0001c0001t0001g0168 others(16): Show |
19 | HG01106.hp2 HG01169.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.517+18586_517+1859 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(5): Show |
11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
11 | HG01109.hp1 HG01361.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+18585_517+1859 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0008g0188 a0001c0001t0021g0235 a0002c0002t0004g0238 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+18584_517+1859 others(17): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(7): Show |
22 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(19): Show |
23 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.517+18583_517+1859 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(8): Show |
45 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0047 others(42): Show |
48 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.517+18582_517+1859 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(9): Show |
30 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0063 others(27): Show |
30 | HG00741.hp1 HG01071.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.517+18581_517+1859 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(10): Show |
7 | a0001c0001t0001g0099 a0001c0001t0001g0112 a0001c0001t0012g0031 others(4): Show |
7 | HG00673.hp1 HG02273.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+18580_517+1859 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(11): Show |
5 | a0001c0001t0018g0100 a0001c0003t0003g0127 a0001c0013t0003g0211 others(2): Show |
5 | HG01123.hp1 HG01928.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+18579_517+1859 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(13): Show |
2 | a0001c0003t0003g0189 a0001c0003t0008g0111 |
2 | HG02055.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.517+18577_517+1859 others(24): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.517+18576_517+1859 others(25): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667289 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.517+18575_517+1859 others(26): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | |||||||
| chr7:15667303 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0006g0175 a0001c0001t0018g0176 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.517+18582_517+1858 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667303 | |||||||
| chr7:15667349 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+18537G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667349 | |||||||
| chr7:15667490 | T | G | 1 | a0001c0001t0012g0031 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517+18396A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667490 | |||||||
| chr7:15667505 | C | T | 3 | a0001c0001t0009g0222 a0002c0002t0004g0244 a0002c0002t0010g0248 |
3 | HG02486.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+18381G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667505 | |||||||
| chr7:15667506 | G | A | 1 | a0001c0001t0016g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.517+18380C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667506 | |||||||
| chr7:15667820 | G | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.517+18066C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667820 | |||||||
| chr7:15667881 | T | C | 1 | a0001c0001t0021g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517+18005A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667881 | |||||||
| chr7:15668025 | G | A | 1 | a0002c0002t0002g0328 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.517+17861C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668025 | |||||||
| chr7:15668217 | C | T | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+17669G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668217 | |||||||
| chr7:15668426 | T | C | 2 | a0001c0001t0006g0175 a0001c0001t0018g0176 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.517+17460A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668426 | |||||||
| chr7:15668548 | C | T | 33 | a0001c0001t0009g0229 a0001c0001t0009g0230 a0001c0001t0009g0231 others(30): Show |
34 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.517+17338G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668548 | |||||||
| chr7:15668638 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.517+17248G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668638 | |||||||
| chr7:15668639 | G | T | 1 | a0002c0002t0002g0296 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.517+17247C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668639 | |||||||
| chr7:15668677 | T | A | 9 | a0002c0002t0002g0270 a0002c0002t0002g0279 a0002c0002t0002g0280 others(6): Show |
9 | NA18940.hp2 NA18950.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+17209A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668677 | |||||||
| chr7:15668856 | T | C | 2 | a0001c0001t0020g0228 a0001c0001t0021g0224 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.517+17030A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668856 | |||||||
| chr7:15669025 | A | C | 15 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0126 others(12): Show |
15 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.517+16861T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669025 | |||||||
| chr7:15669228 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.517+16658A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669228 | |||||||
| chr7:15669343 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.517+16543A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669343 | |||||||
| chr7:15669360 | A | C | 35 | a0001c0001t0009g0229 a0001c0001t0009g0230 a0001c0001t0009g0231 others(32): Show |
36 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+16526T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669360 | |||||||
| chr7:15669879 | T | C | 1 | a0001c0003t0003g0118 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.517+16007A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669879 | |||||||
| chr7:15670147 | A | G | 1 | a0001c0008t0007g0177 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517+15739T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670147 | |||||||
| chr7:15670162 | T | G | 2 | a0001c0001t0001g0075 a0001c0009t0001g0079 |
2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.517+15724A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670162 | |||||||
| chr7:15670234 | G | A | 3 | a0001c0001t0018g0101 a0002c0002t0005g0271 a0002c0002t0005g0272 |
3 | NA18944.hp2 NA18990.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.517+15652C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670234 | |||||||
| chr7:15670314 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.517+15572T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670314 | |||||||
| chr7:15670429 | G | A | 1 | a0002c0002t0002g0287 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.517+15457C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670429 | |||||||
| chr7:15670483 | T | G | 1 | a0002c0002t0004g0237 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.517+15403A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670483 | |||||||
| chr7:15670488 | C | T | 1 | a0003c0004t0011g0310 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.517+15398G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670488 | |||||||
| chr7:15670599 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.517+15287G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670599 | |||||||
| chr7:15670600 | G | A | 2 | a0001c0001t0019g0116 a0001c0001t0019g0117 |
2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.517+15286C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670600 | |||||||
| chr7:15670633 | T | A | 3 | a0001c0001t0007g0072 a0002c0002t0004g0245 a0002c0002t0010g0246 |
3 | HG01081.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.517+15253A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670633 | |||||||
| chr7:15670635 | T | G | 19 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0078 others(16): Show |
20 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.517+15251A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670635 | |||||||
| chr7:15670831 | G | A | 1 | a0002c0002t0004g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517+15055C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670831 | |||||||
| chr7:15670936 | A | G | 1 | a0001c0001t0014g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.517+14950T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670936 | |||||||
| chr7:15671123 | A | G | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+14763T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671123 | |||||||
| chr7:15671227 | A | G | 1 | a0001c0009t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.517+14659T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671227 | |||||||
| chr7:15671310 | A | G | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+14576T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671310 | |||||||
| chr7:15671399 | A | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18983.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.517+14487T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671399 | |||||||
| chr7:15671403 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+14483A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671403 | |||||||
| chr7:15671495 | A | G | 1 | a0001c0001t0021g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517+14391T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671495 | |||||||
| chr7:15671529 | T | C | 7 | a0001c0001t0007g0008 a0001c0001t0007g0178 a0001c0001t0007g0179 others(4): Show |
8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+14357A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671529 | |||||||
| chr7:15671792 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0044 others(26): Show |
31 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.517+14094G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671792 | |||||||
| chr7:15671851 | G | A | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+14035C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671851 | |||||||
| chr7:15671924 | C | G | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+13962G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671924 | |||||||
| chr7:15671960 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(86): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+13926C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671960 | |||||||
| chr7:15671984 | G | A | 1 | a0001c0001t0009g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+13902C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671984 | |||||||
| chr7:15671987 | G | A | 2 | a0002c0002t0005g0271 a0002c0002t0005g0272 |
2 | NA18944.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.517+13899C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671987 | |||||||
| chr7:15672087 | C | T | 2 | a0002c0002t0004g0258 a0002c0002t0004g0259 |
2 | NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.517+13799G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672087 | |||||||
| chr7:15672283 | T | C | 1 | a0002c0002t0002g0300 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.517+13603A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672283 | |||||||
| chr7:15672363 | A | T | 10 | a0001c0001t0001g0045 a0001c0001t0006g0057 a0001c0001t0006g0175 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+13523T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672363 | |||||||
| chr7:15672467 | A | T | 2 | a0001c0001t0015g0018 a0001c0003t0038g0233 |
2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.517+13419T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672467 | |||||||
| chr7:15672629 | A | G | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+13257T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672629 | |||||||
| chr7:15672689 | A | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+13197T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672689 | |||||||
| chr7:15672771 | A | C | 9 | a0001c0001t0006g0175 a0001c0001t0007g0008 a0001c0001t0007g0178 others(6): Show |
10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+13115T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672771 | |||||||
| chr7:15672797 | C | T | 4 | a0002c0002t0002g0304 a0002c0002t0002g0305 a0002c0002t0002g0330 others(1): Show |
4 | HG01361.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+13089G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672797 | |||||||
| chr7:15672854 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(75): Show |
82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.517+13032G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672854 | |||||||
| chr7:15672870 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+13016G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672870 | |||||||
| chr7:15672871 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+13015T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672871 | |||||||
| chr7:15672879 | G | A | 1 | a0001c0001t0034g0216 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.517+13007C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672879 | |||||||
| chr7:15672892 | G | GA | 9 | a0001c0001t0006g0175 a0001c0001t0007g0008 a0001c0001t0007g0178 others(6): Show |
10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+12993dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672892 | |||||||
| chr7:15672892 | GAAAAA | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(86): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+12989_517+1299 others(9): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672892 | |||||||
| chr7:15672928 | C | T | 15 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 others(12): Show |
17 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.517+12958G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672928 | |||||||
| chr7:15672947 | C | G | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+12939G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672947 | |||||||
| chr7:15673054 | C | T | 1 | a0001c0003t0003g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.517+12832G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673054 | |||||||
| chr7:15673201 | G | A | 1 | a0001c0001t0018g0076 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.517+12685C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673201 | |||||||
| chr7:15673227 | C | T | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.517+12659G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673227 | |||||||
| chr7:15673319 | T | C | 1 | a0001c0003t0003g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517+12567A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673319 | |||||||
| chr7:15673329 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.517+12557A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673329 | |||||||
| chr7:15673344 | G | A | 1 | a0003c0004t0011g0239 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.517+12542C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673344 | |||||||
| chr7:15673414 | G | A | 23 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0009g0232 others(20): Show |
25 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.517+12472C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673414 | |||||||
| chr7:15673439 | G | A | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.517+12447C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673439 | |||||||
| chr7:15673480 | G | C | 258 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.517+12406C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673480 | |||||||
| chr7:15673522 | C | G | 2 | a0002c0002t0004g0244 a0002c0002t0010g0248 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+12364G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673522 | |||||||
| chr7:15673556 | AT | A | 16 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 others(13): Show |
18 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.517+12329delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673556 | |||||||
| chr7:15673597 | C | CA | 127 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.517+12288dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | |||||||
| chr7:15673597 | C | CAA | 27 | a0001c0001t0001g0049 a0001c0001t0001g0107 a0001c0001t0001g0108 others(24): Show |
27 | HG00639.hp1 HG01074.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.517+12287_517+1228 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | |||||||
| chr7:15673597 | CA | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(88): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.517+12288delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | |||||||
| chr7:15673597 | CAA | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0164 others(23): Show |
27 | HG00408.hp2 HG01081.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.517+12287_517+1228 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | |||||||
| chr7:15673597 | CAAA | C | 27 | a0001c0001t0001g0186 a0001c0001t0009g0232 a0001c0001t0014g0220 others(24): Show |
27 | HG00673.hp1 HG00735.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.517+12286_517+1228 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | |||||||
| chr7:15673597 | CAAAA | C | 10 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 others(7): Show |
11 | HG01109.hp1 HG02630.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+12285_517+1228 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | |||||||
| chr7:15673597 | CAAAAA | C | 6 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(3): Show |
7 | HG00738.hp1 HG01069.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+12284_517+1228 others(9): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | |||||||
| chr7:15673658 | C | T | 1 | a0002c0002t0004g0332 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.517+12228G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673658 | |||||||
| chr7:15673659 | G | A | 1 | a0002c0002t0002g0331 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.517+12227C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673659 | |||||||
| chr7:15673672 | C | G | 1 | a0002c0002t0026g0249 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517+12214G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673672 | |||||||
| chr7:15673679 | G | T | 8 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(5): Show |
9 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+12207C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673679 | |||||||
| chr7:15673703 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0006g0069 |
2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.517+12183A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673703 | |||||||
| chr7:15673755 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.517+12131G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673755 | |||||||
| chr7:15673931 | A | T | 8 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+11955T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673931 | |||||||
| chr7:15673976 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.517+11910G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673976 | |||||||
| chr7:15673992 | T | A | 2 | a0002c0002t0025g0333 a0002c0002t0025g0334 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.517+11894A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673992 | |||||||
| chr7:15674200 | T | C | 9 | a0001c0001t0006g0175 a0001c0001t0007g0008 a0001c0001t0007g0178 others(6): Show |
10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+11686A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674200 | |||||||
| chr7:15674242 | A | G | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+11644T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674242 | |||||||
| chr7:15674309 | T | C | 170 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(167): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.517+11577A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674309 | |||||||
| chr7:15674384 | G | A | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.517+11502C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674384 | |||||||
| chr7:15674394 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517+11492A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674394 | |||||||
| chr7:15674470 | G | A | 3 | a0001c0001t0016g0015 a0001c0001t0016g0016 a0001c0001t0016g0017 |
3 | HG01891.hp1 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.517+11416C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674470 | |||||||
| chr7:15674476 | T | A | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+11410A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674476 | |||||||
| chr7:15674554 | T | TTG | 107 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.517+11331_517+1133 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | |||||||
| chr7:15674554 | T | TTGTG | 8 | a0001c0001t0001g0161 a0001c0003t0003g0160 a0001c0003t0003g0189 others(5): Show |
8 | HG00408.hp2 HG01099.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+11331_517+1133 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | |||||||
| chr7:15674554 | TTC | T | 6 | a0001c0001t0001g0186 a0001c0001t0012g0003 a0001c0001t0012g0032 others(3): Show |
7 | HG02273.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+11330_517+1133 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | |||||||
| chr7:15674554 | TTCTGTG | T | 20 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0009g0232 others(17): Show |
21 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.517+11326_517+1133 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | |||||||
| chr7:15674556 | C | CTG | 27 | a0001c0001t0001g0063 a0001c0001t0008g0073 a0001c0003t0003g0058 others(24): Show |
28 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.517+11328_517+1132 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674556 | |||||||
| chr7:15674556 | C | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(137): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.517+11330G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674556 | |||||||
| chr7:15674559 | T | C | 1 | a0001c0001t0008g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.517+11327A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674559 | |||||||
| chr7:15674793 | T | A | 3 | a0002c0002t0004g0332 a0002c0002t0025g0333 a0002c0002t0025g0334 |
3 | HG01106.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.517+11093A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674793 | |||||||
| chr7:15674900 | A | T | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+10986T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674900 | |||||||
| chr7:15674989 | GT | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(177): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.517+10896delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674989 | |||||||
| chr7:15675112 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.517+10774G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675112 | |||||||
| chr7:15675431 | T | C | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.517+10455A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675431 | |||||||
| chr7:15675455 | T | C | 10 | a0001c0001t0001g0183 a0001c0001t0006g0175 a0001c0001t0007g0008 others(7): Show |
11 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+10431A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675455 | |||||||
| chr7:15675516 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.517+10370A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675516 | |||||||
| chr7:15675520 | G | C | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+10366C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675520 | |||||||
| chr7:15675618 | G | T | 4 | a0001c0001t0014g0219 a0001c0001t0019g0116 a0001c0001t0019g0117 others(1): Show |
4 | HG01074.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+10268C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675618 | |||||||
| chr7:15675639 | G | C | 8 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0009g0232 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+10247C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675639 | |||||||
| chr7:15675776 | G | C | 1 | a0003c0004t0011g0276 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.517+10110C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675776 | |||||||
| chr7:15676016 | A | G | 16 | a0001c0001t0006g0152 a0001c0003t0003g0058 a0001c0003t0003g0122 others(13): Show |
16 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.517+9870T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676016 | |||||||
| chr7:15676094 | A | G | 171 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(168): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.517+9792T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676094 | |||||||
| chr7:15676248 | A | G | 6 | a0002c0002t0002g0011 a0002c0002t0002g0283 a0002c0002t0002g0284 others(3): Show |
7 | NA18942.hp2 NA18954.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+9638T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676248 | |||||||
| chr7:15676569 | C | T | 32 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0009g0221 others(29): Show |
34 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.517+9317G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676569 | |||||||
| chr7:15676570 | T | C | 1 | a0001c0001t0020g0228 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.517+9316A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676570 | |||||||
| chr7:15676596 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(89): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.517+9290G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676596 | |||||||
| chr7:15676698 | G | A | 1 | a0002c0002t0002g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.517+9188C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676698 | |||||||
| chr7:15676700 | G | C | 7 | a0002c0002t0002g0010 a0002c0002t0002g0252 a0002c0002t0004g0253 others(4): Show |
8 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.517+9186C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676700 | |||||||
| chr7:15676782 | C | T | 1 | a0001c0010t0029g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.517+9104G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676782 | |||||||
| chr7:15676808 | A | C | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+9078T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676808 | |||||||
| chr7:15676836 | C | T | 1 | a0001c0001t0035g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.517+9050G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676836 | |||||||
| chr7:15676839 | C | A | 8 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(5): Show |
9 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+9047G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676839 | |||||||
| chr7:15676857 | C | CA | 21 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0009g0221 others(18): Show |
22 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.517+9028dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676857 | |||||||
| chr7:15677086 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.517+8800G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677086 | |||||||
| chr7:15677182 | A | G | 1 | a0001c0011t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+8704T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677182 | |||||||
| chr7:15677184 | G | T | 8 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(5): Show |
9 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+8702C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677184 | |||||||
| chr7:15677227 | A | G | 1 | a0001c0003t0003g0190 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.517+8659T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677227 | |||||||
| chr7:15677348 | A | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(34): Show |
38 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.517+8538T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677348 | |||||||
| chr7:15677429 | T | C | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+8457A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677429 | |||||||
| chr7:15677499 | G | A | 9 | a0001c0001t0001g0186 a0001c0001t0013g0022 a0001c0001t0013g0023 others(6): Show |
9 | HG01255.hp2 HG01261.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+8387C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677499 | |||||||
| chr7:15677505 | T | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0008g0110 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+8381A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677505 | |||||||
| chr7:15677633 | G | A | 1 | a0002c0002t0002g0336 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.517+8253C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677633 | |||||||
| chr7:15677863 | T | A | 1 | a0001c0001t0014g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.517+8023A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677863 | |||||||
| chr7:15678306 | A | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+7580T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678306 | |||||||
| chr7:15678374 | CTGT | C | 9 | a0001c0001t0006g0175 a0001c0001t0007g0008 a0001c0001t0007g0178 others(6): Show |
10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+7509_517+7511d others(5): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678374 | |||||||
| chr7:15678413 | C | T | 1 | a0001c0001t0007g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517+7473G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678413 | |||||||
| chr7:15678529 | C | T | 1 | a0002c0002t0002g0282 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.517+7357G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678529 | |||||||
| chr7:15678828 | T | C | 1 | a0006c0012t0005g0339 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.517+7058A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678828 | |||||||
| chr7:15678859 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.517+7027G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678859 | |||||||
| chr7:15678879 | CG | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0003t0008g0111 |
3 | HG01243.hp1 HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.517+7006delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678879 | |||||||
| chr7:15678887 | A | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+6999T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678887 | |||||||
| chr7:15678906 | C | T | 264 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.517+6980G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678906 | |||||||
| chr7:15678957 | A | T | 1 | a0001c0003t0003g0189 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.517+6929T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678957 | |||||||
| chr7:15678982 | A | G | 1 | a0001c0003t0003g0118 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.517+6904T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678982 | |||||||
| chr7:15679000 | T | A | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6886A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679000 | |||||||
| chr7:15679071 | A | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+6815T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679071 | |||||||
| chr7:15679118 | A | G | 1 | a0002c0002t0004g0338 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.517+6768T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679118 | |||||||
| chr7:15679191 | G | A | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6695C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679191 | |||||||
| chr7:15679197 | G | A | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+6689C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679197 | |||||||
| chr7:15679402 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+6484A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679402 | |||||||
| chr7:15679440 | T | A | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6446A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679440 | |||||||
| chr7:15679494 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0009g0232 a0001c0003t0038g0233 |
3 | HG02896.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+6392T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679494 | |||||||
| chr7:15679562 | G | A | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6324C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679562 | |||||||
| chr7:15679575 | T | C | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6311A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679575 | |||||||
| chr7:15679721 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(260): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.517+6165T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679721 | |||||||
| chr7:15679746 | T | C | 2 | a0002c0002t0004g0244 a0002c0002t0010g0248 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+6140A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679746 | |||||||
| chr7:15679782 | A | G | 29 | a0001c0001t0009g0221 a0001c0001t0009g0222 a0001c0001t0009g0223 others(26): Show |
30 | HG00639.hp1 HG00639.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.517+6104T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679782 | |||||||
| chr7:15679840 | T | C | 16 | a0001c0001t0009g0222 a0001c0001t0009g0223 a0001c0001t0009g0226 others(13): Show |
16 | HG00639.hp1 HG01255.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.517+6046A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679840 | |||||||
| chr7:15679965 | G | C | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+5921C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679965 | |||||||
| chr7:15680011 | A | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0039 others(182): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.517+5875T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680011 | |||||||
| chr7:15680135 | C | G | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+5751G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680135 | |||||||
| chr7:15680161 | A | G | 1 | a0001c0001t0006g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.517+5725T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680161 | |||||||
| chr7:15680162 | C | T | 1 | a0001c0003t0003g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.517+5724G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680162 | |||||||
| chr7:15680216 | A | T | 10 | a0001c0001t0001g0183 a0001c0001t0006g0175 a0001c0001t0007g0008 others(7): Show |
11 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+5670T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680216 | |||||||
| chr7:15680251 | C | A | 2 | a0001c0001t0009g0232 a0001c0003t0038g0233 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+5635G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680251 | |||||||
| chr7:15680406 | C | T | 12 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.517+5480G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680406 | |||||||
| chr7:15680465 | A | G | 2 | a0001c0001t0001g0183 a0002c0002t0005g0257 |
2 | HG02129.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.517+5421T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680465 | |||||||
| chr7:15680470 | T | C | 16 | a0001c0001t0009g0222 a0001c0001t0009g0223 a0001c0001t0009g0226 others(13): Show |
16 | HG00639.hp1 HG01255.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.517+5416A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680470 | |||||||
| chr7:15680514 | C | T | 1 | a0001c0003t0027g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+5372G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680514 | |||||||
| chr7:15680552 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.517+5334G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680552 | |||||||
| chr7:15680727 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+5159C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680727 | |||||||
| chr7:15680729 | A | G | 12 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.517+5157T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680729 | |||||||
| chr7:15680749 | T | C | 9 | a0001c0001t0006g0175 a0001c0001t0007g0008 a0001c0001t0007g0178 others(6): Show |
10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+5137A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680749 | |||||||
| chr7:15680845 | T | C | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+5041A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680845 | |||||||
| chr7:15680903 | T | C | 12 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.517+4983A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680903 | |||||||
| chr7:15681017 | A | G | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+4869T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681017 | |||||||
| chr7:15681019 | C | CA | 34 | a0001c0001t0001g0186 a0001c0001t0009g0221 a0001c0001t0009g0222 others(31): Show |
35 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.517+4866dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681019 | |||||||
| chr7:15681088 | G | A | 1 | a0001c0003t0003g0163 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.517+4798C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681088 | |||||||
| chr7:15681112 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.517+4774A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681112 | |||||||
| chr7:15681152 | T | C | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+4734A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681152 | |||||||
| chr7:15681272 | T | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0051 others(89): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.517+4614A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681272 | |||||||
| chr7:15681369 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.517+4517C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681369 | |||||||
| chr7:15681380 | A | G | 1 | a0002c0002t0004g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.517+4506T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681380 | |||||||
| chr7:15681465 | ATTTC | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.517+4417_517+4420d others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681465 | |||||||
| chr7:15681477 | C | CA | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+4408dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681477 | |||||||
| chr7:15681477 | CA | C | 14 | a0001c0001t0001g0070 a0001c0001t0006g0069 a0002c0002t0002g0010 others(11): Show |
15 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+4408delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681477 | |||||||
| chr7:15681486 | AT | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0164 a0001c0001t0001g0165 others(6): Show |
10 | HG01081.hp2 HG01106.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+4399delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681486 | |||||||
| chr7:15681514 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0033g0212 |
3 | HG01496.hp2 HG01978.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.517+4372G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681514 | |||||||
| chr7:15681553 | C | T | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.517+4333G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681553 | |||||||
| chr7:15681651 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+4235C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681651 | |||||||
| chr7:15681653 | C | G | 9 | a0001c0001t0006g0175 a0001c0001t0007g0008 a0001c0001t0007g0178 others(6): Show |
10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+4233G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681653 | |||||||
| chr7:15681761 | T | C | 1 | a0002c0002t0002g0337 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.517+4125A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681761 | |||||||
| chr7:15681841 | G | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0051 others(116): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.517+4045C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681841 | |||||||
| chr7:15681916 | C | T | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+3970G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681916 | |||||||
| chr7:15682131 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.517+3755C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682131 | |||||||
| chr7:15682134 | GT | G | 5 | a0001c0001t0001g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+3751delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682134 | |||||||
| chr7:15682276 | C | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG01071.hp2 HG01167.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+3610G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682276 | |||||||
| chr7:15682301 | T | C | 32 | a0001c0001t0001g0186 a0001c0001t0009g0221 a0001c0001t0009g0222 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.517+3585A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682301 | |||||||
| chr7:15682430 | T | C | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+3456A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682430 | |||||||
| chr7:15682533 | C | T | 2 | a0001c0001t0006g0061 a0001c0001t0006g0062 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.517+3353G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682533 | |||||||
| chr7:15682534 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0051 others(85): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.517+3352C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682534 | |||||||
| chr7:15682624 | C | T | 49 | a0001c0001t0001g0186 a0001c0001t0009g0221 a0001c0001t0009g0222 others(46): Show |
51 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.517+3262G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682624 | |||||||
| chr7:15682681 | C | G | 183 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0051 others(180): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.517+3205G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682681 | |||||||
| chr7:15682711 | T | G | 2 | a0001c0001t0008g0042 a0001c0001t0008g0043 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.517+3175A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682711 | |||||||
| chr7:15682813 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0051 others(86): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+3073C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682813 | |||||||
| chr7:15682824 | T | G | 1 | a0001c0001t0008g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517+3062A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682824 | |||||||
| chr7:15682842 | C | T | 1 | a0001c0001t0006g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517+3044G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682842 | |||||||
| chr7:15682879 | C | T | 2 | a0001c0001t0009g0232 a0001c0003t0038g0233 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+3007G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682879 | |||||||
| chr7:15682941 | A | G | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+2945T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682941 | |||||||
| chr7:15683042 | T | C | 3 | a0001c0001t0009g0229 a0001c0001t0009g0230 a0001c0001t0009g0231 |
3 | HG03139.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.517+2844A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683042 | |||||||
| chr7:15683049 | G | T | 2 | a0001c0001t0014g0219 a0001c0001t0036g0218 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.517+2837C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683049 | |||||||
| chr7:15683074 | G | A | 1 | a0001c0001t0016g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517+2812C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683074 | |||||||
| chr7:15683098 | G | C | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+2788C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683098 | |||||||
| chr7:15683211 | G | A | 98 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0039 others(95): Show |
101 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.517+2675C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683211 | |||||||
| chr7:15683255 | G | A | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+2631C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683255 | |||||||
| chr7:15683263 | A | G | 9 | a0001c0001t0006g0175 a0001c0001t0007g0008 a0001c0001t0007g0178 others(6): Show |
10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+2623T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683263 | |||||||
| chr7:15683305 | A | T | 4 | a0002c0002t0002g0279 a0002c0002t0002g0280 a0002c0002t0002g0281 others(1): Show |
4 | NA18940.hp2 NA18955.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+2581T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683305 | |||||||
| chr7:15683525 | A | G | 3 | a0001c0001t0006g0175 a0001c0001t0018g0176 a0001c0008t0007g0177 |
3 | HG02818.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.517+2361T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683525 | |||||||
| chr7:15683727 | C | T | 177 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0051 others(174): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.517+2159G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683727 | |||||||
| chr7:15683763 | C | A | 267 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.517+2123G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683763 | |||||||
| chr7:15683782 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.517+2104C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683782 | |||||||
| chr7:15683806 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.517+2080A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683806 | |||||||
| chr7:15683885 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+2001T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683885 | |||||||
| chr7:15683974 | T | A | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+1912A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683974 | |||||||
| chr7:15683980 | G | A | 1 | a0001c0001t0016g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517+1906C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683980 | |||||||
| chr7:15683994 | G | C | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+1892C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683994 | |||||||
| chr7:15684018 | T | A | 2 | a0001c0001t0001g0186 a0001c0001t0006g0172 |
2 | HG02976.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.517+1868A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684018 | |||||||
| chr7:15684019 | A | T | 1 | a0002c0002t0022g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.517+1867T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684019 | |||||||
| chr7:15684026 | T | A | 2 | a0001c0001t0009g0232 a0001c0003t0038g0233 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+1860A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684026 | |||||||
| chr7:15684105 | T | C | 2 | a0001c0001t0001g0174 a0001c0003t0003g0173 |
2 | HG02074.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.517+1781A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684105 | |||||||
| chr7:15684119 | C | T | 5 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+1767G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684119 | |||||||
| chr7:15684128 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0051 others(114): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.517+1758G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684128 | |||||||
| chr7:15684370 | C | A | 12 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.517+1516G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684370 | |||||||
| chr7:15684383 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+1503T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684383 | |||||||
| chr7:15684390 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+1496C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684390 | |||||||
| chr7:15684493 | C | T | 1 | a0001c0003t0003g0050 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.517+1393G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684493 | |||||||
| chr7:15684532 | G | C | 179 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0123 others(176): Show |
187 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.517+1354C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684532 | |||||||
| chr7:15684584 | T | G | 48 | a0001c0001t0001g0186 a0001c0001t0009g0221 a0001c0001t0009g0222 others(45): Show |
50 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.517+1302A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684584 | |||||||
| chr7:15684704 | G | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | NA18939.hp2 NA18957.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+1182C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684704 | |||||||
| chr7:15684914 | T | C | 7 | a0002c0002t0002g0010 a0002c0002t0002g0252 a0002c0002t0004g0253 others(4): Show |
8 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.517+972A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684914 | |||||||
| chr7:15684923 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517+963G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684923 | |||||||
| chr7:15685058 | TCTAA | T | 16 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(13): Show |
17 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.517+824_517+827del others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685058 | |||||||
| chr7:15685281 | T | C | 3 | a0001c0001t0012g0003 a0001c0001t0012g0032 a0001c0001t0012g0033 |
4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+605A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685281 | |||||||
| chr7:15685353 | T | TA | 45 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0001c0001t0021g0235 others(42): Show |
46 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.517+532dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685353 | |||||||
| chr7:15685404 | T | C | 24 | a0001c0001t0001g0192 a0001c0001t0024g0197 a0001c0003t0003g0001 others(21): Show |
27 | HG00558.hp2 NA18940.hp1 NA18941.hp1 others(24): Show |
intron_variant | MODIFIER | c.517+482A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685404 | |||||||
| chr7:15685479 | C | G | 42 | a0002c0002t0002g0010 a0002c0002t0002g0247 a0002c0002t0002g0252 others(39): Show |
43 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.517+407G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685479 | |||||||
| chr7:15685501 | G | A | 1 | a0001c0001t0015g0020 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.517+385C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685501 | |||||||
| chr7:15685517 | G | T | 5 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0217 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+369C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685517 | |||||||
| chr7:15685531 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+355G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685531 | |||||||
| chr7:15685661 | A | G | 10 | a0001c0001t0001g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+225T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685661 |