Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57787 |
| ensemblid | ENSG00000007047.16 |
| hgncid | 13538 |
| symbol | MARK4 |
| name | microtubule affinity regulating kinase 4 |
| refseq_nuc | NM_001199867.2 |
| refseq_prot | NP_001186796.1 |
| ensembl_nuc | ENST00000262891.9 |
| ensembl_prot | ENSP00000262891.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 45251271 |
| end | 45305284 |
| strand | + |
| ver | v1.2 |
| region | chr19:45251271-45305284 |
| region5000 | chr19:45246271-45310284 |
| regionname0 | MARK4_chr19_45251271_45305284 |
| regionname5000 | MARK4_chr19_45246271_45310284 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 752 | 256 | 89 | 49 | 67 | 14 | 35 | 45 | MARK4_chr19_45246271_45310284 | MARK4 | MSSRT others(747): Show |
chr19 | 45246271 | 45310284 |
| a0002 | 0/0 | 752 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | MSSRT others(747): Show |
chr19 | 45246271 | 45310284 |
| a0003 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | MSSRT others(747): Show |
chr19 | 45246271 | 45310284 |
| a0004 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | MSSRT others(747): Show |
chr19 | 45246271 | 45310284 |
| a0005 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | MSSRT others(747): Show |
chr19 | 45246271 | 45310284 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2256 | 242 | 81 | 48 | 66 | 14 | 32 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0001c0002 | 0/0 | 2256 | 7 | 6 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0001c0003 | 0/0 | 2256 | 2 | 0 | 0 | 0 | 0 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0001c0004 | 1/0 | 2256 | 2 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0001c0008 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0001c0009 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0001c0010 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0002c0007 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0003c0011 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0004c0005 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 | ||
| a0005c0006 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | ATGTC others(2251): Show |
chr19 | 45246271 | 45310284 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5151 | 50 | 6 | 16 | 19 | 4 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0002 | 0/0 | 5151 | 35 | 22 | 2 | 10 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0003 | 0/0 | 5152 | 23 | 2 | 4 | 12 | 0 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0004 | 0/0 | 5152 | 21 | 12 | 1 | 4 | 0 | 4 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0005 | 0/0 | 5151 | 21 | 2 | 4 | 11 | 2 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0006 | 0/0 | 5151 | 17 | 15 | 2 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0007 | 0/1 | 5152 | 12 | 0 | 2 | 6 | 1 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0008 | 0/0 | 5150 | 11 | 0 | 5 | 0 | 1 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5145): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0009 | 0/0 | 5151 | 8 | 0 | 3 | 0 | 2 | 3 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0010 | 0/0 | 5152 | 6 | 1 | 3 | 0 | 0 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0011 | 0/0 | 5147 | 6 | 6 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5142): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0013 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5149): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0014 | 0/0 | 5151 | 2 | 0 | 0 | 1 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0015 | 0/0 | 5151 | 2 | 0 | 1 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0016 | 0/0 | 5151 | 2 | 0 | 0 | 0 | 1 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0017 | 0/0 | 5151 | 2 | 0 | 1 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0018 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0019 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0020 | 0/0 | 5152 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0023 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5150): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0024 | 0/0 | 5151 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0025 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0026 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0027 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5145): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0028 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0029 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0030 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0031 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0032 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0033 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0034 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0035 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0036 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0037 | 0/0 | 5152 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0001t0038 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0002t0012 | 0/0 | 5151 | 4 | 4 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0002t0021 | 0/0 | 5152 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0002t0039 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0003t0002 | 0/0 | 5151 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0003t0004 | 0/0 | 5152 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0004t0022 | 1/0 | 5151 | 2 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0008t0006 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0001c0009t0010 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0001c0010t0001 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0002c0007t0003 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0003c0011t0006 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| a0004c0005t0003 | 0/0 | 5152 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5147): Show |
chr19 | 45246271 | 45310284 |
| a0005c0006t0002 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | CTCCC others(5146): Show |
chr19 | 45246271 | 45310284 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0015g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0016g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0017g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0019g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0020g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0023g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0025g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0026g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0027g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0028g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0029g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0030g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0031g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0032g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0033g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0034g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0035g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0036g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0037g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0038g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0021g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0021g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0039g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0003t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0004t0022g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0004t0022g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0008t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0009t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0010t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0002c0007t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0003c0011t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0004c0005t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0005c0006t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0129 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0119 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0075 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00280 | hp1 | a0001 | c0001 | t0017 | g0229 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0251 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00323 | hp1 | a0001 | c0001 | t0024 | g0141 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0043 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0060 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0254 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00642 | hp2 | a0001 | c0001 | t0030 | g0241 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0050 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0208 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0067 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01074 | hp1 | a0001 | c0002 | t0039 | g0019 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0068 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01099 | hp1 | a0001 | c0001 | t0038 | g0127 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0113 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01106 | hp2 | a0001 | c0001 | t0015 | g0037 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01109 | hp1 | a0002 | c0007 | t0003 | g0158 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0072 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0187 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0073 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0188 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01192 | hp1 | a0001 | c0001 | t0036 | g0160 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01192 | hp2 | a0001 | c0001 | t0017 | g0228 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0071 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0256 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0255 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0195 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0032 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01358 | hp1 | a0001 | c0001 | t0008 | g0085 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01358 | hp2 | a0001 | c0001 | t0027 | g0253 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0172 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0243 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0041 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0074 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01934 | hp1 | a0001 | c0001 | t0009 | g0245 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02145 | hp1 | a0001 | c0002 | t0021 | g0013 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0227 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02258 | hp1 | a0001 | c0002 | t0021 | g0016 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0140 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0081 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02622 | hp2 | a0003 | c0011 | t0006 | g0006 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02647 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0249 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02723 | hp1 | a0001 | c0008 | t0006 | g0165 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02723 | hp2 | a0001 | c0001 | t0031 | g0026 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0058 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0051 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02818 | hp2 | a0001 | c0001 | t0033 | g0023 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02895 | hp1 | a0001 | c0001 | t0020 | g0192 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02895 | hp2 | a0001 | c0001 | t0035 | g0161 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02897 | hp2 | a0001 | c0001 | t0026 | g0190 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0025 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0052 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0033 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03130 | hp2 | a0001 | c0002 | t0012 | g0017 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03195 | hp2 | a0001 | c0002 | t0012 | g0018 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03225 | hp1 | a0001 | c0001 | t0034 | g0012 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03225 | hp2 | a0001 | c0002 | t0012 | g0014 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0257 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0049 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0206 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0246 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03491 | hp2 | a0004 | c0005 | t0003 | g0157 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0242 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03516 | hp1 | a0001 | c0001 | t0020 | g0191 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0024 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03579 | hp1 | a0001 | c0001 | t0032 | g0005 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03579 | hp2 | a0001 | c0009 | t0010 | g0166 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0031 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03669 | hp1 | a0001 | c0001 | t0037 | g0111 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0184 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0183 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03704 | hp1 | a0001 | c0004 | t0022 | g0155 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0169 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0247 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03942 | hp1 | a0001 | c0001 | t0010 | g0030 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0107 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0027 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0220 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0248 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04228 | hp1 | a0001 | c0003 | t0004 | g0211 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04228 | hp2 | a0001 | c0001 | t0009 | g0244 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18522 | hp1 | a0001 | c0002 | t0012 | g0015 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | CHB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0021 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18942 | hp2 | a0005 | c0006 | t0002 | g0226 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18963 | hp1 | a0001 | c0001 | t0025 | g0185 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18966 | hp2 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18974 | hp1 | a0001 | c0001 | t0029 | g0145 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0239 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0053 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19054 | hp1 | a0001 | c0001 | t0028 | g0152 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19054 | hp2 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19068 | hp2 | a0001 | c0001 | t0007 | g0035 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19074 | hp2 | a0001 | c0010 | t0001 | g0150 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ASW | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20129 | hp2 | a0001 | c0001 | t0023 | g0022 | AFR | ASW | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20805 | hp2 | a0001 | c0001 | t0009 | g0250 | EUR | TSI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0048 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0171 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0044 | REF | REF | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0022 | g0154 | REF | REF | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45297684 | C | G | 1 | a0003 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1607C>G | p.Thr536Ser | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 1925/5151 | 1607/2259 | 536/752 | chr19 | 45297684 | |||
| chr19:45297807 | G | A | 1 | a0004 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1730G>A | p.Arg577Gln | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 2048/5151 | 1730/2259 | 577/752 | chr19 | 45297807 | |||
| chr19:45297893 | G | A | 1 | a0005 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.1816G>A | p.Ala606Thr | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 2134/5151 | 1816/2259 | 606/752 | chr19 | 45297893 | |||
| chr19:45302385 | C | T | 1 | a0002 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1934C>T | p.Pro645Leu | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2252/5151 | 1934/2259 | 645/752 | chr19 | 45302385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45271582 | A | G | 1 | a0003c0011 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.660A>G | p.Pro220Pro | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/17 | 978/5151 | 660/2259 | 220/752 | chr19 | 45271582 | |||
| chr19:45271600 | G | A | 1 | a0001c0002 | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
synonymous_variant | LOW | c.678G>A | p.Leu226Leu | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/17 | 996/5151 | 678/2259 | 226/752 | chr19 | 45271600 | |||
| chr19:45277928 | G | C | 1 | a0001c0003 | 2 | HG03490.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.792G>C | p.Leu264Leu | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 9/17 | 1110/5151 | 792/2259 | 264/752 | chr19 | 45277928 | |||
| chr19:45280589 | G | T | 1 | a0001c0010 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.1131G>T | p.Arg377Arg | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/17 | 1449/5151 | 1131/2259 | 377/752 | chr19 | 45280589 | |||
| chr19:45287553 | C | T | 1 | a0001c0009 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1383C>T | p.Thr461Thr | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/17 | 1701/5151 | 1383/2259 | 461/752 | chr19 | 45287553 | |||
| chr19:45294420 | C | T | 1 | a0001c0008 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1566C>T | p.Arg522Arg | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/17 | 1884/5151 | 1566/2259 | 522/752 | chr19 | 45294420 | |||
| chr19:45297760 | T | C | 10 | a0001c0001 a0001c0002 a0001c0003 others(7): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
synonymous_variant | LOW | c.1683T>C | p.Arg561Arg | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 2001/5151 | 1683/2259 | 561/752 | chr19 | 45297760 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45251300 | T | TCCG | 2 | a0001c0001t0013 a0001c0001t0023 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-281_-279dupCGC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 278 | INFO_REALIGN_3_PRIME | chr19 | 45251300 | |||||
| chr19:45251311 | T | C | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(44): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-278T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | chr19 | 45251311 | |||||||
| chr19:45251363 | G | A | 1 | a0001c0001t0024 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-226G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 226 | chr19 | 45251363 | ||||||
| chr19:45251386 | C | G | 3 | a0001c0002t0012 a0001c0002t0021 a0001c0002t0039 |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-203C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 203 | chr19 | 45251386 | ||||||
| chr19:45251545 | G | C | 3 | a0001c0001t0014 a0001c0001t0025 a0001c0001t0026 |
4 | HG02602.hp2 HG02897.hp2 NA18963.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-44G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 44 | chr19 | 45251545 | ||||||
| chr19:45251545 | G | GC | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(12): Show |
81 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(78): Show |
5_prime_UTR_variant | MODIFIER | c.-36dupC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 35 | INFO_REALIGN_3_PRIME | chr19 | 45251545 | |||||
| chr19:45302904 | CG | C | 3 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0027 |
20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*200delG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 200 | INFO_REALIGN_3_PRIME | chr19 | 45302904 | |||||
| chr19:45303264 | C | T | 3 | a0001c0001t0034 a0001c0001t0035 a0001c0001t0038 |
3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*554C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 554 | chr19 | 45303264 | ||||||
| chr19:45303351 | A | G | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(33): Show |
172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*641A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 641 | chr19 | 45303351 | ||||||
| chr19:45303467 | C | T | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0026 |
5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*757C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 757 | chr19 | 45303467 | ||||||
| chr19:45303539 | G | A | 2 | a0001c0001t0015 a0001c0001t0036 |
3 | HG00099.hp2 HG01106.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 829 | chr19 | 45303539 | ||||||
| chr19:45303643 | C | A | 1 | a0001c0001t0030 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*933C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 933 | chr19 | 45303643 | ||||||
| chr19:45303692 | C | G | 1 | a0001c0001t0033 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*982C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 982 | chr19 | 45303692 | ||||||
| chr19:45303728 | CTCTG | C | 1 | a0001c0001t0011 | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1024_*1027delCTGT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1024 | INFO_REALIGN_3_PRIME | chr19 | 45303728 | |||||
| chr19:45303901 | C | G | 1 | a0001c0001t0011 | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1191C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1191 | chr19 | 45303901 | ||||||
| chr19:45303968 | C | T | 1 | a0001c0001t0032 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1258C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1258 | chr19 | 45303968 | ||||||
| chr19:45304130 | G | A | 1 | a0001c0001t0017 | 2 | HG00280.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1420G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1420 | chr19 | 45304130 | ||||||
| chr19:45304470 | C | T | 1 | a0001c0001t0031 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1760 | chr19 | 45304470 | ||||||
| chr19:45304577 | A | T | 1 | a0001c0002t0039 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1867A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1867 | chr19 | 45304577 | ||||||
| chr19:45304588 | C | G | 1 | a0001c0001t0031 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1878C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1878 | chr19 | 45304588 | ||||||
| chr19:45304673 | T | C | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(11): Show |
87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1963T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1963 | chr19 | 45304673 | ||||||
| chr19:45304687 | G | A | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0024 |
33 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1977G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1977 | chr19 | 45304687 | ||||||
| chr19:45304860 | T | A | 1 | a0001c0001t0027 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2150T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2150 | chr19 | 45304860 | ||||||
| chr19:45304884 | T | C | 1 | a0001c0001t0028 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2174T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2174 | chr19 | 45304884 | ||||||
| chr19:45304884 | T | G | 35 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(32): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*2174T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2174 | chr19 | 45304884 | ||||||
| chr19:45305171 | A | C | 1 | a0001c0001t0029 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2461A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2461 | chr19 | 45305171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45251732 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.51+93C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45251732 | |||||||
| chr19:45251757 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.51+118C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45251757 | |||||||
| chr19:45252034 | C | T | 1 | a0001c0001t0009g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.51+395C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252034 | |||||||
| chr19:45252110 | G | T | 19 | a0001c0001t0001g0252 a0001c0001t0002g0240 a0001c0001t0008g0242 others(16): Show |
19 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.51+471G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252110 | |||||||
| chr19:45252203 | G | A | 1 | a0001c0001t0011g0002 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.51+564G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252203 | |||||||
| chr19:45252374 | T | C | 25 | a0001c0001t0002g0001 a0001c0001t0004g0001 a0001c0001t0006g0003 others(22): Show |
25 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.51+735T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252374 | |||||||
| chr19:45252449 | G | A | 1 | a0001c0001t0031g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.51+810G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252449 | |||||||
| chr19:45252948 | T | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.51+1309T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252948 | |||||||
| chr19:45252997 | C | T | 2 | a0001c0001t0018g0024 a0001c0001t0018g0025 |
2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.51+1358C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252997 | |||||||
| chr19:45253033 | A | G | 5 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0004g0234 others(2): Show |
5 | HG02145.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+1394A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253033 | |||||||
| chr19:45253118 | G | C | 81 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.51+1479G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253118 | |||||||
| chr19:45253178 | G | A | 2 | a0001c0001t0003g0076 a0001c0001t0009g0075 |
2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.51+1539G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253178 | |||||||
| chr19:45253190 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.51+1551C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253190 | |||||||
| chr19:45253191 | A | C | 63 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(60): Show |
63 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.51+1552A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253191 | |||||||
| chr19:45253192 | C | CA | 51 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(48): Show |
51 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.51+1554dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45253192 | ||||||
| chr19:45253192 | C | CCA | 8 | a0001c0001t0005g0071 a0001c0001t0005g0073 a0001c0001t0005g0074 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+1553_51+1554ins others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253192 | |||||||
| chr19:45253193 | AC | A | 3 | a0001c0001t0018g0024 a0001c0001t0018g0025 a0001c0001t0034g0012 |
3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.51+1555delC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253193 | |||||||
| chr19:45253236 | C | T | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+1597C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253236 | |||||||
| chr19:45253298 | T | G | 1 | a0001c0001t0002g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.51+1659T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253298 | |||||||
| chr19:45253495 | A | G | 62 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(59): Show |
62 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.51+1856A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253495 | |||||||
| chr19:45253505 | C | T | 62 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(59): Show |
62 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.51+1866C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253505 | |||||||
| chr19:45253856 | G | A | 4 | a0001c0001t0001g0080 a0001c0001t0003g0078 a0001c0001t0003g0079 others(1): Show |
4 | HG02080.hp1 HG02135.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2217G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253856 | |||||||
| chr19:45254117 | T | G | 1 | a0001c0001t0006g0082 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51+2478T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254117 | |||||||
| chr19:45254139 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0008g0068 |
3 | HG01081.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.51+2500C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254139 | |||||||
| chr19:45254192 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.51+2553G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254192 | |||||||
| chr19:45254215 | G | A | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.51+2576G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254215 | |||||||
| chr19:45254754 | A | G | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.51+3115A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254754 | |||||||
| chr19:45255030 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.51+3391A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255030 | |||||||
| chr19:45255106 | A | G | 168 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(165): Show |
168 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.51+3467A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255106 | |||||||
| chr19:45255180 | G | A | 59 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(56): Show |
59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.51+3541G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255180 | |||||||
| chr19:45255202 | C | CA | 6 | a0001c0001t0001g0084 a0001c0001t0002g0164 a0001c0001t0006g0003 others(3): Show |
6 | HG01358.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+3577dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255202 | ||||||
| chr19:45255336 | A | G | 95 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(92): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.52-3653A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255336 | |||||||
| chr19:45255342 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.52-3647C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255342 | |||||||
| chr19:45255413 | T | C | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.52-3576T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255413 | |||||||
| chr19:45255433 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.52-3556C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255433 | |||||||
| chr19:45255559 | C | CA | 70 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(67): Show |
70 | HG00642.hp1 HG01071.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.52-3406dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | ||||||
| chr19:45255559 | C | CAA | 10 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0002g0077 others(7): Show |
10 | HG00408.hp2 HG00642.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-3407_52-3406dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | ||||||
| chr19:45255559 | CA | C | 15 | a0001c0001t0001g0159 a0001c0001t0002g0001 a0001c0001t0002g0222 others(12): Show |
15 | HG01192.hp1 HG02602.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-3406delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | ||||||
| chr19:45255559 | CAAAAAAA others(4): Show |
C | 17 | a0001c0001t0001g0252 a0001c0001t0008g0242 a0001c0001t0008g0246 others(14): Show |
17 | HG00280.hp2 HG00639.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.52-3416_52-3406del others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | ||||||
| chr19:45255613 | G | A | 2 | a0001c0001t0018g0024 a0001c0001t0018g0025 |
2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.52-3376G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255613 | |||||||
| chr19:45255798 | C | T | 2 | a0001c0001t0006g0007 a0001c0001t0006g0011 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.52-3191C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255798 | |||||||
| chr19:45255822 | C | A | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.52-3167C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255822 | |||||||
| chr19:45255869 | G | A | 3 | a0001c0001t0002g0001 a0001c0001t0004g0001 a0003c0011t0006g0006 |
3 | HG02615.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.52-3120G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255869 | |||||||
| chr19:45255897 | G | GAC | 82 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.52-3090_52-3089dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255897 | ||||||
| chr19:45256086 | G | A | 82 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.52-2903G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256086 | |||||||
| chr19:45256203 | C | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.52-2786C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256203 | |||||||
| chr19:45256291 | A | G | 85 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(82): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.52-2698A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256291 | |||||||
| chr19:45256342 | G | A | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.52-2647G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256342 | |||||||
| chr19:45256352 | C | T | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.52-2637C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256352 | |||||||
| chr19:45256353 | G | C | 50 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(47): Show |
50 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.52-2636G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256353 | |||||||
| chr19:45256384 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-2605G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256384 | |||||||
| chr19:45256429 | C | T | 1 | a0005c0006t0002g0226 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52-2560C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256429 | |||||||
| chr19:45256636 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.52-2353C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256636 | |||||||
| chr19:45256930 | T | C | 1 | a0001c0001t0006g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52-2059T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256930 | |||||||
| chr19:45256959 | T | C | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.52-2030T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256959 | |||||||
| chr19:45256960 | CT | C | 17 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0005g0040 others(14): Show |
17 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.52-2019delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45256960 | ||||||
| chr19:45257158 | C | T | 1 | a0001c0001t0006g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52-1831C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257158 | |||||||
| chr19:45257162 | T | C | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-1827T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257162 | |||||||
| chr19:45257290 | A | G | 47 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(44): Show |
47 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.52-1699A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257290 | |||||||
| chr19:45257352 | G | A | 82 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.52-1637G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257352 | |||||||
| chr19:45257383 | C | CT | 42 | a0001c0001t0001g0252 a0001c0001t0002g0083 a0001c0001t0002g0186 others(39): Show |
42 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.52-1588dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257383 | ||||||
| chr19:45257383 | C | CTT | 47 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(44): Show |
47 | HG00408.hp1 HG00609.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.52-1589_52-1588dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257383 | ||||||
| chr19:45257383 | CT | C | 43 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.52-1588delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257383 | ||||||
| chr19:45257530 | C | T | 1 | a0001c0001t0008g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.52-1459C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257530 | |||||||
| chr19:45257572 | C | T | 1 | a0001c0001t0005g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52-1417C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257572 | |||||||
| chr19:45257573 | G | A | 6 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 others(3): Show |
6 | HG01099.hp2 HG01255.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-1416G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257573 | |||||||
| chr19:45257607 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0004g0001 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.52-1382C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257607 | |||||||
| chr19:45257662 | C | T | 20 | a0001c0001t0001g0252 a0001c0001t0002g0240 a0001c0001t0008g0242 others(17): Show |
20 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.52-1327C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257662 | |||||||
| chr19:45257675 | G | A | 82 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.52-1314G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257675 | |||||||
| chr19:45257688 | TA | T | 23 | a0001c0001t0001g0252 a0001c0001t0002g0240 a0001c0001t0008g0242 others(20): Show |
23 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.52-1300delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257688 | |||||||
| chr19:45257689 | A | AT | 29 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0002g0083 others(26): Show |
29 | HG00738.hp1 HG02074.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.52-1282dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257689 | ||||||
| chr19:45257689 | A | T | 1 | a0001c0001t0009g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.52-1300A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257689 | |||||||
| chr19:45257689 | AT | A | 6 | a0001c0001t0001g0159 a0001c0001t0002g0204 a0001c0001t0002g0205 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-1282delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257689 | ||||||
| chr19:45257689 | ATT | A | 56 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(53): Show |
56 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.52-1283_52-1282del others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257689 | ||||||
| chr19:45257693 | T | A | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.52-1296T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257693 | |||||||
| chr19:45257720 | C | T | 1 | a0001c0001t0006g0173 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.52-1269C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257720 | |||||||
| chr19:45257753 | G | C | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.52-1236G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257753 | |||||||
| chr19:45257835 | G | A | 2 | a0001c0001t0005g0045 a0001c0001t0010g0195 |
2 | HG01261.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.52-1154G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257835 | |||||||
| chr19:45257958 | G | C | 15 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0196 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.52-1031G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257958 | |||||||
| chr19:45257988 | C | CT | 23 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0196 others(20): Show |
23 | HG01433.hp1 HG01517.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.52-985dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257988 | ||||||
| chr19:45257988 | CT | C | 25 | a0001c0001t0001g0252 a0001c0001t0002g0240 a0001c0001t0005g0046 others(22): Show |
25 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.52-985delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257988 | ||||||
| chr19:45258103 | A | T | 1 | a0001c0001t0005g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.52-886A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258103 | |||||||
| chr19:45258179 | T | G | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.52-810T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258179 | |||||||
| chr19:45258199 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0004g0001 a0003c0011t0006g0006 |
3 | HG02615.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.52-790C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258199 | |||||||
| chr19:45258231 | C | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.52-758C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258231 | |||||||
| chr19:45258235 | T | A | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.52-754T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258235 | |||||||
| chr19:45258321 | A | G | 1 | a0001c0001t0003g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52-668A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258321 | |||||||
| chr19:45258368 | G | A | 1 | a0001c0001t0005g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.52-621G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258368 | |||||||
| chr19:45258478 | A | G | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.52-511A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258478 | |||||||
| chr19:45258493 | G | A | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.52-496G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258493 | |||||||
| chr19:45258831 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.52-158T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258831 | |||||||
| chr19:45259245 | G | A | 3 | a0001c0001t0018g0024 a0001c0001t0018g0025 a0001c0001t0034g0012 |
3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.252+56G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259245 | |||||||
| chr19:45259245 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.252+56G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259245 | |||||||
| chr19:45259360 | A | G | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.252+171A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259360 | |||||||
| chr19:45259383 | T | C | 86 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(83): Show |
86 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.252+194T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259383 | |||||||
| chr19:45259434 | G | A | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.252+245G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259434 | |||||||
| chr19:45259436 | G | A | 50 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(47): Show |
50 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.252+247G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259436 | |||||||
| chr19:45259490 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.252+301A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259490 | |||||||
| chr19:45259501 | C | T | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+312C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259501 | |||||||
| chr19:45259628 | A | G | 20 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+439A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259628 | |||||||
| chr19:45259689 | C | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.252+500C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259689 | |||||||
| chr19:45259715 | C | T | 1 | a0001c0001t0015g0037 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.252+526C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259715 | |||||||
| chr19:45259885 | G | A | 1 | a0001c0001t0010g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.252+696G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259885 | |||||||
| chr19:45259923 | T | C | 86 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(83): Show |
86 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.252+734T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259923 | |||||||
| chr19:45260053 | C | T | 1 | a0001c0001t0010g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.252+864C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260053 | |||||||
| chr19:45260246 | T | C | 50 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(47): Show |
50 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.252+1057T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260246 | |||||||
| chr19:45260360 | G | A | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.252+1171G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260360 | |||||||
| chr19:45260389 | C | CA | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.252+1218dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45260389 | ||||||
| chr19:45260413 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.252+1224C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260413 | |||||||
| chr19:45260540 | T | A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.252+1351T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260540 | |||||||
| chr19:45260542 | C | CTGAAAAA | 3 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0032g0005 |
3 | HG01891.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.252+1353_252+1354i others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260542 | |||||||
| chr19:45260636 | G | A | 2 | a0001c0001t0006g0187 a0001c0001t0006g0188 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.252+1447G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260636 | |||||||
| chr19:45260678 | C | G | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.252+1489C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260678 | |||||||
| chr19:45260692 | C | G | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1503C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260692 | |||||||
| chr19:45260697 | AAAATAAA others(1): Show |
A | 81 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.252+1526_252+1533d others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45260697 | ||||||
| chr19:45261056 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.252+1867C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261056 | |||||||
| chr19:45261093 | C | G | 1 | a0001c0001t0002g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.252+1904C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261093 | |||||||
| chr19:45261396 | C | T | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.253-1717C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261396 | |||||||
| chr19:45261542 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.253-1571C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261542 | |||||||
| chr19:45261662 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.253-1451G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261662 | |||||||
| chr19:45261794 | A | G | 96 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(93): Show |
96 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.253-1319A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261794 | |||||||
| chr19:45261874 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.253-1239G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261874 | |||||||
| chr19:45261887 | T | C | 96 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(93): Show |
96 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.253-1226T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261887 | |||||||
| chr19:45261933 | CA | C | 39 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0001g0252 others(36): Show |
39 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.253-1167delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45261933 | ||||||
| chr19:45262037 | T | A | 1 | a0001c0001t0002g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.253-1076T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262037 | |||||||
| chr19:45262050 | C | T | 1 | a0001c0001t0010g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.253-1063C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262050 | |||||||
| chr19:45262074 | C | G | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.253-1039C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262074 | |||||||
| chr19:45262140 | C | T | 1 | a0001c0001t0003g0219 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.253-973C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262140 | |||||||
| chr19:45262197 | T | C | 3 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0032g0005 |
3 | HG01891.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.253-916T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262197 | |||||||
| chr19:45262298 | A | C | 1 | a0001c0001t0005g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.253-815A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262298 | |||||||
| chr19:45262299 | C | G | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.253-814C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262299 | |||||||
| chr19:45262299 | C | T | 1 | a0001c0001t0005g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.253-814C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262299 | |||||||
| chr19:45262353 | C | CG | 24 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0109 others(21): Show |
24 | HG00408.hp1 HG00609.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.253-753dupG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45262353 | ||||||
| chr19:45262449 | A | G | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.253-664A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262449 | |||||||
| chr19:45262584 | A | G | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.253-529A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262584 | |||||||
| chr19:45262741 | C | T | 58 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(55): Show |
58 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.253-372C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262741 | |||||||
| chr19:45262791 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.253-322G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262791 | |||||||
| chr19:45262868 | G | A | 1 | a0001c0001t0003g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.253-245G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262868 | |||||||
| chr19:45262964 | C | T | 1 | a0001c0001t0008g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.253-149C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262964 | |||||||
| chr19:45263010 | C | G | 4 | a0001c0001t0005g0029 a0001c0001t0005g0045 a0001c0001t0007g0036 others(1): Show |
4 | NA19000.hp1 NA19074.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-103C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45263010 | |||||||
| chr19:45263011 | C | G | 4 | a0001c0001t0005g0029 a0001c0001t0005g0045 a0001c0001t0007g0036 others(1): Show |
4 | NA19000.hp1 NA19074.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-102C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45263011 | |||||||
| chr19:45263012 | G | A | 3 | a0001c0001t0018g0024 a0001c0001t0018g0025 a0001c0001t0034g0012 |
3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-101G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45263012 | |||||||
| chr19:45263177 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.306+11G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 3/16 | chr19 | 45263177 | |||||||
| chr19:45263249 | C | T | 2 | a0001c0001t0005g0063 a0001c0001t0007g0035 |
2 | NA18994.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.307-70C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 3/16 | chr19 | 45263249 | |||||||
| chr19:45263267 | C | T | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-52C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 3/16 | chr19 | 45263267 | |||||||
| chr19:45263468 | G | A | 1 | a0001c0001t0014g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.355+101G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263468 | |||||||
| chr19:45263471 | G | A | 20 | a0001c0001t0001g0252 a0001c0001t0002g0240 a0001c0001t0008g0085 others(17): Show |
20 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.355+104G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263471 | |||||||
| chr19:45263634 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0004g0001 a0003c0011t0006g0006 |
3 | HG02615.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.355+267C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263634 | |||||||
| chr19:45263741 | CA | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0221 a0001c0001t0002g0201 others(3): Show |
6 | HG01167.hp1 HG01361.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+390delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr19 | 45263741 | ||||||
| chr19:45263956 | G | A | 99 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(96): Show |
99 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.355+589G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263956 | |||||||
| chr19:45264037 | G | A | 1 | a0001c0001t0009g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.356-647G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264037 | |||||||
| chr19:45264119 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.356-565G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264119 | |||||||
| chr19:45264146 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.356-538C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264146 | |||||||
| chr19:45264177 | C | T | 1 | a0001c0001t0004g0220 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.356-507C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264177 | |||||||
| chr19:45264281 | G | C | 63 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(60): Show |
63 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.356-403G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264281 | |||||||
| chr19:45264288 | G | A | 3 | a0001c0001t0018g0024 a0001c0001t0018g0025 a0001c0001t0034g0012 |
3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.356-396G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264288 | |||||||
| chr19:45264290 | T | C | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.356-394T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264290 | |||||||
| chr19:45264490 | C | CA | 41 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0084 others(38): Show |
41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.356-182dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr19 | 45264490 | ||||||
| chr19:45264612 | G | T | 5 | a0001c0001t0010g0195 a0001c0001t0019g0175 a0001c0001t0020g0191 others(2): Show |
5 | HG01261.hp1 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-72G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264612 | |||||||
| chr19:45265110 | C | T | 2 | a0001c0001t0023g0022 a0001c0001t0032g0005 |
2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.492+200C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265110 | |||||||
| chr19:45265113 | T | A | 1 | a0001c0001t0009g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.492+203T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265113 | |||||||
| chr19:45265145 | C | T | 1 | a0001c0001t0005g0062 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.492+235C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265145 | |||||||
| chr19:45265203 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.492+293G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265203 | |||||||
| chr19:45265213 | TGGG | T | 5 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0018g0024 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+306_492+308del others(3): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr19 | 45265213 | ||||||
| chr19:45265218 | G | A | 5 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0018g0024 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+308G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265218 | |||||||
| chr19:45265428 | G | A | 1 | a0001c0001t0031g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.492+518G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265428 | |||||||
| chr19:45265604 | T | TATGTGCA others(193): Show |
1 | a0001c0001t0003g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.493-599_493-400dup others(200): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr19 | 45265604 | ||||||
| chr19:45265688 | T | C | 60 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(57): Show |
60 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.493-537T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265688 | |||||||
| chr19:45265784 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.493-441C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265784 | |||||||
| chr19:45265884 | T | C | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493-341T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265884 | |||||||
| chr19:45265886 | C | T | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493-339C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265886 | |||||||
| chr19:45265897 | G | C | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493-328G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265897 | |||||||
| chr19:45265923 | G | A | 54 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(51): Show |
54 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.493-302G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265923 | |||||||
| chr19:45265961 | G | A | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-264G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265961 | |||||||
| chr19:45266043 | A | G | 69 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(66): Show |
69 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.493-182A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45266043 | |||||||
| chr19:45266066 | G | T | 5 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0018g0024 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-159G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45266066 | |||||||
| chr19:45266128 | G | C | 54 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(51): Show |
54 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.493-97G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45266128 | |||||||
| chr19:45266317 | G | A | 69 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(66): Show |
69 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.549+36G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266317 | |||||||
| chr19:45266484 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.549+203G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266484 | |||||||
| chr19:45266488 | G | C | 1 | a0001c0001t0014g0086 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.549+207G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266488 | |||||||
| chr19:45266491 | G | A | 92 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.549+210G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266491 | |||||||
| chr19:45266511 | A | G | 1 | a0001c0001t0025g0185 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.549+230A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266511 | |||||||
| chr19:45266603 | G | A | 1 | a0001c0001t0004g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.549+322G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266603 | |||||||
| chr19:45266730 | C | CT | 72 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(69): Show |
72 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.549+469dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45266730 | ||||||
| chr19:45266730 | C | CTT | 6 | a0001c0001t0005g0038 a0001c0001t0005g0045 a0001c0001t0005g0067 others(3): Show |
6 | HG00738.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+468_549+469dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45266730 | ||||||
| chr19:45266730 | CT | C | 5 | a0001c0001t0001g0221 a0001c0001t0003g0136 a0001c0001t0004g0235 others(2): Show |
5 | HG01074.hp1 HG02145.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+469delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45266730 | ||||||
| chr19:45266796 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0004g0001 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.549+515G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266796 | |||||||
| chr19:45266802 | C | G | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+521C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266802 | |||||||
| chr19:45266819 | G | T | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+538G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266819 | |||||||
| chr19:45266820 | C | A | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+539C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266820 | |||||||
| chr19:45266825 | T | C | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+544T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266825 | |||||||
| chr19:45266893 | C | T | 1 | a0001c0001t0004g0203 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.549+612C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266893 | |||||||
| chr19:45266978 | C | T | 1 | a0001c0001t0009g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.549+697C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266978 | |||||||
| chr19:45267008 | A | G | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+727A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267008 | |||||||
| chr19:45267042 | G | C | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+761G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267042 | |||||||
| chr19:45267048 | A | G | 55 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(52): Show |
55 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.549+767A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267048 | |||||||
| chr19:45267179 | C | T | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.549+898C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267179 | |||||||
| chr19:45267192 | G | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.549+911G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267192 | |||||||
| chr19:45267256 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0008g0113 |
2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.549+975C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267256 | |||||||
| chr19:45267310 | C | T | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+1029C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267310 | |||||||
| chr19:45267476 | T | C | 1 | a0001c0001t0010g0050 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.549+1195T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267476 | |||||||
| chr19:45267505 | C | T | 7 | a0001c0001t0002g0001 a0001c0001t0004g0001 a0001c0001t0010g0195 others(4): Show |
7 | HG01261.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+1224C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267505 | |||||||
| chr19:45267600 | G | A | 1 | a0001c0001t0013g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.549+1319G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267600 | |||||||
| chr19:45267835 | G | GT | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.549+1560dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45267835 | ||||||
| chr19:45268009 | T | C | 1 | a0001c0001t0006g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.549+1728T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268009 | |||||||
| chr19:45268029 | T | C | 47 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(44): Show |
47 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.549+1748T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268029 | |||||||
| chr19:45268300 | A | G | 15 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0196 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.549+2019A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268300 | |||||||
| chr19:45268364 | A | G | 1 | a0001c0001t0008g0251 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.549+2083A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268364 | |||||||
| chr19:45268453 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.549+2172G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268453 | |||||||
| chr19:45268575 | C | T | 1 | a0003c0011t0006g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.549+2294C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268575 | |||||||
| chr19:45268650 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.549+2369C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268650 | |||||||
| chr19:45268982 | C | T | 47 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(44): Show |
47 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.550-2490C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268982 | |||||||
| chr19:45269059 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.550-2413G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269059 | |||||||
| chr19:45269269 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.550-2203C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269269 | |||||||
| chr19:45269433 | C | T | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.550-2039C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269433 | |||||||
| chr19:45269456 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.550-2016G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269456 | |||||||
| chr19:45269608 | C | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.550-1864C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269608 | |||||||
| chr19:45269710 | C | G | 44 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(41): Show |
44 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.550-1762C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269710 | |||||||
| chr19:45269888 | G | A | 4 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0023g0022 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1584G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269888 | |||||||
| chr19:45269931 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.550-1541C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269931 | |||||||
| chr19:45270041 | T | C | 1 | a0001c0001t0014g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.550-1431T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270041 | |||||||
| chr19:45270050 | A | C | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.550-1422A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270050 | |||||||
| chr19:45270090 | A | G | 5 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0018g0024 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-1382A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270090 | |||||||
| chr19:45270118 | G | T | 2 | a0001c0001t0018g0024 a0001c0001t0018g0025 |
2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.550-1354G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270118 | |||||||
| chr19:45270123 | C | T | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.550-1349C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270123 | |||||||
| chr19:45270164 | G | C | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-1308G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270164 | |||||||
| chr19:45270216 | C | T | 1 | a0001c0001t0006g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-1256C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270216 | |||||||
| chr19:45270641 | T | C | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.550-831T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270641 | |||||||
| chr19:45270848 | G | A | 3 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0023g0022 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.550-624G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270848 | |||||||
| chr19:45270895 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.550-577C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270895 | |||||||
| chr19:45270896 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550-576G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270896 | |||||||
| chr19:45270927 | C | T | 1 | a0001c0002t0039g0019 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.550-545C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270927 | |||||||
| chr19:45271098 | G | T | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.550-374G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271098 | |||||||
| chr19:45271119 | C | T | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.550-353C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271119 | |||||||
| chr19:45271210 | C | A | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-262C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271210 | |||||||
| chr19:45271251 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0004g0001 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.550-221G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271251 | |||||||
| chr19:45271311 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.550-161A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271311 | |||||||
| chr19:45271422 | A | G | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.550-50A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271422 | |||||||
| chr19:45271772 | C | A | 1 | a0001c0003t0004g0211 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.786+64C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45271772 | |||||||
| chr19:45271814 | A | G | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.786+106A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45271814 | |||||||
| chr19:45272032 | A | G | 3 | a0001c0001t0002g0001 a0001c0001t0004g0001 a0001c0001t0010g0195 |
3 | HG01261.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.786+324A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272032 | |||||||
| chr19:45272049 | TG | T | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.786+343delG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45272049 | ||||||
| chr19:45272097 | G | A | 257 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.786+389G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272097 | |||||||
| chr19:45272315 | G | A | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.786+607G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272315 | |||||||
| chr19:45272331 | C | T | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.786+623C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272331 | |||||||
| chr19:45272364 | G | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0003g0101 others(2): Show |
5 | HG00642.hp1 HG01109.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+656G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272364 | |||||||
| chr19:45272431 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.786+723C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272431 | |||||||
| chr19:45272524 | G | A | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.786+816G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272524 | |||||||
| chr19:45272650 | G | A | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.786+942G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272650 | |||||||
| chr19:45272700 | CA | C | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+994delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45272700 | ||||||
| chr19:45272842 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.786+1134T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272842 | |||||||
| chr19:45272875 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0004g0001 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.786+1167G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272875 | |||||||
| chr19:45272883 | G | A | 1 | a0001c0001t0009g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.786+1175G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272883 | |||||||
| chr19:45272934 | C | T | 3 | a0001c0002t0012g0014 a0001c0002t0012g0017 a0001c0002t0012g0018 |
3 | HG03130.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.786+1226C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272934 | |||||||
| chr19:45273242 | C | A | 3 | a0001c0001t0018g0024 a0001c0001t0018g0025 a0001c0001t0034g0012 |
3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.786+1534C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273242 | |||||||
| chr19:45273250 | T | G | 1 | a0001c0001t0018g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.786+1542T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273250 | |||||||
| chr19:45273317 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.786+1609G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273317 | |||||||
| chr19:45273323 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.786+1615T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273323 | |||||||
| chr19:45273367 | G | C | 14 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0017g0228 others(11): Show |
14 | HG00280.hp1 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.786+1659G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273367 | |||||||
| chr19:45273369 | G | C | 39 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0006g0003 others(36): Show |
39 | HG00280.hp1 HG01074.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.786+1661G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273369 | |||||||
| chr19:45273519 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.786+1811T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273519 | |||||||
| chr19:45273702 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.786+1994C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273702 | |||||||
| chr19:45273722 | T | C | 44 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(41): Show |
44 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.786+2014T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273722 | |||||||
| chr19:45273772 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.786+2064C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273772 | |||||||
| chr19:45273843 | C | G | 20 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0006g0082 others(17): Show |
20 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.786+2135C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273843 | |||||||
| chr19:45273973 | G | C | 3 | a0001c0001t0018g0024 a0001c0001t0018g0025 a0001c0001t0034g0012 |
3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.786+2265G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273973 | |||||||
| chr19:45273987 | C | T | 45 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.786+2279C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273987 | |||||||
| chr19:45274010 | G | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.786+2302G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274010 | |||||||
| chr19:45274044 | G | T | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+2336G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274044 | |||||||
| chr19:45274064 | A | G | 15 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0006g0082 others(12): Show |
15 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+2356A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274064 | |||||||
| chr19:45274249 | AAAAC | A | 5 | a0001c0001t0001g0094 a0001c0001t0002g0034 a0001c0001t0002g0061 others(2): Show |
5 | NA18974.hp1 NA18974.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2553_786+2556d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45274249 | ||||||
| chr19:45274583 | A | G | 1 | a0001c0001t0015g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.786+2875A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274583 | |||||||
| chr19:45274676 | C | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0003g0101 others(2): Show |
5 | HG00642.hp1 HG01109.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2968C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274676 | |||||||
| chr19:45274822 | C | A | 1 | a0001c0001t0003g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.787-3101C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274822 | |||||||
| chr19:45275087 | C | A | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.787-2836C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275087 | |||||||
| chr19:45275126 | C | T | 4 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0225 others(1): Show |
4 | HG02970.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2797C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275126 | |||||||
| chr19:45275142 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.787-2781T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275142 | |||||||
| chr19:45275297 | C | T | 1 | a0001c0001t0035g0161 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.787-2626C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275297 | |||||||
| chr19:45275487 | TA | T | 57 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.787-2423delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45275487 | ||||||
| chr19:45275591 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.787-2332G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275591 | |||||||
| chr19:45275630 | G | A | 3 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0023g0022 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.787-2293G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275630 | |||||||
| chr19:45275683 | T | C | 7 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(4): Show |
7 | HG00280.hp1 HG01192.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.787-2240T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275683 | |||||||
| chr19:45275814 | G | A | 3 | a0001c0001t0004g0183 a0001c0003t0002g0206 a0001c0003t0004g0211 |
3 | HG03490.hp2 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.787-2109G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275814 | |||||||
| chr19:45275986 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.787-1937G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275986 | |||||||
| chr19:45276057 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.787-1866G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276057 | |||||||
| chr19:45276170 | G | C | 1 | a0001c0001t0002g0204 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.787-1753G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276170 | |||||||
| chr19:45276336 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.787-1587T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276336 | |||||||
| chr19:45276377 | T | C | 107 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(104): Show |
107 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.787-1546T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276377 | |||||||
| chr19:45276397 | C | T | 1 | a0001c0001t0004g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.787-1526C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276397 | |||||||
| chr19:45276518 | C | T | 1 | a0001c0001t0003g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.787-1405C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276518 | |||||||
| chr19:45276519 | G | A | 1 | a0001c0001t0013g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.787-1404G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276519 | |||||||
| chr19:45276558 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.787-1365G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276558 | |||||||
| chr19:45276622 | A | AT | 15 | a0001c0001t0001g0121 a0001c0001t0001g0130 a0001c0001t0001g0143 others(12): Show |
15 | HG00735.hp1 HG01361.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.787-1280dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276622 | ||||||
| chr19:45276622 | AT | A | 29 | a0001c0001t0001g0080 a0001c0001t0001g0109 a0001c0001t0001g0123 others(26): Show |
29 | HG00639.hp1 HG01074.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.787-1280delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276622 | ||||||
| chr19:45276800 | A | AT | 6 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(3): Show |
6 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-1109dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276800 | ||||||
| chr19:45276823 | TG | T | 5 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0018g0024 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-1096delG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276823 | ||||||
| chr19:45277107 | G | A | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.787-816G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277107 | |||||||
| chr19:45277329 | C | T | 36 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0005g0029 others(33): Show |
36 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.787-594C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277329 | |||||||
| chr19:45277423 | T | A | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.787-500T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277423 | |||||||
| chr19:45277433 | A | AT | 34 | a0001c0001t0001g0120 a0001c0001t0001g0156 a0001c0001t0002g0186 others(31): Show |
34 | HG01071.hp1 HG01071.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.787-471dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277433 | ||||||
| chr19:45277433 | A | ATT | 23 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0006g0082 others(20): Show |
23 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.787-472_787-471dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277433 | ||||||
| chr19:45277526 | A | G | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-397A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277526 | |||||||
| chr19:45277555 | A | G | 7 | a0001c0001t0002g0001 a0001c0001t0004g0001 a0001c0001t0010g0195 others(4): Show |
7 | HG01261.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-368A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277555 | |||||||
| chr19:45277693 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-230C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277693 | |||||||
| chr19:45277694 | G | A | 1 | a0001c0001t0004g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787-229G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277694 | |||||||
| chr19:45277775 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.787-148T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277775 | |||||||
| chr19:45277823 | T | TTG | 16 | a0001c0001t0001g0151 a0001c0001t0001g0252 a0001c0001t0002g0205 others(13): Show |
16 | HG00280.hp2 HG00639.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.787-54_787-53dupGT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | T | TTGTG | 2 | a0001c0001t0002g0204 a0001c0001t0005g0062 |
2 | HG02970.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.787-56_787-53dupGT others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | TTG | T | 109 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.787-54_787-53delGT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | TTGTG | T | 26 | a0001c0001t0001g0088 a0001c0001t0001g0100 a0001c0001t0001g0142 others(23): Show |
26 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.787-56_787-53delGT others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | TTGTGTG | T | 27 | a0001c0001t0001g0092 a0001c0001t0001g0138 a0001c0001t0001g0194 others(24): Show |
27 | HG01884.hp1 HG01891.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.787-58_787-53delGT others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | TTGTGTGT others(1): Show |
T | 18 | a0001c0001t0001g0221 a0001c0001t0006g0167 a0001c0001t0006g0173 others(15): Show |
18 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.787-60_787-53delGT others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | TTGTGTGT others(3): Show |
T | 8 | a0001c0001t0001g0189 a0001c0001t0006g0082 a0001c0001t0006g0170 others(5): Show |
8 | HG01433.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.787-62_787-53delGT others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | TTGTGTGT others(7): Show |
T | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-66_787-53delGT others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277823 | TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.787-68_787-53delGT others(14): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | ||||||
| chr19:45277867 | G | A | 6 | a0001c0001t0006g0167 a0001c0001t0006g0168 a0001c0001t0006g0173 others(3): Show |
6 | HG01433.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-56G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277867 | |||||||
| chr19:45277868 | T | A | 6 | a0001c0001t0006g0167 a0001c0001t0006g0168 a0001c0001t0006g0173 others(3): Show |
6 | HG01433.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-55T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277868 | |||||||
| chr19:45277886 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.787-37G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277886 | |||||||
| chr19:45278279 | G | T | 1 | a0001c0001t0008g0249 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.906+237G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 9/16 | chr19 | 45278279 | |||||||
| chr19:45278434 | G | A | 1 | a0001c0009t0010g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.907-82G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 9/16 | chr19 | 45278434 | |||||||
| chr19:45278658 | C | A | 17 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0006g0082 others(14): Show |
17 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006+43C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278658 | |||||||
| chr19:45278777 | T | C | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1006+162T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278777 | |||||||
| chr19:45278906 | A | T | 44 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(41): Show |
44 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1006+291A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278906 | |||||||
| chr19:45278911 | C | T | 8 | a0001c0001t0002g0001 a0001c0001t0002g0259 a0001c0001t0004g0001 others(5): Show |
8 | HG01261.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+296C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278911 | |||||||
| chr19:45278955 | A | C | 1 | a0001c0001t0002g0217 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1006+340A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278955 | |||||||
| chr19:45279042 | G | A | 2 | a0001c0001t0008g0242 a0001c0001t0008g0246 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1006+427G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279042 | |||||||
| chr19:45279330 | A | C | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1006+715A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279330 | |||||||
| chr19:45279336 | A | G | 9 | a0001c0001t0002g0001 a0001c0001t0002g0259 a0001c0001t0004g0001 others(6): Show |
9 | HG01261.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+721A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279336 | |||||||
| chr19:45279664 | A | G | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1007-710A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279664 | |||||||
| chr19:45279863 | T | C | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1007-511T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279863 | |||||||
| chr19:45279904 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1007-470G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279904 | |||||||
| chr19:45280169 | C | A | 1 | a0001c0009t0010g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1007-205C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45280169 | |||||||
| chr19:45280234 | C | T | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007-140C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45280234 | |||||||
| chr19:45280789 | T | TA | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+56dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45280789 | ||||||
| chr19:45280890 | G | A | 3 | a0001c0001t0018g0024 a0001c0001t0018g0025 a0001c0001t0034g0012 |
3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1276+156G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280890 | |||||||
| chr19:45280939 | G | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0010g0030 others(1): Show |
4 | HG03654.hp2 HG03831.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276+205G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280939 | |||||||
| chr19:45280983 | C | T | 1 | a0001c0001t0028g0152 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1276+249C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280983 | |||||||
| chr19:45280995 | G | A | 5 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0018g0024 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+261G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280995 | |||||||
| chr19:45281174 | T | C | 4 | a0001c0001t0013g0020 a0001c0001t0013g0021 a0001c0001t0023g0022 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+440T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281174 | |||||||
| chr19:45281300 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1276+566C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281300 | |||||||
| chr19:45281367 | C | CTTTTTT | 9 | a0001c0001t0006g0009 a0001c0002t0012g0014 a0001c0002t0012g0015 others(6): Show |
9 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276+639_1276+644d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45281367 | ||||||
| chr19:45281367 | C | CTTTTTTT | 89 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(86): Show |
89 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.1276+638_1276+644d others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45281367 | ||||||
| chr19:45281367 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0189 a0001c0001t0002g0177 a0001c0001t0006g0007 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276+637_1276+644d others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45281367 | ||||||
| chr19:45281444 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1276+710T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281444 | |||||||
| chr19:45281592 | C | T | 1 | a0001c0001t0009g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1276+858C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281592 | |||||||
| chr19:45281859 | G | T | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1276+1125G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281859 | |||||||
| chr19:45281935 | G | A | 15 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0196 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+1201G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281935 | |||||||
| chr19:45281974 | A | C | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1276+1240A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281974 | |||||||
| chr19:45282028 | G | A | 15 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0196 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+1294G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282028 | |||||||
| chr19:45282041 | T | C | 2 | a0001c0001t0008g0247 a0001c0001t0009g0027 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1276+1307T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282041 | |||||||
| chr19:45282178 | A | G | 2 | a0001c0001t0006g0187 a0001c0001t0006g0188 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1276+1444A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282178 | |||||||
| chr19:45282229 | TA | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0194 a0001c0001t0002g0196 others(2): Show |
5 | HG00323.hp1 HG02451.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+1511delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45282229 | ||||||
| chr19:45282245 | A | AT | 4 | a0001c0001t0005g0029 a0001c0001t0005g0045 a0001c0001t0007g0036 others(1): Show |
4 | NA19000.hp1 NA19074.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276+1511_1276+151 others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282245 | |||||||
| chr19:45282260 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1276+1526A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282260 | |||||||
| chr19:45282337 | A | T | 1 | a0001c0001t0010g0050 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1276+1603A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282337 | |||||||
| chr19:45282413 | C | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276+1679C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282413 | |||||||
| chr19:45282590 | A | G | 257 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0069 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1276+1856A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282590 | |||||||
| chr19:45282654 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1276+1920T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282654 | |||||||
| chr19:45282723 | G | A | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276+1989G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282723 | |||||||
| chr19:45282833 | T | C | 2 | a0001c0001t0019g0239 a0001c0001t0034g0012 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1276+2099T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282833 | |||||||
| chr19:45282946 | C | T | 7 | a0001c0001t0006g0227 a0001c0001t0011g0002 a0001c0001t0011g0033 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+2212C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282946 | |||||||
| chr19:45283207 | C | T | 35 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0005g0029 others(32): Show |
35 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1276+2473C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283207 | |||||||
| chr19:45283297 | T | C | 79 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1276+2563T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283297 | |||||||
| chr19:45283409 | C | CA | 15 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0159 others(12): Show |
15 | HG01109.hp1 HG01258.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276+2702dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | ||||||
| chr19:45283409 | CA | C | 15 | a0001c0001t0001g0142 a0001c0001t0001g0252 a0001c0001t0001g0258 others(12): Show |
15 | HG01099.hp1 HG01168.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+2702delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | ||||||
| chr19:45283409 | CAAAAAAA | C | 39 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0002g0236 others(36): Show |
39 | HG00738.hp1 HG01074.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1276+2696_1276+270 others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | ||||||
| chr19:45283409 | CAAAAAAA others(1): Show |
C | 33 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0005g0029 others(30): Show |
33 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1276+2695_1276+270 others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | ||||||
| chr19:45283409 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1276+2691_1276+270 others(16): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | ||||||
| chr19:45283743 | C | T | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1276+3009C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283743 | |||||||
| chr19:45283744 | G | A | 72 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0189 others(69): Show |
72 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1276+3010G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283744 | |||||||
| chr19:45283788 | G | A | 167 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0189 others(164): Show |
167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1276+3054G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283788 | |||||||
| chr19:45283824 | T | C | 166 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0189 others(163): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1276+3090T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283824 | |||||||
| chr19:45283900 | A | G | 1 | a0001c0001t0014g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1276+3166A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283900 | |||||||
| chr19:45284150 | A | G | 2 | a0001c0001t0019g0239 a0001c0001t0034g0012 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-3297A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284150 | |||||||
| chr19:45284308 | A | G | 162 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0189 others(159): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1277-3139A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284308 | |||||||
| chr19:45284311 | C | G | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-3136C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284311 | |||||||
| chr19:45284325 | C | CT | 15 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(12): Show |
15 | HG01099.hp1 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1277-3108dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45284325 | ||||||
| chr19:45284349 | G | A | 33 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0005g0029 others(30): Show |
33 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1277-3098G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284349 | |||||||
| chr19:45284350 | T | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-3097T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284350 | |||||||
| chr19:45284618 | G | A | 2 | a0001c0001t0008g0249 a0001c0001t0009g0244 |
2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1277-2829G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284618 | |||||||
| chr19:45284629 | G | A | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277-2818G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284629 | |||||||
| chr19:45284647 | T | G | 9 | a0001c0001t0006g0227 a0001c0001t0011g0002 a0001c0001t0011g0033 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1277-2800T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284647 | |||||||
| chr19:45284840 | C | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1277-2607C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284840 | |||||||
| chr19:45285191 | C | T | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-2256C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285191 | |||||||
| chr19:45285261 | C | CA | 39 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0121 others(36): Show |
39 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1277-2162dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | ||||||
| chr19:45285261 | CA | C | 20 | a0001c0001t0001g0066 a0001c0001t0001g0087 a0001c0001t0001g0093 others(17): Show |
20 | HG00408.hp1 HG00408.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1277-2162delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | ||||||
| chr19:45285261 | CAAAAA | C | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277-2166_1277-216 others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | ||||||
| chr19:45285261 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-2174_1277-216 others(17): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | ||||||
| chr19:45285354 | T | C | 80 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0189 others(77): Show |
80 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.1277-2093T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285354 | |||||||
| chr19:45285511 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0003g0099 a0001c0001t0029g0145 |
3 | HG02027.hp2 NA18974.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1277-1936G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285511 | |||||||
| chr19:45285659 | G | A | 2 | a0001c0001t0019g0239 a0001c0001t0034g0012 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-1788G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285659 | |||||||
| chr19:45285659 | G | GTATCATA others(18): Show |
6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1787_1277-178 others(29): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285659 | ||||||
| chr19:45285665 | A | T | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1782A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285665 | |||||||
| chr19:45285666 | C | CATATG | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1781_1277-178 others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285666 | |||||||
| chr19:45285667 | C | G | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1780C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285667 | |||||||
| chr19:45285791 | A | G | 6 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0004g0208 others(3): Show |
6 | HG00738.hp1 HG02257.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277-1656A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285791 | |||||||
| chr19:45285895 | T | A | 2 | a0001c0001t0019g0239 a0001c0001t0034g0012 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-1552T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285895 | |||||||
| chr19:45286212 | T | C | 2 | a0001c0001t0019g0239 a0001c0001t0034g0012 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-1235T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286212 | |||||||
| chr19:45286252 | T | C | 1 | a0001c0001t0014g0086 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1277-1195T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286252 | |||||||
| chr19:45286253 | G | A | 1 | a0001c0001t0014g0086 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1277-1194G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286253 | |||||||
| chr19:45286278 | T | A | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1277-1169T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286278 | |||||||
| chr19:45286289 | T | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-1158T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286289 | |||||||
| chr19:45286743 | T | A | 167 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0189 others(164): Show |
167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1277-704T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286743 | |||||||
| chr19:45286774 | T | C | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1277-673T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286774 | |||||||
| chr19:45286856 | A | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-591A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286856 | |||||||
| chr19:45286856 | A | G | 7 | a0001c0001t0006g0227 a0001c0001t0011g0002 a0001c0001t0011g0033 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-591A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286856 | |||||||
| chr19:45286870 | G | T | 1 | a0001c0001t0004g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1277-577G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286870 | |||||||
| chr19:45286916 | G | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1277-531G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286916 | |||||||
| chr19:45286963 | A | C | 1 | a0001c0001t0005g0073 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1277-484A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286963 | |||||||
| chr19:45287042 | C | T | 1 | a0001c0001t0008g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1277-405C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287042 | |||||||
| chr19:45287095 | T | G | 9 | a0001c0001t0002g0177 a0001c0001t0002g0196 a0001c0001t0002g0200 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1277-352T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287095 | |||||||
| chr19:45287129 | A | G | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1277-318A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287129 | |||||||
| chr19:45287181 | C | T | 3 | a0001c0001t0002g0077 a0001c0001t0002g0207 a0001c0001t0004g0214 |
3 | HG02071.hp1 HG02080.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1277-266C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287181 | |||||||
| chr19:45287202 | C | CA | 20 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0002g0238 others(17): Show |
20 | HG00738.hp1 HG01167.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1277-225dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45287202 | ||||||
| chr19:45287202 | CA | C | 12 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0123 others(9): Show |
12 | HG00280.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1277-225delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45287202 | ||||||
| chr19:45287433 | A | AC | 5 | a0001c0001t0002g0083 a0001c0001t0002g0222 a0001c0001t0003g0108 others(2): Show |
5 | HG02074.hp1 HG02145.hp1 HG02738.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1277-9dupC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45287433 | ||||||
| chr19:45287749 | C | T | 1 | a0001c0001t0009g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1494+85C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287749 | |||||||
| chr19:45287750 | G | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1494+86G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287750 | |||||||
| chr19:45287870 | A | G | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1494+206A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287870 | |||||||
| chr19:45287910 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1494+246G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287910 | |||||||
| chr19:45287945 | A | G | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1494+281A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287945 | |||||||
| chr19:45288267 | A | C | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1494+603A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288267 | |||||||
| chr19:45288279 | A | G | 3 | a0001c0001t0034g0012 a0001c0001t0035g0161 a0001c0001t0038g0127 |
3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1494+615A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288279 | |||||||
| chr19:45288421 | C | T | 22 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0002g0236 others(19): Show |
22 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1494+757C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288421 | |||||||
| chr19:45288432 | A | G | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+768A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288432 | |||||||
| chr19:45288543 | A | G | 2 | a0001c0001t0002g0001 a0001c0001t0004g0001 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1494+879A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288543 | |||||||
| chr19:45288552 | CA | C | 79 | a0001c0001t0001g0070 a0001c0001t0001g0088 a0001c0001t0001g0189 others(76): Show |
79 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1494+905delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288552 | ||||||
| chr19:45288578 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0004g0001 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1494+914C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288578 | |||||||
| chr19:45288580 | A | C | 80 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1494+916A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288580 | |||||||
| chr19:45288774 | C | T | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494+1110C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288774 | |||||||
| chr19:45288849 | C | CA | 5 | a0001c0001t0002g0201 a0001c0001t0003g0115 a0001c0001t0006g0227 others(2): Show |
5 | HG01099.hp2 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+1203dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | ||||||
| chr19:45288849 | C | CAA | 108 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0002g0001 others(105): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1494+1202_1494+120 others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | ||||||
| chr19:45288849 | C | CAAA | 25 | a0001c0001t0002g0164 a0001c0001t0002g0225 a0001c0001t0004g0181 others(22): Show |
25 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1494+1201_1494+120 others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | ||||||
| chr19:45288849 | C | CAAAAAA | 22 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0002g0236 others(19): Show |
22 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1494+1198_1494+120 others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | ||||||
| chr19:45288868 | G | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1204G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288868 | |||||||
| chr19:45288869 | T | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1205T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288869 | |||||||
| chr19:45288870 | C | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1206C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288870 | |||||||
| chr19:45288913 | G | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1249G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288913 | |||||||
| chr19:45288919 | A | G | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1494+1255A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288919 | |||||||
| chr19:45289021 | C | T | 1 | a0001c0001t0006g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1494+1357C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289021 | |||||||
| chr19:45289118 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0003g0095 others(1): Show |
4 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+1454G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289118 | |||||||
| chr19:45289317 | G | A | 2 | a0001c0001t0006g0227 a0001c0008t0006g0165 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1494+1653G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289317 | |||||||
| chr19:45289341 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0004g0103 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1494+1677C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289341 | |||||||
| chr19:45289385 | C | CA | 52 | a0001c0001t0001g0028 a0001c0001t0001g0159 a0001c0001t0002g0179 others(49): Show |
52 | HG00738.hp1 HG01074.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1494+1744dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289385 | ||||||
| chr19:45289385 | CA | C | 11 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0258 others(8): Show |
11 | HG00140.hp2 HG00280.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1494+1744delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289385 | ||||||
| chr19:45289385 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0004g0203 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1494+1734_1494+174 others(15): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289385 | ||||||
| chr19:45289447 | G | A | 50 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1494+1783G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289447 | |||||||
| chr19:45289506 | C | T | 32 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(29): Show |
32 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1494+1842C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289506 | |||||||
| chr19:45289560 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0003g0095 others(1): Show |
4 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+1896G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289560 | |||||||
| chr19:45289640 | C | T | 1 | a0004c0005t0003g0157 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1494+1976C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289640 | |||||||
| chr19:45289648 | T | TA | 3 | a0001c0001t0034g0012 a0001c0001t0035g0161 a0001c0001t0038g0127 |
3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1494+1986dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289648 | ||||||
| chr19:45289712 | G | A | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1494+2048G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289712 | |||||||
| chr19:45289718 | C | T | 3 | a0001c0001t0034g0012 a0001c0001t0035g0161 a0001c0001t0038g0127 |
3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1494+2054C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289718 | |||||||
| chr19:45289856 | C | T | 2 | a0001c0003t0002g0206 a0001c0003t0004g0211 |
2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1494+2192C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289856 | |||||||
| chr19:45289857 | A | G | 164 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(161): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1494+2193A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289857 | |||||||
| chr19:45289864 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1494+2200A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289864 | |||||||
| chr19:45289955 | G | A | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1494+2291G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289955 | |||||||
| chr19:45289971 | G | A | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1494+2307G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289971 | |||||||
| chr19:45290144 | G | T | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494+2480G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290144 | |||||||
| chr19:45290449 | G | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(74): Show |
77 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1494+2785G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290449 | |||||||
| chr19:45290570 | T | C | 20 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0004g0208 others(17): Show |
20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1494+2906T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290570 | |||||||
| chr19:45290574 | A | T | 41 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(38): Show |
41 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1494+2910A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290574 | |||||||
| chr19:45290581 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1494+2917G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290581 | |||||||
| chr19:45290658 | G | C | 1 | a0001c0001t0028g0152 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1494+2994G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290658 | |||||||
| chr19:45290715 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1494+3051G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290715 | |||||||
| chr19:45290786 | G | C | 20 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0004g0208 others(17): Show |
20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1494+3122G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290786 | |||||||
| chr19:45290786 | G | T | 4 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0225 others(1): Show |
4 | HG02970.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+3122G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290786 | |||||||
| chr19:45290790 | C | T | 2 | a0001c0001t0004g0180 a0001c0001t0004g0235 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1494+3126C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290790 | |||||||
| chr19:45290851 | G | A | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1494+3187G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290851 | |||||||
| chr19:45290894 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1494+3230C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290894 | |||||||
| chr19:45291110 | A | G | 5 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-3239A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291110 | |||||||
| chr19:45291141 | T | G | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1495-3208T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291141 | |||||||
| chr19:45291245 | C | T | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-3104C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291245 | |||||||
| chr19:45291463 | TGGCAAAA others(128): Show |
T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1495-2883_1495-274 others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45291463 | ||||||
| chr19:45291511 | G | A | 1 | a0001c0001t0007g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1495-2838G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291511 | |||||||
| chr19:45291554 | G | A | 2 | a0001c0001t0006g0173 a0001c0001t0019g0239 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1495-2795G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291554 | |||||||
| chr19:45291607 | C | G | 1 | a0001c0001t0009g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1495-2742C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291607 | |||||||
| chr19:45291612 | C | T | 1 | a0001c0001t0008g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1495-2737C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291612 | |||||||
| chr19:45291675 | G | A | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1495-2674G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291675 | |||||||
| chr19:45291795 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1495-2554A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291795 | |||||||
| chr19:45291880 | G | A | 2 | a0001c0001t0035g0161 a0001c0001t0038g0127 |
2 | HG01099.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1495-2469G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291880 | |||||||
| chr19:45291928 | G | T | 7 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0001t0006g0009 others(4): Show |
7 | HG01261.hp1 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495-2421G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291928 | |||||||
| chr19:45292028 | A | C | 9 | a0001c0001t0002g0259 a0001c0001t0006g0003 a0001c0001t0006g0004 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1495-2321A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292028 | |||||||
| chr19:45292357 | C | T | 3 | a0001c0001t0034g0012 a0001c0001t0035g0161 a0001c0001t0038g0127 |
3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1495-1992C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292357 | |||||||
| chr19:45292381 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1495-1968C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292381 | |||||||
| chr19:45292694 | T | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0002c0007t0003g0158 |
3 | HG00642.hp1 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1495-1655T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292694 | |||||||
| chr19:45292804 | C | T | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-1545C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292804 | |||||||
| chr19:45292850 | C | T | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-1499C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292850 | |||||||
| chr19:45292972 | G | T | 3 | a0001c0001t0002g0034 a0001c0001t0002g0061 a0001c0001t0002g0064 |
3 | NA18974.hp2 NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1495-1377G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292972 | |||||||
| chr19:45292994 | G | A | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-1355G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292994 | |||||||
| chr19:45293162 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(73): Show |
76 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1495-1187G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293162 | |||||||
| chr19:45293188 | T | C | 40 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(37): Show |
40 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1495-1161T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293188 | |||||||
| chr19:45293269 | A | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG02027.hp1 NA18983.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495-1080A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293269 | |||||||
| chr19:45293363 | A | G | 1 | a0001c0001t0004g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1495-986A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293363 | |||||||
| chr19:45293441 | A | G | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1495-908A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293441 | |||||||
| chr19:45293507 | C | G | 3 | a0001c0001t0008g0242 a0001c0001t0008g0246 a0001c0001t0009g0245 |
3 | HG01934.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1495-842C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293507 | |||||||
| chr19:45293534 | G | T | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1495-815G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293534 | |||||||
| chr19:45293545 | C | T | 1 | a0001c0004t0022g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1495-804C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293545 | |||||||
| chr19:45293617 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1495-732A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293617 | |||||||
| chr19:45293777 | T | C | 5 | a0001c0001t0002g0259 a0001c0001t0019g0175 a0001c0001t0020g0191 others(2): Show |
5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495-572T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293777 | |||||||
| chr19:45293834 | A | C | 40 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(37): Show |
40 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1495-515A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293834 | |||||||
| chr19:45293973 | T | G | 40 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(37): Show |
40 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1495-376T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293973 | |||||||
| chr19:45294122 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1495-227C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45294122 | |||||||
| chr19:45294135 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1495-214G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45294135 | |||||||
| chr19:45294335 | T | C | 38 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(35): Show |
38 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1495-14T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45294335 | |||||||
| chr19:45294476 | T | G | 2 | a0001c0001t0023g0022 a0001c0001t0033g0023 |
2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1598+24T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294476 | |||||||
| chr19:45294734 | A | C | 3 | a0001c0001t0008g0251 a0001c0001t0009g0243 a0001c0001t0009g0250 |
3 | HG00280.hp2 HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1598+282A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294734 | |||||||
| chr19:45294834 | G | A | 38 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(35): Show |
38 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1598+382G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294834 | |||||||
| chr19:45294937 | C | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(74): Show |
77 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1598+485C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294937 | |||||||
| chr19:45295120 | C | T | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1598+668C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295120 | |||||||
| chr19:45295121 | A | G | 164 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(161): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1598+669A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295121 | |||||||
| chr19:45295134 | A | T | 32 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(29): Show |
32 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1598+682A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295134 | |||||||
| chr19:45295194 | CA | C | 12 | a0001c0001t0001g0258 a0001c0001t0010g0169 a0001c0001t0019g0239 others(9): Show |
12 | HG01074.hp1 HG01168.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1598+757delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr19 | 45295194 | ||||||
| chr19:45295227 | T | C | 164 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(161): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1598+775T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295227 | |||||||
| chr19:45295375 | G | A | 2 | a0001c0001t0004g0203 a0001c0001t0006g0174 |
2 | HG03209.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1598+923G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295375 | |||||||
| chr19:45295407 | C | T | 38 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(35): Show |
38 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1598+955C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295407 | |||||||
| chr19:45295438 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1598+986G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295438 | |||||||
| chr19:45295441 | C | T | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1598+989C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295441 | |||||||
| chr19:45295442 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1598+990G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295442 | |||||||
| chr19:45295496 | C | G | 3 | a0001c0001t0034g0012 a0001c0001t0035g0161 a0001c0001t0038g0127 |
3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1598+1044C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295496 | |||||||
| chr19:45295541 | G | A | 38 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(35): Show |
38 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1598+1089G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295541 | |||||||
| chr19:45295715 | G | A | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1598+1263G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295715 | |||||||
| chr19:45295773 | C | T | 20 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0004g0208 others(17): Show |
20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1598+1321C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295773 | |||||||
| chr19:45295820 | A | G | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1598+1368A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295820 | |||||||
| chr19:45296023 | C | G | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1598+1571C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296023 | |||||||
| chr19:45296051 | A | C | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1598+1599A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296051 | |||||||
| chr19:45296184 | T | C | 166 | a0001c0001t0001g0093 a0001c0001t0002g0001 a0001c0001t0002g0034 others(163): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1599-1492T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296184 | |||||||
| chr19:45296435 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1599-1241T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296435 | |||||||
| chr19:45296446 | G | C | 165 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(162): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1599-1230G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296446 | |||||||
| chr19:45296494 | C | T | 6 | a0001c0001t0011g0002 a0001c0001t0011g0033 a0001c0001t0011g0048 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1599-1182C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296494 | |||||||
| chr19:45296534 | C | T | 3 | a0001c0001t0034g0012 a0001c0001t0035g0161 a0001c0001t0038g0127 |
3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1599-1142C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296534 | |||||||
| chr19:45296565 | C | T | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1599-1111C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296565 | |||||||
| chr19:45296652 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0137 |
2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1599-1024C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296652 | |||||||
| chr19:45296717 | G | C | 145 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(142): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1599-959G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296717 | |||||||
| chr19:45296776 | G | A | 1 | a0001c0001t0005g0057 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1599-900G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296776 | |||||||
| chr19:45296832 | C | T | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1599-844C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296832 | |||||||
| chr19:45297048 | C | CA | 91 | a0001c0001t0001g0028 a0001c0001t0001g0194 a0001c0001t0002g0001 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1599-608dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr19 | 45297048 | ||||||
| chr19:45297048 | CA | C | 10 | a0001c0001t0003g0149 a0001c0001t0007g0041 a0001c0001t0007g0135 others(7): Show |
10 | HG01074.hp1 HG01516.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1599-608delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr19 | 45297048 | ||||||
| chr19:45297133 | G | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0071 a0001c0001t0005g0073 others(1): Show |
4 | HG00323.hp2 HG01167.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599-543G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297133 | |||||||
| chr19:45297181 | G | A | 2 | a0001c0001t0006g0003 a0001c0001t0006g0004 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1599-495G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297181 | |||||||
| chr19:45297327 | T | G | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1599-349T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297327 | |||||||
| chr19:45297438 | C | T | 19 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0007 others(16): Show |
19 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1599-238C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297438 | |||||||
| chr19:45297965 | C | A | 4 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1877+11C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45297965 | |||||||
| chr19:45298074 | C | G | 1 | a0001c0001t0005g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+120C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298074 | |||||||
| chr19:45298076 | C | T | 1 | a0001c0001t0005g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+122C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298076 | |||||||
| chr19:45298077 | G | T | 1 | a0001c0001t0005g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+123G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298077 | |||||||
| chr19:45298078 | T | C | 1 | a0001c0001t0005g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+124T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298078 | |||||||
| chr19:45298079 | T | C | 1 | a0001c0001t0005g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+125T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298079 | |||||||
| chr19:45298079 | T | TTCC | 31 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(28): Show |
31 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1877+142_1877+144d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45298079 | ||||||
| chr19:45298179 | C | T | 1 | a0001c0010t0001g0150 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1877+225C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298179 | |||||||
| chr19:45298292 | G | A | 1 | a0001c0001t0011g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1877+338G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298292 | |||||||
| chr19:45298321 | GGGTCTGT others(4): Show |
G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(105): Show |
108 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1877+370_1877+380d others(13): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45298321 | ||||||
| chr19:45298376 | G | A | 1 | a0001c0001t0003g0091 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1877+422G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298376 | |||||||
| chr19:45298470 | G | T | 20 | a0001c0001t0008g0068 a0001c0001t0008g0085 a0001c0001t0008g0113 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1877+516G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298470 | |||||||
| chr19:45298527 | G | A | 1 | a0001c0001t0004g0118 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1877+573G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298527 | |||||||
| chr19:45298651 | G | A | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1877+697G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298651 | |||||||
| chr19:45298693 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(67): Show |
70 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1877+739C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298693 | |||||||
| chr19:45298764 | C | T | 34 | a0001c0001t0002g0077 a0001c0001t0002g0186 a0001c0001t0002g0204 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877+810C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298764 | |||||||
| chr19:45298891 | C | T | 1 | a0001c0001t0007g0072 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1878-920C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298891 | |||||||
| chr19:45298920 | T | C | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1878-891T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298920 | |||||||
| chr19:45299000 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1878-811C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299000 | |||||||
| chr19:45299041 | G | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0088 a0001c0001t0001g0133 others(1): Show |
4 | HG00408.hp1 HG00609.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878-770G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299041 | |||||||
| chr19:45299064 | T | TA | 6 | a0001c0001t0001g0066 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG00323.hp1 HG00408.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1878-721dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | ||||||
| chr19:45299064 | TA | T | 31 | a0001c0001t0001g0028 a0001c0001t0001g0070 a0001c0001t0001g0080 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1878-721delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | ||||||
| chr19:45299064 | TAA | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(93): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1878-722_1878-721d others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | ||||||
| chr19:45299064 | TAAA | T | 11 | a0001c0001t0002g0196 a0001c0001t0002g0201 a0001c0001t0002g0213 others(8): Show |
11 | HG02896.hp1 HG02896.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1878-723_1878-721d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | ||||||
| chr19:45299064 | TAAAAA | T | 5 | a0001c0001t0019g0175 a0001c0001t0020g0191 a0001c0001t0020g0192 others(2): Show |
5 | HG02647.hp2 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1878-725_1878-721d others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | ||||||
| chr19:45299064 | TAAAAAAA others(2): Show |
T | 29 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0043 others(26): Show |
29 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1878-729_1878-721d others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | ||||||
| chr19:45299064 | TAAAAAAA others(3): Show |
T | 3 | a0001c0001t0005g0040 a0001c0001t0005g0056 a0001c0001t0007g0072 |
3 | HG01109.hp2 HG02129.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1878-730_1878-721d others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | ||||||
| chr19:45299152 | G | C | 9 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0011g0002 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1878-659G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299152 | |||||||
| chr19:45299296 | C | T | 1 | a0001c0001t0005g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1878-515C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299296 | |||||||
| chr19:45299333 | A | G | 7 | a0001c0002t0012g0014 a0001c0002t0012g0015 a0001c0002t0012g0017 others(4): Show |
7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1878-478A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299333 | |||||||
| chr19:45299380 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0194 a0001c0001t0003g0215 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1878-431C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299380 | |||||||
| chr19:45299407 | T | A | 9 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0011g0002 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1878-404T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299407 | |||||||
| chr19:45299562 | T | A | 2 | a0001c0003t0002g0206 a0001c0003t0004g0211 |
2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1878-249T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299562 | |||||||
| chr19:45299605 | A | G | 32 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(29): Show |
32 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1878-206A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299605 | |||||||
| chr19:45299750 | G | A | 21 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0004g0208 others(18): Show |
21 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1878-61G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299750 | |||||||
| chr19:45300273 | A | G | 1 | a0001c0010t0001g0150 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1922+418A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300273 | |||||||
| chr19:45300344 | G | GAAA | 42 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0080 others(39): Show |
42 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.1922+513_1922+515d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAA | 46 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0088 others(43): Show |
46 | HG00099.hp1 HG00140.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.1922+512_1922+515d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAA | 8 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0121 others(5): Show |
8 | HG00408.hp2 HG00735.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1922+511_1922+515d others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAA | 6 | a0001c0001t0001g0143 a0001c0001t0003g0076 a0001c0001t0004g0237 others(3): Show |
6 | HG01361.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1922+510_1922+515d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA | 11 | a0001c0001t0002g0236 a0001c0001t0002g0238 a0001c0001t0004g0208 others(8): Show |
11 | HG00738.hp1 HG01169.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1922+509_1922+515d others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA others(1): Show |
17 | a0001c0001t0005g0038 a0001c0001t0005g0040 a0001c0001t0005g0047 others(14): Show |
17 | HG00735.hp2 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1922+508_1922+515d others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA others(2): Show |
15 | a0001c0001t0004g0234 a0001c0001t0005g0029 a0001c0001t0005g0043 others(12): Show |
15 | HG00323.hp2 HG01109.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1922+507_1922+515d others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA others(3): Show |
8 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0054 others(5): Show |
8 | HG00609.hp2 HG00738.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1922+506_1922+515d others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA others(4): Show |
2 | a0001c0001t0035g0161 a0001c0001t0038g0127 |
2 | HG01099.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1922+505_1922+515d others(13): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA others(5): Show |
5 | a0001c0001t0002g0209 a0001c0001t0002g0217 a0001c0001t0004g0203 others(2): Show |
5 | HG02129.hp1 NA18942.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1922+504_1922+515d others(14): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA others(6): Show |
3 | a0001c0001t0002g0179 a0001c0001t0002g0213 a0001c0001t0017g0229 |
3 | HG00280.hp1 HG02074.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1922+503_1922+515d others(15): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | G | GAAAAAAA others(7): Show |
1 | a0001c0001t0017g0228 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1922+502_1922+515d others(16): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | GAAAA | G | 5 | a0001c0001t0002g0222 a0001c0001t0004g0103 a0001c0001t0004g0180 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1922+512_1922+515d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | GAAAAA | G | 62 | a0001c0001t0002g0034 a0001c0001t0002g0061 a0001c0001t0002g0064 others(59): Show |
62 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1922+511_1922+515d others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | GAAAAAA | G | 9 | a0001c0001t0004g0147 a0001c0001t0020g0192 a0001c0002t0012g0014 others(6): Show |
9 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1922+510_1922+515d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300344 | GAAAAAAA others(6): Show |
G | 9 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0011g0002 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1922+503_1922+515d others(15): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | ||||||
| chr19:45300621 | A | C | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1922+766A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300621 | |||||||
| chr19:45300751 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0004g0103 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1922+896A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300751 | |||||||
| chr19:45300865 | C | T | 2 | a0001c0003t0002g0206 a0001c0003t0004g0211 |
2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1922+1010C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300865 | |||||||
| chr19:45301049 | T | A | 167 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(164): Show |
167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1922+1194T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301049 | |||||||
| chr19:45301106 | A | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(67): Show |
70 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1922+1251A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301106 | |||||||
| chr19:45301424 | C | G | 2 | a0001c0001t0002g0001 a0001c0001t0004g0001 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1923-950C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301424 | |||||||
| chr19:45301557 | C | CA | 48 | a0001c0001t0001g0102 a0001c0001t0001g0122 a0001c0001t0001g0142 others(45): Show |
48 | HG00099.hp2 HG00738.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1923-795dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | ||||||
| chr19:45301557 | C | CAA | 41 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0064 others(38): Show |
41 | HG00280.hp1 HG00642.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1923-796_1923-795d others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | ||||||
| chr19:45301557 | C | CAAA | 31 | a0001c0001t0002g0164 a0001c0001t0002g0177 a0001c0001t0002g0193 others(28): Show |
31 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1923-797_1923-795d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | ||||||
| chr19:45301557 | C | CAAAA | 9 | a0001c0001t0008g0085 a0001c0001t0008g0251 a0001c0001t0009g0243 others(6): Show |
9 | HG00280.hp2 HG01257.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1923-798_1923-795d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | ||||||
| chr19:45301557 | C | CAAAAAA | 28 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0043 others(25): Show |
28 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1923-800_1923-795d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | ||||||
| chr19:45301557 | C | CAAAAAAA | 6 | a0001c0001t0005g0040 a0001c0001t0005g0045 a0001c0001t0005g0057 others(3): Show |
6 | HG02572.hp1 HG03654.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1923-801_1923-795d others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | ||||||
| chr19:45301634 | G | A | 1 | a0001c0001t0004g0214 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1923-740G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301634 | |||||||
| chr19:45301676 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1923-698C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301676 | |||||||
| chr19:45301692 | C | T | 10 | a0001c0001t0002g0179 a0001c0001t0002g0209 a0001c0001t0002g0213 others(7): Show |
10 | HG01099.hp1 HG02074.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1923-682C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301692 | |||||||
| chr19:45301749 | C | G | 3 | a0001c0001t0006g0167 a0001c0001t0006g0173 a0001c0001t0010g0172 |
3 | HG01433.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1923-625C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301749 | |||||||
| chr19:45301779 | C | T | 34 | a0001c0001t0005g0029 a0001c0001t0005g0038 a0001c0001t0005g0040 others(31): Show |
34 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1923-595C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301779 | |||||||
| chr19:45301790 | A | C | 2 | a0001c0001t0017g0228 a0001c0001t0017g0229 |
2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1923-584A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301790 | |||||||
| chr19:45301859 | C | A | 1 | a0001c0001t0002g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1923-515C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301859 | |||||||
| chr19:45301861 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1923-513G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301861 | |||||||
| chr19:45301865 | CA | C | 80 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1923-492delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301865 | ||||||
| chr19:45301865 | CAA | C | 84 | a0001c0001t0002g0179 a0001c0001t0002g0209 a0001c0001t0002g0213 others(81): Show |
84 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1923-493_1923-492d others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301865 | ||||||
| chr19:45301889 | G | A | 167 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0061 others(164): Show |
167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1923-485G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301889 | |||||||
| chr19:45301908 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1923-466C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301908 | |||||||
| chr19:45302290 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0011g0002 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1923-84C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45302290 |