Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2355 |
| ensemblid | ENSG00000075426.12 |
| hgncid | 3798 |
| symbol | FOSL2 |
| name | FOS like 2, AP-1 transcription factor subunit |
| refseq_nuc | NM_005253.4 |
| refseq_prot | NP_005244.1 |
| ensembl_nuc | ENST00000264716.9 |
| ensembl_prot | ENSP00000264716.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 28392858 |
| end | 28417317 |
| strand | + |
| ver | v1.2 |
| region | chr2:28392858-28417317 |
| region5000 | chr2:28387858-28422317 |
| regionname0 | FOSL2_chr2_28392858_28417317 |
| regionname5000 | FOSL2_chr2_28387858_28422317 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 326 | 360 | 82 | 76 | 148 | 10 | 42 | 116 | FOSL2_chr2_28387858_28422317 | FOSL2 | MYQDY others(321): Show |
chr2 | 28387858 | 28422317 |
| a0002 | 0/0 | 326 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | MYQDY others(321): Show |
chr2 | 28387858 | 28422317 |
| a0003 | 0/0 | 326 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | MYQDY others(321): Show |
chr2 | 28387858 | 28422317 |
| a0004 | 0/0 | 326 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | MYQDY others(321): Show |
chr2 | 28387858 | 28422317 |
| a0005 | 0/0 | 113 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | MYQDY others(108): Show |
chr2 | 28387858 | 28422317 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 978 | 356 | 79 | 76 | 147 | 10 | 42 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(973): Show |
chr2 | 28387858 | 28422317 | ||
| a0001c0002 | 0/0 | 978 | 2 | 2 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(973): Show |
chr2 | 28387858 | 28422317 | ||
| a0001c0004 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(973): Show |
chr2 | 28387858 | 28422317 | ||
| a0001c0005 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(973): Show |
chr2 | 28387858 | 28422317 | ||
| a0002c0008 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(973): Show |
chr2 | 28387858 | 28422317 | ||
| a0003c0006 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(973): Show |
chr2 | 28387858 | 28422317 | ||
| a0004c0007 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(973): Show |
chr2 | 28387858 | 28422317 | ||
| a0005c0003 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | ATGTA others(1018): Show |
chr2 | 28387858 | 28422317 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6711 | 121 | 9 | 37 | 58 | 3 | 14 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0002 | 0/0 | 6712 | 62 | 6 | 16 | 18 | 6 | 16 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0003 | 0/0 | 6712 | 22 | 0 | 0 | 18 | 1 | 3 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0004 | 0/0 | 6712 | 14 | 1 | 0 | 13 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0005 | 0/0 | 6711 | 11 | 11 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0006 | 0/0 | 6711 | 10 | 1 | 0 | 7 | 0 | 2 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0007 | 0/0 | 6711 | 9 | 3 | 1 | 2 | 0 | 3 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0008 | 0/0 | 6710 | 7 | 0 | 2 | 3 | 0 | 2 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6705): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0009 | 0/0 | 6712 | 6 | 4 | 2 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0010 | 0/0 | 6712 | 6 | 6 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0011 | 0/0 | 6712 | 5 | 5 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0012 | 0/0 | 6712 | 5 | 0 | 0 | 5 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0013 | 0/0 | 6711 | 5 | 4 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0014 | 0/0 | 6710 | 4 | 0 | 2 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6705): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0015 | 0/0 | 6712 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0016 | 0/0 | 6711 | 3 | 0 | 1 | 1 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0017 | 0/0 | 6712 | 3 | 0 | 0 | 3 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0018 | 0/0 | 6711 | 3 | 1 | 0 | 1 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0019 | 0/0 | 6712 | 2 | 0 | 0 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0020 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0021 | 0/0 | 6712 | 2 | 1 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0022 | 0/0 | 6712 | 2 | 2 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0023 | 0/0 | 6711 | 2 | 1 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0024 | 0/1 | 6713 | 2 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6708): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0025 | 0/0 | 6711 | 2 | 1 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0026 | 0/0 | 6712 | 2 | 2 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0027 | 0/0 | 6712 | 2 | 2 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0028 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0029 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0030 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0031 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0032 | 0/0 | 6710 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6705): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0033 | 0/0 | 6710 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6705): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0034 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0035 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0036 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0037 | 0/0 | 6713 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6708): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0038 | 0/0 | 6712 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0039 | 0/0 | 6712 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0040 | 0/0 | 6712 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0041 | 0/0 | 6712 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0042 | 0/0 | 6710 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6705): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0043 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0044 | 0/0 | 6713 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6708): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0045 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0046 | 0/0 | 6713 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6708): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0047 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0048 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0049 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0050 | 0/0 | 6713 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6708): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0051 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0052 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0053 | 0/0 | 6711 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0054 | 0/0 | 6712 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0055 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0056 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0057 | 0/0 | 6712 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0058 | 0/0 | 6711 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0059 | 0/0 | 6711 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0060 | 1/0 | 6713 | 1 | 0 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6708): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0061 | 0/0 | 6711 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0062 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0064 | 0/0 | 6710 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6705): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0065 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0066 | 0/0 | 6712 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0067 | 0/0 | 6712 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0068 | 0/0 | 6711 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0069 | 0/0 | 6711 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0001t0070 | 0/0 | 6711 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0002t0015 | 0/0 | 6712 | 2 | 2 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0001c0004t0063 | 0/0 | 6711 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6706): Show |
chr2 | 28387858 | 28422317 |
| a0001c0005t0002 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0002c0008t0020 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0003c0006t0002 | 0/0 | 6712 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0004c0007t0002 | 0/0 | 6712 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6707): Show |
chr2 | 28387858 | 28422317 |
| a0005c0003t0001 | 0/0 | 6756 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | GTAGT others(6751): Show |
chr2 | 28387858 | 28422317 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0001 | 0/0 | 9 | 0 | 3 | 1 | 2 | 3 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0004g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0004g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0007g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0008g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0009g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0009g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0011g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0012g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0012g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0013g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0014g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0014g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0014g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0014g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0015g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0016g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0016g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0017g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0017g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0018g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0018g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0019g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0019g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0020g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0021g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0021g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0022g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0022g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0023g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0023g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0024g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0024g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0025g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0025g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0026g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0026g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0027g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0028g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0029g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0030g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0031g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0032g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0033g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0034g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0035g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0036g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0037g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0038g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0039g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0040g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0042g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0043g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0044g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0045g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0046g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0047g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0048g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0049g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0050g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0051g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0052g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0053g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0054g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0055g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0056g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0057g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0058g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0059g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0060g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0061g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0062g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0064g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0065g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0066g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0067g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0068g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0069g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0001t0070g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0002t0015g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0004t0063g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0001c0005t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0002c0008t0020g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0003c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0004c0007t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| a0005c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | GBR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | FIN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00597 | hp1 | a0001 | c0001 | t0067 | g0097 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00597 | hp2 | a0001 | c0001 | t0008 | g0032 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00609 | hp1 | a0001 | c0001 | t0030 | g0140 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00639 | hp2 | a0001 | c0001 | t0059 | g0002 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00735 | hp2 | a0001 | c0001 | t0070 | g0085 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00738 | hp2 | a0001 | c0001 | t0013 | g0009 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01069 | hp1 | a0001 | c0001 | t0042 | g0001 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01109 | hp1 | a0001 | c0001 | t0054 | g0061 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01109 | hp2 | a0001 | c0001 | t0039 | g0160 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01167 | hp1 | a0001 | c0001 | t0025 | g0011 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01167 | hp2 | a0001 | c0001 | t0057 | g0131 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0004 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01168 | hp2 | a0001 | c0001 | t0016 | g0026 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0011 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01192 | hp1 | a0001 | c0001 | t0041 | g0001 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01243 | hp1 | a0001 | c0001 | t0069 | g0104 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0019 | AMR | PUR | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01256 | hp2 | a0001 | c0001 | t0014 | g0012 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01257 | hp2 | a0001 | c0001 | t0014 | g0007 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01346 | hp1 | a0001 | c0001 | t0021 | g0202 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01496 | hp2 | a0001 | c0001 | t0053 | g0063 | AMR | CLM | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01884 | hp1 | a0001 | c0001 | t0027 | g0004 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01884 | hp2 | a0001 | c0001 | t0036 | g0042 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0122 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01891 | hp2 | a0001 | c0001 | t0020 | g0060 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01934 | hp1 | a0001 | c0001 | t0068 | g0107 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0077 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02004 | hp2 | a0001 | c0001 | t0061 | g0138 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0108 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02055 | hp1 | a0001 | c0001 | t0051 | g0189 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02055 | hp2 | a0001 | c0001 | t0031 | g0237 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02056 | hp1 | a0001 | c0001 | t0007 | g0178 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02074 | hp2 | a0001 | c0001 | t0018 | g0125 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02083 | hp1 | a0001 | c0001 | t0023 | g0169 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02155 | hp2 | a0001 | c0001 | t0062 | g0084 | EAS | CDX | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CDX | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | CDX | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02257 | hp1 | a0001 | c0001 | t0050 | g0019 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02257 | hp2 | a0001 | c0001 | t0027 | g0004 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02258 | hp1 | a0001 | c0001 | t0048 | g0144 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02280 | hp2 | a0002 | c0008 | t0020 | g0059 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02300 | hp2 | a0001 | c0001 | t0015 | g0124 | AMR | PEL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02451 | hp1 | a0001 | c0001 | t0055 | g0207 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02451 | hp2 | a0001 | c0001 | t0025 | g0145 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02615 | hp2 | a0001 | c0005 | t0002 | g0174 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02622 | hp2 | a0001 | c0001 | t0049 | g0188 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02630 | hp1 | a0001 | c0001 | t0056 | g0004 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02630 | hp2 | a0001 | c0001 | t0058 | g0170 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02647 | hp1 | a0001 | c0001 | t0023 | g0176 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0175 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0010 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0045 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02809 | hp2 | a0001 | c0001 | t0037 | g0233 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02895 | hp1 | a0001 | c0001 | t0033 | g0041 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02895 | hp2 | a0001 | c0001 | t0052 | g0055 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0192 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02965 | hp1 | a0003 | c0006 | t0002 | g0042 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02970 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02970 | hp2 | a0001 | c0002 | t0015 | g0029 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02976 | hp2 | a0001 | c0001 | t0022 | g0187 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0149 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0065 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03139 | hp1 | a0001 | c0001 | t0018 | g0217 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03195 | hp2 | a0001 | c0001 | t0032 | g0046 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03209 | hp1 | a0001 | c0001 | t0026 | g0054 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03225 | hp1 | a0001 | c0001 | t0029 | g0062 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03225 | hp2 | a0001 | c0001 | t0034 | g0008 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0010 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03490 | hp1 | a0001 | c0001 | t0016 | g0162 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0003 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03516 | hp1 | a0001 | c0001 | t0047 | g0045 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | ESN | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0030 | AFR | GWD | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0018 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0018 | SAS | BEB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0219 | SAS | BEB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0078 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0018 | SAS | STU | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18522 | hp1 | a0001 | c0001 | t0026 | g0053 | AFR | YRI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0195 | AFR | YRI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | CHB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | YRI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | YRI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18939 | hp1 | a0001 | c0001 | t0066 | g0036 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18942 | hp2 | a0001 | c0001 | t0045 | g0043 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18944 | hp2 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18947 | hp1 | a0001 | c0001 | t0014 | g0099 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18950 | hp2 | a0001 | c0001 | t0019 | g0225 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18952 | hp1 | a0001 | c0001 | t0038 | g0165 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18953 | hp2 | a0001 | c0001 | t0046 | g0043 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18954 | hp1 | a0001 | c0001 | t0028 | g0049 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18959 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18960 | hp1 | a0001 | c0001 | t0043 | g0184 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18961 | hp1 | a0001 | c0001 | t0064 | g0117 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18961 | hp2 | a0001 | c0001 | t0014 | g0032 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18962 | hp1 | a0001 | c0001 | t0008 | g0211 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18967 | hp2 | a0001 | c0001 | t0024 | g0232 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18969 | hp1 | a0001 | c0001 | t0012 | g0051 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18971 | hp2 | a0001 | c0001 | t0012 | g0179 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18973 | hp2 | a0001 | c0001 | t0065 | g0002 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18978 | hp2 | a0001 | c0001 | t0017 | g0230 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19003 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19005 | hp2 | a0001 | c0001 | t0019 | g0049 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19010 | hp1 | a0004 | c0007 | t0002 | g0155 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19043 | hp1 | a0001 | c0001 | t0021 | g0201 | AFR | LWK | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0030 | AFR | LWK | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19056 | hp2 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19063 | hp1 | a0001 | c0001 | t0016 | g0040 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19066 | hp1 | a0001 | c0001 | t0040 | g0001 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19072 | hp2 | a0005 | c0003 | t0001 | g0110 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19081 | hp1 | a0001 | c0004 | t0063 | g0166 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19090 | hp1 | a0001 | c0001 | t0017 | g0172 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | TSI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0135 | EUR | TSI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20905 | hp1 | a0001 | c0001 | t0018 | g0143 | SAS | GIH | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | GIH | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02486 | hp1 | a0001 | c0001 | t0044 | g0194 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0209 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG02559 | hp2 | a0001 | c0002 | t0015 | g0029 | AFR | ACB | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | USA | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0058 | AFR | USA | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | USA | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| NA20300 | hp2 | a0001 | c0001 | t0035 | g0046 | AFR | USA | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0024 | g0126 | REF | REF | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0060 | g0004 | REF | REF | FOSL2_chr2_28387858_28422317 | FOSL2 | chr2 | 28387858 | 28422317 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28393802 | A | G | 1 | a0002 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.82A>G | p.Ser28Gly | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 945/6713 | 82/981 | 28/326 | chr2 | 28393802 | |||
| chr2:28404112 | C | CAGGTGCT others(38): Show |
1 | a0005 | 1 | NA19072.hp2 | conservative_inframe_insertion | MODERATE | c.108_109insAGGTGCTC others(37): Show |
p.Arg37_Val38insCysS others(41): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 972/6713 | 109/981 | 37/326 | chr2 | 28404112 | |||
| chr2:28404113 | C | T | 1 | a0005 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.109C>T | p.Arg37Trp | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 972/6713 | 109/981 | 37/326 | chr2 | 28404113 | |||
| chr2:28404156 | T | G | 1 | a0005 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.152T>G | p.Ile51Ser | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1015/6713 | 152/981 | 51/326 | chr2 | 28404156 | |||
| chr2:28404173 | A | T | 1 | a0005 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.169A>T | p.Ser57Cys | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1032/6713 | 169/981 | 57/326 | chr2 | 28404173 | |||
| chr2:28404194 | G | C | 1 | a0005 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.190G>C | p.Val64Leu | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1053/6713 | 190/981 | 64/326 | chr2 | 28404194 | |||
| chr2:28404195 | T | A | 1 | a0005 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.191T>A | p.Val64Glu | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1054/6713 | 191/981 | 64/326 | chr2 | 28404195 | |||
| chr2:28404299 | A | T | 1 | a0005 | 1 | NA19072.hp2 | stop_gained | HIGH | c.295A>T | p.Arg99* | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1158/6713 | 295/981 | 99/326 | chr2 | 28404299 | |||
| chr2:28404332 | G | A | 1 | a0003 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.328G>A | p.Val110Met | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1191/6713 | 328/981 | 110/326 | chr2 | 28404332 | |||
| chr2:28408789 | A | T | 1 | a0005 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.385A>T | p.Ile129Phe | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/4 | 1248/6713 | 385/981 | 129/326 | chr2 | 28408789 | |||
| chr2:28412060 | G | A | 1 | a0004 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.593G>A | p.Arg198His | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1456/6713 | 593/981 | 198/326 | chr2 | 28412060 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28404169 | G | C | 1 | a0001c0004 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.165G>C | p.Thr55Thr | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1028/6713 | 165/981 | 55/326 | chr2 | 28404169 | |||
| chr2:28404262 | G | A | 1 | a0001c0005 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.258G>A | p.Pro86Pro | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/4 | 1121/6713 | 258/981 | 86/326 | chr2 | 28404262 | |||
| chr2:28412334 | G | A | 1 | a0001c0002 | 2 | HG02559.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.867G>A | p.Glu289Glu | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1730/6713 | 867/981 | 289/326 | chr2 | 28412334 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28392945 | G | GGA | 11 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(8): Show |
21 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-756_-755dupAG | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 754 | INFO_REALIGN_3_PRIME | chr2 | 28392945 | |||||
| chr2:28392945 | GGAGA | G | 4 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0053 others(1): Show |
8 | HG00738.hp2 HG01109.hp1 HG01496.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-758_-755delAGAG | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 755 | INFO_REALIGN_3_PRIME | chr2 | 28392945 | |||||
| chr2:28392945 | GGAGAGA | G | 4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(1): Show |
11 | HG01934.hp2 HG02040.hp2 HG02886.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-760_-755delAGAGAG | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 755 | INFO_REALIGN_3_PRIME | chr2 | 28392945 | |||||
| chr2:28393012 | C | G | 1 | a0001c0001t0070 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-709C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 709 | chr2 | 28393012 | ||||||
| chr2:28393013 | G | A | 2 | a0001c0001t0019 a0001c0001t0028 |
3 | NA18950.hp2 NA18954.hp1 NA19005.hp2 |
5_prime_UTR_variant | MODIFIER | c.-708G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 708 | chr2 | 28393013 | ||||||
| chr2:28393227 | A | G | 1 | a0001c0001t0069 | 1 | HG01243.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-494A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | chr2 | 28393227 | |||||||
| chr2:28393419 | G | C | 1 | a0001c0001t0029 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-302G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 302 | chr2 | 28393419 | ||||||
| chr2:28393681 | G | A | 1 | a0001c0001t0030 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/4 | 40 | chr2 | 28393681 | ||||||
| chr2:28412873 | T | C | 49 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(46): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*425T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 425 | chr2 | 28412873 | ||||||
| chr2:28412915 | A | G | 2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG01109.hp1 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*467A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 467 | chr2 | 28412915 | ||||||
| chr2:28413261 | G | T | 10 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0025 others(7): Show |
22 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*813G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 813 | chr2 | 28413261 | ||||||
| chr2:28413326 | G | A | 1 | a0001c0001t0031 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 878 | chr2 | 28413326 | ||||||
| chr2:28413777 | A | G | 27 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0015 others(24): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1329A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1329 | chr2 | 28413777 | ||||||
| chr2:28413811 | C | T | 1 | a0001c0001t0028 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1363C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1363 | chr2 | 28413811 | ||||||
| chr2:28413820 | T | C | 1 | a0001c0001t0055 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1372T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1372 | chr2 | 28413820 | ||||||
| chr2:28413873 | A | G | 34 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(31): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1425A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1425 | chr2 | 28413873 | ||||||
| chr2:28413903 | C | G | 1 | a0001c0004t0063 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1455C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1455 | chr2 | 28413903 | ||||||
| chr2:28414152 | G | A | 1 | a0001c0001t0040 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1704G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1704 | chr2 | 28414152 | ||||||
| chr2:28414307 | G | T | 3 | a0001c0001t0012 a0001c0001t0045 a0001c0001t0046 |
7 | NA18942.hp2 NA18944.hp2 NA18953.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1859G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 1859 | chr2 | 28414307 | ||||||
| chr2:28414449 | A | G | 1 | a0001c0001t0067 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2001A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 2001 | chr2 | 28414449 | ||||||
| chr2:28414490 | T | C | 1 | a0001c0001t0053 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2042T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 2042 | chr2 | 28414490 | ||||||
| chr2:28415202 | C | T | 1 | a0001c0001t0062 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2754C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 2754 | chr2 | 28415202 | ||||||
| chr2:28415217 | G | A | 1 | a0001c0001t0022 | 2 | HG02976.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2769G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 2769 | chr2 | 28415217 | ||||||
| chr2:28415275 | C | T | 1 | a0001c0001t0061 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2827C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 2827 | chr2 | 28415275 | ||||||
| chr2:28415491 | G | C | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(70): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
3_prime_UTR_variant | MODIFIER | c.*3043G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 3043 | chr2 | 28415491 | ||||||
| chr2:28415591 | G | C | 1 | a0001c0001t0041 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3143G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 3143 | chr2 | 28415591 | ||||||
| chr2:28415731 | A | G | 1 | a0001c0001t0058 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3283A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 3283 | chr2 | 28415731 | ||||||
| chr2:28416106 | A | G | 2 | a0001c0001t0017 a0001c0001t0040 |
4 | NA18978.hp2 NA19003.hp2 NA19066.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3658A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 3658 | chr2 | 28416106 | ||||||
| chr2:28416217 | C | T | 1 | a0001c0001t0050 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3769C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 3769 | chr2 | 28416217 | ||||||
| chr2:28416444 | C | T | 1 | a0001c0001t0010 | 6 | HG02723.hp1 HG02886.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3996C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 3996 | chr2 | 28416444 | ||||||
| chr2:28416455 | T | C | 1 | a0001c0001t0053 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4007T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4007 | chr2 | 28416455 | ||||||
| chr2:28416463 | C | T | 1 | a0001c0001t0039 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4015C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4015 | chr2 | 28416463 | ||||||
| chr2:28416464 | CT | C | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(28): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*4033delT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4033 | INFO_REALIGN_3_PRIME | chr2 | 28416464 | |||||
| chr2:28416464 | CTT | C | 39 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(36): Show |
209 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*4032_*4033delTT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4032 | INFO_REALIGN_3_PRIME | chr2 | 28416464 | |||||
| chr2:28416464 | CTTT | C | 4 | a0001c0001t0014 a0001c0001t0025 a0001c0001t0032 others(1): Show |
8 | HG01167.hp1 HG01256.hp2 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4031_*4033delTTT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4031 | INFO_REALIGN_3_PRIME | chr2 | 28416464 | |||||
| chr2:28416687 | A | G | 1 | a0001c0001t0011 | 5 | HG02559.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4239A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4239 | chr2 | 28416687 | ||||||
| chr2:28416774 | C | G | 27 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(24): Show |
183 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*4326C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4326 | chr2 | 28416774 | ||||||
| chr2:28416949 | C | CT | 13 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0020 others(10): Show |
23 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4522dupT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4523 | INFO_REALIGN_3_PRIME | chr2 | 28416949 | |||||
| chr2:28416949 | CT | C | 4 | a0001c0001t0008 a0001c0001t0023 a0001c0001t0033 others(1): Show |
11 | HG00597.hp2 HG01069.hp1 HG01168.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4522delT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4522 | INFO_REALIGN_3_PRIME | chr2 | 28416949 | |||||
| chr2:28417029 | C | T | 1 | a0001c0001t0013 | 5 | HG00738.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4581C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 4/4 | 4581 | chr2 | 28417029 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28394137 | GC | G | 114 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0038 others(111): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.102+328delC | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28394137 | ||||||
| chr2:28394137 | GCC | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(88): Show |
125 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.102+327_102+328del others(2): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28394137 | ||||||
| chr2:28394138 | C | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0216 others(2): Show |
12 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.102+316C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394138 | |||||||
| chr2:28394143 | C | G | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.102+321C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394143 | |||||||
| chr2:28394145 | C | A | 21 | a0001c0001t0007g0018 a0001c0001t0007g0064 a0001c0001t0009g0011 others(18): Show |
27 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.102+323C>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394145 | |||||||
| chr2:28394148 | C | G | 1 | a0001c0001t0043g0184 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.102+326C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394148 | |||||||
| chr2:28394150 | CA | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0048 others(6): Show |
10 | HG00621.hp2 HG02602.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.102+329delA | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394150 | |||||||
| chr2:28394150 | CACCCCT | C | 4 | a0001c0001t0005g0028 a0001c0001t0005g0234 a0001c0001t0005g0235 others(1): Show |
6 | HG02280.hp1 HG02622.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+329_102+334del others(6): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394150 | |||||||
| chr2:28394151 | A | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0004g0004 others(2): Show |
13 | HG00438.hp2 HG00609.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+329A>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394151 | |||||||
| chr2:28394156 | T | C | 12 | a0001c0001t0001g0198 a0001c0001t0005g0196 a0001c0001t0005g0197 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.102+334T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394156 | |||||||
| chr2:28394156 | T | G | 1 | a0001c0001t0021g0202 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.102+334T>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394156 | |||||||
| chr2:28394289 | C | A | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | HG01106.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.102+467C>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394289 | |||||||
| chr2:28394299 | A | T | 1 | a0001c0001t0018g0125 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.102+477A>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394299 | |||||||
| chr2:28394416 | T | C | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.102+594T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394416 | |||||||
| chr2:28394448 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.102+626C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394448 | |||||||
| chr2:28394473 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+651C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394473 | |||||||
| chr2:28394578 | G | T | 1 | a0001c0001t0015g0124 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.102+756G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28394578 | |||||||
| chr2:28394996 | TG | T | 44 | a0001c0001t0001g0198 a0001c0001t0005g0028 a0001c0001t0005g0196 others(41): Show |
52 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(49): Show |
intron_variant | MODIFIER | c.102+1181delG | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28394996 | ||||||
| chr2:28395065 | C | T | 9 | a0001c0001t0001g0185 a0001c0001t0002g0026 a0001c0001t0002g0044 others(6): Show |
12 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.102+1243C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395065 | |||||||
| chr2:28395208 | C | T | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0182 |
3 | HG01106.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.102+1386C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395208 | |||||||
| chr2:28395289 | C | T | 4 | a0001c0001t0010g0045 a0001c0001t0047g0045 a0001c0001t0049g0188 others(1): Show |
4 | HG02055.hp1 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1467C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395289 | |||||||
| chr2:28395294 | G | A | 88 | a0001c0001t0001g0120 a0001c0001t0001g0154 a0001c0001t0001g0185 others(85): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.102+1472G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395294 | |||||||
| chr2:28395356 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0127 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.102+1534C>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395356 | |||||||
| chr2:28395381 | T | C | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.102+1559T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395381 | |||||||
| chr2:28395408 | C | A | 4 | a0001c0001t0002g0069 a0001c0001t0002g0203 a0001c0001t0002g0204 others(1): Show |
4 | HG01074.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+1586C>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395408 | |||||||
| chr2:28395622 | C | T | 3 | a0001c0001t0021g0201 a0001c0001t0032g0046 a0001c0001t0035g0046 |
3 | HG03195.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.102+1800C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395622 | |||||||
| chr2:28395811 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.102+1989C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395811 | |||||||
| chr2:28395826 | TGGTGGTT others(5): Show |
T | 1 | a0001c0001t0001g0070 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.102+2007_102+2018d others(14): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28395826 | ||||||
| chr2:28395916 | G | A | 18 | a0001c0001t0006g0193 a0001c0001t0007g0192 a0001c0001t0009g0011 others(15): Show |
22 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.102+2094G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28395916 | |||||||
| chr2:28396221 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.102+2399C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396221 | |||||||
| chr2:28396339 | G | T | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.102+2517G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396339 | |||||||
| chr2:28396435 | C | T | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.102+2613C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396435 | |||||||
| chr2:28396473 | G | GT | 88 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0154 others(85): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.102+2657dupT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396473 | ||||||
| chr2:28396788 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.102+2966A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396788 | |||||||
| chr2:28396789 | G | GAC | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(45): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.102+3015_102+3016d others(4): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACAC | 34 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0024 others(31): Show |
47 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.102+3013_102+3016d others(6): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACAC | 23 | a0001c0001t0001g0014 a0001c0001t0001g0091 a0001c0001t0001g0093 others(20): Show |
28 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.102+3011_102+3016d others(8): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(1): Show |
10 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0002g0051 others(7): Show |
13 | HG00558.hp1 HG00597.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+3009_102+3016d others(10): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(3): Show |
21 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0038 others(18): Show |
32 | HG01074.hp2 HG01255.hp1 HG01952.hp1 others(29): Show |
intron_variant | MODIFIER | c.102+3007_102+3016d others(12): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(5): Show |
18 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0035 others(15): Show |
23 | HG00558.hp2 HG00642.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+3005_102+3016d others(14): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(7): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0111 a0001c0001t0001g0113 others(8): Show |
15 | HG02027.hp1 HG02132.hp1 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.102+3003_102+3016d others(16): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(9): Show |
6 | a0001c0001t0001g0115 a0001c0001t0001g0152 a0001c0001t0004g0016 others(3): Show |
7 | HG01192.hp2 HG02165.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+3001_102+3016d others(18): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(11): Show |
7 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0001g0221 others(4): Show |
9 | HG02027.hp2 HG02074.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.102+2999_102+3016d others(20): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(13): Show |
1 | a0001c0001t0001g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.102+2997_102+3016d others(22): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | G | GACACACA others(15): Show |
1 | a0001c0001t0064g0117 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.102+2995_102+3016d others(24): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GAC | G | 16 | a0001c0001t0001g0027 a0001c0001t0001g0185 a0001c0001t0002g0044 others(13): Show |
19 | HG00735.hp1 HG00741.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.102+3015_102+3016d others(4): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GACAC | G | 9 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0223 others(6): Show |
11 | HG00544.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+3013_102+3016d others(6): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GACACAC | G | 3 | a0001c0001t0002g0157 a0001c0001t0003g0071 a0001c0001t0013g0009 |
7 | HG00738.hp2 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+3011_102+3016d others(8): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0128 a0001c0001t0008g0032 a0001c0001t0014g0032 |
3 | HG00597.hp2 NA18961.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.102+3009_102+3016d others(10): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GACACACA others(3): Show |
G | 5 | a0001c0001t0001g0031 a0001c0001t0002g0040 a0001c0001t0002g0156 others(2): Show |
6 | HG00280.hp1 HG01099.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+3007_102+3016d others(12): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GACACACA others(5): Show |
G | 1 | a0001c0001t0001g0154 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.102+3005_102+3016d others(14): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GACACACA others(7): Show |
G | 1 | a0001c0001t0002g0222 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.102+3003_102+3016d others(16): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396789 | GACACACA others(13): Show |
G | 1 | a0001c0001t0002g0119 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.102+2997_102+3016d others(22): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396789 | ||||||
| chr2:28396801 | C | CACACACA others(9): Show |
1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.102+2994_102+2995i others(18): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396801 | ||||||
| chr2:28396805 | C | CACACACA others(7): Show |
3 | a0001c0001t0010g0045 a0001c0001t0047g0045 a0001c0001t0049g0188 |
3 | HG02622.hp2 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.102+2996_102+2997i others(16): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396805 | ||||||
| chr2:28396805 | C | CACACACA others(9): Show |
1 | a0001c0001t0051g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.102+2998_102+2999i others(18): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396805 | ||||||
| chr2:28396807 | C | CACACACA others(7): Show |
3 | a0001c0001t0021g0201 a0001c0001t0032g0046 a0001c0001t0035g0046 |
3 | HG03195.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.102+2998_102+2999i others(16): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396807 | ||||||
| chr2:28396807 | C | CACACACA others(9): Show |
2 | a0001c0001t0020g0060 a0002c0008t0020g0059 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.102+3000_102+3001i others(18): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396807 | ||||||
| chr2:28396809 | C | CACACACA others(17): Show |
1 | a0001c0001t0029g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102+3010_102+3011i others(26): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396809 | ||||||
| chr2:28396811 | C | CACACACA others(3): Show |
1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.102+2998_102+2999i others(12): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396811 | ||||||
| chr2:28396813 | C | CACACACA others(5): Show |
1 | a0001c0001t0021g0202 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.102+3002_102+3003i others(14): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396813 | ||||||
| chr2:28396813 | C | CACACACA others(15): Show |
1 | a0001c0001t0005g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.102+3012_102+3013i others(24): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396813 | ||||||
| chr2:28396813 | C | CACACACA others(17): Show |
1 | a0001c0001t0005g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.102+3014_102+3015i others(26): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396813 | ||||||
| chr2:28396813 | C | CACACACA others(19): Show |
2 | a0001c0001t0005g0197 a0001c0001t0005g0235 |
2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.102+2993_102+3018d others(28): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396813 | ||||||
| chr2:28396813 | C | CACACACA others(21): Show |
1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.102+3016_102+3017i others(30): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396813 | ||||||
| chr2:28396813 | C | CACACACA others(23): Show |
3 | a0001c0001t0005g0028 a0001c0001t0005g0199 a0001c0001t0007g0064 |
5 | HG01934.hp2 HG02622.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+3016_102+3017i others(32): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396813 | ||||||
| chr2:28396813 | C | CACACACA others(25): Show |
2 | a0001c0001t0005g0200 a0001c0001t0005g0236 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.102+3016_102+3017i others(34): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396813 | ||||||
| chr2:28396815 | C | CACACACA others(11): Show |
1 | a0001c0001t0054g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.102+3010_102+3011i others(20): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396815 | ||||||
| chr2:28396815 | C | CACACACA others(15): Show |
1 | a0001c0001t0053g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.102+3014_102+3015i others(24): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28396815 | ||||||
| chr2:28396838 | A | ACAC | 3 | a0001c0001t0006g0090 a0001c0001t0017g0230 a0001c0001t0061g0138 |
3 | HG02004.hp2 NA18940.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.102+3016_102+3017i others(5): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396838 | |||||||
| chr2:28396838 | A | ACACACAC others(4): Show |
2 | a0001c0001t0010g0057 a0001c0001t0068g0107 |
2 | HG01934.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.102+3016_102+3017i others(13): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396838 | |||||||
| chr2:28396838 | A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.102+3016_102+3017i others(17): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396838 | |||||||
| chr2:28396839 | A | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0148 a0001c0001t0003g0114 others(1): Show |
4 | HG01496.hp1 NA18947.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+3017A>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396839 | |||||||
| chr2:28396840 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102+3018A>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396840 | |||||||
| chr2:28396941 | T | A | 18 | a0001c0001t0006g0193 a0001c0001t0007g0192 a0001c0001t0009g0011 others(15): Show |
22 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.102+3119T>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28396941 | |||||||
| chr2:28397035 | T | G | 1 | a0001c0001t0062g0084 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.102+3213T>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397035 | |||||||
| chr2:28397075 | A | C | 1 | a0001c0001t0006g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.102+3253A>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397075 | |||||||
| chr2:28397221 | T | A | 130 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0154 others(127): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.102+3399T>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397221 | |||||||
| chr2:28397223 | A | T | 110 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0154 others(107): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.102+3401A>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397223 | |||||||
| chr2:28397225 | A | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0052 a0001c0001t0002g0183 |
5 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+3403A>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397225 | |||||||
| chr2:28397225 | A | T | 128 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0154 others(125): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.102+3403A>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397225 | |||||||
| chr2:28397256 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0113 |
3 | HG01978.hp2 NA18955.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.102+3434A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397256 | |||||||
| chr2:28397353 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0003g0083 a0001c0001t0003g0112 others(4): Show |
7 | HG02056.hp2 HG02132.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+3531A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397353 | |||||||
| chr2:28397405 | T | C | 2 | a0001c0001t0053g0063 a0001c0001t0054g0061 |
2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.102+3583T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28397405 | |||||||
| chr2:28398020 | G | A | 3 | a0001c0001t0002g0227 a0001c0001t0007g0178 a0001c0004t0063g0166 |
3 | HG02056.hp1 NA19057.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.102+4198G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398020 | |||||||
| chr2:28398024 | A | G | 5 | a0001c0001t0020g0060 a0001c0001t0021g0201 a0001c0001t0032g0046 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+4202A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398024 | |||||||
| chr2:28398034 | A | G | 1 | a0001c0001t0017g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.102+4212A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398034 | |||||||
| chr2:28398133 | G | T | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.102+4311G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398133 | |||||||
| chr2:28398379 | TG | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0091 a0001c0001t0001g0118 others(2): Show |
6 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+4558delG | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398379 | |||||||
| chr2:28398511 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.102+4689C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398511 | |||||||
| chr2:28398588 | G | T | 1 | a0001c0001t0048g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102+4766G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398588 | |||||||
| chr2:28398610 | C | T | 1 | a0001c0001t0053g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.102+4788C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398610 | |||||||
| chr2:28398687 | G | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0139 a0001c0001t0025g0145 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+4865G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398687 | |||||||
| chr2:28398997 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.103-5110G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28398997 | |||||||
| chr2:28399049 | A | C | 1 | a0001c0001t0029g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.103-5058A>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399049 | |||||||
| chr2:28399118 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.103-4989G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399118 | |||||||
| chr2:28399183 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.103-4924C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399183 | |||||||
| chr2:28399231 | A | G | 1 | a0001c0001t0062g0084 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.103-4876A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399231 | |||||||
| chr2:28399342 | G | T | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.103-4765G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399342 | |||||||
| chr2:28399385 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.103-4722A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399385 | |||||||
| chr2:28399425 | T | C | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.103-4682T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399425 | |||||||
| chr2:28399562 | G | A | 1 | a0001c0001t0005g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.103-4545G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399562 | |||||||
| chr2:28399678 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0005g0234 |
2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.103-4429G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399678 | |||||||
| chr2:28399781 | G | A | 3 | a0001c0001t0021g0201 a0001c0001t0032g0046 a0001c0001t0035g0046 |
3 | HG03195.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.103-4326G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399781 | |||||||
| chr2:28399836 | C | A | 15 | a0001c0001t0007g0064 a0001c0001t0009g0011 a0001c0001t0009g0019 others(12): Show |
18 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.103-4271C>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399836 | |||||||
| chr2:28399844 | T | C | 2 | a0001c0001t0053g0063 a0001c0001t0054g0061 |
2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.103-4263T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399844 | |||||||
| chr2:28399930 | A | G | 1 | a0001c0001t0037g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.103-4177A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28399930 | |||||||
| chr2:28400180 | T | C | 134 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0154 others(131): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.103-3927T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400180 | |||||||
| chr2:28400287 | C | T | 18 | a0001c0001t0006g0193 a0001c0001t0007g0192 a0001c0001t0009g0011 others(15): Show |
22 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.103-3820C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400287 | |||||||
| chr2:28400292 | G | A | 124 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0154 others(121): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-3815G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400292 | |||||||
| chr2:28400303 | C | T | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.103-3804C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400303 | |||||||
| chr2:28400338 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.103-3769G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400338 | |||||||
| chr2:28400393 | C | G | 1 | a0001c0001t0021g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103-3714C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400393 | |||||||
| chr2:28400397 | A | G | 1 | a0001c0001t0049g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.103-3710A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400397 | |||||||
| chr2:28400412 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.103-3695C>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400412 | |||||||
| chr2:28400419 | GTCTGAAT others(8): Show |
G | 111 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0154 others(108): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.103-3661_103-3647d others(17): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28400419 | ||||||
| chr2:28400621 | T | C | 4 | a0001c0001t0021g0201 a0001c0001t0029g0062 a0001c0001t0032g0046 others(1): Show |
4 | HG03195.hp2 HG03225.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-3486T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400621 | |||||||
| chr2:28400662 | C | T | 1 | a0001c0001t0003g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.103-3445C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400662 | |||||||
| chr2:28400737 | G | A | 1 | a0001c0004t0063g0166 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.103-3370G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400737 | |||||||
| chr2:28400753 | G | A | 1 | a0001c0001t0010g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-3354G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28400753 | |||||||
| chr2:28401076 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.103-3031T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401076 | |||||||
| chr2:28401115 | A | G | 130 | a0001c0001t0001g0120 a0001c0001t0001g0154 a0001c0001t0001g0185 others(127): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.103-2992A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401115 | |||||||
| chr2:28401223 | C | T | 10 | a0001c0001t0001g0198 a0001c0001t0005g0028 a0001c0001t0005g0196 others(7): Show |
12 | HG01346.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.103-2884C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401223 | |||||||
| chr2:28401238 | T | TA | 91 | a0001c0001t0001g0033 a0001c0001t0001g0115 a0001c0001t0001g0120 others(88): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.103-2854dupA | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 28401238 | ||||||
| chr2:28401253 | A | G | 17 | a0001c0001t0006g0193 a0001c0001t0007g0192 a0001c0001t0009g0011 others(14): Show |
21 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-2854A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401253 | |||||||
| chr2:28401294 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(52): Show |
80 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.103-2813C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401294 | |||||||
| chr2:28401543 | G | C | 1 | a0001c0001t0003g0083 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.103-2564G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401543 | |||||||
| chr2:28401665 | C | T | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.103-2442C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401665 | |||||||
| chr2:28401851 | C | T | 1 | a0001c0001t0007g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.103-2256C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401851 | |||||||
| chr2:28401966 | A | G | 86 | a0001c0001t0001g0120 a0001c0001t0001g0154 a0001c0001t0001g0185 others(83): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.103-2141A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28401966 | |||||||
| chr2:28402086 | C | G | 14 | a0001c0001t0009g0011 a0001c0001t0009g0019 a0001c0001t0009g0030 others(11): Show |
18 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.103-2021C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28402086 | |||||||
| chr2:28402156 | G | C | 1 | a0001c0001t0003g0206 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.103-1951G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28402156 | |||||||
| chr2:28402266 | G | C | 13 | a0001c0001t0001g0185 a0001c0001t0002g0026 a0001c0001t0002g0044 others(10): Show |
16 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.103-1841G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28402266 | |||||||
| chr2:28402385 | A | G | 1 | a0001c0001t0013g0009 | 5 | HG00738.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-1722A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28402385 | |||||||
| chr2:28402804 | A | T | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.103-1303A>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28402804 | |||||||
| chr2:28402843 | T | G | 1 | a0001c0001t0007g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.103-1264T>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28402843 | |||||||
| chr2:28402999 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.103-1108A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28402999 | |||||||
| chr2:28403227 | A | G | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0182 |
3 | HG01106.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.103-880A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28403227 | |||||||
| chr2:28403502 | C | T | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.103-605C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28403502 | |||||||
| chr2:28403658 | T | C | 1 | a0001c0001t0018g0217 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.103-449T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28403658 | |||||||
| chr2:28403781 | C | T | 2 | a0001c0001t0036g0042 a0003c0006t0002g0042 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.103-326C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28403781 | |||||||
| chr2:28403785 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0007g0192 |
3 | HG02738.hp2 HG02922.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.103-322C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28403785 | |||||||
| chr2:28403993 | G | A | 22 | a0001c0001t0001g0198 a0001c0001t0005g0028 a0001c0001t0005g0196 others(19): Show |
26 | HG01109.hp1 HG01346.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.103-114G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 1/3 | chr2 | 28403993 | |||||||
| chr2:28404426 | T | G | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+68T>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28404426 | |||||||
| chr2:28404486 | G | A | 1 | a0001c0001t0007g0178 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.354+128G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28404486 | |||||||
| chr2:28404762 | C | T | 91 | a0001c0001t0001g0154 a0001c0001t0001g0185 a0001c0001t0002g0001 others(88): Show |
115 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.354+404C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28404762 | |||||||
| chr2:28404835 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354+477C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28404835 | |||||||
| chr2:28404858 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.354+500T>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28404858 | |||||||
| chr2:28404960 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.354+602G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28404960 | |||||||
| chr2:28404988 | G | A | 1 | a0001c0001t0031g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.354+630G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28404988 | |||||||
| chr2:28405022 | T | C | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+664T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405022 | |||||||
| chr2:28405172 | A | T | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+814A>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405172 | |||||||
| chr2:28405293 | C | G | 14 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0128 others(11): Show |
14 | HG00609.hp1 NA18940.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.354+935C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405293 | |||||||
| chr2:28405397 | C | G | 2 | a0001c0001t0032g0046 a0001c0001t0035g0046 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.354+1039C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405397 | |||||||
| chr2:28405486 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.354+1128C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405486 | |||||||
| chr2:28405530 | T | A | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+1172T>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405530 | |||||||
| chr2:28405531 | A | T | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+1173A>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405531 | |||||||
| chr2:28405714 | G | A | 1 | a0001c0001t0021g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.354+1356G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405714 | |||||||
| chr2:28405717 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.354+1359G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405717 | |||||||
| chr2:28405728 | TG | T | 69 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0017 others(66): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.354+1374delG | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 28405728 | ||||||
| chr2:28405912 | A | T | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+1554A>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405912 | |||||||
| chr2:28405958 | T | G | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+1600T>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28405958 | |||||||
| chr2:28406034 | T | G | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+1676T>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406034 | |||||||
| chr2:28406042 | CCCTTTTT others(4): Show |
C | 106 | a0001c0001t0001g0198 a0001c0001t0002g0001 a0001c0001t0002g0008 others(103): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.354+1685_354+1695d others(13): Show |
FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406042 | |||||||
| chr2:28406043 | C | T | 6 | a0001c0001t0007g0192 a0001c0001t0031g0237 a0001c0001t0032g0046 others(3): Show |
6 | HG01109.hp1 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+1685C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406043 | |||||||
| chr2:28406044 | C | CT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0079 a0001c0001t0001g0213 others(5): Show |
8 | HG02074.hp1 HG02970.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.354+1709dupT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 28406044 | ||||||
| chr2:28406044 | CT | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0094 others(8): Show |
11 | HG01099.hp2 HG02055.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.354+1709delT | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 28406044 | ||||||
| chr2:28406055 | T | C | 106 | a0001c0001t0001g0198 a0001c0001t0002g0001 a0001c0001t0002g0008 others(103): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.354+1697T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406055 | |||||||
| chr2:28406092 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.354+1734A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406092 | |||||||
| chr2:28406126 | G | C | 1 | a0005c0003t0001g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.354+1768G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406126 | |||||||
| chr2:28406292 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0072 a0001c0001t0001g0086 others(5): Show |
10 | HG00733.hp1 HG01175.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+1934C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406292 | |||||||
| chr2:28406353 | C | T | 1 | a0001c0001t0006g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.354+1995C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406353 | |||||||
| chr2:28406356 | C | T | 1 | a0001c0001t0006g0151 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.354+1998C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406356 | |||||||
| chr2:28406396 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.354+2038C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406396 | |||||||
| chr2:28406397 | A | G | 1 | a0001c0001t0007g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.354+2039A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406397 | |||||||
| chr2:28406447 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.354+2089T>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406447 | |||||||
| chr2:28406476 | G | T | 105 | a0001c0001t0001g0198 a0001c0001t0002g0001 a0001c0001t0002g0008 others(102): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.354+2118G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406476 | |||||||
| chr2:28406500 | G | C | 106 | a0001c0001t0001g0198 a0001c0001t0002g0001 a0001c0001t0002g0008 others(103): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.354+2142G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406500 | |||||||
| chr2:28406513 | G | T | 1 | a0001c0001t0053g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.354+2155G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406513 | |||||||
| chr2:28406623 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.355-2136G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406623 | |||||||
| chr2:28406904 | C | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0136 others(4): Show |
8 | NA18747.hp2 NA18940.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.355-1855C>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406904 | |||||||
| chr2:28406910 | C | G | 2 | a0001c0001t0032g0046 a0001c0001t0035g0046 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.355-1849C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406910 | |||||||
| chr2:28406970 | G | T | 4 | a0001c0001t0010g0045 a0001c0001t0047g0045 a0001c0001t0049g0188 others(1): Show |
4 | HG02055.hp1 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1789G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28406970 | |||||||
| chr2:28407025 | T | C | 115 | a0001c0001t0001g0198 a0001c0001t0002g0001 a0001c0001t0002g0008 others(112): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.355-1734T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407025 | |||||||
| chr2:28407150 | G | A | 1 | a0001c0001t0003g0101 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.355-1609G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407150 | |||||||
| chr2:28407170 | T | C | 1 | a0001c0001t0037g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.355-1589T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407170 | |||||||
| chr2:28407254 | T | C | 4 | a0001c0001t0010g0045 a0001c0001t0047g0045 a0001c0001t0049g0188 others(1): Show |
4 | HG02055.hp1 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1505T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407254 | |||||||
| chr2:28407624 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0008g0032 a0001c0001t0014g0032 |
3 | HG00597.hp2 NA18961.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.355-1135C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407624 | |||||||
| chr2:28407662 | T | C | 1 | a0001c0001t0037g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.355-1097T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407662 | |||||||
| chr2:28407684 | G | A | 1 | a0001c0001t0007g0175 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.355-1075G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407684 | |||||||
| chr2:28407783 | A | G | 1 | a0001c0001t0021g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.355-976A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407783 | |||||||
| chr2:28407898 | T | C | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.355-861T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28407898 | |||||||
| chr2:28408029 | G | T | 1 | a0001c0001t0006g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.355-730G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28408029 | |||||||
| chr2:28408508 | G | T | 1 | a0001c0001t0023g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.355-251G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28408508 | |||||||
| chr2:28408551 | G | T | 13 | a0001c0001t0009g0011 a0001c0001t0009g0019 a0001c0001t0009g0030 others(10): Show |
16 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-208G>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 2/3 | chr2 | 28408551 | |||||||
| chr2:28408882 | T | C | 1 | a0001c0001t0052g0055 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.462+16T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28408882 | |||||||
| chr2:28409060 | G | A | 1 | a0001c0002t0015g0029 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.462+194G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409060 | |||||||
| chr2:28409232 | A | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
5 | HG02040.hp2 HG02886.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+366A>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409232 | |||||||
| chr2:28409324 | G | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0072 a0001c0001t0001g0086 others(5): Show |
10 | HG00733.hp1 HG01175.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.462+458G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409324 | |||||||
| chr2:28409351 | G | A | 1 | a0001c0001t0006g0108 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.462+485G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409351 | |||||||
| chr2:28409483 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0098 |
2 | HG01070.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.462+617C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409483 | |||||||
| chr2:28409510 | G | A | 69 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0017 others(66): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.462+644G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409510 | |||||||
| chr2:28409770 | C | T | 1 | a0001c0001t0018g0125 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.462+904C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409770 | |||||||
| chr2:28409888 | C | T | 1 | a0001c0002t0015g0029 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.462+1022C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28409888 | |||||||
| chr2:28410146 | G | A | 20 | a0001c0001t0009g0011 a0001c0001t0009g0019 a0001c0001t0009g0030 others(17): Show |
23 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.462+1280G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410146 | |||||||
| chr2:28410281 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.462+1415T>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410281 | |||||||
| chr2:28410337 | G | A | 23 | a0001c0001t0007g0018 a0001c0001t0009g0011 a0001c0001t0009g0019 others(20): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.462+1471G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410337 | |||||||
| chr2:28410356 | A | G | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.462+1490A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410356 | |||||||
| chr2:28410384 | C | T | 1 | a0001c0001t0007g0018 | 3 | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.462+1518C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410384 | |||||||
| chr2:28410540 | G | C | 2 | a0001c0001t0002g0044 a0001c0001t0002g0052 |
4 | HG01070.hp2 HG01071.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.463-1390G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410540 | |||||||
| chr2:28410576 | G | A | 1 | a0001c0001t0054g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.463-1354G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410576 | |||||||
| chr2:28410646 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.463-1284C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410646 | |||||||
| chr2:28410684 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0142 others(3): Show |
11 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.463-1246C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410684 | |||||||
| chr2:28410685 | G | A | 1 | a0001c0001t0013g0009 | 5 | HG00738.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.463-1245G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410685 | |||||||
| chr2:28410706 | G | A | 20 | a0001c0001t0009g0011 a0001c0001t0009g0019 a0001c0001t0009g0030 others(17): Show |
23 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.463-1224G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410706 | |||||||
| chr2:28410875 | G | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0119 a0001c0001t0002g0158 others(2): Show |
6 | HG01261.hp1 HG02273.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.463-1055G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410875 | |||||||
| chr2:28410968 | G | A | 20 | a0001c0001t0009g0011 a0001c0001t0009g0019 a0001c0001t0009g0030 others(17): Show |
23 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.463-962G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28410968 | |||||||
| chr2:28411003 | C | T | 20 | a0001c0001t0009g0011 a0001c0001t0009g0019 a0001c0001t0009g0030 others(17): Show |
23 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.463-927C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411003 | |||||||
| chr2:28411100 | G | A | 22 | a0001c0001t0007g0018 a0001c0001t0009g0011 a0001c0001t0009g0019 others(19): Show |
28 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.463-830G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411100 | |||||||
| chr2:28411149 | C | CA | 5 | a0001c0001t0001g0094 a0001c0001t0007g0018 a0001c0001t0010g0195 others(2): Show |
8 | HG02559.hp2 HG02970.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.463-767dupA | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 28411149 | ||||||
| chr2:28411272 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.463-658G>C | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411272 | |||||||
| chr2:28411319 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.463-611C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411319 | |||||||
| chr2:28411376 | G | A | 1 | a0001c0001t0011g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.463-554G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411376 | |||||||
| chr2:28411395 | G | A | 1 | a0002c0008t0020g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463-535G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411395 | |||||||
| chr2:28411457 | C | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0142 others(3): Show |
11 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.463-473C>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411457 | |||||||
| chr2:28411666 | C | T | 1 | a0001c0001t0061g0138 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.463-264C>T | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411666 | |||||||
| chr2:28411721 | A | AC | 20 | a0001c0001t0009g0011 a0001c0001t0009g0019 a0001c0001t0009g0030 others(17): Show |
23 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.463-204dupC | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 28411721 | ||||||
| chr2:28411802 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0055g0207 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.463-128G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411802 | |||||||
| chr2:28411909 | A | G | 17 | a0001c0001t0002g0037 a0001c0001t0002g0051 a0001c0001t0002g0119 others(14): Show |
20 | HG01261.hp1 HG02083.hp1 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.463-21A>G | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411909 | |||||||
| chr2:28411923 | G | A | 72 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0017 others(69): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
splice_region_variant&intron_variant | LOW | c.463-7G>A | FOSL2 | ENSG00000075426.12 | transcript | ENST00000264716.9 | protein_coding | 3/3 | chr2 | 28411923 |