Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55732 |
| ensemblid | ENSG00000000460.17 |
| hgncid | 25565 |
| symbol | FIRRM |
| name | FIGNL1 interacting regulator of recombination and mitosis |
| refseq_nuc | NM_001320047.2 |
| refseq_prot | NP_001306976.1 |
| ensembl_nuc | ENST00000359326.9 |
| ensembl_prot | ENSP00000352276.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 169795040 |
| end | 169854080 |
| strand | + |
| ver | v1.2 |
| region | chr1:169795040-169854080 |
| region5000 | chr1:169790040-169859080 |
| regionname0 | FIRRM_chr1_169795040_169854080 |
| regionname5000 | FIRRM_chr1_169790040_169859080 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 853 | 385 | 82 | 61 | 188 | 13 | 39 | 145 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| a0002 | 0/0 | 853 | 15 | 0 | 5 | 5 | 2 | 3 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| a0003 | 0/0 | 853 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| a0004 | 0/0 | 853 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| a0005 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| a0006 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| a0007 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| a0008 | 0/0 | 853 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | MFLPH others(848): Show |
chr1 | 169790040 | 169859080 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2559 | 328 | 78 | 45 | 159 | 13 | 31 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0001c0002 | 0/0 | 2559 | 54 | 3 | 14 | 29 | 0 | 8 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0001c0006 | 0/0 | 2559 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0001c0009 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0002c0003 | 0/0 | 2559 | 14 | 0 | 5 | 4 | 2 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0002c0012 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0003c0004 | 0/0 | 2559 | 10 | 10 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0004c0005 | 0/0 | 2559 | 6 | 0 | 0 | 6 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0005c0011 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0006c0010 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0007c0007 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 | ||
| a0008c0008 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATGTT others(2554): Show |
chr1 | 169790040 | 169859080 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4011 | 81 | 21 | 15 | 25 | 6 | 14 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0002 | 1/0 | 4011 | 103 | 19 | 11 | 66 | 2 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0003 | 0/0 | 4011 | 50 | 7 | 14 | 16 | 4 | 9 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0004 | 0/0 | 4020 | 57 | 2 | 2 | 48 | 1 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4015): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0006 | 0/0 | 4016 | 9 | 9 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4011): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0007 | 0/0 | 4020 | 5 | 5 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4015): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0008 | 0/0 | 4011 | 5 | 5 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0009 | 0/0 | 3996 | 4 | 4 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(3991): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0010 | 0/0 | 4020 | 4 | 4 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4015): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0011 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0012 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0014 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0015 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0016 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0017 | 0/0 | 4011 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0018 | 0/0 | 4011 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0019 | 0/0 | 4011 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0020 | 0/1 | 4012 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4007): Show |
chr1 | 169790040 | 169859080 |
| a0001c0001t0021 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ATTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0002t0001 | 0/0 | 4011 | 53 | 3 | 14 | 28 | 0 | 8 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0002t0013 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0006t0002 | 0/0 | 4011 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0001c0009t0001 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0002c0003t0005 | 0/0 | 4016 | 14 | 0 | 5 | 4 | 2 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4011): Show |
chr1 | 169790040 | 169859080 |
| a0002c0012t0005 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4011): Show |
chr1 | 169790040 | 169859080 |
| a0003c0004t0003 | 0/0 | 4011 | 10 | 10 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0004c0005t0001 | 0/0 | 4011 | 6 | 0 | 0 | 6 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0005c0011t0002 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0006c0010t0004 | 0/0 | 4020 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4015): Show |
chr1 | 169790040 | 169859080 |
| a0007c0007t0001 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| a0008c0008t0002 | 0/0 | 4011 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | ACTGC others(4006): Show |
chr1 | 169790040 | 169859080 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0010g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0010g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0012g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0014g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0015g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0016g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0017g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0018g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0019g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0020g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0021g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0013g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0006t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0006t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0009t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0012t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0005c0011t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0006c0010t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0007c0007t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0008c0008t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0138 | EUR | GBR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0137 | EUR | GBR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0234 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00423 | hp2 | a0004 | c0005 | t0001 | g0161 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00609 | hp2 | a0004 | c0005 | t0001 | g0157 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00741 | hp1 | a0002 | c0003 | t0005 | g0353 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01069 | hp2 | a0001 | c0006 | t0002 | g0042 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01071 | hp2 | a0001 | c0006 | t0002 | g0043 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01109 | hp1 | a0001 | c0001 | t0017 | g0041 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01168 | hp2 | a0002 | c0003 | t0005 | g0347 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01169 | hp1 | a0002 | c0003 | t0005 | g0350 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01175 | hp2 | a0001 | c0001 | t0019 | g0144 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0309 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0284 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01361 | hp2 | a0002 | c0003 | t0005 | g0355 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01516 | hp1 | a0002 | c0003 | t0005 | g0352 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01517 | hp2 | a0002 | c0003 | t0005 | g0349 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01891 | hp1 | a0003 | c0004 | t0003 | g0022 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01981 | hp1 | a0002 | c0003 | t0005 | g0354 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02015 | hp2 | a0001 | c0001 | t0011 | g0029 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02027 | hp2 | a0005 | c0011 | t0002 | g0077 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02074 | hp1 | a0002 | c0003 | t0005 | g0357 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0342 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02258 | hp1 | a0003 | c0004 | t0003 | g0025 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0341 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0210 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02293 | hp1 | a0001 | c0001 | t0018 | g0094 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0230 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02523 | hp1 | a0002 | c0003 | t0005 | g0348 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0337 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02615 | hp1 | a0006 | c0010 | t0004 | g0150 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0213 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02630 | hp2 | a0003 | c0004 | t0003 | g0022 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02647 | hp2 | a0003 | c0004 | t0003 | g0141 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02717 | hp2 | a0007 | c0007 | t0001 | g0273 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02723 | hp1 | a0003 | c0004 | t0003 | g0128 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02818 | hp1 | a0003 | c0004 | t0003 | g0345 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02886 | hp1 | a0003 | c0004 | t0003 | g0148 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02895 | hp1 | a0003 | c0004 | t0003 | g0343 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0317 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02897 | hp1 | a0003 | c0004 | t0003 | g0344 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0208 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0154 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03130 | hp2 | a0003 | c0004 | t0003 | g0025 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03225 | hp2 | a0001 | c0009 | t0001 | g0006 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03239 | hp1 | a0002 | c0003 | t0005 | g0351 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0212 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03491 | hp2 | a0002 | c0003 | t0005 | g0356 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0209 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0338 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0110 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0296 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0310 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0314 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0288 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04199 | hp1 | a0002 | c0003 | t0005 | g0346 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0289 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0227 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0207 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18939 | hp1 | a0004 | c0005 | t0001 | g0159 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18943 | hp2 | a0002 | c0012 | t0005 | g0039 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18953 | hp1 | a0001 | c0002 | t0013 | g0270 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18953 | hp2 | a0002 | c0003 | t0005 | g0358 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18956 | hp2 | a0004 | c0005 | t0001 | g0158 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18997 | hp1 | a0001 | c0001 | t0015 | g0075 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19002 | hp2 | a0001 | c0001 | t0016 | g0063 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19005 | hp2 | a0001 | c0001 | t0021 | g0162 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19075 | hp2 | a0004 | c0005 | t0001 | g0156 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19088 | hp2 | a0004 | c0005 | t0001 | g0160 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0146 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0131 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20805 | hp2 | a0008 | c0008 | t0002 | g0089 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | GIH | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | GIH | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0211 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0339 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0223 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0334 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0340 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18955 | hp1 | a0002 | c0003 | t0005 | g0039 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0020 | g0167 | REF | REF | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0085 | REF | REF | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169804196 | A | G | 1 | a0005 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.434A>G | p.Asp145Gly | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/25 | 790/4011 | 434/2562 | 145/853 | chr1 | 169804196 | |||
| chr1:169806067 | A | G | 1 | a0006 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.542A>G | p.Asn181Ser | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/25 | 898/4011 | 542/2562 | 181/853 | chr1 | 169806067 | |||
| chr1:169807852 | A | G | 1 | a0004 | 6 | HG00423.hp2 HG00609.hp2 NA18939.hp1 others(3): Show |
missense_variant | MODERATE | c.625A>G | p.Ser209Gly | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/25 | 981/4011 | 625/2562 | 209/853 | chr1 | 169807852 | |||
| chr1:169827056 | T | C | 1 | a0003 | 10 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.854T>C | p.Phe285Ser | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/25 | 1210/4011 | 854/2562 | 285/853 | chr1 | 169827056 | |||
| chr1:169830739 | G | T | 1 | a0002 | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
missense_variant | MODERATE | c.1441G>T | p.Ala481Ser | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/25 | 1797/4011 | 1441/2562 | 481/853 | chr1 | 169830739 | |||
| chr1:169837087 | G | A | 1 | a0008 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1700G>A | p.Arg567His | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/25 | 2056/4011 | 1700/2562 | 567/853 | chr1 | 169837087 | |||
| chr1:169851914 | A | C | 1 | a0007 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2342A>C | p.Glu781Ala | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/25 | 2698/4011 | 2342/2562 | 781/853 | chr1 | 169851914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169803198 | A | C | 1 | a0002c0012 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.201A>C | p.Thr67Thr | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/25 | 557/4011 | 201/2562 | 67/853 | chr1 | 169803198 | |||
| chr1:169804176 | G | A | 2 | a0001c0002 a0007c0007 |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
synonymous_variant | LOW | c.414G>A | p.Leu138Leu | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/25 | 770/4011 | 414/2562 | 138/853 | chr1 | 169804176 | |||
| chr1:169827718 | A | C | 1 | a0001c0009 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1005A>C | p.Pro335Pro | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/25 | 1361/4011 | 1005/2562 | 335/853 | chr1 | 169827718 | |||
| chr1:169851858 | T | A | 1 | a0001c0006 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.2286T>A | p.Arg762Arg | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/25 | 2642/4011 | 2286/2562 | 762/853 | chr1 | 169851858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169795041 | C | T | 1 | a0001c0001t0021 | 1 | NA19005.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-355C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/25 | chr1 | 169795041 | |||||||
| chr1:169795875 | A | G | 1 | a0001c0001t0008 | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-234A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/25 | 5031 | chr1 | 169795875 | ||||||
| chr1:169795911 | C | G | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(3): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
5_prime_UTR_variant | MODIFIER | c.-198C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/25 | 4995 | chr1 | 169795911 | ||||||
| chr1:169798892 | T | C | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
5_prime_UTR_variant | MODIFIER | c.-90T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/25 | 2014 | chr1 | 169798892 | ||||||
| chr1:169798897 | G | A | 1 | a0001c0001t0014 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/25 | 2009 | chr1 | 169798897 | ||||||
| chr1:169798939 | C | A | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
5_prime_UTR_variant | MODIFIER | c.-43C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/25 | 1967 | chr1 | 169798939 | ||||||
| chr1:169852999 | A | AGGCAGAA others(2): Show |
4 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(1): Show |
67 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*15_*23dupCAGAACTG others(1): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 24 | INFO_REALIGN_3_PRIME | chr1 | 169852999 | |||||
| chr1:169853231 | A | G | 1 | a0001c0001t0009 | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*244A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 244 | chr1 | 169853231 | ||||||
| chr1:169853312 | A | G | 1 | a0001c0002t0013 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 325 | chr1 | 169853312 | ||||||
| chr1:169853344 | T | G | 1 | a0001c0001t0015 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 357 | chr1 | 169853344 | ||||||
| chr1:169853347 | T | TAAAGA | 2 | a0002c0003t0005 a0002c0012t0005 |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*362_*366dupAAGAA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 367 | INFO_REALIGN_3_PRIME | chr1 | 169853347 | |||||
| chr1:169853402 | A | G | 2 | a0002c0003t0005 a0002c0012t0005 |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*415A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 415 | chr1 | 169853402 | ||||||
| chr1:169853415 | A | T | 1 | a0001c0001t0018 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 428 | chr1 | 169853415 | ||||||
| chr1:169853709 | A | G | 1 | a0001c0001t0010 | 4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*722A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 722 | chr1 | 169853709 | ||||||
| chr1:169853751 | C | G | 1 | a0001c0001t0017 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 764 | chr1 | 169853751 | ||||||
| chr1:169853819 | T | C | 1 | a0001c0001t0011 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 832 | chr1 | 169853819 | ||||||
| chr1:169853842 | A | T | 2 | a0001c0001t0009 a0001c0001t0012 |
5 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*855A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 855 | chr1 | 169853842 | ||||||
| chr1:169853890 | C | T | 1 | a0001c0001t0016 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*903C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 903 | chr1 | 169853890 | ||||||
| chr1:169853905 | AACTTAGA others(8): Show |
A | 1 | a0001c0001t0009 | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*920_*934delCTTAGA others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 920 | INFO_REALIGN_3_PRIME | chr1 | 169853905 | |||||
| chr1:169854007 | T | G | 1 | a0001c0001t0019 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1020T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 1020 | chr1 | 169854007 | ||||||
| chr1:169854036 | T | TTTTTC | 1 | a0001c0001t0006 | 9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1054_*1058dupCTTT others(1): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 1059 | INFO_REALIGN_3_PRIME | chr1 | 169854036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169795279 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-281+164C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795279 | |||||||
| chr1:169795361 | A | AAAGTGAG others(12): Show |
3 | a0003c0004t0003g0343 a0003c0004t0003g0344 a0003c0004t0003g0345 |
3 | HG02818.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-281+250_-281+268d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr1 | 169795361 | ||||||
| chr1:169795427 | C | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-281+312C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795427 | |||||||
| chr1:169795448 | C | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-281+333C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795448 | |||||||
| chr1:169795485 | C | T | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-280-344C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795485 | |||||||
| chr1:169795747 | A | G | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-280-82A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795747 | |||||||
| chr1:169795782 | CTTCT | C | 5 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-280-36_-280-33del others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr1 | 169795782 | ||||||
| chr1:169795998 | T | C | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.-126+15T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169795998 | |||||||
| chr1:169796098 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0006g0337 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-126+115T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796098 | |||||||
| chr1:169796102 | G | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-126+119G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796102 | |||||||
| chr1:169796170 | C | A | 1 | a0001c0001t0002g0040 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-126+187C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796170 | |||||||
| chr1:169796186 | A | G | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18981.hp2 NA18991.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-126+203A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796186 | |||||||
| chr1:169796199 | G | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-126+216G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796199 | |||||||
| chr1:169796207 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-126+224C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796207 | |||||||
| chr1:169796292 | G | A | 1 | a0001c0001t0017g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-126+309G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796292 | |||||||
| chr1:169796321 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-126+338C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796321 | |||||||
| chr1:169796450 | A | G | 2 | a0001c0001t0002g0095 a0001c0001t0018g0094 |
2 | HG00735.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-126+467A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796450 | |||||||
| chr1:169796582 | T | A | 1 | a0001c0001t0003g0021 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-126+599T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796582 | |||||||
| chr1:169796635 | A | G | 1 | a0001c0001t0002g0336 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-126+652A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796635 | |||||||
| chr1:169796758 | G | A | 55 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0023 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-126+775G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796758 | |||||||
| chr1:169796861 | T | G | 1 | a0001c0001t0003g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-126+878T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796861 | |||||||
| chr1:169796936 | A | G | 2 | a0001c0002t0001g0334 a0001c0002t0001g0335 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-126+953A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796936 | |||||||
| chr1:169797137 | C | T | 50 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(47): Show |
61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-126+1154C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797137 | |||||||
| chr1:169797157 | G | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-126+1174G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797157 | |||||||
| chr1:169797224 | A | C | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | NA18972.hp2 NA18973.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+1241A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797224 | |||||||
| chr1:169797231 | G | C | 2 | a0001c0006t0002g0042 a0001c0006t0002g0043 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-126+1248G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797231 | |||||||
| chr1:169797474 | T | A | 2 | a0001c0002t0001g0264 a0001c0002t0001g0265 |
2 | HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.-125-1383T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797474 | |||||||
| chr1:169797487 | G | A | 2 | a0001c0006t0002g0042 a0001c0006t0002g0043 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-125-1370G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797487 | |||||||
| chr1:169797618 | G | A | 1 | a0001c0001t0004g0220 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-125-1239G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797618 | |||||||
| chr1:169797670 | G | A | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-125-1187G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797670 | |||||||
| chr1:169797741 | A | C | 1 | a0003c0004t0003g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-125-1116A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797741 | |||||||
| chr1:169797822 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-125-1035G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797822 | |||||||
| chr1:169797883 | A | T | 6 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | HG00544.hp2 HG00735.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-125-974A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797883 | |||||||
| chr1:169797884 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-125-973T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797884 | |||||||
| chr1:169797888 | G | A | 6 | a0004c0005t0001g0156 a0004c0005t0001g0157 a0004c0005t0001g0158 others(3): Show |
6 | HG00423.hp2 HG00609.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.-125-969G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797888 | |||||||
| chr1:169798062 | CTT | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-125-794_-125-793d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798062 | |||||||
| chr1:169798237 | T | C | 1 | a0001c0001t0003g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-125-620T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798237 | |||||||
| chr1:169798268 | G | T | 3 | a0001c0001t0004g0256 a0001c0001t0004g0257 a0001c0001t0004g0258 |
3 | NA18989.hp2 NA19005.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-125-589G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798268 | |||||||
| chr1:169798278 | C | CT | 18 | a0001c0001t0002g0333 a0001c0001t0017g0041 a0002c0003t0005g0039 others(15): Show |
18 | HG00741.hp1 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-125-564dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr1 | 169798278 | ||||||
| chr1:169798280 | T | C | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-125-577T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798280 | |||||||
| chr1:169798298 | C | T | 2 | a0001c0001t0006g0013 a0001c0001t0006g0219 |
4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-125-559C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798298 | |||||||
| chr1:169798320 | T | G | 2 | a0001c0001t0001g0163 a0001c0001t0021g0162 |
2 | NA18957.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-125-537T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798320 | |||||||
| chr1:169798345 | G | A | 1 | a0001c0001t0018g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-125-512G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798345 | |||||||
| chr1:169798485 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0164 others(3): Show |
11 | HG00323.hp2 HG00741.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-125-372G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798485 | |||||||
| chr1:169798561 | T | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-125-296T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798561 | |||||||
| chr1:169798636 | G | A | 1 | a0003c0004t0003g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-125-221G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798636 | |||||||
| chr1:169798683 | G | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-125-174G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798683 | |||||||
| chr1:169798990 | C | T | 1 | a0002c0003t0005g0358 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-24+32C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169798990 | |||||||
| chr1:169799220 | G | A | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-24+262G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799220 | |||||||
| chr1:169799227 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-24+269G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799227 | |||||||
| chr1:169799231 | C | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-24+273C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799231 | |||||||
| chr1:169799338 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-24+380G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799338 | |||||||
| chr1:169799338 | G | T | 4 | a0001c0001t0002g0329 a0001c0001t0002g0330 a0001c0001t0002g0331 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+380G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799338 | |||||||
| chr1:169799359 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24+401C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799359 | |||||||
| chr1:169799421 | A | G | 6 | a0001c0001t0001g0126 a0001c0001t0006g0337 a0001c0001t0006g0338 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+463A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799421 | |||||||
| chr1:169799424 | C | G | 1 | a0001c0001t0003g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-24+466C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799424 | |||||||
| chr1:169799440 | A | G | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-24+482A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799440 | |||||||
| chr1:169799708 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24+750C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799708 | |||||||
| chr1:169799744 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-24+786G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799744 | |||||||
| chr1:169799812 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-24+854A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799812 | |||||||
| chr1:169799833 | G | A | 5 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+875G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799833 | |||||||
| chr1:169799840 | G | A | 354 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(351): Show |
411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.-24+882G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799840 | |||||||
| chr1:169799847 | C | A | 1 | a0001c0002t0001g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-24+889C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799847 | |||||||
| chr1:169799904 | G | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24+946G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799904 | |||||||
| chr1:169799935 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-23-948C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799935 | |||||||
| chr1:169799969 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
5 | NA18944.hp1 NA18954.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-914C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799969 | |||||||
| chr1:169800025 | G | A | 284 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-23-858G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800025 | |||||||
| chr1:169800029 | T | TTTTG | 5 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-842_-23-839dup others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800029 | ||||||
| chr1:169800092 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-23-791C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800092 | |||||||
| chr1:169800173 | G | A | 3 | a0001c0001t0002g0315 a0001c0001t0002g0316 a0001c0001t0014g0317 |
3 | HG02896.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-23-710G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800173 | |||||||
| chr1:169800233 | A | G | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23-650A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800233 | |||||||
| chr1:169800239 | T | G | 1 | a0001c0001t0002g0046 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-23-644T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800239 | |||||||
| chr1:169800259 | G | A | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-23-624G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800259 | |||||||
| chr1:169800339 | G | A | 2 | a0001c0001t0004g0221 a0001c0001t0004g0222 |
2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-23-544G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800339 | |||||||
| chr1:169800425 | G | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-23-458G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800425 | |||||||
| chr1:169800613 | T | C | 1 | a0001c0001t0007g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-23-270T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800613 | |||||||
| chr1:169800661 | A | T | 1 | a0001c0001t0002g0328 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-23-222A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800661 | |||||||
| chr1:169800709 | TTC | T | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-168_-23-167del others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800709 | ||||||
| chr1:169800715 | C | CT | 7 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0001g0169 others(4): Show |
8 | HG02559.hp2 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-153dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | ||||||
| chr1:169800715 | C | CTT | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-23-154_-23-153dup others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | ||||||
| chr1:169800715 | C | CTTT | 5 | a0001c0001t0006g0337 a0001c0001t0008g0030 a0001c0001t0008g0207 others(2): Show |
6 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-155_-23-153dup others(3): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | ||||||
| chr1:169800715 | C | CTTTT | 53 | a0001c0001t0002g0333 a0001c0001t0004g0001 a0001c0001t0004g0033 others(50): Show |
64 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-23-156_-23-153dup others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | ||||||
| chr1:169801159 | C | T | 1 | a0001c0001t0009g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.66+188C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801159 | |||||||
| chr1:169801178 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+207C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801178 | |||||||
| chr1:169801336 | T | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+365T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801336 | |||||||
| chr1:169801433 | G | A | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+462G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801433 | |||||||
| chr1:169801445 | C | CA | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(149): Show |
173 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.66+496dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801445 | ||||||
| chr1:169801445 | C | CAA | 22 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(19): Show |
25 | HG01884.hp1 HG01975.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.66+495_66+496dupAA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801445 | ||||||
| chr1:169801445 | CA | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0206 a0001c0001t0002g0045 others(11): Show |
14 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+496delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801445 | ||||||
| chr1:169801496 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+525C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801496 | |||||||
| chr1:169801505 | C | T | 1 | a0001c0001t0004g0225 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.66+534C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801505 | |||||||
| chr1:169801597 | C | CA | 14 | a0001c0001t0002g0049 a0002c0003t0005g0039 a0002c0003t0005g0346 others(11): Show |
14 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+646dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801597 | ||||||
| chr1:169801597 | CAAA | C | 59 | a0001c0001t0001g0164 a0001c0001t0003g0020 a0001c0001t0003g0021 others(56): Show |
65 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.66+644_66+646delAA others(1): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801597 | ||||||
| chr1:169801597 | CAAAA | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
222 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.66+643_66+646delAA others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801597 | ||||||
| chr1:169801679 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.66+708A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801679 | |||||||
| chr1:169801731 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.66+760A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801731 | |||||||
| chr1:169801810 | T | C | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-811T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801810 | |||||||
| chr1:169801863 | A | T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-758A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801863 | |||||||
| chr1:169802057 | T | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0175 a0001c0001t0021g0162 |
3 | NA18957.hp1 NA18960.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.67-564T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802057 | |||||||
| chr1:169802068 | A | G | 3 | a0001c0001t0003g0102 a0001c0001t0003g0124 a0001c0001t0003g0125 |
3 | NA18964.hp1 NA18974.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.67-553A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802068 | |||||||
| chr1:169802109 | A | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.67-512A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802109 | |||||||
| chr1:169802221 | G | A | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-400G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802221 | |||||||
| chr1:169802236 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-385A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802236 | |||||||
| chr1:169802288 | A | G | 2 | a0001c0001t0006g0013 a0001c0001t0006g0219 |
4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-333A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802288 | |||||||
| chr1:169802295 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67-326T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802295 | |||||||
| chr1:169802477 | G | A | 3 | a0001c0002t0001g0272 a0001c0002t0001g0274 a0007c0007t0001g0273 |
3 | HG00642.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-144G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802477 | |||||||
| chr1:169802797 | G | A | 1 | a0006c0010t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.171+72G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802797 | |||||||
| chr1:169802824 | C | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.171+99C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802824 | |||||||
| chr1:169802867 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0263 |
7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+142A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802867 | |||||||
| chr1:169802883 | A | G | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+158A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802883 | |||||||
| chr1:169802898 | TAAG | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
90 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.171+178_171+180del others(3): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr1 | 169802898 | ||||||
| chr1:169803093 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.172-76C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169803093 | |||||||
| chr1:169803144 | G | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-25G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169803144 | |||||||
| chr1:169803504 | T | TG | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.312+199dupG | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr1 | 169803504 | ||||||
| chr1:169803521 | A | T | 1 | a0001c0001t0008g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.312+212A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | chr1 | 169803521 | |||||||
| chr1:169803651 | TC | T | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.312+344delC | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr1 | 169803651 | ||||||
| chr1:169803836 | C | T | 269 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.313-239C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | chr1 | 169803836 | |||||||
| chr1:169804019 | T | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.313-56T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | chr1 | 169804019 | |||||||
| chr1:169804294 | A | G | 6 | a0001c0001t0001g0126 a0001c0001t0006g0337 a0001c0001t0006g0338 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+54A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804294 | |||||||
| chr1:169804344 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.478+104A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804344 | |||||||
| chr1:169804460 | A | G | 1 | a0001c0001t0009g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.478+220A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804460 | |||||||
| chr1:169804475 | A | G | 2 | a0001c0006t0002g0042 a0001c0006t0002g0043 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.478+235A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804475 | |||||||
| chr1:169804524 | AT | A | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.478+291delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr1 | 169804524 | ||||||
| chr1:169804556 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.478+316G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804556 | |||||||
| chr1:169804589 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
90 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.478+349G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804589 | |||||||
| chr1:169804722 | A | C | 16 | a0001c0001t0002g0333 a0002c0003t0005g0039 a0002c0003t0005g0346 others(13): Show |
16 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.478+482A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804722 | |||||||
| chr1:169804782 | A | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.478+542A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804782 | |||||||
| chr1:169804863 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.478+623A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804863 | |||||||
| chr1:169804966 | A | G | 6 | a0001c0001t0001g0126 a0001c0001t0006g0337 a0001c0001t0006g0338 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+726A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804966 | |||||||
| chr1:169805143 | C | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.479-861C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805143 | |||||||
| chr1:169805179 | T | C | 2 | a0001c0001t0004g0226 a0001c0001t0004g0227 |
2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.479-825T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805179 | |||||||
| chr1:169805182 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.479-822A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805182 | |||||||
| chr1:169805193 | A | G | 5 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.479-811A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805193 | |||||||
| chr1:169805374 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.479-630T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805374 | |||||||
| chr1:169805375 | A | G | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-629A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805375 | |||||||
| chr1:169805435 | G | T | 1 | a0001c0001t0002g0081 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.479-569G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805435 | |||||||
| chr1:169805521 | C | T | 2 | a0001c0002t0001g0271 a0001c0002t0001g0312 |
2 | NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.479-483C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805521 | |||||||
| chr1:169805522 | C | T | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.479-482C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805522 | |||||||
| chr1:169805628 | T | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.479-376T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805628 | |||||||
| chr1:169806001 | C | T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.479-3C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169806001 | |||||||
| chr1:169806176 | A | G | 4 | a0001c0001t0004g0252 a0001c0001t0004g0253 a0001c0001t0004g0254 others(1): Show |
4 | HG02015.hp1 HG02080.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.563+88A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806176 | |||||||
| chr1:169806483 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.563+395A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806483 | |||||||
| chr1:169806563 | A | T | 1 | a0001c0001t0004g0225 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.563+475A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806563 | |||||||
| chr1:169806577 | T | C | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(8): Show |
11 | HG00423.hp2 HG00609.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.563+489T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806577 | |||||||
| chr1:169806940 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.564-851A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806940 | |||||||
| chr1:169807056 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.564-735T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807056 | |||||||
| chr1:169807094 | T | A | 1 | a0001c0002t0001g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.564-697T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807094 | |||||||
| chr1:169807234 | T | A | 1 | a0001c0001t0002g0093 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.564-557T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807234 | |||||||
| chr1:169807242 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.564-549A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807242 | |||||||
| chr1:169807315 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0263 |
7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.564-476A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807315 | |||||||
| chr1:169807485 | A | C | 66 | a0001c0001t0001g0026 a0001c0001t0001g0126 a0001c0001t0001g0151 others(63): Show |
68 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.564-306A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807485 | |||||||
| chr1:169807493 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.564-298G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807493 | |||||||
| chr1:169807603 | T | A | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.564-188T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807603 | |||||||
| chr1:169808028 | T | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+99T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808028 | |||||||
| chr1:169808030 | T | C | 1 | a0001c0001t0002g0050 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.702+101T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808030 | |||||||
| chr1:169808284 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0202 others(3): Show |
8 | HG02015.hp2 HG02056.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+355A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808284 | |||||||
| chr1:169808438 | T | A | 1 | a0001c0001t0004g0228 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.702+509T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808438 | |||||||
| chr1:169808608 | G | GT | 210 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.702+693dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169808608 | ||||||
| chr1:169808608 | G | GTT | 55 | a0001c0001t0001g0151 a0001c0001t0002g0333 a0001c0001t0003g0123 others(52): Show |
56 | HG00408.hp1 HG00621.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.702+692_702+693dup others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169808608 | ||||||
| chr1:169808660 | A | G | 1 | a0001c0001t0004g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.702+731A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808660 | |||||||
| chr1:169808971 | A | G | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG02056.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.702+1042A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808971 | |||||||
| chr1:169808986 | G | A | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.702+1057G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808986 | |||||||
| chr1:169809014 | C | T | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.702+1085C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809014 | |||||||
| chr1:169809095 | A | G | 1 | a0001c0001t0014g0317 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.702+1166A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809095 | |||||||
| chr1:169809292 | C | T | 1 | a0001c0002t0001g0311 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.702+1363C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809292 | |||||||
| chr1:169809351 | A | G | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+1422A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809351 | |||||||
| chr1:169809360 | G | A | 1 | a0001c0002t0001g0279 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.702+1431G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809360 | |||||||
| chr1:169809376 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.702+1447C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809376 | |||||||
| chr1:169809413 | A | C | 2 | a0001c0002t0001g0264 a0001c0002t0001g0265 |
2 | HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.702+1484A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809413 | |||||||
| chr1:169809418 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.702+1489C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809418 | |||||||
| chr1:169809539 | A | G | 1 | a0005c0011t0002g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.702+1610A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809539 | |||||||
| chr1:169809604 | A | G | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.702+1675A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809604 | |||||||
| chr1:169809615 | A | G | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.702+1686A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809615 | |||||||
| chr1:169809872 | A | C | 1 | a0001c0002t0001g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.702+1943A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809872 | |||||||
| chr1:169809998 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.702+2069C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809998 | |||||||
| chr1:169810116 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.702+2187G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810116 | |||||||
| chr1:169810173 | C | A | 1 | a0001c0001t0007g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.702+2244C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810173 | |||||||
| chr1:169810202 | T | G | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+2273T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810202 | |||||||
| chr1:169810348 | G | A | 3 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0002t0001g0282 |
3 | NA18940.hp2 NA19076.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.702+2419G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810348 | |||||||
| chr1:169810360 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.702+2431C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810360 | |||||||
| chr1:169810446 | T | C | 6 | a0001c0001t0001g0126 a0001c0001t0006g0337 a0001c0001t0006g0338 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+2517T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810446 | |||||||
| chr1:169810523 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+2594A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810523 | |||||||
| chr1:169810525 | T | G | 1 | a0001c0001t0003g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2596T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810525 | |||||||
| chr1:169810583 | G | T | 1 | a0001c0001t0003g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2654G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810583 | |||||||
| chr1:169810649 | T | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+2720T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810649 | |||||||
| chr1:169810669 | T | C | 52 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(49): Show |
53 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.702+2740T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810669 | |||||||
| chr1:169810703 | C | G | 1 | a0001c0001t0003g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.702+2774C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810703 | |||||||
| chr1:169810731 | A | T | 1 | a0001c0001t0003g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2802A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810731 | |||||||
| chr1:169810764 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.702+2835G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810764 | |||||||
| chr1:169810798 | A | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+2869A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810798 | |||||||
| chr1:169810815 | T | C | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.702+2886T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810815 | |||||||
| chr1:169810832 | C | A | 1 | a0001c0001t0004g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.702+2903C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810832 | |||||||
| chr1:169810834 | A | AT | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(34): Show |
52 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.702+2941dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATT | 23 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(20): Show |
23 | HG00408.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.702+2940_702+2941d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTT | 7 | a0001c0001t0001g0101 a0001c0001t0001g0197 a0001c0001t0002g0093 others(4): Show |
7 | HG00323.hp1 HG01884.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+2939_702+2941d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTT | 18 | a0001c0001t0001g0100 a0001c0001t0002g0321 a0001c0001t0004g0001 others(15): Show |
23 | HG00423.hp1 HG00673.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.702+2938_702+2941d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTT | 19 | a0001c0001t0004g0035 a0001c0001t0004g0220 a0001c0001t0004g0225 others(16): Show |
20 | HG00438.hp2 HG02015.hp1 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.702+2937_702+2941d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(1): Show |
7 | a0001c0001t0002g0322 a0001c0001t0002g0329 a0001c0001t0002g0330 others(4): Show |
9 | HG02602.hp1 HG02647.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.702+2934_702+2941d others(10): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(3): Show |
7 | a0001c0001t0003g0103 a0001c0001t0003g0104 a0001c0001t0003g0113 others(4): Show |
7 | HG02083.hp2 NA18964.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+2932_702+2941d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(4): Show |
9 | a0001c0001t0003g0020 a0001c0001t0003g0105 a0001c0001t0003g0114 others(6): Show |
10 | HG03942.hp1 NA18959.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+2931_702+2941d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(5): Show |
4 | a0001c0001t0003g0116 a0001c0002t0001g0303 a0001c0002t0001g0304 others(1): Show |
4 | HG00408.hp1 NA18994.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+2930_702+2941d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0117 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.702+2929_702+2941d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0002g0323 a0001c0001t0002g0333 a0001c0001t0003g0124 others(1): Show |
4 | HG02970.hp1 HG02976.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2928_702+2941d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(8): Show |
2 | a0001c0002t0001g0281 a0001c0002t0001g0282 |
2 | NA18940.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.702+2927_702+2941d others(17): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0002t0001g0268 others(1): Show |
4 | HG01074.hp1 HG01167.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+2926_702+2941d others(18): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0004g0262 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.702+2925_702+2941d others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(11): Show |
4 | a0001c0001t0003g0120 a0001c0001t0003g0123 a0001c0002t0001g0307 others(1): Show |
4 | HG03471.hp1 NA18977.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2924_702+2941d others(20): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(12): Show |
1 | a0001c0002t0001g0308 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.702+2923_702+2941d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(13): Show |
4 | a0001c0001t0002g0319 a0001c0001t0002g0324 a0001c0001t0003g0125 others(1): Show |
4 | HG01258.hp2 HG02145.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2922_702+2941d others(22): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(14): Show |
1 | a0001c0002t0001g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.702+2921_702+2941d others(23): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0003g0121 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.702+2920_702+2941d others(24): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0003g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.702+2918_702+2941d others(26): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(19): Show |
1 | a0001c0001t0003g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.702+2916_702+2941d others(28): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | ATTTTTTT others(25): Show |
1 | a0001c0002t0001g0265 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.702+2910_702+2941d others(34): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | A | T | 2 | a0001c0001t0002g0076 a0001c0001t0004g0229 |
2 | HG00597.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.702+2905A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810834 | |||||||
| chr1:169810834 | AT | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0126 others(23): Show |
32 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.702+2941delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATT | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0169 others(10): Show |
14 | HG01123.hp1 HG01981.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.702+2940_702+2941d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTT | A | 10 | a0001c0001t0001g0200 a0001c0001t0002g0315 a0001c0001t0002g0316 others(7): Show |
11 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+2939_702+2941d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTT | A | 7 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0003g0145 others(4): Show |
7 | HG01175.hp2 HG01978.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+2937_702+2941d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTT | A | 35 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(32): Show |
39 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.702+2936_702+2941d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT | A | 10 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0213 others(7): Show |
10 | HG01168.hp2 HG01517.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+2935_702+2941d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0181 a0001c0001t0003g0110 a0001c0001t0004g0231 others(4): Show |
7 | HG00642.hp2 HG02717.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+2932_702+2941d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0276 |
2 | HG00597.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.702+2931_702+2941d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(5): Show |
A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02027.hp1 HG02132.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.702+2930_702+2941d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.702+2929_702+2941d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(7): Show |
A | 8 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(5): Show |
9 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2928_702+2941d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0002g0052 a0001c0001t0003g0109 |
2 | HG00544.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.702+2927_702+2941d others(17): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(9): Show |
A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0003g0107 others(5): Show |
9 | HG02145.hp1 HG02559.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2926_702+2941d others(18): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810834 | ATTTTTTT others(10): Show |
A | 2 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
2 | HG00733.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.702+2925_702+2941d others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | ||||||
| chr1:169810845 | T | A | 1 | a0001c0001t0003g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2916T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810845 | |||||||
| chr1:169810871 | G | T | 1 | a0001c0002t0001g0279 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.702+2942G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810871 | |||||||
| chr1:169810872 | A | T | 1 | a0001c0002t0001g0279 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.702+2943A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810872 | |||||||
| chr1:169810887 | C | G | 3 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 |
3 | NA18973.hp2 NA19062.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.702+2958C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810887 | |||||||
| chr1:169810892 | G | A | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2963G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810892 | |||||||
| chr1:169810926 | C | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+2997C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810926 | |||||||
| chr1:169810985 | G | A | 1 | a0001c0001t0006g0338 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702+3056G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810985 | |||||||
| chr1:169811014 | C | T | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3085C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811014 | |||||||
| chr1:169811016 | C | T | 1 | a0001c0002t0001g0267 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.702+3087C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811016 | |||||||
| chr1:169811020 | C | T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+3091C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811020 | |||||||
| chr1:169811349 | A | C | 2 | a0001c0001t0003g0103 a0001c0001t0003g0113 |
2 | NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.702+3420A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811349 | |||||||
| chr1:169811362 | T | G | 1 | a0001c0001t0002g0047 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.702+3433T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811362 | |||||||
| chr1:169811674 | A | AATCTAAA others(17): Show |
10 | a0001c0001t0003g0107 a0001c0001t0003g0114 a0001c0001t0006g0338 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+3871_702+3894d others(26): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811674 | ||||||
| chr1:169811674 | AATCTAAA others(17): Show |
A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
210 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.702+3871_702+3894d others(26): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811674 | ||||||
| chr1:169811674 | AATCTAAA others(41): Show |
A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
9 | HG00280.hp1 HG00673.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+3847_702+3894d others(50): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811674 | ||||||
| chr1:169811693 | C | T | 10 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+3764C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811693 | |||||||
| chr1:169811704 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3775A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811704 | |||||||
| chr1:169811717 | C | T | 1 | a0001c0002t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.702+3788C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811717 | |||||||
| chr1:169811722 | T | A | 1 | a0001c0002t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.702+3793T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811722 | |||||||
| chr1:169811728 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3799A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811728 | |||||||
| chr1:169811752 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3823A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811752 | |||||||
| chr1:169811761 | TAGACAGA others(21): Show |
T | 1 | a0001c0002t0001g0296 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.702+3836_702+3863d others(30): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811761 | ||||||
| chr1:169811765 | C | CAGATTAT others(61): Show |
2 | a0002c0003t0005g0354 a0002c0003t0005g0355 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.702+3846_702+3847i others(70): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811765 | ||||||
| chr1:169811765 | C | CAGATTAT others(85): Show |
13 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(10): Show |
13 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.702+3846_702+3847i others(94): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811765 | ||||||
| chr1:169811765 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3836C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811765 | |||||||
| chr1:169811766 | A | T | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3837A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811766 | |||||||
| chr1:169811767 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3838G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811767 | |||||||
| chr1:169811768 | A | T | 51 | a0001c0001t0002g0333 a0001c0001t0004g0001 a0001c0001t0004g0033 others(48): Show |
62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.702+3839A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811768 | |||||||
| chr1:169811769 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3840T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811769 | |||||||
| chr1:169811776 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3847A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811776 | |||||||
| chr1:169811785 | TAGACAGA others(21): Show |
T | 1 | a0001c0001t0001g0166 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.702+3860_702+3887d others(30): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811785 | ||||||
| chr1:169811789 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3860C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811789 | |||||||
| chr1:169811790 | A | T | 1 | a0001c0001t0004g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3861A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811790 | |||||||
| chr1:169811791 | G | A | 1 | a0001c0001t0004g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3862G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811791 | |||||||
| chr1:169811792 | A | T | 1 | a0001c0001t0004g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3863A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811792 | |||||||
| chr1:169811793 | T | C | 1 | a0001c0001t0004g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3864T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811793 | |||||||
| chr1:169811797 | CTAAATAG others(37): Show |
C | 20 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 others(17): Show |
30 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.702+3871_702+3914d others(46): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811797 | ||||||
| chr1:169811800 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3871A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811800 | |||||||
| chr1:169811811 | G | GATTATCT others(13): Show |
1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3883_702+3884i others(22): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(157): Show |
2 | a0001c0001t0004g0001 a0006c0010t0004g0150 |
2 | HG00673.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.702+3883_702+3884i others(166): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(181): Show |
3 | a0001c0001t0010g0032 a0001c0001t0010g0223 a0001c0001t0010g0230 |
4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(190): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(205): Show |
6 | a0001c0001t0004g0001 a0001c0001t0004g0221 a0001c0001t0004g0222 others(3): Show |
6 | HG00323.hp1 HG02155.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(214): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(229): Show |
10 | a0001c0001t0004g0001 a0001c0001t0004g0220 a0001c0001t0004g0224 others(7): Show |
11 | HG01943.hp1 HG02135.hp2 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(238): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(253): Show |
16 | a0001c0001t0004g0001 a0001c0001t0004g0034 a0001c0001t0004g0225 others(13): Show |
18 | HG00423.hp1 HG00438.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(262): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(277): Show |
5 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(2): Show |
6 | HG02129.hp2 HG04204.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(286): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(301): Show |
5 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0229 others(2): Show |
5 | HG02602.hp1 NA18959.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(310): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(325): Show |
2 | a0001c0001t0004g0037 a0001c0001t0004g0227 |
2 | HG04228.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.702+3883_702+3884i others(334): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811811 | G | GATTATCT others(349): Show |
3 | a0001c0001t0004g0037 a0001c0001t0004g0226 a0001c0001t0004g0233 |
3 | HG02683.hp2 NA18966.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.702+3883_702+3884i others(358): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | ||||||
| chr1:169811813 | C | CAGATTAT others(109): Show |
1 | a0001c0001t0007g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.702+3894_702+3895i others(118): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811813 | ||||||
| chr1:169811813 | C | CAGTTTAT others(301): Show |
4 | a0001c0001t0004g0252 a0001c0001t0004g0253 a0001c0001t0004g0254 others(1): Show |
4 | HG02015.hp1 HG02080.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+3886_702+3887i others(310): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811813 | ||||||
| chr1:169811813 | C | T | 47 | a0001c0001t0002g0333 a0001c0001t0004g0001 a0001c0001t0004g0033 others(44): Show |
58 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.702+3884C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811813 | |||||||
| chr1:169811816 | ATTATCTA others(16): Show |
A | 1 | a0001c0001t0002g0053 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.702+3888_702+3910d others(25): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811816 | |||||||
| chr1:169811821 | C | CTAAATAG others(13): Show |
1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3894_702+3895i others(22): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811821 | ||||||
| chr1:169811828 | A | T | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3899A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811828 | |||||||
| chr1:169811829 | A | C | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3900A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811829 | |||||||
| chr1:169811841 | T | TTATC | 50 | a0001c0001t0002g0333 a0001c0001t0004g0001 a0001c0001t0004g0033 others(47): Show |
61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.702+3915_702+3918d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811841 | ||||||
| chr1:169811841 | T | TTATCTAT others(257): Show |
1 | a0001c0001t0004g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.702+3918_702+3919i others(266): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811841 | ||||||
| chr1:169811869 | T | TTAGA | 4 | a0001c0001t0003g0108 a0001c0001t0003g0114 a0001c0001t0003g0124 others(1): Show |
4 | HG02572.hp2 HG03579.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+3961_702+3964d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811869 | ||||||
| chr1:169812100 | G | A | 1 | a0003c0004t0003g0141 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.702+4171G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812100 | |||||||
| chr1:169812150 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+4221A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812150 | |||||||
| chr1:169812384 | G | C | 1 | a0001c0001t0004g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.702+4455G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812384 | |||||||
| chr1:169812400 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0263 |
7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+4471G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812400 | |||||||
| chr1:169812436 | C | G | 1 | a0001c0001t0004g0242 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.702+4507C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812436 | |||||||
| chr1:169812465 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.702+4536T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812465 | |||||||
| chr1:169812528 | A | T | 1 | a0001c0001t0004g0258 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.702+4599A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812528 | |||||||
| chr1:169812547 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0186 |
3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+4618A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812547 | |||||||
| chr1:169812728 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0186 |
3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+4799G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812728 | |||||||
| chr1:169812856 | C | CA | 6 | a0001c0001t0002g0093 a0001c0001t0004g0258 a0001c0002t0001g0279 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+4941dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169812856 | ||||||
| chr1:169812968 | T | G | 30 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(27): Show |
35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+5039T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812968 | |||||||
| chr1:169812972 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+5043A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812972 | |||||||
| chr1:169813048 | C | T | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.702+5119C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813048 | |||||||
| chr1:169813102 | A | G | 26 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(23): Show |
27 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.702+5173A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813102 | |||||||
| chr1:169813265 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.702+5336T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813265 | |||||||
| chr1:169813268 | A | G | 12 | a0001c0001t0002g0315 a0001c0001t0002g0316 a0001c0001t0002g0318 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+5339A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813268 | |||||||
| chr1:169813424 | G | A | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.702+5495G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813424 | |||||||
| chr1:169813451 | C | T | 2 | a0001c0001t0003g0138 a0001c0001t0003g0139 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.702+5522C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813451 | |||||||
| chr1:169813486 | G | A | 3 | a0001c0002t0001g0296 a0001c0002t0001g0297 a0001c0002t0001g0311 |
3 | HG02735.hp2 HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.702+5557G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813486 | |||||||
| chr1:169813706 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.702+5777A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813706 | |||||||
| chr1:169813879 | C | G | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+5950C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813879 | |||||||
| chr1:169813917 | A | T | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.702+5988A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813917 | |||||||
| chr1:169813927 | C | T | 1 | a0004c0005t0001g0160 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.702+5998C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813927 | |||||||
| chr1:169813959 | C | G | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+6030C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813959 | |||||||
| chr1:169814105 | G | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6176G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814105 | |||||||
| chr1:169814403 | T | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6474T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814403 | |||||||
| chr1:169814407 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.702+6478A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814407 | |||||||
| chr1:169814498 | G | A | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.702+6569G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814498 | |||||||
| chr1:169814513 | C | G | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+6584C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814513 | |||||||
| chr1:169814518 | G | A | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+6589G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814518 | |||||||
| chr1:169814599 | A | C | 1 | a0001c0001t0002g0318 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702+6670A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814599 | |||||||
| chr1:169814604 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6675A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814604 | |||||||
| chr1:169814616 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6687A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814616 | |||||||
| chr1:169814639 | C | T | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+6710C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814639 | |||||||
| chr1:169814661 | G | A | 65 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0006g0337 others(62): Show |
67 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.702+6732G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814661 | |||||||
| chr1:169814847 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.703-6832C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814847 | |||||||
| chr1:169815024 | G | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-6655G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815024 | |||||||
| chr1:169815026 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.703-6653G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815026 | |||||||
| chr1:169815206 | G | A | 1 | a0001c0001t0004g0236 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.703-6473G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815206 | |||||||
| chr1:169815251 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.703-6428G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815251 | |||||||
| chr1:169815252 | C | T | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.703-6427C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815252 | |||||||
| chr1:169815295 | C | CA | 16 | a0001c0001t0002g0093 a0002c0003t0005g0039 a0002c0003t0005g0346 others(13): Show |
16 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-6370dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169815295 | ||||||
| chr1:169815422 | C | G | 30 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(27): Show |
35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.703-6257C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815422 | |||||||
| chr1:169815562 | A | T | 1 | a0001c0001t0002g0093 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.703-6117A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815562 | |||||||
| chr1:169815563 | T | A | 1 | a0001c0001t0002g0093 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.703-6116T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815563 | |||||||
| chr1:169815593 | C | T | 2 | a0001c0001t0002g0325 a0001c0001t0002g0326 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.703-6086C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815593 | |||||||
| chr1:169815697 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.703-5982T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815697 | |||||||
| chr1:169815739 | A | C | 51 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(48): Show |
62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.703-5940A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815739 | |||||||
| chr1:169815933 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-5746A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815933 | |||||||
| chr1:169816074 | A | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-5605A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816074 | |||||||
| chr1:169816133 | A | T | 51 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(48): Show |
62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.703-5546A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816133 | |||||||
| chr1:169816204 | CT | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.703-5474delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816204 | |||||||
| chr1:169816363 | A | T | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-5316A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816363 | |||||||
| chr1:169816437 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703-5242A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816437 | |||||||
| chr1:169816446 | TTCTC | T | 5 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0001t0002g0327 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-5228_703-5225d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169816446 | ||||||
| chr1:169816793 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.703-4886A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816793 | |||||||
| chr1:169817022 | A | G | 50 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(47): Show |
61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.703-4657A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817022 | |||||||
| chr1:169817096 | A | C | 2 | a0001c0002t0001g0292 a0001c0002t0001g0293 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.703-4583A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817096 | |||||||
| chr1:169817163 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-4516A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817163 | |||||||
| chr1:169817206 | T | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-4473T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817206 | |||||||
| chr1:169817337 | C | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
88 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.703-4342C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817337 | |||||||
| chr1:169817380 | C | T | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-4299C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817380 | |||||||
| chr1:169817386 | T | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-4293T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817386 | |||||||
| chr1:169817776 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.703-3903T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817776 | |||||||
| chr1:169817781 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.703-3898A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817781 | |||||||
| chr1:169817891 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.703-3788G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817891 | |||||||
| chr1:169817951 | A | AT | 256 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(253): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.703-3717dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169817951 | ||||||
| chr1:169818067 | C | T | 51 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(48): Show |
62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.703-3612C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818067 | |||||||
| chr1:169818306 | A | G | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.703-3373A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818306 | |||||||
| chr1:169818388 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.703-3291G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818388 | |||||||
| chr1:169818449 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-3230G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818449 | |||||||
| chr1:169818480 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.703-3199A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818480 | |||||||
| chr1:169818730 | A | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0019 |
4 | HG00673.hp2 NA18950.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-2949A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818730 | |||||||
| chr1:169818743 | A | G | 2 | a0001c0001t0004g0034 a0001c0001t0004g0247 |
3 | NA18612.hp1 NA18963.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.703-2936A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818743 | |||||||
| chr1:169818764 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-2915G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818764 | |||||||
| chr1:169818793 | T | A | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2886T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818793 | |||||||
| chr1:169818912 | C | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-2767C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818912 | |||||||
| chr1:169819058 | C | T | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.703-2621C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819058 | |||||||
| chr1:169819060 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0263 |
7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-2619G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819060 | |||||||
| chr1:169819121 | G | A | 1 | a0001c0001t0004g0237 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.703-2558G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819121 | |||||||
| chr1:169819168 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-2511A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819168 | |||||||
| chr1:169819184 | A | G | 1 | a0001c0001t0003g0114 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.703-2495A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819184 | |||||||
| chr1:169819266 | G | T | 1 | a0001c0002t0001g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703-2413G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819266 | |||||||
| chr1:169819282 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.703-2397G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819282 | |||||||
| chr1:169819311 | C | T | 3 | a0001c0001t0002g0327 a0001c0001t0002g0328 a0001c0001t0002g0336 |
3 | HG01109.hp2 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.703-2368C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819311 | |||||||
| chr1:169819373 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.703-2306C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819373 | |||||||
| chr1:169819424 | A | T | 1 | a0006c0010t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.703-2255A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819424 | |||||||
| chr1:169819443 | T | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-2236T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819443 | |||||||
| chr1:169819613 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.703-2066C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819613 | |||||||
| chr1:169819695 | C | T | 59 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(56): Show |
60 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.703-1984C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819695 | |||||||
| chr1:169819702 | AC | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.703-1974delC | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169819702 | ||||||
| chr1:169819705 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-1974C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819705 | |||||||
| chr1:169819718 | G | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-1961G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819718 | |||||||
| chr1:169819720 | C | T | 1 | a0001c0001t0002g0336 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703-1959C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819720 | |||||||
| chr1:169819740 | C | T | 44 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(41): Show |
54 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.703-1939C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819740 | |||||||
| chr1:169819873 | G | GC | 9 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0017 others(6): Show |
13 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-1804dupC | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169819873 | ||||||
| chr1:169819887 | G | A | 1 | a0001c0001t0009g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.703-1792G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819887 | |||||||
| chr1:169819899 | A | G | 1 | a0001c0001t0019g0144 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.703-1780A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819899 | |||||||
| chr1:169820001 | G | C | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-1678G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820001 | |||||||
| chr1:169820008 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(52): Show |
65 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.703-1671A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820008 | |||||||
| chr1:169820195 | A | G | 2 | a0001c0001t0006g0013 a0001c0001t0006g0219 |
4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-1484A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820195 | |||||||
| chr1:169820321 | G | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-1358G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820321 | |||||||
| chr1:169820373 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.703-1306G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820373 | |||||||
| chr1:169820483 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.703-1196C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820483 | |||||||
| chr1:169820563 | A | G | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1116A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820563 | |||||||
| chr1:169820625 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.703-1054G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820625 | |||||||
| chr1:169820637 | C | T | 1 | a0004c0005t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.703-1042C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820637 | |||||||
| chr1:169820698 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.703-981A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820698 | |||||||
| chr1:169820743 | C | T | 14 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0271 others(11): Show |
14 | NA18940.hp2 NA18959.hp1 NA18979.hp2 others(11): Show |
intron_variant | MODIFIER | c.703-936C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820743 | |||||||
| chr1:169821020 | T | G | 56 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0023 others(53): Show |
62 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-659T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821020 | |||||||
| chr1:169821194 | G | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-485G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821194 | |||||||
| chr1:169821210 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.703-469A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821210 | |||||||
| chr1:169821260 | T | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-419T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821260 | |||||||
| chr1:169821404 | A | G | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.703-275A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821404 | |||||||
| chr1:169821404 | A | T | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-275A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821404 | |||||||
| chr1:169821451 | C | G | 2 | a0001c0001t0002g0321 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.703-228C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821451 | |||||||
| chr1:169821527 | G | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-152G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821527 | |||||||
| chr1:169822073 | A | G | 2 | a0001c0001t0006g0013 a0001c0001t0006g0219 |
4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+314A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822073 | |||||||
| chr1:169822121 | G | A | 1 | a0001c0001t0002g0015 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.783+362G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822121 | |||||||
| chr1:169822190 | C | T | 26 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(23): Show |
27 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.783+431C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822190 | |||||||
| chr1:169822191 | C | G | 1 | a0001c0001t0003g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.783+432C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822191 | |||||||
| chr1:169822192 | C | T | 14 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0271 others(11): Show |
14 | NA18940.hp2 NA18959.hp1 NA18979.hp2 others(11): Show |
intron_variant | MODIFIER | c.783+433C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822192 | |||||||
| chr1:169822246 | G | A | 2 | a0001c0001t0002g0325 a0001c0001t0002g0326 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.783+487G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822246 | |||||||
| chr1:169822685 | A | G | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.784-723A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822685 | |||||||
| chr1:169822796 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0186 |
3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.784-612G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822796 | |||||||
| chr1:169822846 | C | T | 1 | a0001c0002t0001g0312 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.784-562C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822846 | |||||||
| chr1:169822897 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.784-511T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822897 | |||||||
| chr1:169823049 | C | T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0050 others(6): Show |
14 | NA18941.hp2 NA18945.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.784-359C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823049 | |||||||
| chr1:169823156 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-252C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823156 | |||||||
| chr1:169823190 | T | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.784-218T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823190 | |||||||
| chr1:169823284 | C | A | 1 | a0001c0001t0002g0072 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.784-124C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823284 | |||||||
| chr1:169823322 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0186 |
3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.784-86A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823322 | |||||||
| chr1:169823501 | A | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+29A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823501 | |||||||
| chr1:169823551 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+79T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823551 | |||||||
| chr1:169823692 | T | TAATA | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+222_848+225dup others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169823692 | ||||||
| chr1:169823749 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.848+277A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823749 | |||||||
| chr1:169823752 | CG | C | 29 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(26): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.848+281delG | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823752 | |||||||
| chr1:169823961 | A | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+489A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823961 | |||||||
| chr1:169824061 | A | G | 3 | a0001c0001t0003g0102 a0001c0001t0003g0124 a0001c0001t0003g0125 |
3 | NA18964.hp1 NA18974.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.848+589A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824061 | |||||||
| chr1:169824107 | A | G | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.848+635A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824107 | |||||||
| chr1:169824158 | GA | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+691delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169824158 | ||||||
| chr1:169824170 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+698C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824170 | |||||||
| chr1:169824272 | C | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0029 others(9): Show |
18 | HG01192.hp1 HG02015.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.848+800C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824272 | |||||||
| chr1:169824274 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0186 a0001c0001t0001g0200 |
4 | HG02818.hp2 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+802A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824274 | |||||||
| chr1:169824446 | A | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+974A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824446 | |||||||
| chr1:169824495 | C | T | 1 | a0001c0001t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.848+1023C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824495 | |||||||
| chr1:169824716 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+1244G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824716 | |||||||
| chr1:169824725 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+1253G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824725 | |||||||
| chr1:169824774 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+1302C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824774 | |||||||
| chr1:169824884 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.848+1412C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824884 | |||||||
| chr1:169824931 | A | G | 1 | a0001c0002t0001g0282 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.848+1459A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824931 | |||||||
| chr1:169824942 | T | A | 1 | a0001c0001t0002g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.848+1470T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824942 | |||||||
| chr1:169825196 | C | T | 2 | a0001c0001t0003g0137 a0001c0001t0003g0146 |
2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.848+1724C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825196 | |||||||
| chr1:169825218 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.848+1746A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825218 | |||||||
| chr1:169825357 | C | T | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.849-1694C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825357 | |||||||
| chr1:169825364 | A | G | 1 | a0002c0003t0005g0354 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.849-1687A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825364 | |||||||
| chr1:169825547 | T | C | 55 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0023 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.849-1504T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825547 | |||||||
| chr1:169825567 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849-1484A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825567 | |||||||
| chr1:169825641 | T | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.849-1410T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825641 | |||||||
| chr1:169825721 | A | T | 55 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0023 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.849-1330A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825721 | |||||||
| chr1:169825781 | A | C | 1 | a0001c0001t0002g0046 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.849-1270A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825781 | |||||||
| chr1:169825989 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-1062A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825989 | |||||||
| chr1:169826064 | T | A | 7 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0053 others(4): Show |
9 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-987T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826064 | |||||||
| chr1:169826073 | CT | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.849-969delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826073 | ||||||
| chr1:169826074 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.849-977T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826074 | |||||||
| chr1:169826103 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.849-948G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826103 | |||||||
| chr1:169826112 | G | C | 1 | a0001c0001t0002g0328 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.849-939G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826112 | |||||||
| chr1:169826135 | A | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.849-916A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826135 | |||||||
| chr1:169826180 | C | A | 1 | a0001c0001t0002g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.849-871C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826180 | |||||||
| chr1:169826189 | C | G | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-862C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826189 | |||||||
| chr1:169826260 | C | T | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.849-791C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826260 | |||||||
| chr1:169826305 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-746C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826305 | |||||||
| chr1:169826338 | C | A | 2 | a0001c0001t0003g0107 a0001c0001t0003g0108 |
2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.849-713C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826338 | |||||||
| chr1:169826342 | C | T | 1 | a0001c0001t0003g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.849-709C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826342 | |||||||
| chr1:169826343 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-708G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826343 | |||||||
| chr1:169826358 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.849-693C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826358 | |||||||
| chr1:169826362 | A | AT | 279 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(276): Show |
317 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.849-673dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826362 | ||||||
| chr1:169826362 | A | ATT | 9 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0218 others(6): Show |
9 | HG02055.hp2 HG02074.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.849-674_849-673dup others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826362 | ||||||
| chr1:169826401 | C | T | 2 | a0001c0002t0001g0292 a0001c0002t0001g0293 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849-650C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826401 | |||||||
| chr1:169826414 | G | A | 7 | a0003c0004t0003g0022 a0003c0004t0003g0128 a0003c0004t0003g0141 others(4): Show |
8 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.849-637G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826414 | |||||||
| chr1:169826487 | C | T | 1 | a0001c0001t0002g0331 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.849-564C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826487 | |||||||
| chr1:169826500 | T | A | 2 | a0004c0005t0001g0157 a0004c0005t0001g0161 |
2 | HG00423.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.849-551T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826500 | |||||||
| chr1:169826659 | C | T | 4 | a0001c0001t0003g0102 a0001c0001t0003g0124 a0001c0001t0003g0125 others(1): Show |
4 | NA18964.hp1 NA18974.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.849-392C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826659 | |||||||
| chr1:169826854 | TGTTTA | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-190_849-186del others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826854 | ||||||
| chr1:169827275 | T | C | 1 | a0004c0005t0001g0157 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.997+76T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827275 | |||||||
| chr1:169827400 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.997+201G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827400 | |||||||
| chr1:169827410 | G | C | 1 | a0001c0001t0004g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.997+211G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827410 | |||||||
| chr1:169827463 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.998-248C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827463 | |||||||
| chr1:169827555 | T | G | 3 | a0001c0001t0002g0327 a0001c0001t0002g0328 a0001c0001t0002g0336 |
3 | HG01109.hp2 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.998-156T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827555 | |||||||
| chr1:169827666 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.998-45T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827666 | |||||||
| chr1:169827688 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.998-23A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827688 | |||||||
| chr1:169827926 | G | GT | 5 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0153 others(2): Show |
6 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1127+96dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr1 | 169827926 | ||||||
| chr1:169827965 | G | A | 2 | a0001c0001t0007g0153 a0001c0001t0007g0154 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1127+125G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169827965 | |||||||
| chr1:169827980 | T | C | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+140T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169827980 | |||||||
| chr1:169827986 | G | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1127+146G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169827986 | |||||||
| chr1:169828138 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1127+298C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828138 | |||||||
| chr1:169828139 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+299G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828139 | |||||||
| chr1:169828163 | A | G | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1127+323A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828163 | |||||||
| chr1:169828254 | A | C | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1127+414A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828254 | |||||||
| chr1:169828281 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0263 |
7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1127+441C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828281 | |||||||
| chr1:169828371 | T | G | 59 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(56): Show |
60 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1127+531T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828371 | |||||||
| chr1:169828409 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1127+569A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828409 | |||||||
| chr1:169828522 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1127+682A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828522 | |||||||
| chr1:169828623 | A | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1128-640A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828623 | |||||||
| chr1:169828749 | A | G | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-514A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828749 | |||||||
| chr1:169828781 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1128-482A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828781 | |||||||
| chr1:169828793 | G | A | 4 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0115 others(1): Show |
4 | NA18985.hp1 NA18985.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-470G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828793 | |||||||
| chr1:169828815 | G | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1128-448G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828815 | |||||||
| chr1:169828883 | C | CT | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1128-379dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr1 | 169828883 | ||||||
| chr1:169828894 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1128-369C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828894 | |||||||
| chr1:169829591 | G | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1314+142G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | chr1 | 169829591 | |||||||
| chr1:169829604 | C | G | 29 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(26): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1314+155C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | chr1 | 169829604 | |||||||
| chr1:169829928 | AAG | A | 5 | a0002c0003t0005g0349 a0002c0003t0005g0351 a0002c0003t0005g0352 others(2): Show |
5 | HG00741.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-328_1315-327d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr1 | 169829928 | ||||||
| chr1:169830074 | A | G | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-185A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | chr1 | 169830074 | |||||||
| chr1:169830431 | C | CTA | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1397+91_1397+92ins others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr1 | 169830431 | ||||||
| chr1:169830688 | T | C | 2 | a0001c0001t0003g0132 a0001c0001t0003g0142 |
2 | HG03831.hp2 HG06807.hp2 |
splice_region_variant&intron_variant | LOW | c.1398-8T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 15/24 | chr1 | 169830688 | |||||||
| chr1:169830689 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.1398-7A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 15/24 | chr1 | 169830689 | |||||||
| chr1:169830820 | A | G | 1 | a0001c0002t0001g0312 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1449+73A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830820 | |||||||
| chr1:169830838 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1449+91G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830838 | |||||||
| chr1:169830860 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1449+113G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830860 | |||||||
| chr1:169830921 | C | T | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1449+174C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830921 | |||||||
| chr1:169830949 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449+202C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830949 | |||||||
| chr1:169830979 | A | C | 2 | a0001c0002t0001g0334 a0001c0002t0001g0335 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1449+232A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830979 | |||||||
| chr1:169831013 | A | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449+266A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831013 | |||||||
| chr1:169831164 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1449+417G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831164 | |||||||
| chr1:169831259 | A | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1449+512A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831259 | |||||||
| chr1:169831272 | C | A | 4 | a0001c0001t0002g0329 a0001c0001t0002g0330 a0001c0001t0002g0331 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+525C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831272 | |||||||
| chr1:169831294 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1449+547A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831294 | |||||||
| chr1:169831549 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449+802A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831549 | |||||||
| chr1:169831604 | T | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1450-813T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831604 | |||||||
| chr1:169831621 | A | T | 1 | a0001c0001t0010g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1450-796A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831621 | |||||||
| chr1:169831877 | C | G | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1450-540C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831877 | |||||||
| chr1:169832025 | C | T | 1 | a0001c0001t0002g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1450-392C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832025 | |||||||
| chr1:169832038 | T | G | 1 | a0001c0001t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1450-379T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832038 | |||||||
| chr1:169832080 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1450-337G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832080 | |||||||
| chr1:169832238 | A | G | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1450-179A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832238 | |||||||
| chr1:169832633 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0263 |
7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+127C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832633 | |||||||
| chr1:169832634 | G | A | 1 | a0001c0001t0004g0238 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1539+128G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832634 | |||||||
| chr1:169832839 | C | T | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+333C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832839 | |||||||
| chr1:169832971 | G | A | 29 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(26): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1539+465G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832971 | |||||||
| chr1:169833340 | G | C | 1 | a0001c0001t0008g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1539+834G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833340 | |||||||
| chr1:169833370 | C | T | 10 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1539+864C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833370 | |||||||
| chr1:169833396 | G | A | 1 | a0002c0003t0005g0355 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1539+890G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833396 | |||||||
| chr1:169833619 | G | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1539+1113G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833619 | |||||||
| chr1:169833707 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0181 a0001c0001t0001g0188 others(3): Show |
7 | HG01168.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+1201G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833707 | |||||||
| chr1:169833737 | C | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1539+1231C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833737 | |||||||
| chr1:169833757 | A | G | 1 | a0001c0001t0002g0093 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1539+1251A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833757 | |||||||
| chr1:169833760 | A | G | 7 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0053 others(4): Show |
9 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1539+1254A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833760 | |||||||
| chr1:169833773 | C | G | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1539+1267C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833773 | |||||||
| chr1:169833781 | CT | C | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+1277delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833781 | ||||||
| chr1:169833807 | A | C | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1539+1301A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833807 | |||||||
| chr1:169833815 | C | G | 55 | a0001c0001t0001g0178 a0001c0001t0003g0020 a0001c0001t0003g0021 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1539+1309C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833815 | |||||||
| chr1:169833846 | C | CT | 19 | a0001c0001t0002g0080 a0001c0001t0002g0096 a0001c0001t0002g0315 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1539+1365dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | ||||||
| chr1:169833846 | C | CTTT | 40 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(37): Show |
41 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1539+1363_1539+136 others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | ||||||
| chr1:169833846 | C | CTTTT | 7 | a0001c0002t0001g0271 a0001c0002t0001g0275 a0001c0002t0001g0278 others(4): Show |
7 | HG01169.hp2 HG03831.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+1362_1539+136 others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | ||||||
| chr1:169833846 | CT | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1539+1365delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | ||||||
| chr1:169833846 | CTT | C | 21 | a0001c0001t0001g0189 a0001c0001t0001g0205 a0001c0001t0003g0104 others(18): Show |
21 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1539+1364_1539+136 others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | ||||||
| chr1:169833846 | CTTT | C | 50 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(47): Show |
61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1539+1363_1539+136 others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | ||||||
| chr1:169833846 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0011g0029 |
3 | HG02015.hp2 HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1539+1351_1539+136 others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | ||||||
| chr1:169833928 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1539+1422C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833928 | |||||||
| chr1:169833978 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0164 others(3): Show |
11 | HG00323.hp2 HG00741.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1539+1472A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833978 | |||||||
| chr1:169834076 | T | C | 1 | a0001c0002t0001g0296 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1539+1570T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834076 | |||||||
| chr1:169834266 | A | C | 1 | a0001c0001t0007g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1539+1760A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834266 | |||||||
| chr1:169834443 | C | T | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1539+1937C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834443 | |||||||
| chr1:169834473 | C | CT | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
88 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1539+1975dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169834473 | ||||||
| chr1:169834549 | A | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1539+2043A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834549 | |||||||
| chr1:169834576 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1539+2070C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834576 | |||||||
| chr1:169834640 | C | T | 1 | a0001c0001t0006g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1539+2134C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834640 | |||||||
| chr1:169834743 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0151 |
3 | HG02559.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1540-2184C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834743 | |||||||
| chr1:169834982 | A | G | 1 | a0001c0001t0017g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1540-1945A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834982 | |||||||
| chr1:169835014 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1540-1913G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835014 | |||||||
| chr1:169835221 | G | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1540-1706G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835221 | |||||||
| chr1:169835258 | A | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540-1669A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835258 | |||||||
| chr1:169835338 | C | G | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-1589C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835338 | |||||||
| chr1:169835485 | A | C | 2 | a0001c0001t0003g0024 a0001c0001t0003g0140 |
3 | HG01081.hp2 HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1540-1442A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835485 | |||||||
| chr1:169835579 | T | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1540-1348T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835579 | |||||||
| chr1:169835611 | A | G | 2 | a0001c0001t0003g0135 a0001c0001t0003g0136 |
2 | HG00642.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1540-1316A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835611 | |||||||
| chr1:169835745 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1540-1182A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835745 | |||||||
| chr1:169835980 | A | G | 3 | a0001c0001t0010g0032 a0001c0001t0010g0223 a0001c0001t0010g0230 |
4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-947A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835980 | |||||||
| chr1:169836053 | AT | A | 60 | a0001c0001t0002g0057 a0001c0001t0002g0321 a0001c0001t0002g0333 others(57): Show |
67 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1540-856delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169836053 | ||||||
| chr1:169836053 | ATT | A | 115 | a0001c0001t0002g0322 a0001c0001t0004g0001 a0001c0001t0004g0033 others(112): Show |
127 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.1540-857_1540-856d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169836053 | ||||||
| chr1:169836053 | ATTT | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
114 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1540-858_1540-856d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169836053 | ||||||
| chr1:169836161 | C | T | 1 | a0001c0001t0004g0258 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1540-766C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836161 | |||||||
| chr1:169836225 | C | T | 55 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0023 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1540-702C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836225 | |||||||
| chr1:169836228 | T | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0201 others(6): Show |
11 | HG02015.hp2 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1540-699T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836228 | |||||||
| chr1:169836347 | G | C | 1 | a0003c0004t0003g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1540-580G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836347 | |||||||
| chr1:169836392 | C | G | 1 | a0001c0001t0009g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1540-535C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836392 | |||||||
| chr1:169836408 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1540-519T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836408 | |||||||
| chr1:169836422 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0195 a0001c0001t0001g0214 others(2): Show |
6 | HG02735.hp1 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-505C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836422 | |||||||
| chr1:169836570 | T | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1540-357T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836570 | |||||||
| chr1:169836641 | T | A | 1 | a0001c0001t0003g0134 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1540-286T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836641 | |||||||
| chr1:169836794 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1540-133G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836794 | |||||||
| chr1:169836825 | C | G | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1540-102C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836825 | |||||||
| chr1:169836924 | C | T | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.1540-3C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836924 | |||||||
| chr1:169837313 | T | C | 1 | a0004c0005t0001g0158 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1725+201T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837313 | |||||||
| chr1:169837395 | G | T | 4 | a0001c0001t0003g0130 a0001c0001t0003g0137 a0001c0001t0003g0146 others(1): Show |
4 | HG00140.hp2 HG01175.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+283G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837395 | |||||||
| chr1:169837448 | A | G | 1 | a0001c0001t0004g0242 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1725+336A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837448 | |||||||
| chr1:169837487 | C | G | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1725+375C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837487 | |||||||
| chr1:169837752 | A | G | 1 | a0001c0002t0001g0314 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1725+640A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837752 | |||||||
| chr1:169837803 | G | C | 2 | a0001c0001t0004g0239 a0001c0001t0004g0240 |
2 | HG00423.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1725+691G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837803 | |||||||
| chr1:169837931 | C | G | 16 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0018 others(13): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1725+819C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837931 | |||||||
| chr1:169837939 | T | C | 9 | a0001c0001t0002g0018 a0001c0001t0002g0049 a0001c0001t0002g0057 others(6): Show |
10 | HG00597.hp1 HG00609.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.1725+827T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837939 | |||||||
| chr1:169837954 | G | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1725+842G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837954 | |||||||
| chr1:169837968 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1725+856G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837968 | |||||||
| chr1:169838031 | G | A | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1725+919G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838031 | |||||||
| chr1:169838117 | T | A | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+1005T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838117 | |||||||
| chr1:169838228 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1725+1116T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838228 | |||||||
| chr1:169838351 | T | C | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1725+1239T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838351 | |||||||
| chr1:169838459 | C | A | 1 | a0001c0001t0003g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1725+1347C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838459 | |||||||
| chr1:169838480 | T | C | 30 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(27): Show |
35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1725+1368T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838480 | |||||||
| chr1:169838490 | T | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1725+1378T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838490 | |||||||
| chr1:169838538 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1725+1426A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838538 | |||||||
| chr1:169838559 | G | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1725+1447G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838559 | |||||||
| chr1:169838608 | G | A | 16 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0018 others(13): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1725+1496G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838608 | |||||||
| chr1:169838720 | C | T | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1725+1608C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838720 | |||||||
| chr1:169838848 | C | T | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1725+1736C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838848 | |||||||
| chr1:169838928 | C | CATCT | 4 | a0001c0001t0002g0329 a0001c0001t0002g0330 a0001c0001t0002g0331 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+1817_1725+182 others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169838928 | ||||||
| chr1:169839020 | G | A | 2 | a0001c0001t0008g0208 a0001c0001t0008g0209 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1725+1908G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839020 | |||||||
| chr1:169839259 | C | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1725+2147C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839259 | |||||||
| chr1:169839510 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1725+2398C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839510 | |||||||
| chr1:169839528 | G | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1725+2416G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839528 | |||||||
| chr1:169839617 | A | G | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18981.hp2 NA18991.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1725+2505A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839617 | |||||||
| chr1:169839794 | T | C | 1 | a0001c0001t0004g0235 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1726-2623T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839794 | |||||||
| chr1:169839825 | C | T | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1726-2592C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839825 | |||||||
| chr1:169839897 | T | A | 1 | a0001c0002t0001g0277 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1726-2520T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839897 | |||||||
| chr1:169839990 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-2427T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839990 | |||||||
| chr1:169840040 | T | C | 2 | a0001c0002t0001g0298 a0001c0002t0001g0299 |
2 | NA18983.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1726-2377T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840040 | |||||||
| chr1:169840128 | TTATAG | T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-2282_1726-227 others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169840128 | ||||||
| chr1:169840144 | A | G | 1 | a0003c0004t0003g0025 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1726-2273A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840144 | |||||||
| chr1:169840192 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1726-2225C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840192 | |||||||
| chr1:169840335 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-2082C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840335 | |||||||
| chr1:169840389 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1726-2028A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840389 | |||||||
| chr1:169840439 | C | G | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1726-1978C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840439 | |||||||
| chr1:169840445 | G | T | 1 | a0001c0001t0015g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1726-1972G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840445 | |||||||
| chr1:169840461 | A | T | 1 | a0001c0001t0003g0110 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1726-1956A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840461 | |||||||
| chr1:169840472 | T | C | 65 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0006g0337 others(62): Show |
67 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1726-1945T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840472 | |||||||
| chr1:169840475 | A | T | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1726-1942A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840475 | |||||||
| chr1:169840511 | C | CT | 24 | a0001c0001t0001g0204 a0001c0001t0002g0327 a0001c0001t0002g0328 others(21): Show |
25 | HG00741.hp1 HG01109.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1726-1892dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169840511 | ||||||
| chr1:169840533 | C | T | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1726-1884C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840533 | |||||||
| chr1:169840542 | G | A | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(49): Show |
61 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1726-1875G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840542 | |||||||
| chr1:169840542 | G | T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-1875G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840542 | |||||||
| chr1:169840543 | C | T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-1874C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840543 | |||||||
| chr1:169840632 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1726-1785T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840632 | |||||||
| chr1:169840660 | G | A | 3 | a0001c0001t0003g0137 a0001c0001t0003g0146 a0001c0001t0019g0144 |
3 | HG00140.hp2 HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1726-1757G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840660 | |||||||
| chr1:169840667 | C | T | 1 | a0001c0001t0009g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1726-1750C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840667 | |||||||
| chr1:169840700 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1726-1717T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840700 | |||||||
| chr1:169840731 | C | T | 2 | a0001c0001t0004g0221 a0001c0001t0004g0222 |
2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1726-1686C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840731 | |||||||
| chr1:169840751 | C | G | 2 | a0001c0001t0007g0152 a0001c0001t0007g0155 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1726-1666C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840751 | |||||||
| chr1:169840772 | A | G | 1 | a0001c0001t0015g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1726-1645A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840772 | |||||||
| chr1:169840773 | G | T | 1 | a0001c0001t0015g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1726-1644G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840773 | |||||||
| chr1:169840802 | G | A | 253 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1726-1615G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840802 | |||||||
| chr1:169840833 | G | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-1584G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840833 | |||||||
| chr1:169840933 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-1484T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840933 | |||||||
| chr1:169841027 | C | T | 4 | a0002c0003t0005g0039 a0002c0003t0005g0348 a0002c0003t0005g0357 others(1): Show |
4 | HG02074.hp1 HG02523.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-1390C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841027 | |||||||
| chr1:169841028 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-1389A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841028 | |||||||
| chr1:169841040 | G | T | 3 | a0001c0001t0010g0032 a0001c0001t0010g0223 a0001c0001t0010g0230 |
4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-1377G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841040 | |||||||
| chr1:169841342 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1726-1075T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841342 | |||||||
| chr1:169841459 | G | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-958G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841459 | |||||||
| chr1:169841745 | C | T | 1 | a0006c0010t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1726-672C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841745 | |||||||
| chr1:169842069 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0067 |
2 | HG02257.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1726-348G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842069 | |||||||
| chr1:169842124 | C | T | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1726-293C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842124 | |||||||
| chr1:169842166 | T | C | 5 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0001t0002g0327 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-251T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842166 | |||||||
| chr1:169842174 | C | CA | 18 | a0001c0001t0002g0080 a0001c0001t0004g0262 a0002c0003t0005g0039 others(15): Show |
18 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1726-228dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169842174 | ||||||
| chr1:169842358 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1726-59C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842358 | |||||||
| chr1:169842701 | T | A | 1 | a0001c0001t0015g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1848+162T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842701 | |||||||
| chr1:169842736 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1848+197C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842736 | |||||||
| chr1:169842799 | A | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1848+260A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842799 | |||||||
| chr1:169842825 | T | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1848+286T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842825 | |||||||
| chr1:169842855 | T | A | 2 | a0001c0001t0004g0256 a0001c0001t0004g0258 |
2 | NA18989.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1848+316T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842855 | |||||||
| chr1:169842887 | T | C | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+348T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842887 | |||||||
| chr1:169843090 | T | C | 3 | a0001c0001t0002g0327 a0001c0001t0002g0328 a0001c0001t0002g0336 |
3 | HG01109.hp2 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1848+551T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843090 | |||||||
| chr1:169843122 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1849-552A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843122 | |||||||
| chr1:169843186 | A | G | 1 | a0001c0002t0013g0270 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1849-488A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843186 | |||||||
| chr1:169843260 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0196 |
2 | NA18950.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1849-414T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843260 | |||||||
| chr1:169843287 | T | G | 1 | a0001c0001t0010g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1849-387T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843287 | |||||||
| chr1:169843393 | C | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1849-281C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843393 | |||||||
| chr1:169843442 | T | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1849-232T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843442 | |||||||
| chr1:169843471 | A | G | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849-203A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843471 | |||||||
| chr1:169843524 | C | T | 2 | a0001c0001t0004g0224 a0001c0001t0004g0232 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1849-150C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843524 | |||||||
| chr1:169843575 | A | G | 2 | a0002c0003t0005g0347 a0002c0003t0005g0350 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1849-99A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843575 | |||||||
| chr1:169843624 | ATTC | A | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1849-47_1849-45del others(3): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr1 | 169843624 | ||||||
| chr1:169843778 | A | G | 4 | a0001c0002t0001g0276 a0001c0002t0001g0285 a0001c0002t0001g0286 others(1): Show |
4 | HG00597.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944+9A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169843778 | |||||||
| chr1:169843797 | T | C | 1 | a0001c0002t0001g0301 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1944+28T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169843797 | |||||||
| chr1:169844048 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1944+279A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844048 | |||||||
| chr1:169844205 | G | A | 2 | a0001c0002t0001g0334 a0001c0002t0001g0335 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1944+436G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844205 | |||||||
| chr1:169844212 | T | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1944+443T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844212 | |||||||
| chr1:169844228 | A | G | 6 | a0001c0001t0004g0228 a0001c0001t0004g0242 a0001c0001t0004g0252 others(3): Show |
6 | HG02015.hp1 HG02080.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944+459A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844228 | |||||||
| chr1:169844246 | A | G | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1944+477A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844246 | |||||||
| chr1:169844505 | G | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1944+736G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844505 | |||||||
| chr1:169844619 | A | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1944+850A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844619 | |||||||
| chr1:169844631 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1944+862A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844631 | |||||||
| chr1:169844850 | G | A | 5 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944+1081G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844850 | |||||||
| chr1:169844887 | A | C | 1 | a0001c0002t0001g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1944+1118A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844887 | |||||||
| chr1:169844920 | T | C | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944+1151T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844920 | |||||||
| chr1:169845219 | A | G | 1 | a0001c0001t0009g0210 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1944+1450A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845219 | |||||||
| chr1:169845392 | C | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1944+1623C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845392 | |||||||
| chr1:169845407 | A | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1944+1638A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845407 | |||||||
| chr1:169845591 | G | A | 5 | a0001c0001t0006g0337 a0001c0001t0006g0338 a0001c0001t0006g0339 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944+1822G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845591 | |||||||
| chr1:169845687 | C | CTTCCA | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1944+1921_1944+192 others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169845687 | ||||||
| chr1:169845689 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1944+1920T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845689 | |||||||
| chr1:169845931 | C | T | 284 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1945-1759C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845931 | |||||||
| chr1:169846101 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1945-1589T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846101 | |||||||
| chr1:169846107 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0186 |
3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1945-1583T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846107 | |||||||
| chr1:169846120 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1945-1570C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846120 | |||||||
| chr1:169846219 | A | G | 4 | a0001c0001t0002g0329 a0001c0001t0002g0330 a0001c0001t0002g0331 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945-1471A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846219 | |||||||
| chr1:169846231 | A | G | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 |
3 | HG03491.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1945-1459A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846231 | |||||||
| chr1:169846670 | C | T | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1945-1020C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846670 | |||||||
| chr1:169846971 | G | A | 9 | a0001c0001t0003g0102 a0001c0001t0003g0106 a0001c0001t0003g0109 others(6): Show |
9 | HG00544.hp1 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.1945-719G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846971 | |||||||
| chr1:169847032 | C | T | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-658C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847032 | |||||||
| chr1:169847041 | G | T | 29 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(26): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1945-649G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847041 | |||||||
| chr1:169847060 | T | C | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-630T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847060 | |||||||
| chr1:169847163 | A | G | 54 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0023 others(51): Show |
60 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1945-527A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847163 | |||||||
| chr1:169847176 | G | A | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1945-514G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847176 | |||||||
| chr1:169847234 | C | A | 1 | a0001c0001t0002g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1945-456C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847234 | |||||||
| chr1:169847290 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1945-400A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847290 | |||||||
| chr1:169847313 | T | TA | 6 | a0001c0001t0002g0060 a0001c0001t0002g0068 a0001c0001t0002g0076 others(3): Show |
6 | HG00597.hp1 HG02647.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945-350dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | ||||||
| chr1:169847313 | TA | T | 6 | a0001c0001t0001g0172 a0001c0001t0002g0045 a0001c0001t0002g0047 others(3): Show |
6 | HG01515.hp2 HG01975.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945-350delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | ||||||
| chr1:169847313 | TAAA | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(53): Show |
66 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1945-352_1945-350d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | ||||||
| chr1:169847313 | TAAAA | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0029 others(71): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1945-353_1945-350d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | ||||||
| chr1:169847313 | TAAAAA | T | 112 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0003g0020 others(109): Show |
120 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1945-354_1945-350d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | ||||||
| chr1:169847313 | TAAAAAA | T | 23 | a0001c0001t0003g0127 a0001c0001t0009g0210 a0001c0001t0009g0211 others(20): Show |
23 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1945-355_1945-350d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | ||||||
| chr1:169847317 | A | T | 2 | a0001c0001t0008g0030 a0001c0001t0008g0207 |
3 | HG01884.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1945-373A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847317 | |||||||
| chr1:169847318 | A | T | 2 | a0001c0001t0008g0208 a0001c0001t0008g0209 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1945-372A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847318 | |||||||
| chr1:169847340 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1945-350A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847340 | |||||||
| chr1:169847484 | G | A | 2 | a0001c0001t0003g0145 a0001c0001t0003g0147 |
2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1945-206G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847484 | |||||||
| chr1:169847521 | T | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-169T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847521 | |||||||
| chr1:169847560 | T | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0007g0152 others(3): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1945-130T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847560 | |||||||
| chr1:169847850 | A | G | 1 | a0006c0010t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2058+47A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169847850 | |||||||
| chr1:169847882 | T | C | 3 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0121 |
3 | HG00733.hp2 HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.2058+79T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169847882 | |||||||
| chr1:169848191 | C | T | 1 | a0001c0001t0008g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2058+388C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848191 | |||||||
| chr1:169848210 | G | A | 4 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058+407G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848210 | |||||||
| chr1:169848427 | A | C | 54 | a0001c0002t0001g0038 a0001c0002t0001g0264 a0001c0002t0001g0265 others(51): Show |
55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2058+624A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848427 | |||||||
| chr1:169848430 | T | C | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | NA18970.hp1 NA19058.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058+627T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848430 | |||||||
| chr1:169848495 | T | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.2058+692T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848495 | |||||||
| chr1:169848638 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2058+835G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848638 | |||||||
| chr1:169848953 | C | T | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2059-547C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848953 | |||||||
| chr1:169849049 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.2059-451A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849049 | |||||||
| chr1:169849051 | G | T | 1 | a0002c0003t0005g0356 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2059-449G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849051 | |||||||
| chr1:169849053 | T | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2059-447T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849053 | |||||||
| chr1:169849077 | T | C | 2 | a0001c0001t0007g0153 a0001c0001t0007g0154 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2059-423T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849077 | |||||||
| chr1:169849215 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2059-285G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849215 | |||||||
| chr1:169849238 | T | G | 2 | a0001c0001t0008g0030 a0001c0001t0008g0207 |
3 | HG01884.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2059-262T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849238 | |||||||
| chr1:169849263 | A | G | 6 | a0001c0001t0002g0315 a0001c0001t0002g0316 a0001c0001t0002g0318 others(3): Show |
6 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059-237A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849263 | |||||||
| chr1:169849338 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2059-162G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849338 | |||||||
| chr1:169849622 | T | G | 5 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0001t0002g0327 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163+18T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849622 | |||||||
| chr1:169849717 | T | C | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163+113T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849717 | |||||||
| chr1:169849738 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2163+134C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849738 | |||||||
| chr1:169849739 | G | A | 54 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0023 others(51): Show |
60 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.2163+135G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849739 | |||||||
| chr1:169849785 | T | C | 25 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(22): Show |
26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2163+181T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849785 | |||||||
| chr1:169849924 | A | G | 65 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0006g0337 others(62): Show |
67 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.2163+320A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849924 | |||||||
| chr1:169849976 | C | G | 4 | a0001c0001t0009g0210 a0001c0001t0009g0211 a0001c0001t0009g0212 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164-289C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849976 | |||||||
| chr1:169850035 | C | T | 11 | a0001c0001t0003g0020 a0001c0001t0003g0103 a0001c0001t0003g0104 others(8): Show |
12 | NA18973.hp1 NA18977.hp2 NA18978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2164-230C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169850035 | |||||||
| chr1:169850143 | G | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2164-122G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169850143 | |||||||
| chr1:169850417 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2244+72C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850417 | |||||||
| chr1:169850464 | A | G | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2244+119A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850464 | |||||||
| chr1:169850525 | C | T | 2 | a0001c0001t0004g0241 a0001c0001t0004g0245 |
2 | NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2244+180C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850525 | |||||||
| chr1:169850529 | G | A | 15 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(12): Show |
15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2244+184G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850529 | |||||||
| chr1:169850641 | C | G | 1 | a0001c0001t0007g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2244+296C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850641 | |||||||
| chr1:169850689 | G | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2244+344G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850689 | |||||||
| chr1:169850751 | A | G | 295 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(292): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.2244+406A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850751 | |||||||
| chr1:169850870 | A | G | 1 | a0001c0001t0004g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2244+525A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850870 | |||||||
| chr1:169850912 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2244+567T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850912 | |||||||
| chr1:169850936 | G | GAGA | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2244+592_2244+594d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850936 | ||||||
| chr1:169850974 | G | A | 24 | a0001c0001t0003g0020 a0001c0001t0003g0102 a0001c0001t0003g0103 others(21): Show |
25 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2244+629G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850974 | |||||||
| chr1:169850980 | C | CT | 6 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0009g0210 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244+661dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTT | 18 | a0001c0001t0002g0321 a0001c0001t0002g0331 a0001c0001t0003g0109 others(15): Show |
18 | HG00408.hp1 HG00544.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244+658_2244+661d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTT | 22 | a0001c0001t0002g0322 a0001c0001t0002g0324 a0001c0001t0002g0329 others(19): Show |
23 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.2244+657_2244+661d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTT | 13 | a0001c0001t0002g0315 a0001c0001t0003g0125 a0001c0001t0014g0317 others(10): Show |
13 | HG00642.hp2 HG00733.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2244+656_2244+661d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT | 10 | a0001c0001t0002g0316 a0001c0001t0002g0318 a0001c0001t0002g0319 others(7): Show |
10 | HG01258.hp2 HG01261.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244+655_2244+661d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0285 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2244+652_2244+661d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0323 a0001c0001t0003g0020 a0001c0001t0003g0104 others(2): Show |
6 | HG02970.hp1 NA18973.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244+651_2244+661d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0105 a0001c0001t0003g0115 |
2 | NA19009.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2244+650_2244+661d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0003g0114 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2244+649_2244+661d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0103 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2244+646_2244+661d others(18): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0003g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2244+643_2244+661d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0006g0338 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2244+641_2244+661d others(23): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0003g0120 a0001c0001t0006g0339 |
2 | HG02486.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2244+639_2244+661d others(25): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2244+661_2244+662i others(32): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | CTTTTTTT others(61): Show |
C | 1 | a0002c0003t0005g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2244+661_2244+728d others(70): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850980 | CTTTTTTT others(62): Show |
C | 14 | a0002c0003t0005g0039 a0002c0003t0005g0346 a0002c0003t0005g0347 others(11): Show |
14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2244+660_2244+728d others(71): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | ||||||
| chr1:169850982 | TTTTTTTT others(56): Show |
T | 1 | a0001c0001t0003g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2244+662_2244+724d others(65): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850982 | ||||||
| chr1:169850985 | TTTTTTTT others(53): Show |
T | 9 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0127 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2244+662_2244+721d others(62): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850985 | ||||||
| chr1:169850986 | TTTTTTTT others(52): Show |
T | 12 | a0001c0001t0003g0023 a0001c0001t0003g0132 a0001c0001t0003g0133 others(9): Show |
12 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.2244+662_2244+720d others(61): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850986 | ||||||
| chr1:169850987 | TTTTTTTT others(51): Show |
T | 7 | a0001c0001t0003g0129 a0001c0001t0003g0130 a0001c0001t0003g0143 others(4): Show |
7 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244+662_2244+719d others(60): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850987 | ||||||
| chr1:169850988 | TTTTTTTT others(50): Show |
T | 2 | a0001c0001t0003g0145 a0003c0004t0003g0025 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2244+662_2244+718d others(59): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850988 | ||||||
| chr1:169850989 | TTTTTTTT others(49): Show |
T | 1 | a0001c0001t0003g0023 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2244+662_2244+717d others(58): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850989 | ||||||
| chr1:169850990 | TTTTTTTT others(48): Show |
T | 1 | a0003c0004t0003g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2244+662_2244+716d others(57): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850990 | ||||||
| chr1:169850996 | TTTTTTTT others(8): Show |
T | 4 | a0001c0001t0008g0030 a0001c0001t0008g0207 a0001c0001t0008g0208 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2244+652_2244+666d others(17): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850996 | |||||||
| chr1:169850997 | TTTTTTTT others(7): Show |
T | 2 | a0001c0001t0003g0113 a0001c0002t0001g0307 |
2 | NA19063.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2244+653_2244+666d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850997 | |||||||
| chr1:169850998 | TTTTTTTT others(6): Show |
T | 1 | a0001c0002t0001g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2244+654_2244+666d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850998 | |||||||
| chr1:169851001 | TTTTTTAT others(3): Show |
T | 1 | a0001c0001t0003g0118 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2244+657_2244+666d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851001 | |||||||
| chr1:169851003 | TTTTA | T | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
46 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.2244+662_2244+665d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851003 | ||||||
| chr1:169851004 | TTTA | T | 62 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(59): Show |
70 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2244+662_2244+664d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851004 | ||||||
| chr1:169851004 | TTTATTTG | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
74 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.2244+660_2244+666d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851004 | |||||||
| chr1:169851005 | TTA | T | 27 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(24): Show |
30 | HG01109.hp2 HG02071.hp2 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.2244+662_2244+663d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851005 | ||||||
| chr1:169851005 | TTATTTG | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(12): Show |
15 | HG01361.hp1 HG02004.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2244+661_2244+666d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851005 | |||||||
| chr1:169851006 | TA | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0091 a0001c0001t0002g0095 others(2): Show |
5 | HG00544.hp2 HG00735.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+662delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851006 | |||||||
| chr1:169851007 | A | T | 100 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0002g0315 others(97): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.2244+662A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851007 | |||||||
| chr1:169851011 | G | T | 141 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0002g0333 others(138): Show |
155 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.2244+666G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851011 | |||||||
| chr1:169851045 | C | CT | 48 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(45): Show |
50 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.2244+728dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTT | 7 | a0001c0001t0002g0044 a0001c0001t0002g0069 a0001c0001t0018g0094 others(4): Show |
7 | HG02040.hp2 HG02293.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244+727_2244+728d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0287 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2244+719_2244+728d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(4): Show |
2 | a0001c0002t0001g0276 a0001c0002t0001g0285 |
2 | HG00597.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2244+718_2244+728d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(5): Show |
1 | a0001c0002t0001g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2244+717_2244+728d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0286 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2244+715_2244+728d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(10): Show |
3 | a0001c0002t0001g0277 a0001c0002t0001g0297 a0001c0002t0001g0310 |
3 | HG03239.hp2 HG03834.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2244+712_2244+728d others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(11): Show |
3 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0296 |
3 | HG00733.hp1 HG01261.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2244+711_2244+728d others(20): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(12): Show |
1 | a0001c0002t0001g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2244+710_2244+728d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(14): Show |
1 | a0001c0002t0001g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2244+708_2244+728d others(23): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(18): Show |
1 | a0007c0007t0001g0273 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2244+704_2244+728d others(27): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(19): Show |
1 | a0001c0002t0001g0314 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2244+703_2244+728d others(28): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(25): Show |
1 | a0001c0002t0001g0308 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2244+728_2244+729i others(34): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(26): Show |
1 | a0001c0002t0001g0309 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2244+728_2244+729i others(35): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | C | CTTTTTTT others(29): Show |
1 | a0001c0002t0001g0279 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2244+728_2244+729i others(38): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | CT | C | 23 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0315 others(20): Show |
24 | HG00544.hp1 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2244+728delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | CTTTTT | C | 14 | a0001c0001t0004g0247 a0001c0001t0004g0260 a0001c0001t0006g0338 others(11): Show |
15 | HG00408.hp1 HG01123.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.2244+724_2244+728d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | CTTTTTT | C | 49 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(46): Show |
60 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2244+723_2244+728d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | CTTTTTTT others(3): Show |
C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(52): Show |
65 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2244+719_2244+728d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851045 | CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0029 others(13): Show |
24 | HG01192.hp1 HG01891.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.2244+718_2244+728d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | ||||||
| chr1:169851077 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2244+732A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851077 | |||||||
| chr1:169851173 | C | A | 1 | a0001c0001t0003g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2245-644C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851173 | |||||||
| chr1:169851270 | A | C | 1 | a0001c0001t0004g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2245-547A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851270 | |||||||
| chr1:169851374 | G | C | 1 | a0001c0001t0012g0342 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2245-443G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851374 | |||||||
| chr1:169851416 | C | T | 2 | a0002c0003t0005g0349 a0002c0003t0005g0352 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2245-401C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851416 | |||||||
| chr1:169851499 | A | G | 2 | a0001c0002t0001g0334 a0001c0002t0001g0335 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2245-318A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851499 | |||||||
| chr1:169851541 | C | T | 3 | a0001c0001t0010g0032 a0001c0001t0010g0223 a0001c0001t0010g0230 |
4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-276C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851541 | |||||||
| chr1:169851569 | A | T | 2 | a0001c0001t0002g0321 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2245-248A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851569 | |||||||
| chr1:169851994 | C | T | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2364+58C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169851994 | |||||||
| chr1:169852261 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0263 |
7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2364+325T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852261 | |||||||
| chr1:169852347 | T | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2364+411T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852347 | |||||||
| chr1:169852395 | ATAGTAAT | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0164 others(3): Show |
11 | HG00323.hp2 HG00741.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.2365-389_2365-383d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr1 | 169852395 | ||||||
| chr1:169852527 | T | C | 1 | a0001c0001t0002g0329 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2365-263T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852527 | |||||||
| chr1:169852709 | T | C | 1 | a0001c0001t0002g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2365-81T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852709 |