Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221421 |
| ensemblid | ENSG00000172426.16 |
| hgncid | 21057 |
| symbol | RSPH9 |
| name | radial spoke head component 9 |
| refseq_nuc | NM_152732.5 |
| refseq_prot | NP_689945.2 |
| ensembl_nuc | ENST00000372163.5 |
| ensembl_prot | ENSP00000361236.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 43645036 |
| end | 43672600 |
| strand | + |
| ver | v1.2 |
| region | chr6:43645036-43672600 |
| region5000 | chr6:43640036-43677600 |
| regionname0 | RSPH9_chr6_43645036_43672600 |
| regionname5000 | RSPH9_chr6_43640036_43677600 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 276 | 260 | 85 | 49 | 88 | 11 | 25 | 71 | RSPH9_chr6_43640036_43677600 | RSPH9 | MDADS others(271): Show |
chr6 | 43640036 | 43677600 |
| a0002 | 0/0 | 276 | 71 | 3 | 4 | 50 | 3 | 11 | 36 | RSPH9_chr6_43640036_43677600 | RSPH9 | MDADS others(271): Show |
chr6 | 43640036 | 43677600 |
| a0003 | 0/0 | 276 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | MDADS others(271): Show |
chr6 | 43640036 | 43677600 |
| a0004 | 0/0 | 276 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | MDADS others(271): Show |
chr6 | 43640036 | 43677600 |
| a0005 | 0/0 | 276 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | MDAGS others(271): Show |
chr6 | 43640036 | 43677600 |
| a0006 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | MDADS others(271): Show |
chr6 | 43640036 | 43677600 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 828 | 257 | 84 | 48 | 87 | 11 | 25 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0001c0007 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0001c0008 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0001c0009 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0002c0002 | 0/0 | 828 | 70 | 3 | 4 | 50 | 3 | 10 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0002c0005 | 0/0 | 828 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0003c0003 | 0/0 | 828 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0004c0004 | 0/0 | 828 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0005c0010 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 | ||
| a0006c0006 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | ATGGA others(823): Show |
chr6 | 43640036 | 43677600 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2545 | 189 | 34 | 41 | 80 | 10 | 22 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0003 | 0/0 | 2545 | 15 | 4 | 3 | 7 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0004 | 0/0 | 2545 | 10 | 10 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0005 | 0/0 | 2545 | 8 | 8 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0006 | 0/0 | 2545 | 7 | 6 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0007 | 0/0 | 2545 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0008 | 0/0 | 2545 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0009 | 0/0 | 2545 | 3 | 3 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0010 | 0/0 | 2545 | 3 | 3 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0011 | 0/0 | 2545 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0012 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0013 | 0/0 | 2545 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0015 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0016 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0017 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0020 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0021 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0001t0022 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0007t0003 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0008t0012 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0001c0009t0003 | 0/0 | 2545 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0002c0002t0002 | 0/0 | 2545 | 68 | 2 | 4 | 49 | 3 | 10 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0002c0002t0014 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0002c0002t0019 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0002c0005t0002 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0003c0003t0001 | 0/0 | 2545 | 4 | 4 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0003c0003t0009 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0003c0003t0018 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0004c0004t0001 | 0/0 | 2545 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0005c0010t0001 | 0/0 | 2545 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| a0006c0006t0001 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | AGGTC others(2540): Show |
chr6 | 43640036 | 43677600 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 18 | 1 | 4 | 11 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 3 | 2 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0026 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0137 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0008g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0010g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0011g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0013g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0015g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0016g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0017g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0020g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0021g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0022g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0007t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0008t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0009t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0001 | 0/0 | 21 | 0 | 2 | 18 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0014g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0019g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0005t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0018g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0004c0004t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0004c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0004c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0005c0010t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0006c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0203 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0132 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01257 | hp2 | a0001 | c0001 | t0011 | g0013 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01258 | hp2 | a0001 | c0001 | t0011 | g0013 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0083 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01516 | hp1 | a0001 | c0001 | t0020 | g0110 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0084 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01993 | hp1 | a0001 | c0009 | t0003 | g0226 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02056 | hp2 | a0004 | c0004 | t0001 | g0012 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | CDX | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0102 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02258 | hp2 | a0003 | c0003 | t0018 | g0063 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0070 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0233 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0100 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0099 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0018 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02717 | hp1 | a0001 | c0001 | t0016 | g0243 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02723 | hp1 | a0001 | c0008 | t0012 | g0239 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02738 | hp1 | a0001 | c0001 | t0015 | g0192 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02809 | hp2 | a0002 | c0002 | t0019 | g0080 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0240 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02965 | hp2 | a0003 | c0003 | t0009 | g0061 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0098 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0068 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0246 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0231 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0062 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0248 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0018 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03688 | hp2 | a0002 | c0005 | t0002 | g0095 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0049 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0085 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0128 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0208 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0082 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18951 | hp1 | a0001 | c0007 | t0003 | g0230 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18957 | hp2 | a0004 | c0004 | t0001 | g0161 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18984 | hp2 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0232 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0064 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19088 | hp1 | a0002 | c0002 | t0014 | g0197 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ASW | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01123 | hp2 | a0005 | c0010 | t0001 | g0177 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0026 | REF | REF | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0137 | REF | REF | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645109 | A | G | 1 | a0005 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.11A>G | p.Asp4Gly | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/5 | 74/2545 | 11/831 | 4/276 | chr6 | 43645109 | |||
| chr6:43650410 | C | T | 1 | a0003 | 6 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
missense_variant | MODERATE | c.263C>T | p.Ala88Val | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/5 | 326/2545 | 263/831 | 88/276 | chr6 | 43650410 | |||
| chr6:43655589 | G | A | 1 | a0004 | 3 | HG02056.hp2 NA18946.hp1 NA18957.hp2 |
missense_variant | MODERATE | c.421G>A | p.Val141Met | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/5 | 484/2545 | 421/831 | 141/276 | chr6 | 43655589 | |||
| chr6:43655640 | G | A | 1 | a0006 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.472G>A | p.Ala158Thr | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/5 | 535/2545 | 472/831 | 158/276 | chr6 | 43655640 | |||
| chr6:43670899 | G | A | 1 | a0002 | 71 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
missense_variant | MODERATE | c.781G>A | p.Val261Ile | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 844/2545 | 781/831 | 261/276 | chr6 | 43670899 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645227 | G | A | 1 | a0002c0005 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.129G>A | p.Arg43Arg | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/5 | 192/2545 | 129/831 | 43/276 | chr6 | 43645227 | |||
| chr6:43656579 | C | T | 1 | a0001c0009 | 1 | HG01993.hp1 | splice_region_variant&synonymous_variant | LOW | c.526C>T | p.Leu176Leu | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/5 | 589/2545 | 526/831 | 176/276 | chr6 | 43656579 | |||
| chr6:43670898 | C | T | 1 | a0001c0008 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.780C>T | p.Tyr260Tyr | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 843/2545 | 780/831 | 260/276 | chr6 | 43670898 | |||
| chr6:43670937 | C | T | 1 | a0001c0007 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.819C>T | p.Pro273Pro | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 882/2545 | 819/831 | 273/276 | chr6 | 43670937 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645081 | A | G | 5 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0012 others(2): Show |
12 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-18A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/5 | 18 | chr6 | 43645081 | ||||||
| chr6:43671279 | T | C | 2 | a0001c0001t0007 a0001c0001t0022 |
7 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*330T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 330 | chr6 | 43671279 | ||||||
| chr6:43671363 | C | T | 1 | a0001c0001t0021 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 414 | chr6 | 43671363 | ||||||
| chr6:43671375 | G | A | 1 | a0001c0001t0013 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 426 | chr6 | 43671375 | ||||||
| chr6:43671437 | A | G | 1 | a0001c0001t0020 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 488 | chr6 | 43671437 | ||||||
| chr6:43671483 | C | T | 1 | a0001c0001t0021 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 534 | chr6 | 43671483 | ||||||
| chr6:43671726 | C | G | 1 | a0001c0001t0005 | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*777C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 777 | chr6 | 43671726 | ||||||
| chr6:43671781 | G | C | 1 | a0002c0002t0014 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 832 | chr6 | 43671781 | ||||||
| chr6:43671896 | G | A | 1 | a0001c0001t0015 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*947G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 947 | chr6 | 43671896 | ||||||
| chr6:43671971 | G | A | 2 | a0001c0001t0004 a0001c0001t0016 |
11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1022G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1022 | chr6 | 43671971 | ||||||
| chr6:43671995 | C | T | 1 | a0002c0002t0019 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1046C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1046 | chr6 | 43671995 | ||||||
| chr6:43672117 | G | A | 1 | a0001c0001t0016 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1168G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1168 | chr6 | 43672117 | ||||||
| chr6:43672141 | G | T | 2 | a0001c0001t0008 a0003c0003t0018 |
7 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1192G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1192 | chr6 | 43672141 | ||||||
| chr6:43672149 | C | T | 7 | a0001c0001t0003 a0001c0007t0003 a0001c0009t0003 others(4): Show |
88 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1200C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1200 | chr6 | 43672149 | ||||||
| chr6:43672302 | C | T | 7 | a0001c0001t0003 a0001c0007t0003 a0001c0009t0003 others(4): Show |
88 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1353C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1353 | chr6 | 43672302 | ||||||
| chr6:43672327 | A | G | 10 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(7): Show |
104 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1378A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1378 | chr6 | 43672327 | ||||||
| chr6:43672360 | G | A | 1 | a0001c0001t0017 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1411 | chr6 | 43672360 | ||||||
| chr6:43672362 | A | G | 7 | a0001c0001t0003 a0001c0007t0003 a0001c0009t0003 others(4): Show |
88 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1413 | chr6 | 43672362 | ||||||
| chr6:43672441 | G | T | 3 | a0001c0001t0009 a0001c0001t0010 a0003c0003t0009 |
7 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1492G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1492 | chr6 | 43672441 | ||||||
| chr6:43672485 | A | G | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0007t0003 others(1): Show |
19 | HG01074.hp2 HG01099.hp1 HG01257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1536A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1536 | chr6 | 43672485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645367 | C | T | 7 | a0001c0001t0001g0247 a0001c0001t0001g0252 a0001c0001t0004g0250 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+42C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645367 | |||||||
| chr6:43645408 | G | A | 1 | a0001c0001t0006g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.227+83G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645408 | |||||||
| chr6:43645443 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(26): Show |
36 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.227+118G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645443 | |||||||
| chr6:43645591 | T | TC | 28 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0075 others(25): Show |
29 | HG00639.hp2 HG01175.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.227+271dupC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43645591 | ||||||
| chr6:43645591 | TC | T | 18 | a0001c0001t0001g0034 a0001c0001t0001g0242 a0001c0001t0001g0247 others(15): Show |
20 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.227+271delC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43645591 | ||||||
| chr6:43645613 | C | A | 1 | a0001c0001t0006g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227+288C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645613 | |||||||
| chr6:43645653 | A | T | 1 | a0001c0001t0007g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.227+328A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645653 | |||||||
| chr6:43645928 | T | C | 1 | a0002c0002t0002g0088 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.227+603T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645928 | |||||||
| chr6:43646125 | TTTATTA | T | 7 | a0002c0002t0002g0082 a0002c0002t0002g0083 a0002c0002t0002g0084 others(4): Show |
7 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+818_227+823del others(6): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646125 | ||||||
| chr6:43646128 | A | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.227+803A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646128 | |||||||
| chr6:43646242 | C | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0234 a0001c0001t0001g0236 others(4): Show |
8 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+917C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646242 | |||||||
| chr6:43646328 | G | T | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.227+1003G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646328 | |||||||
| chr6:43646336 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0089 a0001c0001t0001g0090 |
5 | NA18747.hp1 NA18974.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.227+1011G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646336 | |||||||
| chr6:43646468 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.227+1143G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646468 | |||||||
| chr6:43646496 | C | T | 7 | a0001c0001t0001g0224 a0001c0001t0001g0228 a0001c0001t0001g0229 others(4): Show |
7 | HG01978.hp2 HG01993.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.227+1171C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646496 | |||||||
| chr6:43646570 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.227+1245C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646570 | |||||||
| chr6:43646664 | C | CA | 24 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(21): Show |
28 | HG00738.hp1 HG01192.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.227+1355dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646664 | ||||||
| chr6:43646664 | C | CAA | 11 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0004g0065 others(8): Show |
11 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.227+1354_227+1355d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646664 | ||||||
| chr6:43646687 | GTGTGGTG others(25): Show |
G | 1 | a0001c0001t0001g0247 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.227+1365_227+1396d others(34): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646687 | ||||||
| chr6:43646776 | C | T | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.227+1451C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646776 | |||||||
| chr6:43646829 | G | A | 1 | a0003c0003t0009g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.227+1504G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646829 | |||||||
| chr6:43646863 | G | A | 2 | a0001c0001t0004g0073 a0001c0001t0006g0072 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.227+1538G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646863 | |||||||
| chr6:43646930 | G | C | 6 | a0002c0002t0002g0082 a0002c0002t0002g0083 a0002c0002t0002g0084 others(3): Show |
6 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.227+1605G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646930 | |||||||
| chr6:43646949 | C | G | 3 | a0001c0001t0001g0034 a0001c0001t0005g0245 a0001c0001t0006g0036 |
4 | HG02895.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.227+1624C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646949 | |||||||
| chr6:43646954 | CA | C | 7 | a0001c0001t0001g0216 a0001c0001t0001g0219 a0001c0001t0001g0236 others(4): Show |
7 | HG01255.hp1 NA18942.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+1642delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646954 | ||||||
| chr6:43646968 | G | A | 1 | a0001c0001t0006g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227+1643G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646968 | |||||||
| chr6:43646968 | GA | G | 76 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(73): Show |
91 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.227+1654delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646968 | ||||||
| chr6:43646969 | A | G | 1 | a0001c0001t0006g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227+1644A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646969 | |||||||
| chr6:43647077 | A | G | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(67): Show |
85 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.227+1752A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647077 | |||||||
| chr6:43647095 | G | A | 4 | a0003c0003t0001g0062 a0003c0003t0001g0064 a0003c0003t0009g0061 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.227+1770G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647095 | |||||||
| chr6:43647109 | ACAGAGCG others(58): Show |
A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
8 | HG00140.hp2 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+1788_227+1852d others(67): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43647109 | ||||||
| chr6:43647182 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.227+1857G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647182 | |||||||
| chr6:43647359 | C | A | 8 | a0001c0001t0001g0103 a0001c0001t0008g0006 a0001c0001t0008g0101 others(5): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.227+2034C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647359 | |||||||
| chr6:43647407 | G | A | 3 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0005g0067 |
3 | HG02615.hp1 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.227+2082G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647407 | |||||||
| chr6:43647697 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.227+2372A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647697 | |||||||
| chr6:43647890 | C | T | 17 | a0001c0001t0001g0034 a0001c0001t0001g0242 a0001c0001t0001g0247 others(14): Show |
19 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.228-2485C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647890 | |||||||
| chr6:43647904 | C | T | 25 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(22): Show |
30 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.228-2471C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647904 | |||||||
| chr6:43647933 | A | T | 5 | a0001c0001t0004g0073 a0001c0001t0005g0078 a0001c0001t0005g0079 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-2442A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647933 | |||||||
| chr6:43647999 | G | A | 1 | a0001c0001t0006g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.228-2376G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647999 | |||||||
| chr6:43648223 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0004g0105 |
3 | NA19043.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.228-2152C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648223 | |||||||
| chr6:43648269 | C | CA | 10 | a0001c0001t0001g0069 a0001c0001t0004g0065 a0001c0001t0004g0066 others(7): Show |
10 | HG02258.hp2 HG02615.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.228-2092dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43648269 | ||||||
| chr6:43648283 | A | G | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.228-2092A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648283 | |||||||
| chr6:43648451 | T | A | 1 | a0002c0002t0002g0108 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.228-1924T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648451 | |||||||
| chr6:43648865 | G | A | 4 | a0001c0001t0004g0073 a0001c0001t0005g0078 a0001c0001t0005g0079 others(1): Show |
4 | HG02486.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1510G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648865 | |||||||
| chr6:43648890 | G | A | 7 | a0002c0002t0002g0082 a0002c0002t0002g0083 a0002c0002t0002g0084 others(4): Show |
7 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-1485G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648890 | |||||||
| chr6:43649055 | T | C | 1 | a0001c0001t0003g0109 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.228-1320T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649055 | |||||||
| chr6:43649194 | T | G | 1 | a0001c0001t0007g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.228-1181T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649194 | |||||||
| chr6:43649258 | C | T | 1 | a0001c0001t0003g0200 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.228-1117C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649258 | |||||||
| chr6:43649266 | T | G | 14 | a0001c0001t0001g0242 a0001c0001t0001g0247 a0001c0001t0001g0252 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.228-1109T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649266 | |||||||
| chr6:43649412 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
8 | HG02486.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.228-963G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649412 | |||||||
| chr6:43649466 | C | T | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.228-909C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649466 | |||||||
| chr6:43649496 | T | C | 1 | a0002c0002t0002g0009 | 3 | NA18747.hp2 NA18945.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.228-879T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649496 | |||||||
| chr6:43649571 | T | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
7 | HG00741.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-804T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649571 | |||||||
| chr6:43649643 | G | A | 1 | a0001c0001t0017g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.228-732G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649643 | |||||||
| chr6:43649817 | A | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(70): Show |
88 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(85): Show |
intron_variant | MODIFIER | c.228-558A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649817 | |||||||
| chr6:43649850 | TCATTTAA others(6): Show |
T | 1 | a0001c0001t0020g0110 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.228-521_228-509del others(13): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43649850 | ||||||
| chr6:43649950 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.228-425G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649950 | |||||||
| chr6:43649972 | G | A | 1 | a0002c0002t0019g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.228-403G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649972 | |||||||
| chr6:43649978 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(70): Show |
88 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(85): Show |
intron_variant | MODIFIER | c.228-397G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649978 | |||||||
| chr6:43649989 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.228-386C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649989 | |||||||
| chr6:43650258 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.228-117A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43650258 | |||||||
| chr6:43650273 | C | T | 6 | a0001c0001t0001g0242 a0001c0001t0003g0241 a0001c0001t0004g0244 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-102C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43650273 | |||||||
| chr6:43650289 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(70): Show |
88 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(85): Show |
intron_variant | MODIFIER | c.228-86C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43650289 | |||||||
| chr6:43650634 | C | T | 2 | a0001c0001t0006g0203 a0001c0001t0006g0204 |
2 | HG00741.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.393+94C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650634 | |||||||
| chr6:43650639 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.393+99G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650639 | |||||||
| chr6:43650694 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.393+154C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650694 | |||||||
| chr6:43650734 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.393+194G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650734 | |||||||
| chr6:43650760 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0004g0073 a0001c0001t0005g0078 others(2): Show |
5 | HG02486.hp1 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+220G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650760 | |||||||
| chr6:43650860 | G | A | 1 | a0001c0001t0004g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+320G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650860 | |||||||
| chr6:43650905 | T | TA | 61 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(58): Show |
75 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.393+379dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43650905 | ||||||
| chr6:43650905 | T | TAA | 14 | a0001c0001t0001g0242 a0001c0001t0001g0247 a0001c0001t0001g0252 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+378_393+379dup others(2): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43650905 | ||||||
| chr6:43650947 | CA | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.393+409delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43650947 | ||||||
| chr6:43651118 | G | A | 1 | a0001c0001t0022g0098 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.393+578G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651118 | |||||||
| chr6:43651311 | G | A | 6 | a0001c0001t0001g0242 a0001c0001t0003g0241 a0001c0001t0004g0244 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+771G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651311 | |||||||
| chr6:43651441 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0005g0245 a0001c0001t0006g0036 |
4 | HG02895.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+901G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651441 | |||||||
| chr6:43651489 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.393+949T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651489 | |||||||
| chr6:43651546 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.393+1006T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651546 | |||||||
| chr6:43651633 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0097 |
3 | HG01192.hp2 HG02698.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.393+1093C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651633 | |||||||
| chr6:43651700 | T | C | 44 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0069 others(41): Show |
54 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+1160T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651700 | |||||||
| chr6:43651756 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.393+1216C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651756 | |||||||
| chr6:43651828 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.393+1288C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651828 | |||||||
| chr6:43651845 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(46): Show |
62 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(59): Show |
intron_variant | MODIFIER | c.393+1305A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651845 | |||||||
| chr6:43651914 | T | A | 1 | a0002c0002t0002g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.393+1374T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651914 | |||||||
| chr6:43651942 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.393+1402T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651942 | |||||||
| chr6:43651994 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+1454T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651994 | |||||||
| chr6:43652261 | G | A | 2 | a0001c0001t0005g0245 a0001c0001t0006g0036 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.393+1721G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652261 | |||||||
| chr6:43652285 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.393+1745G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652285 | |||||||
| chr6:43652373 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.393+1833C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652373 | |||||||
| chr6:43652406 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.393+1866G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652406 | |||||||
| chr6:43652464 | C | T | 1 | a0002c0002t0014g0197 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.393+1924C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652464 | |||||||
| chr6:43652519 | G | A | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.393+1979G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652519 | |||||||
| chr6:43652643 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.393+2103C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652643 | |||||||
| chr6:43652661 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.393+2121G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652661 | |||||||
| chr6:43652672 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.393+2132C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652672 | |||||||
| chr6:43652728 | CG | C | 14 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0221 others(11): Show |
14 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+2190delG | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652728 | ||||||
| chr6:43652729 | GGT | G | 9 | a0001c0001t0001g0106 a0001c0001t0003g0081 a0001c0001t0004g0105 others(6): Show |
13 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.393+2190_393+2191d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652729 | |||||||
| chr6:43652730 | G | GT | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(76): Show |
113 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.393+2207dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652730 | ||||||
| chr6:43652730 | G | GTT | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG02738.hp1 NA18940.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+2206_393+2207d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652730 | ||||||
| chr6:43652730 | GT | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(32): Show |
45 | HG00642.hp2 HG01081.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.393+2207delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652730 | ||||||
| chr6:43652807 | C | T | 3 | a0001c0001t0004g0244 a0001c0001t0007g0246 a0001c0001t0016g0243 |
3 | HG02717.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.393+2267C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652807 | |||||||
| chr6:43652808 | G | A | 1 | a0002c0002t0002g0074 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.393+2268G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652808 | |||||||
| chr6:43652818 | T | A | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.393+2278T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652818 | |||||||
| chr6:43652903 | C | A | 2 | a0001c0001t0005g0245 a0001c0001t0006g0036 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.393+2363C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652903 | |||||||
| chr6:43653008 | T | TG | 15 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0004g0073 others(12): Show |
16 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.393+2472dupG | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653008 | ||||||
| chr6:43653095 | T | C | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-2467T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653095 | |||||||
| chr6:43653153 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0004g0105 |
2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.394-2409A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653153 | |||||||
| chr6:43653259 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.394-2303G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653259 | |||||||
| chr6:43653279 | G | A | 1 | a0002c0002t0002g0150 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.394-2283G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653279 | |||||||
| chr6:43653371 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(15): Show |
26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.394-2191C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653371 | |||||||
| chr6:43653379 | G | A | 6 | a0003c0003t0001g0062 a0003c0003t0001g0064 a0003c0003t0001g0068 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-2183G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653379 | |||||||
| chr6:43653401 | C | T | 1 | a0002c0002t0002g0220 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.394-2161C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653401 | |||||||
| chr6:43653409 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0107 a0001c0001t0001g0151 others(3): Show |
9 | HG00597.hp1 NA18940.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-2153T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653409 | |||||||
| chr6:43653434 | A | G | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-2128A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653434 | |||||||
| chr6:43653441 | C | T | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-2121C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653441 | |||||||
| chr6:43653446 | C | CA | 25 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0092 others(22): Show |
27 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.394-2097dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | ||||||
| chr6:43653446 | C | CAA | 19 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0106 others(16): Show |
23 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.394-2098_394-2097d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | ||||||
| chr6:43653446 | CA | C | 8 | a0001c0001t0001g0060 a0001c0001t0001g0103 a0001c0001t0001g0187 others(5): Show |
8 | HG01256.hp2 HG02257.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-2097delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | ||||||
| chr6:43653446 | CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0041 others(7): Show |
12 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-2105_394-2097d others(11): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | ||||||
| chr6:43653469 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.394-2093C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653469 | |||||||
| chr6:43653489 | T | TGTGTGTA others(9): Show |
1 | a0001c0001t0001g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.394-2072_394-2057d others(18): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653489 | ||||||
| chr6:43653532 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-2030C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653532 | |||||||
| chr6:43653586 | AAGCACAG others(3): Show |
A | 1 | a0001c0007t0003g0230 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.394-1975_394-1966d others(12): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653586 | |||||||
| chr6:43653748 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.394-1814A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653748 | |||||||
| chr6:43653788 | A | G | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-1774A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653788 | |||||||
| chr6:43653872 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(71): Show |
89 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.394-1690G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653872 | |||||||
| chr6:43653904 | T | C | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-1658T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653904 | |||||||
| chr6:43654177 | G | C | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394-1385G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654177 | |||||||
| chr6:43654188 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-1374G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654188 | |||||||
| chr6:43654238 | A | G | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394-1324A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654238 | |||||||
| chr6:43654302 | A | G | 24 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(21): Show |
28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-1260A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654302 | |||||||
| chr6:43654516 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0004g0073 a0001c0001t0005g0078 others(3): Show |
6 | HG02486.hp1 HG02809.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-1046C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654516 | |||||||
| chr6:43654548 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0027 others(24): Show |
37 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.394-1014C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654548 | |||||||
| chr6:43654549 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
8 | HG00140.hp2 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-1013G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654549 | |||||||
| chr6:43654695 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.394-867C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654695 | |||||||
| chr6:43654763 | C | T | 6 | a0003c0003t0001g0062 a0003c0003t0001g0064 a0003c0003t0001g0068 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-799C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654763 | |||||||
| chr6:43654783 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394-779A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654783 | |||||||
| chr6:43655019 | A | G | 6 | a0001c0001t0005g0032 a0001c0001t0005g0078 a0001c0001t0005g0079 others(3): Show |
7 | HG02257.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-543A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655019 | |||||||
| chr6:43655064 | T | C | 16 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0103 others(13): Show |
16 | HG01106.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.394-498T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655064 | |||||||
| chr6:43655099 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.394-463A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655099 | |||||||
| chr6:43655118 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0027 others(110): Show |
159 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.394-444G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655118 | |||||||
| chr6:43655188 | A | G | 37 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0118 others(34): Show |
38 | HG00597.hp2 HG00639.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.394-374A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655188 | |||||||
| chr6:43655217 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.394-345C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655217 | |||||||
| chr6:43655365 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(14): Show |
25 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.394-197C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655365 | |||||||
| chr6:43655377 | C | T | 73 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0118 others(70): Show |
103 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.394-185C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655377 | |||||||
| chr6:43655392 | G | T | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-170G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655392 | |||||||
| chr6:43655405 | A | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0030 others(48): Show |
65 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(62): Show |
intron_variant | MODIFIER | c.394-157A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655405 | |||||||
| chr6:43655406 | T | C | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-156T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655406 | |||||||
| chr6:43655537 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0004g0182 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.394-25G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655537 | |||||||
| chr6:43655786 | C | T | 1 | a0002c0005t0002g0095 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.523+95C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655786 | |||||||
| chr6:43655911 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0048 |
4 | HG00140.hp1 HG01192.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+220A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655911 | |||||||
| chr6:43655988 | A | ACTTC | 17 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0033 others(14): Show |
24 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.523+343_523+346dup others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | ||||||
| chr6:43655988 | A | ACTTCCTT others(1): Show |
27 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(24): Show |
32 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.523+339_523+346dup others(8): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | ||||||
| chr6:43655988 | A | ACTTCCTT others(5): Show |
7 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0059 others(4): Show |
7 | HG01256.hp2 HG01891.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.523+335_523+346dup others(12): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | ||||||
| chr6:43655988 | A | ACTTCCTT others(9): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0146 a0001c0001t0011g0013 |
5 | HG01257.hp2 HG01258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+331_523+346dup others(16): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | ||||||
| chr6:43655988 | A | ACTTCCTT others(13): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.523+327_523+346dup others(20): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | ||||||
| chr6:43655988 | ACTTC | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0029 others(15): Show |
21 | HG00280.hp1 HG01192.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.523+343_523+346del others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | ||||||
| chr6:43655992 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.523+301C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655992 | |||||||
| chr6:43655992 | C | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(55): Show |
71 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.523+301C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655992 | |||||||
| chr6:43656028 | CCTTCCTT others(10): Show |
C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(20): Show |
33 | HG00642.hp2 HG01884.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.523+339_523+355del others(17): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656028 | ||||||
| chr6:43656032 | CCTTCCCC others(6): Show |
C | 11 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0136 others(8): Show |
14 | HG01081.hp2 HG01106.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.523+343_523+355del others(13): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656032 | ||||||
| chr6:43656034 | T | G | 3 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0207 |
4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+343T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656034 | |||||||
| chr6:43656035 | TC | T | 28 | a0001c0001t0001g0126 a0001c0001t0001g0142 a0001c0001t0001g0252 others(25): Show |
42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.523+348delC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656035 | ||||||
| chr6:43656036 | C | CCTTCCTT others(4): Show |
2 | a0001c0001t0001g0046 a0001c0001t0020g0110 |
2 | HG01516.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.523+346_523+347ins others(11): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656036 | ||||||
| chr6:43656036 | CCCCTT | C | 20 | a0001c0001t0001g0106 a0001c0001t0001g0143 a0001c0001t0005g0078 others(17): Show |
23 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.523+347_523+351del others(5): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656036 | ||||||
| chr6:43656036 | CCCCTTCT others(2): Show |
C | 8 | a0001c0001t0001g0103 a0001c0001t0004g0073 a0001c0001t0004g0105 others(5): Show |
9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.523+368_523+376del others(9): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656036 | ||||||
| chr6:43656037 | C | CTT | 19 | a0001c0001t0001g0104 a0001c0001t0001g0221 a0001c0001t0007g0035 others(16): Show |
23 | HG00621.hp1 HG00639.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.523+346_523+347ins others(2): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | |||||||
| chr6:43656037 | C | CTTCCTT | 7 | a0001c0001t0007g0035 a0001c0001t0007g0248 a0001c0001t0007g0249 others(4): Show |
8 | HG02109.hp2 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+346_523+347ins others(6): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | |||||||
| chr6:43656037 | C | CTTCCTTC others(3): Show |
3 | a0001c0001t0004g0244 a0001c0001t0007g0246 a0002c0002t0002g0010 |
3 | HG02683.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.523+346_523+347ins others(10): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | |||||||
| chr6:43656037 | C | CTTCCTTC others(10): Show |
1 | a0001c0001t0001g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.523+346_523+347ins others(17): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | |||||||
| chr6:43656038 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0113 |
2 | HG01346.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.523+347C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656038 | |||||||
| chr6:43656039 | C | T | 28 | a0001c0001t0001g0126 a0001c0001t0001g0142 a0001c0001t0001g0252 others(25): Show |
42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.523+348C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656039 | |||||||
| chr6:43656041 | T | C | 28 | a0001c0001t0001g0126 a0001c0001t0001g0142 a0001c0001t0001g0252 others(25): Show |
42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.523+350T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656041 | |||||||
| chr6:43656041 | T | TC | 23 | a0001c0001t0001g0104 a0001c0001t0001g0221 a0001c0001t0004g0244 others(20): Show |
31 | HG00621.hp1 HG02109.hp2 HG02273.hp2 others(28): Show |
intron_variant | MODIFIER | c.523+351dupC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656041 | ||||||
| chr6:43656043 | T | C | 4 | a0002c0002t0002g0083 a0002c0002t0002g0084 a0002c0002t0002g0086 others(1): Show |
4 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+352T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656043 | |||||||
| chr6:43656043 | T | G | 4 | a0001c0001t0005g0078 a0001c0001t0005g0079 a0001c0001t0005g0245 others(1): Show |
4 | HG02965.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+352T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656043 | |||||||
| chr6:43656045 | T | C | 67 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0126 others(64): Show |
96 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.523+354T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656045 | |||||||
| chr6:43656048 | C | T | 5 | a0002c0002t0002g0083 a0002c0002t0002g0084 a0002c0002t0002g0086 others(2): Show |
5 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+357C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656048 | |||||||
| chr6:43656050 | T | C | 5 | a0002c0002t0002g0083 a0002c0002t0002g0084 a0002c0002t0002g0086 others(2): Show |
5 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+359T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656050 | |||||||
| chr6:43656054 | T | C | 6 | a0001c0001t0001g0118 a0002c0002t0002g0083 a0002c0002t0002g0084 others(3): Show |
6 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+363T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656054 | |||||||
| chr6:43656057 | CTTCTTTC others(6): Show |
C | 1 | a0003c0003t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.523+368_523+380del others(13): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656057 | ||||||
| chr6:43656070 | TTCCC | T | 6 | a0002c0002t0002g0087 a0003c0003t0001g0064 a0003c0003t0001g0068 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.523+397_523+400del others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656070 | ||||||
| chr6:43656074 | C | T | 1 | a0003c0003t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.523+383C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656074 | |||||||
| chr6:43656093 | T | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(94): Show |
140 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.523+402T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656093 | |||||||
| chr6:43656108 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0030 others(13): Show |
22 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.523+417G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656108 | |||||||
| chr6:43656121 | T | C | 36 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
47 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.523+430T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656121 | |||||||
| chr6:43656129 | A | C | 1 | a0002c0002t0002g0053 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.523+438A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656129 | |||||||
| chr6:43656221 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(30): Show |
46 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.524-356G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656221 | |||||||
| chr6:43656242 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.524-335C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656242 | |||||||
| chr6:43656280 | T | G | 1 | a0002c0002t0002g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.524-297T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656280 | |||||||
| chr6:43656314 | G | A | 13 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0109 others(10): Show |
15 | HG01074.hp2 HG01099.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.524-263G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656314 | |||||||
| chr6:43656348 | A | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(36): Show |
52 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.524-229A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656348 | |||||||
| chr6:43656398 | T | C | 1 | a0002c0002t0002g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.524-179T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656398 | |||||||
| chr6:43656413 | C | T | 6 | a0001c0001t0001g0106 a0001c0001t0006g0201 a0001c0001t0006g0202 others(3): Show |
6 | HG00741.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-164C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656413 | |||||||
| chr6:43656996 | G | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0191 a0001c0001t0001g0216 |
3 | NA18942.hp2 NA18997.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.670+273G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43656996 | |||||||
| chr6:43657057 | A | G | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+334A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657057 | |||||||
| chr6:43657248 | C | T | 7 | a0001c0001t0001g0139 a0001c0001t0008g0006 a0001c0001t0008g0101 others(4): Show |
11 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+525C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657248 | |||||||
| chr6:43657286 | G | T | 36 | a0001c0001t0001g0126 a0002c0002t0002g0001 a0002c0002t0002g0009 others(33): Show |
65 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.670+563G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657286 | |||||||
| chr6:43657308 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(32): Show |
48 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.670+585T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657308 | |||||||
| chr6:43657514 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.670+791C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657514 | |||||||
| chr6:43657566 | C | T | 37 | a0001c0001t0001g0126 a0002c0002t0002g0001 a0002c0002t0002g0009 others(34): Show |
66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.670+843C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657566 | |||||||
| chr6:43657569 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.670+846T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657569 | |||||||
| chr6:43657701 | T | C | 1 | a0001c0001t0007g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.670+978T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657701 | |||||||
| chr6:43657817 | C | T | 5 | a0001c0001t0001g0106 a0001c0001t0006g0201 a0001c0001t0006g0202 others(2): Show |
5 | HG00741.hp1 HG02630.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+1094C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657817 | |||||||
| chr6:43658155 | T | C | 37 | a0001c0001t0001g0126 a0001c0001t0003g0081 a0002c0002t0002g0001 others(34): Show |
66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.670+1432T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658155 | |||||||
| chr6:43658276 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.670+1553C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658276 | |||||||
| chr6:43658291 | CAA | C | 7 | a0001c0001t0001g0106 a0001c0001t0006g0072 a0001c0001t0006g0201 others(4): Show |
7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1586_670+1587d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43658291 | ||||||
| chr6:43658303 | A | AG | 65 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(62): Show |
79 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.670+1580_670+1581i others(3): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658303 | |||||||
| chr6:43658311 | G | A | 43 | a0001c0001t0001g0118 a0001c0001t0001g0126 a0001c0001t0003g0081 others(40): Show |
72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+1588G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658311 | |||||||
| chr6:43658312 | A | AG | 11 | a0001c0001t0001g0118 a0002c0002t0002g0010 a0002c0002t0002g0083 others(8): Show |
13 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+1589_670+1590i others(3): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658312 | |||||||
| chr6:43658312 | A | G | 31 | a0001c0001t0001g0126 a0001c0001t0003g0081 a0002c0002t0002g0001 others(28): Show |
58 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.670+1589A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658312 | |||||||
| chr6:43658360 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(113): Show |
159 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.670+1637C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658360 | |||||||
| chr6:43658389 | G | A | 1 | a0001c0001t0006g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.670+1666G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658389 | |||||||
| chr6:43658396 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(21): Show |
35 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.670+1673A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658396 | |||||||
| chr6:43658471 | T | C | 1 | a0002c0005t0002g0095 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.670+1748T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658471 | |||||||
| chr6:43658601 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0006g0036 |
2 | HG02965.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.670+1878C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658601 | |||||||
| chr6:43658686 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.670+1963C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658686 | |||||||
| chr6:43658810 | C | T | 1 | a0001c0001t0005g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.670+2087C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658810 | |||||||
| chr6:43659167 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.670+2444T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659167 | |||||||
| chr6:43659202 | G | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(62): Show |
79 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.670+2479G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659202 | |||||||
| chr6:43659225 | C | CT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(37): Show |
53 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.670+2515dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43659225 | ||||||
| chr6:43659225 | C | CTT | 28 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0142 others(25): Show |
29 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.670+2514_670+2515d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43659225 | ||||||
| chr6:43659371 | G | A | 2 | a0001c0001t0008g0006 a0001c0001t0008g0102 |
5 | HG02258.hp1 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+2648G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659371 | |||||||
| chr6:43659386 | C | CT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0133 others(5): Show |
9 | HG00621.hp1 HG01192.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+2677dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43659386 | ||||||
| chr6:43659414 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.670+2691G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659414 | |||||||
| chr6:43659678 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.670+2955G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659678 | |||||||
| chr6:43659944 | C | T | 1 | a0001c0001t0011g0013 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.670+3221C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659944 | |||||||
| chr6:43659961 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.670+3238C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659961 | |||||||
| chr6:43659983 | G | A | 1 | a0001c0001t0003g0218 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.670+3260G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659983 | |||||||
| chr6:43660015 | G | A | 16 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0081 others(13): Show |
18 | HG01074.hp2 HG01099.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.670+3292G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660015 | |||||||
| chr6:43660039 | C | CT | 25 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(22): Show |
26 | HG01192.hp1 HG01358.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.670+3338dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | ||||||
| chr6:43660039 | C | CTT | 42 | a0001c0001t0001g0118 a0001c0001t0001g0126 a0001c0001t0005g0032 others(39): Show |
72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+3337_670+3338d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | ||||||
| chr6:43660039 | C | CTTT | 6 | a0002c0002t0002g0087 a0002c0002t0002g0124 a0002c0002t0002g0128 others(3): Show |
6 | HG01123.hp1 HG02071.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3336_670+3338d others(5): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | ||||||
| chr6:43660039 | CTTTTTT | C | 11 | a0001c0001t0001g0103 a0001c0001t0001g0142 a0001c0001t0001g0143 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+3333_670+3338d others(8): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | ||||||
| chr6:43660039 | CTTTTTTT | C | 5 | a0001c0001t0009g0232 a0001c0001t0009g0233 a0001c0001t0010g0018 others(2): Show |
6 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3332_670+3338d others(9): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | ||||||
| chr6:43660192 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(55): Show |
71 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.670+3469G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660192 | |||||||
| chr6:43660495 | G | A | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+3772G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660495 | |||||||
| chr6:43660594 | G | T | 1 | a0001c0001t0017g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.670+3871G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660594 | |||||||
| chr6:43660609 | G | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(55): Show |
71 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.670+3886G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660609 | |||||||
| chr6:43660636 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.670+3913T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660636 | |||||||
| chr6:43660686 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(55): Show |
71 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.670+3963A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660686 | |||||||
| chr6:43660774 | A | G | 1 | a0001c0001t0006g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.670+4051A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660774 | |||||||
| chr6:43660831 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.670+4108C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660831 | |||||||
| chr6:43660833 | C | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(55): Show |
71 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.670+4110C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660833 | |||||||
| chr6:43660889 | TA | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.670+4171delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660889 | ||||||
| chr6:43660894 | A | C | 1 | a0002c0002t0002g0053 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670+4171A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660894 | |||||||
| chr6:43660937 | G | A | 11 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0073 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+4214G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660937 | |||||||
| chr6:43660979 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.670+4256C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660979 | |||||||
| chr6:43660995 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.670+4272C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660995 | |||||||
| chr6:43661342 | A | T | 1 | a0002c0002t0002g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.670+4619A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661342 | |||||||
| chr6:43661356 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01256.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.670+4633A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661356 | |||||||
| chr6:43661398 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0171 a0001c0001t0001g0242 |
3 | HG01243.hp2 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.670+4675C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661398 | |||||||
| chr6:43661427 | G | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.670+4704G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661427 | |||||||
| chr6:43661436 | G | A | 7 | a0001c0001t0001g0106 a0001c0001t0006g0072 a0001c0001t0006g0201 others(4): Show |
7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+4713G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661436 | |||||||
| chr6:43661486 | C | T | 12 | a0001c0001t0001g0054 a0001c0001t0004g0065 a0001c0001t0004g0066 others(9): Show |
12 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.670+4763C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661486 | |||||||
| chr6:43661489 | C | T | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+4766C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661489 | |||||||
| chr6:43661518 | G | A | 6 | a0001c0001t0001g0118 a0002c0002t0002g0083 a0002c0002t0002g0084 others(3): Show |
6 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+4795G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661518 | |||||||
| chr6:43661538 | G | A | 1 | a0002c0002t0002g0053 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670+4815G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661538 | |||||||
| chr6:43661567 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.670+4844A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661567 | |||||||
| chr6:43661653 | T | A | 37 | a0001c0001t0001g0126 a0002c0002t0002g0001 a0002c0002t0002g0009 others(34): Show |
66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.670+4930T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661653 | |||||||
| chr6:43661653 | T | C | 1 | a0001c0001t0013g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.670+4930T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661653 | |||||||
| chr6:43661660 | C | CA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
165 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.670+4958dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43661660 | ||||||
| chr6:43661660 | C | CAA | 28 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0041 others(25): Show |
30 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.670+4957_670+4958d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43661660 | ||||||
| chr6:43661660 | CA | C | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0142 others(24): Show |
27 | HG01934.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.670+4958delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43661660 | ||||||
| chr6:43661759 | G | A | 1 | a0001c0001t0017g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.670+5036G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661759 | |||||||
| chr6:43661759 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0048 |
4 | HG00140.hp1 HG01192.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+5036G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661759 | |||||||
| chr6:43661809 | G | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.670+5086G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661809 | |||||||
| chr6:43661811 | A | G | 1 | a0001c0001t0004g0250 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670+5088A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661811 | |||||||
| chr6:43661948 | C | T | 38 | a0001c0001t0001g0126 a0001c0001t0001g0221 a0002c0002t0002g0001 others(35): Show |
67 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.670+5225C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661948 | |||||||
| chr6:43662064 | G | A | 36 | a0001c0001t0001g0126 a0002c0002t0002g0001 a0002c0002t0002g0009 others(33): Show |
65 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.670+5341G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662064 | |||||||
| chr6:43662080 | A | G | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+5357A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662080 | |||||||
| chr6:43662269 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.670+5546T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662269 | |||||||
| chr6:43662370 | C | CTT | 35 | a0001c0001t0001g0126 a0002c0002t0002g0001 a0002c0002t0002g0009 others(32): Show |
64 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.670+5660_670+5661d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43662370 | ||||||
| chr6:43662370 | CT | C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0057 others(10): Show |
14 | HG00140.hp2 HG01346.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.670+5661delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43662370 | ||||||
| chr6:43662380 | T | C | 11 | a0001c0001t0001g0103 a0001c0001t0001g0142 a0001c0001t0001g0143 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+5657T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662380 | |||||||
| chr6:43662658 | C | T | 4 | a0002c0002t0002g0114 a0002c0002t0002g0150 a0002c0002t0002g0215 others(1): Show |
4 | HG00621.hp1 NA18945.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+5935C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662658 | |||||||
| chr6:43662823 | G | T | 16 | a0001c0001t0001g0103 a0001c0001t0001g0142 a0001c0001t0001g0143 others(13): Show |
17 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+6100G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662823 | |||||||
| chr6:43662940 | C | T | 1 | a0001c0001t0006g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.670+6217C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662940 | |||||||
| chr6:43662954 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(54): Show |
70 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(67): Show |
intron_variant | MODIFIER | c.670+6231G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662954 | |||||||
| chr6:43662968 | A | AT | 106 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(103): Show |
149 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.670+6255dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43662968 | ||||||
| chr6:43663018 | A | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.670+6295A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663018 | |||||||
| chr6:43663065 | T | C | 16 | a0001c0001t0001g0103 a0001c0001t0001g0142 a0001c0001t0001g0143 others(13): Show |
17 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+6342T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663065 | |||||||
| chr6:43663227 | AT | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.670+6513delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43663227 | ||||||
| chr6:43663352 | G | A | 1 | a0002c0002t0002g0001 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.670+6629G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663352 | |||||||
| chr6:43663510 | C | T | 1 | a0002c0002t0002g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.670+6787C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663510 | |||||||
| chr6:43663522 | G | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.670+6799G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663522 | |||||||
| chr6:43663576 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670+6853G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663576 | |||||||
| chr6:43663592 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.670+6869G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663592 | |||||||
| chr6:43663643 | T | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.670+6920T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663643 | |||||||
| chr6:43663659 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0001g0149 others(3): Show |
6 | HG01346.hp2 HG01433.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+6936C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663659 | |||||||
| chr6:43663737 | AC | A | 5 | a0001c0001t0007g0035 a0001c0001t0007g0246 a0001c0001t0007g0248 others(2): Show |
6 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+7015delC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663737 | |||||||
| chr6:43663757 | C | T | 7 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-7032C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663757 | |||||||
| chr6:43663795 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.671-6994C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663795 | |||||||
| chr6:43663847 | T | C | 37 | a0001c0001t0001g0126 a0002c0002t0002g0001 a0002c0002t0002g0009 others(34): Show |
66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.671-6942T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663847 | |||||||
| chr6:43663858 | C | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(105): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.671-6931C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663858 | |||||||
| chr6:43663916 | C | G | 3 | a0001c0001t0008g0006 a0001c0001t0008g0101 a0001c0001t0008g0102 |
6 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-6873C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663916 | |||||||
| chr6:43663936 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(62): Show |
79 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.671-6853C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663936 | |||||||
| chr6:43663969 | C | T | 7 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-6820C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663969 | |||||||
| chr6:43664024 | C | CT | 5 | a0001c0001t0007g0035 a0001c0001t0007g0246 a0001c0001t0007g0248 others(2): Show |
6 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-6764dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43664024 | ||||||
| chr6:43664026 | C | A | 5 | a0001c0001t0007g0035 a0001c0001t0007g0246 a0001c0001t0007g0248 others(2): Show |
6 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-6763C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664026 | |||||||
| chr6:43664026 | C | CA | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(69): Show |
113 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.671-6763_671-6762i others(3): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664026 | |||||||
| chr6:43664026 | C | CAG | 7 | a0001c0001t0005g0032 a0001c0001t0005g0078 a0001c0001t0005g0079 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-6763_671-6762i others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664026 | |||||||
| chr6:43664027 | G | A | 30 | a0001c0001t0001g0118 a0001c0001t0001g0210 a0001c0001t0004g0065 others(27): Show |
31 | HG00597.hp2 HG00639.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.671-6762G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664027 | |||||||
| chr6:43664028 | A | G | 22 | a0001c0001t0001g0118 a0001c0001t0001g0210 a0001c0001t0004g0065 others(19): Show |
22 | HG00597.hp2 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.671-6761A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664028 | |||||||
| chr6:43664174 | T | G | 1 | a0001c0001t0001g0016 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.671-6615T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664174 | |||||||
| chr6:43664177 | G | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(104): Show |
150 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.671-6612G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664177 | |||||||
| chr6:43664182 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.671-6607G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664182 | |||||||
| chr6:43664203 | GTGATGA | G | 10 | a0001c0001t0003g0024 a0001c0001t0003g0109 a0001c0001t0003g0135 others(7): Show |
12 | HG01257.hp2 HG01258.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.671-6566_671-6561d others(8): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43664203 | ||||||
| chr6:43664220 | G | T | 3 | a0001c0001t0008g0006 a0001c0001t0008g0101 a0001c0001t0008g0102 |
6 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-6569G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664220 | |||||||
| chr6:43664223 | G | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(28): Show |
42 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.671-6566G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664223 | |||||||
| chr6:43664226 | G | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(61): Show |
77 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
intron_variant | MODIFIER | c.671-6563G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664226 | |||||||
| chr6:43664322 | C | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(18): Show |
29 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.671-6467C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664322 | |||||||
| chr6:43664364 | G | A | 36 | a0002c0002t0002g0001 a0002c0002t0002g0009 a0002c0002t0002g0010 others(33): Show |
65 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.671-6425G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664364 | |||||||
| chr6:43664536 | G | A | 1 | a0002c0002t0019g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-6253G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664536 | |||||||
| chr6:43664539 | C | T | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-6250C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664539 | |||||||
| chr6:43664596 | C | A | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-6193C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664596 | |||||||
| chr6:43664646 | T | G | 6 | a0001c0001t0001g0118 a0002c0002t0002g0083 a0002c0002t0002g0084 others(3): Show |
6 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-6143T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664646 | |||||||
| chr6:43664652 | T | C | 43 | a0001c0001t0001g0118 a0002c0002t0002g0001 a0002c0002t0002g0009 others(40): Show |
72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.671-6137T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664652 | |||||||
| chr6:43664711 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.671-6078G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664711 | |||||||
| chr6:43664748 | G | C | 7 | a0001c0001t0001g0106 a0001c0001t0006g0072 a0001c0001t0006g0201 others(4): Show |
7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-6041G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664748 | |||||||
| chr6:43664874 | G | A | 1 | a0001c0001t0009g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.671-5915G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664874 | |||||||
| chr6:43664950 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0169 |
2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.671-5839C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664950 | |||||||
| chr6:43665205 | G | C | 7 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-5584G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665205 | |||||||
| chr6:43665248 | G | T | 1 | a0003c0003t0001g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671-5541G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665248 | |||||||
| chr6:43665305 | G | A | 1 | a0001c0001t0006g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.671-5484G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665305 | |||||||
| chr6:43665365 | A | G | 1 | a0001c0001t0004g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.671-5424A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665365 | |||||||
| chr6:43665466 | T | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(106): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.671-5323T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665466 | |||||||
| chr6:43665483 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.671-5306A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665483 | |||||||
| chr6:43665558 | G | A | 6 | a0001c0001t0009g0168 a0001c0001t0009g0232 a0001c0001t0009g0233 others(3): Show |
7 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-5231G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665558 | |||||||
| chr6:43665560 | G | C | 7 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-5229G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665560 | |||||||
| chr6:43665710 | A | T | 1 | a0001c0001t0006g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.671-5079A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665710 | |||||||
| chr6:43665823 | C | T | 50 | a0001c0001t0001g0106 a0001c0001t0006g0036 a0001c0001t0006g0072 others(47): Show |
77 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.671-4966C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665823 | |||||||
| chr6:43665833 | T | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0206 |
7 | HG02486.hp2 HG02559.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-4956T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665833 | |||||||
| chr6:43665876 | T | C | 4 | a0002c0002t0002g0114 a0002c0002t0002g0150 a0002c0002t0002g0215 others(1): Show |
4 | HG00621.hp1 NA18945.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-4913T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665876 | |||||||
| chr6:43665980 | C | A | 1 | a0002c0002t0002g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.671-4809C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665980 | |||||||
| chr6:43665983 | G | A | 7 | a0001c0001t0001g0106 a0001c0001t0006g0072 a0001c0001t0006g0201 others(4): Show |
7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-4806G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665983 | |||||||
| chr6:43666232 | CT | C | 7 | a0001c0001t0001g0106 a0001c0001t0006g0072 a0001c0001t0006g0201 others(4): Show |
7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-4554delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43666232 | ||||||
| chr6:43666448 | A | G | 1 | a0002c0002t0002g0124 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.671-4341A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666448 | |||||||
| chr6:43666530 | C | T | 5 | a0002c0002t0002g0083 a0002c0002t0002g0084 a0002c0002t0002g0086 others(2): Show |
5 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-4259C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666530 | |||||||
| chr6:43666637 | C | T | 7 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-4152C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666637 | |||||||
| chr6:43666771 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.671-4018G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666771 | |||||||
| chr6:43666910 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(19): Show |
30 | HG00597.hp2 HG00642.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.671-3879A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666910 | |||||||
| chr6:43666987 | G | T | 7 | a0001c0001t0001g0106 a0001c0001t0006g0072 a0001c0001t0006g0201 others(4): Show |
7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-3802G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666987 | |||||||
| chr6:43666996 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.671-3793A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666996 | |||||||
| chr6:43667005 | A | C | 5 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0011g0013 others(2): Show |
6 | HG01257.hp2 HG01258.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-3784A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667005 | |||||||
| chr6:43667428 | C | CCTGCCTG others(1): Show |
121 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(118): Show |
164 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.671-3355_671-3354i others(10): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43667428 | ||||||
| chr6:43667494 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(31): Show |
46 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.671-3295G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667494 | |||||||
| chr6:43667514 | C | T | 1 | a0001c0001t0006g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.671-3275C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667514 | |||||||
| chr6:43667658 | G | A | 11 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0073 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-3131G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667658 | |||||||
| chr6:43667681 | C | CCCT | 44 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(41): Show |
74 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.671-3094_671-3092d others(5): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43667681 | ||||||
| chr6:43667737 | C | T | 6 | a0001c0001t0009g0168 a0001c0001t0009g0232 a0001c0001t0009g0233 others(3): Show |
7 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-3052C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667737 | |||||||
| chr6:43667864 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(31): Show |
46 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.671-2925T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667864 | |||||||
| chr6:43668089 | AG | A | 6 | a0001c0001t0006g0072 a0001c0001t0006g0201 a0001c0001t0006g0202 others(3): Show |
6 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-2695delG | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43668089 | ||||||
| chr6:43668120 | A | C | 11 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0073 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-2669A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668120 | |||||||
| chr6:43668158 | G | A | 1 | a0004c0004t0001g0161 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.671-2631G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668158 | |||||||
| chr6:43668165 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.671-2624T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668165 | |||||||
| chr6:43668183 | C | T | 1 | a0002c0002t0019g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-2606C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668183 | |||||||
| chr6:43668374 | G | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(31): Show |
46 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.671-2415G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668374 | |||||||
| chr6:43668435 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671-2354C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668435 | |||||||
| chr6:43668435 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.671-2354C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668435 | |||||||
| chr6:43668441 | C | T | 8 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(5): Show |
9 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-2348C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668441 | |||||||
| chr6:43668502 | C | T | 1 | a0001c0001t0005g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.671-2287C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668502 | |||||||
| chr6:43668515 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.671-2274G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668515 | |||||||
| chr6:43668920 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.671-1869C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668920 | |||||||
| chr6:43669047 | A | C | 1 | a0001c0001t0005g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.671-1742A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669047 | |||||||
| chr6:43669276 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.671-1513G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669276 | |||||||
| chr6:43669326 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(31): Show |
46 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.671-1463T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669326 | |||||||
| chr6:43669406 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0089 a0001c0001t0001g0090 |
5 | NA18747.hp1 NA18974.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1383G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669406 | |||||||
| chr6:43669482 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.671-1307G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669482 | |||||||
| chr6:43669633 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.671-1156C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669633 | |||||||
| chr6:43669663 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.671-1126G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669663 | |||||||
| chr6:43669678 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0046 others(7): Show |
12 | HG01106.hp1 HG01192.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.671-1111G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669678 | |||||||
| chr6:43669862 | A | G | 42 | a0002c0002t0002g0001 a0002c0002t0002g0009 a0002c0002t0002g0010 others(39): Show |
71 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.671-927A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669862 | |||||||
| chr6:43669892 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0194 |
3 | NA18961.hp1 NA19062.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.671-897G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669892 | |||||||
| chr6:43669906 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0141 |
2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.671-883G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669906 | |||||||
| chr6:43670024 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0140 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.671-765C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670024 | |||||||
| chr6:43670133 | G | A | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-656G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670133 | |||||||
| chr6:43670198 | C | G | 1 | a0001c0001t0021g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-591C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670198 | |||||||
| chr6:43670327 | C | T | 1 | a0002c0002t0002g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.671-462C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670327 | |||||||
| chr6:43670366 | C | T | 1 | a0002c0002t0002g0237 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.671-423C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670366 | |||||||
| chr6:43670421 | G | C | 1 | a0002c0002t0002g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.671-368G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670421 | |||||||
| chr6:43670455 | T | C | 17 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0142 others(14): Show |
18 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.671-334T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670455 | |||||||
| chr6:43670667 | C | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671-122C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670667 | |||||||
| chr6:43670677 | T | A | 1 | a0001c0001t0006g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.671-112T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670677 | |||||||
| chr6:43670685 | T | C | 6 | a0001c0001t0006g0072 a0001c0001t0006g0201 a0001c0001t0006g0202 others(3): Show |
6 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-104T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670685 | |||||||
| chr6:43670748 | C | A | 8 | a0001c0001t0005g0032 a0001c0001t0005g0067 a0001c0001t0005g0078 others(5): Show |
9 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-41C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670748 |