Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1271 |
| ensemblid | ENSG00000122756.15 |
| hgncid | 2170 |
| symbol | CNTFR |
| name | ciliary neurotrophic factor receptor |
| refseq_nuc | NM_147164.3 |
| refseq_prot | NP_671693.1 |
| ensembl_nuc | ENST00000378980.8 |
| ensembl_prot | ENSP00000368265.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 34551433 |
| end | 34589724 |
| strand | - |
| ver | v1.2 |
| region | chr9:34551433-34589724 |
| region5000 | chr9:34546433-34594724 |
| regionname0 | CNTFR_chr9_34551433_34589724 |
| regionname5000 | CNTFR_chr9_34546433_34594724 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 372 | 400 | 95 | 82 | 164 | 14 | 43 | 126 | CNTFR_chr9_34546433_34594724 | CNTFR | MAAPV others(367): Show |
chr9 | 34546433 | 34594724 |
| a0002 | 0/0 | 372 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | MAAPV others(367): Show |
chr9 | 34546433 | 34594724 |
| a0003 | 0/0 | 372 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | MAAPV others(367): Show |
chr9 | 34546433 | 34594724 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1116 | 379 | 93 | 79 | 151 | 14 | 40 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0001c0002 | 0/0 | 1116 | 13 | 0 | 1 | 12 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0001c0003 | 0/0 | 1116 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0001c0004 | 0/0 | 1116 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0001c0007 | 0/0 | 1116 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0001c0008 | 0/0 | 1116 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0001c0009 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0001c0010 | 0/0 | 1116 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0002c0005 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 | ||
| a0003c0006 | 0/0 | 1116 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | ATGGC others(1111): Show |
chr9 | 34546433 | 34594724 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2038 | 260 | 68 | 53 | 98 | 14 | 25 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0002 | 0/0 | 2038 | 73 | 13 | 4 | 46 | 0 | 10 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0003 | 0/0 | 2038 | 30 | 2 | 19 | 5 | 0 | 4 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0004 | 0/0 | 2038 | 8 | 7 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0005 | 0/0 | 2038 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0006 | 0/0 | 2038 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0007 | 0/0 | 2038 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0008 | 0/0 | 2038 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0001t0009 | 0/0 | 2038 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0002t0002 | 0/0 | 2038 | 13 | 0 | 1 | 12 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0003t0001 | 0/0 | 2038 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0004t0001 | 0/0 | 2038 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0007t0003 | 0/0 | 2038 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0008t0002 | 0/0 | 2038 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0009t0001 | 0/0 | 2038 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0001c0010t0001 | 0/0 | 2038 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0002c0005t0001 | 0/0 | 2038 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| a0003c0006t0001 | 0/0 | 2038 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | GCAGA others(2033): Show |
chr9 | 34546433 | 34594724 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 0 | 9 | 1 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0002 | 0/0 | 11 | 1 | 6 | 0 | 1 | 3 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0005 | 0/0 | 7 | 3 | 4 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0039 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0011 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0003 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0004g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0006g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0002t0002g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0003t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0007t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0008t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0009t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0001c0010t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0002c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| a0003c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01074 | hp1 | a0001 | c0008 | t0002 | g0251 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0110 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0087 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0235 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02723 | hp1 | a0002 | c0005 | t0001 | g0192 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0093 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0038 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03491 | hp1 | a0001 | c0007 | t0003 | g0246 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0245 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03654 | hp1 | a0003 | c0006 | t0001 | g0214 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19000 | hp2 | a0001 | c0010 | t0001 | g0259 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19089 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | GIH | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG02559 | hp2 | a0001 | c0009 | t0001 | g0061 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0159 | REF | REF | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0039 | REF | REF | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34564643 | C | T | 1 | a0003 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.275G>A | p.Arg92His | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 556/2038 | 275/1119 | 92/372 | chr9 | 34564643 | |||
| chr9:34564745 | C | T | 1 | a0002 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.173G>A | p.Arg58Gln | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 454/2038 | 173/1119 | 58/372 | chr9 | 34564745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34556348 | C | T | 1 | a0001c0007 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.675G>A | p.Thr225Thr | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/10 | 956/2038 | 675/1119 | 225/372 | chr9 | 34556348 | |||
| chr9:34556393 | C | T | 1 | a0001c0003 | 2 | HG01243.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.630G>A | p.Val210Val | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/10 | 911/2038 | 630/1119 | 210/372 | chr9 | 34556393 | |||
| chr9:34557905 | G | A | 1 | a0001c0002 | 13 | HG00558.hp2 HG00642.hp2 HG02074.hp1 others(10): Show |
synonymous_variant | LOW | c.399C>T | p.Thr133Thr | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 5/10 | 680/2038 | 399/1119 | 133/372 | chr9 | 34557905 | |||
| chr9:34564723 | G | C | 1 | a0001c0008 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.195C>G | p.Ala65Ala | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 476/2038 | 195/1119 | 65/372 | chr9 | 34564723 | |||
| chr9:34564813 | G | A | 1 | a0001c0004 | 2 | HG02698.hp1 HG02738.hp1 |
synonymous_variant | LOW | c.105C>T | p.Tyr35Tyr | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 386/2038 | 105/1119 | 35/372 | chr9 | 34564813 | |||
| chr9:34568928 | T | G | 1 | a0001c0009 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.54A>C | p.Ala18Ala | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/10 | 335/2038 | 54/1119 | 18/372 | chr9 | 34568928 | |||
| chr9:34568937 | G | A | 1 | a0001c0010 | 1 | NA19000.hp2 | synonymous_variant | LOW | c.45C>T | p.Ala15Ala | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/10 | 326/2038 | 45/1119 | 15/372 | chr9 | 34568937 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34551448 | G | A | 1 | a0001c0001t0006 | 2 | HG01106.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*623C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 623 | chr9 | 34551448 | ||||||
| chr9:34551762 | C | T | 1 | a0001c0001t0008 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 309 | chr9 | 34551762 | ||||||
| chr9:34551898 | G | A | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0008t0002 |
87 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*173C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 173 | chr9 | 34551898 | ||||||
| chr9:34551921 | C | T | 1 | a0001c0001t0009 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 150 | chr9 | 34551921 | ||||||
| chr9:34551922 | G | A | 1 | a0001c0001t0007 | 2 | HG02258.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 149 | chr9 | 34551922 | ||||||
| chr9:34551931 | G | A | 1 | a0001c0001t0009 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 140 | chr9 | 34551931 | ||||||
| chr9:34552020 | G | C | 2 | a0001c0001t0003 a0001c0007t0003 |
31 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*51C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 51 | chr9 | 34552020 | ||||||
| chr9:34589563 | C | T | 1 | a0001c0001t0005 | 2 | NA18946.hp1 NA19089.hp2 |
5_prime_UTR_variant | MODIFIER | c.-120G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/10 | 20582 | chr9 | 34589563 | ||||||
| chr9:34589662 | G | C | 1 | a0001c0001t0004 | 8 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-219C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/10 | 20681 | chr9 | 34589662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34552075 | T | C | 1 | a0001c0001t0001g0045 | 2 | NA18973.hp2 NA18993.hp1 |
splice_region_variant&intron_variant | LOW | c.1119-4A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 9/9 | chr9 | 34552075 | |||||||
| chr9:34552368 | T | TG | 7 | a0001c0001t0001g0019 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
9 | HG02647.hp2 HG02965.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.950-40dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552368 | |||||||
| chr9:34552383 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.950-54A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552383 | |||||||
| chr9:34552439 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(116): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.950-110G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552439 | |||||||
| chr9:34552660 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.949+14C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552660 | |||||||
| chr9:34552913 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.769-59G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34552913 | |||||||
| chr9:34553219 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.769-365C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553219 | |||||||
| chr9:34553279 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.769-425G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553279 | |||||||
| chr9:34553413 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769-559A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553413 | |||||||
| chr9:34553613 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0107 |
3 | HG02486.hp1 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.769-759C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553613 | |||||||
| chr9:34553650 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0243 others(1): Show |
8 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.769-796C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553650 | |||||||
| chr9:34553669 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.769-815A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553669 | |||||||
| chr9:34553940 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.769-1086C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553940 | |||||||
| chr9:34553970 | G | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
161 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.769-1116C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553970 | |||||||
| chr9:34554002 | G | A | 22 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0236 others(19): Show |
34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.769-1148C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554002 | |||||||
| chr9:34554015 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0176 |
5 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.769-1161C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554015 | |||||||
| chr9:34554017 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.769-1163C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554017 | |||||||
| chr9:34554022 | G | A | 1 | a0001c0001t0007g0087 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769-1168C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554022 | |||||||
| chr9:34554040 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.769-1186C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554040 | |||||||
| chr9:34554062 | G | A | 22 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0236 others(19): Show |
34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.769-1208C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554062 | |||||||
| chr9:34554146 | C | T | 5 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0080 others(2): Show |
5 | HG00738.hp1 HG02735.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-1292G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554146 | |||||||
| chr9:34554156 | C | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0070 others(2): Show |
7 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.769-1302G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554156 | |||||||
| chr9:34554229 | G | C | 24 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0147 others(21): Show |
36 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.769-1375C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554229 | |||||||
| chr9:34554261 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.769-1407G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554261 | |||||||
| chr9:34554335 | G | A | 1 | a0001c0001t0003g0053 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.769-1481C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554335 | |||||||
| chr9:34554355 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.769-1501T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554355 | |||||||
| chr9:34554426 | G | A | 1 | a0001c0001t0009g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.769-1572C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554426 | |||||||
| chr9:34554471 | T | A | 1 | a0001c0001t0001g0042 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.769-1617A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554471 | |||||||
| chr9:34554603 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0003g0050 |
3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.768+1652G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554603 | |||||||
| chr9:34554636 | A | G | 24 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0147 others(21): Show |
36 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.768+1619T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554636 | |||||||
| chr9:34554718 | C | T | 22 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0236 others(19): Show |
34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+1537G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554718 | |||||||
| chr9:34554737 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.768+1518A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554737 | |||||||
| chr9:34554893 | G | C | 4 | a0001c0001t0001g0085 a0001c0001t0004g0009 a0001c0001t0004g0264 others(1): Show |
9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+1362C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554893 | |||||||
| chr9:34554941 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG02647.hp1 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.768+1314G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554941 | |||||||
| chr9:34555001 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.768+1254A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555001 | |||||||
| chr9:34555028 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0152 |
2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.768+1227G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555028 | |||||||
| chr9:34555108 | C | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0036 others(8): Show |
16 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.768+1147G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555108 | |||||||
| chr9:34555334 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.768+921C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555334 | |||||||
| chr9:34555447 | T | C | 22 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0236 others(19): Show |
34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+808A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555447 | |||||||
| chr9:34555464 | G | A | 1 | a0003c0006t0001g0214 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.768+791C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555464 | |||||||
| chr9:34555483 | C | T | 22 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0236 others(19): Show |
34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+772G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555483 | |||||||
| chr9:34555502 | G | C | 22 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0236 others(19): Show |
34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+753C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555502 | |||||||
| chr9:34555818 | T | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(29): Show |
48 | HG00639.hp2 HG00738.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.768+437A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555818 | |||||||
| chr9:34555883 | G | GCCCGCCA others(9): Show |
1 | a0001c0001t0001g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.768+356_768+371dup others(16): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555883 | |||||||
| chr9:34555903 | GCCATCTC others(41): Show |
G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(1): Show |
6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+304_768+351del others(48): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555903 | |||||||
| chr9:34555918 | T | C | 21 | a0001c0001t0001g0152 a0001c0001t0001g0236 a0001c0001t0003g0003 others(18): Show |
33 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.768+337A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555918 | |||||||
| chr9:34555933 | C | T | 21 | a0001c0001t0001g0152 a0001c0001t0001g0236 a0001c0001t0003g0003 others(18): Show |
33 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.768+322G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555933 | |||||||
| chr9:34555935 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0219 |
2 | HG01891.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.768+320C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555935 | |||||||
| chr9:34555935 | GCCATCTC others(9): Show |
G | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.768+304_768+319del others(16): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555935 | |||||||
| chr9:34555963 | C | CCCCGCCA others(13): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0137 a0001c0001t0009g0245 |
3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.768+272_768+291dup others(20): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555963 | |||||||
| chr9:34555973 | T | G | 1 | a0001c0001t0001g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.768+282A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555973 | |||||||
| chr9:34556024 | C | G | 25 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(22): Show |
39 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.768+231G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34556024 | |||||||
| chr9:34556049 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.768+206G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34556049 | |||||||
| chr9:34556194 | C | CCACTCAC others(15): Show |
12 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(9): Show |
24 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.768+39_768+60dupTT others(20): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34556194 | |||||||
| chr9:34556455 | A | T | 25 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(22): Show |
39 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.605-37T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556455 | |||||||
| chr9:34556795 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.605-377G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556795 | |||||||
| chr9:34556844 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.605-426T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556844 | |||||||
| chr9:34556935 | C | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.605-517G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556935 | |||||||
| chr9:34557073 | G | A | 4 | a0001c0001t0002g0122 a0001c0001t0002g0140 a0001c0001t0002g0141 others(1): Show |
4 | HG00609.hp2 NA18970.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+453C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557073 | |||||||
| chr9:34557099 | T | TG | 68 | a0001c0001t0001g0036 a0001c0001t0001g0117 a0001c0001t0001g0133 others(65): Show |
95 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.604+426dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557099 | |||||||
| chr9:34557122 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.604+404C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557122 | |||||||
| chr9:34557141 | C | T | 2 | a0001c0002t0002g0127 a0001c0002t0002g0225 |
2 | NA19066.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.604+385G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557141 | |||||||
| chr9:34557192 | T | TG | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.604+333dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557192 | |||||||
| chr9:34557194 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0152 others(1): Show |
6 | HG01891.hp1 HG02965.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.604+332C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557194 | |||||||
| chr9:34557249 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.604+277G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557249 | |||||||
| chr9:34557314 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.604+212G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557314 | |||||||
| chr9:34557315 | G | A | 27 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(24): Show |
39 | HG00099.hp1 HG00544.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.604+211C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557315 | |||||||
| chr9:34557392 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.604+134G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557392 | |||||||
| chr9:34557817 | G | A | 1 | a0001c0001t0004g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.437+50C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 5/9 | chr9 | 34557817 | |||||||
| chr9:34558080 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.320-96G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558080 | |||||||
| chr9:34558235 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.320-251G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558235 | |||||||
| chr9:34558518 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0212 others(1): Show |
6 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-534C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558518 | |||||||
| chr9:34558576 | T | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.320-592A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558576 | |||||||
| chr9:34558644 | A | G | 23 | a0001c0001t0001g0064 a0001c0001t0001g0152 a0001c0001t0001g0186 others(20): Show |
35 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.320-660T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558644 | |||||||
| chr9:34558667 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.320-683T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558667 | |||||||
| chr9:34558751 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.320-767A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558751 | |||||||
| chr9:34558913 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
7 | HG01891.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-929G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558913 | |||||||
| chr9:34558914 | G | A | 3 | a0001c0001t0002g0051 a0001c0001t0002g0132 a0001c0001t0002g0231 |
4 | HG00597.hp2 NA18949.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-930C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558914 | |||||||
| chr9:34559031 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.320-1047G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559031 | |||||||
| chr9:34559092 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.320-1108G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559092 | |||||||
| chr9:34559100 | G | A | 5 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0080 others(2): Show |
5 | HG00738.hp1 HG02735.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-1116C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559100 | |||||||
| chr9:34559503 | T | C | 145 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(142): Show |
211 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.320-1519A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559503 | |||||||
| chr9:34559503 | T | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0212 |
5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1519A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559503 | |||||||
| chr9:34559524 | C | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0212 |
5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1540G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559524 | |||||||
| chr9:34559563 | T | C | 23 | a0001c0001t0001g0064 a0001c0001t0001g0096 a0001c0001t0001g0097 others(20): Show |
35 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.320-1579A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559563 | |||||||
| chr9:34559614 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0100 |
4 | HG03516.hp1 NA18522.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-1630G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559614 | |||||||
| chr9:34559835 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.320-1851G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559835 | |||||||
| chr9:34559888 | T | A | 4 | a0001c0001t0001g0085 a0001c0001t0004g0009 a0001c0001t0004g0264 others(1): Show |
9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.320-1904A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559888 | |||||||
| chr9:34559914 | C | G | 22 | a0001c0001t0001g0064 a0001c0001t0001g0152 a0001c0001t0001g0236 others(19): Show |
34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.320-1930G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559914 | |||||||
| chr9:34559918 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.320-1934T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559918 | |||||||
| chr9:34559924 | C | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0023 others(15): Show |
29 | HG02083.hp1 HG02132.hp2 HG02523.hp2 others(26): Show |
intron_variant | MODIFIER | c.320-1940G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559924 | |||||||
| chr9:34560275 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0112 |
3 | NA18946.hp2 NA18988.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.320-2291G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560275 | |||||||
| chr9:34560322 | G | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(81): Show |
124 | HG00099.hp1 HG00544.hp1 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.320-2338C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560322 | |||||||
| chr9:34560351 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.320-2367C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560351 | |||||||
| chr9:34560544 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0063 others(7): Show |
14 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.320-2560C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560544 | |||||||
| chr9:34560605 | A | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(1): Show |
6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-2621T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560605 | |||||||
| chr9:34560620 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0260 others(1): Show |
13 | NA18941.hp2 NA18942.hp1 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.320-2636C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560620 | |||||||
| chr9:34560647 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.320-2663A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560647 | |||||||
| chr9:34560715 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0212 |
5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-2731G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560715 | |||||||
| chr9:34560737 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.320-2753C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560737 | |||||||
| chr9:34560798 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.320-2814G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560798 | |||||||
| chr9:34560827 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0091 others(5): Show |
15 | HG00733.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.320-2843C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560827 | |||||||
| chr9:34560981 | C | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.320-2997G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560981 | |||||||
| chr9:34561069 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(23): Show |
39 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.320-3085G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561069 | |||||||
| chr9:34561162 | G | A | 66 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0117 others(63): Show |
94 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.320-3178C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561162 | |||||||
| chr9:34561250 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(11): Show |
26 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.320-3266G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561250 | |||||||
| chr9:34561341 | G | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02615.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+3258C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561341 | |||||||
| chr9:34561470 | T | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0064 others(28): Show |
46 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.319+3129A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561470 | |||||||
| chr9:34561531 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.319+3068C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561531 | |||||||
| chr9:34561562 | T | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.319+3037A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561562 | |||||||
| chr9:34561744 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.319+2855C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561744 | |||||||
| chr9:34561810 | C | T | 66 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0117 others(63): Show |
94 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.319+2789G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561810 | |||||||
| chr9:34561885 | A | C | 1 | a0001c0001t0002g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.319+2714T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561885 | |||||||
| chr9:34562095 | A | G | 29 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(26): Show |
41 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.319+2504T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562095 | |||||||
| chr9:34562127 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0212 |
5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+2472G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562127 | |||||||
| chr9:34562193 | T | C | 1 | a0001c0001t0002g0142 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.319+2406A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562193 | |||||||
| chr9:34562212 | A | G | 2 | a0001c0001t0006g0047 a0001c0001t0009g0245 |
3 | HG01106.hp1 HG03239.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.319+2387T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562212 | |||||||
| chr9:34562268 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.319+2331C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562268 | |||||||
| chr9:34562269 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319+2330G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562269 | |||||||
| chr9:34562350 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.319+2249C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562350 | |||||||
| chr9:34562501 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.319+2098G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562501 | |||||||
| chr9:34562588 | G | A | 1 | a0001c0001t0003g0050 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.319+2011C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562588 | |||||||
| chr9:34562592 | C | G | 52 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(49): Show |
77 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.319+2007G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562592 | |||||||
| chr9:34562639 | C | T | 1 | a0001c0009t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.319+1960G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562639 | |||||||
| chr9:34562816 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.319+1783G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562816 | |||||||
| chr9:34562833 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0212 |
5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+1766G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562833 | |||||||
| chr9:34562915 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA18959.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.319+1684A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562915 | |||||||
| chr9:34563172 | G | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(2): Show |
7 | HG01891.hp1 HG02965.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+1427C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563172 | |||||||
| chr9:34563235 | C | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0216 |
3 | HG01255.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.319+1364G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563235 | |||||||
| chr9:34563301 | GTGCTGGG others(15): Show |
G | 1 | a0001c0001t0002g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.319+1276_319+1297d others(24): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563301 | |||||||
| chr9:34563321 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.319+1278G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563321 | |||||||
| chr9:34563466 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.319+1133C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563466 | |||||||
| chr9:34563565 | A | G | 27 | a0001c0001t0001g0028 a0001c0001t0001g0064 a0001c0001t0001g0072 others(24): Show |
39 | HG00099.hp1 HG00544.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.319+1034T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563565 | |||||||
| chr9:34563657 | C | A | 2 | a0001c0001t0003g0073 a0001c0001t0003g0086 |
2 | HG01167.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.319+942G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563657 | |||||||
| chr9:34563657 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0255 |
2 | HG01928.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.319+942G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563657 | |||||||
| chr9:34563727 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.319+872G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563727 | |||||||
| chr9:34563758 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0133 |
2 | HG01109.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.319+841C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563758 | |||||||
| chr9:34563760 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.319+839G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563760 | |||||||
| chr9:34563830 | T | A | 1 | a0001c0001t0002g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.319+769A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563830 | |||||||
| chr9:34563868 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.319+731A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563868 | |||||||
| chr9:34564027 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.319+572C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564027 | |||||||
| chr9:34564117 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.319+482C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564117 | |||||||
| chr9:34564181 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(1): Show |
6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+418G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564181 | |||||||
| chr9:34564276 | G | A | 66 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0117 others(63): Show |
94 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.319+323C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564276 | |||||||
| chr9:34564394 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(1): Show |
6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+205C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564394 | |||||||
| chr9:34564842 | G | A | 1 | a0001c0001t0003g0053 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.86-10C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564842 | |||||||
| chr9:34564848 | G | T | 1 | a0001c0001t0001g0208 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.86-16C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564848 | |||||||
| chr9:34564895 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(9): Show |
24 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.86-63G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564895 | |||||||
| chr9:34564940 | G | T | 1 | a0001c0001t0003g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.86-108C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564940 | |||||||
| chr9:34565082 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(15): Show |
29 | HG00733.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-250G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565082 | |||||||
| chr9:34565083 | G | C | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-251C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565083 | |||||||
| chr9:34565096 | T | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0133 |
2 | HG01109.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.86-264A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565096 | |||||||
| chr9:34565134 | A | T | 1 | a0001c0001t0002g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.86-302T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565134 | |||||||
| chr9:34565212 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 others(1): Show |
6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-380C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565212 | |||||||
| chr9:34565298 | A | T | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-466T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565298 | |||||||
| chr9:34565300 | T | C | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-468A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565300 | |||||||
| chr9:34565301 | C | A | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-469G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565301 | |||||||
| chr9:34565302 | C | G | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-470G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565302 | |||||||
| chr9:34565303 | T | G | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-471A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565303 | |||||||
| chr9:34565304 | T | A | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-472A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565304 | |||||||
| chr9:34565305 | T | G | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-473A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565305 | |||||||
| chr9:34565307 | T | C | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-475A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565307 | |||||||
| chr9:34565308 | C | G | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-476G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565308 | |||||||
| chr9:34565311 | T | G | 1 | a0001c0001t0002g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-479A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565311 | |||||||
| chr9:34565367 | AC | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 |
5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-536delG | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565367 | |||||||
| chr9:34565445 | G | A | 1 | a0001c0009t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.86-613C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565445 | |||||||
| chr9:34565572 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 |
5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-740C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565572 | |||||||
| chr9:34565783 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.86-951T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565783 | |||||||
| chr9:34565935 | A | G | 1 | a0001c0001t0002g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.86-1103T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565935 | |||||||
| chr9:34565981 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.86-1149G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565981 | |||||||
| chr9:34566030 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 |
5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-1198A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566030 | |||||||
| chr9:34566152 | C | CT | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0147 |
5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-1321dupA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566152 | |||||||
| chr9:34566192 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.86-1360T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566192 | |||||||
| chr9:34566226 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0003t0001g0038 |
4 | HG01243.hp1 HG03098.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-1394C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566226 | |||||||
| chr9:34566231 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.86-1399G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566231 | |||||||
| chr9:34566259 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.86-1427C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566259 | |||||||
| chr9:34566619 | A | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(6): Show |
21 | HG02056.hp2 HG02523.hp1 NA18941.hp2 others(18): Show |
intron_variant | MODIFIER | c.86-1787T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566619 | |||||||
| chr9:34566729 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0001g0173 others(2): Show |
8 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-1897G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566729 | |||||||
| chr9:34566736 | G | A | 146 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(143): Show |
216 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(213): Show |
intron_variant | MODIFIER | c.86-1904C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566736 | |||||||
| chr9:34566744 | A | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0070 a0001c0001t0001g0083 others(2): Show |
6 | HG00639.hp2 HG00738.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-1912T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566744 | |||||||
| chr9:34566801 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.86-1969C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566801 | |||||||
| chr9:34566884 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02615.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+2013G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566884 | |||||||
| chr9:34566971 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.85+1926C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566971 | |||||||
| chr9:34567050 | C | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG02258.hp1 HG02738.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1847G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567050 | |||||||
| chr9:34567182 | AT | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.85+1714delA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567182 | |||||||
| chr9:34567202 | A | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
379 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(376): Show |
intron_variant | MODIFIER | c.85+1695T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567202 | |||||||
| chr9:34567422 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.85+1475T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567422 | |||||||
| chr9:34567542 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.85+1355G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567542 | |||||||
| chr9:34567670 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85+1227C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567670 | |||||||
| chr9:34567748 | C | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG02258.hp1 HG02738.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1149G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567748 | |||||||
| chr9:34567849 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.85+1048C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567849 | |||||||
| chr9:34568008 | C | A | 1 | a0001c0001t0007g0087 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.85+889G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568008 | |||||||
| chr9:34568340 | A | G | 2 | a0001c0001t0002g0090 a0001c0004t0001g0093 |
2 | HG02738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.85+557T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568340 | |||||||
| chr9:34568497 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+400A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568497 | |||||||
| chr9:34568570 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0137 |
3 | HG01891.hp2 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.85+327G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568570 | |||||||
| chr9:34568742 | A | G | 1 | a0001c0009t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85+155T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568742 | |||||||
| chr9:34568859 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+38C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568859 | |||||||
| chr9:34568869 | T | C | 1 | a0001c0009t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85+28A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568869 | |||||||
| chr9:34568995 | C | A | 1 | a0001c0001t0003g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1-14G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34568995 | |||||||
| chr9:34569012 | T | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
377 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(374): Show |
intron_variant | MODIFIER | c.1-31A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569012 | |||||||
| chr9:34569124 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0004g0009 a0001c0001t0004g0264 others(1): Show |
9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-143G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569124 | |||||||
| chr9:34569299 | T | C | 65 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0117 others(62): Show |
93 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1-318A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569299 | |||||||
| chr9:34569473 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(103): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1-492C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569473 | |||||||
| chr9:34569496 | G | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-515C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569496 | |||||||
| chr9:34569668 | G | T | 1 | a0001c0001t0002g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1-687C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569668 | |||||||
| chr9:34569669 | T | G | 1 | a0001c0001t0002g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1-688A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569669 | |||||||
| chr9:34569670 | G | T | 1 | a0001c0001t0002g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1-689C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569670 | |||||||
| chr9:34569679 | C | A | 1 | a0001c0001t0002g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1-698G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569679 | |||||||
| chr9:34569701 | C | T | 44 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(41): Show |
63 | HG00639.hp2 HG00738.hp2 HG01175.hp2 others(60): Show |
intron_variant | MODIFIER | c.1-720G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569701 | |||||||
| chr9:34569963 | C | G | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-982G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569963 | |||||||
| chr9:34570352 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1-1371G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570352 | |||||||
| chr9:34570356 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
379 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(376): Show |
intron_variant | MODIFIER | c.1-1375G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570356 | |||||||
| chr9:34570442 | C | T | 4 | a0001c0001t0001g0184 a0001c0001t0002g0075 a0001c0001t0002g0076 others(1): Show |
4 | HG00280.hp1 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-1461G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570442 | |||||||
| chr9:34570533 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0063 others(6): Show |
13 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-1552G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570533 | |||||||
| chr9:34570574 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1-1593C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570574 | |||||||
| chr9:34570747 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1-1766A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570747 | |||||||
| chr9:34570836 | G | C | 8 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(5): Show |
10 | HG01074.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1-1855C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570836 | |||||||
| chr9:34570856 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.1-1875T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570856 | |||||||
| chr9:34570863 | T | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0133 |
2 | HG01109.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1-1882A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570863 | |||||||
| chr9:34570990 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1-2009G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570990 | |||||||
| chr9:34570992 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(61): Show |
98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1-2011G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570992 | |||||||
| chr9:34570993 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1-2012G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570993 | |||||||
| chr9:34571015 | T | G | 7 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
9 | HG01074.hp1 HG01496.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1-2034A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571015 | |||||||
| chr9:34571176 | C | T | 1 | a0001c0001t0003g0050 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1-2195G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571176 | |||||||
| chr9:34571437 | T | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0017 others(58): Show |
84 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(81): Show |
intron_variant | MODIFIER | c.1-2456A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571437 | |||||||
| chr9:34571465 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(11): Show |
26 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-2484A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571465 | |||||||
| chr9:34571546 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(3): Show |
7 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-2565C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571546 | |||||||
| chr9:34571553 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1-2572G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571553 | |||||||
| chr9:34571558 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0195 |
2 | HG03540.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1-2577C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571558 | |||||||
| chr9:34571559 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1-2578G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571559 | |||||||
| chr9:34571561 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1-2580A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | T | TAC | 48 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0025 others(45): Show |
72 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1-2582_1-2581dupGT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | T | TACAC | 8 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0052 others(5): Show |
12 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1-2584_1-2581dupGT others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | T | TACACAC | 26 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0064 others(23): Show |
48 | HG00544.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1-2586_1-2581dupGT others(4): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0229 a0001c0001t0002g0121 a0001c0001t0003g0088 |
3 | HG00741.hp2 HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1-2588_1-2581dupGT others(6): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0260 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1-2590_1-2581dupGT others(8): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | TAC | T | 33 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0043 others(30): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1-2582_1-2581delGT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | TACAC | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0063 others(6): Show |
13 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-2584_1-2581delGT others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0080 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1-2590_1-2581delGT others(8): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571561 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1-2592_1-2581delGT others(10): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | |||||||
| chr9:34571588 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1-2607T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571588 | |||||||
| chr9:34571602 | G | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0028 others(13): Show |
21 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1-2621C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571602 | |||||||
| chr9:34571644 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0158 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1-2663G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571644 | |||||||
| chr9:34571665 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-2684G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571665 | |||||||
| chr9:34571680 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0105 |
3 | HG02895.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-2699G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571680 | |||||||
| chr9:34571747 | A | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2766T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571747 | |||||||
| chr9:34571753 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1-2772T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571753 | |||||||
| chr9:34571800 | A | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0028 others(13): Show |
21 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1-2819T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571800 | |||||||
| chr9:34571815 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0063 others(6): Show |
13 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-2834C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571815 | |||||||
| chr9:34571868 | T | C | 1 | a0001c0002t0002g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1-2887A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571868 | |||||||
| chr9:34571964 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-2983C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571964 | |||||||
| chr9:34572151 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-3170G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572151 | |||||||
| chr9:34572216 | C | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG02258.hp1 HG02738.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-3235G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572216 | |||||||
| chr9:34572373 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1-3392G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572373 | |||||||
| chr9:34572450 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1-3469T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572450 | |||||||
| chr9:34572687 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1-3706C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572687 | |||||||
| chr9:34572769 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(100): Show |
166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1-3788A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572769 | |||||||
| chr9:34572817 | C | T | 63 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0117 others(60): Show |
91 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1-3836G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572817 | |||||||
| chr9:34572827 | G | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1-3846C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572827 | |||||||
| chr9:34572909 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1-3928C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572909 | |||||||
| chr9:34572922 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1-3941C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572922 | |||||||
| chr9:34572927 | C | T | 1 | a0001c0001t0009g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1-3946G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572927 | |||||||
| chr9:34572931 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1-3950T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572931 | |||||||
| chr9:34572993 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(4): Show |
8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-4012G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572993 | |||||||
| chr9:34573032 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1-4051C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573032 | |||||||
| chr9:34573146 | CG | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1-4166delC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573146 | |||||||
| chr9:34573286 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1-4305T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573286 | |||||||
| chr9:34573330 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1-4349A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573330 | |||||||
| chr9:34573336 | C | T | 1 | a0001c0001t0001g0055 | 2 | NA18947.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1-4355G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573336 | |||||||
| chr9:34573472 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1-4491T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573472 | |||||||
| chr9:34573596 | G | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0064 others(27): Show |
49 | HG00544.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1-4615C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573596 | |||||||
| chr9:34573608 | C | G | 1 | a0001c0001t0003g0050 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1-4627G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573608 | |||||||
| chr9:34573814 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1-4833G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573814 | |||||||
| chr9:34573918 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1-4937C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573918 | |||||||
| chr9:34574087 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(20): Show |
36 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.1-5106G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574087 | |||||||
| chr9:34574102 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(11): Show |
26 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-5121G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574102 | |||||||
| chr9:34574103 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
6 | HG01496.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-5122C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574103 | |||||||
| chr9:34574121 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0105 |
3 | HG02895.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-5140C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574121 | |||||||
| chr9:34574141 | G | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-5160C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574141 | |||||||
| chr9:34574212 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1-5231G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574212 | |||||||
| chr9:34574306 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | NA18977.hp1 NA18994.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1-5325C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574306 | |||||||
| chr9:34574568 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0114 |
3 | NA19060.hp2 NA19077.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1-5587T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574568 | |||||||
| chr9:34574647 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1-5666C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574647 | |||||||
| chr9:34574666 | G | T | 1 | a0001c0001t0002g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1-5685C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574666 | |||||||
| chr9:34574672 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1-5691A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574672 | |||||||
| chr9:34574682 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1-5701G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574682 | |||||||
| chr9:34574707 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1-5726G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574707 | |||||||
| chr9:34574718 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1-5737A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574718 | |||||||
| chr9:34574745 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1-5764A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574745 | |||||||
| chr9:34574765 | C | CTG | 12 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-5785_1-5784insCA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574765 | |||||||
| chr9:34574849 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1-5868C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574849 | |||||||
| chr9:34574852 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1-5871G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574852 | |||||||
| chr9:34574912 | C | T | 12 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-5931G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574912 | |||||||
| chr9:34575104 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-1+5991G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575104 | |||||||
| chr9:34575153 | T | A | 1 | a0001c0001t0002g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-1+5942A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575153 | |||||||
| chr9:34575349 | T | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+5746A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575349 | |||||||
| chr9:34575378 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-1+5717G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575378 | |||||||
| chr9:34575516 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-1+5579C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575516 | |||||||
| chr9:34575524 | T | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+5571A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575524 | |||||||
| chr9:34575659 | T | TCA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | HG01891.hp2 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+5434_-1+5435dup others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575659 | |||||||
| chr9:34575666 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-1+5429G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575666 | |||||||
| chr9:34575671 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0137 others(2): Show |
5 | HG01891.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+5424G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575671 | |||||||
| chr9:34575687 | C | A | 1 | a0001c0001t0002g0231 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-1+5408G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575687 | |||||||
| chr9:34575691 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1+5404T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575691 | |||||||
| chr9:34575701 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1+5394T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575701 | |||||||
| chr9:34575812 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.-1+5283T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575812 | |||||||
| chr9:34575854 | T | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0052 others(30): Show |
53 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+5241A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575854 | |||||||
| chr9:34575885 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02615.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5210A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575885 | |||||||
| chr9:34575987 | G | GT | 57 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0117 others(54): Show |
85 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.-1+5107dupA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575987 | |||||||
| chr9:34576076 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-1+5019G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576076 | |||||||
| chr9:34576216 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG01891.hp2 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+4879C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576216 | |||||||
| chr9:34576228 | T | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+4867A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576228 | |||||||
| chr9:34576287 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-1+4808G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576287 | |||||||
| chr9:34576374 | C | A | 1 | a0001c0001t0001g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1+4721G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576374 | |||||||
| chr9:34576384 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-1+4711G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576384 | |||||||
| chr9:34576456 | A | G | 1 | a0001c0001t0003g0232 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-1+4639T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576456 | |||||||
| chr9:34576467 | G | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(27): Show |
58 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-1+4628C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576467 | |||||||
| chr9:34576517 | G | A | 1 | a0001c0002t0002g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-1+4578C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576517 | |||||||
| chr9:34576518 | A | G | 1 | a0001c0002t0002g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-1+4577T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576518 | |||||||
| chr9:34576584 | T | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+4511A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576584 | |||||||
| chr9:34576817 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1+4278G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576817 | |||||||
| chr9:34576841 | A | T | 1 | a0001c0002t0002g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-1+4254T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576841 | |||||||
| chr9:34576890 | A | C | 58 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0117 others(55): Show |
86 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-1+4205T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576890 | |||||||
| chr9:34576981 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-1+4114G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576981 | |||||||
| chr9:34577130 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0002g0250 others(1): Show |
4 | HG01074.hp1 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+3965C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577130 | |||||||
| chr9:34577137 | T | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0216 |
3 | HG01255.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-1+3958A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577137 | |||||||
| chr9:34577153 | C | G | 1 | a0001c0001t0005g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-1+3942G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577153 | |||||||
| chr9:34577383 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1+3712C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577383 | |||||||
| chr9:34577413 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0222 a0001c0001t0001g0223 |
6 | HG02083.hp1 HG02523.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+3682C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577413 | |||||||
| chr9:34577461 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-1+3634A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577461 | |||||||
| chr9:34577531 | G | T | 4 | a0001c0001t0001g0085 a0001c0001t0004g0009 a0001c0001t0004g0264 others(1): Show |
9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+3564C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577531 | |||||||
| chr9:34577567 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
5 | NA18945.hp1 NA19000.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+3528G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577567 | |||||||
| chr9:34577586 | GAT | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-1+3507_-1+3508del others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577586 | |||||||
| chr9:34577650 | G | GC | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
161 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.-1+3444dupG | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577650 | |||||||
| chr9:34577683 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1+3412G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577683 | |||||||
| chr9:34577715 | C | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG02257.hp1 HG03453.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-1+3380G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577715 | |||||||
| chr9:34577829 | C | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0001c0001t0001g0069 others(9): Show |
13 | HG01891.hp2 HG02615.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+3266G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577829 | |||||||
| chr9:34577836 | GAGAAA | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0034 others(65): Show |
101 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-1+3254_-1+3258del others(5): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577836 | |||||||
| chr9:34577841 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(181): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-1+3254T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577841 | |||||||
| chr9:34577894 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.-1+3201T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577894 | |||||||
| chr9:34577910 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-1+3185C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577910 | |||||||
| chr9:34577977 | C | CG | 7 | a0001c0001t0001g0117 a0001c0001t0001g0169 a0001c0001t0001g0171 others(4): Show |
9 | HG00621.hp2 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+3117dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577977 | |||||||
| chr9:34577979 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-1+3116C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577979 | |||||||
| chr9:34577997 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0107 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-1+3098C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577997 | |||||||
| chr9:34578139 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0084 others(5): Show |
9 | HG00738.hp1 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+2956T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578139 | |||||||
| chr9:34578162 | C | CGGGTGGG others(10): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0229 a0001c0001t0002g0228 |
3 | HG01884.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-1+2916_-1+2932dup others(17): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578162 | |||||||
| chr9:34578403 | A | G | 2 | a0001c0001t0001g0023 a0001c0002t0002g0168 |
4 | NA18964.hp2 NA18980.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+2692T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578403 | |||||||
| chr9:34578555 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-1+2540A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578555 | |||||||
| chr9:34578646 | T | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
8 | HG02615.hp2 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+2449A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578646 | |||||||
| chr9:34578676 | C | T | 1 | a0001c0002t0002g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-1+2419G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578676 | |||||||
| chr9:34578709 | G | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-1+2386C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578709 | |||||||
| chr9:34578800 | T | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0102 others(9): Show |
18 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1+2295A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578800 | |||||||
| chr9:34578979 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1+2116G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578979 | |||||||
| chr9:34579096 | C | A | 1 | a0001c0001t0001g0262 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-1+1999G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579096 | |||||||
| chr9:34579194 | G | A | 7 | a0001c0001t0001g0243 a0001c0001t0003g0003 a0001c0001t0003g0037 others(4): Show |
16 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+1901C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579194 | |||||||
| chr9:34579363 | G | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0067 a0001c0001t0001g0072 others(10): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+1732C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579363 | |||||||
| chr9:34579369 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-1+1726G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579369 | |||||||
| chr9:34579537 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-1+1558C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579537 | |||||||
| chr9:34579847 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-1+1248A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579847 | |||||||
| chr9:34580115 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(12): Show |
27 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1+980G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580115 | |||||||
| chr9:34580259 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(56): Show |
92 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-1+836C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580259 | |||||||
| chr9:34580438 | C | T | 2 | a0001c0001t0003g0226 a0001c0001t0003g0227 |
2 | HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-1+657G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580438 | |||||||
| chr9:34580528 | C | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(61): Show |
109 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-1+567G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580528 | |||||||
| chr9:34580688 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0212 |
3 | HG02647.hp2 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-1+407G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580688 | |||||||
| chr9:34580896 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.-1+199C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580896 | |||||||
| chr9:34580927 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-1+168C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580927 | |||||||
| chr9:34580984 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1+111T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580984 | |||||||
| chr9:34581006 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-1+89G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34581006 | |||||||
| chr9:34581524 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-111-319G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581524 | |||||||
| chr9:34581527 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
23 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-111-322G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581527 | |||||||
| chr9:34581680 | A | T | 1 | a0001c0001t0002g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-111-475T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581680 | |||||||
| chr9:34581821 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(89): Show |
137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-111-616T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581821 | |||||||
| chr9:34581864 | C | A | 2 | a0001c0001t0007g0244 a0001c0001t0009g0245 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-111-659G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581864 | |||||||
| chr9:34582091 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-111-886A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582091 | |||||||
| chr9:34582276 | C | CA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0233 others(3): Show |
9 | HG01081.hp2 HG01346.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-1072dupT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582276 | C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0029 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
11 | HG02615.hp2 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-111-1079_-111-107 others(12): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582276 | C | CAAAAAAA others(2): Show |
4 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0100 others(1): Show |
7 | HG01175.hp2 HG02572.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111-1080_-111-107 others(13): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582276 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0019 a0001c0001t0004g0264 |
2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-111-1081_-111-107 others(14): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582276 | CAA | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(10): Show |
23 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.-111-1073_-111-107 others(6): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582276 | CAAAA | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(15): Show |
24 | HG00741.hp2 HG01071.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-111-1075_-111-107 others(8): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582276 | CAAAAA | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): Show |
163 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-111-1076_-111-107 others(9): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582276 | CAAAAAA | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-111-1077_-111-107 others(10): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | |||||||
| chr9:34582279 | A | C | 1 | a0001c0001t0002g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-111-1074T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582279 | |||||||
| chr9:34582296 | A | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01255.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-111-1091T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582296 | |||||||
| chr9:34582297 | A | AAAAAAAA others(4): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0002g0080 others(1): Show |
4 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-1093_-111-109 others(15): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582297 | |||||||
| chr9:34582297 | A | AAAAAAAA others(3): Show |
9 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0078 others(6): Show |
10 | HG00099.hp1 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-111-1093_-111-109 others(14): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582297 | |||||||
| chr9:34582556 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
310 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.-111-1351C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582556 | |||||||
| chr9:34582601 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-111-1396C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582601 | |||||||
| chr9:34582682 | A | AG | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.-111-1478dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582682 | |||||||
| chr9:34582851 | G | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0091 others(6): Show |
9 | HG00741.hp2 HG02258.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-111-1646C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582851 | |||||||
| chr9:34582885 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
311 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-111-1680A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582885 | |||||||
| chr9:34582949 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(260): Show |
399 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.-111-1744A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582949 | |||||||
| chr9:34582952 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-111-1747C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582952 | |||||||
| chr9:34583051 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-111-1846T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583051 | |||||||
| chr9:34583069 | C | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(16): Show |
31 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.-111-1864G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583069 | |||||||
| chr9:34583120 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-111-1915G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583120 | |||||||
| chr9:34583145 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-111-1940G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583145 | |||||||
| chr9:34583154 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-111-1949G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583154 | |||||||
| chr9:34583275 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-111-2070C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583275 | |||||||
| chr9:34583283 | T | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(10): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-111-2078A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583283 | |||||||
| chr9:34583479 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-111-2274C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583479 | |||||||
| chr9:34583583 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(17): Show |
32 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.-111-2378G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583583 | |||||||
| chr9:34583638 | G | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
192 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-111-2433C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583638 | |||||||
| chr9:34583799 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-2594C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583799 | |||||||
| chr9:34583833 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0002g0112 |
3 | HG02486.hp1 HG02572.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.-111-2628T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583833 | |||||||
| chr9:34583880 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-111-2675A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583880 | |||||||
| chr9:34583964 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(56): Show |
88 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-111-2759T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583964 | |||||||
| chr9:34584016 | A | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0064 others(29): Show |
52 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-111-2811T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584016 | |||||||
| chr9:34584016 | A | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
36 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-111-2811T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584016 | |||||||
| chr9:34584107 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(56): Show |
88 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-111-2902A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584107 | |||||||
| chr9:34584137 | G | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(10): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-111-2932C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584137 | |||||||
| chr9:34584321 | G | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
120 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.-111-3116C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584321 | |||||||
| chr9:34584465 | C | T | 1 | a0001c0001t0003g0049 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-111-3260G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584465 | |||||||
| chr9:34584629 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-111-3424T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584629 | |||||||
| chr9:34584755 | A | T | 1 | a0001c0001t0001g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-111-3550T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584755 | |||||||
| chr9:34584780 | A | ATGACCTC | 46 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0029 others(43): Show |
74 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.-111-3582_-111-357 others(11): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584780 | |||||||
| chr9:34585068 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-111-3863G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585068 | |||||||
| chr9:34585387 | G | A | 27 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
36 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-112+4168C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585387 | |||||||
| chr9:34585392 | A | G | 1 | a0001c0002t0002g0225 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-112+4163T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585392 | |||||||
| chr9:34585850 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0064 others(27): Show |
49 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-112+3705G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585850 | |||||||
| chr9:34585854 | CA | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(10): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-112+3700delT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585854 | |||||||
| chr9:34585864 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(17): Show |
32 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.-112+3691G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585864 | |||||||
| chr9:34585930 | G | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0100 others(11): Show |
22 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.-112+3625C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585930 | |||||||
| chr9:34585992 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-112+3563C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585992 | |||||||
| chr9:34586039 | C | G | 1 | a0001c0001t0001g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112+3516G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586039 | |||||||
| chr9:34586084 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-112+3471T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586084 | |||||||
| chr9:34586136 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-112+3419C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586136 | |||||||
| chr9:34586169 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(12): Show |
27 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-112+3386G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586169 | |||||||
| chr9:34586253 | C | A | 1 | a0001c0001t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-112+3302G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586253 | |||||||
| chr9:34586279 | C | A | 1 | a0001c0002t0002g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-112+3276G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586279 | |||||||
| chr9:34586346 | A | T | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3209T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586346 | |||||||
| chr9:34586361 | A | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3194T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586361 | |||||||
| chr9:34586362 | G | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3193C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586362 | |||||||
| chr9:34586428 | C | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3127G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586428 | |||||||
| chr9:34586464 | A | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(10): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-112+3091T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586464 | |||||||
| chr9:34586469 | C | T | 2 | a0001c0001t0001g0062 a0001c0009t0001g0061 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-112+3086G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586469 | |||||||
| chr9:34586491 | T | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3064A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586491 | |||||||
| chr9:34586492 | T | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3063A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586492 | |||||||
| chr9:34586493 | C | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3062G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586493 | |||||||
| chr9:34586495 | C | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3060G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586495 | |||||||
| chr9:34586497 | C | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3058G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586497 | |||||||
| chr9:34586498 | C | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3057G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586498 | |||||||
| chr9:34586499 | C | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3056G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586499 | |||||||
| chr9:34586500 | C | T | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3055G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586500 | |||||||
| chr9:34586502 | C | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3053G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586502 | |||||||
| chr9:34586503 | C | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3052G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586503 | |||||||
| chr9:34586504 | C | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3051G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586504 | |||||||
| chr9:34586507 | C | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3048G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586507 | |||||||
| chr9:34586508 | C | G | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3047G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586508 | |||||||
| chr9:34586509 | T | A | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3046A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586509 | |||||||
| chr9:34586512 | G | T | 1 | a0001c0001t0008g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3043C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586512 | |||||||
| chr9:34586542 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112+3013C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586542 | |||||||
| chr9:34586605 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-112+2950T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586605 | |||||||
| chr9:34586792 | G | A | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | NA18939.hp2 NA18946.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112+2763C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586792 | |||||||
| chr9:34586816 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-112+2739A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586816 | |||||||
| chr9:34586947 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-112+2608C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586947 | |||||||
| chr9:34587113 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-112+2442C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587113 | |||||||
| chr9:34587243 | C | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0091 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112+2312G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587243 | |||||||
| chr9:34587312 | T | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0091 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112+2243A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587312 | |||||||
| chr9:34587332 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-112+2223A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587332 | |||||||
| chr9:34587466 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-112+2089A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587466 | |||||||
| chr9:34587487 | C | T | 49 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0019 others(46): Show |
70 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.-112+2068G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587487 | |||||||
| chr9:34587689 | C | T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0091 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112+1866G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587689 | |||||||
| chr9:34587705 | G | T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0077 others(10): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-112+1850C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587705 | |||||||
| chr9:34587808 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0222 a0001c0001t0001g0223 |
6 | HG02083.hp1 HG02523.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112+1747C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587808 | |||||||
| chr9:34588008 | C | T | 164 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
252 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.-112+1547G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588008 | |||||||
| chr9:34588013 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-112+1542C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588013 | |||||||
| chr9:34588022 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-112+1533A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588022 | |||||||
| chr9:34588033 | G | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0064 others(27): Show |
49 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-112+1522C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588033 | |||||||
| chr9:34588126 | G | A | 6 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
8 | HG01074.hp1 HG01496.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+1429C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588126 | |||||||
| chr9:34588240 | C | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-112+1315G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588240 | |||||||
| chr9:34588270 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-112+1285T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588270 | |||||||
| chr9:34588414 | C | A | 1 | a0001c0001t0001g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112+1141G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588414 | |||||||
| chr9:34588509 | G | A | 1 | a0001c0001t0001g0054 | 2 | NA19064.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-112+1046C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588509 | |||||||
| chr9:34588509 | G | T | 1 | a0001c0001t0005g0056 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-112+1046C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588509 | |||||||
| chr9:34588598 | C | T | 1 | a0001c0001t0003g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-112+957G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588598 | |||||||
| chr9:34588607 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-112+948G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588607 | |||||||
| chr9:34588621 | C | CT | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG01891.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+933dupA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588621 | |||||||
| chr9:34588696 | GGGGAGGG others(6): Show |
G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-112+846_-112+858d others(15): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588696 | |||||||
| chr9:34588708 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112+847T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588708 | |||||||
| chr9:34588799 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-112+756G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588799 | |||||||
| chr9:34589054 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-112+501G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589054 | |||||||
| chr9:34589057 | GCA | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0062 others(2): Show |
9 | HG01496.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-112+496_-112+497d others(4): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589057 | |||||||
| chr9:34589067 | A | ACGCG | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG02258.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-112+484_-112+487d others(6): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589067 | |||||||
| chr9:34589090 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-112+465G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589090 | |||||||
| chr9:34589141 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0027 others(12): Show |
27 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-112+414C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589141 |