Item | Value |
---|---|
geneid | 55743 |
ensemblid | ENSG00000072609.18 |
hgncid | 20455 |
symbol | CHFR |
name | checkpoint with forkhead and ring finger domains |
refseq_nuc | NM_001161346.2 |
refseq_prot | NP_001154818.1 |
ensembl_nuc | ENST00000450056.7 |
ensembl_prot | ENSP00000398735.2 |
mane_status | MANE Select |
chr | chr12 |
start | 132832356 |
end | 132887605 |
strand | - |
ver | v1.2 |
region | chr12:132832356-132887605 |
region5000 | chr12:132827356-132892605 |
regionname0 | CHFR_chr12_132832356_132887605 |
regionname5000 | CHFR_chr12_132827356_132892605 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 652 | 221 | 49 | 39 | 111 | 7 | 14 | 81 | CHFR_chr12_132827356_132892605 | CHFR | MERPE others(647): Show |
chr12 | 132827356 | 132892605 |
a0002 | 0/0 | 652 | 89 | 17 | 21 | 33 | 5 | 13 | 24 | CHFR_chr12_132827356_132892605 | CHFR | MERPE others(647): Show |
chr12 | 132827356 | 132892605 |
a0003 | 0/1 | 652 | 55 | 19 | 13 | 7 | 6 | 9 | 4 | CHFR_chr12_132827356_132892605 | CHFR | MERPE others(647): Show |
chr12 | 132827356 | 132892605 |
a0004 | 0/0 | 652 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | CHFR_chr12_132827356_132892605 | CHFR | MERPE others(647): Show |
chr12 | 132827356 | 132892605 |
a0005 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | MERPE others(647): Show |
chr12 | 132827356 | 132892605 |
a0006 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | MERPE others(647): Show |
chr12 | 132827356 | 132892605 |
a0007 | 0/0 | 652 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | MERPE others(647): Show |
chr12 | 132827356 | 132892605 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1956 | 152 | 33 | 26 | 84 | 3 | 6 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0001c0004 | 0/0 | 1956 | 51 | 2 | 11 | 26 | 4 | 8 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0001c0005 | 1/0 | 1956 | 15 | 14 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0001c0010 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0001c0015 | 0/0 | 1956 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0001c0016 | 0/0 | 1956 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0002c0002 | 0/0 | 1956 | 85 | 17 | 21 | 32 | 5 | 10 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0002c0007 | 0/0 | 1956 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0002c0011 | 0/0 | 1956 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0002c0013 | 0/0 | 1956 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0003c0003 | 0/1 | 1956 | 53 | 17 | 13 | 7 | 6 | 9 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0003c0008 | 0/0 | 1956 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0004c0006 | 0/0 | 1956 | 9 | 0 | 0 | 9 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0005c0009 | 0/0 | 1956 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0006c0014 | 0/0 | 1956 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 | ||
a0007c0012 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | ATGGA others(1951): Show |
chr12 | 132827356 | 132892605 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0006 | 0/0 | 11429 | 11 | 0 | 7 | 2 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0007 | 0/0 | 11651 | 10 | 0 | 0 | 10 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0009 | 0/0 | 11651 | 8 | 0 | 4 | 4 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0010 | 0/0 | 11231 | 7 | 7 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11226): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0011 | 0/0 | 11721 | 7 | 0 | 0 | 7 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11716): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0012 | 0/0 | 11464 | 7 | 0 | 0 | 6 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11459): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0014 | 0/0 | 11686 | 6 | 4 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11681): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0015 | 0/0 | 11651 | 6 | 0 | 1 | 4 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0016 | 0/0 | 11651 | 5 | 5 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0023 | 0/0 | 11231 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11226): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0025 | 0/0 | 11686 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11681): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0026 | 0/0 | 11651 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0027 | 0/0 | 11721 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11716): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0033 | 0/0 | 11429 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0040 | 0/0 | 11616 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11611): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0041 | 0/0 | 11651 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0042 | 0/0 | 11721 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11716): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0043 | 0/0 | 11651 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0049 | 0/0 | 11429 | 2 | 0 | 0 | 0 | 2 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0050 | 0/0 | 11359 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11354): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0051 | 0/0 | 11429 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0052 | 0/0 | 11429 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0069 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0071 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11122): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0072 | 0/0 | 11232 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11227): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0073 | 0/0 | 11231 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11226): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0078 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0079 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0080 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0081 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0082 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0083 | 0/0 | 11651 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0084 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0085 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0086 | 0/0 | 11686 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11681): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0087 | 0/0 | 11652 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11647): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0088 | 0/0 | 11617 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11612): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0089 | 0/0 | 11651 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0090 | 0/0 | 11406 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11401): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0091 | 0/0 | 11687 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11682): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0092 | 0/0 | 11651 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0093 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0094 | 0/0 | 11651 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0095 | 0/0 | 11651 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0096 | 0/0 | 11651 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0097 | 0/0 | 11687 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11682): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0098 | 0/0 | 11616 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11611): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0099 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11681): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0100 | 0/0 | 11722 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11717): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0101 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11681): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0102 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0103 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0104 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0105 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0106 | 0/0 | 11651 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0107 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11681): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0108 | 0/0 | 11652 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11647): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0109 | 0/0 | 11616 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11611): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0110 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0111 | 0/0 | 11721 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11716): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0112 | 0/0 | 11722 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11717): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0113 | 0/0 | 11721 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11716): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0114 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0115 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0116 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11646): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0117 | 0/0 | 11231 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11226): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0141 | 0/0 | 11429 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0142 | 0/0 | 11464 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11459): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0143 | 0/0 | 11499 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11494): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0144 | 0/0 | 11430 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11425): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0145 | 0/0 | 11429 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0146 | 0/0 | 11430 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11425): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0147 | 0/0 | 11430 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11425): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0148 | 0/0 | 11429 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0149 | 0/0 | 11366 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11361): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0150 | 0/0 | 11395 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11390): Show |
chr12 | 132827356 | 132892605 |
a0001c0001t0151 | 0/0 | 11394 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11389): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0003 | 0/0 | 11266 | 22 | 0 | 3 | 15 | 1 | 3 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0008 | 0/0 | 11266 | 8 | 1 | 2 | 0 | 2 | 3 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0017 | 0/0 | 11266 | 3 | 0 | 2 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0018 | 0/0 | 11196 | 4 | 0 | 0 | 4 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11191): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0022 | 0/0 | 11267 | 3 | 0 | 0 | 2 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11262): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0034 | 0/0 | 11266 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0035 | 0/0 | 11266 | 2 | 1 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0036 | 0/0 | 11266 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0055 | 0/0 | 11267 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11262): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0056 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0057 | 0/0 | 11267 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11262): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0058 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0004t0059 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0021 | 0/0 | 11193 | 4 | 4 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11188): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0024 | 0/0 | 11229 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11224): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0038 | 1/0 | 11228 | 2 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11223): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0039 | 0/0 | 11228 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11223): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0074 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11223): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0075 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11223): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0076 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11223): Show |
chr12 | 132827356 | 132892605 |
a0001c0005t0077 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11223): Show |
chr12 | 132827356 | 132892605 |
a0001c0010t0033 | 0/0 | 11429 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11424): Show |
chr12 | 132827356 | 132892605 |
a0001c0015t0003 | 0/0 | 11266 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0001c0016t0017 | 0/0 | 11266 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0002 | 0/0 | 11374 | 22 | 8 | 8 | 1 | 2 | 3 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0004 | 0/0 | 11374 | 13 | 1 | 2 | 10 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0005 | 0/0 | 11374 | 12 | 0 | 3 | 9 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0028 | 0/0 | 11374 | 3 | 0 | 1 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0029 | 0/0 | 11375 | 3 | 2 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11370): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0030 | 0/0 | 11374 | 3 | 0 | 0 | 0 | 3 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0044 | 0/0 | 11339 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11334): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0045 | 0/0 | 11374 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0046 | 0/0 | 11374 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0047 | 0/0 | 11374 | 2 | 0 | 1 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0048 | 0/0 | 11409 | 2 | 1 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11404): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0118 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0119 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0120 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0121 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0123 | 0/0 | 11375 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11370): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0124 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0125 | 0/0 | 11339 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11334): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0126 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11370): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0127 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0128 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0130 | 0/0 | 11374 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0131 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0134 | 0/0 | 11410 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11405): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0135 | 0/0 | 11304 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11299): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0136 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11370): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0137 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0138 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11370): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0139 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0002t0140 | 0/0 | 11374 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0007t0002 | 0/0 | 11374 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0011t0122 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0002c0013t0005 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0001 | 0/1 | 11266 | 30 | 0 | 10 | 4 | 6 | 9 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0013 | 0/0 | 11266 | 6 | 5 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0019 | 0/0 | 11266 | 2 | 1 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0020 | 0/0 | 11371 | 4 | 3 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11366): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0037 | 0/0 | 11266 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0060 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0061 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0062 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0063 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0064 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0065 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0066 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0067 | 0/0 | 11371 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11366): Show |
chr12 | 132827356 | 132892605 |
a0003c0003t0068 | 0/0 | 11371 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11366): Show |
chr12 | 132827356 | 132892605 |
a0003c0008t0019 | 0/0 | 11266 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11261): Show |
chr12 | 132827356 | 132892605 |
a0004c0006t0031 | 0/0 | 11374 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0004c0006t0032 | 0/0 | 11374 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0004c0006t0129 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0004c0006t0132 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11370): Show |
chr12 | 132827356 | 132892605 |
a0004c0006t0133 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11370): Show |
chr12 | 132827356 | 132892605 |
a0005c0009t0053 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11429): Show |
chr12 | 132827356 | 132892605 |
a0005c0009t0054 | 0/0 | 11574 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11569): Show |
chr12 | 132827356 | 132892605 |
a0006c0014t0002 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11369): Show |
chr12 | 132827356 | 132892605 |
a0007c0012t0070 | 0/0 | 11231 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | GCAAT others(11226): Show |
chr12 | 132827356 | 132892605 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0009g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0009g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0009g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0010g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0011g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0011g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0011g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0011g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0011g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0012g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0012g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0012g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0014g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0014g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0015g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0015g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0015g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0015g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0015g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0015g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0016g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0016g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0016g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0023g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0025g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0025g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0025g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0026g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0026g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0027g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0027g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0033g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0033g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0040g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0040g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0041g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0041g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0042g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0042g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0043g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0049g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0049g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0050g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0050g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0051g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0051g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0052g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0052g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0069g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0071g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0072g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0073g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0078g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0079g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0080g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0081g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0082g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0083g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0084g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0085g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0086g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0087g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0088g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0089g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0090g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0091g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0092g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0093g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0094g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0095g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0096g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0097g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0098g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0099g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0100g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0101g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0102g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0103g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0104g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0105g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0106g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0107g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0108g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0109g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0110g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0111g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0112g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0113g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0114g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0115g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0116g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0117g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0141g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0142g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0143g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0144g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0145g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0146g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0147g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0148g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0149g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0150g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0001t0151g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0008g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0008g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0008g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0008g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0017g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0017g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0017g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0018g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0018g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0018g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0022g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0022g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0022g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0034g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0034g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0035g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0035g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0036g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0036g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0055g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0056g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0057g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0058g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0004t0059g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0021g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0024g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0024g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0038g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0038g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0039g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0039g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0074g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0075g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0076g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0005t0077g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0010t0033g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0015t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0001c0016t0017g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0028g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0028g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0029g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0029g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0029g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0030g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0030g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0030g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0044g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0045g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0045g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0046g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0047g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0047g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0048g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0048g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0118g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0119g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0120g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0121g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0123g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0124g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0125g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0126g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0127g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0128g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0130g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0131g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0134g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0135g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0136g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0137g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0138g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0139g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0002t0140g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0007t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0007t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0011t0122g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0002c0013t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0332 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0013g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0013g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0019g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0019g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0020g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0020g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0020g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0020g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0037g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0037g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0060g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0061g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0062g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0063g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0064g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0065g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0066g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0067g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0003t0068g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0008t0019g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0003c0008t0019g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0031g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0031g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0031g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0032g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0032g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0032g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0129g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0132g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0004c0006t0133g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0005c0009t0053g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0005c0009t0054g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0006c0014t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
a0007c0012t0070g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0102 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00099 | hp2 | a0002 | c0002 | t0030 | g0103 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00140 | hp1 | a0003 | c0003 | t0001 | g0349 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00140 | hp2 | a0001 | c0001 | t0049 | g0135 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00280 | hp1 | a0001 | c0004 | t0003 | g0224 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0314 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00323 | hp1 | a0001 | c0001 | t0015 | g0297 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00323 | hp2 | a0001 | c0004 | t0008 | g0017 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00408 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00408 | hp2 | a0001 | c0001 | t0042 | g0274 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00423 | hp1 | a0001 | c0001 | t0107 | g0298 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00423 | hp2 | a0002 | c0002 | t0046 | g0013 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00438 | hp1 | a0001 | c0001 | t0050 | g0148 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00438 | hp2 | a0003 | c0003 | t0001 | g0315 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00544 | hp1 | a0001 | c0004 | t0003 | g0191 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00544 | hp2 | a0001 | c0004 | t0003 | g0192 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00558 | hp1 | a0001 | c0001 | t0103 | g0271 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00558 | hp2 | a0001 | c0001 | t0078 | g0240 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00597 | hp1 | a0001 | c0001 | t0082 | g0270 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00597 | hp2 | a0001 | c0001 | t0011 | g0018 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00609 | hp1 | a0002 | c0002 | t0004 | g0100 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00609 | hp2 | a0001 | c0001 | t0007 | g0252 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00642 | hp1 | a0002 | c0002 | t0005 | g0116 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00642 | hp2 | a0001 | c0001 | t0148 | g0130 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00673 | hp1 | a0002 | c0002 | t0005 | g0109 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0307 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00733 | hp1 | a0002 | c0002 | t0120 | g0061 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00733 | hp2 | a0006 | c0014 | t0002 | g0055 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00735 | hp1 | a0001 | c0004 | t0003 | g0202 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0115 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0312 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00741 | hp1 | a0002 | c0002 | t0123 | g0068 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG00741 | hp2 | a0001 | c0001 | t0108 | g0260 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01069 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01070 | hp2 | a0001 | c0004 | t0036 | g0204 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01071 | hp1 | a0001 | c0004 | t0036 | g0205 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0324 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01099 | hp1 | a0001 | c0015 | t0003 | g0203 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01099 | hp2 | a0002 | c0002 | t0028 | g0008 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01106 | hp1 | a0003 | c0003 | t0013 | g0033 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01106 | hp2 | a0001 | c0001 | t0151 | g0156 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01109 | hp1 | a0001 | c0004 | t0017 | g0220 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01109 | hp2 | a0002 | c0002 | t0048 | g0048 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01167 | hp1 | a0001 | c0001 | t0014 | g0277 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01167 | hp2 | a0002 | c0002 | t0005 | g0073 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01168 | hp1 | a0001 | c0004 | t0003 | g0015 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0147 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01169 | hp1 | a0001 | c0001 | t0014 | g0005 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01169 | hp2 | a0001 | c0004 | t0003 | g0015 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01175 | hp1 | a0001 | c0004 | t0035 | g0210 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01175 | hp2 | a0003 | c0003 | t0068 | g0316 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01192 | hp2 | a0002 | c0002 | t0119 | g0063 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01243 | hp1 | a0001 | c0004 | t0055 | g0209 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01243 | hp2 | a0001 | c0001 | t0083 | g0289 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0145 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0336 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01256 | hp1 | a0001 | c0004 | t0008 | g0217 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0118 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01257 | hp1 | a0003 | c0003 | t0001 | g0023 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01257 | hp2 | a0002 | c0002 | t0118 | g0089 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01258 | hp1 | a0003 | c0003 | t0001 | g0023 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01258 | hp2 | a0001 | c0004 | t0008 | g0216 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0137 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01346 | hp1 | a0001 | c0016 | t0017 | g0221 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01346 | hp2 | a0001 | c0001 | t0144 | g0136 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01433 | hp1 | a0002 | c0002 | t0047 | g0049 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01433 | hp2 | a0001 | c0001 | t0145 | g0138 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0259 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0323 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01515 | hp1 | a0002 | c0002 | t0030 | g0105 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01515 | hp2 | a0001 | c0004 | t0008 | g0017 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01516 | hp1 | a0003 | c0003 | t0001 | g0348 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01516 | hp2 | a0001 | c0001 | t0049 | g0141 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01517 | hp1 | a0002 | c0002 | t0030 | g0104 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01517 | hp2 | a0003 | c0003 | t0001 | g0347 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01884 | hp1 | a0001 | c0001 | t0149 | g0146 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01884 | hp2 | a0001 | c0005 | t0024 | g0177 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01891 | hp1 | a0001 | c0001 | t0023 | g0001 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01891 | hp2 | a0003 | c0003 | t0063 | g0034 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01928 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0151 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01934 | hp1 | a0001 | c0001 | t0088 | g0280 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01934 | hp2 | a0003 | c0003 | t0020 | g0320 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0335 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01943 | hp2 | a0002 | c0002 | t0004 | g0010 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01952 | hp1 | a0001 | c0001 | t0015 | g0291 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0167 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01975 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01975 | hp2 | a0001 | c0001 | t0095 | g0290 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01978 | hp1 | a0001 | c0001 | t0009 | g0303 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01981 | hp1 | a0001 | c0001 | t0092 | g0283 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01981 | hp2 | a0001 | c0001 | t0146 | g0129 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02004 | hp1 | a0001 | c0001 | t0094 | g0292 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02004 | hp2 | a0001 | c0004 | t0017 | g0219 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02015 | hp1 | a0001 | c0001 | t0025 | g0238 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02015 | hp2 | a0002 | c0002 | t0138 | g0093 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02027 | hp1 | a0001 | c0004 | t0003 | g0190 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02027 | hp2 | a0001 | c0001 | t0007 | g0306 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02040 | hp1 | a0001 | c0001 | t0050 | g0155 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02040 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0117 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02056 | hp2 | a0001 | c0001 | t0009 | g0301 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02071 | hp2 | a0001 | c0001 | t0025 | g0258 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02074 | hp1 | a0001 | c0001 | t0104 | g0237 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02074 | hp2 | a0002 | c0002 | t0044 | g0011 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02083 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0253 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02129 | hp1 | a0002 | c0002 | t0131 | g0047 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0330 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02132 | hp1 | a0003 | c0003 | t0019 | g0344 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02132 | hp2 | a0002 | c0002 | t0044 | g0011 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02145 | hp1 | a0002 | c0002 | t0130 | g0053 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02145 | hp2 | a0001 | c0005 | t0039 | g0182 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0328 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02148 | hp2 | a0001 | c0001 | t0006 | g0139 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02155 | hp1 | a0002 | c0002 | t0005 | g0091 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02155 | hp2 | a0001 | c0001 | t0012 | g0125 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02165 | hp1 | a0001 | c0001 | t0093 | g0268 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02165 | hp2 | a0001 | c0001 | t0079 | g0235 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02257 | hp1 | a0003 | c0003 | t0060 | g0026 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02257 | hp2 | a0002 | c0002 | t0029 | g0074 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02258 | hp1 | a0003 | c0003 | t0013 | g0027 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02280 | hp2 | a0001 | c0001 | t0086 | g0279 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02293 | hp1 | a0002 | c0002 | t0005 | g0009 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0140 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02523 | hp1 | a0001 | c0001 | t0097 | g0293 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02523 | hp2 | a0001 | c0001 | t0141 | g0126 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0325 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02602 | hp2 | a0002 | c0002 | t0121 | g0111 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02615 | hp1 | a0001 | c0001 | t0117 | g0041 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02615 | hp2 | a0002 | c0002 | t0135 | g0069 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02622 | hp1 | a0003 | c0003 | t0013 | g0032 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02622 | hp2 | a0001 | c0001 | t0016 | g0245 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02630 | hp1 | a0001 | c0005 | t0077 | g0181 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02630 | hp2 | a0001 | c0001 | t0043 | g0022 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02647 | hp1 | a0001 | c0001 | t0091 | g0281 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02647 | hp2 | a0002 | c0002 | t0029 | g0094 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02698 | hp1 | a0002 | c0002 | t0047 | g0046 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0143 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02717 | hp1 | a0001 | c0001 | t0069 | g0180 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02717 | hp2 | a0001 | c0001 | t0043 | g0022 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02723 | hp1 | a0001 | c0001 | t0071 | g0345 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02723 | hp2 | a0001 | c0001 | t0023 | g0001 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02735 | hp1 | a0001 | c0004 | t0008 | g0214 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02735 | hp2 | a0003 | c0003 | t0001 | g0311 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02738 | hp1 | a0001 | c0004 | t0022 | g0201 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02738 | hp2 | a0001 | c0001 | t0052 | g0150 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02809 | hp1 | a0003 | c0003 | t0013 | g0030 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02809 | hp2 | a0003 | c0003 | t0020 | g0318 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02818 | hp1 | a0003 | c0003 | t0062 | g0338 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02818 | hp2 | a0001 | c0001 | t0089 | g0045 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02886 | hp1 | a0003 | c0003 | t0019 | g0339 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02886 | hp2 | a0001 | c0005 | t0024 | g0173 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02895 | hp1 | a0001 | c0001 | t0016 | g0246 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02895 | hp2 | a0003 | c0008 | t0019 | g0343 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02896 | hp1 | a0001 | c0001 | t0090 | g0067 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02896 | hp2 | a0002 | c0002 | t0045 | g0079 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02897 | hp1 | a0002 | c0002 | t0045 | g0080 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02897 | hp2 | a0003 | c0008 | t0019 | g0342 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02922 | hp1 | a0001 | c0001 | t0014 | g0005 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0090 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02965 | hp1 | a0001 | c0001 | t0010 | g0036 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02965 | hp2 | a0001 | c0001 | t0096 | g0282 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02970 | hp1 | a0001 | c0005 | t0024 | g0176 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02970 | hp2 | a0001 | c0001 | t0023 | g0001 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02976 | hp1 | a0003 | c0003 | t0064 | g0029 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02976 | hp2 | a0001 | c0005 | t0021 | g0014 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03017 | hp1 | a0002 | c0011 | t0122 | g0062 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0024 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03041 | hp1 | a0003 | c0003 | t0067 | g0319 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03041 | hp2 | a0003 | c0003 | t0013 | g0031 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03130 | hp1 | a0003 | c0003 | t0037 | g0340 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0075 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03139 | hp1 | a0001 | c0005 | t0076 | g0186 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03139 | hp2 | a0003 | c0003 | t0013 | g0028 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03195 | hp1 | a0005 | c0009 | t0054 | g0108 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03195 | hp2 | a0001 | c0005 | t0021 | g0014 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0278 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03209 | hp2 | a0001 | c0001 | t0010 | g0039 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03225 | hp2 | a0003 | c0003 | t0061 | g0035 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03453 | hp1 | a0002 | c0002 | t0048 | g0050 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03453 | hp2 | a0001 | c0005 | t0021 | g0184 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03486 | hp1 | a0005 | c0009 | t0053 | g0120 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03486 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03490 | hp1 | a0003 | c0003 | t0001 | g0310 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03490 | hp2 | a0001 | c0004 | t0008 | g0212 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03491 | hp1 | a0002 | c0002 | t0134 | g0082 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03491 | hp2 | a0001 | c0004 | t0008 | g0222 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03516 | hp1 | a0001 | c0005 | t0038 | g0179 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0276 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03540 | hp1 | a0003 | c0003 | t0020 | g0317 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03654 | hp1 | a0003 | c0003 | t0001 | g0024 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0078 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03669 | hp1 | a0002 | c0007 | t0002 | g0066 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03669 | hp2 | a0002 | c0002 | t0128 | g0092 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0327 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03831 | hp1 | a0001 | c0001 | t0012 | g0131 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03831 | hp2 | a0002 | c0002 | t0028 | g0060 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03834 | hp1 | a0001 | c0001 | t0052 | g0127 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03834 | hp2 | a0002 | c0002 | t0028 | g0008 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0076 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0346 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0337 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03942 | hp2 | a0001 | c0004 | t0003 | g0016 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG04115 | hp1 | a0001 | c0004 | t0057 | g0187 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG04115 | hp2 | a0001 | c0001 | t0147 | g0128 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0313 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG04199 | hp2 | a0001 | c0004 | t0003 | g0016 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0142 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG04204 | hp2 | a0001 | c0004 | t0003 | g0200 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18522 | hp1 | a0001 | c0001 | t0073 | g0040 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18522 | hp2 | a0001 | c0001 | t0016 | g0232 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18747 | hp1 | a0002 | c0002 | t0005 | g0009 | EAS | CHB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18747 | hp2 | a0001 | c0001 | t0007 | g0275 | EAS | CHB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18906 | hp1 | a0003 | c0003 | t0020 | g0321 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18906 | hp2 | a0001 | c0001 | t0072 | g0038 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18939 | hp1 | a0002 | c0002 | t0005 | g0097 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18939 | hp2 | a0001 | c0004 | t0022 | g0194 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18942 | hp1 | a0001 | c0004 | t0018 | g0083 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18942 | hp2 | a0001 | c0004 | t0003 | g0189 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18943 | hp1 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18943 | hp2 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18944 | hp1 | a0002 | c0002 | t0004 | g0110 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18944 | hp2 | a0002 | c0002 | t0005 | g0085 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18946 | hp1 | a0003 | c0003 | t0001 | g0322 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18946 | hp2 | a0001 | c0004 | t0003 | g0223 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18947 | hp1 | a0001 | c0001 | t0027 | g0019 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18947 | hp2 | a0001 | c0004 | t0034 | g0197 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18948 | hp1 | a0002 | c0002 | t0005 | g0087 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18948 | hp2 | a0001 | c0001 | t0098 | g0250 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18950 | hp1 | a0002 | c0002 | t0124 | g0119 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18950 | hp2 | a0001 | c0001 | t0011 | g0284 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18951 | hp1 | a0001 | c0010 | t0033 | g0133 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0286 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18952 | hp1 | a0001 | c0001 | t0110 | g0230 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18952 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18954 | hp1 | a0001 | c0001 | t0009 | g0249 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18954 | hp2 | a0004 | c0006 | t0032 | g0161 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18956 | hp1 | a0001 | c0004 | t0056 | g0211 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18956 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18959 | hp1 | a0001 | c0004 | t0058 | g0193 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18959 | hp2 | a0001 | c0001 | t0105 | g0288 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18960 | hp1 | a0002 | c0002 | t0005 | g0114 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18960 | hp2 | a0001 | c0001 | t0102 | g0272 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18962 | hp1 | a0004 | c0006 | t0031 | g0164 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18962 | hp2 | a0001 | c0001 | t0080 | g0247 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18963 | hp1 | a0001 | c0001 | t0033 | g0153 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18963 | hp2 | a0001 | c0001 | t0112 | g0285 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18967 | hp1 | a0001 | c0001 | t0027 | g0304 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18967 | hp2 | a0001 | c0004 | t0018 | g0207 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18968 | hp1 | a0004 | c0006 | t0031 | g0163 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18968 | hp2 | a0001 | c0001 | t0116 | g0266 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18969 | hp1 | a0001 | c0001 | t0099 | g0294 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18969 | hp2 | a0004 | c0006 | t0129 | g0160 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18970 | hp1 | a0001 | c0001 | t0011 | g0263 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18970 | hp2 | a0002 | c0002 | t0005 | g0101 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18973 | hp1 | a0002 | c0002 | t0004 | g0169 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18973 | hp2 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18975 | hp1 | a0002 | c0002 | t0139 | g0081 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18975 | hp2 | a0001 | c0001 | t0026 | g0269 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18977 | hp1 | a0001 | c0001 | t0015 | g0243 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18977 | hp2 | a0001 | c0004 | t0059 | g0228 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18979 | hp1 | a0001 | c0004 | t0003 | g0226 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18979 | hp2 | a0001 | c0001 | t0087 | g0267 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18980 | hp1 | a0001 | c0001 | t0040 | g0248 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18980 | hp2 | a0002 | c0002 | t0136 | g0086 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18983 | hp1 | a0001 | c0001 | t0027 | g0019 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18983 | hp2 | a0001 | c0001 | t0011 | g0257 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18984 | hp2 | a0001 | c0001 | t0051 | g0171 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18985 | hp1 | a0001 | c0001 | t0025 | g0261 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18985 | hp2 | a0001 | c0004 | t0022 | g0227 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18986 | hp1 | a0001 | c0004 | t0018 | g0206 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18986 | hp2 | a0001 | c0001 | t0114 | g0308 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18990 | hp1 | a0001 | c0001 | t0051 | g0172 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18990 | hp2 | a0002 | c0002 | t0125 | g0099 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18991 | hp1 | a0001 | c0004 | t0003 | g0188 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18991 | hp2 | a0001 | c0001 | t0115 | g0231 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18992 | hp1 | a0001 | c0001 | t0015 | g0233 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18992 | hp2 | a0001 | c0004 | t0003 | g0195 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18994 | hp1 | a0001 | c0001 | t0143 | g0309 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18994 | hp2 | a0001 | c0001 | t0084 | g0262 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0326 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18998 | hp2 | a0001 | c0001 | t0109 | g0255 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18999 | hp1 | a0001 | c0001 | t0041 | g0251 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA18999 | hp2 | a0002 | c0013 | t0005 | g0123 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19000 | hp1 | a0004 | c0006 | t0133 | g0166 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19000 | hp2 | a0001 | c0001 | t0100 | g0302 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19002 | hp1 | a0002 | c0002 | t0004 | g0113 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19002 | hp2 | a0001 | c0001 | t0041 | g0300 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19004 | hp1 | a0001 | c0004 | t0034 | g0196 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19004 | hp2 | a0003 | c0003 | t0066 | g0329 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19005 | hp1 | a0002 | c0002 | t0004 | g0058 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19005 | hp2 | a0001 | c0001 | t0111 | g0256 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19006 | hp1 | a0001 | c0004 | t0003 | g0229 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19006 | hp2 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19009 | hp1 | a0002 | c0002 | t0004 | g0088 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19009 | hp2 | a0001 | c0001 | t0040 | g0264 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19010 | hp1 | a0001 | c0004 | t0003 | g0225 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19010 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19012 | hp1 | a0001 | c0001 | t0015 | g0295 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19012 | hp2 | a0002 | c0002 | t0137 | g0065 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19043 | hp1 | a0001 | c0005 | t0075 | g0175 | AFR | LWK | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | LWK | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19055 | hp1 | a0003 | c0003 | t0065 | g0331 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19055 | hp2 | a0004 | c0006 | t0132 | g0159 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19056 | hp1 | a0002 | c0002 | t0005 | g0084 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0287 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19057 | hp1 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19057 | hp2 | a0002 | c0002 | t0046 | g0013 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19058 | hp1 | a0001 | c0001 | t0015 | g0241 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19058 | hp2 | a0001 | c0001 | t0012 | g0152 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19060 | hp1 | a0002 | c0002 | t0004 | g0122 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19060 | hp2 | a0001 | c0001 | t0113 | g0265 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19063 | hp1 | a0004 | c0006 | t0031 | g0165 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19063 | hp2 | a0001 | c0001 | t0142 | g0132 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19065 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19065 | hp2 | a0001 | c0001 | t0026 | g0020 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19066 | hp1 | a0001 | c0001 | t0011 | g0239 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19066 | hp2 | a0002 | c0002 | t0004 | g0072 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19077 | hp1 | a0001 | c0001 | t0101 | g0305 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19077 | hp2 | a0001 | c0004 | t0003 | g0199 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19083 | hp1 | a0001 | c0001 | t0026 | g0020 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19083 | hp2 | a0002 | c0002 | t0004 | g0112 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19084 | hp1 | a0004 | c0006 | t0032 | g0158 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19084 | hp2 | a0001 | c0004 | t0018 | g0213 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19086 | hp1 | a0001 | c0001 | t0033 | g0134 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19086 | hp2 | a0001 | c0001 | t0009 | g0236 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19087 | hp1 | a0001 | c0001 | t0085 | g0296 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19087 | hp2 | a0001 | c0001 | t0012 | g0170 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19088 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19088 | hp2 | a0001 | c0001 | t0081 | g0242 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19090 | hp1 | a0002 | c0002 | t0126 | g0057 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19090 | hp2 | a0001 | c0004 | t0003 | g0198 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19091 | hp1 | a0001 | c0001 | t0042 | g0273 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19091 | hp2 | a0004 | c0006 | t0032 | g0162 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19240 | hp1 | a0003 | c0003 | t0037 | g0341 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA19240 | hp2 | a0002 | c0002 | t0140 | g0070 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | ASW | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20129 | hp2 | a0001 | c0001 | t0150 | g0157 | AFR | ASW | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20752 | hp1 | a0003 | c0003 | t0001 | g0333 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0077 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20805 | hp1 | a0003 | c0003 | t0001 | g0334 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20805 | hp2 | a0001 | c0004 | t0017 | g0218 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20905 | hp1 | a0002 | c0002 | t0127 | g0121 | SAS | GIH | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20905 | hp2 | a0002 | c0007 | t0002 | g0071 | SAS | GIH | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01123 | hp1 | a0001 | c0001 | t0106 | g0254 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG01123 | hp2 | a0002 | c0002 | t0029 | g0168 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02109 | hp2 | a0001 | c0001 | t0016 | g0244 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02486 | hp1 | a0001 | c0001 | t0010 | g0042 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0299 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG02559 | hp2 | a0001 | c0005 | t0021 | g0185 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03471 | hp1 | a0007 | c0012 | t0070 | g0025 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG03471 | hp2 | a0001 | c0005 | t0074 | g0174 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG06807 | hp1 | a0001 | c0004 | t0035 | g0208 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
HG06807 | hp2 | a0001 | c0005 | t0039 | g0183 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20300 | hp1 | a0002 | c0002 | t0004 | g0098 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
NA20300 | hp2 | a0001 | c0004 | t0008 | g0215 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0332 | REF | REF | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
homoSapiens | grch38p0 | a0001 | c0005 | t0038 | g0178 | REF | REF | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132847076 | C | T | 1 | a0003 | 54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
missense_variant | MODERATE | c.1702G>A | p.Val568Met | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/18 | 1773/11228 | 1702/1959 | 568/652 | chr12 | 132847076 | |||
chr12:132851656 | G | A | 3 | a0002 a0004 a0006 |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
missense_variant | MODERATE | c.1454C>T | p.Ala485Val | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/18 | 1525/11228 | 1454/1959 | 485/652 | chr12 | 132851656 | |||
chr12:132853460 | G | A | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1343C>T | p.Ala448Val | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/18 | 1414/11228 | 1343/1959 | 448/652 | chr12 | 132853460 | |||
chr12:132859207 | C | T | 1 | a0004 | 9 | NA18954.hp2 NA18962.hp1 NA18968.hp1 others(6): Show |
missense_variant | MODERATE | c.772G>A | p.Gly258Arg | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/18 | 843/11228 | 772/1959 | 258/652 | chr12 | 132859207 | |||
chr12:132861523 | G | A | 1 | a0006 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.695C>T | p.Ser232Leu | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/18 | 766/11228 | 695/1959 | 232/652 | chr12 | 132861523 | |||
chr12:132861611 | G | A | 1 | a0005 | 2 | HG03195.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.607C>T | p.Pro203Ser | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/18 | 678/11228 | 607/1959 | 203/652 | chr12 | 132861611 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132847109 | A | G | 3 | a0001c0004 a0001c0015 a0001c0016 |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
synonymous_variant | LOW | c.1669T>C | p.Leu557Leu | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/18 | 1740/11228 | 1669/1959 | 557/652 | chr12 | 132847109 | |||
chr12:132848657 | G | A | 1 | a0001c0010 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.1560C>T | p.Cys520Cys | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 13/18 | 1631/11228 | 1560/1959 | 520/652 | chr12 | 132848657 | |||
chr12:132851694 | C | T | 1 | a0003c0008 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1416G>A | p.Leu472Leu | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/18 | 1487/11228 | 1416/1959 | 472/652 | chr12 | 132851694 | |||
chr12:132851733 | G | A | 1 | a0002c0011 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.1377C>T | p.Val459Val | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/18 | 1448/11228 | 1377/1959 | 459/652 | chr12 | 132851733 | |||
chr12:132853522 | C | T | 1 | a0002c0007 | 2 | HG03669.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1281G>A | p.Ala427Ala | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/18 | 1352/11228 | 1281/1959 | 427/652 | chr12 | 132853522 | |||
chr12:132856587 | T | C | 15 | a0001c0001 a0001c0004 a0001c0010 others(12): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
synonymous_variant | LOW | c.1110A>G | p.Arg370Arg | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/18 | 1181/11228 | 1110/1959 | 370/652 | chr12 | 132856587 | |||
chr12:132857472 | G | A | 1 | a0002c0013 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.999C>T | p.Pro333Pro | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/18 | 1070/11228 | 999/1959 | 333/652 | chr12 | 132857472 | |||
chr12:132859130 | T | G | 3 | a0001c0004 a0001c0015 a0001c0016 |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
synonymous_variant | LOW | c.849A>C | p.Pro283Pro | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/18 | 920/11228 | 849/1959 | 283/652 | chr12 | 132859130 | |||
chr12:132869644 | T | C | 1 | a0001c0015 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.558A>G | p.Ala186Ala | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/18 | 629/11228 | 558/1959 | 186/652 | chr12 | 132869644 | |||
chr12:132869761 | G | C | 1 | a0001c0016 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.441C>G | p.Pro147Pro | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/18 | 512/11228 | 441/1959 | 147/652 | chr12 | 132869761 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132832496 | G | GA | 1 | a0001c0005t0024 | 3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9057dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 9057 | chr12 | 132832496 | ||||||
chr12:132832636 | A | G | 1 | a0003c0003t0063 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8918T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8918 | chr12 | 132832636 | ||||||
chr12:132832810 | G | A | 1 | a0001c0001t0051 | 2 | NA18984.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8744C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8744 | chr12 | 132832810 | ||||||
chr12:132832860 | C | T | 1 | a0001c0001t0103 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8694G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8694 | chr12 | 132832860 | ||||||
chr12:132832998 | G | A | 35 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(32): Show |
91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*8556C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8556 | chr12 | 132832998 | ||||||
chr12:132833117 | A | G | 2 | a0005c0009t0053 a0005c0009t0054 |
2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8437T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8437 | chr12 | 132833117 | ||||||
chr12:132833153 | C | T | 38 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0005 others(35): Show |
98 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*8401G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8401 | chr12 | 132833153 | ||||||
chr12:132833176 | C | T | 26 | a0001c0004t0003 a0001c0004t0008 a0001c0004t0017 others(23): Show |
97 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*8378G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8378 | chr12 | 132833176 | ||||||
chr12:132833304 | G | A | 1 | a0001c0001t0104 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8250C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8250 | chr12 | 132833304 | ||||||
chr12:132833465 | G | A | 1 | a0001c0001t0050 | 2 | HG00438.hp1 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8089C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8089 | chr12 | 132833465 | ||||||
chr12:132833549 | C | T | 1 | a0002c0002t0131 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8005G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8005 | chr12 | 132833549 | ||||||
chr12:132833830 | G | A | 1 | a0001c0004t0059 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7724C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7724 | chr12 | 132833830 | ||||||
chr12:132833840 | A | G | 149 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(146): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*7714T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7714 | chr12 | 132833840 | ||||||
chr12:132833849 | T | C | 1 | a0003c0003t0067 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7705A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7705 | chr12 | 132833849 | ||||||
chr12:132833854 | C | A | 21 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(18): Show |
42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*7700G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7700 | chr12 | 132833854 | ||||||
chr12:132834097 | T | C | 1 | a0001c0001t0105 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7457A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7457 | chr12 | 132834097 | ||||||
chr12:132834174 | C | G | 3 | a0003c0003t0001 a0003c0003t0065 a0003c0003t0066 |
31 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*7380G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7380 | chr12 | 132834174 | ||||||
chr12:132834255 | G | C | 1 | a0001c0001t0071 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7299C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7299 | chr12 | 132834255 | ||||||
chr12:132834267 | G | A | 1 | a0002c0002t0119 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7287C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7287 | chr12 | 132834267 | ||||||
chr12:132834532 | T | C | 14 | a0001c0004t0003 a0001c0004t0008 a0001c0004t0017 others(11): Show |
49 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*7022A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7022 | chr12 | 132834532 | ||||||
chr12:132834712 | C | CT | 21 | a0001c0001t0072 a0001c0001t0087 a0001c0001t0088 others(18): Show |
25 | HG00741.hp1 HG00741.hp2 HG01123.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*6841dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6841 | chr12 | 132834712 | ||||||
chr12:132834739 | A | G | 149 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(146): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*6815T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6815 | chr12 | 132834739 | ||||||
chr12:132834779 | G | A | 1 | a0001c0001t0145 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6775C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6775 | chr12 | 132834779 | ||||||
chr12:132834802 | G | A | 1 | a0002c0002t0135 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6752C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6752 | chr12 | 132834802 | ||||||
chr12:132834889 | G | T | 149 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(146): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*6665C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6665 | chr12 | 132834889 | ||||||
chr12:132834939 | G | T | 1 | a0001c0001t0102 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6615C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6615 | chr12 | 132834939 | ||||||
chr12:132834959 | C | T | 61 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0010 others(58): Show |
118 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*6595G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6595 | chr12 | 132834959 | ||||||
chr12:132834963 | C | T | 1 | a0001c0004t0059 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6591G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6591 | chr12 | 132834963 | ||||||
chr12:132835009 | G | A | 1 | a0001c0005t0075 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6545C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6545 | chr12 | 132835009 | ||||||
chr12:132835174 | C | T | 1 | a0001c0001t0023 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6380G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6380 | chr12 | 132835174 | ||||||
chr12:132835401 | G | C | 149 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(146): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*6153C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6153 | chr12 | 132835401 | ||||||
chr12:132835536 | C | G | 21 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(18): Show |
42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*6018G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6018 | chr12 | 132835536 | ||||||
chr12:132835555 | A | G | 3 | a0003c0003t0001 a0003c0003t0065 a0003c0003t0066 |
31 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5999T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5999 | chr12 | 132835555 | ||||||
chr12:132835585 | G | A | 1 | a0001c0001t0146 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5969C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5969 | chr12 | 132835585 | ||||||
chr12:132835751 | C | T | 27 | a0001c0004t0003 a0001c0004t0008 a0001c0004t0017 others(24): Show |
101 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5803G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5803 | chr12 | 132835751 | ||||||
chr12:132835779 | G | A | 1 | a0001c0001t0071 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5775C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5775 | chr12 | 132835779 | ||||||
chr12:132835803 | G | A | 1 | a0002c0002t0045 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5751C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5751 | chr12 | 132835803 | ||||||
chr12:132835828 | CAGGCTCC others(28): Show |
C | 1 | a0001c0001t0050 | 2 | HG00438.hp1 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5691_*5725delATCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5691 | chr12 | 132835828 | ||||||
chr12:132835834 | C | T | 1 | a0001c0001t0091 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5720G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5720 | chr12 | 132835834 | ||||||
chr12:132835842 | A | G | 18 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(15): Show |
38 | HG00140.hp2 HG00642.hp2 HG01106.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*5712T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5712 | chr12 | 132835842 | ||||||
chr12:132835842 | AGCGCACG others(28): Show |
A | 1 | a0001c0004t0035 | 2 | HG01175.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5677_*5711delCGTG others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5677 | chr12 | 132835842 | ||||||
chr12:132835848 | C | T | 1 | a0001c0001t0007 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5706G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5706 | chr12 | 132835848 | ||||||
chr12:132835852 | C | A | 1 | a0001c0001t0099 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5702G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5702 | chr12 | 132835852 | ||||||
chr12:132835852 | C | CCTCACAG others(63): Show |
1 | a0001c0001t0025 | 3 | HG02015.hp1 HG02071.hp2 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5701_*5702insTGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5701 | chr12 | 132835852 | ||||||
chr12:132835862 | A | C | 8 | a0001c0001t0010 a0001c0001t0023 a0001c0001t0025 others(5): Show |
18 | HG01891.hp1 HG02015.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5692T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5692 | chr12 | 132835862 | ||||||
chr12:132835863 | T | C | 9 | a0001c0001t0010 a0001c0001t0023 a0001c0001t0025 others(6): Show |
19 | HG01891.hp1 HG02015.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5691A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5691 | chr12 | 132835863 | ||||||
chr12:132835863 | T | TAGGCTCC others(28): Show |
29 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0014 others(26): Show |
61 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | ||||||
chr12:132835863 | T | TAGGCTCC others(28): Show |
2 | a0001c0001t0089 a0001c0001t0096 |
2 | HG02818.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | ||||||
chr12:132835863 | T | TAGGCTCC others(63): Show |
1 | a0001c0001t0088 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | ||||||
chr12:132835863 | T | TAGGCTCC others(273): Show |
1 | a0001c0001t0090 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(276): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | ||||||
chr12:132835863 | T | TAGGCTCC others(63): Show |
1 | a0002c0002t0140 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGTCA others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | ||||||
chr12:132835863 | T | TAGGCTCC others(28): Show |
4 | a0001c0001t0007 a0001c0001t0082 a0001c0001t0103 others(1): Show |
6 | HG00558.hp1 HG00597.hp1 HG02027.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5656_*5690dupGGCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | ||||||
chr12:132835877 | G | A | 46 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0027 others(43): Show |
134 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*5677C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5677 | chr12 | 132835877 | ||||||
chr12:132835883 | C | G | 15 | a0001c0004t0003 a0001c0004t0008 a0001c0004t0017 others(12): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*5671G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5671 | chr12 | 132835883 | ||||||
chr12:132835887 | A | C | 2 | a0002c0002t0127 a0002c0002t0128 |
2 | HG03669.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5667T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5667 | chr12 | 132835887 | ||||||
chr12:132835897 | C | A | 3 | a0001c0001t0050 a0001c0001t0090 a0001c0001t0093 |
4 | HG00438.hp1 HG02040.hp1 HG02165.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5657G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5657 | chr12 | 132835897 | ||||||
chr12:132835912 | G | A | 5 | a0001c0004t0008 a0001c0004t0018 a0001c0004t0035 others(2): Show |
17 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5642C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5642 | chr12 | 132835912 | ||||||
chr12:132835917 | A | ACGGCACT others(29): Show |
1 | a0001c0001t0097 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5636_*5637insGTGC others(32): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5636 | chr12 | 132835917 | ||||||
chr12:132835932 | A | ACAGGCTC others(28): Show |
1 | a0001c0001t0089 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5621_*5622insGCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5621 | chr12 | 132835932 | ||||||
chr12:132835932 | A | ACAGGCTC others(98): Show |
1 | a0005c0009t0054 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5621_*5622insGCAC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5621 | chr12 | 132835932 | ||||||
chr12:132835932 | A | C | 20 | a0001c0001t0027 a0001c0001t0042 a0001c0001t0050 others(17): Show |
29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5622T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5622 | chr12 | 132835932 | ||||||
chr12:132835962 | C | CAGTGCCA others(28): Show |
1 | a0002c0002t0134 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5591_*5592insCTGA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5591 | chr12 | 132835962 | ||||||
chr12:132835962 | C | G | 1 | a0002c0002t0125 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5592G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5592 | chr12 | 132835962 | ||||||
chr12:132835967 | A | ACAGGCTC others(28): Show |
1 | a0002c0002t0048 | 2 | HG01109.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5586_*5587insGCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5586 | chr12 | 132835967 | ||||||
chr12:132835967 | A | C | 69 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0012 others(66): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*5587T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5587 | chr12 | 132835967 | ||||||
chr12:132835997 | G | C | 76 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(73): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*5557C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5557 | chr12 | 132835997 | ||||||
chr12:132835997 | G | GAGTGCCA others(28): Show |
1 | a0002c0002t0135 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5522_*5556dupGTGA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5556 | chr12 | 132835997 | ||||||
chr12:132835997 | GAGTGCCA others(28): Show |
G | 1 | a0001c0005t0021 | 4 | HG02559.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5522_*5556delGTGA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5522 | chr12 | 132835997 | ||||||
chr12:132836002 | C | A | 13 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0042 others(10): Show |
24 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5552G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5552 | chr12 | 132836002 | ||||||
chr12:132836037 | C | A | 8 | a0001c0001t0027 a0001c0001t0042 a0001c0001t0100 others(5): Show |
39 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5517G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5517 | chr12 | 132836037 | ||||||
chr12:132836054 | C | T | 1 | a0001c0001t0107 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5500G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5500 | chr12 | 132836054 | ||||||
chr12:132836062 | A | ACTCACAG others(28): Show |
13 | a0001c0001t0006 a0001c0001t0033 a0001c0001t0049 others(10): Show |
26 | HG00140.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5491_*5492insGGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5491 | chr12 | 132836062 | ||||||
chr12:132836062 | A | C | 3 | a0001c0001t0050 a0001c0001t0150 a0001c0001t0151 |
4 | HG00438.hp1 HG01106.hp2 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5492T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5492 | chr12 | 132836062 | ||||||
chr12:132836067 | C | G | 1 | a0002c0002t0127 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5487G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5487 | chr12 | 132836067 | ||||||
chr12:132836072 | C | A | 79 | a0001c0001t0010 a0001c0001t0023 a0001c0001t0041 others(76): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*5482G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5482 | chr12 | 132836072 | ||||||
chr12:132836072 | C | CCAGGCTC others(28): Show |
11 | a0001c0001t0007 a0001c0001t0040 a0001c0001t0043 others(8): Show |
21 | HG00558.hp1 HG00609.hp2 HG01243.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5481_*5482insTCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5481 | chr12 | 132836072 | ||||||
chr12:132836072 | C | CCAGGCTC others(378): Show |
4 | a0001c0001t0009 a0001c0001t0092 a0001c0001t0093 others(1): Show |
11 | HG00741.hp2 HG01496.hp1 HG01928.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5481_*5482insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5481 | chr12 | 132836072 | ||||||
chr12:132836097 | A | ACTCACAG others(378): Show |
1 | a0001c0001t0026 | 3 | NA18975.hp2 NA19065.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | ||||||
chr12:132836097 | A | ACTCACAG others(378): Show |
2 | a0001c0001t0011 a0001c0001t0112 |
8 | HG00597.hp2 NA18950.hp2 NA18963.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | ||||||
chr12:132836097 | A | ACTCACAG others(343): Show |
2 | a0001c0001t0079 a0001c0001t0098 |
2 | HG02165.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | ||||||
chr12:132836097 | A | ACTCACAG others(378): Show |
1 | a0001c0001t0014 | 6 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | ||||||
chr12:132836097 | A | C | 4 | a0001c0001t0012 a0001c0001t0033 a0001c0001t0090 others(1): Show |
10 | HG02040.hp2 HG02155.hp2 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5457T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5457 | chr12 | 132836097 | ||||||
chr12:132836097 | ACTCACAG others(133): Show |
A | 1 | a0001c0001t0071 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5317_*5456del | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836097 | ||||||
chr12:132836107 | C | A | 68 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(65): Show |
160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*5447G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5447 | chr12 | 132836107 | ||||||
chr12:132836107 | C | CCAGGCTC others(413): Show |
1 | a0001c0001t0027 | 3 | NA18947.hp1 NA18967.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | ||||||
chr12:132836107 | C | CCAGGCTC others(413): Show |
2 | a0001c0001t0042 a0001c0001t0113 |
3 | HG00408.hp2 NA19060.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | ||||||
chr12:132836107 | C | CCAGGCTC others(378): Show |
1 | a0001c0001t0101 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | ||||||
chr12:132836107 | C | CCAGGCTC others(413): Show |
1 | a0001c0001t0100 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | ||||||
chr12:132836107 | C | CCAGGCTC others(343): Show |
1 | a0001c0001t0102 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | ||||||
chr12:132836107 | C | CCAGGCTC others(343): Show |
1 | a0001c0001t0114 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | ||||||
chr12:132836107 | C | CCAGGCTC others(378): Show |
1 | a0001c0001t0091 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | ||||||
chr12:132836107 | CCAGGCTC others(28): Show |
C | 4 | a0001c0001t0010 a0001c0001t0072 a0001c0001t0073 others(1): Show |
10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5412_*5446delTCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5412 | chr12 | 132836107 | ||||||
chr12:132836121 | C | CGGCGCAC others(378): Show |
2 | a0001c0001t0110 a0001c0001t0115 |
2 | NA18952.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5432_*5433insCTGC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5432 | chr12 | 132836121 | ||||||
chr12:132836121 | C | CGGCGCAC others(378): Show |
8 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0016 others(5): Show |
17 | HG00323.hp1 HG00597.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5432_*5433insCTGC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5432 | chr12 | 132836121 | ||||||
chr12:132836132 | A | ACTCACAG others(378): Show |
1 | a0001c0001t0111 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5421_*5422insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5421 | chr12 | 132836132 | ||||||
chr12:132836132 | A | ACTCACAG others(413): Show |
1 | a0001c0001t0086 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5421_*5422insGGCC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5421 | chr12 | 132836132 | ||||||
chr12:132836132 | A | ACTCACAG others(98): Show |
1 | a0001c0001t0143 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5421_*5422insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5421 | chr12 | 132836132 | ||||||
chr12:132836132 | A | C | 18 | a0001c0001t0006 a0001c0001t0033 a0001c0001t0049 others(15): Show |
32 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5422T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5422 | chr12 | 132836132 | ||||||
chr12:132836142 | A | C | 38 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0012 others(35): Show |
70 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*5412T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5412 | chr12 | 132836142 | ||||||
chr12:132836156 | C | CGGCGCAC others(343): Show |
1 | a0001c0001t0078 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5397_*5398insCTGC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5397 | chr12 | 132836156 | ||||||
chr12:132836156 | C | CGGCGCAC others(98): Show |
1 | a0001c0001t0090 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5397_*5398insCTGC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5397 | chr12 | 132836156 | ||||||
chr12:132836156 | C | G | 11 | a0001c0001t0014 a0001c0001t0027 a0001c0001t0042 others(8): Show |
19 | HG00408.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5398G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5398 | chr12 | 132836156 | ||||||
chr12:132836167 | A | C | 18 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(15): Show |
39 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5387T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5387 | chr12 | 132836167 | ||||||
chr12:132836167 | ACTCACAG others(63): Show |
A | 1 | a0001c0004t0018 | 4 | NA18942.hp1 NA18967.hp2 NA18986.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5317_*5386delGGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836167 | ||||||
chr12:132836177 | A | C | 27 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0012 others(24): Show |
54 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*5377T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5377 | chr12 | 132836177 | ||||||
chr12:132836177 | A | CCAGGCTC others(28): Show |
1 | a0001c0001t0033 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5377_*5378insCACT others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5377 | chr12 | 132836177 | ||||||
chr12:132836202 | A | C | 22 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(19): Show |
44 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5352T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5352 | chr12 | 132836202 | ||||||
chr12:132836202 | ACTCACAG others(28): Show |
A | 2 | a0001c0001t0023 a0007c0012t0070 |
4 | HG01891.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5317_*5351delGGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836202 | ||||||
chr12:132836212 | C | A | 82 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0033 others(79): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*5342G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5342 | chr12 | 132836212 | ||||||
chr12:132836212 | C | CCAGGCTC others(63): Show |
2 | a0001c0001t0012 a0001c0001t0142 |
8 | HG02040.hp2 HG02155.hp2 HG03831.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5341_*5342insTCAC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5341 | chr12 | 132836212 | ||||||
chr12:132836237 | C | A | 121 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0010 others(118): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*5317G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836237 | ||||||
chr12:132836242 | C | G | 9 | a0001c0004t0003 a0001c0004t0017 a0001c0004t0022 others(6): Show |
35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*5312G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5312 | chr12 | 132836242 | ||||||
chr12:132836247 | C | A | 24 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0025 others(21): Show |
47 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*5307G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5307 | chr12 | 132836247 | ||||||
chr12:132836247 | C | CCAGGCTC others(98): Show |
1 | a0005c0009t0053 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5306_*5307insTCAC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5306 | chr12 | 132836247 | ||||||
chr12:132836247 | C | CCAGGCTC others(133): Show |
1 | a0005c0009t0054 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5306_*5307insTCAC others(136): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5306 | chr12 | 132836247 | ||||||
chr12:132836272 | A | C | 51 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(48): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*5282T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5282 | chr12 | 132836272 | ||||||
chr12:132836282 | C | A | 38 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(35): Show |
78 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5272G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5272 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(413): Show |
2 | a0001c0001t0025 a0001c0001t0107 |
4 | HG00423.hp1 HG02015.hp1 HG02071.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(378): Show |
1 | a0001c0001t0094 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(413): Show |
1 | a0001c0001t0099 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(378): Show |
1 | a0001c0001t0096 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(28): Show |
10 | a0001c0001t0014 a0001c0001t0042 a0001c0001t0078 others(7): Show |
16 | HG00408.hp2 HG00558.hp2 HG01167.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5237_*5271dupTCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(63): Show |
2 | a0001c0001t0011 a0001c0001t0111 |
8 | HG00597.hp2 NA18950.hp2 NA18970.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5202_*5271dupTCAC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(343): Show |
1 | a0001c0001t0109 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(343): Show |
1 | a0001c0001t0095 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(343): Show |
6 | a0001c0001t0007 a0001c0001t0043 a0001c0001t0083 others(3): Show |
15 | HG00558.hp1 HG00609.hp2 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(343): Show |
2 | a0001c0001t0080 a0001c0001t0116 |
2 | NA18962.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(378): Show |
1 | a0001c0001t0041 | 2 | NA18999.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(343): Show |
1 | a0001c0001t0089 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(378): Show |
1 | a0001c0001t0106 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836282 | C | CCAGGCTC others(343): Show |
1 | a0001c0001t0088 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | ||||||
chr12:132836307 | C | A | 5 | a0001c0001t0071 a0004c0006t0032 a0004c0006t0129 others(2): Show |
7 | HG02723.hp1 NA18954.hp2 NA18969.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5247G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5247 | chr12 | 132836307 | ||||||
chr12:132836317 | A | C | 4 | a0002c0002t0121 a0002c0002t0127 a0003c0003t0062 others(1): Show |
4 | HG02602.hp2 HG02818.hp1 NA18969.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5237T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5237 | chr12 | 132836317 | ||||||
chr12:132836342 | C | A | 1 | a0001c0001t0016 | 5 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5212G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5212 | chr12 | 132836342 | ||||||
chr12:132836347 | C | G | 1 | a0001c0001t0085 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5207G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5207 | chr12 | 132836347 | ||||||
chr12:132836357 | C | CTCCCAGC others(343): Show |
1 | a0001c0001t0097 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5196_*5197insATGA others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5196 | chr12 | 132836357 | ||||||
chr12:132836372 | A | T | 2 | a0002c0002t0044 a0002c0002t0125 |
3 | HG02074.hp2 HG02132.hp2 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5182T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5182 | chr12 | 132836372 | ||||||
chr12:132836401 | C | G | 2 | a0002c0002t0044 a0002c0002t0125 |
3 | HG02074.hp2 HG02132.hp2 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5153G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5153 | chr12 | 132836401 | ||||||
chr12:132836405 | G | A | 3 | a0001c0001t0071 a0002c0002t0121 a0002c0011t0122 |
3 | HG02602.hp2 HG02723.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5149C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5149 | chr12 | 132836405 | ||||||
chr12:132836407 | T | A | 56 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(53): Show |
105 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*5147A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5147 | chr12 | 132836407 | ||||||
chr12:132836410 | G | GCCCTCAC others(64): Show |
1 | a0001c0001t0112 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5143_*5144insGCCG others(67): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5143 | chr12 | 132836410 | ||||||
chr12:132836412 | C | A | 2 | a0002c0002t0044 a0002c0002t0125 |
3 | HG02074.hp2 HG02132.hp2 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5142G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5142 | chr12 | 132836412 | ||||||
chr12:132836412 | C | CCTCACAG others(28): Show |
2 | a0001c0001t0027 a0001c0001t0113 |
4 | NA18947.hp1 NA18967.hp1 NA18983.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5107_*5141dupTGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5141 | chr12 | 132836412 | ||||||
chr12:132836412 | C | CCTCACAG others(63): Show |
1 | a0004c0006t0129 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5072_*5141dupTGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5141 | chr12 | 132836412 | ||||||
chr12:132836412 | C | CCTCACAG others(28): Show |
1 | a0002c0002t0136 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5141_*5142insTGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5141 | chr12 | 132836412 | ||||||
chr12:132836436 | C | A | 1 | a0003c0003t0068 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5118G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5118 | chr12 | 132836436 | ||||||
chr12:132836436 | C | G | 7 | a0002c0002t0004 a0002c0002t0044 a0002c0002t0046 others(4): Show |
21 | HG00423.hp2 HG00609.hp1 HG01943.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5118G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5118 | chr12 | 132836436 | ||||||
chr12:132836447 | A | C | 32 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(29): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*5107T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5107 | chr12 | 132836447 | ||||||
chr12:132836471 | G | C | 3 | a0001c0001t0096 a0003c0003t0061 a0004c0006t0129 |
3 | HG02965.hp2 HG03225.hp2 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5083C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5083 | chr12 | 132836471 | ||||||
chr12:132836482 | A | ACTCACAG others(98): Show |
12 | a0002c0002t0047 a0002c0002t0048 a0002c0002t0130 others(9): Show |
21 | HG01109.hp2 HG01175.hp2 HG01433.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | ||||||
chr12:132836482 | A | ACTCACAG others(98): Show |
1 | a0002c0002t0123 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | ||||||
chr12:132836482 | A | ACTCACAG others(63): Show |
3 | a0002c0002t0044 a0002c0002t0125 a0002c0002t0136 |
4 | HG02074.hp2 HG02132.hp2 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | ||||||
chr12:132836482 | A | ACTCACAG others(28): Show |
1 | a0004c0006t0129 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | ||||||
chr12:132836482 | A | ACTCACAG others(98): Show |
1 | a0002c0002t0134 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | ||||||
chr12:132836482 | A | ACTCACAG others(98): Show |
23 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0005 others(20): Show |
76 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | ||||||
chr12:132836482 | A | C | 5 | a0001c0001t0033 a0001c0001t0142 a0001c0001t0143 others(2): Show |
6 | HG03225.hp2 NA18951.hp1 NA18963.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5072T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5072 | chr12 | 132836482 | ||||||
chr12:132836506 | C | CGGCGCAC others(308): Show |
1 | a0001c0001t0040 | 2 | NA18980.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5047_*5048insCTGC others(311): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5047 | chr12 | 132836506 | ||||||
chr12:132836506 | C | G | 1 | a0003c0003t0061 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5048G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5048 | chr12 | 132836506 | ||||||
chr12:132836545 | G | A | 30 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(27): Show |
60 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5009C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5009 | chr12 | 132836545 | ||||||
chr12:132836563 | C | G | 2 | a0001c0001t0043 a0001c0001t0083 |
3 | HG01243.hp2 HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4991G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4991 | chr12 | 132836563 | ||||||
chr12:132836661 | G | A | 1 | a0003c0003t0065 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4893C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4893 | chr12 | 132836661 | ||||||
chr12:132837038 | G | A | 1 | a0002c0002t0046 | 2 | HG00423.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4516C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4516 | chr12 | 132837038 | ||||||
chr12:132837066 | T | G | 2 | a0005c0009t0053 a0005c0009t0054 |
2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4488A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4488 | chr12 | 132837066 | ||||||
chr12:132837087 | G | T | 2 | a0002c0002t0123 a0002c0002t0140 |
2 | HG00741.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4467C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4467 | chr12 | 132837087 | ||||||
chr12:132837094 | C | G | 19 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(16): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4460G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4460 | chr12 | 132837094 | ||||||
chr12:132837468 | T | C | 134 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(131): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*4086A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4086 | chr12 | 132837468 | ||||||
chr12:132837513 | G | C | 1 | a0001c0001t0114 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4041C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4041 | chr12 | 132837513 | ||||||
chr12:132837543 | A | G | 9 | a0003c0003t0013 a0003c0003t0019 a0003c0003t0037 others(6): Show |
17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4011T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4011 | chr12 | 132837543 | ||||||
chr12:132837647 | G | A | 1 | a0007c0012t0070 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3907C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3907 | chr12 | 132837647 | ||||||
chr12:132837665 | C | T | 21 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(18): Show |
42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3889G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3889 | chr12 | 132837665 | ||||||
chr12:132837697 | T | C | 157 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(154): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*3857A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3857 | chr12 | 132837697 | ||||||
chr12:132837715 | G | C | 2 | a0002c0002t0047 a0002c0002t0048 |
4 | HG01109.hp2 HG01433.hp1 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3839C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3839 | chr12 | 132837715 | ||||||
chr12:132837718 | G | T | 2 | a0005c0009t0053 a0005c0009t0054 |
2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3836C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3836 | chr12 | 132837718 | ||||||
chr12:132837974 | C | A | 15 | a0001c0004t0003 a0001c0004t0008 a0001c0004t0017 others(12): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3580G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3580 | chr12 | 132837974 | ||||||
chr12:132837974 | C | T | 1 | a0003c0003t0060 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3580G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3580 | chr12 | 132837974 | ||||||
chr12:132838129 | C | T | 1 | a0001c0004t0057 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3425G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3425 | chr12 | 132838129 | ||||||
chr12:132838184 | G | A | 2 | a0005c0009t0053 a0005c0009t0054 |
2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3370C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3370 | chr12 | 132838184 | ||||||
chr12:132838283 | C | T | 1 | a0001c0001t0082 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3271G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3271 | chr12 | 132838283 | ||||||
chr12:132838311 | T | C | 1 | a0001c0005t0077 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3243A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3243 | chr12 | 132838311 | ||||||
chr12:132838321 | C | T | 1 | a0001c0001t0023 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3233G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3233 | chr12 | 132838321 | ||||||
chr12:132838453 | G | A | 1 | a0003c0003t0066 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3101C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3101 | chr12 | 132838453 | ||||||
chr12:132838470 | C | T | 1 | a0001c0001t0081 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3084G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3084 | chr12 | 132838470 | ||||||
chr12:132838535 | A | G | 13 | a0002c0002t0119 a0003c0003t0001 a0003c0003t0013 others(10): Show |
49 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3019T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3019 | chr12 | 132838535 | ||||||
chr12:132838549 | G | A | 2 | a0005c0009t0053 a0005c0009t0054 |
2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3005C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3005 | chr12 | 132838549 | ||||||
chr12:132838856 | G | A | 1 | a0001c0001t0071 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2698C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2698 | chr12 | 132838856 | ||||||
chr12:132838915 | A | G | 1 | a0001c0001t0141 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2639T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2639 | chr12 | 132838915 | ||||||
chr12:132839152 | G | A | 7 | a0001c0004t0003 a0001c0004t0022 a0001c0004t0034 others(4): Show |
31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2402C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2402 | chr12 | 132839152 | ||||||
chr12:132839225 | G | A | 7 | a0002c0002t0005 a0002c0002t0118 a0002c0002t0136 others(4): Show |
18 | HG00642.hp1 HG00673.hp1 HG01167.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2329C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2329 | chr12 | 132839225 | ||||||
chr12:132839253 | C | T | 2 | a0001c0001t0080 a0007c0012t0070 |
2 | HG03471.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2301G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2301 | chr12 | 132839253 | ||||||
chr12:132839317 | G | A | 1 | a0001c0001t0069 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2237 | chr12 | 132839317 | ||||||
chr12:132839357 | C | A | 58 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0010 others(55): Show |
112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2197G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2197 | chr12 | 132839357 | ||||||
chr12:132839539 | C | T | 15 | a0001c0004t0003 a0001c0004t0008 a0001c0004t0017 others(12): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2015G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2015 | chr12 | 132839539 | ||||||
chr12:132839686 | C | G | 1 | a0001c0004t0034 | 2 | NA18947.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1868G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1868 | chr12 | 132839686 | ||||||
chr12:132839877 | T | C | 60 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(57): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1677A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1677 | chr12 | 132839877 | ||||||
chr12:132839928 | T | C | 1 | a0001c0004t0036 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1626A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1626 | chr12 | 132839928 | ||||||
chr12:132839934 | C | CGCCCCTG others(31): Show |
98 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0012 others(95): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*1619_*1620insAAGG others(34): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1619 | chr12 | 132839934 | ||||||
chr12:132839951 | G | GGGACCTC others(31): Show |
52 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(49): Show |
98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1602_*1603insGGAG others(34): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1602 | chr12 | 132839951 | ||||||
chr12:132840100 | G | A | 1 | a0001c0001t0117 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1454 | chr12 | 132840100 | ||||||
chr12:132840132 | A | G | 5 | a0002c0002t0028 a0002c0002t0119 a0002c0002t0120 others(2): Show |
7 | HG00733.hp1 HG01099.hp2 HG01192.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1422T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1422 | chr12 | 132840132 | ||||||
chr12:132840327 | C | CA | 40 | a0001c0001t0071 a0002c0002t0002 a0002c0002t0004 others(37): Show |
100 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1226dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1226 | chr12 | 132840327 | ||||||
chr12:132840492 | T | C | 1 | a0001c0001t0043 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1062A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1062 | chr12 | 132840492 | ||||||
chr12:132840540 | C | T | 2 | a0001c0001t0078 a0001c0001t0079 |
2 | HG00558.hp2 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1014G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1014 | chr12 | 132840540 | ||||||
chr12:132840628 | T | C | 1 | a0001c0001t0147 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*926A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 926 | chr12 | 132840628 | ||||||
chr12:132840671 | G | C | 1 | a0002c0002t0140 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*883C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 883 | chr12 | 132840671 | ||||||
chr12:132840699 | T | C | 39 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0005 others(36): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*855A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 855 | chr12 | 132840699 | ||||||
chr12:132840705 | T | TGGGGCTG others(119): Show |
1 | a0001c0001t0049 | 2 | HG00140.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*848_*849insGAGCCT others(120): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 848 | chr12 | 132840705 | ||||||
chr12:132840725 | C | CAAGGGAG others(119): Show |
1 | a0001c0001t0148 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*828_*829insCTGTGA others(120): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 828 | chr12 | 132840725 | ||||||
chr12:132840725 | C | CAAGGGAG others(119): Show |
16 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(13): Show |
36 | HG00438.hp1 HG01106.hp2 HG01168.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*828_*829insCTGTGA others(120): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 828 | chr12 | 132840725 | ||||||
chr12:132840725 | C | CAAGGGAG others(56): Show |
3 | a0001c0001t0149 a0005c0009t0053 a0005c0009t0054 |
3 | HG01884.hp1 HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*828_*829insCTGTGA others(57): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 828 | chr12 | 132840725 | ||||||
chr12:132840725 | C | G | 1 | a0001c0001t0049 | 2 | HG00140.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*829G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 829 | chr12 | 132840725 | ||||||
chr12:132840776 | C | T | 90 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(87): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*778G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 778 | chr12 | 132840776 | ||||||
chr12:132840838 | G | A | 1 | a0001c0001t0115 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 716 | chr12 | 132840838 | ||||||
chr12:132840882 | C | T | 1 | a0002c0002t0118 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 672 | chr12 | 132840882 | ||||||
chr12:132840883 | G | A | 2 | a0001c0001t0072 a0001c0001t0073 |
2 | NA18522.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*671C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 671 | chr12 | 132840883 | ||||||
chr12:132841203 | A | G | 150 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(147): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
3_prime_UTR_variant | MODIFIER | c.*351T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 351 | chr12 | 132841203 | ||||||
chr12:132841216 | T | C | 52 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(49): Show |
98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*338A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 338 | chr12 | 132841216 | ||||||
chr12:132841280 | G | A | 2 | a0001c0001t0150 a0001c0001t0151 |
2 | HG01106.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*274C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 274 | chr12 | 132841280 | ||||||
chr12:132841322 | C | T | 39 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0005 others(36): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*232G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 232 | chr12 | 132841322 | ||||||
chr12:132841323 | G | A | 1 | a0001c0001t0116 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*231C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 231 | chr12 | 132841323 | ||||||
chr12:132841361 | C | A | 1 | a0001c0001t0117 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 193 | chr12 | 132841361 | ||||||
chr12:132841396 | T | TAA | 58 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0033 others(55): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*156_*157dupTT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 157 | chr12 | 132841396 | ||||||
chr12:132841429 | T | C | 1 | a0001c0001t0052 | 2 | HG02738.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 125 | chr12 | 132841429 | ||||||
chr12:132841483 | C | T | 17 | a0001c0004t0003 a0001c0004t0008 a0001c0004t0017 others(14): Show |
55 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*71G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 71 | chr12 | 132841483 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132841634 | T | C | 10 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(7): Show |
11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-38A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841634 | |||||||
chr12:132841713 | A | G | 11 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(8): Show |
14 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1917-117T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841713 | |||||||
chr12:132841810 | A | G | 292 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(289): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1917-214T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841810 | |||||||
chr12:132841814 | G | A | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1917-218C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841814 | |||||||
chr12:132841878 | G | A | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1917-282C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841878 | |||||||
chr12:132841883 | G | A | 1 | a0003c0003t0001g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1917-287C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841883 | |||||||
chr12:132841885 | T | C | 1 | a0001c0001t0097g0293 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1917-289A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841885 | |||||||
chr12:132841970 | T | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1917-374A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841970 | |||||||
chr12:132842067 | CCTCTATA | C | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1917-478_1917-472d others(9): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842067 | |||||||
chr12:132842095 | C | T | 3 | a0003c0003t0019g0339 a0003c0008t0019g0342 a0003c0008t0019g0343 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1917-499G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842095 | |||||||
chr12:132842108 | CA | C | 140 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(137): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1917-513delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842108 | |||||||
chr12:132842108 | CAA | C | 176 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(173): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1917-514_1917-513d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842108 | |||||||
chr12:132842132 | G | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1917-536C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842132 | |||||||
chr12:132842365 | C | T | 1 | a0001c0004t0003g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1916+646G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842365 | |||||||
chr12:132842425 | G | A | 1 | a0001c0001t0011g0257 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1916+586C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842425 | |||||||
chr12:132842441 | G | A | 1 | a0001c0001t0084g0262 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1916+570C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842441 | |||||||
chr12:132842453 | C | T | 1 | a0001c0004t0018g0207 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1916+558G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842453 | |||||||
chr12:132842454 | A | G | 17 | a0001c0004t0008g0017 a0001c0004t0008g0212 a0001c0004t0008g0214 others(14): Show |
18 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1916+557T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842454 | |||||||
chr12:132842487 | A | C | 1 | a0001c0001t0010g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1916+524T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842487 | |||||||
chr12:132842507 | C | A | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1916+504G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842507 | |||||||
chr12:132842580 | C | T | 1 | a0002c0002t0135g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1916+431G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842580 | |||||||
chr12:132842710 | G | A | 90 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0252 others(87): Show |
99 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1916+301C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842710 | |||||||
chr12:132842832 | G | A | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1916+179C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842832 | |||||||
chr12:132842856 | G | A | 1 | a0001c0004t0057g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1916+155C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842856 | |||||||
chr12:132843160 | C | A | 1 | a0003c0003t0001g0322 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1844-77G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843160 | |||||||
chr12:132843178 | G | A | 1 | a0007c0012t0070g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1844-95C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843178 | |||||||
chr12:132843222 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1844-139C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843222 | |||||||
chr12:132843223 | G | C | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1844-140C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843223 | |||||||
chr12:132843252 | A | G | 31 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(28): Show |
35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1844-169T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843252 | |||||||
chr12:132843600 | G | A | 1 | a0006c0014t0002g0055 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1843+427C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843600 | |||||||
chr12:132843688 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1843+339G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843688 | |||||||
chr12:132843766 | T | C | 1 | a0001c0001t0007g0234 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1843+261A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843766 | |||||||
chr12:132843805 | C | T | 1 | a0001c0001t0014g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1843+222G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843805 | |||||||
chr12:132843809 | C | T | 14 | a0002c0002t0047g0046 a0002c0002t0047g0049 a0002c0002t0048g0048 others(11): Show |
14 | HG01109.hp2 HG01433.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1843+218G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843809 | |||||||
chr12:132843937 | G | A | 1 | a0001c0001t0112g0285 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1843+90C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843937 | |||||||
chr12:132843947 | C | CA | 5 | a0003c0003t0001g0007 a0003c0003t0001g0333 a0003c0003t0001g0334 others(2): Show |
6 | HG00738.hp2 HG01069.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1843+79dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843947 | |||||||
chr12:132843947 | CA | C | 48 | a0001c0001t0042g0273 a0001c0001t0096g0282 a0001c0004t0003g0003 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1843+79delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843947 | |||||||
chr12:132844157 | CCCAGCAA others(2): Show |
C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1736-32_1736-24del others(9): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844157 | |||||||
chr12:132844323 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1736-189G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844323 | |||||||
chr12:132844452 | T | TG | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-319_1736-318i others(3): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844452 | |||||||
chr12:132844456 | T | A | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-322A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844456 | |||||||
chr12:132844458 | G | A | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-324C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844458 | |||||||
chr12:132844459 | T | C | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-325A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844459 | |||||||
chr12:132844460 | A | T | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-326T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844460 | |||||||
chr12:132844468 | T | G | 2 | a0001c0005t0074g0174 a0001c0005t0075g0175 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1736-334A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844468 | |||||||
chr12:132844474 | C | T | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-340G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844474 | |||||||
chr12:132844475 | T | G | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-341A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844475 | |||||||
chr12:132844486 | G | A | 52 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(49): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1736-352C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844486 | |||||||
chr12:132844491 | A | G | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-357T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844491 | |||||||
chr12:132844498 | A | C | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-364T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844498 | |||||||
chr12:132844506 | G | A | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-372C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844506 | |||||||
chr12:132844508 | T | A | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-374A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844508 | |||||||
chr12:132844512 | C | T | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-378G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844512 | |||||||
chr12:132844515 | A | T | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-381T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844515 | |||||||
chr12:132844519 | C | CAG | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-386_1736-385i others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844519 | |||||||
chr12:132844520 | G | A | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-386C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844520 | |||||||
chr12:132844527 | A | G | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-393T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844527 | |||||||
chr12:132844539 | C | T | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-405G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844539 | |||||||
chr12:132844547 | G | A | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-413C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844547 | |||||||
chr12:132844556 | T | C | 1 | a0001c0004t0003g0195 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1736-422A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844556 | |||||||
chr12:132844580 | G | A | 1 | a0001c0005t0021g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1736-446C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844580 | |||||||
chr12:132844618 | G | A | 1 | a0002c0002t0047g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1736-484C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844618 | |||||||
chr12:132844627 | A | C | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-493T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844627 | |||||||
chr12:132844755 | C | T | 11 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(8): Show |
14 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1736-621G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844755 | |||||||
chr12:132844791 | C | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1736-657G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844791 | |||||||
chr12:132844813 | A | G | 1 | a0001c0004t0003g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1736-679T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844813 | |||||||
chr12:132844816 | A | G | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1736-682T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844816 | |||||||
chr12:132844923 | A | G | 231 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(228): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1736-789T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844923 | |||||||
chr12:132844929 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1736-795C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844929 | |||||||
chr12:132844957 | T | C | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1736-823A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844957 | |||||||
chr12:132845021 | C | T | 1 | a0003c0003t0001g0007 | 2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1736-887G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845021 | |||||||
chr12:132845050 | A | G | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1736-916T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845050 | |||||||
chr12:132845080 | TTAAAA | T | 231 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(228): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1736-951_1736-947d others(7): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845080 | |||||||
chr12:132845194 | G | A | 1 | a0001c0001t0147g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1736-1060C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845194 | |||||||
chr12:132845195 | C | G | 1 | a0003c0003t0020g0317 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1736-1061G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845195 | |||||||
chr12:132845222 | G | A | 1 | a0003c0003t0066g0329 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1736-1088C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845222 | |||||||
chr12:132845252 | G | A | 3 | a0002c0002t0002g0059 a0002c0002t0002g0064 a0002c0002t0002g0115 |
3 | HG00735.hp2 HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1736-1118C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845252 | |||||||
chr12:132845464 | A | T | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1736-1330T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845464 | |||||||
chr12:132845465 | A | T | 53 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(50): Show |
56 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1736-1331T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845465 | |||||||
chr12:132845467 | A | AT | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1736-1334_1736-133 others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845467 | |||||||
chr12:132845467 | A | T | 3 | a0001c0001t0088g0280 a0001c0001t0089g0045 a0001c0001t0090g0067 |
3 | HG01934.hp1 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1736-1333T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845467 | |||||||
chr12:132845469 | T | A | 323 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(320): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1736-1335A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845469 | |||||||
chr12:132845477 | T | A | 332 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(329): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1736-1343A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845477 | |||||||
chr12:132845478 | A | T | 10 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(7): Show |
11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1736-1344T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845478 | |||||||
chr12:132845571 | G | A | 48 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1736-1437C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845571 | |||||||
chr12:132845614 | C | T | 1 | a0001c0001t0069g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1735+1429G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845614 | |||||||
chr12:132845629 | G | A | 140 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(137): Show |
152 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1735+1414C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845629 | |||||||
chr12:132845781 | G | GGGTGACT others(1): Show |
48 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1735+1261_1735+126 others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845781 | |||||||
chr12:132845808 | C | T | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1735+1235G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845808 | |||||||
chr12:132845817 | G | C | 1 | a0002c0011t0122g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1735+1226C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845817 | |||||||
chr12:132846159 | G | A | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1735+884C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846159 | |||||||
chr12:132846220 | T | C | 3 | a0001c0001t0025g0238 a0001c0001t0025g0258 a0001c0001t0025g0261 |
3 | HG02015.hp1 HG02071.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1735+823A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846220 | |||||||
chr12:132846242 | T | C | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1735+801A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846242 | |||||||
chr12:132846263 | C | CT | 9 | a0001c0001t0010g0043 a0001c0004t0003g0223 a0001c0004t0017g0219 others(6): Show |
9 | HG02004.hp2 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735+779dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | |||||||
chr12:132846263 | C | CTT | 90 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(87): Show |
98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1735+778_1735+779d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | |||||||
chr12:132846263 | C | CTTT | 8 | a0001c0001t0015g0241 a0001c0001t0041g0300 a0001c0001t0078g0240 others(5): Show |
8 | HG00558.hp2 HG02132.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1735+777_1735+779d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | |||||||
chr12:132846263 | C | CTTTT | 58 | a0001c0001t0007g0044 a0001c0001t0007g0234 a0001c0001t0007g0252 others(55): Show |
63 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1735+776_1735+779d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | |||||||
chr12:132846263 | CTT | C | 128 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(125): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1735+778_1735+779d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | |||||||
chr12:132846292 | T | C | 1 | a0001c0001t0073g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1735+751A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846292 | |||||||
chr12:132846294 | G | A | 49 | a0001c0001t0009g0259 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1735+749C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846294 | |||||||
chr12:132846301 | C | G | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1735+742G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846301 | |||||||
chr12:132846302 | C | G | 233 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(230): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1735+741G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846302 | |||||||
chr12:132846380 | A | G | 142 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(139): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1735+663T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846380 | |||||||
chr12:132846408 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1735+635C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846408 | |||||||
chr12:132846411 | C | T | 1 | a0001c0001t0104g0237 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1735+632G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846411 | |||||||
chr12:132846412 | G | A | 144 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(141): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1735+631C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846412 | |||||||
chr12:132846414 | C | T | 142 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(139): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1735+629G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846414 | |||||||
chr12:132846419 | C | T | 142 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(139): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1735+624G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846419 | |||||||
chr12:132846476 | T | C | 231 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(228): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1735+567A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846476 | |||||||
chr12:132846479 | CCAGGATG others(18): Show |
C | 1 | a0001c0001t0142g0132 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1735+539_1735+563d others(27): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846479 | |||||||
chr12:132846512 | C | T | 4 | a0002c0002t0028g0008 a0002c0002t0028g0060 a0002c0002t0121g0111 others(1): Show |
5 | HG01099.hp2 HG02602.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735+531G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846512 | |||||||
chr12:132846516 | C | A | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1735+527G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846516 | |||||||
chr12:132846548 | GC | G | 33 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(30): Show |
36 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1735+494delG | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846548 | |||||||
chr12:132846618 | C | T | 1 | a0001c0001t0069g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1735+425G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846618 | |||||||
chr12:132846920 | A | G | 7 | a0002c0002t0005g0009 a0002c0002t0005g0073 a0002c0002t0005g0084 others(4): Show |
8 | HG00642.hp1 HG01167.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1735+123T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846920 | |||||||
chr12:132846993 | C | T | 2 | a0001c0001t0110g0230 a0001c0001t0115g0231 |
2 | NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1735+50G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846993 | |||||||
chr12:132847280 | G | A | 334 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1648-150C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847280 | |||||||
chr12:132847298 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1648-168C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847298 | |||||||
chr12:132847593 | G | A | 1 | a0001c0001t0006g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1648-463C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847593 | |||||||
chr12:132847917 | CATGCAGA others(87): Show |
C | 1 | a0001c0005t0038g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1647+74_1647+167de others(95): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847917 | |||||||
chr12:132847962 | C | T | 1 | a0001c0004t0008g0212 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1647+123G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847962 | |||||||
chr12:132848317 | T | C | 1 | a0002c0002t0002g0012 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1577-162A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 13/17 | chr12 | 132848317 | |||||||
chr12:132848361 | T | C | 1 | a0001c0001t0088g0280 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1577-206A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 13/17 | chr12 | 132848361 | |||||||
chr12:132848761 | C | T | 2 | a0002c0002t0002g0056 a0002c0002t0002g0075 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1493-37G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132848761 | |||||||
chr12:132848857 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1493-133G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132848857 | |||||||
chr12:132849124 | A | G | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1493-400T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849124 | |||||||
chr12:132849187 | G | C | 1 | a0002c0002t0136g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1493-463C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849187 | |||||||
chr12:132849363 | G | A | 54 | a0001c0005t0024g0173 a0001c0005t0024g0176 a0001c0005t0024g0177 others(51): Show |
57 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1493-639C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849363 | |||||||
chr12:132849375 | G | A | 1 | a0002c0002t0123g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1493-651C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849375 | |||||||
chr12:132849376 | T | C | 1 | a0002c0002t0123g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1493-652A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849376 | |||||||
chr12:132849380 | G | A | 1 | a0001c0004t0018g0083 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1493-656C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849380 | |||||||
chr12:132849512 | C | T | 1 | a0002c0002t0127g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1493-788G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849512 | |||||||
chr12:132849526 | C | T | 100 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(97): Show |
112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1493-802G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849526 | |||||||
chr12:132849578 | C | A | 1 | a0002c0002t0125g0099 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1493-854G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849578 | |||||||
chr12:132849599 | C | CT | 56 | a0001c0001t0012g0131 a0001c0004t0003g0198 a0001c0004t0003g0226 others(53): Show |
59 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1493-876dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849599 | |||||||
chr12:132849638 | T | G | 10 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(7): Show |
11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1493-914A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849638 | |||||||
chr12:132849651 | A | C | 1 | a0003c0003t0001g0023 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1493-927T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849651 | |||||||
chr12:132849832 | C | T | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1493-1108G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849832 | |||||||
chr12:132849897 | T | C | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1493-1173A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849897 | |||||||
chr12:132850015 | G | A | 2 | a0003c0003t0037g0340 a0003c0003t0037g0341 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1493-1291C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850015 | |||||||
chr12:132850054 | C | T | 2 | a0001c0001t0150g0157 a0001c0001t0151g0156 |
2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1493-1330G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850054 | |||||||
chr12:132850144 | G | A | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1493-1420C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850144 | |||||||
chr12:132850266 | TATA | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1492+1349_1492+135 others(7): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850266 | |||||||
chr12:132850333 | G | A | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1492+1285C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850333 | |||||||
chr12:132850359 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1492+1259G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850359 | |||||||
chr12:132850480 | T | C | 1 | a0001c0004t0059g0228 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1492+1138A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850480 | |||||||
chr12:132850496 | G | A | 10 | a0002c0002t0131g0047 a0004c0006t0031g0163 a0004c0006t0031g0164 others(7): Show |
10 | HG02129.hp1 NA18954.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492+1122C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850496 | |||||||
chr12:132850519 | G | A | 1 | a0001c0001t0069g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1492+1099C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850519 | |||||||
chr12:132850525 | C | T | 5 | a0001c0001t0007g0021 a0001c0001t0007g0306 a0001c0001t0082g0270 others(2): Show |
6 | HG00558.hp1 HG00597.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1492+1093G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850525 | |||||||
chr12:132850563 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1492+1055C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850563 | |||||||
chr12:132850759 | C | T | 5 | a0003c0003t0001g0007 a0003c0003t0001g0333 a0003c0003t0001g0334 others(2): Show |
6 | HG00738.hp2 HG01069.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1492+859G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850759 | |||||||
chr12:132850964 | C | CAT | 8 | a0001c0001t0069g0180 a0001c0005t0076g0186 a0003c0003t0001g0312 others(5): Show |
8 | HG00738.hp1 HG01255.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1492+652_1492+653d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | C | CATAT | 9 | a0001c0005t0021g0014 a0001c0005t0021g0185 a0001c0005t0038g0179 others(6): Show |
10 | HG02132.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492+650_1492+653d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | C | CATATATA others(1): Show |
3 | a0001c0005t0021g0184 a0001c0005t0077g0181 a0003c0003t0001g0337 |
3 | HG02630.hp1 HG03453.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1492+646_1492+653d others(10): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | C | CATATATA others(3): Show |
1 | a0001c0005t0074g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1492+644_1492+653d others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | C | CATATATA others(5): Show |
1 | a0001c0005t0024g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1492+642_1492+653d others(14): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | C | CATATATA others(17): Show |
2 | a0001c0005t0024g0176 a0001c0005t0075g0175 |
2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1492+630_1492+653d others(26): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | CAT | C | 46 | a0001c0004t0003g0191 a0001c0004t0008g0017 a0001c0004t0008g0215 others(43): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1492+652_1492+653d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | CATAT | C | 57 | a0001c0001t0083g0289 a0001c0004t0003g0195 a0001c0004t0008g0212 others(54): Show |
61 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1492+650_1492+653d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | CATATAT | C | 12 | a0001c0001t0088g0280 a0001c0001t0089g0045 a0001c0001t0090g0067 others(9): Show |
12 | HG00544.hp2 HG00733.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1492+648_1492+653d others(8): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | CATATATA others(1): Show |
C | 35 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(32): Show |
40 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1492+646_1492+653d others(10): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | CATATATA others(3): Show |
C | 36 | a0001c0001t0007g0234 a0001c0001t0010g0006 a0001c0001t0010g0036 others(33): Show |
42 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1492+644_1492+653d others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | CATATATA others(5): Show |
C | 78 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0252 others(75): Show |
84 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1492+642_1492+653d others(14): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132850964 | CATATATA others(7): Show |
C | 40 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(37): Show |
42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1492+640_1492+653d others(16): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | |||||||
chr12:132851022 | C | T | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1492+596G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851022 | |||||||
chr12:132851025 | C | T | 2 | a0001c0001t0082g0270 a0001c0001t0103g0271 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.1492+593G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851025 | |||||||
chr12:132851029 | C | T | 1 | a0001c0001t0146g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1492+589G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851029 | |||||||
chr12:132851446 | G | A | 89 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(86): Show |
98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1492+172C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851446 | |||||||
chr12:132851545 | C | T | 48 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1492+73G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851545 | |||||||
chr12:132851595 | C | T | 3 | a0001c0001t0006g0140 a0001c0001t0006g0145 a0001c0001t0006g0149 |
3 | HG01255.hp1 HG01261.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1492+23G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851595 | |||||||
chr12:132851770 | G | A | 1 | a0002c0002t0139g0081 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1373-33C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851770 | |||||||
chr12:132851840 | G | C | 1 | a0001c0001t0105g0288 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1373-103C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851840 | |||||||
chr12:132851904 | G | A | 1 | a0001c0001t0006g0145 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1373-167C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851904 | |||||||
chr12:132851908 | A | T | 6 | a0001c0005t0021g0014 a0001c0005t0021g0184 a0001c0005t0021g0185 others(3): Show |
7 | HG02145.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-171T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851908 | |||||||
chr12:132852006 | CAG | C | 89 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(86): Show |
98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1373-271_1373-270d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852006 | |||||||
chr12:132852132 | T | C | 2 | a0001c0001t0050g0148 a0001c0001t0050g0155 |
2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1373-395A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852132 | |||||||
chr12:132852147 | AT | A | 94 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(91): Show |
103 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1373-411delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852147 | |||||||
chr12:132852268 | A | G | 10 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0013g0030 others(7): Show |
10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-531T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852268 | |||||||
chr12:132852382 | G | A | 1 | a0003c0003t0060g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1373-645C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852382 | |||||||
chr12:132852458 | A | AG | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1373-722dupC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852458 | |||||||
chr12:132852489 | G | A | 1 | a0001c0001t0149g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1373-752C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852489 | |||||||
chr12:132852519 | T | TG | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1373-783dupC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852519 | |||||||
chr12:132852692 | T | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1372+739A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852692 | |||||||
chr12:132852763 | G | A | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1372+668C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852763 | |||||||
chr12:132852815 | G | A | 1 | a0002c0002t0140g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1372+616C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852815 | |||||||
chr12:132853017 | T | C | 1 | a0002c0002t0130g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1372+414A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132853017 | |||||||
chr12:132853048 | C | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1372+383G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132853048 | |||||||
chr12:132853049 | G | A | 3 | a0004c0006t0031g0163 a0004c0006t0031g0164 a0004c0006t0031g0165 |
3 | NA18962.hp1 NA18968.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1372+382C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132853049 | |||||||
chr12:132853619 | T | C | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1230-46A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853619 | |||||||
chr12:132853706 | G | A | 1 | a0001c0001t0104g0237 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1230-133C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853706 | |||||||
chr12:132853762 | G | A | 2 | a0001c0004t0003g0224 a0001c0004t0003g0225 |
2 | HG00280.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230-189C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853762 | |||||||
chr12:132853831 | G | C | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1230-258C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853831 | |||||||
chr12:132853904 | G | A | 1 | a0001c0001t0007g0275 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1230-331C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853904 | |||||||
chr12:132853919 | C | T | 6 | a0003c0003t0020g0317 a0003c0003t0020g0318 a0003c0003t0020g0320 others(3): Show |
6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-346G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853919 | |||||||
chr12:132853924 | A | T | 1 | a0001c0001t0089g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1230-351T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853924 | |||||||
chr12:132853951 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1230-378C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853951 | |||||||
chr12:132853957 | C | T | 2 | a0001c0001t0050g0148 a0001c0001t0050g0155 |
2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1230-384G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853957 | |||||||
chr12:132854010 | C | T | 184 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(181): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1230-437G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854010 | |||||||
chr12:132854159 | G | A | 1 | a0003c0003t0001g0326 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1230-586C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854159 | |||||||
chr12:132854202 | T | A | 17 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0013g0030 others(14): Show |
17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.1230-629A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854202 | |||||||
chr12:132854248 | TCTC | T | 10 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(7): Show |
11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230-678_1230-676d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854248 | |||||||
chr12:132854398 | G | A | 6 | a0001c0001t0015g0291 a0001c0001t0015g0295 a0001c0001t0015g0297 others(3): Show |
6 | HG00323.hp1 HG01952.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-825C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854398 | |||||||
chr12:132854409 | G | C | 89 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(86): Show |
98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1230-836C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854409 | |||||||
chr12:132854770 | C | A | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1230-1197G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854770 | |||||||
chr12:132854812 | C | T | 9 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(6): Show |
10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230-1239G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854812 | |||||||
chr12:132854871 | G | A | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1230-1298C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854871 | |||||||
chr12:132854982 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1230-1409G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854982 | |||||||
chr12:132855118 | C | T | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1229+1350G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855118 | |||||||
chr12:132855233 | C | A | 100 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(97): Show |
112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1229+1235G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855233 | |||||||
chr12:132855242 | GA | G | 135 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(132): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1229+1225delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855242 | |||||||
chr12:132855273 | T | A | 1 | a0001c0001t0147g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1229+1195A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855273 | |||||||
chr12:132855393 | G | A | 100 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(97): Show |
112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1229+1075C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855393 | |||||||
chr12:132855416 | C | A | 1 | a0001c0001t0015g0233 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1229+1052G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855416 | |||||||
chr12:132855491 | C | T | 1 | a0001c0004t0034g0196 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1229+977G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855491 | |||||||
chr12:132855501 | C | A | 1 | a0001c0004t0003g0195 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1229+967G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855501 | |||||||
chr12:132855510 | C | CA | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1229+957dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855510 | |||||||
chr12:132855537 | T | C | 1 | a0003c0003t0001g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1229+931A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855537 | |||||||
chr12:132855560 | G | A | 2 | a0001c0001t0052g0127 a0001c0001t0052g0150 |
2 | HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1229+908C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855560 | |||||||
chr12:132855622 | G | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1229+846C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855622 | |||||||
chr12:132855688 | T | G | 1 | a0001c0001t0110g0230 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1229+780A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855688 | |||||||
chr12:132855853 | GT | G | 47 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1229+614delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855853 | |||||||
chr12:132855914 | C | T | 1 | a0001c0001t0091g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1229+554G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855914 | |||||||
chr12:132855999 | C | T | 5 | a0002c0002t0002g0106 a0002c0002t0002g0107 a0002c0002t0030g0103 others(2): Show |
5 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1229+469G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855999 | |||||||
chr12:132856067 | A | T | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1229+401T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856067 | |||||||
chr12:132856158 | C | T | 100 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(97): Show |
112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1229+310G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856158 | |||||||
chr12:132856186 | C | A | 1 | a0001c0001t0006g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1229+282G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856186 | |||||||
chr12:132856267 | C | T | 1 | a0001c0001t0078g0240 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1229+201G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856267 | |||||||
chr12:132856406 | G | A | 41 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1229+62C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856406 | |||||||
chr12:132856651 | C | T | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1067-21G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856651 | |||||||
chr12:132856654 | C | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1067-24G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856654 | |||||||
chr12:132856662 | G | A | 2 | a0002c0002t0127g0121 a0002c0002t0128g0092 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1067-32C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856662 | |||||||
chr12:132856714 | C | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1067-84G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856714 | |||||||
chr12:132856877 | C | T | 3 | a0001c0001t0026g0020 a0001c0001t0026g0269 a0001c0001t0093g0268 |
4 | HG02165.hp1 NA18975.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-247G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856877 | |||||||
chr12:132856905 | G | A | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1067-275C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856905 | |||||||
chr12:132856976 | C | A | 11 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(8): Show |
14 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1067-346G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856976 | |||||||
chr12:132856989 | G | A | 1 | a0001c0001t0103g0271 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1067-359C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856989 | |||||||
chr12:132857005 | GCCCTCAC others(26): Show |
G | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1066+367_1067-376d others(35): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857005 | |||||||
chr12:132857018 | T | C | 283 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(280): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1066+387A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857018 | |||||||
chr12:132857045 | C | T | 1 | a0001c0001t0052g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1066+360G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857045 | |||||||
chr12:132857071 | A | G | 1 | a0002c0002t0002g0124 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1066+334T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857071 | |||||||
chr12:132857107 | C | T | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1066+298G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857107 | |||||||
chr12:132857112 | G | A | 1 | a0001c0004t0018g0207 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1066+293C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857112 | |||||||
chr12:132857118 | G | T | 3 | a0001c0005t0024g0173 a0001c0005t0024g0176 a0001c0005t0024g0177 |
3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1066+287C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857118 | |||||||
chr12:132857120 | G | A | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1066+285C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857120 | |||||||
chr12:132857144 | C | T | 5 | a0003c0003t0001g0007 a0003c0003t0001g0333 a0003c0003t0001g0334 others(2): Show |
6 | HG00738.hp2 HG01069.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066+261G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857144 | |||||||
chr12:132857145 | G | A | 2 | a0001c0001t0148g0130 a0001c0001t0149g0146 |
2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1066+260C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857145 | |||||||
chr12:132857279 | G | A | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1066+126C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857279 | |||||||
chr12:132857332 | C | A | 1 | a0001c0001t0006g0154 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1066+73G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857332 | |||||||
chr12:132857630 | A | G | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.912-71T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132857630 | |||||||
chr12:132857917 | A | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.912-358T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132857917 | |||||||
chr12:132857967 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.912-408G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132857967 | |||||||
chr12:132858220 | T | C | 184 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(181): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.912-661A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858220 | |||||||
chr12:132858600 | C | T | 49 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(46): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.911+468G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858600 | |||||||
chr12:132858718 | C | T | 2 | a0001c0005t0074g0174 a0001c0005t0075g0175 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.911+350G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858718 | |||||||
chr12:132858725 | T | TA | 36 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0188 others(33): Show |
39 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.911+342dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | |||||||
chr12:132858725 | T | TAA | 14 | a0001c0004t0003g0016 a0001c0004t0003g0189 a0001c0004t0003g0198 others(11): Show |
15 | HG00280.hp1 HG03942.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.911+341_911+342dup others(2): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | |||||||
chr12:132858725 | TA | T | 105 | a0001c0001t0006g0140 a0001c0001t0006g0142 a0001c0001t0006g0144 others(102): Show |
114 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.911+342delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | |||||||
chr12:132858725 | TAA | T | 53 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0143 others(50): Show |
57 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.911+341_911+342del others(2): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | |||||||
chr12:132858725 | TAAA | T | 32 | a0001c0001t0006g0147 a0001c0001t0150g0157 a0001c0001t0151g0156 others(29): Show |
35 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.911+340_911+342del others(3): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | |||||||
chr12:132858744 | A | G | 1 | a0001c0001t0078g0240 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.911+324T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858744 | |||||||
chr12:132858778 | T | TA | 7 | a0003c0003t0019g0339 a0003c0003t0037g0340 a0003c0003t0037g0341 others(4): Show |
7 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.911+289dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858778 | |||||||
chr12:132858816 | C | T | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.911+252G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858816 | |||||||
chr12:132858859 | G | A | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.911+209C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858859 | |||||||
chr12:132858863 | A | G | 332 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(329): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.911+205T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858863 | |||||||
chr12:132858920 | CCACCCAC others(2): Show |
C | 3 | a0002c0002t0047g0049 a0002c0002t0048g0048 a0002c0002t0048g0050 |
3 | HG01109.hp2 HG01433.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.911+139_911+147del others(9): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858920 | |||||||
chr12:132858948 | C | T | 27 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(24): Show |
31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.911+120G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858948 | |||||||
chr12:132859009 | C | T | 53 | a0001c0001t0150g0157 a0001c0001t0151g0156 a0003c0003t0001g0007 others(50): Show |
56 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.911+59G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132859009 | |||||||
chr12:132859012 | G | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.911+56C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132859012 | |||||||
chr12:132859052 | G | A | 4 | a0001c0001t0088g0280 a0001c0001t0089g0045 a0001c0001t0090g0067 others(1): Show |
4 | HG01934.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.911+16C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132859052 | |||||||
chr12:132859275 | C | T | 7 | a0002c0002t0002g0076 a0002c0002t0002g0077 a0002c0002t0002g0078 others(4): Show |
7 | HG00733.hp2 HG03491.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.752-48G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859275 | |||||||
chr12:132859410 | G | C | 3 | a0001c0005t0024g0173 a0001c0005t0024g0176 a0001c0005t0024g0177 |
3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-183C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859410 | |||||||
chr12:132859463 | T | A | 3 | a0002c0002t0004g0072 a0002c0002t0004g0100 a0002c0002t0004g0110 |
3 | HG00609.hp1 NA18944.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.752-236A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859463 | |||||||
chr12:132859638 | C | A | 1 | a0001c0001t0089g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.752-411G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859638 | |||||||
chr12:132859809 | A | C | 1 | a0001c0001t0089g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.752-582T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859809 | |||||||
chr12:132859913 | C | T | 36 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(33): Show |
38 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.752-686G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859913 | |||||||
chr12:132859938 | G | A | 1 | a0001c0004t0018g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.752-711C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859938 | |||||||
chr12:132860280 | CT | C | 48 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.752-1054delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860280 | |||||||
chr12:132860288 | A | G | 11 | a0001c0001t0007g0234 a0001c0001t0007g0252 a0001c0001t0007g0286 others(8): Show |
11 | HG00609.hp2 HG00673.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.752-1061T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860288 | |||||||
chr12:132860365 | AAGT | A | 10 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(7): Show |
11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.751+1099_751+1101d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860365 | |||||||
chr12:132860378 | G | A | 1 | a0001c0005t0039g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.751+1089C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860378 | |||||||
chr12:132860494 | C | T | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.751+973G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860494 | |||||||
chr12:132860654 | G | A | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.751+813C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860654 | |||||||
chr12:132860875 | T | A | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.751+592A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860875 | |||||||
chr12:132860903 | C | G | 1 | a0001c0001t0052g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.751+564G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860903 | |||||||
chr12:132861104 | G | C | 1 | a0001c0016t0017g0221 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.751+363C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861104 | |||||||
chr12:132861133 | C | T | 1 | a0003c0003t0001g0337 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.751+334G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861133 | |||||||
chr12:132861344 | C | T | 1 | a0002c0002t0121g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.751+123G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861344 | |||||||
chr12:132861393 | G | A | 1 | a0001c0001t0096g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.751+74C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861393 | |||||||
chr12:132861395 | A | C | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.751+72T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861395 | |||||||
chr12:132861688 | C | G | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.584-54G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861688 | |||||||
chr12:132861691 | T | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.584-57A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861691 | |||||||
chr12:132861910 | C | T | 5 | a0001c0001t0012g0002 a0001c0001t0012g0125 a0001c0001t0012g0131 others(2): Show |
7 | HG02040.hp2 HG02155.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.584-276G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861910 | |||||||
chr12:132861940 | C | T | 1 | a0001c0001t0116g0266 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.584-306G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861940 | |||||||
chr12:132861995 | G | A | 1 | a0001c0001t0011g0263 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.584-361C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861995 | |||||||
chr12:132862136 | G | T | 1 | a0003c0003t0062g0338 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.584-502C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862136 | |||||||
chr12:132862250 | G | A | 1 | a0001c0001t0009g0303 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.584-616C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862250 | |||||||
chr12:132862262 | C | T | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.584-628G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862262 | |||||||
chr12:132862399 | C | A | 2 | a0001c0001t0150g0157 a0001c0001t0151g0156 |
2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.584-765G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862399 | |||||||
chr12:132862408 | C | T | 1 | a0001c0001t0143g0309 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.584-774G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862408 | |||||||
chr12:132862416 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.584-782C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862416 | |||||||
chr12:132862529 | G | A | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.584-895C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862529 | |||||||
chr12:132862680 | C | G | 23 | a0003c0003t0001g0023 a0003c0003t0001g0024 a0003c0003t0001g0310 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.584-1046G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862680 | |||||||
chr12:132862754 | G | A | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.584-1120C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862754 | |||||||
chr12:132862833 | G | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.584-1199C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862833 | |||||||
chr12:132862860 | A | G | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.584-1226T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862860 | |||||||
chr12:132862895 | T | C | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.584-1261A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862895 | |||||||
chr12:132862958 | G | A | 3 | a0001c0001t0088g0280 a0001c0001t0089g0045 a0001c0001t0090g0067 |
3 | HG01934.hp1 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.584-1324C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862958 | |||||||
chr12:132862998 | G | A | 3 | a0001c0001t0147g0128 a0001c0001t0148g0130 a0001c0001t0149g0146 |
3 | HG00642.hp2 HG01884.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.584-1364C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862998 | |||||||
chr12:132863010 | C | T | 2 | a0001c0001t0150g0157 a0001c0001t0151g0156 |
2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.584-1376G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863010 | |||||||
chr12:132863054 | G | A | 17 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0013g0030 others(14): Show |
17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.584-1420C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863054 | |||||||
chr12:132863188 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.584-1554C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863188 | |||||||
chr12:132863192 | G | A | 1 | a0001c0004t0008g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.584-1558C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863192 | |||||||
chr12:132863209 | TA | T | 11 | a0001c0001t0009g0236 a0001c0001t0009g0249 a0001c0001t0016g0232 others(8): Show |
11 | HG00280.hp2 HG01517.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.584-1576delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863209 | |||||||
chr12:132863453 | G | A | 2 | a0003c0003t0001g0007 a0003c0003t0001g0334 |
3 | HG00738.hp2 HG01069.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.584-1819C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863453 | |||||||
chr12:132863460 | G | A | 1 | a0007c0012t0070g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.584-1826C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863460 | |||||||
chr12:132863594 | T | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.584-1960A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863594 | |||||||
chr12:132863602 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.584-1968C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863602 | |||||||
chr12:132863701 | G | A | 4 | a0003c0003t0001g0310 a0003c0003t0001g0311 a0003c0003t0001g0312 others(1): Show |
4 | HG00738.hp1 HG02735.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-2067C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863701 | |||||||
chr12:132863718 | G | A | 1 | a0001c0001t0006g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.584-2084C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863718 | |||||||
chr12:132863912 | C | T | 1 | a0002c0002t0048g0048 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.584-2278G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863912 | |||||||
chr12:132864094 | T | C | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.584-2460A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864094 | |||||||
chr12:132864101 | A | C | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.584-2467T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864101 | |||||||
chr12:132864115 | T | G | 9 | a0001c0004t0008g0017 a0001c0004t0008g0215 a0001c0004t0008g0216 others(6): Show |
10 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.584-2481A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864115 | |||||||
chr12:132864176 | G | GA | 91 | a0001c0001t0012g0125 a0001c0001t0085g0296 a0002c0002t0002g0012 others(88): Show |
97 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.584-2543dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864176 | |||||||
chr12:132864188 | C | A | 184 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(181): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.584-2554G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864188 | |||||||
chr12:132864199 | G | T | 1 | a0001c0001t0052g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.584-2565C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864199 | |||||||
chr12:132864244 | C | T | 2 | a0001c0004t0008g0216 a0001c0004t0008g0217 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.584-2610G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864244 | |||||||
chr12:132864329 | C | T | 1 | a0001c0004t0056g0211 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.584-2695G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864329 | |||||||
chr12:132864343 | G | A | 1 | a0001c0001t0097g0293 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.584-2709C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864343 | |||||||
chr12:132864353 | G | A | 1 | a0001c0001t0010g0006 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.584-2719C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864353 | |||||||
chr12:132864374 | A | C | 1 | a0001c0001t0069g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.584-2740T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864374 | |||||||
chr12:132864436 | TTG | T | 4 | a0001c0001t0033g0134 a0001c0001t0033g0153 a0001c0001t0142g0132 others(1): Show |
4 | NA18951.hp1 NA18963.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-2804_584-2803d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864436 | |||||||
chr12:132864467 | TAGA | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.584-2836_584-2834d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864467 | |||||||
chr12:132864540 | G | C | 2 | a0003c0008t0019g0342 a0003c0008t0019g0343 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.584-2906C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864540 | |||||||
chr12:132864733 | A | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.584-3099T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864733 | |||||||
chr12:132864792 | G | T | 6 | a0001c0004t0008g0017 a0001c0004t0035g0208 a0001c0004t0035g0210 others(3): Show |
7 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.584-3158C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864792 | |||||||
chr12:132864830 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.584-3196C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864830 | |||||||
chr12:132864844 | G | A | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.584-3210C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864844 | |||||||
chr12:132864866 | T | C | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.584-3232A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864866 | |||||||
chr12:132864938 | G | A | 1 | a0001c0001t0040g0264 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.584-3304C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864938 | |||||||
chr12:132865101 | C | T | 334 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.584-3467G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865101 | |||||||
chr12:132865194 | C | T | 27 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(24): Show |
31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.584-3560G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865194 | |||||||
chr12:132865294 | G | A | 1 | a0002c0002t0126g0057 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.584-3660C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865294 | |||||||
chr12:132865387 | G | T | 1 | a0001c0001t0016g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.584-3753C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865387 | |||||||
chr12:132865497 | T | C | 339 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.584-3863A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865497 | |||||||
chr12:132865498 | G | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.584-3864C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865498 | |||||||
chr12:132865518 | G | A | 2 | a0002c0002t0002g0056 a0002c0002t0002g0075 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.584-3884C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865518 | |||||||
chr12:132865652 | TC | T | 66 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(63): Show |
75 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.583+3966delG | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865652 | |||||||
chr12:132865653 | C | CT | 39 | a0001c0001t0006g0142 a0001c0001t0012g0131 a0001c0001t0050g0148 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.583+3965dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | |||||||
chr12:132865653 | C | T | 20 | a0001c0001t0007g0306 a0001c0001t0009g0303 a0001c0001t0011g0284 others(17): Show |
20 | HG00423.hp1 HG01123.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.583+3966G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | |||||||
chr12:132865653 | CT | C | 135 | a0001c0001t0049g0141 a0001c0001t0071g0345 a0001c0001t0149g0146 others(132): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.583+3965delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | |||||||
chr12:132865653 | CTT | C | 12 | a0001c0001t0010g0006 a0001c0001t0010g0037 a0001c0001t0010g0039 others(9): Show |
15 | HG01167.hp2 HG01168.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.583+3964_583+3965d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | |||||||
chr12:132865658 | T | G | 3 | a0001c0001t0027g0019 a0001c0001t0027g0304 a0001c0001t0113g0265 |
4 | NA18947.hp1 NA18967.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+3961A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865658 | |||||||
chr12:132865747 | C | T | 1 | a0004c0006t0132g0159 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.583+3872G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865747 | |||||||
chr12:132866001 | T | G | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+3618A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866001 | |||||||
chr12:132866070 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.583+3549G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866070 | |||||||
chr12:132866237 | C | T | 3 | a0003c0003t0001g0333 a0003c0003t0001g0335 a0003c0003t0001g0336 |
3 | HG01255.hp2 HG01943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.583+3382G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866237 | |||||||
chr12:132866253 | C | G | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+3366G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866253 | |||||||
chr12:132866254 | G | A | 2 | a0001c0004t0008g0216 a0001c0004t0008g0217 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.583+3365C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866254 | |||||||
chr12:132866300 | C | T | 10 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0013g0030 others(7): Show |
10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+3319G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866300 | |||||||
chr12:132866317 | G | A | 1 | a0002c0002t0004g0122 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.583+3302C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866317 | |||||||
chr12:132866419 | A | C | 48 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.583+3200T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866419 | |||||||
chr12:132866493 | T | G | 1 | a0001c0001t0147g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.583+3126A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866493 | |||||||
chr12:132866564 | C | T | 17 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0013g0030 others(14): Show |
17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.583+3055G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866564 | |||||||
chr12:132866577 | T | TGTTACAA others(11): Show |
7 | a0001c0001t0071g0345 a0001c0004t0017g0218 a0001c0004t0017g0219 others(4): Show |
7 | HG01109.hp1 HG01346.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.583+3024_583+3041d others(20): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866577 | |||||||
chr12:132866577 | TGTTACAA others(11): Show |
T | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.583+3024_583+3041d others(20): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866577 | |||||||
chr12:132866626 | C | G | 1 | a0001c0001t0014g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.583+2993G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866626 | |||||||
chr12:132866627 | G | A | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.583+2992C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866627 | |||||||
chr12:132866697 | C | T | 1 | a0001c0004t0003g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.583+2922G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866697 | |||||||
chr12:132866907 | G | A | 33 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(30): Show |
33 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.583+2712C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866907 | |||||||
chr12:132866932 | G | T | 56 | a0001c0001t0012g0002 a0001c0001t0012g0125 a0001c0001t0012g0131 others(53): Show |
61 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.583+2687C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866932 | |||||||
chr12:132866991 | G | A | 1 | a0001c0001t0025g0238 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.583+2628C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866991 | |||||||
chr12:132867120 | C | G | 6 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(3): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.583+2499G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867120 | |||||||
chr12:132867182 | G | A | 1 | a0003c0003t0013g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.583+2437C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867182 | |||||||
chr12:132867205 | C | A | 1 | a0001c0001t0033g0153 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.583+2414G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867205 | |||||||
chr12:132867289 | G | T | 233 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(230): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.583+2330C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867289 | |||||||
chr12:132867329 | A | G | 1 | a0001c0001t0102g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.583+2290T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867329 | |||||||
chr12:132867403 | T | C | 1 | a0003c0003t0019g0339 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.583+2216A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867403 | |||||||
chr12:132867442 | A | C | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.583+2177T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867442 | |||||||
chr12:132867730 | C | T | 1 | a0001c0001t0096g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.583+1889G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867730 | |||||||
chr12:132867733 | G | A | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.583+1886C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867733 | |||||||
chr12:132867824 | A | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.583+1795T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867824 | |||||||
chr12:132867848 | C | T | 3 | a0001c0004t0003g0015 a0001c0004t0003g0200 a0002c0002t0135g0069 |
4 | HG01168.hp1 HG01169.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+1771G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867848 | |||||||
chr12:132867872 | C | G | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.583+1747G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867872 | |||||||
chr12:132867957 | AT | A | 46 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0310 others(43): Show |
48 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.583+1661delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867957 | |||||||
chr12:132867958 | T | TA | 31 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(28): Show |
35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.583+1660_583+1661i others(3): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867958 | |||||||
chr12:132867959 | T | A | 286 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(283): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.583+1660A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867959 | |||||||
chr12:132867969 | T | A | 48 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0310 others(45): Show |
50 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.583+1650A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867969 | |||||||
chr12:132867969 | TA | T | 3 | a0003c0003t0001g0024 a0003c0003t0001g0327 a0003c0003t0064g0029 |
4 | HG02976.hp1 HG03017.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+1649delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867969 | |||||||
chr12:132868021 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.583+1598G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868021 | |||||||
chr12:132868220 | G | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+1399C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868220 | |||||||
chr12:132868262 | G | C | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.583+1357C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868262 | |||||||
chr12:132868266 | A | G | 184 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(181): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.583+1353T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868266 | |||||||
chr12:132868270 | C | T | 100 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(97): Show |
112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.583+1349G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868270 | |||||||
chr12:132868351 | G | A | 2 | a0001c0001t0026g0020 a0001c0001t0026g0269 |
3 | NA18975.hp2 NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.583+1268C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868351 | |||||||
chr12:132868367 | G | A | 1 | a0001c0001t0099g0294 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.583+1252C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868367 | |||||||
chr12:132868388 | C | CTGAGGCA others(5): Show |
3 | a0002c0002t0047g0049 a0002c0002t0048g0048 a0002c0002t0048g0050 |
3 | HG01109.hp2 HG01433.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.583+1219_583+1230d others(14): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868388 | |||||||
chr12:132868406 | G | A | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.583+1213C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868406 | |||||||
chr12:132868424 | C | T | 1 | a0001c0001t0107g0298 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.583+1195G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868424 | |||||||
chr12:132868464 | C | T | 233 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(230): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.583+1155G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868464 | |||||||
chr12:132868479 | G | C | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.583+1140C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868479 | |||||||
chr12:132868521 | C | CA | 39 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(36): Show |
41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.583+1097dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868521 | |||||||
chr12:132868573 | G | GGGAGGCT others(175): Show |
182 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(179): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.583+1045_583+1046i others(184): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868573 | |||||||
chr12:132868581 | G | A | 3 | a0001c0001t0014g0005 a0001c0001t0014g0277 a0001c0001t0014g0278 |
5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.583+1038C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868581 | |||||||
chr12:132868656 | A | G | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+963T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868656 | |||||||
chr12:132868663 | G | C | 3 | a0001c0001t0014g0005 a0001c0001t0014g0277 a0001c0001t0014g0278 |
5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.583+956C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868663 | |||||||
chr12:132868675 | G | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+944C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868675 | |||||||
chr12:132868681 | A | AAACAAAC others(172): Show |
2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+937_583+938ins others(179): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868681 | |||||||
chr12:132868683 | A | C | 48 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.583+936T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868683 | |||||||
chr12:132868806 | ATGGGGCC others(305): Show |
A | 89 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(86): Show |
98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.583+501_583+812del | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868806 | |||||||
chr12:132868812 | CCGAGGGG others(227): Show |
C | 2 | a0001c0004t0017g0219 a0001c0004t0017g0220 |
2 | HG01109.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.583+573_583+806del | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868812 | |||||||
chr12:132868837 | G | A | 3 | a0001c0001t0010g0039 a0001c0001t0010g0042 a0001c0001t0117g0041 |
3 | HG02486.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.583+782C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868837 | |||||||
chr12:132868841 | G | A | 1 | a0002c0002t0002g0124 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.583+778C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868841 | |||||||
chr12:132868868 | T | C | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+751A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868868 | |||||||
chr12:132868907 | T | C | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+712A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868907 | |||||||
chr12:132868917 | CTGCTGGT others(32): Show |
C | 1 | a0001c0004t0003g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.583+663_583+701del others(39): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868917 | |||||||
chr12:132868923 | G | C | 1 | a0001c0001t0073g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+696C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868923 | |||||||
chr12:132868929 | C | T | 1 | a0001c0001t0073g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+690G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868929 | |||||||
chr12:132868948 | GGGAGTGA others(71): Show |
G | 1 | a0001c0001t0073g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+593_583+670del others(78): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868948 | |||||||
chr12:132868956 | T | C | 47 | a0001c0001t0069g0180 a0001c0001t0071g0345 a0001c0004t0003g0003 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.583+663A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868956 | |||||||
chr12:132868961 | G | C | 9 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(6): Show |
10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+658C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868961 | |||||||
chr12:132868988 | G | A | 6 | a0002c0002t0002g0059 a0002c0002t0028g0008 a0002c0002t0028g0060 others(3): Show |
7 | HG00733.hp1 HG01099.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.583+631C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868988 | |||||||
chr12:132869008 | T | C | 1 | a0001c0004t0003g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.583+611A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869008 | |||||||
chr12:132869040 | C | G | 1 | a0001c0001t0073g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+579G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869040 | |||||||
chr12:132869046 | T | TCGAGGGG others(32): Show |
121 | a0001c0001t0071g0345 a0002c0002t0002g0012 a0002c0002t0002g0051 others(118): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.583+534_583+572dup others(39): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869046 | |||||||
chr12:132869046 | TCGAGGGG others(32): Show |
T | 12 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(9): Show |
15 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+534_583+572del others(39): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869046 | |||||||
chr12:132869124 | C | T | 9 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(6): Show |
10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+495G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869124 | |||||||
chr12:132869151 | C | T | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+468G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869151 | |||||||
chr12:132869163 | C | CCGAGGGG others(344): Show |
2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+455_583+456ins others(351): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869163 | |||||||
chr12:132869164 | C | T | 1 | a0001c0001t0026g0020 | 2 | NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.583+455G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869164 | |||||||
chr12:132869260 | T | G | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+359A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869260 | |||||||
chr12:132869266 | C | G | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+353G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869266 | |||||||
chr12:132869570 | A | G | 1 | a0001c0001t0117g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.583+49T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869570 | |||||||
chr12:132869827 | G | C | 3 | a0001c0001t0014g0005 a0001c0001t0014g0277 a0001c0001t0014g0278 |
5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-29C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132869827 | |||||||
chr12:132869852 | C | T | 1 | a0001c0001t0086g0279 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.404-54G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132869852 | |||||||
chr12:132870075 | G | A | 4 | a0001c0005t0024g0173 a0001c0005t0024g0176 a0001c0005t0024g0177 others(1): Show |
4 | HG01106.hp1 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-277C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870075 | |||||||
chr12:132870081 | G | A | 11 | a0002c0002t0047g0046 a0002c0002t0131g0047 a0004c0006t0031g0163 others(8): Show |
11 | HG02129.hp1 HG02698.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.404-283C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870081 | |||||||
chr12:132870099 | T | G | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.404-301A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870099 | |||||||
chr12:132870123 | C | T | 1 | a0003c0003t0001g0326 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.404-325G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870123 | |||||||
chr12:132870236 | C | T | 100 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(97): Show |
112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.404-438G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870236 | |||||||
chr12:132870256 | G | T | 1 | a0001c0001t0080g0247 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.404-458C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870256 | |||||||
chr12:132870257 | C | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.404-459G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870257 | |||||||
chr12:132870276 | C | T | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.403+448G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870276 | |||||||
chr12:132870293 | A | G | 1 | a0002c0002t0030g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.403+431T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870293 | |||||||
chr12:132870354 | A | AAAAC | 48 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0310 others(45): Show |
50 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.403+366_403+369dup others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870354 | |||||||
chr12:132870530 | T | C | 1 | a0003c0003t0001g0348 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403+194A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870530 | |||||||
chr12:132870531 | C | CA | 35 | a0001c0001t0015g0291 a0001c0001t0042g0274 a0001c0001t0087g0267 others(32): Show |
39 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.403+192dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870531 | |||||||
chr12:132870531 | C | T | 1 | a0003c0003t0001g0348 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403+193G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870531 | |||||||
chr12:132870531 | CA | C | 95 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(92): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.403+192delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870531 | |||||||
chr12:132870532 | A | C | 1 | a0003c0003t0001g0348 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403+192T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870532 | |||||||
chr12:132870552 | T | A | 5 | a0001c0001t0007g0021 a0001c0001t0007g0306 a0001c0001t0082g0270 others(2): Show |
6 | HG00558.hp1 HG00597.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+172A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870552 | |||||||
chr12:132870570 | G | T | 6 | a0003c0003t0019g0339 a0003c0003t0037g0340 a0003c0003t0037g0341 others(3): Show |
6 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+154C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870570 | |||||||
chr12:132870609 | G | A | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.403+115C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870609 | |||||||
chr12:132870638 | T | C | 51 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.403+86A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870638 | |||||||
chr12:132870652 | T | C | 2 | a0001c0004t0003g0015 a0001c0004t0003g0200 |
3 | HG01168.hp1 HG01169.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.403+72A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870652 | |||||||
chr12:132870656 | T | C | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.403+68A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870656 | |||||||
chr12:132871102 | C | T | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.344-319G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871102 | |||||||
chr12:132871218 | G | A | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.344-435C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871218 | |||||||
chr12:132871223 | G | A | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.344-440C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871223 | |||||||
chr12:132871269 | C | T | 231 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(228): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.344-486G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871269 | |||||||
chr12:132871308 | C | T | 93 | a0002c0002t0002g0012 a0002c0002t0002g0051 a0002c0002t0002g0052 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.344-525G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871308 | |||||||
chr12:132871351 | C | T | 1 | a0003c0003t0001g0326 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.344-568G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871351 | |||||||
chr12:132871408 | C | T | 1 | a0003c0003t0001g0312 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.344-625G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871408 | |||||||
chr12:132871413 | T | C | 1 | a0002c0002t0134g0082 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.344-630A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871413 | |||||||
chr12:132871415 | G | C | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.344-632C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871415 | |||||||
chr12:132871428 | C | G | 184 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(181): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.344-645G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871428 | |||||||
chr12:132871429 | G | A | 1 | a0001c0004t0003g0198 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.344-646C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871429 | |||||||
chr12:132871600 | C | T | 1 | a0003c0003t0020g0317 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343+685G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871600 | |||||||
chr12:132871628 | C | T | 37 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(34): Show |
39 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.343+657G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871628 | |||||||
chr12:132871630 | G | T | 4 | a0002c0002t0005g0084 a0002c0002t0005g0085 a0002c0002t0005g0087 others(1): Show |
4 | NA18944.hp2 NA18948.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+655C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871630 | |||||||
chr12:132871665 | A | G | 334 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.343+620T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871665 | |||||||
chr12:132871744 | C | T | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.343+541G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871744 | |||||||
chr12:132871805 | G | A | 46 | a0001c0001t0071g0345 a0001c0004t0003g0003 a0001c0004t0003g0015 others(43): Show |
51 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.343+480C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871805 | |||||||
chr12:132871915 | T | C | 1 | a0003c0003t0001g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.343+370A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871915 | |||||||
chr12:132871935 | A | G | 4 | a0001c0001t0016g0246 a0003c0003t0019g0339 a0003c0008t0019g0342 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+350T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871935 | |||||||
chr12:132871967 | G | C | 223 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(220): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.343+318C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871967 | |||||||
chr12:132872192 | T | C | 1 | a0001c0001t0006g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.343+93A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872192 | |||||||
chr12:132872217 | C | T | 1 | a0005c0009t0054g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.343+68G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872217 | |||||||
chr12:132872226 | A | G | 5 | a0001c0001t0014g0276 a0001c0001t0016g0244 a0001c0001t0016g0245 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+59T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872226 | |||||||
chr12:132872229 | G | A | 65 | a0001c0001t0006g0151 a0001c0001t0006g0154 a0001c0001t0007g0021 others(62): Show |
72 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.343+56C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872229 | |||||||
chr12:132872237 | G | A | 2 | a0002c0002t0028g0008 a0002c0002t0028g0060 |
3 | HG01099.hp2 HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.343+48C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872237 | |||||||
chr12:132872432 | A | G | 1 | a0001c0005t0024g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234-38T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872432 | |||||||
chr12:132872577 | G | A | 1 | a0002c0002t0004g0072 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.234-183C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872577 | |||||||
chr12:132872591 | G | A | 77 | a0001c0001t0014g0005 a0001c0001t0014g0277 a0001c0001t0014g0278 others(74): Show |
82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.234-197C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872591 | |||||||
chr12:132872781 | C | A | 48 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(45): Show |
51 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.234-387G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872781 | |||||||
chr12:132872863 | G | A | 85 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(82): Show |
93 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.234-469C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872863 | |||||||
chr12:132873035 | T | A | 1 | a0001c0005t0074g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234-641A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873035 | |||||||
chr12:132873063 | A | G | 1 | a0002c0002t0123g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.234-669T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873063 | |||||||
chr12:132873251 | A | C | 49 | a0001c0001t0015g0297 a0001c0001t0085g0296 a0001c0004t0003g0003 others(46): Show |
54 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.234-857T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873251 | |||||||
chr12:132873358 | G | A | 1 | a0003c0003t0019g0344 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.234-964C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873358 | |||||||
chr12:132873443 | G | C | 88 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(85): Show |
97 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.234-1049C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873443 | |||||||
chr12:132873448 | G | A | 74 | a0001c0004t0018g0083 a0002c0002t0002g0012 a0002c0002t0002g0051 others(71): Show |
80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.234-1054C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873448 | |||||||
chr12:132873459 | C | T | 3 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0060g0026 |
3 | HG02257.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.234-1065G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873459 | |||||||
chr12:132873506 | TGCTGGAC others(83): Show |
T | 123 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(120): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.234-1202_234-1113d others(92): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873506 | |||||||
chr12:132873558 | G | A | 94 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(91): Show |
100 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.234-1164C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873558 | |||||||
chr12:132873612 | T | C | 8 | a0002c0002t0002g0054 a0002c0002t0002g0102 a0002c0002t0002g0106 others(5): Show |
8 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-1218A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873612 | |||||||
chr12:132873620 | CCTGCTCC others(82): Show |
C | 1 | a0001c0001t0105g0288 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.234-1315_234-1227d others(91): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873620 | |||||||
chr12:132873634 | C | T | 4 | a0001c0001t0011g0239 a0001c0001t0011g0257 a0001c0001t0011g0284 others(1): Show |
4 | NA18950.hp2 NA18983.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-1240G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873634 | |||||||
chr12:132873648 | G | A | 1 | a0002c0002t0047g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.234-1254C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873648 | |||||||
chr12:132873744 | T | C | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.234-1350A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873744 | |||||||
chr12:132873745 | G | A | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.234-1351C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873745 | |||||||
chr12:132873795 | G | A | 10 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0013g0030 others(7): Show |
10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.234-1401C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873795 | |||||||
chr12:132874048 | C | T | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.234-1654G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874048 | |||||||
chr12:132874336 | G | A | 1 | a0001c0005t0076g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.234-1942C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874336 | |||||||
chr12:132874366 | T | G | 1 | a0001c0001t0117g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.234-1972A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874366 | |||||||
chr12:132874511 | C | T | 1 | a0001c0001t0015g0243 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.234-2117G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874511 | |||||||
chr12:132874552 | C | T | 3 | a0001c0005t0024g0173 a0001c0005t0024g0176 a0001c0005t0024g0177 |
3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.234-2158G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874552 | |||||||
chr12:132874583 | G | A | 1 | a0002c0002t0137g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.234-2189C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874583 | |||||||
chr12:132874601 | AGAACAGG others(46): Show |
A | 80 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(77): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.234-2260_234-2208d others(55): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874601 | |||||||
chr12:132874691 | G | A | 31 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(28): Show |
35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.234-2297C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874691 | |||||||
chr12:132874857 | C | G | 2 | a0001c0001t0007g0234 a0001c0001t0007g0286 |
2 | NA18943.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.234-2463G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874857 | |||||||
chr12:132874901 | GCGGGGAA others(46): Show |
G | 1 | a0001c0001t0102g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.234-2560_234-2508d others(55): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874901 | |||||||
chr12:132874954 | A | G | 41 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(38): Show |
43 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.234-2560T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874954 | |||||||
chr12:132874955 | C | T | 41 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(38): Show |
43 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.234-2561G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874955 | |||||||
chr12:132874958 | G | GGAAGCCA others(46): Show |
1 | a0002c0002t0002g0012 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.233+2544_234-2565d others(55): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874958 | |||||||
chr12:132875006 | C | T | 1 | a0002c0002t0130g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+2549G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875006 | |||||||
chr12:132875033 | C | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233+2522G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875033 | |||||||
chr12:132875081 | G | T | 41 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.233+2474C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875081 | |||||||
chr12:132875098 | G | A | 10 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(7): Show |
11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+2457C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875098 | |||||||
chr12:132875305 | C | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233+2250G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875305 | |||||||
chr12:132875382 | T | G | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.233+2173A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875382 | |||||||
chr12:132875483 | C | T | 48 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(45): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.233+2072G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875483 | |||||||
chr12:132875489 | G | A | 41 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.233+2066C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875489 | |||||||
chr12:132875670 | C | T | 4 | a0001c0001t0015g0241 a0001c0001t0078g0240 a0001c0001t0079g0235 others(1): Show |
4 | HG00558.hp2 HG02165.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+1885G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875670 | |||||||
chr12:132875897 | G | A | 96 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.233+1658C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875897 | |||||||
chr12:132876173 | C | CA | 106 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(103): Show |
118 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.233+1381dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876173 | |||||||
chr12:132876182 | A | G | 47 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.233+1373T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876182 | |||||||
chr12:132876251 | T | C | 1 | a0001c0001t0006g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.233+1304A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876251 | |||||||
chr12:132876367 | T | C | 1 | a0004c0006t0133g0166 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.233+1188A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876367 | |||||||
chr12:132876749 | T | C | 1 | a0003c0003t0001g0335 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.233+806A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876749 | |||||||
chr12:132876763 | A | G | 2 | a0002c0007t0002g0066 a0002c0007t0002g0071 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.233+792T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876763 | |||||||
chr12:132876951 | C | G | 1 | a0001c0001t0090g0067 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.233+604G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876951 | |||||||
chr12:132876952 | G | A | 39 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(36): Show |
41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.233+603C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876952 | |||||||
chr12:132876955 | C | A | 1 | a0001c0005t0038g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.233+600G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876955 | |||||||
chr12:132876955 | C | T | 41 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.233+600G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876955 | |||||||
chr12:132877090 | C | T | 6 | a0003c0003t0020g0317 a0003c0003t0020g0318 a0003c0003t0020g0320 others(3): Show |
6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+465G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877090 | |||||||
chr12:132877302 | G | A | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233+253C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877302 | |||||||
chr12:132877303 | G | A | 1 | a0003c0003t0065g0331 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.233+252C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877303 | |||||||
chr12:132877321 | G | C | 1 | a0001c0001t0006g0145 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.233+234C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877321 | |||||||
chr12:132877362 | T | C | 2 | a0001c0001t0148g0130 a0001c0001t0149g0146 |
2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.233+193A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877362 | |||||||
chr12:132877708 | C | T | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.134-54G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877708 | |||||||
chr12:132877768 | TA | T | 41 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.134-115delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877768 | |||||||
chr12:132877769 | A | T | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-115T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877769 | |||||||
chr12:132877804 | A | G | 3 | a0001c0001t0011g0239 a0001c0001t0011g0284 a0001c0001t0011g0287 |
3 | NA18950.hp2 NA19056.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.134-150T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877804 | |||||||
chr12:132877833 | C | T | 1 | a0001c0005t0074g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134-179G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877833 | |||||||
chr12:132877834 | GC | G | 15 | a0001c0001t0089g0045 a0002c0002t0047g0046 a0002c0002t0047g0049 others(12): Show |
15 | HG01109.hp2 HG01433.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.134-181delG | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877834 | |||||||
chr12:132877924 | T | G | 1 | a0001c0001t0069g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.134-270A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877924 | |||||||
chr12:132877966 | C | G | 1 | a0001c0001t0010g0036 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.134-312G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877966 | |||||||
chr12:132877981 | T | G | 47 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.134-327A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877981 | |||||||
chr12:132877992 | C | T | 1 | a0003c0003t0001g0324 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.134-338G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877992 | |||||||
chr12:132878068 | C | T | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-414G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878068 | |||||||
chr12:132878097 | C | T | 6 | a0003c0003t0020g0317 a0003c0003t0020g0318 a0003c0003t0020g0320 others(3): Show |
6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-443G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878097 | |||||||
chr12:132878338 | G | A | 5 | a0004c0006t0032g0158 a0004c0006t0032g0161 a0004c0006t0032g0162 others(2): Show |
5 | NA18954.hp2 NA18969.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-684C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878338 | |||||||
chr12:132878384 | G | A | 76 | a0001c0004t0018g0083 a0002c0002t0002g0012 a0002c0002t0002g0051 others(73): Show |
82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.134-730C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878384 | |||||||
chr12:132878448 | G | A | 1 | a0001c0004t0003g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.134-794C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878448 | |||||||
chr12:132878473 | T | TA | 6 | a0001c0001t0042g0273 a0001c0001t0042g0274 a0001c0001t0101g0305 others(3): Show |
6 | HG00408.hp2 HG02602.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-820dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878473 | |||||||
chr12:132878473 | TA | T | 49 | a0001c0001t0015g0297 a0001c0001t0025g0238 a0001c0004t0003g0003 others(46): Show |
54 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.134-820delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878473 | |||||||
chr12:132878479 | A | G | 1 | a0001c0001t0090g0067 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134-825T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878479 | |||||||
chr12:132878583 | A | G | 334 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.134-929T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878583 | |||||||
chr12:132878595 | A | G | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.134-941T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878595 | |||||||
chr12:132878616 | G | A | 34 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(31): Show |
37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.134-962C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878616 | |||||||
chr12:132878642 | A | G | 1 | a0002c0002t0004g0110 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.134-988T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878642 | |||||||
chr12:132878686 | G | C | 1 | a0001c0001t0071g0345 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.134-1032C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878686 | |||||||
chr12:132878692 | G | A | 96 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1038C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878692 | |||||||
chr12:132878711 | T | C | 2 | a0001c0001t0043g0022 a0001c0001t0083g0289 |
3 | HG01243.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.134-1057A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878711 | |||||||
chr12:132878745 | G | A | 96 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1091C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878745 | |||||||
chr12:132878832 | A | G | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1178T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878832 | |||||||
chr12:132878832 | AG | A | 28 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(25): Show |
30 | HG00140.hp2 HG01168.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.134-1179delC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878832 | |||||||
chr12:132878833 | G | A | 12 | a0001c0001t0006g0151 a0001c0001t0050g0148 a0001c0001t0052g0127 others(9): Show |
12 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1179C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878833 | |||||||
chr12:132878833 | G | GA | 40 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(37): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.134-1180dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878833 | |||||||
chr12:132878884 | C | T | 1 | a0001c0004t0057g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.134-1230G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878884 | |||||||
chr12:132878902 | G | A | 1 | a0001c0004t0018g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.134-1248C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878902 | |||||||
chr12:132878998 | T | G | 1 | a0001c0001t0083g0289 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.134-1344A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878998 | |||||||
chr12:132878999 | G | T | 1 | a0002c0007t0002g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.134-1345C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878999 | |||||||
chr12:132879005 | G | T | 96 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1351C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879005 | |||||||
chr12:132879009 | G | T | 2 | a0002c0007t0002g0066 a0004c0006t0031g0163 |
2 | HG03669.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.134-1355C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879009 | |||||||
chr12:132879009 | GT | G | 193 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(190): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.134-1356delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879009 | |||||||
chr12:132879010 | T | G | 2 | a0002c0007t0002g0066 a0004c0006t0031g0163 |
2 | HG03669.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.134-1356A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879010 | |||||||
chr12:132879011 | T | G | 4 | a0003c0003t0001g0315 a0003c0003t0001g0322 a0003c0003t0001g0330 others(1): Show |
4 | HG00438.hp2 HG02129.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1357A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879011 | |||||||
chr12:132879070 | T | A | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1416A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879070 | |||||||
chr12:132879074 | G | A | 1 | a0001c0004t0003g0200 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.134-1420C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879074 | |||||||
chr12:132879153 | C | T | 1 | a0004c0006t0032g0158 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.134-1499G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879153 | |||||||
chr12:132879275 | T | A | 1 | a0001c0001t0012g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.134-1621A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879275 | |||||||
chr12:132879275 | T | G | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.134-1621A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879275 | |||||||
chr12:132879297 | C | G | 47 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.134-1643G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879297 | |||||||
chr12:132879353 | T | C | 1 | a0001c0001t0006g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.134-1699A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879353 | |||||||
chr12:132879370 | T | C | 2 | a0005c0009t0053g0120 a0005c0009t0054g0108 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1716A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879370 | |||||||
chr12:132879380 | T | G | 1 | a0001c0001t0115g0231 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.134-1726A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879380 | |||||||
chr12:132879395 | C | CT | 14 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(11): Show |
15 | HG00735.hp2 HG01070.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-1742dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879395 | |||||||
chr12:132879431 | C | T | 6 | a0001c0001t0015g0291 a0001c0001t0015g0295 a0001c0001t0015g0297 others(3): Show |
6 | HG00323.hp1 HG01952.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-1777G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879431 | |||||||
chr12:132879459 | C | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.134-1805G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879459 | |||||||
chr12:132879460 | A | G | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.134-1806T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879460 | |||||||
chr12:132879484 | G | A | 1 | a0001c0001t0007g0275 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.134-1830C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879484 | |||||||
chr12:132879627 | G | A | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.134-1973C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879627 | |||||||
chr12:132879636 | G | A | 96 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1982C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879636 | |||||||
chr12:132879641 | G | A | 1 | a0001c0001t0006g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.134-1987C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879641 | |||||||
chr12:132879892 | A | G | 77 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(74): Show |
83 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.134-2238T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879892 | |||||||
chr12:132880147 | T | G | 1 | a0003c0003t0062g0338 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.134-2493A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880147 | |||||||
chr12:132880182 | A | C | 1 | a0003c0003t0001g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.134-2528T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880182 | |||||||
chr12:132880246 | C | G | 6 | a0002c0002t0002g0059 a0002c0002t0028g0008 a0002c0002t0028g0060 others(3): Show |
7 | HG00733.hp1 HG01099.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-2592G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880246 | |||||||
chr12:132880431 | G | T | 2 | a0001c0005t0074g0174 a0001c0005t0075g0175 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-2777C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880431 | |||||||
chr12:132880518 | C | T | 1 | a0002c0002t0004g0058 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-2864G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880518 | |||||||
chr12:132880526 | C | T | 95 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(92): Show |
101 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.134-2872G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880526 | |||||||
chr12:132880548 | C | T | 1 | a0001c0004t0018g0207 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.134-2894G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880548 | |||||||
chr12:132880595 | T | C | 1 | a0001c0001t0092g0283 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.134-2941A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880595 | |||||||
chr12:132880615 | G | A | 1 | a0001c0001t0009g0236 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.134-2961C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880615 | |||||||
chr12:132880616 | C | T | 1 | a0001c0001t0009g0236 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.134-2962G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880616 | |||||||
chr12:132880663 | AAG | A | 102 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(99): Show |
113 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.134-3011_134-3010d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880663 | |||||||
chr12:132880664 | AG | A | 5 | a0001c0001t0009g0004 a0001c0001t0084g0262 a0001c0001t0085g0296 others(2): Show |
5 | HG02257.hp1 NA18952.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-3011delC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880664 | |||||||
chr12:132880709 | G | C | 98 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.134-3055C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880709 | |||||||
chr12:132880783 | G | A | 41 | a0003c0003t0001g0007 a0003c0003t0001g0023 a0003c0003t0001g0024 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.134-3129C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880783 | |||||||
chr12:132880834 | G | A | 6 | a0001c0005t0021g0014 a0001c0005t0021g0184 a0001c0005t0021g0185 others(3): Show |
7 | HG02145.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-3180C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880834 | |||||||
chr12:132880922 | G | A | 100 | a0001c0001t0050g0148 a0001c0001t0050g0155 a0001c0001t0089g0045 others(97): Show |
106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.134-3268C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880922 | |||||||
chr12:132880930 | A | G | 1 | a0003c0003t0060g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.134-3276T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880930 | |||||||
chr12:132880979 | A | G | 1 | a0001c0004t0018g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.134-3325T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880979 | |||||||
chr12:132881025 | G | T | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0059g0228 |
3 | HG00280.hp1 NA18977.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.134-3371C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881025 | |||||||
chr12:132881035 | G | A | 87 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(84): Show |
96 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.134-3381C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881035 | |||||||
chr12:132881056 | C | G | 2 | a0001c0004t0036g0204 a0001c0004t0036g0205 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.134-3402G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881056 | |||||||
chr12:132881058 | G | C | 1 | a0002c0002t0004g0110 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.134-3404C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881058 | |||||||
chr12:132881065 | G | A | 44 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(41): Show |
47 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.134-3411C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881065 | |||||||
chr12:132881111 | A | G | 1 | a0001c0001t0079g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.134-3457T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881111 | |||||||
chr12:132881196 | T | G | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.134-3542A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881196 | |||||||
chr12:132881257 | C | CA | 145 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0252 others(142): Show |
159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.134-3604dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881257 | |||||||
chr12:132881568 | C | G | 33 | a0003c0003t0001g0023 a0003c0003t0001g0024 a0003c0003t0001g0310 others(30): Show |
35 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.134-3914G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881568 | |||||||
chr12:132881589 | C | T | 27 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(24): Show |
31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.134-3935G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881589 | |||||||
chr12:132881596 | G | A | 6 | a0004c0006t0032g0158 a0004c0006t0032g0161 a0004c0006t0032g0162 others(3): Show |
6 | NA18954.hp2 NA18969.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-3942C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881596 | |||||||
chr12:132881724 | C | T | 99 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(96): Show |
106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.134-4070G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881724 | |||||||
chr12:132881725 | G | A | 1 | a0001c0001t0006g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.134-4071C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881725 | |||||||
chr12:132881731 | G | A | 1 | a0002c0002t0127g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.134-4077C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881731 | |||||||
chr12:132881792 | C | T | 108 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(105): Show |
120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.134-4138G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881792 | |||||||
chr12:132881800 | G | A | 99 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(96): Show |
106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.134-4146C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881800 | |||||||
chr12:132881831 | G | A | 1 | a0002c0002t0002g0124 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.134-4177C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881831 | |||||||
chr12:132881867 | CA | C | 55 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.134-4214delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881867 | |||||||
chr12:132881867 | CAA | C | 266 | a0001c0001t0007g0021 a0001c0001t0007g0234 a0001c0001t0007g0252 others(263): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.134-4215_134-4214d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881867 | |||||||
chr12:132881940 | G | A | 1 | a0001c0001t0050g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.134-4286C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881940 | |||||||
chr12:132882070 | G | C | 2 | a0001c0001t0043g0022 a0001c0001t0083g0289 |
3 | HG01243.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.134-4416C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882070 | |||||||
chr12:132882432 | C | T | 1 | a0001c0001t0089g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133+4764G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882432 | |||||||
chr12:132882609 | C | T | 10 | a0003c0003t0013g0027 a0003c0003t0013g0028 a0003c0003t0013g0030 others(7): Show |
10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+4587G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882609 | |||||||
chr12:132882638 | A | G | 1 | a0001c0005t0076g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.133+4558T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882638 | |||||||
chr12:132882653 | C | T | 39 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(36): Show |
41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+4543G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882653 | |||||||
chr12:132882684 | C | T | 40 | a0003c0003t0001g0023 a0003c0003t0001g0024 a0003c0003t0001g0310 others(37): Show |
42 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.133+4512G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882684 | |||||||
chr12:132882701 | A | G | 1 | a0001c0001t0089g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133+4495T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882701 | |||||||
chr12:132882706 | GT | G | 176 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(173): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.133+4489delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882706 | |||||||
chr12:132882759 | G | T | 40 | a0003c0003t0001g0023 a0003c0003t0001g0024 a0003c0003t0001g0310 others(37): Show |
42 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.133+4437C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882759 | |||||||
chr12:132882929 | T | C | 99 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(96): Show |
106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+4267A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882929 | |||||||
chr12:132882976 | A | G | 6 | a0003c0003t0020g0317 a0003c0003t0020g0318 a0003c0003t0020g0320 others(3): Show |
6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+4220T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882976 | |||||||
chr12:132883092 | T | C | 1 | a0003c0003t0001g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.133+4104A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883092 | |||||||
chr12:132883387 | T | C | 47 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+3809A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883387 | |||||||
chr12:132883407 | T | C | 334 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(331): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.133+3789A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883407 | |||||||
chr12:132883422 | G | A | 39 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(36): Show |
41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+3774C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883422 | |||||||
chr12:132883426 | C | CA | 10 | a0001c0001t0015g0295 a0001c0001t0069g0180 a0001c0001t0071g0345 others(7): Show |
10 | HG00642.hp1 HG00735.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+3769dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883426 | |||||||
chr12:132883426 | C | CAA | 37 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(34): Show |
39 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.133+3768_133+3769d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883426 | |||||||
chr12:132883446 | C | T | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.133+3750G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883446 | |||||||
chr12:132883563 | A | G | 1 | a0001c0001t0015g0233 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.133+3633T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883563 | |||||||
chr12:132883595 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.133+3601G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883595 | |||||||
chr12:132883626 | T | C | 108 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(105): Show |
120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133+3570A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883626 | |||||||
chr12:132883649 | C | G | 39 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(36): Show |
41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+3547G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883649 | |||||||
chr12:132883830 | T | C | 39 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(36): Show |
41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+3366A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883830 | |||||||
chr12:132883866 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.133+3330C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883866 | |||||||
chr12:132883883 | C | G | 1 | a0002c0002t0127g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.133+3313G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883883 | |||||||
chr12:132883917 | A | C | 38 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(35): Show |
40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.133+3279T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883917 | |||||||
chr12:132884312 | G | T | 1 | a0006c0014t0002g0055 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.133+2884C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884312 | |||||||
chr12:132884313 | G | C | 99 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(96): Show |
106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+2883C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884313 | |||||||
chr12:132884415 | C | CA | 130 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(127): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.133+2780dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884415 | |||||||
chr12:132884670 | T | G | 1 | a0001c0001t0007g0307 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.133+2526A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884670 | |||||||
chr12:132884929 | T | C | 2 | a0001c0001t0150g0157 a0001c0001t0151g0156 |
2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.133+2267A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884929 | |||||||
chr12:132884973 | A | C | 1 | a0003c0003t0001g0315 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.133+2223T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884973 | |||||||
chr12:132884981 | G | A | 99 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(96): Show |
106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+2215C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884981 | |||||||
chr12:132885148 | G | A | 2 | a0002c0002t0046g0013 a0002c0002t0124g0119 |
3 | HG00423.hp2 NA18950.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.133+2048C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885148 | |||||||
chr12:132885265 | G | A | 1 | a0005c0009t0053g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.133+1931C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885265 | |||||||
chr12:132885366 | G | A | 1 | a0001c0005t0076g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.133+1830C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885366 | |||||||
chr12:132885419 | T | TATAA | 93 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(90): Show |
103 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.133+1773_133+1776d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885419 | |||||||
chr12:132885419 | T | TATAAATA others(1): Show |
6 | a0001c0001t0015g0297 a0001c0001t0085g0296 a0002c0002t0002g0124 others(3): Show |
6 | HG00323.hp1 NA18984.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+1769_133+1776d others(10): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885419 | |||||||
chr12:132885419 | TATAA | T | 108 | a0001c0001t0016g0232 a0001c0001t0089g0045 a0001c0004t0003g0003 others(105): Show |
115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.133+1773_133+1776d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885419 | |||||||
chr12:132885436 | A | G | 1 | a0001c0005t0024g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+1760T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885436 | |||||||
chr12:132885454 | A | C | 1 | a0001c0004t0003g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.133+1742T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885454 | |||||||
chr12:132885596 | G | A | 47 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+1600C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885596 | |||||||
chr12:132885743 | C | A | 108 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(105): Show |
120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133+1453G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885743 | |||||||
chr12:132885776 | G | T | 1 | a0001c0004t0057g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.133+1420C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885776 | |||||||
chr12:132885778 | T | C | 1 | a0003c0003t0065g0331 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.133+1418A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885778 | |||||||
chr12:132885861 | T | C | 3 | a0001c0004t0003g0226 a0001c0004t0003g0229 a0001c0004t0022g0227 |
3 | NA18979.hp1 NA18985.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.133+1335A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885861 | |||||||
chr12:132886141 | A | G | 333 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.133+1055T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886141 | |||||||
chr12:132886173 | A | C | 108 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(105): Show |
120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133+1023T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886173 | |||||||
chr12:132886182 | C | T | 1 | a0003c0003t0001g0314 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.133+1014G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886182 | |||||||
chr12:132886309 | TCAAAAAA others(5): Show |
T | 2 | a0001c0001t0110g0230 a0001c0001t0115g0231 |
2 | NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.133+875_133+886del others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886309 | |||||||
chr12:132886339 | C | A | 11 | a0001c0001t0007g0044 a0003c0003t0013g0027 a0003c0003t0013g0028 others(8): Show |
11 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.133+857G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886339 | |||||||
chr12:132886341 | A | C | 1 | a0001c0001t0007g0044 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133+855T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886341 | |||||||
chr12:132886342 | G | A | 1 | a0001c0001t0007g0044 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133+854C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886342 | |||||||
chr12:132886347 | A | C | 99 | a0001c0001t0089g0045 a0001c0001t0090g0067 a0001c0004t0018g0083 others(96): Show |
106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+849T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886347 | |||||||
chr12:132886360 | G | A | 1 | a0001c0001t0107g0298 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.133+836C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886360 | |||||||
chr12:132886374 | C | CA | 9 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(6): Show |
10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+821dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886374 | |||||||
chr12:132886374 | CA | C | 143 | a0001c0001t0007g0021 a0001c0001t0007g0234 a0001c0001t0007g0252 others(140): Show |
157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.133+821delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886374 | |||||||
chr12:132886374 | CAA | C | 157 | a0001c0001t0006g0137 a0001c0001t0006g0139 a0001c0001t0006g0140 others(154): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.133+820_133+821del others(2): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886374 | |||||||
chr12:132886500 | C | A | 47 | a0001c0004t0003g0003 a0001c0004t0003g0015 a0001c0004t0003g0016 others(44): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+696G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886500 | |||||||
chr12:132886557 | T | G | 87 | a0001c0001t0007g0021 a0001c0001t0007g0044 a0001c0001t0007g0234 others(84): Show |
96 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.133+639A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886557 | |||||||
chr12:132886584 | G | T | 1 | a0001c0001t0007g0044 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133+612C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886584 | |||||||
chr12:132886661 | T | C | 1 | a0001c0001t0114g0308 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.133+535A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886661 | |||||||
chr12:132886817 | T | C | 1 | a0001c0001t0143g0309 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.133+379A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886817 | |||||||
chr12:132886923 | A | G | 54 | a0001c0001t0010g0006 a0001c0001t0010g0036 a0001c0001t0010g0037 others(51): Show |
59 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.133+273T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886923 | |||||||
chr12:132887189 | C | T | 4 | a0003c0003t0001g0310 a0003c0003t0001g0311 a0003c0003t0001g0312 others(1): Show |
4 | HG00738.hp1 HG02735.hp2 HG03490.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.133+7G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132887189 | |||||||
chr12:132887383 | G | A | 41 | a0001c0001t0071g0345 a0003c0003t0001g0023 a0003c0003t0001g0024 others(38): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-12-43C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 1/17 | chr12 | 132887383 | |||||||
chr12:132887529 | C | A | 4 | a0003c0003t0001g0346 a0003c0003t0001g0347 a0003c0003t0001g0348 others(1): Show |
4 | HG00140.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+18G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 1/17 | chr12 | 132887529 |