Variant report
Variant | rs5749414 |
---|---|
Chromosome Location | chr22:32774960-32774961 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:121)
- CpG islands (count:0)
- Chromatin interactive region (count:15)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | CTCF | chr22:32774708-32775005 | Hela-S3 | cervix: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
2 | MAX | chr22:32774709-32775006 | K562 | blood: | n/a | n/a |
3 | TBL1XR1 | chr22:32774748-32774991 | K562 | blood: | n/a | n/a |
4 | CTCF | chr22:32774559-32775047 | H1-hESC | embryonic stem cell: | n/a | chr22:32774880-32774898 chr22:32774615-32774628 chr22:32774883-32774896 |
5 | MYC | chr22:32774735-32775000 | K562 | blood: | n/a | n/a |
6 | ZNF143 | chr22:32774656-32775061 | K562 | blood: | n/a | n/a |
7 | YY1 | chr22:32774653-32775137 | H1-hESC | embryonic stem cell: | n/a | n/a |
8 | CTCF | chr22:32774537-32775060 | HepG2 | liver: | n/a | chr22:32774880-32774898 chr22:32774615-32774628 chr22:32774883-32774896 |
9 | CTCF | chr22:32774578-32775091 | K562 | blood: | n/a | chr22:32774880-32774898 chr22:32774615-32774628 chr22:32774883-32774896 |
10 | RAD21 | chr22:32774738-32774961 | GM12878 | blood: | n/a | chr22:32774881-32774900 chr22:32774882-32774896 |
11 | CTCF | chr22:32774820-32774970 | BJ | skin: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
12 | ELF1 | chr22:32774657-32774976 | K562 | blood: | n/a | n/a |
13 | RAD21 | chr22:32774552-32775089 | ECC-1 | luminal epithelium: | n/a | chr22:32774881-32774900 chr22:32774882-32774896 |
14 | CTCFL | chr22:32774751-32774967 | K562 | blood: | n/a | n/a |
15 | CTCF | chr22:32774840-32774990 | GM12864 | blood: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
16 | MAFK | chr22:32774907-32774972 | Hela-S3 | cervix: | n/a | n/a |
17 | CTCF | chr22:32774703-32775020 | Medullo | brain: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
18 | RAD21 | chr22:32774636-32775081 | HepG2 | liver: | n/a | chr22:32774881-32774900 chr22:32774882-32774896 |
19 | RAD21 | chr22:32774620-32775091 | H1-hESC | embryonic stem cell: | n/a | chr22:32774881-32774900 chr22:32774882-32774896 |
20 | CTCF | chr22:32774468-32775279 | MCF-7 | breast: | n/a | chr22:32774880-32774898 chr22:32775157-32775170 chr22:32774615-32774628 chr22:32774883-32774896 |
21 | HDAC2 | chr22:32774639-32775037 | H1-hESC | embryonic stem cell: | n/a | n/a |
22 | UBTF | chr22:32774739-32775020 | K562 | blood: | n/a | n/a |
23 | CTCF | chr22:32774650-32774974 | ECC-1 | luminal epithelium: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
24 | CTCF | chr22:32774700-32775037 | A549 | lung: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
25 | CTCF | chr22:32774590-32775063 | T-47D | breast: | n/a | chr22:32774880-32774898 chr22:32774615-32774628 chr22:32774883-32774896 |
26 | CTCF | chr22:32774728-32774973 | SK-N-SH_RA | brain: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
27 | YY1 | chr22:32774647-32775058 | H1-hESC | embryonic stem cell: | n/a | n/a |
28 | CTCF | chr22:32774554-32775069 | H1-hESC | embryonic stem cell: | n/a | chr22:32774880-32774898 chr22:32774615-32774628 chr22:32774883-32774896 |
29 | SMC3 | chr22:32774679-32775041 | HepG2 | liver: | n/a | chr22:32774882-32774896 |
30 | TBL1XR1 | chr22:32774928-32775036 | K562 | blood: | n/a | n/a |
31 | CTCF | chr22:32774820-32774970 | Hela-S3 | cervix: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
32 | MAZ | chr22:32774760-32774981 | HepG2 | liver: | n/a | n/a |
33 | JUND | chr22:32774715-32775438 | K562 | blood: | n/a | chr22:32775325-32775335 chr22:32775324-32775336 chr22:32775325-32775335 chr22:32775326-32775334 |
34 | CTCF | chr22:32774558-32775189 | HCT-116 | colon: | n/a | chr22:32774880-32774898 chr22:32775157-32775170 chr22:32774615-32774628 chr22:32774883-32774896 |
35 | ZNF143 | chr22:32774714-32775012 | GM12878 | blood: | n/a | n/a |
36 | RAD21 | chr22:32774668-32775010 | K562 | blood: | n/a | chr22:32774881-32774900 chr22:32774882-32774896 |
37 | CTCF | chr22:32774731-32774994 | ProgFib | skin: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
38 | CTCF | chr22:32774753-32774974 | Pancreas_OC | pancreas: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
39 | CTCF | chr22:32774727-32774994 | GM12878 | blood: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
40 | RCOR1 | chr22:32774824-32774983 | HepG2 | liver: | n/a | n/a |
41 | CTCF | chr22:32774654-32775063 | IMR90 | lung: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
42 | RCOR1 | chr22:32774701-32775022 | K562 | blood: | n/a | n/a |
43 | CTCF | chr22:32774734-32774973 | GM19240 | blood: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
44 | MAX | chr22:32774795-32775035 | K562 | blood: | n/a | n/a |
45 | CTCF | chr22:32774683-32775025 | H1-hESC | embryonic stem cell: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
46 | CTCF | chr22:32774725-32774998 | HepG2 | liver: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
47 | RAD21 | chr22:32774554-32775053 | SK-N-SH_RA | brain: | n/a | chr22:32774881-32774900 chr22:32774882-32774896 |
48 | CTCF | chr22:32774724-32775010 | Fibrobl | skin: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
49 | RAD21 | chr22:32774647-32775001 | SK-N-SH_RA | brain: | n/a | chr22:32774881-32774900 chr22:32774882-32774896 |
50 | CTCF | chr22:32774728-32774972 | Lung_OC | lung: | n/a | chr22:32774880-32774898 chr22:32774883-32774896 |
No data |
(count:15 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | 22:31829733-31836635..22:32764253-32784733 | K562 | blood: | |
2 | chr22:32774461..32775315-chr22:33599131..33599713,2 | MCF-7 | breast: | |
3 | 22:31936958-31958600..22:32764253-32784733 | K562 | blood: | |
4 | chr22:32774466..32775412-chr22:32914589..32915237,2 | K562 | blood: | |
5 | chr22:32774801..32777723-chr22:32782145..32784494,2 | MCF-7 | breast: | |
6 | chr22:32774444..32775309-chr22:32839813..32840801,8 | MCF-7 | breast: | |
7 | chr22:32366399..32367270-chr22:32774385..32775272,2 | MCF-7 | breast: | |
8 | 22:32529813-32538538..22:32764253-32784733 | H1-hESC | embryonic stem cell: | embryo |
9 | chr22:32774655..32775289-chr22:32840154..32841027,2 | MCF-7 | breast: | |
10 | chr22:32598513..32599181-chr22:32774588..32775254,2 | MCF-7 | breast: | |
11 | chr22:32598041..32599019-chr22:32774399..32775272,3 | MCF-7 | breast: | |
12 | 22:32513817-32522138..22:32764253-32784733 | H1-hESC | embryonic stem cell: | embryo |
13 | 22:32360288-32405313..22:32764253-32784733 | K562 | blood: | |
14 | chr22:32774484..32775191-chr22:32869003..32869550,2 | MCF-7 | breast: | |
15 | chr22:32499507..32500361-chr22:32774175..32775330,4 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000241954 | TF binding region |
ENSG00000239674 | Chromatin interaction |
ENSG00000234479 | Chromatin interaction |
ENSG00000184708 | Chromatin interaction |
ENSG00000232707 | Chromatin interaction |
ENSG00000230866 | Chromatin interaction |
ENSG00000240647 | Chromatin interaction |
ENSG00000214093 | Chromatin interaction |
ENSG00000232218 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11089557 | 1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11089560 | 0.86[EUR][1000 genomes] |
rs11635 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12160141 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12160986 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12628702 | 0.95[EUR][1000 genomes] |
rs13110 | 0.85[AFR][1000 genomes] |
rs136471 | 0.89[AMR][1000 genomes] |
rs16987625 | 1.00[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs16990258 | 1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs16990262 | 1.00[CEU][hapmap];0.87[CHB][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs16990269 | 1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs16990428 | 0.82[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs16990430 | 0.83[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs1810450 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2014356 | 0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2072815 | 0.88[CHB][hapmap] |
rs2072816 | 0.83[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes] |
rs2076041 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2076045 | 0.83[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2142720 | 0.87[CHB][hapmap] |
rs2281034 | 1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2281035 | 0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2294311 | 0.87[ASN][1000 genomes] |
rs2294313 | 0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes] |
rs2294314 | 0.85[ASN][1000 genomes] |
rs2413110 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2413111 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2413113 | 0.87[CHB][hapmap] |
rs28404482 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs2899184 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2899185 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap] |
rs35003092 | 0.82[AFR][1000 genomes] |
rs35207231 | 0.86[EUR][1000 genomes] |
rs4140572 | 1.00[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap] |
rs45593940 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4577392 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs56088001 | 0.85[AFR][1000 genomes] |
rs56164445 | 0.85[AFR][1000 genomes] |
rs56241612 | 0.82[AFR][1000 genomes] |
rs56257111 | 0.85[AFR][1000 genomes] |
rs56273567 | 0.85[AFR][1000 genomes] |
rs56300131 | 0.82[AFR][1000 genomes] |
rs56304230 | 0.82[AFR][1000 genomes] |
rs56835150 | 0.85[AFR][1000 genomes] |
rs56870764 | 0.85[AFR][1000 genomes] |
rs56946080 | 0.85[AFR][1000 genomes] |
rs57313377 | 0.85[AFR][1000 genomes] |
rs5749408 | 0.89[EUR][1000 genomes] |
rs5749409 | 1.00[CEU][hapmap];0.86[CHB][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5749410 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5749411 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5749413 | 1.00[CEU][hapmap];0.87[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5749416 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes] |
rs5749426 | 0.83[CHB][hapmap] |
rs5749427 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs5749428 | 0.92[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes] |
rs5749429 | 0.92[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs5749433 | 0.92[EUR][1000 genomes] |
rs5749436 | 0.90[JPT][hapmap] |
rs57526188 | 0.82[AFR][1000 genomes] |
rs5753988 | 0.80[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs5754000 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs5754001 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs5754003 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs5754005 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs5754006 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs5754007 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs5754008 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs5754009 | 1.00[CEU][hapmap];0.87[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs5754010 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs5754011 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs5754012 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs5754017 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754018 | 1.00[CEU][hapmap];0.87[CHB][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754019 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs5754021 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs5754023 | 0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754025 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754029 | 1.00[CEU][hapmap];0.87[CHB][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754031 | 0.84[EUR][1000 genomes] |
rs5754032 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754033 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754035 | 1.00[CEU][hapmap];0.87[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754039 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754042 | 0.88[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754045 | 1.00[CEU][hapmap];0.87[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754046 | 0.86[EUR][1000 genomes] |
rs5754047 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5754048 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs5754050 | 1.00[CEU][hapmap];0.86[CHB][hapmap];0.80[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs5754063 | 0.83[CHB][hapmap] |
rs5754065 | 0.92[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs5754066 | 0.84[CHB][hapmap] |
rs57606003 | 0.81[EUR][1000 genomes] |
rs58028985 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs58329990 | 0.85[AFR][1000 genomes] |
rs58500302 | 0.86[AMR][1000 genomes] |
rs58747874 | 0.82[AFR][1000 genomes] |
rs58917959 | 0.82[AFR][1000 genomes] |
rs59540071 | 0.85[AFR][1000 genomes] |
rs59570290 | 0.85[AFR][1000 genomes] |
rs59895149 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs5998434 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs5998453 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5998457 | 1.00[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5998459 | 1.00[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs5998471 | 0.87[CHB][hapmap] |
rs5998475 | 0.92[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes] |
rs60284718 | 0.85[AFR][1000 genomes] |
rs60614590 | 0.85[AFR][1000 genomes] |
rs61036457 | 0.85[AFR][1000 genomes] |
rs61060987 | 0.82[AFR][1000 genomes] |
rs713790 | 1.00[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs72137940 | 0.86[ASN][1000 genomes] |
rs72617300 | 0.81[AMR][1000 genomes] |
rs72617301 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs72617302 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs72620403 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs72620404 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs72620405 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs72620406 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs72620407 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs72620408 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7284713 | 0.85[AFR][1000 genomes] |
rs7284743 | 0.93[YRI][hapmap];0.85[AFR][1000 genomes] |
rs7285750 | 0.85[AFR][1000 genomes] |
rs7287452 | 0.83[CHB][hapmap] |
rs7288743 | 0.94[YRI][hapmap];0.85[AFR][1000 genomes] |
rs7289526 | 0.94[YRI][hapmap];0.82[AFR][1000 genomes] |
rs7289656 | 0.94[YRI][hapmap];0.82[AFR][1000 genomes] |
rs7290295 | 0.94[YRI][hapmap];0.82[AFR][1000 genomes] |
rs7291359 | 0.81[ASN][1000 genomes] |
rs7292163 | 0.86[EUR][1000 genomes] |
rs7293064 | 0.85[AFR][1000 genomes] |
rs737779 | 0.88[CHB][hapmap] |
rs73881659 | 0.86[AFR][1000 genomes] |
rs73881660 | 0.86[AFR][1000 genomes] |
rs73881661 | 0.86[AFR][1000 genomes] |
rs73881662 | 0.86[AFR][1000 genomes] |
rs73881663 | 0.85[AFR][1000 genomes] |
rs73881664 | 0.83[AFR][1000 genomes] |
rs73881665 | 0.82[AFR][1000 genomes] |
rs73881666 | 0.85[AFR][1000 genomes] |
rs73881668 | 0.85[AFR][1000 genomes] |
rs73881669 | 0.85[AFR][1000 genomes] |
rs73881670 | 0.85[AFR][1000 genomes] |
rs73881671 | 0.85[AFR][1000 genomes] |
rs73881673 | 0.85[AFR][1000 genomes] |
rs73881674 | 0.85[AFR][1000 genomes] |
rs73881675 | 0.85[AFR][1000 genomes] |
rs73881676 | 0.85[AFR][1000 genomes] |
rs73881677 | 0.85[AFR][1000 genomes] |
rs73881678 | 0.85[AFR][1000 genomes] |
rs73881679 | 0.82[AFR][1000 genomes] |
rs73881680 | 0.82[AFR][1000 genomes] |
rs73881682 | 0.82[AFR][1000 genomes] |
rs73881683 | 0.82[AFR][1000 genomes] |
rs73881684 | 0.82[AFR][1000 genomes] |
rs73881685 | 0.82[AFR][1000 genomes] |
rs73881686 | 0.82[AFR][1000 genomes] |
rs73881688 | 0.82[AFR][1000 genomes] |
rs73881689 | 0.82[AFR][1000 genomes] |
rs73881690 | 0.82[AFR][1000 genomes] |
rs73881691 | 0.82[AFR][1000 genomes] |
rs73881694 | 0.82[AFR][1000 genomes] |
rs73881695 | 0.82[AFR][1000 genomes] |
rs73881696 | 0.82[AFR][1000 genomes] |
rs73881697 | 0.82[AFR][1000 genomes] |
rs742096 | 0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs8139992 | 1.00[YRI][hapmap];0.86[AFR][1000 genomes] |
rs8141096 | 0.82[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2422247 | chr22:32486448-32788258 | Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
2 | nsv459874 | chr22:32574274-32866934 | Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
3 | nsv588895 | chr22:32574274-32866934 | Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
4 | nsv1064737 | chr22:32603912-32829725 | Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 38 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr22:32755800-32781600 | Weak transcription | Ovary | ovary |
2 | chr22:32762800-32788200 | Weak transcription | Psoas Muscle | Psoas |
3 | chr22:32772000-32781200 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
4 | chr22:32772200-32781400 | Weak transcription | Fetal Intestine Small | intestine |
5 | chr22:32772600-32781400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
6 | chr22:32772800-32780800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
7 | chr22:32772800-32781400 | Weak transcription | Brain Germinal Matrix | brain |
8 | chr22:32772800-32781600 | Weak transcription | Placenta Amnion | Placenta Amnion |
9 | chr22:32773200-32781400 | Weak transcription | Gastric | stomach |
10 | chr22:32773200-32781400 | Weak transcription | Lung | lung |
11 | chr22:32773600-32775000 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
12 | chr22:32773800-32781600 | Weak transcription | Esophagus | oesophagus |
13 | chr22:32774000-32782000 | Weak transcription | Primary B cells from cord blood | blood |
14 | chr22:32774400-32775200 | Enhancers | Brain Hippocampus Middle | brain |
15 | chr22:32774400-32775400 | Enhancers | Fetal Muscle Trunk | muscle |
16 | chr22:32774400-32775400 | Enhancers | Fetal Muscle Leg | muscle |
17 | chr22:32774400-32775400 | Enhancers | Spleen | Spleen |
18 | chr22:32774400-32781200 | Weak transcription | Primary T cells from cord blood | blood |
19 | chr22:32774400-32781400 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
20 | chr22:32774600-32775200 | Enhancers | HUES6 Cell Line | embryonic stem cell |
21 | chr22:32774600-32775200 | Enhancers | Brain Cingulate Gyrus | brain |
22 | chr22:32774600-32775400 | Enhancers | Brain Substantia Nigra | brain |
23 | chr22:32774600-32780800 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
24 | chr22:32774800-32775000 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin01 | Skin |
25 | chr22:32774800-32775200 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
26 | chr22:32774800-32775400 | Enhancers | Brain Angular Gyrus | brain |
27 | chr22:32774800-32775400 | Enhancers | Brain Inferior Temporal Lobe | brain |
28 | chr22:32774800-32775400 | Enhancers | K562 | blood |