Variant report
Variant | rs1638561 |
---|---|
Chromosome Location | chr11:67221710-67221711 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:61)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
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No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:67221691-67221741 | ovcar-3 | ovarian: | n/a |
2 | chr11:67221691-67221741 | AG09309 | skin: | n/a |
3 | chr11:67221691-67221741 | AoSMC | blood vessel: | n/a |
4 | chr11:67221691-67221741 | LNCaP | prostate: | n/a |
5 | chr11:67221691-67221741 | Hepatocyte | liver: | n/a |
6 | chr11:67221691-67221741 | PFSK-1 | brain: | n/a |
7 | chr11:67221691-67221741 | ProgFib | skin: | n/a |
8 | chr11:67221691-67221741 | HAEpiC | amniotic membrane: | n/a |
9 | chr11:67221691-67221741 | HCPEpiC | choroid plexus: | n/a |
10 | chr11:67221691-67221741 | HRPEpiC | eye: | n/a |
11 | chr11:67221691-67221741 | MCF-7 | breast: | n/a |
12 | chr11:67221691-67221741 | IMR90 | lung: | fetal |
13 | chr11:67221691-67221741 | SK-N-SH | brain: | n/a |
14 | chr11:67221691-67221741 | PrEC | prostate: | n/a |
15 | chr11:67221691-67221741 | NT2-D1 | testis: | n/a |
16 | chr11:67221691-67221741 | Caco-2 | colon: | n/a |
17 | chr11:67221691-67221741 | K562 | blood: | n/a |
18 | chr11:67221691-67221741 | CMK | blood: | n/a |
19 | chr11:67221691-67221741 | HCM | heart: | n/a |
20 | chr11:67221691-67221741 | HepG2 | liver: | n/a |
21 | chr11:67221691-67221741 | HEEpiC | esophagus: | n/a |
22 | chr11:67221691-67221741 | SK-N-SH_RA | brain: | n/a |
23 | chr11:67221691-67221741 | NHBE | bronchial: | n/a |
24 | chr11:67221691-67221741 | T-47D | breast: | n/a |
25 | chr11:67221691-67221741 | GM12878 | blood: | n/a |
26 | chr11:67221691-67221741 | Hela-S3 | cervix: | n/a |
27 | chr11:67221691-67221741 | BE2_C | brain: | n/a |
28 | chr11:67221691-67221741 | AG04450 | lung: | fetal |
29 | chr11:67221691-67221741 | GM12892 | blood: | n/a |
30 | chr11:67221691-67221741 | HEK293 | kidney: | embryo |
31 | chr11:67221691-67221741 | SKMC | muscle: | n/a |
32 | chr11:67221691-67221741 | RPTEC | kidney: | n/a |
33 | chr11:67221691-67221741 | AG10803 | skin: | n/a |
34 | chr11:67221691-67221741 | NB4 | blood: | n/a |
35 | chr11:67221691-67221741 | HCT-116 | colon: | n/a |
36 | chr11:67221691-67221741 | HRE | kidney: | n/a |
37 | chr11:67221691-67221741 | GM06990 | blood: | n/a |
38 | chr11:67221691-67221741 | MCF10A-Er-Src | breast: | n/a |
39 | chr11:67221691-67221741 | SK-N-MC | brain: | n/a |
40 | chr11:67221691-67221741 | HRCEpiC | kidney: | n/a |
41 | chr11:67221691-67221741 | GM19239 | blood: | n/a |
42 | chr11:67221691-67221741 | HMEC | breast: | n/a |
43 | chr11:67221691-67221741 | HPAEpiC | pulmonary alveolar: | n/a |
44 | chr11:67221691-67221741 | U87 | brain: | n/a |
45 | chr11:67221691-67221741 | GM12891 | blood: | n/a |
46 | chr11:67221691-67221741 | HL-60 | blood: | n/a |
47 | chr11:67221691-67221741 | AG09319 | gingival: | n/a |
48 | chr11:67221691-67221741 | HUVEC | blood vessel: | n/a |
49 | chr11:67221691-67221741 | HCF | heart: | n/a |
50 | chr11:67221691-67221741 | AG04449 | skin: | fetal |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:67221211..67222819-chr11:67229683..67232141,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
GPR152 | TF binding region |
CABP4 | TF binding region |
CABP4 | CpG island |
GPR152 | CpG island |
ENSG00000270169 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10896175 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11227796 | 1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11227804 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11821703 | 1.00[EUR][1000 genomes] |
rs12293606 | 0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1382089 | 1.00[EUR][1000 genomes] |
rs1618605 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1620333 | 1.00[EUR][1000 genomes] |
rs1624189 | 1.00[EUR][1000 genomes] |
rs1625032 | 1.00[EUR][1000 genomes] |
rs1625892 | 1.00[EUR][1000 genomes] |
rs1630068 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1632616 | 1.00[EUR][1000 genomes] |
rs1638558 | 0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1638559 | 0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1638560 | 1.00[EUR][1000 genomes] |
rs1638562 | 0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1638563 | 1.00[EUR][1000 genomes] |
rs1638570 | 1.00[EUR][1000 genomes] |
rs1638572 | 1.00[EUR][1000 genomes] |
rs1638575 | 1.00[EUR][1000 genomes] |
rs1638576 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1638577 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1638581 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1638584 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1638587 | 1.00[EUR][1000 genomes] |
rs1790729 | 1.00[EUR][1000 genomes] |
rs1790730 | 1.00[EUR][1000 genomes] |
rs1790734 | 1.00[EUR][1000 genomes] |
rs1790736 | 0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1790741 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1790743 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1790744 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1790745 | 1.00[EUR][1000 genomes] |
rs1790749 | 1.00[EUR][1000 genomes] |
rs1790750 | 1.00[EUR][1000 genomes] |
rs1790754 | 1.00[EUR][1000 genomes] |
rs1790756 | 0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1790763 | 0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1790764 | 0.89[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1790765 | 1.00[EUR][1000 genomes] |
rs1824712 | 1.00[EUR][1000 genomes] |
rs2054409 | 1.00[EUR][1000 genomes] |
rs2447590 | 1.00[EUR][1000 genomes] |
rs2447591 | 1.00[EUR][1000 genomes] |
rs2447597 | 1.00[EUR][1000 genomes] |
rs2511058 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2511059 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2514013 | 1.00[EUR][1000 genomes] |
rs2514014 | 1.00[EUR][1000 genomes] |
rs2514015 | 1.00[EUR][1000 genomes] |
rs2514024 | 1.00[EUR][1000 genomes] |
rs2514045 | 1.00[EUR][1000 genomes] |
rs2514064 | 1.00[EUR][1000 genomes] |
rs2514259 | 0.93[AFR][1000 genomes] |
rs2514262 | 1.00[EUR][1000 genomes] |
rs2514263 | 1.00[EUR][1000 genomes] |
rs2885171 | 1.00[EUR][1000 genomes] |
rs3016861 | 1.00[EUR][1000 genomes] |
rs35363135 | 0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs36052107 | 1.00[EUR][1000 genomes] |
rs56050553 | 1.00[EUR][1000 genomes] |
rs56102510 | 1.00[EUR][1000 genomes] |
rs56405884 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57047868 | 1.00[EUR][1000 genomes] |
rs57748654 | 1.00[EUR][1000 genomes] |
rs57749415 | 1.00[EUR][1000 genomes] |
rs57757103 | 1.00[EUR][1000 genomes] |
rs57955602 | 1.00[EUR][1000 genomes] |
rs58999825 | 1.00[EUR][1000 genomes] |
rs59500232 | 1.00[EUR][1000 genomes] |
rs596431 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs596944 | 1.00[EUR][1000 genomes] |
rs601363 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60136955 | 1.00[EUR][1000 genomes] |
rs602220 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs60251934 | 1.00[EUR][1000 genomes] |
rs602720 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs604540 | 0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60521870 | 1.00[EUR][1000 genomes] |
rs60751057 | 1.00[EUR][1000 genomes] |
rs611697 | 1.00[EUR][1000 genomes] |
rs61282424 | 1.00[EUR][1000 genomes] |
rs61429992 | 1.00[EUR][1000 genomes] |
rs61610719 | 1.00[EUR][1000 genomes] |
rs618633 | 1.00[EUR][1000 genomes] |
rs641081 | 1.00[EUR][1000 genomes] |
rs6591267 | 1.00[EUR][1000 genomes] |
rs7104627 | 1.00[EUR][1000 genomes] |
rs7121803 | 1.00[EUR][1000 genomes] |
rs7124630 | 1.00[EUR][1000 genomes] |
rs73490545 | 1.00[EUR][1000 genomes] |
rs73490554 | 1.00[EUR][1000 genomes] |
rs73501797 | 1.00[EUR][1000 genomes] |
rs73501800 | 1.00[EUR][1000 genomes] |
rs73506004 | 0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73506015 | 1.00[EUR][1000 genomes] |
rs73506054 | 1.00[EUR][1000 genomes] |
rs73506056 | 1.00[EUR][1000 genomes] |
rs73506069 | 1.00[EUR][1000 genomes] |
rs73506074 | 1.00[EUR][1000 genomes] |
rs743679 | 1.00[EUR][1000 genomes] |
rs7934566 | 1.00[EUR][1000 genomes] |
rs7941752 | 0.95[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs7947114 | 1.00[EUR][1000 genomes] |
rs8191436 | 1.00[EUR][1000 genomes] |
rs8191446 | 1.00[EUR][1000 genomes] |
rs8191449 | 1.00[EUR][1000 genomes] |
rs949250 | 0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs949251 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs949252 | 1.00[EUR][1000 genomes] |
rs949253 | 1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs949254 | 0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs949255 | 0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531397 | chr11:66653381-67465721 | Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 271 gene(s) | inside rSNPs | diseases |
2 | nsv897797 | chr11:67023040-67293234 | Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 206 gene(s) | inside rSNPs | diseases |
3 | nsv1043037 | chr11:67027193-67357425 | Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 213 gene(s) | inside rSNPs | diseases |
4 | nsv897801 | chr11:67033076-67432479 | Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 236 gene(s) | inside rSNPs | diseases |
5 | nsv1048230 | chr11:67058231-67252397 | Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 146 gene(s) | inside rSNPs | diseases |
6 | nsv897804 | chr11:67090571-67224278 | Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 103 gene(s) | inside rSNPs | diseases |
7 | nsv1039205 | chr11:67135246-67252397 | Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 122 gene(s) | inside rSNPs | diseases |
8 | esv1818769 | chr11:67138811-67300457 | Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 167 gene(s) | inside rSNPs | diseases |
9 | esv1798859 | chr11:67139954-67272983 | Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 154 gene(s) | inside rSNPs | diseases |
10 | nsv897805 | chr11:67155210-67283891 | ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 148 gene(s) | inside rSNPs | diseases |
11 | nsv897806 | chr11:67155210-67294308 | Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 148 gene(s) | inside rSNPs | diseases |
12 | nsv897807 | chr11:67155210-67414492 | Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 176 gene(s) | inside rSNPs | diseases |
13 | nsv897808 | chr11:67155210-67419855 | Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 176 gene(s) | inside rSNPs | diseases |
14 | nsv897809 | chr11:67156875-67276235 | Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 148 gene(s) | inside rSNPs | diseases |
15 | nsv555254 | chr11:67164495-67288594 | Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 146 gene(s) | inside rSNPs | diseases |
16 | nsv534229 | chr11:67164667-67411909 | Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 175 gene(s) | inside rSNPs | diseases |
17 | nsv897813 | chr11:67175692-67283891 | Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 132 gene(s) | inside rSNPs | diseases |
18 | nsv521723 | chr11:67175692-67311258 | Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 132 gene(s) | inside rSNPs | diseases |
19 | nsv524096 | chr11:67186000-67224988 | Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 52 gene(s) | inside rSNPs | diseases |
20 | nsv468604 | chr11:67186000-67283891 | Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 132 gene(s) | inside rSNPs | diseases |
21 | nsv555256 | chr11:67186000-67283891 | Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 132 gene(s) | inside rSNPs | diseases |
22 | nsv527056 | chr11:67207426-67294308 | Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 115 gene(s) | inside rSNPs | diseases |
23 | esv1813337 | chr11:67217703-67235815 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 37 gene(s) | inside rSNPs | diseases |
24 | nsv983155 | chr11:67220251-67251432 | Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 56 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:67211800-67231200 | Weak transcription | Right Atrium | heart |
2 | chr11:67211800-67232000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr11:67212400-67226800 | Enhancers | Primary B cells from peripheral blood | blood |
4 | chr11:67215400-67227200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr11:67215800-67230600 | Weak transcription | Fetal Intestine Small | intestine |
6 | chr11:67217200-67231400 | Weak transcription | Thymus | Thymus |
7 | chr11:67218600-67221800 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
8 | chr11:67218600-67227000 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
9 | chr11:67219000-67231400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
10 | chr11:67219200-67225800 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
11 | chr11:67219800-67226800 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
12 | chr11:67220400-67224400 | Weak transcription | Pancreas | Pancrea |
13 | chr11:67220400-67231400 | Weak transcription | Gastric | stomach |
14 | chr11:67220400-67231400 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
15 | chr11:67220400-67231400 | Weak transcription | Right Ventricle | heart |
16 | chr11:67221200-67222000 | Enhancers | Spleen | Spleen |
17 | chr11:67221400-67222200 | Enhancers | Primary B cells from cord blood | blood |
18 | chr11:67221400-67222600 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
19 | chr11:67221400-67222800 | Bivalent/Poised TSS | Foreskin Fibroblast Primary Cells skin02 | Skin |
20 | chr11:67221400-67230800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
21 | chr11:67221600-67222200 | Genic enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
22 | chr11:67221600-67222400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
23 | chr11:67221600-67222400 | Bivalent Enhancer | Fetal Muscle Trunk | muscle |