Variant report
Variant | rs10904566 |
---|---|
Chromosome Location | chr10:821662-821663 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:817104..818718-chr10:820025..821722,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1013504 | 1.00[ASN][1000 genomes] |
rs10904544 | 1.00[ASN][1000 genomes] |
rs10904545 | 1.00[ASN][1000 genomes] |
rs10904546 | 1.00[ASN][1000 genomes] |
rs10904547 | 1.00[ASN][1000 genomes] |
rs10904550 | 1.00[ASN][1000 genomes] |
rs10904552 | 1.00[ASN][1000 genomes] |
rs10904555 | 1.00[ASN][1000 genomes] |
rs10904556 | 1.00[ASN][1000 genomes] |
rs10904557 | 1.00[ASN][1000 genomes] |
rs10904558 | 1.00[ASN][1000 genomes] |
rs10904564 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10904565 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253329 | 1.00[ASN][1000 genomes] |
rs11253331 | 1.00[ASN][1000 genomes] |
rs11253332 | 1.00[ASN][1000 genomes] |
rs11253339 | 1.00[ASN][1000 genomes] |
rs11253340 | 1.00[ASN][1000 genomes] |
rs11253341 | 1.00[ASN][1000 genomes] |
rs11253342 | 1.00[ASN][1000 genomes] |
rs11253343 | 1.00[ASN][1000 genomes] |
rs11253344 | 1.00[ASN][1000 genomes] |
rs11253346 | 1.00[ASN][1000 genomes] |
rs11253347 | 1.00[ASN][1000 genomes] |
rs11253349 | 1.00[ASN][1000 genomes] |
rs11253350 | 1.00[ASN][1000 genomes] |
rs11253352 | 1.00[ASN][1000 genomes] |
rs11253353 | 1.00[ASN][1000 genomes] |
rs11253355 | 1.00[ASN][1000 genomes] |
rs11253361 | 1.00[ASN][1000 genomes] |
rs11253362 | 1.00[ASN][1000 genomes] |
rs11253363 | 1.00[ASN][1000 genomes] |
rs11253366 | 1.00[ASN][1000 genomes] |
rs11253367 | 1.00[ASN][1000 genomes] |
rs11253369 | 1.00[ASN][1000 genomes] |
rs11253370 | 1.00[ASN][1000 genomes] |
rs11253372 | 1.00[ASN][1000 genomes] |
rs11253373 | 1.00[ASN][1000 genomes] |
rs11253374 | 1.00[ASN][1000 genomes] |
rs11253379 | 1.00[ASN][1000 genomes] |
rs11253388 | 1.00[ASN][1000 genomes] |
rs11253390 | 1.00[ASN][1000 genomes] |
rs11253391 | 1.00[ASN][1000 genomes] |
rs11253392 | 1.00[ASN][1000 genomes] |
rs11253393 | 1.00[ASN][1000 genomes] |
rs11253394 | 1.00[ASN][1000 genomes] |
rs11253395 | 1.00[ASN][1000 genomes] |
rs11253396 | 1.00[ASN][1000 genomes] |
rs11253397 | 1.00[ASN][1000 genomes] |
rs11253398 | 1.00[ASN][1000 genomes] |
rs11253399 | 1.00[ASN][1000 genomes] |
rs11253401 | 1.00[ASN][1000 genomes] |
rs11253403 | 1.00[ASN][1000 genomes] |
rs11253414 | 1.00[ASN][1000 genomes] |
rs11253419 | 1.00[ASN][1000 genomes] |
rs11253420 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253421 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253424 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253425 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253430 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253434 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253435 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253440 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253441 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11253504 | 1.00[ASN][1000 genomes] |
rs11253518 | 1.00[ASN][1000 genomes] |
rs11253530 | 1.00[ASN][1000 genomes] |
rs11253537 | 1.00[ASN][1000 genomes] |
rs11253538 | 1.00[ASN][1000 genomes] |
rs11253539 | 1.00[ASN][1000 genomes] |
rs11253540 | 1.00[ASN][1000 genomes] |
rs11593836 | 1.00[ASN][1000 genomes] |
rs11595057 | 0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11595385 | 1.00[ASN][1000 genomes] |
rs11595507 | 1.00[ASN][1000 genomes] |
rs11595510 | 1.00[ASN][1000 genomes] |
rs11596346 | 1.00[ASN][1000 genomes] |
rs11599043 | 1.00[ASN][1000 genomes] |
rs11599917 | 1.00[ASN][1000 genomes] |
rs12219807 | 1.00[ASN][1000 genomes] |
rs12354872 | 1.00[ASN][1000 genomes] |
rs12354914 | 1.00[ASN][1000 genomes] |
rs12356155 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12356709 | 1.00[ASN][1000 genomes] |
rs12356744 | 1.00[ASN][1000 genomes] |
rs12357016 | 1.00[ASN][1000 genomes] |
rs12357633 | 1.00[ASN][1000 genomes] |
rs12357963 | 1.00[ASN][1000 genomes] |
rs12357995 | 1.00[ASN][1000 genomes] |
rs12358255 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12358513 | 1.00[ASN][1000 genomes] |
rs12358875 | 1.00[ASN][1000 genomes] |
rs12358966 | 1.00[ASN][1000 genomes] |
rs12359731 | 1.00[ASN][1000 genomes] |
rs12761180 | 1.00[ASN][1000 genomes] |
rs12762228 | 1.00[ASN][1000 genomes] |
rs12763443 | 1.00[ASN][1000 genomes] |
rs12765073 | 1.00[ASN][1000 genomes] |
rs12765343 | 1.00[ASN][1000 genomes] |
rs12767043 | 1.00[ASN][1000 genomes] |
rs12767062 | 1.00[ASN][1000 genomes] |
rs12767172 | 1.00[ASN][1000 genomes] |
rs12767287 | 1.00[ASN][1000 genomes] |
rs12768348 | 1.00[ASN][1000 genomes] |
rs12768599 | 1.00[ASN][1000 genomes] |
rs12769002 | 1.00[ASN][1000 genomes] |
rs12771179 | 1.00[ASN][1000 genomes] |
rs12771845 | 1.00[ASN][1000 genomes] |
rs12772911 | 1.00[ASN][1000 genomes] |
rs12774985 | 1.00[ASN][1000 genomes] |
rs12775643 | 1.00[ASN][1000 genomes] |
rs12776447 | 1.00[ASN][1000 genomes] |
rs12777021 | 1.00[ASN][1000 genomes] |
rs12777155 | 1.00[ASN][1000 genomes] |
rs12778271 | 1.00[ASN][1000 genomes] |
rs12779159 | 1.00[ASN][1000 genomes] |
rs12781100 | 1.00[ASN][1000 genomes] |
rs12781329 | 1.00[ASN][1000 genomes] |
rs12782447 | 1.00[ASN][1000 genomes] |
rs12782936 | 1.00[ASN][1000 genomes] |
rs1536336 | 1.00[ASN][1000 genomes] |
rs17293517 | 1.00[ASN][1000 genomes] |
rs1769242 | 1.00[ASN][1000 genomes] |
rs2004478 | 1.00[ASN][1000 genomes] |
rs2004479 | 1.00[ASN][1000 genomes] |
rs2253475 | 1.00[ASN][1000 genomes] |
rs2265529 | 1.00[ASN][1000 genomes] |
rs2265530 | 1.00[ASN][1000 genomes] |
rs2486578 | 1.00[ASN][1000 genomes] |
rs2486579 | 1.00[ASN][1000 genomes] |
rs2766013 | 1.00[ASN][1000 genomes] |
rs2790388 | 1.00[ASN][1000 genomes] |
rs34251037 | 1.00[ASN][1000 genomes] |
rs34257857 | 1.00[ASN][1000 genomes] |
rs34270668 | 1.00[ASN][1000 genomes] |
rs34318754 | 1.00[ASN][1000 genomes] |
rs34383514 | 1.00[ASN][1000 genomes] |
rs34487581 | 1.00[ASN][1000 genomes] |
rs34527494 | 1.00[ASN][1000 genomes] |
rs34652870 | 1.00[ASN][1000 genomes] |
rs34778553 | 1.00[ASN][1000 genomes] |
rs34848170 | 1.00[ASN][1000 genomes] |
rs34885925 | 1.00[ASN][1000 genomes] |
rs34912955 | 1.00[ASN][1000 genomes] |
rs34982663 | 1.00[ASN][1000 genomes] |
rs35028518 | 1.00[ASN][1000 genomes] |
rs35117541 | 1.00[ASN][1000 genomes] |
rs35306767 | 1.00[ASN][1000 genomes] |
rs35342920 | 1.00[ASN][1000 genomes] |
rs35363972 | 1.00[ASN][1000 genomes] |
rs35443149 | 1.00[ASN][1000 genomes] |
rs35666723 | 1.00[ASN][1000 genomes] |
rs35667562 | 1.00[ASN][1000 genomes] |
rs35670857 | 1.00[ASN][1000 genomes] |
rs35709890 | 1.00[ASN][1000 genomes] |
rs35743076 | 1.00[ASN][1000 genomes] |
rs35865720 | 1.00[ASN][1000 genomes] |
rs35872126 | 1.00[ASN][1000 genomes] |
rs35927768 | 1.00[ASN][1000 genomes] |
rs35957139 | 1.00[ASN][1000 genomes] |
rs35967867 | 1.00[ASN][1000 genomes] |
rs36064821 | 1.00[ASN][1000 genomes] |
rs4133015 | 1.00[ASN][1000 genomes] |
rs4504989 | 1.00[ASN][1000 genomes] |
rs4579862 | 1.00[ASN][1000 genomes] |
rs4636581 | 1.00[ASN][1000 genomes] |
rs55697724 | 1.00[ASN][1000 genomes] |
rs55708963 | 1.00[ASN][1000 genomes] |
rs55727503 | 1.00[ASN][1000 genomes] |
rs55742421 | 1.00[ASN][1000 genomes] |
rs56222464 | 1.00[ASN][1000 genomes] |
rs57454320 | 0.80[EUR][1000 genomes] |
rs61830900 | 1.00[ASN][1000 genomes] |
rs61830926 | 1.00[ASN][1000 genomes] |
rs61830931 | 1.00[ASN][1000 genomes] |
rs61830933 | 1.00[ASN][1000 genomes] |
rs61831436 | 1.00[ASN][1000 genomes] |
rs61833260 | 1.00[ASN][1000 genomes] |
rs61833265 | 1.00[ASN][1000 genomes] |
rs67467327 | 1.00[ASN][1000 genomes] |
rs7069720 | 1.00[ASN][1000 genomes] |
rs7071974 | 1.00[ASN][1000 genomes] |
rs7071982 | 1.00[ASN][1000 genomes] |
rs7072970 | 1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7079164 | 1.00[ASN][1000 genomes] |
rs7079299 | 1.00[ASN][1000 genomes] |
rs7079450 | 1.00[ASN][1000 genomes] |
rs7083589 | 1.00[ASN][1000 genomes] |
rs7085476 | 1.00[ASN][1000 genomes] |
rs7088956 | 1.00[ASN][1000 genomes] |
rs7092353 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7092652 | 1.00[ASN][1000 genomes] |
rs7092976 | 1.00[ASN][1000 genomes] |
rs7092986 | 1.00[ASN][1000 genomes] |
rs71489279 | 1.00[ASN][1000 genomes] |
rs71489301 | 1.00[ASN][1000 genomes] |
rs71491303 | 1.00[ASN][1000 genomes] |
rs71491304 | 1.00[ASN][1000 genomes] |
rs71494928 | 1.00[ASN][1000 genomes] |
rs72778228 | 1.00[ASN][1000 genomes] |
rs7475589 | 1.00[ASN][1000 genomes] |
rs749842 | 1.00[ASN][1000 genomes] |
rs7904978 | 1.00[ASN][1000 genomes] |
rs7914758 | 1.00[ASN][1000 genomes] |
rs7923867 | 1.00[ASN][1000 genomes] |
rs877280 | 1.00[ASN][1000 genomes] |
rs877281 | 1.00[ASN][1000 genomes] |
rs877282 | 1.00[ASN][1000 genomes] |
rs957642 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916591 | chr10:224406-1088734 | Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
2 | nsv540386 | chr10:224406-1197416 | Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 51 gene(s) | inside rSNPs | diseases |
3 | nsv1035580 | chr10:248463-832240 | Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
4 | nsv540392 | chr10:248463-832240 | Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
5 | nsv1050252 | chr10:375035-839594 | Genic enhancers Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
6 | nsv540397 | chr10:375035-839594 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
7 | nsv1048859 | chr10:442805-887622 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
8 | nsv1039958 | chr10:450753-889167 | Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
9 | nsv540400 | chr10:450753-889167 | Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
10 | nsv549753 | chr10:458477-894838 | Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
11 | nsv1039849 | chr10:535309-829217 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 14 gene(s) | inside rSNPs | diseases |
12 | nsv1044857 | chr10:577396-856059 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 16 gene(s) | inside rSNPs | diseases |
13 | nsv540402 | chr10:577396-856059 | Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 16 gene(s) | inside rSNPs | diseases |
14 | nsv528733 | chr10:577444-838378 | Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 15 gene(s) | inside rSNPs | diseases |
15 | nsv1036675 | chr10:600206-839594 | Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 15 gene(s) | inside rSNPs | diseases |
16 | nsv1054659 | chr10:611444-1133578 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 43 gene(s) | inside rSNPs | diseases |
17 | nsv1042115 | chr10:641343-825145 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 13 gene(s) | inside rSNPs | diseases |
18 | nsv540405 | chr10:641343-825145 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 13 gene(s) | inside rSNPs | diseases |
19 | nsv948602 | chr10:708293-944641 | Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
20 | nsv949063 | chr10:708293-974870 | Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
21 | nsv466697 | chr10:734229-1129527 | ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
22 | nsv549765 | chr10:734229-1129527 | Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
23 | nsv1036316 | chr10:748848-849979 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
24 | nsv894717 | chr10:763714-834736 | Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
25 | nsv894718 | chr10:763714-861390 | Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
26 | nsv1045119 | chr10:766867-855251 | Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
27 | nsv1043812 | chr10:776547-981126 | Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
28 | nsv540406 | chr10:776547-981126 | Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
29 | nsv530116 | chr10:776548-1401075 | Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 41 gene(s) | inside rSNPs | diseases |
30 | nsv948978 | chr10:813426-1019115 | Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
31 | esv32889 | chr10:818451-834608 | Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:817400-821800 | Weak transcription | Spleen | Spleen |
2 | chr10:818400-830600 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr10:820800-822400 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
4 | chr10:821000-821800 | Genic enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr10:821000-821800 | Enhancers | A549 | lung |
6 | chr10:821000-822000 | Enhancers | Esophagus | oesophagus |
7 | chr10:821200-821800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
8 | chr10:821200-821800 | Active TSS | Rectal Smooth Muscle | rectum |
9 | chr10:821200-821800 | Flanking Active TSS | Skeletal Muscle Male | skeletal muscle |
10 | chr10:821200-821800 | Enhancers | HSMMtube | muscle |
11 | chr10:821200-822000 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
12 | chr10:821200-822000 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
13 | chr10:821200-822000 | Flanking Active TSS | Muscle Satellite Cultured Cells | -- |
14 | chr10:821200-822000 | Enhancers | Skeletal Muscle Female | skeletal muscle |
15 | chr10:821200-822000 | Flanking Active TSS | Stomach Smooth Muscle | stomach |
16 | chr10:821200-822000 | Enhancers | NH-A | brain |
17 | chr10:821400-821800 | Enhancers | Hela-S3 | cervix |
18 | chr10:821400-821800 | Enhancers | HMEC | breast |
19 | chr10:821400-822000 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin01 | Skin |
20 | chr10:821400-822000 | Enhancers | HUVEC | blood vessel |
21 | chr10:821400-824000 | Weak transcription | Brain Dorsolateral Prefrontal Cortex | brain |
22 | chr10:821600-821800 | Flanking Bivalent TSS/Enh | Foreskin Keratinocyte Primary Cells skin02 | Skin |
23 | chr10:821600-821800 | Flanking Bivalent TSS/Enh | Foreskin Keratinocyte Primary Cells skin03 | Skin |
24 | chr10:821600-821800 | ZNF genes & repeats | Foreskin Melanocyte Primary Cells skin01 | Skin |
25 | chr10:821600-821800 | Enhancers | Fetal Brain Male | brain |
26 | chr10:821600-822000 | Bivalent Enhancer | Breast Myoepithelial Primary Cells | Breast |
27 | chr10:821600-822000 | Flanking Bivalent TSS/Enh | Foreskin Fibroblast Primary Cells skin02 | Skin |
28 | chr10:821600-822000 | Enhancers | Osteobl | bone |