Variant report
Variant | rs10896351 |
---|---|
Chromosome Location | chr11:68386896-68386897 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000260808 | TF binding region |
ENSG00000266854 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10047412 | 0.81[ASN][1000 genomes] |
rs10501398 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10750827 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10791981 | 0.86[ASN][1000 genomes] |
rs10791982 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10896326 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10896327 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10896328 | 0.83[ASN][1000 genomes] |
rs10896329 | 0.83[ASN][1000 genomes] |
rs10896330 | 0.83[ASN][1000 genomes] |
rs10896331 | 0.88[ASN][1000 genomes] |
rs10896334 | 0.88[ASN][1000 genomes] |
rs10896337 | 0.88[ASN][1000 genomes] |
rs10896338 | 0.86[ASN][1000 genomes] |
rs10896339 | 0.93[ASN][1000 genomes] |
rs10896340 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10896341 | 0.87[ASN][1000 genomes] |
rs10896342 | 0.87[ASN][1000 genomes] |
rs10896343 | 0.87[ASN][1000 genomes] |
rs10896346 | 0.89[ASN][1000 genomes] |
rs10896347 | 0.89[ASN][1000 genomes] |
rs10896348 | 0.91[ASN][1000 genomes] |
rs10896350 | 1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11228251 | 0.86[ASN][1000 genomes] |
rs11228256 | 0.83[ASN][1000 genomes] |
rs11228258 | 0.84[ASN][1000 genomes] |
rs11228262 | 0.86[ASN][1000 genomes] |
rs11228268 | 0.86[ASN][1000 genomes] |
rs11228269 | 0.86[ASN][1000 genomes] |
rs11228275 | 0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11228276 | 0.85[ASN][1000 genomes] |
rs11228277 | 0.89[ASN][1000 genomes] |
rs11228278 | 0.88[ASN][1000 genomes] |
rs11228279 | 0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11228284 | 0.87[ASN][1000 genomes] |
rs11228287 | 0.91[ASN][1000 genomes] |
rs11228288 | 0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11228291 | 0.88[ASN][1000 genomes] |
rs11228292 | 0.89[ASN][1000 genomes] |
rs11228293 | 0.90[ASN][1000 genomes] |
rs11822059 | 0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1193699 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1201557 | 0.88[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs12226585 | 0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12271290 | 0.89[ASN][1000 genomes] |
rs12272917 | 0.84[ASN][1000 genomes] |
rs12274114 | 0.84[ASN][1000 genomes] |
rs12277225 | 0.89[ASN][1000 genomes] |
rs12281742 | 0.89[ASN][1000 genomes] |
rs12283755 | 0.89[ASN][1000 genomes] |
rs12284933 | 0.89[ASN][1000 genomes] |
rs12285993 | 0.87[ASN][1000 genomes] |
rs12294029 | 0.86[ASN][1000 genomes] |
rs12360903 | 0.83[ASN][1000 genomes] |
rs12363722 | 0.83[ASN][1000 genomes] |
rs12364620 | 0.83[ASN][1000 genomes] |
rs12365160 | 0.83[ASN][1000 genomes] |
rs12941 | 0.89[ASN][1000 genomes] |
rs1685688 | 0.82[EUR][1000 genomes] |
rs17603185 | 0.88[ASN][1000 genomes] |
rs2155730 | 0.86[ASN][1000 genomes] |
rs2156463 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2236708 | 0.88[ASN][1000 genomes] |
rs2282563 | 0.87[ASN][1000 genomes] |
rs2472420 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2510384 | 0.89[ASN][1000 genomes] |
rs2510392 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2513277 | 0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2513285 | 0.92[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2840367 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3018713 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3740628 | 0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3740629 | 0.87[ASN][1000 genomes] |
rs3740631 | 0.87[ASN][1000 genomes] |
rs3758643 | 0.92[ASN][1000 genomes] |
rs3824850 | 0.87[ASN][1000 genomes] |
rs4084149 | 0.86[ASN][1000 genomes] |
rs4316515 | 0.87[ASN][1000 genomes] |
rs4340059 | 0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs488381 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs498782 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4988291 | 0.89[ASN][1000 genomes] |
rs510772 | 0.83[EUR][1000 genomes] |
rs55767696 | 0.91[ASN][1000 genomes] |
rs55816191 | 0.86[ASN][1000 genomes] |
rs55883802 | 0.86[ASN][1000 genomes] |
rs55953412 | 0.87[ASN][1000 genomes] |
rs59056571 | 0.86[ASN][1000 genomes] |
rs596494 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs60212556 | 0.87[ASN][1000 genomes] |
rs624003 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs643609 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6591340 | 0.87[ASN][1000 genomes] |
rs6591341 | 0.89[ASN][1000 genomes] |
rs6591344 | 0.89[ASN][1000 genomes] |
rs6591346 | 0.92[ASN][1000 genomes] |
rs66752716 | 0.86[ASN][1000 genomes] |
rs67005337 | 0.87[ASN][1000 genomes] |
rs67101048 | 0.86[ASN][1000 genomes] |
rs67605986 | 0.87[ASN][1000 genomes] |
rs67947146 | 0.87[ASN][1000 genomes] |
rs7101691 | 0.84[ASN][1000 genomes] |
rs7102273 | 0.93[ASN][1000 genomes] |
rs7102898 | 0.87[ASN][1000 genomes] |
rs7104345 | 0.87[ASN][1000 genomes] |
rs7104877 | 0.90[ASN][1000 genomes] |
rs7106010 | 0.91[ASN][1000 genomes] |
rs7106259 | 0.86[ASN][1000 genomes] |
rs7106339 | 0.83[ASN][1000 genomes] |
rs7107622 | 0.91[ASN][1000 genomes] |
rs7108376 | 0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7109294 | 0.87[ASN][1000 genomes] |
rs7113287 | 0.91[ASN][1000 genomes] |
rs7115374 | 0.87[ASN][1000 genomes] |
rs7116899 | 0.93[ASN][1000 genomes] |
rs7116994 | 0.84[ASN][1000 genomes] |
rs7119422 | 0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7120557 | 0.86[ASN][1000 genomes] |
rs7120635 | 0.86[ASN][1000 genomes] |
rs7120876 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7123564 | 0.89[ASN][1000 genomes] |
rs7124078 | 0.89[ASN][1000 genomes] |
rs7126340 | 0.86[ASN][1000 genomes] |
rs7126451 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7127948 | 0.89[ASN][1000 genomes] |
rs7129248 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs73506204 | 0.89[ASN][1000 genomes] |
rs73516838 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs73516862 | 0.86[ASN][1000 genomes] |
rs73518807 | 0.85[ASN][1000 genomes] |
rs7925275 | 0.86[ASN][1000 genomes] |
rs7927592 | 0.91[ASN][1000 genomes] |
rs7936582 | 0.89[ASN][1000 genomes] |
rs7944870 | 0.85[ASN][1000 genomes] |
rs7950900 | 0.89[ASN][1000 genomes] |
rs871212 | 0.91[ASN][1000 genomes] |
rs948315 | 0.89[ASN][1000 genomes] |
rs948316 | 0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3431317 | chr11:68282676-68411867 | Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | esv3478641 | chr11:68282679-68411856 | Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
3 | esv3478652 | chr11:68282679-68411856 | Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
4 | esv3425206 | chr11:68282708-68411817 | Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
5 | esv3511614 | chr11:68282726-68411806 | Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
6 | esv3511615 | chr11:68282726-68411806 | Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
7 | esv3348204 | chr11:68282891-68411839 | Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
8 | nsv832195 | chr11:68286383-68474611 | Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
9 | nsv430403 | chr11:68297201-68448324 | Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
10 | nsv897864 | chr11:68367007-68453429 | Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers 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 regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:68380800-68391200 | Weak transcription | K562 | blood |
2 | chr11:68383000-68387200 | Weak transcription | HepG2 | liver |
3 | chr11:68383400-68387400 | Weak transcription | Ovary | ovary |
4 | chr11:68384000-68387200 | Weak transcription | Primary T cells fromperipheralblood | blood |
5 | chr11:68384200-68389000 | Weak transcription | Stomach Smooth Muscle | stomach |
6 | chr11:68384200-68389400 | Weak transcription | Duodenum Mucosa | Duodenum |
7 | chr11:68384400-68387200 | Weak transcription | HSMMtube | muscle |
8 | chr11:68384400-68387400 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
9 | chr11:68384400-68387400 | Weak transcription | Esophagus | oesophagus |
10 | chr11:68384400-68387400 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
11 | chr11:68384400-68387600 | Weak transcription | Spleen | Spleen |
12 | chr11:68384600-68387200 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
13 | chr11:68384600-68387400 | Weak transcription | Primary B cells from cord blood | blood |
14 | chr11:68384800-68387600 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
15 | chr11:68385400-68387000 | Strong transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |