Tag | Content |
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EnhancerAtlas ID | HS099-16232 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr3:156505320-156506640 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU4F2 | MA0683.1 | chr3:156506469-156506485 | ATGCATAGTTAATTAC | + | 6.57 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_36276 | chr3:156498702-156508470 | HMEC | SE_37869 | chr3:156503954-156507566 | HSMMtube | SE_45647 | chr3:156504542-156507624 | Osteoblasts | SE_64780 | chr3:156504644-156508244 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I156786 | chr3 | 156503980 | 156508135 |
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Enhancer Sequence | ATCCAAATTA TCAGAGAGTA GACTGGTGCG AGGTTCCACG TGAGTGGAAA AAATTTCTCC 60 AACACCGTTA CTCACCACCA CTGTTACCAA CACCATCACC AGCATTACTA CTACCATAAT 120 TGTTACTATT ATAGGCGGTC TTCCATATCC ACAAGTGCCA CATCCATGGT TTCAACCAAC 180 CACTGATGGA AAATATTTGA AAAATAAAAA ATAACAATGC AACAATACAA GTAAAAAAAT 240 ACAGTATAAC AACTACTTAC ATAGCACTTA CATTGTATTA GGCATTATAA GTAAACTAGA 300 GATGATTTAA AGTATATGGG AGTATATGGG TCGATTATAT GCAAACACTA TATTATTTTA 360 CATAAGGGAC TTGAGCATCG CAGATTTTGG TGTTGGGGAG GTGCTTCCTA GAACCAATTC 420 CCTGTGGATA CTGAGGGAAA ATTGTACCAC CATCATCACC ACCACCAACA TGCCTCTCCT 480 TCCATTTATC TGCTCCATGT GGTTGGGAAA AGGACCTAGG AAAATAACAT TTTGTGGGGA 540 GCTTCTTTTG CACTTAGGGC TACATCTTCC CAGCAGGTTA CAGGGTCATG GTGTGGTAGG 600 AATTGGAAAG TGCAGCATCT GTAAACCAAT CCACAACCCA AACAATTTTT TCCTATTCTA 660 TAATGATGAA AAGTCACTTG CTGAGCTACC ATCGAACAGC AGAATAGAAA AGTCTAAGAA 720 AGCAATTAAC TAGCAGGGTG AAAATACAAG TCAGAGATGA CTGCTGCTGA AACCCCATGG 780 GGAGTAATGA GATAAGAATT CTTAGGACTT AATTCATAAC AGAGACAGTC AGAGTGTGGA 840 GGAGTGGATG GGTAGGCAAT GACTCATGTT CCCTGCCCAG GGTACAACCT CAAAATAGTG 900 AGACTGATCC TACAGGCATA TATGAAAACC AGTCTCAGAA CTGCACTCAC TAGTCATGGA 960 TGATCTTTGT GCTGGTTAAT TTCTAAGACT GCTTTTGTAA CAGAGTGGTG CCCTGATCAC 1020 AGCTAGTTTA CAATCAGAAG CAGCTGAGGA GGCTGGTTCT TCAACATGTA TGATCTTGAG 1080 CAAGCTTCCT AATTCTCTGA ACCTGTGTCT TCATCTGCAA AATGAGAATA ATTCAGTATA 1140 AATTAGAAAA TGCATAGTTA ATTACATAGA ATCTTCAAAA CATATTGGGA ATGATGGTGA 1200 TAATGTGGAC CTTGTTTACT AGCAGAATGC TTGCCTTATC TCTATTCATC TCCTCTACAT 1260 TCCTAGGAAA TAGGTACTAT TATTATCTCC ATTTTACAAA TGAGCAAGGT TACTAAAGCT 1320
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