Tag | Content |
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EnhancerAtlas ID | HS184-20726 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:111809460-111810490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr3:111810280-111810291 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28388 | chr3:111808522-111810716 | Fetal_Intestine | SE_29441 | chr3:111808484-111812275 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 111809791 | 111810097 | chr3 | 111810061 | 111810276 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I112089 | chr3 | 111808811 | 111812371 |
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Enhancer Sequence | TATAGATGAC GGCTGTAAAA TTTTAAGCTG AGTTCCTCCA GGAAGTCATA GAGTAATTAG 60 TGGTTTTTTT CAACACACCA GAGTCCTAAT TTGTGATCTC TAAGGGACAG CATAAATAAA 120 GGCATGAGAG GCCAAGGAGG TGCATTGACA CTCATTCTAT GGCTCATTTG AAACTAGATA 180 TTTCCTTTTG TGCTAATCTT TATGGGTCCC AGCTGCCTTT TATGAGGGCT GAAAATAGCA 240 CCAGGGCTTT GGCCTCAGGA GCTCTGTAAA TGGGGAGATG TTTCTGTCCC CTGAGAAACT 300 GAAGATTCTT TGTACTGGGA TGTCTTTTTC CCGTGTGGCT TCCCCTGGCT TTGAAGCAGT 360 TCTGCAGGTT TTGAGTGGGG ATGAGAGGTG ACCCTATCCC TGGATTCCAG AAATGCACTT 420 AACTCAAGAG GGATTTCCTC TGTCAAGATA TCCCTAGGGC CTTTAAGTGC TCCCCTCGCA 480 CCTCTGACAG GCTAGGCCTC AGAGTCAGTG TAAAGTGCAC TTGGGAAATC CAACATTTGT 540 CCCCTCATCT AGATTTTCTC AAAGTCCATT CTTAAAATTT CTGGGAGGCC TCTACAACTA 600 AACAGCCCAC AATCGTTAAA TGTATATTAC TTGTAGAAGG CACAGGTGTG GAATATAAGA 660 ACAGGGCAGT TTAAGAGCAC CCCTCCTCTA TGTGGTTTCA GTTTACGCAG GAAGATAAGG 720 CCAGGCTCTG TTTGTTTTTG AACCTGAAAC CGGACAGGGC AGTCAGTGGC AACAGCAGAT 780 GGGCTATGTG GACAGCTCAG GTATTGGAAG ATCTCACTAA GGGCAGGTGG GGAGGGAGGC 840 TTCCACCAAA GGGGAGATTT GACCTAACTC CCGAAAGGTG GGAGGCCTCA GACCAGAGGT 900 CTGCCATGGC CTCCTCCCAC CTCCCTTACA ATCTGGTCCA CTAGGTGCAG GTGGGGCCTA 960 GGTATGTGTC AGTTAAAATC CTTACCCAGT GATTCTGATG TGCAGCCAGG CTTGGGCACC 1020 TCTAATTGAG 1030
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