Tag | Content |
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EnhancerAtlas ID | HS194-00048 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr1:20091270-20092720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:20092650-20092671 | CCCTCCTTTTTTCCCTCCATC | - | 6.73 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_52839 | chr1:20091300-20092944 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 20091379 | 20091715 | chr1 | 20091332 | 20091506 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I019764 | chr1 | 20090998 | 20093283 |
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Enhancer Sequence | CCGGGAGGTG GAGGTTGCAG TGAGCCAAGA TTGCGCCATT GCACTCAAGA GTGAAACTCT 60 GTCTCAAAAA AAAAAAAAAA AAAAAAAAAA AGGATGTTGA TGGAGAACCC AGCAGCCAGG 120 TGACAATATT TGCATTTTAC CACAACCTAA GACTAACACC TCAAGTCTTT CTGATTCATC 180 AGGGAGGCAG GGTTTGCAAT CCAGTAATAA ATACCAGGCC AGAAAGCAGA GCCACGTCTG 240 CGGTAGAGAG TGCCGTGGCT CAAGTGTGTG TGCCTCCTGC AGTTCCAGGG CCTAGAGGTG 300 ATCCTCCCTT TGGATTCAGA GATCAGAGGG CAAAAATCAT GACGCAGTTT AAGTCTCCCA 360 GGGACCAATA CAGAGTTCAC GGTGAGATTC ACTTGGCCTT AAATGGAGTT TTGAAACTTA 420 CTTTGAAATG TAATCCTGGG CTACTCACTT AACCTGCAGA ACCTTCATTT TCTCCCCTGT 480 AAGAGCAGGT TAACAGTACC AGTCTCAGCA GCAGATCTGA TGATCATCTA CTCTGCAATA 540 ACTCAGAATC TATGTAAGCG GCCTAGAAGA GCAACTAGAA GAACTTAGGA AGATTACCAA 600 ATGCAAGTAA ACCAGCCCCA CCTGAGATGG CCGTATTTTC AGTTTTGCAA CCTAGAGGAC 660 ATTGGCAACC TAGAGGACAT TGGAGCCATT TCTGGTTATC GCAGCTCAGG AATGTCTACT 720 GGCACCTAGT GGGTAGAGGC CAGGGATGTG GCTAAGCAGC CCATGGCACA CAGAATAGCC 780 CCCCACAACA GAATGATCCA GCCTCAAACA TCAATTGTGT GGAGGTTGAG AGTTATCAGC 840 TCAGATTTAG TTTAACTTTC ATCACGTAAA AGACTTATTT TTTCGGTTGT GTGGGCAAAG 900 CGCTTCGTGG GTTGCTACTA GATGAGGAGA AGGAAATGAT TAGCATGCAC AAAAAATTCC 960 GCCCAGCTGC CAATATGGCA CCGTTCGGTG ACTAACATCC CAAAACTCTC AGTAAAGGTC 1020 AACCTTCCAG GAAGTTCTGA GAAATGCAGC TTTTCATGCT AATTTCCTGG GCTGACTCCG 1080 TGACTAATCA GCCCGTCTCA CACCCAGGGA GAAATCCTGC AGCACAGATA GCCTCCTCCT 1140 CTGCCCCCAT CAATCTCTGT AGAAGGAAGA CATTCAGCAA ATCATGCTGC TCAGCATCTA 1200 AGCTCATTCT CCAAAGAAGG GTCGCCCACC CATCCTTCTA TTGCTCTCGC CCTCCTTCTC 1260 TCCATCCAAC AAGTACCAAG TGTCCACCAT GCATCCGTCA GAAGACATTC AGCAAATCAT 1320 GCTGCTCAGC ATCTAAGCTC ATTCTCCAAA GAAGTGTCGC CCACCCATCT TTCTATTGCA 1380 CCCTCCTTTT TTCCCTCCAT CCAACAAATA CTAATGCCCA CCATGCGTCC ATCCGTGTTG 1440 CACTTGCTGG 1450
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