Tag | Content |
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EnhancerAtlas ID | HS194-00059 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr1:23158140-23159480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:23159451-23159464 | GAATGTTCTGGAA | - | 6.62 | TBX21 | MA0690.1 | chr1:23158262-23158272 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:23158262-23158273 | AAGGTGTGAAA | + | 6.62 |
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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 |
GH01I022824 | chr1 | 23151232 | 23159621 |
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Enhancer Sequence | ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA TTATAAGGGG AGGGCCAAAA 60 TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA TGCTGACCTG GGCTTCCTCA 120 GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC AAGGGCTCAA GAGGGGCTGT 180 GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT TCCAGAGGGA GCTATCCACC 240 CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG ATTCTCTGCC CCACATAAAC 300 CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG GAAGAATTGG GCTTCCCCAG 360 GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT GCAGTCCAGG AGGACCTTCG 420 AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG GAGAGCCAGA AAGTAGGGAC 480 AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG AACAGGGTGC ACGTCATCAG 540 AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG CATGGCCCTG GGTGAGTCAT 600 GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG GCAAACCAAT GCCACCTCTC 660 AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA TGGTGGCTGT TGCCAATGCT 720 ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT TGCAAGCCAC ATTCATCCTT 780 TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA GGATTCTTAC CAGAGAGGTT 840 AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC CTGGGATGCA CCCCTAGTGA 900 TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC TTCTTCAGTC TGGGTGGTTG 960 CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC CAGGAATCCC TCCCTGACCA 1020 CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA CCTTTGAGAC ATTTATCAGA 1080 GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC CTAAGACTTT GAGGGTTCAG 1140 CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA TTTTGTTAAT GACTACAGCA 1200 CCTGTACAAA GGGACAGATA GGTGTCCACA GACTCACATG TATAAGTAAC AGTCATGCAT 1260 GCACAGCCAT GCACATGTGG CTTAGTGAAT ACACATGTAT ACAGACAGGG AGAATGTTCT 1320 GGAACATGAA TTGTGCTCAT 1340
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