Tag | Content |
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EnhancerAtlas ID | HS026-03252 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:232454530-232455960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr1:232455410-232455422 | CCATCAATCATT | + | 6.07 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27584 | chr1:232454562-232456994 | Esophagus |
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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: 2 | ID | Chromosome | Start | End |
GH01I232318 | chr1 | 232453950 | 232454548 | GH01I232319 | chr1 | 232454898 | 232455086 |
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Enhancer Sequence | GCCACAGACT TGGAAATAAT AATTTTAAAA AGAGTTTATG TGACTCTATT AGGGAAATGG 60 TGTGCTAATC CAGGTTTTGT TATCATTTCA GCCTGATGGC AGATTGTCCA TGAAATCTTT 120 CTAGATTCAT GGAGGGAGAA GCTTTGAGGA AATGAATTCA GGAATCTAAC GCAAAGAAAA 180 GAAAGCGGCA TAAACTTTCC CCCACCCCAG ACCTGACATG AAACCCTAGG CGATCCCTCC 240 TTCTCAAATG TTCATACCAT GTGCCCTGAG TTATTTACCT AACAATGGTC ATTCTTCTAA 300 TAACAGATCC TGGGATTCCT GAAACCATGC TTTCTCTCAG TGCTGTTGTC TCTGGGCACA 360 TACGCTGTTG AGATGGCGAC ATCACACACC CTTGAAATAG CAGTTGCACA AAGCAAACGT 420 TTGCCCCAAG CATGTCAGAC TTTTGACAGG CTGCAACATG ATAAGTTACC AGACGTGTTC 480 CCACAGGAGC CTGCGTGAAT TGATTGCAAC CAGACTCACC CGATGACAAG TGACAGACAG 540 CGGATAATGC AGGGAGGTCA GGTGGGCTGC CAGGCCCAGG GCCAATTGCT CCCTGGAGCC 600 CATCAACAAG GGACAGGACT CGGCAGGACC AGGCCGGCAG CCATCCTGGT TGGCTTCCAG 660 CGGGTACAAG GAGAAATTGC AGCTGGCAGA AGCGCAGACT CCTGGTGCCA CTCCAACACA 720 GTGAGGGTAG AGGAAGGTGA GAGGAGGGTG TTACTCTTTA AAAGAACTCA GATTGCATAT 780 GAAATGCATC TCTTTCTTCT TGCTTTTGAT CCCAAAATGA AAAGAGCTTA ATCTCCTATC 840 TGAAAAGAAG CTTTTCCTAT GCTCTGCTGA CACGAACAAA CCATCAATCA TTGCCTGGAT 900 TTCCTGAACC TCTCAGTACA GAGGCTTCCA GGCCAAGAAG GGTTGAGAAA GGCCTCCTTC 960 CAGCTGAGGA CAGTGAAGTG TGGTAGGAAG CAGGAGTCTC CCAGAAAGGG CATACCCTGT 1020 CTGATCCCTC CCTCTGACAA CCTGCTCCAC AAAATGATGT GGGGAGAGAG GGGTCATGGC 1080 TCAGACTCTG GGAAAACAGT GGCTTAGAAA TTGATAAGTA TTCAGACTGG ACTTGGTTCC 1140 GAAACTGATT AAGCCAAACA TCCTTTTCCC AGCTCTTCTG ACTTCTCACT GCTGTTTCAA 1200 AGACCGCTCT TGGCACAGCA ATGGGCAATT TCTCTCTTGT AAAACAGACC ATAAAAAATG 1260 AAAGCACCAG ATTTAAGGGG CACACAAACA TGCACACACA CACACACAAA CACACACACA 1320 TGCACACATA TAAATACACA CACATGCACG CATAAATACA TACACATGCA TGCATACAAA 1380 TACACACAAA ACCACAGCTA AAATCCTTTG TAATCCCAAC CCAGCTATTT 1430
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