Tag | Content |
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EnhancerAtlas ID | HS180-00111 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:3201070-3202450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr1:3201898-3201913 | TGCCCTCTGCCCTCA | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_31389 | chr1:3198815-3202505 | Gastric |
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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 |
GH01I003284 | chr1 | 3200746 | 3202437 |
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Enhancer Sequence | AGGTGGGCTT CTCCTGGCAC TGTCGCCGTG AAGCCTTCGG GAGCCAGGAC CTGCCAGCAG 60 CCAGAGTTCA GCCCTGCAGG GAAAGGGGCG GCCAGGGGGA GCCCCACACC CTGAGAACGT 120 GGGAGTGCGG TCTTGATACA GATCATCTTC AGATAGACTC TGTGGCCTTA TGATGGGGAA 180 TCTGAGGGTT CATTCTCAGC CAGAGAGGAG GATAAGGGGT GTTGCTTCTA GAAACGGCCA 240 TGCGTCTTGG GGGCTTCACG GAGCACCTGT GAGCCTGGGG TGGCCAAGCC TGGGAAACCC 300 AGCGTGGTCC CGCCCAGGCC AGGGCAGAGC AGAGAAGGGT CAGAGCTGGA GGCCGGGCTG 360 AGGAGTCTGC AGCCGCCAGG GCAGCTTCCG AGCTTGGTGC ACCTACTCAC CACGCTGGCC 420 CTTCCTGGGC TGTAAGCCCT GAGTGACCTG CTCCCCTCTG GGCCCGGGCT TTCGGAGGCG 480 AATGTTGGTA GGTTTCTCTG GCCGGTATAG CCCTTGAGCA TGGAACGCTT CACCTGGTGC 540 CCTGGACGGG GTGCAAGGGA GGCAGGCTGG CACTCTCTGG CCCCCCCAAG TTCTGGGCCA 600 GCCCCCAGCA TTTCCTGCTG AGAGTCCCAA GGTCCTTGGT GAGGTTTTCA GAGCCCACTG 660 GGCAAACCTA GGGTGAGGTG GGCTGTGTGG ACTGCAGCCA GGAGCAAAGT CTGGCCTGGG 720 GCACCCCAGC CCTCTGGCCC CAGCCCCGTG GAGGCCCCTG CCTCTCCCCT CCAGCTGGCC 780 ACCTGGGCGT TCTGATTACC TCTCCAGGTG TGGCTGGGAA AGCAGCTCTG CCCTCTGCCC 840 TCACCCCATT GTTCCCCAGG CTCTGCCTTT CAGGTCGTTT TACGTTTTCA CCTGATCCCT 900 GTGATGCTGC AAAGCATTCC CAGGCCACTG AGCAGCCCTG CCACAGCCGC TGTGTCGCCC 960 CCACTCACAA ATCTCGGGAC GGACATGTCC CCTGCCTTCC TGGGAGCAGG CATGCTCCCA 1020 GGAAGCTGTG ACATGCTCGC TCGGGAGCTT GGAGCTGTGA CATGCTCGCT CGGGCTTCTT 1080 CGCTCACACC CGCGACATCC ACATTGGCCG TGGTCATAGC CAGCCTGAGC CCAGGGCGTG 1140 CTTGAGCCCC TCCGTCTCTG GTCCCTGGAC GGCCAAGGTC AGTTTCCTCC CCCTGGAAAT 1200 GGCTAGATGA AGGTCTGCTT CTCCAGATGC CAGCCTTGCT CCCAGGCCAT GGCAGAGGAA 1260 AGCCCCCCCA CCACCGGACA CCTGGCATGT CCACCTGGGG AAAGGGCACT GGCCCTCTCT 1320 GGCAAGAGCT TCTCAGACCC CAGGGTAGGT GGACTTTGTG GTTTTCATCT CTGCCGAGCG 1380
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