Tag | Content |
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EnhancerAtlas ID | HS050-39234 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:182628900-182629960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr2:182629882-182629892 | GCCATATGGT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34305 | chr2:182628767-182629980 | HCT-116 |
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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 |
GH02I181764 | chr2 | 182628921 | 182629070 |
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Enhancer Sequence | CTAGAATATT TTGATGAACC ATTTGCTGCC ACATCTGCAT GCCAGACTTC TTATCTGATT 60 TCCTACACTG CATGAAAACA CCGTCAGCCA GGGGACGTGC CTTATCTGTC TGTTGCAGAG 120 AAGGCTCCAT CTGTCCTTTG CAGAAGAAAC TGAAGGCCTT GTCTGTAACA GCTCTTGGCT 180 GTAGCATCTT GGCTCCCCAA AAGAAGAGCA TCTTCCCTCT TCTCTACTAG CCCCAGAACG 240 AGTGTGCCTG CAAGCAATTC CACAGTGACC CCTTTTCACA ACAATTTGGA GCCAAATAAA 300 TAATTAAGAA AGATAAAGGA TTCAGAGAGG CCTGTCTCAG TCCTCTCCTC CCACATGGGG 360 GCTGGGAACA CCACCCCAGG ACCTGTGTCT CATGTGACAA GAGCATCAGA CCTGGCTTTG 420 TGCAGGTTTT CAGGCAGAGC CCAGCAGCCT TAGTATCTAT GCTTTGTGGA CTGGAGCAAA 480 CTGTAACCAG AAAGCCGGTC AGCTAGTCCT GGGAAACAAT AGAAGTCACT ATTGAAAGGA 540 GCTTGCTTGT CAAAGACTAA TCTTTAATAA CTTTCAAAGG GCTTGGCCCT CTCATTAGTC 600 TTTGTTCCAC CTGCTGGAGG GGATAATGCT GCCATTCTTT TGTTACAATG TCCAGGCCTT 660 GCTTTTGACT AGCCACACTT GATAAACACT GAACTTTCTC CTCTGTCATT GAGGGCCCCA 720 GTTGCCAAAC CAATGTCTAC AAACTAATAA AGGGCATGCA ATTTTGTGTA TTGAAAACAT 780 GGAAATAAGA CTACCATATA TCTATTTCTA TGCATATTTT CAGGGGTGTC TCCCCAACCA 840 GATTCCTAAG AAAGAGCTGC CCATCACCAA GAGCTTTATG CTCGTCATAG GCTGGGTGTG 900 GTGGCTCATG CCTGTAATCC TAGCACTTTG GAAGGCCAAA GCAGGTGGAT TGCTTGAGCT 960 CAGGAGTTCA AGACCAGCCT GGGCCATATG GTGAAACCTT GTCTCTACTA AAATACAAAA 1020 AAATTAGCTG GGCACGGCGG CATGTGCCTG TAATCCCAGC 1060
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