Tag | Content |
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EnhancerAtlas ID | HS180-02802 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:117003140-117004170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:117003694-117003705 | CCTTCCCGCCC | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28774 | chr1:117003286-117004264 | Fetal_Intestine_Large |
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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 |
GH01I116460 | chr1 | 117003287 | 117004264 |
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Enhancer Sequence | CTTGGTGTTT GCTTTTCTCT CCCGGTTCTC AGATTCTTGC TTCTGTGCCC AGGATCCTTT 60 ATCATCTGGC TCCTTTGACT TGGAAAATCC CCAAATTCTA GCCTTTGGGG CTTCTTAAAT 120 GATCTTAGCT CAACCCACAA AACTCCTTGC TTTATTCTCT AGCAGTGAAG GACAGCATCT 180 CCACTCCTAC AGTGCAACTC CCCCTTATGC TCCTCCCAGA AGAGGCAGAA AGAGCCTGCC 240 CTCCAGGTCT TTTTGAGAAG ACACCTGTGC ACTGAGATGT TGAATGCTAG GTCCCCACCC 300 TACAAGGTAG AGGGAGAGCA CTGGCCGCTG CAGAAGCCAA GCCTGGAGAG ATGGGCTTCC 360 TGACCTCTGC ACAGAGCAGA GTCCTGGACC TTCAGACCCA GAGGCTTTAA GATCAGGGGC 420 CAATCTGGAA TCATCTCTGC AGTGAAATAA CTGGGTGTCA GTGATGGCAG CGGCTCCCTG 480 CCTCTGTCAT CACACCTGCC AGATTGCTTT CAGGGCAAGG GGCTCCCTTT GGCCTCCTAG 540 TTCCTCAGCA TTCACCTTCC CGCCCTGCTT GTGTCTCTCT CTCTGTTCCA CATTAGAACT 600 GGTTGCATTT CAGAGATTCA GAGACATCTA GCCTCAAACA GACCTAGGGA ATCTGACCTA 660 TGAACTTCTG CGTGACTGGC CTGGCCCAGG TTCTGCTGAT TACCCTCAGT GAATAATAAA 720 CTTTAGCCAA GTCTGATACA GTTGCTAAAG ATCACTTACT CCACTGAAGA TCTAACTTGG 780 CTTGTGGGTC CCTATGATTA CCATCTGCTT GGGGAAAGAG GAGAAAGTAA TGCAGAGTTG 840 CTAAGAGCGC CTGCAAGAGA GATGTCCTGT TAAGTCTCTC CTGCCTTTTC TCTATAGGCA 900 ACCCACCCAA AGAGTCTCAC CCTTGACAGC TGAACTGGCT GTGAACCAGA AACCAAACAC 960 ATAAATTTTC ACACACACAT GTATACACAC ATACATGTAT GTGACTATAT ACACACATAT 1020 ATACATTCAA 1030
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