Tag | Content |
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EnhancerAtlas ID | HS007-13778 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr5:134712600-134713730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Atoh1 | MA0461.2 | chr5:134712700-134712710 | AACATATGTT | + | 6.02 | Atoh1 | MA0461.2 | chr5:134712700-134712710 | AACATATGTT | - | 6.02 | Foxd3 | MA0041.1 | chr5:134713023-134713035 | GTATGTTTGTTT | + | 6.37 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_09262 | chr5:134700061-134716574 | CD14 | SE_12944 | chr5:134711830-134712824 | CD34_Primary_RO01480 | SE_12944 | chr5:134713179-134713925 | CD34_Primary_RO01480 | SE_13384 | chr5:134703830-134716872 | CD34_Primary_RO01536 | SE_14143 | chr5:134711917-134713658 | CD34_Primary_RO01549 | SE_25667 | chr5:134702231-134716696 | DND41 | SE_27598 | chr5:134712665-134713842 | Esophagus | SE_42046 | chr5:134713126-134714357 | LNCaP | SE_66430 | chr5:134712249-134714666 | Jurkat |
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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 |
GH05I135376 | chr5 | 134712619 | 134714058 |
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Enhancer Sequence | TTTCGATGGA TGGATTTGTG CCAAAAGGAG GAAAAAAGCA ACAGAAAACC TGGTGTTTCC 60 TCTGCCAATA GTTTACTCTT TGCTGTTATG CTTAACAGTT AACATATGTT TGAAAAATGC 120 ACTTGAACTC GATTAACCTC GGTGCTGCCA GACCTGCCTT GATGGAACAC AGCACCCAGG 180 GCGCCCCCAC AGGCATCTCT ACCTTGGAAT GAGGTCTGGG GCTTTTGTCT GACCACAGCA 240 GAGCGTGCAG AGCCAGTGGC TCAGGCAGTA GAAGTCAAGG CCCTGGGAAG GAGAAGGTGC 300 CTGGGGAGGC CCTGAGAAAC CTGTTCTACT CCAAGGCCTG GCTGGCAGCT GGGCAGGACC 360 TCTGACCCAC CAATCACTTG CTGTCAAGGA CTCTCAATTA AGTTACAAGG AAATGGTTAA 420 TATGTATGTT TGTTTTGATA GGGAAAACCA CAGCCATTTG TTCTTAATTC ATCTCAGGAA 480 GGGGTGAACA ATCAGCGATG TCTGCTGAAA TGAAATGATT TGAAGAGTAT AATGTAAAGA 540 GGAAACTCAT TTAAGGAGCC CTGTCATGGT ACGGTTTCCC AGATGGACTC AAAGCGAAAG 600 AGCGAGGAGC AGAACAGTGA GTTTCGTGGG CTGCACTGTG TTGGGGGAGG AGGCGACGTC 660 TGCAATCGGG CTACACATGT TCATCAAGAC AGGGGAGCAG CTTCGCCCAC TGGGAGCAGA 720 ATCAGGGACT TGGTCAGAGG GAGACGTTTT GCTCTACTCC CTTTTGTGCT GTTTGAATTT 780 ATCTTCTGCA TATTTTCCTT TCAAAATGAA AATAATTATA ACACTGGATA GATGAGAAGC 840 TGCAGGCACT TCTGCTATCG GCTGCCCCAG CTGGCCTTTG GTACCACAGG TCACAAGCCC 900 CCTTACCCTC AGACACTCTG TCCCAGCCTG CTTAATCCTG CTTCTCCCAA AAAATGGTTC 960 TGAGCATGCG AAGACTTTCT AGGTTCTTTT TTCATGGCTG TTTTTAGAGC AGTGTGAGTG 1020 TGTCATAGAA AGGGAGGCCC CTGAGAGGGC ACTATAGCTC CTGAGGTCTT TACCAGCCTG 1080 GCCTCTGTGC TGTCTGCCGG TGTGGATTCC CGATGCTGAG GACTGCTTGT 1130
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