Tag | Content |
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EnhancerAtlas ID | HS082-21134 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr20:23426000-23426990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr20:23426698-23426708 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr20:23426698-23426708 | GGCACGTGCC | - | 6.02 | IRF1 | MA0050.2 | chr20:23426880-23426901 | CCTTTCTTTCTTTTTTTTTTT | + | 6.1 |
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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 |
GH20I023445 | chr20 | 23426341 | 23426450 |
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Enhancer Sequence | CACCTTAGCC TCCCAAGTAG CTGAGATTAC AGGTGCACAC CGCTTTGTCC AGCTAATTTT 60 TTAAAACACT TTTTTTGTGG AGACAATATC TCCCTTTCTT GCCTAGGCTG GTCATGGACT 120 CCTGGGCTCA AGTAATCCTC CTGCCTCAGT CTCCCAAAGT GTTGGGATTA TAGGCGTGAG 180 CTACCGCACC CACCCAGCTG ATGCAATTAG AACAGAATGT TCATAATCAT TGGGGAAACC 240 TCATCATTCT TTCTACGCCA CCCCACATCT CTATGGCTTT TCTGAATTTA GCATGTCCCT 300 GAGCTCTGAC CCTAGTGTGG GGAGCCCTAT TTCTTCCCAG CACACACACA ACACTGTGAC 360 TCACACACAT TTTTGTGAGT GTGTCTGAGA TTCCCAATAC CAAATTCACA TTGAGTGACT 420 CACTAGAGGA CTCACAGGAC TTAGCCTAGA GTCATTCTCA TGGCTGTGAT ATGACAGCAA 480 TGGGACACAG GGCAAAACCA GCAAAGGCAA AAGGTGCATG GCGCTAGGTC AGGAGAAAAC 540 CAGCCAGGAG CTTCCAGAGT TCTCTCTCGG TGCCGTCACA CAGAGCACGC TCAATTCCCC 600 CAGAAGTGAG CTGTGGCAGT ATGTGTCACA AGGAAGCTCC TTAAGACCCA GCAGCCAGGG 660 TTTTTACCGG GGACTGGTCA TGAAGGTAGT CTCTGCCTGG CACGTGCCAA AATTCCAGAC 720 TCCCAGAGGA TAGCAGGGGT TCAATGTCAA CCTCACTGCT GTACAGAGAA TGTAAACACA 780 CTGAGGCCCT CTTCTCATGC AGGAAAAGTT TTCTATCAGT GTAGGGAACT GTTGACCCTC 840 CAAGTTCTCA AACTCCATCC AAGGCCAGCC TTGCAAGCAG CCTTTCTTTC TTTTTTTTTT 900 TTCTTTTTTT TGAGACGAAG TCTCGCTCTG TCGCCAGGCT GGAGTGCCGT GGCACGATCT 960 TGGCTCACTG CAGTCTCCGC CTCCCAGGTT 990
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