Tag | Content |
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EnhancerAtlas ID | HS052-23216 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr20:23425930-23427050 |
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 | CAATCACTGA AGCCTCCGCT AAAGTGGAGC TCACTGAAGC CTTGACTTCC CCGGGCTCAA 60 GTGATTCTTT CACCTTAGCC TCCCAAGTAG CTGAGATTAC AGGTGCACAC CGCTTTGTCC 120 AGCTAATTTT TTAAAACACT TTTTTTGTGG AGACAATATC TCCCTTTCTT GCCTAGGCTG 180 GTCATGGACT CCTGGGCTCA AGTAATCCTC CTGCCTCAGT CTCCCAAAGT GTTGGGATTA 240 TAGGCGTGAG CTACCGCACC CACCCAGCTG ATGCAATTAG AACAGAATGT TCATAATCAT 300 TGGGGAAACC TCATCATTCT TTCTACGCCA CCCCACATCT CTATGGCTTT TCTGAATTTA 360 GCATGTCCCT GAGCTCTGAC CCTAGTGTGG GGAGCCCTAT TTCTTCCCAG CACACACACA 420 ACACTGTGAC TCACACACAT TTTTGTGAGT GTGTCTGAGA TTCCCAATAC CAAATTCACA 480 TTGAGTGACT CACTAGAGGA CTCACAGGAC TTAGCCTAGA GTCATTCTCA TGGCTGTGAT 540 ATGACAGCAA TGGGACACAG GGCAAAACCA GCAAAGGCAA AAGGTGCATG GCGCTAGGTC 600 AGGAGAAAAC CAGCCAGGAG CTTCCAGAGT TCTCTCTCGG TGCCGTCACA CAGAGCACGC 660 TCAATTCCCC CAGAAGTGAG CTGTGGCAGT ATGTGTCACA AGGAAGCTCC TTAAGACCCA 720 GCAGCCAGGG TTTTTACCGG GGACTGGTCA TGAAGGTAGT CTCTGCCTGG CACGTGCCAA 780 AATTCCAGAC TCCCAGAGGA TAGCAGGGGT TCAATGTCAA CCTCACTGCT GTACAGAGAA 840 TGTAAACACA CTGAGGCCCT CTTCTCATGC AGGAAAAGTT TTCTATCAGT GTAGGGAACT 900 GTTGACCCTC CAAGTTCTCA AACTCCATCC AAGGCCAGCC TTGCAAGCAG CCTTTCTTTC 960 TTTTTTTTTT TTCTTTTTTT TGAGACGAAG TCTCGCTCTG TCGCCAGGCT GGAGTGCCGT 1020 GGCACGATCT TGGCTCACTG CAGTCTCCGC CTCCCAGGTT CAACCAATTC TTCTGCCTCA 1080 GCCTCCCTAG TAGCTGGGAC TACAGGCGTG CACTGCCACG 1120
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