Tag | Content |
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EnhancerAtlas ID | HS187-24009 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:94997600-94998710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat4 | MA0518.1 | chr8:94997672-94997686 | TTTCCAAGAAATGA | + | 6.04 | TCF7L2 | MA0523.1 | chr8:94998543-94998557 | ATTCTTTGATGTTT | - | 6.16 |
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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: 2 | ID | Chromosome | Start | End |
GH08I093985 | chr8 | 94998028 | 94998428 | GH08I093986 | chr8 | 94998629 | 95000270 |
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Enhancer Sequence | AGATGGGCTG CATTCACTGG TGAGGAACAT GTTCTAGGCT CAAATCTTTC CAGATGGAGA 60 CCTCTGTAGA CATTTCCAAG AAATGACTCT GATTCCTTAG CCACAGACTC TTGCCCAGTT 120 TAGGCCAATC ACAGGCCAGT GGGAGGAGGT ACTACACGTG GCTCAGCCTG CATCATGGGA 180 CAGCCCTGTG GGCCGGTAGT GGCATAGTGA GGCTTTGGGG AAATCACTAC AAGTTGTCCC 240 AACCTGTCCA CTCCCTCACA GCACTTTTGT GATTTGAAGG AAGCCACACA GTCACATAGC 300 TCCTCGAATA GTCTCTGTGG TGATTTTCCT CCTAGAGGAA GCTTTGGGGA GAATGTGGGC 360 ACCTCAGCCT CTCTGTTCCT TTGACCCTTC AGACTCATTA AGTGCAGTGT GGTTCTTACA 420 GTTCTCTCCG TGTAGCTTCC TGACTCACTG CATCTGCAGA TGGCCCCACC CCAGACCTGA 480 AGCATGGCAG CGCCTTTGGT ATCTCCAGGG CTCCCACAGC CAACGTGTCT TCTACCACAG 540 GCATGCAGCT CTTTTTCTGC ATCCTGTTTC ATCCCTGTGG CTGTCACTGT GGTCTGTTAC 600 CTCACAGCCT CCTAAACAGG GGCCAGCTCT GATCACATTG GTCTGCTGCT TCCAAGTGAC 660 AGTGGCTCTC CATTATCTCT CAAATTAGTG GGAGACTCCA GGGCTTGGCA TTCAAGGACT 720 GCCACGATCT TATCCCAAAC AACTTCCAAG CCACTCTTGC GGGCATTGGG TGTTTAGATC 780 CTGCTACTGT AGGACAAACA AGTAGGAAAG CCTTTGGGGA CCAGTGTAAG GAAATGAGCA 840 GGAAGGAGTG AGACTGGCTG GTGGCAGGTT GCTAGGCAGC CATACAGCAA GAAAAGCAAC 900 CTGCATGAGG CAGATGATCC TAGAAGCCAG TGAGCACTCC CGCATTCTTT GATGTTTGTT 960 TTAGCTAAGA TCAGCCAACT TAGGGTACTA ACCAATGGAA TTTTGTGAAC CCATTTAACT 1020 CTGATATTTA ATATGTTGAG GCTCAAGACA TTTTTCCCTC TTTGGTGGTG AAAAAACCCA 1080 TAAACTACTA TTGTTTTTAC TGGGGAATGT 1110
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