Tag | Content |
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EnhancerAtlas ID | HS101-20987 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:8516380-8517610 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr19:8517317-8517328 | TTTCCAGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr19:8517317-8517331 | TTTCCAGGAAAGAG | + | 6.67 | ZNF263 | MA0528.1 | chr19:8516407-8516428 | TCCCTCCCCTTCCCCTTCCCC | - | 6.23 | ZNF263 | MA0528.1 | chr19:8516408-8516429 | CCCTCCCCTTCCCCTTCCCCT | - | 6.63 |
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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 |
GH19I008451 | chr19 | 8516118 | 8517705 |
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Enhancer Sequence | CTATCACATC ATCTAAACTT GAATATGTCC CTCCCCTTCC CCTTCCCCTT CCCTTGCCGA 60 GACAGGGTCT CCCGCTGTTA CCCCCGGCTG GAGTGTAGTG GTGCAATCAT GGCTTACTGT 120 ACCCTTGACC TCCTGGAGCC AGACTGTCTT CTTTCTGCAT AGCTGGGACC GCAGTTGTGC 180 ACCAACATAC CTGGCTAATT TTTTGTATTT TTTTTGTAGG GACACGGTTT TGCCATGTTA 240 CCCAGGCTGG TCTCAAGACT CCTGGATTCA AGCACTCAGC TCACCTCAGC CTCCCAAACT 300 GCTGGGACTG CAGGCATGAG CCACCATGGC CAGTCTGCTT GAATATGTGT CTCGAATGAT 360 ATTTCTTTGA GGGTCATTCT CTACAAGTCT GTCAAGAATT AGTTGGTGGT GGTAGATTTC 420 CAAAAAGGTC AATTTTTTAA AAGTTGGAAA TGACAAGAGA TAGTTCTAAT CTCTTTACTG 480 AGGAAACCTC TCAGAGGGAA TGATTAGCCA GGGAAGGATT TGTTTGCAGA GGTGCTGTGC 540 CCATTAAGCA TGGTGAGAGC CGCTTTCTCA ATGGTGAGTC ATGTGATGTG GATTAACCCC 600 AAACCAAATG CTCAGCTTCT GTGGTTAGAT TGGATAGTTT ATTCGTAGCC ATGGTATGCA 660 CCTGTGGAAT ATAGGTTAGA CACTTTGTTA CCTGCTTTGG CTGTAATTAT TTATTTATAC 720 ATTTCGTAGT TTATAGGTGA GCTTAAGCAG TCTGGTGAAA GACTGGAAAT AATTCATCAT 780 GGACTCTGTC AGAATGTTTT TTATTGTAAA TCTTAAAGTA TTTGGGACTT CAAAAGTAAC 840 AATATTAAAA TTCATTTCCA TCTGTGAATC CTCTGGTGGA CCATGATGTG TAGATTCTGT 900 TATGTTTTAT GATTTTTTCT AACACAGTCG TCGTCATTTT CCAGGAAAGA GTAGGAGATG 960 ATTTGGCAGA TAGATTTTGT TTGGCAGACT TTGGTGAAGG ACTTTCTTTT GGAGTAGACA 1020 AGTGGCCTGG GTAACAGTTG TAGGTCTCCT GTGGGACCTG CTTTGTGGTG TGAAGCCAGT 1080 CTTGTGGACT CAGGTAGATT GCGTTCTAGG CATCTAGGGA TTGGAGCTGC CATAACATCA 1140 CCTTATCTGC CAGCCCGTGG GAAGGGAAGC CTGTTGATTG TGTATTGGTA TAGTTGAGAG 1200 ATCACAGAGG AAGCTGCTTT CCTTGGTTTT 1230
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