Tag | Content |
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EnhancerAtlas ID | HS037-35517 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr7:30598680-30600200 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr7:30599377-30599389 | TGCCTCAGGGCA | + | 6.18 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH07I030559 | chr7 | 30599301 | 30599450 |
| Enhancer Sequence | GTCCTGTTGG CTCTGGCCTA GCACAGTGGC TCAGGCCTGT AATTCCAATG CTTTGGAAGG 60 CCAGGGCAGG CAGAAGGCTT GAGCCCAGAA GTTCAAGACC AGCCTGGGTA ACATGGTGAG 120 ACCCATATCT CCATAAATAC AAAAATTAGC TGGGTGTGGT GGCATGCACC CATAGTCCCA 180 GCTGCTTGGG AGGCTGAGAG GTGGGAGGAT ACCTTGATCC AGGAGGTCAA GGCTGCAGTG 240 AGCCATGATT GCACCAGTGC ACTACAGCCT GGGCAACAAG CGAGACCCAG TCTAAAAAAA 300 AAAGTCCTGT TAGCTCTAAC TTGATCACTC TCTAATCTGC CCCACCAAGA TCTCTGAGGG 360 CCGAGCCACC CTCCTGTCTG GTCTGGGCTA CTCCTGTAGC CTCCTAACTG GCTGCCCCTC 420 ACCTCTACTT CTGCCCCCTG CTTTTTTCCT CCACACTTCA GCCAACGGGA TGATTCTAAA 480 ATGCGGGTCA GATCACACCA CCCCTCCTCA AAACCCTCCA ACTGCTTCCC ATCCACACTT 540 ACAGGAAAAT CTAAAGAACT CAATGTGACT TACACAGCCC TGTATGTTCT GGCCCCTGCC 600 TCTCTCTCCA GCCTCATTTA CTACTTTTCC CTCTCCTTCA CCACATTCCA GAGGCCCTGG 660 CTTCTTTCCT GTTTCCAGGA CACGCCAAAC ACAGTCCTGC CTCAGGGCAG TTTGCTGTCT 720 GGAAGAGCCT TGCCCAGGCC TCAGTAAGGT TCTATGCTCA CTGCATTCAG CTCTCTGCTC 780 TTCTGAGGGG TCCTCATGAC AATCACAAAC AAAACAGCAC CGCTTCACTC GCTGCACTCA 840 AACATTGCTT CACGTTTCCA TAGTGCTCAT CACCGCTTGC CAGTACATTG TATTAAATAG 900 TTCTGAGTTT TTTTTTTTTT TTTCTTTTGA GATGGAGTCT CACTCTGTTG CCCAGGCTGG 960 AGTGCAGCGG TGCAATCTCG GCTCACTGCT ACTTCTGCCT CCCGGGTTCA AGCAATTCTC 1020 CAGCCTCAGC CTCCCGAGTA GTTGGGACTA TAGGCAACCG CCACCATGCC CAGCTAATTT 1080 TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CATGTTAGCC AGGATGGTCT CAATCTCCTG 1140 ACCTCAAGAT CTTCCTGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACCA 1200 CACCCGGCCC AGGGTTGTTT TTGAGATGGG ATCTGTCACT CAGGTTGAAG TCCAGTGTCA 1260 CAACCTCAGC TCACTGCAAC CTCTGCCTCC CAGGCTCAAG AGATCCTTCC ACCTCAGCCT 1320 CCCAAGTTGC TGAGACCACA GGCATGTGCT ACCACACCTG GTTAATTTTT TATGTTTTTG 1380 TTAGAGATGG GATTGTTGCC CAGGCTGGTC TTGAACTCCT GAGCTCAGGT GATCCACCTG 1440 CCTTGACCTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCATGCCCAG CCTAAACACT 1500 TTCATTTGTC TTTCTCTCCT 1520
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