Tag | Content |
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EnhancerAtlas ID | HS092-14383 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:40809900-40811320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr13:40810848-40810860 | TGCCCTCGGGCA | + | 6.27 | TFAP2C | MA0524.2 | chr13:40810848-40810860 | TGCCCTCGGGCA | - | 6.52 |
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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 |
GH13I040232 | chr13 | 40806390 | 40811154 |
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Enhancer Sequence | TGAAAGATAC CATTTTAGCC TTTAAAATGT TGGTCATTTA TATGTGCACA CTTTTTGTAG 60 TCCTGTATTT CTCCTAGTGG TAGCACATGT ATGTGGACAC ACATGCAATA GATGAGTTTT 120 ATCTCCTAAA AGGTTTAAAC TCTGGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 180 GTGTGTTCTT ATACCATTGC CTGGAGTGTA AGGACTTGCA AGGAAATTCT CTTTGACCAG 240 GAGGATTCAA GAATGCAGAG CAAATGTCCA GGAGTCGCAG CCAAATTGGT AGCTTTTCTT 300 GCTCCTTTCC ACTGCATTAG CATGCCCCTA GCCAAAACAA GATGGCACCA TGCCCCGGCC 360 AACTTGATCT CAATGTTCTC CACAGCTGTG TGTCCCCACT GGGGTGAGTA TTGGAGCAAT 420 GTCTCATGTC TAGTCTAGCC AGGAAGATTG TCACTTTGGA CCCTAACCCT TTCTGAGGTT 480 TGAGCCTCCA ATTCACTCAT GTCTGGCCAG CACGAGTCAT GCCATCCATG TATCCTCACT 540 CCCAAAAGAA ATGACACCCT TGGCAAATTC TTGAACTACG TTTTGGAAGC CGCCGCTGAG 600 GTTGCGCAAA CACATTTGGC ACAGGCTTCA GGGACCAAGC AGTTCTCTGG GTTGAATCGC 660 AGAAACAAAA TGTACTTGTC CTGCTTCCGA GATGGTGTCT GAGGACTTGG CTCCCTCGGC 720 CGAGGAACTG CCTCCTCGCT GATGTCATCC TGCCACGGAA AGGCAAACAT CTCTGGGTTC 780 AGCAGTTCAG AACCAGAAGT GAGAAAAGTT GGGGATCCAA AGGGCATCCA CCCAGGCTTA 840 ACTCCATCGG GACAACGTAG AGAGACATGC ACTCAATTCT TAACAACTAA ATCATCTTAA 900 AATAAAATGT ATTGAAGCAG TTTGTGAGGA GGAATCATGC TGCTGAAATG CCCTCGGGCA 960 AGGATTACTG GTCGTGATGC TACCTCCATC CAGTGGGGTT TTGTGGGGCT CCACGTGCTG 1020 CCACATGCAC CCCATAGGAG CACAAGTTCC CAGAGGCCCA GGAGAATATT CAACATCCAA 1080 CCCTAAGGAA GAAATAATTT CCATGTAGCA CTCGTGCCTC ACATTCATGT CACTGCGTAA 1140 TATCTCAGAC ATCCAGTGAC TGCACTTTCC TGGCCAAATT GAGGCGGGTG CTTCTGGAGT 1200 CTGGTACATT TCTCAACTCC AGGTTATTTC TCAGCACACA AAGTACCAGG GCTGCTTCAG 1260 TCTCCTCAGA GGAGCCATTC TCGAGATGGA GTTTCTTTTT TGTTTTATTT TACTTTAAGT 1320 TCTGGGATAC ATGTGCCGAA CGTGCAGGTT TGTTATATAG GTATACGTGT GCCATGGTGG 1380 TTTGCTGCAC CTATCAACCC AAGACGGAGC TTCTTTTACC 1420
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