Tag | Content |
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EnhancerAtlas ID | HS147-01350 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:44348660-44349630 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr1:44349183-44349194 | AGCCTCAGGCA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 44349345 | 44349459 | chr1 | 44349112 | 44349325 |
| Enhancer Sequence | TCTCACTCTG TTGCCCAGGC TGGAGTGCAG TGGCAAGATC ATAGCTCACT GCAGCCTCGA 60 CCCTTCCAGG CTCAAGCGGT CCTCCTGCCT CAGCCTCCCA AGTAACTGGG ACTACAGGCG 120 TGCACTACCA TGACTGGCTA AATTTTTCAA TTTTATTTTT CATAATGACA GGGTCTCAGT 180 GTGTTGCCTA GGCTGGTCTC AAACTCCTAG GTTCAAACAG TTCTCCCACC TCAGCCTTCT 240 AAAGTGCTGG GATTACAGGC ATGAGCCACC GTGCCTGGCT AGGTGCCCAT TCCTGAGCCA 300 CTTAGGAAGG GGTCTCCTGA TTGGTCAGCC CAGACATGTG CCCATCCCAG TAGCAGTGGT 360 GGGGATCAGC CGAACCAGGA GCATATGGAA TGAAAAGGGG GATGCTATTG TAGAAGACAG 420 GGGAAGAGAT GTGGATATCC ACTGCAACGT GCCAACAAGA AAGAGCATGA ACTGAGTGCC 480 TGAAAGTACC AGTGATGATC CAGCTTGAAA TTGGTCCTGA CACAGCCTCA GGCACCAGGC 540 CAGCCCTGCA GTGCTGATGC ACGCCCTGCC TGGCCTTTTC CTTCTGTGCA GTATTTGCAT 600 CTCAGCTGCT TTGTTTACAC CTAGTCAGAA TGCACTTGCC TGCCCATTCT TCCTCACACA 660 TTGCTCCACC TGCCTGGGTG GAACTAGAGG GCAGAGTTAC AAGGGTGCGG GGTGGGGAGG 720 GTGCCAGGCT GAAGTTCCTC TGCCGTTGAT GGGGGCTACT TCCCTCCTCC AGCCTCAGCA 780 TTCTCTCTCC TTATCTTGAA GGGACAGTTA CTTATGGTTC TCTTCTCTTC TGTGCCTTTG 840 TCTTACAACT ACCCTTCTGA ACATTCTCCA CCAGGCTTAA CGTTTATTTA CTTGTCTTTC 900 AAGGCTTAGC TCAGCTTTGC CATTATCTCC TTTGAGATGT CTTTCCAGTA CCCTCAAGTT 960 GGTCAGTGAC 970
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