Tag | Content |
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EnhancerAtlas ID | HS053-13108 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr14:104042560-104044000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr14:104043866-104043877 | ATATTTACATA | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 104043691 | 104043827 | chr14 | 104042726 | 104043413 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103576 | chr14 | 104042351 | 104043998 |
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Enhancer Sequence | TGAACCCAGG AGGCGGAGGT TGCGGTGAGC CGAGATTGCG CCACTGCACT CCAGCCTGGG 60 TGACAGAGCG AGACTCTGTC TCAAAAAAAT AAAAAAAGAA AGTCGATTGT TTATGGATTA 120 AAGAGTTAGA TACATAGTTC GCAGCTGTAG AGCATCTAAT AGGATATAAC AGACTCACCA 180 TTATCTGGAG GAATGATACC GTCCTGAGCT TGAGGGTGAA GACAGAGATA TTCAAGAACA 240 TAAAAGCTGA AAACGTCTGT GTTAAGACTC CTTTTGATCC AGGTTTCTGG ACAGGAGAGT 300 TTGCTGAGCA TATGTGGAGG TGGCTCAGTA CCCAGAGGCG GGTGGAGCTG GCCCCAGTCA 360 TGGCCTGTGC TCAGACGCTA GGACCAGAGC AATTTCTTCC TCATGTTTAA ACTTTTCTCC 420 TAGGCCACTG CCTTACCTTT CTCATGCTAT AAACTGGCTT TCTCTGCCTC CTTGTTTATC 480 CCTCCTAAGT TCAAAGAAGC AGTCAGCTGA GGAGGCTGCC TTTCCTCAGG CTGGCTCCAG 540 CCCGGTTGGG AGGTGCCCGG ATTAGCTGAG GCAGAGGTGG GGCTTGTGCA GAGAGCCTGG 600 CTGCTGCCAT GGAGACGGGA GGAAGCAGGC AAAAGAGCAG GCCTGCTGGC AAAGGATCAG 660 AGGGCTGGGT AGGCGCAGGG ATCAGTGTCC CGGAAATGTG AGGAAGGGCA AGTGCTGGCA 720 GCAAAACAAC ATGGGCAATT TGGACTTCAG GAAAAGCTGC CACAAATACT CAGAAATAAC 780 ACACATTTAT AGACAAATAA CGTGACTACA AGAAGAAAAA ATTGTTCAAA CTCTAAATTT 840 TACAAGGCAT ATTTGTTTAT TTTTTTGAGA TGGAGTCTCA CTCTGTCACC AGGCTGGAGT 900 GCAGTGGCGT GATCTCGGCT CACTGCAGTC TCCACCTCCG GGTTCAAGCA ATTCTCCTGT 960 CTCAGCCTTC CAAGTAGCTG GGATTATAGG CACCCGCCCC CACACCTGGC TAATTTGTGT 1020 GTGTGTGTGT GTTTCGTAGA CGGAGTTTCA CCATGTTGAC CAGGCTGGTC TCAAACTCCT 1080 GACCTCAAGT GATCTTCTCA TCTCAGTCTC CCAAAGTGGT GGGATTACAG GCATGAGCCA 1140 CCGCGCCCAG CCTACAGTGC ATATGCAACA AGAAGTCATC ATTTCATGCT TACTCAGTTC 1200 ATGGGGGAAT GTTTTCAGTC TTGAGACTCA GTGCTGGCGG AGTTACATCA AAGGTGGATG 1260 GCAGCAGAAA ATCCTCAGCC CCTTTTCCAG AAGAATTTAG CTACACATAT TTACATATAC 1320 CCCAGGAAGC AGGCAAATGA TGCTCATGAA TCATCTCTAA GAATTCATGT GAGAGCCAGG 1380 CTTGGTGGCT CATACCTGTA ATCCCACCAC TTTGTGAGGC TGAGGTGGGT GGATCACTTG 1440
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