Tag | Content |
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EnhancerAtlas ID | HS052-18606 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:16961020-16962220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr19:16961265-16961277 | GTTTGTTTGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH19I016850 | chr19 | 16961041 | 16961190 | GH19I016851 | chr19 | 16961284 | 16962172 |
| Enhancer Sequence | TGGTAAAAAT AGTATACACT AATGAAAAAA TAAGTATTAG CAAGAGTATC AAATTTTTAA 60 TGCAAACTTC CTCTCCCTTG ACTCAGTTCT TAGTCATTCT TCTCAGAGGT TAGCACTTCT 120 AAGTGTCTTG TATATCTTTC CAGAAATTTC CTCTGCATGT GTAACAAATA CTTTTTACAA 180 AGCGACACAC GGCATCCTAT TTGTTCTGCC CCTTGGGTTT TTGGGGTTTT TCCTTGTTTT 240 TTTTTGTTTG TTTGTTTTAT TTCAGGTATG CCTGTCCCTA ACAGCAGCCC AGAGCCAGCC 300 CATAGTATCT GATCGCTGCG GGCTGATTTG TTCAGATGCA CCATGACTTG TCCATCTCAC 360 CCACACTTTA GGTCTTTGGG GGTGTCTTTG CATCCAGGTC CTGTGGTGGC AGGGGAAGGC 420 GGAGTACGAT GGAGGTGACC GCAGTGGCAC AGAACGTTGT AGGGCCTCTC CAGCTCTGCC 480 CACGTCCTGC AGAAAAGCTG CGGTCTGTCC ATCGTCCCCT GCCTGTCCAG CCTTCCAGTA 540 TGTTCATAGT AGACTGTTGC AGAACAGTTC TTTGTAAATG TCATTGGCAC CCTGTAGGCA 600 CCCTGCTCGG GACAAGCATC CTCGACCTGT TAGCCGATGG CTGGAGCCTG GGAGGCAGGC 660 CCCGAACCAG CCACGAGCCC CACTCTGCTC CCAGCAAGTG ACGACATCAT CCCCCAGAAA 720 CGTTTTGTCA TTCATAGAAA AGACTTCAAA ACCTGGCCCC AAGGCCCCCA CCAGTGCCCT 780 GGCAAACATC AGCCACTTCC CCTTGCTGCC TGTTTCTCTG TCCACTGCAC CTTGTGTTTC 840 TGTGGTGCCG GCATGCACAC GGCGAGATGC CCCACCAGTG GCCGCCACAT GAGCCCCCGC 900 ACGGGAAGAC CCAACTCAGC TGTCTCCCTC CTGAAACCCC CAGCCCTTCT CCCTCCCTTA 960 TCCATAAAGG CCTCACAGGA GCTTTCTCCC AGCCTGGCAG TGTTAGTCTG TGATGATTCG 1020 GTTACCTTGG AATGTGAGCA TCTTGCTGGA GTCACCTCAC GCATGGACGG AGCATCTGGC 1080 CTGGTGCCCG TGGCCACCAT TGCCCACCGG GCTGTGGGCT GAGCTGGAAG CAGCTCTGCA 1140 TGCTCAGGTG CATGGGTCCA GCCACGTCTC CGGTGCTGAC CACCTCCCAC ATGTGTCCTT 1200
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