Tag | Content |
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EnhancerAtlas ID | HS047-03990 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr10:35242800-35244290 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLTF | MA0109.1 | chr10:35244102-35244112 | ATATAAGGTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr10 | 35243112 | 35243399 | chr10 | 35243779 | 35243914 | chr10 | 35244020 | 35244090 |
| | Number: 1 | ID | Chromosome | Start | End |
GH10I034953 | chr10 | 35242868 | 35243481 |
| Enhancer Sequence | AACTAACCGA GTTCCGAGAA TTATACAGAG AGGCGGCACA CTGGGTTGGT GGGGAGCATG 60 AGCTTCGGAA TAAAGCAGAG CTGAACTTCA GTCCCATCCT TGCTGCTCAC CAGCTCTGTT 120 ACTTGCTGGA CCTCCCAGTT CCTTGTCTGC AAAATAGCAA ACCTGATCAC TAAGGTAAGG 180 AAGCATCTGC CAACCCACAG TAGGTACATT AACATCAGAT TATTGCCTCA TAATGTCGTT 240 TGGAGGACTG AATTGATATT TGCTCAAACA TCTTGTAAAC TGTAAAGTGC TATAGGAACT 300 TTTTAGTAGC AACTTATTTA GGCTGCTGGG AGGCCCTTGA GGTGGAAGAA CCTAGAAAAG 360 GTAAATTGCT CTCTTCAGTC CCCAAGTGCC TGGTTCACTG CCAAGAAACC ACTCCCGAAC 420 TCAGGCTGCT CACCTGGGCT GCTGGCAGGA GGAAGCAGCC CCAGAACGGA GCCAAGCCAG 480 AGCCGGAGAA ACAGGTTCCT GCCTTCTCCG CTGACAGCCT GAGGCTCATG CTCTAATCTG 540 CAAAAATGGC AGAAGTCGCT GTAGTGTTGT AGAACTGAAC TGGGGTTGGC TCCCTGGTGT 600 GGTAAGACCA GATATTTATA TTGACCTGGA TAGTGGGAGA AAGCAAAGTG TTTATTTGTA 660 GGGAGCCAAG TGAGGAGGAA AGGGAGTCCC CACCTTTCTG ATGGCTTGTA GATAAGGATT 720 TTTTTTCCTT TTTTTTTTTT TTTTTGTTTT GAGACAGGGT CTCAACGCTG TTGCCCAGGC 780 TGGAGTGCAG TAGCATGATC TCGGCTCACT GCAACCTCCA CCTCCCAGGT TCAAGTGATT 840 CTTGTGCCTC AGCCTCCCAA GTAGCTGGGA TTACAGGAGC TCGCCACCAC GCCCAGCTAA 900 TTTTTGTATT TTTAGTAGAG ACGGGGTGTC ACCATGTTGG CCAGGCTGGT CTCGAACTTC 960 GGGGCTCAAG TGATCCACCC GCCTCAGCCT CCTAAAGTGC TGGGGCTCCA GGTGTCCACT 1020 GCCGCTCTGG CCTAAAGTGG CTTTTAAGAA AAGTTGCCAC CTAGAGTATG GCATGCTCCA 1080 TACCTTGGCA TTTTGCTCTT TGCTCGCCTG GTTCCACTGG AAGCTCAGCA AGCTCACAGG 1140 TTCTCTCCCA CACCCTGACT CAGGTCCCAC GTCCATTTCC TCAGGCTCCA GAGAAAGTCC 1200 TCACCCCTGG GCCTCCCCAG GACCCCGGGG ACACTGTACA GGGAAGACAC ATTGGAGACA 1260 ACAGCCATGG TAGTCACAGG GCCCTCAACA GTGACATCAA TTATATAAGG TTTGATGGCC 1320 TCACTTTCTC ACTATAAAGC AAAGAATGCT GCCCATCTGG CAGCCAGGGA AAGTTCTGGA 1380 GTTGGGGACC CGGCCATCCT GTGGTGCTGC CTCAGGCTTT GACTTGGAGA CTCACTGGGG 1440 CTCGGGAGAT AGCCAGCCTG GAGCTGCCTC CTCTTCCTTT GCTTTGACAG 1490
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