Tag | Content |
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EnhancerAtlas ID | HS047-31291 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:99058050-99059080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr7:99058382-99058392 | GGTGCCAAGT | + | 6.02 | USF1 | MA0093.2 | chr7:99058235-99058246 | GCCACGTGACC | + | 6.62 | USF2 | MA0526.2 | chr7:99058233-99058249 | GGGCCACGTGACCAAA | - | 7.21 | ZNF263 | MA0528.1 | chr7:99058199-99058220 | AAAGGAGGGGAGGGGGGATAG | + | 6.12 |
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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 |
GH07I099460 | chr7 | 99058401 | 99058550 |
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Enhancer Sequence | TGAGTAACAG CTTGCTGGGA GTAACTCCAG AAAAGGGTCT CGAAAAAAGC AGTAACGTGG 60 CGGACAGGAA AGATTACTGC AAAGCTAACA TTTACTTGAC ATTATTAGCT TATTTAATCT 120 TCACAACAAG CACTTCATGT CTTTACCTTA AAGGAGGGGA GGGGGGATAG ACTCAGAGAG 180 GTTGGGCCAC GTGACCAAAG TCACACACAC AACGTGGGGT CAGGACTGGC CCTCCTATGT 240 CCCTGAAGCC AATATGAGGG TGCCCTGTCC AACCCTGGGG ATGTGTCGCT GGAGAACGTA 300 CAAGAGGGGA TGTGGAAGGA GAGCGGTGTG ACGGTGCCAA GTGTCTCACT CAGACTTGAC 360 GCACTTGTTT ACTGGGGAAG GGCTTCAAAC AGCACCTGGG TTCACACAGC TGGCAGACTC 420 ACCAGATGGG CCAGCCCGAG CAAGTATAAT GAAAGAAACC CAAGGAATTT CCACCTCCAG 480 CATCCTGGGA CCACGGACAC CAACAATTTC CAGAGATAAA AATAAGAGAT AACACATTCC 540 GAGAAGTCAA GTGACGAAAA ACCACTCCAA ATGACTGAAC GGCCCCAGAT CGTATTCCAA 600 TGGGAGTCTG AGAACAAGGA ATCAGAAGGG CTCCTGGCTG AGGCTGTACT GTCCTCACAT 660 TTGGGCCCAG GAGGAGACTA TGGAGGGCCA GGGAGTGGGT GGGCCTGTGG GCGTCAAGGA 720 GATGCATTTA AGAAAGGAAT CGTCTCCCCT GTTCTCCCTG CAAAGATTTA TTTATTTATT 780 TCTGAGAGAC AGGGTCTCAC TCCATTACCC AGGCTGGAGT GCACTGGTTA TTCACAGGTG 840 TGGTCACAGC TCACTGCAGC CTCACTGAGC CTCCTGGACT CAAGTGATCC TCCTGCCTCA 900 ACCTCCTGAA CAGCTGGGAC TACAGGTGTG TGCCACCACA CCCAGCTAAT GATAAGTTTT 960 AAAAAGCTTT TAGCAGATGT CCTATTGAGG GCAAAGAGTC TAGGACCACG GTGCCTTCTC 1020 AAAGATAACC 1030
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