Tag | Content |
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EnhancerAtlas ID | HS176-02987 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:184985890-184987330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr1:184986798-184986815 | TAGGTCATGGTGACACT | - | 6.54 | JUN(var.2) | MA0489.1 | chr1:184986583-184986597 | AATGAATGACTCAT | + | 6.12 | JUN(var.2) | MA0489.1 | chr1:184986588-184986602 | ATGACTCATTCCTT | - | 6.8 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 184986019 | 184986474 | chr1 | 184986501 | 184986896 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I185015 | chr1 | 184984232 | 184987451 |
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Enhancer Sequence | CTGAAGAAAT CATGGTGGAA GGCAAGGAGG GGCAAGTCAC ATCTTACGTG GATGGTGGCA 60 GTCAAAAAAA AACTTGCACA GGGAAACTGC CATTTTTAAA AGCATCGAAT CTCCTAAGAC 120 TCATTCACTA TCATGAGAAC AGTGCAGGAA AGACCCACCC CCCGTGATTC AATCATCTCC 180 CACTGGGCTC CTCCCATGAC AAGTGGGAAC TGTGGGAGTT ACAATTCAAG ATGAGATCTG 240 GGTGGAGACA CAGCCAAATC ATGTCACCAG CATTCCTCCT GTTTCAAGGT CTGCTTCCTG 300 ATGTAACTAC TTGGACAGAA TATGCACACC TCCACAAGGA CAAGCAGCTG ATGGTTGGCA 360 GGGCATAGTT TGAAGCCATT ACTACTCAAG GATCATTCTT CCAAAGGAAA CACAGTCTAC 420 AGAAATGCAG CTCTACCTGC ATCAGTTTTT TATTCCTGCA CAGAATACAT TAGCCTTTAG 480 AGCCACGATT CTGAGAAATA ATCCTGACAC CCCCTCACTG GATTAAACCA GTTCCCCTTG 540 TCCTCGGAGA CCCTAAAAGC TAAGAAAAAG TTCACTGAGA TACTGGCCAT GCAGAATGGA 600 AGATGGTTAT GCCTCAGTAT ACCCCTTCCT TATTAACCTT TAACCAGAAT TCTTTCCTAA 660 GGAGTAAGCA GAAACCAGCT CTGGAAAACA AGAAATGAAT GACTCATTCC TTTATTGCTG 720 TTAGCCAGTC ATCGCAGGCC ATGACTGGAT GTTTTGCAAT TTCTGTACCA CAACTGACCA 780 GCATTTCTTC TTAACAAGAG ACCTTCAACC ATGGGGGGGG TACTGGTTGA TCTATGGAAG 840 ATGCACAGTG AGGGTTTTCC TGTCCTCTGC TTCACATGTT GACATCAGAG AGCTAAAAAC 900 TCCACCCTTA GGTCATGGTG ACACTGCTAT TTTTTGAACC TGCGATCCAT GAAGAGGCCT 960 AAAGCTCAAT TGTGCATATG CATGTTTCTC CTTTCATAAA CATTCATGAT GCCTCATATA 1020 GCTTATTAAA TATATCTATT TGGGTACCCC ATCCAGCATA AATTCCTGTT CCTTTTACCC 1080 CTCCCTTGAA GCACTGTGTC TTCATGTCCA CTGGAAGCTC CGCTTCCTCC TACGGGTTTT 1140 GGTACCTTTA GGAATAAAGC TCTCTATTTT AAATTTATAG AATATTGTTA CTTTTGTGGT 1200 CCACAGTTCC TCAAGATCTC CATTAAGATG TCAGAGTCTT AGTGTCGAGT TGTGGAAATG 1260 AGAAACACAC AGAGACAGTT GCTGCCATCA TTAGCCACCT GCCAGCATCT GTCCTCACAC 1320 TCTGCCTTCC TGTTTCTGTA GCAGAATTAC CCATACCCTT ATCTAAAGCT GTTCTTTCAT 1380 CTGTACACTG GAGCTCAACC CTTGTCACCT ACTCAAGGGT ATCATTCCAG TAATTCTCTC 1440
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