Tag | Content |
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EnhancerAtlas ID | HS073-03593 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr12:132077080-132078690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GRHL1 | MA0647.1 | chr12:132077478-132077490 | AAAACCGGTTTG | - | 6.62 | GRHL1 | MA0647.1 | chr12:132077478-132077490 | AAAACCGGTTTG | + | 6.74 | Nfe2l2 | MA0150.2 | chr12:132077678-132077693 | TGCTTAGTCATCCTG | - | 6.68 | RARA | MA0729.1 | chr12:132078184-132078202 | GAGGTCCTAATGTCAAGG | + | 6.26 | TFCP2 | MA0145.3 | chr12:132077479-132077489 | AAACCGGTTT | + | 6.02 | TFCP2 | MA0145.3 | chr12:132077479-132077489 | AAACCGGTTT | - | 6.02 |
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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 |
GH12I131592 | chr12 | 132077543 | 132077872 |
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Enhancer Sequence | CCCCTGATAA GGAGGGAGGC CCAGCCAACC CCTTTTTCTT CTGCTGGCCG TTGTAGGTTG 60 GGGCAGGTGC TGGGGGCCTG CAGCCGGGTG GAAACAGTGT GGCTTTACCT GGGACTAAGA 120 CAAATCCCCC GAGGTGGTAC TTCCAGTGCT AAAACCATAA GTCCAGACAG ACCTGCAAAT 180 GGGCCCCAGG CGGGAGGCAG AGCCTGGTAG GCAAGCGAGA CCCTGCCCCA CCGAGGACTG 240 GATTCAGGCC TCCCTGGAGT CACCTGCCTC TGAGCTTCTT GTCAGGCAGA GTGAGCAAAT 300 GACCTAAGCC TATTTTAAGC ATATTGTCCT GTTACTTGCA GCCAAAAGCA TCTAAGACCT 360 TATGACTTAT GAGCTAACGA TCCCCTTGTC AAGGTGTTAA AACCGGTTTG CAGAGATAAA 420 TAACTTGGCC AAGGATACAG CCCTGGGAGT GATGGAGCTG GGAGTTAAAC CCAAGGCTTT 480 CTGACTGCAG AACCACTGGA CTCCCGCAGC TCCATGCACG GCCCTTCGCG GTGCTTCTCA 540 GTGGCCTGCC TTTGCCCTCA ACCCTGAGCC TCTTGAGCCT CTTCAAAGCA GGAAGTGGTG 600 CTTAGTCATC CTGAACCCCC AGAACCTAGC ATGTTCTATG TCTAAATGAG TGAATGAAAC 660 CTGAGCAGTC TAACTAGCTT CCCTGGCCTC ACACAGGGAG GTTTCTGGGT GCCTCCCACC 720 ACTCTGGGGC CTATTGAACA CACGTCATCA TGTGTTTCTT TGGATCCGTC TTCAGCAAGG 780 AAAACAGAAG AGAAAACCCT TAAAAAGTGC TCACTTATGT GGCAGACACT GATCTATGCC 840 TTTTACACTT AAGGACCCAT TTGATCATCA CAATAGGCAG ATGACATTTG GGATTGGAAT 900 GCATCTAGAC TGGTCTAGGG AAGGTGCAGG GAATATGCTC CCCAGGGGAT GTAAATGTTA 960 ATAGAACTCT CTCCTGAGTC CCCCAACAAT CGAATGTCAC CTTCACCAAG GCAGGGACTG 1020 AACTGCATGC ATGATTGAGT AGCAGAACCT TCCTGAAATG CTGCATTGCG AAGAGGAGAC 1080 GGAGGCTCTG TGTCCTTGAG CTGAGAGGTC CTAATGTCAA GGGTTTGCTG TGACAGTTAC 1140 ACAAACCAGA AACAATGGCA CCTCTTCCCA ATGTTATTAA AACAGTAAAC TATCAGGAAA 1200 GGATTTGAGG CTTTCCATAA CAAATACAAG TGACATCTTG GTCACAAAGT GACAATTCTT 1260 CAAATCCTAG GCAATAAAAT ACAGTAGATT GATATCCATT TTTCTTTTAA GGACACTATA 1320 TTTTGTTCTT ATGTCACTTC TGTGAAAGGA AATGAAATCT GTTTTTCTCA GTGGAAGCTG 1380 GAAGATGAGA ATGTCAAAGG CTACAAGGCA CACATGCTGC TTTTCCCTGC CAGTGGCTGT 1440 TCCCTCTTCT GAGACCAGTA TCTCTGGTCC CTCTCTGAGG AGTCCCCTTT CCTCCACATC 1500 TTTGGGATGA GCCTTACTGC AGGACCGTGT CAGAGGTGGA TTTTGAACCC GGCTCACACC 1560 AACCAGCGTC TACATTTCAT CCCATCTCTT CTTCCCCAGT CAAGGTGACT 1610
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