| Tag | Content |
|---|
EnhancerAtlas ID | HS060-09004 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr12:132076250-132078220 |
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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I131592 | chr12 | 132077543 | 132077872 |
|
Enhancer Sequence | AGGAGGGGGC CACAGAGGGG TCACGCAGCC CAGTCACCAG GGCCATGCGG CTCCACGGCT 60
TCTACGCTTG GGCACTGAGG ACCGAGGGGT TCAATCAGGT CCCAGCTCCA GTCCAACCTT 120
GGAAGCCAAG TGTTGGGAAG GGAGCATCCG AGGACAGACA GAGCCAGGGC CCCTGAGTCA 180
CTGCAGGAGG ACGCCCCCGC TGGGACTCGG CGTCCGCTGC GCTGAGCCGC TAAGGAGCCG 240
GTCTACTTGC TCCCGCAGCA GCCCGGGGGC CGGAGCTGCC GACACCAGGG AGACGCGTTT 300
TCTGCACTGA CTCCTACGCT CCCGCGTGGA CATCCCCAGC ATGATTTCTG TCTCCACCCA 360
CTTCGCACAC ACCCCGCCCC GGCCAGACAC CCCCAAACCC ACACAGGGTG CAGGGACACC 420
GCCCTGGCCT TGGCTGTGGC TGTCACACTC GCCTGTCCCG CCTTGGCCCC AAGTCCTGCC 480
AGCCCGGCTC CGTCCCCGCC CCACTCCCAG TGGCTCTGTG CCTGCCTCCC TCCCGGGCTC 540
TGCCAGCCCT GCCTCTCCCG CCACGCACAG CTCAGGCGCC TGTGGCTTGT GCGGGGATAA 600
CTTCTAGGAC ACAGACTTCC GGAAGATTCT TTCCCAGCCA ACACTGCCCC ACCCTTCCGG 660
TGGGAGCTCC CAAGTGGACA GACAGGAGAG GAGCTTCTTT ATGATTGGCT GAGCCATCCA 720
GCCAATCCCA CTCCCCTTGG TTAGTGATTG GCCCAGGGAT GGTCATAAGA CTCAGCTAAG 780
ACCAATGAGA TGCAAGGAGC TATCTGCAAG GGGAACCATG AGAATGATAT CCCCTGATAA 840
GGAGGGAGGC CCAGCCAACC CCTTTTTCTT CTGCTGGCCG TTGTAGGTTG GGGCAGGTGC 900
TGGGGGCCTG CAGCCGGGTG GAAACAGTGT GGCTTTACCT GGGACTAAGA CAAATCCCCC 960
GAGGTGGTAC TTCCAGTGCT AAAACCATAA GTCCAGACAG ACCTGCAAAT GGGCCCCAGG 1020
CGGGAGGCAG AGCCTGGTAG GCAAGCGAGA CCCTGCCCCA CCGAGGACTG GATTCAGGCC 1080
TCCCTGGAGT CACCTGCCTC TGAGCTTCTT GTCAGGCAGA GTGAGCAAAT GACCTAAGCC 1140
TATTTTAAGC ATATTGTCCT GTTACTTGCA GCCAAAAGCA TCTAAGACCT TATGACTTAT 1200
GAGCTAACGA TCCCCTTGTC AAGGTGTTAA AACCGGTTTG CAGAGATAAA TAACTTGGCC 1260
AAGGATACAG CCCTGGGAGT GATGGAGCTG GGAGTTAAAC CCAAGGCTTT CTGACTGCAG 1320
AACCACTGGA CTCCCGCAGC TCCATGCACG GCCCTTCGCG GTGCTTCTCA GTGGCCTGCC 1380
TTTGCCCTCA ACCCTGAGCC TCTTGAGCCT CTTCAAAGCA GGAAGTGGTG CTTAGTCATC 1440
CTGAACCCCC AGAACCTAGC ATGTTCTATG TCTAAATGAG TGAATGAAAC CTGAGCAGTC 1500
TAACTAGCTT CCCTGGCCTC ACACAGGGAG GTTTCTGGGT GCCTCCCACC ACTCTGGGGC 1560
CTATTGAACA CACGTCATCA TGTGTTTCTT TGGATCCGTC TTCAGCAAGG AAAACAGAAG 1620
AGAAAACCCT TAAAAAGTGC TCACTTATGT GGCAGACACT GATCTATGCC TTTTACACTT 1680
AAGGACCCAT TTGATCATCA CAATAGGCAG ATGACATTTG GGATTGGAAT GCATCTAGAC 1740
TGGTCTAGGG AAGGTGCAGG GAATATGCTC CCCAGGGGAT GTAAATGTTA ATAGAACTCT 1800
CTCCTGAGTC CCCCAACAAT CGAATGTCAC CTTCACCAAG GCAGGGACTG AACTGCATGC 1860
ATGATTGAGT AGCAGAACCT TCCTGAAATG CTGCATTGCG AAGAGGAGAC GGAGGCTCTG 1920
TGTCCTTGAG CTGAGAGGTC CTAATGTCAA GGGTTTGCTG TGACAGTTAC 1970
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