| Tag | Content |
|---|
EnhancerAtlas ID | HS059-12135 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr12:132076820-132078880 |
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 | CTCAGGCGCC TGTGGCTTGT GCGGGGATAA CTTCTAGGAC ACAGACTTCC GGAAGATTCT 60
TTCCCAGCCA ACACTGCCCC ACCCTTCCGG TGGGAGCTCC CAAGTGGACA GACAGGAGAG 120
GAGCTTCTTT ATGATTGGCT GAGCCATCCA GCCAATCCCA CTCCCCTTGG TTAGTGATTG 180
GCCCAGGGAT GGTCATAAGA CTCAGCTAAG ACCAATGAGA TGCAAGGAGC TATCTGCAAG 240
GGGAACCATG AGAATGATAT CCCCTGATAA GGAGGGAGGC CCAGCCAACC CCTTTTTCTT 300
CTGCTGGCCG TTGTAGGTTG GGGCAGGTGC TGGGGGCCTG CAGCCGGGTG GAAACAGTGT 360
GGCTTTACCT GGGACTAAGA CAAATCCCCC GAGGTGGTAC TTCCAGTGCT AAAACCATAA 420
GTCCAGACAG ACCTGCAAAT GGGCCCCAGG CGGGAGGCAG AGCCTGGTAG GCAAGCGAGA 480
CCCTGCCCCA CCGAGGACTG GATTCAGGCC TCCCTGGAGT CACCTGCCTC TGAGCTTCTT 540
GTCAGGCAGA GTGAGCAAAT GACCTAAGCC TATTTTAAGC ATATTGTCCT GTTACTTGCA 600
GCCAAAAGCA TCTAAGACCT TATGACTTAT GAGCTAACGA TCCCCTTGTC AAGGTGTTAA 660
AACCGGTTTG CAGAGATAAA TAACTTGGCC AAGGATACAG CCCTGGGAGT GATGGAGCTG 720
GGAGTTAAAC CCAAGGCTTT CTGACTGCAG AACCACTGGA CTCCCGCAGC TCCATGCACG 780
GCCCTTCGCG GTGCTTCTCA GTGGCCTGCC TTTGCCCTCA ACCCTGAGCC TCTTGAGCCT 840
CTTCAAAGCA GGAAGTGGTG CTTAGTCATC CTGAACCCCC AGAACCTAGC ATGTTCTATG 900
TCTAAATGAG TGAATGAAAC CTGAGCAGTC TAACTAGCTT CCCTGGCCTC ACACAGGGAG 960
GTTTCTGGGT GCCTCCCACC ACTCTGGGGC CTATTGAACA CACGTCATCA TGTGTTTCTT 1020
TGGATCCGTC TTCAGCAAGG AAAACAGAAG AGAAAACCCT TAAAAAGTGC TCACTTATGT 1080
GGCAGACACT GATCTATGCC TTTTACACTT AAGGACCCAT TTGATCATCA CAATAGGCAG 1140
ATGACATTTG GGATTGGAAT GCATCTAGAC TGGTCTAGGG AAGGTGCAGG GAATATGCTC 1200
CCCAGGGGAT GTAAATGTTA ATAGAACTCT CTCCTGAGTC CCCCAACAAT CGAATGTCAC 1260
CTTCACCAAG GCAGGGACTG AACTGCATGC ATGATTGAGT AGCAGAACCT TCCTGAAATG 1320
CTGCATTGCG AAGAGGAGAC GGAGGCTCTG TGTCCTTGAG CTGAGAGGTC CTAATGTCAA 1380
GGGTTTGCTG TGACAGTTAC ACAAACCAGA AACAATGGCA CCTCTTCCCA ATGTTATTAA 1440
AACAGTAAAC TATCAGGAAA GGATTTGAGG CTTTCCATAA CAAATACAAG TGACATCTTG 1500
GTCACAAAGT GACAATTCTT CAAATCCTAG GCAATAAAAT ACAGTAGATT GATATCCATT 1560
TTTCTTTTAA GGACACTATA TTTTGTTCTT ATGTCACTTC TGTGAAAGGA AATGAAATCT 1620
GTTTTTCTCA GTGGAAGCTG GAAGATGAGA ATGTCAAAGG CTACAAGGCA CACATGCTGC 1680
TTTTCCCTGC CAGTGGCTGT TCCCTCTTCT GAGACCAGTA TCTCTGGTCC CTCTCTGAGG 1740
AGTCCCCTTT CCTCCACATC TTTGGGATGA GCCTTACTGC AGGACCGTGT CAGAGGTGGA 1800
TTTTGAACCC GGCTCACACC AACCAGCGTC TACATTTCAT CCCATCTCTT CTTCCCCAGT 1860
CAAGGTGACT GGCTCATGGA AGACACATGG ACAGTTACTG ACAAAGCTGG ACCCCCAAAA 1920
GATGGGGTCT TTCCCTGTTA GTGTTGGGTG TCACTAACCC AATACATGAA ACCAAAAGTG 1980
TCAAGTAGTG CAGGTGTTAT TCAATGGCCA TGAAATTGAC AAACGGAAGC ATCACTCACA 2040
AGTCAACTTC TTGACATGTG 2060
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