| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06498 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:132077140-132078300 |
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 | GGGCAGGTGC TGGGGGCCTG CAGCCGGGTG GAAACAGTGT GGCTTTACCT GGGACTAAGA 60
CAAATCCCCC GAGGTGGTAC TTCCAGTGCT AAAACCATAA GTCCAGACAG ACCTGCAAAT 120
GGGCCCCAGG CGGGAGGCAG AGCCTGGTAG GCAAGCGAGA CCCTGCCCCA CCGAGGACTG 180
GATTCAGGCC TCCCTGGAGT CACCTGCCTC TGAGCTTCTT GTCAGGCAGA GTGAGCAAAT 240
GACCTAAGCC TATTTTAAGC ATATTGTCCT GTTACTTGCA GCCAAAAGCA TCTAAGACCT 300
TATGACTTAT GAGCTAACGA TCCCCTTGTC AAGGTGTTAA AACCGGTTTG CAGAGATAAA 360
TAACTTGGCC AAGGATACAG CCCTGGGAGT GATGGAGCTG GGAGTTAAAC CCAAGGCTTT 420
CTGACTGCAG AACCACTGGA CTCCCGCAGC TCCATGCACG GCCCTTCGCG GTGCTTCTCA 480
GTGGCCTGCC TTTGCCCTCA ACCCTGAGCC TCTTGAGCCT CTTCAAAGCA GGAAGTGGTG 540
CTTAGTCATC CTGAACCCCC AGAACCTAGC ATGTTCTATG TCTAAATGAG TGAATGAAAC 600
CTGAGCAGTC TAACTAGCTT CCCTGGCCTC ACACAGGGAG GTTTCTGGGT GCCTCCCACC 660
ACTCTGGGGC CTATTGAACA CACGTCATCA TGTGTTTCTT TGGATCCGTC TTCAGCAAGG 720
AAAACAGAAG AGAAAACCCT TAAAAAGTGC TCACTTATGT GGCAGACACT GATCTATGCC 780
TTTTACACTT AAGGACCCAT TTGATCATCA CAATAGGCAG ATGACATTTG GGATTGGAAT 840
GCATCTAGAC TGGTCTAGGG AAGGTGCAGG GAATATGCTC CCCAGGGGAT GTAAATGTTA 900
ATAGAACTCT CTCCTGAGTC CCCCAACAAT CGAATGTCAC CTTCACCAAG GCAGGGACTG 960
AACTGCATGC ATGATTGAGT AGCAGAACCT TCCTGAAATG CTGCATTGCG AAGAGGAGAC 1020
GGAGGCTCTG TGTCCTTGAG CTGAGAGGTC CTAATGTCAA GGGTTTGCTG TGACAGTTAC 1080
ACAAACCAGA AACAATGGCA CCTCTTCCCA ATGTTATTAA AACAGTAAAC TATCAGGAAA 1140
GGATTTGAGG CTTTCCATAA 1160
|
