| Tag | Content |
|---|
EnhancerAtlas ID | HS076-12818 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr12:9966180-9967320 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:9966645-9966665 | CCCCACAACACCCCACACAC | + | 6.86 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 9966772 | 9967089 | | chr12 | 9966400 | 9966894 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH12I009813 | chr12 | 9966197 | 9967510 |
| Enhancer Sequence | TGTCTACAGG CCCTCAGTAC TTTCCTCCAC AAAGAAGAAC CAAAACACCC AGTAGAAAAT 60
CAGACTTGGA ATACAGCATC TAAAAGAACA CATTCGAATT AAGCAGAGAA GCGACAGGAA 120
AGCTCTGAGG CAGGAAAGAG ACAGAGGGGA GGCAGGTAGC TCAGCTGAAA CTGTCTGGGA 180
GCCCAGAGAC TTCTTAGTGC AGGGAAAGTG TGTCCACATT CCCACCGCAG ACTCCTGCAG 240
TCGTAGCCAT GGGAGAGCCC TGGGGGCCCC GAGACTAGGA TGGGGAGCTG CCTGGAGCCT 300
GCACCGCGCA ACAGCACTGT TCCAGGACGG AGCTCAGGCG AGGTCCCACA CACCTCCTGG 360
ACCAGGCTAT TTGGAGCCCA GCCCCAACAA GACTTCATCC TGCCTCGGGT CTCAACAGCT 420
TCCGCATCTC CACATCCCTG GAGCCCCGCA GACATCCTTC ACTTCCCCCA CAACACCCCA 480
CACACCGGGA GGGCTGTAGT GGCACAAGGC TGATTGGTGC CAGCCGTGTG GCTGGGTCCC 540
TGGCACTCTA GCCCCAAAGG TGTTCTACAC CCCGGGGGAA TCGGCAGTGC AGTGCACTGG 600
GGAGGCTGCC TCCAGTCAAA GGGAGCCAAA ACGCAAGCTC CCCAGAGCCT GACAGCCACT 660
TGAGTGAGGT CGCTGCCACT GACAGCCACC CCGACTCCCA ATAGCAAAGC AGCTGCGCAC 720
CGACAGGCTT TCTCCACCCA CTGCCATCTC CACAGCCGGG ACTGCCACCA CCCAAGCACG 780
CCGCTGGGAG GCGCCTGGGG ATTGCCCACT CTGCCAACCA CAGCCTGAGC CCTGAGCACA 840
ACATAGGGGA TTGGGTTGTC TGAGGGTAGG ACCACACCAC CAAGCAAAGC CTCTCCCAGT 900
GCCTGAGCAC ACTGCCCAGG GGCCTGGGGA TCCATGGCCC TGTCCCACCC GTAGCTCCGC 960
GTATGCTCCT GCACCATCAG GAGGCCTGAC TGAAGACCCA GCCTGGCTGC TCGCAAGCCC 1020
CACCTACCAC AGCCTGTGTG CACCATCAGG AGGCCTGAGG TTGGACCCGC AAAGCCTGGT 1080
ACGGCCCACA AGTGCCCAAG TGCATCATTC AGTGGCCTGG GGACCGCCTT TCCACCACCG 1140
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