Tag | Content |
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EnhancerAtlas ID | HS042-11442 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr12:117770710-117772420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr12:117771332-117771352 | AATGGGGGGGTGTGTGGGGG | - | 6.38 | RREB1 | MA0073.1 | chr12:117771334-117771354 | TGGGGGGGTGTGTGGGGGGG | - | 6.72 | SPI1 | MA0080.4 | chr12:117771193-117771207 | CACTTCCTCATTTC | - | 6.22 |
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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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Enhancer Sequence | TCTTAACTCC TAACTTTCTC CCTGAAATGC TGGAATCTTG CAAGTCACTG ACTCTCTCAG 60 GCTCAAAGAA ATGGGGTCTG GTTGGGGTAC CAAAGGCCAA TGGGGGCCCA GCTGGAGATG 120 CTGTGGCCCA GGTGAGGGGC AAGCACCTGT AGCATGTGCC CACGGGGCCG TGTACATGCA 180 CAGTGTGGCA CATCTGGGAT GGGGCAGGTG ATCTGTGGGT GTGGGTAGGG TGGGAAGTAG 240 CCGCCCGTCC CTACTTGTAA TTATTAGTTT GTTGCAAGTT CAAAAAGATA GGTTTGGTCA 300 CACTACAAAC ATCAATACCA GCAAGATGGG TAGGAGACAT CAGAGAACCC TTCCATCTCT 360 TTCCCTGCTC CCCACTCAAG TGCTACTTCC ATCTCTGTCC CAAAGCCCCT TCCTGCCAGC 420 AACCTCACCA TGCTTCAGCA CCAGGAGGGA GCCCCCATCT GCCATGACTA ACAAACTGAC 480 ACTCACTTCC TCATTTCCCT TTTAGCGACT TCCCAGGGTC ACCCCAGGGC TGAGGCAGCT 540 GACAAGCTCC TGCTGCCTCT GAGAGCAGAA GGTGGGTGCA GAGACCCCTC CCAGAGGGAG 600 GTGCCACCTC CTGGATCCCC TCAATGGGGG GGTGTGTGGG GGGGATAATT AGCAAGTTCA 660 GCCTCCCCTT TGCAGCCTGC ATTACGTAAC TCTGTCAGCC CCTCTGTGTG GGTGAGGAAA 720 TAATGAATCC CCGGGCTCAG CCTGGGCTGC GTTCTCCATC TGGCGTTGCT CTGTGTGTGT 780 GTTTCTGTGT ATTCATGCGT CGCCCGCGTG CTGTGTCATT TCTCTGCTGT GTGTGGCCCG 840 GGTGTCAACC GGCTGAGTGT CTTTCGGCAT CTTGCTGCTG GGTTCTGGTT TGCAGGGAAA 900 CCCATCCAGG ACCGCTGTGC CCTTCTCTCT CCTTGCTTCC TTAACCCTCC CCAAGCCCCA 960 TGTCCTGCAG GTACCAAACC CAGGATGCTC ACTGTTCAGT TGGTGGCAGA GACAGCCGGG 1020 ACCTCCAGAG CTCTCTTGAG CATCCCGTTT GGCATTAAGG CTTAATTCTT TAATGAAAGA 1080 AGCAACTGAA AGGCGACCTC TTGGGGAGGC AAGGCCCCCA AGCTGACTTC CTCCAGACTC 1140 TGGCTTGGGC CAGACCTTAC TAAAGGACAG AGGCGGGAAT TAGCCTTTGG TGTACTTTGC 1200 TTAAGGAAAA AAGAAAACAG AAATGAAGCA ATTGGCAACA GCCCCTGGCC ACTCTCAGCA 1260 CGTTCTTCTC TCTTTCTCTG CTGCATCCTA GAATCAGGGA GGGCTCTGGG CTGGTGCTTG 1320 GGAAATTGGT GTGCTGTTTC TCTCTCACAC CTTGGCTGTA GAAAGGAAAC TTGATCTTTG 1380 GAAGGAGTTG GAAGGAAGCT GGGCTGGGGA GAGGCAGATA TATTTTCTGT CTGCTGAGAG 1440 ACAGAGACAG AGAGGGAGGG AGACAGCAAG CTCTGGGTCT GAGCTCTGTC AATTAGCTTC 1500 TTTTTTTTTT AGACAGAGTC TCACTCTGTC GCCCAGGCTG GAATGCAGTG GTGCGATCTC 1560 AGCTCACTGC AACCTCCACC TCCTGGAATC AAACAATTCT CTAGCCTCAG CCTCCCGAGT 1620 AGCTGGGATT ACGGCTCCCG CCACCACACC TGGCTAATTT TGTATTTTTA GTAGAGATAG 1680 GGTTTTGCCA TGTTGGACAG GCTGGTCTCG 1710
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