| Tag | Content |
|---|
EnhancerAtlas ID | HS139-04925 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr1:224390720-224391780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:224391013-224391033 | GGTGAGTGTGTGGGTTGGGG | - | 7.16 |
| | | 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 |
| GH01I224202 | chr1 | 224390586 | 224394441 |
| Enhancer Sequence | CCTGTCTAGT TTTTGTATTT TTAGTAGAGA TGGGGTTTCA TGACGTTGGC CTCGAACTCC 60
TGATCTCAGG TGATCTGCCC ACCTCAACCT CCCAAAGTGC TGGGATTACA GGCGTGAACC 120
ACTATGCCCG GCCCAAAGTT TGTATTTCTT AAAAAGGATT TTACAATGAT AATTTTCCTC 180
AAATTCAGAG CCCGCTTTCT ACTTAGTATA ACTGATGGGG TTTTCTAATG ATAATATGAA 240
CCGTCCCACT CCCAGGAACA CAGGCAGCAG GCCAAGCAGT GGCTCTCAGT GAGGGTGAGT 300
GTGTGGGTTG GGGGAGGGGC AGCCCATGAA CACCCCAAGC TACTTCCACA CTCCAATGGT 360
CAGGAGAATG CAGAATTGAA AGCAGGAACA GGAGTCTGTG GCCTGGAGCT CACATTTAAC 420
CAAATAGTTT TCAGAGCTGG CTCAGAAACA GTTCTCCAAA CCACAGCACT CTGCAAAGCC 480
CAGCTGAGAT CATCAGATGG CCATCCCAGG ACAAGCAAGC AGAACTCCTC GGCCTGGGGT 540
CCTGTTTGCC AAAAGGAATC TGGATGTTGT GAGTGCCTCA AGTCACTGAC TCCCCCTCCT 600
CATGACCAGG GGATGATGAG CAGCTGTTTA ATAAGCCACC GGTGTCAAAC CCGGTGGCCG 660
GGGGCCCAGG AAGAACCCCG ACTTGGGAGT GCAGCCCCTT AGGCATCTCA GAGCCAGGGA 720
CAGGAAAGAA AGACAGGTTG TGTTGCCAGT GTGACTGAAG CAAATTACCT TCCCTGGGCT 780
GGTTTCCTTT ATCTATCTTG TCTATCTTTT CTTACCTCCC TCCCGGGACC TTGAGATGCC 840
TTGGAAATCA GATGGGAAAA GCACTGTCAC TCACTGCAGG GGTTGTGGTA ATGCTGGTTA 900
CTGATGCCAC TGGGAACACC AAGCTACAGG AGTCAGTCAT TTGGGACAGT GCCAGCAGTC 960
AGAGCACAGG TCACACTTGT TCCAAACCAT GGCAGTCGGT GCTTGCTGCC CAAACTATTG 1020
TCTGAGTTTA TTTTTTAAGA AATAAAAAAA AAAATTATCA 1060
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