Tag | Content |
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EnhancerAtlas ID | HS129-38198 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr9:139119920-139120830 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr9:139120092-139120106 | TGGTGACGTGTCAT | - | 6.78 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_58526 | chr9:139098731-139137766 | Ly1 | SE_60916 | chr9:139111911-139138466 | DHL6 | SE_65679 | chr9:139119306-139125149 | Pancreatic_islets |
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| 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 |
GH09I136227 | chr9 | 139119619 | 139120821 |
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Enhancer Sequence | CCCGGACTCC TGGCATTTCT GTAACAGGGC ACTCAGATCT AGATTCTTGT CTGATTTGTT 60 TGGTGACATT ACTTTGTAGG TAGTGGAACA TGCTTCCACC CAGAGGCAAG CGACGCCTCT 120 CTCCTTAGTG ATCACGACCT AAATGCATTA ATGCACCAGG GCTGCAGTGA AATGGTGACG 180 TGTCATCTCT CACCGTTTGC TCATGATGAG CTGGGACAAT TCTGTAAAGA GAGACCTGCC 240 CTCACTGCAA CCCAGCGGAA TGACTCACAT GAGGAAGGGG AGTGCCTGGC TCGTGCTTCA 300 GTCACCAGTA TCAAAGTCAT GGTTTCCGAA GCTGACCAGT GAGGTTTTCT TTTTAAAAGA 360 TTTGTGTTCT TCCTCTGGGA TGTAAAAATT GCACTGCCAA CAATTCACAA ATATTTCCTG 420 GCTCCTCACT CTGTAGGGGT CCTTCCAGGC CCTGAGACTT TGAGGGGACA GCCTAAAGGG 480 GCACCACTGG GTCAAGGGAT GGGTGCTGGC TATCCTGGAG CCTGGAGGCC TCAGCAGAGT 540 CGGCAGTGTG GCAGGGCACG CCGCACCGTG GGAGAGGCAG GTGCAGAGGC GAGACCCAGG 600 CACCCAGCAA ATGGACCTGC CTGGAGGAAT GGAGCCAGCC ACGTGGGGTG CTGCCCTGGC 660 ACAGCCTTGT GACCGGAAGC CCAGTGATTT CTGAACGGGA GGGAACGTTA TGTCTGCCTG 720 TCACTGAGAT ACTGATGAGG CTCTTTTTTG CCTTGTATTC CGATTCTGCC CACTTGTCTA 780 AATCAATGAT TCCACTATAA ATCATGTAAA AAGAGTAAGA GTCTTTTCTG AGAGCGAGCT 840 ATGATCTCAA ACTCCAGAGG TTCTGTTAAA AGCATGCCTG GAAGAGACGG AACATATCAC 900 CAGACTCTGT 910
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