Tag | Content |
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EnhancerAtlas ID | HS129-11258 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:34960190-34961140 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr14:34960393-34960404 | TGTTGTGCAAT | - | 6.14 |
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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 |
GH14I034491 | chr14 | 34960841 | 34960895 |
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Enhancer Sequence | TCGCCATATT AGCCAGACTG GTCTCAAACT CCTGACCTCA GGTGATCCGC CTGCCTTGGC 60 CTCCCAAAGT GCTAGGATTA CAGGCGTGAG CCACCCGCAC CTGTATTGTT GAAAAACAAC 120 AGCTTTTCAA CTCCCTCTAG GAATCAGTGG GGAAGGTGTA CCTGTTCCCC TCAGGCACCT 180 CCCACAGAGC CTCCCCACAC CCTTGTTGTG CAATGAGCTT CATTAGCCTC ATACCTCATC 240 TTCCTCTCTT GTCCTCTAAC CCTATCTTCC TTCACTGCTG CCTGAGTGTA TCTTCCTAGA 300 ACCTTTCTAT GATTTTTCGT CATCTCAGTA GGATAGGCAA GGTTCTTCAT GCTTTTACTC 360 TGGCCTCTCC CCACCAGGCA CACTGAATTA TGACTCCTCT CTGTGGAACA CGTTCTTTCT 420 CACTTCCCTG TGCCGGGCAG CACCTGAGTC CTCCTGGTGA ATTCCAGCTC ATCTGTTAAG 480 GATTAGCTCC ACTGTCTCCT CCTTCATGCT GCCTTTGTTA CTTCCTTCAG GCCCCAAGCA 540 CCCCTTTCTC CCTGAACAAG GACACAGGCC CTAGCACACC CCTCCCCTGG AGCACCTGCT 600 ACCTGCATTG TCACAGTCTA CCCAGGGGTT GCACCCACCG TTCAGTGAGC TCCTGGATGA 660 CAAGCCCTAG ACTTTTTGAT CTTTATGTTC CCCGCACTGC CAGGAACAAA AATAGACTCA 720 ACAAATGCTT GTTGAATGAA TAAGTAAAAG AATGAAGAGT TCATGGCCAC GTGCAGTGGC 780 TCACGCCTGT AATCCCAGCA CTTTGGGAGG GTGAGGCAGG CAGATCACAA GGTCAGGAAT 840 TCAAGACAAG CCTGGCCAAC ATGGTGAAGC CCCGTCTCTA CTAAAAATAA TTTTAAAAAA 900 AATTAGGCGG GCATGGTGTC ACAACCCTGT AATCCCAGCT ACTTGGCAGG 950
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