Tag | Content |
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EnhancerAtlas ID | HS150-03395 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr12:125677030-125677980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:125677619-125677637 | GAAAGGAGGCAAGAAAGG | + | 6.17 | EWSR1-FLI1 | MA0149.1 | chr12:125677623-125677641 | GGAGGCAAGAAAGGAAGG | + | 6.59 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH12I125192 | chr12 | 125677481 | 125677630 |
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Enhancer Sequence | CCATTTATTT TAGAAATGAG GTCTTGCTCT GTTTCCAGGC TGGAGTGCAT TGGCTCAGTC 60 ATAGCACACT GCAGCCTCAG ACTCCCGGGC TGAAGACATT CTCTTGCCTT GGCCTCTCAA 120 AGTGCTGGGA TTATAGGTGT TGAGCCACCA TGCCTGGCTG AAACCTGTCC CTTCTAAAGT 180 CCACCTCCTC ATTCGGGAGC CCCGGCCTGC TTCGGCAGGA GGGACTTGGC GTTTGTGGAA 240 ACAGCAGATG TGGAAGGCCC CTGGAAGGCG GATGGCTGCA AACTTCTCTT GTTAGTCACC 300 AGGATTTACA AATTCAGAGA TGTCAGTGTC ACAATCCAGT TTCTGTCTTT GCTCAATAAA 360 TTGGGAGATC TTGGAATACT GGTTTAGCCC CTTGGCCTCT GTGAGACTCA GTTTTCCCAT 420 CTGTAAAATG GGCGCCGAAA TTCTCCCTGG CTGTTCTCAT TACAAGGCTG GGTGGTTCAG 480 CAAGAAAGAG GTTTGTAAAC AACAACGGCG TGCTGATGCC ATTGTTGTGC TAACAACAAC 540 AGCCTAACAG CCCTGAGGCT GTTAGCACAG GGCACGAGTC CCAGGACAGG AAAGGAGGCA 600 AGAAAGGAAG GGCTGACTGG GGACACATGC AACCATCACA GCTGCAAAGA GAAGAATCAT 660 GAACCATCAG CCGTCTGCCA AGTGGTTTCT CACTTCAGGA TTTCATGGGA TTCTTGGGCA 720 ACTGTTGAGT GAGGGGTAGG ATGTGTCCTC AGATGGGGAC ACTGAGGCTC AGAGGAACCT 780 AGGGACTGAC TCAAGATAAG TCAATCCATG AATGGCAAGG TAGGGTCTCC TCCCCAGAGC 840 TCATGACTTC TGCCCTGATG GTGCCTTCTT GTCCTGGAGT TTTGCCTCAA TTTCCCTGCC 900 CTCAGGCCTG GGTGCCTGTG ATCTCCAGGG CTTGTGTTCT AGGGCAGGTT 950
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