Tag | Content |
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EnhancerAtlas ID | HS139-38503 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr3:128316100-128317450 |
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) |
CTCF | MA0139.1 | chr3:128316619-128316638 | TGCCCAGCAGGGGGTGGTG | + | 6.17 | HES2 | MA0616.2 | chr3:128317270-128317280 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr3:128317270-128317280 | GGCACGTGCC | - | 6.02 | ZIC1 | MA0696.1 | chr3:128316621-128316635 | CCCAGCAGGGGGTG | - | 6.06 | ZIC3 | MA0697.1 | chr3:128316620-128316635 | GCCCAGCAGGGGGTG | - | 6.26 | ZIC4 | MA0751.1 | chr3:128316620-128316635 | GCCCAGCAGGGGGTG | - | 6.02 |
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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 | AATCAGAGGA AGCACTGAGG AGCAGAGGCA GCGGTCCTGC TTGCAGGGTC TTAGGTCTAT 60 TGTCCCATTA CTCCTGACAA GGTAGTTGCT ATGAGTCCCC CCACTCCAAA GATGGAAAAG 120 CTGAGGCACA CAGAGGGTAA GTCATCTGCC AAAGGTCATT GAGCCAGGAG GTTGGCCAGG 180 GAGATCTCTG CTCACCGAGT TGGGACTGAG GAGTGGCAAG GGGGAGAGTA GTGTTTAGGG 240 AGACCCACTG CGTGCCTGCC ACCAGGCTAA GTGCCCTCTG CACTAAGCTA CTCTCATCCT 300 CGAGCAATAT TAAGAGGCTG GCATCGTGCA CCCAATTTTA GAGATGAAGA AGCAGGGCCT 360 CCGGGACCAG AAGCCTCAGC TCACACAGGA TTGAGTGCAG AGCTAAGGCT AGAGCCTGTC 420 TGCCTGGCTG CAGGGCCTAA CCCCTGGAGA GAGAAGACAA CATCACCCTG CTGGTGCTGT 480 CCTCTCAGCC CCCTCCATGC CCTGGGCACT GGGGCCGGAT GCCCAGCAGG GGGTGGTGGC 540 CTTGGCCCTG GGCAGACATT CTAGAAAGCC AGCAGTTCAT TAGGTCCCCT GCTCCAAAAC 600 ACAAGGGCCA TGCTTGAGAC TCATGGGTGA GGGCAGGGGT CTGCTGCTTC TTCCAACCCC 660 CACAACCAAG ATGGGCAGGG TGGACACTGG TGTTTCTCAG GCTCCTGTGA GTGCCCAGCC 720 CTTGCCATAC CAACCGGTGA CAGATGTTGC TGTCCCAGCT GCTTCTCCAC GCCTGGTGCA 780 GCCCTCCAGC GAGCTTTGTC AGGCCTACAT GGTGATTCAA ACACATCTGA GTCAACATAT 840 AAATATCAAA GGATTGCACT TTTTAAAATC CAAATTTCAC ATTTCTCTAG GAAAAAAGTA 900 GATCTGCCAG CCCTAGGCCC ATACTCTCAC AGATCCCCAG TCAGCTAGTG CTGAGCAGCA 960 GCTACCTCTT TGCGTGAAAC ATGTGAGCAT CAGTTTGCCC CAGTCCCCGC CACCTGCAGC 1020 CGAACTACTG TTTTCTTTCT TTTCTGGAGG CAGAGTCTTG CTCTTTCACC CAGGCTGGAA 1080 TGCAGCGGTG CGATCTCAGC TCACTTTAAC CTCCGCCTCC CGGGTTCAAG CGATTCTTCT 1140 GCCTCAGCCT CCCAAGTAGC TGGGATCACA GGCACGTGCC ACCACGCCCA GCTAATTTTT 1200 TGTACTTTAG AAGAGATGGA GTTTCACCAT GTTGCCCAGG CTGGCCTCGA ACTTCTGATC 1260 TCAGGCCTCC CAAAGTACTA GGATTACAGG TGTGAGCCAC CACACCCAAC CCTACTGTTT 1320 TCATTTTTAA GGGCCCTTAT GCTGTTGGTC 1350
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