Tag | Content |
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EnhancerAtlas ID | HS139-04770 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:218594730-218595620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:218595515-218595533 | CCTTCCTTCTTTCTTTCT | - | 6.56 | EWSR1-FLI1 | MA0149.1 | chr1:218595503-218595521 | GATGCCTTCCTTCCTTCC | - | 7.66 | EWSR1-FLI1 | MA0149.1 | chr1:218595511-218595529 | CCTTCCTTCCTTCTTTCT | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr1:218595507-218595525 | CCTTCCTTCCTTCCTTCT | - | 9.09 | JUN | MA0488.1 | chr1:218595082-218595095 | GAGATGAGGTCAT | + | 6.11 | JUND(var.2) | MA0492.1 | chr1:218595081-218595096 | TGAGATGAGGTCATC | + | 6.6 |
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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 |
GH01I218421 | chr1 | 218594650 | 218595535 |
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Enhancer Sequence | ATCACTATAA AAGACCGATT GTTCAGGGGC TTATTTGTCA CTTGATCAAA TGTGTCTTTC 60 TAATGAAGTC TGTTAACTAA TAAGAATATA CCAAGCAGGG ATTGGGTAAG CTGCCATGAA 120 AAATACTCTG TGGGGGTAAT AAGAGAGAGA AAGAACATTT TTTGCTTTGA AGGAGCTCAT 180 AGTTAGATTG AGCATTATAC TCCCCACAGT ATAATTTATG AATCACTACT GTTAGAAGTG 240 GGATTGTGTC CCTTCCCCTA CACATAAAAA AAAGATATGT TGAAGTCATA ATCCCCAGTA 300 CTTTGGAATG TGATCTGATT TGAAAATAGG CTCATTGCAG ATATAATTAG TTGAGATGAG 360 GTCATCCTGC AGGAGGGTGG GTCCCTAATC CAGTATGACT GGTGTCCTTA TAAAAAGACA 420 GCCATGTGAA GACTCAGTCA CAGGGAGCCT GCCATGTGAA GATGAAGGCA GAAATTGAAG 480 CTATGCAACT ATAGCCAAGG AACACCAAAA ATTGCCAGCA AACCACCAGA TGCTAGAAGA 540 GGCAAAGAAG GATCCTCCCT GGAGGCGTCA GAGAGATCAT GGCCCAGCCA ACACCGTGAT 600 TTCAGACTTC TAGCCCCCAG ATTTGTGACA GGATAAGTTA GTGTTATAAG TCACCCAGTT 660 TGTGGTACTT TGTTACTACA GTTCTAGGTT ACCCATACAC CTATCAAGCC AACTCTCCCT 720 AAATCCTAGT ATATATTGTT AGAAAAGATA AAAGGGCACT GAAGAGAGAG GAGGATGCCT 780 TCCTTCCTTC CTTCTTTCTT TCTTTCTTCT TGTTTTTTTT GTTTTTTTGT TTTCTTTTTT 840 TTTGTTTTTG ACAGAGTCTC GCTCTGTCAC CCAGGCTGGA ATGCAGTGGT 890
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