Tag | Content |
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EnhancerAtlas ID | HS176-23433 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:239505210-239506430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:239505419-239505437 | GCTTTCTCCCTTCCTCCC | - | 6.11 | EWSR1-FLI1 | MA0149.1 | chr2:239505654-239505672 | CCTTCCTTTTTTCCCTCC | - | 6.57 | EWSR1-FLI1 | MA0149.1 | chr2:239505650-239505668 | CATTCCTTCCTTTTTTCC | - | 7.41 | IRF1 | MA0050.2 | chr2:239506215-239506236 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | NFYA | MA0060.3 | chr2:239505228-239505239 | TCTGATTGGCC | - | 6.02 | SPI1 | MA0080.4 | chr2:239506314-239506328 | AACTTCCTCTTTCC | - | 6.31 |
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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 |
GH02I238595 | chr2 | 239504406 | 239507476 |
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Enhancer Sequence | AGTTATGGAA GTTTTACTTC TGATTGGCCA AGACTCAATA AACTCTGGTT TGATGTACTC 60 TAATTTATAG GCGTGCAAAG CCAACTCTTT GGCATCAGAG AGGCCGTTAA CGTTGTAATG 120 ATGTTTAAAC GCTGACAAAT GAGCTGCTTG GGCGGCACCT TCAGCCCTGA GAATGGAACT 180 GTTGGAGCTG GAGGACTTGC CTGTCCCCAG CTTTCTCCCT TCCTCCCGTG CTGGTGGAGC 240 AGGTTAAGGG CAGGAGGACT GTTCATTGGG GCGACTGCTC CCCATCGGTT GAGGGGAGGG 300 CACAAAGGGG ACCCATGGCT TCTTTTTCAC TGTTGTCCCT AATTATGGTC TTTCTCATTA 360 AAATAACAAG GACCATTTCT GCTAGAAACG CTGACACATG TTTTTACTTT TCTGGGCCGA 420 TGGAAACCAC ATGTAGAATC CATTCCTTCC TTTTTTCCCT CCAAAATGCA AATGGAAGAG 480 CTGGTCCAGG GGGTCCCCGG TTGCCCAGCC CTGAACAGAG GCTTGGGGAA GCCCCCTACT 540 CCCACGCCAA GACGTGACTT GCGCTTCTCT GGGCACTTTG TGCCAGCCCT ACCAGGGAGT 600 GCTGCCCCGC TCCCCAGGTC TCCCTCTGCT TGCTGGCACT GGGCACTCCC AGCAGGCATA 660 ACCCGAGCAG AGCTGAGTGG TTATTTATAA ACTCTCTTGA ATGCCAAAGC GCCAGGAACA 720 ATCCATTCCC CCCGTTTGCA GGAACATACT TTCAGCATAA CTCATCACTT TGAAGATGGG 780 TCCAAACTTT TGTTCACATT TATTGACAGG AAGTTGTTTT TCAAAGCTCA AGTCAGCAGG 840 CAGGCCCCGG GCCAAGAGGC TCCGCCACCT CAAGCTGGCG CGGCTCTGAG GGCCCATAAA 900 TTGTGTTAGC CTCCCACCCA CCCCTCTCTC TCCCTTTTTC CGCTAGAATT TGCCCAGAGG 960 TTGAACATTA CGTTTTCCCT TTGTAAAGTT TCTTCTTAAA CTTTTTCTTT CTTTCTTTTT 1020 TTTTTTTTTA AGAGAAAATC ACCTATTGGA AGTGTTAAGA GGTTCTTTTC CTCTCTGAAA 1080 TTCTAACCCT TTATGGTGCT CTTGAACTTC CTCTTTCCCG CATAAGCCAC TCTGAGCCCT 1140 CCTTACTGCA TGAAATTTCT CGGCCAAGGG TCCTCCTTCT CATCCCCCTA CTTGAGCCTT 1200 GAAGCAAGAA TGTCCTCCCG 1220
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