Tag | Content |
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EnhancerAtlas ID | HS108-30952 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr4:124364570-124365990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr4:124365376-124365394 | CCCTCCTTCCCTCTCTCC | - | 6.23 | EWSR1-FLI1 | MA0149.1 | chr4:124365368-124365386 | GATTTCTTCCCTCCTTCC | - | 6.38 | Nr2f6(var.2) | MA0728.1 | chr4:124365686-124365701 | TGACCTTTTGCCCTT | - | 6.91 | RARA | MA0729.1 | chr4:124365683-124365701 | AAGTGACCTTTTGCCCTT | - | 7.2 | ZNF263 | MA0528.1 | chr4:124365585-124365606 | CCCTCCTTCCTCCCCAGCTCC | - | 6.3 | ZNF263 | MA0528.1 | chr4:124365588-124365609 | TCCTTCCTCCCCAGCTCCTCC | - | 6.4 | ZNF263 | MA0528.1 | chr4:124365577-124365598 | CCCTTTTGCCCTCCTTCCTCC | - | 6.6 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28125 | chr4:124364087-124366119 | Fetal_Intestine |
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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 |
GH04I123442 | chr4 | 124363971 | 124366138 |
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Enhancer Sequence | ACACAGCCAT TTAAAAAAAA GATGCTTATA TTGAAAAACA TGAATATCAA ACAGTGGCCC 60 ACCCTGAACA GTCCCAGATC TGCTGGTCTG TTAGCCATGC TGCACTTCTC TTCCTCCACC 120 CCCTCAAAAA AGAGAAACAA GTCTGAAGAT GATCAGGCTT CCTGTTCTGT AGATTTTGAA 180 TTACTGTAAT CAGGATCTCA TGTCTGCAGC CACACAGCCA GCGGTGATCT CTCAGCCTGG 240 GCACTTTCTA TTTCAGTTGG TAATTACTCA GTAGTAAAAA AAAAAAAAAA AAAAAAAAAA 300 AAAAAATTAA AAATCACAGA TAGGAGAATT GAGGACATAG TCTACTTGGT GCTGACTCTT 360 TTGTGGGTGG GGAGGGTGGG GAAAATAGGG TACACTATCT GTAATTCTAG TTTTCCCCAG 420 ACCAAAGCAA CTAGGCTGAA TATAATAGGC CCTTTAATTT CCTCGCACCC ATTCAAAGGT 480 GCTTCAATAA GAACAAGTGA AAAGACTCTG GAAGCCAGAA GATTGGTGAT GGGGGAAGGG 540 AGTGGTGCAG CAGAAGTAGC TCCTGGGAGG ACGGAAGATG TTAGCACAGC AGTATCACCA 600 AAACGGAATT TTATATTCTT TAAAAACTGT GTGTGCATGT GTTTTAAGTT AAGGTTAACT 660 TCAAATAATA ATTAAACACC AGTTGCTGGA TCGTCTACTT AGTGCTTATC AAGAGAGTTT 720 ATTTACTGAT CTGCTGAGAC CAAAAGCAGC AGTTCCTCTG GTTAACATTT GCTAAGACAA 780 ATCCTTCCAT TTGGGAAAGA TTTCTTCCCT CCTTCCCTCT CTCCCTGATT TTTCTAGGTC 840 TGGGAAAGCT GGTTTTATAT TATGCAAAAG TGTGAATCGC ACAGCCCAGA GTCACTGTCC 900 CCTTTAAAGG GGGCTTTCTC TCTTGTCTTA AAAAACAGAC CTCAGAAGGA GCCAGATGGT 960 TCCCGTCTGC TGCCTTGAGT CAATGCACTT CCTCCCACAG ACTGGAGCCC TTTTGCCCTC 1020 CTTCCTCCCC AGCTCCTCCC CACATTCTAC CCCCCACCAC TGGGCCTCCC TGTTTTGTCG 1080 CTAGAAATAA TCTTTTATTG CCCAGTTGTT CGGAAGTGAC CTTTTGCCCT TGATTAGATA 1140 GCACCAGGCT CCATCACCGG ATTGCTTTTG AGCGGGCAGT TGCTTTTTTG TGTGGGCTGA 1200 TCCGGTGTCA GGGAGAACAA TGCAAGGCTT TGCAAAATTT TAGTATAGCT CAGGCCTCAT 1260 GTGGAACAGG TGGGGGCGGG GAGACGCGGG GTTGAATAAA GCAGCCCAGT GGATCCTGGT 1320 TGCAAAAATA CATTTTCTTT AGTAAACTGA AAAACAAATG GCATTTTAAA AAATTCACTT 1380 GTACATATTT AACTCATTCC TTAATAACCA TGTATTTCAG 1420
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