Tag | Content |
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EnhancerAtlas ID | HS108-38455 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr7:150788050-150789210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr7:150788707-150788722 | GCAGGGCAAAGGTCA | + | 6.4 | Nr2f6 | MA0677.1 | chr7:150788708-150788722 | CAGGGCAAAGGTCA | + | 6.45 | Rxra | MA0512.2 | chr7:150788708-150788722 | CAGGGCAAAGGTCA | + | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 150788768 | 150788800 | chr7 | 150788464 | 150788850 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I151091 | chr7 | 150788288 | 150788887 |
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Enhancer Sequence | CAAAACAAAA CGGCATACGC CCTGGCATCC CACAGCCCTC AGCCCTTAGG CACACCTGGG 60 GTTTTAGTGT TTGTGTCTGT TTCTGTTCGT CCTGTGACTT GATCCTGGAG GACTGGCATG 120 ATGGTCCCCA TGTTTGTGCC AGGGTGCTCT CTTGAGCTTT CCTTACTGTT CCTGGGTGGG 180 CACTCCCTGG CCGGGCCCTG CATTCCGCCG TGGGCCCTGC TGCACCACAC ACTGCTGAGG 240 TTCCCTTCAA AGATGAGGAC TGGGGGGGTC TGGGATGGGT GCCGGGGACA TGCATCTGGA 300 GCCAGCCCAG GCCCCTCTGG CAATTCGTTG GTTTAGGGAC TGAGTGTCTC ATGGGGGCCT 360 GGTTGCTTAT GCAGGACTTT GCTCGCAAGA GTTCTAGCAA TTCTGAAAAA GAGCATAACC 420 ATGTGGGTGC TAGTAGCCAG GGAAAGCTTC ATTTGTTCCA GATACATTCA TTTAGCTCCT 480 ACTGTGCGGC CCAGTTGCAT CTAGCACAGT GAAAAGCAGA CAATCAAAGG AGAGACAGGG 540 AGCGAAGGGG CCAGAAGGTC TGGGCTTGGT GCACCTGGAG AGAACGACTC AGCCTGTAGG 600 AGGTGCCAGA GAGGCACTGG GAGTCCAGAA GGAGACCTAG ATTTTCAGAA GACCAGGGCA 660 GGGCAAAGGT CAGAGACTTG GGAAACCTCA TCACGACTTC TTTCTTCCGG GTCAGAAGCC 720 AGAACAGGAA GACCTGTCCA GCCTGATCTC AGGCTGCATG GCCTCGTGGG AACCCCTGGT 780 ACCCTGCTCC ATCCAGGGTC TCAGCTCTGG CTCTCCCCAG CAGTGGTACC CCACAGATGA 840 AGCAGTCCTT GTCCCTATGA TGCCACCTGG CAATCTTCCT GTATCATTTA TTTCTTTCCT 900 CAAACGTGTG CCAGGCCTGG GGGTCCGGAG GATTCCCACA TAGAGGAAAC AGGATGATGA 960 AGATAACGGA GGCAGGAGAA CATAGTGTGG CTCTCGGAAC GGCAAGTTGG ACTCTGCAGC 1020 TCGGGTGTTG AGTTGTAGGA GATGGGTGGG TGAGGTGGGC AGGACCCTGG TGAAGGAGTA 1080 TTTCATGCTT TCTCCAGTAT TTATTTCCAC CCTGCCGTGT TCCTAGAAAC CGCAGGAGTT 1140 GGTGCGTCAT TCTGCGAAAG 1160
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