Tag | Content |
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EnhancerAtlas ID | HS154-22870 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chrX:41112230-41113420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chrX:41113118-41113137 | TGCTGCCCTCTAGAGGCCG | - | 6.91 | Foxd3 | MA0041.1 | chrX:41113318-41113330 | GTTTGTTTGTTT | + | 6.32 |
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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 |
GH0XI041253 | chrX | 41112254 | 41113453 |
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Enhancer Sequence | CCCTGAGTTC CAGCGATCAA AGATAAAATT GAAAACATTA GCTATGCCCA CTGCTCCCTG 60 GTGGAAGGCA GCCACCTTCT GAGGAGGTCC CATGGGAGAG TGAGTCCCCT CCCCGTGCAT 120 AACCCGACCC CCAAATTGGG GGCTCTTCAG ACCTCATCAG ATCCTGCACA GGCCCCCCAG 180 GATAGGTGCT TGGGGTGCAG CAGCTGGCCA AGGCGCTGTG CCTTGTTGTC TAGGTGGTGT 240 GCCCACCCGG GCTCCCGGTC CCGCCTGGTC ACAAGCATCC CCGCGTCAGC TGATGAACAC 300 CCCTGTCCAG CAGGTGCCAG ACACCCGAAA TCAAGAGGAG TGTCCTGTGC TCCAGGAGCC 360 TGAGAGGTGG CAAAGTCCCC GGGGGGAGGC GTGATGGTAG GGAAGGCTTC TGACATACCT 420 CTGCAGGGGC CAGGGCCCTG AGTCCCGGGT CCCCATGGTG TGTTTCTGTG TGAAGTCAGT 480 GGCACTGCCA GCGCCGTGGT CATATTACCT AGGCCACAGC TGCCAGGCCT GCAAGCTCTT 540 TCCTACTTCC CTTAGGTGCC CAGACCCAAA GTCAAGAGGA CCTTGACCCG TGGGGGTCGT 600 GGGGAATGAA AACCGTCCTG CGAACTTGAA CTTCACTAGG GAGGCGGCGC TCTCTCTGCC 660 CCGGTTCTAT CACGCGCATC CGTTAGGAAC TAAGCGGCAC CTGCGCGAGG CTAGGCTTGT 720 TGACATATTT CTTGCTGGCG GCGTCCTCTC GCGTGGAGCA CGACTGCGCA AAGCGCCGAC 780 AGTCCCCCGA GCGAGGACGG CAGCGAGACT CCGAAGCCCC CTTAGCAACC AAGCCGGTGC 840 CGCTGCCCTT GCGCCGGGAC TGCAGCCGGG TCTTCCGAAG TGAGGATATG CTGCCCTCTA 900 GAGGCCGCGG GGTGACATGG CCCATGAGGC TGTCTGGGCA GGGTGGGTTC GGGTGGGAGG 960 AACCAAGGTG GACAAGCCTC GAAGTAAGAG ATCTGTTCAA GGTCACAGGG AGTCGGGACT 1020 CATGCGGAGG CACAGATCCA AGCTCTCTGT ACTGGGCCCT TTGGTATTCT GTTGGCTCCT 1080 ATTTTTTTGT TTGTTTGTTT TTTGTTTTTT GTTTTAGATG GAATCTCTGT AGCCCAGGCT 1140 GGAGGGCAGT GGCGCGATCT CGGCTCACCA CAACCTCCAC TGCTGGGATC 1190
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