Tag | Content |
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EnhancerAtlas ID | HS154-11993 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr2:12964050-12965590 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:12964732-12964750 | AGAAGGAGGGAAGAAAGG | + | 6.75 |
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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 |
GH02I012824 | chr2 | 12964201 | 12965530 |
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Enhancer Sequence | GGCCTGGCTG GGTGATGAGG CCAGTCCTGG GGTCTTTGCT CTGACAACAC CTTGCTGAGC 60 TGTTCTGGGC AAATCTCTTA ACTTCTCTGG GTGCTCTCAG AATTCTTATT TATGCAATGA 120 AATAACCTCT ATGGGTCCTT TCCAGGATCA TGATGTGAAG GAAAAGGTGG AATATTGGGC 180 TGCATTTGTG GTGCTCTGCC AGTGCAGGTG AGGAGTGTGT GAGCATCCTA GGAGTGCATC 240 CAGGTAGTTA GGAGGGAGAG GACAACACAT AGTCTCCTAG GTGCAGGCGG CGGGGGAAGT 300 CCGGTGGACA CCTGTGAAGC TAAGTTCCAG GACCTTCTGG GGGCTGTGGA GAGGAAGGGG 360 ACCTTCTCCA GAGGGGCCGT GTTGATTGAC TCATTCTTCT CTGACTCCTC AGAAGCCAGT 420 TCATTGCAGT AGAGGGGCTG TCCTGCAAGT CATATGCTTC TCCTCCTTGC CTTAACTACA 480 GGAATTCCAA GATGTTTACA CAAACTTCAA GGAGTGAACC AAGTTATTAA AAGAGTAGCA 540 ATTAGGGTGG CCCATCCCAG CAATTTAGTT TCCTGTCTAA GGAAGCATGA AGGGGGAGGG 600 GTTTCCAGGG AGGGGAGAGG GAGGGAGCAT TCTTGTCTCC TGATTGGACC GCCCCAGGAT 660 TTCCATTTCT GAACACAGAC ACAGAAGGAG GGAAGAAAGG TTGCCAGATG CCAGCTCCCA 720 GCTCCCTGGA GGAGTTACTC GCCGCCACAG ATGCTCCAGC AGCTGGTTGG GCCCCTCCTC 780 AAAGTGTCTC TCCTGCTTCC TTCTTTTGGG GGATTCTGGC TCAGCTTTGA AAGCCTTTTG 840 GCATCTTTTG CCTGCCTCCA AAAATTAAGC TGTGTTGGAA GCTGCCTGAT AAATCACTCT 900 TTGCACCGTG GCTGCCATGG GGCTTGCAGA GAGTGGCTGC CTAGTGATTT ACCGCGGCTG 960 TCTGAGAGGG CTTTTCCAAG CAGCCAGCGT AGACCAGGGA GTCATCTCTG GCAAAAGGAG 1020 CATTTTGTCT AGCTCAAATG GACACTACAG AGAGGAAGTG GGATTGCTTT GTTCAAAACT 1080 TGTTGGTCAT CCATTCCTCA AGCCAGCCGG AATCTCCAAG TTCATTTCTT CCATGCAACT 1140 TGAGCTCAAG AAAAGAGGTC CAGAAAAGTG GTTTTTCATG ACAGGCCTGC TGGAGCCTTT 1200 CCTAGGGGAA GGAGAACTTT CTGGTTCTGA ACTGCAGTTA CACAATGCTG GGCAGGCCCT 1260 CTGATTTGTG GTCATAGTTT CCCAGAACCC CAAGGGACCC ATCCAGGAAA ACGCCCATGT 1320 CCCCTCGCCT GCGTTGTCAT CTGCTCCCTC CCAAGGGGAT TTTGTTTCCT TGATTGTGTT 1380 CCATAGTGGC TGTTGGAAGT CAGGTGCCCT GGACGCAGCT TGGACAGGAA CCATGTGGTG 1440 TGAGGACCTG AGCCTTGTGC ATACGTGGCT TTTGCTTCTG GTTCTGGCTT GACAGTGTGA 1500 CGAGTTAATT AACCTCTTTC ACCTCTAAAT CTTCATCTCC 1540
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