Tag | Content |
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EnhancerAtlas ID | HS154-13598 | Organism | Homo sapiens | Tissue/cell | Osteoblast | Coordinate | chr20:2188170-2189610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr20:2189089-2189100 | TTTCCTAGAAA | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH20I002208 | chr20 | 2189150 | 2189298 |
| Enhancer Sequence | GGGAGGCCGC AGGGACCTGA GGGCGGAGAG GGGAATTCAG AAAGTGCCGG GCGGCGGCTT 60 CCGCTTCCTC TGCGGGGTCT CTGGGTGGTC GTGGCTGGGA GCTGCCGGGG CCCGGTGGCC 120 GTGCGCCTCT GCTCCGGGCA AGCTCTCCCT GCAAGGCCCG GGCGGCGGCA GGGGGCAGTA 180 GCGGCCCGCG ATGCTCAGAG GCTCGCTGGC ACGGAGCTCC CGGGCTGGGG CGTCCAGATC 240 TGGAGAAGCC GGGGGCCTTG GTCACACTCA GAGCTGACGT CCAGTGCGGC CCTTGCTGAG 300 GACTCGAGCG AACAGATCTC TACCCAGCCC CCGCCCCACG CGCACCCAGC CTGGGTCAGC 360 TCGCCCTGCC CGCAGCCACG CAGCTGGTGG CTAAGCGCGG GCTCCGGGTT CAGGCTGCCT 420 TGAGCTCTGT TGGTTCCCTC TGAAAGTGCT GATAATGATA GCAGGTATCT TGGGATTGCT 480 TTGAGTATTA AACGAGTTAA TCGTACTTAG TACAATTTCT GGACTTAGTT TCTAGCACGT 540 GGGAAGTGCT CATGGGCTTG CCTGGGGCAA GTTAGTTGAC CTCTCAACCT TGCCTCATTA 600 AAAAGTGGGG ATAATAATAG TACCCACTTA ATACCGTTAT AATAATTACA GTAGTTAATA 660 TTTGTAAAGC CCCTTGCCTT CAAGAACTTA GGACATTAAA AAAAAGATTG TGAAGTCCCT 720 AGAATGGTGC CAGGCACATA GTAAGCTGCC TCTATTATTA CCATGGTCAT ATTGTTGTTA 780 TCACTATGTT AAATAAAATT TATAAGAGGC TATTGGTTTG GACTGAGCTC CTGCACTATG 840 CCCAACAGAT CAACCCAACA TGGAGTCACT TATGCTGAAG TTCCGTGCCA CCAAGCTGAA 900 ACTAAGTTGC TTATTTGACT TTCCTAGAAA TTAGGAGAGA GAGACAGTTA ATATAGCCAA 960 ATGCCCAAGT AAACCAGCTT TAGCTGGCAT GATGAGGAAG TCCTCTCTGC TTTAACCTTT 1020 ACAAGGAAAA TAACTTTGAA ACAACCAATT CGCTTTTTGT TCTGTGTTTC TGCTTTCTTC 1080 AGCCCTTTTC TGTCTATAAA GCCAGCCTCC TCAGCTCAGC TCATCAGAGC ACTCATTCTG 1140 TTTTATAGAA CGAGGCATCG GCTGATTCTA GAATGCAAAT ATAAGCCAAT TAAGATTTTA 1200 AACTAAATTT CTTGTAATTT TTGTCTTTTG ACAACTATTA TCGTCTGTTT GCCTTGTGAG 1260 GTTGGAAAGG ATTGCACTTG TCCTGCTACA AGGACTCTTA GTCTCTGGCT GGATTACAGA 1320 AACATTTGCC TGCATTTCTC CTTTTATTTC CCAAAGTTTT TCAGCGTCTT ACATGGTTCT 1380 GTAGAAGAGG CAGGATCGTG TCCTTAAAAG ACCACTGGGC TGTGAGTCAG GTGGATTTTG 1440
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