Tag | Content |
---|
EnhancerAtlas ID | HS098-07924 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr10:94362040-94363460 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr10:94362065-94362076 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr10:94362065-94362076 | TTTCTGGGAAA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGTGTTCTC TCCTTTGCCA GATTTTTTCT GGGAAAAGAT TGAGAAGAAC TGGTATTAGA 60 TCTTCTTGAA ATGTTTTATA GAATTCACCT ATGAAACTAT CAGATCTAGG GCTTTTCTTT 120 GTCAGGAGAT TTTTGGTTAG TGAGTCCATC TCTTTACTGG TTATAGCTCC ATTCAGAATT 180 TCCATTTCTT TGTGATTTAG TCTTTGTAAG TATTGTGTTT CTAGGAATTT GTTCAGCTGG 240 GTTATCCGAT TTGTTGGCAT ACAATTGTTG AAAATACTCT TTCAACAATA AGAGAGAAGA 300 CACAAATAAC TAGTTCTTTT GTTTCCAGTT CCTTAAGTTG TAAAGTTAGG GTGTTGATAT 360 GAGATCTTTC TTGCTTTTTA ATGTAAGCAT TCATAGCTAT AAATTTCCCC CTTAGCACTG 420 CTTTTGCTGT GTCCCGTAAG TTTTGGTATG TTGTATTTTC ATTTTCATTA ATCTCTAAAA 480 TTTTCTAATT TTCCTTGTGA TGTCTTTGAA CCCTGGTTAC TTAAACACAC ACACACACAC 540 ACGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGGTTTTTT GTTTGTTTTG AGACTGAGTT 600 TCGCTCTTGT TGCCCAGGCT GGGGTGCAAT GGCGCGATCT CGGCTCACTG CAACCTCTGC 660 CTCCCGGTTC AAGCGATTCT CCTGTCTCAG CCTCCAGAGT AGCTGGGATT ACAGGCGCCT 720 GCCACCACGC CTGGCTAATT TCACACACAC ATTTAAAAAA TACATCTACC TGCTTTTACT 780 TCAGAATCTT TGCAATTTCT GTTCTCTCTG CCTGAAAATT TTTTCCACCA AAATATCTAC 840 AGGGCCTGGC TCCCTTGCTT TTTAGGTTCT GCTTAAATAT CACCTGCGTA GAAGCATTCC 900 CTAACTACCC TAAAATAGCA ACCAACTATC TTCCACCCTC AACACTTCCT ATCCCCCTTA 960 AACTGCTTTC TTTTCTTTTC TTTTTTTTTT TTTTTTTTTG AGACAGAGTC TCGCTCTGTT 1020 GCCCAGGCCT GGAGTGCAGT GGCGCATTCT TGGCTCACCG CAACCTCCAC TTCAGCCTCC 1080 CAAGTAGCTG GGACTGTAGG TGGCTGCCAC CATGCCTGGC TAATTTTTTT TTTTTTGAGA 1140 TGGAGTCTCA CTCTTTCACC CAGGCTGGAG TGTAGTGGCA CAGTCTCGGC TCACTGCAGC 1200 CTCCATCTCC CAGGTTCAAG TGATTTCTGG CTAATTTTTG TATTTTTAGT AGAGATGAGG 1260 TTTCACCATA TTGGCCAGGG CTAGTTTCGA ACTTCTGACC TCAAGTGATC TGCCCACCTT 1320 GGCCTCCCAA AGTGCTAGGA TTACAGGTGT GAGCCACTGT GCCTGGCCTA ATTTTTGTAT 1380 TTTTAATAGT GATGGGTTTT TACTATGTTG GCCAGGCTGA 1420
|
| |
|
|
|