| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10033 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr2:70414900-70416530 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr2:70416208-70416219 | CTTCCCAGAAA | - | 6.02 |
| | | 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 |
| GH02I070188 | chr2 | 70415218 | 70416397 |
| Enhancer Sequence | CAACCTCCGC CTCCCGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCGAT TAACTGAGAC 60
TACAGGCACA TGCCACCACG CCCAGCTAAT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA 120
CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCAGAT GATCCACCCA CCTCGGCCTC 180
CCAAAGCTCT GGGATTACAG GCATAAGCCA CCATACCCGA CTGCATTTTG GCTTTTATAG 240
GAAAGCTAAA GACAGTACAG AGACTTCCTA CCTACCTTTC ACACAGACTC CCCAAATGTT 300
AACATCTCAC ATAACTATGG GGCATTTGTC AAAAATAAGG TCTTAACATT GGTACAACAC 360
TATTAACTCT ACTACAGGCT TTATTCAGAT TTTACCAGTT GTCCACTAAT GCCCCTTTTT 420
ATTTTATTTA TTTTTTTGAG ACGGAGTCTT GCTCTGTCAC CCAGGCTGGA GTGCAGTGGC 480
GTGATCTTGG CTCACTGCAA CCTCTGCCTC CCGGGTTCAA GCAATTCTCC TGCCTCAGCC 540
TCCTGAGTAG CTGGGATTAC AGGCGTCCAC CACCAAGCCC GGCTAATTTT TCTGTATTTT 600
TAGTTGAGAC GGGGTTTCTC CATGTTGGCC AGGCTGGTCT CGAACTCCTG ACCTCAAGTG 660
ATCTGCCTGT CTCGGCCTCC CAAAGTACTG GGATTACAGG CGTGAGCCGC TATGCCTGGC 720
CTCAATCTCC CTTTTAAAAA AGAATAAATC TTTTAGACTA ATTTTAGATT TTCAGAAAAG 780
TGGCAGATAG AACACAGTTC CCAAACACCA CTCACCCAGT TTCCCAATGT TAACATCATA 840
TATAAACATG GGACATTTGT CAAAACCAAG GGACCAACAT TGCCACATTA TTATTAACTG 900
AACTCTAGAC TTTGCCCCTT TTTTCTGTTT CTGGATCAAA TCCAAGATAC CACATTGCAT 960
TGAGTCATCA CGTCTCCTTA GTCCCCTCAA GTCCGTGAGT TTGTCTTTCT TTTTCCTAAT 1020
CTTGACAGTT TTGAAGAGTC GAATATTTTA CAAAATGTCC CTCAATTTGA GCTTGTTTGA 1080
TATCTTCCTT GCATATTTGG AATCAGTATA TTTTGATTTG ATATTCTGAC CCAGCAATTA 1140
CACTACTAAG AATTTATTTT ACAGACTGAC TCCCACATGT GTGAAATGAG GGAAATTATA 1200
AGGCAACTCA ATGAAGAATA TTTGTAGCAG CAAAATATAA GAAACAACCT GATGTCCCTC 1260
AAGAAGATAC TGGTGTAATT AATTATGGTA TGCCTACAAA ATGGAATACT TCCCAGAAAA 1320
TAAAATATTT TTACAGCTGT TTAAAAAAAA ATGGCATGGC CGGGCACGGT GGCTCACACC 1380
TGTAATCCCA GCACTTTGGG AGGCGAGGCA GGCGGATCAC CTGAGGTCGG GAGTTCCTGA 1440
CCAGCCTGAA CAACATGGAG AAACCCTATC TCTACTAAAA ATACAAAATT AGCCGGGCGT 1500
GGTGACGTAT GCCTGTAATC CCAGCTACTC CGGAGGCTGA GGCAGGAGGA TCGCTTGAAC 1560
CCGGGAGCCA GAGGTTGCGG TGAGCCAAGA TCGTGCCATT GCACTCCAGC CTGGGGAACA 1620
AGAGAGAAAC 1630
|
| |
|
|
|
