| Tag | Content |
|---|
EnhancerAtlas ID | HS091-29443 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr2:238683110-238684550 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LHX6 | MA0658.1 | chr2:238684326-238684336 | ACTAATTAGC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 238683255 | 238683771 | | chr2 | 238683790 | 238683844 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I237774 | chr2 | 238683501 | 238683650 |
| Enhancer Sequence | TTTCCTAGGC AATTTCTAGG AAGAGAATGG CTGCCAGTAT TTCTCTAGTG GGGACGGTAC 60
AGAGAGGATT TACTACTGTG ACATCTGCCC CTGGGCTGGT CATTGTCAGA TCATCCCACA 120
CCACTCTGCA GTGCCGGTGT CTTAATAAAG GAAGGCATGG CGCAGCCAGT TAGGGCTTAG 180
GGCTAGACCC TTGCTGGCAT CAACTAGTTC ATCTGTCAGT TTTGAGCATC TCCTATAGGT 240
CTTGTCCGTA AACGTCAAGA GAATGAGATA AAGGAGTAGC CAGGCCTCTT ATGCTCCGAA 300
TATTTTTTGT GTCATGCAGA ATGAGCCCAG GTGGAGGACC AGGAGCCCAT GGGCCTGCTG 360
TGGCCAAGAG CTGGGTGTGG CACCAGGGCC AGGCCACAGC TGTCTCAGGT CACCCTATGG 420
AGAGTGCCCT TGAGAAGCCG AGCTGCTGTT ACTCCACCTG CTGGTCACAC TCCCAAATTA 480
CCATGCTTGC CAATTAAAAC ACATACTTTA CCTTACTGAA GACACTTGGC AAAGTTGTTT 540
GTTCAACAAA TATTTACAGC ACCCGTTGCA TGCCGGGCAC GGGTTCAGGT GCTGGAGATG 600
CAGCTGTGAC CTTACAGACA GGAGTCTCCG CCTCCATAGA GCCTGTGCTC TGGAAGAGGG 660
AGGTCCATAA AAGTGACCAC AGGCAGGAGA GGGGCTGGGG TGCGGAATGG CCCAGGCCAG 720
GGCAGTTCTA GGTAGGTGGC CAAGGAAGAC TTTCCTTCTT GTGGCATATA AGGACAGGCC 780
TGAACAGCCC AGGGAGTGAG CCAGGCAGAA CTGGGAGAAA GCCTTCCGCG CAAAGGATCA 840
GCACGTGCAG GGGAGCTCGG GGCAAGGCAC TGCCTTTGTC AAGGAACAGT CAGAGCGGTG 900
GAGGCCAAGT GAGCAGGGGG TGAGGGGGTG GAGGGAGCAG TGAGAGCACC TCAGCCCGTG 960
AGGCAGGGCC CTGGAGGCCA TGGACAGGAC TTGGGATCCT CCTGTGCATA AAGTGGGAGC 1020
TACTGCAGGG TTTTGAGCAA AGGAGTGGCT TATGTTGATT TATGTTTCAA TAGGATCACT 1080
CGGGCCGGGC GCGGTGGCTC ACGCCTATAA TCCCAGCACT TTGGGAGGCC AAGGTGAGCA 1140
AATCGCTTGA GCTCAGGAGT TCAAGACCAG TGTGGGCAAC ATAGTGAAAA CCTGTCTTTA 1200
CATAAAGTGC AAAAAAACTA ATTAGCCGGG TGCGGTGGCC CGTGCCTGTA GTCTCAGCTA 1260
CTTGGGAGGC TGAGGCAGGA GGATTGCTTG AGCCTGGGAG GTGAAAGCTG CTTTGACACA 1320
TGAGCGTGCC ACTGCACTCC AGCATGGGGC GACAGAGTGA GACCGTTTTT CATTAAAAAA 1380
AAGGAAAGAA TCACTCATTT TATATTTAAA CTGTAGGAAA GGGACTGTGG AGGAGAAACC 1440
|
| |
|
|
|
