| Tag | Content |
|---|
EnhancerAtlas ID | HS091-03492 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr1:180157050-180158020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr1:180157882-180157893 | TGCTGTGATTT | - | 6.62 | | HEY2 | MA0649.1 | chr1:180157696-180157706 | GGCACGTGTC | - | 6.02 | | Klf1 | MA0493.1 | chr1:180157271-180157282 | AGCCACACCCA | + | 6.14 | | Npas2 | MA0626.1 | chr1:180157696-180157706 | GGCACGTGTC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTAGCTTCT TCCTGAATAG TAGTATCCTA GCAGCTATCA TTTCTTCAGC CCTGCCGGTG 60
CCTGCAGTGT TCTTTGTATA TTAGCTCCTC ATTCTGTTTC TCAGAGAAGA TTCCACAGCA 120
TGGCTTCTAG TATGATCTCC GTTTCATAGA AGGTGAAACA AAGCCCCAGA GAACTAAAGC 180
ACCTTGCCAG GGTCTTCCAG CTAGTGAGGG GCTGGGCAGG GAGCCACACC CACTCGCATC 240
CAGCCCATGC CCATTACCAC CAAGTGCATG GTGCTCACAG GCCCGAACCC CTAAGGGTGC 300
CAGTGGACAC TGCTGGCTCC CCCTGGCTAG CTGCCAGCCC TGCAGGTGCC CGGTCAGTCA 360
GGAGGCCCTC TGCATGTCCT GCCGGTGCCT TCCCACCCGG CCTCTCCCAG CCTGTGCTCC 420
CTCCTGTGAG CAGCTGGTAG GAGTGGCCAC TGGGTGGCGT GTGGGCACCA GGGTTTCCTT 480
GCTCCCAGTT GTCCAGAGCT CCTTAATTCA TCCATCCTTC TGGCACTGTC GCCTTAGAAG 540
GCGGAAGTTT CTAAGTCAGG ATGATGGCAA AGGTCAGTGA GAAATGCTGA CTTCAAGCTG 600
TAAATTTGTG TGTGAGTTCC AGAGGCCCGT GTGGGCTCAC CAGGAGGGCA CGTGTCAAAG 660
CGTGGTCTTT TCCGGCCATT TCTCACTCTG GGGGAAGGTG TCCAGCCCAA CGTTTGATAG 720
GAATATTTAA TGGCTTTCTC AGAGGAATGG ATCTGTTAGC AGGTTTTCCT GTTCAGTTAC 780
CATTCGTGTC TCCAGTATCC TTCTCCTCTC AAATGTTTGT CTTTGCTTTC TTTGCTGTGA 840
TTTTCTCAGG GTCCTCATCC CCTCGGCCAG CCTCTTTGTG GTTTTATCTG ATCAGCCTGC 900
TGCTGTGTCC CTCTTTCTCC TGCCCTCCGC CCCTTGTGCT GTGCACGTGC ACACACGCAC 960
ACACACACAC 970
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