| Tag | Content |
|---|
EnhancerAtlas ID | HS091-27980 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr2:165970480-165971960 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:165971000-165971021 | TCTTTCCCTTTGTCCTCCCCC | - | 6.44 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTAAAAATCA AATATAGTTA ATTAAAAAAT ATATTTTAAT CTTAAATAGG AAAAAATAAA 60
CTTTCTTGCC CCTTCCCCAC TCCACTTCCA GGTAATCATT TCATAGGGTA ACCATCTCCT 120
TCATTTCCTA GTTATCGTCA GCATCCCTCC TGTATAATGA ATTATTCTCA GACTTATATA 180
CTCAGCCAGC TACTTAGAAT TCAAGGAAAT ATTTTATCTA GATTTGCTTA AGTAACAATG 240
GTTTCATTCT TCACCACCAG TCAGGATTAT TTTGCCTCAA GGCCATTGAT GAAAATAGTC 300
CAGGTGCATC TCTCAGGTTT GAGGCAAAAA CTACATGTTC GATTTGTTTA TTCATATTTT 360
GATGTGATCC TGGGTTTTTA ATTCTTTTCA TGCACACATG CACAGAAAAT CTCGCTGTCT 420
TCCCAGGCAT CAGCCACTGT CAATTTTCCG AAGCTAATTT ATTTTTCAGC CTCAGTGCTT 480
CTCTTAGTCA CACCTATGAC TCAGCTCGTC AGTCAGTATC TCTTTCCCTT TGTCCTCCCC 540
CTCCTAGCTT TCGCATTATT TCTAACTCCC ATCCACTCTT CTGCTGTAAG TCTCTGAGCT 600
ACTACTCATC TGATTAAGTC CAGTCACATT GAATAATAGA TATTCATTGA TTTGTGTTCA 660
AGACATTGTG CTGCTTTCTG TGAGAACAGC TATTGCTTTC CCTGCCAAAG CTTCACAATA 720
CAGTTACATC TCAAAACAGC TCTAGCCAAA GCACATTAAC CACATTGGAA CTGTAAGGGA 780
GGGAATGTAA TTACTGTAGC ATCTATAAAT CAAATCACAC CATTGCCAAG GAGTTCTGAA 840
GGGATTACAA TATCAATGAC ATGACATTCT AGAATGCCAT TTATCTCATA GGGTCAGCTT 900
CCTCACATTA TGGAGAATGA GAAAACAAAA AGACCTATCA GATCATTTTA ACTGTCCAGG 960
AATAGTCACT GCCATAAGTA TAATCCAGAA ATCTAGAGAG ATTAACTTTT TAAAAGACAA 1020
AAAAGGAAAA TAAAGATAAA CATGCCTTCA CTATTTATTT TAAATATTTT TCTTATTTAA 1080
TTTAATTTAT GTATTTATTT TGAGACAGGG TCTTGCTCTA TTGCCCAGGC TGAAGTGCAG 1140
TGGCATAATC ATGGCTCACT GTAGCCTCGA CTCCCTGCAA AAGCTCTAAG ATACAGCTGT 1200
GGCTGAGGTA GCAGCGACTA CAGGCATGTA CCACCATGTT GAGCTAATTT ATTTTTTCTT 1260
TCTTTATTTT TTTTTTTGTA GAGGCAAAGC CTTACTACAT TTCCCAGGGT GGTCTCAAAC 1320
TCCTGGGGTC AAGCAATCCT CCTACCGTAG CCTCCCAAAA TTTTGGGGTT ACAGGCATAA 1380
GCCACCACAC CTCGTTTCAT AAATTTTTTT TTTTAAATGA GGCATATTCA GTCTCCGTAA 1440
AGAACAAGGG GAGATTGTAT TTAATCACAT CAGAGCTTGT 1480
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