| Tag | Content |
|---|
EnhancerAtlas ID | HS091-36581 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:39816900-39819080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr4:39817779-39817791 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr4:39817783-39817795 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr4:39817787-39817799 | AAACAAACAAAC | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr4:39818396-39818411 | TGAACTCCTGACCTC | - | 6.22 | | PPARG | MA0066.1 | chr4:39818887-39818907 | CTAGGTAACTGTGACCCTTA | + | 6.17 | | Zfx | MA0146.2 | chr4:39817042-39817056 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 39816936 | 39817327 | | chr4 | 39817078 | 39817414 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH04I039814 | chr4 | 39815929 | 39817284 | | GH04I039816 | chr4 | 39818481 | 39818630 |
|
Enhancer Sequence | TGCCATTCTC CTGCCTCAGC CTTCTGAGTA GCTGGGACTA CAGGCGCCGC CACCACGCCC 60
TGCTCATTTT TGCTATTTTC AGTTGAGACG AGCTTTCACC GTGTTAGCCA GGATGGTCTC 120
GATCTCCTGA CCTCGTGATC TGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT 180
GAGCCACCGC GCCCAGCCCG AAACTGGAGA CTTTATACCC TGGCTCAAGA AAGCCTGATG 240
CAGGCCCAGA GCCTGGAGAG CAGATGCTGC ACCAAGCAGG AACAGCGGAG TCTGCGAGCG 300
CGCCCACCTG CTGCCTGAGG ATGTCCTGGC TGGGGACACC CCTTCTGCTT CAGCAGTGGT 360
AGCCGCTGCG AGCAGGCGAG CGGAGGCGGA TCATGAGGAC GCCCTGGCCG GCTGTCCCTG 420
CGCTTCCCAG AGCTCACTCG AACTCAGCCG CCAGGGAGAC TTCCCATGCA GAGAGCAAGA 480
AGCCATCCAT CATGAACATA TGGGCTTCTG GTTACACAGT CTTTTGTGTC TTTGCCTTAT 540
CATAAGGGCA GTCTTGAGTG TGGCCATGAG TGCGTGGAGG AAACTTTCAA GATCTTTAGG 600
CCGGGCGCGG TGGATCACGC CTGTAATCCC AGCACTTTGG AAGGCTGAGG TGGGCAGATC 660
ACAAGGTCAA GAGATGGAGA CCATCCTGGC TAACACGGTG AAATCCTGTC TCTACTAAAA 720
ATACAAAAAA TTAGCCGGGC GTGGCGGCAT GCGCCTGTAG TCCCAGCCAC TTGGGAGGCT 780
GAGGCAGCAG AATGGCATGA ACCCGGGAGG CGGAGATTGC AGTGAGCCAA GATCATGCCA 840
CTGCACTTCA GCCTGGGCGA CAGAGCGAGA CTGTCTCACA AACAAACAAA CAAACAAACG 900
AACAAACAAA CAGATCTTTA AAGGTGGCTG GGCGCAGTAG CTTACACCTG TAATCCCAGC 960
AATCTGGGGG GCCAAGGTGG GTGATCACTT GAGGCCTGGA GTTCGAGACC AGCCTGGCCA 1020
ACATGGCAAA ACCCTGTCTC TAGGAAAAAT ACAAAAACTA GCCAGGCATG GTGGCGGGCG 1080
CCTGTAGTCC CAGCTACTCA TATAACTCGG TATATGTCAT GCATATCATT GAATTGTACA 1140
TTTAAAGCAA GTGGATTTTA TGGTATGTAA CTTGTATATA AGTCCCCTCC TGAGTAACAG 1200
GGTAGGTGGG AGGGCTTCCT AAGAACTCCT TTGTCCAGGA GCCCCAGCTT TAGTCTCCTG 1260
AGTTGGACTC TGCATCATTT TATTTGTTTA TTTATGAGAC ACAGTCTCAC ACTGTCACCC 1320
AGGCTGGAGT GCAGTGGTAC AACCTCGGCT CACTGCAACC TCTGTCTCCC AGGTCCAGGC 1380
GATTCTCATG CCTCAGCCTC CCGAGTAGCT GGGATTATAG GCATGCACCA CCATGCCTGG 1440
TTAATTTTTG TATTTTTAGT AGAGACGGGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA 1500
CTCCTGACCT CAGGCGATCT GACTGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG 1560
AGCCACCATA CCCGGTCTTG CATCATTTTA AAGGCACATT TCCACCCCTG CCTGGTTGCT 1620
GCCACTTGAC TGACACCGTA AGGTATTCAA CCCTTGCCTT ACAGGATTCC TGCCGGAATT 1680
TACACAGCAA ATGTTTCTCT TATATTTGAG GATTCCTAAG GCGCAGAGAA TCGAGTTTCA 1740
ATGCCAGCCC TTTCTGGGCT TCTGCTGAAT TATCATTGTT GTATGATATT AATCATAAGC 1800
AGGGACATTA AAATGGAAAT GAACTCAGGC AGAAATCCTG ATCTGCTCTT CCTCTGCTGT 1860
CAGAATCCTG CTCTCCCCAA AGCCAAATGG CAGTGCAGGC CATGTGTGTG CACAATGGCT 1920
TCCTCTTGTT TCTACCTGTT CTGGAATATC TGTAATTCCT TTCATCCTTC TATATGAACT 1980
GTAAAATCTA GGTAACTGTG ACCCTTAAAA CACAATAATT GTCAGTAAGA TAGAAATCAT 2040
GCATCAGTGA AGAATAAGGT CTTCAGAGGC TGGGCACGGT GGCTCACGCC TGCAATCCCA 2100
GCACTTTAGG AGGCTGAAGC AGGCGGATCA CGAGGTCAGG AGTTCGAGAT CAGCCTGGCC 2160
AACATGTTGA AACCCCCTTT 2180
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