| Tag | Content |
|---|
EnhancerAtlas ID | HS091-35802 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:186331140-186333470 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:186332821-186332840 | TCGCCAGCAGGGGGAAGTA | + | 6.98 | | EWSR1-FLI1 | MA0149.1 | chr3:186332943-186332961 | GGAAGGAAGGAAAGCAAA | + | 6.44 | | EWSR1-FLI1 | MA0149.1 | chr3:186332939-186332957 | CGGAGGAAGGAAGGAAAG | + | 7.22 | | RUNX1 | MA0002.2 | chr3:186331233-186331244 | AAACCACAGAG | - | 6.14 |
|
| | 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 |
| GH03I186614 | chr3 | 186332341 | 186333150 |
|
Enhancer Sequence | CAGGTAAGTG GACCTGCTGT CTATGAGCTG AAATAATGTG TACATGGAGC TCAATCAGGT 60
GCCTCAAAAA ATCACCATCA CCCAGTGCAA ATGAAACCAC AGAGGAGTAA ATTCTCTGAT 120
TTCTTCCCAG GAGTGAGGGA AGGGGCAGGC AGAGGGCAGG AGAGGAGACA TTCTGTATGG 180
CAGTCATGGG TGTCAGGAGG GAGCTGGGTG GGGTGTGAGG TGGTGTGCAG GAGAAAAAGT 240
GCTTCAAATG GTAGTGTGCA GATCACAGAC AGAAAGTGTA ACTTGCTGGA AAAACTAGGA 300
CCCAAGAGAC CAGCTCCTAG TTGCCAAGTT ACCACTGGCT GAAAATCACG TATCTGTCTT 360
TGGTTTGGTT TCTCTCTAAC AAAGACTGAG AATGAATAAA ACTAGCATCT GGCAGATGCC 420
TACTATATGC CAGGCCCATT CACATAGATT ATCTCATTTA CTCTTTCCCG GTCCTGCCTC 480
CTGGTGCTGT GTGGTACATA TATTGTTCTT GTCTTACCCA AGAGGAGACC AAGGCTCTGT 540
TGTGTGTGTG TGTGCAGTTT TTTTGTTTTT TGTTTTTGTC TTTTTTTTTT TGGTCCAAAA 600
TCATATAATT ACTAAGTCTT CAGGCTGGGA TTTGATTCCA TATCTGTGTT CCTTCTTCTA 660
CACAAACTGC CTCCCAAAGA GAGTTACCCA CATCCCAGAG AGAAGTCTTG GCATAAACAC 720
AATTCACCTC CTCACACACT AGACAGGAAA CCAACGCAGC TTGAAGCCAG TGACAAGAAA 780
AATCAAGCTG GAAATATGCC TCGGGGATCA GTCAAGAGAT TTGGAGAGGT GGAAAGAAGC 840
TGTCTGCCTA CTGCCTGTTT TGAAATTAGA TTTATTTCTG ATTAAGGACA ATTCTTTCAG 900
CAAATATGTA TTACAAGCCT TCCTTGGACA AGAACCAGAG ATATTAGGTT GAACCATATA 960
AAACTGCCAT TTTTCTATAT CAAAAGCAAC CAAATATTGG CCGTTTTAAT GGTTCAACCT 1020
AATACAGTGG TGAAAAAGGC ACAATATGTG CCCACAAGAG CTTACAATCT AGGTTGGAAA 1080
ATAAGGTCAA CAACAGGAAG CCTGGACCGA CTGACGACTG CCATCCGTCT CACAAAGAGA 1140
CAAAATATTT GAAATCAGGA TTGCTCCGGA TGGATTTTAA GAGTGCTGCA GCCATATTAA 1200
AGCACAGTGG TGGTTAGGAG GAAACGCTGA TCAAGTCAGG GGAAATGAAC ACGCAACACG 1260
CACATCTGAG GGAAAAGGTA ATCATGAATG GGCATTGTGA CTTTTACTAA AGGCAGAGCT 1320
TCAGAGTTGG TTCCCTTGAG AAACCCAGGT GTACCCGGTT CCTGTTCGCC AGAGCTGTGA 1380
ACGCTTTCAG GCAGTCACTC TGGGCACACC TGGACATCAT AAAATGCGGA GCTTCTCCCA 1440
GGGGAGGGGA TGCTGAGGCT TCAGGTACTA GTGAATCAGG CAGAACCAAT GAGAGGCAAA 1500
CAGAGCTGGG CTGAGAGGAG AAAAGGCATA CTTGTACCTT CTGGATTTTT CAGGCTTCGA 1560
AGACAAGATA CAGAAACAGG TGAACTCACA AGAATATCTC CAAGGATTGT TGCAAGCTCC 1620
CTCGTGTCTA CACTAGTGAC ATCCAGTTTC CTGTCAGAGG GAGACATGCC CTTCCCCATT 1680
ATCGCCAGCA GGGGGAAGTA GAGAGCAGCA TCGTTGCATG CCGGCACCTG CTGCACAAGC 1740
CAAGACAAAG GAAAAACCAA GGACAACAGC AGCAAAAACC TCTAGGAGGG AAAAGAAAAC 1800
GGAGGAAGGA AGGAAAGCAA ATAATGAAAA GGAAGAAAGA AAGAAGGAGA GGGAGGGATA 1860
GAGGAGATTA AAAAAAGACA GTAAGATATT ACCCTACACC ACCTTATTTT GCAGCTTGTC 1920
TGAGAAAAAT CCAAACTTGC ATTTTCCAAA GCACTGCTTG AAGAGTGAAA TCTTAAAAAA 1980
TTAAATAAAT AATAAATACA AATAAGTGTT AACACCCATT TGTAGTTTTC AAATAGAGCT 2040
CAGAGTGAGG GCTGTGGCTC CATCGACTTG TTCAAGCCCA GGACCCCGTC TGCTTTGCGA 2100
GCATCATCTG GTGCTTCCTT AATCAACAGA CGAAGACCAG ACAAGCCCTG GTCATTGTCC 2160
TGCCCACAGG CCAGTTCAGA GCTAGACGGA GTTGCAGACT GACAGTAAGA ATGACATTTC 2220
CCTCACCTCT CCAAAAGCGG GGTGCTCTCA AGCCCAATGA GGGCGCATAC CGTGGACCGC 2280
ACCACAGGAT CAGGGGAATA GGTTGCTCAC GGCTTCACTC TTTGTCTCCA 2330
|
