| Tag | Content |
|---|
EnhancerAtlas ID | HS091-16021 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:2479500-2481130 |
Target genes | | Number: 44 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:2480235-2480253 | GGAAGGAAGGATGGATAG | + | 7.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGTGCGGGG CGATGTCCGC TGGTTTCTGC CCCACACCCC TTCTGCCTGC CCTGCGGGGC 60
GGACGGTGGG TCCCGCGGGA GGGGAGGCCC TGGCGGCCTG AAGAGGGCTG GCTCGAGCTC 120
TTTAACCCGG GGCGGATGTC GCGTCCCGCG CAGGGAGCCC CGGCGGCCGG GCGCGCGGTT 180
TAAATGCCCG GCGGGCGCCC GAGCCCCTCG GAGCCTTCCC CCGCGGCGAC GTTTTCCGGC 240
CCTTTCCTGG GGCAACGATC GGGTCCCGGG GCAGCGATCC GGCGATCGGG TCCCGGGGCG 300
GCGATCGGGT CTCGGGGAGC CAAACACCAG CGCCTCCTGG TCGGGGAAAG GGCTGCGGAG 360
CGCGTGGGGG CGAAGCGATC CCGCAGCCCG GCCGGGCCCT GACCGAGCCT CAGTCCAGCG 420
GGGCCGTGGA CCTAGCTCTG TGGAAAGCAG CGTTCGGCCC CGCGCGCGTT GAGGCACAGG 480
AAACACGAAC TGTGGTTTCA GCTATTATCA TAGTATCTGT CCTGGAGCCG GAGAATGAGG 540
AATATTTTAT GGAGAGGTCT ATAGAATCTT TGAGAATTCG TCGCCCTGGA ATACGTTTGG 600
CTTTTGCAGC TGATTTAATT GCTAACAGGA AGACCCCGGT CAAGAGAGGG GAGCCGGGAG 660
CAATCGCTAG GAAGTCCTAG CAAGGCGGGG AGGGATTTGG GCCCACAGAG GGGAGTGGCG 720
CTTCCTTTCA GGACTGGAAG GAAGGATGGA TAGAAAGGTA GATTTGTAGA TGGGGAGGCA 780
GGATCCTGAG GTTCCTGTCT GAGGGCTTCT GTTTCCCTGT GAAATAAGGG CTAAGGTCAT 840
CTGCTTAGAG TGAGGAAGGG GTTGCTGGAG TAGGAGTTGG AAAATCCGGC TGTGGGAAGA 900
GGAGAGAGCA CATCTGAGAA GCATGTCCGG GCTGCCTGCC TGGTGGGTGG AATGCCCGTC 960
TCACCTTTAA TGATTGCATC TGTACACAAA CCTACAGGTC TAGGTTTGTG TTGGGACCTG 1020
AGCAACAACC TTACTGCGTA GCTGTCAACT CCGCATTCTA CAATAGAGGG CACACTGAGA 1080
CTCTGCAGAG CTGAGACTTG GACGCACACT GCCCCGGCCT CCAAGTCTGT GGCTTCTCTC 1140
CAGGGCCGAC CCTTCTAATT TGGACTTGAA AACCAGACTC TTCAAGCCCA CAGATCTTTA 1200
TTGAACATTA TGCACCTTGG TCACGTGTGC AAAAAGCAAA GCTATCCAGC AAAGGCCCCA 1260
GGAGTTTTCC TGAGAGTGAA ATAGAAGGAA AACCGTCCTC AGCTTCGGCA GCTTTTTCCC 1320
CTTCCTGCCT GTCATGTGGG CTCTGGATCA GAAAGTTTCC CAATAGCCAA GTTACATGAC 1380
ATGCGCTATT TGCCATAAAT ATTTGTTGAA TATTTGAAAA TGAATGATCT CTTCTGTAAT 1440
TTGTGCAATG CCACTCCTTT ACATAATCTT TGTTTGGGAC AAGAAGCATA GTTCCATCTT 1500
TTGTGGCACA GGGAATAGTA ACCATTAGAT CATCTTCAGA TGTAACTTTT ATCCTTTTTT 1560
TTTCCCTTCA AGGGTGTGTA TATAGAATAA TTTTTCATCT TATCAAGGCT TCTGTCTTTT 1620
TTTCCTTCAG 1630
|
