| Tag | Content |
|---|
EnhancerAtlas ID | HS091-38572 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:78851400-78852880 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr5:78851538-78851556 | TTTTCATTCCTTCCTTGC | - | 6.18 | | NFKB1 | MA0105.4 | chr5:78852810-78852823 | AGGGAATTCCCCT | + | 6.07 | | NFKB1 | MA0105.4 | chr5:78852810-78852823 | AGGGAATTCCCCT | - | 6.18 |
|
| | 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 |
| GH05I079556 | chr5 | 78852024 | 78852423 |
|
Enhancer Sequence | TGCCCTTGTA GCCAGTTTCG CGTGGTACTG AACCAAGTCT TTATATAGCA CTACTCTTCT 60
AAGGAACATG ATATTCTTTA CCAACGTTCA ACTCACTAAT CTTTATGATG TCCCTGGCAT 120
TTCAACAGAC ATCAAGAATT TTCATTCCTT CCTTGCAAAT AAAGAAACTC AATCTTAAAG 180
TAGTTAAGTC TGTTTCCAAG AATTTTACAA AGTAGATCAA TGCCATTCTC TTTAATCTAC 240
TAGAAACCTC AGACTCCAAC TGAAAAAAAA AGTGTTTTCT TTTTCAGATT CATAGTCATA 300
CCCATTTAAC CCATTTTGAA AGCCTCCTAT GGGTTGAGTA CTACGTAAGT TATTTTGTTT 360
AATCCTCAGG AATTCTCTAG TCTTTGATCT ATTTATATGA TGATTAATGA CATTAATTTA 420
GTTGTACTGT AATGCATCAG TAAATTTGTT TTTTCATCTT AGGAGCAGAA GCGCTGAACC 480
TTTTTTCTTC ACTTTTTATT GAAAGTGAGT TGCATTTACA GAAAAAGTAA ATGCAAAAAT 540
TTTAAGCGTA CAGCTAAAAG ACACGATTGC TAAGACGAAA TGTTAATTCT TATCTGAGAA 600
AAATAATTTT TCATTTACGT GTGTTTTCAA AAATTGTAGT AACTTCACAA AAAGCCTTAA 660
TTTTTTACTA TTTTTAAAAT TATAATGCCT AAAATGTTTT GCTCAGGGAT TTGAGGCAAT 720
AACCACCATT TTAAGCTGGT TTCTCTAGTT GCAAGACCAG AAGGGGAACC ACTAGGGGGC 780
GTGCAAAACT GTCATTTCCA AAAGTATTCT GCAATTACTG AATCGGAATT TTAGAGAGGG 840
AAGTGACCTG GAGGTCATCA AATCAGAACT TCATATTTTT TGGACATAAA AACTGAGATC 900
CCATGAGATT ACCTGATTTG CCCAAGATCA CACAGCCATC TGTAAATCTA TAAGAGGCAC 960
TTTAGAGGGC AAGCTTTTTT TGTACCTGTC CAGCTCATAT TCTTCCTGGT AGTAGTGAGA 1020
TTTCAGTTCT TTCTATAATA TCACTTGTCG AATATTTACC ATCACTTGGT AAACCACTTC 1080
ACTGAATTTC CCATCCTTCC AGATTTTGCT TCCTAGGTGG AAAAACCTAG AGACTTGTTT 1140
TAAGTGTCTT GGAATGTCTT CTTATGGGGC TGGTGATAAT AATAATATTT TGAAGCCAAA 1200
ACAGTAAGCA CAGCATAAGC ACTCCCTATT ATATCATTAT TCAGCAAGGA AATCATCATC 1260
ATCTTAAATA CATGTTCTGT GAATACGGTA GTTTGGAATT GCTTTGAATT TTTATTTTTC 1320
ATTGATTGAT TGATTGATTG AGATGAAGTC TCACTCTGTC ACCCAGGCTG GAGCGATCTC 1380
GGCTCATTGC AGCCTCTGCC TCCCTGTTCA AGGGAATTCC CCTGCCTCAG CCTCCTGAAT 1440
AGTTGGGACT ACAGGTGCAC AGCACCACGC CCTGCTAATT 1480
|
