| Tag | Content |
|---|
EnhancerAtlas ID | HS091-27331 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:114457350-114458650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:114457928-114457947 | TAGTACCCTCTTCTGGCCG | - | 6.32 | | Foxd3 | MA0041.1 | chr2:114457503-114457515 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:114457507-114457519 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:114457511-114457523 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:114457515-114457527 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:114457519-114457531 | AAACAAACAAAC | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 114457813 | 114458179 | | chr2 | 114457868 | 114458149 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I113699 | chr2 | 114457378 | 114458177 |
|
Enhancer Sequence | AATTAGTCGG GTGTGGTGGC GCATGCCTGT AATCTCAGCT ACTCAGGAGG CTGAGGCAGA 60
AGAATCGCCT GAACCCGGGA GGCGGAGGTT GCAGTGAGCC GAGATCAAGC CACTGCACTC 120
CAGCCTGGGC GACAGAGTGA GACTCTATCT CAAAAACAAA CAAACAAACA AACAAACAAA 180
CAAAAAACCA TAAGATTCCA ACCTTTTGGG CTCAGCAATT ACACTCCCAG AAGTCATGCC 240
TCAAATGCAC TTTTCTGTCT TCTAGGTCTT TTCTCCTCTC TGTCCTAATC TCCTCTCCAT 300
GCCTCAAGTG ATGCCAATAA ATGGGTAATA ATTCCCTTAA ACTCCGTGGA ATTAATTTCT 360
TTTTGACTAC AGGAATTCAC AGTTCAAAAC AAAATAACCC CAGATTCCTT AATAAATAGA 420
AACCTTAAAG TTCCTTCTAA AAAGATTCAC GGCTATAAAA GTAATAAATG AATCGCCCAA 480
AATATCGCGC TGTGGGTCGG GTTAATAACC CTATTGGACA GGAGCTGGCA TTACTCGGTT 540
TGGGCGGCCG AGCCCAGACA TCAGCATATG TGCTACCGTA GTACCCTCTT CTGGCCGAAT 600
ACAAAATCAA GTTTATGGGG CCGCTTTTAG TCAAGTTTTC CATAGCTGCT TACAAGCACC 660
GAGTTTCCTG CGACTTCCTG TTTATCGCCT CTGCTCTCCT CAAGTTCTCA GCTTTTTCTT 720
GCATCAGCTA GGCTTGCCTC CTCCTCCTCA GGGAAGATCA GGATCCCCTG ATATTCCTAA 780
TCTCAGCTCC CAAGATTTGC CCCTTGCACT ACCCTGTTTC CTGGCTGTTT GCACCATAGC 840
CTCCCACCTT GAGTAAGTCT AGTTCCATCT GTTCTCTCTT ATCTATCTGC CTCCGTACTG 900
GCCATTTACC ATATGCCCAC ATTGCATCTG GGCCTCTGCA CTCATGACCT ACCTGCCGTT 960
CCCTCACTCA CTGCCCCATC TCACCTGCAC TTGCCTGAGC ACTCTCCGTT GATTCCTTGA 1020
TCCAGGGTTT TATAAAATGA GGTCTGTGGA CAATCTACAT TCTCTCCACC TGGCTGCTTG 1080
CTACCTGAGC TCCCTGAATC AGACCTTCTG GAATCCTGGA ACCCGCATTT ATAATAAATA 1140
CCCTGAATAA TTTTTATGTA CATGCACACA CATACACACA AACACACACA CAACATAAAA 1200
ACCACCCTGG GCTGGGCACA GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGACCGAG 1260
GCGGGTGGAC CATGAGGTCA GGAGATCGAG ACCATCCTGG 1300
|
