| Tag | Content |
|---|
EnhancerAtlas ID | HS007-10124 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr20:36497070-36498120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr20:36497697-36497712 | AGGGGTGAGAGGTCA | + | 7.11 | | TCF3 | MA0522.2 | chr20:36497749-36497759 | AGCAGGTGTT | - | 6.02 |
|
| | 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 |
| GH20I037868 | chr20 | 36497301 | 36498022 |
|
Enhancer Sequence | TGTGTACCGT CGGCATATGT AAGCGAGGCC TCGGCACAGG TGATTCGGCA AAGGGATTGA 60
TGCAGGTGTG GGTTCCCTCT GCTTCGTACA TCCCTAGAAA GAACTCAGGG AAGCCGGCTT 120
TACTGTTGGA AAATCACTGC CCCACAGCAT CGGACTGTTT CTCCACTTCC CTCTCTCCTG 180
GGTCTGAGAA GACATTAGGA GAGCAAAGTG TTAGCTCAAT CCATTAAGAC TCCTGCTTCC 240
AGACCATGCC TCCGGGGATA TTAGATGCCA TAATGGTCAT TTCTCTCTCT CCTGGGGCAG 300
CAACTATATC ATTCACATGT GAGTAAGAGA TACCACTTAC ACACAGCCCC AGAGCCTTCT 360
GCCAAAGCTC AGTTCCTGTC TCCATCACCC TGGCCCTCTC TCTAAGGGGC CTTAATAGGA 420
GGCATCACAA CCACTTGCTG TTGGAGGTGA TGGATGGGCC TAACAGAAGA GGATTTCTGG 480
GGGTAGACAC ACAGCTGGCA CATGCCTGAA TCCCACATCC CATTTTCTGG CACACGACCA 540
AAGTAATAAA GAGGAACGGG GCAAAATAAA GAGGTAGCAG GAGCAAAATT ACTTCCCCAG 600
CATTGGCAGG GGTGGGGCTG ACAGGGGAGG GGTGAGAGGT CACATGCTTT GTCTCCCCAG 660
TCTTTGTCTG GTTTGGATCA GCAGGTGTTT TATTATGCAA AAGCCTCTTA CTAGAGAGTT 720
CTCTCCATTT TCTTTCTCAA GCCAGGCCCC AGTAAGGGAC CAGGGGGCAG AAGTGCAGGC 780
AGCCATCCTA GTCACCCACT GCAGGAGATC CTTCAGCACG ACACTCTGCT GGGGGGCCCT 840
CGGCCAGGCT TAGCTGGGAG GAAGGCGAAA GCCCCTGCCT TCATGCAGCT CTCTGTCTAG 900
GGAGAGAGGG GCTGGGTGGA GGATGGTCTA GCAGTCAGGC CCACATGTGC TGGAGGCAGT 960
GGCCTGGGGC CGGGTGTGGG AGTGAGAGGT GACCAGGCAG GCTTTCACAG AGAAGACATC 1020
TCAGGAGGGG ACCCGGAGGA GGTGTGGGAC 1050
|
