| Tag | Content |
|---|
EnhancerAtlas ID | HS086-08529 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr20:37302340-37303720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr20:37303138-37303153 | CAAGCCCCGCCCATC | + | 6.34 | | SP2 | MA0516.2 | chr20:37303137-37303154 | TCAAGCCCCGCCCATCC | + | 6.3 | | SP2 | MA0516.2 | chr20:37303157-37303174 | CCAAGTCCCGCCCCCAC | + | 7.2 | | SP4 | MA0685.1 | chr20:37303138-37303155 | CAAGCCCCGCCCATCCA | + | 6.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 37302978 | 37303466 | | chr20 | 37303200 | 37303600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I038673 | chr20 | 37302244 | 37303683 |
|
Enhancer Sequence | CAGGACGCTA TCATACAGAA TAACGGAGGG GTGGGGCTCC ACTTCTGATC AGAGGGTCAG 60
GGAGGACCTC TTGGAGGCGG TGATAGTTAA GCTGACACCT GAAGAAGCCA GTCATGCAAA 120
GAGTGGGTCA ACAGCTTTCC AAGGCAGAGG GAATCAGGAA AGCGATGGGC TTGTCTGAGG 180
AACAGAAAGG ACAACGAACG TGTGAGTCAC ACTAAGGGGC GCCGTGGTGC GGCATGAGGC 240
TGGAGCCTGA TCACTCGGGG TCTTACTGGC CACGGTGAGG AGTCAGGGTT TCATGCGCCC 300
CTGCAGTCAG AAAGCATGGC CCAACCCCAG TGCCCTAAGT CCGGAAACAT TCAAAGCTGG 360
ACCCAGGGTA GCGGGATCCG GGGCCTCTGG GGACCCGAGA GGGACGTTAA GTTCAGGGCT 420
TCAGGGTGCA GCCCTGGGGT CGGTACCCCC AGCCTCCAAC CCAGAGCTGG CAGCGCTCGC 480
CCCCTTCTCC GCGCGGGCCC TCAGCTCAGC TCCCTCTTCG CTCCCCGTGT CCCCGCGAGC 540
GGGAGGGAGG GGATGCTAGG ACGCCCTGTC GGCGTCGTCG CCGCTTTCCG CCATTGTTTA 600
GTCGTGATGC TCTCATTTTC TCTGAATCAA CAATTTTCTG CTCGGCTCCG CGCCGACCGG 660
CGAACGCGGG GCTTTTCCTC GCCCGCCTGA TGACAGCAGA GCGGCGCGGA GCAGCTGGTC 720
CGGAAGGAAG CGCCAGGCGC CTGCCCGGTC CCAGGCGTCC GCTGCCGCCC ACCCACACCA 780
GACCCCGCCC CCGCGCGTCA AGCCCCGCCC ATCCATACCA AGTCCCGCCC CCACACCCTC 840
ACCCACACAC CAGGCCGTCC CCACCCCGCC CCCAGAGCCC CGGGGCGCCC CGCCCGCTAG 900
CCGCGCACGC GCAGTGAGCA CGGCGACCCC CGGTGGTCGG GTGTCTCCGC AGGCCGAACA 960
CGCTGCTCGC CCAGCTGCGG ATCATTACCG CCCTTTTGTT CTCCGTCGCG CGCTCGCCCC 1020
ACGCTAGGAA TGCAAACTGT AGGCGCCGCC AGCCCCCCCT TCCTGTTTCC CTGGGTGGGA 1080
GTGGGAAGGG AGTTTTAAAC TGAATTGTGC TCAGACTCCC AGCCCAGTCT TCCCGGAGCC 1140
ATCCGTTCCT TCATCCAATG CGGACACCCA TATCTAAGGT TCGGGCAGGA TTTCCGGGGC 1200
ACCCTCAAAC CCAGCCCGTG GGATCCGGGA AGGCCTCCTG GAGGAGAGTC CACGAGGCAC 1260
GGAGCCGAGG ATGGGGTTGG GGTTAGGTCT TGGAGGGCTT CGAATTTCCG GCAAAGGGTC 1320
TGGGATGGTT CTTGAGGACA GCAGGGATTT GCAGGGAGGC TGGGGGTGGA GGTGGGCAGA 1380
|
