| Tag | Content |
|---|
EnhancerAtlas ID | HS082-21332 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr20:37302260-37303500 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I038673 | chr20 | 37302244 | 37303683 |
|
Enhancer Sequence | GAGGTCCCTG ATCTTATGAA GTTTATGGAA AACTACCTAA TTACAAAATT ACTTCACGCC 60
TTGAAAAAGA ACGGAATGAA CAGGACGCTA TCATACAGAA TAACGGAGGG GTGGGGCTCC 120
ACTTCTGATC AGAGGGTCAG GGAGGACCTC TTGGAGGCGG TGATAGTTAA GCTGACACCT 180
GAAGAAGCCA GTCATGCAAA GAGTGGGTCA ACAGCTTTCC AAGGCAGAGG GAATCAGGAA 240
AGCGATGGGC TTGTCTGAGG AACAGAAAGG ACAACGAACG TGTGAGTCAC ACTAAGGGGC 300
GCCGTGGTGC GGCATGAGGC TGGAGCCTGA TCACTCGGGG TCTTACTGGC CACGGTGAGG 360
AGTCAGGGTT TCATGCGCCC CTGCAGTCAG AAAGCATGGC CCAACCCCAG TGCCCTAAGT 420
CCGGAAACAT TCAAAGCTGG ACCCAGGGTA GCGGGATCCG GGGCCTCTGG GGACCCGAGA 480
GGGACGTTAA GTTCAGGGCT TCAGGGTGCA GCCCTGGGGT CGGTACCCCC AGCCTCCAAC 540
CCAGAGCTGG CAGCGCTCGC CCCCTTCTCC GCGCGGGCCC TCAGCTCAGC TCCCTCTTCG 600
CTCCCCGTGT CCCCGCGAGC GGGAGGGAGG GGATGCTAGG ACGCCCTGTC GGCGTCGTCG 660
CCGCTTTCCG CCATTGTTTA GTCGTGATGC TCTCATTTTC TCTGAATCAA CAATTTTCTG 720
CTCGGCTCCG CGCCGACCGG CGAACGCGGG GCTTTTCCTC GCCCGCCTGA TGACAGCAGA 780
GCGGCGCGGA GCAGCTGGTC CGGAAGGAAG CGCCAGGCGC CTGCCCGGTC CCAGGCGTCC 840
GCTGCCGCCC ACCCACACCA GACCCCGCCC CCGCGCGTCA AGCCCCGCCC ATCCATACCA 900
AGTCCCGCCC CCACACCCTC ACCCACACAC CAGGCCGTCC CCACCCCGCC CCCAGAGCCC 960
CGGGGCGCCC CGCCCGCTAG CCGCGCACGC GCAGTGAGCA CGGCGACCCC CGGTGGTCGG 1020
GTGTCTCCGC AGGCCGAACA CGCTGCTCGC CCAGCTGCGG ATCATTACCG CCCTTTTGTT 1080
CTCCGTCGCG CGCTCGCCCC ACGCTAGGAA TGCAAACTGT AGGCGCCGCC AGCCCCCCCT 1140
TCCTGTTTCC CTGGGTGGGA GTGGGAAGGG AGTTTTAAAC TGAATTGTGC TCAGACTCCC 1200
AGCCCAGTCT TCCCGGAGCC ATCCGTTCCT TCATCCAATG 1240
|
