| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29568 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:37592350-37593490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrrg | MA0643.1 | chr2:37592901-37592911 | TCAAGGTCAT | + | 6.02 | | MEOX2 | MA0706.1 | chr2:37592458-37592468 | AGTAATTAAC | + | 6.02 | | RORA | MA0071.1 | chr2:37592900-37592910 | ATCAAGGTCA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGGCTCTCT AGTGTGAAGA GGGAAGGGAG ATGAAGGGAG CCATTAGTGC TAAGGTAGGA 60
GGAATATGGT ATCTTAGGAA CCAAATGAAG CAAGTGTAGC CAGGAGGGAG TAATTAACTG 120
TGTTGAATGC TGACAATAAG TCAAGAGAGA TGAAGACTGA GAGTTGACCA CTGGATGTAG 180
CCATGTAGAG TCATTGGTGT CTTGACAAGA GCAGTTTCAG TACACGGTGG AGATAAAACC 240
CAACTGGGCT AAGTTTAAGA AGTGGGATTG GAGACAGCGT GAATAGACAA CTCCTTCAAG 300
GGGTTTTGCT ATAAATGGGA TTACAAAATT GGGCAGTAGA TGGTGGAGAT AGTGAGGTCA 360
AATATTTTAA GATGAGAAAA GCAACAGCAT GTTTGTTGGC CGATGGGAAT TATCCAGCAG 420
AGATAGAAAA ATTGATGATG TAGGAGAGAA ATGGTATTTG CTAGAGCAAT GTCCTTGAGC 480
AGATGAGAGA GGATAGGATT TTGTGCATAA GCAGGGAGAC TGGCATCTGA TATGAGCATG 540
ACAGAAAGAA ATCAAGGTCA TCGGTTGGGA ATGAAGATGG GTGAGGTGGC AGGGAGAGGA 600
GGAATGTGAA ATCCTAGAAG AGTGCCAGAG TGACTGAACT AAGAAAATAC AAATGACTTG 660
CCAGTCAACA TGAAAGGCCA ATGTGAGGTT TGTGGTCATG AACTTTAAGC AAGGCCAGAC 720
AGTGTGGTTA TATATTTTTT TCTCTGGTGA GGTTTAGCTG CACGAGTGCT GGCACAAAGT 780
AGGTAGAGTA TGTTTTTGCC ATGAAAGTTT GACAAAGGCA GAAAGGGGCA AGGGAGTTGA 840
GGGTGTATGC TAGTGAGTGA TTGGCATGAT TGACTGGAAT TTAAGCCAAA TATAGAGTGA 900
AGTGAGGACA TTATGGGGGT GAAGGACCAT GAAAAGGTGA AACATTCAGT AGATTAGGGG 960
TTCCAGTGGG ATTGAAGGAC TTTGGAGTTT AGAGTACCAG GACCAATCTG AAAGACAGGG 1020
GTTATTGTCA GACGGAGGAA AGTGTAAAAT CAGTTAGAAT CCTAGTCACT CTTTTTAGTT 1080
CCATTCAAAT ACTGTCTTTT TCATAAAGCC CTCCTTGACA CCCCCAGGAT TTTGCTTCTC 1140
|
