| Tag | Content |
|---|
EnhancerAtlas ID | HS176-14026 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr15:65872000-65873400 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr15:65872268-65872280 | AGTCAGCACTTT | - | 6.32 |
|
| | 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 |
| GH15I065578 | chr15 | 65871246 | 65873515 |
|
Enhancer Sequence | AAACAAGACA GAAAATCACC AATGCTCCTG AAATGTGTTC CTAACACATA CTTTCTAAGT 60
GCTCAGCTTA GCATAAGTTC TCCTTGACTG AACTTTAGGG AGCAATTTTA TATGAGAACA 120
AATGTTTATT TAGGGATGCC AGTAACAAGA ATGTGATGGT TTTACTGGGA AGTGGTTCCT 180
CTGCAGGTGA CCAGAAGCAG GCTAAGGAAG ACAGCTGAAT GAAACAACGT CATCATCACA 240
GTTAATGAGC ATTTATGCCA CATGTGGTAG TCAGCACTTT GCATCCATCA TTTCGTTACT 300
CCTAACTTTA AGGAGGAGTA CTTTTCCCCT GTTATTTAGG TATGGAAAAG ACTTGCCCTC 360
AATCTGAAAA CGCTCTTAAC CCTCTGATGC CACTGTGGTG GGGCCTCAGG CTAAGACAAT 420
AAACAGGCTC AAGAGGAGGC CCTGGAGGAG TCAGAGTGGA AAGACCAACA AAAAGAAAGG 480
CTGGTTACTG ATAGAAGCAG AGAAATATGA AGTGCCCCAA CAACCCCTTA GTGGAGTGGT 540
CTGGGCAAGT TATATAGCCT CTCTGGGTCT CAAAGGCCTC ATTTATAAAA TGAGGAGAAT 600
AACCCCTTCC TTACCCACTG CAGAGGCTGA AGCACTTTCC CTAGGCCCTT TTGAGCTCTA 660
ATATGTAGCA TTATATAAAA CCAGAAAAGA GAAATGGGCT CTCTGACCAT CTTTCTACTA 720
TCATCTGTTA AAAAAGTGGA AAGTTAAGAA GAAGGCCAAA CAAGTGTGTC ATCATGAGTA 780
AATAGCTGAT GACTGTAGGA AGCTCTGCAG GGAGGATGGA CTGTGTGGAT TATGGGCTTC 840
AGTTTAGGGA GGGGCCTGGC TGGCTAAGAA GCTCTCCAGT TGAACTCTTG ATTAAAGCTG 900
TTTTATTTCA CCAGCTTACT ACATAATTAA GTTTGAAGAC AACAGTGACA TAAAGGTAAT 960
GAGATAACAC CCAGACAAAG TAGCATGTAT CTTCTCTGGT TAAGATGCTA GCCTAAGGCT 1020
GGCTGTGTGT GCCACATTTT AGAATTAGAA AGCTAAGACA CAAATGACAT ACTTTATGCT 1080
GCACTTAATT TAATTCCAGC CAAACACCAG AACAATAGGG GAGAATCAAG GAGCAAACCT 1140
AAATGTTCCC CACTCTACCC CACCCCCTGT AACTTAACAG TCTCTTCACC AATCGTTCTG 1200
GATTAGCTGC ATATGATTCT GCAGGGCTAT CTCCTCTGCA ATTCATAAAT GTGTAATGTT 1260
AGATATCATT CCTAGAAGCA GAGTCTCTGG TGCAATAAAA ATGTTCTGGG GTGGCCAGGT 1320
GGGGTGGCTC ACGCTTGTAA TCCCAGCACT TTGGGTGGAT CACCTGAGGT CAGGAGTTCG 1380
GGACCAGCCT GGCCAACACA 1400
|
