| Tag | Content |
|---|
EnhancerAtlas ID | HS082-15048 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr17:54776200-54777540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr17:54776336-54776347 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr17:54776337-54776347 | TCAAGGTCAT | + | 6.02 | | RARA(var.2) | MA0730.1 | chr17:54776329-54776346 | AGGCCAAGTCAAGGTCA | + | 6.36 |
|
| | 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 |
| GH17I056697 | chr17 | 54774751 | 54777998 |
|
Enhancer Sequence | CTAGTTGGTA AGGGGGGCCT GGATCCAAAT TCTGTGCTCC TTTGATTTCA CTATGCTCTA 60
TTTCCACCGA GGAAGTGGGT TCCCTGGTGG GGCCAGGGAG GTGGCTCTAT GGCTATGAGC 120
CAAGATTTTA GGCCAAGTCA AGGTCATGGA CTCTTGGGAT CAGCCCTGGG GCCAACAGGC 180
TGCCAGAAGT GACAGAACGA AGAAAGGAAA GGAAGGAGAG AAACAGGAGA CAAATCTTGA 240
TGGCTTCCCC ATATTGCCAT TGTCCTACTT GGGGAGTTCC ACCTTCATCT GTTTTACCCT 300
TTTTTTCCTT TACCTTCGAG CTCTACGTCT CTTTATCAGT AAACTAGCCT TGCAGACAAG 360
TGCAAACTGT GCCAGCCCTT AGGCTGCAAA GGAAATGAAG TTGGCATTCT GTAGTCCTCA 420
CCTGGCATGA ATCACACACA GCCCCAAGGG ACCGGGACAA GGCTACATGT CAGACTGATG 480
GACTATTGTC TGGAGCTTTG AGAGAGGAAA AAGGGAAGGC TGCTTGCAGG AGAAAGGTGA 540
ACAGGTTGGC CCCGGCCCAA GAATGACAGA GGCGCCTTGC TCCTGCCACC CGGCTCTGCT 600
CCTCTGGCCC AGGAACAATA ACAAGGCGCT GTCAGGAAGT GACACTAAAA TGCCTTTCCC 660
CTTATACCTC GTTCAGCCTC TGGCAAAAGG AGGTTCCCGG AGGGAATATT TTTAGTTTGA 720
CAAATGAAAG CCTGGGACCG AGGACAGGAG GGATAAAGGG AGCTCTTCTC TGACACTCCT 780
GGAGACGGGG AGATGATGAG TCAGATACAG AGGGCTTAGG CACGACTTCT CAAGACATTC 840
CTCAGGCATG AGCACAAGCC AGCCGCTCGA ATTCCTCCTG CAAGGCCCGC CACCCGGCAA 900
TCAGGGCGGA GGGGCCGGGC CAGAGGAGCA GCTCTGCTCT GTCTTCCTCT TGGCACATTG 960
TTGGACAGCA GCTTTGGAAG ATCAAAGCAG CCGCCTGTGT TGCTTTCCGG AACTGGGACT 1020
CAGGAGGCCT GGGTTCAAGT CCAGGCTTCA CCATTTGCCG GCTGTGACAT TAAGTGTCCT 1080
CATTTCTCCC TTTATGCCTC AGTTTCCTCA TCACCAAATT GAGAGTATTA TAACACCTTG 1140
GAATTATTAT TATGAGGTTG TACATTTGGA AAAAAAAACC TTGAGAATGC AGTGTTTAAA 1200
AGCATTGGTT TTCTGTATTG CTCCCAGTAC CCCATATGCA GATGGACTCA AAATCTCACA 1260
CTGGTGGCCA CGTGCAGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCAAAGGTGG 1320
GTGGATCACC TGAGGTCAGG 1340
|
