| Tag | Content |
|---|
EnhancerAtlas ID | HS098-24531 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:54776220-54777740 |
SNPs | | Number: 2 | 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 | GGATCCAAAT TCTGTGCTCC TTTGATTTCA CTATGCTCTA TTTCCACCGA GGAAGTGGGT 60
TCCCTGGTGG GGCCAGGGAG GTGGCTCTAT GGCTATGAGC CAAGATTTTA GGCCAAGTCA 120
AGGTCATGGA CTCTTGGGAT CAGCCCTGGG GCCAACAGGC TGCCAGAAGT GACAGAACGA 180
AGAAAGGAAA GGAAGGAGAG AAACAGGAGA CAAATCTTGA TGGCTTCCCC ATATTGCCAT 240
TGTCCTACTT GGGGAGTTCC ACCTTCATCT GTTTTACCCT TTTTTTCCTT TACCTTCGAG 300
CTCTACGTCT CTTTATCAGT AAACTAGCCT TGCAGACAAG TGCAAACTGT GCCAGCCCTT 360
AGGCTGCAAA GGAAATGAAG TTGGCATTCT GTAGTCCTCA CCTGGCATGA ATCACACACA 420
GCCCCAAGGG ACCGGGACAA GGCTACATGT CAGACTGATG GACTATTGTC TGGAGCTTTG 480
AGAGAGGAAA AAGGGAAGGC TGCTTGCAGG AGAAAGGTGA ACAGGTTGGC CCCGGCCCAA 540
GAATGACAGA GGCGCCTTGC TCCTGCCACC CGGCTCTGCT CCTCTGGCCC AGGAACAATA 600
ACAAGGCGCT GTCAGGAAGT GACACTAAAA TGCCTTTCCC CTTATACCTC GTTCAGCCTC 660
TGGCAAAAGG AGGTTCCCGG AGGGAATATT TTTAGTTTGA CAAATGAAAG CCTGGGACCG 720
AGGACAGGAG GGATAAAGGG AGCTCTTCTC TGACACTCCT GGAGACGGGG AGATGATGAG 780
TCAGATACAG AGGGCTTAGG CACGACTTCT CAAGACATTC CTCAGGCATG AGCACAAGCC 840
AGCCGCTCGA ATTCCTCCTG CAAGGCCCGC CACCCGGCAA TCAGGGCGGA GGGGCCGGGC 900
CAGAGGAGCA GCTCTGCTCT GTCTTCCTCT TGGCACATTG TTGGACAGCA GCTTTGGAAG 960
ATCAAAGCAG CCGCCTGTGT TGCTTTCCGG AACTGGGACT CAGGAGGCCT GGGTTCAAGT 1020
CCAGGCTTCA CCATTTGCCG GCTGTGACAT TAAGTGTCCT CATTTCTCCC TTTATGCCTC 1080
AGTTTCCTCA TCACCAAATT GAGAGTATTA TAACACCTTG GAATTATTAT TATGAGGTTG 1140
TACATTTGGA AAAAAAAACC TTGAGAATGC AGTGTTTAAA AGCATTGGTT TTCTGTATTG 1200
CTCCCAGTAC CCCATATGCA GATGGACTCA AAATCTCACA CTGGTGGCCA CGTGCAGTGG 1260
CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCAAAGGTGG GTGGATCACC TGAGGTCAGG 1320
AGTTCGAGAC CAGTGTGGCC AACATGGTGA AACCCTGTCT CCACCAAAAA TACAAAAATT 1380
AGCCAGGCAT GATAAATAGG TGCACGCCTG TAATCCCAGC TACTGGGGAG GCTGAGGCAC 1440
GAGAATAGCT TAAACCTGGG AGGCAGTGGT TGCAGTGAGC CGAGATTGCA CCACGGCACC 1500
CCAGGCTGGG CAACAGAGCG 1520
|
