| Tag | Content |
|---|
EnhancerAtlas ID | HS105-34914 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:54776060-54777570 |
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 | GACAGGCATA GTATGACTTA TTTTATACAC ACCACCTTAT TTATTCTTCA CAATAGCCTG 60
GTATAATGGG TACTATTATC CACCCATATA GATGAGGAAA CAGGCTCAGA GAATGAGATA 120
CCTTACTCAA ATTCACACAG CTAGTTGGTA AGGGGGGCCT GGATCCAAAT TCTGTGCTCC 180
TTTGATTTCA CTATGCTCTA TTTCCACCGA GGAAGTGGGT TCCCTGGTGG GGCCAGGGAG 240
GTGGCTCTAT GGCTATGAGC CAAGATTTTA GGCCAAGTCA AGGTCATGGA CTCTTGGGAT 300
CAGCCCTGGG GCCAACAGGC TGCCAGAAGT GACAGAACGA AGAAAGGAAA GGAAGGAGAG 360
AAACAGGAGA CAAATCTTGA TGGCTTCCCC ATATTGCCAT TGTCCTACTT GGGGAGTTCC 420
ACCTTCATCT GTTTTACCCT TTTTTTCCTT TACCTTCGAG CTCTACGTCT CTTTATCAGT 480
AAACTAGCCT TGCAGACAAG TGCAAACTGT GCCAGCCCTT AGGCTGCAAA GGAAATGAAG 540
TTGGCATTCT GTAGTCCTCA CCTGGCATGA ATCACACACA GCCCCAAGGG ACCGGGACAA 600
GGCTACATGT CAGACTGATG GACTATTGTC TGGAGCTTTG AGAGAGGAAA AAGGGAAGGC 660
TGCTTGCAGG AGAAAGGTGA ACAGGTTGGC CCCGGCCCAA GAATGACAGA GGCGCCTTGC 720
TCCTGCCACC CGGCTCTGCT CCTCTGGCCC AGGAACAATA ACAAGGCGCT GTCAGGAAGT 780
GACACTAAAA TGCCTTTCCC CTTATACCTC GTTCAGCCTC TGGCAAAAGG AGGTTCCCGG 840
AGGGAATATT TTTAGTTTGA CAAATGAAAG CCTGGGACCG AGGACAGGAG GGATAAAGGG 900
AGCTCTTCTC TGACACTCCT GGAGACGGGG AGATGATGAG TCAGATACAG AGGGCTTAGG 960
CACGACTTCT CAAGACATTC CTCAGGCATG AGCACAAGCC AGCCGCTCGA ATTCCTCCTG 1020
CAAGGCCCGC CACCCGGCAA TCAGGGCGGA GGGGCCGGGC CAGAGGAGCA GCTCTGCTCT 1080
GTCTTCCTCT TGGCACATTG TTGGACAGCA GCTTTGGAAG ATCAAAGCAG CCGCCTGTGT 1140
TGCTTTCCGG AACTGGGACT CAGGAGGCCT GGGTTCAAGT CCAGGCTTCA CCATTTGCCG 1200
GCTGTGACAT TAAGTGTCCT CATTTCTCCC TTTATGCCTC AGTTTCCTCA TCACCAAATT 1260
GAGAGTATTA TAACACCTTG GAATTATTAT TATGAGGTTG TACATTTGGA AAAAAAAACC 1320
TTGAGAATGC AGTGTTTAAA AGCATTGGTT TTCTGTATTG CTCCCAGTAC CCCATATGCA 1380
GATGGACTCA AAATCTCACA CTGGTGGCCA CGTGCAGTGG CTCACGCCTG TAATCCCAGC 1440
ACTTTGGGAG GCAAAGGTGG GTGGATCACC TGAGGTCAGG AGTTCGAGAC CAGTGTGGCC 1500
AACATGGTGA 1510
|
