| Tag | Content |
|---|
EnhancerAtlas ID | HS105-14814 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:68309390-68311230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:68310184-68310202 | GGAGGGAGGGAAGGAGAG | + | 6.44 | | Nr2f6(var.2) | MA0728.1 | chr11:68310080-68310095 | TGAACTCCTGACCTC | - | 6.22 | | SP2 | MA0516.2 | chr11:68309610-68309627 | GAGTGGGCGGGGGTGGG | - | 6.25 | | ZNF263 | MA0528.1 | chr11:68310571-68310592 | CCTTTTTTACTCCCCTCCTCC | - | 6.5 | | ZNF263 | MA0528.1 | chr11:68310181-68310202 | TAAGGAGGGAGGGAAGGAGAG | + | 7.36 |
|
| | 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 |
| GH11I068541 | chr11 | 68309116 | 68311390 |
|
Enhancer Sequence | GGCCCAGGTG AAAGCCTGGA GGCAAGCAGA GACAACTCTT TGAAGTGATT TCTTGTAACA 60
GGAGCAGAGA GGAAGTGGTA GGTCGAGGCA GATTTGGAGT CAGGGGTGGT GTGGGGTTTT 120
GTTTTTTCCT AAATGGAAGT GATGACCTGT GAGAACGTTG CAGCACAGAG GAAACACAGC 180
CAGTGTGAGG GAGCAGGCCG CCGAGTGATG CATTGTGCTG GAGTGGGCGG GGGTGGGGGC 240
ATGTGGTCCA GAGCATACAT GCAGGAGATG ACCTCAGGAG CAAGGGCCAC TCCCCTGGAG 300
CGAGGAGGAA GTGCCCAGCT GTAGGTGGGG ATGTGATAGG GCTGGGTTCC CTTCTGATTG 360
CCTTCTCTGT GTTCTCAGGC AAAGGAAGCG AGGTCAGAGC CTATGGAGGA GGAGGGGTCT 420
TGCCGAGGGT GGAGTGGAGG CATCTTTGGG TGCTTGAGAA GCTGCTGTTT TTTTTTTTTT 480
TTTTTTTTTA AGACAGAGTC TTGCTCTGTC ATCCAGGCTG GAGTGCAGTG GCGCAGTCAC 540
AGCTGGCTGC AACCTCTGCC TCCCAGGTTC AAGTGATTCC TGTGCCTCAG CCTCCTGAAT 600
AGCTGAGACT ACAGGTGTGT GCCACCACAC CTGGCTAATT TTTGTGTTTT TAGTAGAGAT 660
GGGGTTTTGC CACATTGGCC AGGCTGGTCA TGAACTCCTG ACCTCTGGTG ATCCATCCAT 720
CTTGGCCTCC CAAAGTGCTG GGACTATTGG TGTGCGCCAC CGCGCTCGGC CTTGAGAAGC 780
TTCTTGAATG TTAAGGAGGG AGGGAAGGAG AGTAGCCCCA GCCTGTCTGG AACCAGAACT 840
CTGAGCTTTT TGTGTAATGG CTAACATTAT GCATGCTTCT TGAGTTAGGT CATACCACCC 900
AGTCACCTAG AAAAAGTGAA CAAATTTTAA AGTTGCTCAT CTGGACTTTC TCTGTCAGAG 960
TTTGGAGAAA ACACTCATGC ATTTGATTCA CAGCCAGGAG TCCGCTTGCC TTTTACTGAT 1020
CTTCTGTTTG TCAGCAGTTT CCACATTAAG ACAGTTGAGT GAGTGCATCT CCCCAACCCA 1080
CTCTAGCAGC ATTCTGCCAT TTTATAGTGA AAATAAAGAG GAATGAAAAC AGCTGTCATT 1140
TATTAAACAC TTATTTACTT TATGCCAGGC CCTCTTCCCA GCCTTTTTTA CTCCCCTCCT 1200
CCATAAGATA AGGACTATTG TCTTAATCTT ACTAACTTGG AAACTGAGGC CCAGAGAGGT 1260
TAAGTAACTT GTCCAAGGTT ATACAGCATG TAAGTGGTAG AGGCCGGTTT TGAACTTAGC 1320
TAGTGTGACT CTAGTAGCTG CACCTGTAAC CGCTGCATCA GCCCACTCCT GGGATAATGG 1380
GTACTTTACA GGGGTTTATA TTCTGGCATC TTGAAGCCCA TGCTACGTAA ATTGAGGGAG 1440
GAGACTTTAC TTCCCAAAGA CCCATACATC TGCCAGGTCT GTTTTTTTTT TTTTCCTTTT 1500
CTGTTTTCTT TATACAAAGA CTCATTTTGG GACCTTCTCA TACTCTTCTG TCTTTAGGCC 1560
TCACACCAGA GCCTGTCAAG TGCCGTGGCT TTCTGGTTCG TCACCAGTGG TCTTTTTGTG 1620
CCAGGGTCTT GCTGCAGGCA GCACTTGCTT GCCTTGGATG CCCCAGGTGT GTCGTATACG 1680
TGTCCCTCCT GCCCCAGTCT TCCCTGGTTT CTTTTGTCAT GCAGCCACGT TTGGCTATTT 1740
TGCCATCTCT CTGTCTTGCT CAGCTTTTGA GCTTGCCACT CCTGATGACT TGTTGGGGCG 1800
CTGGGTCCTG GCTGTCCAGC AGGGAGGAGT GTAAGAGCAG 1840
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