| Tag | Content |
|---|
EnhancerAtlas ID | HS060-14485 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:29390470-29391830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr17:29390625-29390640 | TGACCTTTCACCTGG | - | 6.39 | | Nr2f6(var.2) | MA0728.1 | chr17:29390699-29390714 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6 | MA0677.1 | chr17:29390625-29390639 | TGACCTTTCACCTG | - | 6.17 | | Rxra | MA0512.2 | chr17:29390625-29390639 | TGACCTTTCACCTG | - | 6.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTTGGGAGGC ATAATATAAT GCTGATTTTT TAGGTGTTGT AGGGATACCA AGATGAATGC 60
AGTCTGGAAT GCACTACACA CAGCGCATGA GAATACGGGC TCCGTAGTGA GACAGGCTTC 120
AGTTCACCTC TTGCCTCTGC CACTTACTAG CTGGGTGACC TTTCACCTGG TCTTTTATCA 180
TTGCTGGGTT TCATTTCCTC GTCTGTAAAA TGGAGTTACT AAATGGTCTT GAACTCCTGA 240
CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC 300
GCTCCTGGCC TTGATAATGA TTCTTAACTT CAAGGAATTT ATAATCTTGT AGGTCTGGCT 360
CATATTCACT AGTTCTTTTC AAACTTCCAT GGTAGAGATT CAAGGACAAC TGATGCTGTA 420
ACAAAAGGCA ATCACTAATT GGGGTCTAGA AATGGAGAGC CAAAGCATAA GGCCACGTGT 480
CAGTCATTCA ACAAATAAGA CCCACAGATA TGTATTCAGA TGCTTATTGA GCTCCTATTA 540
TATGCCATGA CCTTACTAAG GATGATTTCA GTGGTCTCTA ATGGTGAAAA GAAAGCTGTA 600
TGTAGAAGAA ATATGCACTA AAAGAAAACA AGGTTAATTT TCCAGCCTAA AAGAAGTGAA 660
TTCCTCTCAA AACCAAGCTC TTTCTTTTGT CATCAAATGG GCTTCTGAAT ACTCACTAAT 720
TTACTTTCCC AGGGACCTCA CAGTCAGGAA GTAGACATCC TCTAAGTGTA GTTATTAGGA 780
ATCCTGTTCC AGGTGCTGGC CTTCCATGAA AAATTAAGTT TCTAAACTTG CAAAGATAAA 840
GACCAGATCC AACACTGACG GTTGACCTCA CCAAGAAGCA GAAAACCTGT GAAACCTATC 900
CTGCCCAGAT ACACCATATA CTCAAATACT TTTTGAGCTC ATCTTGTGTG TCTGGCGTCA 960
GGCTAAGCAC AGGGAATATC ACAGTGAATC AACTAGGATG GCCCCTGCTG TCTTGGTGCT 1020
TACTCTGTGT TGAGGAAGGG AGATGCTTAC CAAATAATTA CACAGTCGGC TGGGCATGGT 1080
GGCTCACACC TGTAATCCCA GCACTTTGGG AGGCCTAGGT GGGCAGATCA CGAGGTCAGG 1140
AGATTGAGAT CATCCTGGCC AACATGGTGG AACCTTGTCT CTACTAATAA AAATACAAAA 1200
ATTAGCTGGG CATGGTGGTG CATGCCTGTA ATCCCAGCTA CTCAGGAGGC TGAGGCAGAA 1260
GAATAGCTTG AACCAGGGAG CCGGAGGTTG CTGTGAGCTG AGATTTTGCC ACTGCACTCC 1320
AGTCTGGCAA CAGAGCAAGA CTACGTGTCA AAAAAAAAGA 1360
|
