| Tag | Content |
|---|
EnhancerAtlas ID | HS065-02161 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr17:29389860-29390780 |
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 | TCTCTACTAA AAATACAAAA ATTAACTGGG CATGGTGGCA TGAGCCTGTA ATCCCAGCTA 60
CCCAGGAGGC TGAGGCAGGA GAATCTCTGG AACCCAGGAG GCAGAGGCTA CAGTGAGCTG 120
AGATTGCGCC ACTGCACCCC AGCCTGGGTG ACAGGGCAAG ACTCCATCTC AAAAAAAAAA 180
AAAAAAGAAT CCATGTGCAT TGGAAGGATC TGGCCAAGGC ATGCTGGTAG GTTTTTTCCT 240
GCTCAAAGAT GATTATCTTG TATTCTGCTC CTTGGGCCCC TGTCTCTATT GGTTTTTGGC 300
CCATATAGTT CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT TTCTCTCTCT 360
GTGTGTGTGT GTTTGATGGC AAATTTCAAA TATACAGTAC ATTATTATCA ATCATAGTCC 420
CCATACTGTA CAGCTTATCC CTATCGTCAT TCTTCACCTT CTAATAATGT TTGTTGCTTC 480
TTACATATTT TGAAGCCTCA TAGAAACTTG AAACTATTTA ATTCAAAGTG GCCTCTTAGT 540
CTCTTTTCTG CTTACGATAA TCGGAGTGGT TTTCTGCTGC TTGCAACCAA CAATTGACTA 600
TATAGACATG TTTGGGAGGC ATAATATAAT GCTGATTTTT TAGGTGTTGT AGGGATACCA 660
AGATGAATGC AGTCTGGAAT GCACTACACA CAGCGCATGA GAATACGGGC TCCGTAGTGA 720
GACAGGCTTC AGTTCACCTC TTGCCTCTGC CACTTACTAG CTGGGTGACC TTTCACCTGG 780
TCTTTTATCA TTGCTGGGTT TCATTTCCTC GTCTGTAAAA TGGAGTTACT AAATGGTCTT 840
GAACTCCTGA CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTACAGGC 900
GTGAGCCACC GCTCCTGGCC 920
|
