| Tag | Content |
|---|
EnhancerAtlas ID | HS142-01593 |
Organism | Homo sapiens |
Tissue/cell | NCCIT |
Coordinate | chr11:43709720-43710500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr11:43709963-43709979 | CGTTGTCATGGTAACT | + | 7.23 | | RFX1 | MA0509.2 | chr11:43709963-43709979 | CGTTGTCATGGTAACT | - | 7.2 | | RFX2 | MA0600.2 | chr11:43709963-43709979 | CGTTGTCATGGTAACT | + | 6.86 | | RFX2 | MA0600.2 | chr11:43709963-43709979 | CGTTGTCATGGTAACT | - | 6.94 | | RFX5 | MA0510.2 | chr11:43709963-43709979 | CGTTGTCATGGTAACT | + | 6.49 | | RFX5 | MA0510.2 | chr11:43709963-43709979 | CGTTGTCATGGTAACT | - | 6.58 |
|
| | 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 |
| GH11I043686 | chr11 | 43707841 | 43709749 |
|
Enhancer Sequence | CACTGCGCTC CAGAGTGGGC AACTGAGCAA CACTCTGTCT CAAAAAAAAA AAAAATTTAA 60
TGAATACAAT AAAATGGGAA TTTATGCTTT TTGTAAGGGA TGCTACTTTT GTGCACTTCT 120
TAGTTATCAT CTCTCAGAGA CCATTTCTGT CTGGGGGAAA AGTCTGATCA CTGTGGTATG 180
GGAAGTTCTT CTCTTACAGG GACTGAGTGA TGGGGTTATT GAAACACTGA AACTAGGTTA 240
TTGCGTTGTC ATGGTAACTC CATAATACCA TGGTGTGGTA GTTGAGAAGC TTGCCACAAA 300
TCTGTATCAG AAAGAACGCT TTGTTTTATT TGTCGATTTT TGTCTACAAA ACAATGCGTT 360
TGCCCTATCT CTAACTGGCA ATTCCAGGAA AACTATCCAG TTTCTGGAAA GTTATCTTTG 420
CCACCATTTA GTGAAGTTAT TTCCATTTAA ATAACCTAGT CATTGTGGAA GAGAGGAAGG 480
GCTAGACAGT TTAAGAACTT GAACAATTGG TGCCTCTCAA GAGTATTACA TTGGGAAACA 540
GTATAGCTAA CAAACAGATT GGCTTTGGAG TCAGTGGGCA AGCTGTGCTG TTACTAAGCT 600
GGTTGACCTT AGGCAAAAAT AGTTAACCTC TGAGCATAAC TTCTTTCATT TTTTAGGGGG 660
ATGATACTTT TCGGGATTAT TATGACAATT AAATGAGATG TAAATGAGGT TCTAGTATAG 720
TCCTTACTGT ATTTTTATGA ATATTAAGTA ACATATATTT AAGAGCATCA TTTGTTTGTA 780
|
