| Tag | Content |
|---|
EnhancerAtlas ID | HS147-18059 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr17:41777540-41778480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr17:41778018-41778029 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr17:41778018-41778029 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr17:41777960-41777975 | CGATCTCTTGACCTC | - | 6 |
|
| | 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 |
| GH17I043700 | chr17 | 41778001 | 41779211 |
|
Enhancer Sequence | CTCCTACCTG ACTGTGGGAT TCTAGCCCCC AGTGGGGTGG GGGACCAAGG GTGACAATTA 60
CCTGGGACCT TGACTATTGA AAGGCTAATC AGGTTTGATT GGGAAAAAAG AGTTGCTAAA 120
AAGGATTGTA TTGGATAATT GGTGAGATTT GAACATGGAT TTTATATTAG TATTGTGTTA 180
TTACATTTTC TGATATTAGT CATTCTTTTT TTTTTTTTTT TTTGACGGAG TTTGCTCTGT 240
CACCAGGCTG GAGTGCAATA GTGTGATCTC GGCTCACTGC AACCTCTGCC ACCCGGGTTC 300
AAGCGATTCC CCTGCTTCGG CCTCCTGAGT AGCTGGGACT ACAGGCGGGT GCCACCACAC 360
CCAGCTTGTT TTTGTACTTT TAGTAGAGAC AGGGTTTCAA CATGTTGGCC AGGATGGTCT 420
CGATCTCTTG ACCTCGTGAT CTGCCCGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCA 480
TGAGTCACCG CTCCCGGCCG TTAGTCATTC TTATAGGTAT GTAAGAAAAT GTCCTTGAGG 540
TATTTAGCAG GGAAGTTCAT GATCTCTGCA GCTTACTCAC AAATGGTTAA ACAGAATGAG 600
ACTAAGAACA GACTAGTAAG AAAAGACTGA AGAATATAAT TATTAGGCCA GGTGCAGTGA 660
CTCACACCTG TAAATCCCAA CATTTTGGGA AGCTGAGATA GGAGGATCAC TTGAGGCCAG 720
GAGTTTGAGA CCAGCCTGGG CAACATAGTG AGACCCCATC TCTACAAAAA AAAAAAAAAG 780
TAAAAATTAC GTGGGCACGG TGGTATACGC CTGTACTTCC AGCTTCTTGG GAGGCTGAAG 840
TGGGATGATC AGAGGACCTC AGGAGTTTGA GGCTGCAGTG AGCTATGATT GCAGCACTGC 900
ACTCCAGCCA GGGAGACAGA CTGAGGCCCG GTCTCTAAAA 940
|
