| Tag | Content |
|---|
EnhancerAtlas ID | HS080-25363 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr3:183672570-183673360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr3:183672833-183672844 | ACAGGGTGTGG | - | 6.14 | | NR2C2 | MA0504.1 | chr3:183672726-183672741 | AAAGGTCAAAGGTGA | + | 6.25 | | Nr2f6 | MA0677.1 | chr3:183672727-183672741 | AAGGTCAAAGGTGA | + | 6.54 | | PBX1 | MA0070.1 | chr3:183672648-183672660 | ACATCAATCAAT | + | 6.44 | | Rxra | MA0512.2 | chr3:183672727-183672741 | AAGGTCAAAGGTGA | + | 6.33 |
|
| | 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 |
| GH03I183954 | chr3 | 183672761 | 183672910 |
|
Enhancer Sequence | CGCAGCCTCA GGAGGTCCTG AGAACAGGCC CAAGGCAGTT GGATTACAGC TTGGTTTTAT 60
GTTTTAGGGA GACATGAGAC ATCAATCAAT ATAAGTGGGG TAATCACTGG TTTGATCCGG 120
AAAGGTGGGG CAACATGGGG CAGGGAGGTG CAGCTTAAAG GTCAAAGGTG AATTCAAAGA 180
TTTTCTGATT GGCAATTGGT TGAAAGGGTT AAGCTCTGCC TGAAGAGTTG AAATTAGCTT 240
GAGTGGTGGG GGAGTGGTGG GGGACAGGGT GTGGACGCCA AGGTTCTTGT CATGTAGATG 300
AAGCCTCCCA GTAGCAGACG TCAGAGAGAA CAGATGTGAA TGTCTCCTAT CAAAGGTGTC 360
AGACCCTCTG GAGAGACCTA GTAAAGGAAG GAGATTCTCT ACGTAATGCA GAACTTCCCC 420
TTCAACAGAC AGCTTTGCAG AGACATTTCA AAATATGCAT TTCTTCCAGG GCCCTGCTAT 480
CTGTCCTGTG ATGCTCTATT ATTTTAATAG AGTGAGGTTG GAATTAGGTA TCTTACAGCT 540
ACAAAGAGAC TGTTCTGTCA GTCTTAGGAT CTCTATATAA ATGTTAATGC TCGTCAGTTG 600
TGTGCCTGAA CTCTAAAGGC AGGGGAGTAT AATAAGGCAC GTCCAACATT GTCTTCCCTT 660
CATGGTCTGA ATAGATTTTC AGGTTCCATT GGGTACCCTT GGCCTAGAGG AGAGTTTATT 720
CAGTTAGTTG CAGGGCACAG AATTTAATTT TTCATTTGCA AGAGAAACAG CTATACAGGA 780
AGATTTTCCC 790
|
