Tag | Content |
---|
EnhancerAtlas ID | HS150-11743 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chrX:47180560-47181260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chrX:47180976-47180990 | AGCCACGCCCACCC | + | 6.17 | SP1 | MA0079.4 | chrX:47180974-47180989 | TTAGCCACGCCCACC | + | 7.88 | SP3 | MA0746.2 | chrX:47180976-47180989 | AGCCACGCCCACC | + | 6.78 | SP4 | MA0685.1 | chrX:47180974-47180991 | TTAGCCACGCCCACCCC | + | 7.38 | SP8 | MA0747.1 | chrX:47180977-47180989 | GCCACGCCCACC | + | 6.62 | YY1 | MA0095.2 | chrX:47180920-47180932 | GCCGCCATGTTG | - | 6.37 | YY1 | MA0095.2 | chrX:47180883-47180895 | CAAAATGGCGGC | + | 6.92 |
|
| 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 |
GH0XI047321 | chrX | 47180401 | 47182135 |
|
Enhancer Sequence | TCAGGCTCGT CTCGAACTCC CCACCTCAGG TGACCCACCC GCCTCGGACT CCCAAAGTGC 60 TGGGATTACA GGCGTGAGCC ACTGCGCCCA GCCTTCTTCT CTTTAAAAGT ATGGTCTGCC 120 ATTGAGATTT TATTAAGTTA ACCATGTTCT TAAACTTGGC ACAATTCCCA TAGGCTCCAT 180 CTAGAAAGCT GACAATCTCC TTCGGGCAAG CTCACTGGGG ATTTGCGGTT GTAGACCAGG 240 GGAGTAGGGG GCGATTTCAA CGAACATAGC CCTCCCGACA GCGGTGCTAC TCGTCCTTCA 300 GCATCCTTTG CCTTAACCTC AAACAAAATG GCGGCGCCCA CACTGTAGCC TTCCTCGGGC 360 GCCGCCATGT TGGATGACGT TTAGCCTCTC CCTCCCCCGA GAGTCAGCTC CTTGTTAGCC 420 ACGCCCACCC CTGGGCTTGC GTGATTCCCC CTCCCCCGGA TGCACTAGGC CTGAATCCCA 480 TTCTCCTCAC CACACCTGGC CAGGCCTGGG TACGATCCAG TCTCCAGCAC ATATGTACTC 540 TGCTGAGCAT TCTGTCTCTG ATCGTGACCT CCAGGCCTCA GCGTGACCTG CCAAATGTTC 600 CCATGGGAGA TCTGAGGCCT GCATTGCTAG TGCCCCCACT GTAACTAAGG GGCTGGCTTG 660 TTGCTAGGAG TTTCCTTGTA GCTAAATTCC AGTTTAGGAA 700
|