Tag | Content |
---|
EnhancerAtlas ID | HS053-13419 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr15:41913190-41914480 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr15:41914257-41914267 | GGTCACGTGC | + | 6.02 | Arntl | MA0603.1 | chr15:41913676-41913686 | GCACGTGACC | - | 6.02 | KLF16 | MA0741.1 | chr15:41914245-41914256 | GGGGGCGTGGC | - | 6.62 | NRF1 | MA0506.1 | chr15:41913790-41913801 | TGCGCAGGCGC | - | 6.62 | RREB1 | MA0073.1 | chr15:41914229-41914249 | GGGTAGGGGGAGGGTGGGGG | - | 6.59 | SP3 | MA0746.2 | chr15:41914244-41914257 | GGGGGGCGTGGCG | - | 7.22 | SP8 | MA0747.1 | chr15:41914244-41914256 | GGGGGGCGTGGC | - | 6.44 | YY1 | MA0095.2 | chr15:41914135-41914147 | CAAAATGGCTGC | + | 6.52 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGGTTAAAC GGTTTCCCCA AGACCACACA GATCAAACAA GTGGGAGAGG AGGGGCTGAA 60 AGTGCCTGGT ATACCTCGCC ACACTCCCAT AATTACCCAA ACCGTCTCAT TCCAAGCCCA 120 AGGACCGGGC TTTCAAGGGG ACACGAAAGG AACGCCCGGG AGGTGAGCGC CAGGAGATCG 180 GGAGAGGTGC CTTTCCCGGC ATGCTCTGCA GCACACCGAG GGGCGCCAGG CGTATCCCGG 240 CGTGCATCGG GGAGCGCCCA AGGGCGATGG TTCCCGGCTC CTGGAGAGGC GTGCGAAGTT 300 AAGCCGGTAG GTGCGAGCTT CCTTAGCTTT GAGCCTCTGG TTTCTCGTTT CCTCTTTATG 360 GGTTTAAATC CATAACGGCA GAAAAGGATG GCCCTCTAAC TACCCTCCCT CTCCGCGTGC 420 GAACGACTCG GCGCCGCTTC GAGCTCGGTG CCAGGTGATT AGCGGGTAGG GGCGGGCTTG 480 CGACCAGCAC GTGACCCGAA CTGGCAGCCA ATGACTAGCC GGGTGGTCCA GCAGCGCGAG 540 GATTCCGGGA CCCGCGAGCG GAGCGGCGCG TGGGTCGGTT GCGGTCGGCC CCGGCAGGTA 600 TGCGCAGGCG CCTTGCTTGC CACGCGCTAC GCCCGTCCCC ACGCGCCTGG TGGCGTGTTC 660 TTGGCGCGAA GTGTTAAGAG TCTGGGTGTT TTTGTGCGTT GGGGGGAAGG AGAGGGTGGC 720 GGGGGCGGGG GGGCGCTGAG GCGTCACGTG GACGCCACAG CCAATCTCAG GCCGAGGCGC 780 ACCCACAGCT TTCCCCGGCG CCCCGGGGTG CGACGTGTTC ACTGAGGTTC GACCGGGCCC 840 TGACGGCCTG AGCGGTCTTT CGAAGCGCGT GTGCGGCCTG TAAATTCTGG CCGCGGCTTT 900 TCGTGGCGTC CTGCTCCGCG GTGAGCACAG ACGACAAGTT CTCAGCAAAA TGGCTGCTGG 960 AAAGAGTCGC CAAGCAGGGG GAGTGCTGGG GCCGCGTGAA GGTCACATGA CGAGGTTGGC 1020 AGCGCGTGCT GCTGGCGCGG GGTAGGGGGA GGGTGGGGGG CGTGGCGGGT CACGTGCCTT 1080 CGACTGCGCC GGCCTGTGGT TTTCCAGCGT CTTTGCTGCG GTCGGATTGC CTGTTTTTAC 1140 TCCTCCCACA TCGAAGCGTG GCAAGCGTCG GTGAGAAGCT GTGTGGTGTA CTGGGATGAG 1200 CCGAGATCTG GGAATTCGGA GGCCTGGGGT CCAGGCCTTT GGCTAGTTTC ATCTTGCCAC 1260 CCTCGGCTTC CATTTCTCAT TCAGCTCGGT 1290
|
| |
|
|
|