Tag | Content |
---|
EnhancerAtlas ID | HS042-29386 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr21:38903020-38904370 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:38903988-38904006 | CCCTCCTTCCCTCCCTGC | - | 6.04 | EWSR1-FLI1 | MA0149.1 | chr21:38903980-38903998 | CTGTCCTGCCCTCCTTCC | - | 6.45 | EWSR1-FLI1 | MA0149.1 | chr21:38903984-38904002 | CCTGCCCTCCTTCCCTCC | - | 6.94 | ZNF263 | MA0528.1 | chr21:38904073-38904094 | AGAGGAGGGGAGGAAGGGGGC | + | 6.88 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 38903168 | 38903400 | chr21 | 38903217 | 38904297 |
| Enhancer Sequence | AGGTCTGGGG GAAAAGCTAT ACATATTTCC AAGGGAGATT GAGCGCATGG GCAATAGGCA 60 AACGTGTAAC ATGCATCCCA TGTCCACTTG GGGGTGAGGT TCTAGCATTA AAATGAGGTG 120 GATTTGGCTT TTGACTTCAA AAGGTGAGCT ATAGGGCACA AAGTTGGTGC ACACCCTGTC 180 GGCGCTCAAG CTGGCCCCGG GTCTGCAGTG TTATGAGGAG AGCCGGTAGG GCCGCCCTCG 240 GTCCCAGCAG AGTTGTAATG GTCTGTGTTG TAAATCAGAG TTAGGAGGGG TCTGACAACT 300 TTCCTGTTAG TGCGGAGTTT AGCCCCAGTG TGGTTTGTCC TGCAGCTCAG GAATCTAGGG 360 GGTTGCCTGC CCACTGAGCT TAGACCCTGG AGCCCAGGGA GCTCTTAATT GACAGAAGGG 420 TGTCCTTTTG GTCTCAGATC ATACCGGTAA CGCTCCTGCC AAGCAGCCCT GGACAGGGGC 480 CCAGCCTACC GCCAGGAGCC ACCTGTCAAA CGGCGGCTTA GGGGGTTTAA AAAGGAAATT 540 AATCCCTCTT CAAGACCACA TAGATAAACC TCTGGTTGGG AGGTGACAGC AAATCTTATC 600 AAAGCAAATT GTCTAGACGT TTCGAGGAGC TCTAGGACGT GGACCTGCTC AATCTTTCTA 660 GAAAGGCCTG CGGCTGCAGG GGCCAGGTTA AGGGGCCCCT TAACCTGCTT CAGAAGAGGC 720 AAGACTGCGT CCTTCCCCGC TGCCCACTGG GACTGACTTG GAGGCCCGAG GAAGGATTTG 780 TTCCCGCAGG ACCAAGTTCC CTCAGGCCAC ACCAGCCTGG GAACCAAAAC AGGATTGCAG 840 TGACAGAACA CAGCGTCTCT GGCTCTGCGC CTACCCTGTT CTTGCTGTGC CCCCAGCGCT 900 CTTGAAGCTG TGTCCTTCCC TGCCTGCCTC CCTCCAGCTG GGCCCCCCTC TCCAGCCACC 960 CTGTCCTGCC CTCCTTCCCT CCCTGCCTGG GTCTTGTGGC TGCGGAGGCC AGAAAGTGGA 1020 GTGGCCCCTA TGTTACCACA AGTCCCGCAG GGCAGAGGAG GGGAGGAAGG GGGCGCGCAG 1080 GAAGCCTGGG AACACCCACC CTTCAGGGCT CAGGACAACC CCACTCCTGG ACAGCCTCCA 1140 GCCCTGGCAG CGACAATCCT GGGCCCCGCC CAGTACTGCA TGGGCACTGC CAAGACAGAG 1200 CTGGACACAT GCCCACGGGG TAGAGTTTGA TTTGGGGGCC ATTTTTGCCC CTTTCTACAA 1260 TGACGTTTTC TCTGACAAAA TTTAGACTGT AATTTAAAAA ATAGTTTCTG ACTGTGATGA 1320 GAAGGAAAAG GCAACATGCT TCCCAAACTA 1350
|
| |
|
|
|