Tag | Content |
---|
EnhancerAtlas ID | HS024-10735 | Organism | Homo sapiens | Tissue/cell | Cerebellum | Coordinate | chr21:44104040-44105680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr21:44104358-44104379 | CCTTCCTCTTCTTCCACCCCT | - | 6.17 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 44104281 | 44105400 | chr21 | 44104688 | 44105340 |
| | Number: 1 | ID | Chromosome | Start | End |
GH21I042683 | chr21 | 44103652 | 44105461 |
| Enhancer Sequence | AAGGCGTCAT TTGCTGCGGC CACCCAGGTT GGAACACAGG GACCACAGGG CCCCCCGCCT 60 TCTGCAGGAC CACCCCGCTC ATCTGAGGGA GACACTGTAG AAACACATCT TTGAGCAGTG 120 GCTTCTAATC CAAGAAACCC AATAGAAGTC AAACGCAGAT TCCTAGGGCC CAACCCGGAC 180 CCACTGCGTG GGAATCCCTC AGCCGGGGCC AGAAGCACGC TTTGAAGACA CCAACCTCCT 240 CAGCAAGCCT CTTGCAAACC ACATCCTGCT TCTCCAGAAG CTGCAGATCC AGAATGTTCA 300 AAGAAAGAGC CCTCCTTGCC TTCCTCTTCT TCCACCCCTG CCCTCTGCAG ACTGGGGTTC 360 TGTAGACCCC CAAAGTAAGT CCGCCACACC GGAAGGAAGT GAGTTACACA GGGGCCCACA 420 TGGGAACCGC TTTTTGTCCT GTCTTGGTGG GAAAATGGCC ACGACCCCAG CCCAGGCTCT 480 GCCACGCCAC AACTCCACGG GCATAGCCTG GGAGGCCGCA GCGTGAACTG TGACTAGGGC 540 TGAGGATGGT GCCATGGTAG AAGTGAGGGC CTGGCACCCG GCCAAGTGCA GGACTCCTCG 600 GCAGTGGGGT TGGGAGAAGC AGCCTCTGCA GGCGAGGCCA GGAACCAGGA CACAGGAGGA 660 GAAGCACATC TCAGAGGAGG GAGCTCTGGG AGGAGCCAGC AGAGTCCTGC AAAGGAGGAT 720 GTGGGGGAAA TGGGGTGAGG CCAAAGTGGG GGCTGCTGAA GGGGCTACTG CACCCGTGCG 780 AGCAGGGCCA GGACCAAGCT GCATAGGCAG CCAGGGACAC AGCCGATGCC ACAGACGTCA 840 GGAACCACGC AATGACACAG GCCACCTTTG ACCGACCGTT ACCCCTGGGG CAAATACCAG 900 TGGGGATAAC GGGCAAGGAG AGGTGCTGTT TACTGTCTTA TTGTTGCCAG TTCAGCAGCC 960 CACAGGAAAT GGTGTTAGTC ACAGAAAAAA AAAATCTGTT TTCTATATTT CACTGTTTCC 1020 AAGTAAAGAA AAAAGAAAAC TAATCTTAGC TTAAAAAAAA AAAAAATGGT GCGCTGGGCA 1080 CCGAAAAATA ACCATCTTCC TAGGCCTGCG TTTCCCCCAC ACCGGGGACT TGTGCTGGAA 1140 AGAAAAGCTG CGTTGGCAGC CAGGAGCCGG GGAAACTGTC CAGGGAGGCA TCCTCTGCGA 1200 TGAAGGCGGG GCCTCGGCGT GGCCCGTTCC GCGCTCTGTC CAGCCCTGGA GAAGCCCCAC 1260 CCTCACCGAG CTCGAAATAC CCCCTCCCTG AGAGCCGAGA CTCATGGCCG GGACCCCTTG 1320 GACAGAAGAT GCGGATGCTA ACCCGGCGCT TCCACCACAG CCCCGGCGGC ACTGGGGAGC 1380 GAGCGCGGCC ATCCCGCGCG TAGGTGGTGT TTCTCTGCAG GCGCCAGTTT CACCGCGGGC 1440 GCCCAGGATC CTCAACGGTT CTGTTGTGAT GTGATTCCCC TCTTCGACTT CGTCATTCAG 1500 CCTCAGTCCC TCAGTCCCCA AATACCGAAA GGCAGTCTTT TTTTTTTTTT TTTGAGACGG 1560 AGTTTCACTC TTGTTGCCCA GGCTGGAGTG CAATGGTGCG ATCTCGGTTC ACTGCAACCT 1620 CCGTCTCCCT GGCTCAAGCG 1640
|
| |
|
|
|