Tag | Content |
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EnhancerAtlas ID | HS042-19501 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr17:46246500-46247970 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:46247146-46247167 | GGAGAAGGAGCAGGGAGGGAA | + | 6.32 | ZNF263 | MA0528.1 | chr17:46247149-46247170 | GAAGGAGCAGGGAGGGAAAGA | + | 7.01 | ZNF263 | MA0528.1 | chr17:46247152-46247173 | GGAGCAGGGAGGGAAAGAGGG | + | 7.87 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAGCTGTAGG AACAGTTAAG AAATAAATCT CCTCTCACCT CCCAGATATA ACCTTAGAGA 60 AAGAGGTGGA AGGAGGAAAT GAGATGAGGG AGGAGTCTGA AACTGGATTC TAGACTTTGC 120 TAAAAGATCA ATGCTTTCTG AATGGAGTTT AATATGAAAT TGGCCATAGG AAGCTTACAG 180 TTACTCCACC CAAGCTGTCC ACATGAAGTG TTTCTTTTCT GCACTGGTGA TGGAAGTTGG 240 TTGAGAAAAG ATATATGTGG AACATGGGCG GGTCAGAACA GATTTTCATT TGGAATTCTG 300 TACAGTAAGT AGACAACAGA AGGAAATAGG TTTCAGAATG GACCTAATCA CATGTGTTCA 360 CTATCATGAG GTACTTGCAG CTACACTCAC ATCCGTGCAT CACACCCGCC TCCACTGCTT 420 TCTTTCTCTC CTGCTTTGGC GCATGACTTC TGAGGCTGCA TCTTCGTTGT CTCTTCTCTT 480 CCCTGGGAGA AGCTGGACCC TTAGGAAGTT GGGTCCTGAA CCTTTTAAGT ATTCACTTTC 540 TGTAGAGAAT GAACCTAGAA ATGGGGGTTT TGCTGGATGG ATAAGGAGAG AAGAAAAAGC 600 ACAAGGAAAG GAGAGAGGAG AATAGGAAAA GACAGGGCTA GATAATGGAG AAGGAGCAGG 660 GAGGGAAAGA GGGCAAGAAT TCCTAGGCTT AAGATTTTCA TAGACTCCCT AAGAAAAATA 720 TCAGCCAGTA TCTAAATCAG TCATGATTAG GGCTCTGCCG ACGGAACGAA TGTCCTTGAG 780 GTGGCCCTTG CAATGTGCAG CATTCCTTTA CTGACAACCA TGGAATAGGT CCTTGGTCCA 840 CTTAAGGAGG CTTCAGAGGG GCATCTGACC TTAGAAAGGA TGGGCTCACT AACAGCCTGA 900 AGCATGGTTA ACAGTCTGGG ATGAATAAGA TGTAATTTTA TATTCAACAA ACCTGTTACA 960 TATTCATTTC CAAATGTGCC TGGAATCAAA CCAGGCTATC AGAAGTCAGC ATCACCAAGG 1020 AATTTTATCT TTCACCCTGT GTTCACTTTT CAGATCTGAC ACATTTCCAT TCCCCTCTGA 1080 ACTTGCAATC TCCGGGCCTC TCAGAGAGGA GACATTTCCA TTCTTTCCAT TCTCAATCCT 1140 CTGATCTCTT AGAGATGAGG CAATTCTATT TTCACTGTAC TGATATAAGA AATATTGATA 1200 GGAAAAAATA AATGTCTGGT TTGGCTTCCC ACCCGCTCTA GGATAAATCT TGGCTGTTCT 1260 GGGAACATTA ATTAAAGTGA ATGTATGGCT GCTTTTAAAG TTTAGGTATT TCCCTACCCA 1320 GTCACTTTAT TTAGGGCTTT GGGGTTCACA CACAGGTACC CTCTTAATTA TTGAGTTCAG 1380 TAATTTTTGT AGTCTCAGAG AAAGGTGCTT TCTCTAATCA GAAGCCCATA ATGTCCTACC 1440 CAGTGCCTGT GCATTTAGAA GCTCTTATAC 1470
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