Tag | Content |
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EnhancerAtlas ID | HS086-01197 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr1:203026080-203027030 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:203026685-203026706 | TTTCCTTCCTGTTCCTCCACC | - | 6.33 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 203026104 | 203026375 | chr1 | 203026461 | 203026871 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I203057 | chr1 | 203026643 | 203029528 |
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Enhancer Sequence | CTCTGTCCCC TTCCTAACGG AGGTCTGGGC GGGCATTGGG GCATCAGAAG CAGGAAGGTG 60 TACTTGGACT GGCCTTCTCT GCCTGCGTCC CAGGGACCAG TTGGGGGAAG CCCCAGGCAG 120 GTTACCTCAG ATCTGCAGAA GCAGTTTTTG GTTAGAGCTA TTCATGGCGG GGTGGATTGC 180 CTTGTGAGGG GGTAAGCTTC TGCCTCTGCA AGCGTCAGGA AGTGGCTGGA TGGCTTTATT 240 TGGCATGCTG TGGAAAGGTC TCCTGTATTG AGTGAAAGAT TGGGTGTCTG GGGTTTCTTT 300 GAATTTGGAG ATTTTCTGAG GTACTGTGCT CGGGACCTTC AGGAGAAATC TCTTGGTTGT 360 TTCTTTAGAA GAGTCAGTTC TTGATTGGAA CTTATTTCTG GGTACATCTG GCCTCTGGGA 420 CTCAAAATGT GATAACACCT AATTATAGCT TTGTAGACAT TAAATTCAAG GAAGAGCTTA 480 GGCAAGCGTG GCATCGTTAT CACCTCTGTG ATAGTATAAA TGTCTAGTAC ATGCTTGGCA 540 TGTGGTGAGT ACACGTTAAA TGTTAGCTTT CATCTGCCCC CTCTCTTCTA TTTCTTCTTT 600 TCTCTTTTCC TTCCTGTTCC TCCACCTTTT CTTTCTGTCA TCTATTCAGC CATTTGTTCC 660 ACAAACATTT ATTGAGTAAC TACTGTATGT CTTAGTAACA GGTGCTGACC AACAGTTCAC 720 TCCTTCAAGG AGTTCAGTGT CTAATGAAAA GGAAGAAGAG ACAATTCCAG AACAACCTAT 780 TGATAGAGAT GTGCCCAGGG TGCTTGTGGG ACTCAGAACT CGGCTATGGA ATGGTGGGGA 840 CAACAGGGGC GGCCTCCTTT GGTAGCGACA CCTGAGCTAA AGTGTGAGGG CCACATAGGA 900 ATTAGCCGAG CCAGGGAGAC ATCTGTGTGT GGAGGAAGGG GTTGGTCTGG 950
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