| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00713 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:23781420-23782370 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:23781947-23781958 | TGTGGATTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr1:23782151-23782172 | GAAGGAGGAGAACAGAGAGAA | + | 6.13 | | ZNF263 | MA0528.1 | chr1:23782154-23782175 | GGAGGAGAACAGAGAGAAGAG | + | 6.14 | | ZNF263 | MA0528.1 | chr1:23781973-23781994 | GAGGGAGTGAGGAGAGGAGGA | + | 6.84 | | ZNF263 | MA0528.1 | chr1:23782142-23782163 | GGGTGAAGAGAAGGAGGAGAA | + | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCCAAGGTT GGGTGCTTAA CCACTGAGCA CACTGCCTCT CAAGGATGAT GTGGCCCCTG 60
CCAACCAGGG AGGATGCTGG GTAGGACTGG AGCCACAAGA GCTGGTCCAG TGCCATGGAG 120
CCTGGAGGGA GATGAGAGGC TTTCCTGGGA GGCAGTGTAG CCAGGCTTAT GCTTGGACTC 180
TGGAGCCAGA CAACCTGGGT TCAAACCGAA CCGTGTGACC TCGGGCAAGC TGCTTAACCT 240
TGAGGTCCTA GTTTCCTAGC CTGTAAGGTG GAGACAACAG TCACACCAGC CCCACAGAGC 300
TGTGCATCCG GATCGAATGA GTGAACACAT GAACTAGTGA GAACTGTGCC TGCACATGGG 360
AAGAGCTGCT GTCACAGGGT GGCCTTGAGG AAAGGACTTG AAGGACCAGA GAGGAGGCAG 420
TCACCAAGGA GGCCATCGGG AAGCAACCCG AGGCCACTGG GCCATGTACA GGGGCTGAGA 480
CGCTTGTGGA GGCAGGGACA GGTCCTGGGA TTTAAGTACG AAGCAGATGT GGATTGGGAA 540
AGCAGAGGAC AAAGAGGGAG TGAGGAGAGG AGGAGGCGGT GGCAGCGGTG GTGGTGGCAG 600
TGGCAGCAGT AGTGGTATAA AGGTAGGAAC CCCCGAGCCT GTCTCTCCTT TATCCCAAAG 660
CTCCTCCAGG GAACCCTCCC TTGCACGGGG CTCTTCCCTG CTGTGAGACC CCCTCTGCTC 720
CTGGGTGAAG AGAAGGAGGA GAACAGAGAG AAGAGTTAGT TGGGTAAGAA GCCAGAGAGA 780
AAGGAGGATT ATCCAAAAGA AGGGTCAGGG CTGGAAAGGG ACCTCAGGTC TGAACTCAGG 840
TCAGAGATCA AGGGCAAATT GGGAGAAGGA AGGAAACGGA CCCTTTCCCA GTCAGGTTCT 900
TAAGACCACT AGATTTACCC TGAGTCTGGG CAAGGAAGAG ACAGGGGCCT 950
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