Tag | Content |
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EnhancerAtlas ID | HS147-00083 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:1489420-1491120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr1:1490566-1490581 | GGAGGTCAGAGGTCT | + | 6.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I001554 | chr1 | 1489709 | 1491347 |
| Enhancer Sequence | CGGAGACCAC GTGTCAGTGG CCAGGGCCTC TAAAGAGAAA CGAGGAGGAA GTGCAGCTCC 60 AGGGAGTGGA GCGGTTGTGA GATTCACCAT CAGCAAAAAG TGAAGCTGAG CACGAGGCGG 120 ATCCGGACCA CTAAGGGGTC CCCACGAAGC TGAGCACGAG GCGGATCCGG ACCACTAAGG 180 GGTCCCCACG AAGCTGAGCA TGAGGCGGAC CCGGACCACT CGGGGGCCCC CACGAAGCTG 240 AGCACGAGAC GGATCCGGAC CACTCGGGGG TCCCCACGAA GCTGAGCATG AGGCGGATCC 300 GGACCACTCG GGGGTCCCCA CGAAGCTGAG CATGAGGCGG ATCCGGCCCA TTTGGGGGTC 360 CCCACGAGCC CTCGCTGACC ACCCACACCC ATTTGATGTG GTTGCTCTCA GGATAAACCA 420 CCCAGGGCCC CAAGGTGCCA GGACATACCA GGAAACGCCC CAAACACAGC TCGGTTTTCC 480 TTACCAAGGT TTTCTCTTTT CACTCCCTAG GGGCCTTAGT GGGACCAGAA CATCCCGGGG 540 AGTTAGAATG AGCGCAGCTG CCCATCCCAC AGGAGAACCG AGAGGCCAGG ACCACACTAC 600 CCTGCTATGA GTCACCAGGG ACTTGAAAGG GAACCCACAG GCACTGCCAC GCCAGTGTGG 660 CTGGCACCAG GGACCGCACT CTCCCACCAC GGCCTGGGAA AAAGCCATGT CAGGTGCAGC 720 ACGCTGGCCA CAGGCACTGG AGCCACGAAA GCAACAGCCC TGGGCAGCCC AGCACCATCC 780 TGGGTTCCCT GCTGCCGGCG CCAGCCCCAC GTACCCCCGA CCACCTCAGC TCCTGGCCCT 840 CAGCCTCTCC TTTGCAAACC GTGGCTGGCA GCAGAGACTT CCTTGACGTC AAGTCTCCTG 900 AAGGTGTTGA TGCTCCGTGG AAGCCTTGGT CCTTCCCCGG AAGGCCACAC CATCTTCCCT 960 GCACGTATGA CTCATCCCAG AGCATGCTAA GTGCTGCTGC CCTGACAGAC ACACCCACGA 1020 GGGGGGCCAG CTATCACCTT ATTGGCCAGA TTGTCCCGGT AACTGAGTGA CGGGACACAC 1080 AGGAACACTG CAGAGCCTGA CAGCCATGCC CCTGCCACAC ACACAGAAGA CTCCCCACAT 1140 CAGAGGGGAG GTCAGAGGTC TCAAAGGTCA GGTTAGAGCT GGGTCAATCC GTTTCCATGG 1200 CAAAACTCAA AGCACCGACA CAGGAGGCTC CGGTATCTGT GCTCCTGGTG CATGGCGGGG 1260 ATGAGACAGC CTCGGCGGCG CTGGTGGAGC TCCTGGGAGC CTCGCTCCAG CGAGGACAGA 1320 GCTGCAGCTC AGCACAGTGA CTGCCCAGGG CTCTGACCCA GATGCCAACA GCCTGGGCAG 1380 TGGCACCTCG GCCAAGAAAG GAGGAACCAG TGCTGCAGGG GCCAGGTGGC GGCTGTGGCA 1440 GGCATGTCTG GAGGGAGTGT CGTGCATGTG GGTGACAAGA ACAGCCGAGT GTGCCACAAG 1500 CGTGGACGGC AGCTCCGTAC TCAGAAGGGC ACGGTGAGAA GAGCAGGTGA CACCGACACG 1560 GCTGTGCACA GCACGATGCT CTGGGCTCCC GGGATGGACT GGGATCCACT CACCACACTA 1620 TGCCACAAGC TTGCCAGCTA CCACTTCCAT GTCAACGTAT CAAGAAATAC ATCTGGGCCG 1680 GGCACAGTGG CTGACACCTG 1700
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