Tag | Content |
---|
EnhancerAtlas ID | HS053-00030 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:1489640-1491320 | 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 | CGGGGGCCCC CACGAAGCTG AGCACGAGAC GGATCCGGAC CACTCGGGGG TCCCCACGAA 60 GCTGAGCATG AGGCGGATCC GGACCACTCG GGGGTCCCCA CGAAGCTGAG CATGAGGCGG 120 ATCCGGCCCA TTTGGGGGTC CCCACGAGCC CTCGCTGACC ACCCACACCC ATTTGATGTG 180 GTTGCTCTCA GGATAAACCA CCCAGGGCCC CAAGGTGCCA GGACATACCA GGAAACGCCC 240 CAAACACAGC TCGGTTTTCC TTACCAAGGT TTTCTCTTTT CACTCCCTAG GGGCCTTAGT 300 GGGACCAGAA CATCCCGGGG AGTTAGAATG AGCGCAGCTG CCCATCCCAC AGGAGAACCG 360 AGAGGCCAGG ACCACACTAC CCTGCTATGA GTCACCAGGG ACTTGAAAGG GAACCCACAG 420 GCACTGCCAC GCCAGTGTGG CTGGCACCAG GGACCGCACT CTCCCACCAC GGCCTGGGAA 480 AAAGCCATGT CAGGTGCAGC ACGCTGGCCA CAGGCACTGG AGCCACGAAA GCAACAGCCC 540 TGGGCAGCCC AGCACCATCC TGGGTTCCCT GCTGCCGGCG CCAGCCCCAC GTACCCCCGA 600 CCACCTCAGC TCCTGGCCCT CAGCCTCTCC TTTGCAAACC GTGGCTGGCA GCAGAGACTT 660 CCTTGACGTC AAGTCTCCTG AAGGTGTTGA TGCTCCGTGG AAGCCTTGGT CCTTCCCCGG 720 AAGGCCACAC CATCTTCCCT GCACGTATGA CTCATCCCAG AGCATGCTAA GTGCTGCTGC 780 CCTGACAGAC ACACCCACGA GGGGGGCCAG CTATCACCTT ATTGGCCAGA TTGTCCCGGT 840 AACTGAGTGA CGGGACACAC AGGAACACTG CAGAGCCTGA CAGCCATGCC CCTGCCACAC 900 ACACAGAAGA CTCCCCACAT CAGAGGGGAG GTCAGAGGTC TCAAAGGTCA GGTTAGAGCT 960 GGGTCAATCC GTTTCCATGG CAAAACTCAA AGCACCGACA CAGGAGGCTC CGGTATCTGT 1020 GCTCCTGGTG CATGGCGGGG ATGAGACAGC CTCGGCGGCG CTGGTGGAGC TCCTGGGAGC 1080 CTCGCTCCAG CGAGGACAGA GCTGCAGCTC AGCACAGTGA CTGCCCAGGG CTCTGACCCA 1140 GATGCCAACA GCCTGGGCAG TGGCACCTCG GCCAAGAAAG GAGGAACCAG TGCTGCAGGG 1200 GCCAGGTGGC GGCTGTGGCA GGCATGTCTG GAGGGAGTGT CGTGCATGTG GGTGACAAGA 1260 ACAGCCGAGT GTGCCACAAG CGTGGACGGC AGCTCCGTAC TCAGAAGGGC ACGGTGAGAA 1320 GAGCAGGTGA CACCGACACG GCTGTGCACA GCACGATGCT CTGGGCTCCC GGGATGGACT 1380 GGGATCCACT CACCACACTA TGCCACAAGC TTGCCAGCTA CCACTTCCAT GTCAACGTAT 1440 CAAGAAATAC ATCTGGGCCG GGCACAGTGG CTGACACCTG TAATCCCAGC ACTCTGGGAG 1500 GCCAAGGCAG GCAGACTGCT TGAGTTCAGG AATCCAAGAC CAGCCTGGGC AACAGGGCGA 1560 AACCTCATTT CTACTAAAAA TAAAAAAATC AGGCCAGGTG GGGTGGCTCA TGGCTGGAGT 1620 CCCAGCTACT CAGGAGGCTG AGGTGGGAGG ATTGAGCCCA GGGACATAAG GCTACAGGGA 1680
|
| |
|
|
|