| Tag | Content |
|---|
EnhancerAtlas ID | HS145-15562 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr22:20123380-20124420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr22:20123452-20123462 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr22:20123452-20123462 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr22:20123452-20123462 | ATTTTCCATT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACGGGCGAGT GCCACTCATA CACAAACAGT GCTAATGAAG AACCTGATTT AAATGAAAAC 60
GTCTGAGTTA AAATTTTCCA TTCCACATTT AGCTGTGGCG GACATTCTGC CCCTAAGCCA 120
CCCCTCTTGC TCGGCGGTAT CTCCCTGCCA GCCCAGGCGG GACTTGGGGC CTCAGCCCGG 180
GTGGGGCCTA TGGTGGTGGT GCATGTCCCT GCCTGTGGCC CTGGAGGAGG GATTGGAACC 240
TCGGGGCTGG GCCCCCTGGA CCTGCCCTCC ACCCGTAGCT TGGCTGGAGC CAGCCAGGAG 300
GGGCTCAGAG GGACATGGCG GGCCAGACAC TCCACCTCCA GCCCAGGCCC AGAGCCTGTC 360
TTTGCCTGGC CCTCCGGCAG GCGAGCCTGG TGTGCACCAT CAGGTCTGGG TGGGAGTGGA 420
GCCTCCCCGA GCCTGGACCC AGACTACTGC CTGCTAGGCC CTGCCTGTGG GAATGCGTGT 480
CTTTGAGTGT CCCTGAGCAT CCACACATGG CCTCCCCTGT CCCCATGTGT CCTCATGCAT 540
CCTTGCATGT CCTTGTGTGT CCTCCCGTGT TCTTGCGCAC CCTGAGAGTG CTTGTGTGTC 600
CTCACACTTG CCCTATCCAC AGAGGGGCAA AGGGAAGCCC AGAGAGTGGG AGGGCCGTGT 660
CTGAGGCCCA GAGTGAGGGG CAGCCGAGCC GAGGCTGGAT AGGGCTGGGT GCAGTGTGAG 720
GAGGCATGTG TCTATGCATG CCTGTGTTCA CGCGTGTTCA CACATAGGTC TTGGTGGGTG 780
AGTGATGTGC AGGCGTGTCT GCGTTCATGC ATGTGCACCA GTGTGTGCAC GTGTGCATGT 840
CTGCATGCAA GTGTTCATGC ATGTATATGT GTTTTGTATG CAGACATGAT TGCATGTGTG 900
CATGTGTGCC TTCTGTGCAC CAGAACAGGT TGTCTGTGTG TTTATGTGTG TACATGCCTG 960
TATATTTGTG TGTGTGCACA CATACCCATG CACATGTGCC CTGGAGCATG TTTGTGTGTG 1020
TGTCCATGTC TTCACACGTG 1040
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