| Tag | Content |
|---|
EnhancerAtlas ID | HS105-39450 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr19:17666780-17667710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr19:17667426-17667436 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr19:17667426-17667436 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr19:17667426-17667436 | AATGGAAAAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGTGAGTCG AGCCCGCTGT CCCCATCAGG CGGGTCACGC GAGCCCCTGC TTGCTGTCCC 60
CATAGGGGTG GGTCCACGCG AGCCCCTGCC CGCTGTCCTC TTCTGGGCGG GTCCGCGCGT 120
GCTTCCTGCT CGCTACCCCC ATCGGGACGG TTCTACGCAT GCCCCTGCCC GCTGCCCCCA 180
TCGGGACGGG TCCACGCGTG CCCCCTGCCT GCTGTCCTCC CATGGGGCCA GACACAGCCC 240
TCCCCACAAC ACAAGCGGGA CCGAGTTCCT CCTGCTGGCT CCTTTGGGGT GGGCTGGGCA 300
CCGCTTCTGC CTGCTGGACC CTACTAGGGC AGCTCCGGCC TCACTAACTG GGGCTCTAAC 360
TCCCTCTGGG GCACGTACAC CTCCAAAGGA CGGAGCCCAG AGCCCCCACT GGGGCGTTGC 420
CAGAGGCCAC ATCTAACAGC AAGCCTTTCT GTGCCGGCTG CTGCCCTTAA GCTTGAACTC 480
AGCCTGGCTC CAGGCCCCAG TCAAACCCCT GCCCTCAGAC CGGCGTGGGT GGAGTCCAGG 540
ACCAGATGGC CCAGGAGGAA GTGGATGCTT TCTTGGTAGG GAATGGGGCA GAGCTCTGAA 600
GAAACCTTTG ACTGGTGACT TCTCACTCCC TGCCTCAGTT TTCTCAAATG GAAAATGGGT 660
CCGGGTGCAG TGGCTCACGC AGTAATCCTA GCAATTTGGG AGGCCAAGGT AAGCGGGTCA 720
CTTGAGCTCA GGAGTTCGAC ACCAGCCTTG CCAACATGGC AAAACCCCGT CTCTAGAAAA 780
AAAATACAAA AATTAGCCAG GTGCGGTGGT GTGTGCCTGT AGTCCCAGCT ATTCAGGAGG 840
CTGACGCAGG AGAATCGCTT GAGCCCAGGA GTTCGAGGCT GCAGTGACCT ATGATTGCAC 900
CACTGCACTC CAGCCTGGGC TACAGAGTAA 930
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