| Tag | Content |
|---|
EnhancerAtlas ID | HS187-19402 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr5:42908400-42909400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr5:42908664-42908675 | CCACACCCTGC | + | 6.62 | | NRF1 | MA0506.1 | chr5:42909111-42909122 | GCGCATGCGCA | + | 6.32 | | NRF1 | MA0506.1 | chr5:42909110-42909121 | TGCGCATGCGC | - | 6.32 | | RREB1 | MA0073.1 | chr5:42909016-42909036 | GGTGTGGGGATGGTTTCGGG | - | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTACCCATT CCAGTGCTTC TCAGCCTTTA TTAGCATTTG AAGATATTGT ACTTGTCTTC 60
AGTTCTTCAA GGTAACTGCT GAGGCTGATT CTTTTCACAA TGATTGTGGT TTCTTGAGTC 120
AAAATAGTTT TTTTTCTGGG TCCTGAAGAC TATGTTTTGG CTCTTGCTGC AACAGTAAGG 180
GACTTGCAGT TCCCACTCTG TGCAGAGAAG TCTGTGGCCT TGCAACTTTC CAGAGGGATC 240
TATATATCCT TCCAACACAT CAACCCACAC CCTGCTCAGG TTCGCAGGGC TTGGGTATTT 300
GTGCATTGCA GCTGTTGTAA CAGTTTCCCA CGGGTGGTGA AAGACGTGCT CTGCAGTCCA 360
GATCTTGATG GTGCAGGCAG TCTGCTAGAT GTCTGTGAAG CGCAGGGGAA AATGAGGTGA 420
GGAGGCTACA CCTGTCCCAC CCCGTCGGGG GCCCTTCAAC CAGCTTCGCT GTGCGCAGGT 480
GCCGTCGGCT CCAAGTGAGG CGGTCCTCCA CTCTTCGTTA CAATGTAACA TTTAAACCAT 540
TTAAAGCAGA GATCCGCAAC GTTTTTGGCA CCAGGGACCA GTTTAGTGGA ATACAATTTT 600
TCTACGGATG GAGAGGGGTG TGGGGATGGT TTCGGGATGA AGGTGTTAGA AATCAAATAA 660
TCAGGCACGC AATAGATTCT CAAAAGGAGA GCAAAAGCTA GTCTTGGTCC TGCGCATGCG 720
CAGTTCACAA TAGGGTTCGC ACTCCTGTGA GAATTTAATG CAGCAGATCT GACGCTAGGC 780
GGAGCTCAGC CAGTAATGCT CGCTTGCCCA CTGCTCAGCT CCTGCTTTGG GGCCGGGTTC 840
CTAACCGGTC CGTGGTGGGG GGGATTGGGG ACCCCTGATT TAAAGAACAG TGCTAATGCC 900
TGTTTTCTGC CTTTATTTGG AGGGCCACAG TCAGTTTCAA AGCAACTCCA GCATATGATC 960
CACCCAGCTG TCCCCTCCCA CCCTGTTAGT ATCCACAGCT 1000
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