| Tag | Content |
|---|
EnhancerAtlas ID | HS187-10508 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:42004540-42005870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr17:42004908-42004919 | CCTTCCCGCCC | - | 6.62 | | KLF5 | MA0599.1 | chr17:42004796-42004806 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr17:42004915-42004925 | GCCCCGCCCC | + | 6.02 | | ZNF263 | MA0528.1 | chr17:42004554-42004575 | GGAGGAGCGAGGAGCGGGAAG | + | 6.2 |
|
| | 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 |
| GH17I043926 | chr17 | 42004199 | 42006952 |
|
Enhancer Sequence | TCCCACGGGA GATGGGAGGA GCGAGGAGCG GGAAGACCAG GGCTCAGTCG GCCGCAGGGG 60
ATTAGAGGTC AGCTGGAGCG GGTCTTTGAT CCACTCCAGA GGCTGAGCCT ACTGGACTAG 120
TAGCCACAAT AGTTGCCACG TGAGGAGGGG CCGTGGGCCC CAGGGACGCT GCTGGGACAT 180
GACATGCGCT GGCGCCGTGC ACTGAGCGGG AGCCATTCTG GCAGCCTCCA GACGCTCGTG 240
CCCCTGACAA ACACGCGCCC CGCCCCGTCG TTAATGACAC CTTTATTTAC GCCACCTTTA 300
TTAGGTTGGG GTCCAGATCT GCTCCATGTC ACCAGGGCGA TCTTAAGTCA CAATCCCGCC 360
CAAGGTCCCC TTCCCGCCCC GCCCCGCTGG AACACCCCTC CCCTCCCCTT AGTGAGGAAG 420
GATTTGGGCC GCAGACCTGG GTGGTCTCAG GACTCCAGCG GCCTGTTGGG GTGAAGTGGG 480
GTGGGGTCGG GGCGCGGCAC AGCTTCCCAA GGAAGTCACA GGACCTCGCC TCGGGATATT 540
CAGAAGTGCT AGTCCAGTTC TGGCAGCCTG AACTCTTCCT CCTCCAAGGT GAAATCCGAG 600
AATACTCTTC CTTCCAGGGA GAGCGACTGA CCTGCAAAAT GGGTGCCAGT TAGGGTGGCA 660
GGGAGGACGC ACATTACAAT CATTTATTCC AAAATGTTGC CATTTTCGCT AAACTTTCGG 720
TATCTTTTGT TGCATGTTTG ATAATTAATT CACCACCCTG TTAGGTAGGG GCTGCCAGGG 780
AATGAGCGAG GACTCCAGAT TTTCTGTAGG AGGGGTGTTG GGGGTAGGCA AGTCGGTCTG 840
GGAGAGAAGG TTTTAATCCG AGTGAAGAGC CCTTTGCACT AGCCTGGGAG GAGGCTGAAC 900
TGTCATCCTG CCTTGACTCA ACACAGCCAT TCCCCTAGAA GTTACAGTGT CACCCTTCAG 960
AGATCTACCC CGTGTGCACA CATAGAGAAG AGGCTTAGGT TGTTAGAGTC AGCATGTTAA 1020
ATCATTTCCT GAAATGCGAC TGTAACTAGA ACCCAGCTGA CTTCCCCCAC AGCCATTCTT 1080
ACCTATTTTA TTACTGTCTG GCATAATTAC CAGCATGTAA ACTCCAAGAA GGTGCTTCAT 1140
CTTCTTCCAG TGCCTAGCAT AGGCATAGGG TGCATAGTGA TGGCTTTAAA GTGGAAGGGA 1200
TTCCAAGGTT CGCCTCATTT AGGGATGGAG CTATTGTTAT AATCAGTTTT CTGAAATCAT 1260
TGCTGACTTC CTCTCACATT TCACAGGAAG CTAGACTTCT TAAAGCTTAA GGTTTCCTTG 1320
GTGGGTTTTA 1330
|
