| Tag | Content |
|---|
EnhancerAtlas ID | HS187-07213 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr14:24521700-24522910 |
Target genes | | Number: 39 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr14:24521833-24521843 | GCCCCGCCCC | + | 6.02 | | REST | MA0138.2 | chr14:24521780-24521801 | GGAGCTGCCCCTGGTCCTGAC | - | 7.7 | | RREB1 | MA0073.1 | chr14:24522531-24522551 | ACACCCCACACCCCCACACA | + | 6.44 |
|
| | 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 |
| GH14I024053 | chr14 | 24522541 | 24522630 |
|
Enhancer Sequence | TCGGCGAAGC GTCCAGTCTC CCATCCGGAG AGTCCCCGCT TCCCCGCCGG GCGGGGCCAA 60
GCCCGCCCCT CCCTGCGATG GGAGCTGCCC CTGGTCCTGA CCGCTGCGTG GCTTAACACC 120
CTCCCTCCTC CCGGCCCCGC CCCGGAACTG GCCCTGAAGA GCCCCTTAGG AGCTGGGCAG 180
CGCCCAGGCC AGTGGGGCAA AGAAAGGAGT CAGGGAAGAG GCCCTGGATT GGAGCTAAAA 240
CCAAGAGCAG GAGGGTCTCT GAGGCTCGCC TCCCACAGCC CCGTCCCAGC CTGCTTCCTT 300
CTCGCTACCC ACCACCCACA CATCAAGGCT TCTCCCGTTT GCATGGTTCT CAGACCTAGC 360
CCAAACCCAG GCCCGGCCAC CCAGCACTGC CACAACCCTG ACCCCCAGAG ACGGGAGCAC 420
AGGCTAGCCC ACGCAAAGCG CAGGATGCTC GTGGATACTC AGAGGCATGC TGCGCCGTGG 480
CAATCTCCCA CACCTGCACA CACACACAGC ACAATCATTA GACGTGTGTA AACACATCTT 540
CACAGAGATG GCACCCCAGC ACACGCGCGT GCACACACAC ACACACACAC TATATCTGGG 600
TGGTTCTGCC AGCAGATGGG TATGGGGCTC ATTTAAACAT TAATTCTTCT CCCCGCCCAA 660
CACACACAGA GGAAGTGTCT GGCTCTGTGC CCCTTCCACA GCATACTCAT TCACACTTAC 720
CTGTCCCCAC CAATGCCACA CTCAGGCTCC CTGACATCTC CAGGAGGCAT GCACACTCTC 780
ATAGTAAAGG CAGACACTCA CACCCGGACC ACCTAGAATA TAGTCAAAGG GACACCCCAC 840
ACCCCCACAC AGTGACTCAC TTTGTATGTG TCAATGGCTG TTGTAGTGCA TGGGTTGGAA 900
AAATTCTTCA CACCCTCAGA AGTGTGAGAC ACACCCTCCC ACAGACAGTC AGCAACCGTC 960
CCCTGACTCA GGGACATCAG GAGCCGGAGT TTTCTCCACA CCCTACTCCC TCTCTAATAG 1020
GAAGAGAAAA GTCAAAAAAG AGACAGTGTG AAAAGTCACC CAAGAAGGAA TGCCCTCTGT 1080
CCCTGTCCTC CCTTCTTTGT CTCTCTGTTT CTCTCTTATC CCATTTGACC CTGACCCTGC 1140
CTCTATCTGG AGAGCTCTGG GAGGTGGGGG TGGCCAGGGT AAGGTGAAGC TCTGAGCAGG 1200
CTCCCACCCC 1210
|
