| Tag | Content |
|---|
EnhancerAtlas ID | HS187-11702 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:1363050-1364500 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr19:1363450-1363464 | CTTCCAGGAAATCA | + | 6.74 |
|
| | 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 |
| GH19I001360 | chr19 | 1360058 | 1364670 |
|
Enhancer Sequence | CAAAAATAGT AAAGGGAGGT GAGGGGGCTT CTCACCCGGG CTTCCCCACT GGCAGCATCC 60
GTAAGGCGCA GGATGTCCCC GGCCAGGAAG CTGGTGCGTG TGCAGCCTCG GGAGCGCCAT 120
TCCACGCACA CTTGCGTGCC GGTGGCCTTG TTATGTCGTT CTTTTTTTGT CTACACTGTT 180
TGAGTGCTTT TCCATCATTG AAAGGGCTTC ATTACAGTCT CACATTTTCC CTTTTTTTTG 240
CCTAATGCTA ATGGTCAGAC TTTTTAACAG TTTTCCACAT GCTCTTCTGA TCCTTTTCCT 300
CTGGGGTGAG CAGTCACCAC TCACCAAACC CTGCCCCACC CATTGGGCAC CTGTCTGGAT 360
GGTCCCAGGA CCGCAGGTGC TGTGGGGCAC CCATTGGGGA CTTCCAGGAA ATCATTTCTG 420
CAGGATCCGT TCGCACACAC GAAGAGCACA GTGCCCTCGG GAAGGGCCCT TTCCGACCAC 480
GCTGCCCCAC TGGGGTTGGG TCACCGGGAC ATACAGAGGC TGGTGCTGCC TGGCTTCTCC 540
TGCCTGCGGT GGGAGCTGGG TTTTGCTCCC GTTTGGTTTT GTTTTCTACC TGTCAGGCTG 600
GGCGTCTTTC TGAGGGTTCC CTGACCGGCC TCTGAATTGA TTGTTTGTCC ACGTGGGCCT 660
GGAAGTTTCT CTTAAAGACT AAATGCCCCT CACTGGGGAA ACGACGCTGT GCCATGTTCA 720
CAGCAGACAC TCACCCCAGT GGGCCTCCCT TTTTCTCTGG TCACGTTGGT TACTTCATAG 780
GCCTTTAGGT TTTGATCTGT GTTTATGGAC CACGGCACTT CCTTCCTTCC ACAGTGCGGT 840
CAGACACAGG CTTTGTGTGT CTAACGACAG ACTGTTTCCA GTAGTTTTTC TAATACTTTA 900
GTTTTAAAAT TTTAAATAAT TCACTTGTTT TTTGGCATTG AAAATATTTC ATTCATAAAT 960
AGTTTCTAGT TATGATTTAA ATAATTTTCC CATTTTTGAC TGTAGTTTCC CAGAATCCTC 1020
TTTAGAATCT CAGTCCTTGT GTTTGGGTCT TCTCCGCGTG CCATTACCTC ACCTCTGTTT 1080
TGTGCCACAC ACTCTTTAAA AGTGTCTTCC CGCGGGGTTT AGAGTTAGGA AAGTCGCGCA 1140
CACATAGGAC AGAGCCCCAG CCGCCCCTCG TGGCACCCCT CCCATCCCAA GGGTGCGTTT 1200
GTCGCAGCTG GGAACCCAGT GCAGCACCCC ACTCAGCTGC TGGTTTCACT GTCTCATCAT 1260
TGGTGGTTAG ACTCAAGTAG TGTGGGGTAT GTGAATCTGC CTTTCAGATT CTCCTGATCT 1320
TTTAAGCGAA TGACACAAAG TCAGGTTTTA ACAATATCGT GCTAACTGTG TTTTCTCAGG 1380
CTGTTACACC TGGTGCTTGA TATGGATTTG ACTTGTCTAT TCTTTTTTTT TTGTTTTTCT 1440
TTTTTCTTTA 1450
|
