| Tag | Content |
|---|
EnhancerAtlas ID | HS148-11916 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr3:16224800-16225960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr3:16225341-16225352 | TGTGACTCATT | + | 6.62 | | Stat6 | MA0520.1 | chr3:16225000-16225015 | CACTTCCTGAGAACA | + | 6.78 |
|
| | 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 |
| GH03I016181 | chr3 | 16222907 | 16225969 |
|
Enhancer Sequence | TGCAAGCTTC TTCATCCATT CTTCTAAGGC CTCAGCTCCA GGCTGTGTCC CAGCCCTAGC 60
AGCCTCAGGC CTGGCCTAGA AGTTGGTATG GTGTTCCCAA GATAAGTGCC ACCAATTACA 120
GGCAAGCTAG GATTTTCTTG CAATGGAGGA ACTTGGCTCT GTGGGATTAC TCCCCTGTTA 180
ATCTTGACAA CCAACTTACA CACTTCCTGA GAACAAGTTC AGTGTCTTTC TTCCTTCAGT 240
GAACAAATAG CTATTGAACA ACTATCAGAA GTAAGAAGGT AAGCAATACC CAGCCCCAAC 300
CCCAAGAAGC TTGGGGTGCA CTGGGGGATG CAGACAAGCA AACAGGCTGG TACATCAGTG 360
GGATCAGGGC TGAGATAGAG AAGCCTATCC GAGTGGGGCG CCTCCACTGA TTTGATAGGA 420
ACTGGGAGTC AGTATCCCCA AAACAGCTTT AGGAAACCTG GCAGAAACCT TTCTACTCTG 480
GCCAGGCAAG GGGAGGGAGG GAAGAGCGTC AGTACTACAG CCAGGCCATC TGGTGCAATG 540
CTGTGACTCA TTCTCTTCAG AGCCATCATC CAAATGCATT TTTCCAAGTT CACAGGGGAT 600
CCTGGAGCTG CAGGAAAAGA GGGTGTGCAT CTGTATGTAA ACACAAGACA CCAGACTCCT 660
CTGATCTTGG AGTGTGAAGA TATAAAGCTA GCCTGCAGAA CAGCTCTCTT AGGCTAAGAT 720
TATCCCTTTC AATCCAGGAC ACACCCCTGG GCTGGAGAAA GGTATCAACA TCCCTGTGTT 780
GGCTAATTAG GGATTAAGCC CAGGTTGATT TGAGTCCAAA GCCCTTGGTT GTTCCTGTCC 840
CGCTGCTCCC ACTCAAAGGA TGAACAAAGG AGGTCAGGGG TGGGGTTTTG GACACTTGAG 900
TGACACATAC AAACCGAGAT AGTAAAATAT TCACCGGATA TTTCGTTGAA GCAGAGAAGT 960
TAGCCTCATT ATTTAACAAT AAAAACATAC ATTTCTTCCT GGATCCTCTG CATAAGTCCC 1020
TAGTCACTTG GGGCCTTGCT TTATGATGTT CAAGAGCCTT TGCCATGCTC TGCCTCATTG 1080
GTTGGCTCAG CAATGCTATG AATGTCTTTC CTTCAGTTCC TGGTACATGC CAGCCCTTTC 1140
CCACCTCTGG GCCTTAGCAG 1160
|
