| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17749 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:141658640-141659960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr3:141659122-141659133 | GGGAGATAAGA | - | 6.62 | | KLF4 | MA0039.3 | chr3:141659268-141659279 | CCACACCCTCC | + | 6.32 | | NKX2-5 | MA0063.2 | chr3:141658740-141658750 | ACCACTTGAG | + | 6.02 | | RREB1 | MA0073.1 | chr3:141659257-141659277 | GCCCCCACCACCCACACCCT | + | 6.16 | | RREB1 | MA0073.1 | chr3:141659261-141659281 | CCACCACCCACACCCTCCCC | + | 6.74 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 141658675 | 141659613 | | chr3 | 141659495 | 141659587 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I141938 | chr3 | 141657661 | 141662058 |
|
Enhancer Sequence | GCATGGGCAA CATAGTGAGA CCCTGTCTCT ACACAAAATA AAAAAACAAG CCAGGTGTGG 60
TGGTGCACAC CACGGCTACT GTGGAGACTG AGGTGGGAGG ACCACTTGAG CCCAGGAATT 120
CGAAGTTACA GTGAGCTGTG ATGGTGTCAC TGCATTCCAG CCTGTGACAG AGCAAGACCT 180
TGTCTCTGCA AGGAAAAAAA TCATCCTGTA AAATTACTTT TTGTTGTACT CAGACTGAGG 240
AAAACCTTTG CTGGAGGTTT GAAAGCAAAT CTATGATGTA TTAGCAGAAC CAGAAAGTCC 300
TTCCTGTGGA GATGGGACCT TTTCGGTATT GTCATTTTTG GATTTTAGTG CACAAACTTC 360
TCATGATTGA GTTTCGGCTT TTGAGAGCCA TGACCAAGTG GTAGGTAGGG CATGAAAGAA 420
GAAAACAAAT CTCCTGACCT TAGCATAATG TGTCACAGTA CTTTAGGCCC CTTAGCCAAG 480
GCGGGAGATA AGAAGGCAAT AAGGAAATGG TTGGATGAAT CACTGTGCCC CAGTGGCAAA 540
AATGTCCTGA AGCAATTTGG ATGAAAGTGA GAAAGTGGAT ATGACAAATG CTGCTCTACA 600
CTAACCGGAT TGGTTGTGCC CCCACCACCC ACACCCTCCC CAACTACAGG ACTTCCTTCA 660
CCACTGTGCA TTTTCCACTG AGATGCTCTC CTGAAAGCAA GTTTCAGCAA GAGGCTGGAA 720
AGGCCTCTCA GAGAGAAGGC TGAGCTGGCA GTGATCAGGG AGCCCCCGGG CATTTGGCAG 780
CCGTCCACAG TAAGACCGGC AGATGGAGCC TTCATCTGGC AAGAAACTGG GGAAGCTGGC 840
GGTGTCGTCA GGTGCAAGCT TCAGTGAGAA GTGCCAGCAC TCTGAGAAGA TGCACAGAAA 900
TACAGAAGCA GCTCCCGTAG GAGAAGGAAT GGAGGCCGCA CGCGGTAGCT CACGCCTGTA 960
ATCCCAGCAC TTTGAGAGGC TGAGGTGGGT GGATTACTTA AGGTCAGGAG TTTGAGACCA 1020
GCCTGACCAA CATGGTGAAA ACCCGTCTCT ACTAAAAATA CAAAATATTA TCCAGGCGTG 1080
GTGGTATGTG ACTGTAGTCC GAGCTACTCG AGAGGCTGAG GCAAGAGAAT CACTTGAACT 1140
CAGGAGGTGG AGGTTGCAGT GAGCCAAGAT GGTGCCATTG CACCTCCTGC CTGGGCAATA 1200
GAGCAAGACT CTGTCTCAAA AAAAAAGGAA TGGAGAAAAC ATAGCCATAG CTCTGGGAGT 1260
AGGAACAGAA GCAAGCAAGC TGACTGCCAG TCGGGTTCTT TCTTCTGGAA AAGGCTCTGG 1320
|
