Tag | Content |
---|
EnhancerAtlas ID | HS180-17709 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr16:1806740-1808140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr16:1808098-1808116 | CCTTTGTCCCTTCCTTCC | - | 6.68 | HNF4G | MA0484.1 | chr16:1808095-1808110 | TGACCTTTGTCCCTT | - | 6.23 | KLF4 | MA0039.3 | chr16:1807791-1807802 | CCACACCCTGC | + | 6.62 | Nr2f6 | MA0677.1 | chr16:1808095-1808109 | TGACCTTTGTCCCT | - | 6.19 | Rxra | MA0512.2 | chr16:1808095-1808109 | TGACCTTTGTCCCT | - | 6.05 | SCRT2 | MA0744.1 | chr16:1806939-1806952 | AAACCTGTTGCTT | - | 6.03 | Zfx | MA0146.2 | chr16:1807348-1807362 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr16:1807934-1807948 | GGCGCCTGGGCCTG | + | 6.41 |
|
| 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 |
GH16I001757 | chr16 | 1807745 | 1808509 |
|
Enhancer Sequence | TGAGCCTGGG AGGTCAACGT TGCAGTAAGC TATGATAGTG CCACTGCACT CCAGCCTGAG 60 CAACAGAGTG AGACCCCGTC TCAAAAAATA AATAAAGGCA TCCAGGAACC TCAGCACAGG 120 AAAGTCCCAT AAAAGTGCTG AGTGGAACAC AGGAAGCCTC CCAGAGAGAT GGATAATGGG 180 GTCCCGTTTT TGTTCTTTGA AACCTGTTGC TTATCTAGAA GGAAACCTGA GAGGAGAATA 240 TTGGCCGTGA GCAGTGGTTG CCCTGGGAAG CCGAGATGAG AGAGAAGGAC ATCTGCTCTC 300 GAATTGGGAA TTGCTTTATT ATTGGAATTC CGATAACAAA CAGCCGTTTT GTCATCTAAA 360 TCAAGTGACA TTTTTTTTTT AATTGAGGCG GAGTCTTGCT CTGTCGCCCA GGCTGGAGTG 420 CAGTGGCGTG ATCTCAGCTC ACTGCAAGCT CTGCCTCCCG GGTTCAGCCA CTCTCCTGCC 480 TCAGCCGCCC GAGTAGCTGG GACTACAGGT GCCCGCTACC AGGTCTGGCT GATTTTTTGT 540 ATTTTTAGTA GAGACGGGGT TTCACCGCAT TAGCCAGGAT GGTCTCAATC TCCTGACCTT 600 GTGATCCGCC CGCCTCGGCC TCCTAAAGTG CTGGGATTAC AGGCGTGAGC CACCACGCCC 660 TGCTCAAGTG ACTTTTTAAT GCCATTTTCC TTTCTGTGTG AAACAACCAA GTAGAAGAGA 720 ACCGCGTCCT CACCTCTGTT GGAGGAAGTG GTGTTTTCCC GCAGAGCGTT TCCCTCGCCA 780 GCCTCCTGTG CAGGGAGGGG CCAGGACCCA GTGAGGATGC CTCGCCCGCC CCACGCTCCC 840 CAGCCCTCCT CTGCTTTCTG GCATGTTCTC TCTGCCCTCC ACAGTGGGGC CCTTGCTCCC 900 ATTGTGACTT CAGTCATCCT TCACCGAGGT CCTGCCCTAC CCAGGCTGAC CCAGAAGCCT 960 AGGAGTCCAG CTCCAGGCCT GCGTCTGCGG TGTCTCCCTC GCCGCTCTCT CCCTCGCCCA 1020 CGCTGGGGGG CTTTTGGAGA CTGGGTACCT GCCACACCCT GCCACACACA CTCTCCTCTT 1080 CACAGGCCTG CATCATGGGG GCTGCGGGGG GCCTGCCCTC CTGATGGGCG ATGGGAGCAG 1140 AGGGCAGCAG GCTTCCGGGT CAGGGCTCGG CAACACAGCC CTGGGCTGGA CCACGGCGCC 1200 TGGGCCTGGT TCCCTGCAGG CCTCTGCCTG GGCACACGGG GCACCGGGAC CTGCTGGAGG 1260 CTGCTCCCTC TCTCTCCTGC CCTGCAACAT GGGAGCAGCC GAATCATTGC TGGGTTTTCT 1320 GTAATAAGAA TGTATTGTTA GTTCCAGTCC CTAATTGACC TTTGTCCCTT CCTTCCCCTG 1380 CCTCTCTGTG CGTCGCTGGA 1400
|