| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00221 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:8352750-8354280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:8353862-8353873 | AGTGACTCATG | + | 6.14 | | MEF2A | MA0052.3 | chr1:8353564-8353576 | TCTATTTTTAGG | - | 6.14 | | MEF2C | MA0497.1 | chr1:8353726-8353741 | GAAATAAAAATAGAA | + | 6.18 |
|
| | 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 |
| GH01I008292 | chr1 | 8352860 | 8355312 |
|
Enhancer Sequence | CGTCTCTCTC TGTCACCCAG GCTGCTGCAG TGCAATGGCA TGATCTCCGC TCACTGCAAC 60
CTCCACCTCC CGGGTTCAAG CAATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGGATTACA 120
GGCATGAGCC ACCATAGCAG GCTAATTTTT GTATTTTTAG CACAGATGGG GTTTCGCCAT 180
GTTGGCCAGG CTGGTCTCCA ACCCCTGACC TCAAGTGATC CACCTGCCTC GGCCTCCCAC 240
AGTGCTGGGA TTATAGGTGT GAGCCACCAC GCCCGGCCTC TACCTCTTAC TTTGAATCAG 300
GAGATCCTGG ACTTACATCC TAATTGGGCT TTAGATGTCC AACCCTGCCT GGGACTGGGG 360
GATACTTCTA ACCTGAGAGG GAACTTATTT GGCCACAAAT CTGAGGTGTG TTCTCCAATT 420
CACTTGATCA CAACTAAACC TCATGTTGAT ATTGCCATAT TCCTGACTCT TTGCCTCCTT 480
TGGGATGGAA CTTGGAAGAG AAGTTTCACA CACTTATTAC AAGAAGTTGG AAGTCCTCAA 540
CACTTAATGT AAGAAAGGTA ATAAAATTCA CGTGTGCTGG GAGGTGCCAC TCACACAGGC 600
CTACTTTGTA CTTCTGCATC AGCCGCGCCT TCATTCCTGG CACCCCCACC CTCCAGAGTC 660
TACACTGATG TCAGCCAGTG AGGCTTCCCC CATCCCCCCT CCCCGCTCAA GTCTCCCCGG 720
TCCACACCTT CTTCATGGGT CCTGGATTTG GAGCTTAGCT AGTGGAGACT ACACATTCTT 780
TTCCAGCATA CGTAGAATGT TTCTAAAAAT TGACTCTATT TTTAGGCTGT AAAGAAATCT 840
CAGTAAATTT CATGGAATTG ATATCATACA TACCATATTC TCTAAACATT ATGTAATTAA 900
CTCAGAAGGT TTTTTTTTCT TTTAACAGAG CTTTAGAAAA AAAGACCACA ATTCTAATAA 960
TATACAAGAT AAAATAGAAA TAAAAATAGA AATGACTCCT TTGCATCTAC TTTCTTGCCA 1020
TTGTTCTAAG TTTCTGGGAG GCAGGAGAGT GGAGAAGATG ATGTGCTGAG GTCCTATCTA 1080
GCGCTTAAAA TGTTTGACTT TTGGTCAGGC GCAGTGACTC ATGCCTGTAA TCCCAACACT 1140
TTGGGAGGCT AAGGTGGGAG GATCGCTTGA AGCCAGGAGT TTGAGACCAG CCTGGGCAAC 1200
ATTGCCAGAC CTCATCTCTA CAAAAAATAC AAAAATTAGC TGGGCATGAT GGCACCTGCC 1260
TGTAGTCTCA GCTACTCAGG AGGTCAAGGC AGGAGGATTG CTTGAGTCCA GGAGGTCAAG 1320
GCTGCAGTGA GTCATGATCG CACCACTGTG CTCCAACCTG GGCAACAGAG TGAGCAACAG 1380
AGTGGGACCC TGTCTCAAAA AAAAAAAAGC TTGACTCTCT CATTTAAATC CTTAAATCAT 1440
TCACTTGGAT GATCTGTTCT TTGGAGATGC TGAGAGCTGT CCCCTCCTGC GTGTGTCTCC 1500
CCACGTTTCT CCTGCCGTCT CAGCAGAGCC 1530
|
