Tag | Content |
---|
EnhancerAtlas ID | HS101-00193 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:6536100-6537580 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:6536713-6536728 | AGGGACCAAAGTCCA | + | 6.95 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68825 | chr1:6536821-6537975 | H9 |
|
| 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 |
GH01I006475 | chr1 | 6535661 | 6537893 |
|
Enhancer Sequence | GGAGAAAGCA GGAGAGGGTT GTGCCTCCCC CGCCCCTCCT TAGCCTGCAG CATGGCTGCC 60 TCCAGAGGGA CCACAGCCTG TTACCCTGGA ACCCCCAGAT TAAAGGTAGC AAGGGCCCTT 120 CAGTTCTGTG AGGAGAGGGG CTCAGTCATT GTTTTTTGTT TTTGTTTTGA GATAGGGTCT 180 CACTCTGTCA CCCAGGCTGG AGTGCAGTGG CATGATCTCG GCTCACTGCA ACCTCCACCT 240 CCTGGGTTCA AGCAATTCTC ATGCTTCAGC CTCTTGAGTA GCTGGGATTG CAGGCGTGTG 300 CCACCACACC CGGCTCATTT TTTTGTATTT TTAGTAATGA CAGGGTTTCA ACATGTTGGC 360 CAGGCTGTTC TCAAACTCCT GACCTGAAGT GATCCACCCA CCTCAGCCTC CCAAAGGGCT 420 GGGATTACAG GTGTGAGCCA CCTTGCCTGG CCTTAGTCAT TGCTGTCTAT CCCCACAGAC 480 CCAAAAGGAC ACAAAGGCCC TGGGATGACA CCCATGGTGA AGCTCCACCC CAAAAACAAA 540 CTCACCTGTG GCCTCAGTTT ACCCTTCTAT AAAATAAGGA TAAGGAAGCC TTGCCTCTGA 600 GGTTATTACA GGAAGGGACC AAAGTCCATG GCTCTTTCTT CCAGGCCTCC CCTCCCCCAT 660 GCTGTGACCA CACCTGAATT CCCAAGGGGC CCTGGCAGTG GGAGAGAGTC TTTTGTTTGT 720 TTATTGTTTT TTAAGACAGG GTCTTGCTCT GTCGCTCAGG CTGGAGTGCA GTGGCACGAT 780 CAGGGCTCAC TGGAGCCTCC ATTGTCGGGG TTCAAGCGAT CCTTCCACCT CAGCCTCCGA 840 GCAGCTGGGA CCACAAGTGT GTGCCACCAC ACCTGGCTAA TTTTTGTATT TTTTGTATTC 900 CAGACATGAG CCACCGTGCC CAACCAGAAG AATCCTTTTG TTCCTCTGAT CAGCTGGGAA 960 AGGACTCGGG GGTTGGCATT TCTCACCAGG CCTGGGTGCC TGCGAGCCAC TCCTCCATAG 1020 GCAGTTGATG GTGGGCCTGA GCTGGGTCCC TGCTCAGCAA GAGGAATTTC TTATTTCCTG 1080 CTCCAAGTGC CTCCTGACCT GGCCACCCCC ACTCCACACT GCCTCTGCTA GGCCCACAGC 1140 CTGGCTTGCA GGACTTGTCC AGAAGTCCCC TGCCCTGAGG ATAGGCAGAA CTAGAAAGAA 1200 AGGGGCCTTC TCTGTGTGGG CCACAGGCCA GGGGCAAAAG CAGCTGGGGG AGGTGAGAAC 1260 CAGTGAGAGC ACAGCACCAG ATAGAGAAAG GCCTGCCTCT GGAAGGGGCA CGCTCATGGA 1320 CTTTCTCTCT TGCTAAAAAA CATTTGGAAC AAAAGGAACC GTAACATACT CGGGTTTCAT 1380 TATTTACAGT CGACTTGTCC TTATGACGCC CTAGCACGTT TCCGACAGTT ACTGAAACAC 1440 TGACACAGGA GCTCTGGGGG CCGAGCTGCG GCTCCCGCCT 1480
|