| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00182 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:6411680-6412660 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:6412510-6412520 | GCCCCGCCCC | + | 6.02 | | ZNF263 | MA0528.1 | chr1:6412412-6412433 | CTTCCCCTCCCCACCTCCCTC | - | 6.02 | | ZNF263 | MA0528.1 | chr1:6412416-6412437 | CCCTCCCCACCTCCCTCATTC | - | 6.68 | | ZNF263 | MA0528.1 | chr1:6412404-6412425 | CCCTCCCTCTTCCCCTCCCCA | - | 6.82 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23464 | chr1:6411485-6412692 | Colon_Crypt_1 | | SE_24052 | chr1:6411536-6412670 | Colon_Crypt_2 | | SE_37032 | chr1:6406618-6415653 | HSMMtube | | SE_50714 | chr1:6411474-6412754 | Sigmoid_Colon | | SE_53099 | chr1:6411468-6412739 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I006351 | chr1 | 6411760 | 6411944 | | GH01I006353 | chr1 | 6412321 | 6412530 |
|
Enhancer Sequence | GAGCAGGGCC CAGCTCCTGG TTCTAGAGCA GTGAGGAAAC ATCAGCCCAG CATTTCCCAG 60
GAGCAGCAGA GCCAGCCTCC AGAGCAGCCT GAATGACTGC TGCAGGCCTC ACTTTGCCTG 120
TCTGTGAAGT GGAGCCACAC ACAGCAGGCT GGCCCCCAGG AATGACACAA GGCCAGGGAG 180
AGAAGACGCG GGCCAAGGGC TGCAGAGCAG CGGAGGAAGT GCTTTCATGC GGTGGGCACT 240
GAAGACAGGA CAGATATGTG GGTAGCCTTT AAGACAGAAG ACCAGGGACA GTGCCTGAGG 300
CCCCGAGGAA GAGCCTGGAG CCACCTGGCA ACAAAGTGAG GACTCGGCAC TTGGCGCTGT 360
GCCATCAGGA GTACATGCCA GGAACTGCAG ACCGCACGCC AGCTGGCTAC CACGGGCCTG 420
GCCGCCTTTC TTCGGCACCT TGGGTCCTGC ACCAAGGACC ATCCTAACTC CCCAACTGAC 480
CACCCAGGAA GCCAGCCCCT GCCCTCAAGG TCAGACACAA CCCTCTCCCC TACAGGACCT 540
GACTCCTGCC TGGGGACTGT GCTGTCACCT CCAATGCACA AGGCTCAAAG CCCAACTCAC 600
TTACCCCTTC TCCCTTTCCC CAAATCAGAC ACCTTCCCTC CAAGCCAGGG CAGCCAGTGA 660
GTCCCAGCCT CAGCTGGGAT TCCTTCCCAT CCTGCATACC ACCACCAGCT GCTCCACACC 720
TGGCCCCTCC CTCTTCCCCT CCCCACCTCC CTCATTCCTT CCAAACAGCT CAGGAACCGC 780
TGGATCCAGC CAGCCTCCAG GACCCATAAA CAGCTCTGTC ACTCTCTCAG GCCCCGCCCC 840
ATGGCCTGGC CAAGGCCAAC CGTGTCCATC CCAGGACAGG GTCATGACTG CCTCTGTCTA 900
AAGGCAGGCA GGGGTGAGAG CCAGGGAGCC AGGGAAGCTG CTGCGTCTCA CTGGAGACTT 960
CGTTTTCCCA TTTCTTTTTT 980
|
