| Tag | Content |
|---|
EnhancerAtlas ID | HS101-33136 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr4:101789200-101790090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr4:101789629-101789645 | CTTTGTTTACACTGTG | - | 6 | | Nkx2-5(var.2) | MA0503.1 | chr4:101789645-101789656 | AGCCACTCAAG | + | 6.62 | | REL | MA0101.1 | chr4:101789889-101789899 | GGAAATCCCC | - | 6.02 | | YY1 | MA0095.2 | chr4:101790074-101790086 | TCAGCCATCTTG | - | 6.04 |
|
| | 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 |
| GH04I100869 | chr4 | 101789367 | 101789884 | | GH04I100868 | chr4 | 101789999 | 101791141 |
|
Enhancer Sequence | GACCCCTCAG CTGCAGGTCT GCTGGAGTTT GCTGGAGGTC CACTCCAGAC CCTGTTTCCC 60
TGAGCATCAC CAGCGGAGGC TGCAGAACAG CAAATATTGC TCCTTAATCC TTCCTCTGGA 120
AGCTTTGTCC CAGAGAGGCA ACCGCCTGTT TGAGGTGTCT GTCAGCCCCT ATTGTGAGGT 180
GTTTCCCATT CAGGCTACAC GGGGGTCAGG AACCCGCTTG AAGAAGCAGT CGGTCCATTC 240
TCACAGCTCA AACGTCATGC TGAGAGAACC ACTGCTCTCT TCAGAGCTGT CAGACAGGTA 300
TGTTTAAGTC TGCAGAAGCT GTCTGCTGCC TTTTGTTCTA CTATGACCTG ACCCCAGAGG 360
TGGAATCTAT AGAAGCAGTA GGCCTTGCTG AGCTGTGGTG GGCTCCACCC AGTTTGTGCT 420
TCTAGGCCTC TTTGTTTACA CTGTGAGCCA CTCAAGCCTC AGCAATGGCA GACGCCCCTC 480
CCCCTTCCAG CTGCAGCATA GCAGGTGGAT CTCAGATTGC TGCACTGGCA GTAAGCAAGG 540
CTCTGTGGGT GTGGGACCTG CCGAGCCAGG CACGGGAGGG TATCTCCTGG TCTGCCAGTT 600
GCTAAGACTG TGGGAATAAT GCAGTATTTG GTCAGGAGTG AACCGTTTCT CCAGATACAG 660
TCTGTCACAG CGTCCCTTGT CTAGGAAAGG GAAATCCCCC GGCCCCTTGT GCTTCCGGGA 720
TAAGGCGATG CCCCACCCTG CTTCAGCTCG CCCTCCATGG GCTGTACCCA CTGTCCAACC 780
AGTCCCAGTG AGATGAACCC TCAGTTGGAA ATGCAGAAAT CACCCGTCTT CTGCGTCAAT 840
CTTGCTGGGA GCTGCAGACC GGAGCTGTTC CTATTCAGCC ATCTTGGCAG 890
|
