| Tag | Content |
|---|
EnhancerAtlas ID | HS012-15335 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:2810770-2811590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr19:2811294-2811308 | GTTGCGTGGGCGTG | - | 6.64 | | EGR2 | MA0472.2 | chr19:2811296-2811307 | TGCGTGGGCGT | - | 6.62 | | EGR3 | MA0732.1 | chr19:2811294-2811309 | GTTGCGTGGGCGTGC | - | 6.5 | | EGR4 | MA0733.1 | chr19:2811293-2811309 | TGTTGCGTGGGCGTGC | - | 6.45 | | ZNF263 | MA0528.1 | chr19:2811541-2811562 | GGAGGAGCATGGGGTGGGGGC | + | 6.18 | | ZNF263 | MA0528.1 | chr19:2811538-2811559 | GGAGGAGGAGCATGGGGTGGG | + | 6.65 |
|
| | 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 |
| GH19I002810 | chr19 | 2810682 | 2812574 |
|
Enhancer Sequence | CCACCCTTGA GCCGGGCACA CCCTGGAATT TGGAGCCTCA GCTGCTTCCC TGGGAAGGTG 60
AAGGGAGTTG GTCCCCATGC TTCACTTAGC AAGTGCAGGA GTCCCTGCTG GGGAGCCACG 120
GAGCGCGTCC CAGGCTCCTC GGGGGACAGC CCCAGCTGAG ATGCAGCTGC AGGCCCAGGG 180
TCGGGGACGG GTGTGCGGCC CCAGCCCCCA GGAGGAGTGT GTTCCCTGGA GCCTCTGCTT 240
TGAATGAAGC TGGCGTTTTC CTGATTGAAA TGTATGACAC ATGCTTTGTA AAAAGCCTGG 300
AGAAGTACAG GAAGGCCTAG GAATTTCCGA TCCTAATGAT GAGAAGTGGG CCCTGTTTCC 360
ATGCTCACCT GTTGTCCTGT GTGCATGTGT GTTCACACAC GCTTGCGAGG ATCCAGAATT 420
TGGAAATACA GCATGATTTT AACATGGGTG GTGTTTTGCT GGCTTAACAC TCCATAGACT 480
TCAAAAATCT TTCCAAAAGC GTTTTCAGCA GCGTGGCCTG TGATGTTGCG TGGGCGTGCC 540
TTGCTTTATT GACGCAGTCT CAAAATGGGG ACTTTGCTCT GTGGCAGCTG ACAGCCCCGT 600
TAAATGAGCT CCTGTCCTTC CAGGAGAGGG GGCGGAGACT TGTGGCCCTC GCTTTGTGGC 660
TGACTCTGGT TCTAGAAGTA TCCAGCTGGT CTCGGCCCTC ACCGTGATCC TCCAGCTTCT 720
CCCTGTTCCG GGCAGGGGTC TCAGGAGTCT GGCTGGTTGT CTTCTCCTGG AGGAGGAGCA 780
TGGGGTGGGG GCTACAGCGT GAACCCTGCC ATGTGTCCGC 820
|
