| Tag | Content |
|---|
EnhancerAtlas ID | HS101-20677 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:883430-884420 |
Target genes | | Number: 34 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr19:884099-884111 | CCCCACGTGCCC | + | 6.07 | | MYC | MA0147.3 | chr19:883478-883490 | GGGCACGTGGGG | - | 6.07 | | ZEB1 | MA0103.3 | chr19:884091-884102 | CCCACCTGCCC | + | 6.14 |
|
| | 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 |
| GH19I000883 | chr19 | 883600 | 884759 |
|
Enhancer Sequence | GCGGTGCGTG AAGAGCTGGG CATGGCGGGG ACCAAAGCCT GGCATGGTGG GCACGTGGGG 60
CGGTAGGGGG AGAGATGGGG GAGAGATGGG TGCGGTGGGG ACTGTCCCAG TGACCCCCAG 120
CTGCCAGGGA TGTGAGACCT GAGAAAGGCT GTGGCATGTG TGTGAGACGT GGCTCTCGGG 180
CGGGTAACAG CTGGGCCAGC AGGTGAGGAC GGCTGCAGGA GACGAGGAGG AGTGTCGGAG 240
CCCAGGACTG CCCAGTGGCT TGGCTGTGGG CAGATGGTAG ACACAGACGT GCCCAGCGGG 300
GGCACCGGGC AGTGAAGGTG CAGGTCTGTG CAGCCACACG GGGTGGCGCC AGGTGCTGCT 360
GCAGGAGCCA GCGCAGCCCA AACTGCCTGG TGACTCACCA CGAGGCCCAG GGGAAGGAAT 420
GAGGCCCAAC AAGGCCCTGG GGACCGGGCG AAGGAACGAG CCCTGGGAGA AGGAATGGCA 480
GCAGCCCTCT TCACCTGCCT GGTGACTCAC TACAAGCCCT GGGGGAAGGA ATGGCAGTGG 540
CCCTCTTCAC CTTTACTGCC TCTGCGGCCA CAATGGGCAG TTGACATAAC CACCTGCAGG 600
CCCCGGGAGC CATCGGGGCC TCTTGACACG TGCTCATTAG TGGCTTCTGA GGAGCGCCTG 660
CCCCACCTGC CCCACGTGCC CCCACGTCTG GCCACTCCAG GGTCCATTAG CGCTAATCGG 720
CAAATGCCTG TGCTCTCATC TACCGGGAAA ACATCTCCCT TCTCCAGAGC GGAGGCCAGC 780
CTAAAAACCA GGCCCGCAGC CTCCGAGGCT CTGAAAACCA AGCGGCTGTT CTGGTCCCCG 840
GTCATAGCAG GCGGGCGTCC CTGCTTCGCT CCAGCCCCAG GATTTTGTGC CGGAGGTGGG 900
GATGACGGGC TTGGCTCCGT GGGTGCGGGG GGCCCATCGG GCGGATAGAG ATGGGAATGG 960
GGGCCCCAGA AGAGGCTGCT GGAGAGGTGG 990
|
