| Tag | Content |
|---|
EnhancerAtlas ID | HS012-17352 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr20:39969640-39970450 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr20:39969706-39969724 | CCATCCTACATTCCTTCC | - | 6.75 | | EWSR1-FLI1 | MA0149.1 | chr20:39969714-39969732 | CATTCCTTCCTTCCTGTC | - | 7.16 | | EWSR1-FLI1 | MA0149.1 | chr20:39969710-39969728 | CCTACATTCCTTCCTTCC | - | 8.01 | | Klf1 | MA0493.1 | chr20:39970112-39970123 | AGCCACACCCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGTAGGGCC CAACTCGGGG GGAGAAGAGA TGACCCTCTC CCCTCCCGCC CTGCCCATCT 60
GTCCTGCCAT CCTACATTCC TTCCTTCCTG TCCGCGGGCC TGGGTCCACC CCTAGCTGTA 120
AGATGGGGAC GCAGGGGTGG AGGGACTGGC CTCATTTTGT CCCTTTTTCC CTGGCCCAGC 180
GGCTGCAGGC CCCCTGGACA CCCAGAACGT AGAGTCTGGA GAGGAGACGT CGAAACCTCC 240
CAGGGGAGGC TGGCCCAGCT TTACCCCAGC CTGACTGTGT GACCTTGAGG AGGACAGCCA 300
CTTTCTCTGG TACCCAGTGT CCTCAGTTGC AAAACAGTGA CTGGCCCTTG CCCTGCTTGC 360
CCTGAGACTG GGCAGATCAG ATGCTGTAGC TGCTGGGGGC TGGGGTGGCG CTTTCTCTCT 420
ACTGGGGCAC TAGGAGTGCT TACTCTCCTG CTCCCTCTGG TCCTCGGTGG AGAGCCACAC 480
CCTTCATCCA CCCAAACCTG GGAGCCCCGA GGGCTGAGAG CCTAGTCCTA GGGCAGCTTG 540
CTCTGGCTTC CCTGTGCTAG AGTTGTAGTC TAGCCTGGAA GGCCTGTGAA CATCCCCAAG 600
GTGGGGTGTG AGGCCTACGT GGAGTGCACA TGCTCGTTTT GCAAATAGTG GTGCCACCAT 660
TGTGCATGGC CTTGAGTGCC AAGTTAAGAA GTCCAAACTC CGCTGGGCGC GGTGGCTCAC 720
GCCTGTAATC CCAGCACTTT GGAGACTGAG GCGGGTGGAT CATGAGGTCA GGAGATCGAG 780
ACCATCCTAA CACGGTGAAA CCCCGTCTCC 810
|
