| Tag | Content |
|---|
EnhancerAtlas ID | HS012-14599 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr17:41038160-41039260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:41038465-41038483 | CCTCCCTCCCTTCCTTCC | - | 8.13 | | KLF4 | MA0039.3 | chr17:41039168-41039179 | GCAGGGTGTGG | - | 6.62 | | ZNF263 | MA0528.1 | chr17:41039028-41039049 | GAGGCAGCAGGAAGAGGGAGA | + | 6.05 | | ZNF263 | MA0528.1 | chr17:41038491-41038512 | CTTCCTCTTTCCTCTTCCTTC | - | 6.12 | | ZNF263 | MA0528.1 | chr17:41038497-41038518 | CTTTCCTCTTCCTTCTCCATC | - | 6.33 | | ZNF263 | MA0528.1 | chr17:41038465-41038486 | CCTCCCTCCCTTCCTTCCTCT | - | 6.81 | | ZNF263 | MA0528.1 | chr17:41038464-41038485 | TCCTCCCTCCCTTCCTTCCTC | - | 6.83 | | ZNF263 | MA0528.1 | chr17:41038494-41038515 | CCTCTTTCCTCTTCCTTCTCC | - | 6.96 |
|
| | 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 |
| GH17I042885 | chr17 | 41037984 | 41039286 |
|
Enhancer Sequence | TTGCCCAGGC TGGTCTTGAA CCTTGAGCTC AATGGATCTT CCTGCCTTGG CCTCTGAAAG 60
CACTGGGTTT ATAGGTGTGA GCAACTATGC CTGGCCCCCT CCTATAGTTT TTCCCTGGCC 120
AATATCCCTC TTATAAATCC ACAGAGCTTC TCACTCTCTG CAGGGAATAT TAGGTCATTC 180
ACATACCTGG GTTCAGTCCC TACACCGCAG TCATCGTGAT GCTTACACCC CAGACACCCC 240
AGACGTGTGT CCTCCTTCAA ACAGCCTATT CCCACCCACT AAGCCTCTGC CCATGTGTTC 300
CGACTCCTCC CTCCCTTCCT TCCTCTGCTT CCTTCCTCTT TCCTCTTCCT TCTCCATCTA 360
GTGACAGCTT ATTCACTGTC TAAAACCCAA CTCGAATCCC ACTCTCTCGA CCTTTCCCTG 420
AACAACATTA TTTACTTTGT TGTCTCTGCT CCCATAGTAC TTTGGACAGA ACTCTGCCAT 480
GGAGGTTCAC AAACTGAACT CTAGTTCCTT GACCACGTGT GTCCTCCCCT CACTCCCCAC 540
ACTGAACCTG GCTTTGGTGG CCTGGTGCCC AGCATGGTGT TGTGCCCGTG TGTGGATGCT 600
TAAATACATC TTTGAAATTT GAATAAATAG TAAACATTGT TATACATGAG TCATGTTTTT 660
CTCTTTAAAA GCCACATCAT ATCCATTTGC TCATTGGACT ACTTCAAAAG AGAAGCTCTA 720
AGGACATCCA AAGATCCTAA GTGAAAAATC ACCCTGGCTG CACGGGTCAA GCCAGGACAC 780
AGGGCCAAAG GTCGGTCAGC ACTGACACGC TGAGCCCAGG CGTTTGCTTT CCAGATGAGA 840
CCTGCACCGC TGGACCAGCA ATGCAGCAGA GGCAGCAGGA AGAGGGAGAT GGAGCCAAAG 900
GGTTTCTGGA CAGGCGGTTG CTGGCAGATC TATAAATCGA TGCCCCACAA TGGGCTGTCA 960
CTGAAACAGG CCAGGAGTAG CCCAGAGCCT GGAGGTAGAC CTGAGAGGGC AGGGTGTGGG 1020
AAGATTAGAA GCATAGGCTA GGCCAGGCAC AGCGGATCGT GCCTGTAATC CCAGCACTTT 1080
GGGAGGCCGA GGCAGGTGGA 1100
|
