| Tag | Content |
|---|
EnhancerAtlas ID | HS028-00211 |
Organism | Homo sapiens |
Tissue/cell | Colo829 |
Coordinate | chr1:161645900-161647110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:161646596-161646614 | CCTTCCGTCCCTCCCTTC | - | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr1:161646605-161646623 | CCTCCCTTCCTCCCTTTC | - | 7.04 | | IRF1 | MA0050.2 | chr1:161646625-161646646 | ACTCACTCTCTCTTTCTTTTT | + | 6.11 | | Stat6 | MA0520.1 | chr1:161646470-161646485 | GACTTCCTGAGAAAT | + | 7.77 | | ZNF263 | MA0528.1 | chr1:161646790-161646811 | CCCTCCCCCACCTCTTCCCCA | - | 6.18 | | ZNF263 | MA0528.1 | chr1:161646787-161646808 | CCCCCCTCCCCCACCTCTTCC | - | 6.8 |
|
| | 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 |
| GH01I161675 | chr1 | 161645425 | 161647563 |
|
Enhancer Sequence | GGATGCCAGG CAACTTCCAG ACTGTAGTTA AAGTCAGAGC ACAAAGGAAA CCAGTGCTTT 60
CTCTGGGGGC TTCCATGACA GTAAGAACAG GCAGAAAAAA GAGGCTGTCA AAGACCCCAC 120
CTCAGATGGC TGGAGTATGA TTCAGAGCAG AGCCAACAGA TTTAAGAGCT TGAGCAAAAT 180
ATCACTTGTT CAGCTGTGCT TGCAGCAAGG TCGCATGTCT GCTGGCCAGG CCCAGTGGTG 240
ATAGGGGCCT GTGTTCACAC CAGGGCCAAA ACAGATCTGG AAAAAACAAA GTCCAAGCAA 300
CTGGATTATC CATCTTGTTG TGTGGTTCTG TCTGCACTGG CATAAGCACA TTTCACAAGG 360
CACTTTTGCA GCCAGGCATT GGGGCTGCAT AAATGGTTTT TTAAAAATCC TTTCCCAAAA 420
GGCAAAGCTG GGTTGCTGGG ATTCTTGGGA AATGTAATAG AATGGGAATT CAGAATGCGG 480
TTTACTGCAG AATTTACAGC ATGGCAATAA AGGCTCTCTA TGTTCAGGGG GTGAGAGAAG 540
AGACTAGATG CATTGTCTCA GATGTCTCCT GACTTCCTGA GAAATGCCAC TTTGCAGATA 600
TGGGGCTGCT TTTCACACTG GCTAAGTCAG TTCATGGCAA AATATGAGGG AATTCAGTGT 660
GTTTCAGACA CTAACCAAAG TCCATCCTTC CTTTCTCCTT CCGTCCCTCC CTTCCTCCCT 720
TTCTCACTCA CTCTCTCTTT CTTTTTAATG CCATGGAGTA CCATATTTTT CAAAGTTCCA 780
ACAAAGATGC ACTACATTTA GACAATGTGG AAATGGCCCT CAGCCTTCTC TCCCTGAAGT 840
CTGTGGCCAG CAAAAATCTG GACTTTACTT CACTCTGATG CTGAACACCC CCCTCCCCCA 900
CCTCTTCCCC AATATCTCAG ATCCCAAGCC TCCCTGGTTT GCTTCTAGGA AAGCTCAGCA 960
ATTCCCTGAA AAGAATGCAG CTCAAGTGAC TGCTCCACTT TTTCACCTTG GCCTTTGCGG 1020
AAGGCTGTGG CTGGGCTACC CTATGCATCG ATCAATGAGG TCATATTTAC CCAGTGCTTG 1080
GCCTAGAGGC CCAAGACAGG GTCAGCAGTG CTTGCTTTGG CTCTAGTTTG GGCGTTGGTT 1140
TTGCAGCCTC AGCATCAGCA CAGGCAGGCC CTCTTCTCCA GCAGTGCTCT GGCTGATATT 1200
TCTTCTTTTT 1210
|
