| Tag | Content |
|---|
EnhancerAtlas ID | HS105-22193 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr13:45741830-45742940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BARHL2 | MA0635.1 | chr13:45742217-45742227 | ACCGTTTAGC | - | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr13:45742913-45742931 | GCTTCCTTCCTTCCTTCC | - | 10.05 | | EWSR1-FLI1 | MA0149.1 | chr13:45742917-45742935 | CCTTCCTTCCTTCCTTCC | - | 10.83 | | EWSR1-FLI1 | MA0149.1 | chr13:45742921-45742939 | CCTTCCTTCCTTCCTTCC | - | 10.83 | | EWSR1-FLI1 | MA0149.1 | chr13:45742905-45742923 | CCTGGCTGGCTTCCTTCC | - | 6.45 | | EWSR1-FLI1 | MA0149.1 | chr13:45742909-45742927 | GCTGGCTTCCTTCCTTCC | - | 7.61 | | SPIC | MA0687.1 | chr13:45742692-45742706 | TTCTTCCTCATTTT | - | 6.42 | | ZNF263 | MA0528.1 | chr13:45742917-45742938 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 |
|
| | 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 |
| GH13I045167 | chr13 | 45741594 | 45743130 |
|
Enhancer Sequence | GCCCCCCAGC TGATTTTTGT GTTTTAAGTA GCAATAGGCT TTCACCATGT TGGCCAGGCT 60
GGTTTCAAAC TCCTGACCTC AAGTGATCCT CCCACCTCAG GCCTCCCAAA CCTCCCAAGT 120
GCTGGAATTA CAGGCATGAG CCACCACGCC CAGCCTCACT TGTTTCCCCC CAGTCTAAAA 180
GAACCTTTCT TGAGAATATT TTATGGTTGA AAGTTGTGGC ATTTTCTGTT GATAGAGGGA 240
AAAAAAAGTA CACCACCCAG TGTTGTTTAC AGCTTCAGTT TCTTTTATAT AGCTATGCAG 300
AACTTAATGA CTATGATGAT TTGACACATT TTTTTCCTTA CTGTATAATG TGTTATGTGT 360
CAGACTTTTC TTGAGAGAAA GATCTGTACC GTTTAGCAAA GAAAAAAGTC TGGTTTAGAG 420
CACTTCTCAA CCCCTTTTCT GCTGCTTCTA GGTGAAGGCT GATGTGTCTT TACATTCACA 480
AGTTTGGGAC AGACTCCTAT AGATTAGGGG CTGTGGCATA GATGCCCCAG GTGCTGTCAG 540
TGTTCGCCCA TAGCCTCTCA AGGCCTTGCC GTTACTGTGC ACACTAGCCA ACTTTTACAT 600
CTCGGCACCT TTGTCTGCCT GAGAGCTTCT CTTGCTGCCA ACTACTCTGC CTGCCTGGAG 660
GGCAGGCCAG AAATGCCAGG ATTTTAACAC TCACTTTGGG AGTGGCGTTC AGCCAATATC 720
TGCCAGGAGT TGTTAGTTGA TAAACACCCA GCTCCTTTAA TCCTCAGGTA GGGTGACTAA 780
GGCACATATT AAGCAACAGT TGTCCTTAGT AGTATCCAGC TGGTACTGGT TTTCTACACT 840
AATCATTTTA TAGGCTCATT TCTTCTTCCT CATTTTTCCA ACCCTCAGTG TTTTCTGACA 900
AATAAACTAC CTGAACTTTA TTTATTTATT TTTTTGAGAC AGGTTTTCAC TCTGTCACCC 960
AGGCTGTAGT GCAGTGCCCC GATCTCGGTT CATGGCACCC CCTACCTCTG GGGCTCTAGT 1020
GATTTCCCCA CCTCAGCCTC CTGAGTAGCT GGAGCTGCAA GTGTGTGCCA CCACACCTGG 1080
CTGGCTTCCT TCCTTCCTTC CTTCCTTCCT 1110
|
