| Tag | Content |
|---|
EnhancerAtlas ID | HS148-03603 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr11:114248270-114249460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:114249171-114249189 | GGAAGGAAGGCAGAAGGA | + | 6.37 | | EWSR1-FLI1 | MA0149.1 | chr11:114249167-114249185 | GGAGGGAAGGAAGGCAGA | + | 7.52 | | EWSR1-FLI1 | MA0149.1 | chr11:114249163-114249181 | GGGAGGAGGGAAGGAAGG | + | 8.45 |
|
| | 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 |
| GH11I114377 | chr11 | 114248059 | 114249489 |
|
Enhancer Sequence | CTTACCAGGC CTGGTCATCC TAGCAGCACC CACACTCTGG GAAGTGTGTG GAACTCAGTG 60
AGCCATCTCA CTGGACTGGC AACCCCTCAG GGCCCAAGCA ACCCTGCTGT GGGAGTCCCC 120
TAAGGGCGTG AAACAGTAGA GGAAGTGTTT CTCTGTTCAA CCCTTGACAG GTCAGGGAGC 180
TTGGGGCACA GAGGACTATG AGCAATGAGG GTTGAGTATC TTTTCCTTGG AAGGAGCAGA 240
GGCCCACAGA GGGAGTGCAT GTTAGAGTAG CAGAGGCCCG AGAAGGCGGC CCTGAAACAT 300
GAACATGTGT CAGACAGCCC CTTCTCCCAT ACTCTCAGAA GGGCTTCGGG GCTGGGGTTT 360
TAGAAGGAAC TGGAATTACT TTTATGAGTC ATCAAAGCCC AGAATTAATA AGATTTTGAT 420
TTGAATCTCA AGGAACCCCA AGCTTGAGTC CACAGGCTGC TGATGCTTGG AAATGTCTGA 480
GTCACATCAC GTAAAATCAC TGGTTTCAGG ATGATTTCCT GTAGGAGTCC TGGTAGGAGG 540
GAGCTGGCTG GGATAGTCAT TGTCATGCAT GCCAATGCAG GAGAGGACAG AGCATAATTG 600
CTTCAATCTG TGTCTCTTTT GCCTACTGAA TTCCTACTCT CCGTAGACTG ATTATAGTGG 660
AGAAACAGTC AAGAGCCTAA GGAATTCTAA AATAATAGAA GCCGGTGGGA ACTGGAATAG 720
TCATAGAAAA ACATTTGTGG CAGAGGTAGA TGACCTGAGA AGGCTAGTAA AAAGAGTGAG 780
AGAAGGGCTT TTACCAATAT CTCTGCTTGA TTCTGTATAT CTGTACGCAG TCACTCTCCA 840
AAGCCTAGGA CCCCAGCAGG CAGTGCAGCC ACCAGCTTGG AGTCTTTGTC CTTGGGAGGA 900
GGGAAGGAAG GCAGAAGGAG TGACAATGCT GTCACTCTCC AGCACCCACA ACTTTTGACT 960
TCCTGGGTGG GTGTTAATAA CACCCCAGCC TTTCCAGGGC AGCTCTAATT TCAAATGATC 1020
TGTCCCAACG TCTTGGAAGA ATGGTAGCCA TAAGAAAAGA ACCGAGGAGC CATAACCAAT 1080
GCCATTGCTC CAGTGCTGTC TCTTTGCTAG CTGCACTGTG GGTCCTTGAT TGAGTCACTT 1140
CTCCTCTCTA ACCCTGTTTC CTAGTCTGTA GAAAGAAAGA CTAATACTGA 1190
|
