| Tag | Content |
|---|
EnhancerAtlas ID | HS138-08145 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr11:114248030-114249460 |
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: 2 | Chromosome | Start | End |
| chr11 | 114248201 | 114248251 | | chr11 | 114248584 | 114248922 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I114377 | chr11 | 114248059 | 114249489 |
|
Enhancer Sequence | TCATTTAATT TCCTGGGCTC TATTAGCCAA GATTCCTCCT GGAAAAAGAG TAAGTCATGT 60
CAGTGCCCGG GATACACACT GAATTGTGAC AAACTAGGGA TGGATGGATG CTCCAGGAGA 120
GCCAATTTGC AGAGAGGGCA GGGCACAGAA AATTCATCCG AAGGTGAGAG AACATGTGGA 180
ATGAGCGTCA GGGCCTAGGG TCAATGCATG GGCAGGTGTA GGCAGCCCTT GGTCCTGGGA 240
CTTACCAGGC CTGGTCATCC TAGCAGCACC CACACTCTGG GAAGTGTGTG GAACTCAGTG 300
AGCCATCTCA CTGGACTGGC AACCCCTCAG GGCCCAAGCA ACCCTGCTGT GGGAGTCCCC 360
TAAGGGCGTG AAACAGTAGA GGAAGTGTTT CTCTGTTCAA CCCTTGACAG GTCAGGGAGC 420
TTGGGGCACA GAGGACTATG AGCAATGAGG GTTGAGTATC TTTTCCTTGG AAGGAGCAGA 480
GGCCCACAGA GGGAGTGCAT GTTAGAGTAG CAGAGGCCCG AGAAGGCGGC CCTGAAACAT 540
GAACATGTGT CAGACAGCCC CTTCTCCCAT ACTCTCAGAA GGGCTTCGGG GCTGGGGTTT 600
TAGAAGGAAC TGGAATTACT TTTATGAGTC ATCAAAGCCC AGAATTAATA AGATTTTGAT 660
TTGAATCTCA AGGAACCCCA AGCTTGAGTC CACAGGCTGC TGATGCTTGG AAATGTCTGA 720
GTCACATCAC GTAAAATCAC TGGTTTCAGG ATGATTTCCT GTAGGAGTCC TGGTAGGAGG 780
GAGCTGGCTG GGATAGTCAT TGTCATGCAT GCCAATGCAG GAGAGGACAG AGCATAATTG 840
CTTCAATCTG TGTCTCTTTT GCCTACTGAA TTCCTACTCT CCGTAGACTG ATTATAGTGG 900
AGAAACAGTC AAGAGCCTAA GGAATTCTAA AATAATAGAA GCCGGTGGGA ACTGGAATAG 960
TCATAGAAAA ACATTTGTGG CAGAGGTAGA TGACCTGAGA AGGCTAGTAA AAAGAGTGAG 1020
AGAAGGGCTT TTACCAATAT CTCTGCTTGA TTCTGTATAT CTGTACGCAG TCACTCTCCA 1080
AAGCCTAGGA CCCCAGCAGG CAGTGCAGCC ACCAGCTTGG AGTCTTTGTC CTTGGGAGGA 1140
GGGAAGGAAG GCAGAAGGAG TGACAATGCT GTCACTCTCC AGCACCCACA ACTTTTGACT 1200
TCCTGGGTGG GTGTTAATAA CACCCCAGCC TTTCCAGGGC AGCTCTAATT TCAAATGATC 1260
TGTCCCAACG TCTTGGAAGA ATGGTAGCCA TAAGAAAAGA ACCGAGGAGC CATAACCAAT 1320
GCCATTGCTC CAGTGCTGTC TCTTTGCTAG CTGCACTGTG GGTCCTTGAT TGAGTCACTT 1380
CTCCTCTCTA ACCCTGTTTC CTAGTCTGTA GAAAGAAAGA CTAATACTGA 1430
|
