| Tag | Content |
|---|
EnhancerAtlas ID | HS041-01886 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:150185350-150186050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr1:150185928-150185939 | CGCGCATGCGC | - | 6.02 | | NRF1 | MA0506.1 | chr1:150185929-150185940 | GCGCATGCGCA | + | 6.32 | | SPI1 | MA0080.4 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.04 | | SPIB | MA0081.2 | chr1:150185880-150185892 | AAAGCGGAAGTA | + | 6.37 | | SPIC | MA0687.1 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.11 | | USF2 | MA0526.2 | chr1:150186010-150186026 | GGACCACGTGACTGGG | - | 6.06 |
|
| | 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 |
| GH01I150213 | chr1 | 150185372 | 150186896 |
|
Enhancer Sequence | GACAAGAAGA GAAATTCACT TAAGCAAAGG TCACCTAAGT GCAAACTTGA ACCAGACTGT 60
GCACAAACAA GTGACAGAAG CGAAAGTGGC CTCAGCTGCA AACGCAGCAC TTGATAAACC 120
ACACTCATGA TCAGCCCTCA TTTCCACCTT AGAGAGATTG AAAACATACC TAACTCCACC 180
ATTTATAGCT GCTGAGCAGG TGGATGACAT TCGTCAACGT GGGGTTTAGA ATAATGCAAT 240
GTTTGAAATA AAATTAGAAA GAAAATAAGG CCAGGCACGG TGGCTCACGC CTCGAACCCC 300
AGCATTTTGG GAGGCCGAGG CAGGAGGATC GCTTGAGCCC AAGAATTCGA GACCAACCTG 360
GGCAACAGGA CAAGACTCCA TGTGTATTAA AAAAAAAAAA TTAAGAAAAC AAAAGCTTTG 420
TTAATCGTTA AGTAAGGATT GCAAAATGGA AGACAGTAAA GAAAAGGAAG GTCCTAAGAA 480
TCTGACCCAC GAGTTTCAGT CCAAGTAACC TGGACCTGCC CAGAGGAAGC AAAGCGGAAG 540
TAGGATCCAA AACGCTTTCA GCAGGCCGCC TGCGCCCCCG CGCATGCGCA GGTCTCTGAC 600
TTTGACCGTT TTGGCGGGTG CGCGCCAGCC CTAGTTTATC TAGAGGGGAA GGGCGGTGCG 660
GGACCACGTG ACTGGGGTTG CGGCATTTCT GGCCCAATCC 700
|
