| Tag | Content |
|---|
EnhancerAtlas ID | HS103-01933 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr1:204616170-204617550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:204616264-204616282 | GAAAGGAAGCAAGGAGGT | + | 6.37 | | NFE2L1 | MA0089.2 | chr1:204616836-204616851 | CTATGACTCAGCAGG | + | 6.6 | | Nfe2l2 | MA0150.2 | chr1:204616834-204616849 | CTCTATGACTCAGCA | + | 6.84 |
|
| | 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 |
| GH01I204647 | chr1 | 204616528 | 204617430 |
|
Enhancer Sequence | ACGAGTGTGG CTGGCTTGAC TTTTGCTGCA ATAGGCAAGG GGGTGCCCAA GAACTTGGCC 60
TGCAGTGACT GGGATTGCAA GATTCTGATT CCAGGAAAGG AAGCAAGGAG GTTAAAAAAA 120
AAAAAAAAAG GCTAGAAAGT TAAGGAGAAA AGAAGGCCTT AAAGAGACTG GTCTGGCAGG 180
GTTAATAGTT TCTTTCCTTC AATAGAGATT TCATGCCACA TTGAATAAAT AAAATACCAC 240
ACAATTGCAA AAGATGCATT CCACAGTATA TTAGATACCA CCACACTGTT ACCCACATCT 300
GTCAGCTACT ACCATCAGAG TGACTGATGA CTTATCAAAA GCCACTCTGA CATTTCCAAA 360
TGAGATATTT TGATAGAGGT GCCATTCAAC AGGGCCAAAA AAGCAGATAG AACTTGAATG 420
TAAATGAGGA ACATTTGTCA CCTTTGTCTC ACCTATTTAA AGGTTTCTTG TCTGACAACA 480
AGGAAAGGGA GAGAGGGAGT GAGGGGAGAG GAGGTGGAGG ATGGGCAGGT AAGAAGGTAA 540
GAGGGAAGGG GAGAGAGCAC CAACTCCAAA AGAGCCCAAA GGAGAAGGGC TGGTCCCTGA 600
GAGCAGTAGG AAGTGAAAGA GAAGCAAAGC CCAGATGGAC GGCTCTGATT TTTATGCGGA 660
GTCACTCTAT GACTCAGCAG GAAGGAGCAG TATCAAGAAC AAAGACCAGA GCTGTCCAAG 720
GTGGCAGCCC CACATGAGGC CACTGGGTAT TTGCAATGTG GCCAGTCCAA ATGGAGATGT 780
GCTGGACATG TAAATGTACA CCAGCTTTCA AAGATTTAAT ATGAAAAAAG AATGTGAAAC 840
ATCTCATTCA TGAATTTGTT ATTGATTGCA TTTTGAAATA TTTTTGCTAT ATTGGGTGAA 900
TATGTTATTA ACTTCACCTG TTTCTTTTTG CCTTTTTAAT GCAGCTTGCA TTATATTTCT 960
ATTGAACATA CATTTCTATA TTCTGACAGA CTGTGGATTA GAAAGACTTA GGTTCAAATC 1020
CCACCTCCAC CACTTACTCA GGGACACTTG GAAGGTGAGC CCAGCTACAG CCACTGAAGA 1080
CAAGATGGGC CAAACCATAG GGAAAGAGCA CAGGGTTGGA ACAGGATGGG CTGGGGTTGG 1140
CAGCATGTGT GGAAACAGAC AGTGGGGAAA ATGTGAAGAG GAAAATGTCA GAGAGGTGCA 1200
GCCAACTGCA CCTTCCCACA GTGAGAGAGG GCCTGGGCAG GGTGCAGAAG AAGCTGTAAC 1260
CTCTCCCAAG GCTGCCCTCA CTACTGGGTA CATCTCAATG CCAAATCCCA GCATGTCAAG 1320
AGTTGGAAGA AGCCTGAAAG AGAATCCAAT CCAGGGACCC CAAGAAAATA GGCCCAGAGC 1380
|
