| Tag | Content |
|---|
EnhancerAtlas ID | HS098-31535 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:136544410-136545410 |
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 | chr2:136545160-136545178 | GGAAAGGAGGAAGGAAAC | + | 6.44 |
|
| | 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 |
| GH02I135786 | chr2 | 136544041 | 136545410 |
|
Enhancer Sequence | GGTGTGCGCC ACCGTGCCCG GCCAACAAAT GTCTTTAATA TCAATTTTAG AACCACCCCC 60
ACCCCCATCT GACAAACTTT TCCAGTCGAT TGATGGAGAA AAATGCTTGT GCACCACAAG 120
CTCCTGACTG CCAGGTTGGG ACTCATGGCG TTGGAATGTT TTGATAGGGA AAGGAATGCT 180
TACAAGAAGC AAATTTCAAG TGTGATCATC CTTTTAAGAC CAGCCCAAAA TTACTCTGTT 240
GTTACAAAAC ATTTTCCCAG CTATCTAGAT GTAATATATG GGCCAATCAA GTGTTTAGGT 300
GTTTCACACT GAGATTGTCT CTCAGCACAT TTGAGGGGAT TATAAAGAAC ATATCTCTGC 360
TCCCACCACT GCCCTGGAAA TGCTATGTGA ATGGGTGAAC ACACGAAAGG AGCATTTGTG 420
CTTTTCATTG CTCTCTCCAA GTTGTGCTTG CCAGAGACAA TGAGACATGG TCCTTGGCCT 480
TAAGAAGCTG ATGATAGAGA AATACGCAAT TCCAGTATAG AAACTGGATG GTCAAGTTGT 540
AATAGGGGAT ATTTACAAGC AAAGCAGACG AAGGAGAATC TGCCTGGGGA TTTCAGGGAA 600
GCCATTCAGA GGAGGAAGTA CATTATTTCA GCTGAGACTT AAAGGCATTT TCAGAAGAAA 660
GGGCATCCTA GGTGGAAGGA GTAGCATTTG GGAAGACACA AAGGAATATG GATAGTTGTC 720
CTATGTGCCG TTTAGAACTA CCACAAATTG GGAAAGGAGG AAGGAAACAG ACTAAATGAA 780
CCAAGGTCAG ATGGGAGAGC TGGGGATGGC ATAAAAAGTG GCAGTGGGGG TGTTCGAGGG 840
GTGGGAAAAG GCCACTTTCT GCATGTTGTG GTATTTGCCC CAAGGAATAT AATGTCAACA 900
GAAAGACTTG GTCTGGTGAG AAAGCTTAAT CGGAGCTCCA GATGGCTTGT GTGACTTCAT 960
AACTTCTCTT GAACCTACTT TCTCAAGGAG GGGCAACCAT 1000
|
