Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region
Chrom. | Start | End | TF Name | Source | Predicted site? | Tissue/Cell line | id | More |
---|---|---|---|---|---|---|---|---|
chr17 | 59337907 | 59337925 | RARA | JASPAR | yes | 21268404 | ||
chr17 | 59337907 | 59337925 | RARA | JASPAR | yes | 55142028 | ||
chr17 | 59337917 | 59337928 | STAT1 | JASPAR | yes | 21268405 | ||
chr17 | 59337917 | 59337928 | STAT1 | JASPAR | yes | 55142030 | ||
chr17 | 59337921 | 59337926 | ETS2 | TRANSFAC | yes | 21268406 | ||
chr17 | 59337921 | 59337926 | ETS2 | TRANSFAC | yes | 55142031 | ||
chr17 | 59337935 | 59337949 | E2F7 | JASPAR | yes | 21268407 | ||
chr17 | 59337935 | 59337949 | E2F7 | JASPAR | yes | 55142032 | ||
chr17 | 59337971 | 59337983 | MEF2A | JASPAR | yes | 21268408 | ||
chr17 | 59337971 | 59337983 | MEF2A | JASPAR | yes | 55142033 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 59337970 | rs148991649 | C | T | no | 4966906 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
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Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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