Enhancers that regulate WNT9B[ENSG00000158955.6]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr17 44807665 44822640 enh4438 44910567 87927
chr17 44846485 44850635 enh91164 44910567 59932
chr17 44847625 44847956 vista24957 44910567 62611
chr17 44848199 44848613 vista24958 44910567 61954
chr17 44848812 44849347 vista24959 44910567 61220
chr17 44849895 44850213 vista24960 44910567 60354
chr17 44850644 44850747 vista24961 44910567 59820
chr17 44853334 44866495 enh17192 44910567 44072
chr17 44869005 44875155 enh86252 44910567 35412
chr17 44884565 44894093 enh44436 44910567 16474
chr17 44896658 44896796 vista24962 44910567 13771
chr17 44899125 44903275 enh91165 44910567 7292
chr17 44940381 44949855 enh44437 44910567 29814
chr17 44970125 44974275 enh88297 44910567 59558
chr17 44981325 44985521 enh65045 44910567 70758
chr17 44990141 44990292 vista24963 44910567 79574
chr17 44993343 44993471 vista24964 44910567 82776

Transcript facotrs that regulate WNT9B[ENSG00000158955.6]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr17 44941366 rs2165846 A G 0 Esophagus 0.00109719 4901644
chr17 45138927 rs35936425 A G 174831 Esophagus 0.148094 4902316
chr17 44947821 rs57986961 G A,T 0 Esophagus 0.246756 4901738
chr17 44941366 rs2165846 A G 0 Heart 0.0716646 4901644
chr17 44972333 rs7212341 G A 8237 Heart 0.0267759 4901827
chr17 44814598 rs117936104 A G 95969 Lung 0.24317 4901032
chr17 45389897 rs58365772 G A 425801 Stomach 0.25783 4904379

Genomic Location chr17:44910567-44964096[+]
TSS 44910567
Gene Name WNT9B
Ensembl ID ENSG00000158955.6
ENTREZID 7484
Uniprot
O14905
E7EPC3
Protein Name
Protein Wnt
Protein Wnt-9b