EnhancerDB

Enhancers that regulate FAM101B[ENSG00000183688.4]

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Chrom.	Start	End	Enhancer ID	TSS of gene	Distance between enhancer and TSS	Tissues that enhancer appears	More
chr17	196245	201695	enh62575	295730	94035	Esophagus Thyroid Uterus
chr17	198472	198837	vista23603	295730	96893	VISTA
chr17	200517	200885	vista23604	295730	94845	VISTA
chr17	202967	210995	enh86230	295730	84735	Colon (HCT116) Brain (SK-N-SH) Prostate (RWPE1) Stomach
chr17	209872	210104	vista23605	295730	85626	VISTA
chr17	215105	219255	enh88268	295730	76475	Pancreas
chr17	220265	224415	enh109739	295730	71315	Stomach
chr17	224801	234915	enh16912	295730	60815	Liver (HepG2) Brain (SK-N-SH) Epithelial (MCF-7) Large Intestine Prostate (RWPE1) Lung Placenta Pancreas Muscle (Myotube) Heart
chr17	232485	232614	vista23606	295730	63116	VISTA
chr17	234794	234851	vista23607	295730	60879	VISTA
chr17	241625	245775	enh92699	295730	49955	Liver (HepG2) Stomach
chr17	260905	270355	enh47990	295730	25375	Liver (HepG2) Peripheral Blood (MM.1S) Thymus Blood (T-cell)

Transcript facotrs that regulate FAM101B[ENSG00000183688.4]

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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	449919	rs7209168	C	A,T	154189	Esophagus	1.34666e-07	4684195
chr17	655293	rs1884726	G	A	359563	Heart	0.0471878	4685363
chr17	436221	rs2304947	G	C	140491	Pancreas	3.18211e-06	4684069
chr17	261549	rs8077865	C	G	28220	Thyroid	0.104852	4683660
chr17	922804	rs75665137	GCT	G	627074	Liver	0.136127	4688543
chr17	699988	rs869050	A	G	404258	Lung	0.134305	4685589
chr17	438650	rs72477027	G	A	142920	Stomach	0.227105	4684098

Genomic Location	chr17:289769-295730[-]
TSS	295730
Gene Name	FAM101B
Ensembl ID	ENSG00000183688.4
ENTREZID
Uniprot
Protein Name
	isoform CRA_a
	member B
	Alternative protein FAM101B
	Family with sequence similarity 101