Variant report

Variant	rs573154090
Chromosome Location	chr17:16396465-16396466
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr17:16395456-16396662	H1-hESC	embryonic stem cell:	n/a	chr17:16395674-16395684
2	CEBPB	chr17:16396459-16396647	K562	blood:	n/a	chr17:16396510-16396523
3	E2F6	chr17:16395451-16396570	H1-hESC	embryonic stem cell:	n/a	chr17:16395667-16395677 chr17:16395631-16395643 chr17:16395630-16395641

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:16116365..16119285-chr17:16395133..16397532,2	K562	blood:
2	chr17:16368821..16370735-chr17:16395780..16397972,2	K562	blood:

Variant related genes	Relation type
FAM211A	TF binding region
ENSG00000141027	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
3	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
5	nsv1063764	chr17:16171649-16662914	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
6	nsv1061463	chr17:16245878-16490691	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
7	nsv543216	chr17:16245878-16490691	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
8	nsv428668	chr17:16265210-16455285	Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
9	nsv1063941	chr17:16357086-16424098	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv1058448	chr17:16389870-16926287	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
11	esv3323619	chr17:16394252-16396800	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	esv3344255	chr17:16394352-16396600	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv574494	chr17:16395083-16398555	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16394800-16396600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr17:16395800-16396600	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr17:16395800-16397200	Enhancers	Small Intestine	intestine
4	chr17:16395800-16397400	Enhancers	K562	blood
5	chr17:16396000-16396600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr17:16396000-16396800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr17:16396000-16401400	Weak transcription	Spleen	Spleen
8	chr17:16396200-16396600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr17:16396200-16396600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
10	chr17:16396200-16396600	Enhancers	Adipose Nuclei	Adipose
11	chr17:16396200-16396600	Enhancers	Colonic Mucosa	Colon
12	chr17:16396200-16396600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr17:16396200-16396600	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr17:16396200-16396800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
15	chr17:16396200-16396800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chr17:16396200-16397400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr17:16396200-16398200	Enhancers	Fetal Intestine Large	intestine
18	chr17:16396200-16399000	Weak transcription	Liver	Liver
19	chr17:16396400-16396600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr17:16396400-16397800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr17:16396400-16398400	Enhancers	Fetal Intestine Small	intestine
22	chr17:16396400-16399800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr17:16396400-16399800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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