Variant report

Variant	rs1981354
Chromosome Location	chr18:13177059-13177060
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1981356	1.00[ASN][1000 genomes]
rs3944554	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4261607	0.92[EUR][1000 genomes]
rs61283323	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61637798	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9947395	0.92[EUR][1000 genomes]
rs9954021	0.92[EUR][1000 genomes]
rs9962778	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062014	chr18:12687210-13183383	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv543655	chr18:12687210-13183383	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	nsv1057083	chr18:12916779-13207538	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv576524	chr18:12918318-13183609	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1056593	chr18:12926314-13183383	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv1064364	chr18:12926314-13207686	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv833591	chr18:13093777-13253748	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv909408	chr18:13122618-13308950	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv909409	chr18:13151544-13240284	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv909410	chr18:13151544-13308950	Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:13173000-13177400	Enhancers	Fetal Thymus	thymus
2	chr18:13173400-13177200	Enhancers	Thymus	Thymus
3	chr18:13174000-13182600	Enhancers	HepG2	liver
4	chr18:13176200-13181800	Weak transcription	Gastric	stomach
5	chr18:13176400-13177200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr18:13176600-13177400	Active TSS	Colonic Mucosa	Colon
7	chr18:13176600-13177400	Enhancers	Fetal Intestine Small	intestine
8	chr18:13176600-13177400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
9	chr18:13176600-13177600	Flanking Active TSS	Duodenum Mucosa	Duodenum
10	chr18:13176800-13177200	Active TSS	Liver	Liver
11	chr18:13176800-13177400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
12	chr18:13176800-13177400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr18:13176800-13177400	Active TSS	Rectal Smooth Muscle	rectum
14	chr18:13177000-13177200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
15	chr18:13177000-13177200	Weak transcription	Fetal Intestine Large	intestine
16	chr18:13177000-13177200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
17	chr18:13177000-13177400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
18	chr18:13177000-13177400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr18:13177000-13177400	Active TSS	Duodenum Smooth Muscle	Duodenum
20	chr18:13177000-13178600	Weak transcription	Small Intestine	intestine

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