Variant report

Variant	rs74085776
Chromosome Location	chr13:52988035-52988036
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:52986828..52988975-chr13:53022775..53024785,2	K562	blood:
2	chr13:52978712..52982217-chr13:52984992..52988158,3	K562	blood:
3	chr13:52985298..52988100-chr13:53012949..53014836,2	K562	blood:

Variant related genes	Relation type
ENSG00000136100	Chromatin interaction
ENSG00000136114	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs55645852	1.00[AFR][1000 genomes]
rs55796806	0.88[AFR][1000 genomes]
rs55924773	1.00[AFR][1000 genomes]
rs56116089	1.00[AFR][1000 genomes]
rs56252739	1.00[AFR][1000 genomes]
rs56758534	0.89[AFR][1000 genomes]
rs57339165	0.88[AFR][1000 genomes]
rs57461595	0.88[AFR][1000 genomes]
rs60539260	0.82[AFR][1000 genomes]
rs60864284	1.00[AFR][1000 genomes]
rs61285838	0.88[AFR][1000 genomes]
rs74085735	0.88[AFR][1000 genomes]
rs74085745	1.00[AFR][1000 genomes]
rs74085746	1.00[AFR][1000 genomes]
rs74085748	1.00[AFR][1000 genomes]
rs74085750	1.00[AFR][1000 genomes]
rs74085767	1.00[AFR][1000 genomes]
rs74085773	0.89[AFR][1000 genomes]
rs74085781	1.00[AFR][1000 genomes]
rs74085783	0.88[AFR][1000 genomes]
rs74087342	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv1040931	chr13:52564792-53350914	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv541773	chr13:52564792-53350914	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv428288	chr13:52728370-53068132	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv900084	chr13:52835231-53119704	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv1838257	chr13:52971893-53231454	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52980200-52988400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr13:52980200-52989800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr13:52980200-53002000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr13:52980200-53021600	Weak transcription	Small Intestine	intestine
5	chr13:52980600-52988200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr13:52980600-52988200	Weak transcription	Esophagus	oesophagus
7	chr13:52980600-52988200	Weak transcription	Fetal Stomach	stomach
8	chr13:52980600-52988200	Weak transcription	Gastric	stomach
9	chr13:52980600-52988200	Weak transcription	Pancreas	Pancrea
10	chr13:52980600-52988400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr13:52980600-52988600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr13:52980600-52989800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr13:52980800-52988200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr13:52980800-52988200	Weak transcription	Brain Anterior Caudate	brain
15	chr13:52980800-52988200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr13:52980800-52988200	Weak transcription	Colonic Mucosa	Colon
17	chr13:52980800-52988200	Weak transcription	Right Ventricle	heart
18	chr13:52980800-52988200	Weak transcription	GM12878-XiMat	blood
19	chr13:52980800-52988400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr13:52980800-52988400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr13:52980800-52988400	Weak transcription	Brain Hippocampus Middle	brain
22	chr13:52980800-52988400	Weak transcription	HUVEC	blood vessel
23	chr13:52980800-52988600	Weak transcription	Fetal Lung	lung
24	chr13:52980800-52992800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr13:52980800-52993200	Weak transcription	Right Atrium	heart
26	chr13:52981000-52988400	Weak transcription	Fetal Thymus	thymus
27	chr13:52981000-53022800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr13:52981200-52988200	Weak transcription	Fetal Kidney	kidney
29	chr13:52981200-52988400	Weak transcription	Thymus	Thymus
30	chr13:52981400-52988400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr13:52981800-52988200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr13:52981800-52988400	Weak transcription	Colon Smooth Muscle	Colon
33	chr13:52982200-52988200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr13:52982600-52988400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr13:52982600-52988400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr13:52982800-52988400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr13:52982800-52996400	Weak transcription	Brain Germinal Matrix	brain
38	chr13:52982800-53012600	Weak transcription	Fetal Brain Male	brain
39	chr13:52983600-53000800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr13:52983800-52988400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr13:52983800-52988400	Weak transcription	Lung	lung
42	chr13:52983800-52988800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr13:52983800-53016600	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr13:52984000-52988200	Weak transcription	Psoas Muscle	Psoas
45	chr13:52984000-52996600	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr13:52984000-53002400	Weak transcription	Hela-S3	cervix
47	chr13:52984400-53023400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr13:52984600-52991000	Strong transcription	Primary hematopoietic stem cells	blood
49	chr13:52984600-52993200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr13:52984800-53013400	Strong transcription	Dnd41	blood

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