Variant report

Variant	rs61972933
Chromosome Location	chr13:96612217-96612218
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs17885267	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs41306037	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41315036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs45454901	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61966715	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61966717	0.85[EUR][1000 genomes]
rs61966754	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61966755	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61966758	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61966759	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61967960	0.84[EUR][1000 genomes]
rs61967961	0.80[EUR][1000 genomes]
rs61967964	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61967995	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61967998	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61968001	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61968003	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61968009	0.80[EUR][1000 genomes]
rs61968010	0.80[EUR][1000 genomes]
rs61968012	0.80[EUR][1000 genomes]
rs61968031	0.80[EUR][1000 genomes]
rs61968032	0.80[EUR][1000 genomes]
rs61972863	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972866	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972867	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972891	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972897	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972899	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972901	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972902	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972903	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972905	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972921	0.87[EUR][1000 genomes]
rs61972926	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972928	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972930	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61972931	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61972943	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61972945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61972946	0.85[EUR][1000 genomes]
rs61972947	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61972950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61972951	0.85[EUR][1000 genomes]
rs61972952	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61972953	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61972954	1.00[EUR][1000 genomes]
rs61973960	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61973962	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61973964	0.85[EUR][1000 genomes]
rs61973968	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61973969	0.85[EUR][1000 genomes]
rs61973970	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832691	chr13:96478098-96659823	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv900935	chr13:96497070-96631221	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1050430	chr13:96508530-97020734	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv541883	chr13:96508530-97020734	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1041165	chr13:96522021-96966520	Enhancers Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1051574	chr13:96550653-96779248	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1040320	chr13:96573646-96790859	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96577000-96623200	Weak transcription	NHLF	lung
2	chr13:96589000-96615600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr13:96591600-96622000	Weak transcription	Hela-S3	cervix
4	chr13:96592200-96616200	Weak transcription	Brain Angular Gyrus	brain
5	chr13:96594600-96613000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:96599000-96623600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr13:96599400-96620600	Weak transcription	HSMM	muscle
8	chr13:96599600-96613000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr13:96599600-96613000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:96600200-96620800	Weak transcription	Osteobl	bone
11	chr13:96601200-96613200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr13:96604000-96613000	Weak transcription	Right Ventricle	heart
13	chr13:96604000-96620600	Weak transcription	Left Ventricle	heart
14	chr13:96609400-96612800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr13:96609400-96623600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr13:96609800-96612800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr13:96609800-96613000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr13:96609800-96636200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr13:96610000-96612400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr13:96611000-96612400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr13:96611000-96612400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr13:96611000-96612600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr13:96611200-96612600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr13:96611200-96613400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr13:96611200-96613400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
26	chr13:96611400-96612400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr13:96611600-96613400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
28	chr13:96611800-96613000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr13:96611800-96613200	ZNF genes & repeats	A549	lung
30	chr13:96611800-96614200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr13:96611800-96620600	Weak transcription	Ovary	ovary
32	chr13:96612000-96612800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
33	chr13:96612000-96613000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr13:96612000-96613200	ZNF genes & repeats	Fetal Intestine Large	intestine
35	chr13:96612000-96613600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
36	chr13:96612000-96620600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr13:96612200-96612400	ZNF genes & repeats	Colon Smooth Muscle	Colon
38	chr13:96612200-96612400	ZNF genes & repeats	Fetal Lung	lung
39	chr13:96612200-96612400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
40	chr13:96612200-96613600	Weak transcription	Gastric	stomach
41	chr13:96612200-96620600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr13:96612200-96620600	Weak transcription	Aorta	Aorta
43	chr13:96612200-96620800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:96612200-96622800	Weak transcription	Spleen	Spleen
45	chr13:96612200-96623600	Weak transcription	Placenta	Placenta
46	chr13:96612200-96655000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr13:96612200-96668600	Weak transcription	Pancreas	Pancrea

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