Variant report

Variant	rs59751965
Chromosome Location	chr3:195033077-195033078
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:195028253..195031997-chr3:195032734..195036397,6	K562	blood:
2	chr3:195025817..195028618-chr3:195031491..195033491,2	MCF-7	breast:
3	chr3:195032015..195035498-chr3:195161704..195164752,3	K562	blood:
4	chr3:195026519..195030688-chr3:195031134..195036189,5	K562	blood:

Variant related genes	Relation type
ENSG00000114331	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs56309159	1.00[AFR][1000 genomes]
rs56911559	0.88[AFR][1000 genomes]
rs60284665	0.91[AFR][1000 genomes]
rs60560609	0.91[AFR][1000 genomes]
rs60584652	0.95[AFR][1000 genomes]
rs6764918	1.00[AFR][1000 genomes]
rs6790118	0.91[AFR][1000 genomes]
rs6809102	0.90[AFR][1000 genomes]
rs73890752	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73890760	1.00[AMR][1000 genomes]
rs73890762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73890763	1.00[AFR][1000 genomes]
rs73890764	0.95[AFR][1000 genomes]
rs73890767	1.00[AFR][1000 genomes]
rs73890782	0.91[AFR][1000 genomes]
rs73890784	0.95[AFR][1000 genomes]
rs73890791	0.95[AFR][1000 genomes]
rs73890793	0.91[AFR][1000 genomes]
rs73893622	0.86[AFR][1000 genomes]
rs73893623	0.90[AFR][1000 genomes]
rs73893628	0.90[AFR][1000 genomes]
rs7611086	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009796	chr3:194737333-195124248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
3	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
4	nsv533904	chr3:194868329-195438728	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
5	nsv1010168	chr3:194874494-195135790	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv536877	chr3:194874494-195135790	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv997956	chr3:194879534-195087539	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
8	nsv536878	chr3:194879534-195087539	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	esv1832781	chr3:194902818-195528226	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
10	nsv432508	chr3:194916131-195478861	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
11	nsv432510	chr3:194935314-195478861	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
12	nsv1005519	chr3:194964301-195340515	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
13	nsv432511	chr3:194986167-195479748	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
14	nsv432512	chr3:195007260-195475989	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194992600-195090000	Weak transcription	Aorta	Aorta
2	chr3:194992800-195039800	Weak transcription	Fetal Brain Male	brain
3	chr3:194992800-195039800	Weak transcription	Right Ventricle	heart
4	chr3:194993000-195038600	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:194993000-195039200	Weak transcription	Brain Germinal Matrix	brain
6	chr3:194993000-195039600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:194993000-195050400	Weak transcription	Colon Smooth Muscle	Colon
8	chr3:194993000-195076000	Weak transcription	Fetal Heart	heart
9	chr3:194995000-195039800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr3:194995400-195040000	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr3:194996400-195033800	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr3:195004000-195039600	Weak transcription	Pancreas	Pancrea
13	chr3:195004000-195066600	Weak transcription	Small Intestine	intestine
14	chr3:195004200-195039600	Weak transcription	Gastric	stomach
15	chr3:195005200-195039600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:195008000-195039800	Weak transcription	NH-A	brain
17	chr3:195010000-195039000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr3:195010000-195039600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr3:195010000-195039800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr3:195010000-195039800	Weak transcription	Brain Substantia Nigra	brain
21	chr3:195010000-195061000	Weak transcription	Fetal Kidney	kidney
22	chr3:195010000-195076400	Weak transcription	Brain Angular Gyrus	brain
23	chr3:195013200-195039400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr3:195014200-195040800	Weak transcription	Hela-S3	cervix
25	chr3:195016000-195039600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr3:195016200-195039800	Weak transcription	NHLF	lung
27	chr3:195016400-195038600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr3:195018200-195034200	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr3:195019400-195034000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr3:195021800-195039600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr3:195021800-195039600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:195022600-195038600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr3:195022600-195073400	Weak transcription	HMEC	breast
34	chr3:195022800-195038600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:195022800-195039600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr3:195022800-195039600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr3:195022800-195039600	Weak transcription	Rectal Smooth Muscle	rectum
38	chr3:195022800-195039800	Weak transcription	Colonic Mucosa	Colon
39	chr3:195022800-195073400	Weak transcription	NHEK	skin
40	chr3:195023000-195033600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr3:195023000-195038200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr3:195023000-195038600	Weak transcription	Fetal Lung	lung
43	chr3:195023000-195039600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr3:195023000-195039600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr3:195023000-195039800	Weak transcription	HepG2	liver
46	chr3:195023000-195040200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr3:195023400-195039400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:195023800-195033600	Weak transcription	Osteobl	bone
49	chr3:195024000-195039600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr3:195024200-195039600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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