Variant report

Variant	rs62395833
Chromosome Location	chr6:31807652-31807653
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
2	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
3	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
4	chr6:31805278..31808004-chr6:31924712..31926962,2	K562	blood:
5	chr6:31807124..31808732-chr6:31933080..31935143,2	K562	blood:
6	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:

Variant related genes	Relation type
ENSG00000204356	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204351	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1062309	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17200969	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2257331	0.83[ASN][1000 genomes]
rs2844451	0.83[ASN][1000 genomes]
rs34431565	0.83[EUR][1000 genomes]
rs544167	0.83[ASN][1000 genomes]
rs62395789	1.00[ASN][1000 genomes]
rs62395791	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62395804	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62395814	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62395823	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62395828	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62395847	1.00[ASN][1000 genomes]
rs62395848	1.00[ASN][1000 genomes]
rs62395849	1.00[ASN][1000 genomes]
rs62395855	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
9	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
10	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
14	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
16	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
18	nsv884461	chr6:31785453-31827045	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
19	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
20	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
21	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
22	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
23	nsv884463	chr6:31797422-31827045	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
24	nsv884464	chr6:31805389-31817114	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
25	nsv884465	chr6:31805389-31818580	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31803000-31817200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:31805000-31808600	Strong transcription	Aorta	Aorta
3	chr6:31805400-31809200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:31805600-31808000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
5	chr6:31805600-31808600	Strong transcription	Brain Cingulate Gyrus	brain
6	chr6:31805600-31808800	Strong transcription	Brain Inferior Temporal Lobe	brain
7	chr6:31805600-31808800	Strong transcription	Brain Substantia Nigra	brain
8	chr6:31805600-31808800	Strong transcription	HSMMtube	muscle
9	chr6:31805600-31809200	Strong transcription	Brain Hippocampus Middle	brain
10	chr6:31805600-31809400	Strong transcription	Ovary	ovary
11	chr6:31805800-31808000	Strong transcription	Fetal Kidney	kidney
12	chr6:31805800-31808600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
13	chr6:31805800-31808600	Strong transcription	Brain Anterior Caudate	brain
14	chr6:31805800-31808600	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr6:31805800-31808800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:31805800-31808800	Strong transcription	Colon Smooth Muscle	Colon
17	chr6:31805800-31809000	Strong transcription	Duodenum Smooth Muscle	Duodenum
18	chr6:31805800-31809000	Strong transcription	Esophagus	oesophagus
19	chr6:31805800-31809000	Weak transcription	Right Atrium	heart
20	chr6:31805800-31810800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr6:31805800-31811000	Strong transcription	Fetal Stomach	stomach
22	chr6:31806000-31808800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:31806000-31808800	Strong transcription	Rectal Smooth Muscle	rectum
24	chr6:31806000-31809000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:31806000-31809000	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr6:31806000-31809000	Strong transcription	Liver	Liver
27	chr6:31806000-31809000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr6:31806000-31809000	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr6:31806000-31809200	Strong transcription	Brain Germinal Matrix	brain
30	chr6:31806000-31809200	Strong transcription	Fetal Lung	lung
31	chr6:31806000-31810200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:31806000-31810800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr6:31806200-31808000	Strong transcription	Small Intestine	intestine
34	chr6:31806200-31808800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:31806200-31808800	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr6:31806200-31809200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:31806200-31810200	Strong transcription	Fetal Brain Female	brain
38	chr6:31806400-31807800	Strong transcription	Primary hematopoietic stem cells	blood
39	chr6:31806400-31807800	Strong transcription	Right Ventricle	heart
40	chr6:31806400-31808200	Strong transcription	H9 Cell Line	embryonic stem cell
41	chr6:31806400-31808600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:31806400-31808800	Weak transcription	Fetal Heart	heart
43	chr6:31806400-31808800	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr6:31806400-31808800	Strong transcription	HSMM	muscle
45	chr6:31806400-31809000	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr6:31806400-31809000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
47	chr6:31806400-31809000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:31806400-31809200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:31806400-31809200	Strong transcription	Fetal Muscle Leg	muscle
50	chr6:31806400-31809400	Strong transcription	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links