Variant report

Variant	rs9500865
Chromosome Location	chr6:30693477-30693478
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:213)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:213 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr6:30693405-30694062	K562	blood:	n/a	n/a
2	POLR2A	chr6:30692296-30694437	K562	blood:	n/a	n/a
3	BCL3	chr6:30692818-30694183	GM12878	blood:	n/a	n/a
4	CHD2	chr6:30692670-30694160	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr6:30693433-30694131	GM10847	blood:	n/a	n/a
6	PML	chr6:30692201-30694187	K562	blood:	n/a	n/a
7	STAT5A	chr6:30692551-30694913	GM12878	blood:	n/a	chr6:30694805-30694819
8	POLR2A	chr6:30687742-30694690	GM12878	blood:	n/a	n/a
9	POLR2A	chr6:30692324-30694192	HCT-116	colon:	n/a	n/a
10	MYBL2	chr6:30692662-30694182	HepG2	liver:	n/a	n/a
11	JUND	chr6:30693465-30694035	HepG2	liver:	n/a	n/a
12	POLR2A	chr6:30690060-30695157	GM12892	blood:	n/a	n/a
13	JUND	chr6:30692960-30694353	HCT-116	colon:	n/a	chr6:30693232-30693243
14	POLR2A	chr6:30687036-30695449	HUVEC	blood vessel:	n/a	n/a
15	POLR2A	chr6:30690176-30694491	HepG2	liver:	n/a	n/a
16	JUND	chr6:30693456-30694143	HepG2	liver:	n/a	n/a
17	JUND	chr6:30692671-30694211	HCT-116	colon:	n/a	chr6:30693232-30693243
18	POLR2A	chr6:30687122-30694167	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr6:30692770-30694169	GM12878	blood:	n/a	n/a
20	POLR2A	chr6:30693154-30694777	HL-60	blood:	n/a	n/a
21	POLR2A	chr6:30692316-30694157	K562	blood:	n/a	n/a
22	POLR2A	chr6:30683610-30695318	SK-N-MC	brain:	n/a	n/a
23	POLR2A	chr6:30691230-30694189	K562	blood:	n/a	n/a
24	TEAD4	chr6:30692284-30694091	K562	blood:	n/a	n/a
25	NFATC1	chr6:30692636-30695046	GM12878	blood:	n/a	n/a
26	MBD4	chr6:30692362-30694218	HepG2	liver:	n/a	n/a
27	POLR2A	chr6:30693204-30694615	ProgFib	skin:	n/a	n/a
28	NFIC	chr6:30692597-30694809	GM12878	blood:	n/a	n/a
29	POLR2A	chr6:30693427-30694196	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr6:30692324-30694533	HCT-116	colon:	n/a	n/a
31	POLR2A	chr6:30690156-30694752	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr6:30690112-30695297	Hela-S3	cervix:	n/a	n/a
33	SIN3AK20	chr6:30692575-30694762	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr6:30686736-30693839	K562	blood:	n/a	n/a
35	POLR2A	chr6:30687488-30695337	Hela-S3	cervix:	n/a	n/a
36	USF1	chr6:30693336-30693850	A549	lung:	n/a	n/a
37	POLR2A	chr6:30692338-30695323	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr6:30692209-30696227	U87	brain:	n/a	n/a
39	TAF1	chr6:30693073-30694044	PFSK-1	brain:	n/a	n/a
40	TEAD4	chr6:30693375-30694302	ECC-1	luminal epithelium:	n/a	n/a
41	SIN3AK20	chr6:30692377-30693953	K562	blood:	n/a	n/a
42	POLR2A	chr6:30692693-30694205	HepG2	liver:	n/a	n/a
43	POLR2A	chr6:30692568-30694207	NB4	blood:	n/a	n/a
44	TEAD4	chr6:30692570-30694191	HepG2	liver:	n/a	n/a
45	GATA3	chr6:30693031-30694286	A549	lung:	n/a	chr6:30693975-30693985
46	POLR2A	chr6:30687419-30696083	PFSK-1	brain:	n/a	n/a
47	HEY1	chr6:30693408-30694086	K562	blood:	n/a	n/a
48	NFIC	chr6:30692953-30693753	HepG2	liver:	n/a	n/a
49	ETS1	chr6:30693134-30694051	A549	lung:	n/a	n/a
50	SP4	chr6:30692613-30694084	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30451219..30453103-chr6:30692483..30694829,2	K562	blood:
2	chr6:30692885..30693719-chr6:43968705..43969609,2	Hela-S3	cervix:
3	chr6:30691897..30694851-chr6:30760025..30762962,2	K562	blood:
4	chr6:30576582..30588788-chr6:30682721..30700088,114	K562	blood:
5	chr6:30634661..30668428-chr6:30680318..30698953,145	MCF-7	breast:
6	chr6:30646432..30647241-chr6:30693199..30694158,2	K562	blood:
7	chr6:30608315..30616989-chr6:30683761..30694958,31	K562	blood:
8	chr6:30693361..30695767-chr6:30895208..30897558,2	K562	blood:
9	chr6:30692214..30695086-chr6:30900554..30903279,2	K562	blood:
10	chr11:62608638..62609358-chr6:30693377..30693999,2	Hela-S3	cervix:
11	chr6:30692018..30694762-chr6:30878588..30881246,2	K562	blood:
12	chr6:30693275..30696224-chr6:30778287..30780136,2	K562	blood:
13	chr6:30692887..30695267-chr6:30900165..30903279,3	K562	blood:
14	chr6:30577862..30587208-chr6:30682997..30696247,43	MCF-7	breast:
15	chr6:30510952..30513795-chr6:30691840..30693915,2	K562	blood:
16	chr13:41956378..41959414-chr6:30690779..30694701,5	K562	blood:
17	chr6:30643326..30660432-chr6:30681522..30696111,127	MCF-7	breast:
18	chr6:30447631..30450065-chr6:30691817..30695001,3	K562	blood:
19	chr6:30577773..30589670-chr6:30680333..30700280,58	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000272540	TF binding region
ENSG00000230449	Chromatin interaction
ENSG00000266183	Chromatin interaction
ENSG00000137343	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000213780	Chromatin interaction
ENSG00000214222	Chromatin interaction
ENSG00000204564	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000222894	Chromatin interaction
ENSG00000137404	Chromatin interaction
ENSG00000252761	Chromatin interaction
ENSG00000146112	Chromatin interaction
ENSG00000204568	Chromatin interaction
ENSG00000204560	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs16867845	0.82[ASN][1000 genomes]
rs17189120	0.82[ASN][1000 genomes]
rs17189134	0.82[ASN][1000 genomes]
rs17189155	0.82[ASN][1000 genomes]
rs17195411	0.82[ASN][1000 genomes]
rs17195474	0.82[ASN][1000 genomes]
rs17195488	0.82[ASN][1000 genomes]
rs17195516	0.82[ASN][1000 genomes]
rs2106069	0.82[ASN][1000 genomes]
rs2239514	0.82[ASN][1000 genomes]
rs2239515	0.82[ASN][1000 genomes]
rs2239516	0.82[ASN][1000 genomes]
rs2267638	0.82[ASN][1000 genomes]
rs2267640	0.82[ASN][1000 genomes]
rs2284172	0.85[AFR][1000 genomes]
rs2302347	0.82[ASN][1000 genomes]
rs2394387	0.82[ASN][1000 genomes]
rs2394388	0.82[ASN][1000 genomes]
rs2394389	0.82[ASN][1000 genomes]
rs25497	0.85[AFR][1000 genomes]
rs3815101	0.82[ASN][1000 genomes]
rs4148247	0.82[ASN][1000 genomes]
rs55810373	0.85[AFR][1000 genomes]
rs59272830	0.82[ASN][1000 genomes]
rs59607822	0.82[ASN][1000 genomes]
rs59913575	0.82[ASN][1000 genomes]
rs60081418	0.82[ASN][1000 genomes]
rs60399658	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61733213	0.94[ASN][1000 genomes]
rs6457246	0.82[ASN][1000 genomes]
rs6457247	0.82[ASN][1000 genomes]
rs6457248	0.82[ASN][1000 genomes]
rs6457249	0.82[ASN][1000 genomes]
rs6899769	0.82[ASN][1000 genomes]
rs6901251	0.82[ASN][1000 genomes]
rs6911174	0.82[ASN][1000 genomes]
rs6917434	0.82[ASN][1000 genomes]
rs6917935	0.82[ASN][1000 genomes]
rs6934466	0.82[ASN][1000 genomes]
rs73727463	0.85[AFR][1000 genomes]
rs7742291	0.82[ASN][1000 genomes]
rs7742650	0.82[ASN][1000 genomes]
rs7742754	0.82[ASN][1000 genomes]
rs7749109	0.82[ASN][1000 genomes]
rs7749807	0.82[ASN][1000 genomes]
rs7749978	0.82[ASN][1000 genomes]
rs7767002	0.82[ASN][1000 genomes]
rs7773711	0.94[ASN][1000 genomes]
rs9262120	0.82[ASN][1000 genomes]
rs9461625	0.85[AFR][1000 genomes]
rs9468812	0.94[ASN][1000 genomes]
rs9468817	0.85[AFR][1000 genomes]
rs9468821	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9468822	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9468823	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9500863	0.85[AFR][1000 genomes]
rs9500864	0.85[AFR][1000 genomes]
rs9500866	0.85[AFR][1000 genomes]
rs9500867	0.85[AFR][1000 genomes]
rs9501027	0.85[AFR][1000 genomes]
rs9671	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' 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	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	esv3430377	chr6:30443802-30814426	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS 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	967 gene(s)	inside rSNPs	diseases
5	nsv830626	chr6:30558064-30732905	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	406 gene(s)	inside rSNPs	diseases
6	esv2758041	chr6:30644693-30816319	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
7	esv2759413	chr6:30644693-30816319	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
8	nsv970736	chr6:30692055-30710740	Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 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	chr6:30689400-30694000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:30689400-30694000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:30690000-30694000	Transcr. at gene 5' and 3'	Brain Germinal Matrix	brain
4	chr6:30690000-30709600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:30690200-30694000	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
6	chr6:30690200-30699200	Strong transcription	Sigmoid Colon	Sigmoid Colon
7	chr6:30690400-30696400	Strong transcription	Gastric	stomach
8	chr6:30690400-30709200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr6:30690600-30693600	Weak transcription	Right Atrium	heart
10	chr6:30690600-30693800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:30690600-30694000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
12	chr6:30690600-30694000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr6:30690600-30694000	Genic enhancers	Adipose Nuclei	Adipose
14	chr6:30690600-30694000	Genic enhancers	Skeletal Muscle Female	skeletal muscle
15	chr6:30690600-30694200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:30690600-30694200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr6:30690600-30694400	Genic enhancers	Primary T cells fromperipheralblood	blood
18	chr6:30690600-30694400	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr6:30690600-30694400	Genic enhancers	Fetal Muscle Leg	muscle
20	chr6:30690600-30694600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:30690600-30698000	Strong transcription	Rectal Mucosa Donor 31	rectum
22	chr6:30690600-30698200	Strong transcription	Left Ventricle	heart
23	chr6:30690600-30698400	Strong transcription	Right Ventricle	heart
24	chr6:30690600-30701200	Strong transcription	Brain Angular Gyrus	brain
25	chr6:30690600-30703800	Strong transcription	Lung	lung
26	chr6:30690800-30693800	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr6:30690800-30693800	Genic enhancers	Stomach Smooth Muscle	stomach
28	chr6:30690800-30694200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:30690800-30694200	Strong transcription	Small Intestine	intestine
30	chr6:30691000-30693600	Strong transcription	Rectal Smooth Muscle	rectum
31	chr6:30691000-30693800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr6:30691000-30693800	Genic enhancers	Fetal Lung	lung
33	chr6:30691000-30694000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr6:30691000-30694000	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr6:30691000-30694000	Strong transcription	Brain Substantia Nigra	brain
36	chr6:30691000-30694000	Genic enhancers	Fetal Brain Male	brain
37	chr6:30691000-30694000	Genic enhancers	Fetal Thymus	thymus
38	chr6:30691000-30694000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
39	chr6:30691000-30695000	Genic enhancers	Osteobl	bone
40	chr6:30691000-30697800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr6:30691000-30698000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr6:30691000-30698000	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr6:30691000-30698200	Strong transcription	Fetal Intestine Large	intestine
44	chr6:30691000-30698400	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr6:30691000-30698400	Strong transcription	Brain Anterior Caudate	brain
46	chr6:30691000-30698400	Strong transcription	Brain Hippocampus Middle	brain
47	chr6:30691000-30703800	Strong transcription	Brain Cingulate Gyrus	brain
48	chr6:30691200-30693800	Genic enhancers	K562	blood
49	chr6:30691200-30697600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:30691200-30697800	Strong transcription	Placenta	Placenta

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