Variant report

Variant	rs9469048
Chromosome Location	chr6:31737701-31737702
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:31737640-31737790	HCT-116	colon:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
2	RCOR1	chr6:31737481-31737998	K562	blood:	n/a	n/a
3	CTCF	chr6:31737533-31737945	GM12878	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
4	SP4	chr6:31737464-31737993	H1-hESC	embryonic stem cell:	n/a	n/a
5	CREB1	chr6:31737575-31737887	A549	lung:	n/a	n/a
6	CTCF	chr6:31737660-31737810	HEEpiC	esophagus:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
7	POLR2A	chr6:31737424-31737962	K562	blood:	n/a	n/a
8	CTCF	chr6:31737700-31737850	BE2_C	brain:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
9	CTCF	chr6:31737434-31737987	HCT-116	colon:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
10	CTCF	chr6:31737604-31737886	MCF-7	breast:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
11	CTCF	chr6:31737680-31737830	K562	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
12	ZC3H11A	chr6:31737411-31737980	K562	blood:	n/a	n/a
13	MAX	chr6:31737629-31737817	Hela-S3	cervix:	n/a	n/a
14	GABPA	chr6:31737367-31737968	K562	blood:	n/a	n/a
15	RAD21	chr6:31737537-31737908	A549	lung:	n/a	chr6:31737723-31737742
16	CTCF	chr6:31737640-31737790	Caco-2	colon:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
17	CTCF	chr6:31737680-31737830	GM12867	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
18	RAD21	chr6:31737493-31737958	K562	blood:	n/a	chr6:31737723-31737742
19	CTCF	chr6:31737505-31737892	H1-hESC	embryonic stem cell:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
20	SIN3AK20	chr6:31737559-31737983	K562	blood:	n/a	n/a
21	RAD21	chr6:31737528-31737935	HepG2	liver:	n/a	chr6:31737723-31737742
22	CTCF	chr6:31737382-31738130	SK-N-SH	brain:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
23	CTCF	chr6:31737680-31737830	GM12874	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
24	CTCF	chr6:31737660-31737810	GM12865	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
25	FOSL1	chr6:31737438-31737934	K562	blood:	n/a	n/a
26	ETS1	chr6:31737313-31738073	K562	blood:	n/a	n/a
27	CTCF	chr6:31737618-31737874	Lung_OC	lung:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
28	CTCF	chr6:31737570-31737906	MCF-7	breast:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
29	CTCF	chr6:31737660-31737810	AG09309	skin:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
30	CTCF	chr6:31737640-31737790	GM12868	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
31	CTCF	chr6:31737660-31737810	AG10803	skin:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
32	MTA3	chr6:31737468-31737973	GM12878	blood:	n/a	n/a
33	CTCF	chr6:31737620-31737770	GM12873	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
34	CBX3	chr6:31736681-31738860	K562	blood:	n/a	n/a
35	CTCF	chr6:31737660-31737810	HMEC	breast:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
36	CTCF	chr6:31737492-31737853	A549	lung:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
37	CTCF	chr6:31737660-31737810	NHEK	skin:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
38	CTCF	chr6:31737660-31737810	GM12870	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
39	EP300	chr6:31737536-31737955	K562	blood:	n/a	n/a
40	E2F6	chr6:31737604-31737815	K562	blood:	n/a	n/a
41	RAD21	chr6:31737496-31738048	A549	lung:	n/a	chr6:31737723-31737742
42	BHLHE40	chr6:31737634-31737840	GM12878	blood:	n/a	n/a
43	CTCF	chr6:31737660-31737810	HA-sp	spinal cord:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
44	CTCF	chr6:31737548-31737891	HepG2	liver:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
45	CTCF	chr6:31737602-31737884	ProgFib	skin:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
46	CTCF	chr6:31737573-31737897	MCF-7	breast:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
47	CTCF	chr6:31737660-31737810	NB4	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
48	CTCF	chr6:31737660-31737810	GM12871	blood:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
49	CTCF	chr6:31737680-31737830	BJ	skin:	n/a	chr6:31737720-31737741 chr6:31737731-31737740 chr6:31737726-31737742 chr6:31737727-31737740 chr6:31737725-31737743 chr6:31737728-31737738
50	JUN	chr6:31737273-31738087	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31700939..31701625-chr6:31737341..31738128,3	K562	blood:
2	chr6:31737659..31738210-chr6:31830118..31830993,2	K562	blood:
3	chr6:31736974..31739294-chr6:31782125..31784587,2	MCF-7	breast:
4	chr6:31647872..31649252-chr6:31737299..31738191,5	MCF-7	breast:
5	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
6	chr6:31648308..31649358-chr6:31737283..31737803,3	MCF-7	breast:
7	chr6:31730833..31734412-chr6:31734807..31737911,5	MCF-7	breast:
8	chr6:31650429..31651074-chr6:31737455..31738004,2	K562	blood:
9	chr6:31679788..31680730-chr6:31737330..31738173,2	MCF-7	breast:
10	chr6:31737648..31740756-chr6:31757248..31760700,3	MCF-7	breast:
11	chr6:31737530..31738235-chr6:31831315..31832267,3	K562	blood:
12	chr6:31736705..31739143-chr6:31864030..31867249,3	K562	blood:
13	chr6:31728460..31729420-chr6:31737290..31738225,3	MCF-7	breast:
14	chr6:31696738..31697585-chr6:31737248..31738174,4	MCF-7	breast:
15	chr6:31737477..31739729-chr6:31793263..31795025,2	MCF-7	breast:
16	chr6:31717928..31719785-chr6:31735295..31738183,2	MCF-7	breast:
17	chr6:31696826..31698523-chr6:31737263..31738269,10	K562	blood:
18	chr6:31736266..31738927-chr6:31762294..31764324,2	MCF-7	breast:
19	chr6:31722088..31725241-chr6:31736236..31738283,4	MCF-7	breast:
20	chr6:31664975..31665752-chr6:31737286..31737856,2	K562	blood:
21	chr6:31647329..31649450-chr6:31737352..31738874,2	MCF-7	breast:
22	chr6:31737503..31739335-chr6:31742183..31744187,2	MCF-7	breast:
23	chr6:31735011..31745595-chr6:31798203..31806127,22	MCF-7	breast:
24	chr6:31647116..31649167-chr6:31737022..31738467,12	K562	blood:
25	chr6:31697098..31697762-chr6:31737428..31738101,2	MCF-7	breast:

Variant related genes	Relation type
SAPCD1-AS1	TF binding region
VWA7	TF binding region
ENSG00000204371	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000235663	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000252743	Chromatin interaction
ENSG00000228727	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000201754	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10947225	1.00[AFR][1000 genomes]
rs17201459	1.00[AMR][1000 genomes]
rs28445017	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56194675	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58368425	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59402363	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73728948	1.00[AMR][1000 genomes]
rs73728988	1.00[AFR][1000 genomes]
rs73728991	1.00[AFR][1000 genomes]
rs73729004	1.00[AMR][1000 genomes]
rs73729005	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9282875	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9332712	1.00[AFR][1000 genomes]
rs9461723	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9461730	1.00[AFR][1000 genomes]
rs9469030	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469035	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469037	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469078	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9501148	1.00[AMR][1000 genomes]
rs9501150	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9501151	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9501153	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription 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 miRNA target site	206 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	esv2763547	chr6:31715882-31738478	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
15	nsv884426	chr6:31728102-31800868	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
16	nsv884427	chr6:31728102-31802465	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers 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 target site	152 gene(s)	inside rSNPs	diseases
17	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
18	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
19	nsv884430	chr6:31731881-31800631	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
20	nsv884431	chr6:31732679-31761386	Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
21	nsv601943	chr6:31733544-31763862	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	55 gene(s)	inside rSNPs	diseases
22	nsv884432	chr6:31734117-31777687	Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
23	nsv884433	chr6:31737701-31777687	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers 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	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31709000-31738200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr6:31716600-31744000	Weak transcription	GM12878-XiMat	blood
3	chr6:31725800-31737800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr6:31727600-31738400	Weak transcription	Primary T cells from cord blood	blood
5	chr6:31729200-31742800	Weak transcription	A549	lung
6	chr6:31731400-31744400	Weak transcription	Left Ventricle	heart
7	chr6:31731600-31743400	Weak transcription	Lung	lung
8	chr6:31731800-31743600	Weak transcription	Right Ventricle	heart
9	chr6:31731800-31749600	Weak transcription	HUVEC	blood vessel
10	chr6:31732000-31739000	Weak transcription	NHEK	skin
11	chr6:31732000-31740000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:31732200-31740000	Weak transcription	Dnd41	blood
13	chr6:31732400-31737800	Weak transcription	Hela-S3	cervix
14	chr6:31732600-31745000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:31732800-31744400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:31734400-31742800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:31734400-31743400	Weak transcription	Right Atrium	heart
18	chr6:31734600-31737800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:31734600-31737800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr6:31734600-31739800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:31734600-31740800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr6:31734600-31740800	Weak transcription	Stomach Mucosa	stomach
23	chr6:31734600-31743600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr6:31734600-31744200	Weak transcription	Brain Anterior Caudate	brain
25	chr6:31734600-31744200	Weak transcription	NH-A	brain
26	chr6:31734600-31744600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr6:31734600-31744600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr6:31734600-31745200	Weak transcription	Brain Germinal Matrix	brain
29	chr6:31734600-31745400	Weak transcription	Fetal Brain Female	brain
30	chr6:31734600-31746600	Weak transcription	Brain Angular Gyrus	brain
31	chr6:31734800-31740800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr6:31734800-31745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr6:31735200-31738000	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr6:31735200-31740800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr6:31735400-31742800	Weak transcription	Fetal Intestine Large	intestine
36	chr6:31735600-31737800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:31735600-31740800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:31735800-31738000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr6:31736200-31738000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:31736200-31739600	Enhancers	Placenta	Placenta
41	chr6:31736600-31737800	Genic enhancers	Fetal Intestine Small	intestine
42	chr6:31736600-31738000	Enhancers	Spleen	Spleen
43	chr6:31736800-31738000	Enhancers	Primary B cells from cord blood	blood
44	chr6:31736800-31738000	Enhancers	Gastric	stomach
45	chr6:31736800-31741600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:31737000-31738200	Enhancers	HepG2	liver
47	chr6:31737200-31741600	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr6:31737200-31744200	Weak transcription	Fetal Stomach	stomach
49	chr6:31737400-31738000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:31737400-31738000	Enhancers	Adipose Nuclei	Adipose

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