Variant report

Variant	rs11602181
Chromosome Location	chr11:63896591-63896592
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:63896507-63897570	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63896557-63896607	SK-N-MC	brain:	n/a
2	chr11:63896557-63896607	RPTEC	kidney:	n/a
3	chr11:63896557-63896607	IMR90	lung:	fetal
4	chr11:63896557-63896607	Hepatocyte	liver:	n/a
5	chr11:63896557-63896607	HCT-116	colon:	n/a
6	chr11:63896557-63896607	HIPEpiC	eye:	n/a
7	chr11:63896557-63896607	Hela-S3	cervix:	n/a
8	chr11:63896557-63896607	ECC-1	luminal epithelium:	n/a
9	chr11:63896557-63896607	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:63896557-63896607	Caco-2	colon:	n/a
11	chr11:63896557-63896607	AG09319	gingival:	n/a
12	chr11:63896557-63896607	GM19239	blood:	n/a
13	chr11:63896557-63896607	H1-hESC	embryonic stem cell:	embryo
14	chr11:63896557-63896607	LNCaP	prostate:	n/a
15	chr11:63896557-63896607	K562	blood:	n/a
16	chr11:63896557-63896607	SK-N-SH	brain:	n/a
17	chr11:63896557-63896607	AG04449	skin:	fetal
18	chr11:63896557-63896607	AG09309	skin:	n/a
19	chr11:63896557-63896607	HAEpiC	amniotic membrane:	n/a
20	chr11:63896557-63896607	SK-N-SH_RA	brain:	n/a
21	chr11:63896557-63896607	HCM	heart:	n/a
22	chr11:63896557-63896607	HepG2	liver:	n/a
23	chr11:63896557-63896607	NH-A	brain:	n/a
24	chr11:63896557-63896607	HUVEC	blood vessel:	n/a
25	chr11:63896557-63896607	ovcar-3	ovarian:	n/a
26	chr11:63896557-63896607	MCF10A-Er-Src	breast:	n/a
27	chr11:63896557-63896607	BJ	skin:	n/a
28	chr11:63896557-63896607	Jurkat	blood:	n/a
29	chr11:63896557-63896607	NHDF-neo	bronchial:	n/a
30	chr11:63896557-63896607	AG04450	lung:	fetal
31	chr11:63896557-63896607	HRE	kidney:	n/a
32	chr11:63896557-63896607	NHBE	bronchial:	n/a
33	chr11:63896557-63896607	GM12891	blood:	n/a
34	chr11:63896557-63896607	A549	lung:	n/a
35	chr11:63896557-63896607	HL-60	blood:	n/a
36	chr11:63896557-63896607	PFSK-1	brain:	n/a
37	chr11:63896557-63896607	HNPCEpiC	eye:	n/a
38	chr11:63896557-63896607	GM12892	blood:	n/a
39	chr11:63896557-63896607	NT2-D1	testis:	n/a
40	chr11:63896557-63896607	ProgFib	skin:	n/a
41	chr11:63896557-63896607	SAEC	small airway:	n/a
42	chr11:63896557-63896607	HEK293	kidney:	embryo
43	chr11:63896557-63896607	PANC-1	pancreas:	n/a
44	chr11:63896557-63896607	PrEC	prostate:	n/a
45	chr11:63896557-63896607	HRCEpiC	kidney:	n/a
46	chr11:63896557-63896607	U87	brain:	n/a
47	chr11:63896557-63896607	MCF-7	breast:	n/a
48	chr11:63896557-63896607	HEEpiC	esophagus:	n/a
49	chr11:63896557-63896607	HRPEpiC	eye:	n/a
50	chr11:63896557-63896607	T-47D	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63894757..63897753-chr11:63898307..63901137,2	K562	blood:
2	chr11:63743504..63745731-chr11:63895376..63898316,2	K562	blood:
3	chr11:63894649..63896789-chr11:63898167..63901854,5	MCF-7	breast:
4	chr11:63896273..63898593-chr11:63900938..63902757,2	K562	blood:
5	chr11:63891937..63894081-chr11:63896157..63898107,2	K562	blood:
6	chr11:63788062..63790678-chr11:63896459..63899438,2	K562	blood:
7	chr11:63896044..63898939-chr11:63908774..63911161,2	MCF-7	breast:
8	chr11:63888929..63891222-chr11:63896109..63898759,2	MCF-7	breast:

No data

Variant related genes	Relation type
MACROD1	TF binding region
MACROD1	CpG island

Extended variants
information (count: 70 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1058735	0.86[CEU][hapmap];0.87[CHB][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes]
rs1059440	1.00[ASW][hapmap];0.93[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11231701	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11601024	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11601577	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11603042	0.81[CHB][hapmap]
rs11603212	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.88[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11605738	1.00[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.83[YRI][hapmap]
rs11606544	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11607007	0.86[CEU][hapmap];0.87[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes]
rs11607144	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11607165	1.00[ASW][hapmap];0.93[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12418035	0.84[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12574258	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12575642	1.00[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.90[CHD][hapmap];0.88[JPT][hapmap];0.83[LWK][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12787852	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12794145	1.00[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.86[MEX][hapmap];0.83[MKK][hapmap];0.96[TSI][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes]
rs12797120	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12798333	0.87[CHD][hapmap];0.92[GIH][hapmap];0.83[LWK][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes]
rs12802950	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2001003	1.00[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap]
rs2015226	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2070765	1.00[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.90[MEX][hapmap];0.83[MKK][hapmap];0.96[TSI][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes]
rs2154986	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2282490	1.00[ASW][hapmap];0.93[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2286614	1.00[ASW][hapmap]
rs2875749	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34089806	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34113693	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34838337	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35090903	0.86[EUR][1000 genomes]
rs35095324	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35458188	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35524387	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35858916	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3802933	0.93[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3824854	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58632573	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs614035	0.85[YRI][hapmap]
rs643243	0.85[YRI][hapmap]
rs6591837	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs663889	0.85[YRI][hapmap]
rs66648159	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67546972	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs693984	0.85[YRI][hapmap]
rs7102327	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7112277	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7130030	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71479474	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72918475	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72920332	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7939784	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7944061	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7952318	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs882146	1.00[ASW][hapmap];0.93[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
3	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
4	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
5	nsv832184	chr11:63787702-63925084	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
7	nsv897658	chr11:63810944-63897759	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv897659	chr11:63813470-63907079	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv832185	chr11:63819946-63963532	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
10	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
11	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
12	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
13	nsv356	chr11:63868847-63913129	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
15	esv1801661	chr11:63894054-63937949	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS 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	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs11602181	PPP1R14B	Cis_1M	lymphoblastoid	RTeQTL
rs11602181	FKBP2	cis	parietal	SCAN
rs11602181	FAM89B	cis	parietal	SCAN
rs11602181	GPHA2	cis	cerebellum	SCAN
rs11602181	TRPT1	cis	Muscle Skeletal	GTEx
rs11602181	PRDX5	cis	parietal	SCAN
rs11602181	PPP1R14B	cis	multi-tissue	Pritchard
rs11602181	PPP1R14B	cis	lymphoblastoid	seeQTL
rs11602181	ASRGL1	cis	parietal	SCAN
rs11602181	PPP1R14B	cis	Heart Left Ventricle	GTEx
rs11602181	FAU	cis	parietal	SCAN
rs11602181	SLC22A10	cis	parietal	SCAN
rs11602181	CD248	cis	parietal	SCAN

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63885000-63896600	Weak transcription	Hela-S3	cervix
2	chr11:63885400-63898600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:63885600-63911200	Weak transcription	Gastric	stomach
4	chr11:63886800-63908600	Weak transcription	Ovary	ovary
5	chr11:63890000-63899000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr11:63890200-63898000	Weak transcription	Lung	lung
7	chr11:63890200-63899200	Weak transcription	Fetal Lung	lung
8	chr11:63890600-63899200	Weak transcription	Left Ventricle	heart
9	chr11:63890600-63899400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:63890600-63913600	Weak transcription	Esophagus	oesophagus
11	chr11:63890800-63899200	Weak transcription	Brain Angular Gyrus	brain
12	chr11:63890800-63899200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr11:63890800-63899400	Weak transcription	Right Atrium	heart
14	chr11:63891000-63898400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr11:63891000-63899400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:63891200-63897400	Weak transcription	Fetal Brain Male	brain
17	chr11:63891200-63897400	Weak transcription	Stomach Smooth Muscle	stomach
18	chr11:63891200-63898800	Weak transcription	Fetal Brain Female	brain
19	chr11:63891400-63896800	Weak transcription	Liver	Liver
20	chr11:63891600-63896600	Weak transcription	Brain Anterior Caudate	brain
21	chr11:63892000-63915800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr11:63892200-63900400	Enhancers	Pancreas	Pancrea
23	chr11:63892400-63904400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr11:63893000-63899400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr11:63893200-63900400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr11:63893600-63896600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr11:63893600-63897400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr11:63893800-63898200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:63894000-63898200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:63894000-63898400	Weak transcription	Primary hematopoietic stem cells	blood
31	chr11:63894000-63898400	Weak transcription	Fetal Thymus	thymus
32	chr11:63894000-63899000	Weak transcription	Primary T cells from cord blood	blood
33	chr11:63894400-63896600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr11:63894400-63898200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:63894400-63900400	Enhancers	Fetal Intestine Large	intestine
36	chr11:63894600-63899200	Weak transcription	Brain Hippocampus Middle	brain
37	chr11:63894800-63898200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:63894800-63898600	Weak transcription	Brain Substantia Nigra	brain
39	chr11:63894800-63899200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:63895600-63896800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:63895600-63896800	Enhancers	Right Ventricle	heart
42	chr11:63895600-63899600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr11:63895800-63896600	Enhancers	Adipose Nuclei	Adipose
44	chr11:63895800-63899200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr11:63895800-63920000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr11:63896000-63897800	Weak transcription	Fetal Muscle Leg	muscle
47	chr11:63896000-63898000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr11:63896000-63898000	Weak transcription	Brain Germinal Matrix	brain
49	chr11:63896000-63899000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr11:63896000-63899200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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