Variant report

Variant	rs11928558
Chromosome Location	chr3:47044122-47044123
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	RAD21	chr3:47043998-47044543	H1-hESC	embryonic stem cell:	n/a	chr3:47044427-47044436 chr3:47044346-47044359
2	GABPA	chr3:47044035-47044411	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr3:47044067-47044415	K562	blood:	n/a	n/a
4	SIN3A	chr3:47044065-47044398	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr3:47043403-47044758	GM12892	blood:	n/a	n/a
6	CTCF	chr3:47044120-47044270	K562	blood:	n/a	n/a
7	TEAD4	chr3:47044081-47044443	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr3:47044100-47044250	SAEC	small airway:	n/a	n/a
9	CTCF	chr3:47044121-47044394	K562	blood:	n/a	chr3:47044347-47044360
10	CTCF	chr3:47044085-47044385	H1-hESC	embryonic stem cell:	n/a	chr3:47044347-47044360
11	CTCF	chr3:47044120-47044270	NHEK	skin:	n/a	n/a
12	ZNF143	chr3:47044070-47044402	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr3:47044052-47044346	K562	blood:	n/a	n/a
14	POLR2A	chr3:47043689-47044312	GM12878	blood:	n/a	n/a
15	POLR2A	chr3:47043990-47044560	K562	blood:	n/a	n/a
16	CTCF	chr3:47044120-47044270	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr3:47044021-47044443	H1-hESC	embryonic stem cell:	n/a	chr3:47044347-47044360
18	CTCF	chr3:47044080-47044230	HCT-116	colon:	n/a	n/a
19	CTCF	chr3:47044060-47044210	GM12872	blood:	n/a	n/a
20	CTCF	chr3:47044120-47044270	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr3:47044080-47044230	HPF	lung:	n/a	n/a
22	CTCF	chr3:47044100-47044250	GM12870	blood:	n/a	n/a
23	CTCF	chr3:47044120-47044270	HBMEC	blood vessel:	n/a	n/a
24	MAZ	chr3:47044121-47044328	K562	blood:	n/a	n/a
25	CTCF	chr3:47044080-47044230	GM12875	blood:	n/a	n/a
26	POLR2A	chr3:47043864-47044678	K562	blood:	n/a	n/a
27	CTCF	chr3:47044010-47044387	K562	blood:	n/a	chr3:47044016-47044025 chr3:47044347-47044360
28	POLR2A	chr3:47043758-47044183	GM12892	blood:	n/a	n/a
29	ATF2	chr3:47044002-47044388	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr3:47044100-47044250	GM12874	blood:	n/a	n/a
31	CTCF	chr3:47044100-47044250	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr3:47044120-47044270	HA-sp	spinal cord:	n/a	n/a
33	POLR2A	chr3:47043824-47044814	GM12892	blood:	n/a	n/a
34	POLR2A	chr3:47044064-47044672	K562	blood:	n/a	n/a
35	CTCF	chr3:47044080-47044230	GM12872	blood:	n/a	n/a
36	MAX	chr3:47044057-47044476	H1-hESC	embryonic stem cell:	n/a	n/a
37	RAD21	chr3:47044060-47044463	ECC-1	luminal epithelium:	n/a	chr3:47044427-47044436 chr3:47044346-47044359
38	CCNT2	chr3:47044103-47044324	K562	blood:	n/a	chr3:47044124-47044133
39	CTCF	chr3:47044080-47044230	GM12869	blood:	n/a	n/a
40	RAD21	chr3:47043991-47044395	H1-hESC	embryonic stem cell:	n/a	chr3:47044346-47044359
41	RAD21	chr3:47044036-47044458	H1-hESC	embryonic stem cell:	n/a	chr3:47044427-47044436 chr3:47044346-47044359
42	CTCF	chr3:47044084-47044305	GM12878	blood:	n/a	n/a
43	CTCF	chr3:47044028-47044463	H1-hESC	embryonic stem cell:	n/a	chr3:47044347-47044360

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:47030302..47032309-chr3:47043809..47045425,2	MCF-7	breast:
2	chr3:47042301..47045391-chr3:47048299..47050590,3	MCF-7	breast:

Variant related genes	Relation type
NBEAL2	TF binding region
ENSG00000160796	Chromatin interaction

Extended variants
information (count: 164 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:155)

rs_ID	r²[population]
rs1024036	1.00[EUR][1000 genomes]
rs10461017	0.95[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10461019	1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10865945	1.00[EUR][1000 genomes]
rs11130108	0.82[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11130109	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11706212	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11708257	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11709693	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11709876	0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11713537	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11922925	1.00[EUR][1000 genomes]
rs12330516	1.00[EUR][1000 genomes]
rs12487763	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12488371	1.00[EUR][1000 genomes]
rs12631730	0.95[YRI][hapmap]
rs13062185	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13078181	1.00[EUR][1000 genomes]
rs13079416	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13082531	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13323092	0.95[YRI][hapmap];1.00[EUR][1000 genomes]
rs1378818	0.95[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1463394	0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1466272	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1466273	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1466274	0.89[AMR][1000 genomes]
rs1473382	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1473384	1.00[EUR][1000 genomes]
rs1473385	1.00[EUR][1000 genomes]
rs1563431	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1563432	1.00[EUR][1000 genomes]
rs1814564	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1869870	0.90[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1874264	1.00[EUR][1000 genomes]
rs1979736	1.00[EUR][1000 genomes]
rs2124509	0.95[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2124510	1.00[AMR][1000 genomes]
rs2350642	1.00[EUR][1000 genomes]
rs2385863	1.00[EUR][1000 genomes]
rs2385868	0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2385869	0.95[YRI][hapmap];1.00[AMR][1000 genomes]
rs28735306	1.00[EUR][1000 genomes]
rs2891887	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2891893	0.87[YRI][hapmap];0.89[AMR][1000 genomes]
rs34147581	1.00[EUR][1000 genomes]
rs35366910	1.00[EUR][1000 genomes]
rs4018904	0.95[YRI][hapmap];1.00[EUR][1000 genomes]
rs4282092	1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4289375	0.82[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4324490	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4373094	0.95[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4378998	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4389512	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4450857	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4478107	0.95[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4522803	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4525902	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4543047	0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682828	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682832	0.86[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682833	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682834	1.00[EUR][1000 genomes]
rs4682835	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682836	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682838	0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682840	0.89[AMR][1000 genomes]
rs4682841	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682843	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682846	1.00[EUR][1000 genomes]
rs4682847	1.00[EUR][1000 genomes]
rs4683277	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683279	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683282	0.90[YRI][hapmap]
rs4683283	0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683284	1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683285	0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683286	0.82[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683288	1.00[EUR][1000 genomes]
rs4683289	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683290	0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683291	0.85[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683292	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683293	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683303	1.00[EUR][1000 genomes]
rs6442041	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442042	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442043	0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442044	0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442047	0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442048	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442062	1.00[EUR][1000 genomes]
rs6442063	1.00[EUR][1000 genomes]
rs6766676	0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6767868	1.00[EUR][1000 genomes]
rs6768169	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6772449	1.00[EUR][1000 genomes]
rs6775797	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6778673	1.00[EUR][1000 genomes]
rs6778687	1.00[EUR][1000 genomes]
rs6780994	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6785462	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6787210	1.00[EUR][1000 genomes]
rs6804732	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6806521	0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6808052	1.00[EUR][1000 genomes]
rs6808117	1.00[EUR][1000 genomes]
rs6808629	1.00[EUR][1000 genomes]
rs6809904	0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73831482	1.00[EUR][1000 genomes]
rs7615774	1.00[EUR][1000 genomes]
rs7621530	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7624549	0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7625011	0.86[YRI][hapmap];0.89[AMR][1000 genomes]
rs7630154	0.95[YRI][hapmap];1.00[EUR][1000 genomes]
rs7630904	0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7638549	1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7639121	1.00[EUR][1000 genomes]
rs7643150	1.00[EUR][1000 genomes]
rs7643868	0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7644382	0.95[YRI][hapmap];1.00[EUR][1000 genomes]
rs7646076	0.87[YRI][hapmap];1.00[EUR][1000 genomes]
rs7649413	1.00[EUR][1000 genomes]
rs7649941	0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7650142	0.82[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7652492	1.00[EUR][1000 genomes]
rs924009	1.00[EUR][1000 genomes]
rs936173	1.00[EUR][1000 genomes]
rs936177	0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936178	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936179	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936180	0.83[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936181	0.86[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936182	0.85[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936185	1.00[EUR][1000 genomes]
rs936186	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9810881	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9812407	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9819344	1.00[EUR][1000 genomes]
rs9819475	1.00[EUR][1000 genomes]
rs9823480	1.00[EUR][1000 genomes]
rs9826488	1.00[EUR][1000 genomes]
rs9827293	1.00[EUR][1000 genomes]
rs9828473	0.85[YRI][hapmap];1.00[EUR][1000 genomes]
rs9833500	1.00[EUR][1000 genomes]
rs9836801	1.00[EUR][1000 genomes]
rs9850151	1.00[EUR][1000 genomes]
rs9852167	1.00[EUR][1000 genomes]
rs9861247	1.00[EUR][1000 genomes]
rs9861265	1.00[EUR][1000 genomes]
rs9862711	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9869489	1.00[EUR][1000 genomes]
rs9878813	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9883152	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9883909	1.00[EUR][1000 genomes]
rs9990284	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876755	chr3:46895109-47061183	Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	esv3461834	chr3:46977730-47173228	Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	esv3461835	chr3:46977822-47173168	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	esv3461836	chr3:46977822-47173168	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1009396	chr3:46994991-47048166	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv876756	chr3:47002931-47586514	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
7	esv1800172	chr3:47013346-47049306	Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv590209	chr3:47018214-47050784	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
9	nsv876757	chr3:47018214-47058057	Active TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	21 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	chr3:47022600-47049000	Weak transcription	Hela-S3	cervix
2	chr3:47022600-47050600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:47029800-47050600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr3:47030200-47044600	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:47030800-47045600	Weak transcription	Aorta	Aorta
6	chr3:47031000-47049600	Strong transcription	Gastric	stomach
7	chr3:47031000-47050200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr3:47031000-47053000	Strong transcription	Dnd41	blood
9	chr3:47032200-47050000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr3:47033800-47049200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr3:47034200-47049800	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr3:47035400-47049000	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr3:47036800-47044200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:47038000-47050000	Strong transcription	Thymus	Thymus
15	chr3:47038600-47044400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr3:47038600-47044600	Strong transcription	K562	blood
17	chr3:47038600-47050000	Strong transcription	Fetal Stomach	stomach
18	chr3:47038600-47050400	Weak transcription	Fetal Lung	lung
19	chr3:47039000-47050000	Strong transcription	Adipose Nuclei	Adipose
20	chr3:47039800-47050200	Strong transcription	Colonic Mucosa	Colon
21	chr3:47039800-47058000	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr3:47040000-47049400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr3:47040000-47050400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:47040200-47046000	Strong transcription	Primary T killer memory cells from peripheral blood	blood
25	chr3:47040200-47049000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
26	chr3:47040200-47049000	Strong transcription	Stomach Smooth Muscle	stomach
27	chr3:47040200-47049800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr3:47040200-47049800	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr3:47040400-47046400	Strong transcription	Ovary	ovary
30	chr3:47040400-47048800	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr3:47040400-47049200	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr3:47040400-47049600	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr3:47040400-47050000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:47040400-47050000	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr3:47040400-47050000	Strong transcription	Spleen	Spleen
36	chr3:47040400-47050400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr3:47040400-47050400	Strong transcription	Duodenum Mucosa	Duodenum
38	chr3:47040400-47050400	Weak transcription	Right Atrium	heart
39	chr3:47040600-47048000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr3:47040600-47048200	Strong transcription	Primary B cells from peripheral blood	blood
41	chr3:47040600-47048400	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr3:47040600-47049600	Strong transcription	Right Ventricle	heart
43	chr3:47040600-47049800	Strong transcription	Primary T cells from cord blood	blood
44	chr3:47040600-47049800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr3:47040600-47050000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:47040600-47050200	Strong transcription	Stomach Mucosa	stomach
47	chr3:47040600-47050400	Weak transcription	Fetal Kidney	kidney
48	chr3:47040600-47051000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr3:47040600-47051400	Weak transcription	Fetal Heart	heart
50	chr3:47040800-47045000	Strong transcription	Primary T helper naive cells from peripheral blood	blood

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