Variant report

Variant	nsv556281
Chromosome Location	chr11:107197869-107240802
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:65)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:65 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:107240708-107240809	K562	blood:	n/a	n/a
2	CEBPB	chr11:107199128-107199405	IMR90	lung:	n/a	n/a
3	CTCF	chr11:107215290-107215315	GM13976	blood:	n/a	n/a
4	CTCF	chr11:107207073-107207127	Fibrobl	skin:	n/a	n/a
5	CTCF	chr11:107215321-107215330	GM13976	blood:	n/a	n/a
6	CTCF	chr11:107233572-107233629	Kidney_OC	kidney:	n/a	n/a
7	CUX1	chr11:107218932-107218950	GM12878	blood:	n/a	n/a
8	E2F4	chr11:107208494-107208574	MCF10A-Er-Src	breast:	n/a	n/a
9	EBF1	chr11:107205272-107205398	GM12878	blood:	n/a	n/a
10	FOS	chr11:107222374-107222525	MCF10A-Er-Src	breast:	n/a	n/a
11	FOXA1	chr11:107240572-107241011	HepG2	liver:	n/a	n/a
12	FOXA1	chr11:107211694-107212003	HepG2	liver:	n/a	n/a
13	FOXA1	chr11:107240552-107240908	HepG2	liver:	n/a	n/a
14	FOXA2	chr11:107240625-107240831	HepG2	liver:	n/a	n/a
15	FOXA2	chr11:107211680-107211918	HepG2	liver:	n/a	n/a
16	FOXA2	chr11:107232651-107233340	A549	lung:	n/a	n/a
17	GATA3	chr11:107231469-107231532	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr11:107228678-107228906	SH-SY5Y	brain:	n/a	n/a
19	JUN	chr11:107224358-107224368	H1-hESC	embryonic stem cell:	n/a	n/a
20	JUND	chr11:107199997-107200207	HepG2	liver:	n/a	chr11:107200086-107200093 chr11:107200084-107200094 chr11:107200085-107200093 chr11:107200083-107200094
21	JUND	chr11:107222361-107222588	K562	blood:	n/a	n/a
22	MAFK	chr11:107202374-107202438	HepG2	liver:	n/a	n/a
23	MYC	chr11:107202623-107202630	NB4	blood:	n/a	n/a
24	NFYB	chr11:107229613-107229700	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:107232159-107232356	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr11:107231607-107231731	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr11:107228421-107228478	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr11:107232533-107233078	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:107219760-107219777	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr11:107232820-107232834	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr11:107198597-107198822	K562	blood:	n/a	n/a
32	POLR2A	chr11:107203130-107203131	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr11:107214090-107214170	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr11:107203562-107203677	K562	blood:	n/a	n/a
35	POLR2A	chr11:107232831-107233008	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:107232783-107233017	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr11:107232837-107233153	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr11:107217638-107217664	GM12878	blood:	n/a	n/a
39	REST	chr11:107208863-107208950	GM12878	blood:	n/a	n/a
40	REST	chr11:107208851-107209090	GM12878	blood:	n/a	n/a
41	REST	chr11:107208844-107209075	H1-hESC	embryonic stem cell:	n/a	n/a
42	REST	chr11:107208808-107209051	H1-hESC	embryonic stem cell:	n/a	n/a
43	REST	chr11:107208808-107209121	HCT-116	colon:	n/a	n/a
44	REST	chr11:107208728-107209183	ECC-1	luminal epithelium:	n/a	n/a
45	REST	chr11:107208745-107209155	ECC-1	luminal epithelium:	n/a	n/a
46	REST	chr11:107208826-107209016	SK-N-SH	brain:	n/a	n/a
47	RFX5	chr11:107213031-107213042	K562	blood:	n/a	n/a
48	RFX5	chr11:107201866-107201969	K562	blood:	n/a	n/a
49	SPI1	chr11:107202464-107202775	GM12891	blood:	n/a	chr11:107202657-107202670 chr11:107202658-107202671
50	SPI1	chr11:107202481-107202797	GM12891	blood:	n/a	chr11:107202657-107202670 chr11:107202658-107202671

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107232729-107232779	NH-A	brain:	n/a
2	chr11:107232729-107232779	PANC-1	pancreas:	n/a
3	chr11:107232729-107232779	HL-60	blood:	n/a
4	chr11:107232729-107232779	HMEC	breast:	n/a
5	chr11:107232729-107232779	ovcar-3	ovarian:	n/a
6	chr11:107232729-107232779	ECC-1	luminal epithelium:	n/a
7	chr11:107232729-107232779	AG10803	skin:	n/a
8	chr11:107232729-107232779	MCF10A-Er-Src	breast:	n/a
9	chr11:107232729-107232779	NHDF-neo	bronchial:	n/a
10	chr11:107232729-107232779	HRE	kidney:	n/a
11	chr11:107232729-107232779	NT2-D1	testis:	n/a
12	chr11:107232729-107232779	AG09319	gingival:	n/a
13	chr11:107232729-107232779	LNCaP	prostate:	n/a
14	chr11:107232729-107232779	HepG2	liver:	n/a
15	chr11:107232729-107232779	NHBE	bronchial:	n/a
16	chr11:107232729-107232779	SK-N-SH_RA	brain:	n/a
17	chr11:107232729-107232779	HCF	heart:	n/a
18	chr11:107232729-107232779	CMK	blood:	n/a
19	chr11:107232729-107232779	AoSMC	blood vessel:	n/a
20	chr11:107232729-107232779	K562	blood:	n/a
21	chr11:107232729-107232779	SK-N-MC	brain:	n/a
22	chr11:107232729-107232779	GM19239	blood:	n/a
23	chr11:107232729-107232779	HUVEC	blood vessel:	n/a
24	chr11:107232729-107232779	PrEC	prostate:	n/a
25	chr11:107232729-107232779	BJ	skin:	n/a
26	chr11:107232729-107232779	Hepatocyte	liver:	n/a
27	chr11:107232729-107232779	ProgFib	skin:	n/a
28	chr11:107232729-107232779	A549	lung:	n/a
29	chr11:107232729-107232779	HEK293	kidney:	embryo
30	chr11:107232729-107232779	U87	brain:	n/a
31	chr11:107232729-107232779	AG09309	skin:	n/a
32	chr11:107232729-107232779	SAEC	small airway:	n/a
33	chr11:107232729-107232779	HEEpiC	esophagus:	n/a
34	chr11:107232729-107232779	SK-N-SH	brain:	n/a
35	chr11:107232729-107232779	NB4	blood:	n/a
36	chr11:107232729-107232779	H1-hESC	embryonic stem cell:	embryo
37	chr11:107232729-107232779	AG04449	skin:	fetal
38	chr11:107232729-107232779	RPTEC	kidney:	n/a
39	chr11:107232729-107232779	HRCEpiC	kidney:	n/a
40	chr11:107232729-107232779	IMR90	lung:	fetal
41	chr11:107232729-107232779	BE2_C	brain:	n/a
42	chr11:107232729-107232779	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:107232729-107232779	GM12891	blood:	n/a
44	chr11:107232729-107232779	GM12878	blood:	n/a
45	chr11:107232729-107232779	HAEpiC	amniotic membrane:	n/a
46	chr11:107232729-107232779	AG04450	lung:	fetal
47	chr11:107232729-107232779	Caco-2	colon:	n/a
48	chr11:107232729-107232779	GM06990	blood:	n/a
49	chr11:107232729-107232779	HCT-116	colon:	n/a
50	chr11:107232729-107232779	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:107215828..107218529-chr11:107218963..107221832,3	K562	blood:
2	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:
3	chr11:107213050..107215630-chr11:107219007..107221031,2	K562	blood:
4	chr11:107216471..107218529-chr11:107219942..107221612,2	K562	blood:
5	chr11:107240491..107241393-chr16:2244600..2245300,2	MCF-7	breast:
6	chr11:107215828..107218529-chr11:107218963..107221832,3	K562	blood:
7	chr11:107216471..107218529-chr11:107219942..107221612,2	K562	blood:
8	chr11:107213050..107215630-chr11:107219007..107221031,2	K562	blood:

No data

Variant related genes	Relation type
CWF19L2	TF binding region
CWF19L2	CpG island

Extended variants
information (count: 1638 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12363600	chr11:107197869-107197870	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574498428	chr11:107197873-107197874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374808010	chr11:107197941-107197942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551969553	chr11:107197960-107197961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535631296	chr11:107198003-107198004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12278038	chr11:107198033-107198034	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575477302	chr11:107198100-107198101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545839751	chr11:107198104-107198105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564037631	chr11:107198105-107198106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572984245	chr11:107198163-107198164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185329604	chr11:107198168-107198169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571228869	chr11:107198192-107198193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373244094	chr11:107198255-107198256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529502733	chr11:107198350-107198351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs665203	chr11:107198386-107198387	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs563066872	chr11:107198431-107198432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138027713	chr11:107198524-107198525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551374924	chr11:107198536-107198537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566485747	chr11:107198546-107198547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531621130	chr11:107198549-107198550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190043204	chr11:107198552-107198553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369534458	chr11:107198561-107198562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142637506	chr11:107198596-107198597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11212162	chr11:107198610-107198611	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs76258765	chr11:107198617-107198618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146034334	chr11:107198670-107198671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181593711	chr11:107198687-107198688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539705179	chr11:107198700-107198701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557789859	chr11:107198702-107198703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11212163	chr11:107198731-107198732	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs567296660	chr11:107198740-107198741	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540223915	chr11:107198744-107198745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115168458	chr11:107198749-107198750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186715714	chr11:107198822-107198823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191919708	chr11:107198830-107198831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11212164	chr11:107198839-107198840	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs369170941	chr11:107198864-107198865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146969533	chr11:107198865-107198866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533451495	chr11:107198877-107198878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59090004	chr11:107198881-107198882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545248590	chr11:107198921-107198922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560408473	chr11:107198945-107198946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555378168	chr11:107198991-107198992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183655147	chr11:107198998-107198999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139988237	chr11:107199008-107199009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149660286	chr11:107199026-107199027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374576716	chr11:107199046-107199047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550512333	chr11:107199092-107199093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59811569	chr11:107199117-107199118	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12796965	chr11:107199134-107199135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107163800-107199000	Weak transcription	K562	blood
2	chr11:107168800-107201000	Weak transcription	NHEK	skin
3	chr11:107169400-107230000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr11:107172800-107204200	Weak transcription	NH-A	brain
5	chr11:107173600-107231400	Weak transcription	Brain Angular Gyrus	brain
6	chr11:107175400-107199400	Weak transcription	NHDF-Ad	bronchial
7	chr11:107179200-107229800	Weak transcription	Psoas Muscle	Psoas
8	chr11:107180000-107233200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr11:107183400-107234400	Weak transcription	HSMMtube	muscle
10	chr11:107189200-107199000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr11:107189400-107201800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:107189800-107200400	Weak transcription	Fetal Brain Male	brain
13	chr11:107189800-107206200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr11:107190000-107198800	Weak transcription	NHLF	lung
15	chr11:107190000-107223200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:107191200-107199400	Strong transcription	Fetal Intestine Large	intestine
17	chr11:107191200-107200800	Strong transcription	Primary B cells from cord blood	blood
18	chr11:107191200-107205800	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr11:107191600-107199000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr11:107191600-107200400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:107191600-107200800	Strong transcription	Liver	Liver
22	chr11:107191600-107203200	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr11:107191600-107208600	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr11:107191800-107199200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr11:107191800-107201000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr11:107192000-107198800	Strong transcription	Dnd41	blood
27	chr11:107192000-107200200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr11:107192000-107224200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:107192200-107199000	Weak transcription	Brain Germinal Matrix	brain
30	chr11:107192200-107200200	Strong transcription	Primary T cells from cord blood	blood
31	chr11:107192200-107201000	Strong transcription	Adipose Nuclei	Adipose
32	chr11:107192200-107205400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:107192200-107207400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr11:107192200-107208200	Weak transcription	Spleen	Spleen
35	chr11:107192200-107223800	Weak transcription	Brain Substantia Nigra	brain
36	chr11:107192200-107225600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:107192200-107229000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:107192200-107232200	Weak transcription	Esophagus	oesophagus
39	chr11:107192400-107201800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr11:107192400-107203600	Weak transcription	Pancreas	Pancrea
41	chr11:107192400-107214600	Weak transcription	Fetal Intestine Small	intestine
42	chr11:107192600-107199000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr11:107192600-107207400	Weak transcription	Colonic Mucosa	Colon
44	chr11:107192800-107201800	Weak transcription	HMEC	breast
45	chr11:107193000-107200400	Weak transcription	Brain Hippocampus Middle	brain
46	chr11:107193800-107209600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr11:107193800-107229800	Weak transcription	Right Ventricle	heart
48	chr11:107193800-107237200	Weak transcription	Gastric	stomach
49	chr11:107194000-107198200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr11:107194200-107205400	Weak transcription	HepG2	liver

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