Variant report

Variant	nsv875617
Chromosome Location	chr2:190701869-190724141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:190701263-190701896	A549	lung:	n/a	n/a
2	CEBPB	chr2:190713568-190713802	HepG2	liver:	n/a	chr2:190713706-190713719 chr2:190713707-190713718 chr2:190713708-190713717 chr2:190713706-190713717
3	CEBPB	chr2:190700941-190701871	Hela-S3	cervix:	n/a	chr2:190701542-190701555 chr2:190701468-190701479
4	CTCF	chr2:190705376-190705403	Kidney_OC	kidney:	n/a	n/a
5	EBF1	chr2:190702987-190703115	GM12878	blood:	n/a	chr2:190703055-190703065 chr2:190703056-190703065 chr2:190703054-190703065 chr2:190703054-190703067 chr2:190703056-190703066
6	EP300	chr2:190701192-190701989	A549	lung:	n/a	chr2:190701465-190701479 chr2:190701521-190701531
7	EP300	chr2:190701254-190701876	A549	lung:	n/a	chr2:190701465-190701479 chr2:190701521-190701531
8	FAM48A	chr2:190703531-190703601	GM12878	blood:	n/a	n/a
9	FOS	chr2:190707922-190708072	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr2:190709022-190709275	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr2:190708976-190709234	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr2:190708962-190709177	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr2:190708968-190709248	MCF10A-Er-Src	breast:	n/a	n/a
14	FOSL1	chr2:190708840-190709189	HCT-116	colon:	n/a	n/a
15	FOSL1	chr2:190708802-190709222	HCT-116	colon:	n/a	n/a
16	FOSL2	chr2:190701246-190701949	A549	lung:	n/a	n/a
17	FOSL2	chr2:190708908-190709208	SK-N-SH	brain:	n/a	n/a
18	FOSL2	chr2:190708804-190709208	A549	lung:	n/a	n/a
19	FOSL2	chr2:190719653-190720107	SK-N-SH	brain:	n/a	chr2:190719908-190719915 chr2:190719909-190719920 chr2:190719908-190719917
20	FOXA2	chr2:190701283-190702082	A549	lung:	n/a	n/a
21	FOXA2	chr2:190701324-190701895	A549	lung:	n/a	n/a
22	GATA3	chr2:190701078-190702099	A549	lung:	n/a	chr2:190701197-190701207
23	GATA3	chr2:190701310-190701998	MCF-7	breast:	n/a	n/a
24	GATA3	chr2:190701286-190701963	A549	lung:	n/a	n/a
25	GATA3	chr2:190701144-190702093	MCF-7	breast:	n/a	chr2:190701197-190701207
26	JUND	chr2:190707890-190708090	H1-hESC	embryonic stem cell:	n/a	n/a
27	JUND	chr2:190708649-190709250	Hela-S3	cervix:	n/a	chr2:190709097-190709108
28	JUND	chr2:190709066-190709166	HepG2	liver:	n/a	chr2:190709097-190709108
29	JUND	chr2:190719608-190720074	SK-N-SH	brain:	n/a	chr2:190719908-190719915 chr2:190719909-190719920 chr2:190719908-190719917
30	KAP1	chr2:190700767-190701939	U2OS	brain:	n/a	chr2:190701255-190701263
31	KAP1	chr2:190700782-190701895	HEK293	kidney:	n/a	chr2:190701255-190701263
32	MAFK	chr2:190706951-190707118	IMR90	lung:	n/a	chr2:190707054-190707069
33	MAFK	chr2:190706897-190707200	HepG2	liver:	n/a	chr2:190707054-190707069
34	MAFK	chr2:190706945-190707141	HepG2	liver:	n/a	chr2:190707054-190707069
35	NFIC	chr2:190715853-190716481	ECC-1	luminal epithelium:	n/a	n/a
36	NFYB	chr2:190704989-190705189	GM12878	blood:	n/a	n/a
37	NRF1	chr2:190719816-190719953	K562	blood:	n/a	n/a
38	POLR2A	chr2:190721865-190721872	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr2:190717819-190717873	ProgFib	skin:	n/a	n/a
40	POLR2A	chr2:190715461-190715569	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr2:190723097-190723489	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr2:190718902-190719273	SK-N-MC	brain:	n/a	n/a
43	RCOR1	chr2:190701243-190702057	Hela-S3	cervix:	n/a	n/a
44	REST	chr2:190718334-190718390	PANC-1	pancreas:	n/a	n/a
45	REST	chr2:190701216-190701936	A549	lung:	n/a	n/a
46	SIN3AK20	chr2:190701270-190701989	MCF-7	breast:	n/a	n/a
47	SIX5	chr2:190715987-190716179	H1-hESC	embryonic stem cell:	n/a	n/a
48	SP1	chr2:190701236-190701951	A549	lung:	n/a	n/a
49	SP1	chr2:190715868-190716296	H1-hESC	embryonic stem cell:	n/a	n/a
50	SP1	chr2:190701279-190701876	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:190719470-190719520	A549	lung:	n/a
2	chr2:190715638-190715688	PFSK-1	brain:	n/a
3	chr2:190719470-190719520	HEEpiC	esophagus:	n/a
4	chr2:190715638-190715688	HIPEpiC	eye:	n/a
5	chr2:190706964-190707014	HIPEpiC	eye:	n/a
6	chr2:190706964-190707014	HUVEC	blood vessel:	n/a
7	chr2:190715638-190715688	ProgFib	skin:	n/a
8	chr2:190706964-190707014	H1-hESC	embryonic stem cell:	embryo
9	chr2:190706964-190707014	PrEC	prostate:	n/a
10	chr2:190719470-190719520	NH-A	brain:	n/a
11	chr2:190719470-190719520	Hela-S3	cervix:	n/a
12	chr2:190706964-190707014	SK-N-MC	brain:	n/a
13	chr2:190715638-190715688	MCF10A-Er-Src	breast:	n/a
14	chr2:190706964-190707014	NT2-D1	testis:	n/a
15	chr2:190715638-190715688	HEEpiC	esophagus:	n/a
16	chr2:190715638-190715688	HRCEpiC	kidney:	n/a
17	chr2:190706964-190707014	GM12892	blood:	n/a
18	chr2:190715638-190715688	SAEC	small airway:	n/a
19	chr2:190715638-190715688	CMK	blood:	n/a
20	chr2:190719470-190719520	RPTEC	kidney:	n/a
21	chr2:190706964-190707014	HEK293	kidney:	embryo
22	chr2:190719470-190719520	Jurkat	blood:	n/a
23	chr2:190715638-190715688	AoSMC	blood vessel:	n/a
24	chr2:190719470-190719520	HRCEpiC	kidney:	n/a
25	chr2:190706964-190707014	HCF	heart:	n/a
26	chr2:190719470-190719520	HMEC	breast:	n/a
27	chr2:190715638-190715688	HL-60	blood:	n/a
28	chr2:190706964-190707014	GM19239	blood:	n/a
29	chr2:190706964-190707014	HCPEpiC	choroid plexus:	n/a
30	chr2:190719470-190719520	GM12878	blood:	n/a
31	chr2:190719470-190719520	HCPEpiC	choroid plexus:	n/a
32	chr2:190719470-190719520	ovcar-3	ovarian:	n/a
33	chr2:190706964-190707014	PFSK-1	brain:	n/a
34	chr2:190719470-190719520	MCF-7	breast:	n/a
35	chr2:190706964-190707014	BJ	skin:	n/a
36	chr2:190719470-190719520	HCT-116	colon:	n/a
37	chr2:190715638-190715688	U87	brain:	n/a
38	chr2:190706964-190707014	ProgFib	skin:	n/a
39	chr2:190715638-190715688	AG10803	skin:	n/a
40	chr2:190715638-190715688	NHBE	bronchial:	n/a
41	chr2:190715638-190715688	SK-N-MC	brain:	n/a
42	chr2:190719470-190719520	PrEC	prostate:	n/a
43	chr2:190715638-190715688	GM12892	blood:	n/a
44	chr2:190715638-190715688	HCM	heart:	n/a
45	chr2:190715638-190715688	AG04449	skin:	fetal
46	chr2:190715638-190715688	RPTEC	kidney:	n/a
47	chr2:190715638-190715688	HRE	kidney:	n/a
48	chr2:190706964-190707014	HRPEpiC	eye:	n/a
49	chr2:190715638-190715688	HRPEpiC	eye:	n/a
50	chr2:190719470-190719520	NHDF-neo	bronchial:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:190702622..190704522-chr2:191400412..191402253,2	K562	blood:
2	chr2:190647331..190649036-chr2:190714080..190716253,2	MCF-7	breast:
3	chr2:190615507..190617110-chr2:190708783..190711521,2	K562	blood:
4	chr2:190648774..190650494-chr2:190701394..190702901,2	MCF-7	breast:
5	chr2:190713621..190715990-chr2:190716646..190719108,2	MCF-7	breast:
6	chr2:190707467..190709544-chr2:190709954..190711600,2	K562	blood:
7	chr2:190694673..190697021-chr2:190708610..190710917,2	MCF-7	breast:
8	chr2:190707467..190709544-chr2:190709954..190711600,2	K562	blood:
9	chr2:190715500..190717076-chr2:190721270..190723258,2	K562	blood:
10	chr2:190722858..190725446-chr2:190730351..190732243,2	K562	blood:
11	chr2:190713621..190715990-chr2:190716646..190719108,2	MCF-7	breast:

No data

Variant related genes	Relation type
PMS1	TF binding region
PMS1	CpG island
ENSG00000064933	chromatin interactions
ENSG00000128699	chromatin interactions

Extended variants
information (count: 788 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1233250	chr2:190701869-190701870	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6753164	chr2:190701872-190701873	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs112928963	chr2:190701890-190701891	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs199513735	chr2:190701904-190701905	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs183344759	chr2:190701992-190701993	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115831793	chr2:190702024-190702025	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577722393	chr2:190702047-190702048	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs374081140	chr2:190702057-190702058	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376752786	chr2:190702099-190702100	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs528642678	chr2:190702111-190702112	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570244834	chr2:190702121-190702122	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs1233251	chr2:190702160-190702161	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs552454421	chr2:190702179-190702180	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs188404924	chr2:190702193-190702194	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534711438	chr2:190702197-190702198	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540764490	chr2:190702232-190702233	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553033172	chr2:190702291-190702292	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs568566325	chr2:190702299-190702300	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191745200	chr2:190702360-190702361	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557158105	chr2:190702406-190702407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs575354521	chr2:190702548-190702549	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs138492504	chr2:190702601-190702602	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs78056333	chr2:190702651-190702652	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs377406699	chr2:190702676-190702677	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540262131	chr2:190702692-190702693	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs561626725	chr2:190702695-190702696	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573722957	chr2:190702703-190702704	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543982291	chr2:190702749-190702750	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs554400843	chr2:190702868-190702869	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs563859269	chr2:190702888-190702889	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs531032807	chr2:190702903-190702904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182476450	chr2:190702911-190702912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558992223	chr2:190702979-190702980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564473143	chr2:190703047-190703048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534785581	chr2:190703065-190703066	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74462916	chr2:190703074-190703075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74356037	chr2:190703114-190703115	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568451121	chr2:190703166-190703167	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535900321	chr2:190703289-190703290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150682695	chr2:190703348-190703349	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74645111	chr2:190703349-190703350	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539682684	chr2:190703366-190703367	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs57920919	chr2:190703367-190703368	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139886376	chr2:190703374-190703375	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569944169	chr2:190703428-190703429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12617253	chr2:190703437-190703438	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs192540730	chr2:190703442-190703443	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533761938	chr2:190703469-190703470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555303773	chr2:190703513-190703514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73042337	chr2:190703535-190703536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Colorectal cancer	16912164	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190649800-190713400	Weak transcription	Gastric	stomach
2	chr2:190650400-190711400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr2:190656800-190721000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr2:190658200-190743800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr2:190659800-190743600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr2:190661400-190717800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr2:190662800-190719000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr2:190663000-190712800	Weak transcription	Aorta	Aorta
9	chr2:190663200-190712400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr2:190664800-190741800	Weak transcription	Brain Angular Gyrus	brain
11	chr2:190669400-190743800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr2:190669600-190709600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr2:190669600-190713200	Weak transcription	Ovary	ovary
14	chr2:190669800-190709000	Weak transcription	Placenta	Placenta
15	chr2:190670800-190712800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr2:190671000-190719600	Weak transcription	NH-A	brain
17	chr2:190676200-190712400	Weak transcription	K562	blood
18	chr2:190677000-190709400	Weak transcription	Fetal Intestine Small	intestine
19	chr2:190681000-190743000	Weak transcription	Brain Germinal Matrix	brain
20	chr2:190683800-190709800	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr2:190684000-190712600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr2:190684000-190712800	Weak transcription	Duodenum Mucosa	Duodenum
23	chr2:190684000-190743600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr2:190684600-190709800	Weak transcription	HMEC	breast
25	chr2:190684600-190712600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr2:190684600-190712600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr2:190685000-190712600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr2:190685000-190736400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:190685200-190706200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:190685200-190708400	Weak transcription	Fetal Intestine Large	intestine
31	chr2:190685400-190712800	Weak transcription	Adipose Nuclei	Adipose
32	chr2:190685400-190739400	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr2:190685400-190741800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr2:190685600-190709600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:190685600-190712800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr2:190685800-190702000	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr2:190685800-190708600	Weak transcription	Liver	Liver
38	chr2:190685800-190708800	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr2:190685800-190709600	Weak transcription	Fetal Muscle Trunk	muscle
40	chr2:190686000-190711400	Weak transcription	Primary B cells from peripheral blood	blood
41	chr2:190687000-190706800	Weak transcription	Left Ventricle	heart
42	chr2:190687000-190712800	Weak transcription	Thymus	Thymus
43	chr2:190687000-190724400	Weak transcription	Esophagus	oesophagus
44	chr2:190687000-190738400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:190687000-190738400	Weak transcription	Lung	lung
46	chr2:190687200-190706800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr2:190687200-190710200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:190687200-190710400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:190687400-190708800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr2:190691000-190706200	Weak transcription	H1 Cell Line	embryonic stem cell

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