Variant report

Variant	nsv593434
Chromosome Location	chr4:2688719-2737140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:775)
CpG islands
(count:734)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:2697995-2698718	GM12878	blood:	n/a	n/a
2	ATF2	chr4:2697871-2698708	GM12878	blood:	n/a	n/a
3	ATF2	chr4:2693689-2694309	GM12878	blood:	n/a	n/a
4	ATF3	chr4:2691673-2691891	GM12878	blood:	n/a	n/a
5	BATF	chr4:2691670-2691928	GM12878	blood:	n/a	n/a
6	BATF	chr4:2714241-2714436	GM12878	blood:	n/a	n/a
7	BATF	chr4:2736380-2736677	GM12878	blood:	n/a	n/a
8	BATF	chr4:2714153-2714433	GM12878	blood:	n/a	n/a
9	BATF	chr4:2698084-2698552	GM12878	blood:	n/a	n/a
10	BATF	chr4:2736340-2736643	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:2698041-2698507	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:2693791-2694131	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:2698095-2698489	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:2736381-2736654	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:2698033-2698657	GM12878	blood:	n/a	n/a
16	BCLAF1	chr4:2713889-2714317	GM12878	blood:	n/a	n/a
17	BCLAF1	chr4:2697963-2698880	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:2693915-2694205	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:2696495-2696661	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:2716278-2716614	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:2698003-2698670	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:2693799-2694411	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:2691521-2692259	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:2699808-2700120	HepG2	liver:	n/a	n/a
25	BHLHE40	chr4:2714283-2714392	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:2733871-2733952	HepG2	liver:	n/a	n/a
27	CCNT2	chr4:2735254-2735459	K562	blood:	n/a	n/a
28	CEBPB	chr4:2704972-2705080	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:2716695-2716951	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:2704957-2705088	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:2698119-2698462	GM12878	blood:	n/a	n/a
32	CEBPB	chr4:2697949-2698638	GM12878	blood:	n/a	n/a
33	CEBPB	chr4:2704978-2705137	K562	blood:	n/a	n/a
34	CEBPB	chr4:2699827-2699925	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:2709418-2709570	K562	blood:	n/a	n/a
36	CHD1	chr4:2694201-2694214	GM12878	blood:	n/a	n/a
37	CHD1	chr4:2691596-2691673	GM12878	blood:	n/a	n/a
38	CHD2	chr4:2691681-2691974	GM12878	blood:	n/a	n/a
39	CHD2	chr4:2735033-2735141	HepG2	liver:	n/a	n/a
40	CHD2	chr4:2693891-2694296	GM12878	blood:	n/a	n/a
41	CHD2	chr4:2698061-2698723	GM12878	blood:	n/a	n/a
42	CREB1	chr4:2698013-2698652	GM12878	blood:	n/a	n/a
43	CTCF	chr4:2714082-2714300	K562	blood:	n/a	n/a
44	CTCF	chr4:2715700-2715850	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr4:2715820-2715970	BJ	skin:	n/a	n/a
46	CTCF	chr4:2715660-2715810	HMF	breast:	n/a	n/a
47	CTCF	chr4:2714140-2714290	AG09309	skin:	n/a	n/a
48	CTCF	chr4:2715780-2715930	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr4:2698280-2698430	GM12801	blood:	n/a	chr4:2698338-2698351
50	CTCF	chr4:2715720-2715870	HPAF	blood vessel:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2696786-2696836	K562	blood:	n/a
2	chr4:2733734-2733784	A549	lung:	n/a
3	chr4:2696786-2696836	K562	blood:	n/a
4	chr4:2733734-2733784	A549	lung:	n/a
5	chr4:2696631-2696681	HRCEpiC	kidney:	n/a
6	chr4:2696631-2696681	HCF	heart:	n/a
7	chr4:2731366-2731416	HIPEpiC	eye:	n/a
8	chr4:2716524-2716574	AG09309	skin:	n/a
9	chr4:2733970-2734020	GM06990	blood:	n/a
10	chr4:2733970-2734020	AG04450	lung:	fetal
11	chr4:2716524-2716574	NT2-D1	testis:	n/a
12	chr4:2733908-2733958	HEK293	kidney:	embryo
13	chr4:2733397-2733447	Hela-S3	cervix:	n/a
14	chr4:2696715-2696765	HCPEpiC	choroid plexus:	n/a
15	chr4:2696715-2696765	Hepatocyte	liver:	n/a
16	chr4:2716524-2716574	MCF10A-Er-Src	breast:	n/a
17	chr4:2736028-2736078	SKMC	muscle:	n/a
18	chr4:2733839-2733889	MCF-7	breast:	n/a
19	chr4:2696715-2696765	HIPEpiC	eye:	n/a
20	chr4:2733839-2733889	BJ	skin:	n/a
21	chr4:2733734-2733784	AG04449	skin:	fetal
22	chr4:2716524-2716574	GM12891	blood:	n/a
23	chr4:2736028-2736078	HL-60	blood:	n/a
24	chr4:2733839-2733889	Jurkat	blood:	n/a
25	chr4:2733970-2734020	AG10803	skin:	n/a
26	chr4:2716524-2716574	SKMC	muscle:	n/a
27	chr4:2696786-2696836	PANC-1	pancreas:	n/a
28	chr4:2731366-2731416	T-47D	breast:	n/a
29	chr4:2716524-2716574	SK-N-SH	brain:	n/a
30	chr4:2733970-2734020	GM12891	blood:	n/a
31	chr4:2731366-2731416	MCF-7	breast:	n/a
32	chr4:2733970-2734020	A549	lung:	n/a
33	chr4:2696631-2696681	SKMC	muscle:	n/a
34	chr4:2696715-2696765	GM19239	blood:	n/a
35	chr4:2716524-2716574	ECC-1	luminal epithelium:	n/a
36	chr4:2733970-2734020	Hela-S3	cervix:	n/a
37	chr4:2716524-2716574	PFSK-1	brain:	n/a
38	chr4:2733397-2733447	HAEpiC	amniotic membrane:	n/a
39	chr4:2733734-2733784	HNPCEpiC	eye:	n/a
40	chr4:2735245-2735295	A549	lung:	n/a
41	chr4:2696786-2696836	NHBE	bronchial:	n/a
42	chr4:2736028-2736078	GM12878	blood:	n/a
43	chr4:2733839-2733889	PrEC	prostate:	n/a
44	chr4:2716524-2716574	K562	blood:	n/a
45	chr4:2733839-2733889	AG04450	lung:	fetal
46	chr4:2733839-2733889	MCF10A-Er-Src	breast:	n/a
47	chr4:2731366-2731416	MCF10A-Er-Src	breast:	n/a
48	chr4:2733908-2733958	HRPEpiC	eye:	n/a
49	chr4:2736028-2736078	HEEpiC	esophagus:	n/a
50	chr4:2736028-2736078	MCF10A-Er-Src	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2686800..2688519-chr4:2692243..2694641,2	MCF-7	breast:
2	chr4:2693061..2695542-chr4:2698679..2700261,2	K562	blood:
3	chr4:2691900..2694094-chr4:2704691..2707252,2	MCF-7	breast:
4	chr4:2684900..2686631-chr4:2732347..2735002,2	MCF-7	breast:
5	chr4:2694438..2696914-chr4:2698682..2700465,2	K562	blood:
6	chr4:2709028..2711083-chr4:2714281..2716848,2	K562	blood:
7	chr4:2729531..2731576-chr4:2736624..2739591,3	K562	blood:
8	chr4:2728834..2731031-chr4:2737580..2740128,2	K562	blood:
9	chr4:2694438..2696914-chr4:2698682..2700465,2	K562	blood:
10	chr11:62608625..62609221-chr4:2723288..2724083,2	NB4	blood:
11	chr4:2686405..2688173-chr4:2690940..2692757,2	K562	blood:
12	chr4:2681997..2685012-chr4:2686552..2689862,4	K562	blood:
13	chr4:2698027..2699882-chr4:2708019..2712089,3	K562	blood:
14	chr4:2698027..2699882-chr4:2708019..2712089,3	K562	blood:
15	chr4:2729531..2731576-chr4:2736624..2739591,3	K562	blood:
16	chr4:2693061..2695542-chr4:2698679..2700261,2	K562	blood:
17	chr4:2714914..2717325-chr4:2756410..2757959,2	MCF-7	breast:
18	chr4:2722338..2725244-chr4:2727735..2730949,3	K562	blood:
19	chr4:2722338..2725244-chr4:2727735..2730949,3	K562	blood:
20	chr4:2728248..2729881-chr4:2757575..2759272,2	MCF-7	breast:
21	chr4:2687414..2693444-chr4:2695682..2700044,5	MCF-7	breast:
22	chr4:2536351..2537886-chr4:2713685..2715325,2	MCF-7	breast:
23	chr4:2734730..2737183-chr4:2738834..2740475,2	K562	blood:
24	chr4:2673139..2674929-chr4:2692013..2693790,2	K562	blood:
25	chr4:2536163..2539003-chr4:2712977..2717563,4	MCF-7	breast:
26	chr4:2691900..2694094-chr4:2704691..2707252,2	MCF-7	breast:
27	chr4:2709028..2711083-chr4:2714281..2716848,2	K562	blood:

No data

Variant related genes	Relation type
FAM193A	TF binding region
FAM193A	CpG island
ENSG00000125386	chromatin interactions
ENSG00000168884	chromatin interactions

Extended variants
information (count: 2209 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2209 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12509340	chr4:2688719-2688720	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs558048571	chr4:2688815-2688816	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192353710	chr4:2688854-2688855	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs573516171	chr4:2688869-2688870	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139419943	chr4:2688899-2688900	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184568253	chr4:2688930-2688931	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117954836	chr4:2688947-2688948	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188932937	chr4:2688992-2688993	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs567287777	chr4:2688995-2688996	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373612557	chr4:2689004-2689005	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7340952	chr4:2689006-2689007	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs553205080	chr4:2689012-2689013	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7340951	chr4:2689061-2689062	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538850800	chr4:2689066-2689067	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs149868318	chr4:2689108-2689109	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574091657	chr4:2689174-2689175	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577644821	chr4:2689238-2689239	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112629707	chr4:2689250-2689251	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144894741	chr4:2689268-2689269	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139837854	chr4:2689275-2689276	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181339673	chr4:2689291-2689292	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143260541	chr4:2689297-2689298	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs544607763	chr4:2689309-2689310	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs114171601	chr4:2689313-2689314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184876365	chr4:2689326-2689327	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs1988706	chr4:2689375-2689376	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551282293	chr4:2689379-2689380	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146705717	chr4:2689408-2689409	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs140328973	chr4:2689422-2689423	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs371615689	chr4:2689423-2689424	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567425137	chr4:2689434-2689435	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs1828803	chr4:2689449-2689450	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs16843203	chr4:2689454-2689455	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs567051028	chr4:2689456-2689457	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539349300	chr4:2689461-2689462	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558872751	chr4:2689498-2689499	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550699138	chr4:2689508-2689509	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372387208	chr4:2689517-2689518	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575756880	chr4:2689558-2689559	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538460938	chr4:2689623-2689624	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs377248462	chr4:2689669-2689670	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557046632	chr4:2689700-2689701	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573787958	chr4:2689703-2689704	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6605352	chr4:2689743-2689744	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs552979399	chr4:2689756-2689757	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373327457	chr4:2689773-2689774	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556056044	chr4:2689800-2689801	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189777249	chr4:2689807-2689808	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570292863	chr4:2689821-2689822	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114973837	chr4:2689822-2689823	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Breast cancer	22522925	CNVD
Cancer	22970210	CNVD
Disease	21248748	CNVD
Gastric cancer	21784958	CNVD
Systemic lupus erythematosus	22942739	CNVD
Breast cancer	20409316	CNVD

Chromatin state (count:1563 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2638200-2724400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:2669600-2692200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:2673600-2714400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:2673800-2698000	Weak transcription	Fetal Heart	heart
5	chr4:2674200-2695600	Weak transcription	Stomach Mucosa	stomach
6	chr4:2675200-2691600	Weak transcription	Small Intestine	intestine
7	chr4:2675200-2698200	Weak transcription	Psoas Muscle	Psoas
8	chr4:2675400-2689200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr4:2675600-2692000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr4:2677200-2692200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:2677400-2698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:2677800-2692600	Weak transcription	Hela-S3	cervix
13	chr4:2679200-2689600	Strong transcription	Fetal Intestine Small	intestine
14	chr4:2679400-2712600	Strong transcription	Fetal Stomach	stomach
15	chr4:2680200-2712800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:2680400-2712200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr4:2680800-2710200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr4:2681600-2712600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr4:2681800-2690000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:2682000-2690400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:2682000-2695200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:2682000-2699400	Strong transcription	Fetal Intestine Large	intestine
23	chr4:2682000-2706000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr4:2682000-2707600	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr4:2682000-2708000	Strong transcription	Dnd41	blood
26	chr4:2682200-2690400	Strong transcription	Fetal Muscle Trunk	muscle
27	chr4:2682200-2708000	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr4:2682600-2689600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:2682600-2707200	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr4:2682600-2709800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr4:2682800-2710000	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr4:2683000-2699200	Strong transcription	Liver	Liver
33	chr4:2683000-2707200	Strong transcription	Placenta	Placenta
34	chr4:2683200-2706400	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr4:2683200-2710000	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr4:2683400-2690000	Strong transcription	K562	blood
37	chr4:2683400-2710400	Strong transcription	Osteobl	bone
38	chr4:2684000-2706800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr4:2684000-2707000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:2684200-2690800	Strong transcription	Primary B cells from peripheral blood	blood
41	chr4:2684200-2693200	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr4:2684400-2706600	Strong transcription	Primary T cells from cord blood	blood
43	chr4:2684600-2690600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr4:2684600-2698600	Strong transcription	HepG2	liver
45	chr4:2684600-2710400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:2684600-2710800	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr4:2684800-2690600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:2684800-2707000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:2685000-2691000	Strong transcription	Fetal Muscle Leg	muscle
50	chr4:2685000-2696200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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