Variant report

Variant	nsv829839
Chromosome Location	chr4:2624422-2659610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:335)
CpG islands
(count:672)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:2655375-2655768	GM12878	blood:	n/a	n/a
2	BATF	chr4:2655469-2655722	GM12878	blood:	n/a	n/a
3	CBX3	chr4:2653079-2653411	K562	blood:	n/a	n/a
4	CTCF	chr4:2626160-2626310	AoAF	blood vessel:	n/a	chr4:2626285-2626292
5	CTCF	chr4:2632647-2633052	K562	blood:	n/a	n/a
6	CTCF	chr4:2626088-2626373	H1-hESC	embryonic stem cell:	n/a	chr4:2626285-2626292
7	CTCF	chr4:2632780-2632930	GM12873	blood:	n/a	n/a
8	CTCF	chr4:2632740-2632890	GM12870	blood:	n/a	n/a
9	CTCF	chr4:2632792-2632903	MCF-7	breast:	n/a	n/a
10	CTCF	chr4:2632740-2632933	GM19240	blood:	n/a	n/a
11	CTCF	chr4:2626140-2626290	GM12864	blood:	n/a	n/a
12	CTCF	chr4:2632740-2632890	GM12873	blood:	n/a	n/a
13	CTCF	chr4:2626173-2626354	H1-hESC	embryonic stem cell:	n/a	chr4:2626285-2626292
14	CTCF	chr4:2632735-2632952	K562	blood:	n/a	n/a
15	CTCF	chr4:2632827-2632901	LNCaP	prostate:	n/a	n/a
16	CTCF	chr4:2626180-2626330	Hela-S3	cervix:	n/a	chr4:2626285-2626292
17	CTCF	chr4:2650352-2650444	GM12892	blood:	n/a	n/a
18	CTCF	chr4:2626180-2626330	GM06990	blood:	n/a	chr4:2626285-2626292
19	CTCF	chr4:2632741-2632937	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:2626240-2626390	GM12864	blood:	n/a	chr4:2626285-2626292
21	CTCF	chr4:2632780-2632930	BE2_C	brain:	n/a	n/a
22	CTCF	chr4:2631392-2631600	IMR90	lung:	n/a	chr4:2631479-2631500
23	CTCF	chr4:2632784-2632888	NHEK	skin:	n/a	n/a
24	CTCF	chr4:2632469-2633189	HCT-116	colon:	n/a	chr4:2632621-2632630
25	CTCF	chr4:2632740-2632890	GM12878	blood:	n/a	n/a
26	CTCF	chr4:2632800-2632950	GM12874	blood:	n/a	n/a
27	CTCF	chr4:2632760-2632910	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr4:2626220-2626370	SAEC	small airway:	n/a	chr4:2626285-2626292
29	CTCF	chr4:2626180-2626330	HBMEC	blood vessel:	n/a	chr4:2626285-2626292
30	CTCF	chr4:2632700-2632850	GM12866	blood:	n/a	n/a
31	CTCF	chr4:2626160-2626310	HMF	breast:	n/a	chr4:2626285-2626292
32	CTCF	chr4:2632540-2632690	GM12874	blood:	n/a	chr4:2632621-2632630
33	CTCF	chr4:2632600-2632750	K562	blood:	n/a	chr4:2632621-2632630
34	CTCF	chr4:2632761-2632910	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:2626213-2626296	GM19240	blood:	n/a	chr4:2626285-2626292
36	CTCF	chr4:2626240-2626390	A549	lung:	n/a	chr4:2626285-2626292
37	CTCF	chr4:2632611-2633073	MCF-7	breast:	n/a	chr4:2632621-2632630
38	CTCF	chr4:2632780-2632930	A549	lung:	n/a	n/a
39	CTCF	chr4:2626180-2626330	HCPEpiC	choroid plexus:	n/a	chr4:2626285-2626292
40	CTCF	chr4:2626220-2626370	GM06990	blood:	n/a	chr4:2626285-2626292
41	CTCF	chr4:2626220-2626370	GM12865	blood:	n/a	chr4:2626285-2626292
42	CTCF	chr4:2626160-2626310	WERI-Rb-1	eye:	n/a	chr4:2626285-2626292
43	CTCF	chr4:2626220-2626370	HCFaa	heart:	n/a	chr4:2626285-2626292
44	CTCF	chr4:2650311-2650340	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr4:2626214-2626305	GM19238	blood:	n/a	chr4:2626285-2626292
46	CTCF	chr4:2650380-2650439	GM19238	blood:	n/a	n/a
47	CTCF	chr4:2632760-2632910	GM12874	blood:	n/a	n/a
48	CTCF	chr4:2626220-2626370	HPAF	blood vessel:	n/a	chr4:2626285-2626292
49	CTCF	chr4:2626260-2626410	HAc	cerebellar:	n/a	chr4:2626285-2626292
50	CTCF	chr4:2632559-2632975	H1-hESC	embryonic stem cell:	n/a	chr4:2632621-2632630

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2627057-2627107	HMEC	breast:	n/a
2	chr4:2627057-2627107	HMEC	breast:	n/a
3	chr4:2625790-2625840	PANC-1	pancreas:	n/a
4	chr4:2627014-2627064	HUVEC	blood vessel:	n/a
5	chr4:2627118-2627168	SKMC	muscle:	n/a
6	chr4:2628771-2628821	U87	brain:	n/a
7	chr4:2627057-2627107	HEEpiC	esophagus:	n/a
8	chr4:2627246-2627296	GM12878	blood:	n/a
9	chr4:2627118-2627168	SK-N-SH_RA	brain:	n/a
10	chr4:2625790-2625840	SK-N-SH_RA	brain:	n/a
11	chr4:2627014-2627064	CMK	blood:	n/a
12	chr4:2627039-2627089	HCPEpiC	choroid plexus:	n/a
13	chr4:2626256-2626306	AG04450	lung:	fetal
14	chr4:2628771-2628821	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:2627039-2627089	MCF-7	breast:	n/a
16	chr4:2627039-2627089	GM12892	blood:	n/a
17	chr4:2627118-2627168	K562	blood:	n/a
18	chr4:2627194-2627244	AG04450	lung:	fetal
19	chr4:2627194-2627244	NHDF-neo	bronchial:	n/a
20	chr4:2627142-2627192	PFSK-1	brain:	n/a
21	chr4:2627246-2627296	HCF	heart:	n/a
22	chr4:2625790-2625840	IMR90	lung:	fetal
23	chr4:2627039-2627089	GM06990	blood:	n/a
24	chr4:2627057-2627107	GM12892	blood:	n/a
25	chr4:2627142-2627192	Jurkat	blood:	n/a
26	chr4:2627194-2627244	HEEpiC	esophagus:	n/a
27	chr4:2625790-2625840	PFSK-1	brain:	n/a
28	chr4:2627142-2627192	GM12892	blood:	n/a
29	chr4:2627039-2627089	SAEC	small airway:	n/a
30	chr4:2628771-2628821	HCM	heart:	n/a
31	chr4:2626256-2626306	HepG2	liver:	n/a
32	chr4:2627039-2627089	AG09319	gingival:	n/a
33	chr4:2627057-2627107	A549	lung:	n/a
34	chr4:2627057-2627107	AG04450	lung:	fetal
35	chr4:2626256-2626306	HCF	heart:	n/a
36	chr4:2627142-2627192	PANC-1	pancreas:	n/a
37	chr4:2627246-2627296	HepG2	liver:	n/a
38	chr4:2627142-2627192	Hela-S3	cervix:	n/a
39	chr4:2626256-2626306	U87	brain:	n/a
40	chr4:2627246-2627296	HEEpiC	esophagus:	n/a
41	chr4:2628771-2628821	Jurkat	blood:	n/a
42	chr4:2627142-2627192	HMEC	breast:	n/a
43	chr4:2628771-2628821	HL-60	blood:	n/a
44	chr4:2628771-2628821	ovcar-3	ovarian:	n/a
45	chr4:2627118-2627168	HL-60	blood:	n/a
46	chr4:2627014-2627064	GM19239	blood:	n/a
47	chr4:2627194-2627244	GM06990	blood:	n/a
48	chr4:2626256-2626306	BE2_C	brain:	n/a
49	chr4:2626239-2626289	Jurkat	blood:	n/a
50	chr4:2628771-2628821	HEK293	kidney:	embryo

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2536061..2538974-chr4:2638260..2639987,2	K562	blood:
2	chr4:2538499..2541036-chr4:2633041..2634919,2	MCF-7	breast:
3	chr4:2443170..2444011-chr4:2631001..2632008,3	MCF-7	breast:
4	chr4:2652789..2655769-chr4:2658106..2659944,2	K562	blood:
5	chr4:2640027..2642177-chr4:2642653..2645301,2	K562	blood:
6	chr4:2643967..2645489-chr4:2745808..2748370,2	MCF-7	breast:
7	chr4:2652789..2655769-chr4:2658106..2659944,2	K562	blood:
8	chr4:2652130..2653752-chr4:2654894..2657353,2	K562	blood:
9	chr4:2634391..2637399-chr4:2638186..2641197,3	K562	blood:
10	chr4:2631087..2633393-chr4:2638925..2641589,2	K562	blood:
11	chr4:2652130..2654569-chr4:2654894..2657353,4	K562	blood:
12	chr4:2541446..2543494-chr4:2621946..2624670,2	K562	blood:
13	chr4:2652789..2655769-chr4:2657386..2659944,4	K562	blood:
14	chr4:2639557..2641367-chr4:2647223..2650179,2	MCF-7	breast:
15	chr4:2639377..2642131-chr4:2743539..2746245,2	K562	blood:
16	chr4:2652789..2655769-chr4:2657386..2659944,4	K562	blood:
17	chr4:2652183..2654453-chr4:2660198..2662180,2	MCF-7	breast:
18	chr4:2640027..2642177-chr4:2642653..2645301,2	K562	blood:
19	chr4:2658066..2659602-chr4:2743104..2745272,2	K562	blood:
20	chr4:2562540..2564110-chr4:2632419..2633973,2	K562	blood:
21	chr4:2631087..2633393-chr4:2638925..2641589,2	K562	blood:
22	chr4:2625863..2628714-chr4:2636142..2638423,2	MCF-7	breast:
23	chr4:2639557..2641367-chr4:2647223..2650179,2	MCF-7	breast:
24	chr4:2656644..2658573-chr4:2660984..2662891,3	K562	blood:
25	chr4:2626484..2629580-chr4:2631999..2636135,3	K562	blood:
26	chr4:2634391..2637399-chr4:2638186..2641197,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF4-1	chr4:2650229-2650734	NONHSAT094802
2	lnc-RNF4-1	chr4:2649906-2649952	NONHSAT094802

No data

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

Extended variants
information (count: 1594 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1594 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551415522	chr4:2624440-2624441	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180946760	chr4:2624458-2624459	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536646449	chr4:2624459-2624460	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs117706425	chr4:2624462-2624463	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs113839292	chr4:2624480-2624481	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536168692	chr4:2624511-2624512	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs371710287	chr4:2624524-2624525	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs553011494	chr4:2624532-2624533	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs572957527	chr4:2624545-2624546	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs544882001	chr4:2624555-2624556	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs558960063	chr4:2624607-2624608	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115371388	chr4:2624611-2624612	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs185071670	chr4:2624617-2624618	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs561297489	chr4:2624618-2624619	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs530140748	chr4:2624622-2624623	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs540888357	chr4:2624667-2624668	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs560631419	chr4:2624689-2624690	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532692580	chr4:2624694-2624695	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs149347123	chr4:2624698-2624699	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs574794269	chr4:2624741-2624742	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs535925208	chr4:2624765-2624766	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs550137585	chr4:2624786-2624787	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs144189723	chr4:2624791-2624792	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs535883485	chr4:2624831-2624832	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs553188306	chr4:2624932-2624933	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566655284	chr4:2624933-2624934	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538820641	chr4:2624954-2624955	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558508210	chr4:2624958-2624959	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148273118	chr4:2624959-2624960	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191052821	chr4:2624990-2624991	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs555118008	chr4:2625032-2625033	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574846756	chr4:2625045-2625046	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs540271574	chr4:2625050-2625051	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs183099756	chr4:2625055-2625056	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs571239482	chr4:2625079-2625080	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs532277357	chr4:2625143-2625144	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs141302822	chr4:2625234-2625235	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532116962	chr4:2625274-2625275	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs547528462	chr4:2625276-2625277	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs546363076	chr4:2625280-2625281	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs186986822	chr4:2625297-2625298	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs191480811	chr4:2625340-2625341	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs550225272	chr4:2625344-2625345	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs2857798	chr4:2625354-2625355	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs529643069	chr4:2625355-2625356	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs546323690	chr4:2625360-2625361	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs566746040	chr4:2625361-2625362	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs183342196	chr4:2625430-2625431	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs372503758	chr4:2625458-2625459	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs188081696	chr4:2625479-2625480	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1367 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2589200-2627200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr4:2599400-2627200	Weak transcription	HSMM	muscle
3	chr4:2600600-2627800	Weak transcription	NHDF-Ad	bronchial
4	chr4:2600800-2627000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr4:2601000-2627000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr4:2601400-2627000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr4:2601400-2628200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr4:2602600-2626600	Weak transcription	Placenta	Placenta
9	chr4:2602600-2627000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr4:2602600-2627000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr4:2602800-2627600	Weak transcription	Brain Germinal Matrix	brain
12	chr4:2604200-2625200	Weak transcription	Adipose Nuclei	Adipose
13	chr4:2604200-2627000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr4:2604400-2625200	Weak transcription	Fetal Stomach	stomach
15	chr4:2604400-2627000	Weak transcription	Fetal Intestine Large	intestine
16	chr4:2604600-2627200	Weak transcription	Fetal Thymus	thymus
17	chr4:2605400-2625200	Weak transcription	Thymus	Thymus
18	chr4:2607000-2627200	Weak transcription	Primary B cells from cord blood	blood
19	chr4:2607200-2627000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:2607400-2625400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr4:2607400-2627000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:2608000-2627000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr4:2608400-2627000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr4:2609000-2627000	Weak transcription	Liver	Liver
25	chr4:2609000-2627000	Weak transcription	Fetal Kidney	kidney
26	chr4:2609200-2626400	Weak transcription	Fetal Lung	lung
27	chr4:2609200-2627000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr4:2609600-2627000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr4:2609600-2627600	Weak transcription	Fetal Brain Female	brain
30	chr4:2609800-2627000	Weak transcription	Dnd41	blood
31	chr4:2610000-2626800	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr4:2610200-2626800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:2610400-2625200	Weak transcription	Fetal Muscle Trunk	muscle
34	chr4:2610400-2626800	Weak transcription	Colon Smooth Muscle	Colon
35	chr4:2610600-2626800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr4:2610600-2627200	Weak transcription	GM12878-XiMat	blood
37	chr4:2616600-2625200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:2616600-2626600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:2616600-2627600	Weak transcription	A549	lung
40	chr4:2616600-2627800	Weak transcription	Osteobl	bone
41	chr4:2617000-2627800	Weak transcription	Rectal Smooth Muscle	rectum
42	chr4:2617200-2627000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:2617200-2627000	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr4:2618000-2626400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:2619800-2628000	Weak transcription	Small Intestine	intestine
46	chr4:2620000-2627000	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr4:2620000-2627000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr4:2620000-2627000	Weak transcription	NH-A	brain
49	chr4:2620000-2627800	Weak transcription	Aorta	Aorta
50	chr4:2620000-2628000	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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