Variant report

Variant	nsv2696
Chromosome Location	chr2:39988381-40033288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:782)
CpG islands
(count:671)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:782 , 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	ARID3A	chr2:40005724-40006822	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:40009729-40010336	K562	blood:	n/a	n/a
3	ARID3A	chr2:40008059-40008584	K562	blood:	n/a	n/a
4	ARID3A	chr2:40008118-40008121	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:40005350-40005786	K562	blood:	n/a	n/a
6	ATF1	chr2:40009768-40010682	K562	blood:	n/a	n/a
7	ATF3	chr2:40006159-40006496	HepG2	liver:	n/a	chr2:40006399-40006419
8	ATF3	chr2:40010278-40010499	K562	blood:	n/a	chr2:40010448-40010457 chr2:40010419-40010428
9	BACH1	chr2:40009533-40009999	K562	blood:	n/a	n/a
10	BACH1	chr2:39998576-39998577	K562	blood:	n/a	n/a
11	BACH1	chr2:40026039-40026076	K562	blood:	n/a	n/a
12	BACH1	chr2:40005996-40006438	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr2:40008233-40008413	K562	blood:	n/a	n/a
14	BCL3	chr2:40010306-40010883	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:40010283-40010625	HepG2	liver:	n/a	chr2:40010442-40010463 chr2:40010448-40010457 chr2:40010446-40010459 chr2:40010449-40010458 chr2:40010413-40010434 chr2:40010448-40010457
16	BHLHE40	chr2:40006150-40006705	HepG2	liver:	n/a	n/a
17	BHLHE40	chr2:40009871-40010944	K562	blood:	n/a	chr2:40010442-40010463 chr2:40010448-40010457 chr2:40010446-40010459 chr2:40010449-40010458 chr2:40010413-40010434 chr2:40010448-40010457
18	BHLHE40	chr2:40006144-40006601	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:40006244-40006476	A549	lung:	n/a	n/a
20	BHLHE40	chr2:40005730-40007145	K562	blood:	n/a	n/a
21	CBX3	chr2:40007750-40008704	K562	blood:	n/a	n/a
22	CBX3	chr2:40017638-40017847	K562	blood:	n/a	n/a
23	CBX3	chr2:40017551-40017840	K562	blood:	n/a	n/a
24	CBX3	chr2:40009992-40010630	K562	blood:	n/a	n/a
25	CBX3	chr2:40005981-40006949	K562	blood:	n/a	n/a
26	CCNT2	chr2:40006079-40006710	K562	blood:	n/a	n/a
27	CCNT2	chr2:40007710-40008576	K562	blood:	n/a	n/a
28	CEBPB	chr2:40006636-40006699	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:40019411-40019643	K562	blood:	n/a	n/a
30	CEBPB	chr2:40008177-40008178	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:40008839-40009169	IMR90	lung:	n/a	chr2:40008985-40008998 chr2:40008986-40008997 chr2:40008985-40008996
32	CEBPB	chr2:39997911-39998111	A549	lung:	n/a	chr2:39998009-39998026
33	CEBPB	chr2:39996659-39996871	HepG2	liver:	n/a	chr2:39996792-39996803
34	CEBPB	chr2:40002725-40002987	K562	blood:	n/a	chr2:40002969-40002982
35	CEBPB	chr2:40006265-40006313	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr2:39996659-39996878	Hela-S3	cervix:	n/a	chr2:39996792-39996803
37	CEBPB	chr2:40002987-40003009	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:40014356-40014578	HepG2	liver:	n/a	chr2:40014437-40014448
39	CEBPB	chr2:40008797-40009157	K562	blood:	n/a	chr2:40008985-40008998 chr2:40008986-40008997 chr2:40008985-40008996
40	CEBPB	chr2:39996657-39996965	H1-hESC	embryonic stem cell:	n/a	chr2:39996792-39996803
41	CEBPB	chr2:39996728-39996834	HepG2	liver:	n/a	chr2:39996792-39996803
42	CEBPB	chr2:39999526-39999900	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:40008756-40009176	HepG2	liver:	n/a	chr2:40008985-40008998 chr2:40008986-40008997 chr2:40008985-40008996
44	CEBPB	chr2:40008802-40009186	K562	blood:	n/a	chr2:40008985-40008998 chr2:40008986-40008997 chr2:40008985-40008996
45	CEBPB	chr2:39996732-39996956	MCF-7	breast:	n/a	chr2:39996792-39996803
46	CEBPB	chr2:40033097-40033413	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:40008783-40009170	A549	lung:	n/a	chr2:40008985-40008998 chr2:40008986-40008997 chr2:40008985-40008996
48	CEBPB	chr2:39996787-39996867	K562	blood:	n/a	chr2:39996792-39996803
49	CEBPB	chr2:39997898-39998106	HepG2	liver:	n/a	chr2:39998009-39998026
50	CEBPD	chr2:40006155-40006500	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40009501-40009551	HRE	kidney:	n/a
2	chr2:40006217-40006267	GM06990	blood:	n/a
3	chr2:40006334-40006384	ovcar-3	ovarian:	n/a
4	chr2:39999331-39999381	HCF	heart:	n/a
5	chr2:39999331-39999381	HNPCEpiC	eye:	n/a
6	chr2:40006891-40006941	AG04450	lung:	fetal
7	chr2:40001222-40001272	HRPEpiC	eye:	n/a
8	chr2:40007061-40007111	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:40006561-40006611	ECC-1	luminal epithelium:	n/a
10	chr2:40006334-40006384	HCM	heart:	n/a
11	chr2:40006561-40006611	NHDF-neo	bronchial:	n/a
12	chr2:40006543-40006593	CMK	blood:	n/a
13	chr2:39999331-39999381	IMR90	lung:	fetal
14	chr2:40007061-40007111	AG04449	skin:	fetal
15	chr2:39999331-39999381	NHDF-neo	bronchial:	n/a
16	chr2:40006891-40006941	T-47D	breast:	n/a
17	chr2:40001222-40001272	HIPEpiC	eye:	n/a
18	chr2:40006891-40006941	HNPCEpiC	eye:	n/a
19	chr2:40001222-40001272	K562	blood:	n/a
20	chr2:40006561-40006611	HMEC	breast:	n/a
21	chr2:40005788-40005838	RPTEC	kidney:	n/a
22	chr2:40006561-40006611	GM19239	blood:	n/a
23	chr2:39999331-39999381	HMEC	breast:	n/a
24	chr2:40006891-40006941	HL-60	blood:	n/a
25	chr2:39999331-39999381	BJ	skin:	n/a
26	chr2:40006543-40006593	BE2_C	brain:	n/a
27	chr2:40006543-40006593	HAEpiC	amniotic membrane:	n/a
28	chr2:40006561-40006611	HRE	kidney:	n/a
29	chr2:40006334-40006384	GM12878	blood:	n/a
30	chr2:40006217-40006267	AG04449	skin:	fetal
31	chr2:40006217-40006267	HCPEpiC	choroid plexus:	n/a
32	chr2:40009501-40009551	U87	brain:	n/a
33	chr2:40001222-40001272	T-47D	breast:	n/a
34	chr2:40006314-40006364	NHDF-neo	bronchial:	n/a
35	chr2:40006543-40006593	AG04450	lung:	fetal
36	chr2:40006561-40006611	ovcar-3	ovarian:	n/a
37	chr2:40007061-40007111	HMEC	breast:	n/a
38	chr2:40006314-40006364	ProgFib	skin:	n/a
39	chr2:39999331-39999381	HRE	kidney:	n/a
40	chr2:40006891-40006941	RPTEC	kidney:	n/a
41	chr2:40006334-40006384	NHDF-neo	bronchial:	n/a
42	chr2:40007061-40007111	PANC-1	pancreas:	n/a
43	chr2:40006334-40006384	PrEC	prostate:	n/a
44	chr2:40006891-40006941	CMK	blood:	n/a
45	chr2:40006561-40006611	Caco-2	colon:	n/a
46	chr2:40006543-40006593	HEK293	kidney:	embryo
47	chr2:40006891-40006941	SK-N-SH	brain:	n/a
48	chr2:40006891-40006941	AG10803	skin:	n/a
49	chr2:39999331-39999381	Hela-S3	cervix:	n/a
50	chr2:40006314-40006364	T-47D	breast:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:39956738..39958463-chr2:40003948..40005760,2	K562	blood:
2	chr2:39541547..39543631-chr2:39997665..39999926,2	K562	blood:
3	chr2:39961424..39963272-chr2:40004019..40005990,2	K562	blood:
4	chr2:39999247..40000027-chr6:14903249..14904079,2	MCF-7	breast:
5	chr2:39996045..39997746-chr3:50647710..50649775,2	MCF-7	breast:
6	chr2:40026913..40028511-chr2:40029938..40031858,2	MCF-7	breast:
7	chr2:39981401..39983374-chr2:39998682..40001306,2	K562	blood:
8	chr2:39662097..39664715-chr2:39993095..39995663,2	K562	blood:
9	chr2:40001641..40002163-chr3:101263430..101263949,2	MCF-7	breast:
10	chr2:39997806..40003955-chr2:40003961..40007756,6	MCF-7	breast:
11	chr2:40005279..40007772-chr2:40018373..40020937,3	K562	blood:
12	chr2:40026913..40028511-chr2:40029938..40031858,2	MCF-7	breast:
13	chr2:40002526..40004161-chr2:40026691..40028627,2	K562	blood:
14	chr2:40005279..40008048-chr2:40019437..40021577,2	K562	blood:
15	chr2:40002526..40004161-chr2:40026691..40028627,2	K562	blood:
16	chr2:39975048..39977790-chr2:39997360..39998912,2	K562	blood:
17	chr2:39739040..39741917-chr2:40004865..40006467,2	K562	blood:
18	chr2:39909390..39911752-chr2:39999764..40002592,2	K562	blood:
19	chr2:39986915..39988908-chr2:40004711..40006490,2	MCF-7	breast:
20	chr2:39990318..39993221-chr2:40005644..40007529,2	MCF-7	breast:
21	chr14:105957090..105957996-chr2:40006019..40006535,2	Hela-S3	cervix:
22	chr2:39987488..39989422-chr2:39993351..39995786,2	MCF-7	breast:
23	chr2:40006031..40007593-chr2:40009599..40011683,2	MCF-7	breast:
24	chr2:40004284..40008257-chr2:40008263..40012278,6	MCF-7	breast:
25	chr2:40000146..40001663-chr3:101262826..101264500,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40003494-40003533	ucscGeneNc_uc002rrw_2

No data

Variant related genes	Relation type
SLC8A1-AS1	TF binding region
THUMPD2	TF binding region
SLC8A1-AS1	CpG island
THUMPD2	CpG island
ENSG00000114737	chromatin interactions
ENSG00000114738	chromatin interactions
ENSG00000138050	chromatin interactions
ENSG00000231312	chromatin interactions
ENSG00000011566	chromatin interactions
ENSG00000185347	chromatin interactions

Extended variants
information (count: 2029 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2029 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568253786	chr2:39988395-39988396	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115749704	chr2:39988402-39988403	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547594859	chr2:39988414-39988415	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376984934	chr2:39988419-39988420	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs369266584	chr2:39988440-39988441	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs143247738	chr2:39988471-39988472	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs578006539	chr2:39988478-39988479	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs200258471	chr2:39988479-39988480	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374861467	chr2:39988489-39988490	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369257127	chr2:39988491-39988492	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141776919	chr2:39988494-39988495	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142811748	chr2:39988501-39988502	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373324639	chr2:39988502-39988503	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147366386	chr2:39988519-39988520	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569674526	chr2:39988527-39988528	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs537090300	chr2:39988578-39988579	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368580431	chr2:39988590-39988591	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs555492317	chr2:39988594-39988595	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184163745	chr2:39988607-39988608	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573816504	chr2:39988611-39988612	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573908853	chr2:39988629-39988630	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532381976	chr2:39988682-39988683	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554358500	chr2:39988688-39988689	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572608395	chr2:39988689-39988690	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546479609	chr2:39988701-39988702	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564487267	chr2:39988702-39988703	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs3732122	chr2:39988703-39988704	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs58750710	chr2:39988711-39988712	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs148590193	chr2:39988730-39988731	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142767915	chr2:39988739-39988740	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529409102	chr2:39988760-39988761	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547242320	chr2:39988792-39988793	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs3732121	chr2:39988804-39988805	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533034227	chr2:39988859-39988860	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551652682	chr2:39988917-39988918	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs570006527	chr2:39988922-39988923	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189393514	chr2:39988941-39988942	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146540200	chr2:39988963-39988964	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567924192	chr2:39988966-39988967	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567342780	chr2:39989018-39989019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs534724431	chr2:39989102-39989103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141251674	chr2:39989109-39989110	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572596015	chr2:39989161-39989162	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6753279	chr2:39989244-39989245	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558011297	chr2:39989278-39989279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs180982887	chr2:39989282-39989283	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs997976	chr2:39989355-39989356	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs571746778	chr2:39989381-39989382	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184862463	chr2:39989404-39989405	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs118043682	chr2:39989465-39989466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39962200-39993200	Strong transcription	Liver	Liver
2	chr2:39965200-40005000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:39965200-40005400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:39967600-39991200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr2:39969800-39999800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr2:39971000-39999800	Weak transcription	Right Ventricle	heart
7	chr2:39971600-39998800	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:39972400-39998600	Strong transcription	HMEC	breast
9	chr2:39972400-39998800	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr2:39973000-39998800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:39974200-39998600	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:39974600-39994000	Strong transcription	Fetal Thymus	thymus
13	chr2:39975000-39998400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:39975000-39999800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr2:39975200-39989000	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr2:39975200-39989800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:39975200-39993800	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr2:39975400-39997000	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr2:39975800-39989400	Strong transcription	A549	lung
20	chr2:39975800-39994600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr2:39976000-39988600	Strong transcription	HepG2	liver
22	chr2:39976000-39988800	Strong transcription	Duodenum Mucosa	Duodenum
23	chr2:39976000-39989800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:39976000-39993200	Strong transcription	Placenta	Placenta
25	chr2:39976000-39993400	Strong transcription	Adipose Nuclei	Adipose
26	chr2:39976200-39995400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:39976200-39998800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr2:39976400-39992000	Strong transcription	K562	blood
29	chr2:39976600-39992000	Strong transcription	Primary B cells from cord blood	blood
30	chr2:39976800-39988800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr2:39976800-39999000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:39977000-39990000	Strong transcription	Fetal Muscle Leg	muscle
33	chr2:39977200-39989000	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr2:39978200-39988600	Strong transcription	GM12878-XiMat	blood
35	chr2:39978600-40000000	Weak transcription	Fetal Heart	heart
36	chr2:39979800-39989200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:39980000-39992000	Strong transcription	Primary T cells from cord blood	blood
38	chr2:39980400-39989400	Strong transcription	HSMMtube	muscle
39	chr2:39982600-39992600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr2:39982800-39988600	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr2:39982800-39992000	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:39983000-39989600	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr2:39983000-39992000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:39983000-39999200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:39983200-39994000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:39983400-39989400	Strong transcription	Osteobl	bone
47	chr2:39983600-39994200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:39983600-39996400	Strong transcription	NHDF-Ad	bronchial
49	chr2:39983600-39998600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:39983600-39999000	Strong transcription	HSMM	muscle

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