Variant report

Variant	nsv508710
Chromosome Location	chr2:11982971-12028555
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:12007050-12007158	K562	blood:	n/a	n/a
2	ATF1	chr2:11998970-11999497	K562	blood:	n/a	n/a
3	ATF1	chr2:12007054-12007317	K562	blood:	n/a	n/a
4	ATF2	chr2:12003740-12004155	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:12002068-12002625	GM12878	blood:	n/a	n/a
6	ATF2	chr2:12003678-12004413	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:12005451-12005784	GM12878	blood:	n/a	n/a
8	ATF2	chr2:12003203-12004171	GM12878	blood:	n/a	n/a
9	ATF2	chr2:12006944-12007592	GM12878	blood:	n/a	n/a
10	ATF2	chr2:12005434-12005910	GM12878	blood:	n/a	n/a
11	ATF2	chr2:12007151-12007590	GM12878	blood:	n/a	n/a
12	ATF2	chr2:12002112-12002513	GM12878	blood:	n/a	n/a
13	ATF3	chr2:12003736-12004327	K562	blood:	n/a	n/a
14	BATF	chr2:12003804-12004098	GM12878	blood:	n/a	n/a
15	BATF	chr2:12005399-12005774	GM12878	blood:	n/a	n/a
16	BATF	chr2:12005424-12005818	GM12878	blood:	n/a	n/a
17	BATF	chr2:12002147-12002619	GM12878	blood:	n/a	n/a
18	BATF	chr2:12001149-12001504	GM12878	blood:	n/a	chr2:12001420-12001428
19	BATF	chr2:12006924-12007485	GM12878	blood:	n/a	n/a
20	BATF	chr2:12010723-12011050	GM12878	blood:	n/a	n/a
21	BATF	chr2:12002130-12002458	GM12878	blood:	n/a	n/a
22	BCL3	chr2:12007155-12007454	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:12003255-12004124	GM12878	blood:	n/a	n/a
24	BCLAF1	chr2:12002053-12002629	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:12005423-12006000	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:12006696-12007518	GM12878	blood:	n/a	n/a
27	BHLHE40	chr2:11996310-11996510	K562	blood:	n/a	n/a
28	BHLHE40	chr2:12001324-12001737	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:12003817-12004148	K562	blood:	n/a	n/a
30	BHLHE40	chr2:12010136-12010392	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:12019675-12019693	K562	blood:	n/a	n/a
32	BHLHE40	chr2:12006999-12007336	K562	blood:	n/a	n/a
33	BHLHE40	chr2:12013550-12013785	K562	blood:	n/a	n/a
34	BHLHE40	chr2:12003392-12004126	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:12008125-12008395	K562	blood:	n/a	n/a
36	CBX3	chr2:11996188-11996669	K562	blood:	n/a	n/a
37	CBX3	chr2:11998716-11999426	K562	blood:	n/a	n/a
38	CBX3	chr2:12008011-12008489	K562	blood:	n/a	n/a
39	CBX3	chr2:12003599-12004165	K562	blood:	n/a	n/a
40	CBX3	chr2:11988093-11988455	K562	blood:	n/a	n/a
41	CBX3	chr2:12000144-12000538	K562	blood:	n/a	n/a
42	CCNT2	chr2:12008134-12008372	K562	blood:	n/a	n/a
43	CCNT2	chr2:12003877-12004077	K562	blood:	n/a	n/a
44	CEBPB	chr2:12013913-12014301	Hela-S3	cervix:	n/a	chr2:12014095-12014106 chr2:12014118-12014129 chr2:12014097-12014106 chr2:12014097-12014106 chr2:12014095-12014108 chr2:12014117-12014128 chr2:12014097-12014106 chr2:12014096-12014107 chr2:12014119-12014128 chr2:12014097-12014106
45	CEBPB	chr2:12013913-12014300	K562	blood:	n/a	chr2:12014095-12014106 chr2:12014118-12014129 chr2:12014097-12014106 chr2:12014097-12014106 chr2:12014095-12014108 chr2:12014117-12014128 chr2:12014097-12014106 chr2:12014096-12014107 chr2:12014119-12014128 chr2:12014097-12014106
46	CEBPB	chr2:12003821-12004385	K562	blood:	n/a	n/a
47	CEBPB	chr2:12013558-12014335	K562	blood:	n/a	chr2:12014095-12014106 chr2:12014118-12014129 chr2:12014097-12014106 chr2:12014097-12014106 chr2:12014095-12014108 chr2:12014117-12014128 chr2:12014097-12014106 chr2:12014096-12014107 chr2:12014119-12014128 chr2:12014097-12014106
48	CEBPB	chr2:12003630-12004384	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr2:12013908-12014332	ECC-1	luminal epithelium:	n/a	chr2:12014095-12014106 chr2:12014118-12014129 chr2:12014097-12014106 chr2:12014097-12014106 chr2:12014095-12014108 chr2:12014117-12014128 chr2:12014097-12014106 chr2:12014096-12014107 chr2:12014119-12014128 chr2:12014097-12014106
50	CEBPB	chr2:12013746-12014454	A549	lung:	n/a	chr2:12014095-12014106 chr2:12014118-12014129 chr2:12014097-12014106 chr2:12014097-12014106 chr2:12014095-12014108 chr2:12014117-12014128 chr2:12014097-12014106 chr2:12014096-12014107 chr2:12014119-12014128 chr2:12014097-12014106 chr2:12014430-12014442

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11990297-11990347	HEK293	kidney:	embryo
2	chr2:12003848-12003898	HRPEpiC	eye:	n/a
3	chr2:11990393-11990443	HEK293	kidney:	embryo
4	chr2:11989691-11989741	HL-60	blood:	n/a
5	chr2:11989691-11989741	K562	blood:	n/a
6	chr2:11989691-11989741	GM06990	blood:	n/a
7	chr2:11990493-11990543	PANC-1	pancreas:	n/a
8	chr2:11990297-11990347	NHBE	bronchial:	n/a
9	chr2:12013993-12014043	LNCaP	prostate:	n/a
10	chr2:11990393-11990443	T-47D	breast:	n/a
11	chr2:12009793-12009843	SK-N-SH	brain:	n/a
12	chr2:11989691-11989741	HCM	heart:	n/a
13	chr2:12009793-12009843	SK-N-MC	brain:	n/a
14	chr2:12003848-12003898	GM12891	blood:	n/a
15	chr2:11990493-11990543	PrEC	prostate:	n/a
16	chr2:11989691-11989741	SK-N-MC	brain:	n/a
17	chr2:12009793-12009843	HRE	kidney:	n/a
18	chr2:11989691-11989741	MCF10A-Er-Src	breast:	n/a
19	chr2:11990493-11990543	GM06990	blood:	n/a
20	chr2:11990493-11990543	NH-A	brain:	n/a
21	chr2:12003848-12003898	SK-N-MC	brain:	n/a
22	chr2:12013993-12014043	SK-N-SH	brain:	n/a
23	chr2:12009793-12009843	BJ	skin:	n/a
24	chr2:12009793-12009843	AG04450	lung:	fetal
25	chr2:12013993-12014043	Jurkat	blood:	n/a
26	chr2:11990493-11990543	HCPEpiC	choroid plexus:	n/a
27	chr2:11990297-11990347	Caco-2	colon:	n/a
28	chr2:12003848-12003898	AG09319	gingival:	n/a
29	chr2:12013993-12014043	U87	brain:	n/a
30	chr2:11989691-11989741	HRE	kidney:	n/a
31	chr2:12003848-12003898	HIPEpiC	eye:	n/a
32	chr2:12013993-12014043	HCPEpiC	choroid plexus:	n/a
33	chr2:11990297-11990347	AG04450	lung:	fetal
34	chr2:12003848-12003898	SK-N-SH	brain:	n/a
35	chr2:11990493-11990543	NHDF-neo	bronchial:	n/a
36	chr2:11989691-11989741	NT2-D1	testis:	n/a
37	chr2:11990493-11990543	CMK	blood:	n/a
38	chr2:11990393-11990443	GM19239	blood:	n/a
39	chr2:12003848-12003898	HEK293	kidney:	embryo
40	chr2:11990297-11990347	GM12878	blood:	n/a
41	chr2:11990297-11990347	MCF10A-Er-Src	breast:	n/a
42	chr2:11989691-11989741	SKMC	muscle:	n/a
43	chr2:11990297-11990347	HUVEC	blood vessel:	n/a
44	chr2:11989691-11989741	AoSMC	blood vessel:	n/a
45	chr2:11990393-11990443	PrEC	prostate:	n/a
46	chr2:11990297-11990347	U87	brain:	n/a
47	chr2:12003848-12003898	U87	brain:	n/a
48	chr2:11990493-11990543	HCF	heart:	n/a
49	chr2:12013993-12014043	SAEC	small airway:	n/a
50	chr2:12003848-12003898	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:12003738..12004249-chr2:12857486..12858298,2	MCF-7	breast:
2	chr2:11987561..11990167-chr2:11991624..11995278,3	K562	blood:
3	chr2:12013801..12015397-chr2:12017049..12018677,2	K562	blood:
4	chr2:12008707..12011170-chr2:12011267..12015363,3	K562	blood:
5	chr2:12003424..12004525-chr2:12090949..12092302,3	K562	blood:
6	chr2:12012584..12014369-chr2:12014479..12016672,2	K562	blood:
7	chr2:11969450..11970064-chr2:12003506..12004520,3	K562	blood:
8	chr2:12003845..12005351-chr2:12005598..12008038,2	K562	blood:
9	chr2:12004373..12006571-chr2:12008587..12010447,2	MCF-7	breast:
10	chr2:12012584..12014369-chr2:12014479..12016672,2	K562	blood:
11	chr2:12003663..12004307-chr2:13146720..13147387,2	MCF-7	breast:
12	chr2:12013801..12015397-chr2:12017049..12018677,2	K562	blood:
13	chr2:12008707..12011170-chr2:12011267..12015363,3	K562	blood:
14	chr2:11988582..11990167-chr2:11992928..11995278,2	K562	blood:
15	chr2:12003538..12004294-chr2:12091341..12091981,2	MCF-7	breast:
16	chr2:12003714..12004353-chr2:12188666..12189311,2	MCF-7	breast:
17	chr2:12003722..12005269-chr2:12316727..12318905,2	K562	blood:
18	chr2:12003510..12004337-chr2:12188494..12189188,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPIN1-1	chr2:12005976-12006411	NONHSAT069206
2	lnc-LPIN1-1	chr2:12005976-12006410	XLOC_001353
3	lnc-LPIN1-1	chr2:11988748-11988870	XLOC_001353
4	lnc-LPIN1-1	chr2:12005638-12005889	NONHSAT069206
5	lnc-LPIN1-1	chr2:12005976-12006302	XLOC_001353
6	lnc-LPIN1-1	chr2:11996599-11996622	XLOC_001353
7	lnc-LPIN1-3	chr2:12016638-12016845	NONHSAT069208
8	lnc-LPIN1-2	chr2:12000104-12001333	NONHSAT069205

Variant related genes	Relation type
ENSG00000224184	TF binding region
ENSG00000224184	CpG island
ENSG00000224184	chromatin interactions
ENSG00000225649	chromatin interactions
NF1	miRNA target sites
PHLDA2	miRNA target sites

Extended variants
information (count: 1703 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556651412	chr2:11983042-11983043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556677309	chr2:11983063-11983064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188865307	chr2:11983082-11983083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542803525	chr2:11983122-11983123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141541580	chr2:11983131-11983132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181656183	chr2:11983143-11983144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186228497	chr2:11983164-11983165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540158293	chr2:11983197-11983198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34665807	chr2:11983238-11983239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371669637	chr2:11983261-11983262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377549425	chr2:11983265-11983266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1012566	chr2:11983283-11983284	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs536282825	chr2:11983305-11983306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531967164	chr2:11983333-11983334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201542442	chr2:11983373-11983374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567640170	chr2:11983377-11983378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536066359	chr2:11983402-11983403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562602661	chr2:11983404-11983405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12470633	chr2:11983416-11983417	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548725566	chr2:11983429-11983430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550844903	chr2:11983430-11983431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115511215	chr2:11983494-11983495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552879207	chr2:11983518-11983519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571193917	chr2:11983521-11983522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538232138	chr2:11983557-11983558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569543542	chr2:11983562-11983563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574828100	chr2:11983571-11983572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60887696	chr2:11983574-11983575	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs74756448	chr2:11983576-11983577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572930265	chr2:11983620-11983621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74377272	chr2:11983637-11983638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374180535	chr2:11983652-11983653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189327820	chr2:11983667-11983668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78028126	chr2:11983676-11983677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180697141	chr2:11983690-11983691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578160370	chr2:11983699-11983700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186005365	chr2:11983707-11983708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536830090	chr2:11983826-11983827	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs115936891	chr2:11983855-11983856	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs527869720	chr2:11983882-11983883	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs191302811	chr2:11983899-11983900	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs182895680	chr2:11983940-11983941	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs75465793	chr2:11984075-11984076	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs398059949	chr2:11984076-11984077	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs532045818	chr2:11984081-11984082	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs4553790	chr2:11984089-11984090	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs552651523	chr2:11984169-11984170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34194124	chr2:11984182-11984183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186706752	chr2:11984203-11984204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142724248	chr2:11984217-11984218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	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
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11975600-11983200	Weak transcription	Right Atrium	heart
2	chr2:11978800-11987800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:11982400-11983600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:11987800-11988000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:11988000-11988800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:11988200-11988400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:11988600-11989200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
8	chr2:11988800-11989400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:11988800-11989600	Enhancers	Brain Substantia Nigra	brain
10	chr2:11989000-11989400	Bivalent Enhancer	Brain Hippocampus Middle	brain
11	chr2:11989000-11989400	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr2:11989000-11989600	Enhancers	Brain Cingulate Gyrus	brain
13	chr2:11989000-11989800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr2:11989200-11989400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:11989200-11989400	Enhancers	Brain Anterior Caudate	brain
16	chr2:11989200-11989400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr2:11989200-11989600	Enhancers	Brain Angular Gyrus	brain
18	chr2:11989200-11990000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:11989200-11992400	Weak transcription	Primary B cells from peripheral blood	blood
20	chr2:11989400-11989600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:11989400-11989600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:11989400-11989600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
23	chr2:11989400-11989600	Enhancers	NH-A	brain
24	chr2:11989400-11990000	Flanking Active TSS	Brain Anterior Caudate	brain
25	chr2:11989400-11990000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
26	chr2:11989400-11990600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:11989400-11990600	Active TSS	Osteobl	bone
28	chr2:11989600-11989800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:11989600-11989800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr2:11989600-11989800	Bivalent Enhancer	Fetal Brain Male	brain
31	chr2:11989600-11989800	Flanking Active TSS	NH-A	brain
32	chr2:11989600-11990000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:11989600-11990000	Flanking Active TSS	Brain Angular Gyrus	brain
34	chr2:11989600-11990000	Flanking Active TSS	Brain Cingulate Gyrus	brain
35	chr2:11989600-11990000	Flanking Active TSS	Brain Substantia Nigra	brain
36	chr2:11989600-11990000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
37	chr2:11989600-11990200	Flanking Active TSS	Brain Hippocampus Middle	brain
38	chr2:11989600-11990400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
39	chr2:11989600-11990600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:11989600-11990600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:11989800-11990000	Active TSS	NH-A	brain
42	chr2:11989800-11990400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:11989800-11990400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr2:11989800-11990400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr2:11990000-11990200	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
46	chr2:11990000-11990200	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
47	chr2:11990000-11990400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr2:11990000-11990400	Active TSS	Brain Angular Gyrus	brain
49	chr2:11990000-11990400	Active TSS	Brain Cingulate Gyrus	brain
50	chr2:11990000-11990400	Enhancers	Brain Germinal Matrix	brain

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