Variant report

Variant	nsv999704
Chromosome Location	chr2:12153766-12243960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1498)
CpG islands
(count:305)
Chromatin interactive
region (count:32)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:12200260-12200798	K562	blood:	n/a	n/a
2	ARID3A	chr2:12214078-12214735	K562	blood:	n/a	n/a
3	ARID3A	chr2:12215220-12215309	K562	blood:	n/a	n/a
4	ARID3A	chr2:12199810-12200006	K562	blood:	n/a	n/a
5	ARID3A	chr2:12190510-12190853	K562	blood:	n/a	n/a
6	ARID3A	chr2:12224320-12224487	K562	blood:	n/a	n/a
7	ATF1	chr2:12214190-12214878	K562	blood:	n/a	n/a
8	ATF1	chr2:12224211-12224502	K562	blood:	n/a	n/a
9	ATF1	chr2:12190507-12190860	K562	blood:	n/a	n/a
10	ATF2	chr2:12216889-12217266	GM12878	blood:	n/a	n/a
11	ATF2	chr2:12211462-12211854	GM12878	blood:	n/a	n/a
12	ATF2	chr2:12211397-12211889	GM12878	blood:	n/a	n/a
13	ATF2	chr2:12185775-12186473	GM12878	blood:	n/a	n/a
14	ATF2	chr2:12172424-12173014	GM12878	blood:	n/a	n/a
15	ATF2	chr2:12197329-12198127	GM12878	blood:	n/a	n/a
16	ATF2	chr2:12184828-12185404	GM12878	blood:	n/a	n/a
17	ATF2	chr2:12214201-12214689	GM12878	blood:	n/a	n/a
18	ATF2	chr2:12185827-12186453	GM12878	blood:	n/a	n/a
19	ATF2	chr2:12172549-12173049	GM12878	blood:	n/a	n/a
20	ATF2	chr2:12174320-12175009	GM12878	blood:	n/a	n/a
21	ATF3	chr2:12200022-12200450	K562	blood:	n/a	n/a
22	ATF3	chr2:12214161-12214796	K562	blood:	n/a	chr2:12214471-12214491
23	BACH1	chr2:12242794-12243109	K562	blood:	n/a	n/a
24	BACH1	chr2:12197730-12197944	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr2:12197554-12197870	GM12878	blood:	n/a	n/a
26	BATF	chr2:12215757-12216021	GM12878	blood:	n/a	n/a
27	BATF	chr2:12216963-12217290	GM12878	blood:	n/a	n/a
28	BATF	chr2:12190537-12190844	GM12878	blood:	n/a	n/a
29	BATF	chr2:12214284-12214640	GM12878	blood:	n/a	chr2:12214480-12214493
30	BATF	chr2:12215793-12215994	GM12878	blood:	n/a	n/a
31	BATF	chr2:12185988-12186297	GM12878	blood:	n/a	n/a
32	BATF	chr2:12172595-12172856	GM12878	blood:	n/a	n/a
33	BATF	chr2:12185846-12186367	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:12197485-12197956	GM12878	blood:	n/a	chr2:12197932-12197941
35	BCL11A	chr2:12211422-12211829	GM12878	blood:	n/a	chr2:12211643-12211652
36	BCL11A	chr2:12223232-12223426	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr2:12214363-12214649	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:12214269-12214720	GM12878	blood:	n/a	chr2:12214307-12214314
39	BCL11A	chr2:12185952-12186265	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:12211508-12211807	GM12878	blood:	n/a	chr2:12211643-12211652
41	BCL11A	chr2:12197592-12197896	GM12878	blood:	n/a	n/a
42	BCL3	chr2:12237953-12238250	GM12878	blood:	n/a	n/a
43	BCL3	chr2:12197564-12197985	GM12878	blood:	n/a	chr2:12197932-12197941
44	BCL3	chr2:12228185-12228478	GM12878	blood:	n/a	n/a
45	BCLAF1	chr2:12184910-12185348	GM12878	blood:	n/a	n/a
46	BCLAF1	chr2:12185792-12186643	GM12878	blood:	n/a	n/a
47	BCLAF1	chr2:12172416-12173028	GM12878	blood:	n/a	n/a
48	BCLAF1	chr2:12214128-12214778	K562	blood:	n/a	chr2:12214307-12214314
49	BCLAF1	chr2:12190397-12190921	GM12878	blood:	n/a	n/a
50	BCLAF1	chr2:12197493-12198087	GM12878	blood:	n/a	chr2:12197932-12197941

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:12163118-12163168	T-47D	breast:	n/a
2	chr2:12223636-12223686	ProgFib	skin:	n/a
3	chr2:12163619-12163669	AG09309	skin:	n/a
4	chr2:12163118-12163168	NHBE	bronchial:	n/a
5	chr2:12173618-12173668	SAEC	small airway:	n/a
6	chr2:12223636-12223686	HL-60	blood:	n/a
7	chr2:12237012-12237062	AG09319	gingival:	n/a
8	chr2:12163118-12163168	NB4	blood:	n/a
9	chr2:12223636-12223686	ovcar-3	ovarian:	n/a
10	chr2:12237012-12237062	AoSMC	blood vessel:	n/a
11	chr2:12237012-12237062	HRCEpiC	kidney:	n/a
12	chr2:12237012-12237062	SK-N-SH	brain:	n/a
13	chr2:12163619-12163669	SKMC	muscle:	n/a
14	chr2:12223636-12223686	T-47D	breast:	n/a
15	chr2:12237012-12237062	PrEC	prostate:	n/a
16	chr2:12237012-12237062	HEK293	kidney:	embryo
17	chr2:12223636-12223686	HAEpiC	amniotic membrane:	n/a
18	chr2:12223636-12223686	NB4	blood:	n/a
19	chr2:12237012-12237062	K562	blood:	n/a
20	chr2:12173618-12173668	RPTEC	kidney:	n/a
21	chr2:12237012-12237062	U87	brain:	n/a
22	chr2:12237012-12237062	HEEpiC	esophagus:	n/a
23	chr2:12223636-12223686	GM12878	blood:	n/a
24	chr2:12173618-12173668	Hepatocyte	liver:	n/a
25	chr2:12163619-12163669	GM12892	blood:	n/a
26	chr2:12163118-12163168	GM12878	blood:	n/a
27	chr2:12163118-12163168	MCF10A-Er-Src	breast:	n/a
28	chr2:12237012-12237062	HAEpiC	amniotic membrane:	n/a
29	chr2:12173618-12173668	Jurkat	blood:	n/a
30	chr2:12163118-12163168	HUVEC	blood vessel:	n/a
31	chr2:12237012-12237062	BJ	skin:	n/a
32	chr2:12163118-12163168	HIPEpiC	eye:	n/a
33	chr2:12173618-12173668	AG09309	skin:	n/a
34	chr2:12173618-12173668	PrEC	prostate:	n/a
35	chr2:12223636-12223686	NT2-D1	testis:	n/a
36	chr2:12163118-12163168	ovcar-3	ovarian:	n/a
37	chr2:12223636-12223686	BE2_C	brain:	n/a
38	chr2:12223636-12223686	SAEC	small airway:	n/a
39	chr2:12173618-12173668	HCF	heart:	n/a
40	chr2:12163619-12163669	HAEpiC	amniotic membrane:	n/a
41	chr2:12237012-12237062	HL-60	blood:	n/a
42	chr2:12173618-12173668	H1-hESC	embryonic stem cell:	embryo
43	chr2:12223636-12223686	HNPCEpiC	eye:	n/a
44	chr2:12223636-12223686	AoSMC	blood vessel:	n/a
45	chr2:12173618-12173668	BE2_C	brain:	n/a
46	chr2:12237012-12237062	MCF-7	breast:	n/a
47	chr2:12163619-12163669	LNCaP	prostate:	n/a
48	chr2:12163619-12163669	HRE	kidney:	n/a
49	chr2:12237012-12237062	AG04449	skin:	fetal
50	chr2:12163118-12163168	AoSMC	blood vessel:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
2	chr2:12202416..12205140-chr2:12205945..12209401,3	K562	blood:
3	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
4	chr2:12240589..12242524-chr2:12244995..12247436,2	K562	blood:
5	chr2:12155340..12157815-chr2:12177536..12179462,2	MCF-7	breast:
6	chr2:12142937..12145403-chr2:12173680..12175523,2	K562	blood:
7	chr2:12149476..12151758-chr2:12152643..12155527,2	K562	blood:
8	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
9	chr2:12219592..12223181-chr2:12244088..12246187,3	K562	blood:
10	chr2:12233977..12235737-chr2:12241751..12243264,2	K562	blood:
11	chr2:12200110..12202419-chr2:12206699..12209506,2	K562	blood:
12	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
13	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
14	chr2:12233977..12235737-chr2:12241751..12243264,2	K562	blood:
15	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
16	chr2:12180693..12182626-chr2:12190865..12193405,2	K562	blood:
17	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
18	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
19	chr2:12146656..12149397-chr2:12152065..12154381,3	K562	blood:
20	chr2:12194778..12196811-chr2:12221641..12223390,2	K562	blood:
21	chr2:12155340..12157815-chr2:12177536..12179462,2	MCF-7	breast:
22	chr2:12176844..12179370-chr2:12184810..12186635,2	MCF-7	breast:
23	chr2:12176844..12179370-chr2:12184810..12186635,2	MCF-7	breast:
24	chr2:12003510..12004337-chr2:12188494..12189188,2	MCF-7	breast:
25	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
26	chr2:12202416..12205140-chr2:12205945..12209401,3	K562	blood:
27	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
28	chr2:12200110..12202419-chr2:12206699..12209506,2	K562	blood:
29	chr2:12194778..12196811-chr2:12221641..12223390,2	K562	blood:
30	chr2:12146656..12149397-chr2:12152065..12154039,2	K562	blood:
31	chr2:12180693..12182626-chr2:12190865..12193405,2	K562	blood:
32	chr2:12003714..12004353-chr2:12188666..12189311,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GREB1-10	chr2:12164161-12164261	NONHSAT069216
2	lnc-GREB1-10	chr2:12164395-12164528	NONHSAT069216
3	lnc-LPIN1-1	chr2:12223575-12223744	ENSG00000224184
4	lnc-GREB1-10	chr2:12188883-12189162	NONHSAT069209
5	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069196
6	lnc-GREB1-10	chr2:12188883-12189125	NONHSAT069216
7	lnc-LPIN1-1	chr2:12223575-12223743	NR_110198
8	lnc-GREB1-10	chr2:12164395-12164528	NONHSAT069209
9	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069210

No data

Variant related genes	Relation type
ENSG00000238503	TF binding region
ENSG00000224184	TF binding region
ENSG00000238503	CpG island
ENSG00000224184	CpG island
ENSG00000224184	chromatin interactions

Extended variants
information (count: 3579 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3579 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs751579	chr2:12153766-12153767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531750388	chr2:12153783-12153784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568762989	chr2:12153825-12153826	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs140306942	chr2:12153864-12153865	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562246484	chr2:12153903-12153904	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544223596	chr2:12153968-12153969	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534245863	chr2:12153999-12154000	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs1440037	chr2:12154028-12154029	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566554551	chr2:12154091-12154092	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145344300	chr2:12154109-12154110	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552069967	chr2:12154111-12154112	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570087747	chr2:12154119-12154120	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs529844517	chr2:12154123-12154124	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537477128	chr2:12154126-12154127	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs873200	chr2:12154191-12154192	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568187815	chr2:12154210-12154211	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs11692044	chr2:12154230-12154231	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs75437976	chr2:12154248-12154249	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs76464310	chr2:12154255-12154256	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs61580555	chr2:12154305-12154306	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532102113	chr2:12154306-12154307	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572559093	chr2:12154321-12154322	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377488383	chr2:12154354-12154355	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558506818	chr2:12154363-12154364	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114934306	chr2:12154429-12154430	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs568800095	chr2:12154455-12154456	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs111895936	chr2:12154506-12154507	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs193211878	chr2:12154546-12154547	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs542045545	chr2:12154572-12154573	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs185562732	chr2:12154604-12154605	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs529343950	chr2:12154616-12154617	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs148035027	chr2:12154626-12154627	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs560261151	chr2:12154639-12154640	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs73918410	chr2:12154640-12154641	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs188139615	chr2:12154685-12154686	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs570445774	chr2:12154709-12154710	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs141714795	chr2:12154717-12154718	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs527557641	chr2:12154724-12154725	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs549411926	chr2:12154733-12154734	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs73918411	chr2:12154757-12154758	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs150593309	chr2:12154777-12154778	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs138630180	chr2:12154787-12154788	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs566233967	chr2:12154805-12154806	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369139695	chr2:12154901-12154902	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372638976	chr2:12154904-12154905	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376951150	chr2:12154909-12154910	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73918413	chr2:12154933-12154934	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs374913938	chr2:12155019-12155020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180998117	chr2:12155031-12155032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555695918	chr2:12155051-12155052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	19270706	CNVD
Prostate cancer	19258504	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:12147400-12154000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:12147800-12153800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr2:12149200-12154000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:12149800-12154200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:12150000-12153800	Weak transcription	NHDF-Ad	bronchial
6	chr2:12150000-12154000	Weak transcription	K562	blood
7	chr2:12150000-12154000	Weak transcription	Osteobl	bone
8	chr2:12150200-12153800	Weak transcription	NHLF	lung
9	chr2:12150400-12153800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr2:12150400-12153800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:12150400-12154000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr2:12150800-12153800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr2:12151200-12153800	Weak transcription	HSMMtube	muscle
14	chr2:12151800-12154000	Weak transcription	Fetal Muscle Leg	muscle
15	chr2:12152800-12155000	Enhancers	GM12878-XiMat	blood
16	chr2:12153200-12153800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr2:12153600-12155000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr2:12153600-12155000	Enhancers	Primary B cells from cord blood	blood
19	chr2:12153600-12155600	Enhancers	HSMM	muscle
20	chr2:12153800-12154200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
21	chr2:12153800-12154200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr2:12153800-12155000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:12153800-12155000	Enhancers	Primary B cells from peripheral blood	blood
24	chr2:12153800-12155000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:12153800-12155000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr2:12153800-12155200	Enhancers	NHDF-Ad	bronchial
27	chr2:12153800-12155200	Enhancers	NHLF	lung
28	chr2:12153800-12155400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr2:12153800-12155400	Enhancers	HSMMtube	muscle
30	chr2:12154000-12154600	Enhancers	K562	blood
31	chr2:12154000-12154800	Enhancers	Spleen	Spleen
32	chr2:12154000-12155000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:12154000-12155000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr2:12154000-12155000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr2:12154000-12155000	Enhancers	Osteobl	bone
36	chr2:12154000-12155200	Enhancers	Fetal Muscle Leg	muscle
37	chr2:12154000-12155400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:12154200-12154400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr2:12154200-12154400	Enhancers	NH-A	brain
40	chr2:12154200-12154800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:12154200-12155000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr2:12154400-12154800	Enhancers	Stomach Smooth Muscle	stomach
43	chr2:12154400-12155000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr2:12154600-12155000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:12154800-12156400	Weak transcription	Spleen	Spleen
46	chr2:12155000-12158600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:12155000-12158600	Weak transcription	Primary B cells from peripheral blood	blood
48	chr2:12155000-12159200	Weak transcription	Primary B cells from cord blood	blood
49	chr2:12155000-12164000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr2:12155200-12157800	Weak transcription	Fetal Muscle Leg	muscle

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