Variant report

Variant	nsv973131
Chromosome Location	chr12:122848665-122851457
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	ATF2	chr12:122851341-122851791	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr12:122851401-122851840	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr12:122851365-122851965	HCT-116	colon:	n/a	n/a
4	ATF3	chr12:122851291-122851853	A549	lung:	n/a	n/a
5	ATF3	chr12:122851320-122851912	A549	lung:	n/a	n/a
6	ATF3	chr12:122851310-122851900	HCT-116	colon:	n/a	n/a
7	ATF3	chr12:122851393-122851699	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr12:122851426-122851744	K562	blood:	n/a	n/a
9	BCL3	chr12:122851278-122852299	A549	lung:	n/a	n/a
10	BHLHE40	chr12:122851414-122851750	HepG2	liver:	n/a	n/a
11	BHLHE40	chr12:122851414-122851761	K562	blood:	n/a	n/a
12	CBX3	chr12:122851343-122851820	HCT-116	colon:	n/a	n/a
13	CBX3	chr12:122851242-122851882	HCT-116	colon:	n/a	n/a
14	CEBPB	chr12:122848347-122849017	A549	lung:	n/a	chr12:122848509-122848518 chr12:122848507-122848520 chr12:122848507-122848518
15	CEBPB	chr12:122851240-122851968	HCT-116	colon:	n/a	chr12:122851604-122851615
16	CEBPB	chr12:122851389-122851846	K562	blood:	n/a	chr12:122851604-122851615
17	CEBPB	chr12:122848347-122849053	IMR90	lung:	n/a	chr12:122848509-122848518 chr12:122848507-122848520 chr12:122848507-122848518
18	CEBPB	chr12:122851430-122851764	HepG2	liver:	n/a	chr12:122851604-122851615
19	CEBPB	chr12:122851272-122852021	A549	lung:	n/a	chr12:122851604-122851615
20	CEBPB	chr12:122851382-122851836	A549	lung:	n/a	chr12:122851604-122851615
21	CEBPB	chr12:122851418-122851804	A549	lung:	n/a	chr12:122851604-122851615
22	CEBPB	chr12:122851400-122851849	ECC-1	luminal epithelium:	n/a	chr12:122851604-122851615
23	CEBPB	chr12:122848274-122848796	A549	lung:	n/a	chr12:122848509-122848518 chr12:122848507-122848520 chr12:122848507-122848518
24	CEBPB	chr12:122848745-122848956	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:122851413-122851810	IMR90	lung:	n/a	chr12:122851604-122851615
26	CEBPB	chr12:122851413-122851829	K562	blood:	n/a	chr12:122851604-122851615
27	CEBPB	chr12:122851405-122851754	K562	blood:	n/a	chr12:122851604-122851615
28	CEBPB	chr12:122851395-122851830	Hela-S3	cervix:	n/a	chr12:122851604-122851615
29	CEBPB	chr12:122851417-122851797	HepG2	liver:	n/a	chr12:122851604-122851615
30	CEBPB	chr12:122851419-122851811	H1-hESC	embryonic stem cell:	n/a	chr12:122851604-122851615
31	CEBPB	chr12:122851343-122851852	MCF-7	breast:	n/a	chr12:122851604-122851615
32	CEBPB	chr12:122851185-122851987	HCT-116	colon:	n/a	chr12:122851604-122851615
33	CEBPB	chr12:122848336-122849011	MCF-7	breast:	n/a	chr12:122848509-122848518 chr12:122848507-122848520 chr12:122848507-122848518
34	CEBPB	chr12:122851375-122851833	MCF-7	breast:	n/a	chr12:122851604-122851615
35	CEBPB	chr12:122848352-122849030	HepG2	liver:	n/a	chr12:122848509-122848518 chr12:122848507-122848520 chr12:122848507-122848518
36	CEBPB	chr12:122848372-122848954	K562	blood:	n/a	chr12:122848509-122848518 chr12:122848507-122848520 chr12:122848507-122848518
37	CEBPB	chr12:122851372-122851793	ECC-1	luminal epithelium:	n/a	chr12:122851604-122851615
38	CEBPD	chr12:122851427-122851685	HepG2	liver:	n/a	chr12:122851603-122851614
39	CHD2	chr12:122851445-122851767	Hela-S3	cervix:	n/a	n/a
40	E2F6	chr12:122851418-122851692	H1-hESC	embryonic stem cell:	n/a	n/a
41	E2F6	chr12:122851182-122851917	A549	lung:	n/a	n/a
42	E2F6	chr12:122851277-122851796	H1-hESC	embryonic stem cell:	n/a	n/a
43	EP300	chr12:122851396-122851827	Hela-S3	cervix:	n/a	chr12:122851601-122851615
44	EP300	chr12:122851253-122851867	ECC-1	luminal epithelium:	n/a	chr12:122851601-122851615
45	EP300	chr12:122851419-122851745	HepG2	liver:	n/a	chr12:122851601-122851615
46	EP300	chr12:122851420-122851859	K562	blood:	n/a	chr12:122851601-122851615
47	EP300	chr12:122851375-122851951	A549	lung:	n/a	chr12:122851601-122851615
48	EP300	chr12:122851453-122851865	HepG2	liver:	n/a	chr12:122851601-122851615
49	FOS	chr12:122851448-122851757	Hela-S3	cervix:	n/a	n/a
50	FOS	chr12:122851418-122851887	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:122851438-122851488	HCF	heart:	n/a
2	chr12:122851438-122851488	AG04450	lung:	fetal
3	chr12:122851438-122851488	IMR90	lung:	fetal
4	chr12:122851438-122851488	HEEpiC	esophagus:	n/a
5	chr12:122851438-122851488	GM19239	blood:	n/a
6	chr12:122851438-122851488	HPAEpiC	pulmonary alveolar:	n/a
7	chr12:122851438-122851488	Jurkat	blood:	n/a
8	chr12:122851438-122851488	GM06990	blood:	n/a
9	chr12:122851438-122851488	BJ	skin:	n/a
10	chr12:122851438-122851488	AG10803	skin:	n/a
11	chr12:122851438-122851488	ProgFib	skin:	n/a
12	chr12:122851438-122851488	NT2-D1	testis:	n/a
13	chr12:122851438-122851488	MCF-7	breast:	n/a
14	chr12:122851438-122851488	HCPEpiC	choroid plexus:	n/a
15	chr12:122851438-122851488	SKMC	muscle:	n/a
16	chr12:122851438-122851488	PFSK-1	brain:	n/a
17	chr12:122851438-122851488	AoSMC	blood vessel:	n/a
18	chr12:122851438-122851488	HMEC	breast:	n/a
19	chr12:122851438-122851488	HEK293	kidney:	embryo
20	chr12:122851438-122851488	HIPEpiC	eye:	n/a
21	chr12:122851438-122851488	ECC-1	luminal epithelium:	n/a
22	chr12:122851438-122851488	HNPCEpiC	eye:	n/a
23	chr12:122851438-122851488	BE2_C	brain:	n/a
24	chr12:122851438-122851488	NB4	blood:	n/a
25	chr12:122851438-122851488	H1-hESC	embryonic stem cell:	embryo
26	chr12:122851438-122851488	Caco-2	colon:	n/a
27	chr12:122851438-122851488	GM12892	blood:	n/a
28	chr12:122851438-122851488	AG04449	skin:	fetal
29	chr12:122851438-122851488	NHBE	bronchial:	n/a
30	chr12:122851438-122851488	HepG2	liver:	n/a
31	chr12:122851438-122851488	HRCEpiC	kidney:	n/a
32	chr12:122851438-122851488	U87	brain:	n/a
33	chr12:122851438-122851488	MCF10A-Er-Src	breast:	n/a
34	chr12:122851438-122851488	CMK	blood:	n/a
35	chr12:122851438-122851488	K562	blood:	n/a
36	chr12:122851438-122851488	HL-60	blood:	n/a
37	chr12:122851438-122851488	Hela-S3	cervix:	n/a
38	chr12:122851438-122851488	NHDF-neo	bronchial:	n/a
39	chr12:122851438-122851488	ovcar-3	ovarian:	n/a
40	chr12:122851438-122851488	HUVEC	blood vessel:	n/a
41	chr12:122851438-122851488	HCT-116	colon:	n/a
42	chr12:122851438-122851488	PANC-1	pancreas:	n/a
43	chr12:122851438-122851488	SAEC	small airway:	n/a
44	chr12:122851438-122851488	HCM	heart:	n/a
45	chr12:122851438-122851488	AG09319	gingival:	n/a
46	chr12:122851438-122851488	RPTEC	kidney:	n/a
47	chr12:122851438-122851488	A549	lung:	n/a
48	chr12:122851438-122851488	AG09309	skin:	n/a
49	chr12:122851438-122851488	GM12878	blood:	n/a
50	chr12:122851438-122851488	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:122851188..122853354-chr12:122856942..122858649,2	MCF-7	breast:
2	chr12:122847930..122850385-chr12:123009903..123011569,2	MCF-7	breast:
3	chr12:122850554..122853337-chr12:122906112..122908968,4	MCF-7	breast:
4	chr12:122847513..122850050-chr12:122850104..122851693,3	K562	blood:
5	chr12:122850653..122853175-chr12:122883038..122884712,2	K562	blood:

Variant related genes	Relation type
RPL21P1	TF binding region
CLIP1	TF binding region
RPL21P1	CpG island
CLIP1	CpG island
ENSG00000111011	chromatin interactions
ENSG00000214760	chromatin interactions
ENSG00000130779	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563193257	chr12:122848679-122848680	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs369566935	chr12:122848687-122848688	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs184187536	chr12:122848709-122848710	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs190034486	chr12:122848753-122848754	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs548805419	chr12:122848793-122848794	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141440932	chr12:122848824-122848825	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs145197199	chr12:122848869-122848870	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs146423444	chr12:122848918-122848919	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs35729680	chr12:122848953-122848954	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs398077017	chr12:122848967-122848968	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs398021428	chr12:122848968-122848969	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs545878318	chr12:122848984-122848985	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs149044573	chr12:122849114-122849115	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368260844	chr12:122849123-122849124	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs193195422	chr12:122849236-122849237	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556653431	chr12:122849306-122849307	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568812851	chr12:122849313-122849314	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536099992	chr12:122849315-122849316	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372717439	chr12:122849321-122849322	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560125748	chr12:122849344-122849345	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs115476093	chr12:122849345-122849346	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143075881	chr12:122849373-122849374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1818050	chr12:122849392-122849393	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs577232451	chr12:122849425-122849426	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544617587	chr12:122849463-122849464	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112564325	chr12:122849555-122849556	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141248153	chr12:122849588-122849589	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200915086	chr12:122849589-122849590	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530429125	chr12:122849627-122849628	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs146989977	chr12:122849630-122849631	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530529541	chr12:122849638-122849639	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs550617336	chr12:122849654-122849655	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368243382	chr12:122849664-122849665	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs199974353	chr12:122849665-122849666	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114387181	chr12:122849800-122849801	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs527916277	chr12:122849840-122849841	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552458002	chr12:122849860-122849861	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200530713	chr12:122849929-122849930	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138174706	chr12:122849941-122849942	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532062274	chr12:122849969-122849970	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190753389	chr12:122849970-122849971	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373162200	chr12:122849992-122849993	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568551575	chr12:122850005-122850006	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374853497	chr12:122850086-122850087	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535841292	chr12:122850095-122850096	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs7976580	chr12:122850103-122850104	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs566414766	chr12:122850146-122850147	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534006819	chr12:122850163-122850164	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs558440785	chr12:122850189-122850190	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs34314261	chr12:122850224-122850225	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122812800-122850600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:122818400-122852800	Weak transcription	Stomach Mucosa	stomach
3	chr12:122837000-122851200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:122837600-122856000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:122838000-122868000	Weak transcription	Fetal Lung	lung
6	chr12:122838600-122852200	Weak transcription	Small Intestine	intestine
7	chr12:122839400-122850200	Weak transcription	Right Atrium	heart
8	chr12:122839600-122851400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:122839600-122861800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr12:122839600-122871000	Weak transcription	Fetal Kidney	kidney
11	chr12:122840000-122852000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr12:122840000-122861800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr12:122840000-122862600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr12:122840200-122851000	Weak transcription	NH-A	brain
15	chr12:122840200-122857800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:122841000-122872600	Weak transcription	Fetal Brain Male	brain
17	chr12:122843000-122848800	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr12:122843000-122848800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr12:122843000-122849000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr12:122843000-122849200	Strong transcription	Placenta	Placenta
21	chr12:122843200-122849000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:122843200-122849200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:122843400-122848800	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr12:122843400-122848800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:122843400-122851000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr12:122843600-122848800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr12:122843800-122848800	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr12:122843800-122848800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr12:122843800-122848800	Strong transcription	Colon Smooth Muscle	Colon
30	chr12:122843800-122848800	Strong transcription	Duodenum Mucosa	Duodenum
31	chr12:122843800-122849200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr12:122843800-122849200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:122844000-122849200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:122844200-122848800	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr12:122844400-122862000	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr12:122844600-122851000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr12:122844800-122856000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr12:122846000-122851000	Weak transcription	HMEC	breast
39	chr12:122846000-122851200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:122846000-122851200	Weak transcription	Brain Angular Gyrus	brain
41	chr12:122846000-122851400	Weak transcription	Brain Anterior Caudate	brain
42	chr12:122846000-122854000	Weak transcription	GM12878-XiMat	blood
43	chr12:122846000-122865600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:122846000-122883800	Weak transcription	Aorta	Aorta
45	chr12:122846200-122850000	Weak transcription	HUVEC	blood vessel
46	chr12:122846200-122851000	Weak transcription	K562	blood
47	chr12:122846200-122851000	Weak transcription	Osteobl	bone
48	chr12:122846200-122851200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr12:122846200-122851400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr12:122846200-122856000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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