Variant report

Variant	nsv10193
Chromosome Location	chr2:133279818-133308948
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	chr2:133304775-133304963	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133304875-133304890	K562	blood:	n/a	n/a
3	CEBPB	chr2:133280625-133280665	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr2:133304646-133305121	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
5	CTCF	chr2:133304540-133304690	GM12867	blood:	n/a	n/a
6	CTCF	chr2:133304760-133304910	GM12873	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
7	CTCF	chr2:133304780-133304930	HepG2	liver:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
8	CTCF	chr2:133304780-133304930	GM12868	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
9	CTCF	chr2:133304549-133304583	K562	blood:	n/a	n/a
10	CTCF	chr2:133304800-133304950	HBMEC	blood vessel:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
11	CTCF	chr2:133304820-133304970	Hela-S3	cervix:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
12	CTCF	chr2:133304760-133304910	GM12871	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
13	CTCF	chr2:133304140-133304290	AG04450	lung:	n/a	n/a
14	CTCF	chr2:133304800-133304950	Hela-S3	cervix:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
15	CTCF	chr2:133304642-133304644	GM19239	blood:	n/a	n/a
16	CTCF	chr2:133304780-133304930	HUVEC	blood vessel:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
17	CTCF	chr2:133304760-133304910	GM12875	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
18	CTCF	chr2:133304800-133304950	HCT-116	colon:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
19	CTCF	chr2:133304700-133304850	K562	blood:	n/a	n/a
20	CTCF	chr2:133304780-133304930	AG04450	lung:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
21	CTCF	chr2:133304740-133304890	HA-sp	spinal cord:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
22	CTCF	chr2:133304720-133304870	HVMF	connective:	n/a	chr2:133304857-133304870 chr2:133304857-133304866
23	CTCF	chr2:133304780-133304930	GM12864	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
24	CTCF	chr2:133304800-133304950	NHDF-neo	bronchial:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
25	CTCF	chr2:133304800-133304950	HL-60	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
26	CTCF	chr2:133304804-133304927	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
27	CTCF	chr2:133304800-133304950	AG04450	lung:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
28	CTCF	chr2:133304780-133304930	BJ	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
29	CTCF	chr2:133304740-133304997	GM19238	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
30	CTCF	chr2:133304800-133304950	GM12872	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
31	CTCF	chr2:133304520-133304636	GM19239	blood:	n/a	n/a
32	CTCF	chr2:133304100-133304250	AG09319	gingival:	n/a	n/a
33	CTCF	chr2:133304480-133304630	GM12865	blood:	n/a	n/a
34	CTCF	chr2:133304800-133304950	NB4	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
35	CTCF	chr2:133304792-133304954	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
36	CTCF	chr2:133304713-133305007	Medullo	brain:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
37	CTCF	chr2:133304780-133304930	HFF	foreskin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
38	CTCF	chr2:133304785-133304966	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
39	CTCF	chr2:133304800-133304950	RPTEC	kidney:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
40	CTCF	chr2:133304780-133304930	HEK293	kidney:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
41	CTCF	chr2:133304745-133305124	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
42	CTCF	chr2:133289569-133289639	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr2:133304723-133304979	Pancreas_OC	pancreas:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
44	CTCF	chr2:133304527-133304626	GM10266	blood:	n/a	n/a
45	CTCF	chr2:133304719-133304999	GM12878	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
46	CTCF	chr2:133304760-133304910	K562	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
47	CTCF	chr2:133304780-133304930	WERI-Rb-1	eye:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
48	CTCF	chr2:133304800-133304950	NHEK	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
49	CTCF	chr2:133304747-133304976	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
50	CTCF	chr2:133304605-133304649	GM19240	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:133308087..133308889-chr2:133339718..133340292,2	MCF-7	breast:
2	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:
3	chr2:133304876..133306446-chr2:133426520..133428307,2	MCF-7	breast:
4	chr2:133274709..133277168-chr2:133277775..133280190,2	K562	blood:
5	chr2:133304259..133305229-chr2:133647133..133647703,2	MCF-7	breast:
6	chr2:133304640..133305382-chr2:133928983..133929651,2	MCF-7	breast:
7	chr2:133304353..133304857-chr2:134601593..134602264,2	MCF-7	breast:
8	chr2:133304368..133305326-chr2:134601553..134602523,5	K562	blood:
9	chr2:133304762..133308062-chr2:133425978..133429369,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf27A-10	chr2:133281190-133281509	NONHSAT074537

Variant related genes	Relation type
ENSG00000221142	TF binding region
RN7SKP103	TF binding region
ENSG00000150551	chromatin interactions

Extended variants
information (count: 1230 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1230 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141972065	chr2:133279835-133279836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545790500	chr2:133279855-133279856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564096220	chr2:133279948-133279949	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs35332901	chr2:133280013-133280014	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs374149999	chr2:133280020-133280021	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs115239642	chr2:133280028-133280029	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs549926477	chr2:133280033-133280034	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs571389933	chr2:133280040-133280041	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs539433154	chr2:133280049-133280050	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs59871121	chr2:133280096-133280097	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546680443	chr2:133280228-133280229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187207693	chr2:133280231-133280232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566828082	chr2:133280302-133280303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150664657	chr2:133280313-133280314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555836616	chr2:133280351-133280352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72983622	chr2:133280412-133280413	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs537979730	chr2:133280478-133280479	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs569947684	chr2:133280553-133280554	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs556701422	chr2:133280556-133280557	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs557455553	chr2:133280557-133280558	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs6759012	chr2:133280619-133280620	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545267216	chr2:133280647-133280648	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs554045283	chr2:133280661-133280662	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs140096163	chr2:133280730-133280731	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs143674975	chr2:133280793-133280794	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs551118129	chr2:133280817-133280818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191973397	chr2:133280834-133280835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11898943	chr2:133280843-133280844	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs565064826	chr2:133280846-133280847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184719387	chr2:133280852-133280853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547673184	chr2:133280884-133280885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11898952	chr2:133280890-133280891	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs530060385	chr2:133280916-133280917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534519241	chr2:133280932-133280933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146808452	chr2:133280981-133280982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567587966	chr2:133281002-133281003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377481588	chr2:133281007-133281008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538303006	chr2:133281032-133281033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577005044	chr2:133281041-133281042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77971076	chr2:133281051-133281052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367952721	chr2:133281061-133281062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571764506	chr2:133281180-133281181	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs12613678	chr2:133281214-133281215	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs553992046	chr2:133281319-133281320	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs572383027	chr2:133281464-133281465	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs542948321	chr2:133281478-133281479	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs552148466	chr2:133281499-133281500	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs190357521	chr2:133281506-133281507	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs370256887	chr2:133281511-133281512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575972633	chr2:133281519-133281520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133262000-133280400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:133268200-133282800	Weak transcription	Fetal Intestine Small	intestine
3	chr2:133274400-133280200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:133274400-133283200	Weak transcription	Pancreas	Pancrea
5	chr2:133278400-133280800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:133278600-133280600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:133278600-133281000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr2:133278800-133280400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:133279000-133280800	Enhancers	Brain Germinal Matrix	brain
10	chr2:133279000-133282600	Enhancers	Fetal Brain Male	brain
11	chr2:133279200-133280200	Weak transcription	Fetal Brain Female	brain
12	chr2:133279200-133280200	Weak transcription	NHEK	skin
13	chr2:133279200-133281600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:133279200-133283000	Weak transcription	Fetal Heart	heart
15	chr2:133279400-133280400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr2:133279600-133280000	Weak transcription	HMEC	breast
17	chr2:133279800-133281200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr2:133280000-133280800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr2:133280000-133280800	Enhancers	HMEC	breast
20	chr2:133280200-133280600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr2:133280200-133280600	Enhancers	NHEK	skin
22	chr2:133280200-133281000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:133280200-133281400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:133280200-133281400	Enhancers	Fetal Brain Female	brain
25	chr2:133280400-133280600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:133280400-133280800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:133280400-133281200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr2:133280400-133281200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr2:133280800-133281200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:133281200-133281400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:133281200-133281800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:133281400-133296400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:133281800-133282000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:133282000-133284600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:133282800-133284800	ZNF genes & repeats	Fetal Intestine Small	intestine
36	chr2:133283000-133283800	Enhancers	Fetal Heart	heart
37	chr2:133283200-133283400	Genic enhancers	Pancreas	Pancrea
38	chr2:133283400-133283800	Weak transcription	Pancreas	Pancrea
39	chr2:133295600-133297400	Enhancers	Fetal Heart	heart
40	chr2:133295800-133296000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:133295800-133296400	Enhancers	Placenta	Placenta
42	chr2:133295800-133296600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:133295800-133297000	ZNF genes & repeats	Fetal Intestine Small	intestine
44	chr2:133296000-133296600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr2:133296000-133296800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:133296000-133299000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:133296400-133296600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr2:133296400-133296600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:133296600-133300200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:133296600-133301400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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