Variant report

Variant	esv3423868
Chromosome Location	chr2:133280649-133308776
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	chr2:133304780-133304930	GM12869	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
5	CTCF	chr2:133304523-133304980	GM13977	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
6	CTCF	chr2:133304800-133304950	SK-N-SH_RA	brain:	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	chr2:133304800-133304950	HBMEC	blood vessel:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
9	CTCF	chr2:133304800-133304950	GM12865	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
10	CTCF	chr2:133304800-133304950	Hela-S3	cervix:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
11	CTCF	chr2:133304761-133304983	GM12892	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
12	CTCF	chr2:133304780-133304930	GM12864	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
13	CTCF	chr2:133304746-133304947	GM20000	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
14	CTCF	chr2:133304380-133304530	GM12864	blood:	n/a	n/a
15	CTCF	chr2:133296860-133297010	GM12869	blood:	n/a	n/a
16	CTCF	chr2:133304760-133304910	HFF-Myc	foreskin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
17	CTCF	chr2:133304780-133304930	GM12871	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
18	CTCF	chr2:133304800-133304950	AG04450	lung:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
19	CTCF	chr2:133304780-133304930	BE2_C	brain:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
20	CTCF	chr2:133304800-133304950	NB4	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
21	CTCF	chr2:133304740-133304963	LNCaP	prostate:	n/a	chr2:133304857-133304870 chr2:133304857-133304866 chr2:133304854-133304872 chr2:133304856-133304877
22	CTCF	chr2:133304659-133305019	H1-hESC	embryonic stem cell:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
23	CTCF	chr2:133304780-133304930	GM12870	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
24	CTCF	chr2:133304800-133304950	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
25	CTCF	chr2:133304740-133304997	GM19238	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
26	CTCF	chr2:133304760-133304910	GM12865	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
27	CTCF	chr2:133304342-133305304	SK-N-SH	brain:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
28	CTCF	chr2:133304780-133304930	GM12878	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
29	CTCF	chr2:133304320-133304470	HCM	heart:	n/a	n/a
30	CTCF	chr2:133304610-133304618	Lung_OC	lung:	n/a	n/a
31	CTCF	chr2:133304840-133304990	HCM	heart:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
32	CTCF	chr2:133304792-133304954	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
33	CTCF	chr2:133304720-133304870	HVMF	connective:	n/a	chr2:133304857-133304870 chr2:133304857-133304866
34	CTCF	chr2:133304780-133304930	RPTEC	kidney:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
35	CTCF	chr2:133304527-133304626	GM10266	blood:	n/a	n/a
36	CTCF	chr2:133304719-133304992	K562	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
37	CTCF	chr2:133304760-133304910	HepG2	liver:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
38	CTCF	chr2:133304723-133304979	Pancreas_OC	pancreas:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
39	CTCF	chr2:133304760-133304910	HCT-116	colon:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
40	CTCF	chr2:133304820-133304970	GM12869	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
41	CTCF	chr2:133304760-133304910	AG09319	gingival:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
42	CTCF	chr2:133304760-133304910	GM12873	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
43	CTCF	chr2:133304747-133304976	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
44	CTCF	chr2:133304708-133304991	Lung_OC	lung:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
45	CTCF	chr2:133304734-133304976	Fibrobl	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
46	CTCF	chr2:133304760-133304910	GM12871	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
47	CTCF	chr2:133304735-133304947	GM10248	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
48	CTCF	chr2:133304800-133304950	HMF	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
49	CTCF	chr2:133283360-133283510	HepG2	liver:	n/a	n/a
50	CTCF	chr2:133304760-133304910	GM12872	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866

No.	Distal block	Cell Line	Cell type
1	chr2:133304259..133305229-chr2:133647133..133647703,2	MCF-7	breast:
2	chr2:133304640..133305382-chr2:133928983..133929651,2	MCF-7	breast:
3	chr2:133304368..133305326-chr2:134601553..134602523,5	K562	blood:
4	chr2:133304762..133308062-chr2:133425978..133429369,3	MCF-7	breast:
5	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:
6	chr2:133304876..133306446-chr2:133426520..133428307,2	MCF-7	breast:
7	chr2:133304353..133304857-chr2:134601593..134602264,2	MCF-7	breast:
8	chr2:133308087..133308889-chr2:133339718..133340292,2	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: 1196 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1196 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554045283	chr2:133280661-133280662	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs140096163	chr2:133280730-133280731	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs143674975	chr2:133280793-133280794	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs551118129	chr2:133280817-133280818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191973397	chr2:133280834-133280835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11898943	chr2:133280843-133280844	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs565064826	chr2:133280846-133280847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184719387	chr2:133280852-133280853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547673184	chr2:133280884-133280885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11898952	chr2:133280890-133280891	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs530060385	chr2:133280916-133280917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534519241	chr2:133280932-133280933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146808452	chr2:133280981-133280982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567587966	chr2:133281002-133281003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377481588	chr2:133281007-133281008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538303006	chr2:133281032-133281033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577005044	chr2:133281041-133281042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77971076	chr2:133281051-133281052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367952721	chr2:133281061-133281062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571764506	chr2:133281180-133281181	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs12613678	chr2:133281214-133281215	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553992046	chr2:133281319-133281320	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs572383027	chr2:133281464-133281465	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs542948321	chr2:133281478-133281479	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs552148466	chr2:133281499-133281500	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs190357521	chr2:133281506-133281507	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs370256887	chr2:133281511-133281512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575972633	chr2:133281519-133281520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145139077	chr2:133281526-133281527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564839963	chr2:133281552-133281553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577050980	chr2:133281569-133281570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541222903	chr2:133281614-133281615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559612547	chr2:133281616-133281617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529998358	chr2:133281645-133281646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548202020	chr2:133281686-133281687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374212783	chr2:133281690-133281691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531610552	chr2:133281712-133281713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550207399	chr2:133281726-133281727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553079490	chr2:133281734-133281735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571404496	chr2:133281744-133281745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538776764	chr2:133281775-133281776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182547580	chr2:133281778-133281779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10183993	chr2:133281790-133281791	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556964391	chr2:133281797-133281798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536925787	chr2:133281813-133281814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370333541	chr2:133281888-133281889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149108613	chr2:133281894-133281895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536630810	chr2:133281924-133281925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371158090	chr2:133281942-133281943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534925422	chr2:133281967-133281968	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:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133268200-133282800	Weak transcription	Fetal Intestine Small	intestine
2	chr2:133274400-133283200	Weak transcription	Pancreas	Pancrea
3	chr2:133278400-133280800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:133278600-133281000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr2:133279000-133280800	Enhancers	Brain Germinal Matrix	brain
6	chr2:133279000-133282600	Enhancers	Fetal Brain Male	brain
7	chr2:133279200-133281600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr2:133279200-133283000	Weak transcription	Fetal Heart	heart
9	chr2:133279800-133281200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr2:133280000-133280800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:133280000-133280800	Enhancers	HMEC	breast
12	chr2:133280200-133281000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:133280200-133281400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:133280200-133281400	Enhancers	Fetal Brain Female	brain
15	chr2:133280400-133280800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:133280400-133281200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:133280400-133281200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:133280800-133281200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:133281200-133281400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr2:133281200-133281800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:133281400-133296400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:133281800-133282000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:133282000-133284600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:133282800-133284800	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr2:133283000-133283800	Enhancers	Fetal Heart	heart
26	chr2:133283200-133283400	Genic enhancers	Pancreas	Pancrea
27	chr2:133283400-133283800	Weak transcription	Pancreas	Pancrea
28	chr2:133295600-133297400	Enhancers	Fetal Heart	heart
29	chr2:133295800-133296000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:133295800-133296400	Enhancers	Placenta	Placenta
31	chr2:133295800-133296600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:133295800-133297000	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr2:133296000-133296600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr2:133296000-133296800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:133296000-133299000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:133296400-133296600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr2:133296400-133296600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:133296600-133300200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr2:133296600-133301400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:133296800-133297400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:133297200-133298200	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr2:133297400-133297600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:133297400-133301000	Weak transcription	Gastric	stomach
44	chr2:133297800-133298200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:133297800-133299600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:133299000-133303400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:133299200-133302800	Enhancers	Placenta	Placenta
48	chr2:133299600-133300600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr2:133300200-133302000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:133300400-133301000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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