Variant report

Variant	nsv1001299
Chromosome Location	chr2:31428030-31464385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:661)
CpG islands
(count:1589)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:31456595-31457193	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:31456598-31456992	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:31441886-31442907	GM12878	blood:	n/a	n/a
4	BACH1	chr2:31456642-31457042	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:31442483-31442746	GM12878	blood:	n/a	n/a
6	BATF	chr2:31442515-31442799	GM12878	blood:	n/a	n/a
7	BCL3	chr2:31456641-31457247	A549	lung:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
8	BCLAF1	chr2:31441899-31442872	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:31456640-31457127	GM12878	blood:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
10	BHLHE40	chr2:31440475-31440850	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:31456662-31457127	GM12878	blood:	n/a	chr2:31457080-31457096
12	BHLHE40	chr2:31434430-31434614	K562	blood:	n/a	n/a
13	BHLHE40	chr2:31441900-31442892	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:31463632-31463876	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:31430809-31431053	GM12878	blood:	n/a	n/a
16	BRCA1	chr2:31456720-31457019	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr2:31456858-31457304	K562	blood:	n/a	chr2:31457137-31457146
18	CEBPB	chr2:31436089-31436493	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:31456573-31456935	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:31458407-31458725	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:31442574-31442749	A549	lung:	n/a	n/a
22	CEBPZ	chr2:31452816-31452914	HepG2	liver:	n/a	n/a
23	CHD1	chr2:31442065-31442458	GM12878	blood:	n/a	n/a
24	CHD1	chr2:31456869-31457425	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr2:31441888-31442844	GM12878	blood:	n/a	n/a
26	CHD2	chr2:31456531-31457222	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr2:31456890-31456943	HepG2	liver:	n/a	n/a
28	CHD2	chr2:31456757-31457101	GM12878	blood:	n/a	n/a
29	CREB1	chr2:31456606-31457154	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr2:31456527-31457601	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr2:31456659-31457229	A549	lung:	n/a	n/a
32	CREB1	chr2:31456683-31457015	A549	lung:	n/a	n/a
33	CTBP2	chr2:31456608-31457511	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr2:31456700-31456850	BE2_C	brain:	n/a	n/a
35	CTCF	chr2:31456664-31456891	GM13977	blood:	n/a	n/a
36	CTCF	chr2:31458540-31458690	AG04450	lung:	n/a	chr2:31458646-31458655
37	CTCF	chr2:31456590-31456933	K562	blood:	n/a	n/a
38	CTCF	chr2:31456280-31456430	AG10803	skin:	n/a	n/a
39	CTCF	chr2:31458580-31458730	HPF	lung:	n/a	chr2:31458646-31458655
40	CTCF	chr2:31456624-31456888	NHEK	skin:	n/a	n/a
41	CTCF	chr2:31456640-31456790	HFF	foreskin:	n/a	n/a
42	CTCF	chr2:31430733-31430785	NHEK	skin:	n/a	n/a
43	CTCF	chr2:31456700-31456850	HRE	kidney:	n/a	n/a
44	CTCF	chr2:31458480-31458630	RPTEC	kidney:	n/a	n/a
45	CTCF	chr2:31456680-31456830	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr2:31456700-31456850	NHEK	skin:	n/a	n/a
47	CTCF	chr2:31458540-31458690	AG10803	skin:	n/a	chr2:31458646-31458655
48	CTCF	chr2:31456614-31456922	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:31456680-31456830	GM12874	blood:	n/a	n/a
50	CTCF	chr2:31456700-31456850	GM12865	blood:	n/a	n/a

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:31455443-31455493	T-47D	breast:	n/a
2	chr2:31456741-31456791	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:31456789-31456839	T-47D	breast:	n/a
4	chr2:31455443-31455493	T-47D	breast:	n/a
5	chr2:31456741-31456791	HPAEpiC	pulmonary alveolar:	n/a
6	chr2:31456789-31456839	T-47D	breast:	n/a
7	chr2:31456964-31457014	RPTEC	kidney:	n/a
8	chr2:31456964-31457014	HEK293	kidney:	embryo
9	chr2:31456964-31457014	HCM	heart:	n/a
10	chr2:31456217-31456267	AG04450	lung:	fetal
11	chr2:31440451-31440501	HNPCEpiC	eye:	n/a
12	chr2:31449901-31449951	HEEpiC	esophagus:	n/a
13	chr2:31456217-31456267	GM06990	blood:	n/a
14	chr2:31456761-31456811	HIPEpiC	eye:	n/a
15	chr2:31457608-31457658	NH-A	brain:	n/a
16	chr2:31457058-31457108	RPTEC	kidney:	n/a
17	chr2:31455890-31455940	NB4	blood:	n/a
18	chr2:31456775-31456825	GM06990	blood:	n/a
19	chr2:31439687-31439737	HCT-116	colon:	n/a
20	chr2:31456789-31456839	ProgFib	skin:	n/a
21	chr2:31441554-31441604	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:31440451-31440501	SK-N-MC	brain:	n/a
23	chr2:31440349-31440399	HL-60	blood:	n/a
24	chr2:31457287-31457337	GM19239	blood:	n/a
25	chr2:31456775-31456825	HEEpiC	esophagus:	n/a
26	chr2:31441554-31441604	HRCEpiC	kidney:	n/a
27	chr2:31456966-31457016	HRCEpiC	kidney:	n/a
28	chr2:31457061-31457111	Hepatocyte	liver:	n/a
29	chr2:31457608-31457658	SK-N-SH_RA	brain:	n/a
30	chr2:31457608-31457658	GM19239	blood:	n/a
31	chr2:31456741-31456791	T-47D	breast:	n/a
32	chr2:31456217-31456267	HEK293	kidney:	embryo
33	chr2:31449901-31449951	AG09309	skin:	n/a
34	chr2:31456761-31456811	T-47D	breast:	n/a
35	chr2:31456761-31456811	LNCaP	prostate:	n/a
36	chr2:31456217-31456267	GM12878	blood:	n/a
37	chr2:31441312-31441362	Hepatocyte	liver:	n/a
38	chr2:31449901-31449951	MCF-7	breast:	n/a
39	chr2:31456964-31457014	NHDF-neo	bronchial:	n/a
40	chr2:31459843-31459893	HRCEpiC	kidney:	n/a
41	chr2:31440451-31440501	U87	brain:	n/a
42	chr2:31456804-31456854	Jurkat	blood:	n/a
43	chr2:31457058-31457108	NT2-D1	testis:	n/a
44	chr2:31456964-31457014	U87	brain:	n/a
45	chr2:31441588-31441638	AG10803	skin:	n/a
46	chr2:31456775-31456825	LNCaP	prostate:	n/a
47	chr2:31455443-31455493	PrEC	prostate:	n/a
48	chr2:31455443-31455493	AoSMC	blood vessel:	n/a
49	chr2:31456217-31456267	LNCaP	prostate:	n/a
50	chr2:31439687-31439737	MCF-7	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:31456557..31458927-chr2:31463971..31466184,2	MCF-7	breast:
2	chr2:31457912..31460253-chr2:31482759..31484283,2	MCF-7	breast:
3	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
4	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:
5	chr2:31418550..31420224-chr2:31425779..31428465,2	K562	blood:
6	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
7	chr2:31449978..31452625-chr2:31454988..31456954,2	K562	blood:
8	chr17:58816926..58819384-chr2:31448134..31450659,2	MCF-7	breast:
9	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
10	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:
11	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
12	chr2:31407024..31409183-chr2:31430215..31431751,2	MCF-7	breast:
13	chr2:31456683..31458757-chr2:31460645..31462411,2	MCF-7	breast:
14	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
15	chr2:31453246..31458582-chr2:31458844..31463834,9	MCF-7	breast:
16	chr17:63334973..63335809-chr2:31437485..31438063,2	MCF-7	breast:
17	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
18	chr2:31449978..31452625-chr2:31454988..31456954,2	K562	blood:

No data

Variant related genes	Relation type
RNA5SP90	TF binding region
CAPN14	TF binding region
EHD3	TF binding region
RNA5SP90	CpG island
CAPN14	CpG island
EHD3	CpG island
ENSG00000201671	chromatin interactions
ENSG00000214711	chromatin interactions
ENSG00000013016	chromatin interactions

Extended variants
information (count: 1637 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1637 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1867329	chr2:31428030-31428031	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543049917	chr2:31428066-31428067	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200835957	chr2:31428070-31428071	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113482339	chr2:31428112-31428113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368808576	chr2:31428146-31428147	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79600252	chr2:31428191-31428192	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374924641	chr2:31428272-31428273	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527877188	chr2:31428286-31428287	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201825271	chr2:31428320-31428321	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544628010	chr2:31428344-31428345	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374644307	chr2:31428383-31428384	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190025338	chr2:31428458-31428459	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182592991	chr2:31428513-31428514	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528915861	chr2:31428525-31428526	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552279672	chr2:31428540-31428541	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11687767	chr2:31428541-31428542	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs568487772	chr2:31428575-31428576	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531538493	chr2:31428594-31428595	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187293984	chr2:31428623-31428624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571395459	chr2:31428633-31428634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373161899	chr2:31428634-31428635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533992312	chr2:31428647-31428648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553642416	chr2:31428649-31428650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147887955	chr2:31428667-31428668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536714281	chr2:31428668-31428669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556622016	chr2:31428673-31428674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192834299	chr2:31428674-31428675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545418209	chr2:31428685-31428686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559199177	chr2:31428687-31428688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572604200	chr2:31428690-31428691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141644364	chr2:31428753-31428754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561112864	chr2:31428777-31428778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201930581	chr2:31428797-31428798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150436415	chr2:31428807-31428808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542295528	chr2:31428829-31428830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562180747	chr2:31428841-31428842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114629846	chr2:31428882-31428883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200116287	chr2:31428887-31428888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551435585	chr2:31428892-31428893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200934501	chr2:31428895-31428896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145795397	chr2:31428896-31428897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200505995	chr2:31428899-31428900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201440262	chr2:31428900-31428901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201205171	chr2:31428904-31428905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113792962	chr2:31428905-31428906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567444924	chr2:31428908-31428909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375219448	chr2:31428968-31428969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369303934	chr2:31428985-31428986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183756660	chr2:31428987-31428988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556683565	chr2:31429023-31429024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	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
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Medulloblastoma	16968546	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	18927303	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1030 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31411200-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:31420800-31430800	Weak transcription	Primary B cells from cord blood	blood
3	chr2:31421200-31429600	Weak transcription	Dnd41	blood
4	chr2:31423400-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:31424200-31435800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:31424200-31437600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:31425400-31428400	Strong transcription	Primary B cells from peripheral blood	blood
8	chr2:31426400-31428400	Enhancers	Left Ventricle	heart
9	chr2:31427400-31428200	Enhancers	Brain Angular Gyrus	brain
10	chr2:31427600-31430800	Weak transcription	Fetal Heart	heart
11	chr2:31428000-31428800	Strong transcription	Esophagus	oesophagus
12	chr2:31428000-31429000	Weak transcription	Right Ventricle	heart
13	chr2:31428200-31428600	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr2:31428400-31430400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr2:31428400-31431200	Weak transcription	Left Ventricle	heart
16	chr2:31428800-31437400	Weak transcription	Esophagus	oesophagus
17	chr2:31429000-31429200	Enhancers	Right Ventricle	heart
18	chr2:31429800-31430200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:31430000-31432800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:31430200-31441600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:31430400-31431600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:31430400-31432000	Enhancers	Primary B cells from peripheral blood	blood
23	chr2:31430600-31431000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:31430600-31431000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:31430800-31431200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:31430800-31431400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:31430800-31431800	Enhancers	Primary B cells from cord blood	blood
28	chr2:31430800-31432400	Enhancers	Fetal Heart	heart
29	chr2:31431000-31431600	Enhancers	GM12878-XiMat	blood
30	chr2:31431000-31436000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr2:31431000-31436000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr2:31431200-31431400	Enhancers	Left Ventricle	heart
33	chr2:31431200-31436000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr2:31431600-31432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:31431600-31435800	Weak transcription	GM12878-XiMat	blood
36	chr2:31431800-31436800	Weak transcription	Primary B cells from cord blood	blood
37	chr2:31432000-31435800	Weak transcription	Primary B cells from peripheral blood	blood
38	chr2:31432400-31436600	Weak transcription	Fetal Heart	heart
39	chr2:31432600-31433000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:31432800-31435600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:31433000-31433800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:31433800-31434400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:31434400-31435800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:31435600-31436200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:31435800-31436000	Enhancers	Primary B cells from peripheral blood	blood
46	chr2:31435800-31436200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:31435800-31437000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:31435800-31437200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr2:31435800-31439800	Enhancers	GM12878-XiMat	blood
50	chr2:31436000-31436400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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