Variant report

Variant	nsv581268
Chromosome Location	chr2:31425783-31467079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:674)
CpG islands
(count:1589)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:674 , 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	chr2:31441886-31442907	GM12878	blood:	n/a	n/a
2	ATF2	chr2:31456598-31456992	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:31456595-31457193	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:31456642-31457042	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:31442515-31442799	GM12878	blood:	n/a	n/a
6	BATF	chr2:31442483-31442746	GM12878	blood:	n/a	n/a
7	BCL3	chr2:31456641-31457247	A549	lung:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
8	BCLAF1	chr2:31456640-31457127	GM12878	blood:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
9	BCLAF1	chr2:31441899-31442872	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:31430809-31431053	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:31441900-31442892	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:31440475-31440850	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:31434430-31434614	K562	blood:	n/a	n/a
14	BHLHE40	chr2:31463632-31463876	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:31456662-31457127	GM12878	blood:	n/a	chr2:31457080-31457096
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	chr2:31456573-31456935	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:31427031-31427326	IMR90	lung:	n/a	chr2:31427167-31427178
20	CEBPB	chr2:31458407-31458725	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:31465299-31465479	HepG2	liver:	n/a	chr2:31465356-31465369 chr2:31465356-31465367
22	CEBPB	chr2:31426142-31426190	K562	blood:	n/a	n/a
23	CEBPB	chr2:31436089-31436493	MCF-7	breast:	n/a	n/a
24	CEBPB	chr2:31442574-31442749	A549	lung:	n/a	n/a
25	CEBPB	chr2:31427020-31427332	HepG2	liver:	n/a	chr2:31427167-31427178
26	CEBPB	chr2:31426991-31427339	A549	lung:	n/a	chr2:31427167-31427178
27	CEBPB	chr2:31427049-31427251	K562	blood:	n/a	chr2:31427167-31427178
28	CEBPZ	chr2:31452816-31452914	HepG2	liver:	n/a	n/a
29	CHD1	chr2:31456869-31457425	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr2:31442065-31442458	GM12878	blood:	n/a	n/a
31	CHD2	chr2:31456757-31457101	GM12878	blood:	n/a	n/a
32	CHD2	chr2:31441888-31442844	GM12878	blood:	n/a	n/a
33	CHD2	chr2:31456531-31457222	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr2:31456890-31456943	HepG2	liver:	n/a	n/a
35	CREB1	chr2:31456683-31457015	A549	lung:	n/a	n/a
36	CREB1	chr2:31456527-31457601	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr2:31456659-31457229	A549	lung:	n/a	n/a
38	CREB1	chr2:31456606-31457154	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr2:31456608-31457511	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr2:31456640-31456790	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr2:31456660-31456810	HCFaa	heart:	n/a	n/a
42	CTCF	chr2:31458400-31458550	SAEC	small airway:	n/a	n/a
43	CTCF	chr2:31456700-31456850	GM12869	blood:	n/a	n/a
44	CTCF	chr2:31458580-31458730	HBMEC	blood vessel:	n/a	chr2:31458646-31458655
45	CTCF	chr2:31456691-31456776	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr2:31452470-31452489	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:31456620-31456770	A549	lung:	n/a	n/a
48	CTCF	chr2:31456680-31456830	NB4	blood:	n/a	n/a
49	CTCF	chr2:31456640-31456790	HepG2	liver:	n/a	n/a
50	CTCF	chr2:31457500-31457650	NHEK	skin:	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	chr2:31454631-31454681	ProgFib	skin:	n/a
2	chr2:31440349-31440399	HNPCEpiC	eye:	n/a
3	chr2:31458372-31458422	AG09319	gingival:	n/a
4	chr2:31454631-31454681	ProgFib	skin:	n/a
5	chr2:31440349-31440399	HNPCEpiC	eye:	n/a
6	chr2:31458372-31458422	AG09319	gingival:	n/a
7	chr2:31455890-31455940	HRCEpiC	kidney:	n/a
8	chr2:31456217-31456267	GM19239	blood:	n/a
9	chr2:31457608-31457658	Jurkat	blood:	n/a
10	chr2:31440451-31440501	IMR90	lung:	fetal
11	chr2:31449901-31449951	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:31457058-31457108	NT2-D1	testis:	n/a
13	chr2:31456741-31456791	NHDF-neo	bronchial:	n/a
14	chr2:31456217-31456267	SK-N-SH_RA	brain:	n/a
15	chr2:31456964-31457014	HAEpiC	amniotic membrane:	n/a
16	chr2:31441312-31441362	HL-60	blood:	n/a
17	chr2:31457287-31457337	ovcar-3	ovarian:	n/a
18	chr2:31439687-31439737	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:31449901-31449951	PFSK-1	brain:	n/a
20	chr2:31456761-31456811	HCT-116	colon:	n/a
21	chr2:31456741-31456791	HCT-116	colon:	n/a
22	chr2:31441588-31441638	HL-60	blood:	n/a
23	chr2:31457061-31457111	T-47D	breast:	n/a
24	chr2:31456217-31456267	H1-hESC	embryonic stem cell:	embryo
25	chr2:31456741-31456791	RPTEC	kidney:	n/a
26	chr2:31457287-31457337	BJ	skin:	n/a
27	chr2:31441588-31441638	Hepatocyte	liver:	n/a
28	chr2:31456966-31457016	MCF-7	breast:	n/a
29	chr2:31441312-31441362	NHDF-neo	bronchial:	n/a
30	chr2:31456747-31456797	MCF10A-Er-Src	breast:	n/a
31	chr2:31457043-31457093	LNCaP	prostate:	n/a
32	chr2:31455890-31455940	HEK293	kidney:	embryo
33	chr2:31457287-31457337	Caco-2	colon:	n/a
34	chr2:31456217-31456267	AG04449	skin:	fetal
35	chr2:31457061-31457111	HRPEpiC	eye:	n/a
36	chr2:31455890-31455940	K562	blood:	n/a
37	chr2:31439687-31439737	Caco-2	colon:	n/a
38	chr2:31457043-31457093	GM12891	blood:	n/a
39	chr2:31456804-31456854	Jurkat	blood:	n/a
40	chr2:31455443-31455493	GM19239	blood:	n/a
41	chr2:31456761-31456811	HCPEpiC	choroid plexus:	n/a
42	chr2:31454631-31454681	Caco-2	colon:	n/a
43	chr2:31440349-31440399	AG09309	skin:	n/a
44	chr2:31457608-31457658	HEK293	kidney:	embryo
45	chr2:31456966-31457016	BE2_C	brain:	n/a
46	chr2:31441312-31441362	NT2-D1	testis:	n/a
47	chr2:31440451-31440501	GM12878	blood:	n/a
48	chr2:31456775-31456825	HCM	heart:	n/a
49	chr2:31456747-31456797	ProgFib	skin:	n/a
50	chr2:31440451-31440501	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
2	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:
3	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
4	chr2:31418550..31420224-chr2:31425779..31428465,2	K562	blood:
5	chr2:31457912..31460253-chr2:31482759..31484283,2	MCF-7	breast:
6	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
7	chr2:31449978..31452625-chr2:31454988..31456954,2	K562	blood:
8	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
9	chr2:31456683..31458757-chr2:31460645..31462411,2	MCF-7	breast:
10	chr17:58816926..58819384-chr2:31448134..31450659,2	MCF-7	breast:
11	chr2:31407024..31409183-chr2:31430215..31431751,2	MCF-7	breast:
12	chr2:31456557..31458927-chr2:31463971..31466184,2	MCF-7	breast:
13	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
14	chr17:63334973..63335809-chr2:31437485..31438063,2	MCF-7	breast:
15	chr2:31453246..31458582-chr2:31458844..31463834,9	MCF-7	breast:
16	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
17	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:
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
ENSG00000013016	chromatin interactions
ENSG00000214711	chromatin interactions

Extended variants
information (count: 1850 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1373218	chr2:31425783-31425784	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530871891	chr2:31425906-31425907	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs550577225	chr2:31425939-31425940	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs372195179	chr2:31425971-31425972	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs570484260	chr2:31426006-31426007	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs546462559	chr2:31426034-31426035	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs533708103	chr2:31426037-31426038	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs546963620	chr2:31426042-31426043	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs564656539	chr2:31426052-31426053	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs567096409	chr2:31426074-31426075	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs386644493	chr2:31426096-31426097	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs1470335	chr2:31426098-31426099	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146182900	chr2:31426102-31426103	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs369902966	chr2:31426162-31426163	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs139153257	chr2:31426174-31426175	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs557020066	chr2:31426196-31426197	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs562212188	chr2:31426201-31426202	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs60701289	chr2:31426233-31426234	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397960470	chr2:31426236-31426237	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373553750	chr2:31426260-31426261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185494721	chr2:31426274-31426275	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546116591	chr2:31426280-31426281	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552986991	chr2:31426304-31426305	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376773115	chr2:31426364-31426365	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190695828	chr2:31426370-31426371	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561510350	chr2:31426379-31426380	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192215345	chr2:31426382-31426383	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184490379	chr2:31426394-31426395	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564175933	chr2:31426400-31426401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533165225	chr2:31426418-31426419	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73921587	chr2:31426446-31426447	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs7559123	chr2:31426449-31426450	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs34438079	chr2:31426450-31426451	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188393364	chr2:31426461-31426462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79309590	chr2:31426478-31426479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144017816	chr2:31426480-31426481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537173396	chr2:31426489-31426490	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577465261	chr2:31426490-31426491	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535369203	chr2:31426515-31426516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533252465	chr2:31426545-31426546	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570472706	chr2:31426582-31426583	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539063369	chr2:31426601-31426602	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370023259	chr2:31426628-31426629	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552889888	chr2:31426653-31426654	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553277027	chr2:31426655-31426656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573069571	chr2:31426677-31426678	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574662453	chr2:31426696-31426697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541693476	chr2:31426716-31426717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555169692	chr2:31426720-31426721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4527250	chr2:31426741-31426742	Weak transcription Strong 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:1109 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31411000-31427400	Weak transcription	Fetal Brain Female	brain
2	chr2:31411200-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr2:31420800-31430800	Weak transcription	Primary B cells from cord blood	blood
4	chr2:31421200-31429600	Weak transcription	Dnd41	blood
5	chr2:31423400-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:31424200-31435800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:31424200-31437600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:31424800-31428000	Weak transcription	Esophagus	oesophagus
9	chr2:31425200-31427400	Enhancers	Colon Smooth Muscle	Colon
10	chr2:31425400-31426400	Weak transcription	Left Ventricle	heart
11	chr2:31425400-31427600	Enhancers	Fetal Heart	heart
12	chr2:31425400-31428400	Strong transcription	Primary B cells from peripheral blood	blood
13	chr2:31425600-31428000	Enhancers	Right Ventricle	heart
14	chr2:31425800-31426200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr2:31426400-31428400	Enhancers	Left Ventricle	heart
16	chr2:31427400-31427600	Enhancers	Fetal Brain Female	brain
17	chr2:31427400-31428200	Enhancers	Brain Angular Gyrus	brain
18	chr2:31427600-31430800	Weak transcription	Fetal Heart	heart
19	chr2:31428000-31428800	Strong transcription	Esophagus	oesophagus
20	chr2:31428000-31429000	Weak transcription	Right Ventricle	heart
21	chr2:31428200-31428600	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr2:31428400-31430400	Weak transcription	Primary B cells from peripheral blood	blood
23	chr2:31428400-31431200	Weak transcription	Left Ventricle	heart
24	chr2:31428800-31437400	Weak transcription	Esophagus	oesophagus
25	chr2:31429000-31429200	Enhancers	Right Ventricle	heart
26	chr2:31429800-31430200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:31430000-31432800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:31430200-31441600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:31430400-31431600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:31430400-31432000	Enhancers	Primary B cells from peripheral blood	blood
31	chr2:31430600-31431000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:31430600-31431000	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr2:31430800-31431200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr2:31430800-31431400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:31430800-31431800	Enhancers	Primary B cells from cord blood	blood
36	chr2:31430800-31432400	Enhancers	Fetal Heart	heart
37	chr2:31431000-31431600	Enhancers	GM12878-XiMat	blood
38	chr2:31431000-31436000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:31431000-31436000	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr2:31431200-31431400	Enhancers	Left Ventricle	heart
41	chr2:31431200-31436000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr2:31431600-31432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:31431600-31435800	Weak transcription	GM12878-XiMat	blood
44	chr2:31431800-31436800	Weak transcription	Primary B cells from cord blood	blood
45	chr2:31432000-31435800	Weak transcription	Primary B cells from peripheral blood	blood
46	chr2:31432400-31436600	Weak transcription	Fetal Heart	heart
47	chr2:31432600-31433000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:31432800-31435600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:31433000-31433800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:31433800-31434400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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