Variant report

Variant	nsv430635
Chromosome Location	chr2:31420415-31464385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:686)
CpG islands
(count:1588)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:686 , 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	chr2:31456598-31456992	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:31441886-31442907	GM12878	blood:	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	chr2:31442483-31442746	GM12878	blood:	n/a	n/a
6	BATF	chr2:31442515-31442799	GM12878	blood:	n/a	n/a
7	BCL3	chr2:31423822-31424213	GM12878	blood:	n/a	n/a
8	BCL3	chr2:31456641-31457247	A549	lung:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
9	BCLAF1	chr2:31441899-31442872	GM12878	blood:	n/a	n/a
10	BCLAF1	chr2:31456640-31457127	GM12878	blood:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
11	BHLHE40	chr2:31456662-31457127	GM12878	blood:	n/a	chr2:31457080-31457096
12	BHLHE40	chr2:31441900-31442892	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:31463632-31463876	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:31440475-31440850	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:31430809-31431053	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:31434430-31434614	K562	blood:	n/a	n/a
17	BRCA1	chr2:31456720-31457019	H1-hESC	embryonic stem cell:	n/a	n/a
18	CCNT2	chr2:31456858-31457304	K562	blood:	n/a	chr2:31457137-31457146
19	CEBPB	chr2:31427031-31427326	IMR90	lung:	n/a	chr2:31427167-31427178
20	CEBPB	chr2:31442574-31442749	A549	lung:	n/a	n/a
21	CEBPB	chr2:31426142-31426190	K562	blood:	n/a	n/a
22	CEBPB	chr2:31426991-31427339	A549	lung:	n/a	chr2:31427167-31427178
23	CEBPB	chr2:31427049-31427251	K562	blood:	n/a	chr2:31427167-31427178
24	CEBPB	chr2:31456573-31456935	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:31427020-31427332	HepG2	liver:	n/a	chr2:31427167-31427178
26	CEBPB	chr2:31458407-31458725	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:31436089-31436493	MCF-7	breast:	n/a	n/a
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	chr2:31441888-31442844	GM12878	blood:	n/a	n/a
32	CHD2	chr2:31456890-31456943	HepG2	liver:	n/a	n/a
33	CHD2	chr2:31456531-31457222	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr2:31456757-31457101	GM12878	blood:	n/a	n/a
35	CREB1	chr2:31456683-31457015	A549	lung:	n/a	n/a
36	CREB1	chr2:31456659-31457229	A549	lung:	n/a	n/a
37	CREB1	chr2:31456606-31457154	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr2:31456527-31457601	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	chr2:31456620-31456770	HVMF	connective:	n/a	n/a
41	CTCF	chr2:31430695-31430862	GM12892	blood:	n/a	n/a
42	CTCF	chr2:31456660-31456810	GM06990	blood:	n/a	n/a
43	CTCF	chr2:31458580-31458730	HPAF	blood vessel:	n/a	chr2:31458646-31458655
44	CTCF	chr2:31456680-31456830	HEK293	kidney:	n/a	n/a
45	CTCF	chr2:31453800-31453950	HepG2	liver:	n/a	n/a
46	CTCF	chr2:31453820-31453970	AG04450	lung:	n/a	n/a
47	CTCF	chr2:31455940-31456090	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr2:31456620-31456770	RPTEC	kidney:	n/a	n/a
49	CTCF	chr2:31456607-31456918	A549	lung:	n/a	n/a
50	CTCF	chr2:31456680-31456830	AG04450	lung:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:31440349-31440399	HEK293	kidney:	embryo
2	chr2:31457608-31457658	HRCEpiC	kidney:	n/a
3	chr2:31440349-31440399	HEK293	kidney:	embryo
4	chr2:31457608-31457658	HRCEpiC	kidney:	n/a
5	chr2:31457043-31457093	ECC-1	luminal epithelium:	n/a
6	chr2:31449901-31449951	HCF	heart:	n/a
7	chr2:31456217-31456267	HIPEpiC	eye:	n/a
8	chr2:31456775-31456825	HL-60	blood:	n/a
9	chr2:31441554-31441604	HMEC	breast:	n/a
10	chr2:31456804-31456854	AG09319	gingival:	n/a
11	chr2:31456217-31456267	HMEC	breast:	n/a
12	chr2:31456775-31456825	GM12878	blood:	n/a
13	chr2:31455890-31455940	PrEC	prostate:	n/a
14	chr2:31457058-31457108	GM12891	blood:	n/a
15	chr2:31458372-31458422	HCPEpiC	choroid plexus:	n/a
16	chr2:31456964-31457014	BE2_C	brain:	n/a
17	chr2:31456761-31456811	H1-hESC	embryonic stem cell:	embryo
18	chr2:31457608-31457658	CMK	blood:	n/a
19	chr2:31441554-31441604	LNCaP	prostate:	n/a
20	chr2:31457608-31457658	HMEC	breast:	n/a
21	chr2:31441554-31441604	SAEC	small airway:	n/a
22	chr2:31454631-31454681	T-47D	breast:	n/a
23	chr2:31457608-31457658	U87	brain:	n/a
24	chr2:31455890-31455940	HPAEpiC	pulmonary alveolar:	n/a
25	chr2:31455890-31455940	BJ	skin:	n/a
26	chr2:31456804-31456854	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:31458372-31458422	HCM	heart:	n/a
28	chr2:31440349-31440399	HCT-116	colon:	n/a
29	chr2:31457058-31457108	NB4	blood:	n/a
30	chr2:31456747-31456797	SKMC	muscle:	n/a
31	chr2:31455443-31455493	HUVEC	blood vessel:	n/a
32	chr2:31456789-31456839	MCF10A-Er-Src	breast:	n/a
33	chr2:31456964-31457014	NB4	blood:	n/a
34	chr2:31440349-31440399	SAEC	small airway:	n/a
35	chr2:31457608-31457658	MCF-7	breast:	n/a
36	chr2:31457061-31457111	HNPCEpiC	eye:	n/a
37	chr2:31459843-31459893	NHBE	bronchial:	n/a
38	chr2:31439687-31439737	NB4	blood:	n/a
39	chr2:31440451-31440501	PANC-1	pancreas:	n/a
40	chr2:31457058-31457108	K562	blood:	n/a
41	chr2:31440349-31440399	Jurkat	blood:	n/a
42	chr2:31441554-31441604	HCM	heart:	n/a
43	chr2:31457058-31457108	NT2-D1	testis:	n/a
44	chr2:31457061-31457111	GM12892	blood:	n/a
45	chr2:31439687-31439737	Hela-S3	cervix:	n/a
46	chr2:31456804-31456854	NHBE	bronchial:	n/a
47	chr2:31454631-31454681	NT2-D1	testis:	n/a
48	chr2:31455890-31455940	NB4	blood:	n/a
49	chr2:31441588-31441638	LNCaP	prostate:	n/a
50	chr2:31456747-31456797	AG04450	lung:	fetal

(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	chr2:31449978..31452625-chr2:31454988..31456954,2	K562	blood:
3	chr2:31456683..31458757-chr2:31460645..31462411,2	MCF-7	breast:
4	chr17:63334973..63335809-chr2:31437485..31438063,2	MCF-7	breast:
5	chr2:31418550..31420224-chr2:31425779..31428465,2	K562	blood:
6	chr17:58816926..58819384-chr2:31448134..31450659,2	MCF-7	breast:
7	chr2:31453246..31458582-chr2:31458844..31463834,9	MCF-7	breast:
8	chr2:31407024..31409183-chr2:31430215..31431751,2	MCF-7	breast:
9	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:
10	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
11	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
12	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
13	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
14	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
15	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:
16	chr2:31449978..31452625-chr2:31454988..31456954,2	K562	blood:
17	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
18	chr2:31457912..31460253-chr2:31482759..31484283,2	MCF-7	breast:

No data

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

Extended variants
information (count: 2009 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2009 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7595622	chr2:31420415-31420416	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565910722	chr2:31420458-31420459	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117870460	chr2:31420471-31420472	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150934132	chr2:31420474-31420475	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139511613	chr2:31420483-31420484	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182647513	chr2:31420484-31420485	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1443716	chr2:31420485-31420486	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149705002	chr2:31420500-31420501	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7595550	chr2:31420506-31420507	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs187573932	chr2:31420533-31420534	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192814362	chr2:31420580-31420581	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536106375	chr2:31420584-31420585	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555216833	chr2:31420658-31420659	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146719136	chr2:31420664-31420665	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555637606	chr2:31420784-31420785	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117084547	chr2:31420803-31420804	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543116820	chr2:31420834-31420835	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140359411	chr2:31420846-31420847	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34348757	chr2:31420865-31420866	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397871631	chr2:31420871-31420872	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116575804	chr2:31420917-31420918	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184665526	chr2:31420923-31420924	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537608819	chr2:31420959-31420960	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559680613	chr2:31420983-31420984	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528327722	chr2:31420997-31420998	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187308307	chr2:31421005-31421006	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371782786	chr2:31421013-31421014	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561697005	chr2:31421035-31421036	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375208230	chr2:31421070-31421071	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543679667	chr2:31421074-31421075	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531053996	chr2:31421082-31421083	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550636683	chr2:31421085-31421086	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6750359	chr2:31421128-31421129	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs539436304	chr2:31421130-31421131	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192035090	chr2:31421176-31421177	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567159691	chr2:31421183-31421184	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199724343	chr2:31421222-31421223	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs80037410	chr2:31421223-31421224	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35701726	chr2:31421224-31421225	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370157917	chr2:31421225-31421226	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs397784680	chr2:31421226-31421227	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535736572	chr2:31421232-31421233	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555946015	chr2:31421272-31421273	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184535853	chr2:31421276-31421277	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537171476	chr2:31421291-31421292	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6708447	chr2:31421334-31421335	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs576954981	chr2:31421336-31421337	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559068047	chr2:31421400-31421401	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189301390	chr2:31421427-31421428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559045307	chr2:31421454-31421455	Weak transcription Strong transcription	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:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31411000-31421800	Weak transcription	Primary T cells from cord blood	blood
2	chr2:31411000-31427400	Weak transcription	Fetal Brain Female	brain
3	chr2:31411200-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:31413400-31425600	Weak transcription	Right Ventricle	heart
5	chr2:31415400-31420800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr2:31417000-31424200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:31417400-31425400	Weak transcription	Primary B cells from peripheral blood	blood
8	chr2:31419200-31420600	Enhancers	NHEK	skin
9	chr2:31419400-31420800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:31419400-31420800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:31419400-31423400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr2:31419600-31420800	Strong transcription	Primary B cells from cord blood	blood
13	chr2:31419800-31420600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:31420000-31420800	Enhancers	Esophagus	oesophagus
15	chr2:31420000-31421400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:31420200-31420800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:31420400-31423800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:31420800-31421800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:31420800-31422000	Weak transcription	Esophagus	oesophagus
20	chr2:31420800-31423800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:31420800-31430800	Weak transcription	Primary B cells from cord blood	blood
22	chr2:31421200-31429600	Weak transcription	Dnd41	blood
23	chr2:31421800-31422600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:31422000-31422400	ZNF genes & repeats	Esophagus	oesophagus
25	chr2:31422400-31424000	Weak transcription	Esophagus	oesophagus
26	chr2:31422600-31424200	Weak transcription	Brain Germinal Matrix	brain
27	chr2:31423400-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr2:31423800-31424200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:31423800-31424200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:31424000-31424200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr2:31424000-31424800	Strong transcription	Esophagus	oesophagus
32	chr2:31424200-31424400	Enhancers	Brain Germinal Matrix	brain
33	chr2:31424200-31435800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:31424200-31437600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:31424800-31428000	Weak transcription	Esophagus	oesophagus
36	chr2:31425200-31425400	Enhancers	Left Ventricle	heart
37	chr2:31425200-31427400	Enhancers	Colon Smooth Muscle	Colon
38	chr2:31425400-31426400	Weak transcription	Left Ventricle	heart
39	chr2:31425400-31427600	Enhancers	Fetal Heart	heart
40	chr2:31425400-31428400	Strong transcription	Primary B cells from peripheral blood	blood
41	chr2:31425600-31428000	Enhancers	Right Ventricle	heart
42	chr2:31425800-31426200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr2:31426400-31428400	Enhancers	Left Ventricle	heart
44	chr2:31427400-31427600	Enhancers	Fetal Brain Female	brain
45	chr2:31427400-31428200	Enhancers	Brain Angular Gyrus	brain
46	chr2:31427600-31430800	Weak transcription	Fetal Heart	heart
47	chr2:31428000-31428800	Strong transcription	Esophagus	oesophagus
48	chr2:31428000-31429000	Weak transcription	Right Ventricle	heart
49	chr2:31428200-31428600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr2:31428400-31430400	Weak transcription	Primary B cells from peripheral blood	blood

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