Variant report

Variant	nsv582009
Chromosome Location	chr2:53701324-53785037
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:523)
CpG islands
(count:366)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:53718011-53718202	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:53743872-53744174	GM12878	blood:	n/a	n/a
3	BATF	chr2:53743884-53744091	GM12878	blood:	n/a	n/a
4	BRCA1	chr2:53702397-53703247	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr2:53732954-53733393	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr2:53739626-53739837	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr2:53703941-53704510	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr2:53702123-53703068	HCT-116	colon:	n/a	n/a
9	CBX3	chr2:53703850-53704480	HCT-116	colon:	n/a	n/a
10	CBX3	chr2:53701938-53703325	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:53702263-53703112	HCT-116	colon:	n/a	chr2:53703002-53703019
12	CEBPB	chr2:53784458-53784658	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:53781633-53781847	HepG2	liver:	n/a	chr2:53781767-53781778
14	CEBPB	chr2:53725295-53725758	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:53717911-53718214	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:53702175-53703286	Hela-S3	cervix:	n/a	chr2:53703002-53703019
17	CEBPB	chr2:53720034-53720332	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:53739555-53739944	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:53717882-53718254	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:53752634-53752730	K562	blood:	n/a	n/a
21	CEBPB	chr2:53701031-53701420	Hela-S3	cervix:	n/a	chr2:53701315-53701327
22	CEBPB	chr2:53739612-53739812	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:53742616-53743191	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:53739537-53739943	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:53725272-53725726	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:53703905-53704648	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:53743586-53743649	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:53702219-53703198	HCT-116	colon:	n/a	chr2:53703002-53703019
29	CHD2	chr2:53739624-53739824	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr2:53703925-53704545	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr2:53702154-53703199	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr2:53732991-53733366	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr2:53738900-53739050	HRPEpiC	eye:	n/a	chr2:53738900-53738907
34	CTCF	chr2:53742987-53743131	GM12878	blood:	n/a	n/a
35	CTCF	chr2:53742923-53743101	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr2:53742921-53743193	T-47D	breast:	n/a	n/a
37	CTCF	chr2:53742960-53743110	NHEK	skin:	n/a	n/a
38	CTCF	chr2:53742980-53743130	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:53735880-53736030	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr2:53742940-53743090	SAEC	small airway:	n/a	n/a
41	CTCF	chr2:53742999-53743118	LNCaP	prostate:	n/a	n/a
42	CTCF	chr2:53742940-53743090	HMF	breast:	n/a	n/a
43	CTCF	chr2:53738832-53738964	HepG2	liver:	n/a	chr2:53738900-53738907
44	CTCF	chr2:53742940-53743090	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr2:53735932-53736020	K562	blood:	n/a	n/a
46	CTCF	chr2:53738899-53738941	MCF-7	breast:	n/a	chr2:53738900-53738907
47	CTCF	chr2:53742940-53743090	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:53742971-53743116	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr2:53742960-53743110	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr2:53742960-53743110	HEK293	kidney:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53731598-53731648	T-47D	breast:	n/a
2	chr2:53747541-53747591	HL-60	blood:	n/a
3	chr2:53731598-53731648	AG04450	lung:	fetal
4	chr2:53731598-53731648	HCPEpiC	choroid plexus:	n/a
5	chr2:53725202-53725252	HCPEpiC	choroid plexus:	n/a
6	chr2:53725202-53725252	AG09309	skin:	n/a
7	chr2:53747541-53747591	HCT-116	colon:	n/a
8	chr2:53725202-53725252	HRCEpiC	kidney:	n/a
9	chr2:53725202-53725252	SK-N-SH_RA	brain:	n/a
10	chr2:53747541-53747591	Hepatocyte	liver:	n/a
11	chr2:53747541-53747591	Caco-2	colon:	n/a
12	chr2:53725202-53725252	SKMC	muscle:	n/a
13	chr2:53764920-53764970	AoSMC	blood vessel:	n/a
14	chr2:53701531-53701581	HEK293	kidney:	embryo
15	chr2:53764920-53764970	AG09319	gingival:	n/a
16	chr2:53747541-53747591	NHBE	bronchial:	n/a
17	chr2:53714365-53714415	H1-hESC	embryonic stem cell:	embryo
18	chr2:53747541-53747591	HUVEC	blood vessel:	n/a
19	chr2:53714365-53714415	NB4	blood:	n/a
20	chr2:53731598-53731648	U87	brain:	n/a
21	chr2:53701531-53701581	A549	lung:	n/a
22	chr2:53731598-53731648	H1-hESC	embryonic stem cell:	embryo
23	chr2:53725202-53725252	MCF-7	breast:	n/a
24	chr2:53701531-53701581	HCPEpiC	choroid plexus:	n/a
25	chr2:53747541-53747591	AG04449	skin:	fetal
26	chr2:53725202-53725252	GM19239	blood:	n/a
27	chr2:53714365-53714415	PANC-1	pancreas:	n/a
28	chr2:53725202-53725252	Caco-2	colon:	n/a
29	chr2:53714365-53714415	HCPEpiC	choroid plexus:	n/a
30	chr2:53725202-53725252	SAEC	small airway:	n/a
31	chr2:53701531-53701581	GM06990	blood:	n/a
32	chr2:53731598-53731648	NT2-D1	testis:	n/a
33	chr2:53747541-53747591	SAEC	small airway:	n/a
34	chr2:53701531-53701581	ProgFib	skin:	n/a
35	chr2:53725202-53725252	HepG2	liver:	n/a
36	chr2:53731598-53731648	SK-N-SH	brain:	n/a
37	chr2:53747541-53747591	HCPEpiC	choroid plexus:	n/a
38	chr2:53747541-53747591	MCF10A-Er-Src	breast:	n/a
39	chr2:53714365-53714415	HepG2	liver:	n/a
40	chr2:53725202-53725252	NHDF-neo	bronchial:	n/a
41	chr2:53731598-53731648	GM12891	blood:	n/a
42	chr2:53701531-53701581	LNCaP	prostate:	n/a
43	chr2:53747541-53747591	AG04450	lung:	fetal
44	chr2:53714365-53714415	A549	lung:	n/a
45	chr2:53701531-53701581	MCF-7	breast:	n/a
46	chr2:53731598-53731648	HRCEpiC	kidney:	n/a
47	chr2:53764920-53764970	LNCaP	prostate:	n/a
48	chr2:53731598-53731648	Jurkat	blood:	n/a
49	chr2:53747541-53747591	HNPCEpiC	eye:	n/a
50	chr2:53747541-53747591	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:53718351..53720003-chr2:53723225..53725281,2	K562	blood:
2	chr2:53763474..53765231-chr2:53774418..53775976,2	K562	blood:
3	chr2:53774246..53775776-chr2:53777337..53778910,2	K562	blood:
4	chr2:53718351..53720003-chr2:53723225..53725281,2	K562	blood:
5	chr2:53780507..53782864-chr2:53992929..53994536,2	K562	blood:
6	chr2:53757085..53758831-chr2:53762624..53764865,2	K562	blood:
7	chr2:53764669..53766504-chr2:53770937..53773630,2	K562	blood:
8	chr2:53691365..53693137-chr2:53701304..53703137,2	MCF-7	breast:
9	chr2:53771758..53774525-chr2:53776196..53777860,2	MCF-7	breast:
10	chr2:53757085..53758831-chr2:53762624..53764865,2	K562	blood:
11	chr2:53725082..53727239-chr2:53732255..53735113,2	K562	blood:
12	chr2:53764669..53766504-chr2:53770937..53773630,2	K562	blood:
13	chr2:53763474..53765231-chr2:53774418..53775976,2	K562	blood:
14	chr2:53720586..53722714-chr2:53727046..53728819,2	MCF-7	breast:
15	chr2:53720586..53722714-chr2:53727046..53728819,2	MCF-7	breast:
16	chr2:53771758..53774525-chr2:53776196..53777860,2	MCF-7	breast:
17	chr2:53725082..53727239-chr2:53732255..53735113,2	K562	blood:
18	chr2:53774246..53775776-chr2:53777337..53778910,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223897	TF binding region
ENSG00000251942	TF binding region
ENSG00000223897	CpG island
ENSG00000251942	CpG island

Extended variants
information (count: 3531 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3531 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs903227	chr2:53701324-53701325	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs185678111	chr2:53701328-53701329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs558855700	chr2:53701365-53701366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565835104	chr2:53701394-53701395	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs377158618	chr2:53701402-53701403	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561256456	chr2:53701404-53701405	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs530367410	chr2:53701425-53701426	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs534822225	chr2:53701449-53701450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188865219	chr2:53701454-53701455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199969894	chr2:53701548-53701549	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs554766142	chr2:53701556-53701557	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs570060406	chr2:53701572-53701573	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs181716818	chr2:53701581-53701582	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs185442973	chr2:53701620-53701621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116983425	chr2:53701649-53701650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533981620	chr2:53701718-53701719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142043454	chr2:53701745-53701746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573971168	chr2:53701764-53701765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536593595	chr2:53701783-53701784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188393809	chr2:53701784-53701785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181292870	chr2:53701831-53701832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201091666	chr2:53701837-53701838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544743766	chr2:53701946-53701947	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs146289820	chr2:53701958-53701959	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572499304	chr2:53701993-53701994	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs374671749	chr2:53702040-53702041	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs541217478	chr2:53702064-53702065	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs76712330	chr2:53702080-53702081	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs530308218	chr2:53702090-53702091	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs185975190	chr2:53702111-53702112	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs148511496	chr2:53702120-53702121	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs532563467	chr2:53702177-53702178	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs142959542	chr2:53702211-53702212	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190844316	chr2:53702247-53702248	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566172545	chr2:53702250-53702251	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs151110148	chr2:53702338-53702339	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs534147757	chr2:53702352-53702353	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140031944	chr2:53702420-53702421	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs183995598	chr2:53702475-53702476	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536535007	chr2:53702487-53702488	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556437322	chr2:53702512-53702513	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs569521591	chr2:53702593-53702594	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs545867926	chr2:53702642-53702643	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs553885851	chr2:53702668-53702669	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs538631097	chr2:53702695-53702696	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs149824788	chr2:53702707-53702708	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571806835	chr2:53702720-53702721	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs141274843	chr2:53702764-53702765	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs199870965	chr2:53702768-53702769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528731206	chr2:53702784-53702785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53698000-53706400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr2:53698200-53702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:53698200-53702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:53698200-53702200	Weak transcription	HMEC	breast
5	chr2:53698200-53702200	Weak transcription	NHEK	skin
6	chr2:53700000-53703000	Enhancers	Hela-S3	cervix
7	chr2:53700400-53704200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:53700800-53702400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:53701000-53702000	Weak transcription	NHDF-Ad	bronchial
10	chr2:53701000-53702200	Weak transcription	NHLF	lung
11	chr2:53701200-53702200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:53701200-53704000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:53702000-53703200	Enhancers	NHDF-Ad	bronchial
14	chr2:53702200-53702600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:53702200-53703200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:53702200-53703200	Enhancers	A549	lung
17	chr2:53702200-53703200	Enhancers	NHLF	lung
18	chr2:53702200-53703400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr2:53702200-53703600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr2:53702200-53703600	Enhancers	NH-A	brain
21	chr2:53702200-53704000	Enhancers	HMEC	breast
22	chr2:53702200-53704200	Enhancers	NHEK	skin
23	chr2:53702400-53702600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:53702400-53703200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr2:53702600-53703000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:53703000-53703200	Flanking Active TSS	Hela-S3	cervix
27	chr2:53703200-53703400	Enhancers	Hela-S3	cervix
28	chr2:53703400-53703600	Flanking Active TSS	Hela-S3	cervix
29	chr2:53703400-53703800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:53703600-53707200	Enhancers	Hela-S3	cervix
31	chr2:53703800-53704200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:53704000-53704200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:53706400-53708000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr2:53707200-53711400	Weak transcription	Hela-S3	cervix
35	chr2:53708000-53708400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr2:53708400-53708600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:53708600-53712000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr2:53711000-53711600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:53711000-53712000	Enhancers	Stomach Mucosa	stomach
40	chr2:53711400-53712200	Enhancers	Hela-S3	cervix
41	chr2:53712000-53712400	Weak transcription	Stomach Mucosa	stomach
42	chr2:53712000-53713000	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr2:53712200-53717000	Weak transcription	Hela-S3	cervix
44	chr2:53712400-53712600	Enhancers	Stomach Mucosa	stomach
45	chr2:53712400-53713400	Enhancers	Fetal Stomach	stomach
46	chr2:53712400-53717600	Weak transcription	Aorta	Aorta
47	chr2:53712600-53713000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:53712600-53714600	Weak transcription	Stomach Mucosa	stomach
49	chr2:53713000-53713600	Enhancers	Fetal Brain Male	brain
50	chr2:53713000-53714600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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