Variant report

Variant	nsv961452
Chromosome Location	chr2:96195565-96199535
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	ATF2	chr2:96196364-96196820	GM12878	blood:	n/a	n/a
2	ATF2	chr2:96196438-96196882	GM12878	blood:	n/a	n/a
3	BATF	chr2:96196469-96196822	GM12878	blood:	n/a	n/a
4	BATF	chr2:96196382-96197020	GM12878	blood:	n/a	n/a
5	BCL3	chr2:96197262-96197625	GM12878	blood:	n/a	n/a
6	BCL3	chr2:96196371-96196868	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:96196496-96196958	GM12878	blood:	n/a	n/a
8	BRCA1	chr2:96197411-96197504	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:96196346-96196776	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:96195864-96196064	HepG2	liver:	n/a	chr2:96196012-96196023
11	CEBPB	chr2:96196312-96196446	HepG2	liver:	n/a	n/a
12	CHD2	chr2:96196541-96197075	GM12878	blood:	n/a	n/a
13	CHD2	chr2:96197519-96197521	GM12878	blood:	n/a	n/a
14	CREB1	chr2:96196294-96197258	GM12878	blood:	n/a	n/a
15	CREB1	chr2:96196432-96197228	GM12878	blood:	n/a	n/a
16	CTCF	chr2:96199220-96199370	GM12871	blood:	n/a	chr2:96199278-96199287
17	CTCF	chr2:96199200-96199350	GM12865	blood:	n/a	chr2:96199278-96199287
18	CTCF	chr2:96199040-96199190	A549	lung:	n/a	n/a
19	CTCF	chr2:96199220-96199370	HCPEpiC	choroid plexus:	n/a	chr2:96199278-96199287
20	CTCF	chr2:96199180-96199330	GM12872	blood:	n/a	chr2:96199278-96199287
21	CTCF	chr2:96199240-96199390	HCFaa	heart:	n/a	chr2:96199278-96199287
22	CTCF	chr2:96199180-96199330	GM12864	blood:	n/a	chr2:96199278-96199287
23	CTCF	chr2:96199120-96199270	GM12872	blood:	n/a	n/a
24	CTCF	chr2:96199180-96199330	HepG2	liver:	n/a	chr2:96199278-96199287
25	CTCF	chr2:96199180-96199330	GM12873	blood:	n/a	chr2:96199278-96199287
26	CTCF	chr2:96199180-96199330	GM06990	blood:	n/a	chr2:96199278-96199287
27	CTCF	chr2:96199220-96199370	HMF	breast:	n/a	chr2:96199278-96199287
28	CTCF	chr2:96199360-96199510	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr2:96199180-96199330	MCF-7	breast:	n/a	chr2:96199278-96199287
30	CTCF	chr2:96199160-96199310	GM12865	blood:	n/a	chr2:96199278-96199287
31	CTCF	chr2:96199180-96199330	NHEK	skin:	n/a	chr2:96199278-96199287
32	CTCF	chr2:96199180-96199330	Hela-S3	cervix:	n/a	chr2:96199278-96199287
33	CTCF	chr2:96199180-96199330	AoAF	blood vessel:	n/a	chr2:96199278-96199287
34	CTCF	chr2:96199100-96199250	GM12866	blood:	n/a	n/a
35	CTCF	chr2:96199220-96199370	RPTEC	kidney:	n/a	chr2:96199278-96199287
36	CTCF	chr2:96199200-96199350	HBMEC	blood vessel:	n/a	chr2:96199278-96199287
37	CTCF	chr2:96199200-96199350	HPAF	blood vessel:	n/a	chr2:96199278-96199287
38	CTCF	chr2:96199240-96199390	HEEpiC	esophagus:	n/a	chr2:96199278-96199287
39	CTCF	chr2:96199260-96199410	HAc	cerebellar:	n/a	chr2:96199278-96199287
40	CTCF	chr2:96199260-96199410	MCF-7	breast:	n/a	chr2:96199278-96199287
41	CTCF	chr2:96199140-96199290	HCT-116	colon:	n/a	chr2:96199278-96199287
42	CTCF	chr2:96199160-96199310	HMF	breast:	n/a	chr2:96199278-96199287
43	CTCF	chr2:96199180-96199330	HEK293	kidney:	n/a	chr2:96199278-96199287
44	CTCF	chr2:96198960-96199110	AG10803	skin:	n/a	n/a
45	CTCF	chr2:96199253-96199307	K562	blood:	n/a	chr2:96199278-96199287
46	CTCF	chr2:96199160-96199310	GM12878	blood:	n/a	chr2:96199278-96199287
47	EBF1	chr2:96197402-96197685	GM12878	blood:	n/a	n/a
48	EBF1	chr2:96197293-96197708	GM12878	blood:	n/a	n/a
49	EBF1	chr2:96196434-96197023	GM12878	blood:	n/a	chr2:96196791-96196802
50	EBF1	chr2:96196414-96197043	GM12878	blood:	n/a	chr2:96196791-96196802

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96196596-96196646	HRE	kidney:	n/a
2	chr2:96196596-96196646	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:96196596-96196646	K562	blood:	n/a
4	chr2:96196596-96196646	AG04450	lung:	fetal
5	chr2:96196596-96196646	LNCaP	prostate:	n/a
6	chr2:96196596-96196646	Caco-2	colon:	n/a
7	chr2:96196596-96196646	AG04449	skin:	fetal
8	chr2:96196596-96196646	NHBE	bronchial:	n/a
9	chr2:96196596-96196646	GM12891	blood:	n/a
10	chr2:96196596-96196646	A549	lung:	n/a
11	chr2:96196596-96196646	GM12878	blood:	n/a
12	chr2:96196596-96196646	AoSMC	blood vessel:	n/a
13	chr2:96196596-96196646	AG09319	gingival:	n/a
14	chr2:96196596-96196646	HRPEpiC	eye:	n/a
15	chr2:96196596-96196646	Jurkat	blood:	n/a
16	chr2:96196596-96196646	HCF	heart:	n/a
17	chr2:96196596-96196646	SK-N-MC	brain:	n/a
18	chr2:96196596-96196646	NT2-D1	testis:	n/a
19	chr2:96196596-96196646	Hela-S3	cervix:	n/a
20	chr2:96196596-96196646	HAEpiC	amniotic membrane:	n/a
21	chr2:96196596-96196646	SK-N-SH	brain:	n/a
22	chr2:96196596-96196646	T-47D	breast:	n/a
23	chr2:96196596-96196646	HCT-116	colon:	n/a
24	chr2:96196596-96196646	BJ	skin:	n/a
25	chr2:96196596-96196646	HNPCEpiC	eye:	n/a
26	chr2:96196596-96196646	HepG2	liver:	n/a
27	chr2:96196596-96196646	HL-60	blood:	n/a
28	chr2:96196596-96196646	NH-A	brain:	n/a
29	chr2:96196596-96196646	HEK293	kidney:	embryo
30	chr2:96196596-96196646	PFSK-1	brain:	n/a
31	chr2:96196596-96196646	HUVEC	blood vessel:	n/a
32	chr2:96196596-96196646	ProgFib	skin:	n/a
33	chr2:96196596-96196646	U87	brain:	n/a
34	chr2:96196596-96196646	PrEC	prostate:	n/a
35	chr2:96196596-96196646	CMK	blood:	n/a
36	chr2:96196596-96196646	HIPEpiC	eye:	n/a
37	chr2:96196596-96196646	MCF-7	breast:	n/a
38	chr2:96196596-96196646	ovcar-3	ovarian:	n/a
39	chr2:96196596-96196646	GM12892	blood:	n/a
40	chr2:96196596-96196646	SKMC	muscle:	n/a
41	chr2:96196596-96196646	IMR90	lung:	fetal
42	chr2:96196596-96196646	HEEpiC	esophagus:	n/a
43	chr2:96196596-96196646	AG09309	skin:	n/a
44	chr2:96196596-96196646	HMEC	breast:	n/a
45	chr2:96196596-96196646	HCM	heart:	n/a
46	chr2:96196596-96196646	SAEC	small airway:	n/a
47	chr2:96196596-96196646	PANC-1	pancreas:	n/a
48	chr2:96196596-96196646	MCF10A-Er-Src	breast:	n/a
49	chr2:96196596-96196646	GM19239	blood:	n/a
50	chr2:96196596-96196646	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96197171..96199687-chr2:96228199..96230029,2	MCF-7	breast:
2	chr2:96197687..96200374-chr2:96200707..96202651,2	MCF-7	breast:
3	chr2:96193783..96195942-chr2:96197752..96200330,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000273305	TF binding region
ENSG00000272913	TF binding region
ENSG00000273305	CpG island
ENSG00000272913	CpG island
ENSG00000236431	chromatin interactions
ENSG00000229689	chromatin interactions

Extended variants
information (count: 131 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:131 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555550420	chr2:96195612-96195613	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1364395	chr2:96195632-96195633	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541320749	chr2:96195633-96195634	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557675938	chr2:96195645-96195646	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577505070	chr2:96195675-96195676	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs142326189	chr2:96195686-96195687	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs151310139	chr2:96195722-96195723	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1364394	chr2:96195730-96195731	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs185976729	chr2:96195759-96195760	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559910125	chr2:96195767-96195768	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192131526	chr2:96195963-96195964	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs140548795	chr2:96195973-96195974	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs565620203	chr2:96196034-96196035	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs531207839	chr2:96196093-96196094	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs549822535	chr2:96196165-96196166	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576724662	chr2:96196281-96196282	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569632819	chr2:96196297-96196298	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs2216793	chr2:96196322-96196323	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs34906416	chr2:96196334-96196335	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs548757073	chr2:96196374-96196375	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs116034722	chr2:96196385-96196386	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs534555276	chr2:96196391-96196392	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183211308	chr2:96196407-96196408	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs577544574	chr2:96196487-96196488	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs536920424	chr2:96196495-96196496	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs556952101	chr2:96196601-96196602	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs573914186	chr2:96196627-96196628	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs543112464	chr2:96196631-96196632	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs370382279	chr2:96196638-96196639	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs573279356	chr2:96196699-96196700	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs545644122	chr2:96196700-96196701	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs565447746	chr2:96196737-96196738	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs531245541	chr2:96196742-96196743	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551252824	chr2:96196827-96196828	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186449047	chr2:96196849-96196850	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs528927565	chr2:96196850-96196851	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs548953080	chr2:96196894-96196895	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs377294486	chr2:96197026-96197027	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs565670015	chr2:96197029-96197030	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs530046967	chr2:96197033-96197034	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs534694865	chr2:96197066-96197067	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542032209	chr2:96197112-96197113	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571075952	chr2:96197123-96197124	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs543528690	chr2:96197125-96197126	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs556792818	chr2:96197149-96197150	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573879056	chr2:96197150-96197151	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs536292332	chr2:96197178-96197179	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs147734483	chr2:96197198-96197199	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs527505950	chr2:96197206-96197207	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs545482672	chr2:96197207-96197208	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96192200-96197800	Weak transcription	Fetal Heart	heart
2	chr2:96192400-96196800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:96193000-96196400	Weak transcription	Spleen	Spleen
4	chr2:96193200-96195600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr2:96193200-96195600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:96193200-96195600	Weak transcription	Fetal Lung	lung
7	chr2:96193200-96195800	Weak transcription	Brain Substantia Nigra	brain
8	chr2:96193200-96196000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr2:96193200-96196600	Weak transcription	Osteobl	bone
10	chr2:96193200-96196800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr2:96193200-96197000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr2:96193200-96199000	Weak transcription	HSMMtube	muscle
13	chr2:96193400-96195600	Weak transcription	NHLF	lung
14	chr2:96193400-96196000	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr2:96193400-96196200	Weak transcription	Esophagus	oesophagus
16	chr2:96193400-96198000	Weak transcription	Colonic Mucosa	Colon
17	chr2:96193400-96199000	Weak transcription	Fetal Brain Male	brain
18	chr2:96193600-96195800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr2:96193600-96196000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr2:96193600-96196200	Weak transcription	HUVEC	blood vessel
21	chr2:96193600-96196600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr2:96193600-96196800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr2:96193600-96197000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr2:96193600-96198200	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr2:96193600-96198800	Weak transcription	Fetal Thymus	thymus
26	chr2:96193800-96195600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:96193800-96195600	Weak transcription	Brain Hippocampus Middle	brain
28	chr2:96193800-96196400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr2:96193800-96196600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:96193800-96197000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr2:96193800-96197000	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr2:96193800-96197400	Weak transcription	Colon Smooth Muscle	Colon
33	chr2:96193800-96199000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr2:96193800-96200400	Weak transcription	Stomach Mucosa	stomach
35	chr2:96194000-96198000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:96194000-96198400	Weak transcription	HMEC	breast
37	chr2:96194200-96195600	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr2:96194200-96196600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr2:96194200-96197600	Strong transcription	HSMM	muscle
40	chr2:96194400-96195800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr2:96194400-96196000	Strong transcription	Primary T cells from cord blood	blood
42	chr2:96194400-96196200	ZNF genes & repeats	Fetal Intestine Small	intestine
43	chr2:96194400-96196800	Strong transcription	Brain Angular Gyrus	brain
44	chr2:96194400-96197600	ZNF genes & repeats	Aorta	Aorta
45	chr2:96194400-96197800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:96194400-96197800	Strong transcription	Fetal Muscle Trunk	muscle
47	chr2:96194400-96197800	Genic enhancers	Gastric	stomach
48	chr2:96194400-96198000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr2:96194400-96198000	ZNF genes & repeats	Fetal Stomach	stomach
50	chr2:96194400-96207200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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