Variant report

Variant	nsv875619
Chromosome Location	chr2:191062951-191112241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:214)
CpG islands
(count:305)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:191067389-191067740	HepG2	liver:	n/a	n/a
2	ATF1	chr2:191078200-191078828	K562	blood:	n/a	n/a
3	ATF1	chr2:191070482-191070695	K562	blood:	n/a	n/a
4	BRCA1	chr2:191064608-191064740	GM12878	blood:	n/a	n/a
5	CBX3	chr2:191106006-191106303	K562	blood:	n/a	n/a
6	CCNT2	chr2:191078828-191078891	K562	blood:	n/a	n/a
7	CCNT2	chr2:191067349-191067726	K562	blood:	n/a	n/a
8	CEBPB	chr2:191070451-191070728	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:191067001-191067256	K562	blood:	n/a	n/a
10	CEBPB	chr2:191070385-191070759	K562	blood:	n/a	n/a
11	CEBPB	chr2:191103651-191103789	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:191070457-191070689	K562	blood:	n/a	n/a
13	CEBPB	chr2:191070413-191070745	K562	blood:	n/a	n/a
14	CTCF	chr2:191067520-191067670	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr2:191067380-191067530	HepG2	liver:	n/a	n/a
16	CTCF	chr2:191081580-191081730	GM12872	blood:	n/a	chr2:191081647-191081656
17	CTCF	chr2:191081580-191081730	HepG2	liver:	n/a	chr2:191081647-191081656
18	CTCF	chr2:191091243-191091389	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr2:191067380-191067530	HMF	breast:	n/a	n/a
20	CTCF	chr2:191067403-191067586	MCF-7	breast:	n/a	n/a
21	CTCF	chr2:191110432-191110503	GM13976	blood:	n/a	n/a
22	CTCF	chr2:191081600-191081750	HCPEpiC	choroid plexus:	n/a	chr2:191081647-191081656
23	CTCF	chr2:191081597-191081686	MCF-7	breast:	n/a	chr2:191081647-191081656
24	CTCF	chr2:191067400-191067550	HepG2	liver:	n/a	n/a
25	CTCF	chr2:191067421-191067558	MCF-7	breast:	n/a	n/a
26	CTCF	chr2:191067300-191067450	GM06990	blood:	n/a	n/a
27	CTCF	chr2:191067316-191067724	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:191078940-191079090	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr2:191081580-191081730	BE2_C	brain:	n/a	chr2:191081647-191081656
30	CTCF	chr2:191067460-191067610	GM12872	blood:	n/a	n/a
31	CTCF	chr2:191067209-191067271	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr2:191081560-191081710	HA-sp	spinal cord:	n/a	chr2:191081647-191081656
33	CTCF	chr2:191101100-191101250	HL-60	blood:	n/a	n/a
34	CTCF	chr2:191081580-191081730	HRPEpiC	eye:	n/a	chr2:191081647-191081656
35	CTCF	chr2:191067478-191067480	HepG2	liver:	n/a	n/a
36	CTCF	chr2:191067360-191067510	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr2:191067480-191067630	HMEC	breast:	n/a	n/a
38	CTCF	chr2:191067380-191067530	HMEC	breast:	n/a	n/a
39	CTCF	chr2:191072486-191072528	ProgFib	skin:	n/a	n/a
40	CTCF	chr2:191081620-191081770	HAc	cerebellar:	n/a	chr2:191081647-191081656
41	CTCF	chr2:191099545-191099655	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr2:191081640-191081790	HBMEC	blood vessel:	n/a	chr2:191081647-191081656
43	CTCF	chr2:191081620-191081770	HCPEpiC	choroid plexus:	n/a	chr2:191081647-191081656
44	CTCF	chr2:191067400-191067550	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr2:191067380-191067530	BE2_C	brain:	n/a	n/a
46	CTCF	chr2:191067400-191067550	A549	lung:	n/a	n/a
47	CTCF	chr2:191078943-191079143	K562	blood:	n/a	n/a
48	CTCF	chr2:191067465-191067511	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:191067400-191067550	RPTEC	kidney:	n/a	n/a
50	CTCF	chr2:191081580-191081730	HEK293	kidney:	n/a	chr2:191081647-191081656

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:191092628-191092678	K562	blood:	n/a
2	chr2:191079856-191079906	SK-N-SH_RA	brain:	n/a
3	chr2:191069680-191069730	GM12891	blood:	n/a
4	chr2:191092628-191092678	RPTEC	kidney:	n/a
5	chr2:191064776-191064826	ECC-1	luminal epithelium:	n/a
6	chr2:191079856-191079906	HNPCEpiC	eye:	n/a
7	chr2:191064776-191064826	PrEC	prostate:	n/a
8	chr2:191064776-191064826	MCF10A-Er-Src	breast:	n/a
9	chr2:191064776-191064826	HRCEpiC	kidney:	n/a
10	chr2:191069680-191069730	Hela-S3	cervix:	n/a
11	chr2:191079856-191079906	Hepatocyte	liver:	n/a
12	chr2:191064776-191064826	GM06990	blood:	n/a
13	chr2:191092628-191092678	ProgFib	skin:	n/a
14	chr2:191079856-191079906	HIPEpiC	eye:	n/a
15	chr2:191064776-191064826	NH-A	brain:	n/a
16	chr2:191069680-191069730	HIPEpiC	eye:	n/a
17	chr2:191064776-191064826	NHBE	bronchial:	n/a
18	chr2:191092628-191092678	NHDF-neo	bronchial:	n/a
19	chr2:191064776-191064826	MCF-7	breast:	n/a
20	chr2:191092628-191092678	HEK293	kidney:	embryo
21	chr2:191069680-191069730	Jurkat	blood:	n/a
22	chr2:191092628-191092678	HEEpiC	esophagus:	n/a
23	chr2:191064776-191064826	HAEpiC	amniotic membrane:	n/a
24	chr2:191079856-191079906	HCPEpiC	choroid plexus:	n/a
25	chr2:191065479-191065529	SK-N-MC	brain:	n/a
26	chr2:191092628-191092678	PFSK-1	brain:	n/a
27	chr2:191069680-191069730	HRPEpiC	eye:	n/a
28	chr2:191064776-191064826	Hela-S3	cervix:	n/a
29	chr2:191092628-191092678	HMEC	breast:	n/a
30	chr2:191064776-191064826	AG04449	skin:	fetal
31	chr2:191064776-191064826	HCF	heart:	n/a
32	chr2:191065479-191065529	GM19239	blood:	n/a
33	chr2:191064776-191064826	HCM	heart:	n/a
34	chr2:191092628-191092678	AG10803	skin:	n/a
35	chr2:191069680-191069730	HCF	heart:	n/a
36	chr2:191092628-191092678	PrEC	prostate:	n/a
37	chr2:191065479-191065529	RPTEC	kidney:	n/a
38	chr2:191064776-191064826	LNCaP	prostate:	n/a
39	chr2:191064776-191064826	RPTEC	kidney:	n/a
40	chr2:191069680-191069730	NB4	blood:	n/a
41	chr2:191092628-191092678	HNPCEpiC	eye:	n/a
42	chr2:191092628-191092678	BJ	skin:	n/a
43	chr2:191092628-191092678	CMK	blood:	n/a
44	chr2:191092628-191092678	Caco-2	colon:	n/a
45	chr2:191092628-191092678	GM19239	blood:	n/a
46	chr2:191064776-191064826	PFSK-1	brain:	n/a
47	chr2:191092628-191092678	NB4	blood:	n/a
48	chr2:191092628-191092678	MCF-7	breast:	n/a
49	chr2:191092628-191092678	AG04450	lung:	fetal
50	chr2:191079856-191079906	HCM	heart:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:191058213..191060210-chr2:191073885..191076482,2	K562	blood:
2	chr2:191072093..191074775-chr2:191077748..191080618,2	K562	blood:
3	chr2:191058046..191059738-chr2:191062571..191064131,2	MCF-7	breast:
4	chr2:191094730..191097098-chr2:191136539..191139119,2	K562	blood:
5	chr2:191052189..191054750-chr2:191092119..191094674,2	K562	blood:
6	chr2:191067344..191068056-chr2:191141661..191142510,2	MCF-7	breast:
7	chr2:191062978..191067308-chr2:191069746..191072703,3	K562	blood:
8	chr2:191072093..191074775-chr2:191077748..191080618,2	K562	blood:
9	chr2:191066942..191067634-chr2:191184150..191184904,2	MCF-7	breast:
10	chr2:191062034..191064478-chr2:191069746..191072608,2	K562	blood:
11	chr2:191058197..191060868-chr2:191061375..191063080,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MSTN-2	chr2:191073411-191073639	NONHSAT076079
2	lnc-MSTN-2	chr2:191077682-191080835	NONHSAT076079
3	lnc-C2orf88-1	chr2:191064423-191064553	NONHSAT076077
4	lnc-C2orf88-3	chr2:191107786-191108123	l_2008_chr2:191107785-191141547_brain
5	lnc-C2orf88-3	chr2:191108852-191108962	l_2008_chr2:191107785-191141547_brain

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C2orf88	hsa-miR-125b-5p	chr2:191065445-191065451

Variant related genes	Relation type
HIBCH	TF binding region
HIBCH	CpG island
ENSG00000198130	chromatin interactions

Extended variants
information (count: 2024 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:2024 , 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	rs4853684	chr2:191062951-191062952	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557489657	chr2:191062971-191062972	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs193042594	chr2:191063004-191063005	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575710473	chr2:191063014-191063015	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532061228	chr2:191063016-191063017	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146846177	chr2:191063048-191063049	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543000829	chr2:191063053-191063054	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs16832420	chr2:191063071-191063072	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs547913233	chr2:191063086-191063087	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577920599	chr2:191063100-191063101	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566028393	chr2:191063135-191063136	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184383454	chr2:191063138-191063139	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554361951	chr2:191063147-191063148	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140792740	chr2:191063156-191063157	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188769843	chr2:191063164-191063165	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558383744	chr2:191063243-191063244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374871822	chr2:191063252-191063253	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73053733	chr2:191063254-191063255	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs1223	chr2:191063305-191063306	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs181201222	chr2:191063326-191063327	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574469948	chr2:191063349-191063350	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs35125102	chr2:191063357-191063358	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35653488	chr2:191063358-191063359	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71027204	chr2:191063381-191063382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541913249	chr2:191063442-191063443	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs71401240	chr2:191063445-191063446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs147100757	chr2:191063446-191063447	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs386392138	chr2:191063448-191063449	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs10675848	chr2:191063451-191063452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199765613	chr2:191063452-191063453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200496110	chr2:191063453-191063454	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201149580	chr2:191063454-191063455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532729563	chr2:191063466-191063467	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561477558	chr2:191063474-191063475	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183976824	chr2:191063624-191063625	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs16832425	chr2:191063628-191063629	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs565432546	chr2:191063638-191063639	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532576025	chr2:191063696-191063697	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs367853653	chr2:191063701-191063702	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371188415	chr2:191063735-191063736	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547455348	chr2:191063749-191063750	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs7597985	chr2:191063763-191063764	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs368549461	chr2:191063815-191063816	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530147481	chr2:191063831-191063832	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548233681	chr2:191063849-191063850	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569516699	chr2:191063873-191063874	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112797530	chr2:191063886-191063887	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138424235	chr2:191063957-191063958	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552485310	chr2:191063976-191063977	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs570640140	chr2:191064031-191064032	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Ovarian cancer	21720365	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191046000-191074000	Weak transcription	HMEC	breast
2	chr2:191046000-191088400	Weak transcription	HSMMtube	muscle
3	chr2:191046200-191064200	Weak transcription	HSMM	muscle
4	chr2:191046400-191063600	Weak transcription	HepG2	liver
5	chr2:191046400-191064400	Weak transcription	Pancreas	Pancrea
6	chr2:191046400-191064400	Weak transcription	Psoas Muscle	Psoas
7	chr2:191046400-191070400	Weak transcription	Fetal Stomach	stomach
8	chr2:191046600-191064400	Weak transcription	Brain Angular Gyrus	brain
9	chr2:191046600-191086400	Weak transcription	Colonic Mucosa	Colon
10	chr2:191047000-191080400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr2:191047600-191081000	Weak transcription	Brain Anterior Caudate	brain
12	chr2:191048200-191073800	Weak transcription	Aorta	Aorta
13	chr2:191049200-191064400	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:191052000-191108800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr2:191052600-191063000	Weak transcription	Left Ventricle	heart
16	chr2:191053000-191078200	Weak transcription	Right Ventricle	heart
17	chr2:191056600-191070200	Weak transcription	NHDF-Ad	bronchial
18	chr2:191056800-191064400	Weak transcription	Esophagus	oesophagus
19	chr2:191056800-191124600	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr2:191056800-191131800	Weak transcription	NHEK	skin
21	chr2:191057000-191078400	Weak transcription	Thymus	Thymus
22	chr2:191057200-191076200	Weak transcription	Fetal Kidney	kidney
23	chr2:191057800-191087800	Weak transcription	Fetal Brain Female	brain
24	chr2:191058000-191076000	Weak transcription	Colon Smooth Muscle	Colon
25	chr2:191059600-191063800	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr2:191059800-191064400	Weak transcription	Rectal Smooth Muscle	rectum
27	chr2:191059800-191064600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr2:191060000-191107000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr2:191060200-191063600	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr2:191060200-191066600	Weak transcription	Dnd41	blood
31	chr2:191060200-191078600	Weak transcription	NH-A	brain
32	chr2:191060200-191090600	Weak transcription	A549	lung
33	chr2:191060400-191068000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:191060400-191076600	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr2:191060600-191063800	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr2:191060600-191072000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr2:191060600-191074000	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr2:191060600-191078200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:191060600-191084000	Weak transcription	HUVEC	blood vessel
40	chr2:191060600-191087800	Weak transcription	Brain Germinal Matrix	brain
41	chr2:191060800-191063800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:191060800-191079600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:191060800-191180000	Weak transcription	Small Intestine	intestine
44	chr2:191061000-191064400	Weak transcription	Brain Substantia Nigra	brain
45	chr2:191061000-191070200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr2:191061000-191089200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr2:191061200-191070200	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr2:191061400-191064600	Weak transcription	Stomach Smooth Muscle	stomach
49	chr2:191061400-191068600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr2:191061600-191065000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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