Variant report

Variant	nsv832215
Chromosome Location	chr1:194902968-195106134
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:693)
CpG islands
(count:62)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:693 , 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	ATF1	chr1:194963175-194963179	K562	blood:	n/a	n/a
2	ATF1	chr1:194933783-194933793	K562	blood:	n/a	n/a
3	ATF1	chr1:194921272-194921554	K562	blood:	n/a	n/a
4	ATF1	chr1:194979275-194979408	K562	blood:	n/a	n/a
5	ATF1	chr1:194945122-194945347	K562	blood:	n/a	n/a
6	ATF1	chr1:194928895-194928956	K562	blood:	n/a	n/a
7	CBX3	chr1:195066317-195066989	HCT-116	colon:	n/a	n/a
8	CBX3	chr1:194944969-194945511	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:195066119-195066969	HCT-116	colon:	n/a	n/a
10	CCNT2	chr1:195082155-195082271	K562	blood:	n/a	n/a
11	CEBPB	chr1:194959278-194959979	IMR90	lung:	n/a	chr1:194959731-194959743
12	CEBPB	chr1:194927941-194928159	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:194959643-194959906	K562	blood:	n/a	chr1:194959731-194959743
14	CEBPB	chr1:195048707-195048870	A549	lung:	n/a	chr1:195048785-195048798 chr1:195048787-195048796 chr1:195048785-195048796
15	CEBPB	chr1:195065089-195065188	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:194959642-194959946	H1-hESC	embryonic stem cell:	n/a	chr1:194959731-194959743
17	CEBPB	chr1:195104306-195104383	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:194977028-194977083	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:194959301-194959967	A549	lung:	n/a	chr1:194959731-194959743
20	CEBPB	chr1:194974428-194974799	MCF-7	breast:	n/a	n/a
21	CEBPB	chr1:194963996-194964196	HepG2	liver:	n/a	chr1:194964052-194964063
22	CEBPB	chr1:195085449-195085677	HepG2	liver:	n/a	chr1:195085517-195085528 chr1:195085516-195085529 chr1:195085564-195085575 chr1:195085564-195085575
23	CEBPB	chr1:195048669-195048869	K562	blood:	n/a	chr1:195048785-195048798 chr1:195048787-195048796 chr1:195048785-195048796
24	CEBPB	chr1:194919793-194920076	HepG2	liver:	n/a	chr1:194919885-194919896 chr1:194919929-194919940
25	CEBPB	chr1:194959230-194959962	HepG2	liver:	n/a	chr1:194959731-194959743
26	CEBPB	chr1:194919721-194920140	Hela-S3	cervix:	n/a	chr1:194919885-194919896 chr1:194919929-194919940
27	CEBPB	chr1:194959633-194959965	ECC-1	luminal epithelium:	n/a	chr1:194959731-194959743
28	CEBPB	chr1:194959620-194959981	ECC-1	luminal epithelium:	n/a	chr1:194959731-194959743
29	CEBPB	chr1:194909916-194909997	HepG2	liver:	n/a	chr1:194909966-194909979 chr1:194909967-194909978
30	CEBPB	chr1:195048651-195048838	HepG2	liver:	n/a	chr1:195048785-195048798 chr1:195048787-195048796 chr1:195048785-195048796
31	CEBPB	chr1:195016869-195017077	K562	blood:	n/a	chr1:195016980-195016993
32	CEBPB	chr1:194959224-194959964	Hela-S3	cervix:	n/a	chr1:194959731-194959743
33	CEBPB	chr1:194960299-194960553	A549	lung:	n/a	n/a
34	CHD2	chr1:195032724-195032789	K562	blood:	n/a	n/a
35	CHD2	chr1:194905139-194905158	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr1:194905136-194905247	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:194905100-194905250	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr1:194905122-194905259	GM13977	blood:	n/a	n/a
39	CTCF	chr1:195074500-195074650	GM12865	blood:	n/a	n/a
40	CTCF	chr1:194905100-194905250	GM12875	blood:	n/a	n/a
41	CTCF	chr1:194905120-194905270	A549	lung:	n/a	n/a
42	CTCF	chr1:194905120-194905270	GM12868	blood:	n/a	n/a
43	CTCF	chr1:194905160-194905310	GM12864	blood:	n/a	n/a
44	CTCF	chr1:195074500-195074650	GM12878	blood:	n/a	n/a
45	CTCF	chr1:195074540-195074690	GM06990	blood:	n/a	n/a
46	CTCF	chr1:195074600-195074750	GM12872	blood:	n/a	n/a
47	CTCF	chr1:195074580-195074730	GM12865	blood:	n/a	n/a
48	CTCF	chr1:195074540-195074690	GM12871	blood:	n/a	n/a
49	CTCF	chr1:195074600-195074750	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr1:195074527-195074708	GM19239	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:195023534-195023584	ProgFib	skin:	n/a
2	chr1:195023534-195023584	ProgFib	skin:	n/a
3	chr1:195023534-195023584	H1-hESC	embryonic stem cell:	embryo
4	chr1:195023534-195023584	ovcar-3	ovarian:	n/a
5	chr1:195023534-195023584	HEEpiC	esophagus:	n/a
6	chr1:195023534-195023584	SAEC	small airway:	n/a
7	chr1:195023534-195023584	PrEC	prostate:	n/a
8	chr1:195023534-195023584	HNPCEpiC	eye:	n/a
9	chr1:195023534-195023584	BJ	skin:	n/a
10	chr1:195023534-195023584	AoSMC	blood vessel:	n/a
11	chr1:195023534-195023584	HepG2	liver:	n/a
12	chr1:195023534-195023584	Jurkat	blood:	n/a
13	chr1:195023534-195023584	MCF10A-Er-Src	breast:	n/a
14	chr1:195023534-195023584	HRCEpiC	kidney:	n/a
15	chr1:195023534-195023584	GM12878	blood:	n/a
16	chr1:195023534-195023584	AG09309	skin:	n/a
17	chr1:195023534-195023584	HIPEpiC	eye:	n/a
18	chr1:195023534-195023584	U87	brain:	n/a
19	chr1:195023534-195023584	HCM	heart:	n/a
20	chr1:195023534-195023584	GM12892	blood:	n/a
21	chr1:195023534-195023584	NT2-D1	testis:	n/a
22	chr1:195023534-195023584	Hepatocyte	liver:	n/a
23	chr1:195023534-195023584	Hela-S3	cervix:	n/a
24	chr1:195023534-195023584	AG04449	skin:	fetal
25	chr1:195023534-195023584	SK-N-SH_RA	brain:	n/a
26	chr1:195023534-195023584	SKMC	muscle:	n/a
27	chr1:195023534-195023584	A549	lung:	n/a
28	chr1:195023534-195023584	GM19239	blood:	n/a
29	chr1:195023534-195023584	HEK293	kidney:	embryo
30	chr1:195023534-195023584	HCPEpiC	choroid plexus:	n/a
31	chr1:195023534-195023584	NH-A	brain:	n/a
32	chr1:195023534-195023584	RPTEC	kidney:	n/a
33	chr1:195023534-195023584	HL-60	blood:	n/a
34	chr1:195023534-195023584	HRPEpiC	eye:	n/a
35	chr1:195023534-195023584	AG10803	skin:	n/a
36	chr1:195023534-195023584	CMK	blood:	n/a
37	chr1:195023534-195023584	LNCaP	prostate:	n/a
38	chr1:195023534-195023584	NB4	blood:	n/a
39	chr1:195023534-195023584	NHDF-neo	bronchial:	n/a
40	chr1:195023534-195023584	PANC-1	pancreas:	n/a
41	chr1:195023534-195023584	T-47D	breast:	n/a
42	chr1:195023534-195023584	HCF	heart:	n/a
43	chr1:195023534-195023584	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:195023534-195023584	SK-N-SH	brain:	n/a
45	chr1:195023534-195023584	HCT-116	colon:	n/a
46	chr1:195023534-195023584	AG04450	lung:	fetal
47	chr1:195023534-195023584	SK-N-MC	brain:	n/a
48	chr1:195023534-195023584	ECC-1	luminal epithelium:	n/a
49	chr1:195023534-195023584	PFSK-1	brain:	n/a
50	chr1:195023534-195023584	HRE	kidney:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:195076488..195078314-chr16:29816661..29818822,2	MCF-7	breast:
2	chr1:194940992..194943005-chr1:194943083..194945420,2	MCF-7	breast:
3	chr1:195005563..195007915-chr1:195009562..195011162,2	K562	blood:
4	chr1:194956938..194959266-chr1:194974594..194976244,2	K562	blood:
5	chr1:194940992..194943005-chr1:194943083..194945420,2	MCF-7	breast:
6	chr1:194976691..194979568-chr1:194983292..194986112,2	K562	blood:
7	chr1:194894090..194896590-chr1:194908541..194910307,2	MCF-7	breast:
8	chr1:194820017..194822446-chr1:194943208..194945267,2	K562	blood:
9	chr1:195005563..195007915-chr1:195009562..195011162,2	K562	blood:
10	chr1:194975514..194978503-chr1:194979065..194981637,2	MCF-7	breast:
11	chr1:194976691..194979568-chr1:194983292..194986112,2	K562	blood:
12	chr1:194956938..194959266-chr1:194974594..194976244,2	K562	blood:
13	chr1:194927782..194929413-chr1:194932247..194935027,2	MCF-7	breast:
14	chr1:195022148..195022648-chr5:180672971..180673497,2	HCT-116	colon:
15	chr1:194927782..194929413-chr1:194932247..194935027,2	MCF-7	breast:
16	chr1:194975514..194978503-chr1:194979065..194981637,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000265108	TF binding region
ENSG00000265108	CpG island
ENSG00000103495	chromatin interactions

Extended variants
information (count: 1132 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72746014	chr1:194908606-194908607	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189111940	chr1:194908649-194908650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs367807191	chr1:194908730-194908731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190384614	chr1:194908798-194908799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560066663	chr1:194908812-194908813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149177042	chr1:194908853-194908854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572261129	chr1:194908856-194908857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549394809	chr1:194908902-194908903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567845041	chr1:194908928-194908929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538578775	chr1:194908931-194908932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1752790	chr1:194908969-194908970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183008074	chr1:194908977-194908978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12061513	chr1:194909006-194909007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563633789	chr1:194909039-194909040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571879988	chr1:194909046-194909047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199896328	chr1:194909061-194909062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539493496	chr1:194909081-194909082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs180309	chr1:194909088-194909089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1629829	chr1:194909112-194909113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1752791	chr1:194909117-194909118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199863591	chr1:194909135-194909136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557910186	chr1:194909139-194909140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201141829	chr1:194909142-194909143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199987153	chr1:194909143-194909144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12088456	chr1:194909155-194909156	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs555369162	chr1:194909158-194909159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573849878	chr1:194909231-194909232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143264905	chr1:194909262-194909263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139047294	chr1:194909296-194909297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574816	chr1:194909316-194909317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549248871	chr1:194909335-194909336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs386369198	chr1:194909350-194909351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs80002385	chr1:194909351-194909352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61816820	chr1:194909353-194909354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4292939	chr1:194909372-194909373	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs339590	chr1:194909428-194909429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184631	chr1:194909443-194909444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545068944	chr1:194909448-194909449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180310	chr1:194909452-194909453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2174204	chr1:194909456-194909457	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs527815171	chr1:194909463-194909464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532877311	chr1:194909496-194909497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537865	chr1:194909526-194909527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537868	chr1:194909529-194909530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72746016	chr1:194909579-194909580	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs561375270	chr1:194909603-194909604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531871187	chr1:194909635-194909636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550500534	chr1:194909658-194909659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566463363	chr1:194909677-194909678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532767251	chr1:194909678-194909679	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Maculopathy	22022419	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Maculopathy	22355348	CNVD
Schizophrenia	21346763	CNVD
early-passage human iPS cells	21368824	CNVD
Recurrent pregnancy loss	19789632	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Maculopathy	21850184	CNVD
Schizophrenia	20967226	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Asthma	20841430	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194908600-194910800	Enhancers	Fetal Brain Male	brain
2	chr1:194908800-194910000	Enhancers	Fetal Brain Female	brain
3	chr1:194910000-194910400	Weak transcription	Fetal Brain Female	brain
4	chr1:194910400-194910800	Enhancers	Fetal Brain Female	brain
5	chr1:194921200-194921800	Enhancers	Brain Germinal Matrix	brain
6	chr1:194934800-194936400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:194937400-194937800	Enhancers	Brain Germinal Matrix	brain
8	chr1:194951400-194951600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:194976800-194977800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:194976800-194977800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:194977800-194980000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:194977800-194980200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:194980000-194980800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr1:194980200-194980600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:194980200-194980800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:194988600-194989000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr1:194988600-194989000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr1:194988800-194989200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:194999600-195000200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:195005000-195005400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr1:195022600-195023000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
22	chr1:195045000-195045200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:195045200-195045600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:195045600-195046800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:195045600-195046800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:195046800-195047400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:195046800-195047600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:195047400-195050800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:195047600-195050200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:195050200-195051800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:195050800-195051200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:195054200-195054800	Enhancers	Fetal Lung	lung
33	chr1:195063000-195065400	Weak transcription	Right Atrium	heart
34	chr1:195063600-195064000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:195064000-195066200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:195065200-195065600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr1:195065200-195065600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr1:195065400-195065600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr1:195065400-195065600	ZNF genes & repeats	Right Atrium	heart
40	chr1:195066200-195067200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:195066200-195067200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:195066200-195067600	Enhancers	HMEC	breast
43	chr1:195066400-195066800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:195066400-195067000	Enhancers	NHEK	skin
45	chr1:195066400-195067200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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