Variant report

Variant	nsv946461
Chromosome Location	chr1:161372505-161384947
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:112)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:112 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:161373912-161374076	K562	blood:	n/a	n/a
2	ATF1	chr1:161377600-161377723	K562	blood:	n/a	n/a
3	ATF2	chr1:161379562-161380002	GM12878	blood:	n/a	n/a
4	BATF	chr1:161379655-161380102	GM12878	blood:	n/a	n/a
5	BATF	chr1:161379614-161379994	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:161380344-161380544	K562	blood:	n/a	n/a
7	BHLHE40	chr1:161379842-161379970	GM12878	blood:	n/a	n/a
8	CBX3	chr1:161380161-161380430	K562	blood:	n/a	n/a
9	CBX3	chr1:161373726-161374301	K562	blood:	n/a	n/a
10	CBX3	chr1:161379997-161380740	K562	blood:	n/a	n/a
11	CBX3	chr1:161373881-161374212	K562	blood:	n/a	n/a
12	CEBPD	chr1:161380318-161380713	K562	blood:	n/a	n/a
13	CTCF	chr1:161376782-161376821	LNCaP	prostate:	n/a	n/a
14	CTCF	chr1:161380981-161381033	GM13976	blood:	n/a	n/a
15	CTCF	chr1:161376618-161376690	GM13976	blood:	n/a	n/a
16	EBF1	chr1:161379681-161380025	GM12878	blood:	n/a	n/a
17	ELF1	chr1:161379911-161380403	GM12878	blood:	n/a	chr1:161380228-161380241
18	ELF1	chr1:161373829-161374197	K562	blood:	n/a	chr1:161374011-161374024
19	ELF1	chr1:161379978-161380437	K562	blood:	n/a	chr1:161380228-161380241
20	EP300	chr1:161380362-161380750	K562	blood:	n/a	n/a
21	EP300	chr1:161377651-161377712	K562	blood:	n/a	n/a
22	EP300	chr1:161374027-161374148	K562	blood:	n/a	n/a
23	FOS	chr1:161372301-161372638	MCF10A-Er-Src	breast:	n/a	chr1:161372352-161372361
24	FOS	chr1:161372352-161372548	MCF10A-Er-Src	breast:	n/a	chr1:161372352-161372361
25	FOS	chr1:161384212-161384268	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:161372292-161372599	MCF10A-Er-Src	breast:	n/a	chr1:161372352-161372361
27	FOSL2	chr1:161372317-161372555	HepG2	liver:	n/a	chr1:161372352-161372361
28	FOXA2	chr1:161382181-161382377	HepG2	liver:	n/a	n/a
29	FOXA2	chr1:161382356-161382771	A549	lung:	n/a	n/a
30	GATA1	chr1:161380355-161380776	PBDE	blood:	n/a	n/a
31	GATA2	chr1:161380338-161380784	K562	blood:	n/a	n/a
32	GATA2	chr1:161382655-161383152	K562	blood:	n/a	n/a
33	GATA2	chr1:161374082-161374405	K562	blood:	n/a	n/a
34	GATA3	chr1:161373039-161373242	SH-SY5Y	brain:	n/a	chr1:161373092-161373102 chr1:161373094-161373104 chr1:161373094-161373101
35	GATA3	chr1:161384712-161384843	SH-SY5Y	brain:	n/a	n/a
36	HEY1	chr1:161376502-161376863	K562	blood:	n/a	n/a
37	IRF1	chr1:161379706-161379865	K562	blood:	n/a	n/a
38	IRF4	chr1:161379615-161380214	GM12878	blood:	n/a	n/a
39	IRF4	chr1:161379550-161380067	GM12878	blood:	n/a	n/a
40	KAP1	chr1:161380120-161380649	K562	blood:	n/a	n/a
41	MAX	chr1:161377259-161377544	K562	blood:	n/a	n/a
42	MAZ	chr1:161377474-161377669	K562	blood:	n/a	n/a
43	MXI1	chr1:161379703-161379894	GM12878	blood:	n/a	n/a
44	MYC	chr1:161373901-161373944	K562	blood:	n/a	n/a
45	MYC	chr1:161376559-161376564	MCF-7	breast:	n/a	n/a
46	NR2F2	chr1:161380044-161380953	K562	blood:	n/a	n/a
47	NR2F2	chr1:161380367-161380722	K562	blood:	n/a	n/a
48	NR3C1	chr1:161372115-161372548	A549	lung:	n/a	chr1:161372324-161372338 chr1:161372135-161372153
49	PAX5	chr1:161379600-161379975	GM12878	blood:	n/a	n/a
50	PAX5	chr1:161379604-161380196	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161373646-161373696	HRCEpiC	kidney:	n/a
2	chr1:161373646-161373696	RPTEC	kidney:	n/a
3	chr1:161375390-161375440	IMR90	lung:	fetal
4	chr1:161373646-161373696	NT2-D1	testis:	n/a
5	chr1:161373646-161373696	ECC-1	luminal epithelium:	n/a
6	chr1:161373646-161373696	ProgFib	skin:	n/a
7	chr1:161373646-161373696	Caco-2	colon:	n/a
8	chr1:161375390-161375440	Caco-2	colon:	n/a
9	chr1:161375390-161375440	PFSK-1	brain:	n/a
10	chr1:161375390-161375440	NHBE	bronchial:	n/a
11	chr1:161373646-161373696	GM06990	blood:	n/a
12	chr1:161373646-161373696	NHBE	bronchial:	n/a
13	chr1:161375390-161375440	U87	brain:	n/a
14	chr1:161373646-161373696	HIPEpiC	eye:	n/a
15	chr1:161373646-161373696	HL-60	blood:	n/a
16	chr1:161375390-161375440	T-47D	breast:	n/a
17	chr1:161373646-161373696	CMK	blood:	n/a
18	chr1:161375390-161375440	GM06990	blood:	n/a
19	chr1:161375390-161375440	HCPEpiC	choroid plexus:	n/a
20	chr1:161375390-161375440	NB4	blood:	n/a
21	chr1:161373646-161373696	LNCaP	prostate:	n/a
22	chr1:161373646-161373696	A549	lung:	n/a
23	chr1:161373646-161373696	AG04450	lung:	fetal
24	chr1:161373646-161373696	SK-N-MC	brain:	n/a
25	chr1:161373646-161373696	HCT-116	colon:	n/a
26	chr1:161375390-161375440	SK-N-MC	brain:	n/a
27	chr1:161373646-161373696	HRE	kidney:	n/a
28	chr1:161373646-161373696	NHDF-neo	bronchial:	n/a
29	chr1:161373646-161373696	Jurkat	blood:	n/a
30	chr1:161375390-161375440	HMEC	breast:	n/a
31	chr1:161375390-161375440	HepG2	liver:	n/a
32	chr1:161375390-161375440	PrEC	prostate:	n/a
33	chr1:161375390-161375440	CMK	blood:	n/a
34	chr1:161373646-161373696	T-47D	breast:	n/a
35	chr1:161375390-161375440	ovcar-3	ovarian:	n/a
36	chr1:161375390-161375440	Hepatocyte	liver:	n/a
37	chr1:161373646-161373696	Hepatocyte	liver:	n/a
38	chr1:161375390-161375440	HCF	heart:	n/a
39	chr1:161373646-161373696	PANC-1	pancreas:	n/a
40	chr1:161373646-161373696	Hela-S3	cervix:	n/a
41	chr1:161373646-161373696	GM12892	blood:	n/a
42	chr1:161375390-161375440	PANC-1	pancreas:	n/a
43	chr1:161375390-161375440	HRE	kidney:	n/a
44	chr1:161375390-161375440	HEK293	kidney:	embryo
45	chr1:161373646-161373696	K562	blood:	n/a
46	chr1:161375390-161375440	NH-A	brain:	n/a
47	chr1:161373646-161373696	HCM	heart:	n/a
48	chr1:161373646-161373696	ovcar-3	ovarian:	n/a
49	chr1:161375390-161375440	HCM	heart:	n/a
50	chr1:161375390-161375440	Jurkat	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:161122375..161125085-chr1:161376067..161378858,2	K562	blood:
2	chr1:161371806..161374700-chr1:161382431..161384803,2	MCF-7	breast:
3	chr1:161170434..161172328-chr1:161378596..161380361,2	K562	blood:
4	chr1:161381183..161383372-chr1:161391779..161394555,3	K562	blood:
5	chr1:161381959..161384163-chr1:161388654..161390300,2	K562	blood:
6	chr1:161373435..161375369-chr1:161381940..161384249,4	K562	blood:
7	chr1:161367430..161368932-chr1:161384466..161386892,2	MCF-7	breast:
8	chr1:161371806..161374700-chr1:161382431..161384803,2	MCF-7	breast:
9	chr1:161373435..161375369-chr1:161381940..161384249,4	K562	blood:
10	chr1:161372330..161375943-chr1:161377177..161380756,5	K562	blood:
11	chr1:161377159..161380003-chr1:161395367..161397564,2	MCF-7	breast:
12	chr1:161379123..161382070-chr1:161387001..161390523,3	K562	blood:
13	chr1:161358247..161360860-chr1:161371655..161373907,3	K562	blood:
14	chr1:161367523..161369303-chr1:161373719..161375547,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000215840	TF binding region
ENSG00000215840	CpG island
ENSG00000158864	chromatin interactions
ENSG00000215840	chromatin interactions
ENSG00000143222	chromatin interactions

Extended variants
information (count: 489 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556817361	chr1:161372526-161372527	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs567271302	chr1:161372544-161372545	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs7515068	chr1:161372555-161372556	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs145335373	chr1:161372591-161372592	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs188263639	chr1:161372597-161372598	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs7519821	chr1:161372608-161372609	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs114064111	chr1:161372614-161372615	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372393316	chr1:161372620-161372621	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149203326	chr1:161372629-161372630	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs78307098	chr1:161372690-161372691	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs544663201	chr1:161372712-161372713	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs193265952	chr1:161372739-161372740	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552124175	chr1:161372745-161372746	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs111320390	chr1:161372854-161372855	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
15	rs565675189	chr1:161372859-161372860	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs116471833	chr1:161372863-161372864	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs60125968	chr1:161372925-161372926	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551444021	chr1:161372926-161372927	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs10157457	chr1:161372944-161372945	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs566735255	chr1:161372960-161372961	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs76618139	chr1:161372992-161372993	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs57079072	chr1:161372993-161372994	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs12133897	chr1:161373073-161373074	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530526014	chr1:161373125-161373126	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs147785696	chr1:161373132-161373133	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs185484037	chr1:161373173-161373174	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs536111977	chr1:161373264-161373265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141239613	chr1:161373297-161373298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376121776	chr1:161373407-161373408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538484684	chr1:161373452-161373453	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs10157158	chr1:161373472-161373473	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs146922373	chr1:161373511-161373512	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs147988450	chr1:161373589-161373590	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs554957136	chr1:161373605-161373606	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs61410886	chr1:161373642-161373643	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs112500830	chr1:161373646-161373647	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	mRNA abundance
37	rs186893364	chr1:161373658-161373659	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs536532732	chr1:161373731-161373732	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs116301708	chr1:161373747-161373748	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs34550741	chr1:161373788-161373789	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs191407373	chr1:161373791-161373792	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs372211836	chr1:161373792-161373793	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs374874599	chr1:161373794-161373795	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs140874193	chr1:161373796-161373797	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs529673347	chr1:161373804-161373805	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs563342398	chr1:161373810-161373811	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs150177529	chr1:161373817-161373818	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs566700021	chr1:161373908-161373909	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs201807287	chr1:161373912-161373913	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs138585997	chr1:161373949-161373950	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161370400-161375400	Weak transcription	Ovary	ovary
2	chr1:161370400-161379200	Weak transcription	Stomach Mucosa	stomach
3	chr1:161370400-161380000	Weak transcription	Gastric	stomach
4	chr1:161370600-161372800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:161370600-161373600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr1:161370600-161373800	Weak transcription	Small Intestine	intestine
7	chr1:161370600-161375200	Weak transcription	Hela-S3	cervix
8	chr1:161370600-161378600	Weak transcription	Fetal Heart	heart
9	chr1:161370600-161381800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:161370800-161373800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr1:161370800-161373800	Weak transcription	Left Ventricle	heart
12	chr1:161370800-161374400	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr1:161370800-161374800	Weak transcription	Fetal Brain Male	brain
14	chr1:161370800-161379200	Weak transcription	Colonic Mucosa	Colon
15	chr1:161371000-161373800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr1:161371000-161373800	Enhancers	K562	blood
17	chr1:161371000-161374400	Weak transcription	Fetal Lung	lung
18	chr1:161371000-161378800	Weak transcription	Duodenum Mucosa	Duodenum
19	chr1:161371000-161378800	Weak transcription	Fetal Intestine Small	intestine
20	chr1:161371000-161379000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr1:161371000-161379000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:161371000-161379000	Weak transcription	Right Atrium	heart
23	chr1:161371000-161379400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr1:161371000-161381400	Weak transcription	Esophagus	oesophagus
25	chr1:161371000-161387800	Weak transcription	Spleen	Spleen
26	chr1:161371200-161373400	Weak transcription	HepG2	liver
27	chr1:161371200-161373800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr1:161371200-161378800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr1:161371200-161379000	Weak transcription	Psoas Muscle	Psoas
30	chr1:161371400-161378400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr1:161371400-161379000	Weak transcription	Primary B cells from peripheral blood	blood
32	chr1:161371600-161379000	Weak transcription	Right Ventricle	heart
33	chr1:161371800-161373800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:161371800-161374000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:161372000-161372600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:161372200-161372600	Weak transcription	Fetal Intestine Large	intestine
37	chr1:161372200-161372600	Enhancers	A549	lung
38	chr1:161372200-161372600	Enhancers	Osteobl	bone
39	chr1:161372200-161379800	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr1:161372400-161375400	Weak transcription	Pancreas	Pancrea
41	chr1:161372600-161372800	Enhancers	Fetal Intestine Large	intestine
42	chr1:161372600-161374400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:161372800-161377400	Weak transcription	Fetal Intestine Large	intestine
44	chr1:161373400-161374600	Enhancers	HepG2	liver
45	chr1:161373600-161374000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr1:161373800-161374000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr1:161373800-161374000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr1:161373800-161374000	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr1:161373800-161374200	Enhancers	Left Ventricle	heart
50	chr1:161373800-161374200	Enhancers	Small Intestine	intestine

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