Variant report

Variant	nsv600255
Chromosome Location	chr5:167622534-167651603
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	BATF	chr5:167646756-167647108	GM12878	blood:	n/a	n/a
2	BATF	chr5:167625474-167625750	GM12878	blood:	n/a	n/a
3	BHLHE40	chr5:167646775-167647101	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:167622110-167622740	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:167646832-167647104	K562	blood:	n/a	chr5:167646987-167647004
6	CTCF	chr5:167646863-167647035	SK-N-SH_RA	brain:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
7	CTCF	chr5:167646940-167647090	BE2_C	brain:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
8	CTCF	chr5:167646747-167647168	H1-hESC	embryonic stem cell:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
9	CTCF	chr5:167646826-167647132	MCF-7	breast:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
10	CTCF	chr5:167646920-167647070	GM12866	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
11	CTCF	chr5:167638387-167638401	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:167646960-167647110	HAc	cerebellar:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
13	CTCF	chr5:167646765-167647166	K562	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
14	CTCF	chr5:167646843-167647105	HepG2	liver:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
15	CTCF	chr5:167646749-167647186	T-47D	breast:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
16	CTCF	chr5:167646920-167647070	GM12801	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
17	CTCF	chr5:167646835-167647117	Hela-S3	cervix:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
18	CTCF	chr5:167634600-167634750	NHEK	skin:	n/a	chr5:167634634-167634652 chr5:167634637-167634650
19	CTCF	chr5:167646880-167647030	SK-N-SH_RA	brain:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
20	CTCF	chr5:167646840-167646990	GM12870	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
21	CTCF	chr5:167646813-167647129	HUVEC	blood vessel:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
22	CTCF	chr5:167646520-167646670	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr5:167646861-167647106	GM13977	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
24	CTCF	chr5:167646900-167647050	Caco-2	colon:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
25	CTCF	chr5:167646772-167647131	K562	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
26	CTCF	chr5:167646920-167647070	MCF-7	breast:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
27	CTCF	chr5:167638260-167638410	GM12878	blood:	n/a	n/a
28	CTCF	chr5:167646789-167647138	H1-hESC	embryonic stem cell:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
29	CTCF	chr5:167645940-167646090	GM12873	blood:	n/a	n/a
30	CTCF	chr5:167646880-167647030	HMEC	breast:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
31	CTCF	chr5:167646831-167647130	GM12878	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
32	CTCF	chr5:167646880-167647030	HPAF	blood vessel:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
33	CTCF	chr5:167646920-167647070	HCM	heart:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
34	CTCF	chr5:167646900-167647050	NB4	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
35	CTCF	chr5:167647261-167647379	GM10266	blood:	n/a	n/a
36	CTCF	chr5:167646900-167647050	GM06990	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
37	CTCF	chr5:167646899-167647027	GM19238	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
38	CTCF	chr5:167646867-167647124	GM13976	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
39	CTCF	chr5:167646900-167647050	RPTEC	kidney:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
40	CTCF	chr5:167647120-167647270	NHEK	skin:	n/a	n/a
41	CTCF	chr5:167646772-167647143	ECC-1	luminal epithelium:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
42	CTCF	chr5:167646880-167647030	HMF	breast:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
43	CTCF	chr5:167646880-167647030	HepG2	liver:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
44	CTCF	chr5:167646880-167647030	AG09309	skin:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
45	CTCF	chr5:167646830-167647044	A549	lung:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
46	CTCF	chr5:167646744-167647040	ECC-1	luminal epithelium:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
47	CTCF	chr5:167646900-167647050	BJ	skin:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
48	CTCF	chr5:167646760-167647094	A549	lung:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983
49	CTCF	chr5:167646540-167646690	GM12864	blood:	n/a	n/a
50	CTCF	chr5:167646900-167647050	GM12871	blood:	n/a	chr5:167646972-167646980 chr5:167646960-167646981 chr5:167646965-167646983

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:167645394-167645444	NHBE	bronchial:	n/a
2	chr5:167645456-167645506	K562	blood:	n/a
3	chr5:167645456-167645506	Hela-S3	cervix:	n/a
4	chr5:167634748-167634798	BJ	skin:	n/a
5	chr5:167634748-167634798	AG04449	skin:	fetal
6	chr5:167642863-167642913	HIPEpiC	eye:	n/a
7	chr5:167634748-167634798	NT2-D1	testis:	n/a
8	chr5:167645456-167645506	NT2-D1	testis:	n/a
9	chr5:167642863-167642913	HCPEpiC	choroid plexus:	n/a
10	chr5:167642863-167642913	BE2_C	brain:	n/a
11	chr5:167645456-167645506	H1-hESC	embryonic stem cell:	embryo
12	chr5:167642863-167642913	HUVEC	blood vessel:	n/a
13	chr5:167645456-167645506	PFSK-1	brain:	n/a
14	chr5:167634748-167634798	IMR90	lung:	fetal
15	chr5:167645456-167645506	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:167634748-167634798	ECC-1	luminal epithelium:	n/a
17	chr5:167642863-167642913	SAEC	small airway:	n/a
18	chr5:167634748-167634798	HRCEpiC	kidney:	n/a
19	chr5:167645456-167645506	HCF	heart:	n/a
20	chr5:167634748-167634798	AG10803	skin:	n/a
21	chr5:167642863-167642913	LNCaP	prostate:	n/a
22	chr5:167634748-167634798	BE2_C	brain:	n/a
23	chr5:167645394-167645444	HCPEpiC	choroid plexus:	n/a
24	chr5:167642863-167642913	AG09319	gingival:	n/a
25	chr5:167645456-167645506	GM12892	blood:	n/a
26	chr5:167645456-167645506	MCF10A-Er-Src	breast:	n/a
27	chr5:167645394-167645444	Caco-2	colon:	n/a
28	chr5:167634748-167634798	HMEC	breast:	n/a
29	chr5:167645394-167645444	HCF	heart:	n/a
30	chr5:167645394-167645444	ProgFib	skin:	n/a
31	chr5:167645456-167645506	GM19239	blood:	n/a
32	chr5:167645456-167645506	SK-N-SH_RA	brain:	n/a
33	chr5:167645394-167645444	HRE	kidney:	n/a
34	chr5:167645394-167645444	RPTEC	kidney:	n/a
35	chr5:167642863-167642913	Jurkat	blood:	n/a
36	chr5:167634748-167634798	U87	brain:	n/a
37	chr5:167645456-167645506	A549	lung:	n/a
38	chr5:167645456-167645506	AG10803	skin:	n/a
39	chr5:167645394-167645444	HRPEpiC	eye:	n/a
40	chr5:167642863-167642913	HepG2	liver:	n/a
41	chr5:167642863-167642913	HRPEpiC	eye:	n/a
42	chr5:167645456-167645506	HepG2	liver:	n/a
43	chr5:167642863-167642913	HEK293	kidney:	embryo
44	chr5:167634748-167634798	ProgFib	skin:	n/a
45	chr5:167645456-167645506	HAEpiC	amniotic membrane:	n/a
46	chr5:167634748-167634798	GM12878	blood:	n/a
47	chr5:167634748-167634798	AG09309	skin:	n/a
48	chr5:167645456-167645506	IMR90	lung:	fetal
49	chr5:167642863-167642913	U87	brain:	n/a
50	chr5:167645456-167645506	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:167474616..167475298-chr5:167646316..167647289,2	MCF-7	breast:
2	chr5:167351075..167351891-chr5:167646939..167647556,2	MCF-7	breast:
3	chr5:167530827..167533333-chr5:167637920..167639619,2	K562	blood:
4	chr5:167541006..167542085-chr5:167646466..167647492,9	MCF-7	breast:
5	chr5:167638699..167640439-chr5:167642753..167644819,2	K562	blood:
6	chr5:167625904..167627787-chr5:167630198..167633051,2	K562	blood:
7	chr5:167629202..167631723-chr5:167632406..167635349,3	K562	blood:
8	chr5:167649331..167651184-chr5:167653596..167655823,2	K562	blood:
9	chr5:167541464..167542017-chr5:167646588..167647367,2	K562	blood:
10	chr5:167512986..167513910-chr5:167646566..167647140,2	MCF-7	breast:
11	chr5:167617381..167620061-chr5:167621010..167623836,2	K562	blood:
12	chr5:167638699..167640439-chr5:167642753..167644819,2	K562	blood:
13	chr5:167629202..167631723-chr5:167632406..167635349,3	K562	blood:
14	chr5:167541391..167542060-chr5:167646403..167647190,2	MCF-7	breast:
15	chr5:167150201..167150713-chr5:167646626..167647567,2	MCF-7	breast:
16	chr5:167625904..167627787-chr5:167630198..167633051,2	K562	blood:

Variant related genes	Relation type
TENM2	TF binding region
TENM2	CpG island

Extended variants
information (count: 1116 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1116 , 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	rs10516045	chr5:167622534-167622535	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556505359	chr5:167622557-167622558	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12186655	chr5:167622561-167622562	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs143043809	chr5:167622573-167622574	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545863670	chr5:167622607-167622608	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs59946077	chr5:167622609-167622610	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536378743	chr5:167622611-167622612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35040257	chr5:167622613-167622614	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559321578	chr5:167622636-167622637	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114308405	chr5:167622675-167622676	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs80015809	chr5:167622689-167622690	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561964085	chr5:167622708-167622709	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192742930	chr5:167622712-167622713	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563959186	chr5:167622729-167622730	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575895954	chr5:167622771-167622772	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542602875	chr5:167622795-167622796	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368673361	chr5:167622800-167622801	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560982413	chr5:167622803-167622804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4415101	chr5:167622839-167622840	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs60353035	chr5:167622893-167622894	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533292579	chr5:167622901-167622902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs13180204	chr5:167622914-167622915	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566991945	chr5:167622977-167622978	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150719666	chr5:167622990-167622991	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540579528	chr5:167622998-167622999	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535656928	chr5:167623052-167623053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17731087	chr5:167623089-167623090	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569226181	chr5:167623164-167623165	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115333350	chr5:167623280-167623281	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs17632217	chr5:167623283-167623284	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs576760398	chr5:167623359-167623360	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183308274	chr5:167623394-167623395	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532012492	chr5:167623416-167623417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113018205	chr5:167623439-167623440	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572927315	chr5:167623486-167623487	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542054207	chr5:167623489-167623490	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139944473	chr5:167623524-167623525	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575630951	chr5:167623553-167623554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544495609	chr5:167623562-167623563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144964995	chr5:167623638-167623639	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548185356	chr5:167623655-167623656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566444733	chr5:167623696-167623697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147928491	chr5:167623747-167623748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187994941	chr5:167623756-167623757	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192153247	chr5:167623757-167623758	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140112073	chr5:167623759-167623760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184701308	chr5:167623763-167623764	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188703382	chr5:167623803-167623804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145430417	chr5:167623818-167623819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34608084	chr5:167623831-167623832	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16865294	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Pancreatic cancer	17952125	CNVD
Epilepsy	20502679	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167592400-167626000	Weak transcription	HSMM	muscle
2	chr5:167606600-167626800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:167608600-167631800	Weak transcription	NH-A	brain
4	chr5:167615800-167633800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr5:167615800-167646600	Weak transcription	Fetal Heart	heart
6	chr5:167617000-167628200	Strong transcription	NHEK	skin
7	chr5:167618800-167624000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:167618800-167625000	Weak transcription	Right Ventricle	heart
9	chr5:167619200-167646600	Weak transcription	NHDF-Ad	bronchial
10	chr5:167619800-167622800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr5:167620600-167626800	Weak transcription	Brain Angular Gyrus	brain
12	chr5:167620800-167634200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:167620800-167636400	Weak transcription	HSMMtube	muscle
14	chr5:167621200-167636600	Weak transcription	Brain Anterior Caudate	brain
15	chr5:167621400-167622800	Strong transcription	Left Ventricle	heart
16	chr5:167621400-167626800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:167621400-167636600	Weak transcription	Fetal Lung	lung
18	chr5:167621400-167657600	Weak transcription	Fetal Brain Female	brain
19	chr5:167621800-167622600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:167621800-167629000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:167621800-167646400	Weak transcription	Brain Germinal Matrix	brain
22	chr5:167622000-167624200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:167622200-167622800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr5:167622200-167623000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:167622200-167628000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr5:167622200-167636200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:167622200-167636400	Weak transcription	Fetal Brain Male	brain
28	chr5:167622400-167623000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:167622400-167625600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr5:167622600-167636600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr5:167622800-167625600	Weak transcription	Left Ventricle	heart
32	chr5:167622800-167629800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr5:167622800-167634000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:167623000-167634200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:167624000-167631400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:167624000-167636600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr5:167624200-167625600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr5:167624600-167634400	Weak transcription	HMEC	breast
39	chr5:167624600-167646600	Weak transcription	Liver	Liver
40	chr5:167624800-167636800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr5:167625000-167628200	Strong transcription	Right Ventricle	heart
42	chr5:167625600-167627200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr5:167625600-167633200	Strong transcription	Left Ventricle	heart
44	chr5:167625600-167633400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr5:167626000-167628800	Strong transcription	HSMM	muscle
46	chr5:167626400-167636600	Weak transcription	Brain Cingulate Gyrus	brain
47	chr5:167626800-167627200	Strong transcription	Brain Angular Gyrus	brain
48	chr5:167626800-167627400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:167626800-167629200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr5:167627200-167631200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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