Variant report

Variant	nsv515766
Chromosome Location	chr5:17283367-17306790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:464)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr5:17305740-17306793	A549	lung:	n/a	chr5:17306230-17306243 chr5:17305996-17306006
2	ATF3	chr5:17305772-17306632	A549	lung:	n/a	chr5:17306230-17306243 chr5:17305996-17306006
3	ATF3	chr5:17304934-17305682	A549	lung:	n/a	n/a
4	ATF3	chr5:17304997-17305551	A549	lung:	n/a	n/a
5	BCL3	chr5:17283730-17284668	A549	lung:	n/a	n/a
6	BCL3	chr5:17304298-17305641	A549	lung:	n/a	n/a
7	BCL3	chr5:17278591-17283707	A549	lung:	n/a	n/a
8	BCL3	chr5:17284858-17285406	A549	lung:	n/a	n/a
9	BCL3	chr5:17284833-17285128	GM12878	blood:	n/a	n/a
10	BCL3	chr5:17290668-17290872	GM12878	blood:	n/a	n/a
11	BCL3	chr5:17290553-17290971	GM12878	blood:	n/a	n/a
12	BCL3	chr5:17304497-17306914	A549	lung:	n/a	n/a
13	BCL3	chr5:17305724-17307035	A549	lung:	n/a	n/a
14	BRCA1	chr5:17302217-17303213	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr5:17304511-17306729	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr5:17303713-17303758	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:17284874-17285240	A549	lung:	n/a	n/a
18	CEBPB	chr5:17305061-17305575	A549	lung:	n/a	chr5:17305113-17305124 chr5:17305113-17305124 chr5:17305305-17305318
19	CEBPB	chr5:17289635-17290089	MCF-7	breast:	n/a	n/a
20	CEBPB	chr5:17284897-17285356	A549	lung:	n/a	n/a
21	CEBPB	chr5:17306102-17306525	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:17305864-17306750	A549	lung:	n/a	n/a
23	CEBPB	chr5:17302884-17303231	A549	lung:	n/a	chr5:17302995-17303008
24	CEBPB	chr5:17305046-17305553	MCF-7	breast:	n/a	chr5:17305113-17305124 chr5:17305113-17305124 chr5:17305305-17305318
25	CEBPB	chr5:17287786-17287818	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:17305821-17306819	MCF-7	breast:	n/a	n/a
27	CEBPB	chr5:17305051-17305565	MCF-7	breast:	n/a	chr5:17305113-17305124 chr5:17305113-17305124 chr5:17305305-17305318
28	CEBPB	chr5:17306166-17306483	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:17304391-17304701	A549	lung:	n/a	n/a
30	CEBPB	chr5:17290767-17291017	A549	lung:	n/a	chr5:17290902-17290913
31	CEBPB	chr5:17284873-17285138	A549	lung:	n/a	n/a
32	CEBPB	chr5:17305891-17306763	A549	lung:	n/a	n/a
33	CEBPB	chr5:17304876-17306892	A549	lung:	n/a	chr5:17305113-17305124 chr5:17305113-17305124 chr5:17305305-17305318
34	CEBPB	chr5:17302602-17303269	A549	lung:	n/a	chr5:17302995-17303008
35	CEBPB	chr5:17305008-17305659	A549	lung:	n/a	chr5:17305113-17305124 chr5:17305113-17305124 chr5:17305305-17305318
36	CEBPB	chr5:17290275-17290564	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:17284949-17285170	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:17302194-17303260	Hela-S3	cervix:	n/a	chr5:17302995-17303008
39	CEBPB	chr5:17304208-17304809	A549	lung:	n/a	n/a
40	CEBPB	chr5:17284868-17285228	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:17290859-17291018	HepG2	liver:	n/a	chr5:17290902-17290913
42	CEBPB	chr5:17304353-17306743	Hela-S3	cervix:	n/a	chr5:17305113-17305124 chr5:17305113-17305124 chr5:17305305-17305318
43	CEBPB	chr5:17305123-17305512	IMR90	lung:	n/a	chr5:17305305-17305318
44	CEBPB	chr5:17305791-17306779	MCF-7	breast:	n/a	n/a
45	CHD2	chr5:17302101-17303183	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr5:17287987-17288180	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr5:17287848-17287871	HepG2	liver:	n/a	n/a
48	CHD2	chr5:17306618-17306660	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr5:17305038-17305575	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr5:17305917-17306990	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17306335-17306385	CMK	blood:	n/a
2	chr5:17306335-17306385	NH-A	brain:	n/a
3	chr5:17290681-17290731	HEEpiC	esophagus:	n/a
4	chr5:17306335-17306385	PFSK-1	brain:	n/a
5	chr5:17306335-17306385	ProgFib	skin:	n/a
6	chr5:17306335-17306385	HRE	kidney:	n/a
7	chr5:17290681-17290731	HCM	heart:	n/a
8	chr5:17290681-17290731	Hepatocyte	liver:	n/a
9	chr5:17306335-17306385	HRPEpiC	eye:	n/a
10	chr5:17306335-17306385	Hela-S3	cervix:	n/a
11	chr5:17290681-17290731	HAEpiC	amniotic membrane:	n/a
12	chr5:17290681-17290731	NH-A	brain:	n/a
13	chr5:17290681-17290731	AG04449	skin:	fetal
14	chr5:17290681-17290731	U87	brain:	n/a
15	chr5:17290681-17290731	AG10803	skin:	n/a
16	chr5:17306335-17306385	NB4	blood:	n/a
17	chr5:17306335-17306385	AoSMC	blood vessel:	n/a
18	chr5:17306335-17306385	H1-hESC	embryonic stem cell:	embryo
19	chr5:17306335-17306385	U87	brain:	n/a
20	chr5:17290681-17290731	HRE	kidney:	n/a
21	chr5:17306335-17306385	SK-N-MC	brain:	n/a
22	chr5:17306335-17306385	GM12892	blood:	n/a
23	chr5:17290681-17290731	SK-N-MC	brain:	n/a
24	chr5:17290681-17290731	ECC-1	luminal epithelium:	n/a
25	chr5:17306335-17306385	HEK293	kidney:	embryo
26	chr5:17306335-17306385	GM12878	blood:	n/a
27	chr5:17290681-17290731	SKMC	muscle:	n/a
28	chr5:17306335-17306385	AG09309	skin:	n/a
29	chr5:17306335-17306385	HMEC	breast:	n/a
30	chr5:17290681-17290731	NB4	blood:	n/a
31	chr5:17306335-17306385	HUVEC	blood vessel:	n/a
32	chr5:17306335-17306385	K562	blood:	n/a
33	chr5:17306335-17306385	HNPCEpiC	eye:	n/a
34	chr5:17290681-17290731	IMR90	lung:	fetal
35	chr5:17306335-17306385	LNCaP	prostate:	n/a
36	chr5:17306335-17306385	HRCEpiC	kidney:	n/a
37	chr5:17290681-17290731	H1-hESC	embryonic stem cell:	embryo
38	chr5:17290681-17290731	HCPEpiC	choroid plexus:	n/a
39	chr5:17290681-17290731	HNPCEpiC	eye:	n/a
40	chr5:17290681-17290731	BJ	skin:	n/a
41	chr5:17306335-17306385	HCPEpiC	choroid plexus:	n/a
42	chr5:17290681-17290731	GM12878	blood:	n/a
43	chr5:17306335-17306385	AG10803	skin:	n/a
44	chr5:17290681-17290731	MCF10A-Er-Src	breast:	n/a
45	chr5:17306335-17306385	AG04450	lung:	fetal
46	chr5:17290681-17290731	SK-N-SH	brain:	n/a
47	chr5:17290681-17290731	NHBE	bronchial:	n/a
48	chr5:17306335-17306385	HCM	heart:	n/a
49	chr5:17306335-17306385	HCT-116	colon:	n/a
50	chr5:17306335-17306385	AG09319	gingival:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:16934595..16937300-chr5:17301950..17303830,2	MCF-7	breast:
2	chr5:17276120..17278770-chr5:17300938..17303785,2	MCF-7	breast:
3	chr5:17219127..17220679-chr5:17282330..17284104,2	MCF-7	breast:
4	chr5:17282891..17284625-chr5:17285945..17288068,2	MCF-7	breast:
5	chr5:17298640..17300836-chr5:17306560..17308116,2	MCF-7	breast:
6	chr5:17223288..17225551-chr5:17303206..17305533,2	MCF-7	breast:
7	chr5:17282874..17284438-chr5:17301953..17304324,2	MCF-7	breast:
8	chr5:17287620..17289134-chr5:17291849..17294137,2	MCF-7	breast:
9	chr5:17238515..17239072-chr5:17305563..17306451,2	MCF-7	breast:
10	chr12:16671093..16672761-chr5:17295731..17297652,2	MCF-7	breast:
11	chr5:17302539..17304915-chr5:17307997..17309870,2	MCF-7	breast:
12	chr5:16934773..16937451-chr5:17304289..17306411,2	MCF-7	breast:
13	chr5:17298640..17300836-chr5:17306560..17308116,2	MCF-7	breast:
14	chr5:17215446..17220855-chr5:17303141..17309835,13	MCF-7	breast:
15	chr5:17282891..17284625-chr5:17285945..17288068,2	MCF-7	breast:
16	chr5:17279526..17282180-chr5:17283122..17285646,2	K562	blood:
17	chr5:17217787..17219336-chr5:17290050..17291601,2	MCF-7	breast:
18	chr5:17236574..17239004-chr5:17300342..17302444,2	MCF-7	breast:
19	chr5:17282874..17284438-chr5:17301953..17304324,2	MCF-7	breast:
20	chr5:17231132..17233023-chr5:17300531..17302683,2	MCF-7	breast:
21	chr5:17301754..17303834-chr5:17308080..17310804,2	MCF-7	breast:
22	chr5:17287620..17289134-chr5:17291849..17294137,2	MCF-7	breast:
23	chr5:17215544..17223113-chr5:17298591..17308160,18	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000185296	TF binding region
ENSG00000185296	CpG island
ENSG00000176788	chromatin interactions
ENSG00000145555	chromatin interactions
ENSG00000215196	chromatin interactions

Extended variants
information (count: 934 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs298582	chr5:17283367-17283368	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540760044	chr5:17283393-17283394	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs564216551	chr5:17283421-17283422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533139639	chr5:17283457-17283458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543678270	chr5:17283483-17283484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35035907	chr5:17283505-17283506	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184700742	chr5:17283537-17283538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78936435	chr5:17283538-17283539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114243923	chr5:17283541-17283542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139341786	chr5:17283584-17283585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2652654	chr5:17283587-17283588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528530878	chr5:17283601-17283602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373606959	chr5:17283625-17283626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551438246	chr5:17283634-17283635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564875930	chr5:17283637-17283638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77133908	chr5:17283649-17283650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111496740	chr5:17283714-17283715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532211118	chr5:17283724-17283725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537216597	chr5:17283776-17283777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557156539	chr5:17283817-17283818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529873054	chr5:17283822-17283823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567904037	chr5:17283837-17283838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536556145	chr5:17283850-17283851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556523354	chr5:17283868-17283869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553669856	chr5:17283900-17283901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs55858647	chr5:17283903-17283904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189253539	chr5:17283950-17283951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192063631	chr5:17283957-17283958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79182834	chr5:17284013-17284014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560332864	chr5:17284028-17284029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577833128	chr5:17284038-17284039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185048350	chr5:17284040-17284041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs298581	chr5:17284049-17284050	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs138507167	chr5:17284094-17284095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141230288	chr5:17284128-17284129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs298580	chr5:17284132-17284133	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs559624788	chr5:17284143-17284144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs298579	chr5:17284156-17284157	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs189524633	chr5:17284212-17284213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568420474	chr5:17284221-17284222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75618572	chr5:17284222-17284223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530917235	chr5:17284232-17284233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535966531	chr5:17284269-17284270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143629706	chr5:17284306-17284307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567752945	chr5:17284334-17284335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536898856	chr5:17284361-17284362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546957366	chr5:17284375-17284376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567188673	chr5:17284406-17284407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146785303	chr5:17284426-17284427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72738670	chr5:17284450-17284451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17276600-17283800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr5:17276600-17285400	Enhancers	Primary B cells from peripheral blood	blood
3	chr5:17277800-17284800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:17277800-17290600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:17278000-17287400	Weak transcription	Hela-S3	cervix
6	chr5:17279400-17284600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:17282400-17283400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:17282400-17283400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr5:17283000-17283400	Active TSS	Monocytes-CD14+_RO01746	blood
10	chr5:17283000-17284000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:17283000-17284000	Weak transcription	A549	lung
12	chr5:17283200-17283400	Enhancers	GM12878-XiMat	blood
13	chr5:17283200-17284200	Enhancers	Primary B cells from cord blood	blood
14	chr5:17283200-17290200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr5:17283400-17283800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr5:17283800-17284000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr5:17283800-17284000	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr5:17284000-17285200	Enhancers	A549	lung
19	chr5:17284000-17285200	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr5:17284200-17284400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr5:17285200-17285400	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr5:17287400-17287600	Enhancers	Hela-S3	cervix
23	chr5:17287600-17288200	Flanking Active TSS	Hela-S3	cervix
24	chr5:17287600-17288600	Enhancers	Fetal Heart	heart
25	chr5:17288200-17290800	Enhancers	Hela-S3	cervix
26	chr5:17289800-17290600	Enhancers	Stomach Mucosa	stomach
27	chr5:17289800-17291000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:17289800-17291600	Enhancers	Placenta	Placenta
29	chr5:17290200-17291000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr5:17290200-17291000	Enhancers	Placenta Amnion	Placenta Amnion
31	chr5:17290200-17291600	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr5:17290400-17290600	Enhancers	Fetal Heart	heart
33	chr5:17290600-17290800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr5:17290600-17291000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr5:17291600-17292000	Weak transcription	Placenta	Placenta
36	chr5:17292000-17293400	Enhancers	Placenta	Placenta
37	chr5:17292200-17292800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:17292600-17293000	Enhancers	Primary B cells from peripheral blood	blood
39	chr5:17293400-17302000	Weak transcription	Placenta	Placenta
40	chr5:17296600-17306600	Weak transcription	Aorta	Aorta
41	chr5:17298200-17300200	Enhancers	Stomach Mucosa	stomach
42	chr5:17298400-17298600	Enhancers	Gastric	stomach
43	chr5:17298600-17299200	Weak transcription	Gastric	stomach
44	chr5:17298800-17299200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:17299000-17299200	Enhancers	A549	lung
46	chr5:17299200-17299400	Enhancers	Gastric	stomach
47	chr5:17299200-17299600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:17299200-17300200	Weak transcription	A549	lung
49	chr5:17299400-17306600	Weak transcription	Gastric	stomach
50	chr5:17299600-17301000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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