Variant report

Variant	nsv549182
Chromosome Location	chr1:215167236-215248417
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	ATF1	chr1:215183082-215183085	K562	blood:	n/a	n/a
2	ATF2	chr1:215174619-215175413	GM12878	blood:	n/a	n/a
3	ATF2	chr1:215174804-215175522	GM12878	blood:	n/a	n/a
4	BATF	chr1:215175021-215175376	GM12878	blood:	n/a	n/a
5	BATF	chr1:215191913-215192204	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:215174734-215175434	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:215174929-215175338	GM12878	blood:	n/a	n/a
8	BCL3	chr1:215174674-215175424	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:215174877-215175414	GM12878	blood:	n/a	n/a
10	BCLAF1	chr1:215174795-215175435	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:215174834-215175364	GM12878	blood:	n/a	n/a
12	CEBPB	chr1:215192513-215192708	HepG2	liver:	n/a	chr1:215192655-215192666
13	CEBPB	chr1:215176976-215177349	IMR90	lung:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
14	CEBPB	chr1:215244913-215245192	HepG2	liver:	n/a	chr1:215245042-215245053
15	CEBPB	chr1:215176980-215177354	Hela-S3	cervix:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
16	CEBPB	chr1:215176894-215177502	MCF-7	breast:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
17	CEBPB	chr1:215176984-215177328	K562	blood:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
18	CEBPB	chr1:215196834-215197198	A549	lung:	n/a	chr1:215197059-215197068 chr1:215197089-215197100 chr1:215196987-215196996 chr1:215197059-215197068 chr1:215196987-215196996 chr1:215197057-215197070 chr1:215197059-215197068 chr1:215196985-215196998 chr1:215196987-215196996 chr1:215197059-215197070 chr1:215197059-215197070 chr1:215197059-215197068
19	CEBPB	chr1:215176983-215177344	HepG2	liver:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
20	CEBPB	chr1:215192596-215192798	IMR90	lung:	n/a	chr1:215192655-215192666
21	CEBPB	chr1:215174522-215175516	GM12878	blood:	n/a	n/a
22	CEBPB	chr1:215176845-215177475	MCF-7	breast:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
23	CEBPB	chr1:215196799-215197235	IMR90	lung:	n/a	chr1:215197059-215197068 chr1:215197089-215197100 chr1:215196987-215196996 chr1:215197059-215197068 chr1:215196987-215196996 chr1:215197057-215197070 chr1:215197059-215197068 chr1:215196985-215196998 chr1:215196987-215196996 chr1:215197059-215197070 chr1:215197059-215197070 chr1:215197059-215197068
24	CEBPB	chr1:215176065-215176123	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr1:215176974-215177350	A549	lung:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
26	CEBPB	chr1:215243144-215243320	A549	lung:	n/a	n/a
27	CEBPB	chr1:215196914-215197114	K562	blood:	n/a	chr1:215197059-215197068 chr1:215197089-215197100 chr1:215196987-215196996 chr1:215197059-215197068 chr1:215196987-215196996 chr1:215197057-215197070 chr1:215197059-215197068 chr1:215196985-215196998 chr1:215196987-215196996 chr1:215197059-215197070 chr1:215197059-215197070 chr1:215197059-215197068
28	CEBPB	chr1:215196816-215197182	HepG2	liver:	n/a	chr1:215197059-215197068 chr1:215197089-215197100 chr1:215196987-215196996 chr1:215197059-215197068 chr1:215196987-215196996 chr1:215197057-215197070 chr1:215197059-215197068 chr1:215196985-215196998 chr1:215196987-215196996 chr1:215197059-215197070 chr1:215197059-215197070 chr1:215197059-215197068
29	CEBPB	chr1:215225876-215226429	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:215195983-215196572	IMR90	lung:	n/a	chr1:215196177-215196190
31	CEBPB	chr1:215196916-215197162	H1-hESC	embryonic stem cell:	n/a	chr1:215197059-215197068 chr1:215197089-215197100 chr1:215196987-215196996 chr1:215197059-215197068 chr1:215196987-215196996 chr1:215197057-215197070 chr1:215197059-215197068 chr1:215196985-215196998 chr1:215196987-215196996 chr1:215197059-215197070 chr1:215197059-215197070 chr1:215197059-215197068
32	CEBPB	chr1:215171202-215171219	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:215196887-215197238	MCF-7	breast:	n/a	chr1:215197059-215197068 chr1:215197089-215197100 chr1:215196987-215196996 chr1:215197059-215197068 chr1:215196987-215196996 chr1:215197057-215197070 chr1:215197059-215197068 chr1:215196985-215196998 chr1:215196987-215196996 chr1:215197059-215197070 chr1:215197059-215197070 chr1:215197059-215197068
34	CEBPB	chr1:215244919-215245194	IMR90	lung:	n/a	chr1:215245042-215245053
35	CEBPB	chr1:215191916-215192244	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:215228572-215228682	A549	lung:	n/a	n/a
37	CEBPB	chr1:215213631-215213829	H1-hESC	embryonic stem cell:	n/a	chr1:215213689-215213700
38	CEBPB	chr1:215177030-215177283	H1-hESC	embryonic stem cell:	n/a	chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177157-215177170 chr1:215177159-215177168 chr1:215177158-215177169 chr1:215177157-215177168 chr1:215177159-215177168
39	CEBPB	chr1:215213591-215213766	HepG2	liver:	n/a	chr1:215213689-215213700
40	CEBPB	chr1:215196032-215197258	Hela-S3	cervix:	n/a	chr1:215197059-215197068 chr1:215197089-215197100 chr1:215196987-215196996 chr1:215197059-215197068 chr1:215196987-215196996 chr1:215196177-215196190 chr1:215197057-215197070 chr1:215197059-215197068 chr1:215196985-215196998 chr1:215196987-215196996 chr1:215197059-215197070 chr1:215197059-215197070 chr1:215197059-215197068
41	CHD1	chr1:215175003-215175363	GM12878	blood:	n/a	n/a
42	CHD2	chr1:215174882-215175364	GM12878	blood:	n/a	n/a
43	CTCF	chr1:215205617-215205702	Medullo	brain:	n/a	n/a
44	CTCF	chr1:215203990-215204022	GM13976	blood:	n/a	n/a
45	CTCF	chr1:215184704-215184747	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:215197200-215197350	Caco-2	colon:	n/a	n/a
47	CTCF	chr1:215227800-215227950	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:215202400-215202550	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:215205557-215205608	Medullo	brain:	n/a	n/a
50	CTCF	chr1:215197204-215197600	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:215219381-215219431	HIPEpiC	eye:	n/a
2	chr1:215219381-215219431	HIPEpiC	eye:	n/a
3	chr1:215179151-215179201	HL-60	blood:	n/a
4	chr1:215228588-215228638	HUVEC	blood vessel:	n/a
5	chr1:215178658-215178708	LNCaP	prostate:	n/a
6	chr1:215219381-215219431	IMR90	lung:	fetal
7	chr1:215177428-215177478	HRPEpiC	eye:	n/a
8	chr1:215228588-215228638	GM19239	blood:	n/a
9	chr1:215178658-215178708	ProgFib	skin:	n/a
10	chr1:215178854-215178904	HMEC	breast:	n/a
11	chr1:215219381-215219431	PrEC	prostate:	n/a
12	chr1:215178658-215178708	HEK293	kidney:	embryo
13	chr1:215196452-215196502	NT2-D1	testis:	n/a
14	chr1:215178601-215178651	Hepatocyte	liver:	n/a
15	chr1:215177428-215177478	AG10803	skin:	n/a
16	chr1:215177428-215177478	U87	brain:	n/a
17	chr1:215219381-215219431	GM12878	blood:	n/a
18	chr1:215219381-215219431	HEEpiC	esophagus:	n/a
19	chr1:215169182-215169232	HEK293	kidney:	embryo
20	chr1:215177428-215177478	HCF	heart:	n/a
21	chr1:215169182-215169232	GM12878	blood:	n/a
22	chr1:215169182-215169232	HRCEpiC	kidney:	n/a
23	chr1:215178907-215178957	AG09319	gingival:	n/a
24	chr1:215179216-215179266	NH-A	brain:	n/a
25	chr1:215177428-215177478	HUVEC	blood vessel:	n/a
26	chr1:215178907-215178957	BE2_C	brain:	n/a
27	chr1:215169182-215169232	HMEC	breast:	n/a
28	chr1:215196452-215196502	PFSK-1	brain:	n/a
29	chr1:215178601-215178651	AG04450	lung:	fetal
30	chr1:215177428-215177478	HRE	kidney:	n/a
31	chr1:215178907-215178957	SAEC	small airway:	n/a
32	chr1:215178907-215178957	HCT-116	colon:	n/a
33	chr1:215179151-215179201	BJ	skin:	n/a
34	chr1:215179216-215179266	HL-60	blood:	n/a
35	chr1:215178854-215178904	GM19239	blood:	n/a
36	chr1:215219381-215219431	GM12891	blood:	n/a
37	chr1:215169182-215169232	HIPEpiC	eye:	n/a
38	chr1:215179151-215179201	HCT-116	colon:	n/a
39	chr1:215196452-215196502	PANC-1	pancreas:	n/a
40	chr1:215178658-215178708	NHDF-neo	bronchial:	n/a
41	chr1:215178854-215178904	T-47D	breast:	n/a
42	chr1:215179151-215179201	Hepatocyte	liver:	n/a
43	chr1:215177441-215177491	BE2_C	brain:	n/a
44	chr1:215177441-215177491	GM06990	blood:	n/a
45	chr1:215179151-215179201	NHDF-neo	bronchial:	n/a
46	chr1:215179151-215179201	SK-N-SH	brain:	n/a
47	chr1:215177441-215177491	Jurkat	blood:	n/a
48	chr1:215178601-215178651	NB4	blood:	n/a
49	chr1:215178907-215178957	GM19239	blood:	n/a
50	chr1:215177441-215177491	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:215228959..215231778-chr1:215232389..215235318,2	K562	blood:
2	chr1:215195775..215197372-chr1:215199514..215201909,2	K562	blood:
3	chr1:215181552..215183505-chr1:215187538..215189562,2	K562	blood:
4	chr1:215196838..215197537-chr1:215249583..215250160,2	MCF-7	breast:
5	chr1:215181522..215183505-chr1:215186881..215189562,2	K562	blood:
6	chr1:215195775..215197372-chr1:215199514..215201909,2	K562	blood:
7	chr1:215175482..215177146-chr1:215181742..215183576,2	K562	blood:
8	chr1:215181522..215183505-chr1:215186881..215189562,2	K562	blood:
9	chr1:215175482..215177146-chr1:215181742..215183576,2	K562	blood:
10	chr1:215177498..215178498-chr13:40006578..40007578,2	MCF-7	breast:
11	chr1:214773067..214775005-chr1:215239783..215241407,2	K562	blood:
12	chr1:215181552..215183505-chr1:215187538..215189562,2	K562	blood:
13	chr1:215228959..215231778-chr1:215232389..215235318,2	K562	blood:

Variant related genes	Relation type
KCNK2	TF binding region
KCNK2	CpG island

Extended variants
information (count: 3130 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3130 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6662428	chr1:215167236-215167237	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537402327	chr1:215167239-215167240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370200621	chr1:215167263-215167264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530944442	chr1:215167284-215167285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551029820	chr1:215167337-215167338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561314358	chr1:215167367-215167368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57689794	chr1:215167384-215167385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138316887	chr1:215167391-215167392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12119060	chr1:215167414-215167415	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs538939370	chr1:215167445-215167446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74540205	chr1:215167480-215167481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75400779	chr1:215167518-215167519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569171727	chr1:215167579-215167580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370792552	chr1:215167585-215167586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182046721	chr1:215167603-215167604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558759133	chr1:215167619-215167620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573576441	chr1:215167628-215167629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535976273	chr1:215167641-215167642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs61819972	chr1:215167654-215167655	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76316970	chr1:215167685-215167686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185928289	chr1:215167689-215167690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150643853	chr1:215167725-215167726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558771266	chr1:215167752-215167753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575638779	chr1:215167793-215167794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544515886	chr1:215167796-215167797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs117567417	chr1:215167797-215167798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530062907	chr1:215167798-215167799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540372745	chr1:215167837-215167838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80136098	chr1:215167841-215167842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77053917	chr1:215167849-215167850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2841620	chr1:215167862-215167863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543008482	chr1:215167873-215167874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2601649	chr1:215167898-215167899	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs375223455	chr1:215167963-215167964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548826037	chr1:215167978-215167979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs956765	chr1:215167985-215167986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56152266	chr1:215168036-215168037	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371252139	chr1:215168049-215168050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189073653	chr1:215168075-215168076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181167207	chr1:215168104-215168105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376772599	chr1:215168109-215168110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1377182	chr1:215168126-215168127	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538717477	chr1:215168169-215168170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558836730	chr1:215168204-215168205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112293659	chr1:215168216-215168217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575501819	chr1:215168246-215168247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116057500	chr1:215168266-215168267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554801883	chr1:215168282-215168283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17604089	chr1:215168297-215168298	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs114859923	chr1:215168311-215168312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215163800-215168200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:215164200-215167800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:215164200-215174800	Weak transcription	NH-A	brain
4	chr1:215164800-215175000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr1:215166600-215167600	Enhancers	NHDF-Ad	bronchial
6	chr1:215166600-215168000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:215166800-215167400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:215166800-215167400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:215166800-215167600	Enhancers	NHLF	lung
10	chr1:215166800-215168000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:215167200-215170600	Weak transcription	Osteobl	bone
12	chr1:215167400-215174600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:215167600-215168000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:215167800-215168400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr1:215167800-215168600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:215167800-215169000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr1:215168000-215174800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:215168200-215168600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:215168400-215169000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:215168600-215169200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:215170600-215171200	Genic enhancers	Osteobl	bone
22	chr1:215171200-215172800	Strong transcription	Osteobl	bone
23	chr1:215172800-215174600	Weak transcription	Osteobl	bone
24	chr1:215174000-215174800	Enhancers	GM12878-XiMat	blood
25	chr1:215174400-215175200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:215174600-215176000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:215174600-215176200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:215174600-215176400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:215174600-215176400	Enhancers	HMEC	breast
30	chr1:215174600-215176600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr1:215174600-215176600	Enhancers	NHEK	skin
32	chr1:215174600-215177400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:215174600-215178200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:215174600-215178600	Enhancers	Osteobl	bone
35	chr1:215174800-215175400	Enhancers	Esophagus	oesophagus
36	chr1:215174800-215175400	Flanking Active TSS	GM12878-XiMat	blood
37	chr1:215174800-215176400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:215174800-215176600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:215174800-215176800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr1:215174800-215176800	Enhancers	NH-A	brain
41	chr1:215174800-215178000	Enhancers	NHDF-Ad	bronchial
42	chr1:215175000-215176600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:215175000-215176600	Enhancers	NHLF	lung
44	chr1:215175200-215176000	Enhancers	HSMM	muscle
45	chr1:215175200-215176400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:215175200-215176400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr1:215175400-215176200	Enhancers	GM12878-XiMat	blood
48	chr1:215175600-215176000	Enhancers	HSMMtube	muscle
49	chr1:215176000-215178600	Weak transcription	HSMM	muscle
50	chr1:215176000-215178800	Weak transcription	HSMMtube	muscle

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