Variant report

Variant	nsv962445
Chromosome Location	chr17:45397004-45428018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:774)
CpG islands
(count:672)
Chromatin interactive
region (count:20)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45400690-45401184	K562	blood:	n/a	n/a
2	ARID3A	chr17:45401126-45401220	HepG2	liver:	n/a	n/a
3	ATF2	chr17:45401740-45402536	GM12878	blood:	n/a	n/a
4	ATF2	chr17:45400911-45401534	GM12878	blood:	n/a	n/a
5	ATF2	chr17:45401460-45401994	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr17:45401070-45401564	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr17:45401787-45402387	GM12878	blood:	n/a	n/a
8	ATF3	chr17:45401135-45401442	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr17:45400963-45401448	K562	blood:	n/a	n/a
10	ATF3	chr17:45400832-45401848	A549	lung:	n/a	n/a
11	ATF3	chr17:45401079-45401475	HepG2	liver:	n/a	n/a
12	BACH1	chr17:45400672-45401381	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr17:45402164-45402512	GM12878	blood:	n/a	n/a
14	BCL3	chr17:45401228-45402086	A549	lung:	n/a	n/a
15	BCL3	chr17:45400908-45401494	GM12878	blood:	n/a	n/a
16	BCL3	chr17:45400527-45402367	A549	lung:	n/a	n/a
17	BCLAF1	chr17:45400883-45402507	GM12878	blood:	n/a	n/a
18	BHLHE40	chr17:45400783-45401534	HepG2	liver:	n/a	n/a
19	BHLHE40	chr17:45400912-45402336	GM12878	blood:	n/a	n/a
20	BHLHE40	chr17:45400834-45401611	K562	blood:	n/a	n/a
21	BRCA1	chr17:45400643-45401612	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr17:45401192-45401255	HepG2	liver:	n/a	n/a
23	BRCA1	chr17:45401360-45401501	GM12878	blood:	n/a	n/a
24	CBX3	chr17:45398207-45398906	K562	blood:	n/a	n/a
25	CBX3	chr17:45398315-45398717	HCT-116	colon:	n/a	n/a
26	CBX3	chr17:45400547-45402013	K562	blood:	n/a	n/a
27	CBX3	chr17:45401008-45401348	K562	blood:	n/a	n/a
28	CBX3	chr17:45398253-45398725	K562	blood:	n/a	n/a
29	CCNT2	chr17:45400884-45401537	K562	blood:	n/a	n/a
30	CEBPB	chr17:45401251-45401860	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr17:45401719-45401726	K562	blood:	n/a	n/a
32	CEBPB	chr17:45400762-45401549	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr17:45402742-45402817	K562	blood:	n/a	n/a
34	CEBPB	chr17:45401426-45403018	A549	lung:	n/a	n/a
35	CEBPB	chr17:45401653-45402841	A549	lung:	n/a	n/a
36	CEBPB	chr17:45401792-45402102	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr17:45401324-45402847	GM12878	blood:	n/a	n/a
38	CEBPB	chr17:45401760-45402533	MCF-7	breast:	n/a	n/a
39	CEBPD	chr17:45401062-45401313	HepG2	liver:	n/a	n/a
40	CEBPD	chr17:45401314-45401514	HepG2	liver:	n/a	n/a
41	CEBPD	chr17:45400913-45401563	HepG2	liver:	n/a	n/a
42	CHD1	chr17:45400811-45402377	GM12878	blood:	n/a	n/a
43	CHD2	chr17:45400935-45402253	GM12878	blood:	n/a	n/a
44	CHD2	chr17:45400927-45401394	HepG2	liver:	n/a	n/a
45	CHD2	chr17:45400922-45401524	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr17:45400833-45401545	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr17:45402719-45402722	GM12878	blood:	n/a	n/a
48	CHD2	chr17:45400846-45401729	K562	blood:	n/a	n/a
49	CREB1	chr17:45401007-45401411	A549	lung:	n/a	n/a
50	CREB1	chr17:45400695-45401811	HepG2	liver:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45400748-45400798	ovcar-3	ovarian:	n/a
2	chr17:45400748-45400798	ovcar-3	ovarian:	n/a
3	chr17:45401150-45401200	PANC-1	pancreas:	n/a
4	chr17:45401148-45401198	Hepatocyte	liver:	n/a
5	chr17:45400748-45400798	H1-hESC	embryonic stem cell:	embryo
6	chr17:45401150-45401200	AoSMC	blood vessel:	n/a
7	chr17:45400944-45400994	PFSK-1	brain:	n/a
8	chr17:45401397-45401447	CMK	blood:	n/a
9	chr17:45398817-45398867	GM19239	blood:	n/a
10	chr17:45403706-45403756	HRPEpiC	eye:	n/a
11	chr17:45398817-45398867	HRCEpiC	kidney:	n/a
12	chr17:45401312-45401362	AG04449	skin:	fetal
13	chr17:45400944-45400994	HRCEpiC	kidney:	n/a
14	chr17:45403706-45403756	IMR90	lung:	fetal
15	chr17:45401150-45401200	HNPCEpiC	eye:	n/a
16	chr17:45400944-45400994	Hepatocyte	liver:	n/a
17	chr17:45401148-45401198	HNPCEpiC	eye:	n/a
18	chr17:45403706-45403756	PrEC	prostate:	n/a
19	chr17:45398817-45398867	PrEC	prostate:	n/a
20	chr17:45401156-45401206	SKMC	muscle:	n/a
21	chr17:45401156-45401206	CMK	blood:	n/a
22	chr17:45401833-45401883	MCF10A-Er-Src	breast:	n/a
23	chr17:45400944-45400994	BJ	skin:	n/a
24	chr17:45401833-45401883	HIPEpiC	eye:	n/a
25	chr17:45400748-45400798	HMEC	breast:	n/a
26	chr17:45401397-45401447	HRE	kidney:	n/a
27	chr17:45398817-45398867	CMK	blood:	n/a
28	chr17:45401148-45401198	NHBE	bronchial:	n/a
29	chr17:45401148-45401198	SK-N-SH	brain:	n/a
30	chr17:45401833-45401883	HCM	heart:	n/a
31	chr17:45401150-45401200	SKMC	muscle:	n/a
32	chr17:45401397-45401447	ProgFib	skin:	n/a
33	chr17:45401150-45401200	CMK	blood:	n/a
34	chr17:45401148-45401198	H1-hESC	embryonic stem cell:	embryo
35	chr17:45400944-45400994	MCF10A-Er-Src	breast:	n/a
36	chr17:45401733-45401783	LNCaP	prostate:	n/a
37	chr17:45401156-45401206	NHDF-neo	bronchial:	n/a
38	chr17:45400944-45400994	SAEC	small airway:	n/a
39	chr17:45401156-45401206	PANC-1	pancreas:	n/a
40	chr17:45401312-45401362	T-47D	breast:	n/a
41	chr17:45398817-45398867	GM12878	blood:	n/a
42	chr17:45401733-45401783	H1-hESC	embryonic stem cell:	embryo
43	chr17:45401150-45401200	IMR90	lung:	fetal
44	chr17:45400944-45400994	LNCaP	prostate:	n/a
45	chr17:45401312-45401362	SAEC	small airway:	n/a
46	chr17:45401148-45401198	HCT-116	colon:	n/a
47	chr17:45400944-45400994	AG10803	skin:	n/a
48	chr17:45398817-45398867	AG04450	lung:	fetal
49	chr17:45401397-45401447	HUVEC	blood vessel:	n/a
50	chr17:45400944-45400994	GM06990	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45264537..45266755-chr17:45396250..45398578,2	K562	blood:
2	chr17:45401064..45401883-chr20:30194485..30195180,2	Hela-S3	cervix:
3	chr17:45334238..45336850-chr17:45399681..45401766,2	K562	blood:
4	chr17:45346995..45349121-chr17:45397201..45400062,2	K562	blood:
5	chr17:45143352..45146051-chr17:45399301..45401762,3	K562	blood:
6	chr17:45399600..45403116-chr17:45404916..45409576,7	K562	blood:
7	chr17:45400044..45402588-chr17:45412958..45415067,2	MCF-7	breast:
8	chr17:45400573..45401426-chr9:116172200..116173194,2	Hela-S3	cervix:
9	chr17:45382065..45383991-chr17:45399117..45400961,2	K562	blood:
10	chr17:45264972..45267284-chr17:45403808..45405423,2	K562	blood:
11	chr17:45399600..45403116-chr17:45404916..45409576,7	K562	blood:
12	chr17:45406105..45410563-chr17:45415777..45418447,5	K562	blood:
13	chr17:45402601..45404438-chr17:45415492..45418430,2	K562	blood:
14	chr17:45399518..45402231-chr17:45418878..45421613,2	K562	blood:
15	chr17:45414278..45416918-chr17:45428922..45430523,2	K562	blood:
16	chr17:45302015..45304122-chr17:45394820..45397251,2	K562	blood:
17	chr17:45422002..45424871-chr17:45443232..45445313,2	MCF-7	breast:
18	chr17:45234199..45236994-chr17:45399820..45401734,2	MCF-7	breast:
19	chr17:45143352..45144907-chr17:45399301..45401186,2	K562	blood:
20	chr17:45417186..45419360-chr17:45433473..45435862,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYL4-4	chr17:45401820-45401889	NONHSAT054299
2	lnc-MYL4-4	chr17:45407217-45407271	NONHSAT054301
3	lnc-MYL4-4	chr17:45412562-45412722	NONHSAT054301
4	lnc-AC040934.1-2	chr17:45400564-45401497	ENSG00000247683
5	lnc-MYL4-4	chr17:45418757-45418817	NONHSAT054300
6	lnc-MYL4-4	chr17:45417222-45417454	NONHSAT054301
7	lnc-MYL4-4	chr17:45419287-45419393	NONHSAT054299
8	lnc-AC040934.1-2	chr17:45400724-45401156	NONHSAT054295
9	lnc-MYL4-4	chr17:45405635-45405749	NONHSAT054299
10	lnc-MYL4-4	chr17:45405414-45405749	NONHSAT054300
11	lnc-MYL4-4	chr17:45401327-45401440	NONHSAT054299
12	lnc-AC040934.1-2	chr17:45400903-45400979	ENSG00000263293.1
13	lnc-AC040934.1-2	chr17:45401616-45402367	ENSG00000247683
14	lnc-MYL4-4	chr17:45412562-45412722	NONHSAT054300
15	lnc-MYL4-4	chr17:45403592-45403753	NONHSAT054299
16	lnc-AC040934.1-2	chr17:45402274-45403111	NONHSAT054297

No data

Variant related genes	Relation type
ENSG00000263293	TF binding region
EFCAB13	TF binding region
ENSG00000263293	CpG island
EFCAB13	CpG island
ENSG00000262879	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000263293	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000148229	chromatin interactions
ENSG00000238419	chromatin interactions
ENSG00000004897	chromatin interactions
ENSG00000157653	chromatin interactions
GLI2	miRNA target sites

Extended variants
information (count: 1052 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1052 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73322397	chr17:45397047-45397048	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148216983	chr17:45397091-45397092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs544157418	chr17:45397105-45397106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs547721103	chr17:45397113-45397114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72825633	chr17:45397138-45397139	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73322398	chr17:45397146-45397147	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542447350	chr17:45397221-45397222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191827507	chr17:45397225-45397226	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114411816	chr17:45397243-45397244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568843804	chr17:45397272-45397273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184065434	chr17:45397290-45397291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558066251	chr17:45397321-45397322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577898910	chr17:45397328-45397329	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs148130267	chr17:45397350-45397351	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562539787	chr17:45397434-45397435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2873530	chr17:45397440-45397441	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs573788596	chr17:45397441-45397442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566764774	chr17:45397464-45397465	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533986002	chr17:45397472-45397473	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542678206	chr17:45397473-45397474	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188272181	chr17:45397478-45397479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs531397095	chr17:45397481-45397482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200019680	chr17:45397482-45397483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201056790	chr17:45397494-45397495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4968256	chr17:45397513-45397514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs72825634	chr17:45397518-45397519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373644265	chr17:45397649-45397650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145231749	chr17:45397650-45397651	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576006122	chr17:45397670-45397671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545042609	chr17:45397748-45397749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs73322400	chr17:45397754-45397755	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs111395052	chr17:45397873-45397874	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191947587	chr17:45397895-45397896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561293890	chr17:45397912-45397913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs182484215	chr17:45397934-45397935	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549078848	chr17:45397942-45397943	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368070158	chr17:45397943-45397944	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537828932	chr17:45398003-45398004	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs551441028	chr17:45398016-45398017	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113229779	chr17:45398018-45398019	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538305336	chr17:45398023-45398024	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs367653435	chr17:45398025-45398026	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533802963	chr17:45398028-45398029	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564738005	chr17:45398031-45398032	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs34589418	chr17:45398085-45398086	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs187137560	chr17:45398086-45398087	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112547868	chr17:45398091-45398092	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs142988628	chr17:45398123-45398124	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs150837048	chr17:45398124-45398125	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138075275	chr17:45398129-45398130	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	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
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Angelman syndrome	16183798	CNVD

Chromatin state (count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45357200-45398000	Weak transcription	Psoas Muscle	Psoas
2	chr17:45382800-45400800	Weak transcription	Lung	lung
3	chr17:45388400-45398000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr17:45388800-45400800	Weak transcription	Aorta	Aorta
5	chr17:45391200-45400800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr17:45393000-45398000	Weak transcription	Fetal Muscle Leg	muscle
7	chr17:45393000-45398200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr17:45393000-45400600	Weak transcription	Brain Angular Gyrus	brain
9	chr17:45393200-45400600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr17:45393200-45400600	Weak transcription	Colon Smooth Muscle	Colon
11	chr17:45393200-45400600	Weak transcription	Fetal Heart	heart
12	chr17:45393200-45400600	Weak transcription	Pancreas	Pancrea
13	chr17:45393600-45398000	Weak transcription	Fetal Stomach	stomach
14	chr17:45393600-45398400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr17:45394200-45400600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr17:45394200-45400600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr17:45394400-45400000	Weak transcription	HUVEC	blood vessel
18	chr17:45394600-45398400	Weak transcription	Adipose Nuclei	Adipose
19	chr17:45394800-45399800	Weak transcription	Hela-S3	cervix
20	chr17:45394800-45400200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr17:45394800-45400400	Weak transcription	NH-A	brain
22	chr17:45394800-45400600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr17:45394800-45400600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr17:45395000-45400000	Weak transcription	NHDF-Ad	bronchial
25	chr17:45395200-45400600	Weak transcription	Fetal Intestine Small	intestine
26	chr17:45395200-45400600	Weak transcription	Osteobl	bone
27	chr17:45396200-45398400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr17:45396200-45400600	Weak transcription	HSMMtube	muscle
29	chr17:45398000-45398400	ZNF genes & repeats	Fetal Stomach	stomach
30	chr17:45398000-45398800	ZNF genes & repeats	Fetal Muscle Leg	muscle
31	chr17:45398200-45399000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr17:45398400-45398600	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr17:45398400-45398800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr17:45398400-45398800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr17:45398400-45399000	ZNF genes & repeats	A549	lung
36	chr17:45398400-45400600	Weak transcription	Fetal Stomach	stomach
37	chr17:45398600-45400400	Weak transcription	Adipose Nuclei	Adipose
38	chr17:45398800-45400000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr17:45398800-45400600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr17:45398800-45400600	Weak transcription	Fetal Muscle Leg	muscle
41	chr17:45399000-45400200	Weak transcription	A549	lung
42	chr17:45399200-45399400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr17:45399200-45400600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr17:45399400-45400800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr17:45399800-45400200	Enhancers	HepG2	liver
46	chr17:45399800-45400400	Weak transcription	Dnd41	blood
47	chr17:45399800-45400600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr17:45399800-45400600	Enhancers	Hela-S3	cervix
49	chr17:45400000-45400200	Enhancers	HUVEC	blood vessel
50	chr17:45400000-45400200	Enhancers	K562	blood

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