Variant report

Variant	nsv574991
Chromosome Location	chr17:37770005-37831035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3820)
CpG islands
(count:5009)
Chromatin interactive
region (count:187)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3820 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:37820347-37820555	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:37790617-37791026	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:37791605-37791720	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:37786407-37786499	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:37806350-37806698	K562	blood:	n/a	n/a
6	ARID3A	chr17:37828450-37828481	K562	blood:	n/a	n/a
7	ARID3A	chr17:37793415-37793463	K562	blood:	n/a	n/a
8	ARID3A	chr17:37790662-37791006	K562	blood:	n/a	n/a
9	ARID3A	chr17:37778226-37778525	HepG2	liver:	n/a	n/a
10	ARID3A	chr17:37824818-37825041	K562	blood:	n/a	n/a
11	ARID3A	chr17:37810135-37810419	HepG2	liver:	n/a	n/a
12	ARID3A	chr17:37774705-37774830	HepG2	liver:	n/a	chr17:37774718-37774734 chr17:37774719-37774735
13	ATF1	chr17:37805308-37805692	K562	blood:	n/a	n/a
14	ATF1	chr17:37798121-37798336	K562	blood:	n/a	n/a
15	ATF1	chr17:37806264-37806780	K562	blood:	n/a	n/a
16	ATF2	chr17:37778264-37778711	GM12878	blood:	n/a	n/a
17	ATF2	chr17:37828335-37828775	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr17:37793324-37793698	GM12878	blood:	n/a	n/a
19	ATF2	chr17:37801313-37801666	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr17:37778126-37778563	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr17:37806330-37806720	K562	blood:	n/a	n/a
22	ATF3	chr17:37823207-37823417	K562	blood:	n/a	chr17:37823321-37823335
23	ATF3	chr17:37778237-37778557	K562	blood:	n/a	n/a
24	ATF3	chr17:37778158-37778583	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr17:37779702-37779946	K562	blood:	n/a	n/a
26	ATF3	chr17:37778153-37778488	HepG2	liver:	n/a	n/a
27	ATF3	chr17:37806221-37806740	K562	blood:	n/a	n/a
28	ATF3	chr17:37778161-37778758	GM12878	blood:	n/a	n/a
29	ATF3	chr17:37778719-37778910	K562	blood:	n/a	chr17:37778838-37778851
30	ATF3	chr17:37774014-37774192	K562	blood:	n/a	chr17:37774141-37774150 chr17:37774124-37774133
31	ATF3	chr17:37823113-37823503	K562	blood:	n/a	chr17:37823321-37823335
32	ATF3	chr17:37778210-37778523	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr17:37778198-37778494	K562	blood:	n/a	n/a
34	BACH1	chr17:37790962-37790985	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr17:37824819-37825041	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr17:37782605-37782894	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr17:37794403-37794412	K562	blood:	n/a	n/a
38	BACH1	chr17:37820027-37820211	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr17:37806437-37806764	K562	blood:	n/a	n/a
40	BACH1	chr17:37796178-37796185	K562	blood:	n/a	n/a
41	BACH1	chr17:37779646-37780011	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr17:37779732-37779989	K562	blood:	n/a	n/a
43	BATF	chr17:37778601-37778905	GM12878	blood:	n/a	chr17:37778742-37778753
44	BATF	chr17:37778574-37778862	GM12878	blood:	n/a	chr17:37778742-37778753
45	BATF	chr17:37793417-37793746	GM12878	blood:	n/a	n/a
46	BCL3	chr17:37819921-37821125	A549	lung:	n/a	n/a
47	BCL3	chr17:37821874-37822887	A549	lung:	n/a	chr17:37821930-37821938
48	BCL3	chr17:37790526-37791199	A549	lung:	n/a	n/a
49	BCL3	chr17:37828145-37828847	A549	lung:	n/a	n/a
50	BCL3	chr17:37806347-37806601	GM12878	blood:	n/a	n/a

(count:5009 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37782685-37782735	HRCEpiC	kidney:	n/a
2	chr17:37793307-37793357	HRCEpiC	kidney:	n/a
3	chr17:37824526-37824576	SK-N-SH	brain:	n/a
4	chr17:37821478-37821528	AG04450	lung:	fetal
5	chr17:37779789-37779839	SK-N-SH	brain:	n/a
6	chr17:37774934-37774984	U87	brain:	n/a
7	chr17:37793460-37793510	HAEpiC	amniotic membrane:	n/a
8	chr17:37782685-37782735	HRCEpiC	kidney:	n/a
9	chr17:37793307-37793357	HRCEpiC	kidney:	n/a
10	chr17:37824526-37824576	SK-N-SH	brain:	n/a
11	chr17:37821478-37821528	AG04450	lung:	fetal
12	chr17:37779789-37779839	SK-N-SH	brain:	n/a
13	chr17:37774934-37774984	U87	brain:	n/a
14	chr17:37793460-37793510	HAEpiC	amniotic membrane:	n/a
15	chr17:37823631-37823681	HIPEpiC	eye:	n/a
16	chr17:37774893-37774943	HCF	heart:	n/a
17	chr17:37779789-37779839	BE2_C	brain:	n/a
18	chr17:37792770-37792820	H1-hESC	embryonic stem cell:	embryo
19	chr17:37793287-37793337	HPAEpiC	pulmonary alveolar:	n/a
20	chr17:37784024-37784074	GM19239	blood:	n/a
21	chr17:37821536-37821586	HCPEpiC	choroid plexus:	n/a
22	chr17:37783689-37783739	BE2_C	brain:	n/a
23	chr17:37793212-37793262	HRCEpiC	kidney:	n/a
24	chr17:37824238-37824288	ProgFib	skin:	n/a
25	chr17:37793287-37793337	SKMC	muscle:	n/a
26	chr17:37814104-37814154	U87	brain:	n/a
27	chr17:37783488-37783538	HNPCEpiC	eye:	n/a
28	chr17:37827057-37827107	HCT-116	colon:	n/a
29	chr17:37774457-37774507	SK-N-SH_RA	brain:	n/a
30	chr17:37773848-37773898	H1-hESC	embryonic stem cell:	embryo
31	chr17:37793295-37793345	H1-hESC	embryonic stem cell:	embryo
32	chr17:37774934-37774984	LNCaP	prostate:	n/a
33	chr17:37793326-37793376	GM12892	blood:	n/a
34	chr17:37820361-37820411	BJ	skin:	n/a
35	chr17:37809838-37809888	SK-N-SH_RA	brain:	n/a
36	chr17:37774058-37774108	Hepatocyte	liver:	n/a
37	chr17:37802070-37802120	PrEC	prostate:	n/a
38	chr17:37794080-37794130	GM12891	blood:	n/a
39	chr17:37783488-37783538	BJ	skin:	n/a
40	chr17:37813369-37813419	HMEC	breast:	n/a
41	chr17:37820361-37820411	SK-N-SH_RA	brain:	n/a
42	chr17:37820361-37820411	H1-hESC	embryonic stem cell:	embryo
43	chr17:37814104-37814154	HIPEpiC	eye:	n/a
44	chr17:37820361-37820411	SK-N-MC	brain:	n/a
45	chr17:37793215-37793265	T-47D	breast:	n/a
46	chr17:37808339-37808389	U87	brain:	n/a
47	chr17:37794080-37794130	NHDF-neo	bronchial:	n/a
48	chr17:37821478-37821528	NHDF-neo	bronchial:	n/a
49	chr17:37814104-37814154	Hepatocyte	liver:	n/a
50	chr17:37794056-37794106	HEK293	kidney:	embryo

(count:187 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr17:37790210..37790930-chr17:37828221..37828992,2	MCF-7	breast:
2	chr17:37801673..37804556-chr17:37823494..37825971,2	MCF-7	breast:
3	chr17:37792606..37795177-chr17:37810755..37812742,3	MCF-7	breast:
4	chr17:37777847..37779169-chr17:37827001..37829318,18	K562	blood:
5	chr17:37776904..37777847-chr17:37827993..37828988,2	MCF-7	breast:
6	chr17:37796473..37799426-chr17:37809354..37812211,3	MCF-7	breast:
7	chr17:37777435..37780800-chr17:37803920..37808668,4	K562	blood:
8	chr17:37793922..37796197-chr17:37796263..37800246,4	MCF-7	breast:
9	chr17:37776626..37780124-chr17:37818606..37821377,4	K562	blood:
10	chr17:37758356..37760181-chr17:37774194..37775834,2	MCF-7	breast:
11	chr17:37793727..37796192-chr17:37829753..37832726,2	MCF-7	breast:
12	chr17:37829376..37831831-chr17:37883917..37885766,2	K562	blood:
13	chr17:37769208..37773729-chr17:37777189..37781252,6	K562	blood:
14	chr17:37792539..37793245-chr19:13263539..13264259,2	Hela-S3	cervix:
15	chr17:37789315..37792571-chr17:37910228..37913282,4	K562	blood:
16	chr17:37793922..37796197-chr17:37796263..37800246,4	MCF-7	breast:
17	chr17:37763061..37765644-chr17:37767093..37771195,3	K562	blood:
18	chr17:37782428..37784390-chr17:37785390..37788111,2	K562	blood:
19	chr17:37771753..37773281-chr17:37910069..37912599,2	K562	blood:
20	chr17:37769144..37771005-chr17:37773634..37775729,2	MCF-7	breast:
21	chr17:37789952..37790826-chr17:37809840..37810573,2	K562	blood:
22	chr17:37829760..37835390-chr17:37853762..37858979,8	MCF-7	breast:
23	chr17:37778015..37778817-chr17:38136400..38137216,2	MCF-7	breast:
24	chr17:37810058..37810709-chr17:37910120..37910665,2	K562	blood:
25	chr17:37775807..37781695-chr17:37822673..37828377,10	K562	blood:
26	chr17:37779838..37780411-chr17:37790377..37790904,2	K562	blood:
27	chr17:37789952..37790826-chr17:37809840..37810573,2	K562	blood:
28	chr17:37791520..37796368-chr17:37822308..37826994,8	K562	blood:
29	chr17:37777961..37778768-chr17:37910171..37911038,7	MCF-7	breast:
30	chr17:37772115..37773801-chr17:37825160..37827936,2	K562	blood:
31	chr17:37793727..37796192-chr17:37829753..37832726,2	MCF-7	breast:
32	chr17:37827266..37833048-chr17:37842420..37846685,6	MCF-7	breast:
33	chr17:37822303..37824126-chr17:37856298..37859081,2	K562	blood:
34	chr17:37777123..37780362-chr17:37909816..37911514,36	K562	blood:
35	chr17:37806444..37808313-chr17:37808562..37810244,2	K562	blood:
36	chr17:37778774..37780358-chr17:37893179..37896235,3	K562	blood:
37	chr17:37779838..37780411-chr17:37790377..37790904,2	K562	blood:
38	chr17:37779307..37779994-chr17:37809757..37810305,2	K562	blood:
39	chr17:37820269..37822636-chr17:37824547..37827418,2	MCF-7	breast:
40	chr17:37777888..37778610-chr17:37809336..37810309,3	MCF-7	breast:
41	chr17:37792465..37794385-chr17:37800394..37802053,2	MCF-7	breast:
42	chr17:37777847..37779169-chr17:37827001..37829318,18	K562	blood:
43	chr17:37791520..37796368-chr17:37822308..37826994,8	K562	blood:
44	chr17:37824914..37826916-chr17:37844097..37845761,2	K562	blood:
45	chr17:37780595..37782911-chr17:37786267..37787886,2	MCF-7	breast:
46	chr17:37824143..37826951-chr17:37830490..37832127,2	MCF-7	breast:
47	chr17:37777901..37778833-chr17:37828093..37829149,5	MCF-7	breast:
48	chr17:37821804..37826261-chr17:37885454..37888153,4	K562	blood:
49	chr17:37793295..37796255-chr17:37843602..37845450,3	K562	blood:
50	chr17:37773997..37776613-chr17:37779619..37781489,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC087491.2.1-1	chr17:37775866-37775914	ENSG00000214546.3
2	lnc-NEUROD2-3	chr17:37771818-37772115	NONHSAT053461
3	lnc-AC087491.2.1-1	chr17:37776006-37776081	ENSG00000214546.3
4	lnc-AC087491.2.1-1	chr17:37778097-37778149	ENSG00000214546.3
5	lnc-NEUROD2-2	chr17:37769986-37770227	NONHSAT053460
6	lnc-AC087491.2.1-1	chr17:37778329-37778766	ENSG00000214546.3

No data

Variant related genes	Relation type
STARD3	TF binding region
TCAP	TF binding region
PNMT	TF binding region
ENSG00000214546	TF binding region
NEUROD2	TF binding region
PPP1R1B	TF binding region
STARD3	CpG island
TCAP	CpG island
PNMT	CpG island
ENSG00000214546	CpG island
NEUROD2	CpG island
PPP1R1B	CpG island
ENSG00000214546	chromatin interactions
ENSG00000067191	chromatin interactions
ENSG00000131771	chromatin interactions
ENSG00000161395	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000141744	chromatin interactions
ENSG00000141741	chromatin interactions
ENSG00000145494	chromatin interactions
ENSG00000173991	chromatin interactions
ENSG00000131748	chromatin interactions
ENSG00000141738	chromatin interactions
ENSG00000171532	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000108344	chromatin interactions
ENSG00000141736	chromatin interactions
ENSG00000085788	chromatin interactions
ENSG00000167258	chromatin interactions

Extended variants
information (count: 2523 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:2523 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12453682	chr17:37770005-37770006	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558887587	chr17:37770006-37770007	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs574650603	chr17:37770011-37770012	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs577161660	chr17:37770023-37770024	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs574643041	chr17:37770094-37770095	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs12946926	chr17:37770102-37770103	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs78256851	chr17:37770134-37770135	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs553298265	chr17:37770156-37770157	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs540139066	chr17:37770157-37770158	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs138550004	chr17:37770216-37770217	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs78713857	chr17:37770226-37770227	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs186932105	chr17:37770227-37770228	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs530998373	chr17:37770270-37770271	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs191741131	chr17:37770287-37770288	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184790025	chr17:37770292-37770293	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184329828	chr17:37770299-37770300	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144049636	chr17:37770309-37770310	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs72343132	chr17:37770329-37770330	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200739504	chr17:37770330-37770331	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs60658256	chr17:37770341-37770342	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs565648516	chr17:37770347-37770348	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs55942935	chr17:37770356-37770357	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs548297934	chr17:37770365-37770366	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs569911645	chr17:37770376-37770377	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537244620	chr17:37770385-37770386	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545958519	chr17:37770411-37770412	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs139210213	chr17:37770422-37770423	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs534887237	chr17:37770428-37770429	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs9915323	chr17:37770481-37770482	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs574757670	chr17:37770485-37770486	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs188875421	chr17:37770555-37770556	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs149280289	chr17:37770572-37770573	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs193160804	chr17:37770578-37770579	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs555278696	chr17:37770591-37770592	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs564311769	chr17:37770618-37770619	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs528814706	chr17:37770624-37770625	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs75349857	chr17:37770669-37770670	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs74451218	chr17:37770687-37770688	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs529692099	chr17:37770716-37770717	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs144483570	chr17:37770839-37770840	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs563378713	chr17:37770860-37770861	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs79761132	chr17:37770878-37770879	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs185419770	chr17:37770900-37770901	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs377525345	chr17:37770914-37770915	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534644586	chr17:37770930-37770931	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs9891817	chr17:37770987-37770988	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568408551	chr17:37770995-37770996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs535467611	chr17:37771007-37771008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556903190	chr17:37771034-37771035	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs113488714	chr17:37771038-37771039	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
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
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	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
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	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
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Urothelial carcinoma	21177765	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Disease	22962312	CNVD
Mental retardation	20152051	CNVD
Mental retardation	19951919	CNVD
Mental retardation	22817714	CNVD
Mental retardation	21956041	CNVD
Brain cancer	19584924	CNVD
Glioblastoma multiforme	22286061	CNVD
Schizophrenia	21399695	CNVD
Non-syndromic sensorineural hearing loss	19165922	CNVD
Prader-willi syndrome	20588305	CNVD
17q21.31 microdeletion syndrome	16940994	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
17q21.31 microdeletion syndrome	22283845	CNVD
Intellectual disability	22194194	CNVD
17q21.31 microdeletion syndrome	20606400	CNVD
17q21.31 microdeletion syndrome	18628315	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:4194 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37763600-37773600	Weak transcription	Gastric	stomach
2	chr17:37765600-37770400	Enhancers	Fetal Brain Male	brain
3	chr17:37767800-37770200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr17:37767800-37771800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr17:37768000-37773600	Weak transcription	Right Atrium	heart
6	chr17:37769200-37771400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr17:37769800-37770800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr17:37769800-37771800	Weak transcription	Fetal Brain Female	brain
9	chr17:37770000-37770200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
10	chr17:37770000-37770200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
11	chr17:37770000-37770200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr17:37770200-37771800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr17:37770400-37771800	Weak transcription	Fetal Brain Male	brain
14	chr17:37771800-37772000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr17:37771800-37772000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr17:37771800-37772000	Enhancers	Hela-S3	cervix
17	chr17:37771800-37772200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr17:37771800-37772400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr17:37771800-37772400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr17:37771800-37772400	Enhancers	Fetal Brain Female	brain
21	chr17:37771800-37776200	Enhancers	Fetal Brain Male	brain
22	chr17:37772000-37772200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr17:37772000-37772200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr17:37772000-37773200	Weak transcription	Hela-S3	cervix
25	chr17:37772400-37772800	Weak transcription	Fetal Brain Female	brain
26	chr17:37772800-37773400	Enhancers	Fetal Brain Female	brain
27	chr17:37773000-37773600	Bivalent Enhancer	Brain Germinal Matrix	brain
28	chr17:37773200-37773400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
29	chr17:37773200-37773400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr17:37773200-37773400	Enhancers	Hela-S3	cervix
31	chr17:37773200-37773600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
32	chr17:37773200-37773600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
33	chr17:37773200-37773600	Enhancers	Spleen	Spleen
34	chr17:37773200-37773800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr17:37773400-37773600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
36	chr17:37773400-37773600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr17:37773400-37773600	Bivalent Enhancer	Primary T cells from cord blood	blood
38	chr17:37773400-37773600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr17:37773400-37773600	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr17:37773400-37773600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
41	chr17:37773400-37773600	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr17:37773400-37773600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
43	chr17:37773400-37773600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr17:37773400-37773600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
45	chr17:37773400-37773600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr17:37773400-37773600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr17:37773400-37773600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr17:37773400-37773600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr17:37773400-37773600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
50	chr17:37773400-37773600	Enhancers	Adipose Nuclei	Adipose

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