Variant report

Variant	nsv997471
Chromosome Location	chr4:47489412-47895223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4176)
CpG islands
(count:2077)
Chromatin interactive
region (count:115)
LncRNA
region (count:13)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:4176 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:47735208-47736035	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:47688376-47688645	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:47838667-47838904	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:47670805-47671245	K562	blood:	n/a	chr4:47671147-47671163
5	ARID3A	chr4:47788705-47789130	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:47566310-47566738	K562	blood:	n/a	n/a
7	ARID3A	chr4:47881529-47882008	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:47665081-47665333	K562	blood:	n/a	n/a
9	ARID3A	chr4:47884399-47884605	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:47566343-47566703	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:47751721-47752471	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:47717974-47718536	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:47563328-47563680	HepG2	liver:	n/a	n/a
14	ARID3A	chr4:47707563-47707945	HepG2	liver:	n/a	n/a
15	ARID3A	chr4:47878677-47879238	HepG2	liver:	n/a	n/a
16	ATF1	chr4:47567261-47567600	K562	blood:	n/a	n/a
17	ATF2	chr4:47533555-47534185	GM12878	blood:	n/a	n/a
18	ATF2	chr4:47841134-47841615	GM12878	blood:	n/a	n/a
19	ATF2	chr4:47512313-47512968	GM12878	blood:	n/a	n/a
20	ATF2	chr4:47521386-47522151	GM12878	blood:	n/a	n/a
21	ATF2	chr4:47533593-47534069	GM12878	blood:	n/a	n/a
22	ATF2	chr4:47512406-47513246	GM12878	blood:	n/a	n/a
23	ATF2	chr4:47788986-47789548	GM12878	blood:	n/a	n/a
24	ATF2	chr4:47521233-47522006	GM12878	blood:	n/a	n/a
25	ATF2	chr4:47500864-47501370	GM12878	blood:	n/a	n/a
26	ATF2	chr4:47495837-47496260	GM12878	blood:	n/a	n/a
27	ATF2	chr4:47495167-47495817	GM12878	blood:	n/a	n/a
28	BACH1	chr4:47588673-47588680	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:47838507-47839363	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:47578860-47578906	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr4:47567278-47567639	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr4:47688351-47688734	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr4:47567297-47567657	K562	blood:	n/a	n/a
34	BATF	chr4:47512447-47512805	GM12878	blood:	n/a	n/a
35	BATF	chr4:47495830-47496135	GM12878	blood:	n/a	n/a
36	BATF	chr4:47567258-47567627	GM12878	blood:	n/a	chr4:47567444-47567455
37	BATF	chr4:47732634-47732828	GM12878	blood:	n/a	n/a
38	BATF	chr4:47692635-47692950	GM12878	blood:	n/a	n/a
39	BATF	chr4:47619700-47619940	GM12878	blood:	n/a	n/a
40	BATF	chr4:47521527-47521876	GM12878	blood:	n/a	chr4:47521702-47521713
41	BATF	chr4:47500935-47501204	GM12878	blood:	n/a	chr4:47500950-47500961
42	BATF	chr4:47500843-47501151	GM12878	blood:	n/a	chr4:47500950-47500961
43	BATF	chr4:47512488-47512846	GM12878	blood:	n/a	n/a
44	BATF	chr4:47876259-47876454	GM12878	blood:	n/a	n/a
45	BATF	chr4:47619695-47619918	GM12878	blood:	n/a	n/a
46	BATF	chr4:47841192-47841573	GM12878	blood:	n/a	n/a
47	BATF	chr4:47567227-47567642	GM12878	blood:	n/a	chr4:47567444-47567455
48	BATF	chr4:47732587-47732811	GM12878	blood:	n/a	n/a
49	BATF	chr4:47521506-47521847	GM12878	blood:	n/a	chr4:47521702-47521713
50	BCL11A	chr4:47533703-47533967	GM12878	blood:	n/a	n/a

(count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:47840011-47840061	U87	brain:	n/a
2	chr4:47710820-47710870	HRCEpiC	kidney:	n/a
3	chr4:47841314-47841364	AoSMC	blood vessel:	n/a
4	chr4:47840011-47840061	U87	brain:	n/a
5	chr4:47710820-47710870	HRCEpiC	kidney:	n/a
6	chr4:47841314-47841364	AoSMC	blood vessel:	n/a
7	chr4:47706142-47706192	HRE	kidney:	n/a
8	chr4:47839283-47839333	NH-A	brain:	n/a
9	chr4:47843915-47843965	HUVEC	blood vessel:	n/a
10	chr4:47710147-47710197	HRE	kidney:	n/a
11	chr4:47841314-47841364	AG09319	gingival:	n/a
12	chr4:47839218-47839268	U87	brain:	n/a
13	chr4:47708509-47708559	AG04450	lung:	fetal
14	chr4:47512538-47512588	AG04450	lung:	fetal
15	chr4:47837775-47837825	Jurkat	blood:	n/a
16	chr4:47839876-47839926	Jurkat	blood:	n/a
17	chr4:47597617-47597667	AG09319	gingival:	n/a
18	chr4:47865430-47865480	ovcar-3	ovarian:	n/a
19	chr4:47513375-47513425	Hela-S3	cervix:	n/a
20	chr4:47839218-47839268	GM12892	blood:	n/a
21	chr4:47839218-47839268	NT2-D1	testis:	n/a
22	chr4:47533905-47533955	SK-N-MC	brain:	n/a
23	chr4:47513375-47513425	GM12891	blood:	n/a
24	chr4:47806451-47806501	HRE	kidney:	n/a
25	chr4:47840136-47840186	RPTEC	kidney:	n/a
26	chr4:47841314-47841364	SAEC	small airway:	n/a
27	chr4:47845589-47845639	AoSMC	blood vessel:	n/a
28	chr4:47710820-47710870	HepG2	liver:	n/a
29	chr4:47840136-47840186	LNCaP	prostate:	n/a
30	chr4:47512538-47512588	HCT-116	colon:	n/a
31	chr4:47719380-47719430	GM12878	blood:	n/a
32	chr4:47840162-47840212	HRE	kidney:	n/a
33	chr4:47838169-47838219	ovcar-3	ovarian:	n/a
34	chr4:47719380-47719430	RPTEC	kidney:	n/a
35	chr4:47841314-47841364	RPTEC	kidney:	n/a
36	chr4:47512538-47512588	RPTEC	kidney:	n/a
37	chr4:47707064-47707114	HRPEpiC	eye:	n/a
38	chr4:47885045-47885095	HCM	heart:	n/a
39	chr4:47838616-47838666	HEK293	kidney:	embryo
40	chr4:47708509-47708559	Caco-2	colon:	n/a
41	chr4:47719380-47719430	HNPCEpiC	eye:	n/a
42	chr4:47512538-47512588	CMK	blood:	n/a
43	chr4:47840011-47840061	HUVEC	blood vessel:	n/a
44	chr4:47719380-47719430	K562	blood:	n/a
45	chr4:47597617-47597667	HUVEC	blood vessel:	n/a
46	chr4:47710147-47710197	SK-N-SH	brain:	n/a
47	chr4:47838670-47838720	HCM	heart:	n/a
48	chr4:47865430-47865480	HMEC	breast:	n/a
49	chr4:47706142-47706192	AG04450	lung:	fetal
50	chr4:47845589-47845639	HRPEpiC	eye:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:47706456..47708112-chr4:47838146..47839411,13	MCF-7	breast:
2	chr4:47792582..47794260-chr4:47794493..47796071,2	K562	blood:
3	chr4:47688611..47689443-chr4:47936530..47937494,2	K562	blood:
4	chr4:47877395..47879656-chr4:47884028..47886105,2	K562	blood:
5	chr4:47670607..47671485-chr4:47706644..47707642,3	MCF-7	breast:
6	chr4:47500151..47502308-chr4:47567247..47568908,2	MCF-7	breast:
7	chr4:47551527..47553990-chr4:47565795..47567988,3	K562	blood:
8	chr4:47565772..47567712-chr4:47570354..47573060,2	K562	blood:
9	chr4:47536442..47538388-chr4:47538970..47540735,2	K562	blood:
10	chr4:47688063..47688915-chr4:47838342..47839484,4	MCF-7	breast:
11	chr4:47844982..47848045-chr4:47848832..47852694,3	K562	blood:
12	chr4:47555618..47557283-chr4:47565873..47568060,2	K562	blood:
13	chr4:47749490..47752397-chr4:47755183..47756959,2	K562	blood:
14	chr4:47894034..47895961-chr4:47915600..47918104,2	K562	blood:
15	chr4:47837985..47840233-chr4:47840589..47843103,2	MCF-7	breast:
16	chr4:47688906..47691612-chr4:47692853..47694990,2	K562	blood:
17	chr4:47876934..47878897-chr4:47913738..47916807,3	MCF-7	breast:
18	chr4:47648571..47651518-chr4:47651849..47655335,3	K562	blood:
19	chr4:47857858..47861058-chr4:47906882..47908675,3	MCF-7	breast:
20	chr4:47893328..47896289-chr4:47914943..47917180,2	MCF-7	breast:
21	chr4:47562873..47564467-chr4:47565898..47568483,2	K562	blood:
22	chr4:47494690..47496480-chr4:47498763..47501727,2	K562	blood:
23	chr4:47648571..47650880-chr4:47653230..47655335,2	K562	blood:
24	chr4:47688307..47688945-chr4:47841076..47841947,3	MCF-7	breast:
25	chr4:47856515..47858025-chr4:47868614..47870377,2	K562	blood:
26	chr4:47533452..47535756-chr4:47565106..47567780,2	K562	blood:
27	chr4:47582229..47585198-chr4:47587871..47590442,2	K562	blood:
28	chr4:47851196..47853833-chr4:47870828..47872465,2	K562	blood:
29	chr4:47888142..47889697-chr4:47892947..47895362,2	K562	blood:
30	chr4:47551527..47553990-chr4:47565795..47567988,3	K562	blood:
31	chr4:47792582..47794260-chr4:47794493..47796071,2	K562	blood:
32	chr4:47707683..47708302-chr4:47841300..47841809,2	MCF-7	breast:
33	chr4:47856515..47858025-chr4:47868614..47870377,2	K562	blood:
34	chr1:36983678..36984348-chr4:47541449..47542413,2	MCF-7	breast:
35	chr4:47686925..47689964-chr4:47690624..47694621,3	K562	blood:
36	chr4:47691917..47693928-chr4:47696448..47699124,2	MCF-7	breast:
37	chr4:47851196..47853833-chr4:47870828..47872465,2	K562	blood:
38	chr4:47891396..47894348-chr4:47898612..47901449,2	MCF-7	breast:
39	chr4:47706419..47708274-chr4:47838366..47839313,9	MCF-7	breast:
40	chr4:47880953..47884485-chr4:47884558..47887475,3	K562	blood:
41	chr4:47881002..47883818-chr4:47884414..47887354,2	K562	blood:
42	chr4:47559378..47560960-chr4:47564050..47565557,2	K562	blood:
43	chr4:47706458..47708260-chr4:47841005..47842113,10	MCF-7	breast:
44	chr4:47892858..47895013-chr4:47908321..47910117,3	K562	blood:
45	chr4:47706546..47707227-chr4:48088499..48089380,2	MCF-7	breast:
46	chr4:47567303..47570218-chr4:47578983..47580542,2	K562	blood:
47	chr4:47887965..47889707-chr4:47897054..47899233,2	MCF-7	breast:
48	chr4:47562873..47564467-chr4:47565898..47568483,2	K562	blood:
49	chr4:47551527..47553990-chr4:47565971..47567988,2	K562	blood:
50	chr4:47494690..47496480-chr4:47498763..47501727,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096264
2	lnc-NIPAL1-3	chr4:47877223-47877348	NONHSAT096264
3	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096265
4	lnc-NIPAL1-3	chr4:47877194-47877348	NONHSAT096265
5	lnc-NIPAL1-2	chr4:47841939-47846867	NONHSAT096267
6	lnc-CORIN-2	chr4:47562219-47562276	ENSG00000248254.1
7	lnc-NIPAL1-3	chr4:47884259-47884595	NONHSAT096265
8	lnc-COMMD8-1	chr4:47492984-47493488	NONHSAT096253
9	lnc-NIPAL1-3	chr4:47877194-47877348	NONHSAT096263
10	lnc-CORIN-2	chr4:47559659-47559928	ENSG00000248254.1
11	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096263
12	lnc-CORIN-1	chr4:47842139-47846356	ENSG00000259959.1
13	lnc-CORIN-2	chr4:47558748-47559020	ENSG00000248254.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-8053	chr4:47654696-47654719	MIMAT0030980

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATP10D	hsa-miR-192-5p	chr4:47548938-47548960

Variant related genes	Relation type
ENSG00000242431	TF binding region
ENSG00000259959	TF binding region
ATP10D	TF binding region
NFXL1	TF binding region
RN7SKP215	TF binding region
ENSG00000242262	TF binding region
ENSG00000248254	TF binding region
CORIN	TF binding region
ENSG00000242431	CpG island
ENSG00000259959	CpG island
ATP10D	CpG island
NFXL1	CpG island
RN7SKP215	CpG island
ENSG00000242262	CpG island
ENSG00000248254	CpG island
CORIN	CpG island
ENSG00000145246	chromatin interactions
ENSG00000163293	chromatin interactions
ENSG00000170448	chromatin interactions
ENSG00000242262	chromatin interactions
ENSG00000259959	chromatin interactions
ENSG00000242431	chromatin interactions
ENSG00000145244	chromatin interactions
ENSG00000248254	chromatin interactions
ENSG00000169019	chromatin interactions

Extended variants
information (count: 14589 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:14589 , 50 per page) page: 1 2 3 4 5 6 7 ... 292

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550759617	chr4:47489443-47489444	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562506914	chr4:47489461-47489462	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144984840	chr4:47489538-47489539	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187820369	chr4:47489583-47489584	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192746031	chr4:47489624-47489625	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs534744909	chr4:47489630-47489631	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs546543831	chr4:47489655-47489656	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs571618267	chr4:47489716-47489717	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs10010745	chr4:47489726-47489727	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557554040	chr4:47489727-47489728	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs183682131	chr4:47489734-47489735	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs189570578	chr4:47489750-47489751	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs554408191	chr4:47489775-47489776	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs192467052	chr4:47489808-47489809	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs540235601	chr4:47489810-47489811	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs113549977	chr4:47489833-47489834	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs10010904	chr4:47489845-47489846	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570888591	chr4:47489900-47489901	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs190218587	chr4:47489983-47489984	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs142243435	chr4:47490009-47490010	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529890631	chr4:47490011-47490012	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73138044	chr4:47490018-47490019	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs561052272	chr4:47490059-47490060	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181469285	chr4:47490083-47490084	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371813065	chr4:47490161-47490162	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7683828	chr4:47490173-47490174	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs6447555	chr4:47490186-47490187	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs186643738	chr4:47490189-47490190	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189469188	chr4:47490258-47490259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6447556	chr4:47490263-47490264	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs11737854	chr4:47490264-47490265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs145556395	chr4:47490278-47490279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566579052	chr4:47490386-47490387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533835541	chr4:47490387-47490388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6447557	chr4:47490417-47490418	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs148886721	chr4:47490514-47490515	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7679651	chr4:47490611-47490612	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368323646	chr4:47490625-47490626	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373039740	chr4:47490628-47490629	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs200612937	chr4:47490630-47490631	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs78539337	chr4:47490650-47490651	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139050989	chr4:47490652-47490653	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544189380	chr4:47490713-47490714	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7654625	chr4:47490759-47490760	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs536567835	chr4:47490774-47490775	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541671014	chr4:47490792-47490793	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559882358	chr4:47490827-47490828	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs180956901	chr4:47490840-47490841	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35077733	chr4:47490848-47490849	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185026618	chr4:47490861-47490862	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19214233	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Renal cell carcinoma	20952505	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:5395 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47486800-47489600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:47486800-47490000	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr4:47487000-47489600	Active TSS	HSMMtube	muscle
4	chr4:47487200-47489600	Active TSS	HMEC	breast
5	chr4:47487200-47489800	Active TSS	Placenta	Placenta
6	chr4:47488000-47492400	Weak transcription	Spleen	Spleen
7	chr4:47488000-47492600	Weak transcription	Gastric	stomach
8	chr4:47488000-47533800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:47488400-47489800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr4:47488600-47489600	Weak transcription	Fetal Heart	heart
11	chr4:47488600-47490800	Weak transcription	Left Ventricle	heart
12	chr4:47488600-47492400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr4:47488600-47495400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr4:47488600-47495600	Weak transcription	Small Intestine	intestine
15	chr4:47488600-47500000	Weak transcription	Fetal Brain Male	brain
16	chr4:47488600-47514400	Weak transcription	Lung	lung
17	chr4:47488600-47524600	Weak transcription	Fetal Intestine Small	intestine
18	chr4:47488800-47489600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:47488800-47489600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:47488800-47489600	Weak transcription	GM12878-XiMat	blood
21	chr4:47488800-47489800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:47488800-47489800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr4:47488800-47490000	Enhancers	Primary B cells from cord blood	blood
24	chr4:47488800-47490800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr4:47488800-47492400	Weak transcription	Liver	Liver
26	chr4:47488800-47492600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr4:47488800-47492600	Weak transcription	NHDF-Ad	bronchial
28	chr4:47488800-47493400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr4:47488800-47495200	Weak transcription	Fetal Kidney	kidney
30	chr4:47488800-47495400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr4:47488800-47495600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:47488800-47495600	Weak transcription	Fetal Lung	lung
33	chr4:47488800-47500800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr4:47488800-47502400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr4:47488800-47502600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr4:47488800-47559800	Weak transcription	Right Ventricle	heart
37	chr4:47489000-47489600	Weak transcription	Colon Smooth Muscle	Colon
38	chr4:47489000-47489600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr4:47489000-47489800	Weak transcription	NH-A	brain
40	chr4:47489000-47490000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr4:47489000-47490800	Weak transcription	Pancreas	Pancrea
42	chr4:47489000-47490800	Weak transcription	Psoas Muscle	Psoas
43	chr4:47489000-47491800	Weak transcription	Primary B cells from peripheral blood	blood
44	chr4:47489000-47491800	Weak transcription	HUVEC	blood vessel
45	chr4:47489000-47492400	Weak transcription	Aorta	Aorta
46	chr4:47489000-47492400	Weak transcription	Ovary	ovary
47	chr4:47489000-47495400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr4:47489000-47495400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:47489000-47495800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr4:47489000-47500600	Weak transcription	Primary monocytes fromperipheralblood	blood

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