Variant report

Variant	nsv537307
Chromosome Location	chr4:152202627-152498890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3167)
CpG islands
(count:2199)
Chromatin interactive
region (count:101)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3167 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:152245404-152246312	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:152246655-152247366	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:152339395-152339967	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:152330998-152331597	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:152283909-152284178	K562	blood:	n/a	n/a
6	ARID3A	chr4:152283872-152284217	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:152329870-152330087	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:152236357-152236672	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:152443367-152443482	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:152223581-152223988	HepG2	liver:	n/a	n/a
11	ATF2	chr4:152328761-152329347	GM12878	blood:	n/a	n/a
12	ATF2	chr4:152405480-152406188	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:152405446-152406295	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:152339076-152339368	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:152328950-152329378	GM12878	blood:	n/a	n/a
16	ATF2	chr4:152410658-152411028	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr4:152405961-152406194	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr4:152245958-152246238	K562	blood:	n/a	n/a
19	BACH1	chr4:152337183-152337311	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:152329039-152330143	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr4:152410762-152410960	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr4:152252867-152253102	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr4:152205949-152206356	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr4:152283845-152284131	K562	blood:	n/a	n/a
25	BACH1	chr4:152239544-152239715	K562	blood:	n/a	n/a
26	BACH1	chr4:152470311-152470372	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:152246262-152247097	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr4:152317166-152317295	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:152459478-152459498	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:152405613-152406248	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr4:152317107-152317340	K562	blood:	n/a	n/a
32	BATF	chr4:152488331-152488574	GM12878	blood:	n/a	n/a
33	BATF	chr4:152488330-152488532	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:152488306-152488634	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:152405934-152406177	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr4:152488300-152488541	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:152206042-152206370	H1-hESC	embryonic stem cell:	n/a	n/a
38	BCL11A	chr4:152328930-152329199	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:152328858-152329243	GM12878	blood:	n/a	n/a
40	BCL11A	chr4:152405884-152406142	H1-hESC	embryonic stem cell:	n/a	n/a
41	BCL11A	chr4:152470637-152470868	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCLAF1	chr4:152328779-152329357	GM12878	blood:	n/a	chr4:152329249-152329262 chr4:152329297-152329310
43	BCLAF1	chr4:152328836-152329362	GM12878	blood:	n/a	chr4:152329249-152329262 chr4:152329297-152329310
44	BHLHE40	chr4:152329818-152330172	K562	blood:	n/a	chr4:152330106-152330122
45	BHLHE40	chr4:152203362-152203467	GM12878	blood:	n/a	n/a
46	BHLHE40	chr4:152339803-152339854	HepG2	liver:	n/a	n/a
47	BHLHE40	chr4:152245821-152246110	HepG2	liver:	n/a	n/a
48	BHLHE40	chr4:152245896-152246183	HepG2	liver:	n/a	n/a
49	BHLHE40	chr4:152328848-152330160	GM12878	blood:	n/a	chr4:152329357-152329373 chr4:152330106-152330122
50	BHLHE40	chr4:152331006-152331477	HepG2	liver:	n/a	n/a

(count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:152329364-152329414	PFSK-1	brain:	n/a
2	chr4:152217416-152217466	MCF10A-Er-Src	breast:	n/a
3	chr4:152249812-152249862	HRPEpiC	eye:	n/a
4	chr4:152329364-152329414	PFSK-1	brain:	n/a
5	chr4:152217416-152217466	MCF10A-Er-Src	breast:	n/a
6	chr4:152249812-152249862	HRPEpiC	eye:	n/a
7	chr4:152246547-152246597	NHDF-neo	bronchial:	n/a
8	chr4:152246234-152246284	BJ	skin:	n/a
9	chr4:152328900-152328950	NB4	blood:	n/a
10	chr4:152330872-152330922	AG09309	skin:	n/a
11	chr4:152432509-152432559	HRE	kidney:	n/a
12	chr4:152330774-152330824	MCF10A-Er-Src	breast:	n/a
13	chr4:152246857-152246907	HUVEC	blood vessel:	n/a
14	chr4:152217416-152217466	ProgFib	skin:	n/a
15	chr4:152330012-152330062	NT2-D1	testis:	n/a
16	chr4:152327153-152327203	AG04450	lung:	fetal
17	chr4:152330337-152330387	HEK293	kidney:	embryo
18	chr4:152329364-152329414	HAEpiC	amniotic membrane:	n/a
19	chr4:152330774-152330824	GM19239	blood:	n/a
20	chr4:152345440-152345490	HEEpiC	esophagus:	n/a
21	chr4:152332936-152332986	PrEC	prostate:	n/a
22	chr4:152330339-152330389	AG09319	gingival:	n/a
23	chr4:152330349-152330399	PANC-1	pancreas:	n/a
24	chr4:152330774-152330824	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:152246909-152246959	GM06990	blood:	n/a
26	chr4:152330012-152330062	HEK293	kidney:	embryo
27	chr4:152493081-152493131	AoSMC	blood vessel:	n/a
28	chr4:152246857-152246907	HEK293	kidney:	embryo
29	chr4:152246909-152246959	GM12892	blood:	n/a
30	chr4:152475308-152475358	MCF10A-Er-Src	breast:	n/a
31	chr4:152424074-152424124	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:152327153-152327203	HCF	heart:	n/a
33	chr4:152246909-152246959	Hepatocyte	liver:	n/a
34	chr4:152246547-152246597	A549	lung:	n/a
35	chr4:152330337-152330387	AG04450	lung:	fetal
36	chr4:152247150-152247200	HIPEpiC	eye:	n/a
37	chr4:152330107-152330157	PrEC	prostate:	n/a
38	chr4:152329364-152329414	AG10803	skin:	n/a
39	chr4:152242679-152242729	SKMC	muscle:	n/a
40	chr4:152247150-152247200	HAEpiC	amniotic membrane:	n/a
41	chr4:152246909-152246959	ECC-1	luminal epithelium:	n/a
42	chr4:152330339-152330389	MCF10A-Er-Src	breast:	n/a
43	chr4:152330465-152330515	GM12891	blood:	n/a
44	chr4:152246020-152246070	U87	brain:	n/a
45	chr4:152475308-152475358	RPTEC	kidney:	n/a
46	chr4:152330465-152330515	HepG2	liver:	n/a
47	chr4:152432509-152432559	Hela-S3	cervix:	n/a
48	chr4:152424074-152424124	HRE	kidney:	n/a
49	chr4:152330337-152330387	PFSK-1	brain:	n/a
50	chr4:152432509-152432559	MCF10A-Er-Src	breast:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:50936343..50936843-chr4:152377370..152378176,2	K562	blood:
2	chr4:152316714..152318854-chr4:152328707..152331073,2	MCF-7	breast:
3	chr4:152235211..152238517-chr4:152240982..152244208,5	MCF-7	breast:
4	chr4:152371542..152374443-chr4:152375598..152378565,2	MCF-7	breast:
5	chr4:152237261..152239909-chr4:152241388..152243872,3	MCF-7	breast:
6	chr4:152334377..152337765-chr4:152341477..152345908,4	K562	blood:
7	chr4:152342878..152344921-chr4:152349555..152352134,2	MCF-7	breast:
8	chr4:152222898..152227266-chr4:152244180..152247379,4	MCF-7	breast:
9	chr4:152342878..152344921-chr4:152349555..152352134,2	MCF-7	breast:
10	chr12:53844772..53847737-chr4:152264669..152266872,2	MCF-7	breast:
11	chr4:152329542..152330364-chr6:26026932..26027811,2	Hela-S3	cervix:
12	chr4:152478771..152481740-chr4:152484056..152486219,2	MCF-7	breast:
13	chr4:152329894..152331826-chr4:152444189..152446160,2	MCF-7	breast:
14	chr4:152197683..152198608-chr4:152283214..152284436,5	MCF-7	breast:
15	chr4:152389958..152392173-chr4:152395343..152398079,2	K562	blood:
16	chr4:152393445..152396231-chr4:152399034..152401565,3	MCF-7	breast:
17	chr4:152245950..152246651-chr6:27860270..27861013,2	Hela-S3	cervix:
18	chr4:152019186..152022865-chr4:152245245..152246932,3	MCF-7	breast:
19	chr4:152223332..152225331-chr4:152226624..152229579,2	K562	blood:
20	chr4:152451680..152452632-chr4:152566818..152567655,2	K562	blood:
21	chr4:152451909..152453994-chr4:152457176..152459826,2	K562	blood:
22	chr4:152283616..152284269-chr4:152525183..152526125,3	K562	blood:
23	chr1:89149595..89150508-chr4:152329195..152330084,2	Hela-S3	cervix:
24	chr4:152239187..152240739-chr4:152245309..152246828,2	MCF-7	breast:
25	chr4:152248939..152251667-chr4:152260869..152263066,2	MCF-7	breast:
26	chr4:152019364..152021476-chr4:152328335..152331101,2	MCF-7	breast:
27	chr3:186500934..186501586-chr4:152245910..152246549,2	Hela-S3	cervix:
28	chr4:152328180..152331870-chr4:152350239..152352902,3	MCF-7	breast:
29	chr4:152392114..152395056-chr4:152400714..152402332,2	MCF-7	breast:
30	chr4:152215556..152217545-chr4:152227958..152229723,3	MCF-7	breast:
31	chr4:152327541..152330018-chr4:152354907..152357662,2	MCF-7	breast:
32	chr4:152334377..152337765-chr4:152341477..152345908,4	K562	blood:
33	chr4:152329199..152330989-chr4:152430941..152433845,2	MCF-7	breast:
34	chr4:152480645..152483966-chr4:152488462..152492385,3	MCF-7	breast:
35	chr4:152371542..152374443-chr4:152375598..152378565,2	MCF-7	breast:
36	chr4:152424956..152426757-chr4:152427452..152429748,2	K562	blood:
37	chr4:152323872..152326732-chr4:152328496..152330059,3	K562	blood:
38	chr4:152237261..152239909-chr4:152241388..152243872,3	MCF-7	breast:
39	chr4:152389958..152393083-chr4:152394251..152396843,3	K562	blood:
40	chr4:152391915..152393876-chr4:152394170..152396250,2	MCF-7	breast:
41	chr4:152245224..152246809-chr4:152248437..152250003,2	K562	blood:
42	chr4:152391915..152393876-chr4:152394170..152396250,2	MCF-7	breast:
43	chr4:152329639..152330392-chr8:130951751..130952461,2	HCT-116	colon:
44	chr4:152235211..152238517-chr4:152240982..152244208,5	MCF-7	breast:
45	chr4:152038573..152039512-chr4:152283907..152284485,2	MCF-7	breast:
46	chr4:152324300..152327192-chr4:152328168..152330030,2	K562	blood:
47	chr4:152493503..152497006-chr4:152497328..152500411,3	MCF-7	breast:
48	chr4:152405946..152407616-chr4:152409141..152411607,2	MCF-7	breast:
49	chr4:152393445..152396231-chr4:152399034..152401565,3	MCF-7	breast:
50	chr4:152405946..152407616-chr4:152409141..152411607,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3D19-1	chr4:152329787-152330005	XLOC_004122
2	lnc-FAM160A1-8	chr4:152455847-152455928	NONHSAT098761
3	lnc-SH3D19-5	chr4:152254927-152255141	ENSG00000270265.1
4	lnc-SH3D19-5	chr4:152274052-152274376	ENSG00000270265.1
5	lnc-FAM160A1-8	chr4:152330368-152330617	NONHSAT098760
6	lnc-FAM160A1-8	chr4:152375853-152375960	NONHSAT098760
7	lnc-FAM160A1-8	chr4:152487290-152487410	NONHSAT098760
8	lnc-SH3D19-1	chr4:152326596-152330019	NONHSAT098755
9	lnc-FAM160A1-8	chr4:152375853-152375960	NONHSAT098761
10	lnc-PRSS48-2	chr4:152237733-152238350	NONHSAT098752
11	lnc-FAM160A1-8	chr4:152403676-152403800	NONHSAT098760
12	lnc-SH3D19-1	chr4:152328335-152329162	XLOC_004122
13	lnc-SH3D19-1	chr4:152328641-152328859	XLOC_004122
14	lnc-SH3D19-1	chr4:152326672-152326760	XLOC_004122
15	lnc-FAM160A1-8	chr4:152330504-152330617	NONHSAT098761
16	lnc-PRSS48-3	chr4:152244367-152244721	expReg_chr4_7530_+
17	lnc-SH3D19-1	chr4:152326703-152326760	XLOC_004122
18	lnc-SH3D19-1	chr4:152329787-152329987	XLOC_004122
19	lnc-PET112-3	chr4:152493859-152493983	l_2754_chr4:152493858-152548475_thyroid
20	lnc-SH3D19-1	chr4:152328703-152328859	XLOC_004122
21	lnc-FAM160A1-9	chr4:152328665-152329301	NONHSAT098759

No data

Variant related genes	Relation type
FAM160A1	TF binding region
RN7SKP35	TF binding region
RNU6-1282P	TF binding region
ENSG00000251611	TF binding region
ENSG00000270265	TF binding region
ENSG00000250350	TF binding region
SH3D19	TF binding region
ENSG00000221657	TF binding region
FAM160A1	CpG island
RN7SKP35	CpG island
RNU6-1282P	CpG island
ENSG00000251611	CpG island
ENSG00000270265	CpG island
ENSG00000250350	CpG island
SH3D19	CpG island
ENSG00000221657	CpG island
ENSG00000065243	chromatin interactions
ENSG00000253019	chromatin interactions
ENSG00000109686	chromatin interactions
ENSG00000189099	chromatin interactions
ENSG00000124529	chromatin interactions
ENSG00000116266	chromatin interactions
ENSG00000153310	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000197111	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000201264	chromatin interactions
ENSG00000145425	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000164142	chromatin interactions
ENSG00000251611	chromatin interactions
ENSG00000253720	chromatin interactions
CMTM4	miRNA target sites
CSNK1G1	miRNA target sites
NIN	miRNA target sites
RGMB	miRNA target sites

Extended variants
information (count: 9527 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:9527 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368294077	chr4:152202631-152202632	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs563236811	chr4:152202718-152202719	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187291599	chr4:152202722-152202723	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548888064	chr4:152202814-152202815	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148514083	chr4:152202821-152202822	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557618723	chr4:152202847-152202848	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193189737	chr4:152202851-152202852	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184616152	chr4:152202855-152202856	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189932750	chr4:152202858-152202859	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565752535	chr4:152202888-152202889	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73861150	chr4:152202896-152202897	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539162959	chr4:152202900-152202901	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557890984	chr4:152202943-152202944	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576144811	chr4:152202948-152202949	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546451820	chr4:152203001-152203002	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571217990	chr4:152203054-152203055	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374253757	chr4:152203062-152203063	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368485711	chr4:152203125-152203126	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550999454	chr4:152203218-152203219	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569240869	chr4:152203263-152203264	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536781592	chr4:152203293-152203294	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs370412647	chr4:152203323-152203324	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs372652981	chr4:152203338-152203339	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs375690535	chr4:152203367-152203368	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs371043758	chr4:152203376-152203377	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs199896407	chr4:152203378-152203379	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs202018966	chr4:152203399-152203400	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200807354	chr4:152203418-152203419	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs376777805	chr4:152203426-152203427	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs192149727	chr4:152203427-152203428	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs577660606	chr4:152203430-152203431	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs17027505	chr4:152203437-152203438	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs200120511	chr4:152203451-152203452	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs575226053	chr4:152203483-152203484	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs368123924	chr4:152203484-152203485	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs542676890	chr4:152203536-152203537	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs183837737	chr4:152203537-152203538	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs188453537	chr4:152203538-152203539	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs17027509	chr4:152203562-152203563	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372259053	chr4:152203569-152203570	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs560325226	chr4:152203573-152203574	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs564834026	chr4:152203589-152203590	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367571113	chr4:152203601-152203602	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143028832	chr4:152203604-152203605	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550679535	chr4:152203630-152203631	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569207719	chr4:152203642-152203643	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6849871	chr4:152203664-152203665	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548623316	chr4:152203819-152203820	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148209180	chr4:152203855-152203856	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181919490	chr4:152203857-152203858	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3952 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152182600-152211000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:152182800-152206000	Weak transcription	NHEK	skin
3	chr4:152188600-152204000	Weak transcription	Gastric	stomach
4	chr4:152189400-152205800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:152190800-152208600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:152191200-152204200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:152194200-152213200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr4:152196000-152204000	Weak transcription	Fetal Stomach	stomach
9	chr4:152196000-152218400	Weak transcription	Psoas Muscle	Psoas
10	chr4:152197800-152242400	Weak transcription	Aorta	Aorta
11	chr4:152198200-152205800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr4:152198600-152203400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:152198600-152204600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:152198600-152204800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr4:152198600-152205000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr4:152198600-152205000	Weak transcription	Fetal Intestine Large	intestine
17	chr4:152198600-152205800	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr4:152198800-152203200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr4:152198800-152204400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr4:152198800-152221800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:152198800-152242800	Weak transcription	Fetal Lung	lung
22	chr4:152200600-152204200	Weak transcription	HUVEC	blood vessel
23	chr4:152201000-152203400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:152201000-152204400	Genic enhancers	HepG2	liver
25	chr4:152201600-152203000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr4:152201600-152203200	Weak transcription	Left Ventricle	heart
27	chr4:152201600-152203200	Weak transcription	Right Atrium	heart
28	chr4:152201600-152203400	Weak transcription	Lung	lung
29	chr4:152201600-152205800	Weak transcription	Liver	Liver
30	chr4:152201600-152206000	Weak transcription	Right Ventricle	heart
31	chr4:152201600-152228600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:152201800-152204600	Weak transcription	Fetal Intestine Small	intestine
33	chr4:152201800-152205200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:152202000-152202800	Enhancers	Stomach Mucosa	stomach
35	chr4:152202000-152206000	Weak transcription	Ovary	ovary
36	chr4:152202400-152203400	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr4:152202400-152206000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:152202600-152214800	Weak transcription	Small Intestine	intestine
39	chr4:152202800-152206000	Weak transcription	Stomach Mucosa	stomach
40	chr4:152203000-152203600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr4:152203200-152203400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:152203200-152203400	Enhancers	Left Ventricle	heart
43	chr4:152203200-152203600	Enhancers	Esophagus	oesophagus
44	chr4:152203200-152203800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:152203200-152203800	Enhancers	Right Atrium	heart
46	chr4:152203400-152203600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:152203400-152203600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:152203400-152203600	Genic enhancers	Left Ventricle	heart
49	chr4:152203400-152203600	Enhancers	Lung	lung
50	chr4:152203400-152203800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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