Variant report

Variant	nsv461674
Chromosome Location	chr4:147047072-147143572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:967)
CpG islands
(count:976)
Chromatin interactive
region (count:46)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:147096402-147097073	HepG2	liver:	n/a	n/a
2	ATF2	chr4:147096494-147096898	GM12878	blood:	n/a	n/a
3	ATF2	chr4:147053339-147054132	GM12878	blood:	n/a	n/a
4	ATF2	chr4:147096617-147097074	GM12878	blood:	n/a	n/a
5	ATF2	chr4:147053384-147054196	GM12878	blood:	n/a	n/a
6	BACH1	chr4:147096449-147096574	K562	blood:	n/a	n/a
7	BATF	chr4:147076449-147076795	GM12878	blood:	n/a	n/a
8	BATF	chr4:147080620-147081059	GM12878	blood:	n/a	n/a
9	BATF	chr4:147080580-147081116	GM12878	blood:	n/a	chr4:147080606-147080615
10	BATF	chr4:147096706-147096983	GM12878	blood:	n/a	n/a
11	BATF	chr4:147076538-147076733	GM12878	blood:	n/a	n/a
12	BATF	chr4:147053529-147054080	GM12878	blood:	n/a	n/a
13	BATF	chr4:147053453-147054084	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:147053418-147054101	GM12878	blood:	n/a	chr4:147053723-147053732 chr4:147054044-147054053
15	BCL11A	chr4:147053504-147054046	GM12878	blood:	n/a	chr4:147053723-147053732
16	BCL3	chr4:147053451-147054024	GM12878	blood:	n/a	chr4:147053723-147053732
17	BCL3	chr4:147068118-147068485	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:147053463-147054004	GM12878	blood:	n/a	chr4:147053723-147053732
19	BCLAF1	chr4:147053451-147053916	GM12878	blood:	n/a	chr4:147053723-147053732
20	BCLAF1	chr4:147096628-147097235	GM12878	blood:	n/a	chr4:147096971-147096984
21	BCLAF1	chr4:147096677-147097175	GM12878	blood:	n/a	chr4:147096971-147096984
22	BHLHE40	chr4:147096725-147097191	K562	blood:	n/a	n/a
23	BHLHE40	chr4:147080804-147081186	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:147106486-147106729	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:147054270-147054336	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:147053382-147053954	GM12878	blood:	n/a	n/a
27	BRCA1	chr4:147080844-147080955	GM12878	blood:	n/a	n/a
28	BRCA1	chr4:147066139-147066151	HepG2	liver:	n/a	n/a
29	BRCA1	chr4:147096635-147097107	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr4:147096596-147097146	K562	blood:	n/a	n/a
31	CBX3	chr4:147096523-147097139	HCT-116	colon:	n/a	n/a
32	CCNT2	chr4:147096722-147097276	K562	blood:	n/a	n/a
33	CEBPB	chr4:147099279-147099596	K562	blood:	n/a	n/a
34	CEBPB	chr4:147110114-147110268	K562	blood:	n/a	chr4:147110197-147110208
35	CEBPB	chr4:147086944-147087334	A549	lung:	n/a	chr4:147087135-147087146
36	CEBPB	chr4:147068134-147068329	HepG2	liver:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
37	CEBPB	chr4:147068087-147068405	Hela-S3	cervix:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
38	CEBPB	chr4:147087046-147087319	ECC-1	luminal epithelium:	n/a	chr4:147087135-147087146
39	CEBPB	chr4:147068103-147068404	A549	lung:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
40	CEBPB	chr4:147110086-147110323	IMR90	lung:	n/a	chr4:147110197-147110208
41	CEBPB	chr4:147085939-147086011	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:147114678-147114836	A549	lung:	n/a	chr4:147114704-147114717 chr4:147114703-147114720 chr4:147114704-147114715 chr4:147114704-147114717
43	CEBPB	chr4:147087058-147087303	HepG2	liver:	n/a	chr4:147087135-147087146
44	CEBPB	chr4:147087043-147087282	A549	lung:	n/a	chr4:147087135-147087146
45	CEBPB	chr4:147067412-147067608	HepG2	liver:	n/a	chr4:147067526-147067537
46	CEBPB	chr4:147086984-147087347	Hela-S3	cervix:	n/a	chr4:147087135-147087146
47	CEBPB	chr4:147072906-147073185	IMR90	lung:	n/a	chr4:147073012-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073013-147073024 chr4:147073014-147073023
48	CEBPB	chr4:147085824-147086136	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:147053407-147054140	GM12878	blood:	n/a	n/a
50	CEBPB	chr4:147086986-147087379	IMR90	lung:	n/a	chr4:147087135-147087146

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147096787-147096837	HCPEpiC	choroid plexus:	n/a
2	chr4:147099913-147099963	AG09309	skin:	n/a
3	chr4:147095635-147095685	MCF-7	breast:	n/a
4	chr4:147097886-147097936	AG04450	lung:	fetal
5	chr4:147138044-147138094	GM12878	blood:	n/a
6	chr4:147097364-147097414	AG04449	skin:	fetal
7	chr4:147096785-147096835	A549	lung:	n/a
8	chr4:147095635-147095685	PFSK-1	brain:	n/a
9	chr4:147096785-147096835	HAEpiC	amniotic membrane:	n/a
10	chr4:147097364-147097414	CMK	blood:	n/a
11	chr4:147097886-147097936	NT2-D1	testis:	n/a
12	chr4:147097886-147097936	LNCaP	prostate:	n/a
13	chr4:147097443-147097493	PrEC	prostate:	n/a
14	chr4:147056211-147056261	GM19239	blood:	n/a
15	chr4:147097209-147097259	GM12892	blood:	n/a
16	chr4:147095396-147095446	ProgFib	skin:	n/a
17	chr4:147096787-147096837	GM12892	blood:	n/a
18	chr4:147096820-147096870	NHBE	bronchial:	n/a
19	chr4:147099913-147099963	PrEC	prostate:	n/a
20	chr4:147097364-147097414	HL-60	blood:	n/a
21	chr4:147096820-147096870	HAEpiC	amniotic membrane:	n/a
22	chr4:147095396-147095446	HRE	kidney:	n/a
23	chr4:147097886-147097936	HL-60	blood:	n/a
24	chr4:147097364-147097414	Jurkat	blood:	n/a
25	chr4:147095635-147095685	HRPEpiC	eye:	n/a
26	chr4:147096787-147096837	Caco-2	colon:	n/a
27	chr4:147096828-147096878	NT2-D1	testis:	n/a
28	chr4:147095396-147095446	HAEpiC	amniotic membrane:	n/a
29	chr4:147097364-147097414	HAEpiC	amniotic membrane:	n/a
30	chr4:147097886-147097936	HEEpiC	esophagus:	n/a
31	chr4:147097886-147097936	GM12891	blood:	n/a
32	chr4:147099913-147099963	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:147097443-147097493	GM12892	blood:	n/a
34	chr4:147056211-147056261	HL-60	blood:	n/a
35	chr4:147106103-147106153	HUVEC	blood vessel:	n/a
36	chr4:147096820-147096870	GM19239	blood:	n/a
37	chr4:147138044-147138094	BJ	skin:	n/a
38	chr4:147099913-147099963	GM19239	blood:	n/a
39	chr4:147096785-147096835	AG10803	skin:	n/a
40	chr4:147096909-147096959	U87	brain:	n/a
41	chr4:147097886-147097936	ProgFib	skin:	n/a
42	chr4:147138044-147138094	HEEpiC	esophagus:	n/a
43	chr4:147097209-147097259	LNCaP	prostate:	n/a
44	chr4:147097364-147097414	BJ	skin:	n/a
45	chr4:147097443-147097493	SKMC	muscle:	n/a
46	chr4:147106103-147106153	T-47D	breast:	n/a
47	chr4:147096909-147096959	PFSK-1	brain:	n/a
48	chr4:147096820-147096870	MCF10A-Er-Src	breast:	n/a
49	chr4:147106103-147106153	GM19239	blood:	n/a
50	chr4:147095396-147095446	GM12892	blood:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:146538731..146541596-chr4:147058799..147061667,2	MCF-7	breast:
2	chr4:147096162..147099903-chr4:147161380..147165203,4	MCF-7	breast:
3	chr4:147131915..147134397-chr4:147145047..147146932,2	MCF-7	breast:
4	chr4:147100998..147102686-chr4:147106253..147108281,2	K562	blood:
5	chr4:147049621..147051937-chr4:147059777..147061735,2	K562	blood:
6	chr4:147103019..147105139-chr4:147110887..147113160,2	K562	blood:
7	chr4:147116335..147119084-chr4:147119994..147121504,2	MCF-7	breast:
8	chr4:147055908..147058873-chr4:147059749..147061908,2	K562	blood:
9	chr4:147086830..147091007-chr4:147091903..147096779,4	K562	blood:
10	chr4:147099369..147101389-chr4:147104400..147106028,2	MCF-7	breast:
11	chr4:147090038..147091690-chr4:147095340..147097162,2	MCF-7	breast:
12	chr4:147100998..147102686-chr4:147106253..147108281,2	K562	blood:
13	chr4:147111066..147113636-chr4:147115907..147120334,4	K562	blood:
14	chr4:147094825..147098572-chr4:147107210..147109613,3	MCF-7	breast:
15	chr4:147032685..147035197-chr4:147045955..147048803,2	K562	blood:
16	chr4:147116009..147117870-chr4:147118795..147120333,2	MCF-7	breast:
17	chr4:147106019..147107613-chr4:147111595..147114491,2	K562	blood:
18	chr4:147055512..147057408-chr4:147060408..147062142,2	K562	blood:
19	chr4:147111066..147113636-chr4:147115907..147120334,4	K562	blood:
20	chr4:147113098..147115033-chr4:147118947..147121819,2	K562	blood:
21	chr4:147096691..147098879-chr4:147107983..147110600,2	MCF-7	breast:
22	chr4:147098952..147101592-chr4:147130358..147132148,2	K562	blood:
23	chr4:147076257..147079097-chr4:147084297..147086831,2	MCF-7	breast:
24	chr4:147111066..147113405-chr4:147115907..147118837,2	K562	blood:
25	chr4:147086830..147091007-chr4:147091903..147096779,4	K562	blood:
26	chr4:147049621..147051937-chr4:147059777..147061735,2	K562	blood:
27	chr4:147106019..147107613-chr4:147111595..147114491,2	K562	blood:
28	chr4:147040989..147042728-chr4:147052779..147055096,2	MCF-7	breast:
29	chr4:147055908..147058873-chr4:147059749..147061908,2	K562	blood:
30	chr4:147088096..147091007-chr4:147093172..147095753,2	K562	blood:
31	chr4:147088096..147091007-chr4:147093172..147095753,2	K562	blood:
32	chr4:147059542..147061750-chr4:147066448..147068340,2	K562	blood:
33	chr4:147113098..147115033-chr4:147118947..147121819,2	K562	blood:
34	chr4:147096699..147098795-chr4:147099511..147101268,2	MCF-7	breast:
35	chr4:147095588..147099041-chr4:147101501..147104102,4	MCF-7	breast:
36	chr4:147103613..147105948-chr4:147107918..147110388,2	K562	blood:
37	chr4:147099369..147101389-chr4:147104400..147106028,2	MCF-7	breast:
38	chr4:147103613..147105948-chr4:147107918..147110388,3	K562	blood:
39	chr4:147116335..147119084-chr4:147119994..147121504,2	MCF-7	breast:
40	chr4:147098952..147101592-chr4:147130358..147132148,2	K562	blood:
41	chr4:147095588..147099041-chr4:147101501..147104102,4	MCF-7	breast:
42	chr4:147076257..147079097-chr4:147084297..147086831,2	MCF-7	breast:
43	chr4:147111066..147113405-chr4:147115907..147118837,2	K562	blood:
44	chr4:147116009..147117870-chr4:147118795..147120333,2	MCF-7	breast:
45	chr4:147059542..147061750-chr4:147066448..147068340,2	K562	blood:
46	chr4:147055512..147057408-chr4:147060408..147062142,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC10A7-2	chr4:147079257-147079602	expReg_chr4_6941_-
2	lnc-RP11-6L6.2.1-3	chr4:147097320-147097838	NONHSAT098665
3	lnc-RP11-6L6.2.1-3	chr4:147096922-147096963	NONHSAT098665
4	lnc-RP11-6L6.2.1-2	chr4:147111638-147114339	NONHSAT098666

No data

Variant related genes	Relation type
LINC01095	TF binding region
ENSG00000216055	TF binding region
ENSG00000250673	TF binding region
LSM6	TF binding region
LINC01095	CpG island
ENSG00000216055	CpG island
ENSG00000250673	CpG island
LSM6	CpG island
ENSG00000251010	chromatin interactions
ENSG00000151611	chromatin interactions
ENSG00000250673	chromatin interactions
ENSG00000164167	chromatin interactions
ENSG00000248809	chromatin interactions

Extended variants
information (count: 3700 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3700 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4835286	chr4:147047072-147047073	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191234218	chr4:147047086-147047087	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575783478	chr4:147047087-147047088	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs79874334	chr4:147047094-147047095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184504599	chr4:147047104-147047105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs574980973	chr4:147047118-147047119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540018186	chr4:147047125-147047126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs547329636	chr4:147047132-147047133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149130447	chr4:147047145-147047146	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189341228	chr4:147047174-147047175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529296892	chr4:147047185-147047186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549452146	chr4:147047266-147047267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs143244498	chr4:147047314-147047315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs377148194	chr4:147047326-147047327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192912100	chr4:147047345-147047346	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550317184	chr4:147047349-147047350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs184896996	chr4:147047359-147047360	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577839129	chr4:147047369-147047370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115382264	chr4:147047389-147047390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552884164	chr4:147047411-147047412	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147845470	chr4:147047422-147047423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535154165	chr4:147047440-147047441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545108224	chr4:147047460-147047461	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555350630	chr4:147047465-147047466	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563922618	chr4:147047493-147047494	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544316156	chr4:147047525-147047526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564632633	chr4:147047532-147047533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369102442	chr4:147047565-147047566	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs56289966	chr4:147047568-147047569	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs540906177	chr4:147047664-147047665	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs114804175	chr4:147047674-147047675	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs76169649	chr4:147047687-147047688	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs549069204	chr4:147047743-147047744	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs562905584	chr4:147047757-147047758	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs531683790	chr4:147047763-147047764	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377321023	chr4:147047780-147047781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188879231	chr4:147047799-147047800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141491797	chr4:147047803-147047804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539278644	chr4:147047826-147047827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546488456	chr4:147047844-147047845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs34784071	chr4:147047863-147047864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371287706	chr4:147047864-147047865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181590591	chr4:147047869-147047870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs11940961	chr4:147047921-147047922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs555032843	chr4:147047939-147047940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs112278754	chr4:147048091-147048092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201726335	chr4:147048098-147048099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs56944179	chr4:147048100-147048101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs200180157	chr4:147048126-147048127	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201224498	chr4:147048130-147048131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1390 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147045800-147055400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:147046600-147047800	Weak transcription	Placenta	Placenta
3	chr4:147047800-147048000	Enhancers	Placenta	Placenta
4	chr4:147052400-147053200	Enhancers	GM12878-XiMat	blood
5	chr4:147052600-147056000	Weak transcription	Right Atrium	heart
6	chr4:147053200-147054200	Flanking Active TSS	GM12878-XiMat	blood
7	chr4:147053400-147053600	Enhancers	HMEC	breast
8	chr4:147053600-147054400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:147053800-147054000	Enhancers	Esophagus	oesophagus
10	chr4:147054000-147054200	Enhancers	Osteobl	bone
11	chr4:147054000-147055600	Weak transcription	Esophagus	oesophagus
12	chr4:147054200-147054600	Enhancers	GM12878-XiMat	blood
13	chr4:147054600-147055800	Weak transcription	Osteobl	bone
14	chr4:147054600-147056600	Enhancers	Fetal Brain Male	brain
15	chr4:147055200-147056600	Enhancers	Fetal Brain Female	brain
16	chr4:147055200-147057400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr4:147055200-147057400	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr4:147055400-147055800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:147055400-147056200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:147055400-147056200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:147055400-147056600	Enhancers	HMEC	breast
22	chr4:147055400-147056800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:147055600-147056600	Enhancers	Esophagus	oesophagus
24	chr4:147055600-147056800	Enhancers	Brain Germinal Matrix	brain
25	chr4:147055600-147057200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:147055800-147056200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:147055800-147056200	Enhancers	NHEK	skin
28	chr4:147055800-147056400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr4:147055800-147056600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:147055800-147056600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr4:147055800-147056600	Enhancers	Osteobl	bone
32	chr4:147055800-147057400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:147055800-147057400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:147055800-147057600	Enhancers	Fetal Muscle Leg	muscle
35	chr4:147055800-147058000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:147055800-147058400	Enhancers	Adipose Nuclei	Adipose
37	chr4:147056000-147056200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr4:147056000-147056600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:147056000-147056600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:147056000-147056600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:147056000-147056600	Enhancers	Right Atrium	heart
42	chr4:147056000-147056800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:147056000-147057200	Enhancers	Brain Cingulate Gyrus	brain
44	chr4:147056200-147056600	Enhancers	Brain Anterior Caudate	brain
45	chr4:147056200-147057600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:147056600-147058000	Weak transcription	Right Atrium	heart
47	chr4:147056600-147064000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:147057200-147057400	Enhancers	Brain Hippocampus Middle	brain
49	chr4:147058000-147058200	Enhancers	Right Atrium	heart
50	chr4:147058400-147062400	Weak transcription	Adipose Nuclei	Adipose

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