Variant report

Variant	nsv461660
Chromosome Location	chr4:143437219-143538179
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:645)
CpG islands
(count:183)
Chromatin interactive
region (count:158)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:143471084-143471686	A549	lung:	n/a	n/a
2	BACH1	chr4:143443920-143443948	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr4:143459206-143459399	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:143484795-143485098	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:143487137-143487163	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:143487866-143488614	GM12878	blood:	n/a	chr4:143488116-143488137 chr4:143488122-143488131 chr4:143488120-143488133 chr4:143488122-143488131 chr4:143488121-143488130
7	BHLHE40	chr4:143490550-143490694	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:143495539-143495817	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:143485342-143485388	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:143489388-143489570	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:143536082-143536931	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr4:143470280-143472567	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:143470749-143471759	HCT-116	colon:	n/a	n/a
14	CEBPB	chr4:143536470-143536755	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:143470896-143471685	ECC-1	luminal epithelium:	n/a	chr4:143470897-143470905
16	CEBPB	chr4:143473007-143473154	A549	lung:	n/a	chr4:143473087-143473104
17	CEBPB	chr4:143522123-143522455	MCF-7	breast:	n/a	n/a
18	CEBPB	chr4:143489253-143489631	A549	lung:	n/a	chr4:143489580-143489593
19	CEBPB	chr4:143522039-143522455	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:143536434-143536886	MCF-7	breast:	n/a	n/a
21	CEBPB	chr4:143470258-143471737	HCT-116	colon:	n/a	chr4:143470897-143470905
22	CEBPB	chr4:143470876-143471324	A549	lung:	n/a	chr4:143470897-143470905
23	CEBPB	chr4:143497072-143497584	HepG2	liver:	n/a	chr4:143497528-143497541 chr4:143497528-143497541 chr4:143497529-143497540 chr4:143497528-143497539
24	CEBPB	chr4:143472929-143473244	IMR90	lung:	n/a	chr4:143473087-143473104
25	CEBPB	chr4:143448685-143448902	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:143470151-143471932	HCT-116	colon:	n/a	chr4:143470897-143470905
27	CEBPB	chr4:143471389-143471641	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:143471013-143471537	A549	lung:	n/a	n/a
29	CEBPB	chr4:143440536-143440955	A549	lung:	n/a	chr4:143440773-143440784
30	CEBPB	chr4:143536291-143536926	MCF-7	breast:	n/a	n/a
31	CHD1	chr4:143487448-143487499	GM12878	blood:	n/a	n/a
32	CHD1	chr4:143485677-143485720	GM12878	blood:	n/a	n/a
33	CHD2	chr4:143487207-143487290	GM12878	blood:	n/a	n/a
34	CHD2	chr4:143489289-143489594	GM12878	blood:	n/a	n/a
35	CHD2	chr4:143484957-143485358	GM12878	blood:	n/a	n/a
36	CHD2	chr4:143476001-143476083	GM12878	blood:	n/a	n/a
37	CTCF	chr4:143488500-143488650	NHEK	skin:	n/a	n/a
38	CTCF	chr4:143471483-143471664	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr4:143488500-143488650	RPTEC	kidney:	n/a	n/a
40	CTCF	chr4:143488440-143488590	NHLF	lung:	n/a	n/a
41	CTCF	chr4:143471501-143471626	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr4:143488540-143488690	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr4:143488557-143488658	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr4:143488460-143488610	GM06990	blood:	n/a	n/a
45	CTCF	chr4:143488560-143488710	HMEC	breast:	n/a	n/a
46	CTCF	chr4:143488484-143488625	NHEK	skin:	n/a	n/a
47	CTCF	chr4:143488470-143488553	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:143520383-143520518	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:143520410-143520503	NHEK	skin:	n/a	n/a
50	CTCF	chr4:143488410-143488715	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:143437493-143437543	HEEpiC	esophagus:	n/a
2	chr4:143470771-143470821	HEEpiC	esophagus:	n/a
3	chr4:143488622-143488672	ECC-1	luminal epithelium:	n/a
4	chr4:143488622-143488672	PANC-1	pancreas:	n/a
5	chr4:143488622-143488672	Caco-2	colon:	n/a
6	chr4:143470771-143470821	AG04450	lung:	fetal
7	chr4:143470771-143470821	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:143488622-143488672	NB4	blood:	n/a
9	chr4:143488622-143488672	HEK293	kidney:	embryo
10	chr4:143437493-143437543	AG09309	skin:	n/a
11	chr4:143470771-143470821	AoSMC	blood vessel:	n/a
12	chr4:143488622-143488672	RPTEC	kidney:	n/a
13	chr4:143470771-143470821	GM06990	blood:	n/a
14	chr4:143488622-143488672	Hepatocyte	liver:	n/a
15	chr4:143437493-143437543	IMR90	lung:	fetal
16	chr4:143437493-143437543	ovcar-3	ovarian:	n/a
17	chr4:143437493-143437543	ProgFib	skin:	n/a
18	chr4:143470771-143470821	PANC-1	pancreas:	n/a
19	chr4:143488622-143488672	SAEC	small airway:	n/a
20	chr4:143488622-143488672	T-47D	breast:	n/a
21	chr4:143470771-143470821	BJ	skin:	n/a
22	chr4:143470771-143470821	ProgFib	skin:	n/a
23	chr4:143437493-143437543	SK-N-MC	brain:	n/a
24	chr4:143488622-143488672	HCM	heart:	n/a
25	chr4:143437493-143437543	HAEpiC	amniotic membrane:	n/a
26	chr4:143470771-143470821	A549	lung:	n/a
27	chr4:143488622-143488672	GM06990	blood:	n/a
28	chr4:143488622-143488672	HIPEpiC	eye:	n/a
29	chr4:143470771-143470821	AG09309	skin:	n/a
30	chr4:143488622-143488672	HCF	heart:	n/a
31	chr4:143470771-143470821	GM12891	blood:	n/a
32	chr4:143488622-143488672	HMEC	breast:	n/a
33	chr4:143470771-143470821	HAEpiC	amniotic membrane:	n/a
34	chr4:143437493-143437543	NHBE	bronchial:	n/a
35	chr4:143470771-143470821	AG04449	skin:	fetal
36	chr4:143488622-143488672	HRCEpiC	kidney:	n/a
37	chr4:143437493-143437543	HL-60	blood:	n/a
38	chr4:143488622-143488672	HEEpiC	esophagus:	n/a
39	chr4:143437493-143437543	T-47D	breast:	n/a
40	chr4:143488622-143488672	BE2_C	brain:	n/a
41	chr4:143488622-143488672	HRPEpiC	eye:	n/a
42	chr4:143437493-143437543	HRCEpiC	kidney:	n/a
43	chr4:143437493-143437543	SK-N-SH	brain:	n/a
44	chr4:143470771-143470821	HCF	heart:	n/a
45	chr4:143488622-143488672	NHBE	bronchial:	n/a
46	chr4:143488622-143488672	GM12892	blood:	n/a
47	chr4:143470771-143470821	NB4	blood:	n/a
48	chr4:143470771-143470821	U87	brain:	n/a
49	chr4:143488622-143488672	H1-hESC	embryonic stem cell:	embryo
50	chr4:143470771-143470821	ECC-1	luminal epithelium:	n/a

(count:158 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:143517914..143520098-chr4:143525876..143528126,2	MCF-7	breast:
2	chr4:143395462..143397095-chr4:143447482..143449703,2	MCF-7	breast:
3	chr4:143522544..143524167-chr4:143536541..143538148,2	MCF-7	breast:
4	chr11:8506706..8507606-chr4:143536248..143536811,2	MCF-7	breast:
5	chr4:143391320..143397090-chr4:143436268..143441588,7	MCF-7	breast:
6	chr4:143461464..143464431-chr4:143476844..143478769,2	MCF-7	breast:
7	chr4:143448680..143450271-chr4:143471628..143474463,2	MCF-7	breast:
8	chr4:143515775..143516713-chr8:125811738..125812411,2	MCF-7	breast:
9	chr4:143387939..143398265-chr4:143528932..143544358,55	MCF-7	breast:
10	chr4:143389462..143399452-chr4:143428707..143442488,28	MCF-7	breast:
11	chr4:143459017..143460718-chr4:143467557..143470331,2	MCF-7	breast:
12	chr4:143431692..143434414-chr4:143436305..143438204,2	MCF-7	breast:
13	chr4:143536517..143538495-chr4:143637512..143640289,2	MCF-7	breast:
14	chr4:143517546..143521080-chr4:143535706..143539870,4	MCF-7	breast:
15	chr4:143444200..143447177-chr4:143456596..143458956,2	MCF-7	breast:
16	chr4:143393408..143395744-chr4:143477847..143480284,3	MCF-7	breast:
17	chr4:143451374..143452924-chr4:143454697..143456261,2	MCF-7	breast:
18	chr4:143431039..143433246-chr4:143529573..143531191,2	MCF-7	breast:
19	chr4:143488759..143491260-chr4:143536558..143538874,2	MCF-7	breast:
20	chr4:143506127..143509971-chr4:143766689..143769613,3	MCF-7	breast:
21	chr4:143535928..143538576-chr4:143767240..143768815,2	MCF-7	breast:
22	chr4:143457460..143459443-chr4:143533756..143535732,2	MCF-7	breast:
23	chr4:143475822..143478119-chr4:143482410..143485244,3	MCF-7	breast:
24	chr4:143469458..143471257-chr4:143473239..143475404,2	MCF-7	breast:
25	chr4:143509941..143511857-chr4:143515159..143518167,3	MCF-7	breast:
26	chr4:143393069..143398763-chr4:143454567..143462510,17	MCF-7	breast:
27	chr4:143518531..143520300-chr4:143521688..143524164,2	MCF-7	breast:
28	chr4:143390775..143397216-chr4:143452311..143461627,17	MCF-7	breast:
29	chr4:143488482..143490655-chr4:143513753..143516838,3	MCF-7	breast:
30	chr4:143469254..143471063-chr4:143535925..143538743,3	MCF-7	breast:
31	chr4:143517583..143519363-chr4:143531947..143533468,2	MCF-7	breast:
32	chr4:143493193..143494838-chr4:143533347..143535926,2	MCF-7	breast:
33	chr4:143438526..143441082-chr4:143443050..143445665,2	MCF-7	breast:
34	chr4:143522544..143524167-chr4:143536541..143538148,2	MCF-7	breast:
35	chr4:143394598..143397673-chr4:143470943..143474173,4	MCF-7	breast:
36	chr4:143515194..143518460-chr4:143519756..143524261,5	MCF-7	breast:
37	chr4:143427468..143430250-chr4:143437553..143439341,2	MCF-7	breast:
38	chr4:143436234..143437895-chr4:143469778..143471517,2	MCF-7	breast:
39	chr4:143537607..143539576-chr4:143628828..143631506,2	MCF-7	breast:
40	chr4:143536781..143539215-chr4:143551772..143553795,2	MCF-7	breast:
41	chr4:143473623..143475385-chr4:143483705..143485634,2	MCF-7	breast:
42	chr4:143517583..143519363-chr4:143531947..143533468,2	MCF-7	breast:
43	chr4:143488759..143491260-chr4:143536558..143538874,2	MCF-7	breast:
44	chr4:143454704..143456916-chr4:143459367..143461134,2	K562	blood:
45	chr4:143392466..143394692-chr4:143481340..143483349,2	MCF-7	breast:
46	chr4:143444200..143447177-chr4:143456596..143458956,2	MCF-7	breast:
47	chr4:143393991..143396854-chr4:143462129..143463666,2	MCF-7	breast:
48	chr4:143463931..143465579-chr4:143468036..143470044,2	MCF-7	breast:
49	chr4:143394033..143395619-chr4:143499692..143501211,2	MCF-7	breast:
50	chr4:143500805..143505474-chr4:143506198..143510194,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP38-2	chr4:143504605-143504776	ENSG00000249806
2	lnc-USP38-2	chr4:143487172-143487343	ENSG00000249806
3	lnc-USP38-3	chr4:143439856-143440136	ENSG00000251248

No data

Variant related genes	Relation type
INPP4B	TF binding region
ENSG00000249806	TF binding region
INPP4B	CpG island
ENSG00000249806	CpG island
ENSG00000249806	chromatin interactions
ENSG00000109452	chromatin interactions

Extended variants
information (count: 3843 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3843 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1364920	chr4:143437219-143437220	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79082619	chr4:143437236-143437237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556981768	chr4:143437284-143437285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376828727	chr4:143437328-143437329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144284164	chr4:143437361-143437362	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1364919	chr4:143437470-143437471	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148674613	chr4:143437493-143437494	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192212850	chr4:143437494-143437495	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs377422467	chr4:143437498-143437499	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs113420144	chr4:143437565-143437566	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs62328330	chr4:143437606-143437607	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs183260831	chr4:143437647-143437648	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143333160	chr4:143437652-143437653	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187968341	chr4:143437672-143437673	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs191955215	chr4:143437713-143437714	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567886022	chr4:143437801-143437802	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs60004938	chr4:143437848-143437849	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs546553765	chr4:143437855-143437856	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs58333696	chr4:143437857-143437858	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs547507739	chr4:143437873-143437874	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs535534494	chr4:143437888-143437889	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557439948	chr4:143437895-143437896	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569295964	chr4:143437896-143437897	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111958329	chr4:143437910-143437911	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs72948719	chr4:143437923-143437924	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184579425	chr4:143437979-143437980	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573159085	chr4:143437993-143437994	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs534097933	chr4:143437998-143437999	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs113800713	chr4:143438007-143438008	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs539369730	chr4:143438069-143438070	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555375506	chr4:143438099-143438100	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573590770	chr4:143438153-143438154	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543909626	chr4:143438220-143438221	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111829249	chr4:143438227-143438228	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs199702990	chr4:143438228-143438229	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs60037426	chr4:143438273-143438274	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs188237189	chr4:143438347-143438348	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs76126070	chr4:143438362-143438363	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546360994	chr4:143438383-143438384	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564352616	chr4:143438423-143438424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528731414	chr4:143438481-143438482	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546890521	chr4:143438515-143438516	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561708388	chr4:143438532-143438533	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529281178	chr4:143438578-143438579	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550748477	chr4:143438587-143438588	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375790932	chr4:143438609-143438610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs569312855	chr4:143438617-143438618	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539584530	chr4:143438618-143438619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551568872	chr4:143438621-143438622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541471137	chr4:143438622-143438623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143428800-143453000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:143431800-143437600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:143433400-143437600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:143433800-143437400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr4:143434000-143437600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr4:143434000-143437600	Weak transcription	Osteobl	bone
7	chr4:143434000-143440600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:143436600-143438000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:143436600-143438800	Enhancers	HMEC	breast
10	chr4:143436600-143440000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:143436600-143440000	Enhancers	Dnd41	blood
12	chr4:143436800-143437600	Weak transcription	Left Ventricle	heart
13	chr4:143437200-143438800	Enhancers	NHEK	skin
14	chr4:143437200-143439000	Enhancers	Fetal Heart	heart
15	chr4:143437400-143438200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:143437400-143438200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr4:143437400-143438200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:143437400-143438600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:143437600-143438000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:143437600-143438000	Enhancers	NHLF	lung
21	chr4:143437600-143438000	Enhancers	Osteobl	bone
22	chr4:143437600-143438200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:143437600-143438200	Enhancers	Fetal Intestine Small	intestine
24	chr4:143437600-143438200	Enhancers	Left Ventricle	heart
25	chr4:143437600-143438600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr4:143437600-143438600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:143437600-143438600	Enhancers	Fetal Intestine Large	intestine
28	chr4:143437600-143438600	Enhancers	A549	lung
29	chr4:143437600-143438600	Enhancers	HSMM	muscle
30	chr4:143437600-143438600	Enhancers	NH-A	brain
31	chr4:143437600-143438800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:143437800-143438200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:143437800-143438200	Enhancers	Right Atrium	heart
34	chr4:143438000-143438200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr4:143438200-143440000	Weak transcription	Left Ventricle	heart
36	chr4:143438600-143438800	Enhancers	Aorta	Aorta
37	chr4:143438600-143440000	Weak transcription	Fetal Intestine Large	intestine
38	chr4:143438600-143440400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr4:143438600-143440600	Weak transcription	HSMM	muscle
40	chr4:143438600-143443600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:143438800-143440600	Weak transcription	NHEK	skin
42	chr4:143438800-143443600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:143438800-143444000	Weak transcription	HMEC	breast
44	chr4:143438800-143462800	Weak transcription	Aorta	Aorta
45	chr4:143439000-143452200	Weak transcription	Fetal Heart	heart
46	chr4:143440000-143440200	Enhancers	Left Ventricle	heart
47	chr4:143440000-143440600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:143440000-143440800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:143440200-143440400	Enhancers	Fetal Intestine Large	intestine
50	chr4:143440400-143441000	Enhancers	Muscle Satellite Cultured Cells	--

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