Variant report

Variant	nsv999041
Chromosome Location	chr3:138148812-138347988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2434)
CpG islands
(count:4030)
Chromatin interactive
region (count:95)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2434 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138161304-138161671	K562	blood:	n/a	n/a
2	ARID3A	chr3:138198251-138198297	K562	blood:	n/a	n/a
3	ARID3A	chr3:138312595-138313897	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:138161260-138161463	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:138335614-138335620	K562	blood:	n/a	n/a
6	ATF1	chr3:138161267-138161641	K562	blood:	n/a	n/a
7	ATF1	chr3:138312992-138313910	K562	blood:	n/a	n/a
8	ATF2	chr3:138312575-138313137	H1-hESC	embryonic stem cell:	n/a	chr3:138313097-138313108
9	ATF2	chr3:138313458-138313922	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr3:138232341-138232746	GM12878	blood:	n/a	n/a
11	BACH1	chr3:138153468-138153646	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:138327502-138327812	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:138312835-138313813	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:138153892-138154114	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr3:138290753-138291213	GM12878	blood:	n/a	n/a
16	BATF	chr3:138232250-138232641	GM12878	blood:	n/a	n/a
17	BATF	chr3:138290836-138291217	GM12878	blood:	n/a	n/a
18	BATF	chr3:138232282-138232701	GM12878	blood:	n/a	n/a
19	BCL11A	chr3:138232380-138232593	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:138232300-138232602	GM12878	blood:	n/a	n/a
21	BCL3	chr3:138307165-138307494	GM12878	blood:	n/a	n/a
22	BCL3	chr3:138328122-138328599	A549	lung:	n/a	n/a
23	BCL3	chr3:138328128-138328619	A549	lung:	n/a	n/a
24	BCL3	chr3:138313278-138313807	A549	lung:	n/a	n/a
25	BCLAF1	chr3:138313432-138313912	GM12878	blood:	n/a	n/a
26	BCLAF1	chr3:138232232-138232651	GM12878	blood:	n/a	n/a
27	BCLAF1	chr3:138327514-138327893	GM12878	blood:	n/a	n/a
28	BCLAF1	chr3:138328174-138328622	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:138335232-138335467	K562	blood:	n/a	n/a
30	BHLHE40	chr3:138153048-138153470	HepG2	liver:	n/a	n/a
31	BHLHE40	chr3:138153202-138153422	HepG2	liver:	n/a	n/a
32	BHLHE40	chr3:138198379-138198526	K562	blood:	n/a	n/a
33	BHLHE40	chr3:138152952-138153745	HepG2	liver:	n/a	n/a
34	BHLHE40	chr3:138161357-138161658	K562	blood:	n/a	n/a
35	BHLHE40	chr3:138314071-138314204	K562	blood:	n/a	n/a
36	BHLHE40	chr3:138327464-138327904	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:138313023-138313788	K562	blood:	n/a	n/a
38	BHLHE40	chr3:138313037-138314138	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:138174985-138175101	K562	blood:	n/a	n/a
40	BRCA1	chr3:138313631-138313846	HepG2	liver:	n/a	n/a
41	BRCA1	chr3:138312883-138313083	GM12878	blood:	n/a	n/a
42	BRCA1	chr3:138313027-138313947	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr3:138226822-138227373	Hela-S3	cervix:	n/a	chr3:138226971-138226978
44	BRCA1	chr3:138327538-138327832	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr3:138313007-138313374	HepG2	liver:	n/a	n/a
46	BRCA1	chr3:138313788-138314017	GM12878	blood:	n/a	n/a
47	CBX3	chr3:138321611-138321992	K562	blood:	n/a	n/a
48	CBX3	chr3:138312845-138313897	K562	blood:	n/a	n/a
49	CBX3	chr3:138313178-138313841	K562	blood:	n/a	n/a
50	CBX3	chr3:138327482-138327730	K562	blood:	n/a	n/a

(count:4030 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138153439-138153489	NB4	blood:	n/a
2	chr3:138196760-138196810	GM19239	blood:	n/a
3	chr3:138326610-138326660	HEK293	kidney:	embryo
4	chr3:138160066-138160116	K562	blood:	n/a
5	chr3:138153439-138153489	NB4	blood:	n/a
6	chr3:138196760-138196810	GM19239	blood:	n/a
7	chr3:138326610-138326660	HEK293	kidney:	embryo
8	chr3:138160066-138160116	K562	blood:	n/a
9	chr3:138311508-138311558	HL-60	blood:	n/a
10	chr3:138152902-138152952	NHBE	bronchial:	n/a
11	chr3:138174025-138174075	AG04449	skin:	fetal
12	chr3:138153168-138153218	Hela-S3	cervix:	n/a
13	chr3:138152902-138152952	Caco-2	colon:	n/a
14	chr3:138326610-138326660	ProgFib	skin:	n/a
15	chr3:138153168-138153218	SKMC	muscle:	n/a
16	chr3:138327519-138327569	SK-N-MC	brain:	n/a
17	chr3:138154620-138154670	AoSMC	blood vessel:	n/a
18	chr3:138311416-138311466	CMK	blood:	n/a
19	chr3:138328259-138328309	AoSMC	blood vessel:	n/a
20	chr3:138153278-138153328	K562	blood:	n/a
21	chr3:138160066-138160116	Caco-2	colon:	n/a
22	chr3:138153763-138153813	AG09309	skin:	n/a
23	chr3:138313011-138313061	SK-N-SH_RA	brain:	n/a
24	chr3:138154754-138154804	BE2_C	brain:	n/a
25	chr3:138312356-138312406	K562	blood:	n/a
26	chr3:138316954-138317004	K562	blood:	n/a
27	chr3:138170705-138170755	NB4	blood:	n/a
28	chr3:138313050-138313100	SK-N-SH	brain:	n/a
29	chr3:138327826-138327876	T-47D	breast:	n/a
30	chr3:138152902-138152952	H1-hESC	embryonic stem cell:	embryo
31	chr3:138160066-138160116	GM12892	blood:	n/a
32	chr3:138167430-138167480	HEK293	kidney:	embryo
33	chr3:138153832-138153882	Hepatocyte	liver:	n/a
34	chr3:138325023-138325073	HRE	kidney:	n/a
35	chr3:138311416-138311466	ProgFib	skin:	n/a
36	chr3:138196760-138196810	NHDF-neo	bronchial:	n/a
37	chr3:138313326-138313376	PFSK-1	brain:	n/a
38	chr3:138341122-138341172	HCF	heart:	n/a
39	chr3:138312634-138312684	K562	blood:	n/a
40	chr3:138153127-138153177	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:138174025-138174075	MCF10A-Er-Src	breast:	n/a
42	chr3:138153357-138153407	H1-hESC	embryonic stem cell:	embryo
43	chr3:138170705-138170755	MCF-7	breast:	n/a
44	chr3:138327519-138327569	NT2-D1	testis:	n/a
45	chr3:138172124-138172174	HMEC	breast:	n/a
46	chr3:138328334-138328384	NHBE	bronchial:	n/a
47	chr3:138154620-138154670	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:138153168-138153218	HUVEC	blood vessel:	n/a
49	chr3:138327728-138327778	NHDF-neo	bronchial:	n/a
50	chr3:138313166-138313216	MCF10A-Er-Src	breast:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:138311550..138315468-chr3:138324471..138329332,12	MCF-7	breast:
2	chr3:138335565..138337167-chr3:138338248..138339761,2	MCF-7	breast:
3	chr3:138228056..138229897-chr3:138230355..138233975,3	K562	blood:
4	chr3:138328930..138332756-chr3:138333514..138336895,4	K562	blood:
5	chr12:94235884..94236520-chr3:138149730..138150622,2	MCF-7	breast:
6	chr3:138186020..138187574-chr3:138189253..138191029,2	K562	blood:
7	chr3:138169355..138171117-chr3:138172389..138174530,2	MCF-7	breast:
8	chr3:138153249..138157225-chr3:138162199..138165931,3	K562	blood:
9	chr3:138143800..138147354-chr3:138150796..138153111,3	MCF-7	breast:
10	chr3:138326609..138328476-chr3:138335701..138339758,3	MCF-7	breast:
11	chr3:138152067..138153775-chr3:138169983..138172416,2	MCF-7	breast:
12	chr3:138169355..138171117-chr3:138172389..138174530,2	MCF-7	breast:
13	chr3:138334799..138337572-chr3:138340483..138342350,2	MCF-7	breast:
14	chr3:138308688..138311077-chr3:138311353..138314105,2	MCF-7	breast:
15	chr3:138153677..138156615-chr3:138182530..138184739,2	MCF-7	breast:
16	chr3:138327546..138328111-chr5:53813454..53813969,2	Hela-S3	cervix:
17	chr3:138308891..138310571-chr3:138313902..138316460,2	K562	blood:
18	chr3:138173174..138174919-chr3:138181076..138182864,2	MCF-7	breast:
19	chr3:138185730..138189738-chr3:138190908..138194397,4	MCF-7	breast:
20	chr3:138197115..138197897-chr3:138634489..138635059,2	MCF-7	breast:
21	chr3:138309156..138310798-chr3:138631884..138634871,2	MCF-7	breast:
22	chr3:138312690..138314858-chr3:138552284..138553853,2	K562	blood:
23	chr3:138136047..138137057-chr3:138178340..138179089,3	MCF-7	breast:
24	chr3:138065940..138068792-chr3:138150528..138153476,2	K562	blood:
25	chr3:138152375..138158526-chr3:138160154..138163422,8	MCF-7	breast:
26	chr20:3451237..3451899-chr3:138226141..138226668,2	MCF-7	breast:
27	chr3:137892183..137893942-chr3:138313140..138314743,2	K562	blood:
28	chr3:138222687..138224341-chr3:138230011..138232185,2	MCF-7	breast:
29	chr3:138310855..138313031-chr3:138326538..138329064,2	K562	blood:
30	chr3:138312928..138314956-chr3:138381208..138383898,2	K562	blood:
31	chr3:138320556..138325017-chr3:138325878..138328603,4	K562	blood:
32	chr3:138310314..138312413-chr3:138315463..138317379,2	MCF-7	breast:
33	chr3:138313052..138315422-chr3:138326245..138328582,4	MCF-7	breast:
34	chr14:105717555..105718335-chr3:138200943..138201661,2	MCF-7	breast:
35	chr3:138186886..138189284-chr3:138191772..138193552,2	K562	blood:
36	chr3:138147884..138150331-chr3:138154238..138156616,2	K562	blood:
37	chr19:18391696..18392343-chr3:138327465..138328374,2	Hela-S3	cervix:
38	chr3:138185730..138189738-chr3:138190908..138194397,4	MCF-7	breast:
39	chr2:197162739..197163660-chr3:138306734..138307658,2	MCF-7	breast:
40	chr3:138310855..138313031-chr3:138326538..138329064,2	K562	blood:
41	chr3:138311550..138315468-chr3:138324471..138329332,12	MCF-7	breast:
42	chr3:138328930..138332756-chr3:138333514..138336895,4	K562	blood:
43	chr3:138186020..138187574-chr3:138189253..138191029,2	K562	blood:
44	chr3:138335565..138337167-chr3:138338248..138339761,2	MCF-7	breast:
45	chr3:138326724..138329143-chr3:138336748..138338571,2	MCF-7	breast:
46	chr3:138305622..138307712-chr3:138326146..138327736,2	K562	blood:
47	chr3:137908958..137910626-chr3:138333368..138336043,2	K562	blood:
48	chr3:138159991..138162907-chr3:138171980..138174435,2	MCF-7	breast:
49	chr3:138306522..138308483-chr3:138311202..138313507,2	MCF-7	breast:
50	chr3:138180759..138183381-chr3:138313025..138314933,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ESYT3-3	chr3:138217403-138218541	ucscGeneNc_uc003erl_1
2	lnc-PIK3CB-1	chr3:138310708-138310798	NONHSAT092334
3	lnc-PIK3CB-1	chr3:138311823-138311922	NONHSAT092334
4	lnc-PIK3CB-1	chr3:138313040-138313096	NONHSAT092334
5	lnc-FAIM-2	chr3:138325237-138326255	NONHSAT092335

No data

Variant related genes	Relation type
ESYT3	TF binding region
CEP70	TF binding region
FAIM	TF binding region
ESYT3	CpG island
CEP70	CpG island
FAIM	CpG island
ENSG00000198931	chromatin interactions
ENSG00000051382	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000158186	chromatin interactions
ENSG00000114107	chromatin interactions
ENSG00000106299	chromatin interactions
ENSG00000088812	chromatin interactions
ENSG00000272686	chromatin interactions
ENSG00000173825	chromatin interactions
ENSG00000158234	chromatin interactions
ENSG00000138231	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000178996	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000158220	chromatin interactions

Extended variants
information (count: 7784 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:7784 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142691928	chr3:138148814-138148815	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs537939659	chr3:138148848-138148849	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142230778	chr3:138148897-138148898	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557479915	chr3:138148913-138148914	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs183571674	chr3:138148935-138148936	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs150080702	chr3:138148970-138148971	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138398820	chr3:138148986-138148987	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189083172	chr3:138149006-138149007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72974799	chr3:138149024-138149025	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs58924542	chr3:138149040-138149041	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs36086129	chr3:138149048-138149049	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562098732	chr3:138149068-138149069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530850015	chr3:138149097-138149098	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs139351589	chr3:138149131-138149132	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559385840	chr3:138149149-138149150	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564582283	chr3:138149196-138149197	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs1851701	chr3:138149199-138149200	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs143168674	chr3:138149200-138149201	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566578083	chr3:138149247-138149248	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147514132	chr3:138149264-138149265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs56283986	chr3:138149288-138149289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568834255	chr3:138149289-138149290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537454177	chr3:138149293-138149294	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557387688	chr3:138149304-138149305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558877107	chr3:138149368-138149369	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs577332354	chr3:138149423-138149424	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs148526223	chr3:138149547-138149548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531642434	chr3:138149574-138149575	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201347204	chr3:138149575-138149576	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200730048	chr3:138149601-138149602	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553127144	chr3:138149608-138149609	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs367788323	chr3:138149619-138149620	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542500385	chr3:138149626-138149627	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs56118112	chr3:138149682-138149683	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs552669242	chr3:138149734-138149735	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35198318	chr3:138149735-138149736	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs386398025	chr3:138149741-138149742	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575546494	chr3:138149744-138149745	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570193538	chr3:138149749-138149750	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs372292915	chr3:138149765-138149766	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564543719	chr3:138149775-138149776	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533444122	chr3:138149799-138149800	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567670497	chr3:138149814-138149815	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540767278	chr3:138149820-138149821	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375664944	chr3:138149835-138149836	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560288101	chr3:138149839-138149840	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187643978	chr3:138149849-138149850	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375428382	chr3:138149881-138149882	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs386666287	chr3:138149890-138149891	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150610222	chr3:138149891-138149892	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3968 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138148600-138149000	Enhancers	Fetal Heart	heart
2	chr3:138150200-138150600	Bivalent Enhancer	Fetal Muscle Leg	muscle
3	chr3:138150400-138150600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr3:138151800-138152000	Enhancers	Aorta	Aorta
5	chr3:138151800-138152200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:138152200-138152400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
7	chr3:138152200-138152400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:138152200-138152600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
9	chr3:138152200-138152600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:138152200-138152800	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:138152200-138153200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr3:138152200-138153200	Bivalent Enhancer	Fetal Stomach	stomach
13	chr3:138152200-138155000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
14	chr3:138152400-138153000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
15	chr3:138152400-138154800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:138152600-138152800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
17	chr3:138152600-138152800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:138152600-138152800	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr3:138152600-138152800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
20	chr3:138152600-138152800	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr3:138152600-138152800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr3:138152600-138152800	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
23	chr3:138152600-138152800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
24	chr3:138152600-138152800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
25	chr3:138152600-138152800	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
26	chr3:138152600-138152800	Bivalent/Poised TSS	NHDF-Ad	bronchial
27	chr3:138152600-138153000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
28	chr3:138152600-138153000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
29	chr3:138152600-138153000	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr3:138152600-138153000	Active TSS	Brain Anterior Caudate	brain
31	chr3:138152600-138153000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr3:138152600-138153000	Active TSS	Ovary	ovary
33	chr3:138152600-138153000	Active TSS	Right Ventricle	heart
34	chr3:138152600-138153000	Bivalent Enhancer	Thymus	Thymus
35	chr3:138152600-138153200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
36	chr3:138152600-138153200	Enhancers	Liver	Liver
37	chr3:138152600-138153200	Flanking Active TSS	Brain Hippocampus Middle	brain
38	chr3:138152600-138153200	Bivalent Enhancer	HUVEC	blood vessel
39	chr3:138152600-138153600	Bivalent/Poised TSS	Fetal Brain Female	brain
40	chr3:138152600-138153800	Bivalent Enhancer	Fetal Thymus	thymus
41	chr3:138152600-138154000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr3:138152600-138154600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr3:138152600-138154800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
44	chr3:138152600-138154800	Active TSS	Brain Angular Gyrus	brain
45	chr3:138152800-138153000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:138152800-138153000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
47	chr3:138152800-138153000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
48	chr3:138152800-138153000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
49	chr3:138152800-138153000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
50	chr3:138152800-138153000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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