Variant report

Variant	nsv876598
Chromosome Location	chr3:20242143-20970042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2869)
CpG islands
(count:611)
Chromatin interactive
region (count:186)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2869 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20722557-20722641	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
3	ARID3A	chr3:20914902-20915005	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:20949786-20949796	K562	blood:	n/a	n/a
5	ARID3A	chr3:20931033-20931041	K562	blood:	n/a	n/a
6	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
7	ARID3A	chr3:20630843-20631125	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:20902796-20903296	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:20267278-20267600	K562	blood:	n/a	n/a
11	ARID3A	chr3:20895434-20895683	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:20362800-20363279	K562	blood:	n/a	n/a
13	ARID3A	chr3:20371522-20371864	K562	blood:	n/a	n/a
14	ARID3A	chr3:20364750-20365312	K562	blood:	n/a	n/a
15	ARID3A	chr3:20361861-20362463	HepG2	liver:	n/a	n/a
16	ARID3A	chr3:20363620-20364094	K562	blood:	n/a	chr3:20363734-20363750
17	ARID3A	chr3:20931542-20931909	K562	blood:	n/a	n/a
18	ARID3A	chr3:20368591-20368761	K562	blood:	n/a	n/a
19	ARID3A	chr3:20946660-20947229	K562	blood:	n/a	n/a
20	ARID3A	chr3:20814162-20815382	HepG2	liver:	n/a	n/a
21	ARID3A	chr3:20366598-20367214	K562	blood:	n/a	n/a
22	ARID3A	chr3:20870357-20870611	HepG2	liver:	n/a	n/a
23	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
24	ARID3A	chr3:20894140-20894670	HepG2	liver:	n/a	n/a
25	ARID3A	chr3:20888276-20888579	HepG2	liver:	n/a	n/a
26	ARID3A	chr3:20553373-20553610	HepG2	liver:	n/a	n/a
27	ATF1	chr3:20366606-20366910	K562	blood:	n/a	n/a
28	ATF1	chr3:20346503-20346616	K562	blood:	n/a	n/a
29	ATF1	chr3:20946771-20947039	K562	blood:	n/a	n/a
30	ATF1	chr3:20931617-20932153	K562	blood:	n/a	n/a
31	ATF1	chr3:20521702-20521870	K562	blood:	n/a	n/a
32	ATF1	chr3:20710817-20710996	K562	blood:	n/a	n/a
33	ATF1	chr3:20364790-20365451	K562	blood:	n/a	n/a
34	ATF2	chr3:20288074-20288600	GM12878	blood:	n/a	n/a
35	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr3:20288131-20288515	GM12878	blood:	n/a	n/a
37	ATF3	chr3:20850445-20850672	K562	blood:	n/a	n/a
38	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
39	ATF3	chr3:20946684-20947097	K562	blood:	n/a	n/a
40	ATF3	chr3:20931588-20932045	K562	blood:	n/a	n/a
41	BACH1	chr3:20363669-20363903	K562	blood:	n/a	n/a
42	BACH1	chr3:20699095-20699443	K562	blood:	n/a	n/a
43	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
45	BACH1	chr3:20616608-20616882	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr3:20578833-20579051	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr3:20366536-20366578	K562	blood:	n/a	n/a
48	BACH1	chr3:20649604-20649855	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr3:20492146-20492486	K562	blood:	n/a	n/a
50	BACH1	chr3:20536253-20536368	H1-hESC	embryonic stem cell:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20589671-20589721	HIPEpiC	eye:	n/a
2	chr3:20589671-20589721	HIPEpiC	eye:	n/a
3	chr3:20448283-20448333	PrEC	prostate:	n/a
4	chr3:20321584-20321634	NHBE	bronchial:	n/a
5	chr3:20448283-20448333	SK-N-SH_RA	brain:	n/a
6	chr3:20575513-20575563	BE2_C	brain:	n/a
7	chr3:20589671-20589721	K562	blood:	n/a
8	chr3:20589671-20589721	HRPEpiC	eye:	n/a
9	chr3:20589671-20589721	GM19239	blood:	n/a
10	chr3:20371290-20371340	T-47D	breast:	n/a
11	chr3:20448283-20448333	GM12892	blood:	n/a
12	chr3:20887296-20887346	GM12878	blood:	n/a
13	chr3:20589760-20589810	K562	blood:	n/a
14	chr3:20575513-20575563	IMR90	lung:	fetal
15	chr3:20321584-20321634	HEEpiC	esophagus:	n/a
16	chr3:20589760-20589810	HRE	kidney:	n/a
17	chr3:20589760-20589810	HepG2	liver:	n/a
18	chr3:20418856-20418906	Hela-S3	cervix:	n/a
19	chr3:20412342-20412392	SK-N-SH_RA	brain:	n/a
20	chr3:20589671-20589721	Caco-2	colon:	n/a
21	chr3:20522301-20522351	GM06990	blood:	n/a
22	chr3:20589760-20589810	HMEC	breast:	n/a
23	chr3:20371290-20371340	NT2-D1	testis:	n/a
24	chr3:20575513-20575563	AoSMC	blood vessel:	n/a
25	chr3:20412342-20412392	A549	lung:	n/a
26	chr3:20448283-20448333	H1-hESC	embryonic stem cell:	embryo
27	chr3:20418856-20418906	H1-hESC	embryonic stem cell:	embryo
28	chr3:20575513-20575563	HCPEpiC	choroid plexus:	n/a
29	chr3:20589671-20589721	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:20522301-20522351	SAEC	small airway:	n/a
31	chr3:20589760-20589810	HRCEpiC	kidney:	n/a
32	chr3:20418856-20418906	NB4	blood:	n/a
33	chr3:20448283-20448333	HIPEpiC	eye:	n/a
34	chr3:20412342-20412392	GM12891	blood:	n/a
35	chr3:20321584-20321634	SAEC	small airway:	n/a
36	chr3:20371290-20371340	IMR90	lung:	fetal
37	chr3:20589671-20589721	HEEpiC	esophagus:	n/a
38	chr3:20412342-20412392	ovcar-3	ovarian:	n/a
39	chr3:20589760-20589810	GM06990	blood:	n/a
40	chr3:20589760-20589810	NHBE	bronchial:	n/a
41	chr3:20887296-20887346	NHBE	bronchial:	n/a
42	chr3:20589760-20589810	SK-N-MC	brain:	n/a
43	chr3:20589671-20589721	NH-A	brain:	n/a
44	chr3:20321584-20321634	ECC-1	luminal epithelium:	n/a
45	chr3:20371290-20371340	GM06990	blood:	n/a
46	chr3:20575513-20575563	HNPCEpiC	eye:	n/a
47	chr3:20589760-20589810	A549	lung:	n/a
48	chr3:20575513-20575563	T-47D	breast:	n/a
49	chr3:20522301-20522351	SK-N-SH_RA	brain:	n/a
50	chr3:20418856-20418906	BJ	skin:	n/a

(count:186 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
2	chr1:11967831..11969033-chr3:20886071..20887071,5	HCT-116	colon:
3	chr3:20255206..20257186-chr3:20272224..20273896,2	K562	blood:
4	chr3:20791529..20793078-chr3:20793887..20796565,3	K562	blood:
5	chr3:20267223..20267887-chr3:21592292..21593221,2	MCF-7	breast:
6	chr3:20952300..20954626-chr9:100195157..100197678,2	MCF-7	breast:
7	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
8	chr3:20618172..20620795-chr3:20622169..20624863,2	MCF-7	breast:
9	chr3:20884248..20889854-chr3:20892080..20895253,4	K562	blood:
10	chr3:20780166..20782816-chr3:20783082..20785519,2	K562	blood:
11	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
12	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
13	chr3:20875856..20878691-chr3:20885550..20887328,2	K562	blood:
14	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
15	chr3:20934835..20936645-chr3:20951174..20953297,2	K562	blood:
16	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
17	chr17:57920861..57923845-chr3:20581102..20583235,2	MCF-7	breast:
18	chr3:20266881..20267830-chr3:21935770..21936618,4	MCF-7	breast:
19	chr3:20876604..20878785-chr3:20879848..20882141,2	K562	blood:
20	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
21	chr3:20269133..20272394-chr3:20272728..20275710,3	K562	blood:
22	chr3:20884787..20886669-chr3:20993293..20995378,2	K562	blood:
23	chr3:20927362..20929640-chr3:20931820..20933882,3	K562	blood:
24	chr3:20618172..20620795-chr3:20622169..20624863,2	MCF-7	breast:
25	chr3:20881823..20883921-chr3:20890790..20893677,2	K562	blood:
26	chr3:20552973..20553911-chr3:20970672..20972125,8	MCF-7	breast:
27	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
28	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
29	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
30	chr3:20964849..20967779-chr3:20982374..20984223,2	MCF-7	breast:
31	chr3:20908678..20911215-chr3:20923449..20926169,2	K562	blood:
32	chr3:20369262..20370826-chr3:20371574..20373222,2	K562	blood:
33	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
34	chr3:20876604..20878785-chr3:20879848..20882141,2	K562	blood:
35	chr20:55749599..55750399-chr3:20381742..20382481,2	MCF-7	breast:
36	chr3:20881823..20883921-chr3:20890790..20893677,2	K562	blood:
37	chr3:20795079..20796913-chr3:20797062..20799579,3	MCF-7	breast:
38	chr3:20965735..20967990-chr3:20971658..20973714,2	K562	blood:
39	chr3:20800581..20802290-chr3:20809522..20812257,2	K562	blood:
40	chr3:20687019..20688591-chr3:20688596..20691199,2	K562	blood:
41	chr3:20691277..20693337-chr3:20693426..20695477,2	MCF-7	breast:
42	chr3:20864204..20867034-chr3:20867315..20869207,3	K562	blood:
43	chr3:20924826..20926791-chr3:20930314..20933043,2	K562	blood:
44	chr3:20931783..20933492-chr3:20955039..20957721,2	K562	blood:
45	chr3:20934088..20937595-chr3:20944729..20947553,4	K562	blood:
46	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
47	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
48	chr3:20801549..20804402-chr3:20814292..20816121,2	MCF-7	breast:
49	chr3:20931783..20933492-chr3:20955039..20957721,2	K562	blood:
50	chr3:20920030..20922787-chr3:20928844..20930529,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-6	chr3:20286533-20287951	NONHSAT088619
2	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
3	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1
4	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595
5	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595
6	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
7	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
8	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595
9	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622
10	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
11	lnc-KAT2B-8	chr3:20755529-20756407	NONHSAT088630
12	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
13	lnc-KAT2B-9	chr3:20947004-20947099	NONHSAT088631
14	lnc-KAT2B-8	chr3:20747491-20747580	NONHSAT088630
15	lnc-KAT2B-9	chr3:20931812-20931937	NONHSAT088631

No data

Variant related genes	Relation type
RNU6-815P	TF binding region
RNU6-822P	TF binding region
ENSG00000231304	TF binding region
ENSG00000261734	TF binding region
RNU6-815P	CpG island
RNU6-822P	CpG island
ENSG00000231304	CpG island
ENSG00000261734	CpG island
ENSG00000206807	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000252557	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000244560	chromatin interactions

Extended variants
information (count: 17021 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:17021 , 50 per page) page: 1 2 3 4 5 6 7 ... 341

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs951455	chr3:20242143-20242144	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147682850	chr3:20242175-20242176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140717178	chr3:20242201-20242202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183088609	chr3:20242267-20242268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186352079	chr3:20242268-20242269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191819890	chr3:20242275-20242276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112074500	chr3:20242276-20242277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11128941	chr3:20242385-20242386	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs183595754	chr3:20242403-20242404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377583992	chr3:20242405-20242406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144591994	chr3:20242435-20242436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11128942	chr3:20242454-20242455	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs372634363	chr3:20242490-20242491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539802697	chr3:20242493-20242494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111428295	chr3:20242494-20242495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570708001	chr3:20242528-20242529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147854649	chr3:20242562-20242563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140385928	chr3:20242585-20242586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574253180	chr3:20242628-20242629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75444301	chr3:20242636-20242637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557007441	chr3:20242651-20242652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13317534	chr3:20242668-20242669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73175302	chr3:20242724-20242725	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs540882795	chr3:20242731-20242732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546165594	chr3:20242802-20242803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115868506	chr3:20242817-20242818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573480824	chr3:20242860-20242861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540881468	chr3:20242863-20242864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568828702	chr3:20242877-20242878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529472189	chr3:20242882-20242883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551215927	chr3:20242896-20242897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563374012	chr3:20242903-20242904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550681910	chr3:20242973-20242974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564846741	chr3:20242978-20242979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552139702	chr3:20242987-20242988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570398855	chr3:20243003-20243004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5847046	chr3:20243010-20243011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113861398	chr3:20243020-20243021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397743888	chr3:20243024-20243025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs202030820	chr3:20243025-20243026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200376129	chr3:20243026-20243027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201558982	chr3:20243028-20243029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199570006	chr3:20243029-20243030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200214240	chr3:20243030-20243031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534327326	chr3:20243055-20243056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546455813	chr3:20243096-20243097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537941329	chr3:20243201-20243202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559165957	chr3:20243230-20243231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377725016	chr3:20243235-20243236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535250810	chr3:20243242-20243243	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20241800-20242400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:20241800-20242600	Enhancers	Fetal Stomach	stomach
3	chr3:20241800-20243400	Enhancers	Fetal Lung	lung
4	chr3:20241800-20243600	Enhancers	Ovary	ovary
5	chr3:20242600-20243000	Enhancers	Brain Anterior Caudate	brain
6	chr3:20242600-20243200	Weak transcription	Fetal Stomach	stomach
7	chr3:20243200-20243400	Enhancers	Fetal Stomach	stomach
8	chr3:20243600-20244000	Weak transcription	Ovary	ovary
9	chr3:20244000-20244200	Active TSS	Ovary	ovary
10	chr3:20244200-20244400	Flanking Active TSS	Ovary	ovary
11	chr3:20244400-20244600	Active TSS	Ovary	ovary
12	chr3:20244600-20246000	Enhancers	Ovary	ovary
13	chr3:20246000-20259000	Weak transcription	Ovary	ovary
14	chr3:20248600-20253800	Weak transcription	Aorta	Aorta
15	chr3:20259000-20259200	Enhancers	Ovary	ovary
16	chr3:20259200-20259600	Weak transcription	Ovary	ovary
17	chr3:20259600-20260000	Enhancers	Ovary	ovary
18	chr3:20259800-20260200	Enhancers	Fetal Stomach	stomach
19	chr3:20260200-20265000	Weak transcription	Fetal Stomach	stomach
20	chr3:20262600-20264000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:20262600-20264800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr3:20262600-20265600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr3:20262800-20265200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:20263200-20263400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr3:20263200-20263600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:20263200-20264800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:20263400-20263600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr3:20263400-20263800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr3:20263400-20264000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr3:20263400-20264200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:20263400-20264200	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:20263400-20264200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:20263400-20264400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr3:20263400-20264400	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr3:20263600-20263800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:20263600-20263800	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr3:20263600-20264200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr3:20263800-20264000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:20263800-20264200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr3:20264000-20264200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:20264000-20265000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr3:20264200-20264400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:20264200-20264600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:20264200-20265200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:20264200-20267600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr3:20264600-20265200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:20264800-20265200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr3:20264800-20265600	Enhancers	Adipose Nuclei	Adipose
49	chr3:20264800-20267000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:20265000-20265200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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