Variant report

Variant	esv1829107
Chromosome Location	chr3:20322019-20391205
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:602)
CpG islands
(count:63)
Chromatin interactive
region (count:50)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:602 , 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	ARID3A	chr3:20366598-20367214	K562	blood:	n/a	n/a
2	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
4	ARID3A	chr3:20361861-20362463	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:20362800-20363279	K562	blood:	n/a	n/a
6	ARID3A	chr3:20371522-20371864	K562	blood:	n/a	n/a
7	ARID3A	chr3:20368591-20368761	K562	blood:	n/a	n/a
8	ARID3A	chr3:20364750-20365312	K562	blood:	n/a	n/a
9	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
10	ARID3A	chr3:20363620-20364094	K562	blood:	n/a	chr3:20363734-20363750
11	ATF1	chr3:20346503-20346616	K562	blood:	n/a	n/a
12	ATF1	chr3:20364790-20365451	K562	blood:	n/a	n/a
13	ATF1	chr3:20366606-20366910	K562	blood:	n/a	n/a
14	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:20363669-20363903	K562	blood:	n/a	n/a
16	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
17	BACH1	chr3:20366536-20366578	K562	blood:	n/a	n/a
18	BCL11A	chr3:20371437-20371693	H1-hESC	embryonic stem cell:	n/a	n/a
19	BHLHE40	chr3:20366210-20366396	K562	blood:	n/a	n/a
20	BHLHE40	chr3:20364697-20365365	K562	blood:	n/a	n/a
21	BHLHE40	chr3:20355407-20355580	A549	lung:	n/a	n/a
22	BHLHE40	chr3:20361903-20362390	HepG2	liver:	n/a	n/a
23	BHLHE40	chr3:20381816-20382255	K562	blood:	n/a	n/a
24	BHLHE40	chr3:20371536-20371904	K562	blood:	n/a	n/a
25	BRCA1	chr3:20381852-20382113	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr3:20324344-20324598	K562	blood:	n/a	n/a
27	CBX3	chr3:20366551-20367349	K562	blood:	n/a	n/a
28	CBX3	chr3:20324264-20324647	K562	blood:	n/a	n/a
29	CBX3	chr3:20364770-20365367	K562	blood:	n/a	n/a
30	CBX3	chr3:20347694-20347925	K562	blood:	n/a	n/a
31	CBX3	chr3:20346385-20346769	K562	blood:	n/a	n/a
32	CBX3	chr3:20347626-20347963	K562	blood:	n/a	n/a
33	CCNT2	chr3:20371431-20371945	K562	blood:	n/a	n/a
34	CCNT2	chr3:20361414-20361646	K562	blood:	n/a	n/a
35	CCNT2	chr3:20364768-20365575	K562	blood:	n/a	n/a
36	CCNT2	chr3:20372976-20373098	K562	blood:	n/a	n/a
37	CCNT2	chr3:20366682-20366882	K562	blood:	n/a	n/a
38	CCNT2	chr3:20362758-20363417	K562	blood:	n/a	chr3:20363078-20363098
39	CEBPB	chr3:20369435-20369698	K562	blood:	n/a	chr3:20369583-20369594
40	CEBPB	chr3:20381803-20382270	K562	blood:	n/a	n/a
41	CEBPB	chr3:20356761-20356776	K562	blood:	n/a	n/a
42	CEBPB	chr3:20364589-20365397	K562	blood:	n/a	chr3:20364637-20364646 chr3:20364637-20364648 chr3:20364966-20364977
43	CEBPB	chr3:20339706-20339888	K562	blood:	n/a	n/a
44	CEBPB	chr3:20369432-20369715	Hela-S3	cervix:	n/a	chr3:20369583-20369594
45	CEBPB	chr3:20325107-20325384	HepG2	liver:	n/a	chr3:20325251-20325264 chr3:20325252-20325263 chr3:20325116-20325127 chr3:20325251-20325262 chr3:20325251-20325264 chr3:20325251-20325264
46	CEBPB	chr3:20381826-20382192	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:20325166-20325366	K562	blood:	n/a	chr3:20325251-20325264 chr3:20325252-20325263 chr3:20325251-20325262 chr3:20325251-20325264 chr3:20325251-20325264
48	CEBPB	chr3:20364787-20365122	K562	blood:	n/a	chr3:20364966-20364977
49	CEBPB	chr3:20348990-20349167	K562	blood:	n/a	chr3:20349081-20349092 chr3:20349082-20349091 chr3:20349080-20349093
50	CEBPB	chr3:20363703-20363988	K562	blood:	n/a	n/a

(count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20371290-20371340	SK-N-SH	brain:	n/a
2	chr3:20371290-20371340	Hepatocyte	liver:	n/a
3	chr3:20371290-20371340	SK-N-SH	brain:	n/a
4	chr3:20371290-20371340	Hepatocyte	liver:	n/a
5	chr3:20371290-20371340	K562	blood:	n/a
6	chr3:20371290-20371340	CMK	blood:	n/a
7	chr3:20371290-20371340	LNCaP	prostate:	n/a
8	chr3:20371290-20371340	HRCEpiC	kidney:	n/a
9	chr3:20371290-20371340	HCM	heart:	n/a
10	chr3:20371290-20371340	HEK293	kidney:	embryo
11	chr3:20371290-20371340	ECC-1	luminal epithelium:	n/a
12	chr3:20371290-20371340	HNPCEpiC	eye:	n/a
13	chr3:20371290-20371340	AG09309	skin:	n/a
14	chr3:20371290-20371340	HL-60	blood:	n/a
15	chr3:20371290-20371340	PFSK-1	brain:	n/a
16	chr3:20371290-20371340	Hela-S3	cervix:	n/a
17	chr3:20371290-20371340	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:20371290-20371340	AG09319	gingival:	n/a
19	chr3:20371290-20371340	PrEC	prostate:	n/a
20	chr3:20371290-20371340	SAEC	small airway:	n/a
21	chr3:20371290-20371340	AG10803	skin:	n/a
22	chr3:20371290-20371340	HMEC	breast:	n/a
23	chr3:20371290-20371340	GM06990	blood:	n/a
24	chr3:20371290-20371340	HRE	kidney:	n/a
25	chr3:20371290-20371340	HCT-116	colon:	n/a
26	chr3:20371290-20371340	HEEpiC	esophagus:	n/a
27	chr3:20371290-20371340	HCPEpiC	choroid plexus:	n/a
28	chr3:20371290-20371340	A549	lung:	n/a
29	chr3:20371290-20371340	GM12892	blood:	n/a
30	chr3:20371290-20371340	SKMC	muscle:	n/a
31	chr3:20371290-20371340	ovcar-3	ovarian:	n/a
32	chr3:20371290-20371340	HUVEC	blood vessel:	n/a
33	chr3:20371290-20371340	PANC-1	pancreas:	n/a
34	chr3:20371290-20371340	AG04450	lung:	fetal
35	chr3:20371290-20371340	NH-A	brain:	n/a
36	chr3:20371290-20371340	BJ	skin:	n/a
37	chr3:20371290-20371340	U87	brain:	n/a
38	chr3:20371290-20371340	HCF	heart:	n/a
39	chr3:20371290-20371340	HIPEpiC	eye:	n/a
40	chr3:20371290-20371340	NB4	blood:	n/a
41	chr3:20371290-20371340	HAEpiC	amniotic membrane:	n/a
42	chr3:20371290-20371340	GM12891	blood:	n/a
43	chr3:20371290-20371340	NHBE	bronchial:	n/a
44	chr3:20371290-20371340	Caco-2	colon:	n/a
45	chr3:20371290-20371340	IMR90	lung:	fetal
46	chr3:20371290-20371340	GM12878	blood:	n/a
47	chr3:20371290-20371340	AoSMC	blood vessel:	n/a
48	chr3:20371290-20371340	NHDF-neo	bronchial:	n/a
49	chr3:20371290-20371340	SK-N-MC	brain:	n/a
50	chr3:20371290-20371340	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
2	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
3	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
4	chr3:20365682..20367813-chr3:20369993..20373801,3	K562	blood:
5	chr3:20378280..20380658-chr3:21571258..21574044,2	K562	blood:
6	chr3:20381671..20382483-chr3:21592493..21593315,3	MCF-7	breast:
7	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
8	chr3:20369262..20370826-chr3:20371574..20373222,2	K562	blood:
9	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
10	chr3:20363426..20365605-chr3:20367558..20369154,2	K562	blood:
11	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
12	chr20:55749599..55750399-chr3:20381742..20382481,2	MCF-7	breast:
13	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
14	chr3:20225982..20227551-chr3:20349845..20352725,2	K562	blood:
15	chr3:20365682..20367813-chr3:20369993..20373801,3	K562	blood:
16	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
17	chr3:20358544..20361265-chr3:20365566..20368705,3	K562	blood:
18	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
19	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
20	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
21	chr3:20358544..20361265-chr3:20365566..20368705,3	K562	blood:
22	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
23	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
24	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
25	chr3:20361855..20364563-chr3:20364654..20366618,2	K562	blood:
26	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
27	chr3:20381636..20382451-chr3:20971371..20972187,4	MCF-7	breast:
28	chr3:20248922..20251335-chr3:20323167..20325698,2	K562	blood:
29	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
30	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
31	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
32	chr3:20358467..20362257-chr3:20366935..20370675,4	K562	blood:
33	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
34	chr3:20363426..20365605-chr3:20367558..20369154,2	K562	blood:
35	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
36	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
37	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
38	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
39	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
40	chr3:20352341..20352841-chr6:144261197..144261734,2	MCF-7	breast:
41	chr3:20358467..20362257-chr3:20366935..20370675,4	K562	blood:
42	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
43	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
44	chr3:20381763..20382471-chr3:21525223..21526354,4	MCF-7	breast:
45	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
46	chr3:20369262..20370826-chr3:20371574..20373222,2	K562	blood:
47	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
48	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
49	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
50	chr3:20361855..20364563-chr3:20364654..20366618,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
2	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
3	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595
4	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
5	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
6	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622
7	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595
8	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595

No data

Variant related genes	Relation type
ENSG00000231304	TF binding region
ENSG00000231304	CpG island

Extended variants
information (count: 2322 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11713618	chr3:20322019-20322020	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546539116	chr3:20322035-20322036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568273129	chr3:20322042-20322043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535693115	chr3:20322066-20322067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550456545	chr3:20322067-20322068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7616513	chr3:20322069-20322070	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs62243482	chr3:20322119-20322120	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs76070818	chr3:20322169-20322170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573260772	chr3:20322173-20322174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533956583	chr3:20322206-20322207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs193204368	chr3:20322212-20322213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550325367	chr3:20322216-20322217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138432324	chr3:20322239-20322240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563168967	chr3:20322252-20322253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578231142	chr3:20322341-20322342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372397540	chr3:20322355-20322356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545587219	chr3:20322356-20322357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547557406	chr3:20322366-20322367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185101524	chr3:20322390-20322391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546280847	chr3:20322400-20322401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188247812	chr3:20322416-20322417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528873006	chr3:20322423-20322424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560963052	chr3:20322426-20322427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180991334	chr3:20322447-20322448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568790430	chr3:20322515-20322516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556789326	chr3:20322521-20322522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529660821	chr3:20322542-20322543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564011637	chr3:20322551-20322552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113824218	chr3:20322552-20322553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551129052	chr3:20322553-20322554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79334414	chr3:20322556-20322557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534254855	chr3:20322587-20322588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185612479	chr3:20322600-20322601	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs567694637	chr3:20322636-20322637	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79911590	chr3:20322718-20322719	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532410322	chr3:20322723-20322724	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556916138	chr3:20322738-20322739	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62243483	chr3:20322792-20322793	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs77143329	chr3:20322822-20322823	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs143264064	chr3:20322841-20322842	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs148300714	chr3:20322842-20322843	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs114472199	chr3:20322857-20322858	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs189738255	chr3:20322865-20322866	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs528911889	chr3:20322881-20322882	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs542547753	chr3:20322883-20322884	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs369076660	chr3:20322918-20322919	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs543777722	chr3:20322921-20322922	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs562460000	chr3:20322960-20322961	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs533019029	chr3:20322963-20322964	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs141394855	chr3:20322991-20322992	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20317600-20329000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:20320400-20322400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:20320400-20322600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:20320800-20322200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:20321600-20322200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:20321600-20322200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr3:20321600-20322200	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr3:20321600-20322200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr3:20321600-20322400	Enhancers	Primary B cells from peripheral blood	blood
10	chr3:20321600-20322400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr3:20321800-20322200	Enhancers	Primary T cells fromperipheralblood	blood
12	chr3:20322000-20329800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:20322200-20322600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:20322200-20322600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr3:20322600-20322800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:20322600-20325800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:20322800-20323000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:20324000-20324800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:20325600-20325800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
20	chr3:20325600-20325800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr3:20325800-20330200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr3:20326200-20331000	Weak transcription	Pancreas	Pancrea
23	chr3:20327400-20331000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:20328800-20331200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
25	chr3:20329000-20329800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
26	chr3:20329000-20330200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
27	chr3:20329200-20329600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
28	chr3:20331000-20331200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:20331000-20331200	ZNF genes & repeats	Pancreas	Pancrea
30	chr3:20336600-20337000	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
31	chr3:20337000-20344800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr3:20344000-20344800	Enhancers	Fetal Heart	heart
33	chr3:20344200-20345000	Enhancers	Fetal Brain Male	brain
34	chr3:20347000-20347200	Active TSS	K562	blood
35	chr3:20347200-20347400	Flanking Active TSS	K562	blood
36	chr3:20347400-20347800	Enhancers	K562	blood
37	chr3:20349000-20349400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr3:20350600-20351200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:20351200-20351800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr3:20351200-20353400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr3:20351600-20353000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:20351800-20352600	Enhancers	Adipose Nuclei	Adipose
43	chr3:20351800-20352800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:20352200-20352800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr3:20352800-20357000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:20352800-20357600	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr3:20353400-20357800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:20353800-20354000	Enhancers	Aorta	Aorta
49	chr3:20354000-20381800	Weak transcription	Aorta	Aorta
50	chr3:20357000-20358800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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