Variant report

Variant	nsv830090
Chromosome Location	chr4:141770494-141947764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1540)
CpG islands
(count:550)
Chromatin interactive
region (count:46)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1540 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:141805687-141805835	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:141782528-141782857	K562	blood:	n/a	n/a
3	ARID3A	chr4:141782538-141782877	HepG2	liver:	n/a	n/a
4	ATF3	chr4:141805696-141805854	K562	blood:	n/a	n/a
5	BATF	chr4:141851945-141852158	GM12878	blood:	n/a	n/a
6	BCLAF1	chr4:141772069-141772498	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:141805722-141805930	A549	lung:	n/a	n/a
8	BHLHE40	chr4:141805613-141805972	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:141904268-141904269	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:141805620-141805982	K562	blood:	n/a	n/a
11	BHLHE40	chr4:141805646-141805952	HepG2	liver:	n/a	n/a
12	CBX3	chr4:141800075-141800426	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:141873872-141874221	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:141889561-141889832	IMR90	lung:	n/a	chr4:141889702-141889715 chr4:141889703-141889714
15	CEBPB	chr4:141918032-141918169	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:141873925-141874164	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:141776810-141777036	A549	lung:	n/a	chr4:141776933-141776944
18	CEBPB	chr4:141927574-141927841	K562	blood:	n/a	chr4:141927712-141927723 chr4:141927741-141927754
19	CEBPB	chr4:141777610-141777797	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:141941372-141941572	HepG2	liver:	n/a	chr4:141941475-141941486
21	CEBPB	chr4:141933158-141933279	A549	lung:	n/a	n/a
22	CEBPB	chr4:141846656-141846937	IMR90	lung:	n/a	chr4:141846784-141846795 chr4:141846873-141846881
23	CEBPB	chr4:141776816-141777060	K562	blood:	n/a	chr4:141776933-141776944
24	CEBPB	chr4:141776804-141777052	HepG2	liver:	n/a	chr4:141776933-141776944
25	CEBPB	chr4:141927631-141927772	H1-hESC	embryonic stem cell:	n/a	chr4:141927712-141927723 chr4:141927741-141927754
26	CEBPB	chr4:141873908-141874139	A549	lung:	n/a	n/a
27	CEBPB	chr4:141776803-141777097	IMR90	lung:	n/a	chr4:141776933-141776944
28	CEBPB	chr4:141923680-141923769	A549	lung:	n/a	n/a
29	CEBPB	chr4:141874055-141874080	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:141836176-141836307	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:141834731-141834994	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:141927533-141927886	HepG2	liver:	n/a	chr4:141927712-141927723 chr4:141927741-141927754
33	CEBPB	chr4:141941361-141941595	IMR90	lung:	n/a	chr4:141941475-141941486
34	CEBPB	chr4:141889576-141889770	H1-hESC	embryonic stem cell:	n/a	chr4:141889702-141889715 chr4:141889703-141889714
35	CEBPB	chr4:141813504-141813643	HepG2	liver:	n/a	chr4:141813547-141813558
36	CEBPB	chr4:141884470-141884625	A549	lung:	n/a	n/a
37	CEBPB	chr4:141923474-141923910	IMR90	lung:	n/a	chr4:141923773-141923786
38	CEBPB	chr4:141889599-141889822	HepG2	liver:	n/a	chr4:141889702-141889715 chr4:141889703-141889714
39	CEBPB	chr4:141884482-141884601	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:141923545-141923688	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:141846749-141846819	K562	blood:	n/a	chr4:141846784-141846795
42	CEBPB	chr4:141927571-141927892	K562	blood:	n/a	chr4:141927712-141927723 chr4:141927741-141927754
43	CEBPB	chr4:141778291-141778593	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:141776893-141777003	Hela-S3	cervix:	n/a	chr4:141776933-141776944
45	CEBPB	chr4:141846665-141846919	A549	lung:	n/a	chr4:141846784-141846795 chr4:141846873-141846881
46	CEBPB	chr4:141873863-141874222	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr4:141927522-141927965	Hela-S3	cervix:	n/a	chr4:141927712-141927723 chr4:141927741-141927754
48	CEBPB	chr4:141927593-141927878	A549	lung:	n/a	chr4:141927712-141927723 chr4:141927741-141927754
49	CEBPB	chr4:141927549-141927885	IMR90	lung:	n/a	chr4:141927712-141927723 chr4:141927741-141927754
50	CEBPB	chr4:141846619-141846961	HepG2	liver:	n/a	chr4:141846784-141846795 chr4:141846873-141846881

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:141797676-141797726	Jurkat	blood:	n/a
2	chr4:141797676-141797726	Jurkat	blood:	n/a
3	chr4:141846078-141846128	LNCaP	prostate:	n/a
4	chr4:141859672-141859722	MCF10A-Er-Src	breast:	n/a
5	chr4:141923701-141923751	SK-N-SH	brain:	n/a
6	chr4:141877033-141877083	PFSK-1	brain:	n/a
7	chr4:141859672-141859722	MCF-7	breast:	n/a
8	chr4:141846078-141846128	AG04449	skin:	fetal
9	chr4:141923701-141923751	MCF-7	breast:	n/a
10	chr4:141865108-141865158	HRE	kidney:	n/a
11	chr4:141859672-141859722	T-47D	breast:	n/a
12	chr4:141859672-141859722	HCM	heart:	n/a
13	chr4:141846078-141846128	AG09309	skin:	n/a
14	chr4:141846078-141846128	HAEpiC	amniotic membrane:	n/a
15	chr4:141787753-141787803	HRPEpiC	eye:	n/a
16	chr4:141846078-141846128	NHDF-neo	bronchial:	n/a
17	chr4:141859472-141859522	HRE	kidney:	n/a
18	chr4:141846078-141846128	PFSK-1	brain:	n/a
19	chr4:141859672-141859722	Hela-S3	cervix:	n/a
20	chr4:141923701-141923751	AoSMC	blood vessel:	n/a
21	chr4:141846078-141846128	NT2-D1	testis:	n/a
22	chr4:141859672-141859722	Hepatocyte	liver:	n/a
23	chr4:141923701-141923751	HNPCEpiC	eye:	n/a
24	chr4:141859472-141859522	GM06990	blood:	n/a
25	chr4:141877033-141877083	PrEC	prostate:	n/a
26	chr4:141877033-141877083	SKMC	muscle:	n/a
27	chr4:141923701-141923751	Jurkat	blood:	n/a
28	chr4:141942745-141942795	BE2_C	brain:	n/a
29	chr4:141787753-141787803	GM12891	blood:	n/a
30	chr4:141859472-141859522	AoSMC	blood vessel:	n/a
31	chr4:141797676-141797726	Hela-S3	cervix:	n/a
32	chr4:141942745-141942795	AG10803	skin:	n/a
33	chr4:141859672-141859722	PANC-1	pancreas:	n/a
34	chr4:141787753-141787803	CMK	blood:	n/a
35	chr4:141846078-141846128	SK-N-SH	brain:	n/a
36	chr4:141942745-141942795	HAEpiC	amniotic membrane:	n/a
37	chr4:141797676-141797726	HepG2	liver:	n/a
38	chr4:141797676-141797726	GM19239	blood:	n/a
39	chr4:141859672-141859722	NHBE	bronchial:	n/a
40	chr4:141859672-141859722	AoSMC	blood vessel:	n/a
41	chr4:141859472-141859522	T-47D	breast:	n/a
42	chr4:141942745-141942795	AoSMC	blood vessel:	n/a
43	chr4:141787753-141787803	NH-A	brain:	n/a
44	chr4:141797676-141797726	NHBE	bronchial:	n/a
45	chr4:141859672-141859722	GM06990	blood:	n/a
46	chr4:141923701-141923751	HRE	kidney:	n/a
47	chr4:141846078-141846128	GM06990	blood:	n/a
48	chr4:141797676-141797726	HRCEpiC	kidney:	n/a
49	chr4:141942745-141942795	HIPEpiC	eye:	n/a
50	chr4:141877033-141877083	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:104822380..104823255-chr4:141779931..141780635,2	MCF-7	breast:
2	chr4:141281034..141281686-chr4:141804229..141805061,2	MCF-7	breast:
3	chr4:141679363..141682261-chr4:141769305..141772055,2	MCF-7	breast:
4	chr4:141787778..141789643-chr4:141796789..141798752,2	MCF-7	breast:
5	chr4:141888929..141891016-chr4:141891201..141893150,2	K562	blood:
6	chr4:141782326..141783157-chr4:141884203..141884946,4	MCF-7	breast:
7	chr4:141635808..141637655-chr4:141769565..141771761,2	MCF-7	breast:
8	chr4:141782379..141783151-chr4:141805302..141805804,2	MCF-7	breast:
9	chr4:141783860..141784596-chr4:141805289..141806021,2	K562	blood:
10	chr4:141787778..141789643-chr4:141796789..141798752,2	MCF-7	breast:
11	chr4:141280975..141281570-chr4:141771932..141772838,2	MCF-7	breast:
12	chr4:141280643..141281602-chr4:141805509..141806288,3	MCF-7	breast:
13	chr4:141530860..141531726-chr4:141771963..141772864,3	K562	blood:
14	chr4:141782326..141783157-chr4:141884203..141884946,4	MCF-7	breast:
15	chr4:141779548..141781738-chr4:141783078..141785466,2	K562	blood:
16	chr4:141770788..141774316-chr4:141774374..141777547,3	K562	blood:
17	chr4:141866516..141868304-chr4:141870029..141871688,2	K562	blood:
18	chr4:141945582..141947748-chr4:141959113..141961533,2	K562	blood:
19	chr4:141649186..141651742-chr4:141777396..141779181,2	MCF-7	breast:
20	chr4:141562580..141565413-chr4:141772121..141774639,2	MCF-7	breast:
21	chr4:141578881..141581236-chr4:141769794..141771706,2	MCF-7	breast:
22	chr4:141557512..141560350-chr4:141769351..141771473,2	MCF-7	breast:
23	chr4:141281391..141281921-chr4:141771667..141772400,2	K562	blood:
24	chr4:141857760..141859447-chr4:141874857..141876675,2	K562	blood:
25	chr4:141782262..141783195-chr4:142054318..142055590,4	MCF-7	breast:
26	chr4:141770788..141774316-chr4:141774374..141777547,3	K562	blood:
27	chr4:141781276..141784169-chr4:142052132..142055667,4	MCF-7	breast:
28	chr4:141782379..141783151-chr4:141805302..141805804,2	MCF-7	breast:
29	chr4:141858527..141861200-chr4:141868423..141870294,2	K562	blood:
30	chr4:141858527..141861200-chr4:141868423..141870294,2	K562	blood:
31	chr4:141866516..141868304-chr4:141870029..141871688,2	K562	blood:
32	chr4:139951894..139952451-chr4:141771635..141772412,2	K562	blood:
33	chr4:141870898..141873805-chr4:142207109..142209928,2	K562	blood:
34	chr4:141942691..141944577-chr4:141956813..141958772,2	MCF-7	breast:
35	chr4:141251642..141252163-chr4:141771893..141772416,2	K562	blood:
36	chr4:141857760..141859447-chr4:141874857..141876675,2	K562	blood:
37	chr4:141764448..141767171-chr4:141769164..141770908,2	MCF-7	breast:
38	chr4:141783860..141784596-chr4:141805289..141806021,2	K562	blood:
39	chr4:141864985..141866884-chr4:141889124..141891392,2	K562	blood:
40	chr4:141781761..141783219-chr4:142054304..142055190,6	MCF-7	breast:
41	chr4:141782299..141783199-chr4:142054253..142055164,4	K562	blood:
42	chr4:141676176..141678106-chr4:141769138..141773512,3	MCF-7	breast:
43	chr4:141779548..141781738-chr4:141783078..141785466,2	K562	blood:
44	chr4:141865472..141867411-chr4:142030563..142032115,2	MCF-7	breast:
45	chr4:141559086..141559669-chr4:141772132..141772745,2	MCF-7	breast:
46	chr4:141864985..141866884-chr4:141889124..141891392,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF150-4	chr4:141782330-141782401	NONHSAT098514
2	lnc-RNF150-4	chr4:141783599-141785342	NONHSAT098514

No data

Variant related genes	Relation type
RNF150	TF binding region
RNF150	CpG island
ENSG00000109436	chromatin interactions
ENSG00000170153	chromatin interactions
ENSG00000273472	chromatin interactions

Extended variants
information (count: 6759 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:6759 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188004025	chr4:141770508-141770509	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs6836292	chr4:141770572-141770573	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs193011210	chr4:141770688-141770689	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs184314658	chr4:141770689-141770690	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs150135828	chr4:141770690-141770691	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549118964	chr4:141770717-141770718	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs62346604	chr4:141770736-141770737	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574407731	chr4:141770747-141770748	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544180040	chr4:141770759-141770760	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs556204327	chr4:141770795-141770796	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs188005870	chr4:141770796-141770797	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs372706781	chr4:141770839-141770840	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560222345	chr4:141770851-141770852	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs528366109	chr4:141770855-141770856	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs542825995	chr4:141770881-141770882	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547044789	chr4:141770888-141770889	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs571651757	chr4:141770955-141770956	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs193060646	chr4:141770987-141770988	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs531507777	chr4:141770995-141770996	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564310021	chr4:141771015-141771016	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550522400	chr4:141771018-141771019	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149302705	chr4:141771122-141771123	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs184783460	chr4:141771138-141771139	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs551565362	chr4:141771139-141771140	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116462483	chr4:141771220-141771221	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs115943620	chr4:141771281-141771282	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549601147	chr4:141771330-141771331	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs76983297	chr4:141771341-141771342	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs188798555	chr4:141771343-141771344	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs538528892	chr4:141771346-141771347	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs557178199	chr4:141771414-141771415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs556944835	chr4:141771448-141771449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs377340824	chr4:141771494-141771495	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181574107	chr4:141771546-141771547	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538663722	chr4:141771564-141771565	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs144576376	chr4:141771676-141771677	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs199689691	chr4:141771709-141771710	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs78877852	chr4:141771715-141771716	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374724826	chr4:141771716-141771717	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572129591	chr4:141771717-141771718	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113516671	chr4:141771720-141771721	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376859032	chr4:141771766-141771767	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs542369397	chr4:141771778-141771779	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs536462705	chr4:141771789-141771790	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs560760418	chr4:141771816-141771817	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575875153	chr4:141771834-141771835	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543289042	chr4:141771836-141771837	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs115419467	chr4:141771882-141771883	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs533137154	chr4:141771890-141771891	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs147630687	chr4:141771900-141771901	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Thoracic aortic aneurysm	21092924	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
Prostate cancer	18632612	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:141770200-141770600	Enhancers	Primary B cells from cord blood	blood
2	chr4:141770600-141771200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:141770600-141771200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr4:141770600-141772400	Enhancers	Primary B cells from peripheral blood	blood
5	chr4:141770800-141771000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:141770800-141771200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr4:141771000-141771200	Enhancers	Fetal Lung	lung
8	chr4:141771200-141771600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr4:141771600-141772400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr4:141772000-141772400	Enhancers	GM12878-XiMat	blood
11	chr4:141772000-141772400	Enhancers	HepG2	liver
12	chr4:141774800-141776000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:141775200-141775600	Enhancers	Stomach Smooth Muscle	stomach
14	chr4:141775200-141775800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:141775400-141775800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:141775400-141776400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:141775400-141778200	Enhancers	Fetal Muscle Leg	muscle
18	chr4:141775600-141775800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:141775600-141776000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr4:141775800-141785000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:141775800-141787000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:141776000-141776200	Enhancers	Stomach Smooth Muscle	stomach
23	chr4:141776000-141777600	Enhancers	Fetal Muscle Trunk	muscle
24	chr4:141776000-141777800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:141776000-141778000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:141776200-141777200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr4:141776400-141777600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:141776400-141777800	Enhancers	NHEK	skin
29	chr4:141776400-141778000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:141776600-141777800	Enhancers	HMEC	breast
31	chr4:141776600-141780200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:141776800-141777000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:141776800-141778000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:141776800-141778800	Enhancers	Fetal Heart	heart
35	chr4:141777000-141780200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:141777200-141777400	Enhancers	Right Atrium	heart
37	chr4:141777200-141777600	Active TSS	Stomach Smooth Muscle	stomach
38	chr4:141777200-141777800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:141777200-141778000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr4:141777200-141778000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:141777200-141778400	Enhancers	Fetal Stomach	stomach
42	chr4:141777200-141778400	Enhancers	Left Ventricle	heart
43	chr4:141777200-141778400	Enhancers	Psoas Muscle	Psoas
44	chr4:141777200-141780800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr4:141777400-141778200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:141777400-141778200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:141777400-141778200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:141777400-141778200	Enhancers	HSMMtube	muscle
49	chr4:141777400-141778400	Enhancers	Colon Smooth Muscle	Colon
50	chr4:141777400-141778400	Enhancers	Fetal Lung	lung

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