Variant report

Variant	nsv1011882
Chromosome Location	chr4:88363959-88402477
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:88386953-88387278	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:88386974-88387246	K562	blood:	n/a	n/a
3	BATF	chr4:88390556-88390793	GM12878	blood:	n/a	chr4:88390709-88390720
4	BRCA1	chr4:88382429-88382828	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr4:88401998-88402198	K562	blood:	n/a	n/a
6	CEBPB	chr4:88382327-88382857	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr4:88372857-88372993	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:88375347-88375569	HepG2	liver:	n/a	chr4:88375416-88375427
9	CEBPB	chr4:88371825-88371994	HepG2	liver:	n/a	chr4:88371897-88371908
10	CEBPB	chr4:88397592-88397901	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr4:88382425-88382795	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr4:88387020-88387170	GM12865	blood:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
13	CTCF	chr4:88372800-88372950	HPF	lung:	n/a	n/a
14	CTCF	chr4:88387060-88387210	HVMF	connective:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
15	CTCF	chr4:88386940-88387090	RPTEC	kidney:	n/a	n/a
16	CTCF	chr4:88386995-88387200	Hela-S3	cervix:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
17	CTCF	chr4:88386996-88387151	SK-N-SH_RA	brain:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
18	CTCF	chr4:88387260-88387410	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr4:88387000-88387209	Kidney_OC	kidney:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
20	CTCF	chr4:88386885-88387227	ECC-1	luminal epithelium:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
21	CTCF	chr4:88372820-88372970	AG04449	skin:	n/a	n/a
22	CTCF	chr4:88387220-88387370	GM12866	blood:	n/a	n/a
23	CTCF	chr4:88387060-88387210	BE2_C	brain:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
24	CTCF	chr4:88372700-88372850	HAc	cerebellar:	n/a	n/a
25	CTCF	chr4:88387000-88387150	NHDF-neo	bronchial:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
26	CTCF	chr4:88386720-88386870	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr4:88387000-88387150	K562	blood:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
28	CTCF	chr4:88387327-88387429	GM13977	blood:	n/a	n/a
29	CTCF	chr4:88372766-88372926	HepG2	liver:	n/a	n/a
30	CTCF	chr4:88372800-88372950	AG10803	skin:	n/a	n/a
31	CTCF	chr4:88387240-88387390	GM12875	blood:	n/a	n/a
32	CTCF	chr4:88387020-88387170	HMF	breast:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
33	CTCF	chr4:88386686-88387592	SK-N-SH	brain:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
34	CTCF	chr4:88387040-88387190	HCPEpiC	choroid plexus:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
35	CTCF	chr4:88387200-88387350	SAEC	small airway:	n/a	n/a
36	CTCF	chr4:88386923-88387258	A549	lung:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
37	CTCF	chr4:88387280-88387430	Caco-2	colon:	n/a	n/a
38	CTCF	chr4:88386983-88387206	GM12878	blood:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
39	CTCF	chr4:88386979-88387215	Pancreas_OC	pancreas:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
40	CTCF	chr4:88372840-88372990	HCFaa	heart:	n/a	n/a
41	CTCF	chr4:88387020-88387170	HEEpiC	esophagus:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
42	CTCF	chr4:88387100-88387250	GM12868	blood:	n/a	n/a
43	CTCF	chr4:88372786-88372986	K562	blood:	n/a	n/a
44	CTCF	chr4:88372820-88372970	HMF	breast:	n/a	n/a
45	CTCF	chr4:88387336-88387346	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr4:88387299-88387322	Fibrobl	skin:	n/a	n/a
47	CTCF	chr4:88372819-88372937	HepG2	liver:	n/a	n/a
48	CTCF	chr4:88372780-88372930	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr4:88387005-88387192	LNCaP	prostate:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112
50	CTCF	chr4:88387060-88387210	GM12867	blood:	n/a	chr4:88387097-88387110 chr4:88387090-88387111 chr4:88387098-88387108 chr4:88387095-88387113 chr4:88387096-88387112

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88379316-88379366	IMR90	lung:	fetal
2	chr4:88379316-88379366	AG09319	gingival:	n/a
3	chr4:88379316-88379366	GM12878	blood:	n/a
4	chr4:88379316-88379366	HEEpiC	esophagus:	n/a
5	chr4:88379316-88379366	MCF-7	breast:	n/a
6	chr4:88364394-88364444	RPTEC	kidney:	n/a
7	chr4:88364394-88364444	A549	lung:	n/a
8	chr4:88379316-88379366	AoSMC	blood vessel:	n/a
9	chr4:88364394-88364444	GM12878	blood:	n/a
10	chr4:88364394-88364444	HRE	kidney:	n/a
11	chr4:88379316-88379366	NH-A	brain:	n/a
12	chr4:88379316-88379366	HNPCEpiC	eye:	n/a
13	chr4:88364394-88364444	MCF10A-Er-Src	breast:	n/a
14	chr4:88364394-88364444	HCF	heart:	n/a
15	chr4:88364394-88364444	ProgFib	skin:	n/a
16	chr4:88364394-88364444	HCPEpiC	choroid plexus:	n/a
17	chr4:88379316-88379366	HAEpiC	amniotic membrane:	n/a
18	chr4:88364394-88364444	BE2_C	brain:	n/a
19	chr4:88379316-88379366	K562	blood:	n/a
20	chr4:88379316-88379366	NB4	blood:	n/a
21	chr4:88364394-88364444	SK-N-MC	brain:	n/a
22	chr4:88379316-88379366	ProgFib	skin:	n/a
23	chr4:88379316-88379366	GM19239	blood:	n/a
24	chr4:88379316-88379366	SK-N-MC	brain:	n/a
25	chr4:88379316-88379366	AG10803	skin:	n/a
26	chr4:88364394-88364444	HEEpiC	esophagus:	n/a
27	chr4:88364394-88364444	SK-N-SH_RA	brain:	n/a
28	chr4:88379316-88379366	HL-60	blood:	n/a
29	chr4:88379316-88379366	PFSK-1	brain:	n/a
30	chr4:88379316-88379366	GM06990	blood:	n/a
31	chr4:88364394-88364444	GM19239	blood:	n/a
32	chr4:88364394-88364444	HAEpiC	amniotic membrane:	n/a
33	chr4:88364394-88364444	HepG2	liver:	n/a
34	chr4:88364394-88364444	K562	blood:	n/a
35	chr4:88379316-88379366	AG09309	skin:	n/a
36	chr4:88379316-88379366	AG04449	skin:	fetal
37	chr4:88379316-88379366	GM12892	blood:	n/a
38	chr4:88364394-88364444	PANC-1	pancreas:	n/a
39	chr4:88364394-88364444	GM12891	blood:	n/a
40	chr4:88364394-88364444	CMK	blood:	n/a
41	chr4:88364394-88364444	Jurkat	blood:	n/a
42	chr4:88379316-88379366	HEK293	kidney:	embryo
43	chr4:88364394-88364444	HNPCEpiC	eye:	n/a
44	chr4:88379316-88379366	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:88379316-88379366	GM12891	blood:	n/a
46	chr4:88379316-88379366	BE2_C	brain:	n/a
47	chr4:88364394-88364444	AG04450	lung:	fetal
48	chr4:88364394-88364444	HUVEC	blood vessel:	n/a
49	chr4:88379316-88379366	ECC-1	luminal epithelium:	n/a
50	chr4:88364394-88364444	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:88296948..88297924-chr4:88386736..88387589,3	K562	blood:
2	chr4:88367022..88369969-chr4:88369971..88371877,2	K562	blood:
3	chr4:88367022..88369969-chr4:88369971..88371877,2	K562	blood:
4	chr4:88391725..88393377-chr4:88400606..88403156,2	K562	blood:
5	chr4:88296681..88297512-chr4:88386982..88387860,3	MCF-7	breast:
6	chr4:88274380..88275024-chr4:88386955..88387766,2	MCF-7	breast:
7	chr4:88341987..88343662-chr4:88383872..88386006,2	MCF-7	breast:
8	chr4:88311036..88312677-chr4:88391107..88393586,2	K562	blood:
9	chr4:88072049..88072620-chr4:88386607..88387532,2	K562	blood:
10	chr4:88023177..88025115-chr4:88372900..88374503,2	K562	blood:
11	chr4:88380058..88382518-chr4:88388082..88389915,2	K562	blood:
12	chr4:88342819..88344465-chr4:88375784..88377431,2	MCF-7	breast:
13	chr4:88380058..88382518-chr4:88388082..88389915,2	K562	blood:
14	chr4:88275546..88276371-chr4:88386699..88387600,2	MCF-7	breast:
15	chr4:88394985..88397833-chr4:88400065..88401721,2	K562	blood:
16	chr4:88274390..88275203-chr4:88387077..88388072,3	K562	blood:
17	chr4:88345779..88348484-chr4:88376364..88379281,2	K562	blood:
18	chr4:88391725..88393377-chr4:88400606..88403156,2	K562	blood:
19	chr4:88315473..88317637-chr4:88397561..88399533,2	K562	blood:
20	chr4:88342378..88346157-chr4:88365314..88366974,3	MCF-7	breast:
21	chr4:88361602..88363140-chr4:88363791..88366603,2	MCF-7	breast:
22	chr4:88341784..88343437-chr4:88384944..88387219,2	K562	blood:
23	chr4:88311036..88312581-chr4:88390124..88392607,2	K562	blood:
24	chr4:88394985..88397833-chr4:88400065..88401721,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPARCL1-2	chr4:88383119-88383432	ENSG00000272856.1
2	lnc-SPARCL1-2	chr4:88381959-88382135	ENSG00000272856.1

Variant related genes	Relation type
ENSG00000272856	TF binding region
ENSG00000272856	CpG island
ENSG00000170502	chromatin interactions
ENSG00000198189	chromatin interactions
TAC1	miRNA target sites
ZEB2	miRNA target sites

Extended variants
information (count: 1375 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1375 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564042277	chr4:88363981-88363982	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs529517550	chr4:88364043-88364044	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550867527	chr4:88364088-88364089	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115822950	chr4:88364135-88364136	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540015462	chr4:88364185-88364186	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78593979	chr4:88364206-88364207	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566539707	chr4:88364211-88364212	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533683726	chr4:88364218-88364219	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs74715582	chr4:88364268-88364269	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573699194	chr4:88364324-88364325	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs28535549	chr4:88364331-88364332	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs151213163	chr4:88364369-88364370	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs578027397	chr4:88364395-88364396	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200092698	chr4:88364401-88364402	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192948816	chr4:88364412-88364413	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34697941	chr4:88364413-88364414	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs13145111	chr4:88364414-88364415	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34893260	chr4:88364449-88364450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372214140	chr4:88364480-88364481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529145795	chr4:88364493-88364494	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140398674	chr4:88364503-88364504	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116260158	chr4:88364504-88364505	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185070547	chr4:88364625-88364626	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75888289	chr4:88364631-88364632	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150337695	chr4:88364642-88364643	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs529260247	chr4:88364670-88364671	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138033513	chr4:88364696-88364697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550601977	chr4:88364727-88364728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115003599	chr4:88364757-88364758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533483661	chr4:88364805-88364806	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75193795	chr4:88364816-88364817	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs566965855	chr4:88364834-88364835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533855611	chr4:88364843-88364844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs61556224	chr4:88364874-88364875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187516263	chr4:88364884-88364885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs77280018	chr4:88364913-88364914	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192374040	chr4:88364989-88364990	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372423561	chr4:88365030-88365031	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs149521543	chr4:88365047-88365048	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs72877390	chr4:88365065-88365066	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553906485	chr4:88365072-88365073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373322498	chr4:88365077-88365078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs13119333	chr4:88365083-88365084	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs540683058	chr4:88365103-88365104	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs561837744	chr4:88365168-88365169	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573844536	chr4:88365198-88365199	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147058960	chr4:88365244-88365245	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571426582	chr4:88365291-88365292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562576750	chr4:88365295-88365296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533641163	chr4:88365299-88365300	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88344400-88398600	Weak transcription	Gastric	stomach
2	chr4:88345200-88400000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr4:88345200-88416400	Weak transcription	Colonic Mucosa	Colon
4	chr4:88345400-88372400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:88345400-88378800	Weak transcription	A549	lung
6	chr4:88345800-88372200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr4:88346000-88364200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:88346200-88370600	Weak transcription	Thymus	Thymus
9	chr4:88346200-88382600	Weak transcription	NHLF	lung
10	chr4:88346400-88366200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr4:88346400-88369600	Weak transcription	Right Atrium	heart
12	chr4:88346400-88372200	Weak transcription	Aorta	Aorta
13	chr4:88346400-88379400	Weak transcription	Small Intestine	intestine
14	chr4:88346600-88371600	Weak transcription	Spleen	Spleen
15	chr4:88346600-88372200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:88346600-88410400	Weak transcription	Esophagus	oesophagus
17	chr4:88346800-88371400	Weak transcription	Lung	lung
18	chr4:88347200-88366000	Weak transcription	NH-A	brain
19	chr4:88347200-88372000	Weak transcription	NHEK	skin
20	chr4:88349000-88372400	Weak transcription	HSMMtube	muscle
21	chr4:88349000-88375400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr4:88349400-88381800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr4:88350600-88380600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:88351200-88379000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:88351400-88382400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr4:88351600-88414600	Weak transcription	Psoas Muscle	Psoas
27	chr4:88351800-88366600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr4:88352600-88387200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:88353400-88377000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr4:88354800-88381600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr4:88356000-88377600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:88356200-88365200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:88356200-88367400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr4:88356200-88367600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:88356200-88368000	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:88356400-88376400	Strong transcription	Liver	Liver
37	chr4:88356400-88377200	Weak transcription	Fetal Brain Male	brain
38	chr4:88356600-88382000	Weak transcription	Brain Germinal Matrix	brain
39	chr4:88357000-88366800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:88357000-88367400	Strong transcription	Duodenum Mucosa	Duodenum
41	chr4:88357200-88366800	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr4:88357400-88367200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr4:88357600-88372000	Weak transcription	Hela-S3	cervix
44	chr4:88357600-88380000	Weak transcription	Brain Angular Gyrus	brain
45	chr4:88357800-88367000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:88357800-88381600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr4:88358000-88365600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:88358200-88364800	Weak transcription	GM12878-XiMat	blood
49	chr4:88358400-88370600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:88359200-88367400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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