Variant report

Variant	nsv890621
Chromosome Location	chr8:19173379-19211220
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:587)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:19202604-19203192	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:19176267-19176856	HepG2	liver:	n/a	n/a
3	ATF1	chr8:19179636-19179910	K562	blood:	n/a	n/a
4	BATF	chr8:19205482-19205761	GM12878	blood:	n/a	chr8:19205670-19205681
5	BATF	chr8:19205507-19205805	GM12878	blood:	n/a	chr8:19205670-19205681
6	BHLHE40	chr8:19205315-19205709	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:19179597-19180012	K562	blood:	n/a	n/a
8	CCNT2	chr8:19179623-19179911	K562	blood:	n/a	n/a
9	CEBPB	chr8:19183480-19183924	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr8:19183615-19183842	A549	lung:	n/a	n/a
11	CEBPB	chr8:19183350-19183954	HCT-116	colon:	n/a	n/a
12	CEBPB	chr8:19207827-19207947	IMR90	lung:	n/a	chr8:19207876-19207889
13	CEBPB	chr8:19183640-19183739	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:19205523-19205786	IMR90	lung:	n/a	n/a
15	CEBPB	chr8:19192732-19192940	A549	lung:	n/a	n/a
16	CEBPB	chr8:19183465-19183922	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr8:19176486-19176630	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:19207570-19207950	HepG2	liver:	n/a	chr8:19207658-19207671 chr8:19207876-19207889 chr8:19207660-19207671
19	CEBPB	chr8:19192744-19192783	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:19176427-19176657	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:19183434-19183970	MCF-7	breast:	n/a	n/a
22	CEBPB	chr8:19183453-19184021	MCF-7	breast:	n/a	n/a
23	CEBPD	chr8:19179521-19179997	K562	blood:	n/a	n/a
24	CHD2	chr8:19186652-19186655	HepG2	liver:	n/a	n/a
25	CHD2	chr8:19204067-19204191	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr8:19205414-19205772	GM12878	blood:	n/a	n/a
27	CTCF	chr8:19175014-19175346	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:19204060-19204210	K562	blood:	n/a	n/a
29	CTCF	chr8:19175160-19175310	BJ	skin:	n/a	n/a
30	CTCF	chr8:19176886-19177091	MCF-7	breast:	n/a	chr8:19176992-19177010
31	CTCF	chr8:19204020-19204170	NHEK	skin:	n/a	n/a
32	CTCF	chr8:19176915-19177059	H1-hESC	embryonic stem cell:	n/a	chr8:19176992-19177010
33	CTCF	chr8:19203998-19204230	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr8:19204040-19204190	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr8:19204060-19204210	GM12871	blood:	n/a	n/a
36	CTCF	chr8:19176920-19177070	HEEpiC	esophagus:	n/a	chr8:19176992-19177010
37	CTCF	chr8:19204060-19204210	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr8:19203787-19203842	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:19175040-19175190	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr8:19204000-19204150	GM12866	blood:	n/a	n/a
41	CTCF	chr8:19175118-19175275	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr8:19204040-19204190	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr8:19204006-19204219	GM12878	blood:	n/a	n/a
44	CTCF	chr8:19204339-19204460	GM10248	blood:	n/a	n/a
45	CTCF	chr8:19176900-19177050	HEEpiC	esophagus:	n/a	chr8:19176992-19177010
46	CTCF	chr8:19204060-19204210	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr8:19205415-19205460	GM10248	blood:	n/a	n/a
48	CTCF	chr8:19204100-19204250	HCM	heart:	n/a	n/a
49	CTCF	chr8:19204320-19204470	AG04449	skin:	n/a	n/a
50	CTCF	chr8:19204020-19204170	GM12874	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19177170-19177220	A549	lung:	n/a
2	chr8:19174316-19174366	HIPEpiC	eye:	n/a
3	chr8:19177170-19177220	SK-N-SH	brain:	n/a
4	chr8:19177170-19177220	HCF	heart:	n/a
5	chr8:19177170-19177220	GM12891	blood:	n/a
6	chr8:19203257-19203307	SKMC	muscle:	n/a
7	chr8:19177170-19177220	GM06990	blood:	n/a
8	chr8:19177170-19177220	Caco-2	colon:	n/a
9	chr8:19174316-19174366	Hepatocyte	liver:	n/a
10	chr8:19177170-19177220	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:19174316-19174366	NHDF-neo	bronchial:	n/a
12	chr8:19174316-19174366	HEK293	kidney:	embryo
13	chr8:19203257-19203307	NH-A	brain:	n/a
14	chr8:19174316-19174366	T-47D	breast:	n/a
15	chr8:19177170-19177220	RPTEC	kidney:	n/a
16	chr8:19174316-19174366	K562	blood:	n/a
17	chr8:19174316-19174366	Jurkat	blood:	n/a
18	chr8:19174316-19174366	U87	brain:	n/a
19	chr8:19174316-19174366	ProgFib	skin:	n/a
20	chr8:19174316-19174366	HCT-116	colon:	n/a
21	chr8:19177170-19177220	GM12878	blood:	n/a
22	chr8:19177170-19177220	K562	blood:	n/a
23	chr8:19174316-19174366	CMK	blood:	n/a
24	chr8:19177170-19177220	AG09309	skin:	n/a
25	chr8:19177170-19177220	HRPEpiC	eye:	n/a
26	chr8:19174316-19174366	NH-A	brain:	n/a
27	chr8:19177170-19177220	SAEC	small airway:	n/a
28	chr8:19174316-19174366	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:19177170-19177220	U87	brain:	n/a
30	chr8:19174316-19174366	GM12892	blood:	n/a
31	chr8:19177170-19177220	Hepatocyte	liver:	n/a
32	chr8:19203257-19203307	AG09309	skin:	n/a
33	chr8:19203257-19203307	RPTEC	kidney:	n/a
34	chr8:19203257-19203307	Jurkat	blood:	n/a
35	chr8:19203257-19203307	H1-hESC	embryonic stem cell:	embryo
36	chr8:19174316-19174366	SKMC	muscle:	n/a
37	chr8:19177170-19177220	AoSMC	blood vessel:	n/a
38	chr8:19203257-19203307	HNPCEpiC	eye:	n/a
39	chr8:19174316-19174366	AG04450	lung:	fetal
40	chr8:19177170-19177220	SK-N-SH_RA	brain:	n/a
41	chr8:19174316-19174366	SAEC	small airway:	n/a
42	chr8:19174316-19174366	LNCaP	prostate:	n/a
43	chr8:19203257-19203307	NHBE	bronchial:	n/a
44	chr8:19177170-19177220	HCT-116	colon:	n/a
45	chr8:19203257-19203307	AG09319	gingival:	n/a
46	chr8:19174316-19174366	NT2-D1	testis:	n/a
47	chr8:19203257-19203307	HAEpiC	amniotic membrane:	n/a
48	chr8:19203257-19203307	HepG2	liver:	n/a
49	chr8:19203257-19203307	GM06990	blood:	n/a
50	chr8:19177170-19177220	GM12892	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:12789775..12791275-chr8:19175114..19177596,2	MCF-7	breast:
2	chr8:19168689..19173779-chr8:19180928..19188121,8	MCF-7	breast:
3	chr8:19169455..19173162-chr8:19175391..19178341,5	MCF-7	breast:
4	chr8:19174699..19177695-chr8:19183567..19186086,3	MCF-7	breast:
5	chr8:19126347..19128223-chr8:19186550..19188769,2	K562	blood:
6	chr8:19175184..19177540-chr8:19177821..19179991,2	MCF-7	breast:
7	chr8:19146966..19149051-chr8:19185409..19187470,2	MCF-7	breast:
8	chr8:19198858..19201082-chr8:19203495..19205274,3	K562	blood:
9	chr8:19198858..19201082-chr8:19203495..19205274,3	K562	blood:
10	chr8:18870145..18872043-chr8:19205249..19207721,2	MCF-7	breast:
11	chr8:19155044..19157820-chr8:19172820..19174971,2	MCF-7	breast:
12	chr8:19149962..19152072-chr8:19173164..19175700,2	MCF-7	breast:
13	chr8:19170128..19172258-chr8:19179256..19183513,5	MCF-7	breast:
14	chr8:19142668..19144947-chr8:19171540..19174164,2	MCF-7	breast:

No data

Variant related genes	Relation type
SH2D4A	TF binding region
SH2D4A	CpG island
ENSG00000104611	chromatin interactions
ENSG00000095059	chromatin interactions
ENSG00000156011	chromatin interactions

Extended variants
information (count: 1726 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10107389	chr8:19173379-19173380	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79903815	chr8:19173440-19173441	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs185836618	chr8:19173488-19173489	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs570920556	chr8:19173497-19173498	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs75176532	chr8:19173554-19173555	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs553354648	chr8:19173558-19173559	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs573149465	chr8:19173598-19173599	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs535882278	chr8:19173603-19173604	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs372721482	chr8:19173624-19173625	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs575523723	chr8:19173679-19173680	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs191445693	chr8:19173688-19173689	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs148878204	chr8:19173712-19173713	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs377147930	chr8:19173720-19173721	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs577272922	chr8:19173731-19173732	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs143530516	chr8:19173759-19173760	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs114774498	chr8:19173766-19173767	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs528869123	chr8:19173806-19173807	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs148063751	chr8:19173828-19173829	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs370582917	chr8:19173849-19173850	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs143700458	chr8:19173884-19173885	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs555821625	chr8:19173963-19173964	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182067241	chr8:19173968-19173969	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs551152288	chr8:19173973-19173974	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs571056809	chr8:19173976-19173977	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs556582954	chr8:19173996-19173997	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs7005125	chr8:19174030-19174031	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186990589	chr8:19174043-19174044	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs547103846	chr8:19174044-19174045	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs566988465	chr8:19174068-19174069	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs377657754	chr8:19174069-19174070	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs529955635	chr8:19174097-19174098	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs147212584	chr8:19174107-19174108	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs569017625	chr8:19174121-19174122	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs537751500	chr8:19174145-19174146	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs115612136	chr8:19174161-19174162	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7005298	chr8:19174166-19174167	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs117311305	chr8:19174242-19174243	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs553565891	chr8:19174248-19174249	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs573704860	chr8:19174266-19174267	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs554440886	chr8:19174308-19174309	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs138686272	chr8:19174312-19174313	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs76792542	chr8:19174343-19174344	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs192327189	chr8:19174345-19174346	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs142692134	chr8:19174377-19174378	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs544916842	chr8:19174378-19174379	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573010019	chr8:19174422-19174423	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs564807976	chr8:19174456-19174457	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs116732367	chr8:19174478-19174479	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs115853780	chr8:19174479-19174480	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs183421751	chr8:19174490-19174491	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19171000-19173400	Active TSS	Duodenum Mucosa	Duodenum
2	chr8:19172000-19179600	Weak transcription	Spleen	Spleen
3	chr8:19172200-19173400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:19172200-19173400	Weak transcription	Gastric	stomach
5	chr8:19172200-19173400	Weak transcription	Lung	lung
6	chr8:19172200-19173600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:19172200-19174000	Weak transcription	Aorta	Aorta
8	chr8:19172200-19179800	Weak transcription	Left Ventricle	heart
9	chr8:19172200-19182600	Weak transcription	Esophagus	oesophagus
10	chr8:19172400-19173400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr8:19172400-19173400	Weak transcription	Right Atrium	heart
12	chr8:19172400-19173600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:19172400-19173600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
14	chr8:19172400-19173600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr8:19172400-19173800	Enhancers	Fetal Intestine Small	intestine
16	chr8:19172400-19173800	Weak transcription	HSMMtube	muscle
17	chr8:19172400-19173800	Weak transcription	HUVEC	blood vessel
18	chr8:19172400-19174000	Enhancers	NHEK	skin
19	chr8:19172400-19174200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:19172400-19174200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:19172400-19174200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr8:19172400-19174200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:19172400-19174200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr8:19172400-19174400	Enhancers	Ovary	ovary
25	chr8:19172400-19175800	Enhancers	Pancreas	Pancrea
26	chr8:19172400-19176000	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr8:19172400-19176200	Weak transcription	Fetal Lung	lung
28	chr8:19172400-19176200	Enhancers	Stomach Mucosa	stomach
29	chr8:19172400-19176800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr8:19172400-19176800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:19172400-19177000	Weak transcription	Adipose Nuclei	Adipose
32	chr8:19172400-19180600	Weak transcription	Fetal Stomach	stomach
33	chr8:19172400-19184800	Weak transcription	Stomach Smooth Muscle	stomach
34	chr8:19172400-19187800	Weak transcription	Fetal Heart	heart
35	chr8:19172400-19188000	Weak transcription	Right Ventricle	heart
36	chr8:19172400-19202400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:19172600-19173400	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr8:19172600-19174200	Enhancers	HMEC	breast
39	chr8:19172600-19181200	Weak transcription	NH-A	brain
40	chr8:19172600-19202800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr8:19172800-19173600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
42	chr8:19172800-19173800	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr8:19172800-19173800	Enhancers	NHDF-Ad	bronchial
44	chr8:19172800-19174000	Weak transcription	Small Intestine	intestine
45	chr8:19172800-19174400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr8:19172800-19176800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr8:19172800-19176800	Weak transcription	Fetal Intestine Large	intestine
48	chr8:19172800-19181600	Weak transcription	Placenta	Placenta
49	chr8:19173000-19173400	Weak transcription	NHLF	lung
50	chr8:19173000-19173600	Enhancers	Colonic Mucosa	Colon

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