Variant report

Variant	nsv601464
Chromosome Location	chr6:29912169-29924728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:1343)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29922852-29922901	K562	blood:	n/a	n/a
2	ATF2	chr6:29914800-29915500	GM12878	blood:	n/a	n/a
3	BCL3	chr6:29914873-29915463	GM12878	blood:	n/a	n/a
4	BCLAF1	chr6:29914592-29915546	GM12878	blood:	n/a	n/a
5	BCLAF1	chr6:29916040-29916482	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:29914573-29915557	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:29915021-29915352	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:29920974-29921274	K562	blood:	n/a	n/a
9	BHLHE40	chr6:29920783-29921023	A549	lung:	n/a	n/a
10	CBX3	chr6:29920575-29921454	HCT-116	colon:	n/a	n/a
11	CEBPB	chr6:29919167-29919420	K562	blood:	n/a	n/a
12	CHD2	chr6:29915121-29915474	GM12878	blood:	n/a	n/a
13	CHD2	chr6:29914301-29914707	GM12878	blood:	n/a	n/a
14	CHD2	chr6:29915994-29916686	GM12878	blood:	n/a	n/a
15	CTCF	chr6:29917974-29918105	K562	blood:	n/a	n/a
16	CTCF	chr6:29917940-29918090	K562	blood:	n/a	n/a
17	CUX1	chr6:29914956-29915089	GM12878	blood:	n/a	n/a
18	CUX1	chr6:29913984-29913991	GM12878	blood:	n/a	n/a
19	EBF1	chr6:29914059-29914215	GM12878	blood:	n/a	n/a
20	EBF1	chr6:29912206-29913080	GM12878	blood:	n/a	chr6:29912641-29912652
21	ELF1	chr6:29915020-29915453	GM12878	blood:	n/a	n/a
22	EP300	chr6:29920738-29921236	A549	lung:	n/a	n/a
23	EP300	chr6:29920979-29921212	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr6:29920634-29921267	A549	lung:	n/a	n/a
25	FOS	chr6:29920685-29921275	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr6:29920684-29921270	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr6:29920665-29921284	HUVEC	blood vessel:	n/a	n/a
28	FOS	chr6:29920677-29921326	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr6:29920699-29921264	MCF10A-Er-Src	breast:	n/a	n/a
30	FOSL1	chr6:29920649-29921461	HCT-116	colon:	n/a	n/a
31	FOSL1	chr6:29920598-29921295	HCT-116	colon:	n/a	n/a
32	FOSL2	chr6:29920758-29921244	A549	lung:	n/a	n/a
33	FOSL2	chr6:29920553-29921362	A549	lung:	n/a	n/a
34	FOSL2	chr6:29920563-29921346	SK-N-SH	brain:	n/a	n/a
35	GATA3	chr6:29918761-29919040	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr6:29920615-29921377	A549	lung:	n/a	n/a
37	JUN	chr6:29920751-29921344	HUVEC	blood vessel:	n/a	n/a
38	JUND	chr6:29921013-29921312	K562	blood:	n/a	n/a
39	JUND	chr6:29920569-29921371	HCT-116	colon:	n/a	n/a
40	JUND	chr6:29920645-29921459	HCT-116	colon:	n/a	n/a
41	JUND	chr6:29920600-29921304	SK-N-SH	brain:	n/a	n/a
42	MAFK	chr6:29913273-29913406	Hela-S3	cervix:	n/a	n/a
43	MAX	chr6:29920664-29921326	A549	lung:	n/a	n/a
44	MAX	chr6:29912700-29912727	GM12878	blood:	n/a	n/a
45	MAX	chr6:29913321-29913331	GM12878	blood:	n/a	n/a
46	MAX	chr6:29920664-29921185	A549	lung:	n/a	n/a
47	MAX	chr6:29914766-29914807	GM12878	blood:	n/a	n/a
48	MEF2A	chr6:29920703-29921365	SK-N-SH	brain:	n/a	n/a
49	MTA3	chr6:29913554-29917310	GM12878	blood:	n/a	n/a
50	MTA3	chr6:29912430-29912952	GM12878	blood:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29924299-29924349	Hela-S3	cervix:	n/a
2	chr6:29924299-29924349	Hela-S3	cervix:	n/a
3	chr6:29923913-29923963	IMR90	lung:	fetal
4	chr6:29920309-29920359	HNPCEpiC	eye:	n/a
5	chr6:29924207-29924257	AoSMC	blood vessel:	n/a
6	chr6:29924471-29924521	HIPEpiC	eye:	n/a
7	chr6:29924310-29924360	Hela-S3	cervix:	n/a
8	chr6:29923954-29924004	Hela-S3	cervix:	n/a
9	chr6:29924475-29924525	MCF10A-Er-Src	breast:	n/a
10	chr6:29921779-29921829	HUVEC	blood vessel:	n/a
11	chr6:29913343-29913393	GM12891	blood:	n/a
12	chr6:29924407-29924457	AoSMC	blood vessel:	n/a
13	chr6:29923954-29924004	HL-60	blood:	n/a
14	chr6:29912713-29912763	T-47D	breast:	n/a
15	chr6:29923954-29924004	AG09309	skin:	n/a
16	chr6:29924471-29924521	H1-hESC	embryonic stem cell:	embryo
17	chr6:29924067-29924117	MCF-7	breast:	n/a
18	chr6:29914938-29914988	GM19239	blood:	n/a
19	chr6:29924310-29924360	Jurkat	blood:	n/a
20	chr6:29924247-29924297	NHDF-neo	bronchial:	n/a
21	chr6:29924256-29924306	PrEC	prostate:	n/a
22	chr6:29923695-29923745	U87	brain:	n/a
23	chr6:29924207-29924257	ProgFib	skin:	n/a
24	chr6:29924475-29924525	PANC-1	pancreas:	n/a
25	chr6:29924407-29924457	H1-hESC	embryonic stem cell:	embryo
26	chr6:29913343-29913393	AG10803	skin:	n/a
27	chr6:29924471-29924521	GM19239	blood:	n/a
28	chr6:29924310-29924360	K562	blood:	n/a
29	chr6:29924256-29924306	H1-hESC	embryonic stem cell:	embryo
30	chr6:29914938-29914988	H1-hESC	embryonic stem cell:	embryo
31	chr6:29913098-29913148	HIPEpiC	eye:	n/a
32	chr6:29924310-29924360	BJ	skin:	n/a
33	chr6:29912713-29912763	HAEpiC	amniotic membrane:	n/a
34	chr6:29912713-29912763	GM12891	blood:	n/a
35	chr6:29923952-29924002	SK-N-MC	brain:	n/a
36	chr6:29922522-29922572	NT2-D1	testis:	n/a
37	chr6:29923952-29924002	ECC-1	luminal epithelium:	n/a
38	chr6:29924067-29924117	LNCaP	prostate:	n/a
39	chr6:29924256-29924306	HNPCEpiC	eye:	n/a
40	chr6:29923954-29924004	NHBE	bronchial:	n/a
41	chr6:29924407-29924457	HEEpiC	esophagus:	n/a
42	chr6:29913098-29913148	HRE	kidney:	n/a
43	chr6:29923913-29923963	NHBE	bronchial:	n/a
44	chr6:29924067-29924117	NB4	blood:	n/a
45	chr6:29912713-29912763	SKMC	muscle:	n/a
46	chr6:29914938-29914988	ProgFib	skin:	n/a
47	chr6:29924299-29924349	HIPEpiC	eye:	n/a
48	chr6:29914938-29914988	T-47D	breast:	n/a
49	chr6:29924310-29924360	PrEC	prostate:	n/a
50	chr6:29921779-29921829	RPTEC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
2	chr6:29917150..29919030-chr6:29920403..29922798,2	MCF-7	breast:
3	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
4	chr6:29854712..29856936-chr6:29909499..29912386,4	MCF-7	breast:
5	chr6:29764926..29767618-chr6:29920990..29923179,3	MCF-7	breast:
6	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
7	chr6:29917150..29919030-chr6:29920403..29922798,2	MCF-7	breast:
8	chr6:29917426..29919477-chr6:29924161..29925991,2	K562	blood:
9	chr6:29909870..29912784-chr6:29914733..29916600,2	MCF-7	breast:
10	chr6:29860588..29861572-chr6:29915904..29916650,2	HCT-116	colon:
11	chr6:29820057..29821697-chr6:29920603..29922626,2	K562	blood:
12	chr6:29917977..29920432-chr6:29924161..29926474,2	K562	blood:
13	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HLA-A	hsa-miR-148b-3p	chr6:29913484-29913504

Variant related genes	Relation type
HCG4P5	TF binding region
HLA-W	TF binding region
HCG4P5	CpG island
HLA-W	CpG island
ENSG00000233265	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000206341	chromatin interactions
ENSG00000235290	chromatin interactions
ENSG00000206503	chromatin interactions
ENSG00000227766	chromatin interactions

Extended variants
information (count: 1317 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1317 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41545513	chr6:29912169-29912170	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs567795363	chr6:29912179-29912180	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs9260184	chr6:29912188-29912189	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs113037584	chr6:29912203-29912204	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs2276447	chr6:29912204-29912205	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs9260186	chr6:29912208-29912209	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs199786100	chr6:29912233-29912234	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs113645195	chr6:29912234-29912235	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs188245242	chr6:29912249-29912250	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs538569961	chr6:29912262-29912263	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs1136903	chr6:29912280-29912281	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs1136917	chr6:29912281-29912282	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs376591124	chr6:29912290-29912291	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs1136949	chr6:29912297-29912298	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs41558618	chr6:29912301-29912302	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs200050592	chr6:29912304-29912305	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs41555922	chr6:29912305-29912306	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs41554316	chr6:29912315-29912316	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs1059846	chr6:29912326-29912327	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs3179982	chr6:29912333-29912334	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs1059896	chr6:29912342-29912343	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs1137078	chr6:29912348-29912349	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs1141891	chr6:29912368-29912369	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs116046290	chr6:29912379-29912380	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs41550119	chr6:29912382-29912383	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1137160	chr6:29912386-29912387	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs74408957	chr6:29912394-29912395	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545184037	chr6:29912395-29912396	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs201507150	chr6:29912396-29912397	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs369661979	chr6:29912398-29912399	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs41551619	chr6:29912410-29912411	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs560749565	chr6:29912414-29912415	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs370824210	chr6:29912417-29912418	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551910414	chr6:29912427-29912428	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs9260193	chr6:29912451-29912452	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs9260194	chr6:29912457-29912458	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs554587009	chr6:29912458-29912459	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs9260195	chr6:29912463-29912464	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs9260196	chr6:29912473-29912474	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs9260197	chr6:29912477-29912478	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs183484257	chr6:29912480-29912481	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs386698555	chr6:29912493-29912494	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs9260198	chr6:29912502-29912503	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
44	rs1632885	chr6:29912510-29912511	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
45	rs1655895	chr6:29912517-29912518	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs560389293	chr6:29912522-29912523	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs146309471	chr6:29912526-29912527	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs551996488	chr6:29912527-29912528	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs386698556	chr6:29912562-29912563	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs17885126	chr6:29912564-29912565	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29909000-29912600	Active TSS	Psoas Muscle	Psoas
2	chr6:29909600-29912400	Active TSS	Brain Hippocampus Middle	brain
3	chr6:29909800-29912200	Active TSS	Small Intestine	intestine
4	chr6:29910200-29914800	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
5	chr6:29910400-29913800	Transcr. at gene 5' and 3'	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:29910400-29914200	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
7	chr6:29910400-29914600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
8	chr6:29910600-29913600	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:29910600-29915400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
10	chr6:29910800-29912400	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
11	chr6:29910800-29912800	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
12	chr6:29910800-29913600	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
13	chr6:29910800-29914200	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
14	chr6:29910800-29914200	Transcr. at gene 5' and 3'	Primary T helper cells fromperipheralblood	blood
15	chr6:29910800-29914200	Transcr. at gene 5' and 3'	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:29911000-29912800	Transcr. at gene 5' and 3'	Sigmoid Colon	Sigmoid Colon
17	chr6:29911000-29913000	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:29911000-29913800	Transcr. at gene 5' and 3'	Primary T killer naive cells fromperipheralblood	blood
19	chr6:29911000-29914600	Transcr. at gene 5' and 3'	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:29911000-29915800	Weak transcription	Aorta	Aorta
21	chr6:29911200-29912600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
22	chr6:29911200-29913200	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
23	chr6:29911200-29913200	Transcr. at gene 5' and 3'	Rectal Smooth Muscle	rectum
24	chr6:29911200-29913400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
25	chr6:29911200-29913400	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
26	chr6:29911200-29913400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:29911200-29913400	Transcr. at gene 5' and 3'	Thymus	Thymus
28	chr6:29911200-29914200	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
29	chr6:29911200-29914600	Transcr. at gene 5' and 3'	Primary T helper memory cells from peripheral blood 2	blood
30	chr6:29911200-29920200	Weak transcription	A549	lung
31	chr6:29911200-29921400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:29911400-29912400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr6:29911400-29912400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr6:29911400-29912600	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
35	chr6:29911400-29912800	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:29911400-29912800	Transcr. at gene 5' and 3'	Duodenum Mucosa	Duodenum
37	chr6:29911400-29912800	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach
38	chr6:29911400-29913400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:29911400-29913400	Transcr. at gene 5' and 3'	Adipose Nuclei	Adipose
40	chr6:29911400-29913400	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 29	rectum
41	chr6:29911400-29913600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr6:29911400-29913800	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr6:29911400-29913800	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 31	rectum
44	chr6:29911400-29913800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
45	chr6:29911400-29914200	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
46	chr6:29911400-29914400	Transcr. at gene 5' and 3'	Primary T cells from cord blood	blood
47	chr6:29911400-29915000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:29911600-29912200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:29911600-29912200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:29911600-29912200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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