Variant report

Variant	nsv933704
Chromosome Location	chr6:80657182-80674202
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	chr6:80658906-80659220	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:80658922-80659230	K562	blood:	n/a	n/a
3	ATF3	chr6:80657155-80657502	H1-hESC	embryonic stem cell:	n/a	chr6:80657435-80657444
4	ATF3	chr6:80657092-80657471	H1-hESC	embryonic stem cell:	n/a	chr6:80657435-80657444
5	BACH1	chr6:80657510-80657774	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr6:80657183-80657755	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr6:80657019-80657708	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr6:80657124-80657494	A549	lung:	n/a	n/a
9	CREB1	chr6:80657048-80657737	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr6:80656206-80657733	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr6:80658872-80659245	H1-hESC	embryonic stem cell:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
12	CTCF	chr6:80658721-80659403	HCT-116	colon:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
13	CTCF	chr6:80658951-80659134	GM10248	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
14	CTCF	chr6:80658960-80659110	NB4	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
15	CTCF	chr6:80658902-80659260	K562	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
16	CTCF	chr6:80659000-80659150	BJ	skin:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
17	CTCF	chr6:80658960-80659110	GM12867	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
18	CTCF	chr6:80658220-80658370	HCM	heart:	n/a	n/a
19	CTCF	chr6:80658960-80659110	HA-sp	spinal cord:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
20	CTCF	chr6:80658940-80659090	GM12873	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
21	CTCF	chr6:80659140-80659290	NHLF	lung:	n/a	n/a
22	CTCF	chr6:80658980-80659130	AG09309	skin:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
23	CTCF	chr6:80658979-80659162	GM12892	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
24	CTCF	chr6:80658960-80659110	GM12875	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
25	CTCF	chr6:80658960-80659110	HepG2	liver:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
26	CTCF	chr6:80658940-80659090	HL-60	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
27	CTCF	chr6:80658940-80659090	HepG2	liver:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
28	CTCF	chr6:80659000-80659143	MCF-7	breast:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
29	CTCF	chr6:80658960-80659110	AoAF	blood vessel:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
30	CTCF	chr6:80658975-80659135	GM20000	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
31	CTCF	chr6:80658960-80659110	GM06990	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
32	CTCF	chr6:80658900-80659050	GM12874	blood:	n/a	n/a
33	CTCF	chr6:80659013-80659142	GM12891	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
34	CTCF	chr6:80658893-80659158	HUVEC	blood vessel:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
35	CTCF	chr6:80658920-80659070	RPTEC	kidney:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
36	CTCF	chr6:80658865-80659156	SK-N-SH_RA	brain:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
37	CTCF	chr6:80658960-80659110	GM12869	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
38	CTCF	chr6:80658920-80659070	HFF	foreskin:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
39	CTCF	chr6:80659000-80659150	HFF-Myc	foreskin:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
40	CTCF	chr6:80658960-80659110	GM12872	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
41	CTCF	chr6:80658960-80659110	RPTEC	kidney:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
42	CTCF	chr6:80658940-80659090	Caco-2	colon:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
43	CTCF	chr6:80658920-80659070	HBMEC	blood vessel:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
44	CTCF	chr6:80658960-80659110	GM12865	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
45	CTCF	chr6:80658980-80659130	GM12864	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
46	CTCF	chr6:80658960-80659110	AG10803	skin:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
47	CTCF	chr6:80658915-80659071	GM13977	blood:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
48	CTCF	chr6:80658940-80659090	AG04450	lung:	n/a	chr6:80659035-80659053 chr6:80659037-80659058
49	CTCF	chr6:80659680-80659830	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr6:80658936-80659153	LNCaP	prostate:	n/a	chr6:80659035-80659053 chr6:80659037-80659058

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:80657428-80657478	HRE	kidney:	n/a
2	chr6:80657428-80657478	GM06990	blood:	n/a
3	chr6:80657412-80657462	ovcar-3	ovarian:	n/a
4	chr6:80657412-80657462	NH-A	brain:	n/a
5	chr6:80657826-80657876	IMR90	lung:	fetal
6	chr6:80657826-80657876	SKMC	muscle:	n/a
7	chr6:80657412-80657462	ECC-1	luminal epithelium:	n/a
8	chr6:80657826-80657876	HUVEC	blood vessel:	n/a
9	chr6:80657428-80657478	GM12892	blood:	n/a
10	chr6:80657542-80657592	HAEpiC	amniotic membrane:	n/a
11	chr6:80657412-80657462	HAEpiC	amniotic membrane:	n/a
12	chr6:80657542-80657592	HL-60	blood:	n/a
13	chr6:80657826-80657876	NH-A	brain:	n/a
14	chr6:80657555-80657605	HIPEpiC	eye:	n/a
15	chr6:80657428-80657478	CMK	blood:	n/a
16	chr6:80657542-80657592	AoSMC	blood vessel:	n/a
17	chr6:80657428-80657478	Hepatocyte	liver:	n/a
18	chr6:80657436-80657486	BJ	skin:	n/a
19	chr6:80657542-80657592	T-47D	breast:	n/a
20	chr6:80657412-80657462	T-47D	breast:	n/a
21	chr6:80657428-80657478	NH-A	brain:	n/a
22	chr6:80657428-80657478	RPTEC	kidney:	n/a
23	chr6:80657555-80657605	SK-N-SH	brain:	n/a
24	chr6:80657412-80657462	U87	brain:	n/a
25	chr6:80657415-80657465	RPTEC	kidney:	n/a
26	chr6:80657428-80657478	AG04450	lung:	fetal
27	chr6:80657430-80657480	IMR90	lung:	fetal
28	chr6:80657412-80657462	MCF10A-Er-Src	breast:	n/a
29	chr6:80657415-80657465	Hela-S3	cervix:	n/a
30	chr6:80657430-80657480	HCPEpiC	choroid plexus:	n/a
31	chr6:80657430-80657480	NB4	blood:	n/a
32	chr6:80657436-80657486	AG04449	skin:	fetal
33	chr6:80657826-80657876	K562	blood:	n/a
34	chr6:80657193-80657243	CMK	blood:	n/a
35	chr6:80657193-80657243	AG09309	skin:	n/a
36	chr6:80657193-80657243	K562	blood:	n/a
37	chr6:80657193-80657243	GM12892	blood:	n/a
38	chr6:80657412-80657462	SK-N-SH_RA	brain:	n/a
39	chr6:80657826-80657876	CMK	blood:	n/a
40	chr6:80657826-80657876	BE2_C	brain:	n/a
41	chr6:80657555-80657605	H1-hESC	embryonic stem cell:	embryo
42	chr6:80657542-80657592	PANC-1	pancreas:	n/a
43	chr6:80657415-80657465	HCPEpiC	choroid plexus:	n/a
44	chr6:80657542-80657592	SK-N-MC	brain:	n/a
45	chr6:80657555-80657605	RPTEC	kidney:	n/a
46	chr6:80657193-80657243	AG04449	skin:	fetal
47	chr6:80657555-80657605	HRPEpiC	eye:	n/a
48	chr6:80657555-80657605	HCPEpiC	choroid plexus:	n/a
49	chr6:80657193-80657243	HEK293	kidney:	embryo
50	chr6:80657412-80657462	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:80659127..80661422-chr6:80663652..80666036,2	K562	blood:
2	chr1:149858428..149860800-chr6:80655814..80658112,2	MCF-7	breast:
3	chr6:80658511..80659143-chr6:80803528..80804503,2	K562	blood:
4	chr6:80657745..80660049-chr6:80716512..80719051,2	MCF-7	breast:
5	chr6:80658533..80659818-chr6:80802938..80804495,11	MCF-7	breast:
6	chr6:80658920..80659483-chr6:80801274..80801876,2	K562	blood:
7	chr6:80656144..80658220-chr6:80712686..80714230,2	K562	blood:
8	chr6:80658870..80659475-chr6:80804226..80804935,2	MCF-7	breast:
9	chr6:80658835..80659700-chr6:80713034..80713810,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTK-2	chr6:80673932-80674236	NONHSAT113719

Variant related genes	Relation type
ELOVL4	TF binding region
RPL35AP18	TF binding region
GAPDHP63	TF binding region
ELOVL4	CpG island
RPL35AP18	CpG island
GAPDHP63	CpG island
ENSG00000184260	chromatin interactions
ENSG00000218582	chromatin interactions
ENSG00000112742	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000184270	chromatin interactions

Extended variants
information (count: 694 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370635051	chr6:80657223-80657224	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs240307	chr6:80657232-80657233	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs376652433	chr6:80657241-80657242	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs560742982	chr6:80657245-80657246	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs539142746	chr6:80657248-80657249	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs200403099	chr6:80657255-80657256	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs546271509	chr6:80657264-80657265	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs566258062	chr6:80657276-80657277	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs559131282	chr6:80657288-80657289	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs538376275	chr6:80657307-80657308	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs374411961	chr6:80657332-80657333	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs552115192	chr6:80657348-80657349	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs75912037	chr6:80657423-80657424	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs538486068	chr6:80657428-80657429	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs555010506	chr6:80657446-80657447	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs376515971	chr6:80657457-80657458	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs575077004	chr6:80657507-80657508	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs111607692	chr6:80657526-80657527	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs554289359	chr6:80657568-80657569	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs577386577	chr6:80657639-80657640	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs192646827	chr6:80657684-80657685	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs545998983	chr6:80657706-80657707	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs562862804	chr6:80657771-80657772	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs367632356	chr6:80657779-80657780	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs145531476	chr6:80657800-80657801	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs544484552	chr6:80657875-80657876	Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs560880319	chr6:80657889-80657890	Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs117539312	chr6:80657960-80657961	Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs546361593	chr6:80658003-80658004	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs559931196	chr6:80658005-80658006	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs532191608	chr6:80658039-80658040	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs148065116	chr6:80658089-80658090	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs201185343	chr6:80658091-80658092	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs568834200	chr6:80658119-80658120	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537485388	chr6:80658128-80658129	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs182759679	chr6:80658196-80658197	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568801197	chr6:80658231-80658232	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140692175	chr6:80658261-80658262	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs534522274	chr6:80658263-80658264	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs150096171	chr6:80658298-80658299	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs570968437	chr6:80658356-80658357	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs187862755	chr6:80658359-80658360	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs576367409	chr6:80658369-80658370	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs541883376	chr6:80658374-80658375	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs78318480	chr6:80658391-80658392	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs147378687	chr6:80658422-80658423	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs192552035	chr6:80658463-80658464	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs138227526	chr6:80658491-80658492	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs544933545	chr6:80658524-80658525	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs540145649	chr6:80658561-80658562	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80654400-80657600	Active TSS	Brain Anterior Caudate	brain
2	chr6:80654600-80657400	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr6:80654800-80657800	Active TSS	Brain Angular Gyrus	brain
4	chr6:80655600-80657400	Active TSS	Right Atrium	heart
5	chr6:80655600-80657400	Active TSS	NHDF-Ad	bronchial
6	chr6:80655600-80657600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:80655600-80659400	Active TSS	Thymus	Thymus
8	chr6:80655800-80657400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:80655800-80657400	Active TSS	NHLF	lung
10	chr6:80655800-80657600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:80655800-80657600	Active TSS	Brain Hippocampus Middle	brain
12	chr6:80655800-80657600	Active TSS	Fetal Brain Male	brain
13	chr6:80655800-80657800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:80655800-80657800	Active TSS	Stomach Smooth Muscle	stomach
15	chr6:80655800-80658000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr6:80656000-80657400	Active TSS	H1 Cell Line	embryonic stem cell
17	chr6:80656000-80657400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:80656000-80657400	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr6:80656000-80657400	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr6:80656000-80657400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
21	chr6:80656000-80657400	Active TSS	Brain Cingulate Gyrus	brain
22	chr6:80656000-80657400	Active TSS	Dnd41	blood
23	chr6:80656000-80657600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:80656000-80657600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:80656000-80657600	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr6:80656000-80657600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:80656000-80657600	Active TSS	HSMM	muscle
28	chr6:80656000-80657800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr6:80656000-80657800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:80656000-80657800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr6:80656000-80657800	Active TSS	Aorta	Aorta
32	chr6:80656000-80657800	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr6:80656000-80658000	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr6:80656200-80657200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
35	chr6:80656200-80657400	Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr6:80656200-80657400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:80656200-80657400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
38	chr6:80656200-80657400	Active TSS	Rectal Smooth Muscle	rectum
39	chr6:80656200-80657400	Active TSS	HMEC	breast
40	chr6:80656200-80657400	Active TSS	HSMMtube	muscle
41	chr6:80656200-80657600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:80656200-80657600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:80656200-80657600	Active TSS	H9 Cell Line	embryonic stem cell
44	chr6:80656200-80657600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:80656200-80657600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr6:80656200-80657600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:80656200-80657600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
48	chr6:80656200-80657600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
49	chr6:80656200-80657600	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
50	chr6:80656200-80657600	Active TSS	Colon Smooth Muscle	Colon

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