Variant report

Variant	nsv1027863
Chromosome Location	chr6:163934616-163965216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:255)
CpG islands
(count:122)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:255 , 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	chr6:163957788-163958100	K562	blood:	n/a	n/a
2	ARID3A	chr6:163954423-163954851	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:163933418-163934890	K562	blood:	n/a	n/a
4	ATF3	chr6:163957793-163958162	K562	blood:	n/a	n/a
5	BACH1	chr6:163934548-163934907	K562	blood:	n/a	n/a
6	BACH1	chr6:163934620-163934796	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:163952314-163952396	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr6:163934899-163935276	K562	blood:	n/a	n/a
9	CCNT2	chr6:163950889-163951089	K562	blood:	n/a	n/a
10	CEBPB	chr6:163954494-163954962	IMR90	lung:	n/a	chr6:163954769-163954786
11	CEBPB	chr6:163954511-163954864	A549	lung:	n/a	chr6:163954769-163954786
12	CEBPB	chr6:163934509-163935197	K562	blood:	n/a	n/a
13	CEBPB	chr6:163954522-163954812	A549	lung:	n/a	chr6:163954769-163954786
14	CEBPB	chr6:163954379-163955017	A549	lung:	n/a	chr6:163954769-163954786
15	CEBPB	chr6:163934881-163935217	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:163954487-163954861	Hela-S3	cervix:	n/a	chr6:163954769-163954786
17	CEBPB	chr6:163954515-163954806	K562	blood:	n/a	chr6:163954769-163954786
18	CEBPB	chr6:163934905-163935078	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:163934842-163935247	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:163954494-163954850	HepG2	liver:	n/a	chr6:163954769-163954786
21	CEBPB	chr6:163954544-163954953	HCT-116	colon:	n/a	chr6:163954769-163954786
22	CHD2	chr6:163950637-163950660	K562	blood:	n/a	n/a
23	CHD2	chr6:163952342-163952482	HepG2	liver:	n/a	n/a
24	CREB1	chr6:163954490-163954866	HepG2	liver:	n/a	n/a
25	CREB1	chr6:163954620-163954827	A549	lung:	n/a	n/a
26	CTCF	chr6:163952774-163952823	GM10248	blood:	n/a	n/a
27	CTCF	chr6:163950960-163951110	AG04449	skin:	n/a	n/a
28	CTCF	chr6:163934800-163934950	SAEC	small airway:	n/a	n/a
29	CTCF	chr6:163950980-163951130	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr6:163960537-163960597	GM13976	blood:	n/a	n/a
31	CTCF	chr6:163938578-163938580	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr6:163950880-163951030	AG04449	skin:	n/a	n/a
33	CTCF	chr6:163938589-163938628	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr6:163950740-163950890	HAc	cerebellar:	n/a	n/a
35	CTCF	chr6:163950820-163950970	AG04450	lung:	n/a	n/a
36	CTCF	chr6:163950920-163951070	HPAF	blood vessel:	n/a	n/a
37	CTCFL	chr6:163935049-163935186	K562	blood:	n/a	n/a
38	CUX1	chr6:163938298-163938302	K562	blood:	n/a	n/a
39	CUX1	chr6:163963410-163963535	GM12878	blood:	n/a	n/a
40	CUX1	chr6:163952382-163952573	K562	blood:	n/a	n/a
41	CUX1	chr6:163934265-163935012	K562	blood:	n/a	n/a
42	CUX1	chr6:163957894-163958032	K562	blood:	n/a	n/a
43	E2F4	chr6:163950782-163951029	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr6:163943038-163943130	MCF10A-Er-Src	breast:	n/a	n/a
45	EGR1	chr6:163957843-163958183	HCT-116	colon:	n/a	chr6:163957885-163957894
46	EGR1	chr6:163957841-163958130	K562	blood:	n/a	chr6:163957885-163957894
47	EP300	chr6:163950451-163951302	SK-N-SH	brain:	n/a	chr6:163950564-163950578 chr6:163951113-163951127
48	EP300	chr6:163957826-163957990	K562	blood:	n/a	n/a
49	EP300	chr6:163934484-163935179	K562	blood:	n/a	n/a
50	EP300	chr6:163950796-163950830	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163959346-163959396	HCT-116	colon:	n/a
2	chr6:163951256-163951306	LNCaP	prostate:	n/a
3	chr6:163951256-163951306	HRE	kidney:	n/a
4	chr6:163959346-163959396	HIPEpiC	eye:	n/a
5	chr6:163959346-163959396	HNPCEpiC	eye:	n/a
6	chr6:163959346-163959396	AG04450	lung:	fetal
7	chr6:163959346-163959396	K562	blood:	n/a
8	chr6:163959346-163959396	GM12892	blood:	n/a
9	chr6:163951256-163951306	AoSMC	blood vessel:	n/a
10	chr6:163951256-163951306	BE2_C	brain:	n/a
11	chr6:163951256-163951306	HRPEpiC	eye:	n/a
12	chr6:163959346-163959396	RPTEC	kidney:	n/a
13	chr6:163959346-163959396	IMR90	lung:	fetal
14	chr6:163951256-163951306	PFSK-1	brain:	n/a
15	chr6:163959346-163959396	MCF10A-Er-Src	breast:	n/a
16	chr6:163959346-163959396	HCF	heart:	n/a
17	chr6:163959346-163959396	AG09309	skin:	n/a
18	chr6:163951256-163951306	ovcar-3	ovarian:	n/a
19	chr6:163951256-163951306	NHDF-neo	bronchial:	n/a
20	chr6:163959346-163959396	GM19239	blood:	n/a
21	chr6:163959346-163959396	BJ	skin:	n/a
22	chr6:163959346-163959396	NB4	blood:	n/a
23	chr6:163951256-163951306	HCF	heart:	n/a
24	chr6:163959346-163959396	ProgFib	skin:	n/a
25	chr6:163951256-163951306	HRCEpiC	kidney:	n/a
26	chr6:163951256-163951306	SK-N-SH	brain:	n/a
27	chr6:163951256-163951306	ProgFib	skin:	n/a
28	chr6:163951256-163951306	T-47D	breast:	n/a
29	chr6:163951256-163951306	AG09309	skin:	n/a
30	chr6:163959346-163959396	SK-N-SH_RA	brain:	n/a
31	chr6:163959346-163959396	PrEC	prostate:	n/a
32	chr6:163951256-163951306	Hela-S3	cervix:	n/a
33	chr6:163951256-163951306	AG09319	gingival:	n/a
34	chr6:163951256-163951306	U87	brain:	n/a
35	chr6:163959346-163959396	SK-N-MC	brain:	n/a
36	chr6:163959346-163959396	MCF-7	breast:	n/a
37	chr6:163959346-163959396	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:163951256-163951306	HIPEpiC	eye:	n/a
39	chr6:163959346-163959396	NHBE	bronchial:	n/a
40	chr6:163951256-163951306	HNPCEpiC	eye:	n/a
41	chr6:163951256-163951306	IMR90	lung:	fetal
42	chr6:163951256-163951306	HEK293	kidney:	embryo
43	chr6:163951256-163951306	AG04450	lung:	fetal
44	chr6:163959346-163959396	NHDF-neo	bronchial:	n/a
45	chr6:163951256-163951306	PrEC	prostate:	n/a
46	chr6:163959346-163959396	T-47D	breast:	n/a
47	chr6:163959346-163959396	HRCEpiC	kidney:	n/a
48	chr6:163951256-163951306	A549	lung:	n/a
49	chr6:163951256-163951306	GM12878	blood:	n/a
50	chr6:163951256-163951306	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:163964093..163966401-chr6:163969080..163970781,2	K562	blood:
2	chr6:163941356..163943183-chr6:163944716..163947112,2	K562	blood:
3	chr6:163916682..163919334-chr6:163944719..163947401,2	MCF-7	breast:
4	chr6:163834068..163835581-chr6:163938752..163941095,2	K562	blood:
5	chr6:163933236..163935376-chr6:163942344..163945131,2	MCF-7	breast:
6	chr6:163836950..163839312-chr6:163964461..163966264,2	MCF-7	breast:
7	chr6:163953551..163956028-chr6:163958889..163960899,2	K562	blood:
8	chr6:163889319..163891540-chr6:163964872..163967579,2	K562	blood:
9	chr6:163863869..163866423-chr6:163944458..163946973,2	K562	blood:
10	chr6:163936784..163940539-chr6:163940693..163944816,5	K562	blood:
11	chr6:163935185..163937541-chr6:163947865..163950666,2	K562	blood:
12	chr6:163935196..163937277-chr6:163938981..163941955,2	K562	blood:
13	chr6:163956713..163960069-chr6:163960925..163963530,5	K562	blood:
14	chr6:163832850..163838270-chr6:163950827..163956360,5	K562	blood:
15	chr6:163919801..163922242-chr6:163941031..163943536,2	K562	blood:
16	chr6:163952879..163955434-chr6:163961662..163963741,2	K562	blood:
17	chr6:163956713..163960069-chr6:163960925..163963530,5	K562	blood:
18	chr6:163943184..163945151-chr6:163945835..163948340,2	K562	blood:
19	chr6:163947867..163950430-chr6:163952220..163954736,3	K562	blood:
20	chr6:163943461..163945437-chr6:163948022..163950368,2	MCF-7	breast:
21	chr6:163947867..163950430-chr6:163952220..163954736,3	K562	blood:
22	chr6:163962731..163964246-chr6:163970939..163973748,2	K562	blood:
23	chr6:163959475..163961501-chr6:163964972..163967917,2	K562	blood:
24	chr6:163959475..163961501-chr6:163964972..163967917,2	K562	blood:
25	chr6:163935041..163936837-chr6:163945446..163947162,2	K562	blood:
26	chr6:163963165..163965030-chr6:163966469..163968182,2	K562	blood:
27	chr6:163941356..163943183-chr6:163944716..163947112,2	K562	blood:
28	chr6:163943184..163945151-chr6:163945835..163948340,2	K562	blood:
29	chr6:163957772..163960340-chr6:163964403..163966144,2	MCF-7	breast:
30	chr6:163846486..163849719-chr6:163934600..163936577,3	K562	blood:
31	chr6:163957772..163960340-chr6:163964403..163966144,2	MCF-7	breast:
32	chr6:163936784..163940539-chr6:163940693..163944816,5	K562	blood:
33	chr6:163835622..163837984-chr6:163932902..163934643,2	K562	blood:
34	chr6:163852299..163854392-chr6:163948916..163951173,3	K562	blood:
35	chr6:163947828..163950335-chr6:163953664..163955368,2	K562	blood:
36	chr6:163956231..163958805-chr6:163964495..163966703,2	K562	blood:
37	chr6:163956231..163958805-chr6:163964495..163966703,2	K562	blood:
38	chr6:163957257..163960069-chr6:163960925..163963530,2	K562	blood:
39	chr6:163935185..163937541-chr6:163947865..163950666,2	K562	blood:
40	chr6:163943461..163945437-chr6:163948022..163950368,2	MCF-7	breast:
41	chr6:163947828..163950335-chr6:163953664..163955368,2	K562	blood:
42	chr6:163852299..163854392-chr6:163948916..163950508,2	K562	blood:
43	chr6:163952879..163955434-chr6:163961662..163963741,2	K562	blood:
44	chr6:163957257..163960069-chr6:163960925..163963530,2	K562	blood:
45	chr6:163933236..163935376-chr6:163942344..163945131,2	MCF-7	breast:
46	chr6:163834027..163837000-chr6:163957594..163959485,2	K562	blood:
47	chr6:163951535..163954078-chr6:163954622..163957067,3	K562	blood:
48	chr6:163935196..163937277-chr6:163938981..163941955,2	K562	blood:
49	chr6:163932152..163934277-chr6:163941799..163943537,2	K562	blood:
50	chr6:163935041..163936837-chr6:163945446..163947162,2	K562	blood:

No data

Variant related genes	Relation type
QKI	TF binding region
QKI	CpG island
ENSG00000270419	chromatin interactions
ENSG00000112531	chromatin interactions

Extended variants
information (count: 1158 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2179524	chr6:163934616-163934617	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558756644	chr6:163934618-163934619	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575518507	chr6:163934651-163934652	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs544547025	chr6:163934667-163934668	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs187528715	chr6:163934668-163934669	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs139303462	chr6:163934700-163934701	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs540683029	chr6:163934727-163934728	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs560397554	chr6:163934781-163934782	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs142737671	chr6:163934802-163934803	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs552384769	chr6:163934844-163934845	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs562712352	chr6:163934894-163934895	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs2179523	chr6:163934947-163934948	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548506128	chr6:163935011-163935012	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs9295222	chr6:163935209-163935210	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs190078686	chr6:163935238-163935239	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550632615	chr6:163935245-163935246	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373896946	chr6:163935252-163935253	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547438791	chr6:163935274-163935275	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570428858	chr6:163935293-163935294	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566152889	chr6:163935362-163935363	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6914387	chr6:163935382-163935383	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs75447022	chr6:163935400-163935401	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6913113	chr6:163935422-163935423	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs538105322	chr6:163935432-163935433	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115742128	chr6:163935438-163935439	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375164935	chr6:163935466-163935467	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574743111	chr6:163935527-163935528	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540290528	chr6:163935589-163935590	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182953031	chr6:163935603-163935604	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577407290	chr6:163935607-163935608	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546366291	chr6:163935652-163935653	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562624398	chr6:163935698-163935699	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531542885	chr6:163935715-163935716	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188449863	chr6:163935732-163935733	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561853933	chr6:163935825-163935826	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79196137	chr6:163935831-163935832	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7775850	chr6:163935846-163935847	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs368073665	chr6:163935847-163935848	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532862855	chr6:163935856-163935857	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549471003	chr6:163935883-163935884	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2321701	chr6:163935902-163935903	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs538066138	chr6:163935967-163935968	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555215941	chr6:163935975-163935976	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192233332	chr6:163935976-163935977	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568639480	chr6:163936031-163936032	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184607001	chr6:163936036-163936037	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187586125	chr6:163936056-163936057	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577312358	chr6:163936060-163936061	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541396479	chr6:163936106-163936107	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139596429	chr6:163936113-163936114	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1144 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163911800-163934800	Weak transcription	Pancreas	Pancrea
2	chr6:163920200-163934800	Weak transcription	Ovary	ovary
3	chr6:163926600-163934800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:163926600-163934800	Weak transcription	Lung	lung
5	chr6:163926600-163934800	Weak transcription	Psoas Muscle	Psoas
6	chr6:163926600-163934800	Weak transcription	Right Atrium	heart
7	chr6:163926600-163946200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:163926600-163946600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:163926600-163991800	Weak transcription	Esophagus	oesophagus
10	chr6:163926800-163934800	Weak transcription	Right Ventricle	heart
11	chr6:163927200-163951600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:163928200-163951600	Weak transcription	Spleen	Spleen
13	chr6:163928600-163938400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:163928600-163941000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr6:163928800-163934800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr6:163928800-163942800	Weak transcription	HSMM	muscle
17	chr6:163928800-163944000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr6:163928800-163946600	Weak transcription	HUVEC	blood vessel
19	chr6:163929000-163938000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:163929000-163947200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:163929200-163946600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr6:163929200-163946800	Weak transcription	HMEC	breast
23	chr6:163929400-163943800	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr6:163929400-163946600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:163929600-163934800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr6:163929600-163940000	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr6:163929600-163947200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr6:163929600-163950800	Weak transcription	Fetal Lung	lung
29	chr6:163929600-163951600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr6:163929800-163957000	Weak transcription	Primary B cells from cord blood	blood
31	chr6:163930200-163934800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:163930400-163940400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:163930400-163941000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:163930600-163938000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:163930600-163943600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:163930600-163950200	Weak transcription	Fetal Muscle Leg	muscle
37	chr6:163931000-163934800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:163931600-163934800	Weak transcription	Left Ventricle	heart
39	chr6:163933200-163935000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr6:163933200-163935200	Enhancers	Brain Anterior Caudate	brain
41	chr6:163933200-163935200	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr6:163933400-163939800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:163933800-163934800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr6:163933800-163937800	Weak transcription	Colon Smooth Muscle	Colon
45	chr6:163934000-163934800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr6:163934000-163935000	Flanking Active TSS	K562	blood
47	chr6:163934000-163935200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:163934000-163937800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr6:163934000-163939800	Enhancers	Fetal Heart	heart
50	chr6:163934200-163935200	Enhancers	A549	lung

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