Variant report

Variant	nsv470839
Chromosome Location	chr6:86205323-86279737
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:497)
CpG islands
(count:61)
Chromatin interactive
region (count:58)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:86246818-86247127	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:86225737-86226249	HepG2	liver:	n/a	n/a
3	BATF	chr6:86216073-86216495	GM12878	blood:	n/a	n/a
4	BATF	chr6:86205745-86206176	GM12878	blood:	n/a	n/a
5	BATF	chr6:86205760-86206009	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:86223159-86223173	GM12878	blood:	n/a	n/a
7	BRCA1	chr6:86208585-86208957	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr6:86225935-86226188	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr6:86248658-86248776	K562	blood:	n/a	n/a
10	CEBPB	chr6:86278173-86278463	K562	blood:	n/a	n/a
11	CEBPB	chr6:86225923-86226254	HepG2	liver:	n/a	n/a
12	CEBPB	chr6:86225826-86226298	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr6:86257775-86257998	A549	lung:	n/a	chr6:86257898-86257909
14	CEBPB	chr6:86225952-86226219	A549	lung:	n/a	n/a
15	CEBPB	chr6:86278161-86278480	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr6:86246980-86247026	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr6:86278177-86278481	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:86278204-86278358	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:86278171-86278479	K562	blood:	n/a	n/a
20	CEBPB	chr6:86271489-86271780	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:86225898-86226283	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr6:86278142-86278586	A549	lung:	n/a	n/a
23	CEBPB	chr6:86257737-86258093	HepG2	liver:	n/a	chr6:86257898-86257909
24	CEBPB	chr6:86208372-86209019	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:86278090-86278502	A549	lung:	n/a	n/a
26	CEBPB	chr6:86225924-86226285	MCF-7	breast:	n/a	n/a
27	CEBPB	chr6:86257726-86258057	IMR90	lung:	n/a	chr6:86257898-86257909
28	CEBPB	chr6:86225819-86226365	HCT-116	colon:	n/a	n/a
29	CEBPB	chr6:86225861-86226246	A549	lung:	n/a	n/a
30	CHD2	chr6:86208419-86208983	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr6:86261130-86261183	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr6:86246880-86247030	HMEC	breast:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
33	CTCF	chr6:86255475-86255538	GM10248	blood:	n/a	n/a
34	CTCF	chr6:86246857-86247097	HUVEC	blood vessel:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
35	CTCF	chr6:86246980-86247130	NHEK	skin:	n/a	n/a
36	CTCF	chr6:86246880-86247030	AG10803	skin:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
37	CTCF	chr6:86246589-86247245	K562	blood:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
38	CTCF	chr6:86247220-86247370	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr6:86246840-86246990	GM12864	blood:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
40	CTCF	chr6:86246674-86247326	A549	lung:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
41	CTCF	chr6:86246980-86247130	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:86246920-86247070	HRPEpiC	eye:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
43	CTCF	chr6:86246540-86246690	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr6:86247120-86247270	NB4	blood:	n/a	n/a
45	CTCF	chr6:86247160-86247310	NHLF	lung:	n/a	n/a
46	CTCF	chr6:86246586-86246664	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr6:86246878-86247080	K562	blood:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
48	CTCF	chr6:86266249-86266323	Fibrobl	skin:	n/a	n/a
49	CTCF	chr6:86246900-86247050	GM12871	blood:	n/a	chr6:86246941-86246962 chr6:86246947-86246963 chr6:86246946-86246964 chr6:86246952-86246961 chr6:86246948-86246961
50	CTCF	chr6:86247060-86247210	GM12869	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:86215383-86215433	AG09319	gingival:	n/a
2	chr6:86215383-86215433	SAEC	small airway:	n/a
3	chr6:86215383-86215433	Hela-S3	cervix:	n/a
4	chr6:86215383-86215433	HEK293	kidney:	embryo
5	chr6:86215383-86215433	AG10803	skin:	n/a
6	chr6:86215383-86215433	SK-N-MC	brain:	n/a
7	chr6:86215383-86215433	NB4	blood:	n/a
8	chr6:86215383-86215433	HEEpiC	esophagus:	n/a
9	chr6:86215383-86215433	AG04450	lung:	fetal
10	chr6:86215383-86215433	HCF	heart:	n/a
11	chr6:86215383-86215433	HRE	kidney:	n/a
12	chr6:86215383-86215433	SK-N-SH_RA	brain:	n/a
13	chr6:86215383-86215433	HCPEpiC	choroid plexus:	n/a
14	chr6:86215383-86215433	HCT-116	colon:	n/a
15	chr6:86215383-86215433	GM12892	blood:	n/a
16	chr6:86215383-86215433	GM12891	blood:	n/a
17	chr6:86215383-86215433	HL-60	blood:	n/a
18	chr6:86215383-86215433	SKMC	muscle:	n/a
19	chr6:86215383-86215433	LNCaP	prostate:	n/a
20	chr6:86215383-86215433	ProgFib	skin:	n/a
21	chr6:86215383-86215433	HUVEC	blood vessel:	n/a
22	chr6:86215383-86215433	AG04449	skin:	fetal
23	chr6:86215383-86215433	CMK	blood:	n/a
24	chr6:86215383-86215433	HAEpiC	amniotic membrane:	n/a
25	chr6:86215383-86215433	K562	blood:	n/a
26	chr6:86215383-86215433	NHBE	bronchial:	n/a
27	chr6:86215383-86215433	MCF-7	breast:	n/a
28	chr6:86215383-86215433	HRPEpiC	eye:	n/a
29	chr6:86215383-86215433	AoSMC	blood vessel:	n/a
30	chr6:86215383-86215433	GM12878	blood:	n/a
31	chr6:86215383-86215433	T-47D	breast:	n/a
32	chr6:86215383-86215433	PANC-1	pancreas:	n/a
33	chr6:86215383-86215433	ovcar-3	ovarian:	n/a
34	chr6:86215383-86215433	HNPCEpiC	eye:	n/a
35	chr6:86215383-86215433	RPTEC	kidney:	n/a
36	chr6:86215383-86215433	NHDF-neo	bronchial:	n/a
37	chr6:86215383-86215433	NT2-D1	testis:	n/a
38	chr6:86215383-86215433	IMR90	lung:	fetal
39	chr6:86215383-86215433	ECC-1	luminal epithelium:	n/a
40	chr6:86215383-86215433	Jurkat	blood:	n/a
41	chr6:86215383-86215433	Hepatocyte	liver:	n/a
42	chr6:86215383-86215433	HIPEpiC	eye:	n/a
43	chr6:86215383-86215433	AG09309	skin:	n/a
44	chr6:86215383-86215433	GM19239	blood:	n/a
45	chr6:86215383-86215433	HMEC	breast:	n/a
46	chr6:86215383-86215433	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:86215383-86215433	H1-hESC	embryonic stem cell:	embryo
48	chr6:86215383-86215433	PFSK-1	brain:	n/a
49	chr6:86215383-86215433	BJ	skin:	n/a
50	chr6:86215383-86215433	HCM	heart:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:86262845..86265792-chr6:86354340..86355847,2	K562	blood:
2	chr6:86245425..86248526-chr6:86302419..86304294,3	MCF-7	breast:
3	chr6:86202769..86205694-chr6:86385949..86388710,3	K562	blood:
4	chr1:121483913..121485978-chr6:86260101..86262043,2	MCF-7	breast:
5	chr6:86227398..86231196-chr6:86231483..86235507,4	K562	blood:
6	chr6:86230797..86232766-chr6:86233829..86236046,2	K562	blood:
7	chr6:86278096..86280709-chr6:86299065..86302030,2	K562	blood:
8	chr6:86203775..86205410-chr6:86207113..86209986,2	MCF-7	breast:
9	chr6:86268112..86269653-chr6:86301871..86303765,2	MCF-7	breast:
10	chr6:86215713..86217410-chr6:86218817..86221712,2	K562	blood:
11	chr6:86211598..86213102-chr6:86215561..86217190,2	K562	blood:
12	chr6:86205630..86207293-chr6:86209333..86212533,3	K562	blood:
13	chr6:86263461..86265279-chr6:86276918..86279076,2	K562	blood:
14	chr6:86226272..86228604-chr6:86231901..86233578,2	K562	blood:
15	chr6:86260582..86262333-chr6:86283688..86285782,2	K562	blood:
16	chr6:86244402..86246705-chr6:86351828..86353927,2	K562	blood:
17	chr6:86205630..86207293-chr6:86209333..86212533,3	K562	blood:
18	chr6:86230797..86232766-chr6:86233829..86236046,2	K562	blood:
19	chr6:86215713..86217410-chr6:86218817..86221712,2	K562	blood:
20	chr6:86249376..86250949-chr6:86302957..86305018,2	MCF-7	breast:
21	chr6:86212509..86214733-chr6:86218733..86220237,2	K562	blood:
22	chr6:86256251..86258999-chr6:86261062..86262660,2	K562	blood:
23	chr6:86254209..86255785-chr6:86263781..86265838,2	K562	blood:
24	chr6:86211598..86213102-chr6:86215561..86217190,2	K562	blood:
25	chr6:86252068..86253967-chr6:86254803..86256985,2	MCF-7	breast:
26	chr2:86333196..86333767-chr6:86224978..86225478,2	HCT-116	colon:
27	chr6:86227398..86231196-chr6:86231483..86235507,4	K562	blood:
28	chr6:86212509..86214733-chr6:86218733..86220237,2	K562	blood:
29	chr6:86246870..86249179-chr6:86250224..86253982,4	K562	blood:
30	chr6:86253602..86255869-chr6:86388137..86389916,2	K562	blood:
31	chr6:86252970..86257934-chr6:86299533..86304034,5	K562	blood:
32	chr6:86226272..86228604-chr6:86231901..86233578,2	K562	blood:
33	chr6:86264055..86265860-chr6:86266095..86267988,2	MCF-7	breast:
34	chr6:86207297..86209802-chr6:86213073..86214625,2	K562	blood:
35	chr6:86216856..86218839-chr6:86222143..86224772,2	MCF-7	breast:
36	chr6:86230515..86233270-chr6:86240880..86242983,2	MCF-7	breast:
37	chr6:86246140..86247926-chr6:86387829..86390203,2	K562	blood:
38	chr6:86199220..86200919-chr6:86203979..86206335,3	K562	blood:
39	chr6:86213906..86216612-chr6:86245425..86247790,2	K562	blood:
40	chr6:86272075..86276621-chr6:86278796..86281589,4	K562	blood:
41	chr6:86272075..86276621-chr6:86278796..86281589,4	K562	blood:
42	chr6:86256251..86258999-chr6:86261062..86262660,2	K562	blood:
43	chr6:86264055..86265860-chr6:86266095..86267988,2	MCF-7	breast:
44	chr6:86216856..86218839-chr6:86222143..86224772,2	MCF-7	breast:
45	chr6:86259058..86261534-chr6:86261647..86264216,2	MCF-7	breast:
46	chr6:86244360..86246151-chr6:86281101..86282612,2	K562	blood:
47	chr6:86278825..86281337-chr6:86301829..86304998,5	MCF-7	breast:
48	chr6:86230515..86233270-chr6:86240880..86242983,2	MCF-7	breast:
49	chr6:86277967..86280027-chr6:86387160..86389820,3	K562	blood:
50	chr6:86246106..86247862-chr6:86386298..86390203,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX14-2	chr6:86208159-86208764	NONHSAT113838
2	lnc-SYNCRIP-7	chr6:86216951-86217007	NONHSAT113839
3	lnc-SYNCRIP-7	chr6:86215516-86215723	NONHSAT113839
4	lnc-SYNCRIP-7	chr6:86217686-86218175	NONHSAT113839
5	lnc-FAM165A-1	chr6:86270792-86270928	ENSG00000223998.1
6	lnc-FAM165A-1	chr6:86270033-86270491	ENSG00000223998.1

No data

Variant related genes	Relation type
SNX14	TF binding region
SNX14	CpG island
ENSG00000068654	chromatin interactions
ENSG00000135317	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000135316	chromatin interactions
ENSG00000132300	chromatin interactions

Extended variants
information (count: 2558 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2558 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6922	chr6:86205323-86205324	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150877880	chr6:86205333-86205334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs138351627	chr6:86205375-86205376	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142840005	chr6:86205391-86205392	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562180332	chr6:86205434-86205435	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146065294	chr6:86205515-86205516	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544859299	chr6:86205570-86205571	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140010305	chr6:86205585-86205586	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs12528808	chr6:86205644-86205645	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs184217790	chr6:86205654-86205655	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552485944	chr6:86205664-86205665	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570671158	chr6:86205697-86205698	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs115454013	chr6:86205727-86205728	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs546282830	chr6:86205782-86205783	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs575530449	chr6:86205811-86205812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529522191	chr6:86205875-86205876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568110709	chr6:86205904-86205905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535170750	chr6:86205914-86205915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556686614	chr6:86205958-86205959	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7761762	chr6:86205968-86205969	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs149958569	chr6:86206029-86206030	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558393320	chr6:86206066-86206067	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189024048	chr6:86206085-86206086	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144101557	chr6:86206140-86206141	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555486648	chr6:86206145-86206146	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370929087	chr6:86206179-86206180	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544714219	chr6:86206191-86206192	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562998172	chr6:86206273-86206274	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148688308	chr6:86206313-86206314	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527272131	chr6:86206320-86206321	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182095987	chr6:86206334-86206335	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4501401	chr6:86206396-86206397	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs528387400	chr6:86206420-86206421	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187139001	chr6:86206472-86206473	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532606501	chr6:86206518-86206519	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528886224	chr6:86206519-86206520	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147819921	chr6:86206660-86206661	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568624572	chr6:86206678-86206679	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139573792	chr6:86206720-86206721	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190805612	chr6:86206730-86206731	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569063483	chr6:86206746-86206747	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374001244	chr6:86206747-86206748	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567112839	chr6:86206748-86206749	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145101059	chr6:86206754-86206755	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374408333	chr6:86206758-86206759	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6927475	chr6:86206773-86206774	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs538258926	chr6:86206777-86206778	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556668850	chr6:86206783-86206784	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531546312	chr6:86206803-86206804	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115375667	chr6:86206822-86206823	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	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
Lung adenocarcinoma	21935476	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
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
craniofacial dysmorphism	21918468	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1790 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86176800-86242600	Weak transcription	Gastric	stomach
2	chr6:86178800-86206800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:86186800-86206200	Weak transcription	Lung	lung
4	chr6:86186800-86211000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:86192600-86207000	Weak transcription	Brain Hippocampus Middle	brain
6	chr6:86192800-86221400	Weak transcription	Brain Substantia Nigra	brain
7	chr6:86193000-86221200	Weak transcription	A549	lung
8	chr6:86193200-86212200	Weak transcription	Brain Anterior Caudate	brain
9	chr6:86193400-86208600	Weak transcription	HUVEC	blood vessel
10	chr6:86193400-86219800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr6:86194800-86206000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr6:86194800-86206000	Strong transcription	NHDF-Ad	bronchial
13	chr6:86195000-86211800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr6:86195000-86219800	Weak transcription	Brain Angular Gyrus	brain
15	chr6:86196800-86206800	Weak transcription	Esophagus	oesophagus
16	chr6:86196800-86221600	Weak transcription	Spleen	Spleen
17	chr6:86199600-86219400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr6:86200000-86219200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr6:86200200-86219400	Weak transcription	Colon Smooth Muscle	Colon
20	chr6:86200600-86206600	Weak transcription	Fetal Stomach	stomach
21	chr6:86200600-86207200	Strong transcription	Osteobl	bone
22	chr6:86200600-86207400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:86200600-86208800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:86200600-86220400	Weak transcription	Psoas Muscle	Psoas
25	chr6:86200600-86221800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr6:86200800-86206800	Weak transcription	NH-A	brain
27	chr6:86200800-86212800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr6:86201000-86216600	Weak transcription	Left Ventricle	heart
29	chr6:86201600-86218800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr6:86202600-86212000	Weak transcription	Primary T cells from cord blood	blood
31	chr6:86202800-86206000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:86202800-86206000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:86202800-86208400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr6:86202800-86211800	Weak transcription	Ovary	ovary
35	chr6:86202800-86218800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:86203000-86207000	Weak transcription	Aorta	Aorta
37	chr6:86203400-86219800	Weak transcription	NHLF	lung
38	chr6:86203800-86206000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr6:86204800-86206400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:86204800-86207400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:86204800-86208000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:86204800-86208400	Weak transcription	NHEK	skin
43	chr6:86205000-86205400	Strong transcription	HMEC	breast
44	chr6:86205000-86206000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:86205000-86206000	Strong transcription	Muscle Satellite Cultured Cells	--
46	chr6:86205000-86206000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr6:86205000-86206800	Weak transcription	Fetal Muscle Leg	muscle
48	chr6:86205000-86207000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr6:86205000-86211000	Weak transcription	Adipose Nuclei	Adipose
50	chr6:86205000-86212400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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