Variant report

Variant	nsv1017419
Chromosome Location	chr6:106984669-106997000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:106988592-106989119	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:106996021-106996314	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:106985110-106985286	GM12878	blood:	n/a	n/a
4	CEBPB	chr6:106988811-106989083	HepG2	liver:	n/a	chr6:106988958-106988969
5	CEBPB	chr6:106988709-106989172	MCF-7	breast:	n/a	chr6:106988751-106988764 chr6:106988958-106988969
6	CEBPB	chr6:106988817-106989138	A549	lung:	n/a	chr6:106988958-106988969
7	CEBPB	chr6:106987408-106987625	A549	lung:	n/a	chr6:106987527-106987538
8	CEBPB	chr6:106987384-106987609	HepG2	liver:	n/a	chr6:106987527-106987538
9	CEBPB	chr6:106984874-106985150	IMR90	lung:	n/a	chr6:106985121-106985134
10	CEBPB	chr6:106987539-106987581	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:106988814-106989125	IMR90	lung:	n/a	chr6:106988958-106988969
12	CEBPB	chr6:106994236-106995166	HCT-116	colon:	n/a	n/a
13	CEBPB	chr6:106988356-106989183	Hela-S3	cervix:	n/a	chr6:106988751-106988764 chr6:106988958-106988969
14	CEBPB	chr6:106988811-106989159	HepG2	liver:	n/a	chr6:106988958-106988969
15	CEBPB	chr6:106987433-106987626	Hela-S3	cervix:	n/a	chr6:106987527-106987538
16	CEBPB	chr6:106988834-106989132	HepG2	liver:	n/a	chr6:106988958-106988969
17	CEBPB	chr6:106988756-106989050	A549	lung:	n/a	chr6:106988958-106988969
18	CEBPB	chr6:106987354-106987644	K562	blood:	n/a	chr6:106987527-106987538
19	CEBPB	chr6:106988719-106989156	HepG2	liver:	n/a	chr6:106988751-106988764 chr6:106988958-106988969
20	CEBPB	chr6:106994615-106994833	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:106988731-106989241	MCF-7	breast:	n/a	chr6:106988751-106988764 chr6:106988958-106988969
22	CHD2	chr6:106996125-106996342	HepG2	liver:	n/a	n/a
23	CHD2	chr6:106988971-106989036	HepG2	liver:	n/a	n/a
24	CHD2	chr6:106996102-106996182	K562	blood:	n/a	n/a
25	CTCF	chr6:106995880-106996030	WI-38	lung:	n/a	n/a
26	CTCF	chr6:106995920-106996070	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr6:106995840-106995990	AG04450	lung:	n/a	n/a
28	CTCF	chr6:106995900-106996050	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr6:106995940-106996090	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr6:106995880-106996030	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr6:106995800-106995950	NHEK	skin:	n/a	n/a
32	CTCF	chr6:106995900-106996050	HMEC	breast:	n/a	n/a
33	CTCF	chr6:106995900-106996050	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr6:106995940-106996090	HAc	cerebellar:	n/a	n/a
35	CTCF	chr6:106995880-106996030	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr6:106995840-106995990	SAEC	small airway:	n/a	n/a
37	CTCF	chr6:106995900-106996050	Caco-2	colon:	n/a	n/a
38	CTCF	chr6:106995960-106996110	HCFaa	heart:	n/a	n/a
39	CTCF	chr6:106996180-106996330	AG04450	lung:	n/a	n/a
40	CTCF	chr6:106995940-106996090	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr6:106995860-106996010	HMF	breast:	n/a	n/a
42	CTCF	chr6:106995980-106996130	HepG2	liver:	n/a	n/a
43	CTCF	chr6:106996060-106996210	HVMF	connective:	n/a	n/a
44	CTCF	chr6:106995880-106996030	HPF	lung:	n/a	n/a
45	CTCF	chr6:106995880-106996030	AG04450	lung:	n/a	n/a
46	CTCF	chr6:106995900-106996050	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr6:106995920-106996070	HMEC	breast:	n/a	n/a
48	E2F4	chr6:106995992-106996380	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F6	chr6:106996230-106996526	H1-hESC	embryonic stem cell:	n/a	n/a
50	E2F6	chr6:106996135-106996621	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:106988121-106988171	HRE	kidney:	n/a
2	chr6:106988121-106988171	AoSMC	blood vessel:	n/a
3	chr6:106988121-106988171	AG09319	gingival:	n/a
4	chr6:106988121-106988171	LNCaP	prostate:	n/a
5	chr6:106988121-106988171	GM12891	blood:	n/a
6	chr6:106988121-106988171	SKMC	muscle:	n/a
7	chr6:106988121-106988171	T-47D	breast:	n/a
8	chr6:106988121-106988171	MCF-7	breast:	n/a
9	chr6:106988121-106988171	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:106988121-106988171	NT2-D1	testis:	n/a
11	chr6:106988121-106988171	Jurkat	blood:	n/a
12	chr6:106988121-106988171	GM12878	blood:	n/a
13	chr6:106988121-106988171	K562	blood:	n/a
14	chr6:106988121-106988171	HL-60	blood:	n/a
15	chr6:106988121-106988171	CMK	blood:	n/a
16	chr6:106988121-106988171	GM19239	blood:	n/a
17	chr6:106988121-106988171	HCPEpiC	choroid plexus:	n/a
18	chr6:106988121-106988171	ovcar-3	ovarian:	n/a
19	chr6:106988121-106988171	NHBE	bronchial:	n/a
20	chr6:106988121-106988171	HRPEpiC	eye:	n/a
21	chr6:106988121-106988171	BE2_C	brain:	n/a
22	chr6:106988121-106988171	Hepatocyte	liver:	n/a
23	chr6:106988121-106988171	Caco-2	colon:	n/a
24	chr6:106988121-106988171	AG09309	skin:	n/a
25	chr6:106988121-106988171	HAEpiC	amniotic membrane:	n/a
26	chr6:106988121-106988171	HMEC	breast:	n/a
27	chr6:106988121-106988171	NB4	blood:	n/a
28	chr6:106988121-106988171	NHDF-neo	bronchial:	n/a
29	chr6:106988121-106988171	BJ	skin:	n/a
30	chr6:106988121-106988171	MCF10A-Er-Src	breast:	n/a
31	chr6:106988121-106988171	AG04450	lung:	fetal
32	chr6:106988121-106988171	IMR90	lung:	fetal
33	chr6:106988121-106988171	Hela-S3	cervix:	n/a
34	chr6:106988121-106988171	AG04449	skin:	fetal
35	chr6:106988121-106988171	PFSK-1	brain:	n/a
36	chr6:106988121-106988171	HCT-116	colon:	n/a
37	chr6:106988121-106988171	HCF	heart:	n/a
38	chr6:106988121-106988171	SAEC	small airway:	n/a
39	chr6:106988121-106988171	AG10803	skin:	n/a
40	chr6:106988121-106988171	HEEpiC	esophagus:	n/a
41	chr6:106988121-106988171	HepG2	liver:	n/a
42	chr6:106988121-106988171	PANC-1	pancreas:	n/a
43	chr6:106988121-106988171	RPTEC	kidney:	n/a
44	chr6:106988121-106988171	HRCEpiC	kidney:	n/a
45	chr6:106988121-106988171	ECC-1	luminal epithelium:	n/a
46	chr6:106988121-106988171	A549	lung:	n/a
47	chr6:106988121-106988171	ProgFib	skin:	n/a
48	chr6:106988121-106988171	HIPEpiC	eye:	n/a
49	chr6:106988121-106988171	U87	brain:	n/a
50	chr6:106988121-106988171	HCM	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:106972979..106975776-chr6:106983451..106985409,2	MCF-7	breast:
2	chr6:106982668..106985044-chr6:106987673..106989483,2	K562	blood:
3	chr6:106976336..106978142-chr6:106984891..106987411,2	K562	blood:
4	chr6:106988236..106991971-chr6:106994585..106996382,3	MCF-7	breast:
5	chr6:106982665..106985601-chr6:106993025..106995759,2	MCF-7	breast:
6	chr6:106939256..106941678-chr6:106985710..106988008,2	MCF-7	breast:
7	chr6:106937771..106940207-chr6:106996030..106997572,2	MCF-7	breast:
8	chr6:106958366..106960246-chr6:106994046..106995660,2	MCF-7	breast:
9	chr6:106990837..106993931-chr6:106996769..107001251,4	K562	blood:
10	chr6:106982665..106985601-chr6:106993025..106995759,2	MCF-7	breast:

No data

Variant related genes	Relation type
AIM1	TF binding region
AIM1	CpG island
ENSG00000112297	chromatin interactions

Extended variants
information (count: 532 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9320173	chr6:106984669-106984670	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35546863	chr6:106984725-106984726	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs11153007	chr6:106984739-106984740	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs138372268	chr6:106984812-106984813	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142949603	chr6:106984875-106984876	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs373283606	chr6:106984887-106984888	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556332643	chr6:106984922-106984923	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569750038	chr6:106984945-106984946	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs536082359	chr6:106984967-106984968	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs13210799	chr6:106985056-106985057	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs555702724	chr6:106985105-106985106	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs79463573	chr6:106985148-106985149	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs541368778	chr6:106985149-106985150	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs558382988	chr6:106985156-106985157	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs554075380	chr6:106985188-106985189	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs183285104	chr6:106985236-106985237	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543403426	chr6:106985267-106985268	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs563475209	chr6:106985271-106985272	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs529327799	chr6:106985278-106985279	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs542684655	chr6:106985297-106985298	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs9486388	chr6:106985371-106985372	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs9320174	chr6:106985408-106985409	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs9320175	chr6:106985419-106985420	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs570724163	chr6:106985471-106985472	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs532988893	chr6:106985472-106985473	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs188214174	chr6:106985480-106985481	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs569640610	chr6:106985486-106985487	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs535558038	chr6:106985506-106985507	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs555399636	chr6:106985588-106985589	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs566143612	chr6:106985597-106985598	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs555940768	chr6:106985611-106985612	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535218076	chr6:106985634-106985635	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs536590884	chr6:106985725-106985726	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs577901956	chr6:106985765-106985766	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373600069	chr6:106985785-106985786	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572579802	chr6:106985798-106985799	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs553611252	chr6:106985816-106985817	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs17067219	chr6:106985820-106985821	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs150653791	chr6:106985832-106985833	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs72941340	chr6:106985856-106985857	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs9486389	chr6:106985862-106985863	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs76842459	chr6:106985876-106985877	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs783401	chr6:106985886-106985887	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs564249004	chr6:106985908-106985909	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200960557	chr6:106985911-106985912	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs139757026	chr6:106985957-106985958	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs550063393	chr6:106985967-106985968	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs569676740	chr6:106986024-106986025	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs386704594	chr6:106986034-106986035	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs3841394	chr6:106986037-106986038	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD

Chromatin state (count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106961000-107001400	Weak transcription	Gastric	stomach
2	chr6:106964800-106991000	Weak transcription	Spleen	Spleen
3	chr6:106964800-107029800	Weak transcription	Small Intestine	intestine
4	chr6:106970600-107022400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:106973400-106985600	Weak transcription	Stomach Mucosa	stomach
6	chr6:106973600-106985800	Weak transcription	Thymus	Thymus
7	chr6:106973600-106986000	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:106973600-106992800	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr6:106976400-106986200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr6:106976600-106991400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:106977000-106986400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:106978800-106985600	Weak transcription	Fetal Thymus	thymus
13	chr6:106978800-106993800	Weak transcription	NHLF	lung
14	chr6:106979000-107001400	Weak transcription	Pancreas	Pancrea
15	chr6:106979600-106987200	Weak transcription	HepG2	liver
16	chr6:106980800-106986200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:106980800-106986400	Strong transcription	Liver	Liver
18	chr6:106981400-106988000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr6:106981600-106995600	Weak transcription	Colonic Mucosa	Colon
20	chr6:106981800-106985200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr6:106981800-106985600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:106981800-106985600	Weak transcription	Esophagus	oesophagus
23	chr6:106981800-106987800	Weak transcription	Lung	lung
24	chr6:106982400-106984800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr6:106982400-106984800	Genic enhancers	NHEK	skin
26	chr6:106982400-106986000	Weak transcription	Placenta	Placenta
27	chr6:106982400-106987400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr6:106982400-106987600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
29	chr6:106982400-106987800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:106982400-107000800	Weak transcription	Rectal Smooth Muscle	rectum
31	chr6:106982600-106985600	Weak transcription	Fetal Intestine Large	intestine
32	chr6:106982600-106987200	Weak transcription	Hela-S3	cervix
33	chr6:106982800-106993200	Weak transcription	HUVEC	blood vessel
34	chr6:106983000-106987800	Weak transcription	Adipose Nuclei	Adipose
35	chr6:106983400-106985000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:106983400-106985000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr6:106983400-106985000	Weak transcription	GM12878-XiMat	blood
38	chr6:106983400-106989000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr6:106983400-106989800	Strong transcription	Dnd41	blood
40	chr6:106983600-106985400	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr6:106984000-106985000	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr6:106984000-106985000	Enhancers	NHDF-Ad	bronchial
43	chr6:106984000-106985200	Enhancers	Duodenum Mucosa	Duodenum
44	chr6:106984000-106986000	Enhancers	Fetal Intestine Small	intestine
45	chr6:106984000-106986800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
46	chr6:106984000-106986800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr6:106984000-106987800	Genic enhancers	Primary T cells from cord blood	blood
48	chr6:106984000-106989200	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr6:106984200-106984800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr6:106984200-106984800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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