Variant report

Variant	nsv817322
Chromosome Location	chr6:109933272-110070574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1459)
CpG islands
(count:1894)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:110012148-110012516	K562	blood:	n/a	n/a
2	ARID3A	chr6:109947743-109947775	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:110016756-110017015	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:110011916-110012560	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:110016814-110017014	K562	blood:	n/a	n/a
6	ATF1	chr6:110008403-110008832	K562	blood:	n/a	n/a
7	ATF2	chr6:110011764-110012271	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr6:110008348-110008671	K562	blood:	n/a	n/a
9	BATF	chr6:109953633-109953962	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:110026327-110026828	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:110026282-110026872	GM12878	blood:	n/a	n/a
12	BCLAF1	chr6:110012118-110012892	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:110011547-110012800	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:110008452-110008919	K562	blood:	n/a	n/a
15	BHLHE40	chr6:110012001-110012958	K562	blood:	n/a	n/a
16	BHLHE40	chr6:110026449-110026718	HepG2	liver:	n/a	n/a
17	BHLHE40	chr6:110018469-110018860	K562	blood:	n/a	n/a
18	BHLHE40	chr6:110026358-110026784	GM12878	blood:	n/a	n/a
19	BRCA1	chr6:110012014-110012749	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr6:110026248-110026927	HCT-116	colon:	n/a	n/a
21	CCNT2	chr6:110012207-110012744	K562	blood:	n/a	chr6:110012451-110012460
22	CCNT2	chr6:110011549-110011857	K562	blood:	n/a	n/a
23	CEBPB	chr6:109957671-109957789	A549	lung:	n/a	n/a
24	CEBPB	chr6:110008480-110008680	HepG2	liver:	n/a	chr6:110008552-110008563
25	CEBPB	chr6:110008413-110008730	K562	blood:	n/a	chr6:110008552-110008563
26	CEBPB	chr6:109952629-109952933	A549	lung:	n/a	chr6:109952785-109952796
27	CEBPB	chr6:110062154-110062387	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:110008384-110008743	Hela-S3	cervix:	n/a	chr6:110008552-110008563
29	CEBPB	chr6:110008348-110008719	K562	blood:	n/a	chr6:110008552-110008563
30	CEBPB	chr6:110018560-110018886	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:109952623-109952968	HepG2	liver:	n/a	chr6:109952785-109952796
32	CEBPB	chr6:110062120-110062336	K562	blood:	n/a	n/a
33	CEBPB	chr6:109947555-109947885	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:109957648-109957810	K562	blood:	n/a	n/a
35	CEBPB	chr6:110008251-110009063	HCT-116	colon:	n/a	chr6:110008552-110008563
36	CEBPB	chr6:110008257-110008925	HCT-116	colon:	n/a	chr6:110008552-110008563
37	CEBPB	chr6:109952640-109952967	IMR90	lung:	n/a	chr6:109952785-109952796
38	CEBPB	chr6:110008365-110008934	IMR90	lung:	n/a	chr6:110008552-110008563
39	CEBPB	chr6:110011810-110012545	GM12878	blood:	n/a	chr6:110012343-110012355
40	CEBPB	chr6:110018594-110018882	K562	blood:	n/a	n/a
41	CEBPB	chr6:110062108-110062332	A549	lung:	n/a	n/a
42	CEBPB	chr6:110008450-110008602	K562	blood:	n/a	chr6:110008552-110008563
43	CEBPB	chr6:109952735-109952897	K562	blood:	n/a	chr6:109952785-109952796
44	CHD1	chr6:110011967-110012344	GM12878	blood:	n/a	n/a
45	CHD1	chr6:110026322-110026941	IMR90	lung:	n/a	n/a
46	CHD2	chr6:110011732-110012976	GM12878	blood:	n/a	chr6:110012873-110012880
47	CHD2	chr6:110012187-110012526	K562	blood:	n/a	n/a
48	CHD2	chr6:110000434-110000678	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr6:110012353-110012600	HepG2	liver:	n/a	n/a
50	CHD2	chr6:110011510-110012632	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:110012263-110012313	NH-A	brain:	n/a
2	chr6:109941310-109941360	HAEpiC	amniotic membrane:	n/a
3	chr6:110012723-110012773	AG10803	skin:	n/a
4	chr6:110012263-110012313	NH-A	brain:	n/a
5	chr6:109941310-109941360	HAEpiC	amniotic membrane:	n/a
6	chr6:110012723-110012773	AG10803	skin:	n/a
7	chr6:110011968-110012018	GM12891	blood:	n/a
8	chr6:110011599-110011649	SK-N-SH	brain:	n/a
9	chr6:109941310-109941360	SK-N-SH	brain:	n/a
10	chr6:110008415-110008465	LNCaP	prostate:	n/a
11	chr6:110011968-110012018	NT2-D1	testis:	n/a
12	chr6:110011999-110012049	H1-hESC	embryonic stem cell:	embryo
13	chr6:110011599-110011649	HCM	heart:	n/a
14	chr6:110012386-110012436	HRPEpiC	eye:	n/a
15	chr6:110012574-110012624	GM19239	blood:	n/a
16	chr6:110015052-110015102	IMR90	lung:	fetal
17	chr6:110012386-110012436	IMR90	lung:	fetal
18	chr6:110012591-110012641	AG09319	gingival:	n/a
19	chr6:110011999-110012049	HEEpiC	esophagus:	n/a
20	chr6:110015052-110015102	GM12878	blood:	n/a
21	chr6:110012723-110012773	LNCaP	prostate:	n/a
22	chr6:110012409-110012459	MCF10A-Er-Src	breast:	n/a
23	chr6:110023769-110023819	PANC-1	pancreas:	n/a
24	chr6:110012632-110012682	PANC-1	pancreas:	n/a
25	chr6:110011968-110012018	MCF-7	breast:	n/a
26	chr6:110011968-110012018	LNCaP	prostate:	n/a
27	chr6:110012263-110012313	NT2-D1	testis:	n/a
28	chr6:110011599-110011649	Caco-2	colon:	n/a
29	chr6:110011686-110011736	A549	lung:	n/a
30	chr6:110012874-110012924	NH-A	brain:	n/a
31	chr6:109940408-109940458	ECC-1	luminal epithelium:	n/a
32	chr6:110011968-110012018	AG10803	skin:	n/a
33	chr6:109960018-109960068	HCM	heart:	n/a
34	chr6:110012378-110012428	H1-hESC	embryonic stem cell:	embryo
35	chr6:110009743-110009793	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:109941310-109941360	BJ	skin:	n/a
37	chr6:110015052-110015102	T-47D	breast:	n/a
38	chr6:110012577-110012627	SK-N-SH_RA	brain:	n/a
39	chr6:110009743-110009793	GM19239	blood:	n/a
40	chr6:109953157-109953207	NB4	blood:	n/a
41	chr6:110012263-110012313	ProgFib	skin:	n/a
42	chr6:110011999-110012049	SAEC	small airway:	n/a
43	chr6:109941310-109941360	PrEC	prostate:	n/a
44	chr6:109940408-109940458	HRPEpiC	eye:	n/a
45	chr6:110011999-110012049	HCF	heart:	n/a
46	chr6:110012366-110012416	AG10803	skin:	n/a
47	chr6:109953157-109953207	H1-hESC	embryonic stem cell:	embryo
48	chr6:110012577-110012627	HepG2	liver:	n/a
49	chr6:110015052-110015102	SK-N-SH_RA	brain:	n/a
50	chr6:110012095-110012145	HAEpiC	amniotic membrane:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:110026295..110027102-chr6:110374620..110375475,7	K562	blood:
2	chr6:110001528..110003303-chr6:110005576..110008412,2	MCF-7	breast:
3	chr6:110025954..110027208-chr6:110359665..110362381,41	MCF-7	breast:
4	chr6:110006952..110010658-chr6:110010983..110015603,5	K562	blood:
5	chr6:110026083..110027087-chr6:110374560..110375697,12	MCF-7	breast:
6	chr6:110026208..110027002-chr6:110360378..110361549,3	K562	blood:
7	chr6:110026116..110027123-chr6:110104149..110105170,4	MCF-7	breast:
8	chr6:110026127..110027055-chr6:110711820..110712448,2	MCF-7	breast:
9	chr6:109996616..109999325-chr6:110011516..110013836,2	K562	blood:
10	chr6:110026144..110026871-chr6:110500143..110501053,2	MCF-7	breast:
11	chr6:110024804..110028000-chr6:110359372..110362087,3	MCF-7	breast:
12	chr6:109983707..109985653-chr6:110007788..110010480,2	K562	blood:
13	chr6:110026131..110026685-chr6:110213854..110214493,2	MCF-7	breast:
14	chr6:109926146..109927722-chr6:109932421..109934095,2	MCF-7	breast:
15	chr6:109917095..109917599-chr6:110026112..110027051,2	MCF-7	breast:
16	chr6:110009150..110010856-chr6:110010893..110012924,2	MCF-7	breast:
17	chr6:110012433..110012940-chr8:145634538..145635256,2	Hela-S3	cervix:
18	chr6:110017902..110019926-chr6:110022450..110025001,2	K562	blood:
19	chr6:109847917..109848863-chr6:110026120..110026805,4	MCF-7	breast:
20	chr6:109848106..109848779-chr6:110026265..110026944,2	MCF-7	breast:
21	chr6:109963602..109966014-chr6:110009596..110012309,2	MCF-7	breast:
22	chr6:109927783..109929912-chr6:109931522..109933858,2	K562	blood:
23	chr6:109916966..109917798-chr6:110016397..110017380,5	MCF-7	breast:
24	chr6:109509121..109509682-chr6:110026304..110027085,2	K562	blood:
25	chr6:110026617..110027143-chr6:110372925..110373520,2	MCF-7	breast:
26	chr6:109932824..109934658-chr6:109936171..109939061,2	K562	blood:
27	chr6:110047914..110050234-chr6:110051143..110053248,2	MCF-7	breast:
28	chr6:110026132..110026688-chr6:110711506..110712260,2	MCF-7	breast:
29	chr6:109982568..109985653-chr6:110007788..110010480,3	K562	blood:
30	chr6:109932824..109934658-chr6:109936171..109939061,2	K562	blood:
31	chr6:110025993..110027032-chr6:110374302..110375553,10	MCF-7	breast:
32	chr6:110001528..110003303-chr6:110005576..110008412,2	MCF-7	breast:
33	chr6:109916901..109917812-chr6:110016606..110017379,4	MCF-7	breast:
34	chr6:110025916..110027085-chr6:110711360..110712730,11	K562	blood:
35	chr6:110042492..110045032-chr6:110370097..110372632,2	MCF-7	breast:
36	chr6:110047914..110050234-chr6:110051143..110053248,2	MCF-7	breast:
37	chr6:110026058..110027053-chr6:110360200..110361829,12	MCF-7	breast:
38	chr6:109978242..109980545-chr6:109984478..109986308,2	K562	blood:

No data

Variant related genes	Relation type
AK9	TF binding region
FIG4	TF binding region
AK9	CpG island
FIG4	CpG island
ENSG00000272115	chromatin interactions
ENSG00000112290	chromatin interactions
ENSG00000112367	chromatin interactions
ENSG00000071894	chromatin interactions
ENSG00000155085	chromatin interactions

Extended variants
information (count: 5000 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:5000 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553809064	chr6:109933283-109933284	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs148990878	chr6:109933389-109933390	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs73519236	chr6:109933415-109933416	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558738305	chr6:109933461-109933462	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182661711	chr6:109933485-109933486	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62438268	chr6:109933510-109933511	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374454514	chr6:109933512-109933513	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544528598	chr6:109933553-109933554	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561089805	chr6:109933566-109933567	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530086494	chr6:109933612-109933613	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150229013	chr6:109933619-109933620	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368384163	chr6:109933620-109933621	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188055957	chr6:109933622-109933623	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545551984	chr6:109933637-109933638	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192820632	chr6:109933664-109933665	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184566417	chr6:109933700-109933701	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187486512	chr6:109933783-109933784	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532693156	chr6:109933792-109933793	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552358491	chr6:109933797-109933798	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192682759	chr6:109933833-109933834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184832938	chr6:109933837-109933838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376903687	chr6:109933848-109933849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369449806	chr6:109933854-109933855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548451025	chr6:109933870-109933871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59618833	chr6:109933891-109933892	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs533779961	chr6:109933960-109933961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547120919	chr6:109933994-109933995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570175594	chr6:109934051-109934052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533895116	chr6:109934200-109934201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189596152	chr6:109934228-109934229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371544092	chr6:109934246-109934247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs117657261	chr6:109934249-109934250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374901867	chr6:109934309-109934310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575447089	chr6:109934331-109934332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538088528	chr6:109934352-109934353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1406954	chr6:109934373-109934374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6914498	chr6:109934408-109934409	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs575075536	chr6:109934509-109934510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527252442	chr6:109934545-109934546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180930280	chr6:109934578-109934579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533956812	chr6:109934620-109934621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117314583	chr6:109934662-109934663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577363554	chr6:109934691-109934692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76994278	chr6:109934728-109934729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1321327	chr6:109934760-109934761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs78682204	chr6:109934805-109934806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548132607	chr6:109934811-109934812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562007460	chr6:109934906-109934907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140064748	chr6:109934957-109934958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547325152	chr6:109934972-109934973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
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
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
low-grade B-cell lymphoma tumor	18367492	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
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1981 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109923600-109952600	Weak transcription	Right Ventricle	heart
2	chr6:109926400-109934200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:109926600-109934400	Weak transcription	Brain Substantia Nigra	brain
4	chr6:109926800-109935400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:109927600-109935200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:109928000-109966400	Weak transcription	Pancreas	Pancrea
7	chr6:109931600-109934000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr6:109932000-109933800	Strong transcription	Primary B cells from cord blood	blood
9	chr6:109932200-109936400	Weak transcription	Fetal Kidney	kidney
10	chr6:109932400-109935800	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr6:109932600-109933400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
12	chr6:109932600-109933800	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr6:109932600-109936000	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr6:109933000-109933400	Weak transcription	Fetal Thymus	thymus
15	chr6:109933000-109933600	Weak transcription	Gastric	stomach
16	chr6:109933000-109934400	Weak transcription	Duodenum Mucosa	Duodenum
17	chr6:109933000-109934400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr6:109933000-109935200	Weak transcription	Adipose Nuclei	Adipose
19	chr6:109933000-109935200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr6:109933000-109935200	Weak transcription	Brain Hippocampus Middle	brain
21	chr6:109933000-109935200	Weak transcription	Esophagus	oesophagus
22	chr6:109933000-109935400	Weak transcription	Small Intestine	intestine
23	chr6:109933000-109935600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr6:109933000-109936800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr6:109933000-109936800	Weak transcription	Spleen	Spleen
26	chr6:109933000-109937000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr6:109933000-109939400	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr6:109933000-109948800	Weak transcription	Thymus	Thymus
29	chr6:109933000-109962800	Weak transcription	Left Ventricle	heart
30	chr6:109933000-109966400	Weak transcription	Brain Germinal Matrix	brain
31	chr6:109933000-109985200	Weak transcription	Psoas Muscle	Psoas
32	chr6:109933200-109935000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:109933400-109933600	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr6:109933400-109934000	Strong transcription	Fetal Thymus	thymus
35	chr6:109933600-109933800	ZNF genes & repeats	Aorta	Aorta
36	chr6:109933600-109933800	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr6:109933600-109933800	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr6:109933600-109933800	Enhancers	Gastric	stomach
39	chr6:109933800-109934000	Weak transcription	Gastric	stomach
40	chr6:109933800-109935400	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr6:109933800-109951400	Weak transcription	Primary B cells from cord blood	blood
42	chr6:109934000-109935600	Weak transcription	Fetal Thymus	thymus
43	chr6:109935400-109935600	Active TSS	Small Intestine	intestine
44	chr6:109936400-109936600	Enhancers	Fetal Kidney	kidney
45	chr6:109936600-109937200	Weak transcription	Fetal Kidney	kidney
46	chr6:109944000-109945000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:109944400-109944800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:109944400-109945000	Enhancers	Primary T cells from cord blood	blood
49	chr6:109945400-109966400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr6:109947200-109966800	Weak transcription	Gastric	stomach

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