Variant report

Variant	nsv1029609
Chromosome Location	chr6:5187633-5397254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3062)
CpG islands
(count:1649)
Chromatin interactive
region (count:175)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3062 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5190707-5191119	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:5266696-5266977	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:5231961-5232471	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:5269918-5270747	K562	blood:	n/a	n/a
5	ARID3A	chr6:5380018-5380168	K562	blood:	n/a	n/a
6	ARID3A	chr6:5263118-5263132	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:5230864-5231238	K562	blood:	n/a	n/a
8	ARID3A	chr6:5263034-5263237	K562	blood:	n/a	n/a
9	ARID3A	chr6:5302507-5302854	K562	blood:	n/a	n/a
10	ARID3A	chr6:5299473-5299621	K562	blood:	n/a	n/a
11	ARID3A	chr6:5329295-5329331	K562	blood:	n/a	n/a
12	ARID3A	chr6:5260977-5262130	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:5266169-5266235	K562	blood:	n/a	n/a
14	ARID3A	chr6:5351954-5352010	K562	blood:	n/a	n/a
15	ARID3A	chr6:5333915-5334256	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:5206127-5206777	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:5236019-5236351	HepG2	liver:	n/a	n/a
18	ATF1	chr6:5300478-5300736	K562	blood:	n/a	n/a
19	ATF1	chr6:5260289-5260755	K562	blood:	n/a	n/a
20	ATF1	chr6:5230908-5231258	K562	blood:	n/a	n/a
21	ATF1	chr6:5329106-5329358	K562	blood:	n/a	n/a
22	ATF1	chr6:5302305-5302992	K562	blood:	n/a	n/a
23	ATF1	chr6:5294668-5294952	K562	blood:	n/a	n/a
24	ATF1	chr6:5270252-5270586	K562	blood:	n/a	n/a
25	ATF1	chr6:5211669-5211719	K562	blood:	n/a	n/a
26	ATF2	chr6:5303469-5303900	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:5261445-5261913	GM12878	blood:	n/a	n/a
28	ATF2	chr6:5338294-5338813	GM12878	blood:	n/a	n/a
29	ATF2	chr6:5260895-5261306	GM12878	blood:	n/a	n/a
30	ATF2	chr6:5261451-5261842	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr6:5261233-5262073	GM12878	blood:	n/a	n/a
32	ATF2	chr6:5302657-5303223	GM12878	blood:	n/a	n/a
33	ATF2	chr6:5206132-5206459	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr6:5302721-5303188	GM12878	blood:	n/a	n/a
35	ATF2	chr6:5335131-5335747	GM12878	blood:	n/a	n/a
36	ATF3	chr6:5287879-5288150	K562	blood:	n/a	n/a
37	ATF3	chr6:5262710-5263007	K562	blood:	n/a	n/a
38	BACH1	chr6:5380041-5380208	K562	blood:	n/a	n/a
39	BACH1	chr6:5303473-5303784	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr6:5270366-5270567	K562	blood:	n/a	n/a
41	BACH1	chr6:5260460-5260597	K562	blood:	n/a	n/a
42	BACH1	chr6:5309454-5309486	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr6:5215060-5215664	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr6:5215176-5215774	K562	blood:	n/a	n/a
45	BATF	chr6:5302751-5303177	GM12878	blood:	n/a	n/a
46	BATF	chr6:5287873-5288218	GM12878	blood:	n/a	chr6:5288074-5288085 chr6:5288075-5288085
47	BATF	chr6:5338444-5338732	GM12878	blood:	n/a	n/a
48	BATF	chr6:5280277-5280715	GM12878	blood:	n/a	chr6:5280626-5280635
49	BATF	chr6:5338449-5338757	GM12878	blood:	n/a	n/a
50	BATF	chr6:5335227-5335571	GM12878	blood:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5205542-5205592	NB4	blood:	n/a
2	chr6:5261291-5261341	IMR90	lung:	fetal
3	chr6:5205542-5205592	NB4	blood:	n/a
4	chr6:5261291-5261341	IMR90	lung:	fetal
5	chr6:5261560-5261610	HEK293	kidney:	embryo
6	chr6:5261406-5261456	NT2-D1	testis:	n/a
7	chr6:5261091-5261141	NH-A	brain:	n/a
8	chr6:5262017-5262067	MCF10A-Er-Src	breast:	n/a
9	chr6:5261406-5261456	HIPEpiC	eye:	n/a
10	chr6:5214950-5215000	AG09319	gingival:	n/a
11	chr6:5296249-5296299	MCF-7	breast:	n/a
12	chr6:5205542-5205592	ovcar-3	ovarian:	n/a
13	chr6:5262017-5262067	GM12878	blood:	n/a
14	chr6:5378917-5378967	GM12878	blood:	n/a
15	chr6:5287843-5287893	HRE	kidney:	n/a
16	chr6:5261291-5261341	HL-60	blood:	n/a
17	chr6:5261829-5261879	AG10803	skin:	n/a
18	chr6:5296249-5296299	ovcar-3	ovarian:	n/a
19	chr6:5287843-5287893	PFSK-1	brain:	n/a
20	chr6:5261506-5261556	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:5316922-5316972	SK-N-SH	brain:	n/a
22	chr6:5261829-5261879	Caco-2	colon:	n/a
23	chr6:5287843-5287893	HL-60	blood:	n/a
24	chr6:5287843-5287893	NHDF-neo	bronchial:	n/a
25	chr6:5264929-5264979	GM19239	blood:	n/a
26	chr6:5258521-5258571	Hela-S3	cervix:	n/a
27	chr6:5287843-5287893	Jurkat	blood:	n/a
28	chr6:5261046-5261096	HEK293	kidney:	embryo
29	chr6:5313645-5313695	HCT-116	colon:	n/a
30	chr6:5261829-5261879	K562	blood:	n/a
31	chr6:5261473-5261523	LNCaP	prostate:	n/a
32	chr6:5296249-5296299	HRPEpiC	eye:	n/a
33	chr6:5258521-5258571	SAEC	small airway:	n/a
34	chr6:5241236-5241286	PANC-1	pancreas:	n/a
35	chr6:5260664-5260714	NHBE	bronchial:	n/a
36	chr6:5260950-5261000	SK-N-MC	brain:	n/a
37	chr6:5261560-5261610	U87	brain:	n/a
38	chr6:5261291-5261341	SK-N-SH_RA	brain:	n/a
39	chr6:5313645-5313695	NHDF-neo	bronchial:	n/a
40	chr6:5313645-5313695	BE2_C	brain:	n/a
41	chr6:5261366-5261416	HCT-116	colon:	n/a
42	chr6:5262017-5262067	HCF	heart:	n/a
43	chr6:5261560-5261610	NHBE	bronchial:	n/a
44	chr6:5316922-5316972	CMK	blood:	n/a
45	chr6:5296249-5296299	GM12878	blood:	n/a
46	chr6:5260664-5260714	NHDF-neo	bronchial:	n/a
47	chr6:5261471-5261521	GM12878	blood:	n/a
48	chr6:5313645-5313695	AG09319	gingival:	n/a
49	chr6:5261438-5261488	HRCEpiC	kidney:	n/a
50	chr6:5262017-5262067	HAEpiC	amniotic membrane:	n/a

(count:175 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:5316219..5318124-chr6:5321436..5323216,2	K562	blood:
2	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
3	chr6:5255894..5257705-chr6:5381224..5383041,2	K562	blood:
4	chr6:5244206..5246671-chr6:5260247..5262061,2	MCF-7	breast:
5	chr6:5287945..5289983-chr6:5297023..5298876,2	K562	blood:
6	chr6:5200460..5201968-chr6:5202592..5204399,2	MCF-7	breast:
7	chr6:5243071..5246983-chr6:5247269..5251044,4	MCF-7	breast:
8	chr6:5260357..5262137-chr6:5285896..5288338,2	MCF-7	breast:
9	chr6:5371917..5373549-chr6:5379735..5382475,2	K562	blood:
10	chr6:5259731..5262247-chr6:5263109..5267225,3	MCF-7	breast:
11	chr6:5273787..5275351-chr6:5283823..5285479,2	K562	blood:
12	chr6:5194051..5195705-chr6:5197927..5200504,2	K562	blood:
13	chr6:5212097..5214794-chr6:5261245..5262873,2	K562	blood:
14	chr6:5302902..5305704-chr6:5324020..5325616,2	K562	blood:
15	chr6:5314865..5316963-chr6:5319263..5320833,2	K562	blood:
16	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
17	chr6:5235833..5237389-chr6:5249976..5252772,2	K562	blood:
18	chr6:5271290..5273704-chr6:5277063..5279259,2	K562	blood:
19	chr6:5295190..5297508-chr6:5331125..5333153,2	K562	blood:
20	chr6:5203877..5206736-chr6:5207600..5210343,2	MCF-7	breast:
21	chr6:5284244..5290564-chr6:5292142..5296092,7	K562	blood:
22	chr6:5270189..5272095-chr6:5280821..5282645,2	K562	blood:
23	chr6:5259574..5262375-chr6:5317058..5319115,2	K562	blood:
24	chr6:5285977..5287695-chr6:5316657..5318764,2	MCF-7	breast:
25	chr6:5275045..5278604-chr6:5280944..5282922,3	K562	blood:
26	chr6:5196236..5198103-chr6:5221332..5223439,2	K562	blood:
27	chr6:5194051..5195705-chr6:5197927..5200504,2	K562	blood:
28	chr6:5230386..5232263-chr6:5256966..5259626,3	K562	blood:
29	chr6:5273787..5275351-chr6:5283823..5285479,2	K562	blood:
30	chr6:5380009..5381908-chr6:5391068..5392911,2	K562	blood:
31	chr6:5230156..5232438-chr6:5235968..5238786,2	K562	blood:
32	chr6:5219149..5221377-chr6:5248567..5251892,3	K562	blood:
33	chr6:5258576..5260130-chr6:5278247..5279774,2	K562	blood:
34	chr6:5356672..5358762-chr6:5360755..5363627,2	K562	blood:
35	chr15:91040281..91042340-chr6:5395615..5398410,2	MCF-7	breast:
36	chr6:5232470..5236352-chr6:5241278..5244100,4	K562	blood:
37	chr6:5237216..5240073-chr6:5242175..5245334,3	K562	blood:
38	chr6:5295225..5299115-chr6:5300154..5305822,5	K562	blood:
39	chr6:5243071..5246983-chr6:5247269..5251044,4	MCF-7	breast:
40	chr6:5230815..5235706-chr6:5259906..5263752,5	K562	blood:
41	chr6:5337400..5339933-chr6:5352570..5354341,2	K562	blood:
42	chr6:5254535..5257442-chr6:5259369..5261994,2	MCF-7	breast:
43	chr6:5261565..5263835-chr6:5284540..5287301,3	MCF-7	breast:
44	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
45	chr6:5378186..5380144-chr6:5383015..5385414,2	K562	blood:
46	chr6:5354142..5357037-chr6:5358520..5360420,2	K562	blood:
47	chr6:5295225..5299115-chr6:5300154..5305822,5	K562	blood:
48	chr6:5284244..5290564-chr6:5292142..5296092,7	K562	blood:
49	chr6:5214761..5215392-chr6:5379547..5380560,3	MCF-7	breast:
50	chr6:5323707..5326276-chr6:5329133..5331071,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYRM4-1	chr6:5291263-5291621	NONHSAT107517
2	lnc-PPP1R3G-1	chr6:5237941-5240729	ENSG00000251561
3	lnc-RPP40-5	chr6:5236517-5236694	NONHSAT107516
4	lnc-RPP40-5	chr6:5240759-5240956	NONHSAT107516
5	lnc-RPP40-5	chr6:5260881-5260954	NONHSAT107516

No data

Variant related genes	Relation type
FARS2	TF binding region
ENSG00000264541	TF binding region
LYRM4	TF binding region
ENSG00000220446	TF binding region
FARS2	CpG island
ENSG00000264541	CpG island
LYRM4	CpG island
ENSG00000220446	CpG island
ENSG00000136631	chromatin interactions
ENSG00000072274	chromatin interactions
ENSG00000214113	chromatin interactions
ENSG00000220446	chromatin interactions
ENSG00000145982	chromatin interactions
ENSG00000260063	chromatin interactions
GTF2H2D	miRNA target sites

Extended variants
information (count: 8298 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:8298 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183062901	chr6:5187634-5187635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140795200	chr6:5187635-5187636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111850400	chr6:5187641-5187642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150086709	chr6:5187656-5187657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570396466	chr6:5187734-5187735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113984437	chr6:5187757-5187758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574428339	chr6:5187758-5187759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138411013	chr6:5187826-5187827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574568353	chr6:5187842-5187843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541986764	chr6:5187906-5187907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563426719	chr6:5187927-5187928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143273906	chr6:5187997-5187998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34392558	chr6:5188034-5188035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs202172148	chr6:5188066-5188067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs397731440	chr6:5188075-5188076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376083904	chr6:5188076-5188077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147536962	chr6:5188085-5188086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545747216	chr6:5188086-5188087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564428524	chr6:5188106-5188107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370978288	chr6:5188139-5188140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527749710	chr6:5188307-5188308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371438509	chr6:5188331-5188332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144006431	chr6:5188346-5188347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540219000	chr6:5188359-5188360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561790188	chr6:5188394-5188395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374636410	chr6:5188414-5188415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115589188	chr6:5188484-5188485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186445683	chr6:5188527-5188528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144355027	chr6:5188559-5188560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148737405	chr6:5188571-5188572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79280968	chr6:5188606-5188607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150259999	chr6:5188613-5188614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375929734	chr6:5188614-5188615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs71540852	chr6:5188615-5188616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567131174	chr6:5188629-5188630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534530709	chr6:5188658-5188659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557606756	chr6:5188753-5188754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190610286	chr6:5188805-5188806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568066451	chr6:5188856-5188857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535503281	chr6:5188935-5188936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557109969	chr6:5188997-5188998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182878391	chr6:5189038-5189039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367678755	chr6:5189059-5189060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370027463	chr6:5189083-5189084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571314727	chr6:5189106-5189107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536885643	chr6:5189118-5189119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557704714	chr6:5189121-5189122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187921200	chr6:5189201-5189202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13195652	chr6:5189208-5189209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543329018	chr6:5189222-5189223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3811 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5163800-5189600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:5173000-5190800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:5175800-5193400	Weak transcription	Brain Substantia Nigra	brain
4	chr6:5176200-5190600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:5176200-5192400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:5176200-5201200	Weak transcription	Fetal Muscle Leg	muscle
7	chr6:5176200-5203600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:5176200-5239600	Weak transcription	Thymus	Thymus
9	chr6:5177800-5205200	Weak transcription	Aorta	Aorta
10	chr6:5178400-5190800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:5179200-5207600	Weak transcription	Primary B cells from cord blood	blood
12	chr6:5179800-5190600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:5180000-5201000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr6:5180200-5212200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr6:5180400-5193200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr6:5180600-5192600	Weak transcription	Brain Angular Gyrus	brain
17	chr6:5180600-5195800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr6:5180600-5205000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr6:5180600-5205800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:5180600-5208200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:5181000-5190800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:5181200-5190400	Weak transcription	NHEK	skin
23	chr6:5181200-5204600	Weak transcription	Esophagus	oesophagus
24	chr6:5182000-5187800	Weak transcription	Spleen	Spleen
25	chr6:5182000-5189200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:5182000-5196200	Weak transcription	Pancreas	Pancrea
27	chr6:5182000-5213600	Weak transcription	Gastric	stomach
28	chr6:5182200-5191400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:5182200-5200000	Weak transcription	Left Ventricle	heart
30	chr6:5182400-5189400	Weak transcription	A549	lung
31	chr6:5183600-5189000	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr6:5184200-5192600	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr6:5184600-5190400	Weak transcription	Osteobl	bone
34	chr6:5185200-5190800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:5186000-5192400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:5186400-5193600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:5186400-5195800	Weak transcription	K562	blood
38	chr6:5186400-5205000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:5186600-5190600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:5186600-5190800	Weak transcription	HepG2	liver
41	chr6:5186600-5191400	Weak transcription	Fetal Intestine Small	intestine
42	chr6:5186600-5196200	Weak transcription	Fetal Stomach	stomach
43	chr6:5186600-5200400	Weak transcription	Right Ventricle	heart
44	chr6:5186600-5202600	Weak transcription	Primary T cells from cord blood	blood
45	chr6:5187200-5194000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr6:5189000-5189200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:5189000-5213200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr6:5189200-5189400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:5189200-5189400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:5189200-5190600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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