Variant report

Variant	nsv1030254
Chromosome Location	chr6:5132261-5431585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4751)
CpG islands
(count:2875)
Chromatin interactive
region (count:221)
LncRNA
region (count:5)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:4751 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5380018-5380168	K562	blood:	n/a	n/a
2	ARID3A	chr6:5333915-5334256	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:5351954-5352010	K562	blood:	n/a	n/a
4	ARID3A	chr6:5302507-5302854	K562	blood:	n/a	n/a
5	ARID3A	chr6:5299473-5299621	K562	blood:	n/a	n/a
6	ARID3A	chr6:5260977-5262130	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:5190707-5191119	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:5182330-5182406	K562	blood:	n/a	n/a
9	ARID3A	chr6:5266696-5266977	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:5231961-5232471	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:5263118-5263132	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:5269918-5270747	K562	blood:	n/a	n/a
13	ARID3A	chr6:5236019-5236351	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:5266169-5266235	K562	blood:	n/a	n/a
15	ARID3A	chr6:5230864-5231238	K562	blood:	n/a	n/a
16	ARID3A	chr6:5329295-5329331	K562	blood:	n/a	n/a
17	ARID3A	chr6:5139558-5139834	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:5206127-5206777	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:5263034-5263237	K562	blood:	n/a	n/a
20	ATF1	chr6:5300478-5300736	K562	blood:	n/a	n/a
21	ATF1	chr6:5398731-5399051	K562	blood:	n/a	n/a
22	ATF1	chr6:5294668-5294952	K562	blood:	n/a	n/a
23	ATF1	chr6:5302305-5302992	K562	blood:	n/a	n/a
24	ATF1	chr6:5211669-5211719	K562	blood:	n/a	n/a
25	ATF1	chr6:5400979-5401008	K562	blood:	n/a	n/a
26	ATF1	chr6:5270252-5270586	K562	blood:	n/a	n/a
27	ATF1	chr6:5260289-5260755	K562	blood:	n/a	n/a
28	ATF1	chr6:5329106-5329358	K562	blood:	n/a	n/a
29	ATF1	chr6:5230908-5231258	K562	blood:	n/a	n/a
30	ATF2	chr6:5132901-5133409	GM12878	blood:	n/a	n/a
31	ATF2	chr6:5261451-5261842	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr6:5174096-5174925	GM12878	blood:	n/a	n/a
33	ATF2	chr6:5338294-5338813	GM12878	blood:	n/a	n/a
34	ATF2	chr6:5206132-5206459	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr6:5302721-5303188	GM12878	blood:	n/a	n/a
36	ATF2	chr6:5303469-5303900	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr6:5261445-5261913	GM12878	blood:	n/a	n/a
38	ATF2	chr6:5335131-5335747	GM12878	blood:	n/a	n/a
39	ATF2	chr6:5261233-5262073	GM12878	blood:	n/a	n/a
40	ATF2	chr6:5260895-5261306	GM12878	blood:	n/a	n/a
41	ATF2	chr6:5302657-5303223	GM12878	blood:	n/a	n/a
42	ATF3	chr6:5262710-5263007	K562	blood:	n/a	n/a
43	ATF3	chr6:5287879-5288150	K562	blood:	n/a	n/a
44	BACH1	chr6:5215060-5215664	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr6:5303473-5303784	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr6:5260460-5260597	K562	blood:	n/a	n/a
47	BACH1	chr6:5180101-5180461	K562	blood:	n/a	n/a
48	BACH1	chr6:5180186-5180398	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr6:5309454-5309486	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr6:5270366-5270567	K562	blood:	n/a	n/a

(count:2875 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5133475-5133525	Hepatocyte	liver:	n/a
2	chr6:5282702-5282752	NT2-D1	testis:	n/a
3	chr6:5145569-5145619	HRE	kidney:	n/a
4	chr6:5282702-5282752	PrEC	prostate:	n/a
5	chr6:5135794-5135844	SK-N-SH	brain:	n/a
6	chr6:5192344-5192394	MCF-7	breast:	n/a
7	chr6:5261473-5261523	GM06990	blood:	n/a
8	chr6:5174647-5174697	PFSK-1	brain:	n/a
9	chr6:5133475-5133525	Hepatocyte	liver:	n/a
10	chr6:5282702-5282752	NT2-D1	testis:	n/a
11	chr6:5145569-5145619	HRE	kidney:	n/a
12	chr6:5282702-5282752	PrEC	prostate:	n/a
13	chr6:5135794-5135844	SK-N-SH	brain:	n/a
14	chr6:5192344-5192394	MCF-7	breast:	n/a
15	chr6:5261473-5261523	GM06990	blood:	n/a
16	chr6:5174647-5174697	PFSK-1	brain:	n/a
17	chr6:5261316-5261366	K562	blood:	n/a
18	chr6:5241236-5241286	AG10803	skin:	n/a
19	chr6:5425832-5425882	LNCaP	prostate:	n/a
20	chr6:5133475-5133525	GM12891	blood:	n/a
21	chr6:5181057-5181107	GM12878	blood:	n/a
22	chr6:5313645-5313695	GM12891	blood:	n/a
23	chr6:5378917-5378967	AG09319	gingival:	n/a
24	chr6:5133475-5133525	SK-N-SH	brain:	n/a
25	chr6:5144078-5144128	H1-hESC	embryonic stem cell:	embryo
26	chr6:5258521-5258571	SK-N-MC	brain:	n/a
27	chr6:5260950-5261000	NHBE	bronchial:	n/a
28	chr6:5412087-5412137	ovcar-3	ovarian:	n/a
29	chr6:5145161-5145211	Hela-S3	cervix:	n/a
30	chr6:5261473-5261523	NT2-D1	testis:	n/a
31	chr6:5145614-5145664	HEEpiC	esophagus:	n/a
32	chr6:5404958-5405008	ECC-1	luminal epithelium:	n/a
33	chr6:5205542-5205592	HRE	kidney:	n/a
34	chr6:5412087-5412137	HCM	heart:	n/a
35	chr6:5145019-5145069	AG04449	skin:	fetal
36	chr6:5145071-5145121	HEK293	kidney:	embryo
37	chr6:5261091-5261141	HEK293	kidney:	embryo
38	chr6:5261473-5261523	Hepatocyte	liver:	n/a
39	chr6:5135184-5135234	Hela-S3	cervix:	n/a
40	chr6:5316922-5316972	NH-A	brain:	n/a
41	chr6:5261438-5261488	HRPEpiC	eye:	n/a
42	chr6:5261046-5261096	MCF-7	breast:	n/a
43	chr6:5181057-5181107	PFSK-1	brain:	n/a
44	chr6:5152468-5152518	HL-60	blood:	n/a
45	chr6:5205542-5205592	Caco-2	colon:	n/a
46	chr6:5261829-5261879	ovcar-3	ovarian:	n/a
47	chr6:5264929-5264979	HCT-116	colon:	n/a
48	chr6:5261560-5261610	AG04449	skin:	fetal
49	chr6:5260950-5261000	CMK	blood:	n/a
50	chr6:5133475-5133525	BJ	skin:	n/a

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:5280760..5282906-chr6:5284734..5288197,3	K562	blood:
2	chr6:5156038..5158677-chr6:5160543..5162347,2	K562	blood:
3	chr6:5149373..5152322-chr6:5189165..5191119,2	K562	blood:
4	chr6:5214746..5216032-chr6:5379652..5380557,3	K562	blood:
5	chr6:5143614..5144581-chr6:5379550..5380557,6	MCF-7	breast:
6	chr6:5209168..5211266-chr6:5213691..5215244,2	K562	blood:
7	chr6:5143921..5144506-chr6:5398809..5399361,2	MCF-7	breast:
8	chr6:5273787..5275351-chr6:5283823..5285479,2	K562	blood:
9	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
10	chr6:5360554..5362439-chr6:5363496..5365484,2	K562	blood:
11	chr6:5270189..5272095-chr6:5280821..5282645,2	K562	blood:
12	chr6:5259520..5261609-chr6:5287252..5289754,2	K562	blood:
13	chr6:5156038..5158677-chr6:5160543..5162347,2	K562	blood:
14	chr6:5212097..5214794-chr6:5261245..5262873,2	K562	blood:
15	chr6:5194051..5195705-chr6:5197927..5200504,2	K562	blood:
16	chr6:5287945..5289983-chr6:5297023..5298876,2	K562	blood:
17	chr6:5145534..5146304-chr8:93741632..93742260,2	MCF-7	breast:
18	chr6:5376489..5378009-chr6:5378380..5380035,2	MCF-7	breast:
19	chr6:5235833..5237389-chr6:5249976..5252772,2	K562	blood:
20	chr6:5232933..5235244-chr6:5282951..5285822,2	K562	blood:
21	chr6:5143706..5144466-chr6:5167696..5168623,2	MCF-7	breast:
22	chr6:5268649..5270848-chr6:5278225..5280226,2	K562	blood:
23	chr6:5316219..5318124-chr6:5321436..5323216,2	K562	blood:
24	chr6:5354142..5357037-chr6:5358520..5360420,2	K562	blood:
25	chr6:5371917..5373549-chr6:5379735..5382475,2	K562	blood:
26	chr6:5314865..5316963-chr6:5319263..5320833,2	K562	blood:
27	chr6:5352377..5354120-chr6:5360443..5362372,2	K562	blood:
28	chr6:5380009..5381908-chr6:5391068..5392911,2	K562	blood:
29	chr6:5230753..5233512-chr6:5233653..5235870,3	K562	blood:
30	chr6:5260884..5263189-chr6:5279736..5282482,2	K562	blood:
31	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
32	chr6:5378186..5380144-chr6:5383015..5385414,2	K562	blood:
33	chr6:5235833..5237389-chr6:5249976..5252772,2	K562	blood:
34	chr6:5260024..5261967-chr6:5263819..5265450,3	MCF-7	breast:
35	chr6:5308485..5310755-chr6:5312679..5315010,2	K562	blood:
36	chr6:5143652..5144542-chr6:5175040..5175982,3	MCF-7	breast:
37	chr1:150038831..150039716-chr6:5260490..5261436,2	Hela-S3	cervix:
38	chr6:5333079..5335354-chr6:5335769..5338319,2	K562	blood:
39	chr6:5308101..5310755-chr6:5313510..5315565,2	K562	blood:
40	chr6:5351636..5353650-chr6:5354468..5356338,2	K562	blood:
41	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
42	chr6:5259367..5263928-chr6:5312372..5314632,4	K562	blood:
43	chr6:5200460..5201968-chr6:5202592..5204399,2	MCF-7	breast:
44	chr6:5191188..5193916-chr6:5259998..5262177,2	K562	blood:
45	chr6:5285714..5287859-chr6:5301778..5303462,2	K562	blood:
46	chr6:5378846..5381566-chr6:5383901..5386296,2	K562	blood:
47	chr6:4365316..4368041-chr6:5177218..5180072,2	K562	blood:
48	chr6:5230476..5232022-chr6:5258422..5260596,2	MCF-7	breast:
49	chr6:5285977..5287695-chr6:5316657..5318764,2	MCF-7	breast:
50	chr6:5232470..5236352-chr6:5241278..5244100,4	K562	blood:

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

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3691-3p	chr6:5148480-5148501	MIMAT0019224
hsa-miR-3691-5p	chr6:5148520-5148542	MIMAT0018120

No data

Variant related genes	Relation type
FARS2	TF binding region
ENSG00000264541	TF binding region
MIR3691	TF binding region
LYRM4	TF binding region
ENSG00000220446	TF binding region
FARS2	CpG island
ENSG00000264541	CpG island
MIR3691	CpG island
LYRM4	CpG island
ENSG00000220446	CpG island
ENSG00000145982	chromatin interactions
ENSG00000214113	chromatin interactions
ENSG00000220446	chromatin interactions
ENSG00000260063	chromatin interactions
ENSG00000136631	chromatin interactions
ENSG00000072274	chromatin interactions
CSPG5	Mature miRNA region
GTF2H2D	miRNA target sites

Extended variants
information (count: 12092 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:12092 , 50 per page) page: 1 2 3 4 5 6 7 ... 242

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77067130	chr6:5132267-5132268	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs77697214	chr6:5132268-5132269	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs576757227	chr6:5132325-5132326	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs181027227	chr6:5132332-5132333	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs553132014	chr6:5132386-5132387	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs574835899	chr6:5132405-5132406	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs541961005	chr6:5132443-5132444	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs563875544	chr6:5132487-5132488	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs6937982	chr6:5132515-5132516	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs575064899	chr6:5132533-5132534	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs374501038	chr6:5132537-5132538	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs385315	chr6:5132544-5132545	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs528836910	chr6:5132553-5132554	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs145905581	chr6:5132579-5132580	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs186109842	chr6:5132623-5132624	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs529770260	chr6:5132644-5132645	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs112742488	chr6:5132647-5132648	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs547996305	chr6:5132661-5132662	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs569767465	chr6:5132692-5132693	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs138649284	chr6:5132729-5132730	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs34192149	chr6:5132781-5132782	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs533420192	chr6:5132852-5132853	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs190596155	chr6:5132861-5132862	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs570402821	chr6:5132866-5132867	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs370450914	chr6:5132888-5132889	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs571202860	chr6:5132937-5132938	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs534613091	chr6:5132938-5132939	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs182605332	chr6:5132990-5132991	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs462327	chr6:5133008-5133009	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185327280	chr6:5133055-5133056	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs141135649	chr6:5133060-5133061	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs1076728	chr6:5133145-5133146	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528605738	chr6:5133207-5133208	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs147101892	chr6:5133215-5133216	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs190628267	chr6:5133216-5133217	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs457846	chr6:5133240-5133241	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs540594262	chr6:5133291-5133292	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550468440	chr6:5133319-5133320	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs182814859	chr6:5133329-5133330	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs548197955	chr6:5133348-5133349	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs148172751	chr6:5133356-5133357	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs530558141	chr6:5133380-5133381	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs85204	chr6:5133432-5133433	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs570315805	chr6:5133449-5133450	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs534577262	chr6:5133474-5133475	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs546591441	chr6:5133475-5133476	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs1076729	chr6:5133507-5133508	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs1076730	chr6:5133566-5133567	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs202130577	chr6:5133568-5133569	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs551191621	chr6:5133574-5133575	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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	21293372	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:5041 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5103200-5132800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr6:5112800-5132600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr6:5113400-5132400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:5124800-5133200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:5125000-5133200	Weak transcription	Right Ventricle	heart
6	chr6:5126600-5133200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:5126600-5134000	Weak transcription	NHEK	skin
8	chr6:5126800-5132800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr6:5127200-5132600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:5128600-5132400	Weak transcription	Primary B cells from cord blood	blood
11	chr6:5128800-5132400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr6:5128800-5136200	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr6:5129000-5136800	Weak transcription	Primary T cells from cord blood	blood
14	chr6:5129000-5162000	Weak transcription	K562	blood
15	chr6:5129200-5132600	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr6:5129800-5138000	Weak transcription	HepG2	liver
17	chr6:5130000-5132600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:5130200-5132400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr6:5130600-5132400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr6:5130600-5132800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr6:5130600-5132800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr6:5130600-5140400	Weak transcription	Gastric	stomach
23	chr6:5130600-5172200	Weak transcription	Lung	lung
24	chr6:5130800-5132800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:5130800-5132800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:5130800-5132800	Weak transcription	Fetal Muscle Trunk	muscle
27	chr6:5130800-5132800	Weak transcription	Left Ventricle	heart
28	chr6:5130800-5133200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr6:5130800-5133200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:5130800-5139400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:5130800-5142400	Weak transcription	Fetal Intestine Small	intestine
32	chr6:5131000-5132400	Weak transcription	Fetal Heart	heart
33	chr6:5131000-5132600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr6:5131000-5133000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:5131000-5143000	Weak transcription	Spleen	Spleen
36	chr6:5131400-5132600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr6:5131400-5133800	Enhancers	Brain Cingulate Gyrus	brain
38	chr6:5131600-5132600	Enhancers	Fetal Muscle Leg	muscle
39	chr6:5131600-5133800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:5131800-5133000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr6:5131800-5133400	Enhancers	Brain Angular Gyrus	brain
42	chr6:5131800-5134400	Enhancers	Primary B cells from peripheral blood	blood
43	chr6:5131800-5135200	Weak transcription	Placenta	Placenta
44	chr6:5132000-5132400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:5132000-5132800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr6:5132000-5133200	Flanking Active TSS	Fetal Kidney	kidney
47	chr6:5132000-5133400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:5132000-5133400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr6:5132000-5133600	Enhancers	Fetal Stomach	stomach
50	chr6:5132000-5133800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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