Variant report

Variant	nsv916361
Chromosome Location	chr6:5315853-5695486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3316)
CpG islands
(count:1100)
Chromatin interactive
region (count:159)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3316 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5598639-5598744	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:5542174-5542541	K562	blood:	n/a	n/a
3	ARID3A	chr6:5351954-5352010	K562	blood:	n/a	n/a
4	ARID3A	chr6:5593216-5593360	K562	blood:	n/a	n/a
5	ARID3A	chr6:5512133-5512452	K562	blood:	n/a	n/a
6	ARID3A	chr6:5333915-5334256	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:5380018-5380168	K562	blood:	n/a	n/a
8	ARID3A	chr6:5671496-5671730	K562	blood:	n/a	n/a
9	ARID3A	chr6:5329295-5329331	K562	blood:	n/a	n/a
10	ARID3A	chr6:5466765-5467343	K562	blood:	n/a	n/a
11	ARID3A	chr6:5471245-5471536	K562	blood:	n/a	n/a
12	ATF1	chr6:5646196-5646578	K562	blood:	n/a	n/a
13	ATF1	chr6:5400979-5401008	K562	blood:	n/a	n/a
14	ATF1	chr6:5398731-5399051	K562	blood:	n/a	n/a
15	ATF1	chr6:5522069-5522347	K562	blood:	n/a	n/a
16	ATF1	chr6:5593290-5593491	K562	blood:	n/a	n/a
17	ATF1	chr6:5329106-5329358	K562	blood:	n/a	n/a
18	ATF1	chr6:5542060-5542538	K562	blood:	n/a	n/a
19	ATF1	chr6:5513745-5514079	K562	blood:	n/a	n/a
20	ATF1	chr6:5534822-5535016	K562	blood:	n/a	n/a
21	ATF1	chr6:5672929-5673130	K562	blood:	n/a	n/a
22	ATF1	chr6:5583252-5583384	K562	blood:	n/a	n/a
23	ATF1	chr6:5512189-5512466	K562	blood:	n/a	n/a
24	ATF1	chr6:5671344-5671762	K562	blood:	n/a	n/a
25	ATF2	chr6:5507116-5507755	GM12878	blood:	n/a	n/a
26	ATF2	chr6:5566854-5567419	GM12878	blood:	n/a	n/a
27	ATF2	chr6:5566803-5568144	GM12878	blood:	n/a	n/a
28	ATF2	chr6:5671265-5671809	GM12878	blood:	n/a	n/a
29	ATF2	chr6:5542162-5542589	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr6:5338294-5338813	GM12878	blood:	n/a	n/a
31	ATF2	chr6:5542100-5542555	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr6:5507200-5507833	GM12878	blood:	n/a	n/a
33	ATF2	chr6:5567464-5568036	GM12878	blood:	n/a	n/a
34	ATF2	chr6:5335131-5335747	GM12878	blood:	n/a	n/a
35	ATF2	chr6:5486408-5486752	GM12878	blood:	n/a	n/a
36	ATF2	chr6:5486322-5486870	GM12878	blood:	n/a	n/a
37	BACH1	chr6:5466733-5467034	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr6:5380041-5380208	K562	blood:	n/a	n/a
39	BACH1	chr6:5672424-5672514	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr6:5672781-5673492	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr6:5472378-5472661	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr6:5512684-5512923	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr6:5512790-5513144	K562	blood:	n/a	n/a
44	BATF	chr6:5567584-5567890	GM12878	blood:	n/a	n/a
45	BATF	chr6:5565893-5566144	GM12878	blood:	n/a	n/a
46	BATF	chr6:5554016-5554318	GM12878	blood:	n/a	n/a
47	BATF	chr6:5486405-5486840	GM12878	blood:	n/a	n/a
48	BATF	chr6:5566931-5567329	GM12878	blood:	n/a	n/a
49	BATF	chr6:5335214-5335580	GM12878	blood:	n/a	n/a
50	BATF	chr6:5486359-5486772	GM12878	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5463751-5463801	HCF	heart:	n/a
2	chr6:5510800-5510850	PANC-1	pancreas:	n/a
3	chr6:5463751-5463801	HCF	heart:	n/a
4	chr6:5510800-5510850	PANC-1	pancreas:	n/a
5	chr6:5431669-5431719	HEK293	kidney:	embryo
6	chr6:5672954-5673004	HepG2	liver:	n/a
7	chr6:5672954-5673004	GM06990	blood:	n/a
8	chr6:5412087-5412137	HAEpiC	amniotic membrane:	n/a
9	chr6:5378917-5378967	PANC-1	pancreas:	n/a
10	chr6:5404958-5405008	ProgFib	skin:	n/a
11	chr6:5512308-5512358	PANC-1	pancreas:	n/a
12	chr6:5316922-5316972	AG04449	skin:	fetal
13	chr6:5425832-5425882	HL-60	blood:	n/a
14	chr6:5404958-5405008	CMK	blood:	n/a
15	chr6:5406020-5406070	A549	lung:	n/a
16	chr6:5510697-5510747	T-47D	breast:	n/a
17	chr6:5463751-5463801	Hela-S3	cervix:	n/a
18	chr6:5431669-5431719	MCF-7	breast:	n/a
19	chr6:5512308-5512358	Caco-2	colon:	n/a
20	chr6:5412087-5412137	ovcar-3	ovarian:	n/a
21	chr6:5672954-5673004	ovcar-3	ovarian:	n/a
22	chr6:5510800-5510850	AG10803	skin:	n/a
23	chr6:5672954-5673004	NHBE	bronchial:	n/a
24	chr6:5431669-5431719	HCF	heart:	n/a
25	chr6:5425832-5425882	Hela-S3	cervix:	n/a
26	chr6:5472095-5472145	AG09309	skin:	n/a
27	chr6:5510800-5510850	HCM	heart:	n/a
28	chr6:5378917-5378967	MCF10A-Er-Src	breast:	n/a
29	chr6:5510697-5510747	HMEC	breast:	n/a
30	chr6:5472095-5472145	SK-N-MC	brain:	n/a
31	chr6:5316922-5316972	SK-N-SH	brain:	n/a
32	chr6:5404958-5405008	MCF-7	breast:	n/a
33	chr6:5431669-5431719	HL-60	blood:	n/a
34	chr6:5406020-5406070	AG04450	lung:	fetal
35	chr6:5404958-5405008	AoSMC	blood vessel:	n/a
36	chr6:5431669-5431719	HAEpiC	amniotic membrane:	n/a
37	chr6:5425832-5425882	NHDF-neo	bronchial:	n/a
38	chr6:5378917-5378967	AG09319	gingival:	n/a
39	chr6:5554079-5554129	HAEpiC	amniotic membrane:	n/a
40	chr6:5412087-5412137	NB4	blood:	n/a
41	chr6:5425832-5425882	PANC-1	pancreas:	n/a
42	chr6:5378917-5378967	AG04449	skin:	fetal
43	chr6:5472095-5472145	HEEpiC	esophagus:	n/a
44	chr6:5472095-5472145	SK-N-SH	brain:	n/a
45	chr6:5463751-5463801	U87	brain:	n/a
46	chr6:5510748-5510798	SK-N-SH	brain:	n/a
47	chr6:5425832-5425882	HRCEpiC	kidney:	n/a
48	chr6:5425832-5425882	HMEC	breast:	n/a
49	chr6:5378917-5378967	T-47D	breast:	n/a
50	chr6:5425832-5425882	A549	lung:	n/a

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:5549888..5552504-chr6:5555146..5558122,2	K562	blood:
2	chr6:5214686..5215658-chr6:5401229..5403280,10	K562	blood:
3	chr6:5473023..5474708-chr6:5475378..5477106,2	K562	blood:
4	chr6:5376489..5378009-chr6:5378380..5380035,2	MCF-7	breast:
5	chr6:5316219..5318124-chr6:5321436..5323216,2	K562	blood:
6	chr6:5364826..5367079-chr6:5385611..5387966,2	K562	blood:
7	chr6:5431881..5436604-chr6:5436753..5441713,4	K562	blood:
8	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
9	chr6:5549888..5553907-chr6:5554178..5558122,4	K562	blood:
10	chr6:5364063..5366771-chr6:5369592..5371297,2	K562	blood:
11	chr6:5259536..5262981-chr6:5378329..5381673,4	K562	blood:
12	chr6:5478279..5480478-chr6:5483218..5485001,2	K562	blood:
13	chr6:5670035..5672305-chr6:5675850..5677415,2	K562	blood:
14	chr6:5668378..5671034-chr6:5677672..5680311,2	K562	blood:
15	chr6:5606607..5608411-chr6:5609552..5611263,2	K562	blood:
16	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
17	chr6:5549888..5552504-chr6:5555146..5558122,2	K562	blood:
18	chr6:5056624..5057532-chr6:5398465..5398983,2	K562	blood:
19	chr6:5485806..5488225-chr6:5489962..5492920,2	K562	blood:
20	chr6:5609969..5611663-chr6:5617459..5619947,2	K562	blood:
21	chr6:5571772..5574003-chr6:5575874..5578608,2	MCF-7	breast:
22	chr6:5604267..5607635-chr6:5611344..5613997,3	K562	blood:
23	chr6:5337400..5339933-chr6:5352570..5354341,2	K562	blood:
24	chr6:5360554..5362439-chr6:5363496..5365484,2	K562	blood:
25	chr6:5143921..5144506-chr6:5398809..5399361,2	MCF-7	breast:
26	chr6:5470498..5472871-chr6:6545581..6547972,2	MCF-7	breast:
27	chr6:5499395..5501300-chr6:5509807..5511478,2	K562	blood:
28	chr6:5214744..5215638-chr6:5398420..5399368,7	K562	blood:
29	chr6:5451514..5453139-chr6:5455554..5457510,2	K562	blood:
30	chr6:5554838..5557346-chr6:5557615..5560510,3	K562	blood:
31	chr6:5352377..5354120-chr6:5360443..5362372,2	K562	blood:
32	chr6:5435025..5437230-chr6:5438877..5440438,2	MCF-7	breast:
33	chr6:5668378..5671034-chr6:5677672..5680311,2	K562	blood:
34	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
35	chr6:5471238..5471818-chr6:5519987..5520960,2	K562	blood:
36	chr6:5285977..5287695-chr6:5316657..5318764,2	MCF-7	breast:
37	chr6:5255894..5257705-chr6:5381224..5383041,2	K562	blood:
38	chr6:5513795..5515998-chr6:5521292..5524048,2	K562	blood:
39	chr6:5378846..5381566-chr6:5383901..5386296,2	K562	blood:
40	chr6:5214746..5216032-chr6:5379652..5380557,3	K562	blood:
41	chr6:5511127..5514739-chr6:5516626..5520619,5	K562	blood:
42	chr6:5598894..5600945-chr6:5606990..5609322,2	K562	blood:
43	chr6:5295190..5297508-chr6:5331125..5333153,2	K562	blood:
44	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
45	chr6:5604267..5607635-chr6:5611344..5613997,3	K562	blood:
46	chr6:5220721..5222969-chr6:5379273..5381024,2	K562	blood:
47	chr6:5314865..5316963-chr6:5319263..5320833,2	K562	blood:
48	chr6:5616037..5618304-chr6:5621666..5623191,2	K562	blood:
49	chr6:5549888..5553907-chr6:5554178..5558122,4	K562	blood:
50	chr6:5554838..5557346-chr6:5557615..5559842,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYRM4-3	chr6:5457186-5457261	ENSG00000269985.1
2	lnc-PPP1R3G-7	chr6:5502505-5504640	NONHSAT107521
3	lnc-NRN1-7	chr6:5668270-5668346	ENSG00000270174.1
4	lnc-NRN1-7	chr6:5665218-5665691	ENSG00000270174.1
5	lnc-LYRM4-3	chr6:5452701-5452990	ENSG00000269985.1
6	lnc-NRN1-7	chr6:5695378-5695505	ENSG00000270174.1
7	lnc-LYRM4-3	chr6:5458127-5458278	NONHSAT107520
8	lnc-NRN1-7	chr6:5695115-5695241	ENSG00000270174.1
9	lnc-LYRM4-3	chr6:5458127-5458308	ENSG00000269985.1
10	lnc-LYRM4-3	chr6:5451916-5452990	ENSG00000269985.1
11	lnc-LYRM4-3	chr6:5458127-5458266	ENSG00000269985.1
12	lnc-LYRM4-3	chr6:5457093-5457261	NONHSAT107520

No data

Variant related genes	Relation type
FARS2	TF binding region
HNRNPA1P37	TF binding region
ENSG00000269985	TF binding region
FARS2	CpG island
HNRNPA1P37	CpG island
ENSG00000269985	CpG island
ENSG00000145982	chromatin interactions
ENSG00000218574	chromatin interactions
ENSG00000214113	chromatin interactions

Extended variants
information (count: 15560 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:15560 , 50 per page) page: 1 2 3 4 5 6 7 ... 312

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547336903	chr6:5315937-5315938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565996602	chr6:5315942-5315943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369017393	chr6:5315949-5315950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368796312	chr6:5315950-5315951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71678515	chr6:5315951-5315952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148811522	chr6:5315954-5315955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368308813	chr6:5315959-5315960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs70974188	chr6:5315970-5315971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs68096366	chr6:5315971-5315972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs67341103	chr6:5315974-5315975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9504378	chr6:5315978-5315979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548606966	chr6:5315982-5315983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12210891	chr6:5315986-5315987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs13208318	chr6:5315990-5315991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs70974189	chr6:5315991-5315992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371535441	chr6:5315995-5315996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569726145	chr6:5315999-5316000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537102332	chr6:5316001-5316002	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs552841286	chr6:5316038-5316039	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs150866345	chr6:5316051-5316052	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs534921789	chr6:5316054-5316055	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs553367664	chr6:5316065-5316066	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs575122493	chr6:5316096-5316097	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs79691425	chr6:5316145-5316146	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs808813	chr6:5316152-5316153	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs149622630	chr6:5316193-5316194	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs543511534	chr6:5316207-5316208	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs564985896	chr6:5316250-5316251	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs797145	chr6:5316399-5316400	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs541269210	chr6:5316402-5316403	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs111716570	chr6:5316631-5316632	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs536010509	chr6:5316642-5316643	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs192034599	chr6:5316682-5316683	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs183164626	chr6:5316712-5316713	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs563315667	chr6:5316737-5316738	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs530828986	chr6:5316780-5316781	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs552237289	chr6:5316784-5316785	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs570639341	chr6:5316861-5316862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375074366	chr6:5316911-5316912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534903001	chr6:5316950-5316951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549431235	chr6:5317012-5317013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72815629	chr6:5317058-5317059	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs35203723	chr6:5317069-5317070	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs73718064	chr6:5317120-5317121	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs34715339	chr6:5317134-5317135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs536097244	chr6:5317154-5317155	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs140861329	chr6:5317169-5317170	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs12527769	chr6:5317189-5317190	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144617913	chr6:5317199-5317200	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs537075717	chr6:5317202-5317203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	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
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4581 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5288000-5316200	Weak transcription	Fetal Stomach	stomach
2	chr6:5288400-5324000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:5288400-5331000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:5292800-5334400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:5295400-5325000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:5296200-5316000	Weak transcription	Lung	lung
7	chr6:5301800-5322200	Weak transcription	Ovary	ovary
8	chr6:5302600-5316000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:5302800-5319200	Weak transcription	Aorta	Aorta
10	chr6:5303200-5316000	Weak transcription	Brain Hippocampus Middle	brain
11	chr6:5303200-5368800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:5303600-5316000	Weak transcription	Brain Anterior Caudate	brain
13	chr6:5303600-5317400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:5303600-5319000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr6:5303600-5332400	Weak transcription	Gastric	stomach
16	chr6:5303800-5316000	Weak transcription	Stomach Smooth Muscle	stomach
17	chr6:5303800-5316200	Weak transcription	Left Ventricle	heart
18	chr6:5304000-5320400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr6:5304000-5325400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr6:5304000-5326000	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr6:5304000-5337600	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr6:5304200-5316000	Weak transcription	Fetal Muscle Leg	muscle
23	chr6:5304200-5322800	Weak transcription	Pancreas	Pancrea
24	chr6:5306800-5316000	Weak transcription	Fetal Lung	lung
25	chr6:5306800-5321400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr6:5307000-5320400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr6:5307000-5323800	Weak transcription	HepG2	liver
28	chr6:5307800-5318800	Weak transcription	Fetal Intestine Large	intestine
29	chr6:5308800-5318000	Weak transcription	Primary B cells from cord blood	blood
30	chr6:5308800-5325000	Weak transcription	Primary T cells from cord blood	blood
31	chr6:5308800-5325000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:5309000-5317200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:5309200-5333400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:5309200-5334000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:5312800-5317400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr6:5313000-5316400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr6:5313800-5322800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:5314400-5316000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr6:5314400-5316000	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr6:5314600-5316000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr6:5314800-5316000	Weak transcription	Psoas Muscle	Psoas
42	chr6:5314800-5323800	Weak transcription	GM12878-XiMat	blood
43	chr6:5315000-5326400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr6:5315400-5316000	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr6:5315400-5316400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:5315400-5316400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:5315400-5316800	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr6:5315400-5316800	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr6:5315600-5316000	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr6:5315600-5317400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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