Variant report

Variant	nsv5235
Chromosome Location	chr6:27358498-27404074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:119)
CpG islands
(count:610)
Chromatin interactive
region (count:56)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:119 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:27394018-27394083	HepG2	liver:	n/a	n/a
2	ATF1	chr6:27383778-27384017	K562	blood:	n/a	n/a
3	ATF3	chr6:27383740-27384015	K562	blood:	n/a	n/a
4	BACH1	chr6:27375391-27375515	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:27375350-27375570	K562	blood:	n/a	n/a
6	BHLHE40	chr6:27393868-27394204	HepG2	liver:	n/a	n/a
7	CBX3	chr6:27368598-27369112	K562	blood:	n/a	n/a
8	CEBPB	chr6:27373906-27374224	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:27367781-27367863	HepG2	liver:	n/a	n/a
10	CEBPB	chr6:27373929-27374279	MCF-7	breast:	n/a	n/a
11	CEBPB	chr6:27381881-27382109	K562	blood:	n/a	n/a
12	CEBPB	chr6:27378763-27379055	HepG2	liver:	n/a	chr6:27378930-27378941
13	CEBPB	chr6:27378874-27379053	K562	blood:	n/a	chr6:27378930-27378941
14	CEBPB	chr6:27373892-27374256	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr6:27373829-27374315	MCF-7	breast:	n/a	n/a
16	CEBPB	chr6:27373941-27374301	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr6:27378843-27379048	MCF-7	breast:	n/a	chr6:27378930-27378941
18	CREB1	chr6:27390672-27391067	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr6:27390681-27391237	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr6:27373900-27374050	HEK293	kidney:	n/a	n/a
21	CTCF	chr6:27373982-27374005	GM19239	blood:	n/a	n/a
22	CTCF	chr6:27373926-27374037	K562	blood:	n/a	n/a
23	CTCF	chr6:27373886-27374086	MCF-7	breast:	n/a	n/a
24	CTCF	chr6:27373947-27374031	NHEK	skin:	n/a	n/a
25	CTCF	chr6:27373981-27374018	Gliobla	brain:	n/a	n/a
26	CTCF	chr6:27373894-27374101	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:27373930-27374076	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:27373926-27374072	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:27373959-27374059	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:27373914-27374068	Hela-S3	cervix:	n/a	n/a
31	E2F6	chr6:27389505-27390024	H1-hESC	embryonic stem cell:	n/a	n/a
32	FOS	chr6:27382858-27383201	MCF10A-Er-Src	breast:	n/a	chr6:27383007-27383018
33	FOS	chr6:27382873-27383178	MCF10A-Er-Src	breast:	n/a	chr6:27383007-27383018
34	FOS	chr6:27383746-27384018	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr6:27383772-27384040	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr6:27382907-27383064	MCF10A-Er-Src	breast:	n/a	chr6:27383007-27383018
37	FOS	chr6:27383774-27384043	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:27383772-27384028	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL2	chr6:27393813-27394139	HepG2	liver:	n/a	chr6:27394111-27394122
40	FOSL2	chr6:27375249-27375575	HepG2	liver:	n/a	n/a
41	FOXA1	chr6:27393837-27394126	HepG2	liver:	n/a	n/a
42	FOXA1	chr6:27393898-27394162	HepG2	liver:	n/a	n/a
43	FOXA2	chr6:27393846-27394132	HepG2	liver:	n/a	n/a
44	HCFC1	chr6:27390776-27391082	K562	blood:	n/a	n/a
45	HEY1	chr6:27391959-27392095	HepG2	liver:	n/a	n/a
46	IRF1	chr6:27382164-27382329	K562	blood:	n/a	n/a
47	IRF1	chr6:27374154-27374176	K562	blood:	n/a	n/a
48	JUN	chr6:27393970-27394084	HepG2	liver:	n/a	n/a
49	JUN	chr6:27383776-27384056	HepG2	liver:	n/a	chr6:27383909-27383922
50	JUN	chr6:27383781-27384008	K562	blood:	n/a	chr6:27383909-27383922

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:27390647-27390697	HMEC	breast:	n/a
2	chr6:27368122-27368172	BE2_C	brain:	n/a
3	chr6:27390845-27390895	ProgFib	skin:	n/a
4	chr6:27360506-27360556	Hepatocyte	liver:	n/a
5	chr6:27366902-27366952	SKMC	muscle:	n/a
6	chr6:27360506-27360556	ovcar-3	ovarian:	n/a
7	chr6:27391843-27391893	SK-N-SH	brain:	n/a
8	chr6:27390845-27390895	NH-A	brain:	n/a
9	chr6:27360506-27360556	MCF-7	breast:	n/a
10	chr6:27366902-27366952	NHDF-neo	bronchial:	n/a
11	chr6:27392665-27392715	SK-N-SH	brain:	n/a
12	chr6:27369144-27369194	HMEC	breast:	n/a
13	chr6:27390647-27390697	K562	blood:	n/a
14	chr6:27390890-27390940	HEK293	kidney:	embryo
15	chr6:27369144-27369194	MCF10A-Er-Src	breast:	n/a
16	chr6:27366782-27366832	HEEpiC	esophagus:	n/a
17	chr6:27369144-27369194	Caco-2	colon:	n/a
18	chr6:27366782-27366832	Jurkat	blood:	n/a
19	chr6:27390890-27390940	RPTEC	kidney:	n/a
20	chr6:27390890-27390940	SK-N-SH	brain:	n/a
21	chr6:27392665-27392715	GM12891	blood:	n/a
22	chr6:27390890-27390940	A549	lung:	n/a
23	chr6:27390890-27390940	HEEpiC	esophagus:	n/a
24	chr6:27390845-27390895	MCF10A-Er-Src	breast:	n/a
25	chr6:27390647-27390697	HCT-116	colon:	n/a
26	chr6:27390647-27390697	T-47D	breast:	n/a
27	chr6:27392665-27392715	BJ	skin:	n/a
28	chr6:27369144-27369194	SKMC	muscle:	n/a
29	chr6:27369144-27369194	BE2_C	brain:	n/a
30	chr6:27368122-27368172	HIPEpiC	eye:	n/a
31	chr6:27369144-27369194	T-47D	breast:	n/a
32	chr6:27390845-27390895	NB4	blood:	n/a
33	chr6:27368122-27368172	HCT-116	colon:	n/a
34	chr6:27368122-27368172	Hepatocyte	liver:	n/a
35	chr6:27369144-27369194	HAEpiC	amniotic membrane:	n/a
36	chr6:27368122-27368172	HNPCEpiC	eye:	n/a
37	chr6:27369144-27369194	BJ	skin:	n/a
38	chr6:27360506-27360556	BJ	skin:	n/a
39	chr6:27390890-27390940	HRE	kidney:	n/a
40	chr6:27392665-27392715	SAEC	small airway:	n/a
41	chr6:27366782-27366832	HAEpiC	amniotic membrane:	n/a
42	chr6:27390890-27390940	SK-N-MC	brain:	n/a
43	chr6:27360506-27360556	AG04449	skin:	fetal
44	chr6:27366902-27366952	ECC-1	luminal epithelium:	n/a
45	chr6:27360506-27360556	HNPCEpiC	eye:	n/a
46	chr6:27368122-27368172	RPTEC	kidney:	n/a
47	chr6:27366902-27366952	NT2-D1	testis:	n/a
48	chr6:27392665-27392715	A549	lung:	n/a
49	chr6:27368122-27368172	NHBE	bronchial:	n/a
50	chr6:27369144-27369194	PFSK-1	brain:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:27382004..27384798-chr6:27386646..27388886,2	K562	blood:
2	chr6:27276042..27278512-chr6:27366738..27369712,2	K562	blood:
3	chr6:27356907..27359078-chr6:27397692..27399728,2	K562	blood:
4	chr6:27363554..27367371-chr6:27369337..27372451,5	K562	blood:
5	chr6:27363318..27368170-chr6:27368582..27372451,5	K562	blood:
6	chr6:27362299..27364139-chr6:27382508..27384526,2	K562	blood:
7	chr6:27357105..27360959-chr6:27363374..27365305,4	K562	blood:
8	chr6:27357105..27360959-chr6:27363374..27365305,4	K562	blood:
9	chr6:27368618..27370867-chr6:27411111..27412908,2	K562	blood:
10	chr6:27355567..27357656-chr6:27365756..27367664,2	K562	blood:
11	chr6:27384306..27386881-chr6:27596735..27599221,2	K562	blood:
12	chr6:27356277..27359093-chr6:27439899..27443040,4	MCF-7	breast:
13	chr6:27355079..27357819-chr6:27369323..27370983,2	K562	blood:
14	chr6:27387622..27389400-chr6:27392243..27394109,3	K562	blood:
15	chr6:27384861..27387249-chr6:27388670..27390511,2	K562	blood:
16	chr6:27403637..27406205-chr6:27438159..27440305,2	K562	blood:
17	chr6:27387622..27389345-chr6:27392576..27394109,2	K562	blood:
18	chr6:27360610..27362921-chr6:27368248..27371052,2	MCF-7	breast:
19	chr6:27359046..27360563-chr6:27366041..27368204,2	K562	blood:
20	chr6:27361962..27364399-chr6:27416292..27418860,2	K562	blood:
21	chr6:27364229..27366794-chr6:27416961..27418573,2	K562	blood:
22	chr6:27394554..27397400-chr6:27397468..27400662,4	K562	blood:
23	chr6:27362299..27364139-chr6:27382508..27384526,2	K562	blood:
24	chr6:27389481..27391998-chr6:27409744..27412634,3	K562	blood:
25	chr6:27392162..27394752-chr6:27395413..27397356,2	K562	blood:
26	chr6:27382004..27384798-chr6:27386646..27388886,2	K562	blood:
27	chr6:27387622..27389400-chr6:27392243..27394109,3	K562	blood:
28	chr6:27387622..27389345-chr6:27392576..27394109,2	K562	blood:
29	chr6:27387983..27390252-chr6:27430155..27433045,2	K562	blood:
30	chr6:27359046..27360563-chr6:27366041..27368204,2	K562	blood:
31	chr6:27360610..27362921-chr6:27368248..27371052,2	MCF-7	breast:
32	chr6:27394116..27396577-chr6:27402117..27405995,3	K562	blood:
33	chr6:27374845..27377266-chr6:27859975..27862570,2	K562	blood:
34	chr6:27394222..27397400-chr6:27397468..27400934,4	K562	blood:
35	chr6:27394554..27397400-chr6:27397468..27400662,4	K562	blood:
36	chr6:27343208..27345684-chr6:27358840..27361489,2	K562	blood:
37	chr6:27392162..27394752-chr6:27395413..27397356,2	K562	blood:
38	chr6:27371829..27373336-chr6:27374034..27376555,2	K562	blood:
39	chr6:27100771..27102364-chr6:27363627..27365600,2	K562	blood:
40	chr6:27356362..27358956-chr6:27773296..27775539,3	K562	blood:
41	chr6:27356549..27360030-chr6:27360597..27364786,4	MCF-7	breast:
42	chr6:27383453..27385090-chr6:27415473..27417741,2	K562	blood:
43	chr6:27357897..27360026-chr6:27439101..27441512,2	K562	blood:
44	chr6:27394116..27396577-chr6:27402117..27405995,3	K562	blood:
45	chr6:27386703..27389483-chr6:27429188..27431655,2	K562	blood:
46	chr6:27363554..27367371-chr6:27369337..27372451,5	K562	blood:
47	chr6:27370730..27373329-chr6:27374910..27376555,2	K562	blood:
48	chr6:27279249..27281645-chr6:27389545..27391578,2	K562	blood:
49	chr6:27363318..27368170-chr6:27368582..27372451,5	K562	blood:
50	chr6:27402730..27404689-chr6:27419537..27421092,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS16-3	chr6:27358759-27358911	NONHSAT108379
2	lnc-PRSS16-4	chr6:27368315-27368534	NONHSAT108381
3	lnc-ZNF184-2	chr6:27371789-27374743	ENSG00000271755.1
4	lnc-PRSS16-2	chr6:27357718-27358702	NONHSAT108380
5	lnc-ZNF391-1	chr6:27362796-27362874	NONHSAT108376
6	lnc-PRSS16-5	chr6:27369662-27371681	NONHSAT108382
7	lnc-ZNF391-1	chr6:27367221-27367327	NONHSAT108376

No data

Variant related genes	Relation type
ENSG00000271755	TF binding region
MCFD2P1	TF binding region
ENSG00000271755	CpG island
MCFD2P1	CpG island
ENSG00000237154	chromatin interactions
ENSG00000238648	chromatin interactions
ENSG00000217862	chromatin interactions
ENSG00000271755	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000124613	chromatin interactions
ENSG00000096654	chromatin interactions
ENSG00000158553	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000196331	chromatin interactions

Extended variants
information (count: 1598 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1598 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554335752	chr6:27358561-27358562	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
2	rs184215676	chr6:27358572-27358573	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs189582497	chr6:27358573-27358574	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs181842991	chr6:27358615-27358616	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
5	rs186438072	chr6:27358621-27358622	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs542215911	chr6:27358631-27358632	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs554904268	chr6:27358641-27358642	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs16898958	chr6:27358673-27358674	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs149721214	chr6:27358706-27358707	Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs145558789	chr6:27358718-27358719	Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs148440803	chr6:27358768-27358769	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs545902104	chr6:27358776-27358777	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs190323520	chr6:27358814-27358815	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs374171910	chr6:27358819-27358820	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
15	rs181579271	chr6:27358845-27358846	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
16	rs6936356	chr6:27358853-27358854	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs6936539	chr6:27358917-27358918	Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs13202617	chr6:27358978-27358979	Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs545826835	chr6:27358980-27358981	Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs386406591	chr6:27358981-27358982	Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs186385647	chr6:27358995-27358996	Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs59994175	chr6:27359000-27359001	Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs78669227	chr6:27359001-27359002	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs527976784	chr6:27359040-27359041	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs191280398	chr6:27359066-27359067	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs144030368	chr6:27359074-27359075	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs537522262	chr6:27359122-27359123	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs6936951	chr6:27359131-27359132	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs554214027	chr6:27359142-27359143	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs570116063	chr6:27359184-27359185	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs535857238	chr6:27359248-27359249	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs72843151	chr6:27359268-27359269	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs183382292	chr6:27359311-27359312	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs540496019	chr6:27359316-27359317	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs200058912	chr6:27359326-27359327	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs66664734	chr6:27359327-27359328	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs142231148	chr6:27359330-27359331	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs79590010	chr6:27359331-27359332	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs200818644	chr6:27359332-27359333	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs140120083	chr6:27359333-27359334	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs140146135	chr6:27359334-27359335	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs553750929	chr6:27359435-27359436	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs367669129	chr6:27359492-27359493	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs114338169	chr6:27359517-27359518	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs575755487	chr6:27359526-27359527	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs543182250	chr6:27359527-27359528	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs7754411	chr6:27359584-27359585	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs531298192	chr6:27359640-27359641	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs76050333	chr6:27359655-27359656	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
50	rs11970261	chr6:27359719-27359720	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27357200-27362200	Weak transcription	Aorta	Aorta
2	chr6:27357200-27366600	Weak transcription	Left Ventricle	heart
3	chr6:27357400-27361600	Weak transcription	Colonic Mucosa	Colon
4	chr6:27357400-27363000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:27357400-27363000	Weak transcription	Right Atrium	heart
6	chr6:27357400-27364200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:27357400-27364800	Weak transcription	Fetal Muscle Leg	muscle
8	chr6:27357400-27364800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:27357400-27365000	Weak transcription	Fetal Lung	lung
10	chr6:27357400-27366000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr6:27357400-27367000	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr6:27357400-27367200	Weak transcription	Brain Substantia Nigra	brain
13	chr6:27357400-27367800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr6:27357400-27368000	Weak transcription	Fetal Kidney	kidney
15	chr6:27357600-27360200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr6:27357600-27362000	Weak transcription	Fetal Stomach	stomach
17	chr6:27357600-27362000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr6:27357600-27362800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:27357600-27365000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:27357600-27365000	Weak transcription	Fetal Muscle Trunk	muscle
21	chr6:27357600-27365800	Weak transcription	Stomach Smooth Muscle	stomach
22	chr6:27357600-27367000	Weak transcription	Fetal Brain Male	brain
23	chr6:27357600-27368000	Weak transcription	Brain Angular Gyrus	brain
24	chr6:27357600-27368600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:27357600-27368800	Weak transcription	Pancreas	Pancrea
26	chr6:27357800-27359400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr6:27357800-27361000	Weak transcription	Adipose Nuclei	Adipose
28	chr6:27357800-27361400	Weak transcription	Primary B cells from cord blood	blood
29	chr6:27357800-27362000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:27357800-27362800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:27357800-27366800	Weak transcription	Brain Anterior Caudate	brain
32	chr6:27357800-27367000	Weak transcription	Spleen	Spleen
33	chr6:27357800-27367200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr6:27358000-27358600	Enhancers	Dnd41	blood
35	chr6:27358000-27359600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:27358000-27360000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:27358000-27360200	Weak transcription	NHEK	skin
38	chr6:27358000-27360400	Weak transcription	K562	blood
39	chr6:27358000-27365000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr6:27358000-27367000	Weak transcription	Brain Hippocampus Middle	brain
41	chr6:27358000-27368200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr6:27358200-27359000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr6:27358200-27363000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr6:27358400-27360600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:27359000-27359200	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr6:27359200-27360000	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:27359400-27359800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
48	chr6:27359600-27371200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr6:27359600-27372200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:27360000-27360200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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