Variant report

Variant	nsv5516
Chromosome Location	chr6:144300321-144345812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:605)
CpG islands
(count:1652)
Chromatin interactive
region (count:53)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:144334581-144335006	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:144334532-144334878	K562	blood:	n/a	n/a
3	ATF1	chr6:144327872-144328193	K562	blood:	n/a	n/a
4	ATF3	chr6:144327814-144328153	K562	blood:	n/a	n/a
5	ATF3	chr6:144329435-144329637	K562	blood:	n/a	n/a
6	BHLHE40	chr6:144329488-144330049	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:144329557-144329608	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:144304120-144304418	K562	blood:	n/a	n/a
9	BHLHE40	chr6:144329301-144329697	K562	blood:	n/a	n/a
10	BHLHE40	chr6:144334645-144334908	K562	blood:	n/a	n/a
11	CBX3	chr6:144323387-144323714	K562	blood:	n/a	n/a
12	CBX3	chr6:144334465-144335117	HCT-116	colon:	n/a	n/a
13	CBX3	chr6:144334460-144335139	HCT-116	colon:	n/a	n/a
14	CBX3	chr6:144329322-144329738	K562	blood:	n/a	n/a
15	CCNT2	chr6:144328917-144329845	K562	blood:	n/a	n/a
16	CCNT2	chr6:144327456-144327554	K562	blood:	n/a	n/a
17	CEBPB	chr6:144320468-144320942	IMR90	lung:	n/a	chr6:144320571-144320584 chr6:144320572-144320583 chr6:144320571-144320584
18	CEBPB	chr6:144320504-144320789	HepG2	liver:	n/a	chr6:144320571-144320584 chr6:144320572-144320583 chr6:144320571-144320584
19	CEBPB	chr6:144310809-144311054	HepG2	liver:	n/a	chr6:144310923-144310934
20	CHD1	chr6:144327419-144329527	IMR90	lung:	n/a	n/a
21	CTCF	chr6:144334680-144334830	HCM	heart:	n/a	n/a
22	CTCF	chr6:144334640-144334790	BJ	skin:	n/a	n/a
23	CTCF	chr6:144334620-144334824	T-47D	breast:	n/a	n/a
24	CTCF	chr6:144334620-144334770	HVMF	connective:	n/a	n/a
25	CTCF	chr6:144334660-144334810	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:144334617-144334884	LNCaP	prostate:	n/a	n/a
27	CTCF	chr6:144334451-144335040	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:144334700-144334850	GM12871	blood:	n/a	n/a
29	CTCF	chr6:144334635-144334925	GM12892	blood:	n/a	n/a
30	CTCF	chr6:144334640-144334790	GM12869	blood:	n/a	n/a
31	CTCF	chr6:144334680-144334830	GM12872	blood:	n/a	n/a
32	CTCF	chr6:144334640-144334790	HRE	kidney:	n/a	n/a
33	CTCF	chr6:144334660-144334810	BE2_C	brain:	n/a	n/a
34	CTCF	chr6:144334660-144334810	HMF	breast:	n/a	n/a
35	CTCF	chr6:144334680-144334830	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr6:144334479-144334945	A549	lung:	n/a	n/a
37	CTCF	chr6:144334660-144334899	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:144334660-144334810	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr6:144334700-144334850	HCM	heart:	n/a	n/a
40	CTCF	chr6:144335001-144335014	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr6:144334660-144334810	BJ	skin:	n/a	n/a
42	CTCF	chr6:144334660-144334810	AG10803	skin:	n/a	n/a
43	CTCF	chr6:144334680-144334830	AG09309	skin:	n/a	n/a
44	CTCF	chr6:144334660-144334810	HCFaa	heart:	n/a	n/a
45	CTCF	chr6:144334600-144334916	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:144334620-144334770	WI-38	lung:	n/a	n/a
47	CTCF	chr6:144334617-144334875	GM13977	blood:	n/a	n/a
48	CTCF	chr6:144334660-144334810	HMEC	breast:	n/a	n/a
49	CTCF	chr6:144334539-144334922	HepG2	liver:	n/a	n/a
50	CTCF	chr6:144334498-144334969	IMR90	lung:	n/a	n/a

(count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:144329382-144329432	PFSK-1	brain:	n/a
2	chr6:144328482-144328532	HepG2	liver:	n/a
3	chr6:144329172-144329222	HNPCEpiC	eye:	n/a
4	chr6:144328917-144328967	SAEC	small airway:	n/a
5	chr6:144334733-144334783	LNCaP	prostate:	n/a
6	chr6:144329382-144329432	PFSK-1	brain:	n/a
7	chr6:144328482-144328532	HepG2	liver:	n/a
8	chr6:144329172-144329222	HNPCEpiC	eye:	n/a
9	chr6:144328917-144328967	SAEC	small airway:	n/a
10	chr6:144334733-144334783	LNCaP	prostate:	n/a
11	chr6:144329732-144329782	HAEpiC	amniotic membrane:	n/a
12	chr6:144329052-144329102	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:144334733-144334783	ovcar-3	ovarian:	n/a
14	chr6:144328482-144328532	AG10803	skin:	n/a
15	chr6:144334983-144335033	T-47D	breast:	n/a
16	chr6:144328482-144328532	ECC-1	luminal epithelium:	n/a
17	chr6:144329922-144329972	NH-A	brain:	n/a
18	chr6:144329909-144329959	HRCEpiC	kidney:	n/a
19	chr6:144329962-144330012	HIPEpiC	eye:	n/a
20	chr6:144329473-144329523	ProgFib	skin:	n/a
21	chr6:144329780-144329830	CMK	blood:	n/a
22	chr6:144329780-144329830	ECC-1	luminal epithelium:	n/a
23	chr6:144329052-144329102	A549	lung:	n/a
24	chr6:144329780-144329830	AG10803	skin:	n/a
25	chr6:144334733-144334783	HCM	heart:	n/a
26	chr6:144334983-144335033	ProgFib	skin:	n/a
27	chr6:144329485-144329535	GM19239	blood:	n/a
28	chr6:144329331-144329381	HIPEpiC	eye:	n/a
29	chr6:144329922-144329972	AG10803	skin:	n/a
30	chr6:144329172-144329222	MCF-7	breast:	n/a
31	chr6:144330162-144330212	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:144329732-144329782	GM12892	blood:	n/a
33	chr6:144330233-144330283	HCT-116	colon:	n/a
34	chr6:144329887-144329937	AoSMC	blood vessel:	n/a
35	chr6:144329922-144329972	HRCEpiC	kidney:	n/a
36	chr6:144329909-144329959	HIPEpiC	eye:	n/a
37	chr6:144330233-144330283	GM12891	blood:	n/a
38	chr6:144329780-144329830	ovcar-3	ovarian:	n/a
39	chr6:144330345-144330395	HL-60	blood:	n/a
40	chr6:144329780-144329830	SAEC	small airway:	n/a
41	chr6:144329997-144330047	U87	brain:	n/a
42	chr6:144329766-144329816	HNPCEpiC	eye:	n/a
43	chr6:144329922-144329972	AG04450	lung:	fetal
44	chr6:144328482-144328532	HCPEpiC	choroid plexus:	n/a
45	chr6:144329922-144329972	AG09319	gingival:	n/a
46	chr6:144329887-144329937	GM12878	blood:	n/a
47	chr6:144329172-144329222	IMR90	lung:	fetal
48	chr6:144333219-144333269	MCF10A-Er-Src	breast:	n/a
49	chr6:144328917-144328967	HepG2	liver:	n/a
50	chr6:144329331-144329381	HL-60	blood:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:144261338..144263476-chr6:144332649..144334229,2	K562	blood:
2	chr6:144308289..144311855-chr6:144313891..144316861,3	K562	blood:
3	chr6:144281063..144283369-chr6:144300258..144301921,2	MCF-7	breast:
4	chr17:57922501..57925397-chr6:144320697..144322462,2	MCF-7	breast:
5	chr6:144284653..144286601-chr6:144327499..144329714,2	K562	blood:
6	chr6:144308289..144311855-chr6:144313891..144316861,3	K562	blood:
7	chr6:144307669..144309454-chr6:144321320..144323421,2	K562	blood:
8	chr6:144318653..144320908-chr6:144327115..144329301,2	MCF-7	breast:
9	chr6:144323590..144325654-chr6:144327756..144330869,4	K562	blood:
10	chr6:144317835..144320608-chr6:144321687..144325166,4	K562	blood:
11	chr6:144162948..144166199-chr6:144325900..144330312,6	K562	blood:
12	chr6:144262280..144264649-chr6:144315231..144317847,3	K562	blood:
13	chr6:144317835..144320608-chr6:144321687..144325166,4	K562	blood:
14	chr6:143830342..143833743-chr6:144326901..144329456,3	K562	blood:
15	chr6:144262965..144264005-chr6:144332999..144335668,24	MCF-7	breast:
16	chr1:201278978..201279852-chr6:144334250..144335005,2	MCF-7	breast:
17	chr6:144328273..144330730-chr6:144332408..144334974,3	MCF-7	breast:
18	chr6:144321371..144324041-chr6:144325680..144328312,2	MCF-7	breast:
19	chr6:144321371..144324041-chr6:144325680..144328312,2	MCF-7	breast:
20	chr6:144309639..144311261-chr6:144311360..144313081,2	MCF-7	breast:
21	chr6:144162988..144165888-chr6:144327569..144329475,4	K562	blood:
22	chr6:144263343..144263849-chr6:144314441..144315044,2	MCF-7	breast:
23	chr6:144307669..144309454-chr6:144321320..144323421,2	K562	blood:
24	chr6:144262987..144264027-chr6:144334233..144335108,3	K562	blood:
25	chr6:143896253..143896901-chr6:144334460..144335006,2	MCF-7	breast:
26	chr6:144260683..144261884-chr6:144334204..144335620,11	K562	blood:
27	chr6:144305955..144307809-chr6:144315881..144318184,2	K562	blood:
28	chr11:85195062..85195778-chr6:144328873..144329374,2	HCT-116	colon:
29	chr6:144286319..144288248-chr6:144317369..144319699,2	K562	blood:
30	chr6:144284921..144286601-chr6:144327267..144329714,2	K562	blood:
31	chr6:144317224..144321801-chr6:144325299..144329748,8	K562	blood:
32	chr6:144274204..144276778-chr6:144326473..144328934,2	K562	blood:
33	chr6:144327197..144329498-chr6:144336574..144339323,2	K562	blood:
34	chr6:143896199..143897161-chr6:144334481..144335481,6	K562	blood:
35	chr6:144302101..144303644-chr6:144304485..144306870,2	K562	blood:
36	chr6:144299725..144302101-chr6:144323058..144324849,2	MCF-7	breast:
37	chr6:144163704..144165322-chr6:144301291..144303230,2	MCF-7	breast:
38	chr6:143824207..143826466-chr6:144327937..144329566,2	K562	blood:
39	chr6:144286646..144289265-chr6:144304089..144305699,2	K562	blood:
40	chr6:144262914..144263721-chr6:144334214..144334821,4	MCF-7	breast:
41	chr6:143913267..143914036-chr6:144334250..144334794,2	K562	blood:
42	chr6:144261214..144261795-chr6:144334290..144335183,2	MCF-7	breast:
43	chr6:144318653..144320908-chr6:144327115..144329301,2	MCF-7	breast:
44	chr6:143769099..143771662-chr6:144327770..144329794,2	K562	blood:
45	chr12:54389286..54389956-chr6:144328658..144329549,2	Hela-S3	cervix:
46	chr6:144020099..144020600-chr6:144334156..144334754,2	K562	blood:
47	chr6:144284969..144287872-chr6:144298750..144300717,2	K562	blood:
48	chr6:144342771..144345121-chr6:144347638..144350267,2	MCF-7	breast:
49	chr6:144260927..144262000-chr6:144334479..144335516,6	MCF-7	breast:
50	chr6:144305516..144307905-chr6:144308755..144311303,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SF3B5-2	chr6:144329228-144329255	NONHSAT115368
2	lnc-SF3B5-2	chr6:144306272-144306333	NONHSAT115372
3	lnc-SF3B5-2	chr6:144325474-144329867	NONHSAT115373
4	lnc-SF3B5-2	chr6:144324034-144324633	NONHSAT115373
5	lnc-SF3B5-2	chr6:144306273-144306311	NONHSAT115366

No data

Variant related genes	Relation type
PLAGL1	TF binding region
PLAGL1	CpG island
ENSG00000001036	chromatin interactions
ENSG00000118495	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000223203	chromatin interactions
ENSG00000229036	chromatin interactions
ENSG00000180806	chromatin interactions
ENSG00000250133	chromatin interactions
ENSG00000135521	chromatin interactions

Extended variants
information (count: 1540 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1540 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143112862	chr6:144300333-144300334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs193120617	chr6:144300338-144300339	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185096549	chr6:144300357-144300358	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs6936239	chr6:144300380-144300381	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147015616	chr6:144300467-144300468	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs374272290	chr6:144300469-144300470	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375683959	chr6:144300485-144300486	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537946468	chr6:144300491-144300492	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556570275	chr6:144300492-144300493	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577962612	chr6:144300521-144300522	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114831561	chr6:144300545-144300546	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545770066	chr6:144300546-144300547	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544965704	chr6:144300557-144300558	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568262829	chr6:144300582-144300583	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572380613	chr6:144300604-144300605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs542847841	chr6:144300642-144300643	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530654193	chr6:144300656-144300657	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188976388	chr6:144300677-144300678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531479452	chr6:144300734-144300735	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543154504	chr6:144300740-144300741	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs6570598	chr6:144300779-144300780	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532161546	chr6:144300821-144300822	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547388477	chr6:144300827-144300828	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566008545	chr6:144300849-144300850	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530002752	chr6:144300852-144300853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148274934	chr6:144300855-144300856	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570463771	chr6:144300862-144300863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs77918243	chr6:144300884-144300885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539034133	chr6:144300900-144300901	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs191647276	chr6:144300943-144300944	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs77715917	chr6:144300956-144300957	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs9386054	chr6:144300957-144300958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs62427104	chr6:144301042-144301043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs114178716	chr6:144301071-144301072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35565029	chr6:144301109-144301110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4379308	chr6:144301219-144301220	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs572445785	chr6:144301285-144301286	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs573175597	chr6:144301308-144301309	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs542909602	chr6:144301333-144301334	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs79593986	chr6:144301337-144301338	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150730421	chr6:144301347-144301348	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs543963425	chr6:144301369-144301370	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs376126203	chr6:144301405-144301406	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs532223934	chr6:144301451-144301452	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541061785	chr6:144301460-144301461	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559384906	chr6:144301485-144301486	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530066278	chr6:144301515-144301516	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs71024882	chr6:144301526-144301527	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs551098131	chr6:144301527-144301528	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs398002977	chr6:144301542-144301543	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144269800-144304400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:144284800-144318400	Weak transcription	Aorta	Aorta
3	chr6:144288400-144314800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:144289000-144301800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr6:144292400-144301200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:144293600-144309800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:144294800-144302600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:144294800-144312200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:144294800-144313600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:144294800-144315600	Weak transcription	NHDF-Ad	bronchial
11	chr6:144295000-144304600	Weak transcription	Fetal Stomach	stomach
12	chr6:144295000-144312600	Weak transcription	Fetal Intestine Small	intestine
13	chr6:144295800-144301400	Weak transcription	Fetal Muscle Leg	muscle
14	chr6:144296000-144304200	Weak transcription	Fetal Kidney	kidney
15	chr6:144297200-144300400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:144297600-144301600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:144297600-144302400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr6:144297600-144304600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:144298400-144301400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:144298800-144304000	Weak transcription	Fetal Lung	lung
21	chr6:144300000-144301000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:144300400-144300600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:144301000-144303000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:144301200-144301600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:144301400-144302200	ZNF genes & repeats	Fetal Muscle Leg	muscle
26	chr6:144301400-144302800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:144301600-144302000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:144301600-144303400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:144301800-144302000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
30	chr6:144301800-144304400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:144302000-144302400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:144302200-144302400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:144302200-144305000	Strong transcription	Fetal Muscle Leg	muscle
34	chr6:144302400-144302600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr6:144302400-144305200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr6:144302400-144305800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr6:144302600-144302800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr6:144302600-144302800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:144302600-144302800	Enhancers	Placenta	Placenta
40	chr6:144302600-144305200	Strong transcription	Fetal Muscle Trunk	muscle
41	chr6:144302800-144303000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:144302800-144303800	Weak transcription	Placenta	Placenta
43	chr6:144302800-144307600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:144303000-144303400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:144303000-144304000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:144303400-144304800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:144303400-144312800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:144303800-144304600	Enhancers	Placenta	Placenta
49	chr6:144303800-144305000	Enhancers	K562	blood
50	chr6:144304000-144304600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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