Variant report

Variant	nsv884435
Chromosome Location	chr6:31739881-31750919
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:906)
CpG islands
(count:4766)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31744950-31745207	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:31744791-31745248	K562	blood:	n/a	n/a
3	ARID3A	chr6:31740685-31740937	K562	blood:	n/a	n/a
4	ARID3A	chr6:31740705-31740842	HepG2	liver:	n/a	n/a
5	ATF1	chr6:31744739-31745294	K562	blood:	n/a	chr6:31744920-31744934
6	ATF2	chr6:31744593-31745360	GM12878	blood:	n/a	chr6:31744920-31744934
7	ATF2	chr6:31744662-31745294	GM12878	blood:	n/a	chr6:31744920-31744934
8	ATF3	chr6:31744657-31745504	K562	blood:	n/a	n/a
9	ATF3	chr6:31744570-31745542	K562	blood:	n/a	n/a
10	BACH1	chr6:31740819-31740823	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:31748097-31748139	K562	blood:	n/a	n/a
12	BACH1	chr6:31744775-31745310	K562	blood:	n/a	chr6:31745135-31745149
13	BACH1	chr6:31740721-31740863	K562	blood:	n/a	n/a
14	BATF	chr6:31744874-31745274	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:31744747-31745233	GM12878	blood:	n/a	n/a
16	BCL11A	chr6:31744806-31745124	GM12878	blood:	n/a	n/a
17	BCL3	chr6:31744559-31745342	A549	lung:	n/a	n/a
18	BCL3	chr6:31744547-31745467	K562	blood:	n/a	n/a
19	BCL3	chr6:31744638-31745342	A549	lung:	n/a	n/a
20	BCL3	chr6:31744523-31745345	GM12878	blood:	n/a	n/a
21	BCLAF1	chr6:31744631-31745448	K562	blood:	n/a	n/a
22	BCLAF1	chr6:31744727-31745294	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:31744624-31745537	K562	blood:	n/a	n/a
24	BCLAF1	chr6:31744638-31745283	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:31739703-31740017	K562	blood:	n/a	n/a
26	BHLHE40	chr6:31740655-31741177	K562	blood:	n/a	n/a
27	BHLHE40	chr6:31740671-31740973	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:31744836-31745249	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:31744706-31745227	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:31744537-31745627	K562	blood:	n/a	n/a
31	BHLHE40	chr6:31743765-31744030	HepG2	liver:	n/a	n/a
32	BRCA1	chr6:31744767-31745359	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr6:31740719-31740902	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr6:31744980-31745128	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:31740672-31740964	HepG2	liver:	n/a	n/a
36	BRCA1	chr6:31743138-31743170	HepG2	liver:	n/a	n/a
37	CBX3	chr6:31744203-31746270	K562	blood:	n/a	n/a
38	CBX3	chr6:31744655-31745413	K562	blood:	n/a	n/a
39	CBX3	chr6:31740648-31740946	K562	blood:	n/a	n/a
40	CBX3	chr6:31740525-31741197	K562	blood:	n/a	n/a
41	CCNT2	chr6:31740719-31740920	K562	blood:	n/a	n/a
42	CCNT2	chr6:31744509-31745393	K562	blood:	n/a	chr6:31744819-31744828
43	CEBPB	chr6:31745430-31745585	K562	blood:	n/a	n/a
44	CEBPB	chr6:31744698-31745355	GM12878	blood:	n/a	n/a
45	CEBPB	chr6:31744809-31745176	K562	blood:	n/a	n/a
46	CEBPB	chr6:31742973-31743033	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:31744906-31745115	GM12878	blood:	n/a	n/a
48	CEBPB	chr6:31744914-31745375	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:31744758-31745483	K562	blood:	n/a	n/a
50	CEBPD	chr6:31744644-31745408	HepG2	liver:	n/a	n/a

(count:4766 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31750165-31750215	SKMC	muscle:	n/a
2	chr6:31746114-31746164	HIPEpiC	eye:	n/a
3	chr6:31740970-31741020	AoSMC	blood vessel:	n/a
4	chr6:31744037-31744087	GM12878	blood:	n/a
5	chr6:31747216-31747266	T-47D	breast:	n/a
6	chr6:31747023-31747073	NHDF-neo	bronchial:	n/a
7	chr6:31747257-31747307	PANC-1	pancreas:	n/a
8	chr6:31746874-31746924	GM19239	blood:	n/a
9	chr6:31750165-31750215	SKMC	muscle:	n/a
10	chr6:31746114-31746164	HIPEpiC	eye:	n/a
11	chr6:31740970-31741020	AoSMC	blood vessel:	n/a
12	chr6:31744037-31744087	GM12878	blood:	n/a
13	chr6:31747216-31747266	T-47D	breast:	n/a
14	chr6:31747023-31747073	NHDF-neo	bronchial:	n/a
15	chr6:31747257-31747307	PANC-1	pancreas:	n/a
16	chr6:31746874-31746924	GM19239	blood:	n/a
17	chr6:31740849-31740899	CMK	blood:	n/a
18	chr6:31747237-31747287	GM06990	blood:	n/a
19	chr6:31741184-31741234	H1-hESC	embryonic stem cell:	embryo
20	chr6:31746808-31746858	AG10803	skin:	n/a
21	chr6:31747232-31747282	H1-hESC	embryonic stem cell:	embryo
22	chr6:31743769-31743819	Jurkat	blood:	n/a
23	chr6:31744524-31744574	HL-60	blood:	n/a
24	chr6:31741184-31741234	U87	brain:	n/a
25	chr6:31744927-31744977	NHDF-neo	bronchial:	n/a
26	chr6:31747255-31747305	AG04449	skin:	fetal
27	chr6:31747255-31747305	GM06990	blood:	n/a
28	chr6:31744735-31744785	NT2-D1	testis:	n/a
29	chr6:31740951-31741001	PrEC	prostate:	n/a
30	chr6:31747053-31747103	SKMC	muscle:	n/a
31	chr6:31746941-31746991	HCM	heart:	n/a
32	chr6:31740849-31740899	HEEpiC	esophagus:	n/a
33	chr6:31748160-31748210	HEEpiC	esophagus:	n/a
34	chr6:31744962-31745012	HCT-116	colon:	n/a
35	chr6:31744545-31744595	Hepatocyte	liver:	n/a
36	chr6:31744015-31744065	NHBE	bronchial:	n/a
37	chr6:31746114-31746164	SKMC	muscle:	n/a
38	chr6:31743928-31743978	PrEC	prostate:	n/a
39	chr6:31741184-31741234	HCM	heart:	n/a
40	chr6:31750532-31750582	HRPEpiC	eye:	n/a
41	chr6:31745821-31745871	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:31747216-31747266	SKMC	muscle:	n/a
43	chr6:31745181-31745231	BE2_C	brain:	n/a
44	chr6:31748160-31748210	Hela-S3	cervix:	n/a
45	chr6:31746847-31746897	NHDF-neo	bronchial:	n/a
46	chr6:31743986-31744036	AG04450	lung:	fetal
47	chr6:31746956-31747006	HRPEpiC	eye:	n/a
48	chr6:31744816-31744866	ProgFib	skin:	n/a
49	chr6:31744524-31744574	PFSK-1	brain:	n/a
50	chr6:31746919-31746969	Jurkat	blood:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31508667..31511581-chr6:31742885..31745171,3	MCF-7	breast:
2	chr6:31642643..31644341-chr6:31742570..31744549,2	MCF-7	breast:
3	chr6:31701475..31705916-chr6:31741171..31744372,4	MCF-7	breast:
4	chr6:31502088..31504001-chr6:31743213..31745224,2	MCF-7	breast:
5	chr6:31737963..31740782-chr6:31743505..31746196,3	MCF-7	breast:
6	chr6:31743107..31747994-chr6:31781956..31785553,7	MCF-7	breast:
7	chr6:31743176..31746587-chr6:31939802..31942689,4	K562	blood:
8	chr6:31748274..31750464-chr6:31829000..31831442,2	MCF-7	breast:
9	chr6:31747450..31751295-chr6:31800640..31804723,4	MCF-7	breast:
10	chr6:31741163..31742824-chr6:31743275..31745395,3	MCF-7	breast:
11	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
12	chr6:31706404..31710413-chr6:31739544..31742193,3	MCF-7	breast:
13	chr6:31668602..31672513-chr6:31741310..31744822,4	MCF-7	breast:
14	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
15	chr6:31507944..31511146-chr6:31743964..31746169,3	K562	blood:
16	chr6:31697592..31699245-chr6:31742808..31745377,2	MCF-7	breast:
17	chr6:31632664..31635327-chr6:31741807..31745187,4	MCF-7	breast:
18	chr6:31732922..31735851-chr6:31748037..31750099,2	MCF-7	breast:
19	chr6:31745070..31746845-chr6:31830028..31832915,2	MCF-7	breast:
20	chr6:31742555..31745004-chr6:31773789..31777145,5	MCF-7	breast:
21	chr6:31508578..31511041-chr6:31743489..31745514,2	K562	blood:
22	chr6:31741149..31744902-chr6:31760858..31763694,5	MCF-7	breast:
23	chr6:31620739..31623442-chr6:31750369..31752880,2	MCF-7	breast:
24	chr6:31742944..31744994-chr6:31869511..31871431,2	K562	blood:
25	chr6:31739355..31742514-chr6:31742775..31744985,3	MCF-7	breast:
26	chr6:31735011..31745595-chr6:31798203..31806127,22	MCF-7	breast:
27	chr6:31745758..31747408-chr6:31800818..31802986,2	MCF-7	breast:
28	chr6:31737648..31740756-chr6:31757248..31760700,3	MCF-7	breast:
29	chr6:31739355..31742514-chr6:31742775..31744985,3	MCF-7	breast:
30	chr6:31710678..31714958-chr6:31739473..31744061,4	MCF-7	breast:
31	chr6:31740931..31743197-chr6:31865687..31868469,2	MCF-7	breast:
32	chr6:31742934..31744615-chr6:31773250..31774889,2	MCF-7	breast:
33	chr6:31743287..31747076-chr6:31793437..31796925,5	MCF-7	breast:
34	chr6:31737503..31739335-chr6:31742183..31744187,2	MCF-7	breast:
35	chr6:31742931..31744824-chr6:31926408..31928564,2	K562	blood:
36	chr6:31696116..31699055-chr6:31743914..31747307,3	MCF-7	breast:
37	chr6:31703366..31705147-chr6:31738315..31740489,2	MCF-7	breast:
38	chr6:31750326..31751829-chr6:31829443..31831754,2	MCF-7	breast:
39	chr11:64545106..64547042-chr6:31742109..31744042,2	MCF-7	breast:
40	chr6:31740985..31743056-chr6:31795621..31797863,3	MCF-7	breast:
41	chr6:31730683..31732865-chr6:31738402..31740134,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000201555	TF binding region
VWA7	TF binding region
VARS	TF binding region
ENSG00000201555	CpG island
VWA7	CpG island
VARS	CpG island
ENSG00000204366	chromatin interactions
ENSG00000266776	chromatin interactions
ENSG00000265236	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000213719	chromatin interactions
ENSG00000204410	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000204392	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000263020	chromatin interactions
ENSG00000235663	chromatin interactions
ENSG00000204356	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000269038	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000255152	chromatin interactions
ENSG00000201823	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000234006	chromatin interactions
ENSG00000204351	chromatin interactions
ENSG00000201754	chromatin interactions
ENSG00000204396	chromatin interactions
ENSG00000204427	chromatin interactions
ENSG00000228727	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000204387	chromatin interactions

Extended variants
information (count: 486 )
Associated
traits (count: 132 )

Variant overlapped rSNPs/rCNVs (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536158523	chr6:31739954-31739955	Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs554302771	chr6:31739965-31739966	Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs575835709	chr6:31739979-31739980	Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs558827701	chr6:31740063-31740064	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs577154727	chr6:31740167-31740168	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs541097316	chr6:31740184-31740185	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs137859769	chr6:31740212-31740213	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs185015661	chr6:31740219-31740220	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs80087332	chr6:31740262-31740263	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs563822735	chr6:31740288-31740289	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs376888367	chr6:31740341-31740342	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs368664265	chr6:31740352-31740353	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs373268014	chr6:31740361-31740362	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs531059006	chr6:31740392-31740393	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs190565543	chr6:31740414-31740415	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs199587064	chr6:31740443-31740444	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs192980878	chr6:31740444-31740445	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs139590714	chr6:31740510-31740511	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs565345970	chr6:31740538-31740539	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs536095659	chr6:31740568-31740569	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs548128125	chr6:31740661-31740662	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs377625112	chr6:31740681-31740682	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs373169264	chr6:31740745-31740746	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs201394026	chr6:31740760-31740761	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs139774402	chr6:31740768-31740769	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs377401343	chr6:31740778-31740779	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs565249818	chr6:31740779-31740780	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs577437793	chr6:31740781-31740782	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs370829297	chr6:31740801-31740802	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs536885510	chr6:31740805-31740806	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs149780751	chr6:31740806-31740807	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs374709454	chr6:31740824-31740825	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs149293400	chr6:31740825-31740826	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs368204071	chr6:31740828-31740829	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs535132715	chr6:31740852-31740853	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs146780305	chr6:31740879-31740880	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs574887629	chr6:31740881-31740882	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs542536426	chr6:31740900-31740901	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs113698227	chr6:31740919-31740920	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs181231987	chr6:31740938-31740939	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs564010975	chr6:31740951-31740952	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs575777619	chr6:31740952-31740953	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs185333600	chr6:31740971-31740972	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs373779910	chr6:31740975-31740976	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs367744626	chr6:31740979-31740980	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs188242832	chr6:31740984-31740985	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs532069939	chr6:31741036-31741037	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs372135746	chr6:31741048-31741049	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs139770801	chr6:31741049-31741050	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs547013618	chr6:31741052-31741053	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:132)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	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
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31716600-31744000	Weak transcription	GM12878-XiMat	blood
2	chr6:31729200-31742800	Weak transcription	A549	lung
3	chr6:31731400-31744400	Weak transcription	Left Ventricle	heart
4	chr6:31731600-31743400	Weak transcription	Lung	lung
5	chr6:31731800-31743600	Weak transcription	Right Ventricle	heart
6	chr6:31731800-31749600	Weak transcription	HUVEC	blood vessel
7	chr6:31732000-31740000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr6:31732200-31740000	Weak transcription	Dnd41	blood
9	chr6:31732600-31745000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:31732800-31744400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:31734400-31742800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:31734400-31743400	Weak transcription	Right Atrium	heart
13	chr6:31734600-31740800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:31734600-31740800	Weak transcription	Stomach Mucosa	stomach
15	chr6:31734600-31743600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr6:31734600-31744200	Weak transcription	Brain Anterior Caudate	brain
17	chr6:31734600-31744200	Weak transcription	NH-A	brain
18	chr6:31734600-31744600	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:31734600-31744600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr6:31734600-31745200	Weak transcription	Brain Germinal Matrix	brain
21	chr6:31734600-31745400	Weak transcription	Fetal Brain Female	brain
22	chr6:31734600-31746600	Weak transcription	Brain Angular Gyrus	brain
23	chr6:31734800-31740800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr6:31734800-31745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr6:31735200-31740800	Weak transcription	Duodenum Mucosa	Duodenum
26	chr6:31735400-31742800	Weak transcription	Fetal Intestine Large	intestine
27	chr6:31735600-31740800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:31736800-31741600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr6:31737200-31741600	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr6:31737200-31744200	Weak transcription	Fetal Stomach	stomach
31	chr6:31737400-31741800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr6:31737400-31744400	Weak transcription	Fetal Muscle Leg	muscle
33	chr6:31737400-31744600	Enhancers	Primary T cells fromperipheralblood	blood
34	chr6:31737600-31740000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:31737600-31740200	Weak transcription	Thymus	Thymus
36	chr6:31737600-31740800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:31737600-31740800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:31737800-31740800	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr6:31737800-31741400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr6:31737800-31741600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr6:31738000-31740000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:31738000-31740000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:31738000-31740600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:31738000-31740600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr6:31738000-31740600	Weak transcription	Spleen	Spleen
46	chr6:31738000-31740800	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr6:31738000-31740800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:31738000-31740800	Weak transcription	Liver	Liver
49	chr6:31738000-31740800	Weak transcription	Esophagus	oesophagus
50	chr6:31738000-31741800	Weak transcription	Fetal Muscle Trunk	muscle

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