Variant report

Variant	nsv508401
Chromosome Location	chr6:34669708-34710302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34707133-34707243	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34682463-34682759	K562	blood:	n/a	n/a
3	ARID3A	chr6:34708045-34708073	K562	blood:	n/a	n/a
4	ARID3A	chr6:34699510-34699850	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:34709883-34710222	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:34708281-34708419	HepG2	liver:	n/a	n/a
7	ATF1	chr6:34682476-34682782	K562	blood:	n/a	n/a
8	ATF3	chr6:34682457-34682837	K562	blood:	n/a	n/a
9	BACH1	chr6:34691020-34691511	K562	blood:	n/a	n/a
10	BACH1	chr6:34691059-34691391	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr6:34691509-34691713	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:34682512-34682755	K562	blood:	n/a	n/a
13	BHLHE40	chr6:34708114-34708531	K562	blood:	n/a	n/a
14	BHLHE40	chr6:34708230-34708442	HepG2	liver:	n/a	n/a
15	BHLHE40	chr6:34677264-34677400	K562	blood:	n/a	n/a
16	BRCA1	chr6:34708223-34708553	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr6:34693761-34694109	K562	blood:	n/a	n/a
18	CBX3	chr6:34693680-34694281	K562	blood:	n/a	n/a
19	CBX3	chr6:34682269-34682849	K562	blood:	n/a	n/a
20	CCNT2	chr6:34682475-34682743	K562	blood:	n/a	n/a
21	CEBPB	chr6:34705445-34705524	K562	blood:	n/a	n/a
22	CEBPB	chr6:34706330-34706532	HepG2	liver:	n/a	chr6:34706406-34706417
23	CEBPB	chr6:34708197-34708579	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
24	CEBPB	chr6:34685350-34686027	A549	lung:	n/a	chr6:34685828-34685839
25	CEBPB	chr6:34708167-34708601	Hela-S3	cervix:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
26	CEBPB	chr6:34707065-34707294	HepG2	liver:	n/a	chr6:34707184-34707195
27	CEBPB	chr6:34680760-34680834	K562	blood:	n/a	n/a
28	CEBPB	chr6:34685663-34686041	HepG2	liver:	n/a	chr6:34685828-34685839
29	CEBPB	chr6:34685720-34685893	HepG2	liver:	n/a	chr6:34685828-34685839
30	CEBPB	chr6:34685622-34685960	K562	blood:	n/a	chr6:34685828-34685839
31	CEBPB	chr6:34709955-34710097	A549	lung:	n/a	chr6:34710057-34710068
32	CEBPB	chr6:34707550-34707691	K562	blood:	n/a	n/a
33	CEBPB	chr6:34685629-34685878	HepG2	liver:	n/a	chr6:34685828-34685839
34	CEBPB	chr6:34685659-34686027	K562	blood:	n/a	chr6:34685828-34685839
35	CEBPB	chr6:34708243-34708469	K562	blood:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
36	CEBPB	chr6:34708193-34708564	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
37	CEBPB	chr6:34706363-34706518	K562	blood:	n/a	chr6:34706406-34706417
38	CEBPB	chr6:34708280-34708505	H1-hESC	embryonic stem cell:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
39	CEBPB	chr6:34708209-34708551	MCF-7	breast:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
40	CEBPB	chr6:34685663-34686029	HepG2	liver:	n/a	chr6:34685828-34685839
41	CEBPB	chr6:34708222-34708519	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
42	CEBPB	chr6:34708157-34708498	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
43	CEBPB	chr6:34685681-34685936	IMR90	lung:	n/a	chr6:34685828-34685839
44	CEBPB	chr6:34708280-34708510	IMR90	lung:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
45	CEBPB	chr6:34680707-34680831	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:34708225-34708526	A549	lung:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
47	CEBPB	chr6:34708108-34708643	K562	blood:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
48	CEBPB	chr6:34685217-34686045	Hela-S3	cervix:	n/a	chr6:34685828-34685839
49	CEBPB	chr6:34685762-34685926	K562	blood:	n/a	chr6:34685828-34685839
50	CEBPB	chr6:34708196-34708577	K562	blood:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34691678-34691728	GM19239	blood:	n/a
2	chr6:34677450-34677500	GM12878	blood:	n/a
3	chr6:34677450-34677500	K562	blood:	n/a
4	chr6:34677450-34677500	SK-N-SH_RA	brain:	n/a
5	chr6:34677450-34677500	NB4	blood:	n/a
6	chr6:34691678-34691728	SK-N-SH_RA	brain:	n/a
7	chr6:34691678-34691728	GM12892	blood:	n/a
8	chr6:34691678-34691728	K562	blood:	n/a
9	chr6:34677450-34677500	PrEC	prostate:	n/a
10	chr6:34677450-34677500	MCF10A-Er-Src	breast:	n/a
11	chr6:34691678-34691728	SKMC	muscle:	n/a
12	chr6:34677450-34677500	SKMC	muscle:	n/a
13	chr6:34691678-34691728	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:34677450-34677500	CMK	blood:	n/a
15	chr6:34677450-34677500	AG10803	skin:	n/a
16	chr6:34677450-34677500	HEK293	kidney:	embryo
17	chr6:34691678-34691728	HCF	heart:	n/a
18	chr6:34691678-34691728	HRCEpiC	kidney:	n/a
19	chr6:34677450-34677500	Jurkat	blood:	n/a
20	chr6:34677450-34677500	HRE	kidney:	n/a
21	chr6:34691678-34691728	NHBE	bronchial:	n/a
22	chr6:34677450-34677500	T-47D	breast:	n/a
23	chr6:34691678-34691728	IMR90	lung:	fetal
24	chr6:34677450-34677500	LNCaP	prostate:	n/a
25	chr6:34677450-34677500	BE2_C	brain:	n/a
26	chr6:34691678-34691728	Hela-S3	cervix:	n/a
27	chr6:34677450-34677500	HIPEpiC	eye:	n/a
28	chr6:34691678-34691728	HepG2	liver:	n/a
29	chr6:34691678-34691728	H1-hESC	embryonic stem cell:	embryo
30	chr6:34691678-34691728	NB4	blood:	n/a
31	chr6:34691678-34691728	ProgFib	skin:	n/a
32	chr6:34691678-34691728	AG10803	skin:	n/a
33	chr6:34691678-34691728	HNPCEpiC	eye:	n/a
34	chr6:34691678-34691728	Jurkat	blood:	n/a
35	chr6:34691678-34691728	GM12891	blood:	n/a
36	chr6:34691678-34691728	HCM	heart:	n/a
37	chr6:34691678-34691728	HCT-116	colon:	n/a
38	chr6:34691678-34691728	HCPEpiC	choroid plexus:	n/a
39	chr6:34691678-34691728	CMK	blood:	n/a
40	chr6:34677450-34677500	HRPEpiC	eye:	n/a
41	chr6:34677450-34677500	AoSMC	blood vessel:	n/a
42	chr6:34677450-34677500	NHDF-neo	bronchial:	n/a
43	chr6:34677450-34677500	HEEpiC	esophagus:	n/a
44	chr6:34691678-34691728	T-47D	breast:	n/a
45	chr6:34691678-34691728	HEK293	kidney:	embryo
46	chr6:34677450-34677500	ProgFib	skin:	n/a
47	chr6:34691678-34691728	PrEC	prostate:	n/a
48	chr6:34677450-34677500	GM19239	blood:	n/a
49	chr6:34677450-34677500	HCM	heart:	n/a
50	chr6:34677450-34677500	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:34685141..34687022-chr6:34692903..34695560,2	K562	blood:
2	chr6:34707078..34708583-chr6:34711882..34714603,2	MCF-7	breast:
3	chr6:34690459..34693304-chr6:34723664..34726438,2	K562	blood:
4	chr6:34665467..34667075-chr6:34685677..34688380,2	K562	blood:
5	chr6:34663483..34667506-chr6:34667607..34669948,3	K562	blood:
6	chr6:34707099..34709785-chr6:34713149..34715872,2	K562	blood:
7	chr6:34696691..34699544-chr6:34703628..34706154,2	K562	blood:
8	chr6:34706864..34709056-chr6:34722827..34726268,3	K562	blood:
9	chr6:34694281..34696402-chr6:34696757..34699128,2	K562	blood:
10	chr6:34673308..34675540-chr6:34685613..34688342,2	MCF-7	breast:
11	chr6:34672410..34673961-chr6:34856046..34857679,2	K562	blood:
12	chr6:34663382..34666828-chr6:34670260..34673795,4	K562	blood:
13	chr6:34708225..34709906-chr6:34758782..34761089,2	MCF-7	breast:
14	chr6:34673308..34675540-chr6:34685613..34688342,2	MCF-7	breast:
15	chr6:34657888..34660088-chr6:34685697..34688432,2	MCF-7	breast:
16	chr6:34663482..34665135-chr6:34670765..34672477,2	MCF-7	breast:
17	chr6:34694281..34696402-chr6:34696757..34699128,2	K562	blood:
18	chr6:34696691..34699544-chr6:34703628..34706154,2	K562	blood:
19	chr6:34706320..34708599-chr6:34713149..34715491,2	K562	blood:
20	chr6:34674851..34676937-chr6:34678092..34680234,2	K562	blood:
21	chr6:34677816..34680106-chr6:34720595..34722854,2	MCF-7	breast:
22	chr6:34664626..34667053-chr6:34675137..34677958,3	K562	blood:
23	chr6:34698371..34700265-chr6:34702057..34704593,2	K562	blood:
24	chr6:34671316..34674801-chr6:34727062..34730590,3	K562	blood:
25	chr6:34683902..34686435-chr6:34695998..34698813,2	K562	blood:
26	chr6:34689130..34691156-chr6:34693829..34696616,2	K562	blood:
27	chr6:34709940..34711491-chr6:34711698..34713387,2	K562	blood:
28	chr6:34663129..34665276-chr6:34679494..34681887,3	K562	blood:
29	chr6:34671509..34674335-chr6:34684957..34686904,2	K562	blood:
30	chr6:34683902..34686435-chr6:34695998..34698813,2	K562	blood:
31	chr6:34681066..34682821-chr6:34689773..34692489,2	K562	blood:
32	chr6:34664965..34667279-chr6:34675934..34678672,3	K562	blood:
33	chr6:34671509..34674335-chr6:34684957..34686904,2	K562	blood:
34	chr6:34685141..34688900-chr6:34692903..34695756,4	K562	blood:
35	chr6:34689130..34691156-chr6:34693829..34696616,2	K562	blood:
36	chr6:34685141..34687022-chr6:34692903..34695560,2	K562	blood:
37	chr6:34674851..34676937-chr6:34678092..34680234,2	K562	blood:
38	chr6:34698371..34700265-chr6:34702057..34704593,2	K562	blood:
39	chr6:34685141..34688900-chr6:34692903..34695756,4	K562	blood:
40	chr6:34665132..34667717-chr6:34706629..34708944,2	MCF-7	breast:
41	chr6:34681902..34684168-chr6:34685297..34688228,3	K562	blood:
42	chr6:34681066..34682821-chr6:34689773..34692489,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNRPC-1	chr6:34683390-34683717	NONHSAT112146

Variant related genes	Relation type
ENSG00000217130	TF binding region
ENSG00000186328	TF binding region
ENSG00000217130	CpG island
ENSG00000186328	CpG island
ENSG00000217130	chromatin interactions
ENSG00000186328	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000064999	chromatin interactions
ENSG00000196821	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000272288	chromatin interactions

Extended variants
information (count: 1480 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12208743	chr6:34669729-34669730	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs541814410	chr6:34669742-34669743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563391906	chr6:34669747-34669748	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs150964556	chr6:34669770-34669771	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs149211054	chr6:34669878-34669879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs371560640	chr6:34669880-34669881	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs552558083	chr6:34669904-34669905	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551456702	chr6:34669909-34669910	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs571143663	chr6:34669919-34669920	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs140767600	chr6:34669966-34669967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547180625	chr6:34669986-34669987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571408298	chr6:34670027-34670028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113283033	chr6:34670103-34670104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538108704	chr6:34670114-34670115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568151684	chr6:34670146-34670147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535591683	chr6:34670150-34670151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534359732	chr6:34670154-34670155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187286534	chr6:34670156-34670157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554095828	chr6:34670168-34670169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557740348	chr6:34670172-34670173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540430443	chr6:34670288-34670289	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs202037083	chr6:34670296-34670297	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200052279	chr6:34670339-34670340	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs71544306	chr6:34670340-34670341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs35684630	chr6:34670344-34670345	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs374877845	chr6:34670368-34670369	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs533709515	chr6:34670372-34670373	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555579207	chr6:34670392-34670393	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs7759128	chr6:34670395-34670396	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs113389314	chr6:34670403-34670404	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs193117302	chr6:34670408-34670409	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs575203266	chr6:34670426-34670427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs546179765	chr6:34670457-34670458	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541987261	chr6:34670463-34670464	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs564581961	chr6:34670488-34670489	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs185584931	chr6:34670498-34670499	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140417388	chr6:34670540-34670541	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs187610203	chr6:34670578-34670579	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7759412	chr6:34670584-34670585	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs71567459	chr6:34670603-34670604	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs7741398	chr6:34670623-34670624	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs564444143	chr6:34670627-34670628	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568995917	chr6:34670660-34670661	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs377513995	chr6:34670669-34670670	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192563953	chr6:34670694-34670695	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551368379	chr6:34670719-34670720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs557844104	chr6:34670767-34670768	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7759985	chr6:34670786-34670787	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs534145881	chr6:34670789-34670790	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs184316504	chr6:34670800-34670801	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	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
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
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
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
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34665800-34671600	Weak transcription	A549	lung
2	chr6:34667200-34672200	Weak transcription	K562	blood
3	chr6:34669400-34670200	Enhancers	HepG2	liver
4	chr6:34670200-34672400	Weak transcription	HepG2	liver
5	chr6:34671600-34671800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:34671600-34671800	Enhancers	A549	lung
7	chr6:34671600-34672400	Enhancers	Fetal Muscle Leg	muscle
8	chr6:34671600-34672800	Enhancers	Fetal Heart	heart
9	chr6:34671800-34673000	Weak transcription	A549	lung
10	chr6:34672000-34672200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr6:34672000-34672200	Weak transcription	Ovary	ovary
12	chr6:34672200-34672400	Enhancers	Ovary	ovary
13	chr6:34672200-34672800	Enhancers	Fetal Muscle Trunk	muscle
14	chr6:34672200-34673200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr6:34672200-34673400	Enhancers	Stomach Mucosa	stomach
16	chr6:34672200-34673600	Enhancers	K562	blood
17	chr6:34672400-34673600	Enhancers	Hela-S3	cervix
18	chr6:34672400-34673600	Enhancers	HepG2	liver
19	chr6:34672400-34676400	Weak transcription	Fetal Muscle Leg	muscle
20	chr6:34672400-34676800	Weak transcription	Ovary	ovary
21	chr6:34672800-34673200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:34672800-34673200	Weak transcription	Fetal Heart	heart
23	chr6:34672800-34673600	Enhancers	HUVEC	blood vessel
24	chr6:34672800-34676400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr6:34673000-34673400	Enhancers	A549	lung
26	chr6:34673000-34673600	Enhancers	Osteobl	bone
27	chr6:34673200-34673400	Enhancers	Fetal Heart	heart
28	chr6:34673200-34676400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr6:34673400-34673600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:34673400-34676400	Weak transcription	Fetal Heart	heart
31	chr6:34673400-34676600	Weak transcription	Stomach Mucosa	stomach
32	chr6:34673600-34677200	Weak transcription	K562	blood
33	chr6:34673600-34677200	Weak transcription	Osteobl	bone
34	chr6:34674000-34676800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr6:34676200-34678000	Enhancers	Brain Cingulate Gyrus	brain
36	chr6:34676400-34677600	Enhancers	Fetal Heart	heart
37	chr6:34676400-34677800	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr6:34676400-34677800	Enhancers	Fetal Muscle Trunk	muscle
39	chr6:34676400-34677800	Enhancers	Pancreas	Pancrea
40	chr6:34676400-34678000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:34676400-34678200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr6:34676400-34678200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr6:34676400-34678400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:34676400-34678400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr6:34676400-34678400	Enhancers	Fetal Muscle Leg	muscle
46	chr6:34676600-34676800	Enhancers	Stomach Mucosa	stomach
47	chr6:34676600-34676800	Enhancers	HSMMtube	muscle
48	chr6:34676800-34677200	Weak transcription	Stomach Mucosa	stomach
49	chr6:34676800-34677400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:34676800-34677600	Enhancers	Left Ventricle	heart

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