Variant report

Variant	nsv1021859
Chromosome Location	chr6:34515436-34535289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:610)
Chromatin interactive
region (count:56)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34530717-34531006	K562	blood:	n/a	n/a
2	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
3	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:34535143-34535361	HepG2	liver:	n/a	n/a
5	ATF1	chr6:34530640-34531020	K562	blood:	n/a	n/a
6	ATF1	chr6:34528256-34528770	K562	blood:	n/a	n/a
7	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
8	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
9	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
10	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:34531305-34531454	K562	blood:	n/a	n/a
12	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
13	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
14	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
15	BHLHE40	chr6:34530292-34531071	K562	blood:	n/a	n/a
16	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a
17	BRCA1	chr6:34528656-34528787	HepG2	liver:	n/a	n/a
18	BRCA1	chr6:34534813-34534889	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr6:34528383-34528433	HepG2	liver:	n/a	n/a
20	CBX3	chr6:34528147-34529296	K562	blood:	n/a	n/a
21	CBX3	chr6:34525771-34526610	K562	blood:	n/a	n/a
22	CBX3	chr6:34529829-34530430	K562	blood:	n/a	n/a
23	CBX3	chr6:34525886-34526725	K562	blood:	n/a	n/a
24	CBX3	chr6:34530537-34531593	K562	blood:	n/a	n/a
25	CBX3	chr6:34528238-34529132	K562	blood:	n/a	n/a
26	CBX3	chr6:34524227-34524720	K562	blood:	n/a	n/a
27	CCNT2	chr6:34528207-34528986	K562	blood:	n/a	chr6:34528756-34528765
28	CCNT2	chr6:34530372-34531113	K562	blood:	n/a	n/a
29	CCNT2	chr6:34524999-34525293	K562	blood:	n/a	n/a
30	CCNT2	chr6:34519480-34519561	K562	blood:	n/a	n/a
31	CEBPB	chr6:34528245-34528702	K562	blood:	n/a	n/a
32	CEBPB	chr6:34529800-34530094	K562	blood:	n/a	chr6:34529885-34529898
33	CEBPB	chr6:34530630-34530986	K562	blood:	n/a	n/a
34	CEBPB	chr6:34528488-34528675	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:34530449-34530954	K562	blood:	n/a	n/a
36	CEBPD	chr6:34530475-34531224	K562	blood:	n/a	n/a
37	CEBPD	chr6:34530475-34531566	K562	blood:	n/a	n/a
38	CEBPD	chr6:34524892-34525479	K562	blood:	n/a	n/a
39	CEBPD	chr6:34524939-34525496	K562	blood:	n/a	n/a
40	CEBPD	chr6:34528208-34528720	K562	blood:	n/a	n/a
41	CHD2	chr6:34528783-34528794	HepG2	liver:	n/a	n/a
42	CHD2	chr6:34530625-34530936	K562	blood:	n/a	n/a
43	CHD2	chr6:34524902-34525076	K562	blood:	n/a	n/a
44	CHD2	chr6:34534835-34534865	HepG2	liver:	n/a	n/a
45	CHD2	chr6:34528258-34528859	K562	blood:	n/a	n/a
46	CREB1	chr6:34530413-34531126	K562	blood:	n/a	n/a
47	CTCF	chr6:34528327-34529018	K562	blood:	n/a	chr6:34528811-34528824
48	CTCF	chr6:34528780-34528930	GM12873	blood:	n/a	chr6:34528811-34528824
49	CTCF	chr6:34528660-34528810	HVMF	connective:	n/a	n/a
50	CTCF	chr6:34523800-34523950	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34524698-34524748	HepG2	liver:	n/a
2	chr6:34524597-34524647	AG10803	skin:	n/a
3	chr6:34524597-34524647	AG04449	skin:	fetal
4	chr6:34528827-34528877	PFSK-1	brain:	n/a
5	chr6:34528827-34528877	HEEpiC	esophagus:	n/a
6	chr6:34524766-34524816	H1-hESC	embryonic stem cell:	embryo
7	chr6:34523925-34523975	MCF-7	breast:	n/a
8	chr6:34524278-34524328	SK-N-MC	brain:	n/a
9	chr6:34523925-34523975	U87	brain:	n/a
10	chr6:34524097-34524147	HNPCEpiC	eye:	n/a
11	chr6:34524597-34524647	U87	brain:	n/a
12	chr6:34524095-34524145	HRE	kidney:	n/a
13	chr6:34524278-34524328	ovcar-3	ovarian:	n/a
14	chr6:34524278-34524328	AG09309	skin:	n/a
15	chr6:34523925-34523975	HNPCEpiC	eye:	n/a
16	chr6:34528827-34528877	U87	brain:	n/a
17	chr6:34524097-34524147	SK-N-SH_RA	brain:	n/a
18	chr6:34524698-34524748	SK-N-SH_RA	brain:	n/a
19	chr6:34524698-34524748	NB4	blood:	n/a
20	chr6:34524095-34524145	Hepatocyte	liver:	n/a
21	chr6:34525026-34525076	ovcar-3	ovarian:	n/a
22	chr6:34524290-34524340	NH-A	brain:	n/a
23	chr6:34524290-34524340	HEK293	kidney:	embryo
24	chr6:34523925-34523975	HIPEpiC	eye:	n/a
25	chr6:34524278-34524328	HCT-116	colon:	n/a
26	chr6:34524766-34524816	ProgFib	skin:	n/a
27	chr6:34524698-34524748	A549	lung:	n/a
28	chr6:34524097-34524147	SK-N-SH	brain:	n/a
29	chr6:34523925-34523975	HCPEpiC	choroid plexus:	n/a
30	chr6:34524278-34524328	SKMC	muscle:	n/a
31	chr6:34524698-34524748	ECC-1	luminal epithelium:	n/a
32	chr6:34524278-34524328	SAEC	small airway:	n/a
33	chr6:34524095-34524145	GM12878	blood:	n/a
34	chr6:34524597-34524647	HCF	heart:	n/a
35	chr6:34524290-34524340	GM19239	blood:	n/a
36	chr6:34524097-34524147	IMR90	lung:	fetal
37	chr6:34524097-34524147	T-47D	breast:	n/a
38	chr6:34523925-34523975	ProgFib	skin:	n/a
39	chr6:34524097-34524147	K562	blood:	n/a
40	chr6:34524597-34524647	Caco-2	colon:	n/a
41	chr6:34528827-34528877	AG09309	skin:	n/a
42	chr6:34525026-34525076	SKMC	muscle:	n/a
43	chr6:34524290-34524340	SK-N-SH	brain:	n/a
44	chr6:34525026-34525076	AG04449	skin:	fetal
45	chr6:34524597-34524647	Hepatocyte	liver:	n/a
46	chr6:34524290-34524340	AG04449	skin:	fetal
47	chr6:34524698-34524748	AoSMC	blood vessel:	n/a
48	chr6:34523925-34523975	AG10803	skin:	n/a
49	chr6:34525026-34525076	HUVEC	blood vessel:	n/a
50	chr6:34528827-34528877	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
2	chr6:34514809..34519137-chr6:34522826..34525341,4	K562	blood:
3	chr6:34528906..34533005-chr6:34533870..34536568,4	MCF-7	breast:
4	chr6:34505107..34506692-chr6:34515801..34518168,2	MCF-7	breast:
5	chr6:34427383..34427978-chr6:34528004..34528902,2	MCF-7	breast:
6	chr6:34520436..34525113-chr6:34525166..34530447,6	K562	blood:
7	chr6:34216270..34217861-chr6:34527614..34529829,2	MCF-7	breast:
8	chr6:34535124..34537027-chr6:34540257..34543237,2	K562	blood:
9	chr6:33686485..33689308-chr6:34514444..34516167,2	MCF-7	breast:
10	chr6:34514003..34515621-chr6:34528599..34531450,2	K562	blood:
11	chr6:34531920..34532420-chr9:133836898..133837416,2	Hela-S3	cervix:
12	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
13	chr6:34205000..34207351-chr6:34521778..34524214,3	MCF-7	breast:
14	chr6:34491195..34497458-chr6:34528901..34533837,5	K562	blood:
15	chr6:34527602..34533050-chr6:34533572..34539589,8	K562	blood:
16	chr6:34514736..34516500-chr6:34519380..34521095,2	K562	blood:
17	chr6:34527129..34530623-chr6:34530939..34533511,3	K562	blood:
18	chr6:34511760..34514306-chr6:34515453..34517552,2	K562	blood:
19	chr6:34522438..34524089-chr6:34549801..34552822,3	MCF-7	breast:
20	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
21	chr6:34514095..34516338-chr6:34543578..34545622,2	MCF-7	breast:
22	chr6:34528717..34530463-chr6:34574776..34577421,2	K562	blood:
23	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
24	chr6:34508152..34511012-chr6:34535080..34537020,2	K562	blood:
25	chr6:34535124..34538612-chr6:34540257..34541806,3	K562	blood:
26	chr6:34524749..34526335-chr6:34530684..34532317,2	K562	blood:
27	chr6:34532465..34535112-chr6:34540040..34542974,2	K562	blood:
28	chr6:34503239..34505474-chr6:34519140..34521426,2	MCF-7	breast:
29	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
30	chr6:34496932..34498060-chr6:34528153..34529212,4	MCF-7	breast:
31	chr6:34506980..34511719-chr6:34518115..34520438,4	K562	blood:
32	chr6:34535096..34537769-chr6:34560989..34563955,2	K562	blood:
33	chr6:34481114..34483145-chr6:34525090..34526631,2	K562	blood:
34	chr6:34527129..34530623-chr6:34530939..34533511,3	K562	blood:
35	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
36	chr6:34438209..34440665-chr6:34531080..34532692,2	K562	blood:
37	chr6:34524749..34526335-chr6:34530684..34532317,2	K562	blood:
38	chr20:52484501..52486317-chr6:34526583..34529198,2	MCF-7	breast:
39	chr6:32936553..32938765-chr6:34521756..34523748,2	MCF-7	breast:
40	chr6:34529337..34532289-chr6:34533729..34536883,4	K562	blood:
41	chr6:34527602..34533050-chr6:34533572..34539589,8	K562	blood:
42	chr6:34265209..34267014-chr6:34530646..34533613,2	K562	blood:
43	chr6:34435937..34438924-chr6:34520705..34523320,2	MCF-7	breast:
44	chr6:34529337..34532289-chr6:34533729..34536883,4	K562	blood:
45	chr6:34514003..34515621-chr6:34528599..34531450,2	K562	blood:
46	chr6:34528906..34533005-chr6:34533870..34536568,4	MCF-7	breast:
47	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
48	chr6:34426702..34428652-chr6:34520960..34523550,2	MCF-7	breast:
49	chr6:34518383..34520887-chr6:34564269..34566173,2	MCF-7	breast:
50	chr6:34527129..34529225-chr6:34531595..34533511,2	K562	blood:

No data

Variant related genes	Relation type
SPDEF	TF binding region
SPDEF	CpG island
ENSG00000204256	chromatin interactions
ENSG00000196114	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000124507	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000221635	chromatin interactions

Extended variants
information (count: 811 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556273687	chr6:34515439-34515440	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs571417854	chr6:34515528-34515529	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs79057416	chr6:34515534-34515535	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs374904536	chr6:34515536-34515537	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553803284	chr6:34515578-34515579	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs369149731	chr6:34515585-34515586	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554899471	chr6:34515690-34515691	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs116840405	chr6:34515711-34515712	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs191243898	chr6:34515726-34515727	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs182987946	chr6:34515788-34515789	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs75149985	chr6:34515799-34515800	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs543298762	chr6:34515808-34515809	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562631594	chr6:34515812-34515813	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs557848173	chr6:34515813-34515814	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545840765	chr6:34515834-34515835	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533261254	chr6:34515857-34515858	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544955368	chr6:34515868-34515869	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs560137667	chr6:34515916-34515917	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577697671	chr6:34515932-34515933	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs549638299	chr6:34515944-34515945	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs187657577	chr6:34515974-34515975	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs531933017	chr6:34515985-34515986	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372896268	chr6:34515988-34515989	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs73746683	chr6:34516034-34516035	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs192073084	chr6:34516061-34516062	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538757466	chr6:34516073-34516074	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553766623	chr6:34516145-34516146	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565652518	chr6:34516210-34516211	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs183466273	chr6:34516283-34516284	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2395595	chr6:34516292-34516293	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs3778073	chr6:34516355-34516356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34750257	chr6:34516420-34516421	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113449916	chr6:34516439-34516440	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561201114	chr6:34516450-34516451	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546952494	chr6:34516474-34516475	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4713811	chr6:34516549-34516550	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192354852	chr6:34516585-34516586	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2395596	chr6:34516588-34516589	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs577688084	chr6:34516598-34516599	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545115603	chr6:34516605-34516606	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373394379	chr6:34516609-34516610	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs377550094	chr6:34516615-34516616	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34641105	chr6:34516706-34516707	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560429659	chr6:34516756-34516757	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs527665721	chr6:34516799-34516800	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542704002	chr6:34516847-34516848	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145023881	chr6:34516848-34516849	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531923965	chr6:34516867-34516868	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550366811	chr6:34516877-34516878	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138708116	chr6:34516888-34516889	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34512400-34517600	Enhancers	Duodenum Mucosa	Duodenum
2	chr6:34512600-34516000	Enhancers	Fetal Brain Male	brain
3	chr6:34512600-34522200	Enhancers	Stomach Mucosa	stomach
4	chr6:34512800-34517200	Enhancers	Colonic Mucosa	Colon
5	chr6:34513000-34515800	Enhancers	Lung	lung
6	chr6:34513000-34517200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:34513000-34521400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:34513200-34516000	Enhancers	Fetal Intestine Small	intestine
9	chr6:34513200-34524000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr6:34513600-34515800	Enhancers	Fetal Heart	heart
11	chr6:34513800-34515600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr6:34513800-34515800	Enhancers	Fetal Brain Female	brain
13	chr6:34513800-34520600	Enhancers	Gastric	stomach
14	chr6:34514000-34516000	Enhancers	Fetal Intestine Large	intestine
15	chr6:34514000-34516200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:34514000-34517800	Enhancers	Fetal Muscle Leg	muscle
17	chr6:34514200-34515800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:34514200-34515800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr6:34514200-34516000	Enhancers	Liver	Liver
20	chr6:34514200-34516800	Enhancers	Pancreas	Pancrea
21	chr6:34514400-34515800	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr6:34514600-34521400	Weak transcription	K562	blood
23	chr6:34515000-34516000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr6:34515000-34516000	Flanking Active TSS	A549	lung
25	chr6:34515000-34517800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:34515200-34516200	Bivalent Enhancer	HepG2	liver
27	chr6:34515200-34516600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:34515200-34517000	Weak transcription	Fetal Stomach	stomach
29	chr6:34515200-34517600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr6:34515200-34517800	Weak transcription	Adipose Nuclei	Adipose
31	chr6:34515200-34518000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:34515200-34518600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:34515200-34518800	Weak transcription	Spleen	Spleen
34	chr6:34515200-34520800	Weak transcription	Fetal Lung	lung
35	chr6:34515200-34527600	Weak transcription	Right Atrium	heart
36	chr6:34515400-34515600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
37	chr6:34515600-34516000	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr6:34515800-34516000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:34515800-34516000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr6:34515800-34516200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
41	chr6:34515800-34518600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr6:34516000-34516200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
43	chr6:34516000-34516800	Enhancers	A549	lung
44	chr6:34516000-34519800	Weak transcription	Fetal Intestine Small	intestine
45	chr6:34516000-34520800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr6:34516200-34516400	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr6:34516200-34516800	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr6:34516200-34518000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr6:34516400-34516600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:34516400-34517800	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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