Variant report

Variant	esv3355640
Chromosome Location	chr6:36163199-36165747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:748)
CpG islands
(count:550)
Chromatin interactive
region (count:19)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:36164105-36164309	HepG2	liver:	n/a	n/a
2	ATF1	chr6:36164985-36165311	K562	blood:	n/a	n/a
3	ATF2	chr6:36164947-36165401	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:36164093-36164353	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr6:36164638-36165025	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:36163899-36164515	GM12878	blood:	n/a	chr6:36164234-36164243 chr6:36164197-36164210
7	BHLHE40	chr6:36163798-36164592	HepG2	liver:	n/a	chr6:36164526-36164542 chr6:36164517-36164533
8	BHLHE40	chr6:36163962-36164447	K562	blood:	n/a	n/a
9	BHLHE40	chr6:36164020-36164481	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:36164860-36165317	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:36164860-36165309	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:36165110-36165303	K562	blood:	n/a	n/a
13	BRCA1	chr6:36164116-36164643	HepG2	liver:	n/a	n/a
14	BRCA1	chr6:36163915-36164463	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr6:36165038-36165249	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:36164999-36165325	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr6:36163726-36164276	K562	blood:	n/a	n/a
18	CBX3	chr6:36164788-36165386	K562	blood:	n/a	n/a
19	CBX3	chr6:36165425-36165866	K562	blood:	n/a	n/a
20	CCNT2	chr6:36163950-36165235	K562	blood:	n/a	chr6:36165007-36165016 chr6:36165206-36165215
21	CEBPB	chr6:36165734-36165779	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPD	chr6:36163930-36165300	K562	blood:	n/a	n/a
23	CEBPD	chr6:36163684-36165216	HepG2	liver:	n/a	n/a
24	CEBPD	chr6:36164187-36164807	HepG2	liver:	n/a	n/a
25	CHD1	chr6:36165036-36165279	GM12878	blood:	n/a	n/a
26	CHD1	chr6:36164276-36164397	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr6:36164585-36164762	GM12878	blood:	n/a	n/a
28	CHD1	chr6:36163975-36164306	GM12878	blood:	n/a	n/a
29	CHD2	chr6:36163840-36164499	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:36164086-36165314	K562	blood:	n/a	n/a
31	CHD2	chr6:36164870-36165285	GM12878	blood:	n/a	n/a
32	CHD2	chr6:36164880-36165299	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr6:36164848-36165223	HepG2	liver:	n/a	n/a
34	CHD2	chr6:36163786-36164536	HepG2	liver:	n/a	n/a
35	CHD2	chr6:36165565-36165659	GM12878	blood:	n/a	n/a
36	CHD2	chr6:36164030-36165338	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr6:36163750-36164382	GM12878	blood:	n/a	n/a
38	CREB1	chr6:36164888-36165351	ECC-1	luminal epithelium:	n/a	n/a
39	CREB1	chr6:36164822-36165401	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr6:36164813-36165335	A549	lung:	n/a	n/a
41	CREB1	chr6:36164812-36165428	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr6:36164985-36165440	ECC-1	luminal epithelium:	n/a	n/a
43	CREB1	chr6:36164011-36164461	A549	lung:	n/a	chr6:36164052-36164065
44	CREB1	chr6:36163586-36165456	HepG2	liver:	n/a	chr6:36164052-36164065
45	CREB1	chr6:36164785-36165346	GM12878	blood:	n/a	n/a
46	CREB1	chr6:36165000-36165314	A549	lung:	n/a	n/a
47	CTCF	chr6:36164140-36164290	HCPEpiC	choroid plexus:	n/a	chr6:36164246-36164264
48	CTCF	chr6:36164200-36164350	HCT-116	colon:	n/a	chr6:36164246-36164264
49	CTCF	chr6:36164108-36164400	NHEK	skin:	n/a	chr6:36164246-36164264
50	CTCF	chr6:36164143-36164400	GM10248	blood:	n/a	chr6:36164246-36164264

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:36164058-36164108	H1-hESC	embryonic stem cell:	embryo
2	chr6:36164058-36164108	H1-hESC	embryonic stem cell:	embryo
3	chr6:36165121-36165171	U87	brain:	n/a
4	chr6:36165617-36165667	HNPCEpiC	eye:	n/a
5	chr6:36165382-36165432	A549	lung:	n/a
6	chr6:36164058-36164108	PrEC	prostate:	n/a
7	chr6:36165204-36165254	AG09319	gingival:	n/a
8	chr6:36164803-36164853	PrEC	prostate:	n/a
9	chr6:36164655-36164705	T-47D	breast:	n/a
10	chr6:36164803-36164853	H1-hESC	embryonic stem cell:	embryo
11	chr6:36164024-36164074	NHDF-neo	bronchial:	n/a
12	chr6:36165121-36165171	Hela-S3	cervix:	n/a
13	chr6:36165121-36165171	HepG2	liver:	n/a
14	chr6:36164058-36164108	AG09319	gingival:	n/a
15	chr6:36164655-36164705	Hela-S3	cervix:	n/a
16	chr6:36165204-36165254	BE2_C	brain:	n/a
17	chr6:36164655-36164705	NB4	blood:	n/a
18	chr6:36165121-36165171	NT2-D1	testis:	n/a
19	chr6:36164803-36164853	GM12878	blood:	n/a
20	chr6:36164024-36164074	HepG2	liver:	n/a
21	chr6:36164803-36164853	SAEC	small airway:	n/a
22	chr6:36165204-36165254	HNPCEpiC	eye:	n/a
23	chr6:36165121-36165171	HL-60	blood:	n/a
24	chr6:36164058-36164108	SKMC	muscle:	n/a
25	chr6:36165617-36165667	ovcar-3	ovarian:	n/a
26	chr6:36164024-36164074	BJ	skin:	n/a
27	chr6:36165617-36165667	A549	lung:	n/a
28	chr6:36164655-36164705	GM06990	blood:	n/a
29	chr6:36164058-36164108	HMEC	breast:	n/a
30	chr6:36165617-36165667	GM12878	blood:	n/a
31	chr6:36165617-36165667	HUVEC	blood vessel:	n/a
32	chr6:36165617-36165667	NHBE	bronchial:	n/a
33	chr6:36165617-36165667	RPTEC	kidney:	n/a
34	chr6:36165204-36165254	U87	brain:	n/a
35	chr6:36165204-36165254	HepG2	liver:	n/a
36	chr6:36165204-36165254	NHDF-neo	bronchial:	n/a
37	chr6:36165635-36165685	PANC-1	pancreas:	n/a
38	chr6:36164024-36164074	HCT-116	colon:	n/a
39	chr6:36164058-36164108	T-47D	breast:	n/a
40	chr6:36165382-36165432	U87	brain:	n/a
41	chr6:36164058-36164108	HRE	kidney:	n/a
42	chr6:36165617-36165667	GM12891	blood:	n/a
43	chr6:36165121-36165171	PANC-1	pancreas:	n/a
44	chr6:36164803-36164853	BE2_C	brain:	n/a
45	chr6:36165382-36165432	ECC-1	luminal epithelium:	n/a
46	chr6:36165617-36165667	BE2_C	brain:	n/a
47	chr6:36165635-36165685	IMR90	lung:	fetal
48	chr6:36165382-36165432	HUVEC	blood vessel:	n/a
49	chr6:36164655-36164705	ECC-1	luminal epithelium:	n/a
50	chr6:36165204-36165254	GM06990	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36097129..36099054-chr6:36162391..36164603,2	K562	blood:
2	chr6:36089979..36090632-chr6:36163721..36164348,2	MCF-7	breast:
3	chr6:36093292..36096677-chr6:36162699..36165787,6	K562	blood:
4	chr6:35993989..35997402-chr6:36163188..36166883,8	MCF-7	breast:
5	chr6:35992707..35998254-chr6:36162958..36166458,7	K562	blood:
6	chr6:36133204..36136174-chr6:36161325..36163724,2	K562	blood:
7	chr6:35993265..35998448-chr6:36161633..36166981,11	K562	blood:
8	chr6:36096617..36099142-chr6:36162886..36164936,2	MCF-7	breast:
9	chr6:36164615..36166150-chr6:36409127..36410666,2	K562	blood:
10	chr6:36164534..36167237-chr6:36236407..36238243,2	MCF-7	breast:
11	chr11:82996519..82997293-chr6:36164993..36165533,2	Hela-S3	cervix:
12	chr15:75660425..75661076-chr6:36164710..36165398,2	HCT-116	colon:
13	chr6:36152501..36154693-chr6:36162205..36164087,2	MCF-7	breast:
14	chr6:36105269..36110195-chr6:36162724..36166768,9	MCF-7	breast:
15	chr6:36083240..36096353-chr6:36161490..36168411,30	MCF-7	breast:
16	chr16:68271616..68273577-chr6:36163527..36165172,2	MCF-7	breast:
17	chr6:36098131..36102554-chr6:36163258..36166179,4	K562	blood:
18	chr6:36097672..36103046-chr6:36163327..36166048,5	MCF-7	breast:
19	chr6:35994949..35995828-chr6:36163769..36164278,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf222-1	chr6:36163814-36163947	ENSG00000246982
2	lnc-C6orf222-1	chr6:36164852-36164980	ENSG00000246982
3	lnc-C6orf222-1	chr6:36163814-36164288	NONHSAT112212
4	lnc-C6orf222-1	chr6:36163814-36163947	ENSG00000246982
5	lnc-C6orf222-1	chr6:36164852-36164982	ENSG00000246982

No data

Variant related genes	Relation type
ENSG00000246982	TF binding region
BRPF3	TF binding region
ENSG00000246982	CpG island
BRPF3	CpG island
ENSG00000221743	chromatin interactions
ENSG00000112078	chromatin interactions
ENSG00000156711	chromatin interactions
ENSG00000103067	chromatin interactions
ENSG00000112062	chromatin interactions
ENSG00000260274	chromatin interactions
ENSG00000137500	chromatin interactions
ENSG00000180316	chromatin interactions
ENSG00000140400	chromatin interactions
ENSG00000255234	chromatin interactions
TSPAN33	miRNA target sites
ERLIN1	miRNA target sites

Extended variants
information (count: 80 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138646107	chr6:36163232-36163233	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs550402598	chr6:36163261-36163262	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs571856255	chr6:36163284-36163285	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs377708116	chr6:36163287-36163288	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs539379491	chr6:36163389-36163390	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs554401813	chr6:36163396-36163397	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs370453593	chr6:36163490-36163491	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs566303273	chr6:36163510-36163511	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs74693149	chr6:36163543-36163544	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs189877495	chr6:36163601-36163602	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs373038582	chr6:36163612-36163613	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs554777914	chr6:36163636-36163637	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs576341213	chr6:36163674-36163675	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs182403939	chr6:36163707-36163708	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs573313231	chr6:36163727-36163728	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs111587260	chr6:36163764-36163765	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs142875258	chr6:36163782-36163783	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs28713246	chr6:36163853-36163854	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs558951924	chr6:36163856-36163857	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs576724423	chr6:36163908-36163909	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs376529131	chr6:36163914-36163915	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs185398800	chr6:36163930-36163931	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs9470228	chr6:36163941-36163942	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs76696370	chr6:36163943-36163944	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs541496489	chr6:36163945-36163946	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs113046152	chr6:36163994-36163995	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs368239533	chr6:36164031-36164032	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs115707874	chr6:36164055-36164056	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs59752650	chr6:36164068-36164069	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs149313448	chr6:36164071-36164072	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs9470229	chr6:36164092-36164093	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs144890112	chr6:36164113-36164114	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs373371454	chr6:36164118-36164119	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs539534043	chr6:36164123-36164124	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs117054385	chr6:36164155-36164156	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs566240162	chr6:36164159-36164160	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs536856201	chr6:36164256-36164257	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs555010622	chr6:36164282-36164283	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs570046289	chr6:36164349-36164350	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs537600306	chr6:36164402-36164403	Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs558660360	chr6:36164493-36164494	Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs576861710	chr6:36164620-36164621	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs540893408	chr6:36164686-36164687	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs552871656	chr6:36164707-36164708	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs574246712	chr6:36164873-36164874	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
46	rs541667273	chr6:36164891-36164892	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
47	rs36093387	chr6:36164907-36164908	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
48	rs563538730	chr6:36164927-36164928	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
49	rs188342388	chr6:36164928-36164929	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
50	rs545910339	chr6:36164938-36164939	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Lung cancer	19153074	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36146000-36163400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr6:36149000-36163600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr6:36152600-36163600	Weak transcription	Brain Angular Gyrus	brain
4	chr6:36155600-36163400	Weak transcription	Primary T cells from cord blood	blood
5	chr6:36155600-36163400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:36155800-36163600	Weak transcription	Psoas Muscle	Psoas
7	chr6:36156000-36163400	Weak transcription	Fetal Intestine Small	intestine
8	chr6:36157600-36163800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:36158600-36163400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr6:36159400-36163400	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr6:36159800-36163200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr6:36160200-36163400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr6:36160200-36163600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:36162600-36163400	Weak transcription	HUVEC	blood vessel
15	chr6:36162800-36163200	Enhancers	HepG2	liver
16	chr6:36163000-36163200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr6:36163000-36163400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:36163000-36163400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr6:36163000-36163400	Enhancers	Dnd41	blood
20	chr6:36163000-36163600	Enhancers	Primary B cells from cord blood	blood
21	chr6:36163000-36163600	Enhancers	Fetal Thymus	thymus
22	chr6:36163000-36163800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:36163000-36165800	Active TSS	H9 Cell Line	embryonic stem cell
24	chr6:36163200-36163400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr6:36163200-36163400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:36163200-36163400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:36163200-36163400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr6:36163200-36163400	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr6:36163200-36163400	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr6:36163200-36163400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr6:36163200-36163400	Enhancers	Liver	Liver
32	chr6:36163200-36163400	Enhancers	Brain Cingulate Gyrus	brain
33	chr6:36163200-36163400	Enhancers	Duodenum Mucosa	Duodenum
34	chr6:36163200-36163400	Enhancers	Fetal Kidney	kidney
35	chr6:36163200-36163400	Flanking Active TSS	HepG2	liver
36	chr6:36163200-36163600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr6:36163200-36163600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr6:36163200-36163600	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr6:36163200-36163600	Enhancers	K562	blood
40	chr6:36163200-36163800	Enhancers	Primary hematopoietic stem cells	blood
41	chr6:36163200-36163800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:36163200-36163800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr6:36163200-36163800	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr6:36163200-36165800	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr6:36163200-36166200	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr6:36163400-36163600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr6:36163400-36163600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr6:36163400-36163600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:36163400-36163600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:36163400-36163600	Enhancers	Primary neutrophils fromperipheralblood	blood

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