Variant report

Variant	nsv464027
Chromosome Location	chr6:118768150-118856822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:560)
CpG islands
(count:367)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:560 , 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	chr6:118823438-118823630	K562	blood:	n/a	n/a
2	ARID3A	chr6:118827198-118827857	K562	blood:	n/a	n/a
3	ARID3A	chr6:118830184-118830599	K562	blood:	n/a	n/a
4	ARID3A	chr6:118789925-118790949	HepG2	liver:	n/a	n/a
5	ATF2	chr6:118844367-118844780	GM12878	blood:	n/a	n/a
6	ATF2	chr6:118788378-118788709	GM12878	blood:	n/a	n/a
7	ATF3	chr6:118790642-118790921	K562	blood:	n/a	n/a
8	ATF3	chr6:118827141-118827527	K562	blood:	n/a	n/a
9	BATF	chr6:118844430-118844743	GM12878	blood:	n/a	n/a
10	BATF	chr6:118806735-118807083	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
11	BATF	chr6:118806716-118807107	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
12	BATF	chr6:118844451-118844653	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:118790184-118790852	HepG2	liver:	n/a	n/a
14	BHLHE40	chr6:118826979-118827557	K562	blood:	n/a	n/a
15	BHLHE40	chr6:118806741-118807388	GM12878	blood:	n/a	n/a
16	CBX3	chr6:118809874-118810172	HCT-116	colon:	n/a	n/a
17	CBX3	chr6:118852098-118852469	HCT-116	colon:	n/a	n/a
18	CBX3	chr6:118809864-118810120	K562	blood:	n/a	n/a
19	CBX3	chr6:118809816-118810159	K562	blood:	n/a	n/a
20	CBX3	chr6:118816720-118817275	HCT-116	colon:	n/a	n/a
21	CBX3	chr6:118852090-118852382	K562	blood:	n/a	n/a
22	CCNT2	chr6:118827176-118827545	K562	blood:	n/a	n/a
23	CEBPB	chr6:118790697-118790886	H1-hESC	embryonic stem cell:	n/a	chr6:118790816-118790827
24	CEBPB	chr6:118790707-118791048	A549	lung:	n/a	chr6:118790816-118790827
25	CEBPB	chr6:118807335-118807706	HepG2	liver:	n/a	chr6:118807509-118807520
26	CEBPB	chr6:118826803-118827596	K562	blood:	n/a	chr6:118827005-118827016
27	CEBPB	chr6:118807292-118807772	A549	lung:	n/a	chr6:118807509-118807520
28	CEBPB	chr6:118821758-118822117	HepG2	liver:	n/a	chr6:118821931-118821942
29	CEBPB	chr6:118790676-118791047	MCF-7	breast:	n/a	chr6:118790816-118790827
30	CEBPB	chr6:118790635-118790939	K562	blood:	n/a	chr6:118790816-118790827
31	CEBPB	chr6:118826819-118827546	K562	blood:	n/a	chr6:118827005-118827016
32	CEBPB	chr6:118821757-118822090	IMR90	lung:	n/a	chr6:118821931-118821942
33	CEBPB	chr6:118826847-118827174	HepG2	liver:	n/a	chr6:118827005-118827016
34	CEBPB	chr6:118807337-118807680	Hela-S3	cervix:	n/a	chr6:118807509-118807520
35	CEBPB	chr6:118850928-118851297	IMR90	lung:	n/a	chr6:118851113-118851124 chr6:118851111-118851124 chr6:118851111-118851122
36	CEBPB	chr6:118790618-118791031	A549	lung:	n/a	chr6:118790816-118790827
37	CEBPB	chr6:118821820-118822060	MCF-7	breast:	n/a	chr6:118821931-118821942
38	CEBPB	chr6:118816816-118817405	HCT-116	colon:	n/a	n/a
39	CEBPB	chr6:118790252-118791015	HepG2	liver:	n/a	chr6:118790816-118790827
40	CEBPB	chr6:118851061-118851260	H1-hESC	embryonic stem cell:	n/a	chr6:118851113-118851124 chr6:118851111-118851124 chr6:118851111-118851122
41	CEBPB	chr6:118816873-118817089	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:118850957-118851173	A549	lung:	n/a	chr6:118851113-118851124 chr6:118851111-118851124 chr6:118851111-118851122
43	CEBPB	chr6:118807394-118807584	K562	blood:	n/a	chr6:118807509-118807520
44	CEBPB	chr6:118850942-118851291	HepG2	liver:	n/a	chr6:118851113-118851124 chr6:118851111-118851124 chr6:118851111-118851122
45	CEBPB	chr6:118829330-118829611	K562	blood:	n/a	n/a
46	CEBPB	chr6:118807337-118807684	K562	blood:	n/a	chr6:118807509-118807520
47	CEBPB	chr6:118807323-118807703	IMR90	lung:	n/a	chr6:118807509-118807520
48	CEBPB	chr6:118816703-118817336	HCT-116	colon:	n/a	n/a
49	CEBPB	chr6:118823417-118823791	K562	blood:	n/a	n/a
50	CEBPB	chr6:118807313-118807756	MCF-7	breast:	n/a	chr6:118807509-118807520

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:118821449-118821499	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:118821449-118821499	HPAEpiC	pulmonary alveolar:	n/a
3	chr6:118823964-118824014	MCF-7	breast:	n/a
4	chr6:118822466-118822516	SK-N-SH	brain:	n/a
5	chr6:118822505-118822555	Jurkat	blood:	n/a
6	chr6:118822505-118822555	HL-60	blood:	n/a
7	chr6:118822505-118822555	HNPCEpiC	eye:	n/a
8	chr6:118823964-118824014	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:118821449-118821499	HAEpiC	amniotic membrane:	n/a
10	chr6:118776527-118776577	GM12891	blood:	n/a
11	chr6:118822131-118822181	AG04450	lung:	fetal
12	chr6:118822505-118822555	HCF	heart:	n/a
13	chr6:118822466-118822516	Jurkat	blood:	n/a
14	chr6:118822505-118822555	AoSMC	blood vessel:	n/a
15	chr6:118822466-118822516	HCPEpiC	choroid plexus:	n/a
16	chr6:118776527-118776577	Caco-2	colon:	n/a
17	chr6:118822131-118822181	NB4	blood:	n/a
18	chr6:118822466-118822516	HAEpiC	amniotic membrane:	n/a
19	chr6:118776527-118776577	GM19239	blood:	n/a
20	chr6:118822505-118822555	NHBE	bronchial:	n/a
21	chr6:118822505-118822555	HCPEpiC	choroid plexus:	n/a
22	chr6:118776527-118776577	HEK293	kidney:	embryo
23	chr6:118776527-118776577	IMR90	lung:	fetal
24	chr6:118822505-118822555	NT2-D1	testis:	n/a
25	chr6:118822131-118822181	T-47D	breast:	n/a
26	chr6:118822466-118822516	Caco-2	colon:	n/a
27	chr6:118822131-118822181	SK-N-SH_RA	brain:	n/a
28	chr6:118821449-118821499	GM12892	blood:	n/a
29	chr6:118822466-118822516	GM12891	blood:	n/a
30	chr6:118822505-118822555	A549	lung:	n/a
31	chr6:118821449-118821499	NT2-D1	testis:	n/a
32	chr6:118823964-118824014	HCT-116	colon:	n/a
33	chr6:118821449-118821499	MCF10A-Er-Src	breast:	n/a
34	chr6:118821449-118821499	AG04449	skin:	fetal
35	chr6:118821449-118821499	PFSK-1	brain:	n/a
36	chr6:118822466-118822516	NHDF-neo	bronchial:	n/a
37	chr6:118821449-118821499	ECC-1	luminal epithelium:	n/a
38	chr6:118776527-118776577	PANC-1	pancreas:	n/a
39	chr6:118823964-118824014	HNPCEpiC	eye:	n/a
40	chr6:118822505-118822555	HCM	heart:	n/a
41	chr6:118822466-118822516	A549	lung:	n/a
42	chr6:118822131-118822181	NH-A	brain:	n/a
43	chr6:118822466-118822516	K562	blood:	n/a
44	chr6:118822131-118822181	NHDF-neo	bronchial:	n/a
45	chr6:118822131-118822181	BJ	skin:	n/a
46	chr6:118822466-118822516	HRCEpiC	kidney:	n/a
47	chr6:118823964-118824014	SAEC	small airway:	n/a
48	chr6:118823964-118824014	Caco-2	colon:	n/a
49	chr6:118822131-118822181	NT2-D1	testis:	n/a
50	chr6:118821449-118821499	SK-N-SH_RA	brain:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:118807810..118810020-chr6:118811825..118813344,2	K562	blood:
2	chr6:118604757..118606576-chr6:118829465..118831114,11	MCF-7	breast:
3	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
4	chr6:118826989..118829311-chr6:118938215..118940660,2	K562	blood:
5	chr6:118790912..118793638-chr6:118795834..118798403,2	K562	blood:
6	chr6:118824560..118826306-chr6:118830401..118832913,2	K562	blood:
7	chr6:118604657..118606544-chr6:118829791..118831020,17	MCF-7	breast:
8	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
9	chr6:118845234..118848026-chr6:118887537..118889460,2	K562	blood:
10	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
11	chr6:118830553..118833464-chr6:118833711..118836187,2	K562	blood:
12	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
13	chr6:118829900..118830527-chr6:118872009..118872536,2	MCF-7	breast:
14	chr6:118807810..118810020-chr6:118811825..118813344,2	K562	blood:
15	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
16	chr6:118840065..118842365-chr6:118844866..118846753,2	K562	blood:
17	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
18	chr6:118807029..118809570-chr6:118811844..118815669,3	K562	blood:
19	chr6:118836380..118838045-chr6:118841416..118842970,2	K562	blood:
20	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
21	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
22	chr6:118790912..118793638-chr6:118795834..118798403,2	K562	blood:
23	chr6:118766414..118769352-chr6:118774128..118777684,3	K562	blood:
24	chr6:118829745..118830555-chr6:118939535..118940562,3	MCF-7	breast:
25	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
26	chr6:118840065..118842365-chr6:118844866..118846753,2	K562	blood:
27	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
28	chr6:118605631..118606342-chr6:118829971..118830837,2	K562	blood:
29	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
30	chr6:118836380..118838045-chr6:118841416..118842970,2	K562	blood:
31	chr6:118824560..118826306-chr6:118830401..118832913,2	K562	blood:
32	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
33	chr6:118830553..118833464-chr6:118833711..118836187,2	K562	blood:
34	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
35	chr6:118729437..118730312-chr6:118828228..118829001,2	MCF-7	breast:
36	chr6:118807029..118809570-chr6:118811844..118815669,3	K562	blood:
37	chr6:118829899..118830781-chr6:118901492..118902427,2	MCF-7	breast:
38	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
39	chr6:118630135..118632500-chr6:118803686..118805267,2	K562	blood:
40	chr6:118830553..118833373-chr6:118834538..118836187,2	K562	blood:
41	chr6:118830553..118833373-chr6:118834538..118836187,2	K562	blood:
42	chr6:118827080..118828715-chr6:118830473..118832709,2	K562	blood:
43	chr6:118839207..118841504-chr6:119214917..119216766,2	MCF-7	breast:
44	chr6:118827080..118828715-chr6:118830473..118832709,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLN-1	chr6:118822536-118824996	NR_002730
2	lnc-PLN-2	chr6:118772307-118773627	NONHSAT114692

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C6orf204	hsa-miR-335-5p	chr6:118812647-118812669

Variant related genes	Relation type
ENSG00000216809	TF binding region
BRD7P3	TF binding region
ENSG00000216809	CpG island
BRD7P3	CpG island
ENSG00000216809	chromatin interactions
ENSG00000111875	chromatin interactions
ENSG00000111877	chromatin interactions

Extended variants
information (count: 3326 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3326 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6919887	chr6:118768150-118768151	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536556355	chr6:118768172-118768173	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371820794	chr6:118768229-118768230	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548533764	chr6:118768233-118768234	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150051145	chr6:118768237-118768238	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117838551	chr6:118768277-118768278	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554664768	chr6:118768280-118768281	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185886033	chr6:118768293-118768294	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533705233	chr6:118768326-118768327	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs554019806	chr6:118768342-118768343	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544085845	chr6:118768365-118768366	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201213689	chr6:118768379-118768380	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs75090538	chr6:118768380-118768381	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189430693	chr6:118768397-118768398	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116749987	chr6:118768411-118768412	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556526648	chr6:118768440-118768441	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs180996503	chr6:118768495-118768496	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545425352	chr6:118768497-118768498	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369142578	chr6:118768558-118768559	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12201919	chr6:118768564-118768565	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs527788440	chr6:118768588-118768589	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541183820	chr6:118768609-118768610	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs117261198	chr6:118768616-118768617	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574419151	chr6:118768651-118768652	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185232801	chr6:118768672-118768673	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs62424170	chr6:118768766-118768767	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550037410	chr6:118768775-118768776	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190338297	chr6:118768848-118768849	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531206621	chr6:118768970-118768971	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181143715	chr6:118768978-118768979	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201284670	chr6:118768988-118768989	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs199681508	chr6:118768989-118768990	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200893747	chr6:118768992-118768993	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34081871	chr6:118768993-118768994	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571217270	chr6:118768994-118768995	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533888400	chr6:118768995-118768996	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs397707766	chr6:118769003-118769004	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372465856	chr6:118769004-118769005	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553981343	chr6:118769005-118769006	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574506628	chr6:118769007-118769008	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369157144	chr6:118769043-118769044	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543231852	chr6:118769051-118769052	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs62424171	chr6:118769058-118769059	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs553585732	chr6:118769060-118769061	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560139026	chr6:118769079-118769080	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs536408176	chr6:118769123-118769124	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573617458	chr6:118769181-118769182	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186789999	chr6:118769194-118769195	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs145374178	chr6:118769198-118769199	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191637593	chr6:118769210-118769211	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD

Chromatin state (count:1509 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118763000-118770600	Weak transcription	HSMM	muscle
2	chr6:118763600-118772600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr6:118763800-118770200	Weak transcription	Brain Substantia Nigra	brain
4	chr6:118764800-118772000	Weak transcription	Ovary	ovary
5	chr6:118765400-118769200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:118765600-118769000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:118766600-118769600	Weak transcription	Gastric	stomach
8	chr6:118766600-118771800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:118766800-118769400	ZNF genes & repeats	Primary T cells from cord blood	blood
10	chr6:118767000-118771600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:118767400-118771200	Weak transcription	Left Ventricle	heart
12	chr6:118768000-118768600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:118768800-118769200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr6:118769000-118771200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:118769400-118769800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr6:118772600-118774000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:118773200-118775000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:118773400-118776200	ZNF genes & repeats	Adipose Nuclei	Adipose
19	chr6:118774400-118808600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr6:118775000-118779600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:118775600-118784600	Weak transcription	HSMM	muscle
22	chr6:118776000-118792400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr6:118776200-118786000	Weak transcription	Adipose Nuclei	Adipose
24	chr6:118776600-118785800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr6:118776800-118808800	Weak transcription	Fetal Stomach	stomach
26	chr6:118777000-118780000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:118777400-118786400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:118777600-118777800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
29	chr6:118777600-118790800	Weak transcription	Pancreas	Pancrea
30	chr6:118777800-118778200	Enhancers	Fetal Heart	heart
31	chr6:118777800-118788000	Weak transcription	HMEC	breast
32	chr6:118777800-118791000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr6:118778000-118784800	Weak transcription	Osteobl	bone
34	chr6:118778000-118785000	Weak transcription	Primary T cells from cord blood	blood
35	chr6:118778200-118778600	Flanking Active TSS	Fetal Heart	heart
36	chr6:118778200-118781400	Weak transcription	Fetal Muscle Leg	muscle
37	chr6:118778200-118786000	Weak transcription	Fetal Muscle Trunk	muscle
38	chr6:118778400-118778600	Enhancers	Brain Substantia Nigra	brain
39	chr6:118778400-118784600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:118778600-118778800	Enhancers	Fetal Heart	heart
41	chr6:118778600-118790200	Weak transcription	Stomach Mucosa	stomach
42	chr6:118778800-118781400	Weak transcription	Fetal Heart	heart
43	chr6:118778800-118784600	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr6:118778800-118785600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr6:118779000-118781400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:118779000-118781600	Weak transcription	Dnd41	blood
47	chr6:118779400-118780200	Enhancers	HepG2	liver
48	chr6:118779400-118784600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr6:118779400-118785000	Weak transcription	Primary hematopoietic stem cells	blood
50	chr6:118779400-118785800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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