Variant report

Variant	nsv604555
Chromosome Location	chr6:118695049-118856822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:848)
CpG islands
(count:490)
Chromatin interactive
region (count:47)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:848 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:118789925-118790949	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:118823438-118823630	K562	blood:	n/a	n/a
3	ARID3A	chr6:118830184-118830599	K562	blood:	n/a	n/a
4	ARID3A	chr6:118827198-118827857	K562	blood:	n/a	n/a
5	ATF2	chr6:118788378-118788709	GM12878	blood:	n/a	n/a
6	ATF2	chr6:118844367-118844780	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	BACH1	chr6:118708234-118708493	K562	blood:	n/a	n/a
10	BACH1	chr6:118708219-118708390	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:118721836-118722106	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:118721799-118722067	K562	blood:	n/a	n/a
13	BATF	chr6:118806735-118807083	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
14	BATF	chr6:118806716-118807107	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
15	BATF	chr6:118844430-118844743	GM12878	blood:	n/a	n/a
16	BATF	chr6:118844451-118844653	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:118806741-118807388	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:118790184-118790852	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:118826979-118827557	K562	blood:	n/a	n/a
20	CBX3	chr6:118809864-118810120	K562	blood:	n/a	n/a
21	CBX3	chr6:118809874-118810172	HCT-116	colon:	n/a	n/a
22	CBX3	chr6:118816720-118817275	HCT-116	colon:	n/a	n/a
23	CBX3	chr6:118852098-118852469	HCT-116	colon:	n/a	n/a
24	CBX3	chr6:118852090-118852382	K562	blood:	n/a	n/a
25	CBX3	chr6:118809816-118810159	K562	blood:	n/a	n/a
26	CCNT2	chr6:118827176-118827545	K562	blood:	n/a	n/a
27	CEBPB	chr6:118698883-118699570	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:118698892-118699259	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:118698887-118699258	K562	blood:	n/a	n/a
30	CEBPB	chr6:118790676-118791047	MCF-7	breast:	n/a	chr6:118790816-118790827
31	CEBPB	chr6:118807337-118807684	K562	blood:	n/a	chr6:118807509-118807520
32	CEBPB	chr6:118816801-118817338	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:118790618-118791031	A549	lung:	n/a	chr6:118790816-118790827
34	CEBPB	chr6:118737613-118737852	HepG2	liver:	n/a	chr6:118737735-118737746 chr6:118737733-118737744
35	CEBPB	chr6:118698914-118699234	A549	lung:	n/a	n/a
36	CEBPB	chr6:118790231-118790626	MCF-7	breast:	n/a	n/a
37	CEBPB	chr6:118758660-118758932	IMR90	lung:	n/a	chr6:118758789-118758800
38	CEBPB	chr6:118807292-118807772	A549	lung:	n/a	chr6:118807509-118807520
39	CEBPB	chr6:118790642-118790962	K562	blood:	n/a	chr6:118790816-118790827
40	CEBPB	chr6:118821790-118822086	A549	lung:	n/a	chr6:118821931-118821942
41	CEBPB	chr6:118790252-118791015	HepG2	liver:	n/a	chr6:118790816-118790827
42	CEBPB	chr6:118850942-118851291	HepG2	liver:	n/a	chr6:118851113-118851124 chr6:118851111-118851124 chr6:118851111-118851122
43	CEBPB	chr6:118807337-118807680	Hela-S3	cervix:	n/a	chr6:118807509-118807520
44	CEBPB	chr6:118741797-118741903	A549	lung:	n/a	n/a
45	CEBPB	chr6:118698882-118699254	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:118790202-118791017	IMR90	lung:	n/a	chr6:118790816-118790827
47	CEBPB	chr6:118790683-118790953	A549	lung:	n/a	chr6:118790816-118790827
48	CEBPB	chr6:118790309-118791032	HepG2	liver:	n/a	chr6:118790816-118790827
49	CEBPB	chr6:118803319-118803618	HepG2	liver:	n/a	chr6:118803450-118803461 chr6:118803479-118803490
50	CEBPB	chr6:118807323-118807700	H1-hESC	embryonic stem cell:	n/a	chr6:118807509-118807520

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:118822505-118822555	HRCEpiC	kidney:	n/a
2	chr6:118822131-118822181	HEEpiC	esophagus:	n/a
3	chr6:118822505-118822555	HRCEpiC	kidney:	n/a
4	chr6:118822131-118822181	HEEpiC	esophagus:	n/a
5	chr6:118822131-118822181	HL-60	blood:	n/a
6	chr6:118822131-118822181	ECC-1	luminal epithelium:	n/a
7	chr6:118822466-118822516	Jurkat	blood:	n/a
8	chr6:118822466-118822516	U87	brain:	n/a
9	chr6:118823964-118824014	HL-60	blood:	n/a
10	chr6:118709682-118709732	Caco-2	colon:	n/a
11	chr6:118823964-118824014	Hela-S3	cervix:	n/a
12	chr6:118776527-118776577	ECC-1	luminal epithelium:	n/a
13	chr6:118822131-118822181	GM19239	blood:	n/a
14	chr6:118822131-118822181	SKMC	muscle:	n/a
15	chr6:118821449-118821499	GM12878	blood:	n/a
16	chr6:118776527-118776577	K562	blood:	n/a
17	chr6:118822466-118822516	HIPEpiC	eye:	n/a
18	chr6:118776527-118776577	AoSMC	blood vessel:	n/a
19	chr6:118699056-118699106	AG09319	gingival:	n/a
20	chr6:118709682-118709732	HAEpiC	amniotic membrane:	n/a
21	chr6:118821449-118821499	NH-A	brain:	n/a
22	chr6:118823964-118824014	AG04450	lung:	fetal
23	chr6:118709682-118709732	ECC-1	luminal epithelium:	n/a
24	chr6:118699056-118699106	IMR90	lung:	fetal
25	chr6:118822505-118822555	HNPCEpiC	eye:	n/a
26	chr6:118823964-118824014	NHDF-neo	bronchial:	n/a
27	chr6:118699056-118699106	HNPCEpiC	eye:	n/a
28	chr6:118709682-118709732	PANC-1	pancreas:	n/a
29	chr6:118822505-118822555	IMR90	lung:	fetal
30	chr6:118699056-118699106	HCPEpiC	choroid plexus:	n/a
31	chr6:118822466-118822516	PrEC	prostate:	n/a
32	chr6:118699056-118699106	MCF-7	breast:	n/a
33	chr6:118822505-118822555	AG09319	gingival:	n/a
34	chr6:118776527-118776577	SK-N-MC	brain:	n/a
35	chr6:118699056-118699106	GM12891	blood:	n/a
36	chr6:118822131-118822181	HRPEpiC	eye:	n/a
37	chr6:118699056-118699106	PrEC	prostate:	n/a
38	chr6:118822505-118822555	A549	lung:	n/a
39	chr6:118821449-118821499	CMK	blood:	n/a
40	chr6:118822505-118822555	Caco-2	colon:	n/a
41	chr6:118776527-118776577	ovcar-3	ovarian:	n/a
42	chr6:118776527-118776577	HCT-116	colon:	n/a
43	chr6:118822466-118822516	NHBE	bronchial:	n/a
44	chr6:118699056-118699106	HCM	heart:	n/a
45	chr6:118822505-118822555	BE2_C	brain:	n/a
46	chr6:118822466-118822516	LNCaP	prostate:	n/a
47	chr6:118822466-118822516	SK-N-SH	brain:	n/a
48	chr6:118823964-118824014	GM06990	blood:	n/a
49	chr6:118823964-118824014	CMK	blood:	n/a
50	chr6:118822131-118822181	Hela-S3	cervix:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
2	chr6:118839207..118841504-chr6:119214917..119216766,2	MCF-7	breast:
3	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
4	chr6:118836380..118838045-chr6:118841416..118842970,2	K562	blood:
5	chr6:118790912..118793638-chr6:118795834..118798403,2	K562	blood:
6	chr6:118826989..118829311-chr6:118938215..118940660,2	K562	blood:
7	chr6:118827080..118828715-chr6:118830473..118832709,2	K562	blood:
8	chr6:118720659..118723492-chr6:118725899..118729757,3	K562	blood:
9	chr6:118827080..118828715-chr6:118830473..118832709,2	K562	blood:
10	chr6:118729437..118730312-chr6:118828228..118829001,2	MCF-7	breast:
11	chr6:118840065..118842365-chr6:118844866..118846753,2	K562	blood:
12	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
13	chr6:118766414..118769352-chr6:118774128..118777684,3	K562	blood:
14	chr6:118729437..118730312-chr6:118828228..118829001,2	MCF-7	breast:
15	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
16	chr6:118830553..118833373-chr6:118834538..118836187,2	K562	blood:
17	chr6:118807029..118809570-chr6:118811844..118815669,3	K562	blood:
18	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
19	chr6:118605631..118606342-chr6:118829971..118830837,2	K562	blood:
20	chr6:118807810..118810020-chr6:118811825..118813344,2	K562	blood:
21	chr6:118630135..118632500-chr6:118803686..118805267,2	K562	blood:
22	chr6:118824560..118826306-chr6:118830401..118832913,2	K562	blood:
23	chr6:118720659..118723492-chr6:118725899..118729757,3	K562	blood:
24	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
25	chr6:118830553..118833464-chr6:118833711..118836187,2	K562	blood:
26	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
27	chr6:118840065..118842365-chr6:118844866..118846753,2	K562	blood:
28	chr6:118829900..118830527-chr6:118872009..118872536,2	MCF-7	breast:
29	chr6:118829745..118830555-chr6:118939535..118940562,3	MCF-7	breast:
30	chr6:118829899..118830781-chr6:118901492..118902427,2	MCF-7	breast:
31	chr6:118790912..118793638-chr6:118795834..118798403,2	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	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
36	chr6:118836380..118838045-chr6:118841416..118842970,2	K562	blood:
37	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
38	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
39	chr6:118824560..118826306-chr6:118830401..118832913,2	K562	blood:
40	chr6:118807810..118810020-chr6:118811825..118813344,2	K562	blood:
41	chr6:118845234..118848026-chr6:118887537..118889460,2	K562	blood:
42	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
43	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
44	chr6:118807029..118809570-chr6:118811844..118815669,3	K562	blood:
45	chr6:118830553..118833373-chr6:118834538..118836187,2	K562	blood:
46	chr6:118604657..118606544-chr6:118829791..118831020,17	MCF-7	breast:
47	chr6:118604757..118606576-chr6:118829465..118831114,11	MCF-7	breast:

(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
ENSG00000111877	chromatin interactions
ENSG00000111875	chromatin interactions
ENSG00000216809	chromatin interactions

Extended variants
information (count: 5632 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:5632 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6903177	chr6:118695049-118695050	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557632571	chr6:118695056-118695057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188257053	chr6:118695064-118695065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191611394	chr6:118695125-118695126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141447033	chr6:118695146-118695147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556181101	chr6:118695149-118695150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142430992	chr6:118695172-118695173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569243636	chr6:118695175-118695176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372327278	chr6:118695192-118695193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536613545	chr6:118695234-118695235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556704201	chr6:118695244-118695245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570480787	chr6:118695245-118695246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193150331	chr6:118695270-118695271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553071358	chr6:118695275-118695276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs13206243	chr6:118695296-118695297	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs151303471	chr6:118695316-118695317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555685620	chr6:118695336-118695337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575628508	chr6:118695361-118695362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544568726	chr6:118695386-118695387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs56255677	chr6:118695402-118695403	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs72967572	chr6:118695407-118695408	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558194988	chr6:118695428-118695429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560262250	chr6:118695449-118695450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573328538	chr6:118695468-118695469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529429412	chr6:118695494-118695495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370996805	chr6:118695504-118695505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549179558	chr6:118695540-118695541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562812959	chr6:118695608-118695609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534310781	chr6:118695638-118695639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531882724	chr6:118695666-118695667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115212288	chr6:118695700-118695701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553171085	chr6:118695744-118695745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115621543	chr6:118695770-118695771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35759854	chr6:118695783-118695784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574582027	chr6:118695797-118695798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569949369	chr6:118695813-118695814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535795752	chr6:118695868-118695869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190226569	chr6:118695984-118695985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535610967	chr6:118696026-118696027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372757856	chr6:118696055-118696056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138711526	chr6:118696122-118696123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575563294	chr6:118696227-118696228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537763044	chr6:118696264-118696265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141164258	chr6:118696330-118696331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7767864	chr6:118696338-118696339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs540652265	chr6:118696396-118696397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560178343	chr6:118696444-118696445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117078001	chr6:118696448-118696449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542764036	chr6:118696466-118696467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555590628	chr6:118696469-118696470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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	22522925	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1736 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118688200-118700200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:118691400-118700400	Enhancers	Fetal Heart	heart
3	chr6:118692200-118699000	Weak transcription	Psoas Muscle	Psoas
4	chr6:118693000-118695200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:118694200-118699600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:118694800-118695600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr6:118694800-118696000	Enhancers	Left Ventricle	heart
8	chr6:118694800-118698200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:118695600-118696200	Enhancers	Right Atrium	heart
10	chr6:118695600-118696200	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr6:118696000-118698200	Weak transcription	Left Ventricle	heart
12	chr6:118696200-118698200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr6:118696200-118699000	Weak transcription	Right Atrium	heart
14	chr6:118698200-118698400	Enhancers	Left Ventricle	heart
15	chr6:118698200-118698400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr6:118698200-118699000	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr6:118698200-118699600	Enhancers	Fetal Thymus	thymus
18	chr6:118698200-118699800	Enhancers	Thymus	Thymus
19	chr6:118698400-118698800	Weak transcription	Left Ventricle	heart
20	chr6:118698400-118698800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr6:118698600-118698800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:118698800-118699000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:118698800-118699000	Enhancers	Left Ventricle	heart
24	chr6:118698800-118699000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:118698800-118699800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr6:118698800-118700400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr6:118699000-118699200	Flanking Active TSS	Left Ventricle	heart
28	chr6:118699000-118699400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:118699000-118699400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:118699000-118699400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr6:118699000-118699400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr6:118699000-118699400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
33	chr6:118699000-118699600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:118699000-118699600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:118699000-118699600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:118699000-118699600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:118699000-118699600	Enhancers	Fetal Muscle Trunk	muscle
38	chr6:118699000-118699600	Enhancers	Fetal Muscle Leg	muscle
39	chr6:118699000-118699600	Enhancers	Psoas Muscle	Psoas
40	chr6:118699000-118699600	Enhancers	Right Atrium	heart
41	chr6:118699000-118699800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:118699000-118699800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:118699000-118700000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:118699200-118699400	Enhancers	Left Ventricle	heart
45	chr6:118699400-118699600	Active TSS	Left Ventricle	heart
46	chr6:118699400-118699600	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr6:118699400-118699800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr6:118699600-118700400	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr6:118699600-118707600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:118699600-118716400	Weak transcription	Psoas Muscle	Psoas

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