Variant report

Variant	nsv605232
Chromosome Location	chr6:164994771-165401154
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:165339529-165339854	K562	blood:	n/a	n/a
2	BHLHE40	chr6:165341057-165341386	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:165341052-165341377	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:165341085-165341390	K562	blood:	n/a	n/a
5	BRCA1	chr6:165341191-165341391	HepG2	liver:	n/a	n/a
6	BRCA1	chr6:165341072-165341263	GM12878	blood:	n/a	n/a
7	CBX3	chr6:165055640-165055827	K562	blood:	n/a	n/a
8	CEBPB	chr6:165054168-165054395	HepG2	liver:	n/a	chr6:165054256-165054267
9	CEBPB	chr6:165340972-165341220	HepG2	liver:	n/a	chr6:165341089-165341100 chr6:165341089-165341102 chr6:165341090-165341101
10	CEBPB	chr6:165241508-165241767	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:164996538-164996737	A549	lung:	n/a	chr6:164996578-164996589
12	CEBPB	chr6:165162515-165162798	IMR90	lung:	n/a	chr6:165162656-165162667
13	CEBPB	chr6:165102542-165102851	HepG2	liver:	n/a	chr6:165102690-165102703 chr6:165102692-165102701 chr6:165102690-165102701 chr6:165102692-165102701 chr6:165102690-165102703 chr6:165102692-165102701
14	CEBPB	chr6:165327411-165327418	K562	blood:	n/a	n/a
15	CEBPB	chr6:165114994-165115342	H1-hESC	embryonic stem cell:	n/a	chr6:165115254-165115265 chr6:165115153-165115166
16	CEBPB	chr6:165162502-165162828	HepG2	liver:	n/a	chr6:165162656-165162667
17	CEBPB	chr6:164996421-164996674	HepG2	liver:	n/a	chr6:164996578-164996589
18	CEBPB	chr6:165081130-165081446	HepG2	liver:	n/a	chr6:165081280-165081291
19	CEBPB	chr6:165320320-165320636	HepG2	liver:	n/a	chr6:165320481-165320490 chr6:165320479-165320492 chr6:165320481-165320490 chr6:165320481-165320490 chr6:165320481-165320492 chr6:165320481-165320490 chr6:165320479-165320490 chr6:165320479-165320492
20	CEBPB	chr6:165224152-165224514	HepG2	liver:	n/a	chr6:165224322-165224333
21	CEBPB	chr6:165327180-165327476	HepG2	liver:	n/a	chr6:165327326-165327337
22	CEBPB	chr6:165340979-165341269	K562	blood:	n/a	chr6:165341089-165341100 chr6:165341089-165341102 chr6:165341090-165341101
23	CEBPB	chr6:165340967-165341396	H1-hESC	embryonic stem cell:	n/a	chr6:165341089-165341100 chr6:165341089-165341102 chr6:165341090-165341101
24	CEBPB	chr6:165224170-165224453	IMR90	lung:	n/a	chr6:165224322-165224333
25	CHD2	chr6:165341111-165341307	HepG2	liver:	n/a	n/a
26	CTCF	chr6:165340320-165340470	HBMEC	blood vessel:	n/a	chr6:165340393-165340414
27	CTCF	chr6:165341066-165341403	T-47D	breast:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
28	CTCF	chr6:165341160-165341310	GM12874	blood:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
29	CTCF	chr6:165341180-165341330	HCT-116	colon:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
30	CTCF	chr6:165341097-165341384	Medullo	brain:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
31	CTCF	chr6:165311060-165311210	Hela-S3	cervix:	n/a	chr6:165311187-165311205 chr6:165311189-165311210
32	CTCF	chr6:165150132-165150215	GM13976	blood:	n/a	n/a
33	CTCF	chr6:165340359-165340471	LNCaP	prostate:	n/a	chr6:165340393-165340414
34	CTCF	chr6:165237960-165238110	NHLF	lung:	n/a	n/a
35	CTCF	chr6:165341101-165341375	Gliobla	brain:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
36	CTCF	chr6:165340267-165340554	GM12878	blood:	n/a	chr6:165340393-165340414
37	CTCF	chr6:165341140-165341290	AoAF	blood vessel:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
38	CTCF	chr6:165033820-165033970	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr6:165311160-165311310	HEK293	kidney:	n/a	chr6:165311187-165311205 chr6:165311189-165311210
40	CTCF	chr6:165341091-165341381	GM19239	blood:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
41	CTCF	chr6:165341120-165341270	HRPEpiC	eye:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
42	CTCF	chr6:165340420-165340570	BE2_C	brain:	n/a	n/a
43	CTCF	chr6:165341140-165341290	WERI-Rb-1	eye:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
44	CTCF	chr6:165311185-165311277	GM12878	blood:	n/a	chr6:165311187-165311205 chr6:165311189-165311210
45	CTCF	chr6:165341160-165341310	HUVEC	blood vessel:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
46	CTCF	chr6:165341140-165341290	HCPEpiC	choroid plexus:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
47	CTCF	chr6:165341180-165341330	GM06990	blood:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
48	CTCF	chr6:165341180-165341330	Caco-2	colon:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228
49	CTCF	chr6:165311060-165311210	MCF-7	breast:	n/a	chr6:165311187-165311205 chr6:165311189-165311210
50	CTCF	chr6:165341100-165341250	AG04450	lung:	n/a	chr6:165341212-165341230 chr6:165341214-165341227 chr6:165341207-165341228

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165032068-165032118	AG09309	skin:	n/a
2	chr6:165032068-165032118	AG09309	skin:	n/a
3	chr6:165032124-165032174	HUVEC	blood vessel:	n/a
4	chr6:165032124-165032174	HCT-116	colon:	n/a
5	chr6:165032068-165032118	SK-N-SH_RA	brain:	n/a
6	chr6:165341382-165341432	NHDF-neo	bronchial:	n/a
7	chr6:165341320-165341370	GM12878	blood:	n/a
8	chr6:165115084-165115134	HRCEpiC	kidney:	n/a
9	chr6:165341382-165341432	T-47D	breast:	n/a
10	chr6:165236522-165236572	ovcar-3	ovarian:	n/a
11	chr6:165062070-165062120	HCF	heart:	n/a
12	chr6:165236522-165236572	ProgFib	skin:	n/a
13	chr6:165341320-165341370	SK-N-SH	brain:	n/a
14	chr6:165341382-165341432	Jurkat	blood:	n/a
15	chr6:165032072-165032122	ProgFib	skin:	n/a
16	chr6:165032124-165032174	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:165324747-165324797	Caco-2	colon:	n/a
18	chr6:165032068-165032118	IMR90	lung:	fetal
19	chr6:165032124-165032174	HEK293	kidney:	embryo
20	chr6:165062070-165062120	HEEpiC	esophagus:	n/a
21	chr6:165348000-165348050	HCT-116	colon:	n/a
22	chr6:165348000-165348050	Jurkat	blood:	n/a
23	chr6:165341241-165341291	U87	brain:	n/a
24	chr6:165032068-165032118	HL-60	blood:	n/a
25	chr6:165236522-165236572	HCPEpiC	choroid plexus:	n/a
26	chr6:165341241-165341291	HAEpiC	amniotic membrane:	n/a
27	chr6:165384599-165384649	GM06990	blood:	n/a
28	chr6:165032072-165032122	Hela-S3	cervix:	n/a
29	chr6:165341241-165341291	GM12891	blood:	n/a
30	chr6:165032124-165032174	AoSMC	blood vessel:	n/a
31	chr6:165032124-165032174	NT2-D1	testis:	n/a
32	chr6:165032068-165032118	H1-hESC	embryonic stem cell:	embryo
33	chr6:165384599-165384649	HCT-116	colon:	n/a
34	chr6:165348000-165348050	AG10803	skin:	n/a
35	chr6:165062070-165062120	NH-A	brain:	n/a
36	chr6:165384599-165384649	AG09309	skin:	n/a
37	chr6:165062070-165062120	AG09309	skin:	n/a
38	chr6:165062070-165062120	PFSK-1	brain:	n/a
39	chr6:165324747-165324797	RPTEC	kidney:	n/a
40	chr6:165032124-165032174	K562	blood:	n/a
41	chr6:165115084-165115134	RPTEC	kidney:	n/a
42	chr6:165236522-165236572	ECC-1	luminal epithelium:	n/a
43	chr6:165062070-165062120	GM12891	blood:	n/a
44	chr6:165032072-165032122	PrEC	prostate:	n/a
45	chr6:165062070-165062120	AG04449	skin:	fetal
46	chr6:165341382-165341432	ovcar-3	ovarian:	n/a
47	chr6:165032068-165032118	HUVEC	blood vessel:	n/a
48	chr6:165341382-165341432	K562	blood:	n/a
49	chr6:165384599-165384649	ProgFib	skin:	n/a
50	chr6:165384599-165384649	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:165117997..165120289-chr6:165120644..165122440,2	K562	blood:
2	chr6:165082238..165084641-chr6:165089609..165091881,2	K562	blood:
3	chr6:165085847..165087840-chr6:165089357..165091527,2	K562	blood:
4	chr6:164767711..164769131-chr6:165340232..165341669,7	MCF-7	breast:
5	chr6:165050032..165051589-chr6:165053797..165056474,2	K562	blood:
6	chr6:165160068..165160918-chr8:98129240..98129986,2	MCF-7	breast:
7	chr6:165271396..165272279-chr6:165462865..165463466,2	MCF-7	breast:
8	chr6:165119728..165120228-chrX:107366674..107367661,2	MCF-7	breast:
9	chr6:165110029..165112755-chr6:165114733..165117071,2	K562	blood:
10	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
11	chr6:165082238..165084641-chr6:165089609..165091881,2	K562	blood:
12	chr6:165050032..165051589-chr6:165053797..165056474,2	K562	blood:
13	chr6:165244240..165245853-chr6:165247412..165249558,2	K562	blood:
14	chr6:165259094..165261615-chr6:165279301..165280809,2	K562	blood:
15	chr6:165117997..165120289-chr6:165120644..165122440,2	K562	blood:
16	chr6:165335824..165337632-chr6:165338882..165340730,2	K562	blood:
17	chr6:165259094..165261615-chr6:165279301..165280809,2	K562	blood:
18	chr5:128797111..128797864-chr6:165136910..165137454,2	MCF-7	breast:
19	chr6:165085847..165087840-chr6:165089357..165091527,2	K562	blood:
20	chr6:164768200..164769032-chr6:165340931..165341635,2	MCF-7	breast:
21	chr6:165007452..165009387-chr6:165042540..165044932,2	K562	blood:
22	chr6:164637205..164638102-chr6:165340164..165340958,2	MCF-7	breast:
23	chr6:165249458..165251438-chr6:165253089..165255770,2	K562	blood:
24	chr6:165007452..165009387-chr6:165042540..165044932,2	K562	blood:
25	chr6:164768274..164768906-chr6:165033273..165034147,2	MCF-7	breast:
26	chr6:165110029..165112755-chr6:165114733..165117071,2	K562	blood:
27	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
28	chr6:165249458..165251438-chr6:165253089..165255770,2	K562	blood:
29	chr6:165244240..165245853-chr6:165247412..165249558,2	K562	blood:
30	chr6:165335824..165337632-chr6:165338882..165340730,2	K562	blood:
31	chr6:165375696..165377875-chr6:165438259..165440436,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf118-5	chr6:165139175-165139208	ucscGeneNc_uc003qul_1
2	lnc-QKI-4	chr6:165243009-165243106	NONHSAT115993
3	lnc-C6orf118-5	chr6:165155417-165155532	ucscGeneNc_uc003qul_1
4	lnc-C6orf118-1	chr6:165219185-165219218	NONHSAT115991
5	lnc-C6orf118-1	chr6:165218447-165218582	XLOC_005915
6	lnc-C6orf118-1	chr6:165241067-165241153	XLOC_005915
7	lnc-QKI-4	chr6:165243010-165243106	XLOC_005533
8	lnc-C6orf118-1	chr6:165207066-165207641	NONHSAT115991
9	lnc-C6orf118-1	chr6:165219185-165219218	XLOC_005915
10	lnc-QKI-4	chr6:165244510-165244543	NONHSAT115996
11	lnc-QKI-5	chr6:165341827-165342411	XLOC_005534
12	lnc-C6orf118-1	chr6:165219185-165219218	XLOC_005915
13	lnc-QKI-4	chr6:165241259-165241452	NONHSAT115996
14	lnc-QKI-12	chr6:165163000-165163096	NONHSAT115989
15	lnc-C6orf118-5	chr6:165138435-165138569	ucscGeneNc_uc003qul_1
16	lnc-QKI-4	chr6:165241239-165245119	ENSG00000227455.2
17	lnc-C6orf118-1	chr6:165241067-165241138	NONHSAT115991
18	lnc-QKI-5	chr6:165341407-165341431	NONHSAT115997
19	lnc-C6orf118-1	chr6:165218445-165218579	XLOC_005915
20	lnc-QKI-5	chr6:165341827-165342092	NONHSAT115997
21	lnc-QKI-5	chr6:165341509-165341544	XLOC_005534
22	lnc-QKI-5	chr6:165341449-165341714	FPKM1_group_28841_transcript_1
23	lnc-QKI-12	chr6:165161229-165161442	NONHSAT115989
24	lnc-QKI-5	chr6:165341407-165341431	FPKM1_group_28841_transcript_1
25	lnc-C6orf118-1	chr6:165206864-165207641	XLOC_005915
26	lnc-QKI-4	chr6:165241238-165241452	NONHSAT115993
27	lnc-QKI-4	chr6:165241239-165241452	XLOC_005533
28	lnc-C6orf118-5	chr6:165126854-165127631	ucscGeneNc_uc003qul_1
29	lnc-C6orf118-1	chr6:165218445-165218579	NONHSAT115991
30	lnc-C6orf118-1	chr6:165235427-165235542	XLOC_005915

Variant related genes	Relation type
ENSG00000227455	TF binding region
ENSG00000227455	CpG island
ENSG00000145808	chromatin interactions

Extended variants
information (count: 6466 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:6466 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9347874	chr6:164994771-164994772	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536517346	chr6:164994861-164994862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545370799	chr6:164994862-164994863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565522534	chr6:164994866-164994867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192171216	chr6:164994880-164994881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184729013	chr6:164994934-164994935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554578291	chr6:164994963-164994964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2322492	chr6:164994970-164994971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs35190268	chr6:164994994-164994995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566862773	chr6:164995009-164995010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200658922	chr6:164995022-164995023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200452534	chr6:164995024-164995025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs67077491	chr6:164995025-164995026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397724756	chr6:164995029-164995030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201422137	chr6:164995030-164995031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199576622	chr6:164995031-164995032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142823619	chr6:164995064-164995065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146098842	chr6:164995104-164995105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569066295	chr6:164995106-164995107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537607735	chr6:164995122-164995123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2322493	chr6:164995140-164995141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs376669032	chr6:164995224-164995225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2322494	chr6:164995252-164995253	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2322495	chr6:164995294-164995295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553395094	chr6:164995317-164995318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370475891	chr6:164995328-164995329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545714240	chr6:164995360-164995361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201347325	chr6:164995373-164995374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565424504	chr6:164995391-164995392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575812425	chr6:164995401-164995402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544451453	chr6:164995406-164995407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561370946	chr6:164995407-164995408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188000290	chr6:164995413-164995414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2322496	chr6:164995414-164995415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs2322497	chr6:164995418-164995419	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs9355482	chr6:164995469-164995470	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552458898	chr6:164995485-164995486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6455951	chr6:164995497-164995498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs369080809	chr6:164995531-164995532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546066575	chr6:164995542-164995543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531940506	chr6:164995545-164995546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561764480	chr6:164995548-164995549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145544173	chr6:164995558-164995559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377643243	chr6:164995561-164995562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567907105	chr6:164995563-164995564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572571479	chr6:164995596-164995597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1979780	chr6:164995624-164995625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs372231581	chr6:164995656-164995657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141336231	chr6:164995664-164995665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377443446	chr6:164995674-164995675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164991400-164996400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:164996400-164996800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:164997000-164997200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:164999400-165000200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:165000200-165000400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:165001600-165003400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:165002200-165002800	ZNF genes & repeats	Brain Hippocampus Middle	brain
8	chr6:165002400-165002800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:165016000-165016200	ZNF genes & repeats	Pancreas	Pancrea
10	chr6:165016000-165016400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:165016400-165016800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:165016600-165017000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:165016800-165017000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:165016800-165017000	ZNF genes & repeats	Pancreas	Pancrea
15	chr6:165017000-165020600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:165029000-165029400	Enhancers	Brain Germinal Matrix	brain
17	chr6:165029400-165029800	Weak transcription	Brain Germinal Matrix	brain
18	chr6:165029800-165030600	Enhancers	Brain Germinal Matrix	brain
19	chr6:165031000-165031800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:165033000-165033200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:165033200-165033800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:165033400-165034600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:165033800-165034000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:165033800-165039000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr6:165039000-165039200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:165039800-165040200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:165039800-165041200	Enhancers	Brain Substantia Nigra	brain
28	chr6:165040000-165040800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:165040000-165040800	Enhancers	Brain Hippocampus Middle	brain
30	chr6:165040800-165043000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:165043000-165043600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:165050800-165051000	Enhancers	Brain Anterior Caudate	brain
33	chr6:165051000-165051400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:165051000-165051400	Active TSS	Brain Anterior Caudate	brain
35	chr6:165051000-165051400	Enhancers	Fetal Heart	heart
36	chr6:165051200-165051400	Enhancers	Pancreas	Pancrea
37	chr6:165051400-165052400	Weak transcription	Pancreas	Pancrea
38	chr6:165052400-165052600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:165052400-165052600	Enhancers	Pancreas	Pancrea
40	chr6:165061400-165063000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:165061800-165062000	Enhancers	Brain Hippocampus Middle	brain
42	chr6:165061800-165062400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr6:165061800-165062400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:165061800-165062400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:165061800-165062600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:165062000-165062200	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr6:165062000-165062200	Enhancers	Brain Substantia Nigra	brain
48	chr6:165062000-165062400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr6:165062000-165062400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr6:165062000-165062400	Enhancers	Adipose Nuclei	Adipose

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