Variant report

Variant	esv3349061
Chromosome Location	chr4:22379581-22887563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3305)
CpG islands
(count:2868)
Chromatin interactive
region (count:88)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3305 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:22461719-22462382	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:22514317-22514627	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:22516834-22517061	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:22489028-22489337	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:22457970-22458493	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:22692275-22692679	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:22455972-22456260	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:22436571-22436819	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:22515506-22516172	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:22437299-22437741	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:22476377-22477117	HepG2	liver:	n/a	n/a
12	ATF1	chr4:22719632-22719730	K562	blood:	n/a	n/a
13	ATF2	chr4:22632891-22633274	GM12878	blood:	n/a	n/a
14	ATF2	chr4:22485174-22485556	GM12878	blood:	n/a	n/a
15	ATF2	chr4:22502962-22503259	GM12878	blood:	n/a	n/a
16	ATF2	chr4:22597318-22597734	GM12878	blood:	n/a	n/a
17	BACH1	chr4:22517923-22518017	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:22516640-22517130	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:22698950-22698993	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:22465025-22465108	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr4:22705564-22705832	GM12878	blood:	n/a	chr4:22705743-22705756
22	BATF	chr4:22467709-22468003	GM12878	blood:	n/a	n/a
23	BATF	chr4:22672653-22672907	GM12878	blood:	n/a	chr4:22672831-22672841
24	BATF	chr4:22731779-22732025	GM12878	blood:	n/a	chr4:22731857-22731868
25	BATF	chr4:22601520-22601932	GM12878	blood:	n/a	n/a
26	BATF	chr4:22708980-22709529	GM12878	blood:	n/a	n/a
27	BATF	chr4:22485171-22485506	GM12878	blood:	n/a	n/a
28	BATF	chr4:22746279-22746633	GM12878	blood:	n/a	n/a
29	BATF	chr4:22502998-22503258	GM12878	blood:	n/a	chr4:22503138-22503148 chr4:22503137-22503148
30	BATF	chr4:22632911-22633232	GM12878	blood:	n/a	n/a
31	BATF	chr4:22744976-22745283	GM12878	blood:	n/a	n/a
32	BATF	chr4:22709049-22709228	GM12878	blood:	n/a	n/a
33	BATF	chr4:22601547-22601922	GM12878	blood:	n/a	n/a
34	BATF	chr4:22597162-22597792	GM12878	blood:	n/a	n/a
35	BATF	chr4:22456697-22456973	GM12878	blood:	n/a	n/a
36	BATF	chr4:22606760-22606960	GM12878	blood:	n/a	n/a
37	BATF	chr4:22597407-22597668	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:22632894-22633130	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:22597323-22597768	GM12878	blood:	n/a	n/a
40	BCL11A	chr4:22480127-22480357	GM12878	blood:	n/a	n/a
41	BCL11A	chr4:22597442-22597626	GM12878	blood:	n/a	n/a
42	BCL11A	chr4:22480635-22480793	GM12878	blood:	n/a	n/a
43	BCL11A	chr4:22741560-22741796	GM12878	blood:	n/a	n/a
44	BCL11A	chr4:22885970-22886163	H1-hESC	embryonic stem cell:	n/a	n/a
45	BCL11A	chr4:22485135-22485505	GM12878	blood:	n/a	n/a
46	BCL11A	chr4:22502987-22503282	GM12878	blood:	n/a	chr4:22503140-22503149 chr4:22503081-22503088 chr4:22503141-22503150
47	BCL11A	chr4:22497824-22497994	GM12878	blood:	n/a	n/a
48	BCL11A	chr4:22885743-22886105	H1-hESC	embryonic stem cell:	n/a	n/a
49	BCL11A	chr4:22429384-22429649	GM12878	blood:	n/a	n/a
50	BCL11A	chr4:22485182-22485421	GM12878	blood:	n/a	n/a

(count:2868 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22437783-22437833	K562	blood:	n/a
2	chr4:22437783-22437833	K562	blood:	n/a
3	chr4:22623333-22623383	AG10803	skin:	n/a
4	chr4:22392700-22392750	AG04450	lung:	fetal
5	chr4:22636392-22636442	HAEpiC	amniotic membrane:	n/a
6	chr4:22744871-22744921	AG09319	gingival:	n/a
7	chr4:22517965-22518015	Hepatocyte	liver:	n/a
8	chr4:22517932-22517982	BJ	skin:	n/a
9	chr4:22780491-22780541	ProgFib	skin:	n/a
10	chr4:22623367-22623417	CMK	blood:	n/a
11	chr4:22623367-22623417	NH-A	brain:	n/a
12	chr4:22517094-22517144	CMK	blood:	n/a
13	chr4:22520573-22520623	NH-A	brain:	n/a
14	chr4:22746262-22746312	A549	lung:	n/a
15	chr4:22517195-22517245	GM12878	blood:	n/a
16	chr4:22509445-22509495	NB4	blood:	n/a
17	chr4:22390012-22390062	SK-N-MC	brain:	n/a
18	chr4:22623252-22623302	SAEC	small airway:	n/a
19	chr4:22520573-22520623	Hepatocyte	liver:	n/a
20	chr4:22516158-22516208	PANC-1	pancreas:	n/a
21	chr4:22517094-22517144	Jurkat	blood:	n/a
22	chr4:22516158-22516208	IMR90	lung:	fetal
23	chr4:22520573-22520623	NHDF-neo	bronchial:	n/a
24	chr4:22516158-22516208	HRE	kidney:	n/a
25	chr4:22636203-22636253	CMK	blood:	n/a
26	chr4:22437783-22437833	SKMC	muscle:	n/a
27	chr4:22588665-22588715	GM12878	blood:	n/a
28	chr4:22389706-22389756	CMK	blood:	n/a
29	chr4:22517094-22517144	HL-60	blood:	n/a
30	chr4:22461750-22461800	CMK	blood:	n/a
31	chr4:22483053-22483103	NH-A	brain:	n/a
32	chr4:22636672-22636722	BE2_C	brain:	n/a
33	chr4:22588245-22588295	A549	lung:	n/a
34	chr4:22461750-22461800	AG09309	skin:	n/a
35	chr4:22517932-22517982	GM12878	blood:	n/a
36	chr4:22636672-22636722	HCT-116	colon:	n/a
37	chr4:22590411-22590461	T-47D	breast:	n/a
38	chr4:22517932-22517982	AG04449	skin:	fetal
39	chr4:22517932-22517982	AG09319	gingival:	n/a
40	chr4:22588208-22588258	ECC-1	luminal epithelium:	n/a
41	chr4:22818572-22818622	SK-N-SH	brain:	n/a
42	chr4:22493281-22493331	MCF10A-Er-Src	breast:	n/a
43	chr4:22390012-22390062	NB4	blood:	n/a
44	chr4:22389934-22389984	HCT-116	colon:	n/a
45	chr4:22517094-22517144	NHBE	bronchial:	n/a
46	chr4:22389934-22389984	HCF	heart:	n/a
47	chr4:22588208-22588258	GM12892	blood:	n/a
48	chr4:22744871-22744921	HMEC	breast:	n/a
49	chr4:22818572-22818622	HEEpiC	esophagus:	n/a
50	chr4:22588658-22588708	HRCEpiC	kidney:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:22772449..22775297-chr4:22778279..22780984,3	K562	blood:
2	chr4:22844491..22847403-chr4:22848956..22850580,3	K562	blood:
3	chr4:22407422..22409065-chr4:22411450..22413901,2	K562	blood:
4	chr4:22684475..22686472-chr4:22689943..22692504,2	K562	blood:
5	chr4:22523864..22526257-chr4:22533870..22535996,2	K562	blood:
6	chr4:22465182..22467125-chr4:22517057..22519339,2	MCF-7	breast:
7	chr4:22487490..22489243-chr4:22491775..22493390,2	K562	blood:
8	chr4:22684475..22686472-chr4:22689943..22692504,2	K562	blood:
9	chr4:22515872..22518234-chr4:22557080..22559292,2	MCF-7	breast:
10	chr4:22488399..22490950-chr4:22493521..22495053,2	MCF-7	breast:
11	chr4:22425322..22428021-chr4:22430037..22432573,2	MCF-7	breast:
12	chr4:22843905..22846646-chr4:22849080..22850791,2	K562	blood:
13	chr4:22575405..22577612-chr4:22584979..22587113,2	MCF-7	breast:
14	chr4:22508358..22510140-chr4:22512148..22515141,2	MCF-7	breast:
15	chr4:22507819..22511270-chr4:22511320..22514443,4	MCF-7	breast:
16	chr4:22427307..22429305-chr4:22435269..22437253,2	K562	blood:
17	chr4:22412823..22413341-chr4:22692071..22692819,2	MCF-7	breast:
18	chr4:22391010..22391614-chr4:22608701..22609240,2	MCF-7	breast:
19	chr4:22687079..22688984-chr4:22690023..22692580,2	MCF-7	breast:
20	chr4:21790330..21793132-chr4:22390550..22391689,10	MCF-7	breast:
21	chr4:21790239..21792742-chr4:22389960..22391772,13	MCF-7	breast:
22	chr4:22508358..22510140-chr4:22512148..22515141,2	MCF-7	breast:
23	chr4:22425322..22428021-chr4:22430037..22432573,2	MCF-7	breast:
24	chr4:22471253..22472855-chr4:22515638..22517354,2	MCF-7	breast:
25	chr4:22466667..22470398-chr4:22474006..22476709,3	MCF-7	breast:
26	chr18:24510025..24511017-chr4:22608413..22609080,2	MCF-7	breast:
27	chr4:22407422..22409065-chr4:22411450..22413901,2	K562	blood:
28	chr4:22386027..22387843-chr4:22392194..22394951,2	MCF-7	breast:
29	chr4:22875811..22877491-chr4:22882089..22884830,2	K562	blood:
30	chr4:21791076..21791579-chr4:22691911..22692590,2	K562	blood:
31	chr4:22516473..22518364-chr4:22531777..22533372,2	MCF-7	breast:
32	chr4:22517567..22518315-chr4:76649363..76650054,2	HCT-116	colon:
33	chr4:22452403..22454410-chr4:22458067..22459809,2	MCF-7	breast:
34	chr15:93347439..93348346-chr4:22517806..22518476,2	Hela-S3	cervix:
35	chr4:22796834..22798825-chr4:22803164..22804695,2	K562	blood:
36	chr4:22516426..22520250-chr4:22520676..22526735,6	MCF-7	breast:
37	chr4:22642022..22643894-chr4:22646674..22649581,2	K562	blood:
38	chr4:22412171..22412954-chr4:22692156..22692748,2	K562	blood:
39	chr4:22497592..22500394-chr4:22516759..22518508,2	MCF-7	breast:
40	chr4:22487490..22489243-chr4:22491775..22493390,2	K562	blood:
41	chr4:22816382..22818106-chr4:22821091..22824068,2	K562	blood:
42	chr4:22457536..22463707-chr4:22514115..22518559,7	MCF-7	breast:
43	chr4:22486301..22488142-chr4:22490876..22493757,2	MCF-7	breast:
44	chr4:22412034..22413416-chr4:22608679..22610025,5	MCF-7	breast:
45	chr18:12076450..12076959-chr4:22517248..22517778,2	HCT-116	colon:
46	chr1:148000162..148000856-chr4:22411148..22411799,2	MCF-7	breast:
47	chr4:22501387..22504925-chr4:22515596..22518632,4	MCF-7	breast:
48	chr4:22449726..22452368-chr4:22458347..22461364,3	MCF-7	breast:
49	chr4:22488399..22490950-chr4:22493521..22495053,2	MCF-7	breast:
50	chr4:22505951..22512123-chr4:22514706..22518696,9	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-12	chr4:22666560-22667583	ucscGeneNc_uc003gqr_1
2	lnc-PACRGL-10	chr4:22611966-22612076	NONHSAT095765
3	lnc-PACRGL-12	chr4:22608315-22608334	l_2614_chr4:22608314-22651921_testes
4	lnc-PACRGL-12	chr4:22734103-22734156	l_2614_chr4:22608314-22651921_testes
5	lnc-SOD3-13	chr4:22823158-22825371	NONHSAT095768
6	lnc-PACRGL-11	chr4:22715715-22715773	NONHSAT095766
7	lnc-PACRGL-11	chr4:22716579-22717119	NONHSAT095766
8	lnc-PACRGL-12	chr4:22613871-22613964	ucscGeneNc_uc003gqr_1
9	lnc-PACRGL-12	chr4:22613866-22613964	l_2614_chr4:22608314-22651921_testes
10	lnc-PACRGL-10	chr4:22611344-22611472	NONHSAT095765
11	lnc-PACRGL-10	chr4:22612601-22612686	NONHSAT095765
12	lnc-PACRGL-12	chr4:22610306-22610433	l_2614_chr4:22608314-22651921_testes
13	lnc-SOD3-13	chr4:22825575-22826631	NONHSAT095768
14	lnc-PACRGL-12	chr4:22608272-22608334	ucscGeneNc_uc003gqr_1
15	lnc-PACRGL-10	chr4:22609124-22609169	NONHSAT095765
16	lnc-PACRGL-12	chr4:22731328-22732285	l_2614_chr4:22608314-22651921_testes
17	lnc-PACRGL-9	chr4:22595819-22596073	NONHSAT095763
18	lnc-PACRGL-12	chr4:22731272-22731308	l_2614_chr4:22608314-22651921_testes
19	lnc-PACRGL-12	chr4:22651411-22651921	l_2614_chr4:22608314-22651921_testes
20	lnc-PACRGL-12	chr4:22694418-22694509	l_2614_chr4:22608314-22651921_testes
21	lnc-PACRGL-12	chr4:22731041-22731137	l_2614_chr4:22608314-22651921_testes
22	lnc-PACRGL-12	chr4:22610306-22610433	ucscGeneNc_uc003gqr_1
23	lnc-PACRGL-12	chr4:22733121-22733157	l_2614_chr4:22608314-22651921_testes

No data

Variant related genes	Relation type
ENSG00000244538	TF binding region
GBA3	TF binding region
ENSG00000251516	TF binding region
GPR125	TF binding region
CDC42P6	TF binding region
ENSG00000244538	CpG island
GBA3	CpG island
ENSG00000251516	CpG island
GPR125	CpG island
CDC42P6	CpG island
ENSG00000138757	chromatin interactions
ENSG00000251516	chromatin interactions
ENSG00000223491	chromatin interactions
ENSG00000236756	chromatin interactions
ENSG00000256616	chromatin interactions
ENSG00000152990	chromatin interactions
ENSG00000138768	chromatin interactions

Extended variants
information (count: 17094 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:17094 , 50 per page) page: 1 2 3 4 5 6 7 ... 342

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536213613	chr4:22379587-22379588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541069215	chr4:22379588-22379589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531257272	chr4:22379602-22379603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559320109	chr4:22379640-22379641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73110169	chr4:22379653-22379654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs556183984	chr4:22379660-22379661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192007880	chr4:22379672-22379673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545362459	chr4:22379683-22379684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563973535	chr4:22379707-22379708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531032861	chr4:22379759-22379760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367930535	chr4:22379767-22379768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183817041	chr4:22379790-22379791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567377532	chr4:22379801-22379802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544753744	chr4:22379814-22379815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187931325	chr4:22379824-22379825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546662756	chr4:22379854-22379855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571132481	chr4:22379871-22379872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139847008	chr4:22379891-22379892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538954906	chr4:22379894-22379895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545712368	chr4:22379910-22379911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192497805	chr4:22379919-22379920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569089014	chr4:22379945-22379946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536069719	chr4:22379947-22379948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182099128	chr4:22380017-22380018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186738026	chr4:22380036-22380037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192644982	chr4:22380054-22380055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552986031	chr4:22380067-22380068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577972929	chr4:22380068-22380069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545359020	chr4:22380114-22380115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185033039	chr4:22380131-22380132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572515668	chr4:22380171-22380172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189948769	chr4:22380197-22380198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140622840	chr4:22380301-22380302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373142655	chr4:22380420-22380421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147102415	chr4:22380458-22380459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541735060	chr4:22380467-22380468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546701345	chr4:22380521-22380522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561202481	chr4:22380560-22380561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532030251	chr4:22380589-22380590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377507915	chr4:22380605-22380606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569099875	chr4:22380623-22380624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201722853	chr4:22380716-22380717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193201675	chr4:22380762-22380763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138670717	chr4:22380831-22380832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28790686	chr4:22380874-22380875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs184550828	chr4:22380937-22380938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6842468	chr4:22380942-22380943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs189310977	chr4:22380959-22380960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545082925	chr4:22380973-22380974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370694564	chr4:22380981-22380982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4107 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22329000-22389400	Weak transcription	Pancreas	Pancrea
2	chr4:22336600-22385400	Weak transcription	Fetal Intestine Large	intestine
3	chr4:22365600-22386800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:22365800-22384600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:22366000-22385000	Weak transcription	NHEK	skin
6	chr4:22368800-22418600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:22371600-22449800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:22372000-22400400	Weak transcription	Gastric	stomach
9	chr4:22374800-22383600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:22375000-22385000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr4:22376000-22382200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr4:22376000-22385200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:22376400-22389200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:22377600-22389800	Weak transcription	Colon Smooth Muscle	Colon
15	chr4:22378600-22389200	Weak transcription	Aorta	Aorta
16	chr4:22379800-22380000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:22379800-22384800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:22380000-22381200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr4:22380800-22384600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr4:22381200-22381400	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr4:22381200-22381600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:22381400-22390200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:22381600-22384000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:22381600-22387800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr4:22382000-22384600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:22382200-22382400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:22382200-22386800	Weak transcription	Fetal Intestine Small	intestine
28	chr4:22382400-22385200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr4:22382400-22385400	Weak transcription	Fetal Muscle Leg	muscle
30	chr4:22382400-22389200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:22382400-22389400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr4:22382600-22409600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr4:22382800-22384400	Weak transcription	HSMMtube	muscle
34	chr4:22383000-22384600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:22383000-22384600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:22383200-22388000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr4:22383200-22438000	Weak transcription	Lung	lung
38	chr4:22383400-22385000	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr4:22383400-22385000	Weak transcription	HSMM	muscle
40	chr4:22383400-22386600	Weak transcription	HMEC	breast
41	chr4:22383400-22388200	Weak transcription	Fetal Muscle Trunk	muscle
42	chr4:22383400-22389400	Weak transcription	Stomach Smooth Muscle	stomach
43	chr4:22383600-22383800	Enhancers	Ovary	ovary
44	chr4:22383600-22384200	Enhancers	Right Ventricle	heart
45	chr4:22383600-22384400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:22383600-22385200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:22383600-22389000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:22383600-22389600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr4:22383600-22404200	Weak transcription	Fetal Kidney	kidney
50	chr4:22383600-22442800	Weak transcription	A549	lung

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