Variant report

Variant	nsv821634
Chromosome Location	chr4:22427074-22865948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2709)
CpG islands
(count:2504)
Chromatin interactive
region (count:74)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2709 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:22437299-22437741	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	chr4:22457970-22458493	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:22455972-22456260	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:22476377-22477117	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:22436571-22436819	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:22461719-22462382	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:22489028-22489337	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:22515506-22516172	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:22692275-22692679	HepG2	liver:	n/a	n/a
12	ATF1	chr4:22719632-22719730	K562	blood:	n/a	n/a
13	ATF2	chr4:22502962-22503259	GM12878	blood:	n/a	n/a
14	ATF2	chr4:22485174-22485556	GM12878	blood:	n/a	n/a
15	ATF2	chr4:22632891-22633274	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	chr4:22698950-22698993	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:22465025-22465108	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:22516640-22517130	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr4:22708980-22709529	GM12878	blood:	n/a	n/a
22	BATF	chr4:22467709-22468003	GM12878	blood:	n/a	n/a
23	BATF	chr4:22632911-22633232	GM12878	blood:	n/a	n/a
24	BATF	chr4:22744976-22745283	GM12878	blood:	n/a	n/a
25	BATF	chr4:22502998-22503258	GM12878	blood:	n/a	chr4:22503138-22503148 chr4:22503137-22503148
26	BATF	chr4:22746279-22746633	GM12878	blood:	n/a	n/a
27	BATF	chr4:22485171-22485506	GM12878	blood:	n/a	n/a
28	BATF	chr4:22606760-22606960	GM12878	blood:	n/a	n/a
29	BATF	chr4:22672653-22672907	GM12878	blood:	n/a	chr4:22672831-22672841
30	BATF	chr4:22597407-22597668	GM12878	blood:	n/a	n/a
31	BATF	chr4:22601520-22601932	GM12878	blood:	n/a	n/a
32	BATF	chr4:22705564-22705832	GM12878	blood:	n/a	chr4:22705743-22705756
33	BATF	chr4:22601547-22601922	GM12878	blood:	n/a	n/a
34	BATF	chr4:22709049-22709228	GM12878	blood:	n/a	n/a
35	BATF	chr4:22456697-22456973	GM12878	blood:	n/a	n/a
36	BATF	chr4:22731779-22732025	GM12878	blood:	n/a	chr4:22731857-22731868
37	BATF	chr4:22597162-22597792	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:22597323-22597768	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:22480635-22480793	GM12878	blood:	n/a	n/a
40	BCL11A	chr4:22597442-22597626	GM12878	blood:	n/a	n/a
41	BCL11A	chr4:22502987-22503282	GM12878	blood:	n/a	chr4:22503140-22503149 chr4:22503081-22503088 chr4:22503141-22503150
42	BCL11A	chr4:22485182-22485421	GM12878	blood:	n/a	n/a
43	BCL11A	chr4:22497824-22497994	GM12878	blood:	n/a	n/a
44	BCL11A	chr4:22632894-22633130	GM12878	blood:	n/a	n/a
45	BCL11A	chr4:22765892-22766128	GM12878	blood:	n/a	n/a
46	BCL11A	chr4:22741560-22741796	GM12878	blood:	n/a	n/a
47	BCL11A	chr4:22480127-22480357	GM12878	blood:	n/a	n/a
48	BCL11A	chr4:22429384-22429649	GM12878	blood:	n/a	n/a
49	BCL11A	chr4:22485135-22485505	GM12878	blood:	n/a	n/a
50	BCL3	chr4:22517856-22518353	A549	lung:	n/a	chr4:22518140-22518149

(count:2504 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22623252-22623302	CMK	blood:	n/a
2	chr4:22623333-22623383	Hela-S3	cervix:	n/a
3	chr4:22623252-22623302	SK-N-MC	brain:	n/a
4	chr4:22623252-22623302	CMK	blood:	n/a
5	chr4:22623333-22623383	Hela-S3	cervix:	n/a
6	chr4:22623252-22623302	SK-N-MC	brain:	n/a
7	chr4:22503787-22503837	HCM	heart:	n/a
8	chr4:22694230-22694280	AG10803	skin:	n/a
9	chr4:22517623-22517673	HRCEpiC	kidney:	n/a
10	chr4:22483053-22483103	HUVEC	blood vessel:	n/a
11	chr4:22636392-22636442	HEK293	kidney:	embryo
12	chr4:22437783-22437833	AoSMC	blood vessel:	n/a
13	chr4:22517965-22518015	HCM	heart:	n/a
14	chr4:22694667-22694717	GM06990	blood:	n/a
15	chr4:22590647-22590697	AG09309	skin:	n/a
16	chr4:22636203-22636253	GM06990	blood:	n/a
17	chr4:22517965-22518015	H1-hESC	embryonic stem cell:	embryo
18	chr4:22509445-22509495	HCT-116	colon:	n/a
19	chr4:22514419-22514469	HepG2	liver:	n/a
20	chr4:22636392-22636442	H1-hESC	embryonic stem cell:	embryo
21	chr4:22514419-22514469	A549	lung:	n/a
22	chr4:22780491-22780541	AoSMC	blood vessel:	n/a
23	chr4:22503787-22503837	GM06990	blood:	n/a
24	chr4:22518476-22518526	GM19239	blood:	n/a
25	chr4:22517623-22517673	GM19239	blood:	n/a
26	chr4:22461750-22461800	AG09309	skin:	n/a
27	chr4:22503787-22503837	HNPCEpiC	eye:	n/a
28	chr4:22818572-22818622	HPAEpiC	pulmonary alveolar:	n/a
29	chr4:22590647-22590697	HL-60	blood:	n/a
30	chr4:22517094-22517144	HEK293	kidney:	embryo
31	chr4:22588245-22588295	K562	blood:	n/a
32	chr4:22623367-22623417	Hela-S3	cervix:	n/a
33	chr4:22517965-22518015	CMK	blood:	n/a
34	chr4:22483053-22483103	MCF-7	breast:	n/a
35	chr4:22517623-22517673	HCF	heart:	n/a
36	chr4:22693739-22693789	GM19239	blood:	n/a
37	chr4:22744871-22744921	Hepatocyte	liver:	n/a
38	chr4:22518047-22518097	GM12892	blood:	n/a
39	chr4:22517195-22517245	HRE	kidney:	n/a
40	chr4:22780387-22780437	HIPEpiC	eye:	n/a
41	chr4:22694230-22694280	HIPEpiC	eye:	n/a
42	chr4:22636392-22636442	HL-60	blood:	n/a
43	chr4:22588245-22588295	PANC-1	pancreas:	n/a
44	chr4:22694667-22694717	PrEC	prostate:	n/a
45	chr4:22588658-22588708	HRPEpiC	eye:	n/a
46	chr4:22517094-22517144	NHBE	bronchial:	n/a
47	chr4:22502077-22502127	ECC-1	luminal epithelium:	n/a
48	chr4:22588208-22588258	T-47D	breast:	n/a
49	chr4:22520573-22520623	BJ	skin:	n/a
50	chr4:22518047-22518097	A549	lung:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:22508358..22510140-chr4:22512148..22515141,2	MCF-7	breast:
2	chr4:22497592..22500394-chr4:22516759..22518508,2	MCF-7	breast:
3	chr4:22466142..22467676-chr4:22473054..22475391,2	K562	blood:
4	chr4:22427307..22429305-chr4:22435269..22437253,2	K562	blood:
5	chr4:22516426..22520250-chr4:22520676..22526735,6	MCF-7	breast:
6	chr4:22508358..22510140-chr4:22512148..22515141,2	MCF-7	breast:
7	chr4:22642022..22643894-chr4:22646674..22649581,2	K562	blood:
8	chr4:22687079..22688984-chr4:22690023..22692580,2	MCF-7	breast:
9	chr4:22425322..22428021-chr4:22430037..22432573,2	MCF-7	breast:
10	chr4:22796834..22798825-chr4:22803164..22804695,2	K562	blood:
11	chr4:22487743..22489336-chr4:22491654..22493275,2	K562	blood:
12	chr4:22516555..22518423-chr4:22670641..22673303,2	MCF-7	breast:
13	chr4:22642022..22643894-chr4:22646674..22649581,2	K562	blood:
14	chr4:22505951..22512123-chr4:22514706..22518696,9	MCF-7	breast:
15	chr4:22457536..22463707-chr4:22514115..22518559,7	MCF-7	breast:
16	chr4:22816382..22818106-chr4:22821091..22824068,2	K562	blood:
17	chr4:22433445..22435816-chr4:22516699..22518877,2	MCF-7	breast:
18	chr4:22487490..22489243-chr4:22491775..22493390,2	K562	blood:
19	chr4:22772449..22775297-chr4:22778279..22780984,3	K562	blood:
20	chr4:22684475..22686472-chr4:22689943..22692504,2	K562	blood:
21	chr4:22487490..22489243-chr4:22491775..22493390,2	K562	blood:
22	chr4:22508191..22514199-chr4:22515176..22519559,12	MCF-7	breast:
23	chr4:22575405..22577612-chr4:22584979..22587113,2	MCF-7	breast:
24	chr4:22412171..22412954-chr4:22692156..22692748,2	K562	blood:
25	chr15:93347439..93348346-chr4:22517806..22518476,2	Hela-S3	cervix:
26	chr18:12076450..12076959-chr4:22517248..22517778,2	HCT-116	colon:
27	chr4:22449726..22452368-chr4:22458347..22461364,3	MCF-7	breast:
28	chr4:22465182..22467125-chr4:22517057..22519339,2	MCF-7	breast:
29	chr18:24510025..24511017-chr4:22608413..22609080,2	MCF-7	breast:
30	chr4:22844491..22847403-chr4:22848956..22850580,3	K562	blood:
31	chr4:22507819..22511270-chr4:22511320..22514443,4	MCF-7	breast:
32	chr4:22516473..22518364-chr4:22531777..22533372,2	MCF-7	breast:
33	chr4:22645860..22647619-chr4:22652276..22653871,2	K562	blood:
34	chr4:22466667..22470398-chr4:22474006..22476709,3	MCF-7	breast:
35	chr4:22437735..22439383-chr4:22516765..22518580,2	MCF-7	breast:
36	chr4:22503270..22505334-chr4:22512826..22515443,2	MCF-7	breast:
37	chr4:22452403..22454410-chr4:22458067..22459809,2	MCF-7	breast:
38	chr4:22449726..22452368-chr4:22458347..22461364,3	MCF-7	breast:
39	chr4:22844491..22847403-chr4:22848956..22850580,3	K562	blood:
40	chr10:75007030..75007602-chr4:22476562..22477062,2	Hela-S3	cervix:
41	chr4:22452403..22454410-chr4:22458067..22459809,2	MCF-7	breast:
42	chr4:22466142..22467676-chr4:22473054..22475391,2	K562	blood:
43	chr4:22816382..22818106-chr4:22821091..22824068,2	K562	blood:
44	chr4:22843905..22846646-chr4:22849080..22850791,2	K562	blood:
45	chr4:22488399..22490950-chr4:22493521..22495053,2	MCF-7	breast:
46	chr4:22436354..22437178-chr4:22608677..22609430,4	MCF-7	breast:
47	chr4:22501387..22504925-chr4:22515596..22518632,4	MCF-7	breast:
48	chr4:22796834..22798825-chr4:22803164..22804695,2	K562	blood:
49	chr4:22645860..22647619-chr4:22652276..22653871,2	K562	blood:
50	chr4:22843905..22846646-chr4:22849080..22850791,2	K562	blood:

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

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

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
ENSG00000138768	chromatin interactions
ENSG00000251516	chromatin interactions
ENSG00000256616	chromatin interactions
ENSG00000138757	chromatin interactions
ENSG00000236756	chromatin interactions
ENSG00000152990	chromatin interactions

Extended variants
information (count: 14675 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:14675 , 50 per page) page: 1 2 3 4 5 6 7 ... 294

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571112130	chr4:22427076-22427077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538112930	chr4:22427078-22427079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550374072	chr4:22427089-22427090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369904307	chr4:22427106-22427107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150620850	chr4:22427142-22427143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535580561	chr4:22427160-22427161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs716411	chr4:22427198-22427199	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs572118743	chr4:22427230-22427231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114153009	chr4:22427237-22427238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190273882	chr4:22427255-22427256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1392594	chr4:22427261-22427262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543323296	chr4:22427266-22427267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182903453	chr4:22427307-22427308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572397901	chr4:22427323-22427324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573484049	chr4:22427329-22427330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138677205	chr4:22427351-22427352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187583938	chr4:22427355-22427356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527723721	chr4:22427368-22427369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552547547	chr4:22427373-22427374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564298135	chr4:22427383-22427384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143121494	chr4:22427388-22427389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533818705	chr4:22427424-22427425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550193953	chr4:22427437-22427438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73112127	chr4:22427500-22427501	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs536053727	chr4:22427563-22427564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547555589	chr4:22427598-22427599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370051748	chr4:22427610-22427611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539114651	chr4:22427615-22427616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193229554	chr4:22427649-22427650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184038199	chr4:22427679-22427680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147494219	chr4:22427680-22427681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113480746	chr4:22427717-22427718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139976329	chr4:22427724-22427725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574871859	chr4:22427736-22427737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148366074	chr4:22427757-22427758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543866832	chr4:22427769-22427770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559078450	chr4:22427771-22427772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7669616	chr4:22427773-22427774	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs531490521	chr4:22427778-22427779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370512309	chr4:22427821-22427822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145586307	chr4:22427859-22427860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147295680	chr4:22427928-22427929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551712224	chr4:22428040-22428041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531587682	chr4:22428041-22428042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550543506	chr4:22428058-22428059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74992753	chr4:22428129-22428130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187829536	chr4:22428133-22428134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548014208	chr4:22428150-22428151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148802225	chr4:22428167-22428168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533063675	chr4:22428177-22428178	Weak transcription Strong 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:3417 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22371600-22449800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:22383200-22438000	Weak transcription	Lung	lung
3	chr4:22383600-22442800	Weak transcription	A549	lung
4	chr4:22385400-22430400	Weak transcription	Psoas Muscle	Psoas
5	chr4:22386000-22446600	Weak transcription	Fetal Thymus	thymus
6	chr4:22388200-22432400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:22388200-22442800	Weak transcription	Brain Germinal Matrix	brain
8	chr4:22388400-22473600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr4:22388800-22469600	Weak transcription	Colonic Mucosa	Colon
10	chr4:22389200-22473600	Weak transcription	Fetal Brain Male	brain
11	chr4:22390600-22439600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr4:22390600-22456200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr4:22390600-22459800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr4:22390800-22429400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr4:22393000-22435200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:22393400-22444800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:22393600-22459800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:22393800-22446400	Weak transcription	NH-A	brain
19	chr4:22393800-22453000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:22397000-22428400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:22399800-22442800	Weak transcription	Fetal Brain Female	brain
22	chr4:22400000-22448000	Weak transcription	Left Ventricle	heart
23	chr4:22400800-22429200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr4:22400800-22430000	Weak transcription	Adipose Nuclei	Adipose
25	chr4:22400800-22449600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:22400800-22461800	Weak transcription	Gastric	stomach
27	chr4:22401200-22431000	Weak transcription	Ovary	ovary
28	chr4:22405400-22446000	Weak transcription	Pancreas	Pancrea
29	chr4:22412800-22446000	Weak transcription	Thymus	Thymus
30	chr4:22414600-22430000	Weak transcription	Fetal Heart	heart
31	chr4:22415200-22430200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr4:22416800-22449600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:22417600-22442200	Weak transcription	Hela-S3	cervix
34	chr4:22417800-22436200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr4:22418000-22435200	Strong transcription	Liver	Liver
36	chr4:22418800-22427400	Strong transcription	Rectal Mucosa Donor 31	rectum
37	chr4:22419000-22427200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:22419200-22428800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:22419200-22476200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:22419400-22465800	Weak transcription	HUVEC	blood vessel
41	chr4:22419600-22428200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:22419800-22428000	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr4:22420200-22427400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:22420200-22436400	Weak transcription	Colon Smooth Muscle	Colon
45	chr4:22420600-22488000	Weak transcription	Aorta	Aorta
46	chr4:22420800-22428600	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr4:22420800-22436400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr4:22421200-22442600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr4:22422000-22441400	Weak transcription	Right Ventricle	heart
50	chr4:22422000-22453400	Weak transcription	Esophagus	oesophagus

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