Variant report

Variant	esv3335628
Chromosome Location	chr3:48010796-48074001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:704)
CpG islands
(count:244)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:48057088-48057922	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:48057039-48058435	K562	blood:	n/a	n/a
3	ARID3A	chr3:48069284-48069357	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:48054631-48055618	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:48054505-48055466	K562	blood:	n/a	n/a
6	ARID3A	chr3:48031320-48031798	K562	blood:	n/a	n/a
7	ARID3A	chr3:48031457-48031798	HepG2	liver:	n/a	n/a
8	ATF1	chr3:48054827-48055195	K562	blood:	n/a	n/a
9	ATF3	chr3:48054739-48055164	K562	blood:	n/a	n/a
10	BACH1	chr3:48018552-48018725	K562	blood:	n/a	n/a
11	BATF	chr3:48071750-48071946	GM12878	blood:	n/a	chr3:48071880-48071891
12	BATF	chr3:48071719-48071974	GM12878	blood:	n/a	chr3:48071749-48071758 chr3:48071880-48071891
13	BHLHE40	chr3:48031473-48031793	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:48064950-48065178	HepG2	liver:	n/a	n/a
15	BHLHE40	chr3:48057741-48058426	K562	blood:	n/a	n/a
16	BHLHE40	chr3:48031454-48031801	K562	blood:	n/a	n/a
17	BRCA1	chr3:48025601-48026117	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr3:48046088-48046650	K562	blood:	n/a	n/a
19	CCNT2	chr3:48057781-48058084	K562	blood:	n/a	n/a
20	CCNT2	chr3:48054950-48055415	K562	blood:	n/a	n/a
21	CCNT2	chr3:48031447-48031765	K562	blood:	n/a	n/a
22	CEBPB	chr3:48031437-48031847	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:48047168-48047335	IMR90	lung:	n/a	n/a
24	CEBPB	chr3:48060225-48060832	A549	lung:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
25	CEBPB	chr3:48043494-48043806	K562	blood:	n/a	chr3:48043681-48043692
26	CEBPB	chr3:48060325-48060695	Hela-S3	cervix:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
27	CEBPB	chr3:48070172-48070327	K562	blood:	n/a	n/a
28	CEBPB	chr3:48060321-48060841	HCT-116	colon:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
29	CEBPB	chr3:48041755-48042054	K562	blood:	n/a	chr3:48041917-48041928 chr3:48041919-48041928
30	CEBPB	chr3:48041743-48042079	HepG2	liver:	n/a	chr3:48041917-48041928 chr3:48041919-48041928
31	CEBPB	chr3:48069101-48069375	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:48060310-48060839	IMR90	lung:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
33	CEBPB	chr3:48024419-48024514	H1-hESC	embryonic stem cell:	n/a	chr3:48024443-48024454
34	CEBPB	chr3:48024423-48024443	HepG2	liver:	n/a	n/a
35	CEBPB	chr3:48060470-48060670	H1-hESC	embryonic stem cell:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
36	CEBPB	chr3:48060374-48060626	MCF-7	breast:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
37	CEBPB	chr3:48060345-48060685	HepG2	liver:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
38	CEBPB	chr3:48060333-48060687	A549	lung:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
39	CEBPB	chr3:48024333-48024595	K562	blood:	n/a	chr3:48024443-48024454
40	CEBPB	chr3:48041800-48042018	HepG2	liver:	n/a	chr3:48041917-48041928 chr3:48041919-48041928
41	CEBPB	chr3:48024378-48024537	A549	lung:	n/a	chr3:48024443-48024454
42	CEBPB	chr3:48069178-48069321	K562	blood:	n/a	n/a
43	CEBPB	chr3:48031431-48031827	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr3:48069121-48069379	HepG2	liver:	n/a	n/a
45	CEBPB	chr3:48060346-48060657	K562	blood:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
46	CEBPB	chr3:48024390-48024572	IMR90	lung:	n/a	chr3:48024443-48024454
47	CEBPB	chr3:48043634-48043719	H1-hESC	embryonic stem cell:	n/a	chr3:48043681-48043692
48	CEBPB	chr3:48060245-48060853	HCT-116	colon:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
49	CEBPB	chr3:48060279-48060674	A549	lung:	n/a	chr3:48060496-48060507 chr3:48060495-48060508 chr3:48060495-48060508
50	CEBPB	chr3:48043532-48043844	HepG2	liver:	n/a	chr3:48043681-48043692

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:48056973-48057023	HMEC	breast:	n/a
2	chr3:48031771-48031821	NHDF-neo	bronchial:	n/a
3	chr3:48031771-48031821	U87	brain:	n/a
4	chr3:48018675-48018725	HIPEpiC	eye:	n/a
5	chr3:48016946-48016996	PANC-1	pancreas:	n/a
6	chr3:48056973-48057023	SK-N-SH	brain:	n/a
7	chr3:48031771-48031821	H1-hESC	embryonic stem cell:	embryo
8	chr3:48056973-48057023	AG04450	lung:	fetal
9	chr3:48018675-48018725	K562	blood:	n/a
10	chr3:48056973-48057023	GM12878	blood:	n/a
11	chr3:48016946-48016996	HNPCEpiC	eye:	n/a
12	chr3:48018675-48018725	A549	lung:	n/a
13	chr3:48056973-48057023	AG09319	gingival:	n/a
14	chr3:48056973-48057023	NT2-D1	testis:	n/a
15	chr3:48016946-48016996	H1-hESC	embryonic stem cell:	embryo
16	chr3:48031771-48031821	HL-60	blood:	n/a
17	chr3:48031771-48031821	NT2-D1	testis:	n/a
18	chr3:48018675-48018725	HRPEpiC	eye:	n/a
19	chr3:48056973-48057023	HIPEpiC	eye:	n/a
20	chr3:48018675-48018725	HEEpiC	esophagus:	n/a
21	chr3:48056973-48057023	HCT-116	colon:	n/a
22	chr3:48056973-48057023	GM06990	blood:	n/a
23	chr3:48056973-48057023	ovcar-3	ovarian:	n/a
24	chr3:48056973-48057023	GM12891	blood:	n/a
25	chr3:48056973-48057023	RPTEC	kidney:	n/a
26	chr3:48056973-48057023	LNCaP	prostate:	n/a
27	chr3:48031771-48031821	HEEpiC	esophagus:	n/a
28	chr3:48018675-48018725	AG04450	lung:	fetal
29	chr3:48018675-48018725	PrEC	prostate:	n/a
30	chr3:48031771-48031821	ovcar-3	ovarian:	n/a
31	chr3:48016946-48016996	AG04449	skin:	fetal
32	chr3:48056973-48057023	HAEpiC	amniotic membrane:	n/a
33	chr3:48016946-48016996	Caco-2	colon:	n/a
34	chr3:48056973-48057023	H1-hESC	embryonic stem cell:	embryo
35	chr3:48031771-48031821	T-47D	breast:	n/a
36	chr3:48018675-48018725	HMEC	breast:	n/a
37	chr3:48031771-48031821	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:48018675-48018725	HEK293	kidney:	embryo
39	chr3:48056973-48057023	PFSK-1	brain:	n/a
40	chr3:48018675-48018725	HepG2	liver:	n/a
41	chr3:48016946-48016996	BJ	skin:	n/a
42	chr3:48031771-48031821	HUVEC	blood vessel:	n/a
43	chr3:48031771-48031821	SK-N-SH_RA	brain:	n/a
44	chr3:48031771-48031821	IMR90	lung:	fetal
45	chr3:48018675-48018725	HRE	kidney:	n/a
46	chr3:48031771-48031821	ProgFib	skin:	n/a
47	chr3:48031771-48031821	PANC-1	pancreas:	n/a
48	chr3:48031771-48031821	LNCaP	prostate:	n/a
49	chr3:48056973-48057023	SAEC	small airway:	n/a
50	chr3:48031771-48031821	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:48052490..48054372-chr3:48128789..48131391,2	K562	blood:
2	chr3:48068743..48070956-chr3:48072817..48074815,2	K562	blood:
3	chr3:48051747..48053376-chr3:48056394..48058224,2	K562	blood:
4	chr3:48058679..48060813-chr3:48062111..48064582,2	K562	blood:
5	chr3:48013205..48014837-chr3:48015200..48018193,2	MCF-7	breast:
6	chr13:91363406..91364175-chr3:48057111..48057623,2	MCF-7	breast:
7	chr3:48031080..48034658-chr3:48129847..48131551,3	MCF-7	breast:
8	chr3:47865998..47866940-chr3:48031105..48032038,3	K562	blood:
9	chr3:48043535..48045129-chr3:48052756..48054615,2	MCF-7	breast:
10	chr3:47843567..47845550-chr3:48031640..48033168,2	MCF-7	breast:
11	chr3:48030090..48033252-chr3:48129181..48132220,5	MCF-7	breast:
12	chr3:48029165..48030754-chr3:48040624..48042465,2	K562	blood:
13	chr3:47891319..47892184-chr3:48031144..48032035,2	MCF-7	breast:
14	chr3:47878644..47880081-chr3:48031137..48032073,5	K562	blood:
15	chr3:48058679..48060813-chr3:48062111..48064582,2	K562	blood:
16	chr3:48063591..48066212-chr3:48130578..48132511,2	K562	blood:
17	chr3:48054884..48055678-chr3:48196667..48197285,2	K562	blood:
18	chr3:48043535..48045129-chr3:48052756..48054615,2	MCF-7	breast:
19	chr3:47890032..47891650-chr3:48032292..48034259,2	K562	blood:
20	chr3:48013205..48014837-chr3:48015200..48018193,2	MCF-7	breast:
21	chr12:94728960..94729681-chr3:48014076..48014912,2	MCF-7	breast:
22	chr3:48045100..48046973-chr3:48052739..48054972,2	K562	blood:
23	chr3:47891368..47892453-chr3:48031167..48032088,3	K562	blood:
24	chr3:48054963..48058951-chr3:48128022..48131548,4	MCF-7	breast:
25	chr3:48038125..48041271-chr3:48041821..48047334,6	K562	blood:
26	chr3:48067946..48070956-chr3:48070996..48074815,4	K562	blood:
27	chr3:48057998..48059717-chr3:48060481..48062091,2	K562	blood:
28	chr3:48045100..48046973-chr3:48052739..48054972,2	K562	blood:
29	chr3:48060391..48062688-chr3:48129264..48131215,2	K562	blood:
30	chr3:48067946..48070956-chr3:48070996..48074815,4	K562	blood:
31	chr3:48053192..48056227-chr3:48058255..48061494,4	K562	blood:
32	chr3:47896749..47899036-chr3:48026165..48028320,2	K562	blood:
33	chr3:48058931..48061886-chr3:48063600..48066605,3	MCF-7	breast:
34	chr3:48027401..48029949-chr3:48129327..48132216,3	K562	blood:
35	chr3:48029165..48030754-chr3:48040624..48042465,2	K562	blood:
36	chr3:48053192..48056227-chr3:48058255..48061494,4	K562	blood:
37	chr3:48031116..48033873-chr3:48034462..48037311,3	K562	blood:
38	chr3:48057998..48059717-chr3:48060481..48062091,2	K562	blood:
39	chr3:48058931..48061886-chr3:48063600..48066605,3	MCF-7	breast:
40	chr3:48068743..48070956-chr3:48072817..48074815,2	K562	blood:
41	chr3:48031047..48032105-chr3:48192989..48193632,3	K562	blood:
42	chr3:47889254..47892007-chr3:48021990..48024071,2	MCF-7	breast:
43	chr3:48063591..48066767-chr3:48129911..48132511,3	K562	blood:
44	chr3:48031116..48033873-chr3:48034462..48037311,3	K562	blood:
45	chr3:47884643..47886426-chr3:48028649..48030748,2	K562	blood:
46	chr3:48055864..48058624-chr3:48128858..48131357,3	MCF-7	breast:
47	chr3:48032010..48034336-chr3:48130696..48133167,2	K562	blood:

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MAP4	hsa-miR-23b-3p	chr3:48014618-48014638
2	MAP4	hsa-miR-328-3p	chr3:48016269-48016290
3	MAP4	hsa-miR-23b-3p	chr3:48014798-48014818
4	MAP4	hsa-miR-103a-3p	chr3:48016925-48016919
5	MAP4	hsa-miR-339-5p	chr3:48015903-48015924
6	MAP4	hsa-miR-92a-3p	chr3:48016702-48016724
7	MAP4	hsa-miR-23b-3p	chr3:48014624-48014618

Variant related genes	Relation type
MAP4	TF binding region
MAP4	CpG island
ENSG00000221585	chromatin interactions
ENSG00000132153	chromatin interactions
ENSG00000173588	chromatin interactions
ENSG00000047849	chromatin interactions

Extended variants
information (count: 2103 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2103 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542326477	chr3:48010814-48010815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560681368	chr3:48010904-48010905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11713022	chr3:48010906-48010907	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs200539859	chr3:48010913-48010914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79513108	chr3:48010914-48010915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192895644	chr3:48010915-48010916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs397690298	chr3:48010925-48010926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115907795	chr3:48010930-48010931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571154294	chr3:48010958-48010959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77428280	chr3:48010991-48010992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547735019	chr3:48010999-48011000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190673210	chr3:48011032-48011033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375846606	chr3:48011063-48011064	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182862503	chr3:48011157-48011158	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555179422	chr3:48011223-48011224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149826674	chr3:48011232-48011233	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115391193	chr3:48011237-48011238	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28523573	chr3:48011287-48011288	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs554433576	chr3:48011299-48011300	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572760743	chr3:48011305-48011306	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577114409	chr3:48011325-48011326	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188643386	chr3:48011329-48011330	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553746498	chr3:48011336-48011337	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9882308	chr3:48011337-48011338	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544360818	chr3:48011339-48011340	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77640742	chr3:48011349-48011350	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74427792	chr3:48011350-48011351	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74356863	chr3:48011351-48011352	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576886018	chr3:48011361-48011362	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542450809	chr3:48011366-48011367	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367633479	chr3:48011377-48011378	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531352744	chr3:48011529-48011530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145799627	chr3:48011608-48011609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564907284	chr3:48011637-48011638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9811277	chr3:48011638-48011639	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs192782962	chr3:48011644-48011645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184826916	chr3:48011647-48011648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530401966	chr3:48011702-48011703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563100954	chr3:48011723-48011724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548840015	chr3:48011736-48011737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374492234	chr3:48011742-48011743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570258227	chr3:48011770-48011771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537543771	chr3:48011778-48011779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530311474	chr3:48011805-48011806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs36116563	chr3:48011809-48011810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201551162	chr3:48011814-48011815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187695257	chr3:48011821-48011822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570838534	chr3:48011843-48011844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534678624	chr3:48011923-48011924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553318944	chr3:48011936-48011937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:1904 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47968600-48012600	Weak transcription	Primary B cells from cord blood	blood
2	chr3:47970200-48013000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr3:47970200-48016600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:47974400-48012600	Weak transcription	Osteobl	bone
5	chr3:47989800-48012400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr3:47991600-48016800	Weak transcription	Fetal Intestine Large	intestine
7	chr3:47996400-48018400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:47996600-48014600	Weak transcription	NH-A	brain
9	chr3:47996800-48016000	Weak transcription	HUVEC	blood vessel
10	chr3:47998200-48031400	Weak transcription	Brain Germinal Matrix	brain
11	chr3:48003200-48011200	Weak transcription	HSMMtube	muscle
12	chr3:48003400-48015000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:48003400-48017800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr3:48003400-48029000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:48003800-48012800	Weak transcription	Duodenum Mucosa	Duodenum
16	chr3:48003800-48013000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:48003800-48014400	Weak transcription	HSMM	muscle
18	chr3:48003800-48014800	Weak transcription	Aorta	Aorta
19	chr3:48003800-48017800	Weak transcription	Dnd41	blood
20	chr3:48003800-48018200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr3:48003800-48025600	Weak transcription	Adipose Nuclei	Adipose
22	chr3:48003800-48028400	Weak transcription	Fetal Kidney	kidney
23	chr3:48003800-48032800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr3:48003800-48034400	Weak transcription	Fetal Lung	lung
25	chr3:48003800-48034600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr3:48003800-48037200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr3:48003800-48039800	Weak transcription	Brain Angular Gyrus	brain
28	chr3:48003800-48047200	Weak transcription	Lung	lung
29	chr3:48003800-48060600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr3:48004000-48012800	Weak transcription	Primary T cells from cord blood	blood
31	chr3:48004000-48016600	Weak transcription	Fetal Muscle Leg	muscle
32	chr3:48004000-48016800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr3:48004000-48016800	Weak transcription	Thymus	Thymus
34	chr3:48004000-48017400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr3:48004000-48017600	Weak transcription	Fetal Thymus	thymus
36	chr3:48004000-48021000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr3:48004000-48022400	Weak transcription	Fetal Heart	heart
38	chr3:48004000-48024600	Weak transcription	Right Atrium	heart
39	chr3:48004000-48031400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr3:48004000-48031400	Weak transcription	Fetal Intestine Small	intestine
41	chr3:48004000-48037200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr3:48004000-48037200	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr3:48004000-48037400	Weak transcription	Right Ventricle	heart
44	chr3:48004000-48043600	Weak transcription	Small Intestine	intestine
45	chr3:48004000-48045400	Weak transcription	Placenta	Placenta
46	chr3:48004000-48046200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr3:48004000-48050600	Weak transcription	Pancreas	Pancrea
48	chr3:48004200-48018800	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr3:48004200-48025200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr3:48004200-48028400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

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