Variant report

Variant	esv2755442
Chromosome Location	chr3:17372796-17589896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1537)
CpG islands
(count:61)
Chromatin interactive
region (count:106)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1537 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:17484122-17484922	K562	blood:	n/a	n/a
2	ARID3A	chr3:17506407-17506512	K562	blood:	n/a	n/a
3	ARID3A	chr3:17486399-17486776	K562	blood:	n/a	n/a
4	ARID3A	chr3:17462080-17462754	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:17454500-17454738	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:17414297-17414619	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:17472416-17472770	K562	blood:	n/a	n/a
8	ATF1	chr3:17486434-17486698	K562	blood:	n/a	n/a
9	ATF1	chr3:17520229-17520516	K562	blood:	n/a	n/a
10	ATF1	chr3:17380747-17381109	K562	blood:	n/a	n/a
11	ATF1	chr3:17472550-17472822	K562	blood:	n/a	n/a
12	ATF1	chr3:17484018-17484387	K562	blood:	n/a	n/a
13	ATF1	chr3:17484669-17484932	K562	blood:	n/a	n/a
14	ATF1	chr3:17410725-17410748	K562	blood:	n/a	n/a
15	ATF1	chr3:17375418-17375715	K562	blood:	n/a	n/a
16	ATF2	chr3:17440604-17441083	GM12878	blood:	n/a	n/a
17	ATF2	chr3:17440529-17441152	GM12878	blood:	n/a	n/a
18	ATF3	chr3:17520011-17520619	A549	lung:	n/a	n/a
19	ATF3	chr3:17520058-17520526	A549	lung:	n/a	n/a
20	ATF3	chr3:17484214-17484440	K562	blood:	n/a	n/a
21	ATF3	chr3:17484191-17484365	K562	blood:	n/a	n/a
22	ATF3	chr3:17486331-17486754	K562	blood:	n/a	n/a
23	BACH1	chr3:17474299-17474445	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr3:17473755-17474077	H1-hESC	embryonic stem cell:	n/a	chr3:17473906-17473920
25	BACH1	chr3:17473751-17474065	K562	blood:	n/a	chr3:17473906-17473920
26	BACH1	chr3:17539622-17539654	K562	blood:	n/a	n/a
27	BATF	chr3:17440584-17441027	GM12878	blood:	n/a	n/a
28	BATF	chr3:17440687-17441050	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:17440655-17441034	GM12878	blood:	n/a	chr3:17440792-17440801
30	BCL11A	chr3:17440636-17441099	GM12878	blood:	n/a	chr3:17440792-17440801
31	BCL11A	chr3:17378630-17378839	GM12878	blood:	n/a	n/a
32	BCL3	chr3:17520027-17520714	A549	lung:	n/a	n/a
33	BCL3	chr3:17556772-17557520	A549	lung:	n/a	n/a
34	BCLAF1	chr3:17440538-17441322	GM12878	blood:	n/a	chr3:17440792-17440801
35	BCLAF1	chr3:17440619-17441234	GM12878	blood:	n/a	chr3:17440792-17440801
36	BHLHE40	chr3:17520199-17520344	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:17484668-17485011	K562	blood:	n/a	n/a
38	BHLHE40	chr3:17462222-17462436	K562	blood:	n/a	n/a
39	BHLHE40	chr3:17380693-17381093	K562	blood:	n/a	n/a
40	BHLHE40	chr3:17462223-17462521	HepG2	liver:	n/a	n/a
41	BHLHE40	chr3:17440644-17441042	GM12878	blood:	n/a	n/a
42	BHLHE40	chr3:17428087-17428202	K562	blood:	n/a	n/a
43	BRCA1	chr3:17454624-17454755	HepG2	liver:	n/a	n/a
44	BRCA1	chr3:17556814-17557449	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr3:17519940-17520632	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr3:17484569-17485167	K562	blood:	n/a	n/a
47	CBX3	chr3:17484048-17484463	K562	blood:	n/a	n/a
48	CCNT2	chr3:17472494-17472658	K562	blood:	n/a	n/a
49	CCNT2	chr3:17410588-17410779	K562	blood:	n/a	n/a
50	CCNT2	chr3:17380766-17381064	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:17375660-17375710	HEEpiC	esophagus:	n/a
2	chr3:17375660-17375710	GM12891	blood:	n/a
3	chr3:17375660-17375710	HCT-116	colon:	n/a
4	chr3:17375660-17375710	AG04449	skin:	fetal
5	chr3:17375660-17375710	RPTEC	kidney:	n/a
6	chr3:17375660-17375710	K562	blood:	n/a
7	chr3:17375660-17375710	HRCEpiC	kidney:	n/a
8	chr3:17375660-17375710	PrEC	prostate:	n/a
9	chr3:17375660-17375710	ovcar-3	ovarian:	n/a
10	chr3:17375660-17375710	SK-N-MC	brain:	n/a
11	chr3:17375660-17375710	AG09309	skin:	n/a
12	chr3:17375660-17375710	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:17375660-17375710	Jurkat	blood:	n/a
14	chr3:17375660-17375710	AG04450	lung:	fetal
15	chr3:17375660-17375710	AG09319	gingival:	n/a
16	chr3:17375660-17375710	LNCaP	prostate:	n/a
17	chr3:17375660-17375710	SAEC	small airway:	n/a
18	chr3:17375660-17375710	HIPEpiC	eye:	n/a
19	chr3:17375660-17375710	GM06990	blood:	n/a
20	chr3:17375660-17375710	HRPEpiC	eye:	n/a
21	chr3:17375660-17375710	ECC-1	luminal epithelium:	n/a
22	chr3:17375660-17375710	GM19239	blood:	n/a
23	chr3:17375660-17375710	GM12878	blood:	n/a
24	chr3:17375660-17375710	AoSMC	blood vessel:	n/a
25	chr3:17375660-17375710	H1-hESC	embryonic stem cell:	embryo
26	chr3:17375660-17375710	Hela-S3	cervix:	n/a
27	chr3:17375660-17375710	ProgFib	skin:	n/a
28	chr3:17375660-17375710	HRE	kidney:	n/a
29	chr3:17375660-17375710	NHDF-neo	bronchial:	n/a
30	chr3:17375660-17375710	HUVEC	blood vessel:	n/a
31	chr3:17375660-17375710	NT2-D1	testis:	n/a
32	chr3:17375660-17375710	HCPEpiC	choroid plexus:	n/a
33	chr3:17375660-17375710	T-47D	breast:	n/a
34	chr3:17375660-17375710	A549	lung:	n/a
35	chr3:17375660-17375710	NHBE	bronchial:	n/a
36	chr3:17375660-17375710	MCF10A-Er-Src	breast:	n/a
37	chr3:17375660-17375710	SKMC	muscle:	n/a
38	chr3:17375660-17375710	CMK	blood:	n/a
39	chr3:17375660-17375710	AG10803	skin:	n/a
40	chr3:17375660-17375710	SK-N-SH_RA	brain:	n/a
41	chr3:17375660-17375710	BJ	skin:	n/a
42	chr3:17375660-17375710	PANC-1	pancreas:	n/a
43	chr3:17375660-17375710	HMEC	breast:	n/a
44	chr3:17375660-17375710	SK-N-SH	brain:	n/a
45	chr3:17375660-17375710	BE2_C	brain:	n/a
46	chr3:17375660-17375710	HEK293	kidney:	embryo
47	chr3:17375660-17375710	IMR90	lung:	fetal
48	chr3:17375660-17375710	HCM	heart:	n/a
49	chr3:17375660-17375710	NB4	blood:	n/a
50	chr3:17375660-17375710	HepG2	liver:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:17464487..17468576-chr3:17470106..17473767,3	K562	blood:
2	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
3	chr3:17396023..17398371-chr3:17401669..17406284,4	K562	blood:
4	chr3:17416222..17418689-chr3:177528351..177530087,2	MCF-7	breast:
5	chr3:17568665..17570764-chr3:17576211..17578088,2	K562	blood:
6	chr3:17454364..17456492-chr3:17782379..17784281,3	MCF-7	breast:
7	chr3:17507187..17509434-chr3:17516355..17517975,2	MCF-7	breast:
8	chr3:17472682..17474282-chr3:17477579..17479223,2	K562	blood:
9	chr3:17460223..17462241-chr3:17894481..17896425,2	K562	blood:
10	chr3:17454593..17456440-chr3:17885577..17887079,2	MCF-7	breast:
11	chr3:17568233..17570772-chr3:17578464..17581290,2	K562	blood:
12	chr3:17497865..17499392-chr3:17503466..17506313,2	K562	blood:
13	chr3:17463498..17465841-chr3:17880192..17882882,2	MCF-7	breast:
14	chr3:17348706..17349625-chr3:17454224..17455498,4	K562	blood:
15	chr3:17485709..17487231-chr3:17783472..17786007,2	MCF-7	breast:
16	chr3:17444789..17447315-chr3:17447509..17449518,2	K562	blood:
17	chr3:17422120..17423958-chr3:17425722..17427286,2	MCF-7	breast:
18	chr3:17454330..17455065-chr3:17882486..17883391,2	K562	blood:
19	chr3:17563803..17565634-chr3:17567663..17570561,2	K562	blood:
20	chr3:17568665..17570764-chr3:17576211..17578088,2	K562	blood:
21	chr3:17356582..17359217-chr3:17376177..17378852,2	K562	blood:
22	chr3:17472134..17473149-chr3:17882441..17883393,5	K562	blood:
23	chr3:17379266..17381414-chr3:17386498..17389458,2	K562	blood:
24	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
25	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
26	chr3:17300011..17301671-chr3:17454009..17455084,9	MCF-7	breast:
27	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
28	chr3:17585640..17587263-chr3:17782584..17784641,2	MCF-7	breast:
29	chr3:17561404..17563252-chr3:17564613..17567165,2	K562	blood:
30	chr3:17484813..17486609-chr3:17782332..17783917,2	MCF-7	breast:
31	chr3:17561404..17563252-chr3:17564613..17567165,2	K562	blood:
32	chr3:17464487..17468576-chr3:17470106..17473767,3	K562	blood:
33	chr3:17574853..17577476-chr3:17578727..17581379,2	K562	blood:
34	chr3:17322980..17323870-chr3:17472180..17472688,2	K562	blood:
35	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
36	chr3:17497865..17499392-chr3:17503466..17506313,2	K562	blood:
37	chr3:17463709..17467146-chr3:17467192..17469844,3	K562	blood:
38	chr3:17472139..17473280-chr3:17881966..17883098,4	MCF-7	breast:
39	chr3:17472087..17473109-chr3:17882519..17883281,4	MCF-7	breast:
40	chr3:17299444..17301149-chr3:17449495..17452150,2	K562	blood:
41	chr3:17585835..17588259-chr3:17590207..17593064,3	K562	blood:
42	chr3:17422120..17423958-chr3:17425722..17427286,2	MCF-7	breast:
43	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
44	chr3:17381699..17383887-chr3:17396874..17399021,2	MCF-7	breast:
45	chr3:17459732..17461276-chr3:17463158..17466015,2	MCF-7	breast:
46	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
47	chr3:17374826..17377586-chr3:17377790..17379356,2	K562	blood:
48	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
49	chr3:17379266..17381414-chr3:17386498..17389458,2	K562	blood:
50	chr3:17348679..17349303-chr3:17454556..17455118,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAZL-5	chr3:17413567-17413626	NONHSAT088543
2	lnc-DAZL-5	chr3:17378881-17379128	NONHSAT088543
3	lnc-DAZL-5	chr3:17379941-17380067	NONHSAT088543
4	lnc-SATB1-7	chr3:17567733-17568134	uc_483_-
5	lnc-DAZL-5	chr3:17382147-17382187	NONHSAT088543
6	lnc-PLCL2-7	chr3:17374618-17374923	NONHSAT088542
7	lnc-PLCL2-9	chr3:17567733-17568134	uc_483_+
8	lnc-SATB1-8	chr3:17550041-17550097	NONHSAT088551
9	lnc-PLCL2-8	chr3:17506642-17507002	NONHSAT088548

No data

Variant related genes	Relation type
TBC1D5	TF binding region
ENSG00000231780	TF binding region
ENSG00000227309	TF binding region
TBC1D5	CpG island
ENSG00000231780	CpG island
ENSG00000227309	CpG island
ENSG00000131374	chromatin interactions

Extended variants
information (count: 7807 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:7807 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532758081	chr3:17372813-17372814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543062479	chr3:17372865-17372866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182886380	chr3:17372874-17372875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73145817	chr3:17372887-17372888	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs185483446	chr3:17372896-17372897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189949927	chr3:17372964-17372965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150810989	chr3:17372973-17372974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139143641	chr3:17372977-17372978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571837948	chr3:17372985-17372986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576724457	chr3:17373002-17373003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571206128	chr3:17373068-17373069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546222002	chr3:17373173-17373174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144077368	chr3:17373181-17373182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556630385	chr3:17373200-17373201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146487374	chr3:17373286-17373287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73145818	chr3:17373320-17373321	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs139851015	chr3:17373342-17373343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541971183	chr3:17373343-17373344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143287226	chr3:17373384-17373385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182257026	chr3:17373410-17373411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577546359	chr3:17373424-17373425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542978671	chr3:17373436-17373437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73145819	chr3:17373497-17373498	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs113011540	chr3:17373508-17373509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528934269	chr3:17373523-17373524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112420823	chr3:17373588-17373589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531129057	chr3:17373627-17373628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551191575	chr3:17373634-17373635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564809690	chr3:17373659-17373660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527945336	chr3:17373704-17373705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548036971	chr3:17373714-17373715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547778634	chr3:17373837-17373838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567624241	chr3:17373947-17373948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533685103	chr3:17373952-17373953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550171324	chr3:17374019-17374020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569953677	chr3:17374097-17374098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187512785	chr3:17374118-17374119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555572636	chr3:17374144-17374145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566213650	chr3:17374158-17374159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534490140	chr3:17374225-17374226	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs372583871	chr3:17374335-17374336	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199951693	chr3:17374376-17374377	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374448793	chr3:17374416-17374417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192661767	chr3:17374432-17374433	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577485954	chr3:17374467-17374468	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115559079	chr3:17374484-17374485	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556872897	chr3:17374507-17374508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573543980	chr3:17374582-17374583	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115218466	chr3:17374599-17374600	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552178211	chr3:17374600-17374601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
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
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	21364760	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1672 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17298800-17373000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr3:17330800-17381400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:17333400-17376000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr3:17339400-17442200	Weak transcription	Fetal Intestine Small	intestine
5	chr3:17344400-17439000	Weak transcription	Aorta	Aorta
6	chr3:17352000-17377600	Weak transcription	Dnd41	blood
7	chr3:17354800-17381600	Weak transcription	Ovary	ovary
8	chr3:17356200-17412800	Weak transcription	Left Ventricle	heart
9	chr3:17356800-17390000	Weak transcription	Fetal Muscle Trunk	muscle
10	chr3:17358000-17377600	Weak transcription	Adipose Nuclei	Adipose
11	chr3:17362000-17376200	Weak transcription	Fetal Kidney	kidney
12	chr3:17362800-17382200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr3:17364600-17387600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr3:17364800-17375400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr3:17364800-17381800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr3:17365000-17377800	Weak transcription	Fetal Heart	heart
17	chr3:17365200-17383400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr3:17365400-17390000	Weak transcription	GM12878-XiMat	blood
19	chr3:17365600-17374200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:17365600-17377200	Weak transcription	Primary T cells from cord blood	blood
21	chr3:17365600-17413000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr3:17368400-17381600	Weak transcription	Psoas Muscle	Psoas
23	chr3:17368400-17384200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr3:17370000-17406200	Weak transcription	Primary B cells from peripheral blood	blood
25	chr3:17370800-17411000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr3:17372400-17372800	ZNF genes & repeats	Primary B cells from cord blood	blood
27	chr3:17372400-17372800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr3:17372400-17410600	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr3:17372800-17374200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:17372800-17375800	Strong transcription	Primary B cells from cord blood	blood
31	chr3:17374200-17375000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr3:17374200-17375800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr3:17375000-17380600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr3:17375200-17375600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr3:17375200-17376000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:17375200-17376200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:17375200-17376200	Enhancers	K562	blood
38	chr3:17375400-17376000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr3:17375400-17376000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr3:17375600-17376000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:17375600-17376000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr3:17375800-17377200	Weak transcription	Primary B cells from cord blood	blood
43	chr3:17375800-17377800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:17377000-17377200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr3:17377200-17378000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:17377200-17381200	Strong transcription	Primary B cells from cord blood	blood
47	chr3:17377600-17378000	Enhancers	Adipose Nuclei	Adipose
48	chr3:17377600-17378000	Enhancers	Rectal Smooth Muscle	rectum
49	chr3:17377600-17378200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr3:17377600-17378200	Strong transcription	Dnd41	blood

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