Variant report

Variant	nsv876759
Chromosome Location	chr3:47725315-47830741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1902)
CpG islands
(count:1037)
Chromatin interactive
region (count:112)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1902 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:47823180-47823697	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:47830593-47830912	K562	blood:	n/a	n/a
3	ARID3A	chr3:47824522-47824674	K562	blood:	n/a	n/a
4	ARID3A	chr3:47830586-47830896	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:47821421-47821618	K562	blood:	n/a	n/a
6	ARID3A	chr3:47802732-47802844	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:47803679-47804149	K562	blood:	n/a	n/a
8	ARID3A	chr3:47764408-47764657	K562	blood:	n/a	n/a
9	ATF1	chr3:47764380-47764693	K562	blood:	n/a	n/a
10	ATF1	chr3:47803757-47804142	K562	blood:	n/a	n/a
11	ATF1	chr3:47767259-47767333	K562	blood:	n/a	n/a
12	ATF1	chr3:47830525-47830893	K562	blood:	n/a	n/a
13	ATF2	chr3:47823353-47823818	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr3:47830516-47830898	GM12878	blood:	n/a	n/a
15	ATF2	chr3:47823224-47824309	GM12878	blood:	n/a	n/a
16	ATF2	chr3:47823379-47824042	GM12878	blood:	n/a	n/a
17	ATF2	chr3:47830448-47830905	GM12878	blood:	n/a	n/a
18	ATF3	chr3:47784864-47785095	K562	blood:	n/a	n/a
19	ATF3	chr3:47803657-47804193	K562	blood:	n/a	n/a
20	ATF3	chr3:47830408-47830894	K562	blood:	n/a	n/a
21	ATF3	chr3:47767150-47767384	K562	blood:	n/a	n/a
22	ATF3	chr3:47767154-47767395	K562	blood:	n/a	n/a
23	BACH1	chr3:47822846-47823713	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr3:47823375-47824031	GM12878	blood:	n/a	n/a
25	BATF	chr3:47784422-47784787	GM12878	blood:	n/a	n/a
26	BATF	chr3:47823495-47823776	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:47823445-47823916	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:47823503-47823789	GM12878	blood:	n/a	n/a
29	BCL3	chr3:47823164-47824010	GM12878	blood:	n/a	n/a
30	BCL3	chr3:47823281-47823798	A549	lung:	n/a	n/a
31	BCLAF1	chr3:47822671-47824083	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:47830452-47830879	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:47787738-47788045	GM12878	blood:	n/a	n/a
34	BCLAF1	chr3:47821285-47821812	GM12878	blood:	n/a	chr3:47821556-47821565
35	BCLAF1	chr3:47783229-47783760	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:47822141-47824170	GM12878	blood:	n/a	chr3:47823032-47823048
37	BHLHE40	chr3:47767265-47767426	K562	blood:	n/a	n/a
38	BHLHE40	chr3:47821488-47821702	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:47803848-47804062	K562	blood:	n/a	n/a
40	BHLHE40	chr3:47824471-47824790	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:47822804-47823739	HepG2	liver:	n/a	chr3:47823032-47823048
42	BHLHE40	chr3:47819410-47819570	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:47822472-47823929	K562	blood:	n/a	chr3:47823032-47823048
44	BHLHE40	chr3:47819897-47820060	GM12878	blood:	n/a	n/a
45	BHLHE40	chr3:47764462-47764591	K562	blood:	n/a	n/a
46	BHLHE40	chr3:47830608-47830760	K562	blood:	n/a	n/a
47	BRCA1	chr3:47821939-47822883	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr3:47823134-47823695	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr3:47823134-47823621	HepG2	liver:	n/a	n/a
50	BRCA1	chr3:47823030-47823762	GM12878	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47823638-47823688	NHDF-neo	bronchial:	n/a
2	chr3:47823820-47823870	IMR90	lung:	fetal
3	chr3:47821224-47821274	LNCaP	prostate:	n/a
4	chr3:47823524-47823574	NH-A	brain:	n/a
5	chr3:47823995-47824045	HRE	kidney:	n/a
6	chr3:47823995-47824045	MCF-7	breast:	n/a
7	chr3:47823614-47823664	HRPEpiC	eye:	n/a
8	chr3:47821224-47821274	SKMC	muscle:	n/a
9	chr3:47823674-47823724	NHDF-neo	bronchial:	n/a
10	chr3:47825578-47825628	SK-N-SH_RA	brain:	n/a
11	chr3:47823674-47823724	HepG2	liver:	n/a
12	chr3:47821924-47821974	HCT-116	colon:	n/a
13	chr3:47823121-47823171	CMK	blood:	n/a
14	chr3:47821924-47821974	HL-60	blood:	n/a
15	chr3:47827617-47827667	LNCaP	prostate:	n/a
16	chr3:47823423-47823473	SK-N-SH	brain:	n/a
17	chr3:47823531-47823581	HRE	kidney:	n/a
18	chr3:47821924-47821974	GM12892	blood:	n/a
19	chr3:47823560-47823610	AG09309	skin:	n/a
20	chr3:47823995-47824045	HRCEpiC	kidney:	n/a
21	chr3:47823614-47823664	NHBE	bronchial:	n/a
22	chr3:47823531-47823581	HepG2	liver:	n/a
23	chr3:47823638-47823688	AG04450	lung:	fetal
24	chr3:47823524-47823574	H1-hESC	embryonic stem cell:	embryo
25	chr3:47823524-47823574	AG10803	skin:	n/a
26	chr3:47823531-47823581	BJ	skin:	n/a
27	chr3:47823614-47823664	HCF	heart:	n/a
28	chr3:47823423-47823473	Jurkat	blood:	n/a
29	chr3:47823674-47823724	K562	blood:	n/a
30	chr3:47823067-47823117	ovcar-3	ovarian:	n/a
31	chr3:47823995-47824045	HIPEpiC	eye:	n/a
32	chr3:47823524-47823574	Caco-2	colon:	n/a
33	chr3:47823524-47823574	HL-60	blood:	n/a
34	chr3:47823820-47823870	SKMC	muscle:	n/a
35	chr3:47823067-47823117	HMEC	breast:	n/a
36	chr3:47823674-47823724	PrEC	prostate:	n/a
37	chr3:47823995-47824045	SK-N-SH	brain:	n/a
38	chr3:47823524-47823574	HIPEpiC	eye:	n/a
39	chr3:47823995-47824045	AG09309	skin:	n/a
40	chr3:47823820-47823870	HEEpiC	esophagus:	n/a
41	chr3:47823674-47823724	GM12891	blood:	n/a
42	chr3:47823638-47823688	HMEC	breast:	n/a
43	chr3:47823067-47823117	NT2-D1	testis:	n/a
44	chr3:47823820-47823870	CMK	blood:	n/a
45	chr3:47823674-47823724	HL-60	blood:	n/a
46	chr3:47823067-47823117	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:47823531-47823581	K562	blood:	n/a
48	chr3:47823423-47823473	AG04450	lung:	fetal
49	chr3:47823560-47823610	GM12878	blood:	n/a
50	chr3:47823560-47823610	T-47D	breast:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:47780810..47784890-chr3:47822002..47824979,5	MCF-7	breast:
2	chr3:47720048..47725540-chr3:47728543..47732832,5	K562	blood:
3	chr3:47555041..47556961-chr3:47821638..47825112,3	MCF-7	breast:
4	chr3:47809506..47818715-chr3:47820075..47824996,15	MCF-7	breast:
5	chr3:47783844..47785641-chr3:47821969..47824680,3	K562	blood:
6	chr3:47555986..47558236-chr3:47820565..47823335,2	MCF-7	breast:
7	chr3:47821014..47824119-chr3:47842599..47847365,10	K562	blood:
8	chr3:47807190..47809534-chr3:47813516..47815766,2	K562	blood:
9	chr3:47781011..47782804-chr3:47820824..47822711,2	K562	blood:
10	chr3:47769268..47771270-chr3:47773240..47775597,2	K562	blood:
11	chr3:47787198..47789332-chr3:47822441..47824997,2	K562	blood:
12	chr3:47784697..47786306-chr3:47842799..47844651,2	MCF-7	breast:
13	chr3:47822834..47823428-chr9:115479877..115480684,2	Hela-S3	cervix:
14	chr3:47713394..47715579-chr3:47725306..47727830,2	K562	blood:
15	chr3:47829358..47831275-chr4:101498989..101501516,2	MCF-7	breast:
16	chr3:47555068..47558623-chr3:47821026..47823771,5	K562	blood:
17	chr3:47738086..47739801-chr3:47743562..47745766,3	K562	blood:
18	chr3:47821651..47823502-chr3:172427414..172429681,2	MCF-7	breast:
19	chr3:47807226..47809643-chr3:47821048..47823302,2	MCF-7	breast:
20	chr3:47765531..47768373-chr3:47769962..47773520,5	K562	blood:
21	chr3:47822503..47823283-chr9:96928496..96929478,2	Hela-S3	cervix:
22	chr3:47734956..47737818-chr3:47752172..47754463,2	K562	blood:
23	chr3:47513969..47516839-chr3:47829270..47830805,2	K562	blood:
24	chr3:47819996..47824833-chr3:47866390..47869916,6	K562	blood:
25	chr3:47787622..47789169-chr3:47820606..47823344,2	MCF-7	breast:
26	chr3:47803866..47805515-chr3:47821094..47823324,2	K562	blood:
27	chr3:47787368..47790190-chr3:47793028..47795359,2	MCF-7	breast:
28	chr3:47462219..47463208-chr3:47830258..47831287,4	K562	blood:
29	chr3:47769268..47771270-chr3:47773240..47775597,2	K562	blood:
30	chr3:47798148..47800331-chr3:47801413..47803600,2	K562	blood:
31	chr3:47827524..47829723-chr3:47850586..47853080,2	K562	blood:
32	chr3:47747587..47750464-chr3:47750786..47752967,2	K562	blood:
33	chr17:70588474..70589204-chr3:47822988..47823742,2	HCT-116	colon:
34	chr3:47762182..47765006-chr3:47770740..47772875,2	K562	blood:
35	chr3:47139097..47140627-chr3:47822792..47824576,2	K562	blood:
36	chr3:47579787..47581854-chr3:47822138..47824570,2	K562	blood:
37	chr3:47788667..47790945-chr3:47792935..47794851,2	MCF-7	breast:
38	chr3:47820608..47822821-chr3:47870608..47873437,2	K562	blood:
39	chr3:47807190..47809534-chr3:47813516..47815766,2	K562	blood:
40	chr3:47822067..47822622-chr5:131825519..131826350,2	Hela-S3	cervix:
41	chr3:47830728..47832302-chr3:47832845..47835273,2	K562	blood:
42	chr3:47820857..47823354-chr3:47836932..47839468,2	K562	blood:
43	chr3:47765531..47768373-chr3:47769962..47773520,5	K562	blood:
44	chr3:47762182..47765006-chr3:47770740..47772875,2	K562	blood:
45	chr3:47799964..47802084-chr3:47803507..47806480,3	K562	blood:
46	chr3:47798148..47800331-chr3:47801413..47803600,2	K562	blood:
47	chr3:47791204..47794202-chr3:47822128..47824852,3	MCF-7	breast:
48	chr3:47738843..47740707-chr3:47820955..47824303,3	MCF-7	breast:
49	chr3:47819746..47821257-chr3:47823167..47825022,2	MCF-7	breast:
50	chr3:47772712..47775142-chr3:47820801..47823649,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000266457	TF binding region
SMARCC1	TF binding region
ENSG00000266457	CpG island
SMARCC1	CpG island
ENSG00000029363	chromatin interactions
ENSG00000114646	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000114650	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000181555	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000145012	chromatin interactions
ENSG00000173473	chromatin interactions
ENSG00000270959	chromatin interactions
ENSG00000227036	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000163832	chromatin interactions
ENSG00000266457	chromatin interactions
ENSG00000168710	chromatin interactions
ENSG00000132153	chromatin interactions
ENSG00000266443	chromatin interactions
ENSG00000144959	chromatin interactions
ENSG00000125347	chromatin interactions
ENSG00000148153	chromatin interactions
ENSG00000124688	chromatin interactions
ENSG00000160799	chromatin interactions
ENSG00000260170	chromatin interactions

Extended variants
information (count: 3665 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13063042	chr3:47725315-47725316	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7429162	chr3:47725335-47725336	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs555341973	chr3:47725367-47725368	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574614651	chr3:47725370-47725371	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535759156	chr3:47725398-47725399	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556865545	chr3:47725454-47725455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569416504	chr3:47725465-47725466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575426241	chr3:47725506-47725507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545579618	chr3:47725514-47725515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564211007	chr3:47725538-47725539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376714558	chr3:47725545-47725546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111620415	chr3:47725708-47725709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572984316	chr3:47725817-47725818	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150366419	chr3:47725826-47725827	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138045017	chr3:47725838-47725839	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561682912	chr3:47725854-47725855	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62262128	chr3:47725929-47725930	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79602213	chr3:47725931-47725932	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116026478	chr3:47725956-47725957	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112318728	chr3:47726106-47726107	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551284492	chr3:47726153-47726154	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149497329	chr3:47726170-47726171	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533613733	chr3:47726297-47726298	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183698372	chr3:47726311-47726312	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554864610	chr3:47726416-47726417	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189549981	chr3:47726452-47726453	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527799512	chr3:47726476-47726477	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181819340	chr3:47726496-47726497	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145789859	chr3:47726502-47726503	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533971626	chr3:47726511-47726512	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558525598	chr3:47726514-47726515	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567688367	chr3:47726527-47726528	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147485390	chr3:47726553-47726554	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557270661	chr3:47726578-47726579	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568950281	chr3:47726609-47726610	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539604177	chr3:47726731-47726732	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577296373	chr3:47726733-47726734	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368118957	chr3:47726761-47726762	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557987862	chr3:47726804-47726805	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184559707	chr3:47726823-47726824	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572947767	chr3:47726824-47726825	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9840012	chr3:47726863-47726864	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557209002	chr3:47726908-47726909	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540363618	chr3:47726944-47726945	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377283315	chr3:47727043-47727044	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs34711590	chr3:47727046-47727047	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs555040982	chr3:47727066-47727067	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs573627168	chr3:47727081-47727082	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs544678901	chr3:47727131-47727132	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs544567990	chr3:47727145-47727146	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:3331 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47655800-47765600	Strong transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:47656600-47790800	Strong transcription	Fetal Thymus	thymus
3	chr3:47688200-47763400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr3:47694400-47745800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:47695200-47737200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr3:47698400-47731400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr3:47700200-47757000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr3:47701200-47765000	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr3:47701200-47765600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
10	chr3:47701400-47739800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:47701600-47762200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:47701600-47800400	Strong transcription	Dnd41	blood
13	chr3:47701600-47819800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:47701800-47726800	Weak transcription	Right Atrium	heart
15	chr3:47702200-47790400	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr3:47704000-47788600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:47705600-47727200	Weak transcription	Pancreas	Pancrea
18	chr3:47705600-47742800	Weak transcription	Esophagus	oesophagus
19	chr3:47705800-47739200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr3:47706200-47728000	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr3:47707200-47737000	Strong transcription	H1 Cell Line	embryonic stem cell
22	chr3:47707200-47739400	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr3:47707200-47780800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr3:47707200-47781400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr3:47707600-47737400	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr3:47707600-47762600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr3:47708400-47737400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:47708800-47737000	Strong transcription	Duodenum Mucosa	Duodenum
29	chr3:47709000-47725600	Strong transcription	GM12878-XiMat	blood
30	chr3:47709400-47734200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:47709800-47732400	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr3:47710600-47737200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr3:47710600-47756600	Strong transcription	Placenta	Placenta
34	chr3:47711000-47759400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:47711200-47739400	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr3:47711400-47732800	Weak transcription	Stomach Mucosa	stomach
37	chr3:47711400-47757200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr3:47711600-47740200	Strong transcription	NH-A	brain
39	chr3:47713200-47737200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr3:47713200-47737400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr3:47713600-47739600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr3:47714200-47736800	Strong transcription	Primary B cells from peripheral blood	blood
43	chr3:47714200-47737000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:47714600-47742200	Weak transcription	Psoas Muscle	Psoas
45	chr3:47714800-47737000	Strong transcription	Primary T cells from cord blood	blood
46	chr3:47715400-47737200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:47715600-47725400	Strong transcription	HSMMtube	muscle
48	chr3:47716000-47745800	Weak transcription	Fetal Heart	heart
49	chr3:47716000-47747400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr3:47717800-47736200	Strong transcription	Brain Germinal Matrix	brain

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