Variant report

Variant	nsv999203
Chromosome Location	chr4:48645887-48735512
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:927)
CpG islands
(count:122)
Chromatin interactive
region (count:53)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:927 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48685726-48686787	K562	blood:	n/a	n/a
2	ARID3A	chr4:48682969-48684161	K562	blood:	n/a	chr4:48683524-48683540
3	ARID3A	chr4:48731313-48731501	K562	blood:	n/a	n/a
4	ARID3A	chr4:48669405-48669518	K562	blood:	n/a	n/a
5	ARID3A	chr4:48720801-48721430	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:48701999-48702183	K562	blood:	n/a	n/a
7	ARID3A	chr4:48700373-48700768	K562	blood:	n/a	n/a
8	ARID3A	chr4:48728717-48728995	K562	blood:	n/a	n/a
9	ARID3A	chr4:48689608-48689783	K562	blood:	n/a	n/a
10	ATF1	chr4:48683063-48683464	K562	blood:	n/a	n/a
11	ATF1	chr4:48702001-48702239	K562	blood:	n/a	n/a
12	ATF1	chr4:48700313-48700663	K562	blood:	n/a	n/a
13	ATF1	chr4:48685798-48686486	K562	blood:	n/a	n/a
14	ATF3	chr4:48685726-48686180	K562	blood:	n/a	n/a
15	BACH1	chr4:48728060-48728250	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:48691147-48691178	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:48685835-48686185	K562	blood:	n/a	n/a
18	BACH1	chr4:48701513-48701752	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:48691034-48691195	K562	blood:	n/a	n/a
20	BACH1	chr4:48728776-48728924	K562	blood:	n/a	chr4:48728786-48728800
21	BACH1	chr4:48728808-48728887	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr4:48701979-48702197	GM12878	blood:	n/a	n/a
23	BATF	chr4:48683898-48684198	GM12878	blood:	n/a	n/a
24	BATF	chr4:48655290-48655514	GM12878	blood:	n/a	n/a
25	BATF	chr4:48683946-48684210	GM12878	blood:	n/a	n/a
26	BCL3	chr4:48708896-48709192	GM12878	blood:	n/a	n/a
27	BCL3	chr4:48683910-48684220	GM12878	blood:	n/a	chr4:48684065-48684074
28	BHLHE40	chr4:48685819-48686324	K562	blood:	n/a	n/a
29	BHLHE40	chr4:48700244-48700670	K562	blood:	n/a	n/a
30	BRCA1	chr4:48700270-48700894	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr4:48728627-48728964	HCT-116	colon:	n/a	n/a
32	CBX3	chr4:48731051-48731661	K562	blood:	n/a	n/a
33	CBX3	chr4:48685712-48686197	K562	blood:	n/a	n/a
34	CCNT2	chr4:48685726-48686653	K562	blood:	n/a	chr4:48685965-48685985
35	CCNT2	chr4:48700302-48700990	K562	blood:	n/a	chr4:48700818-48700827 chr4:48700823-48700832
36	CCNT2	chr4:48683199-48683625	K562	blood:	n/a	n/a
37	CEBPB	chr4:48656435-48656564	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:48676926-48677142	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:48728237-48728535	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:48696286-48696533	A549	lung:	n/a	chr4:48696370-48696381
41	CEBPB	chr4:48710462-48710802	MCF-7	breast:	n/a	chr4:48710665-48710676
42	CEBPB	chr4:48700132-48700995	ECC-1	luminal epithelium:	n/a	chr4:48700437-48700445
43	CEBPB	chr4:48700477-48700501	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:48708466-48708744	HepG2	liver:	n/a	chr4:48708587-48708598
45	CEBPB	chr4:48701469-48701813	A549	lung:	n/a	chr4:48701627-48701638 chr4:48701627-48701636 chr4:48701625-48701636
46	CEBPB	chr4:48700215-48700721	K562	blood:	n/a	chr4:48700437-48700445
47	CEBPB	chr4:48696092-48696556	H1-hESC	embryonic stem cell:	n/a	chr4:48696370-48696381
48	CEBPB	chr4:48719515-48719727	K562	blood:	n/a	chr4:48719613-48719624
49	CEBPB	chr4:48700269-48700637	K562	blood:	n/a	chr4:48700437-48700445
50	CEBPB	chr4:48702063-48702458	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48695242-48695292	K562	blood:	n/a
2	chr4:48656001-48656051	HEEpiC	esophagus:	n/a
3	chr4:48695242-48695292	HRPEpiC	eye:	n/a
4	chr4:48695242-48695292	AoSMC	blood vessel:	n/a
5	chr4:48695242-48695292	NHBE	bronchial:	n/a
6	chr4:48695242-48695292	SAEC	small airway:	n/a
7	chr4:48656001-48656051	SK-N-SH_RA	brain:	n/a
8	chr4:48695242-48695292	ovcar-3	ovarian:	n/a
9	chr4:48695242-48695292	HL-60	blood:	n/a
10	chr4:48656001-48656051	LNCaP	prostate:	n/a
11	chr4:48695242-48695292	GM12891	blood:	n/a
12	chr4:48656001-48656051	NH-A	brain:	n/a
13	chr4:48656001-48656051	HL-60	blood:	n/a
14	chr4:48695242-48695292	U87	brain:	n/a
15	chr4:48695242-48695292	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:48695242-48695292	BJ	skin:	n/a
17	chr4:48656001-48656051	MCF-7	breast:	n/a
18	chr4:48656001-48656051	SKMC	muscle:	n/a
19	chr4:48656001-48656051	HRE	kidney:	n/a
20	chr4:48695242-48695292	HEK293	kidney:	embryo
21	chr4:48656001-48656051	U87	brain:	n/a
22	chr4:48695242-48695292	HNPCEpiC	eye:	n/a
23	chr4:48695242-48695292	HCF	heart:	n/a
24	chr4:48656001-48656051	ovcar-3	ovarian:	n/a
25	chr4:48656001-48656051	HCF	heart:	n/a
26	chr4:48695242-48695292	HRCEpiC	kidney:	n/a
27	chr4:48656001-48656051	AoSMC	blood vessel:	n/a
28	chr4:48695242-48695292	AG09319	gingival:	n/a
29	chr4:48656001-48656051	GM12892	blood:	n/a
30	chr4:48656001-48656051	NT2-D1	testis:	n/a
31	chr4:48695242-48695292	Hepatocyte	liver:	n/a
32	chr4:48695242-48695292	NT2-D1	testis:	n/a
33	chr4:48656001-48656051	T-47D	breast:	n/a
34	chr4:48656001-48656051	HMEC	breast:	n/a
35	chr4:48656001-48656051	GM19239	blood:	n/a
36	chr4:48695242-48695292	AG04450	lung:	fetal
37	chr4:48695242-48695292	PANC-1	pancreas:	n/a
38	chr4:48695242-48695292	GM12892	blood:	n/a
39	chr4:48656001-48656051	AG09319	gingival:	n/a
40	chr4:48656001-48656051	GM12878	blood:	n/a
41	chr4:48695242-48695292	Caco-2	colon:	n/a
42	chr4:48656001-48656051	HEK293	kidney:	embryo
43	chr4:48695242-48695292	CMK	blood:	n/a
44	chr4:48656001-48656051	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:48695242-48695292	Jurkat	blood:	n/a
46	chr4:48695242-48695292	HUVEC	blood vessel:	n/a
47	chr4:48656001-48656051	HUVEC	blood vessel:	n/a
48	chr4:48656001-48656051	SK-N-SH	brain:	n/a
49	chr4:48656001-48656051	NHBE	bronchial:	n/a
50	chr4:48656001-48656051	HNPCEpiC	eye:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:48691449..48693997-chr4:48694724..48696610,2	MCF-7	breast:
2	chr4:48687679..48689776-chr4:48780606..48783183,3	MCF-7	breast:
3	chr4:48689702..48692594-chr4:48697555..48699219,2	K562	blood:
4	chr4:48652508..48655525-chr4:48656294..48658905,3	K562	blood:
5	chr4:48653618..48655271-chr4:48662495..48665309,2	K562	blood:
6	chr4:48699623..48702132-chr4:48702246..48704804,2	K562	blood:
7	chr4:48652921..48654969-chr4:48656237..48658200,2	K562	blood:
8	chr4:48447376..48448138-chr4:48683597..48684250,2	K562	blood:
9	chr4:48674728..48678488-chr4:48678619..48683185,5	K562	blood:
10	chr4:48652508..48655525-chr4:48656294..48658905,3	K562	blood:
11	chr4:48699623..48702132-chr4:48702246..48705129,3	K562	blood:
12	chr4:48699623..48702132-chr4:48702246..48705129,3	K562	blood:
13	chr4:48720217..48721926-chr4:48727442..48730398,2	MCF-7	breast:
14	chr4:48685624..48689755-chr4:48691004..48694286,4	K562	blood:
15	chr4:48652921..48654969-chr4:48656237..48658200,2	K562	blood:
16	chr4:48685624..48689755-chr4:48691004..48694286,4	K562	blood:
17	chr4:48700621..48702937-chr4:48705459..48707096,2	MCF-7	breast:
18	chr4:48685998..48688837-chr4:48699802..48703602,5	K562	blood:
19	chr4:48673422..48675692-chr4:48679955..48681969,2	MCF-7	breast:
20	chr4:48699623..48702132-chr4:48702246..48704804,2	K562	blood:
21	chr4:48685998..48688837-chr4:48699802..48703602,5	K562	blood:
22	chr4:48682494..48684841-chr4:48693088..48695162,2	K562	blood:
23	chr4:48691459..48694072-chr4:48776269..48778861,2	K562	blood:
24	chr4:48653618..48655271-chr4:48662495..48665309,2	K562	blood:
25	chr4:48641539..48643469-chr4:48646667..48648214,2	K562	blood:
26	chr4:48702489..48705093-chr4:48707646..48709743,2	MCF-7	breast:
27	chr4:48686253..48688123-chr4:48780643..48783214,2	MCF-7	breast:
28	chr4:48700621..48702937-chr4:48705459..48707096,2	MCF-7	breast:
29	chr4:48684102..48685627-chr4:48698753..48700458,2	K562	blood:
30	chr4:48648727..48651631-chr4:48674696..48676832,2	K562	blood:
31	chr4:48683077..48685040-chr4:48687843..48689972,2	K562	blood:
32	chr4:48689702..48692594-chr4:48697555..48699219,2	K562	blood:
33	chr4:48674728..48678488-chr4:48678619..48683185,5	K562	blood:
34	chr4:48682524..48684809-chr4:48686998..48690088,3	K562	blood:
35	chr4:48702489..48705093-chr4:48707646..48709743,2	MCF-7	breast:
36	chr4:48687862..48689667-chr4:48836444..48838166,2	MCF-7	breast:
37	chr4:48644058..48646870-chr4:48657277..48658947,3	K562	blood:
38	chr4:48659520..48661722-chr4:48662309..48664640,2	MCF-7	breast:
39	chr4:48683162..48685673-chr4:48779626..48783041,3	MCF-7	breast:
40	chr4:48720217..48721926-chr4:48727442..48730398,2	MCF-7	breast:
41	chr4:48722783..48724508-chr4:48831559..48833358,2	MCF-7	breast:
42	chr4:48689938..48695241-chr4:48778784..48782766,5	MCF-7	breast:
43	chr4:48700525..48703151-chr4:48906796..48908721,2	MCF-7	breast:
44	chr4:48691449..48693997-chr4:48694724..48696610,2	MCF-7	breast:
45	chr4:48659520..48661722-chr4:48662309..48664640,2	MCF-7	breast:
46	chr4:48609348..48611174-chr4:48646484..48649204,2	MCF-7	breast:
47	chr4:48699629..48702108-chr4:48781751..48783665,2	MCF-7	breast:
48	chr4:48648727..48651631-chr4:48674696..48676832,2	K562	blood:
49	chr4:48684102..48685627-chr4:48698753..48700458,2	K562	blood:
50	chr4:48673422..48675692-chr4:48679955..48681969,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCIAD2-3	chr4:48729448-48729508	NONHSAT096293
2	lnc-OCIAD2-3	chr4:48686690-48686812	NONHSAT096292
3	lnc-OCIAD2-3	chr4:48712536-48712715	NONHSAT096290
4	lnc-OCIAD2-3	chr4:48686690-48686812	NONHSAT096293
5	lnc-OCIAD2-3	chr4:48686690-48686812	NONHSAT096291
6	lnc-OCIAD2-3	chr4:48647986-48648034	NONHSAT096293
7	lnc-OCIAD2-3	chr4:48712536-48712715	NONHSAT096293

No data

Variant related genes	Relation type
FRYL	TF binding region
FRYL	CpG island
ENSG00000075539	chromatin interactions
ENSG00000109180	chromatin interactions

Extended variants
information (count: 3051 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3051 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141910929	chr4:48645921-48645922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76684825	chr4:48645976-48645977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553170586	chr4:48645991-48645992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146400408	chr4:48646030-48646031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542314884	chr4:48646037-48646038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377630600	chr4:48646063-48646064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563876833	chr4:48646065-48646066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182567012	chr4:48646110-48646111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529429104	chr4:48646158-48646159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185688362	chr4:48646179-48646180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190596490	chr4:48646187-48646188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533210870	chr4:48646237-48646238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551760404	chr4:48646238-48646239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569902651	chr4:48646241-48646242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34084041	chr4:48646244-48646245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148576447	chr4:48646248-48646249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555863252	chr4:48646251-48646252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538615549	chr4:48646282-48646283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567504609	chr4:48646336-48646337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369587892	chr4:48646409-48646410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183927665	chr4:48646450-48646451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188703561	chr4:48646501-48646502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61422049	chr4:48646515-48646516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76059410	chr4:48646530-48646531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76753609	chr4:48646531-48646532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397993303	chr4:48646533-48646534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76778934	chr4:48646534-48646535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577861272	chr4:48646591-48646592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1712763	chr4:48646594-48646595	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77792955	chr4:48646616-48646617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556922003	chr4:48646649-48646650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375972796	chr4:48646727-48646728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575105614	chr4:48646756-48646757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13127769	chr4:48646829-48646830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13127771	chr4:48646830-48646831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368562354	chr4:48646845-48646846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532066999	chr4:48646908-48646909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58976855	chr4:48646917-48646918	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs560626145	chr4:48647001-48647002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546405969	chr4:48647047-48647048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193278315	chr4:48647058-48647059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370252061	chr4:48647075-48647076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541215419	chr4:48647131-48647132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182553582	chr4:48647132-48647133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367866479	chr4:48647139-48647140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73817832	chr4:48647141-48647142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200655696	chr4:48647142-48647143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112711865	chr4:48647163-48647164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533680700	chr4:48647169-48647170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186942213	chr4:48647171-48647172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	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
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Basal cell lymphoma	21115979	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	16272173	CNVD

Chromatin state (count:2443 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48621200-48729400	Weak transcription	Thymus	Thymus
2	chr4:48621800-48655800	Weak transcription	Colonic Mucosa	Colon
3	chr4:48622800-48648400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr4:48627200-48652400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:48627200-48656400	Weak transcription	Fetal Intestine Small	intestine
6	chr4:48635200-48654000	Weak transcription	Fetal Intestine Large	intestine
7	chr4:48635200-48655000	Weak transcription	Dnd41	blood
8	chr4:48637600-48656400	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr4:48637800-48652400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr4:48637800-48653400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:48637800-48664200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr4:48638000-48647200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:48638000-48651600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr4:48638000-48653800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:48638000-48655400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr4:48638000-48655600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:48638000-48657200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr4:48638000-48663000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr4:48638000-48664600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr4:48638400-48686200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr4:48638600-48652400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr4:48638600-48655400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:48638600-48666000	Weak transcription	Primary B cells from cord blood	blood
24	chr4:48639400-48653400	Weak transcription	HMEC	breast
25	chr4:48639600-48647400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr4:48639600-48652200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr4:48642200-48647200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:48642200-48654800	Weak transcription	Stomach Mucosa	stomach
29	chr4:48642400-48647400	Weak transcription	NHEK	skin
30	chr4:48643000-48647200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:48643000-48655200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr4:48643200-48647400	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr4:48643200-48655600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:48643400-48652400	Weak transcription	Primary T cells from cord blood	blood
35	chr4:48644000-48655600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr4:48645000-48648400	Weak transcription	K562	blood
37	chr4:48645000-48652600	Weak transcription	Aorta	Aorta
38	chr4:48645000-48653800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:48645200-48652400	Weak transcription	HSMM	muscle
40	chr4:48645200-48679400	Weak transcription	Rectal Smooth Muscle	rectum
41	chr4:48645400-48647000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr4:48645400-48647200	Weak transcription	Colon Smooth Muscle	Colon
43	chr4:48645400-48647400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr4:48645400-48648400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr4:48645400-48648600	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr4:48645400-48649800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr4:48645400-48650400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr4:48645400-48651000	Weak transcription	Fetal Kidney	kidney
49	chr4:48645400-48651400	Weak transcription	Brain Anterior Caudate	brain
50	chr4:48645400-48651600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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