Variant report

Variant	nsv1039508
Chromosome Location	chr10:49595718-49654403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:990)
CpG islands
(count:733)
Chromatin interactive
region (count:84)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:990 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:49639893-49640966	K562	blood:	n/a	n/a
2	ARID3A	chr10:49632732-49632884	K562	blood:	n/a	n/a
3	ARID3A	chr10:49643331-49643432	K562	blood:	n/a	n/a
4	ARID3A	chr10:49630869-49631301	K562	blood:	n/a	n/a
5	ARID3A	chr10:49638487-49639028	K562	blood:	n/a	n/a
6	ARID3A	chr10:49604342-49604600	K562	blood:	n/a	n/a
7	ARID3A	chr10:49608088-49608879	K562	blood:	n/a	n/a
8	ARID3A	chr10:49652362-49652626	K562	blood:	n/a	n/a
9	ARID3A	chr10:49598569-49598821	K562	blood:	n/a	n/a
10	ARID3A	chr10:49599330-49599433	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:49618323-49618330	K562	blood:	n/a	n/a
12	ARID3A	chr10:49614250-49614916	K562	blood:	n/a	n/a
13	ARID3A	chr10:49599051-49599837	K562	blood:	n/a	n/a
14	ARID3A	chr10:49624983-49625215	HepG2	liver:	n/a	n/a
15	ATF1	chr10:49613877-49614655	K562	blood:	n/a	n/a
16	ATF1	chr10:49630948-49631279	K562	blood:	n/a	n/a
17	ATF1	chr10:49639968-49640274	K562	blood:	n/a	n/a
18	ATF1	chr10:49606467-49606533	K562	blood:	n/a	n/a
19	BACH1	chr10:49614299-49614761	K562	blood:	n/a	n/a
20	BACH1	chr10:49624901-49624971	K562	blood:	n/a	n/a
21	BACH1	chr10:49618488-49618875	K562	blood:	n/a	n/a
22	BATF	chr10:49608340-49608776	GM12878	blood:	n/a	n/a
23	BATF	chr10:49599275-49599643	GM12878	blood:	n/a	chr10:49599429-49599439
24	BATF	chr10:49599066-49599640	GM12878	blood:	n/a	chr10:49599429-49599439
25	BCL3	chr10:49650022-49650484	GM12878	blood:	n/a	n/a
26	BHLHE40	chr10:49631099-49631106	K562	blood:	n/a	n/a
27	BHLHE40	chr10:49652455-49652759	K562	blood:	n/a	n/a
28	BHLHE40	chr10:49614263-49614699	K562	blood:	n/a	n/a
29	BHLHE40	chr10:49599288-49599534	GM12878	blood:	n/a	n/a
30	BHLHE40	chr10:49647917-49648026	K562	blood:	n/a	n/a
31	BHLHE40	chr10:49598536-49598560	K562	blood:	n/a	n/a
32	BHLHE40	chr10:49598133-49598151	K562	blood:	n/a	n/a
33	BRCA1	chr10:49643759-49643781	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr10:49620073-49620512	K562	blood:	n/a	n/a
35	CBX3	chr10:49614124-49614960	K562	blood:	n/a	n/a
36	CBX3	chr10:49619974-49620611	K562	blood:	n/a	n/a
37	CBX3	chr10:49599189-49599653	HCT-116	colon:	n/a	n/a
38	CEBPB	chr10:49648897-49649137	HepG2	liver:	n/a	chr10:49649054-49649067 chr10:49649053-49649070 chr10:49649055-49649066 chr10:49649054-49649065 chr10:49649028-49649039
39	CEBPB	chr10:49638030-49638350	K562	blood:	n/a	n/a
40	CEBPB	chr10:49606855-49607013	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr10:49606832-49607063	A549	lung:	n/a	n/a
42	CEBPB	chr10:49622524-49623145	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:49647786-49648053	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:49612626-49613121	IMR90	lung:	n/a	chr10:49612923-49612934 chr10:49612727-49612744
45	CEBPB	chr10:49639905-49640370	K562	blood:	n/a	n/a
46	CEBPB	chr10:49612616-49613111	K562	blood:	n/a	chr10:49612923-49612934 chr10:49612727-49612744
47	CEBPB	chr10:49606846-49607139	HepG2	liver:	n/a	n/a
48	CEBPB	chr10:49639952-49640326	K562	blood:	n/a	n/a
49	CEBPB	chr10:49622391-49622610	HepG2	liver:	n/a	n/a
50	CEBPB	chr10:49606850-49607378	K562	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49647167-49647217	Jurkat	blood:	n/a
2	chr10:49647167-49647217	Jurkat	blood:	n/a
3	chr10:49643086-49643136	Hepatocyte	liver:	n/a
4	chr10:49642969-49643019	HCM	heart:	n/a
5	chr10:49609776-49609826	AG04450	lung:	fetal
6	chr10:49643086-49643136	GM12878	blood:	n/a
7	chr10:49607582-49607632	HCPEpiC	choroid plexus:	n/a
8	chr10:49624427-49624477	Jurkat	blood:	n/a
9	chr10:49614052-49614102	HNPCEpiC	eye:	n/a
10	chr10:49608952-49609002	HAEpiC	amniotic membrane:	n/a
11	chr10:49608385-49608435	Caco-2	colon:	n/a
12	chr10:49624427-49624477	HepG2	liver:	n/a
13	chr10:49609776-49609826	HCPEpiC	choroid plexus:	n/a
14	chr10:49642969-49643019	GM12892	blood:	n/a
15	chr10:49614052-49614102	HCF	heart:	n/a
16	chr10:49608385-49608435	HL-60	blood:	n/a
17	chr10:49642969-49643019	ovcar-3	ovarian:	n/a
18	chr10:49614052-49614102	HIPEpiC	eye:	n/a
19	chr10:49654342-49654392	MCF10A-Er-Src	breast:	n/a
20	chr10:49624427-49624477	AG04450	lung:	fetal
21	chr10:49609776-49609826	HCF	heart:	n/a
22	chr10:49614052-49614102	AG09309	skin:	n/a
23	chr10:49642969-49643019	Jurkat	blood:	n/a
24	chr10:49614052-49614102	Hepatocyte	liver:	n/a
25	chr10:49643086-49643136	Jurkat	blood:	n/a
26	chr10:49654342-49654392	AoSMC	blood vessel:	n/a
27	chr10:49653080-49653130	IMR90	lung:	fetal
28	chr10:49608557-49608607	SK-N-SH	brain:	n/a
29	chr10:49654342-49654392	SAEC	small airway:	n/a
30	chr10:49647167-49647217	GM12891	blood:	n/a
31	chr10:49642969-49643019	Hepatocyte	liver:	n/a
32	chr10:49608952-49609002	AG09309	skin:	n/a
33	chr10:49653080-49653130	CMK	blood:	n/a
34	chr10:49608952-49609002	A549	lung:	n/a
35	chr10:49642969-49643019	T-47D	breast:	n/a
36	chr10:49608385-49608435	HCM	heart:	n/a
37	chr10:49609776-49609826	IMR90	lung:	fetal
38	chr10:49608385-49608435	BJ	skin:	n/a
39	chr10:49607582-49607632	NHBE	bronchial:	n/a
40	chr10:49624427-49624477	HCM	heart:	n/a
41	chr10:49614052-49614102	GM12891	blood:	n/a
42	chr10:49607582-49607632	IMR90	lung:	fetal
43	chr10:49614052-49614102	SAEC	small airway:	n/a
44	chr10:49608385-49608435	HIPEpiC	eye:	n/a
45	chr10:49654342-49654392	HepG2	liver:	n/a
46	chr10:49608952-49609002	BJ	skin:	n/a
47	chr10:49608952-49609002	HepG2	liver:	n/a
48	chr10:49609776-49609826	AG09309	skin:	n/a
49	chr10:49624427-49624477	IMR90	lung:	fetal
50	chr10:49609776-49609826	BJ	skin:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:49653089..49653710-chr10:49671711..49672225,2	MCF-7	breast:
2	chr10:49600536..49602318-chr10:49619238..49621122,2	K562	blood:
3	chr10:49637793..49639476-chr10:49653673..49655719,2	K562	blood:
4	chr10:49615597..49618030-chr10:49714235..49716218,3	K562	blood:
5	chr10:49625430..49627582-chr10:49637563..49639868,2	K562	blood:
6	chr10:49639013..49641362-chr10:49732442..49734428,2	K562	blood:
7	chr10:49571674..49573268-chr10:49594315..49596996,2	K562	blood:
8	chr10:49597870..49600573-chr10:49685383..49687773,2	K562	blood:
9	chr10:49514542..49516292-chr10:49606736..49609603,3	K562	blood:
10	chr10:49587644..49589610-chr10:49601612..49603267,2	K562	blood:
11	chr10:49514733..49517675-chr10:49606696..49609603,2	K562	blood:
12	chr10:49643859..49645502-chr10:49674672..49677037,2	K562	blood:
13	chr10:49597219..49599872-chr10:49602103..49604352,2	K562	blood:
14	chr10:49629411..49632301-chr10:49684401..49686172,3	K562	blood:
15	chr10:49597669..49599901-chr10:49599925..49601637,2	K562	blood:
16	chr10:49624602..49625302-chr10:49652334..49653265,2	MCF-7	breast:
17	chr10:49646827..49648798-chr10:49677849..49680976,3	K562	blood:
18	chr10:49624602..49625302-chr10:49652334..49653265,2	MCF-7	breast:
19	chr10:49599866..49602810-chr10:49604615..49606169,2	K562	blood:
20	chr10:49571231..49572227-chr10:49652604..49653258,3	MCF-7	breast:
21	chr10:49640741..49644596-chr10:49677175..49679458,3	K562	blood:
22	chr10:49613029..49615967-chr10:49663530..49666398,2	K562	blood:
23	chr10:49571283..49571906-chr10:49652430..49653469,3	MCF-7	breast:
24	chr10:49632219..49636851-chr10:49637055..49643743,11	K562	blood:
25	chr10:49619514..49622153-chr10:49622504..49625064,2	K562	blood:
26	chr10:49605751..49608098-chr10:49638652..49640614,2	K562	blood:
27	chr10:49570787..49573176-chr10:49651060..49654395,3	MCF-7	breast:
28	chr10:49602827..49604920-chr10:49676681..49679745,3	K562	blood:
29	chr10:49596329..49598626-chr10:49641274..49643307,2	K562	blood:
30	chr10:49615995..49618408-chr10:49619011..49621814,2	K562	blood:
31	chr10:49620234..49623060-chr10:49677590..49681287,3	K562	blood:
32	chr10:49600536..49602318-chr10:49619238..49621122,2	K562	blood:
33	chr10:49513543..49515966-chr10:49598483..49600970,2	K562	blood:
34	chr10:49613192..49615301-chr10:49629132..49631884,2	K562	blood:
35	chr10:49619514..49622153-chr10:49622504..49625064,2	K562	blood:
36	chr10:49639661..49642619-chr10:49674798..49676427,2	K562	blood:
37	chr10:49605353..49609385-chr10:49612341..49615386,5	K562	blood:
38	chr10:49620652..49623307-chr10:49629695..49632361,2	K562	blood:
39	chr10:49653221..49653731-chr10:49714626..49715186,2	MCF-7	breast:
40	chr10:49620652..49623307-chr10:49629695..49632361,2	K562	blood:
41	chr10:49615995..49618408-chr10:49619011..49621814,2	K562	blood:
42	chr10:49598612..49601205-chr10:49623829..49626212,2	K562	blood:
43	chr10:49652071..49653009-chr10:49714464..49715277,3	K562	blood:
44	chr10:49652137..49653652-chr10:49714272..49715285,12	MCF-7	breast:
45	chr10:49652115..49653152-chr10:49714314..49715226,3	MCF-7	breast:
46	chr10:49605751..49608098-chr10:49638652..49640614,2	K562	blood:
47	chr10:49649446..49650312-chr10:49714228..49715210,2	MCF-7	breast:
48	chr10:49603654..49605452-chr10:49607238..49610182,2	K562	blood:
49	chr10:49613380..49617347-chr10:49637674..49642930,5	K562	blood:
50	chr10:49639954..49642271-chr10:49642777..49645613,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAPK8-1	chr10:49651168-49652001	XLOC_008482
2	lnc-MAPK8-1	chr10:49649950-49650029	XLOC_008482
3	lnc-ARHGAP22-2	chr10:49651879-49653859	NONHSAT013269

No data

Variant related genes	Relation type
MAPK8	TF binding region
MAPK8	CpG island
ENSG00000107643	chromatin interactions
ENSG00000128805	chromatin interactions

Extended variants
information (count: 2195 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2195 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561676898	chr10:49595719-49595720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187612548	chr10:49595824-49595825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17697960	chr10:49595864-49595865	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs111746267	chr10:49595874-49595875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183178317	chr10:49595890-49595891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142850493	chr10:49595928-49595929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551141654	chr10:49595939-49595940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141931973	chr10:49595942-49595943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144864245	chr10:49595981-49595982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557214755	chr10:49596032-49596033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187022925	chr10:49596055-49596056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148583229	chr10:49596081-49596082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529995437	chr10:49596082-49596083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190261586	chr10:49596118-49596119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182172567	chr10:49596144-49596145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187654965	chr10:49596169-49596170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192789612	chr10:49596238-49596239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558374247	chr10:49596289-49596290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185480210	chr10:49596336-49596337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534046701	chr10:49596346-49596347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576670062	chr10:49596434-49596435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537147002	chr10:49596444-49596445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555475727	chr10:49596448-49596449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34265260	chr10:49596525-49596526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573573797	chr10:49596528-49596529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373253224	chr10:49596558-49596559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189233902	chr10:49596568-49596569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192042500	chr10:49596648-49596649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142927989	chr10:49596672-49596673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555904528	chr10:49596676-49596677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376884755	chr10:49596680-49596681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544859892	chr10:49596754-49596755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184363171	chr10:49596771-49596772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538876833	chr10:49596791-49596792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563143694	chr10:49596843-49596844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150659847	chr10:49596893-49596894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569694687	chr10:49596906-49596907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562194535	chr10:49596907-49596908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188352435	chr10:49596915-49596916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139523632	chr10:49596950-49596951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538361844	chr10:49596974-49596975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74777746	chr10:49596984-49596985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2590388	chr10:49597004-49597005	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552058096	chr10:49597035-49597036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570286073	chr10:49597062-49597063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144342479	chr10:49597083-49597084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2590389	chr10:49597157-49597158	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs147792409	chr10:49597275-49597276	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs534370838	chr10:49597284-49597285	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs552926697	chr10:49597286-49597287	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1571 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49587600-49599600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:49590200-49596400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr10:49590200-49596800	Weak transcription	Left Ventricle	heart
4	chr10:49590200-49598400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr10:49590200-49598800	Weak transcription	A549	lung
6	chr10:49590200-49599600	Weak transcription	Pancreas	Pancrea
7	chr10:49590400-49598600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr10:49590400-49599000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr10:49591400-49599600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:49591800-49597200	Weak transcription	NHDF-Ad	bronchial
11	chr10:49591800-49599000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:49592000-49597600	Weak transcription	HUVEC	blood vessel
13	chr10:49592200-49597400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr10:49592400-49597600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:49592600-49595800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr10:49592600-49597400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr10:49592600-49597600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr10:49592800-49597400	Weak transcription	HMEC	breast
19	chr10:49593000-49596800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr10:49593000-49597400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr10:49593000-49598000	Weak transcription	Right Atrium	heart
22	chr10:49593000-49599000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr10:49593200-49597200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr10:49593200-49597200	Weak transcription	Fetal Heart	heart
25	chr10:49593200-49597600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr10:49593200-49599000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr10:49593200-49607600	Weak transcription	Fetal Lung	lung
28	chr10:49593400-49597400	Weak transcription	Colon Smooth Muscle	Colon
29	chr10:49593400-49597400	Weak transcription	HSMMtube	muscle
30	chr10:49593400-49599000	Weak transcription	HSMM	muscle
31	chr10:49593600-49597200	Weak transcription	GM12878-XiMat	blood
32	chr10:49593600-49597400	Weak transcription	Fetal Kidney	kidney
33	chr10:49593600-49598800	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr10:49595000-49596800	Weak transcription	Ovary	ovary
35	chr10:49595000-49599400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr10:49595000-49616000	Weak transcription	Primary B cells from cord blood	blood
37	chr10:49595400-49595800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr10:49595400-49596400	Weak transcription	Fetal Intestine Large	intestine
39	chr10:49595400-49596800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr10:49595600-49596000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr10:49595600-49597200	Enhancers	K562	blood
42	chr10:49595800-49596000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr10:49595800-49596000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr10:49595800-49597200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr10:49596000-49596200	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr10:49596000-49596800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr10:49596000-49597200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr10:49596200-49597600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr10:49596400-49599600	Enhancers	Fetal Intestine Large	intestine
50	chr10:49596400-49599800	Enhancers	Skeletal Muscle Male	skeletal muscle

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Variant report

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