Variant report

Variant	nsv3916
Chromosome Location	chr3:99186008-99232052
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:99223184-99223477	HepG2	liver:	n/a	n/a
2	ATF2	chr3:99224637-99225315	GM12878	blood:	n/a	n/a
3	ATF2	chr3:99202558-99203147	GM12878	blood:	n/a	n/a
4	ATF2	chr3:99202618-99203076	GM12878	blood:	n/a	n/a
5	ATF2	chr3:99224596-99225255	GM12878	blood:	n/a	n/a
6	BATF	chr3:99202699-99203096	GM12878	blood:	n/a	n/a
7	BATF	chr3:99202574-99203096	GM12878	blood:	n/a	n/a
8	BATF	chr3:99224687-99225114	GM12878	blood:	n/a	n/a
9	BATF	chr3:99224726-99225079	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:99202609-99203107	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:99224723-99225108	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:99224741-99225155	GM12878	blood:	n/a	n/a
13	BCL3	chr3:99202636-99203075	GM12878	blood:	n/a	n/a
14	BCL3	chr3:99224696-99225137	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:99224627-99225139	GM12878	blood:	n/a	n/a
16	BCLAF1	chr3:99224646-99225196	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:99224010-99225208	GM12878	blood:	n/a	n/a
18	CEBPB	chr3:99224888-99225126	K562	blood:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
19	CEBPB	chr3:99223139-99223519	HepG2	liver:	n/a	chr3:99223327-99223338 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223329-99223340 chr3:99223329-99223338
20	CEBPB	chr3:99223138-99223563	IMR90	lung:	n/a	chr3:99223327-99223338 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223329-99223340 chr3:99223329-99223338
21	CEBPB	chr3:99224895-99225208	HepG2	liver:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
22	CEBPB	chr3:99189299-99189600	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:99194111-99194389	IMR90	lung:	n/a	n/a
24	CEBPB	chr3:99189391-99189513	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr3:99223140-99223526	HepG2	liver:	n/a	chr3:99223327-99223338 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223329-99223340 chr3:99223329-99223338
26	CEBPB	chr3:99224883-99225154	K562	blood:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
27	CEBPB	chr3:99202601-99203206	GM12878	blood:	n/a	chr3:99202908-99202920 chr3:99203166-99203179
28	CEBPB	chr3:99224628-99225335	GM12878	blood:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
29	CEBPB	chr3:99223146-99223521	HepG2	liver:	n/a	chr3:99223327-99223338 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223329-99223340 chr3:99223329-99223338
30	CEBPB	chr3:99189280-99189576	HepG2	liver:	n/a	n/a
31	CEBPB	chr3:99224813-99225254	A549	lung:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
32	CEBPB	chr3:99224886-99225206	A549	lung:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
33	CEBPB	chr3:99223186-99223409	HepG2	liver:	n/a	chr3:99223327-99223338 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223329-99223340 chr3:99223329-99223338
34	CEBPB	chr3:99189384-99189537	K562	blood:	n/a	n/a
35	CEBPB	chr3:99223257-99223420	Hela-S3	cervix:	n/a	chr3:99223327-99223338 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223327-99223340 chr3:99223329-99223340 chr3:99223329-99223338
36	CEBPB	chr3:99224893-99225188	Hela-S3	cervix:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
37	CEBPB	chr3:99192182-99192643	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:99224851-99225234	IMR90	lung:	n/a	chr3:99225061-99225074 chr3:99225062-99225073 chr3:99225061-99225072
39	CEBPD	chr3:99223227-99223429	HepG2	liver:	n/a	chr3:99223328-99223339 chr3:99223328-99223339
40	CHD2	chr3:99224720-99225118	GM12878	blood:	n/a	n/a
41	CREB1	chr3:99223128-99223494	HepG2	liver:	n/a	n/a
42	CREB1	chr3:99224629-99225136	GM12878	blood:	n/a	n/a
43	CREB1	chr3:99224568-99225331	GM12878	blood:	n/a	n/a
44	CTCF	chr3:99218160-99218310	GM12866	blood:	n/a	chr3:99218227-99218248 chr3:99218228-99218241 chr3:99218230-99218240 chr3:99218225-99218243 chr3:99218228-99218237
45	CTCF	chr3:99218180-99218330	HepG2	liver:	n/a	chr3:99218227-99218248 chr3:99218228-99218241 chr3:99218230-99218240 chr3:99218225-99218243 chr3:99218228-99218237
46	CTCF	chr3:99218120-99218270	RPTEC	kidney:	n/a	chr3:99218227-99218248 chr3:99218228-99218241 chr3:99218230-99218240 chr3:99218225-99218243 chr3:99218228-99218237
47	CTCF	chr3:99203740-99203890	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr3:99217960-99218505	MCF-7	breast:	n/a	chr3:99218227-99218248 chr3:99218228-99218241 chr3:99218230-99218240 chr3:99218225-99218243 chr3:99218228-99218237
49	CTCF	chr3:99217871-99217987	GM12892	blood:	n/a	n/a
50	CTCF	chr3:99218180-99218330	NHDF-neo	bronchial:	n/a	chr3:99218227-99218248 chr3:99218228-99218241 chr3:99218230-99218240 chr3:99218225-99218243 chr3:99218228-99218237

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:99193044-99193094	NH-A	brain:	n/a
2	chr3:99228156-99228206	IMR90	lung:	fetal
3	chr3:99193044-99193094	NHBE	bronchial:	n/a
4	chr3:99218170-99218220	HUVEC	blood vessel:	n/a
5	chr3:99193044-99193094	AG09309	skin:	n/a
6	chr3:99218170-99218220	MCF-7	breast:	n/a
7	chr3:99228156-99228206	MCF-7	breast:	n/a
8	chr3:99193044-99193094	SK-N-SH	brain:	n/a
9	chr3:99228156-99228206	Jurkat	blood:	n/a
10	chr3:99218170-99218220	GM19239	blood:	n/a
11	chr3:99193044-99193094	HEEpiC	esophagus:	n/a
12	chr3:99228156-99228206	Hepatocyte	liver:	n/a
13	chr3:99228156-99228206	HAEpiC	amniotic membrane:	n/a
14	chr3:99228156-99228206	HRE	kidney:	n/a
15	chr3:99228156-99228206	U87	brain:	n/a
16	chr3:99218170-99218220	GM12892	blood:	n/a
17	chr3:99218170-99218220	HL-60	blood:	n/a
18	chr3:99228156-99228206	GM19239	blood:	n/a
19	chr3:99193044-99193094	AG10803	skin:	n/a
20	chr3:99218170-99218220	U87	brain:	n/a
21	chr3:99193044-99193094	HUVEC	blood vessel:	n/a
22	chr3:99193044-99193094	PFSK-1	brain:	n/a
23	chr3:99193044-99193094	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:99193044-99193094	NB4	blood:	n/a
25	chr3:99218170-99218220	GM06990	blood:	n/a
26	chr3:99193044-99193094	K562	blood:	n/a
27	chr3:99193044-99193094	AG04450	lung:	fetal
28	chr3:99228156-99228206	HUVEC	blood vessel:	n/a
29	chr3:99228156-99228206	SK-N-MC	brain:	n/a
30	chr3:99193044-99193094	RPTEC	kidney:	n/a
31	chr3:99193044-99193094	NHDF-neo	bronchial:	n/a
32	chr3:99218170-99218220	SAEC	small airway:	n/a
33	chr3:99193044-99193094	ECC-1	luminal epithelium:	n/a
34	chr3:99228156-99228206	BJ	skin:	n/a
35	chr3:99228156-99228206	NT2-D1	testis:	n/a
36	chr3:99193044-99193094	HCF	heart:	n/a
37	chr3:99193044-99193094	HMEC	breast:	n/a
38	chr3:99218170-99218220	ECC-1	luminal epithelium:	n/a
39	chr3:99218170-99218220	NB4	blood:	n/a
40	chr3:99193044-99193094	A549	lung:	n/a
41	chr3:99218170-99218220	NH-A	brain:	n/a
42	chr3:99218170-99218220	HEK293	kidney:	embryo
43	chr3:99228156-99228206	NB4	blood:	n/a
44	chr3:99218170-99218220	HRPEpiC	eye:	n/a
45	chr3:99218170-99218220	Jurkat	blood:	n/a
46	chr3:99193044-99193094	IMR90	lung:	fetal
47	chr3:99218170-99218220	GM12891	blood:	n/a
48	chr3:99218170-99218220	PFSK-1	brain:	n/a
49	chr3:99193044-99193094	Hepatocyte	liver:	n/a
50	chr3:99218170-99218220	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:99218147..99219010-chr3:99363822..99364695,3	MCF-7	breast:
2	chr3:99217843..99218709-chr3:99405590..99406505,5	MCF-7	breast:
3	chr3:99217926..99218471-chr3:99250937..99251667,2	MCF-7	breast:
4	chr3:99218086..99218777-chr3:99250976..99251575,3	MCF-7	breast:
5	chr3:99215007..99217420-chr3:99218950..99221198,2	MCF-7	breast:
6	chr3:99217180..99218833-chr3:99471535..99472845,8	MCF-7	breast:
7	chr2:218516301..218518088-chr3:99186166..99188131,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL8A1-2	chr3:99224090-99224352	XLOC_002737
2	lnc-COL8A1-2	chr3:99219191-99219385	XLOC_002737

Variant related genes	Relation type
ENSG00000243296	TF binding region
ENSG00000243296	CpG island
ENSG00000243296	chromatin interactions

Extended variants
information (count: 1437 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1437 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539779685	chr3:99186042-99186043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557870984	chr3:99186085-99186086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148599665	chr3:99186098-99186099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559216266	chr3:99186143-99186144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556474952	chr3:99186200-99186201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115879814	chr3:99186209-99186210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544415396	chr3:99186231-99186232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556398066	chr3:99186241-99186242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578187792	chr3:99186256-99186257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs117968600	chr3:99186274-99186275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563915657	chr3:99186284-99186285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528123372	chr3:99186349-99186350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540307411	chr3:99186356-99186357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192901249	chr3:99186358-99186359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556306516	chr3:99186359-99186360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371643353	chr3:99186389-99186390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56950200	chr3:99186405-99186406	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370108704	chr3:99186447-99186448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533074562	chr3:99186466-99186467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551696702	chr3:99186512-99186513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561843061	chr3:99186521-99186522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566740666	chr3:99186522-99186523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144518016	chr3:99186529-99186530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs5851171	chr3:99186545-99186546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2256606	chr3:99186626-99186627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184924017	chr3:99186627-99186628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538000830	chr3:99186659-99186660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113353548	chr3:99186695-99186696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79806311	chr3:99186739-99186740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76929175	chr3:99186745-99186746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs578154047	chr3:99186751-99186752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545360776	chr3:99186773-99186774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189379077	chr3:99186786-99186787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369647532	chr3:99186804-99186805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542600253	chr3:99186806-99186807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114355089	chr3:99186925-99186926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561727364	chr3:99186955-99186956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573783802	chr3:99186981-99186982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114929519	chr3:99187054-99187055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544064894	chr3:99187066-99187067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11711834	chr3:99187079-99187080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76405146	chr3:99187149-99187150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141361689	chr3:99187154-99187155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145127034	chr3:99187181-99187182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560420384	chr3:99187207-99187208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532562707	chr3:99187239-99187240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180931560	chr3:99187245-99187246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548966741	chr3:99187284-99187285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567365939	chr3:99187288-99187289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555445608	chr3:99187295-99187296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99174800-99187800	Weak transcription	Aorta	Aorta
2	chr3:99186400-99188400	Enhancers	Fetal Heart	heart
3	chr3:99187600-99187800	Enhancers	HSMMtube	muscle
4	chr3:99187600-99187800	Enhancers	NHDF-Ad	bronchial
5	chr3:99187600-99188000	Enhancers	NHEK	skin
6	chr3:99187600-99188800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:99187800-99188000	Enhancers	Aorta	Aorta
8	chr3:99187800-99188200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:99187800-99188400	Enhancers	HMEC	breast
10	chr3:99187800-99191200	Weak transcription	HSMMtube	muscle
11	chr3:99188000-99189800	Weak transcription	NHDF-Ad	bronchial
12	chr3:99188000-99190800	Weak transcription	Aorta	Aorta
13	chr3:99188200-99188600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:99188600-99192400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:99188800-99192000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:99189200-99194600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr3:99189600-99192000	Enhancers	Osteobl	bone
18	chr3:99189800-99191800	Enhancers	NHDF-Ad	bronchial
19	chr3:99190600-99191800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:99190600-99193200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:99190800-99191000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr3:99190800-99191000	ZNF genes & repeats	Aorta	Aorta
23	chr3:99190800-99192200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr3:99190800-99192200	Enhancers	NHLF	lung
25	chr3:99190800-99192400	Enhancers	Adipose Nuclei	Adipose
26	chr3:99190800-99194000	Enhancers	HSMM	muscle
27	chr3:99191000-99192000	Weak transcription	Aorta	Aorta
28	chr3:99191200-99192000	Enhancers	HSMMtube	muscle
29	chr3:99191400-99192800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr3:99191400-99192800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr3:99191800-99192600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:99191800-99192600	Flanking Active TSS	NHDF-Ad	bronchial
33	chr3:99192000-99192200	Flanking Active TSS	HSMMtube	muscle
34	chr3:99192000-99192400	Enhancers	Aorta	Aorta
35	chr3:99192000-99192600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr3:99192000-99192600	Flanking Active TSS	Osteobl	bone
37	chr3:99192200-99192400	Enhancers	HSMMtube	muscle
38	chr3:99192200-99192600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr3:99192200-99193400	Weak transcription	NHLF	lung
40	chr3:99192400-99192600	Flanking Active TSS	HSMMtube	muscle
41	chr3:99192600-99193800	Enhancers	HSMMtube	muscle
42	chr3:99192600-99194000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:99192600-99194000	Enhancers	Osteobl	bone
44	chr3:99192600-99194800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr3:99192600-99194800	Enhancers	NHDF-Ad	bronchial
46	chr3:99192800-99193200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr3:99192800-99193200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr3:99193200-99193600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:99193200-99194000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:99193200-99194000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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