Variant report

Variant	nsv571459
Chromosome Location	chr16:12046899-12062396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:550)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr16:12059908-12060600	GM12878	blood:	n/a	n/a
2	ATF2	chr16:12058461-12059383	GM12878	blood:	n/a	n/a
3	ATF2	chr16:12052745-12053290	GM12878	blood:	n/a	n/a
4	ATF2	chr16:12058525-12059237	GM12878	blood:	n/a	n/a
5	ATF2	chr16:12059973-12060651	GM12878	blood:	n/a	n/a
6	BATF	chr16:12058751-12059152	GM12878	blood:	n/a	n/a
7	BATF	chr16:12058550-12059280	GM12878	blood:	n/a	n/a
8	BATF	chr16:12060041-12060427	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:12060077-12060408	GM12878	blood:	n/a	chr16:12060253-12060262
10	BCL11A	chr16:12056913-12057096	GM12878	blood:	n/a	n/a
11	BCL11A	chr16:12058632-12059097	GM12878	blood:	n/a	n/a
12	BCL11A	chr16:12056877-12057207	GM12878	blood:	n/a	n/a
13	BCL11A	chr16:12060022-12060454	GM12878	blood:	n/a	chr16:12060253-12060262
14	BCL11A	chr16:12058576-12059155	GM12878	blood:	n/a	n/a
15	BCL3	chr16:12056913-12057234	GM12878	blood:	n/a	n/a
16	BCL3	chr16:12058576-12059193	GM12878	blood:	n/a	n/a
17	BCLAF1	chr16:12058547-12059574	GM12878	blood:	n/a	n/a
18	BCLAF1	chr16:12059828-12060647	GM12878	blood:	n/a	chr16:12060253-12060262
19	BCLAF1	chr16:12059933-12060619	GM12878	blood:	n/a	chr16:12060253-12060262
20	BCLAF1	chr16:12058562-12059443	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:12058655-12059413	GM12878	blood:	n/a	n/a
22	BHLHE40	chr16:12056775-12057190	GM12878	blood:	n/a	n/a
23	BHLHE40	chr16:12052908-12053235	GM12878	blood:	n/a	n/a
24	CEBPB	chr16:12059899-12060618	GM12878	blood:	n/a	n/a
25	CEBPB	chr16:12052930-12053249	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr16:12058795-12059231	GM12878	blood:	n/a	chr16:12058947-12058964
27	CEBPB	chr16:12058547-12059481	GM12878	blood:	n/a	chr16:12058947-12058964
28	CEBPB	chr16:12053076-12053103	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:12054698-12054898	K562	blood:	n/a	n/a
30	CEBPB	chr16:12054844-12054878	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:12051689-12051798	K562	blood:	n/a	n/a
32	CEBPB	chr16:12049474-12050227	IMR90	lung:	n/a	chr16:12050003-12050011
33	CEBPB	chr16:12046996-12047188	HepG2	liver:	n/a	chr16:12047058-12047069
34	CEBPB	chr16:12052971-12053190	ECC-1	luminal epithelium:	n/a	n/a
35	CHD1	chr16:12052961-12053174	GM12878	blood:	n/a	n/a
36	CHD1	chr16:12061079-12061225	GM12878	blood:	n/a	n/a
37	CHD1	chr16:12060037-12060754	GM12878	blood:	n/a	n/a
38	CHD1	chr16:12057928-12059527	GM12878	blood:	n/a	n/a
39	CHD2	chr16:12052786-12053173	GM12878	blood:	n/a	n/a
40	CHD2	chr16:12060052-12060502	GM12878	blood:	n/a	n/a
41	CHD2	chr16:12058623-12059258	GM12878	blood:	n/a	n/a
42	CREB1	chr16:12058617-12059299	GM12878	blood:	n/a	n/a
43	CREB1	chr16:12052763-12053296	GM12878	blood:	n/a	n/a
44	CREB1	chr16:12052633-12053443	GM12878	blood:	n/a	n/a
45	CTCF	chr16:12059180-12059330	AG10803	skin:	n/a	n/a
46	CTCF	chr16:12054077-12054370	K562	blood:	n/a	n/a
47	CTCF	chr16:12054020-12054170	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr16:12054180-12054330	HepG2	liver:	n/a	n/a
49	CTCF	chr16:12054180-12054330	K562	blood:	n/a	n/a
50	CTCF	chr16:12054209-12054327	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12057996-12058046	RPTEC	kidney:	n/a
2	chr16:12057996-12058046	RPTEC	kidney:	n/a
3	chr16:12059019-12059069	HL-60	blood:	n/a
4	chr16:12058834-12058884	NH-A	brain:	n/a
5	chr16:12057996-12058046	AG04450	lung:	fetal
6	chr16:12060182-12060232	PFSK-1	brain:	n/a
7	chr16:12060182-12060232	GM19239	blood:	n/a
8	chr16:12058043-12058093	HAEpiC	amniotic membrane:	n/a
9	chr16:12059019-12059069	HCT-116	colon:	n/a
10	chr16:12058834-12058884	Jurkat	blood:	n/a
11	chr16:12060182-12060232	HEEpiC	esophagus:	n/a
12	chr16:12058834-12058884	AG09309	skin:	n/a
13	chr16:12059019-12059069	PANC-1	pancreas:	n/a
14	chr16:12058043-12058093	HRE	kidney:	n/a
15	chr16:12057996-12058046	SK-N-SH_RA	brain:	n/a
16	chr16:12058043-12058093	IMR90	lung:	fetal
17	chr16:12061715-12061765	SK-N-SH_RA	brain:	n/a
18	chr16:12060182-12060232	A549	lung:	n/a
19	chr16:12057996-12058046	SK-N-MC	brain:	n/a
20	chr16:12060182-12060232	HNPCEpiC	eye:	n/a
21	chr16:12060182-12060232	Hela-S3	cervix:	n/a
22	chr16:12061715-12061765	Hepatocyte	liver:	n/a
23	chr16:12061715-12061765	NHDF-neo	bronchial:	n/a
24	chr16:12058001-12058051	MCF10A-Er-Src	breast:	n/a
25	chr16:12059019-12059069	MCF-7	breast:	n/a
26	chr16:12060182-12060232	SK-N-MC	brain:	n/a
27	chr16:12050254-12050304	GM06990	blood:	n/a
28	chr16:12057996-12058046	SAEC	small airway:	n/a
29	chr16:12050254-12050304	HEEpiC	esophagus:	n/a
30	chr16:12050254-12050304	HCT-116	colon:	n/a
31	chr16:12059019-12059069	BJ	skin:	n/a
32	chr16:12058043-12058093	HCT-116	colon:	n/a
33	chr16:12057996-12058046	HNPCEpiC	eye:	n/a
34	chr16:12058834-12058884	AG04450	lung:	fetal
35	chr16:12058043-12058093	HCPEpiC	choroid plexus:	n/a
36	chr16:12061715-12061765	HIPEpiC	eye:	n/a
37	chr16:12058834-12058884	Caco-2	colon:	n/a
38	chr16:12058001-12058051	NHDF-neo	bronchial:	n/a
39	chr16:12059019-12059069	ECC-1	luminal epithelium:	n/a
40	chr16:12059019-12059069	LNCaP	prostate:	n/a
41	chr16:12061715-12061765	ProgFib	skin:	n/a
42	chr16:12058616-12058666	AoSMC	blood vessel:	n/a
43	chr16:12059019-12059069	HCM	heart:	n/a
44	chr16:12059019-12059069	HEEpiC	esophagus:	n/a
45	chr16:12059019-12059069	SK-N-MC	brain:	n/a
46	chr16:12060182-12060232	HEK293	kidney:	embryo
47	chr16:12059019-12059069	NT2-D1	testis:	n/a
48	chr16:12060182-12060232	GM12891	blood:	n/a
49	chr16:12061715-12061765	CMK	blood:	n/a
50	chr16:12058834-12058884	CMK	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12044743..12047515-chr16:12054722..12057306,2	K562	blood:
2	chr16:12051503..12053393-chr16:12070726..12072871,2	MCF-7	breast:
3	chr16:12044743..12047515-chr16:12054722..12057306,2	K562	blood:
4	chr16:12008413..12010461-chr16:12056035..12059014,2	MCF-7	breast:
5	chr16:12012124..12014555-chr16:12045355..12047902,2	K562	blood:
6	chr16:12054203..12056050-chr16:12064634..12067549,2	MCF-7	breast:
7	chr16:12058363..12061770-chr16:12069205..12072370,4	MCF-7	breast:
8	chr16:12050006..12051535-chr16:12068882..12070665,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-166B2.1.1-2	chr16:12050001-12050094	NONHSAT140610
2	lnc-GSPT1-4	chr16:12062365-12062600	NONHSAT140611
3	lnc-RP11-166B2.1.1-2	chr16:12057748-12057883	NONHSAT140610

No data

Variant related genes	Relation type
ENSG00000269121	TF binding region
TNFRSF17	TF binding region
ENSG00000269121	CpG island
TNFRSF17	CpG island
ENSG00000048471	chromatin interactions
ENSG00000266163	chromatin interactions
ENSG00000234719	chromatin interactions
ENSG00000103342	chromatin interactions
ENSG00000260488	chromatin interactions

Extended variants
information (count: 804 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7185307	chr16:12046899-12046900	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373540221	chr16:12046911-12046912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570056621	chr16:12046953-12046954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561854554	chr16:12046954-12046955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147547185	chr16:12046962-12046963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541260170	chr16:12046987-12046988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs386606	chr16:12046995-12046996	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs533442531	chr16:12047012-12047013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550466364	chr16:12047026-12047027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1299500	chr16:12047047-12047048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569640791	chr16:12047063-12047064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74850703	chr16:12047083-12047084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78056338	chr16:12047088-12047089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528898359	chr16:12047091-12047092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77651430	chr16:12047099-12047100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75721856	chr16:12047105-12047106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78586620	chr16:12047109-12047110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74886349	chr16:12047116-12047117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76150347	chr16:12047117-12047118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78417903	chr16:12047126-12047127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369124482	chr16:12047133-12047134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565779173	chr16:12047160-12047161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534745485	chr16:12047175-12047176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566906920	chr16:12047177-12047178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140202343	chr16:12047195-12047196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535872661	chr16:12047223-12047224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571437424	chr16:12047224-12047225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188372174	chr16:12047234-12047235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9922422	chr16:12047249-12047250	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs193185598	chr16:12047252-12047253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71408221	chr16:12047289-12047290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs386789058	chr16:12047290-12047291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs60899454	chr16:12047299-12047300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201158372	chr16:12047300-12047301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541809979	chr16:12047311-12047312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555386965	chr16:12047319-12047320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572425187	chr16:12047371-12047372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376047622	chr16:12047383-12047384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538362102	chr16:12047398-12047399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564486498	chr16:12047428-12047429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144350868	chr16:12047443-12047444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544082955	chr16:12047444-12047445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563963830	chr16:12047519-12047520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs36103994	chr16:12047570-12047571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529660398	chr16:12047597-12047598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548978567	chr16:12047651-12047652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558282314	chr16:12047721-12047722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs199678540	chr16:12047722-12047723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565705394	chr16:12047723-12047724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs578123779	chr16:12047734-12047735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12040400-12065400	Weak transcription	Fetal Intestine Small	intestine
2	chr16:12042000-12049200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr16:12042000-12049600	Weak transcription	A549	lung
4	chr16:12042200-12064400	Weak transcription	Fetal Stomach	stomach
5	chr16:12043200-12049200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr16:12044600-12047400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr16:12044600-12049400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr16:12044800-12048000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr16:12044800-12048800	Weak transcription	NHDF-Ad	bronchial
10	chr16:12044800-12049000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr16:12044800-12049200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr16:12044800-12052400	Weak transcription	GM12878-XiMat	blood
13	chr16:12044800-12056400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr16:12046400-12047600	Enhancers	HepG2	liver
15	chr16:12047400-12048200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr16:12047600-12047800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr16:12047800-12049000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr16:12048000-12049600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr16:12048200-12049200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr16:12048600-12064800	Weak transcription	Thymus	Thymus
21	chr16:12048800-12049800	Enhancers	NHDF-Ad	bronchial
22	chr16:12049000-12049600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:12049000-12049600	Enhancers	Osteobl	bone
24	chr16:12049000-12049800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr16:12049000-12050200	Enhancers	NHLF	lung
26	chr16:12049000-12053400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr16:12049200-12049400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr16:12049200-12049600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr16:12049200-12049600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr16:12049200-12049600	Enhancers	Hela-S3	cervix
31	chr16:12049200-12050200	Enhancers	K562	blood
32	chr16:12049200-12050400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr16:12049200-12050800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr16:12049400-12049600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr16:12049400-12049600	Enhancers	NHEK	skin
36	chr16:12049400-12049800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr16:12049400-12050000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr16:12049400-12050000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr16:12049400-12050200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:12049400-12050200	Enhancers	HSMM	muscle
41	chr16:12049600-12049800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr16:12049600-12049800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr16:12049600-12049800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr16:12049600-12050000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr16:12049600-12050000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr16:12049600-12050000	Enhancers	A549	lung
47	chr16:12049600-12050000	Flanking Active TSS	Osteobl	bone
48	chr16:12049600-12050200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr16:12049600-12050200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr16:12049600-12050200	Flanking Active TSS	Hela-S3	cervix

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