Variant report

Variant	nsv819448
Chromosome Location	chr3:133145453-133165585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 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	ARID3A	chr3:133162962-133163067	K562	blood:	n/a	n/a
2	ARID3A	chr3:133156704-133157073	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:133162975-133163294	HepG2	liver:	n/a	n/a
4	ATF3	chr3:133162944-133163357	A549	lung:	n/a	n/a
5	BACH1	chr3:133163169-133163196	K562	blood:	n/a	n/a
6	BACH1	chr3:133163108-133163230	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr3:133161396-133161659	GM12878	blood:	n/a	n/a
8	BCL3	chr3:133162874-133163354	A549	lung:	n/a	n/a
9	BCL3	chr3:133162950-133163348	A549	lung:	n/a	n/a
10	BCLAF1	chr3:133160617-133161181	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:133160780-133160957	GM12878	blood:	n/a	n/a
12	CEBPB	chr3:133156859-133157194	IMR90	lung:	n/a	n/a
13	CEBPB	chr3:133162950-133163484	HCT-116	colon:	n/a	chr3:133163427-133163435
14	CEBPB	chr3:133156923-133157154	A549	lung:	n/a	n/a
15	CEBPB	chr3:133162969-133163312	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:133156748-133157253	A549	lung:	n/a	n/a
17	CEBPB	chr3:133162957-133163361	A549	lung:	n/a	n/a
18	CEBPB	chr3:133162871-133163463	A549	lung:	n/a	chr3:133163427-133163435
19	CEBPB	chr3:133162994-133163296	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:133159550-133159786	IMR90	lung:	n/a	n/a
21	CEBPB	chr3:133156922-133157253	MCF-7	breast:	n/a	n/a
22	CEBPB	chr3:133145164-133145977	IMR90	lung:	n/a	chr3:133145334-133145343 chr3:133145334-133145345
23	CEBPB	chr3:133163028-133163510	IMR90	lung:	n/a	chr3:133163427-133163435
24	CEBPB	chr3:133156900-133157098	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:133162968-133163397	MCF-7	breast:	n/a	n/a
26	CEBPB	chr3:133156910-133157182	A549	lung:	n/a	n/a
27	CEBPB	chr3:133156907-133157196	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:133160893-133161168	HepG2	liver:	n/a	chr3:133161039-133161050
29	CEBPB	chr3:133145227-133145479	HepG2	liver:	n/a	chr3:133145334-133145343 chr3:133145334-133145345
30	CEBPB	chr3:133160983-133161093	Hela-S3	cervix:	n/a	chr3:133161039-133161050
31	CEBPB	chr3:133162967-133163321	A549	lung:	n/a	n/a
32	CEBPB	chr3:133156962-133157088	HepG2	liver:	n/a	n/a
33	CHD2	chr3:133160707-133160856	GM12878	blood:	n/a	n/a
34	CTCF	chr3:133156520-133156670	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr3:133162923-133163122	A549	lung:	n/a	chr3:133162973-133162991 chr3:133162978-133162986 chr3:133162975-133162996
36	CTCF	chr3:133156520-133156670	AG09309	skin:	n/a	n/a
37	CTCF	chr3:133156560-133156710	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr3:133162860-133163010	AG04450	lung:	n/a	chr3:133162973-133162991 chr3:133162978-133162986 chr3:133162975-133162996
39	CTCF	chr3:133156581-133156656	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr3:133156500-133156650	BE2_C	brain:	n/a	n/a
41	CTCF	chr3:133162988-133163110	K562	blood:	n/a	n/a
42	CTCF	chr3:133162920-133163070	GM12874	blood:	n/a	chr3:133162973-133162991 chr3:133162978-133162986 chr3:133162975-133162996
43	CTCF	chr3:133147933-133147987	GM12892	blood:	n/a	n/a
44	CTCF	chr3:133156480-133156630	HMEC	breast:	n/a	n/a
45	CTCF	chr3:133156480-133156630	HPF	lung:	n/a	n/a
46	CTCF	chr3:133162940-133163090	RPTEC	kidney:	n/a	chr3:133162973-133162991 chr3:133162978-133162986 chr3:133162975-133162996
47	CTCF	chr3:133162940-133163090	GM12875	blood:	n/a	chr3:133162973-133162991 chr3:133162978-133162986 chr3:133162975-133162996
48	CTCF	chr3:133156680-133156830	HCM	heart:	n/a	n/a
49	CTCF	chr3:133162920-133163070	HPF	lung:	n/a	chr3:133162973-133162991 chr3:133162978-133162986 chr3:133162975-133162996
50	CTCF	chr3:133162900-133163050	HEEpiC	esophagus:	n/a	chr3:133162973-133162991 chr3:133162978-133162986 chr3:133162975-133162996

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133160722-133160772	HRCEpiC	kidney:	n/a
2	chr3:133160722-133160772	HCM	heart:	n/a
3	chr3:133160722-133160772	AG09319	gingival:	n/a
4	chr3:133160722-133160772	AG04450	lung:	fetal
5	chr3:133160722-133160772	U87	brain:	n/a
6	chr3:133160722-133160772	LNCaP	prostate:	n/a
7	chr3:133160722-133160772	ProgFib	skin:	n/a
8	chr3:133160722-133160772	HCT-116	colon:	n/a
9	chr3:133160722-133160772	SKMC	muscle:	n/a
10	chr3:133160722-133160772	HEEpiC	esophagus:	n/a
11	chr3:133160722-133160772	HMEC	breast:	n/a
12	chr3:133160722-133160772	IMR90	lung:	fetal
13	chr3:133160722-133160772	HL-60	blood:	n/a
14	chr3:133160722-133160772	HIPEpiC	eye:	n/a
15	chr3:133160722-133160772	ECC-1	luminal epithelium:	n/a
16	chr3:133160722-133160772	NHDF-neo	bronchial:	n/a
17	chr3:133160722-133160772	Jurkat	blood:	n/a
18	chr3:133160722-133160772	AoSMC	blood vessel:	n/a
19	chr3:133160722-133160772	Caco-2	colon:	n/a
20	chr3:133160722-133160772	HEK293	kidney:	embryo
21	chr3:133160722-133160772	BE2_C	brain:	n/a
22	chr3:133160722-133160772	AG04449	skin:	fetal
23	chr3:133160722-133160772	HAEpiC	amniotic membrane:	n/a
24	chr3:133160722-133160772	GM06990	blood:	n/a
25	chr3:133160722-133160772	NT2-D1	testis:	n/a
26	chr3:133160722-133160772	MCF-7	breast:	n/a
27	chr3:133160722-133160772	PFSK-1	brain:	n/a
28	chr3:133160722-133160772	GM19239	blood:	n/a
29	chr3:133160722-133160772	AG10803	skin:	n/a
30	chr3:133160722-133160772	RPTEC	kidney:	n/a
31	chr3:133160722-133160772	HCF	heart:	n/a
32	chr3:133160722-133160772	T-47D	breast:	n/a
33	chr3:133160722-133160772	ovcar-3	ovarian:	n/a
34	chr3:133160722-133160772	CMK	blood:	n/a
35	chr3:133160722-133160772	HNPCEpiC	eye:	n/a
36	chr3:133160722-133160772	NB4	blood:	n/a
37	chr3:133160722-133160772	SK-N-SH	brain:	n/a
38	chr3:133160722-133160772	SAEC	small airway:	n/a
39	chr3:133160722-133160772	PANC-1	pancreas:	n/a
40	chr3:133160722-133160772	HUVEC	blood vessel:	n/a
41	chr3:133160722-133160772	A549	lung:	n/a
42	chr3:133160722-133160772	H1-hESC	embryonic stem cell:	embryo
43	chr3:133160722-133160772	NHBE	bronchial:	n/a
44	chr3:133160722-133160772	MCF10A-Er-Src	breast:	n/a
45	chr3:133160722-133160772	HepG2	liver:	n/a
46	chr3:133160722-133160772	Hela-S3	cervix:	n/a
47	chr3:133160722-133160772	SK-N-MC	brain:	n/a
48	chr3:133160722-133160772	SK-N-SH_RA	brain:	n/a
49	chr3:133160722-133160772	HCPEpiC	choroid plexus:	n/a
50	chr3:133160722-133160772	PrEC	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:133164640..133168534-chr3:133291750..133294077,5	MCF-7	breast:
2	chr3:133146085..133148197-chr3:133291906..133294267,2	MCF-7	breast:
3	chr3:133162782..133163438-chr3:133297156..133297900,2	MCF-7	breast:
4	chr3:133157614..133159681-chr3:133160592..133163349,2	MCF-7	breast:
5	chr3:133162655..133165073-chr3:133302328..133304905,2	MCF-7	breast:
6	chr3:133162579..133164484-chr3:133291508..133294173,3	MCF-7	breast:
7	chr3:133157614..133159681-chr3:133160592..133163349,2	MCF-7	breast:
8	chr3:133153374..133155623-chr3:133178756..133181568,2	MCF-7	breast:
9	chr3:133143999..133146404-chr3:133171252..133173491,2	MCF-7	breast:
10	chr3:133103700..133105206-chr3:133145260..133147537,2	MCF-7	breast:
11	chr3:133161498..133163430-chr3:133177580..133180492,2	MCF-7	breast:
12	chr3:133155512..133157833-chr3:133291235..133293507,2	MCF-7	breast:
13	chr3:133159700..133161367-chr3:133523361..133526240,2	MCF-7	breast:
14	chr3:133161126..133163362-chr3:133716874..133718991,2	MCF-7	breast:
15	chr3:133162582..133163499-chr3:133297110..133297716,3	MCF-7	breast:
16	chr3:133157939..133159842-chr3:133161653..133163728,2	MCF-7	breast:
17	chr3:133157939..133159842-chr3:133161653..133163728,2	MCF-7	breast:
18	chr3:133155354..133158074-chr3:133292278..133293875,2	MCF-7	breast:
19	chr3:133162344..133164568-chr3:133170486..133172340,2	MCF-7	breast:
20	chr3:133162011..133163962-chr3:133171581..133174008,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOPBP1-1	chr3:133164249-133164419	ENSG00000249993.1
2	lnc-TOPBP1-1	chr3:133148113-133148553	ENSG00000249993.1

No data

Variant related genes	Relation type
BFSP2	TF binding region
BFSP2	CpG island
ENSG00000144867	chromatin interactions
ENSG00000091527	chromatin interactions

Extended variants
information (count: 880 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576672469	chr3:133145459-133145460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545416533	chr3:133145461-133145462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142514580	chr3:133145477-133145478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541674450	chr3:133145486-133145487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368492232	chr3:133145489-133145490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147127329	chr3:133145490-133145491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560253492	chr3:133145492-133145493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529011054	chr3:133145546-133145547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs56841612	chr3:133145571-133145572	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs10935062	chr3:133145587-133145588	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs368613295	chr3:133145628-133145629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531545996	chr3:133145657-133145658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551217469	chr3:133145670-133145671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571232565	chr3:133145732-133145733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6804296	chr3:133145755-133145756	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs79134908	chr3:133145770-133145771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144346236	chr3:133145789-133145790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76585288	chr3:133145827-133145828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147792852	chr3:133145861-133145862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79507961	chr3:133145872-133145873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539224946	chr3:133145918-133145919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559265964	chr3:133145930-133145931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572791309	chr3:133145939-133145940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9846931	chr3:133145961-133145962	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78092789	chr3:133145993-133145994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1795110	chr3:133146002-133146003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573676012	chr3:133146053-133146054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542396757	chr3:133146068-133146069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35019506	chr3:133146078-133146079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111839122	chr3:133146087-133146088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562608359	chr3:133146140-133146141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576130550	chr3:133146196-133146197	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs9847509	chr3:133146223-133146224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565661534	chr3:133146247-133146248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs527609222	chr3:133146261-133146262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs59636252	chr3:133146358-133146359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs28615290	chr3:133146422-133146423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530114142	chr3:133146463-133146464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs62280909	chr3:133146527-133146528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs114827910	chr3:133146540-133146541	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs73211865	chr3:133146549-133146550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577077613	chr3:133146555-133146556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554610267	chr3:133146608-133146609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552835975	chr3:133146609-133146610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182379860	chr3:133146651-133146652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535385317	chr3:133146660-133146661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141056814	chr3:133146662-133146663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573511861	chr3:133146704-133146705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536269316	chr3:133146715-133146716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555953806	chr3:133146782-133146783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Hailey-hailey disease	17597066	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133142800-133147000	Weak transcription	Placenta	Placenta
2	chr3:133142800-133147200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:133142800-133147400	Weak transcription	Esophagus	oesophagus
4	chr3:133142800-133151800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:133142800-133154000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:133143000-133145800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:133143400-133145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:133144800-133147200	Weak transcription	Liver	Liver
9	chr3:133145000-133146000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:133145000-133146400	Enhancers	Right Atrium	heart
11	chr3:133145000-133146600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:133145200-133146200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr3:133145200-133146400	Enhancers	Osteobl	bone
14	chr3:133145400-133145600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr3:133145400-133146200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr3:133145400-133146400	Enhancers	HSMMtube	muscle
17	chr3:133145600-133145800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:133145600-133146200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr3:133145800-133147000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:133145800-133148400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr3:133146600-133147600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:133147000-133147600	Enhancers	Placenta	Placenta
23	chr3:133147000-133147800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr3:133147200-133147600	Bivalent Enhancer	HepG2	liver
25	chr3:133147200-133147800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:133147200-133147800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:133147200-133147800	Enhancers	Liver	Liver
28	chr3:133147400-133147600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr3:133147400-133147600	Enhancers	Esophagus	oesophagus
30	chr3:133147400-133147600	Bivalent Enhancer	NHEK	skin
31	chr3:133147400-133147800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:133147400-133147800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:133147400-133147800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr3:133147400-133147800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr3:133147400-133147800	Enhancers	HMEC	breast
36	chr3:133147400-133148400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr3:133147600-133147800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:133147600-133148400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr3:133147600-133148400	Enhancers	HepG2	liver
40	chr3:133147800-133150800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr3:133147800-133151000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:133147800-133152400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr3:133147800-133154200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr3:133148400-133156400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr3:133148400-133159200	Weak transcription	Thymus	Thymus
46	chr3:133149800-133150800	Active TSS	H9 Cell Line	embryonic stem cell
47	chr3:133151000-133151800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:133151000-133152200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr3:133151000-133152200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:133151800-133152200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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