Variant report

Variant	nsv877508
Chromosome Location	chr3:133476852-133482662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr3:133479994-133480008	K562	blood:	n/a	n/a
2	CEBPD	chr3:133482530-133482862	HepG2	liver:	n/a	n/a
3	CHD2	chr3:133479901-133479985	HepG2	liver:	n/a	n/a
4	CREB1	chr3:133480463-133481323	HepG2	liver:	n/a	n/a
5	CREB1	chr3:133482430-133483252	HepG2	liver:	n/a	n/a
6	CREB1	chr3:133476809-133477089	GM12878	blood:	n/a	n/a
7	CTCF	chr3:133478377-133478442	Fibrobl	skin:	n/a	n/a
8	E2F4	chr3:133478743-133478933	MCF10A-Er-Src	breast:	n/a	n/a
9	FOSL2	chr3:133480329-133481334	HepG2	liver:	n/a	n/a
10	FOSL2	chr3:133482442-133483395	HepG2	liver:	n/a	n/a
11	HEY1	chr3:133481157-133481296	HepG2	liver:	n/a	n/a
12	HEY1	chr3:133482177-133483767	HepG2	liver:	n/a	n/a
13	HEY1	chr3:133480476-133480891	HepG2	liver:	n/a	n/a
14	HEY1	chr3:133470261-133482084	HepG2	liver:	n/a	n/a
15	HEY1	chr3:133479740-133479985	HepG2	liver:	n/a	n/a
16	MBD4	chr3:133480265-133482101	HepG2	liver:	n/a	n/a
17	MBD4	chr3:133479369-133483413	HepG2	liver:	n/a	n/a
18	MBD4	chr3:133477652-133478030	HepG2	liver:	n/a	n/a
19	MBD4	chr3:133477352-133477689	HepG2	liver:	n/a	n/a
20	MBD4	chr3:133482345-133483652	HepG2	liver:	n/a	n/a
21	MBD4	chr3:133477931-133478586	HepG2	liver:	n/a	n/a
22	MBD4	chr3:133479421-133480110	HepG2	liver:	n/a	n/a
23	MYBL2	chr3:133480419-133481132	HepG2	liver:	n/a	n/a
24	NFIC	chr3:133480477-133481222	HepG2	liver:	n/a	n/a
25	NFIC	chr3:133482605-133483155	HepG2	liver:	n/a	n/a
26	POLR2A	chr3:133479493-133481361	HepG2	liver:	n/a	n/a
27	POLR2A	chr3:133479294-133484913	HepG2	liver:	n/a	n/a
28	POLR2A	chr3:133481526-133482036	HepG2	liver:	n/a	n/a
29	POLR2A	chr3:133480748-133480882	HepG2	liver:	n/a	n/a
30	POLR2A	chr3:133479792-133479986	HepG2	liver:	n/a	n/a
31	POLR2A	chr3:133479562-133479670	HepG2	liver:	n/a	n/a
32	POLR2A	chr3:133480532-133481275	HepG2	liver:	n/a	n/a
33	POLR2A	chr3:133482481-133484475	HepG2	liver:	n/a	n/a
34	POLR2A	chr3:133478785-133479036	HepG2	liver:	n/a	n/a
35	POLR2A	chr3:133482335-133484568	HepG2	liver:	n/a	n/a
36	POLR2A	chr3:133479991-133480081	HepG2	liver:	n/a	n/a
37	POLR2A	chr3:133464423-133479250	HepG2	liver:	n/a	n/a
38	POLR2A	chr3:133480463-133480553	HepG2	liver:	n/a	n/a
39	POLR2A	chr3:133470213-133490385	HepG2	liver:	n/a	n/a
40	POLR2A	chr3:133477393-133478670	HepG2	liver:	n/a	n/a
41	POLR2A	chr3:133480992-133481080	HepG2	liver:	n/a	n/a
42	POLR2A	chr3:133480189-133480324	HepG2	liver:	n/a	n/a
43	POLR2A	chr3:133479434-133482047	HepG2	liver:	n/a	n/a
44	POLR2A	chr3:133477540-133477672	HepG2	liver:	n/a	n/a
45	POLR2A	chr3:133481110-133481279	HepG2	liver:	n/a	n/a
46	POLR2A	chr3:133476652-133477002	HepG2	liver:	n/a	n/a
47	POLR2A	chr3:133470633-133487808	HepG2	liver:	n/a	n/a
48	POLR2A	chr3:133482564-133483225	HepG2	liver:	n/a	n/a
49	POLR2A	chr3:133476652-133477277	HepG2	liver:	n/a	n/a
50	POLR2A	chr3:133477110-133477205	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133476947-133476997	NHBE	bronchial:	n/a
2	chr3:133476947-133476997	AG09309	skin:	n/a
3	chr3:133476947-133476997	ECC-1	luminal epithelium:	n/a
4	chr3:133476947-133476997	IMR90	lung:	fetal
5	chr3:133476947-133476997	HRE	kidney:	n/a
6	chr3:133476947-133476997	HUVEC	blood vessel:	n/a
7	chr3:133476947-133476997	HPAEpiC	pulmonary alveolar:	n/a
8	chr3:133476947-133476997	NB4	blood:	n/a
9	chr3:133476947-133476997	HRPEpiC	eye:	n/a
10	chr3:133476947-133476997	GM12891	blood:	n/a
11	chr3:133476947-133476997	NHDF-neo	bronchial:	n/a
12	chr3:133476947-133476997	K562	blood:	n/a
13	chr3:133476947-133476997	ProgFib	skin:	n/a
14	chr3:133476947-133476997	NH-A	brain:	n/a
15	chr3:133476947-133476997	NT2-D1	testis:	n/a
16	chr3:133476947-133476997	SAEC	small airway:	n/a
17	chr3:133476947-133476997	AG09319	gingival:	n/a
18	chr3:133476947-133476997	LNCaP	prostate:	n/a
19	chr3:133476947-133476997	MCF-7	breast:	n/a
20	chr3:133476947-133476997	Caco-2	colon:	n/a
21	chr3:133476947-133476997	HAEpiC	amniotic membrane:	n/a
22	chr3:133476947-133476997	Jurkat	blood:	n/a
23	chr3:133476947-133476997	HNPCEpiC	eye:	n/a
24	chr3:133476947-133476997	SK-N-SH	brain:	n/a
25	chr3:133476947-133476997	Hela-S3	cervix:	n/a
26	chr3:133476947-133476997	RPTEC	kidney:	n/a
27	chr3:133476947-133476997	H1-hESC	embryonic stem cell:	embryo
28	chr3:133476947-133476997	PFSK-1	brain:	n/a
29	chr3:133476947-133476997	HCT-116	colon:	n/a
30	chr3:133476947-133476997	U87	brain:	n/a
31	chr3:133476947-133476997	PANC-1	pancreas:	n/a
32	chr3:133476947-133476997	HIPEpiC	eye:	n/a
33	chr3:133476947-133476997	HL-60	blood:	n/a
34	chr3:133476947-133476997	GM12892	blood:	n/a
35	chr3:133476947-133476997	HRCEpiC	kidney:	n/a
36	chr3:133476947-133476997	SK-N-SH_RA	brain:	n/a
37	chr3:133476947-133476997	GM06990	blood:	n/a
38	chr3:133476947-133476997	BE2_C	brain:	n/a
39	chr3:133476947-133476997	AG04449	skin:	fetal
40	chr3:133476947-133476997	HCM	heart:	n/a
41	chr3:133476947-133476997	CMK	blood:	n/a
42	chr3:133476947-133476997	SKMC	muscle:	n/a
43	chr3:133476947-133476997	SK-N-MC	brain:	n/a
44	chr3:133476947-133476997	GM19239	blood:	n/a
45	chr3:133476947-133476997	HMEC	breast:	n/a
46	chr3:133476947-133476997	HepG2	liver:	n/a
47	chr3:133476947-133476997	HCPEpiC	choroid plexus:	n/a
48	chr3:133476947-133476997	A549	lung:	n/a
49	chr3:133476947-133476997	T-47D	breast:	n/a
50	chr3:133476947-133476997	AG10803	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:133380292..133382359-chr3:133479467..133482336,2	K562	blood:
2	chr3:133475218..133478981-chr3:133481312..133484055,3	K562	blood:
3	chr3:133482007..133483955-chr3:133484713..133486913,2	MCF-7	breast:
4	chr3:133475218..133478981-chr3:133481312..133484055,3	K562	blood:
5	chr3:133465852..133468285-chr3:133474499..133477437,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPRB-3	chr3:133479144-133480223	NONHSAT092201
2	lnc-SRPRB-3	chr3:133480371-133481207	NONHSAT092201

No data

Variant related genes	Relation type
TF	TF binding region
ENSG00000244062	TF binding region
TF	CpG island
ENSG00000244062	CpG island
ENSG00000091513	chromatin interactions
ENSG00000163781	chromatin interactions
ENSG00000242337	chromatin interactions

Extended variants
information (count: 226 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:226 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3811658	chr3:133476852-133476853	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371248506	chr3:133476883-133476884	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs533690480	chr3:133476919-133476920	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs189251880	chr3:133476948-133476949	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567212050	chr3:133477030-133477031	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536283108	chr3:133477045-133477046	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs8177239	chr3:133477055-133477056	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576359489	chr3:133477102-133477103	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs35285178	chr3:133477114-133477115	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs41295776	chr3:133477179-133477180	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs558968284	chr3:133477208-133477209	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs181001278	chr3:133477231-133477232	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376758199	chr3:133477250-133477251	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541642405	chr3:133477256-133477257	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs561609908	chr3:133477260-133477261	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575162358	chr3:133477264-133477265	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544066028	chr3:133477330-133477331	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185492672	chr3:133477406-133477407	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs368069498	chr3:133477452-133477453	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs62280595	chr3:133477577-133477578	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs41295778	chr3:133477600-133477601	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190792011	chr3:133477618-133477619	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs8177240	chr3:133477701-133477702	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
24	rs370077835	chr3:133477703-133477704	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs373291188	chr3:133477726-133477727	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs547175702	chr3:133477746-133477747	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs567252954	chr3:133477747-133477748	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs536179950	chr3:133477758-133477759	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs550017522	chr3:133477785-133477786	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs181589522	chr3:133477799-133477800	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs41295780	chr3:133477809-133477810	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs190085055	chr3:133477821-133477822	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs572563809	chr3:133477857-133477858	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs535258360	chr3:133477863-133477864	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577233849	chr3:133477867-133477868	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs72561468	chr3:133477880-133477881	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567683199	chr3:133477897-133477898	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs561630136	chr3:133477903-133477904	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs575052571	chr3:133477918-133477919	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs181329139	chr3:133477926-133477927	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs8177241	chr3:133477961-133477962	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373656369	chr3:133477986-133477987	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs17857483	chr3:133478022-133478023	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs193921099	chr3:133478039-133478040	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs367643653	chr3:133478047-133478048	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201821346	chr3:133478063-133478064	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs575999145	chr3:133478065-133478066	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112157819	chr3:133478077-133478078	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs1804498	chr3:133478101-133478102	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs142766964	chr3:133478112-133478113	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Obesity	21131291	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133465600-133483000	Weak transcription	Brain Germinal Matrix	brain
2	chr3:133471600-133477600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr3:133471800-133477000	Genic enhancers	Brain Cingulate Gyrus	brain
4	chr3:133472400-133480600	Strong transcription	Brain Angular Gyrus	brain
5	chr3:133473400-133480800	Strong transcription	Brain Inferior Temporal Lobe	brain
6	chr3:133473800-133478200	Strong transcription	Liver	Liver
7	chr3:133474000-133480200	Strong transcription	Brain Hippocampus Middle	brain
8	chr3:133475000-133487000	Weak transcription	Fetal Brain Male	brain
9	chr3:133475200-133480800	Strong transcription	HepG2	liver
10	chr3:133475200-133482800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:133475600-133477400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:133476200-133477000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:133476200-133477200	Enhancers	HMEC	breast
14	chr3:133476200-133477800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:133476200-133478600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr3:133476400-133477400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr3:133476400-133478400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr3:133476800-133477000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr3:133476800-133477000	Enhancers	Stomach Smooth Muscle	stomach
20	chr3:133476800-133477000	Bivalent Enhancer	NHEK	skin
21	chr3:133476800-133477200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr3:133476800-133477200	Genic enhancers	Brain Anterior Caudate	brain
23	chr3:133476800-133478200	Strong transcription	Brain Substantia Nigra	brain
24	chr3:133476800-133478800	Strong transcription	Adipose Nuclei	Adipose
25	chr3:133477000-133478000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr3:133477000-133478800	Strong transcription	Brain Cingulate Gyrus	brain
27	chr3:133477000-133490400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr3:133477200-133478400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:133477200-133480400	Strong transcription	Brain Anterior Caudate	brain
30	chr3:133477400-133477600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:133477600-133478200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr3:133477800-133480800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:133478000-133478200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr3:133478200-133478400	Genic enhancers	Liver	Liver
35	chr3:133478200-133478600	Genic enhancers	Brain Substantia Nigra	brain
36	chr3:133478200-133480000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr3:133478400-133478800	Strong transcription	Liver	Liver
38	chr3:133478600-133480400	Strong transcription	Brain Substantia Nigra	brain
39	chr3:133478800-133479000	Genic enhancers	Liver	Liver
40	chr3:133478800-133479400	Weak transcription	Adipose Nuclei	Adipose
41	chr3:133478800-133479600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr3:133478800-133482600	Weak transcription	Left Ventricle	heart
43	chr3:133479000-133480600	Strong transcription	Liver	Liver
44	chr3:133479400-133480000	Strong transcription	Adipose Nuclei	Adipose
45	chr3:133479600-133482400	Strong transcription	Brain Cingulate Gyrus	brain
46	chr3:133480000-133482800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:133480000-133483800	Weak transcription	Adipose Nuclei	Adipose
48	chr3:133480200-133481000	Genic enhancers	Brain Hippocampus Middle	brain
49	chr3:133480400-133480800	Genic enhancers	Brain Anterior Caudate	brain
50	chr3:133480400-133486000	Genic enhancers	Brain Substantia Nigra	brain

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