Variant report

Variant	esv3380897
Chromosome Location	chr3:133473262-133477260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:42)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:42 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CREB1	chr3:133476809-133477089	GM12878	blood:	n/a	n/a
2	CTCF	chr3:133474320-133474470	HepG2	liver:	n/a	n/a
3	EP300	chr3:133472535-133473279	K562	blood:	n/a	n/a
4	FOXA2	chr3:133474162-133474419	HepG2	liver:	n/a	n/a
5	HEY1	chr3:133473097-133473281	HepG2	liver:	n/a	n/a
6	HEY1	chr3:133473291-133473511	HepG2	liver:	n/a	n/a
7	HEY1	chr3:133473752-133474037	HepG2	liver:	n/a	n/a
8	HEY1	chr3:133470261-133482084	HepG2	liver:	n/a	n/a
9	MAFF	chr3:133474007-133474350	HepG2	liver:	n/a	chr3:133474058-133474072 chr3:133474052-133474070
10	MAFK	chr3:133473937-133474137	HepG2	liver:	n/a	chr3:133474058-133474072 chr3:133474055-133474075 chr3:133474057-133474073
11	MAFK	chr3:133474065-133474086	HepG2	liver:	n/a	n/a
12	MAX	chr3:133474031-133474048	HepG2	liver:	n/a	n/a
13	MBD4	chr3:133472924-133473670	HepG2	liver:	n/a	n/a
14	MBD4	chr3:133474519-133475288	HepG2	liver:	n/a	n/a
15	MBD4	chr3:133474511-133475269	HepG2	liver:	n/a	n/a
16	MYBL2	chr3:133473141-133473785	HepG2	liver:	n/a	n/a
17	MYC	chr3:133474182-133474312	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr3:133476652-133477002	HepG2	liver:	n/a	n/a
19	POLR2A	chr3:133476761-133478522	HepG2	liver:	n/a	n/a
20	POLR2A	chr3:133471516-133487597	HepG2	liver:	n/a	n/a
21	POLR2A	chr3:133475253-133475559	HepG2	liver:	n/a	n/a
22	POLR2A	chr3:133473701-133474055	HepG2	liver:	n/a	n/a
23	POLR2A	chr3:133477110-133477205	HepG2	liver:	n/a	n/a
24	POLR2A	chr3:133476996-133477011	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr3:133474847-133476583	HepG2	liver:	n/a	n/a
26	POLR2A	chr3:133476652-133477277	HepG2	liver:	n/a	n/a
27	POLR2A	chr3:133471473-133476552	HepG2	liver:	n/a	n/a
28	POLR2A	chr3:133476920-133477020	GM12878	blood:	n/a	n/a
29	POLR2A	chr3:133470633-133487808	HepG2	liver:	n/a	n/a
30	POLR2A	chr3:133474056-133474741	HepG2	liver:	n/a	n/a
31	POLR2A	chr3:133471573-133479086	HepG2	liver:	n/a	n/a
32	POLR2A	chr3:133474909-133475163	HepG2	liver:	n/a	n/a
33	POLR2A	chr3:133473156-133474810	HepG2	liver:	n/a	n/a
34	POLR2A	chr3:133464423-133479250	HepG2	liver:	n/a	n/a
35	POLR2A	chr3:133475563-133476507	HepG2	liver:	n/a	n/a
36	POLR2A	chr3:133473171-133473686	HepG2	liver:	n/a	n/a
37	POLR2A	chr3:133470213-133490385	HepG2	liver:	n/a	n/a
38	RCOR1	chr3:133473951-133474332	K562	blood:	n/a	n/a
39	STAT3	chr3:133476918-133477118	MCF10A-Er-Src	breast:	n/a	n/a
40	STAT3	chr3:133477006-133477027	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr3:133476953-133477098	MCF10A-Er-Src	breast:	n/a	n/a
42	ZEB1	chr3:133475744-133475962	GM12878	blood:	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	NH-A	brain:	n/a
2	chr3:133476947-133476997	AG09309	skin:	n/a
3	chr3:133476947-133476997	MCF10A-Er-Src	breast:	n/a
4	chr3:133476947-133476997	Hela-S3	cervix:	n/a
5	chr3:133476947-133476997	PANC-1	pancreas:	n/a
6	chr3:133476947-133476997	GM12878	blood:	n/a
7	chr3:133476947-133476997	HRE	kidney:	n/a
8	chr3:133476947-133476997	PrEC	prostate:	n/a
9	chr3:133476947-133476997	HAEpiC	amniotic membrane:	n/a
10	chr3:133476947-133476997	AG10803	skin:	n/a
11	chr3:133476947-133476997	ECC-1	luminal epithelium:	n/a
12	chr3:133476947-133476997	LNCaP	prostate:	n/a
13	chr3:133476947-133476997	ProgFib	skin:	n/a
14	chr3:133476947-133476997	HepG2	liver:	n/a
15	chr3:133476947-133476997	BJ	skin:	n/a
16	chr3:133476947-133476997	AG04450	lung:	fetal
17	chr3:133476947-133476997	NHBE	bronchial:	n/a
18	chr3:133476947-133476997	HRPEpiC	eye:	n/a
19	chr3:133476947-133476997	HMEC	breast:	n/a
20	chr3:133476947-133476997	T-47D	breast:	n/a
21	chr3:133476947-133476997	HEEpiC	esophagus:	n/a
22	chr3:133476947-133476997	RPTEC	kidney:	n/a
23	chr3:133476947-133476997	ovcar-3	ovarian:	n/a
24	chr3:133476947-133476997	HEK293	kidney:	embryo
25	chr3:133476947-133476997	PFSK-1	brain:	n/a
26	chr3:133476947-133476997	GM12892	blood:	n/a
27	chr3:133476947-133476997	HRCEpiC	kidney:	n/a
28	chr3:133476947-133476997	Jurkat	blood:	n/a
29	chr3:133476947-133476997	Hepatocyte	liver:	n/a
30	chr3:133476947-133476997	HCPEpiC	choroid plexus:	n/a
31	chr3:133476947-133476997	HUVEC	blood vessel:	n/a
32	chr3:133476947-133476997	GM06990	blood:	n/a
33	chr3:133476947-133476997	U87	brain:	n/a
34	chr3:133476947-133476997	Caco-2	colon:	n/a
35	chr3:133476947-133476997	AG04449	skin:	fetal
36	chr3:133476947-133476997	K562	blood:	n/a
37	chr3:133476947-133476997	CMK	blood:	n/a
38	chr3:133476947-133476997	MCF-7	breast:	n/a
39	chr3:133476947-133476997	HCF	heart:	n/a
40	chr3:133476947-133476997	SK-N-MC	brain:	n/a
41	chr3:133476947-133476997	SKMC	muscle:	n/a
42	chr3:133476947-133476997	GM12891	blood:	n/a
43	chr3:133476947-133476997	H1-hESC	embryonic stem cell:	embryo
44	chr3:133476947-133476997	SAEC	small airway:	n/a
45	chr3:133476947-133476997	SK-N-SH	brain:	n/a
46	chr3:133476947-133476997	HNPCEpiC	eye:	n/a
47	chr3:133476947-133476997	NHDF-neo	bronchial:	n/a
48	chr3:133476947-133476997	NB4	blood:	n/a
49	chr3:133476947-133476997	NT2-D1	testis:	n/a
50	chr3:133476947-133476997	A549	lung:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:133425971..133428369-chr3:133473525..133475765,2	MCF-7	breast:
2	chr3:133465852..133468285-chr3:133474499..133477437,3	K562	blood:
3	chr3:133472488..133475139-chr3:133486239..133489016,2	K562	blood:
4	chr3:133300041..133302235-chr3:133472033..133474036,2	K562	blood:
5	chr3:133465852..133469783-chr3:133471795..133476120,4	K562	blood:
6	chr3:133475218..133478981-chr3:133481312..133484055,3	K562	blood:

No data

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

Extended variants
information (count: 241 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:241 , 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	rs181704759	chr3:133473267-133473268	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs6778321	chr3:133473272-133473273	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549557016	chr3:133473273-133473274	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs569967495	chr3:133473275-133473276	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377427556	chr3:133473307-133473308	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs8177219	chr3:133473316-133473317	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs41298985	chr3:133473342-133473343	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs150548621	chr3:133473346-133473347	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs199624323	chr3:133473347-133473348	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534968613	chr3:133473365-133473366	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147540361	chr3:133473390-133473391	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377049120	chr3:133473396-133473397	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11549904	chr3:133473421-133473422	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113868497	chr3:133473430-133473431	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs1799830	chr3:133473437-133473438	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574975008	chr3:133473442-133473443	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs41298987	chr3:133473445-133473446	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs34331733	chr3:133473459-133473460	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371174384	chr3:133473498-133473499	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557564745	chr3:133473505-133473506	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113724772	chr3:133473516-133473517	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs75839677	chr3:133473525-133473526	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201033555	chr3:133473527-133473528	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546197673	chr3:133473544-133473545	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs367874174	chr3:133473553-133473554	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559959215	chr3:133473557-133473558	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs149623220	chr3:133473561-133473562	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs540623974	chr3:133473579-133473580	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs8177220	chr3:133473625-133473626	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs8177221	chr3:133473643-133473644	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs549593678	chr3:133473734-133473735	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs8177222	chr3:133473742-133473743	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs8177223	chr3:133473767-133473768	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs552191508	chr3:133473768-133473769	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565959721	chr3:133473769-133473770	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528535342	chr3:133473782-133473783	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs548585036	chr3:133473795-133473796	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs41298989	chr3:133473797-133473798	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568596044	chr3:133473806-133473807	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs8177321	chr3:133473834-133473835	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545614722	chr3:133473870-133473871	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs41298991	chr3:133473933-133473934	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4854759	chr3:133473945-133473946	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs553439136	chr3:133473962-133473963	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573475314	chr3:133473974-133473975	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs8177224	chr3:133474003-133474004	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs554124527	chr3:133474016-133474017	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574067647	chr3:133474101-133474102	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552185567	chr3:133474133-133474134	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144319413	chr3:133474138-133474139	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive 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:69 , 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	chr3:133466800-133476800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:133469600-133473400	Weak transcription	Adipose Nuclei	Adipose
4	chr3:133469600-133473800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr3:133469600-133474400	Weak transcription	Fetal Intestine Small	intestine
6	chr3:133469600-133476400	Weak transcription	Fetal Muscle Leg	muscle
7	chr3:133471200-133473800	Genic enhancers	Liver	Liver
8	chr3:133471400-133474800	Genic enhancers	Brain Substantia Nigra	brain
9	chr3:133471600-133477600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr3:133471800-133474000	Genic enhancers	Brain Hippocampus Middle	brain
11	chr3:133471800-133477000	Genic enhancers	Brain Cingulate Gyrus	brain
12	chr3:133472000-133473400	Genic enhancers	Brain Inferior Temporal Lobe	brain
13	chr3:133472000-133474800	Enhancers	K562	blood
14	chr3:133472000-133476400	Enhancers	Esophagus	oesophagus
15	chr3:133472400-133480600	Strong transcription	Brain Angular Gyrus	brain
16	chr3:133472800-133473600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr3:133473000-133474200	Enhancers	NHEK	skin
18	chr3:133473000-133476800	Strong transcription	Brain Anterior Caudate	brain
19	chr3:133473200-133473800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr3:133473200-133473800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:133473200-133473800	Enhancers	HMEC	breast
22	chr3:133473200-133475200	Genic enhancers	HepG2	liver
23	chr3:133473200-133476200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:133473400-133473600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr3:133473400-133476000	Strong transcription	Adipose Nuclei	Adipose
26	chr3:133473400-133480800	Strong transcription	Brain Inferior Temporal Lobe	brain
27	chr3:133473600-133474600	Enhancers	Fetal Muscle Trunk	muscle
28	chr3:133473600-133475400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr3:133473800-133474000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:133473800-133475200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr3:133473800-133476200	Weak transcription	HMEC	breast
32	chr3:133473800-133478200	Strong transcription	Liver	Liver
33	chr3:133474000-133474600	Bivalent Enhancer	HSMMtube	muscle
34	chr3:133474000-133475600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:133474000-133480200	Strong transcription	Brain Hippocampus Middle	brain
36	chr3:133474200-133475600	Weak transcription	NHEK	skin
37	chr3:133474800-133476400	Strong transcription	Brain Substantia Nigra	brain
38	chr3:133475000-133487000	Weak transcription	Fetal Brain Male	brain
39	chr3:133475200-133480800	Strong transcription	HepG2	liver
40	chr3:133475200-133482800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:133475600-133476000	Enhancers	NHEK	skin
42	chr3:133475600-133477400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:133475800-133476000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr3:133475800-133476600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr3:133476000-133476400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:133476000-133476400	Flanking Active TSS	NHEK	skin
47	chr3:133476000-133476800	Weak transcription	Adipose Nuclei	Adipose
48	chr3:133476200-133477000	Enhancers	H1 Cell Line	embryonic stem cell
49	chr3:133476200-133477200	Enhancers	HMEC	breast
50	chr3:133476200-133477800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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