Variant report

Variant	nsv520818
Chromosome Location	chr3:69401248-69421495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:263)
CpG islands
(count:122)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:69417231-69417873	GM12878	blood:	n/a	n/a
2	ATF2	chr3:69417185-69417831	GM12878	blood:	n/a	n/a
3	BATF	chr3:69402806-69403041	GM12878	blood:	n/a	n/a
4	BATF	chr3:69402729-69403057	GM12878	blood:	n/a	n/a
5	BATF	chr3:69417416-69417782	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:69417370-69417804	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:69417378-69417781	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:69417311-69417899	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:69402548-69403163	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:69417395-69417835	GM12878	blood:	n/a	chr3:69417576-69417592
11	BRCA1	chr3:69403990-69404034	GM12878	blood:	n/a	n/a
12	CEBPB	chr3:69421062-69421637	HepG2	liver:	n/a	chr3:69421498-69421509
13	CEBPB	chr3:69412148-69412487	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:69412159-69412382	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:69412187-69412411	A549	lung:	n/a	n/a
16	CEBPB	chr3:69412321-69412368	K562	blood:	n/a	n/a
17	CEBPB	chr3:69402911-69403237	Hela-S3	cervix:	n/a	chr3:69403048-69403061
18	CEBPB	chr3:69413433-69413807	MCF-7	breast:	n/a	n/a
19	CEBPB	chr3:69402946-69403150	HepG2	liver:	n/a	chr3:69403048-69403061
20	CEBPB	chr3:69412156-69412463	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:69406405-69406753	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr3:69417301-69417880	GM12878	blood:	n/a	n/a
23	CTCF	chr3:69413500-69413650	BE2_C	brain:	n/a	n/a
24	CTCF	chr3:69413440-69413590	AG04449	skin:	n/a	n/a
25	CTCF	chr3:69406472-69406539	GM13976	blood:	n/a	n/a
26	CTCF	chr3:69417651-69417658	GM12878	blood:	n/a	n/a
27	CTCF	chr3:69405511-69405554	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr3:69416142-69416218	GM20000	blood:	n/a	n/a
29	CTCF	chr3:69413482-69413546	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:69405487-69405608	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr3:69413478-69413527	Fibrobl	skin:	n/a	n/a
32	CTCF	chr3:69413380-69413530	NHEK	skin:	n/a	n/a
33	CTCF	chr3:69413503-69413534	ProgFib	skin:	n/a	n/a
34	CTCF	chr3:69413452-69413531	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:69413320-69413470	SK-N-SH_RA	brain:	n/a	n/a
36	CUX1	chr3:69417211-69417817	GM12878	blood:	n/a	n/a
37	E2F4	chr3:69413490-69413794	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr3:69406504-69406666	MCF10A-Er-Src	breast:	n/a	n/a
39	EBF1	chr3:69417493-69417768	GM12878	blood:	n/a	n/a
40	EBF1	chr3:69417373-69417869	GM12878	blood:	n/a	n/a
41	EBF1	chr3:69417424-69417832	GM12878	blood:	n/a	n/a
42	EP300	chr3:69409765-69410145	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr3:69417316-69417814	GM12878	blood:	n/a	chr3:69417520-69417528
44	EP300	chr3:69417365-69417599	SK-N-SH_RA	brain:	n/a	chr3:69417520-69417528
45	EP300	chr3:69404173-69404436	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr3:69402740-69403061	GM12878	blood:	n/a	chr3:69402951-69402960
47	EP300	chr3:69417409-69417834	GM12878	blood:	n/a	chr3:69417520-69417528
48	EP300	chr3:69417385-69417658	SK-N-SH_RA	brain:	n/a	chr3:69417520-69417528
49	EP300	chr3:69413562-69413912	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr3:69417385-69417882	GM12878	blood:	n/a	chr3:69417520-69417528

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:69408925-69408975	MCF10A-Er-Src	breast:	n/a
2	chr3:69402811-69402861	RPTEC	kidney:	n/a
3	chr3:69402811-69402861	PANC-1	pancreas:	n/a
4	chr3:69408925-69408975	PrEC	prostate:	n/a
5	chr3:69408925-69408975	Hela-S3	cervix:	n/a
6	chr3:69408925-69408975	BE2_C	brain:	n/a
7	chr3:69402811-69402861	BE2_C	brain:	n/a
8	chr3:69402811-69402861	HepG2	liver:	n/a
9	chr3:69402811-69402861	Jurkat	blood:	n/a
10	chr3:69402811-69402861	NB4	blood:	n/a
11	chr3:69402811-69402861	ECC-1	luminal epithelium:	n/a
12	chr3:69408925-69408975	NT2-D1	testis:	n/a
13	chr3:69408925-69408975	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:69402811-69402861	T-47D	breast:	n/a
15	chr3:69408925-69408975	SK-N-SH	brain:	n/a
16	chr3:69402811-69402861	SK-N-MC	brain:	n/a
17	chr3:69402811-69402861	ovcar-3	ovarian:	n/a
18	chr3:69402811-69402861	LNCaP	prostate:	n/a
19	chr3:69402811-69402861	HMEC	breast:	n/a
20	chr3:69408925-69408975	NHDF-neo	bronchial:	n/a
21	chr3:69408925-69408975	ECC-1	luminal epithelium:	n/a
22	chr3:69402811-69402861	GM12891	blood:	n/a
23	chr3:69402811-69402861	IMR90	lung:	fetal
24	chr3:69402811-69402861	HCF	heart:	n/a
25	chr3:69408925-69408975	K562	blood:	n/a
26	chr3:69402811-69402861	PFSK-1	brain:	n/a
27	chr3:69408925-69408975	A549	lung:	n/a
28	chr3:69408925-69408975	HCM	heart:	n/a
29	chr3:69402811-69402861	H1-hESC	embryonic stem cell:	embryo
30	chr3:69408925-69408975	IMR90	lung:	fetal
31	chr3:69402811-69402861	ProgFib	skin:	n/a
32	chr3:69408925-69408975	Hepatocyte	liver:	n/a
33	chr3:69408925-69408975	HCF	heart:	n/a
34	chr3:69402811-69402861	MCF-7	breast:	n/a
35	chr3:69402811-69402861	HPAEpiC	pulmonary alveolar:	n/a
36	chr3:69402811-69402861	HEK293	kidney:	embryo
37	chr3:69408925-69408975	GM12878	blood:	n/a
38	chr3:69402811-69402861	AG04449	skin:	fetal
39	chr3:69408925-69408975	NHBE	bronchial:	n/a
40	chr3:69402811-69402861	HNPCEpiC	eye:	n/a
41	chr3:69408925-69408975	HEEpiC	esophagus:	n/a
42	chr3:69408925-69408975	SAEC	small airway:	n/a
43	chr3:69408925-69408975	AG09309	skin:	n/a
44	chr3:69402811-69402861	NH-A	brain:	n/a
45	chr3:69408925-69408975	AoSMC	blood vessel:	n/a
46	chr3:69408925-69408975	H1-hESC	embryonic stem cell:	embryo
47	chr3:69408925-69408975	HL-60	blood:	n/a
48	chr3:69408925-69408975	BJ	skin:	n/a
49	chr3:69402811-69402861	SK-N-SH_RA	brain:	n/a
50	chr3:69408925-69408975	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:69416233..69418620-chr3:69433830..69435946,2	MCF-7	breast:

No data

Variant related genes	Relation type
FRMD4B	TF binding region
FRMD4B	CpG island
ENSG00000114541	chromatin interactions

Extended variants
information (count: 864 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:864 , 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	rs4428187	chr3:69401248-69401249	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2128973	chr3:69401260-69401261	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs550384760	chr3:69401309-69401310	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs149025074	chr3:69401381-69401382	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs1905474	chr3:69401394-69401395	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs9861135	chr3:69401399-69401400	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192992434	chr3:69401459-69401460	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs569833203	chr3:69401490-69401491	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs17350402	chr3:69401498-69401499	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs184676864	chr3:69401500-69401501	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs578108690	chr3:69401502-69401503	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs13323667	chr3:69401503-69401504	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs187967620	chr3:69401524-69401525	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs142068196	chr3:69401528-69401529	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs147787045	chr3:69401564-69401565	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs192205879	chr3:69401578-69401579	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs528507495	chr3:69401651-69401652	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs141231384	chr3:69401673-69401674	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs565204784	chr3:69401690-69401691	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531052029	chr3:69401710-69401711	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs550323220	chr3:69401764-69401765	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs567128954	chr3:69401767-69401768	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs573245803	chr3:69401782-69401783	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs539079185	chr3:69401785-69401786	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs1564758	chr3:69401786-69401787	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1564757	chr3:69401804-69401805	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs553873519	chr3:69401822-69401823	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs374206677	chr3:69401832-69401833	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566448825	chr3:69401842-69401843	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544958035	chr3:69401849-69401850	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs538284405	chr3:69401893-69401894	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs368615496	chr3:69401900-69401901	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs558546907	chr3:69401902-69401903	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs542109437	chr3:69401919-69401920	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs568818421	chr3:69401941-69401942	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs146969375	chr3:69401953-69401954	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs184967323	chr3:69401962-69401963	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs138469020	chr3:69401984-69401985	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs561982327	chr3:69402000-69402001	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs74573438	chr3:69402068-69402069	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs553416487	chr3:69402072-69402073	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs574840779	chr3:69402085-69402086	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs767285	chr3:69402086-69402087	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs545041325	chr3:69402139-69402140	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs1010315	chr3:69402165-69402166	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530869612	chr3:69402188-69402189	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs189288781	chr3:69402229-69402230	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs560740578	chr3:69402232-69402233	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs543067549	chr3:69402244-69402245	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs559119129	chr3:69402253-69402254	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	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
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69372200-69403800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:69393400-69402600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr3:69394000-69403000	Weak transcription	HSMM	muscle
4	chr3:69397800-69406000	Weak transcription	HSMMtube	muscle
5	chr3:69400200-69401800	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr3:69400200-69402400	Enhancers	Brain Angular Gyrus	brain
7	chr3:69400200-69403400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:69400200-69405400	Enhancers	Brain Substantia Nigra	brain
9	chr3:69400400-69401400	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr3:69400400-69401800	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr3:69400400-69401800	Enhancers	Brain Cingulate Gyrus	brain
12	chr3:69400400-69401800	Enhancers	Fetal Thymus	thymus
13	chr3:69400400-69402200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr3:69400400-69403400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:69400400-69403400	Active TSS	Right Atrium	heart
16	chr3:69400400-69403400	Flanking Active TSS	Dnd41	blood
17	chr3:69400600-69401400	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr3:69400600-69402200	Enhancers	Primary B cells from cord blood	blood
19	chr3:69400600-69402800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr3:69400600-69412800	Weak transcription	Esophagus	oesophagus
21	chr3:69400800-69401400	Enhancers	Aorta	Aorta
22	chr3:69400800-69401600	Weak transcription	Thymus	Thymus
23	chr3:69400800-69402600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr3:69401000-69401400	Flanking Active TSS	HUVEC	blood vessel
25	chr3:69401000-69401600	Enhancers	Fetal Heart	heart
26	chr3:69401000-69401800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr3:69401000-69402000	Weak transcription	Fetal Lung	lung
28	chr3:69401000-69402000	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr3:69401000-69402600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr3:69401000-69403200	Active TSS	Adipose Nuclei	Adipose
31	chr3:69401000-69403800	Weak transcription	NHEK	skin
32	chr3:69401200-69401400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr3:69401200-69401800	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr3:69401200-69402000	Enhancers	Primary T cells from cord blood	blood
35	chr3:69401200-69402600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
36	chr3:69401200-69402800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
37	chr3:69401200-69403000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:69401400-69401600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr3:69401400-69401800	Active TSS	Primary hematopoietic stem cells	blood
40	chr3:69401400-69402000	Enhancers	Brain Anterior Caudate	brain
41	chr3:69401400-69402200	Weak transcription	Aorta	Aorta
42	chr3:69401400-69403000	Enhancers	Primary B cells from peripheral blood	blood
43	chr3:69401400-69403000	Active TSS	HUVEC	blood vessel
44	chr3:69401600-69402000	Enhancers	Thymus	Thymus
45	chr3:69401600-69402800	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr3:69401800-69402000	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr3:69401800-69402400	Weak transcription	Brain Cingulate Gyrus	brain
48	chr3:69401800-69402400	Active TSS	Brain Hippocampus Middle	brain
49	chr3:69401800-69402400	Weak transcription	Fetal Thymus	thymus
50	chr3:69401800-69402800	Active TSS	Brain Inferior Temporal Lobe	brain

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