Variant report

Variant	nsv591302
Chromosome Location	chr3:113543081-113600970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1183)
CpG islands
(count:794)
Chromatin interactive
region (count:11)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1183 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:113563487-113563843	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:113592645-113593092	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:113549468-113549777	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:113553861-113554283	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:113557690-113557699	HepG2	liver:	n/a	n/a
6	ATF2	chr3:113551179-113551829	GM12878	blood:	n/a	n/a
7	ATF2	chr3:113557453-113558048	GM12878	blood:	n/a	n/a
8	ATF2	chr3:113549332-113549896	GM12878	blood:	n/a	n/a
9	ATF2	chr3:113557386-113557741	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr3:113557365-113557725	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr3:113551240-113551678	GM12878	blood:	n/a	n/a
12	ATF2	chr3:113543719-113544392	GM12878	blood:	n/a	n/a
13	ATF2	chr3:113543753-113544403	GM12878	blood:	n/a	n/a
14	ATF3	chr3:113549311-113549852	HCT-116	colon:	n/a	n/a
15	BACH1	chr3:113557547-113557988	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr3:113557431-113558104	GM12878	blood:	n/a	n/a
17	BATF	chr3:113549468-113549812	GM12878	blood:	n/a	chr3:113549675-113549686
18	BATF	chr3:113554363-113554694	GM12878	blood:	n/a	chr3:113554538-113554549
19	BATF	chr3:113554376-113554710	GM12878	blood:	n/a	chr3:113554538-113554549
20	BATF	chr3:113551314-113551664	GM12878	blood:	n/a	n/a
21	BATF	chr3:113543809-113544367	GM12878	blood:	n/a	n/a
22	BATF	chr3:113557751-113558078	GM12878	blood:	n/a	n/a
23	BATF	chr3:113549492-113549856	GM12878	blood:	n/a	chr3:113549675-113549686
24	BATF	chr3:113543805-113544297	GM12878	blood:	n/a	n/a
25	BATF	chr3:113551303-113551580	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:113557740-113558032	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:113543875-113544271	GM12878	blood:	n/a	chr3:113544088-113544097 chr3:113544087-113544096
28	BCL11A	chr3:113547546-113547750	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:113543819-113544325	GM12878	blood:	n/a	chr3:113544088-113544097 chr3:113544087-113544096
30	BCL11A	chr3:113551267-113551638	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:113549431-113549885	GM12878	blood:	n/a	n/a
32	BCL3	chr3:113557512-113557849	GM12878	blood:	n/a	n/a
33	BCL3	chr3:113543767-113544250	GM12878	blood:	n/a	chr3:113544088-113544097 chr3:113544087-113544096
34	BCL3	chr3:113551320-113551657	GM12878	blood:	n/a	n/a
35	BCLAF1	chr3:113557338-113558171	GM12878	blood:	n/a	n/a
36	BCLAF1	chr3:113549315-113549852	GM12878	blood:	n/a	n/a
37	BCLAF1	chr3:113543758-113544443	GM12878	blood:	n/a	chr3:113544088-113544097 chr3:113544087-113544096
38	BHLHE40	chr3:113557433-113557669	K562	blood:	n/a	n/a
39	BHLHE40	chr3:113557466-113557770	HepG2	liver:	n/a	n/a
40	BHLHE40	chr3:113563537-113563769	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:113548839-113549838	GM12878	blood:	n/a	n/a
42	BRCA1	chr3:113557473-113558378	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr3:113557443-113557740	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr3:113557594-113557623	HepG2	liver:	n/a	n/a
45	CBX3	chr3:113549370-113549959	HCT-116	colon:	n/a	n/a
46	CBX3	chr3:113550485-113550666	K562	blood:	n/a	n/a
47	CBX3	chr3:113598730-113599055	K562	blood:	n/a	n/a
48	CCNT2	chr3:113556763-113556875	K562	blood:	n/a	n/a
49	CCNT2	chr3:113557519-113557889	K562	blood:	n/a	n/a
50	CEBPB	chr3:113566783-113567371	HCT-116	colon:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:113557582-113557632	HEEpiC	esophagus:	n/a
2	chr3:113557582-113557632	HEEpiC	esophagus:	n/a
3	chr3:113557646-113557696	NHDF-neo	bronchial:	n/a
4	chr3:113557462-113557512	NB4	blood:	n/a
5	chr3:113557462-113557512	AG09319	gingival:	n/a
6	chr3:113557409-113557459	ovcar-3	ovarian:	n/a
7	chr3:113599916-113599966	SK-N-MC	brain:	n/a
8	chr3:113557932-113557982	Hepatocyte	liver:	n/a
9	chr3:113557445-113557495	HCM	heart:	n/a
10	chr3:113557462-113557512	HCM	heart:	n/a
11	chr3:113557569-113557619	GM12892	blood:	n/a
12	chr3:113557646-113557696	MCF-7	breast:	n/a
13	chr3:113557462-113557512	H1-hESC	embryonic stem cell:	embryo
14	chr3:113599916-113599966	Hela-S3	cervix:	n/a
15	chr3:113557445-113557495	GM19239	blood:	n/a
16	chr3:113554391-113554441	HRCEpiC	kidney:	n/a
17	chr3:113560972-113561022	HL-60	blood:	n/a
18	chr3:113599916-113599966	LNCaP	prostate:	n/a
19	chr3:113557792-113557842	HCM	heart:	n/a
20	chr3:113557932-113557982	GM19239	blood:	n/a
21	chr3:113557582-113557632	HRE	kidney:	n/a
22	chr3:113557932-113557982	ovcar-3	ovarian:	n/a
23	chr3:113557792-113557842	ovcar-3	ovarian:	n/a
24	chr3:113557646-113557696	HUVEC	blood vessel:	n/a
25	chr3:113557582-113557632	HAEpiC	amniotic membrane:	n/a
26	chr3:113557638-113557688	AG04450	lung:	fetal
27	chr3:113557932-113557982	K562	blood:	n/a
28	chr3:113557792-113557842	AG04450	lung:	fetal
29	chr3:113557792-113557842	AG04449	skin:	fetal
30	chr3:113560972-113561022	Jurkat	blood:	n/a
31	chr3:113557445-113557495	PrEC	prostate:	n/a
32	chr3:113557409-113557459	NH-A	brain:	n/a
33	chr3:113557409-113557459	HRCEpiC	kidney:	n/a
34	chr3:113557445-113557495	SKMC	muscle:	n/a
35	chr3:113557462-113557512	BE2_C	brain:	n/a
36	chr3:113557569-113557619	NH-A	brain:	n/a
37	chr3:113556717-113556767	HMEC	breast:	n/a
38	chr3:113557445-113557495	Caco-2	colon:	n/a
39	chr3:113557569-113557619	NT2-D1	testis:	n/a
40	chr3:113554391-113554441	BJ	skin:	n/a
41	chr3:113556717-113556767	A549	lung:	n/a
42	chr3:113557792-113557842	T-47D	breast:	n/a
43	chr3:113557582-113557632	CMK	blood:	n/a
44	chr3:113557792-113557842	Hepatocyte	liver:	n/a
45	chr3:113557409-113557459	RPTEC	kidney:	n/a
46	chr3:113557445-113557495	LNCaP	prostate:	n/a
47	chr3:113554391-113554441	NHBE	bronchial:	n/a
48	chr3:113557569-113557619	Hepatocyte	liver:	n/a
49	chr3:113560972-113561022	HCM	heart:	n/a
50	chr3:113557445-113557495	HPAEpiC	pulmonary alveolar:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:113538794..113541088-chr3:113549599..113551887,2	MCF-7	breast:
2	chr3:113546118..113548286-chr3:113550163..113552651,2	MCF-7	breast:
3	chr3:113542536..113544154-chr3:113546826..113548864,2	K562	blood:
4	chr3:113548993..113551007-chr3:113552942..113555704,2	K562	blood:
5	chr3:113563584..113564144-chr3:113631853..113632404,2	MCF-7	breast:
6	chr3:113564891..113567125-chr3:113615091..113617846,2	MCF-7	breast:
7	chr3:113543876..113544661-chr3:113557420..113558376,3	MCF-7	breast:
8	chr3:113557202..113559537-chr3:113665338..113666861,2	MCF-7	breast:
9	chr12:123010884..123011687-chr3:113557598..113558313,2	Hela-S3	cervix:
10	chr3:113548993..113551007-chr3:113552942..113555704,2	K562	blood:
11	chr3:113558122..113560757-chr3:113561345..113564124,3	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1A-2	chr3:113563350-113563496	NONHSAT091246
2	lnc-ATP6V1A-2	chr3:113557665-113557783	NONHSAT091246
3	lnc-NAA50-4	chr3:113569084-113569578	NONHSAT091250
4	lnc-ATP6V1A-2	chr3:113594331-113594714	NONHSAT091246
5	lnc-ATP6V1A-2	chr3:113588354-113588438	NONHSAT091246
6	lnc-ATP6V1A-2	chr3:113563670-113563812	NONHSAT091249
7	lnc-ATP6V1A-2	chr3:113563350-113563496	NONHSAT091249

No data

Variant related genes	Relation type
ENSG00000240776	TF binding region
GRAMD1C	TF binding region
ENSG00000241889	TF binding region
ENSG00000240776	CpG island
GRAMD1C	CpG island
ENSG00000241889	CpG island
ENSG00000178075	chromatin interactions
ENSG00000184307	chromatin interactions
ENSG00000111011	chromatin interactions
ENSG00000273394	chromatin interactions

Extended variants
information (count: 1806 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1806 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7646203	chr3:113543081-113543082	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537704749	chr3:113543106-113543107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35137493	chr3:113543154-113543155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556206805	chr3:113543187-113543188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189520616	chr3:113543214-113543215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139926169	chr3:113543218-113543219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552281214	chr3:113543222-113543223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568441430	chr3:113543231-113543232	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs553877188	chr3:113543235-113543236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572303075	chr3:113543282-113543283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7636168	chr3:113543317-113543318	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs564450761	chr3:113543349-113543350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560198741	chr3:113543402-113543403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144855102	chr3:113543428-113543429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543661074	chr3:113543434-113543435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs561761757	chr3:113543485-113543486	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs2712346	chr3:113543516-113543517	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs554501406	chr3:113543561-113543562	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs563831925	chr3:113543615-113543616	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs559412780	chr3:113543618-113543619	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144206583	chr3:113543631-113543632	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569023778	chr3:113543739-113543740	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568597390	chr3:113543799-113543800	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs570193153	chr3:113543800-113543801	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531129572	chr3:113543847-113543848	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs549672550	chr3:113543865-113543866	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs377747354	chr3:113543914-113543915	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs535424581	chr3:113543986-113543987	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs114690801	chr3:113544028-113544029	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs146045768	chr3:113544070-113544071	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs539471711	chr3:113544114-113544115	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs570851181	chr3:113544135-113544136	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs557678018	chr3:113544182-113544183	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs539852365	chr3:113544186-113544187	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs557936955	chr3:113544187-113544188	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs180999722	chr3:113544200-113544201	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546731044	chr3:113544218-113544219	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs185291214	chr3:113544288-113544289	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs191188844	chr3:113544339-113544340	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs181793719	chr3:113544580-113544581	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs377168403	chr3:113544596-113544597	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs535259653	chr3:113544608-113544609	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533277897	chr3:113544609-113544610	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs186101599	chr3:113544611-113544612	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370519124	chr3:113544621-113544622	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs566682467	chr3:113544627-113544628	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs555521842	chr3:113544632-113544633	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563753798	chr3:113544633-113544634	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs533862462	chr3:113544684-113544685	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs140021483	chr3:113544694-113544695	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Hirschsprung''s Disease	21712996	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
Prostate cancer	21965145	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
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD

Chromatin state (count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113524600-113543800	Weak transcription	HMEC	breast
2	chr3:113525400-113543800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr3:113525400-113548600	Weak transcription	NHLF	lung
4	chr3:113528600-113544000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:113529200-113543800	Weak transcription	HUVEC	blood vessel
6	chr3:113530000-113543600	Weak transcription	Primary B cells from cord blood	blood
7	chr3:113532000-113543600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr3:113532000-113544000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr3:113539000-113549000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:113539200-113543400	Weak transcription	GM12878-XiMat	blood
11	chr3:113543400-113543600	Enhancers	GM12878-XiMat	blood
12	chr3:113543600-113544000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:113543600-113544200	Enhancers	A549	lung
14	chr3:113543600-113544400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr3:113543600-113544400	Enhancers	Primary B cells from cord blood	blood
16	chr3:113543600-113544400	Flanking Active TSS	GM12878-XiMat	blood
17	chr3:113543600-113545000	Enhancers	Primary B cells from peripheral blood	blood
18	chr3:113543800-113544200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:113543800-113544200	Enhancers	Stomach Mucosa	stomach
20	chr3:113543800-113544200	Enhancers	HMEC	breast
21	chr3:113543800-113544400	Enhancers	HUVEC	blood vessel
22	chr3:113544000-113544200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr3:113544000-113544400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr3:113544000-113544400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr3:113544000-113548600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr3:113544200-113548600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr3:113544200-113548600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:113544200-113548600	Weak transcription	HMEC	breast
29	chr3:113544200-113549400	Weak transcription	Stomach Mucosa	stomach
30	chr3:113544400-113545400	Enhancers	GM12878-XiMat	blood
31	chr3:113544400-113547200	Weak transcription	Primary B cells from cord blood	blood
32	chr3:113544400-113548200	Weak transcription	HUVEC	blood vessel
33	chr3:113544400-113548600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr3:113544400-113548800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr3:113544400-113548800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:113545000-113546800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr3:113545400-113546600	Weak transcription	GM12878-XiMat	blood
38	chr3:113546600-113546800	Enhancers	GM12878-XiMat	blood
39	chr3:113546800-113550000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr3:113546800-113550000	Enhancers	Primary B cells from peripheral blood	blood
41	chr3:113546800-113550200	Flanking Active TSS	GM12878-XiMat	blood
42	chr3:113547200-113549000	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr3:113547200-113549200	Enhancers	Primary B cells from cord blood	blood
44	chr3:113548000-113549000	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr3:113548000-113549400	Enhancers	Primary hematopoietic stem cells	blood
46	chr3:113548200-113548600	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr3:113548200-113551200	Enhancers	HUVEC	blood vessel
48	chr3:113548600-113549200	Enhancers	Pancreas	Pancrea
49	chr3:113548600-113549400	Enhancers	NHLF	lung
50	chr3:113548600-113549600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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