Variant report

Variant	nsv524042
Chromosome Location	chr3:98317836-98436188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1137)
CpG islands
(count:671)
Chromatin interactive
region (count:17)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:98331729-98332499	GM12878	blood:	n/a	n/a
2	ATF2	chr3:98331491-98332456	GM12878	blood:	n/a	n/a
3	BACH1	chr3:98397129-98397157	K562	blood:	n/a	n/a
4	BACH1	chr3:98431536-98431728	H1-hESC	embryonic stem cell:	n/a	chr3:98431553-98431567
5	BATF	chr3:98361493-98361992	GM12878	blood:	n/a	n/a
6	BATF	chr3:98331781-98332375	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:98331904-98332354	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:98331844-98332296	GM12878	blood:	n/a	n/a
9	BCL3	chr3:98363038-98363376	GM12878	blood:	n/a	n/a
10	BCL3	chr3:98331295-98332684	GM12878	blood:	n/a	n/a
11	BCL3	chr3:98331814-98332275	GM12878	blood:	n/a	n/a
12	BCLAF1	chr3:98376201-98376680	GM12878	blood:	n/a	chr3:98376421-98376434 chr3:98376499-98376512 chr3:98376513-98376526 chr3:98376506-98376519 chr3:98376426-98376435
13	BCLAF1	chr3:98331388-98332429	GM12878	blood:	n/a	n/a
14	BCLAF1	chr3:98331475-98332451	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:98320926-98321331	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:98376356-98376616	K562	blood:	n/a	chr3:98376427-98376443
17	BHLHE40	chr3:98376344-98376584	GM12878	blood:	n/a	chr3:98376427-98376443
18	BHLHE40	chr3:98331938-98332299	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:98318788-98318886	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:98319242-98319696	GM12878	blood:	n/a	n/a
21	BRCA1	chr3:98331520-98331537	HepG2	liver:	n/a	n/a
22	BRCA1	chr3:98324291-98324404	GM12878	blood:	n/a	n/a
23	CBX3	chr3:98399394-98400238	HCT-116	colon:	n/a	n/a
24	CBX3	chr3:98399453-98400117	HCT-116	colon:	n/a	n/a
25	CEBPB	chr3:98318587-98318748	HepG2	liver:	n/a	chr3:98318689-98318700
26	CEBPB	chr3:98331392-98332538	GM12878	blood:	n/a	n/a
27	CEBPB	chr3:98427505-98427796	H1-hESC	embryonic stem cell:	n/a	chr3:98427634-98427645
28	CEBPB	chr3:98338574-98338890	A549	lung:	n/a	n/a
29	CEBPB	chr3:98418018-98418336	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:98318501-98318876	HepG2	liver:	n/a	chr3:98318689-98318700
31	CEBPB	chr3:98369822-98369921	A549	lung:	n/a	n/a
32	CEBPB	chr3:98318503-98318870	MCF-7	breast:	n/a	chr3:98318689-98318700
33	CEBPB	chr3:98318438-98318944	A549	lung:	n/a	chr3:98318689-98318700
34	CEBPB	chr3:98411685-98411988	IMR90	lung:	n/a	chr3:98411826-98411839 chr3:98411826-98411837
35	CEBPB	chr3:98399520-98400009	HCT-116	colon:	n/a	n/a
36	CEBPB	chr3:98411750-98411902	HepG2	liver:	n/a	chr3:98411826-98411839 chr3:98411826-98411837
37	CEBPB	chr3:98411665-98412022	HepG2	liver:	n/a	chr3:98411826-98411839 chr3:98411826-98411837
38	CEBPB	chr3:98411731-98411899	HepG2	liver:	n/a	chr3:98411826-98411839 chr3:98411826-98411837
39	CEBPB	chr3:98320971-98321433	A549	lung:	n/a	n/a
40	CEBPB	chr3:98399375-98400112	HCT-116	colon:	n/a	n/a
41	CEBPB	chr3:98321062-98321433	K562	blood:	n/a	n/a
42	CEBPB	chr3:98411786-98411900	A549	lung:	n/a	chr3:98411826-98411839 chr3:98411826-98411837
43	CEBPB	chr3:98318525-98318848	H1-hESC	embryonic stem cell:	n/a	chr3:98318689-98318700
44	CEBPB	chr3:98427489-98427749	HepG2	liver:	n/a	chr3:98427634-98427645
45	CEBPB	chr3:98406134-98406357	IMR90	lung:	n/a	chr3:98406273-98406284
46	CEBPB	chr3:98416423-98416557	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:98318505-98318870	IMR90	lung:	n/a	chr3:98318689-98318700
48	CEBPB	chr3:98318528-98318876	Hela-S3	cervix:	n/a	chr3:98318689-98318700
49	CEBPB	chr3:98318506-98318890	K562	blood:	n/a	chr3:98318689-98318700
50	CEBPB	chr3:98418875-98419029	IMR90	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:98343882-98343932	A549	lung:	n/a
2	chr3:98343882-98343932	HMEC	breast:	n/a
3	chr3:98376478-98376528	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:98429487-98429537	HCPEpiC	choroid plexus:	n/a
5	chr3:98342807-98342857	Jurkat	blood:	n/a
6	chr3:98376029-98376079	AG04449	skin:	fetal
7	chr3:98343882-98343932	ProgFib	skin:	n/a
8	chr3:98342807-98342857	GM06990	blood:	n/a
9	chr3:98429487-98429537	HRCEpiC	kidney:	n/a
10	chr3:98376390-98376440	HNPCEpiC	eye:	n/a
11	chr3:98376390-98376440	HMEC	breast:	n/a
12	chr3:98376478-98376528	HNPCEpiC	eye:	n/a
13	chr3:98376938-98376988	Hela-S3	cervix:	n/a
14	chr3:98342807-98342857	HNPCEpiC	eye:	n/a
15	chr3:98372781-98372831	AG04449	skin:	fetal
16	chr3:98429487-98429537	CMK	blood:	n/a
17	chr3:98343882-98343932	SK-N-MC	brain:	n/a
18	chr3:98376938-98376988	HCF	heart:	n/a
19	chr3:98372781-98372831	NHBE	bronchial:	n/a
20	chr3:98376029-98376079	ECC-1	luminal epithelium:	n/a
21	chr3:98376029-98376079	HRPEpiC	eye:	n/a
22	chr3:98343882-98343932	U87	brain:	n/a
23	chr3:98372781-98372831	HCM	heart:	n/a
24	chr3:98429487-98429537	NHDF-neo	bronchial:	n/a
25	chr3:98379208-98379258	GM12892	blood:	n/a
26	chr3:98376938-98376988	AoSMC	blood vessel:	n/a
27	chr3:98379208-98379258	PrEC	prostate:	n/a
28	chr3:98379208-98379258	HCF	heart:	n/a
29	chr3:98376390-98376440	RPTEC	kidney:	n/a
30	chr3:98376427-98376477	PANC-1	pancreas:	n/a
31	chr3:98376574-98376624	ProgFib	skin:	n/a
32	chr3:98343882-98343932	CMK	blood:	n/a
33	chr3:98376938-98376988	PrEC	prostate:	n/a
34	chr3:98376478-98376528	PrEC	prostate:	n/a
35	chr3:98376574-98376624	RPTEC	kidney:	n/a
36	chr3:98379208-98379258	Hela-S3	cervix:	n/a
37	chr3:98429487-98429537	NHBE	bronchial:	n/a
38	chr3:98429487-98429537	IMR90	lung:	fetal
39	chr3:98376390-98376440	HCPEpiC	choroid plexus:	n/a
40	chr3:98429487-98429537	HepG2	liver:	n/a
41	chr3:98379208-98379258	SK-N-SH	brain:	n/a
42	chr3:98376427-98376477	Caco-2	colon:	n/a
43	chr3:98343882-98343932	BJ	skin:	n/a
44	chr3:98376574-98376624	HIPEpiC	eye:	n/a
45	chr3:98376390-98376440	SK-N-SH	brain:	n/a
46	chr3:98379208-98379258	SAEC	small airway:	n/a
47	chr3:98376478-98376528	MCF10A-Er-Src	breast:	n/a
48	chr3:98343882-98343932	HPAEpiC	pulmonary alveolar:	n/a
49	chr3:98372781-98372831	Hepatocyte	liver:	n/a
50	chr3:98376478-98376528	NT2-D1	testis:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:98321530..98322415-chr3:98531181..98531955,2	MCF-7	breast:
2	chr3:98320433..98321618-chr3:98424245..98425562,4	MCF-7	breast:
3	chr20:52332749..52333464-chr3:98352060..98352684,2	MCF-7	breast:
4	chr3:98391064..98393925-chr3:98395948..98398945,2	K562	blood:
5	chr3:98316857..98318853-chr3:98318886..98321058,2	K562	blood:
6	chr3:98394828..98396802-chr3:98418414..98420079,2	MCF-7	breast:
7	chr3:98394828..98396802-chr3:98418414..98420079,2	MCF-7	breast:
8	chr3:98386847..98388821-chr3:98390572..98392318,2	K562	blood:
9	chr3:98320901..98321587-chr3:98530671..98531252,2	MCF-7	breast:
10	chr3:98320682..98321287-chr3:98531748..98532391,2	MCF-7	breast:
11	chr3:98388705..98390319-chr3:98395278..98397892,2	MCF-7	breast:
12	chr3:98386847..98388821-chr3:98390572..98392318,2	K562	blood:
13	chr3:98314191..98315885-chr3:98317245..98319751,3	K562	blood:
14	chr3:98316857..98318853-chr3:98318886..98321058,2	K562	blood:
15	chr3:98391064..98393925-chr3:98395948..98398945,2	K562	blood:
16	chr3:98388705..98390319-chr3:98395278..98397892,2	MCF-7	breast:
17	chr3:98320433..98321618-chr3:98424245..98425562,4	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCBLD2-1	chr3:98434494-98434621	ENSG00000239445.1
2	lnc-DCBLD2-1	chr3:98433177-98433342	NR_046683
3	lnc-DCBLD2-1	chr3:98434494-98434621	NR_046683
4	lnc-DCBLD2-1	chr3:98434494-98434645	NONHSAT147243
5	lnc-DCBLD2-1	chr3:98434220-98434365	NR_046683
6	lnc-DCBLD2-1	chr3:98434149-98434365	ENSG00000239445.1
7	lnc-DCBLD2-1	chr3:98434256-98434365	NONHSAT147243
8	lnc-DCBLD2-1	chr3:98433174-98433342	ENSG00000239445.1
9	lnc-ST3GAL6-4	chr3:98425014-98426540	NONHSAT090809
10	lnc-DCBLD2-1	chr3:98433176-98433342	ENSG00000239445.1
11	lnc-DCBLD2-1	chr3:98434220-98434365	NONHSAT090810
12	lnc-GPR15-2	chr3:98338909-98339462	NONHSAT090806
13	lnc-DCBLD2-1	chr3:98434494-98434621	ENSG00000239445.1
14	lnc-DCBLD2-1	chr3:98434494-98434622	NONHSAT090810
15	lnc-DCBLD2-1	chr3:98434220-98434365	ENSG00000239445.1
16	lnc-ST3GAL6-5	chr3:98376584-98377010	NONHSAT090808
17	lnc-DCBLD2-1	chr3:98434220-98434365	ENSG00000239445.1
18	lnc-DCBLD2-1	chr3:98432741-98433342	NONHSAT090810
19	lnc-DCBLD2-1	chr3:98434494-98434621	ENSG00000239445.1

No data

Variant related genes	Relation type
ENSG00000266233	TF binding region
WWP1P1	TF binding region
ENSG00000240827	TF binding region
ENSG00000266233	CpG island
WWP1P1	CpG island
ENSG00000240827	CpG island
ENSG00000057019	chromatin interactions

Extended variants
information (count: 2861 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2861 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1729987	chr3:98317836-98317837	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs1675528	chr3:98317872-98317873	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549469644	chr3:98317873-98317874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569734823	chr3:98317876-98317877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535175177	chr3:98317912-98317913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370631075	chr3:98317928-98317929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555162441	chr3:98317934-98317935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568654707	chr3:98317947-98317948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185111562	chr3:98317986-98317987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554505862	chr3:98317987-98317988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577353602	chr3:98317989-98317990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542970881	chr3:98317990-98317991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs202246777	chr3:98318014-98318015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564553256	chr3:98318091-98318092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556254050	chr3:98318145-98318146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576495231	chr3:98318159-98318160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113197834	chr3:98318169-98318170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201509900	chr3:98318182-98318183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541940311	chr3:98318243-98318244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113030595	chr3:98318321-98318322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1729988	chr3:98318393-98318394	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190539583	chr3:98318394-98318395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182305356	chr3:98318433-98318434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72924754	chr3:98318483-98318484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148388621	chr3:98318498-98318499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186097925	chr3:98318521-98318522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576980970	chr3:98318551-98318552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569517602	chr3:98318598-98318599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189921076	chr3:98318623-98318624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141569687	chr3:98318632-98318633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568719972	chr3:98318694-98318695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534386271	chr3:98318695-98318696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554368860	chr3:98318709-98318710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571166316	chr3:98318719-98318720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180771342	chr3:98318727-98318728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150601140	chr3:98318729-98318730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201536875	chr3:98318732-98318733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143490818	chr3:98318736-98318737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78437753	chr3:98318750-98318751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539708825	chr3:98318793-98318794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145830838	chr3:98318890-98318891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538781575	chr3:98318915-98318916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185717325	chr3:98318917-98318918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542353489	chr3:98318939-98318940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138395401	chr3:98318940-98318941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142872798	chr3:98318956-98318957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540830083	chr3:98318992-98318993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146082368	chr3:98319045-98319046	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs1675527	chr3:98319068-98319069	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs573521822	chr3:98319077-98319078	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	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
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98313000-98321400	Enhancers	Liver	Liver
2	chr3:98313200-98321200	Weak transcription	Fetal Thymus	thymus
3	chr3:98313200-98322600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:98315200-98321000	Enhancers	HepG2	liver
5	chr3:98315800-98319400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr3:98316000-98319600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr3:98316800-98318000	Enhancers	GM12878-XiMat	blood
8	chr3:98317000-98318000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr3:98317200-98321000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:98317200-98322400	Weak transcription	K562	blood
11	chr3:98317400-98322200	Weak transcription	Thymus	Thymus
12	chr3:98317800-98322400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr3:98318000-98318400	Weak transcription	GM12878-XiMat	blood
14	chr3:98318400-98319000	Enhancers	GM12878-XiMat	blood
15	chr3:98319000-98319600	Flanking Active TSS	GM12878-XiMat	blood
16	chr3:98319400-98321200	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr3:98319600-98320400	Enhancers	GM12878-XiMat	blood
18	chr3:98320400-98321200	Weak transcription	GM12878-XiMat	blood
19	chr3:98320600-98321400	Enhancers	Brain Substantia Nigra	brain
20	chr3:98321200-98321400	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr3:98321200-98321400	Enhancers	GM12878-XiMat	blood
22	chr3:98321200-98322800	Enhancers	Fetal Thymus	thymus
23	chr3:98321400-98322200	Weak transcription	GM12878-XiMat	blood
24	chr3:98322200-98322400	Enhancers	GM12878-XiMat	blood
25	chr3:98322200-98322600	Flanking Active TSS	Thymus	Thymus
26	chr3:98322400-98322800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:98322400-98322800	Enhancers	Stomach Mucosa	stomach
28	chr3:98322400-98322800	Enhancers	K562	blood
29	chr3:98322600-98322800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr3:98322600-98322800	Enhancers	Thymus	Thymus
31	chr3:98324200-98324600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:98331400-98331800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr3:98331400-98332000	Enhancers	Fetal Thymus	thymus
34	chr3:98331400-98332000	Enhancers	GM12878-XiMat	blood
35	chr3:98331400-98332000	Enhancers	HepG2	liver
36	chr3:98331400-98332200	Enhancers	Placenta	Placenta
37	chr3:98331400-98332400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr3:98331400-98332800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr3:98331600-98331800	Enhancers	Duodenum Mucosa	Duodenum
40	chr3:98331600-98331800	Enhancers	Pancreas	Pancrea
41	chr3:98331600-98332200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr3:98331800-98332200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr3:98331800-98332400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:98331800-98332400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr3:98332000-98332400	Enhancers	Adipose Nuclei	Adipose
46	chr3:98332000-98332400	Flanking Active TSS	HepG2	liver
47	chr3:98332400-98336400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr3:98335400-98336400	Enhancers	Brain Angular Gyrus	brain
49	chr3:98335400-98337200	Enhancers	Brain Substantia Nigra	brain
50	chr3:98335400-98337400	Enhancers	Brain Cingulate Gyrus	brain

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