Variant report

Variant	nsv1014962
Chromosome Location	chr2:98704622-98795737
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:366)
Chromatin interactive
region (count:32)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:98751199-98751430	K562	blood:	n/a	n/a
2	ATF1	chr2:98716824-98717232	K562	blood:	n/a	n/a
3	ATF1	chr2:98707651-98707822	K562	blood:	n/a	n/a
4	ATF2	chr2:98750612-98751042	GM12878	blood:	n/a	n/a
5	ATF2	chr2:98750595-98751083	GM12878	blood:	n/a	n/a
6	ATF3	chr2:98751111-98751462	K562	blood:	n/a	n/a
7	BACH1	chr2:98793964-98794164	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr2:98750707-98751062	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:98750539-98751000	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:98765949-98765950	K562	blood:	n/a	n/a
11	BHLHE40	chr2:98750670-98750926	GM12878	blood:	n/a	n/a
12	BRCA1	chr2:98732644-98732672	HepG2	liver:	n/a	n/a
13	BRCA1	chr2:98722843-98722939	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr2:98720913-98720924	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:98765828-98766099	K562	blood:	n/a	n/a
16	CEBPB	chr2:98785690-98785899	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:98747247-98747562	IMR90	lung:	n/a	chr2:98747416-98747427
18	CEBPB	chr2:98787614-98787707	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:98747262-98747586	HepG2	liver:	n/a	chr2:98747416-98747427
20	CEBPB	chr2:98745813-98746013	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:98747289-98747555	A549	lung:	n/a	chr2:98747416-98747427
22	CEBPB	chr2:98747407-98747485	K562	blood:	n/a	chr2:98747416-98747427
23	CEBPB	chr2:98785677-98785917	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:98765693-98766173	HepG2	liver:	n/a	n/a
25	CEBPD	chr2:98746665-98746998	K562	blood:	n/a	n/a
26	CHD2	chr2:98750687-98751228	GM12878	blood:	n/a	n/a
27	CREB1	chr2:98750595-98751157	GM12878	blood:	n/a	n/a
28	CREB1	chr2:98750605-98751143	GM12878	blood:	n/a	n/a
29	CTCF	chr2:98792460-98792610	GM12865	blood:	n/a	n/a
30	CTCF	chr2:98774027-98774375	HepG2	liver:	n/a	n/a
31	CTCF	chr2:98774070-98774337	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr2:98792423-98792622	GM10266	blood:	n/a	n/a
33	CTCF	chr2:98765855-98765956	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:98704824-98704924	GM12892	blood:	n/a	n/a
35	CTCF	chr2:98792400-98792550	MCF-7	breast:	n/a	chr2:98792419-98792427
36	CTCF	chr2:98774160-98774310	BE2_C	brain:	n/a	n/a
37	CTCF	chr2:98774089-98774318	K562	blood:	n/a	n/a
38	CTCF	chr2:98774100-98774250	GM12865	blood:	n/a	n/a
39	CTCF	chr2:98792451-98792525	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:98704797-98704929	GM13976	blood:	n/a	n/a
41	CTCF	chr2:98792420-98792570	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:98704805-98704928	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:98766040-98766190	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr2:98792420-98792570	GM12871	blood:	n/a	n/a
45	CTCF	chr2:98716800-98716809	ProgFib	skin:	n/a	n/a
46	CTCF	chr2:98774120-98774270	BJ	skin:	n/a	n/a
47	CTCF	chr2:98774120-98774270	GM12872	blood:	n/a	n/a
48	CTCF	chr2:98792420-98792570	GM12874	blood:	n/a	n/a
49	CTCF	chr2:98704747-98704976	GM12878	blood:	n/a	n/a
50	CTCF	chr2:98792364-98792605	HepG2	liver:	n/a	chr2:98792419-98792427

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98756447-98756497	Jurkat	blood:	n/a
2	chr2:98793396-98793446	HEEpiC	esophagus:	n/a
3	chr2:98794267-98794317	NH-A	brain:	n/a
4	chr2:98755852-98755902	AG09309	skin:	n/a
5	chr2:98794267-98794317	RPTEC	kidney:	n/a
6	chr2:98707797-98707847	AG10803	skin:	n/a
7	chr2:98794267-98794317	GM12892	blood:	n/a
8	chr2:98756447-98756497	HEEpiC	esophagus:	n/a
9	chr2:98756447-98756497	SKMC	muscle:	n/a
10	chr2:98755852-98755902	GM06990	blood:	n/a
11	chr2:98793396-98793446	HL-60	blood:	n/a
12	chr2:98704858-98704908	HUVEC	blood vessel:	n/a
13	chr2:98707797-98707847	MCF10A-Er-Src	breast:	n/a
14	chr2:98793396-98793446	HNPCEpiC	eye:	n/a
15	chr2:98755852-98755902	GM12891	blood:	n/a
16	chr2:98756447-98756497	Caco-2	colon:	n/a
17	chr2:98793396-98793446	HRCEpiC	kidney:	n/a
18	chr2:98704858-98704908	ProgFib	skin:	n/a
19	chr2:98756447-98756497	HL-60	blood:	n/a
20	chr2:98707797-98707847	K562	blood:	n/a
21	chr2:98794267-98794317	GM12878	blood:	n/a
22	chr2:98707797-98707847	GM12878	blood:	n/a
23	chr2:98704858-98704908	SKMC	muscle:	n/a
24	chr2:98704858-98704908	HEEpiC	esophagus:	n/a
25	chr2:98755852-98755902	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:98707797-98707847	NB4	blood:	n/a
27	chr2:98756447-98756497	K562	blood:	n/a
28	chr2:98793396-98793446	GM19239	blood:	n/a
29	chr2:98755852-98755902	HCM	heart:	n/a
30	chr2:98793396-98793446	SK-N-SH	brain:	n/a
31	chr2:98794267-98794317	HUVEC	blood vessel:	n/a
32	chr2:98793396-98793446	K562	blood:	n/a
33	chr2:98707797-98707847	HEEpiC	esophagus:	n/a
34	chr2:98704858-98704908	NT2-D1	testis:	n/a
35	chr2:98756447-98756497	CMK	blood:	n/a
36	chr2:98755852-98755902	AG10803	skin:	n/a
37	chr2:98756447-98756497	ProgFib	skin:	n/a
38	chr2:98794267-98794317	AG09319	gingival:	n/a
39	chr2:98755852-98755902	H1-hESC	embryonic stem cell:	embryo
40	chr2:98704858-98704908	AG04450	lung:	fetal
41	chr2:98756447-98756497	Hepatocyte	liver:	n/a
42	chr2:98707797-98707847	AG04449	skin:	fetal
43	chr2:98707797-98707847	HUVEC	blood vessel:	n/a
44	chr2:98704858-98704908	NB4	blood:	n/a
45	chr2:98704858-98704908	SK-N-SH	brain:	n/a
46	chr2:98707797-98707847	HRCEpiC	kidney:	n/a
47	chr2:98755852-98755902	SAEC	small airway:	n/a
48	chr2:98793396-98793446	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:98756447-98756497	AG09319	gingival:	n/a
50	chr2:98756447-98756497	ECC-1	luminal epithelium:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:98705628..98707141-chr2:98772756..98775686,2	MCF-7	breast:
2	chr2:98790192..98791719-chr2:98794432..98797427,2	K562	blood:
3	chr2:98600951..98603752-chr2:98713774..98716598,2	K562	blood:
4	chr2:98758686..98760901-chr2:98772249..98774966,2	K562	blood:
5	chr2:98732440..98734489-chr2:98736889..98739713,2	K562	blood:
6	chr2:98739471..98741169-chr2:98745863..98748204,2	MCF-7	breast:
7	chr2:98766384..98769751-chr2:98776231..98780220,5	K562	blood:
8	chr2:98774522..98776569-chr2:98782191..98784432,2	K562	blood:
9	chr2:98704397..98705262-chr2:98850185..98851043,2	MCF-7	breast:
10	chr2:98612119..98614854-chr2:98702248..98705786,3	K562	blood:
11	chr2:98422884..98423763-chr2:98773660..98774512,4	MCF-7	breast:
12	chr2:98610350..98614892-chr2:98700211..98704879,10	MCF-7	breast:
13	chr2:98766384..98768153-chr2:98776231..98777799,2	K562	blood:
14	chr2:98726208..98727848-chr2:98729692..98732563,2	K562	blood:
15	chr2:98774522..98776569-chr2:98782191..98784432,2	K562	blood:
16	chr2:98611064..98613202-chr2:98773939..98776742,2	MCF-7	breast:
17	chr2:98766384..98769751-chr2:98776231..98780220,5	K562	blood:
18	chr2:98790192..98791719-chr2:98794432..98797427,2	K562	blood:
19	chr2:98732440..98734489-chr2:98736889..98739713,2	K562	blood:
20	chr2:98748644..98750375-chr2:98752119..98754106,2	MCF-7	breast:
21	chr2:98748644..98750375-chr2:98752119..98754106,2	MCF-7	breast:
22	chr2:98702427..98705157-chr2:98705401..98707639,3	MCF-7	breast:
23	chr2:98773639..98775254-chr2:98778952..98780537,2	K562	blood:
24	chr2:98726208..98727848-chr2:98729692..98732563,2	K562	blood:
25	chr2:98742448..98743166-chr2:140398071..140398801,2	MCF-7	breast:
26	chr2:98739471..98741169-chr2:98745863..98748204,2	MCF-7	breast:
27	chr2:98758686..98760901-chr2:98772249..98774966,2	K562	blood:
28	chr2:98423370..98423923-chr2:98792023..98792988,2	K562	blood:
29	chr2:98705628..98707141-chr2:98772756..98775686,2	MCF-7	breast:
30	chr2:98610743..98612687-chr2:98718237..98721068,2	MCF-7	breast:
31	chr2:98766384..98768153-chr2:98776231..98777799,2	K562	blood:
32	chr2:98773639..98775254-chr2:98778952..98780537,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM131-3	chr2:98754514-98754975	NONHSAT072694
2	lnc-TMEM131-3	chr2:98751506-98751681	NONHSAT072693
3	lnc-CNGA3-3	chr2:98732115-98732209	NONHSAT072691
4	lnc-TMEM131-3	chr2:98751797-98751905	NONHSAT072693
5	lnc-TMEM131-3	chr2:98744833-98745473	NONHSAT072693
6	lnc-CNGA3-3	chr2:98709524-98709751	NONHSAT072691
7	lnc-CNGA3-3	chr2:98750287-98750360	NONHSAT072691
8	lnc-TMEM131-3	chr2:98751856-98751941	NONHSAT072694

No data

Variant related genes	Relation type
VWA3B	TF binding region
VWA3B	CpG island
ENSG00000075568	chromatin interactions
ENSG00000168658	chromatin interactions

Extended variants
information (count: 3093 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3093 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372651358	chr2:98704647-98704648	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs182948317	chr2:98704733-98704734	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs544060496	chr2:98704749-98704750	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567482291	chr2:98704751-98704752	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563904548	chr2:98704758-98704759	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529602532	chr2:98704808-98704809	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs140826628	chr2:98704859-98704860	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144570971	chr2:98704897-98704898	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186911563	chr2:98704937-98704938	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528508091	chr2:98705000-98705001	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147881004	chr2:98705002-98705003	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190223174	chr2:98705019-98705020	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537124923	chr2:98705045-98705046	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs148517058	chr2:98705076-98705077	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569822884	chr2:98705090-98705091	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182777198	chr2:98705107-98705108	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115744081	chr2:98705132-98705133	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572215823	chr2:98705167-98705168	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534616597	chr2:98705219-98705220	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187746767	chr2:98705226-98705227	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577861815	chr2:98705251-98705252	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543536274	chr2:98705252-98705253	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563198712	chr2:98705294-98705295	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534777531	chr2:98705296-98705297	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs142964588	chr2:98705303-98705304	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542826475	chr2:98705358-98705359	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560011624	chr2:98705383-98705384	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553980632	chr2:98705416-98705417	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs528745838	chr2:98705460-98705461	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs551389156	chr2:98705519-98705520	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545272810	chr2:98705532-98705533	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs151129296	chr2:98705660-98705661	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141040143	chr2:98705692-98705693	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377080160	chr2:98705734-98705735	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs567604256	chr2:98705735-98705736	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs529103914	chr2:98705813-98705814	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145114917	chr2:98705839-98705840	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568342564	chr2:98705848-98705849	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534915154	chr2:98705857-98705858	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369643172	chr2:98705923-98705924	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557830318	chr2:98705954-98705955	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369384827	chr2:98706002-98706003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6705096	chr2:98706004-98706005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs557041203	chr2:98706007-98706008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs62154869	chr2:98706112-98706113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs74515004	chr2:98706114-98706115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs113367766	chr2:98706128-98706129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs548127413	chr2:98706215-98706216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10203048	chr2:98706232-98706233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs140929911	chr2:98706243-98706244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98702800-98705200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
2	chr2:98703000-98704800	Enhancers	Spleen	Spleen
3	chr2:98703200-98706000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr2:98703800-98704800	Flanking Active TSS	Duodenum Mucosa	Duodenum
5	chr2:98703800-98704800	Flanking Active TSS	Stomach Mucosa	stomach
6	chr2:98703800-98705000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
7	chr2:98704000-98704800	Enhancers	Primary hematopoietic stem cells	blood
8	chr2:98704000-98705000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr2:98704000-98705200	Enhancers	Primary B cells from peripheral blood	blood
10	chr2:98704200-98704800	Bivalent Enhancer	Fetal Thymus	thymus
11	chr2:98704200-98705200	Weak transcription	Lung	lung
12	chr2:98704200-98705400	Enhancers	Placenta	Placenta
13	chr2:98704200-98707200	Weak transcription	Gastric	stomach
14	chr2:98704200-98709800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr2:98704400-98704800	Active TSS	Adipose Nuclei	Adipose
16	chr2:98704400-98705400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr2:98704400-98709000	Enhancers	Primary B cells from cord blood	blood
18	chr2:98704600-98704800	Enhancers	HepG2	liver
19	chr2:98704600-98705000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:98704600-98705000	Enhancers	GM12878-XiMat	blood
21	chr2:98704600-98707400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:98704800-98705000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr2:98704800-98705000	ZNF genes & repeats	Adipose Nuclei	Adipose
24	chr2:98704800-98705000	Enhancers	Duodenum Mucosa	Duodenum
25	chr2:98704800-98705000	Enhancers	K562	blood
26	chr2:98704800-98705800	Enhancers	Stomach Mucosa	stomach
27	chr2:98704800-98707400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr2:98705000-98705400	Weak transcription	Adipose Nuclei	Adipose
29	chr2:98705000-98706600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr2:98705200-98706200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr2:98705200-98708200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr2:98705400-98705600	Enhancers	Adipose Nuclei	Adipose
33	chr2:98705400-98705600	Enhancers	Lung	lung
34	chr2:98705400-98707800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:98705600-98707000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:98705600-98708000	Weak transcription	Adipose Nuclei	Adipose
37	chr2:98705800-98706000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:98706000-98706400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr2:98706000-98707800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:98706200-98708800	Enhancers	Primary B cells from peripheral blood	blood
41	chr2:98706400-98707000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr2:98706600-98708800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr2:98707000-98707400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr2:98707000-98707600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:98707200-98708000	Enhancers	Gastric	stomach
46	chr2:98707400-98707800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr2:98707400-98708800	Enhancers	Primary hematopoietic stem cells	blood
48	chr2:98707400-98708800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr2:98707600-98707800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:98707600-98707800	Enhancers	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links