Variant report

Variant	nsv535836
Chromosome Location	chr2:99329084-99353519
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:674)
CpG islands
(count:733)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:99348284-99349093	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99344181-99344479	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:99347710-99347908	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:99351304-99351833	K562	blood:	n/a	n/a
5	ARID3A	chr2:99351261-99351842	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:99352884-99353266	HepG2	liver:	n/a	n/a
7	ATF1	chr2:99351376-99351732	K562	blood:	n/a	n/a
8	ATF2	chr2:99330027-99330608	GM12878	blood:	n/a	n/a
9	ATF2	chr2:99329899-99330733	GM12878	blood:	n/a	n/a
10	BACH1	chr2:99346840-99346973	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:99347838-99348187	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr2:99330023-99330500	GM12878	blood:	n/a	chr2:99330209-99330220
13	BATF	chr2:99329923-99330536	GM12878	blood:	n/a	chr2:99330209-99330220
14	BCL11A	chr2:99329934-99330569	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:99330069-99330355	GM12878	blood:	n/a	n/a
16	BCL3	chr2:99330025-99330478	GM12878	blood:	n/a	n/a
17	BCLAF1	chr2:99329937-99330607	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:99346571-99347012	HepG2	liver:	n/a	chr2:99346971-99346987
19	BHLHE40	chr2:99347751-99348118	GM12878	blood:	n/a	chr2:99348042-99348058
20	BHLHE40	chr2:99330093-99330447	GM12878	blood:	n/a	n/a
21	BRCA1	chr2:99343443-99343614	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr2:99347750-99347916	HepG2	liver:	n/a	n/a
23	BRCA1	chr2:99347882-99347930	GM12878	blood:	n/a	n/a
24	CBX3	chr2:99351253-99351632	K562	blood:	n/a	n/a
25	CCNT2	chr2:99347175-99347456	K562	blood:	n/a	n/a
26	CCNT2	chr2:99351308-99351749	K562	blood:	n/a	chr2:99351739-99351748
27	CEBPB	chr2:99343208-99343574	HepG2	liver:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
28	CEBPB	chr2:99351443-99351657	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:99352912-99353177	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:99329901-99330696	GM12878	blood:	n/a	n/a
31	CEBPB	chr2:99343215-99343547	IMR90	lung:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
32	CEBPB	chr2:99348514-99348710	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:99352906-99353320	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:99348446-99348773	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:99343257-99343478	H1-hESC	embryonic stem cell:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
36	CEBPB	chr2:99331165-99331353	HepG2	liver:	n/a	chr2:99331228-99331239
37	CEBPB	chr2:99343237-99343538	Hela-S3	cervix:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
38	CEBPB	chr2:99343221-99343577	K562	blood:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
39	CEBPB	chr2:99346243-99346870	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:99343232-99343529	A549	lung:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
41	CEBPB	chr2:99352837-99353271	A549	lung:	n/a	n/a
42	CEBPB	chr2:99352867-99353318	MCF-7	breast:	n/a	n/a
43	CEBPB	chr2:99348249-99348809	HepG2	liver:	n/a	n/a
44	CEBPD	chr2:99351255-99351835	K562	blood:	n/a	n/a
45	CEBPD	chr2:99346652-99347301	HepG2	liver:	n/a	n/a
46	CEBPD	chr2:99351301-99351703	K562	blood:	n/a	n/a
47	CEBPD	chr2:99347639-99347979	HepG2	liver:	n/a	n/a
48	CEBPD	chr2:99347647-99347927	HepG2	liver:	n/a	n/a
49	CHD1	chr2:99348067-99348246	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr2:99347958-99347989	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99346902-99346952	HL-60	blood:	n/a
2	chr2:99346902-99346952	HL-60	blood:	n/a
3	chr2:99348232-99348282	HMEC	breast:	n/a
4	chr2:99342685-99342735	AG09319	gingival:	n/a
5	chr2:99351550-99351600	GM12878	blood:	n/a
6	chr2:99348232-99348282	SAEC	small airway:	n/a
7	chr2:99346635-99346685	PANC-1	pancreas:	n/a
8	chr2:99342685-99342735	GM12891	blood:	n/a
9	chr2:99351550-99351600	AG09319	gingival:	n/a
10	chr2:99351550-99351600	H1-hESC	embryonic stem cell:	embryo
11	chr2:99348176-99348226	A549	lung:	n/a
12	chr2:99346635-99346685	Caco-2	colon:	n/a
13	chr2:99347987-99348037	NHBE	bronchial:	n/a
14	chr2:99347854-99347904	HUVEC	blood vessel:	n/a
15	chr2:99347854-99347904	HRE	kidney:	n/a
16	chr2:99351550-99351600	HEK293	kidney:	embryo
17	chr2:99347854-99347904	LNCaP	prostate:	n/a
18	chr2:99351550-99351600	BE2_C	brain:	n/a
19	chr2:99342685-99342735	HMEC	breast:	n/a
20	chr2:99346818-99346868	A549	lung:	n/a
21	chr2:99346635-99346685	ProgFib	skin:	n/a
22	chr2:99346818-99346868	HUVEC	blood vessel:	n/a
23	chr2:99348232-99348282	LNCaP	prostate:	n/a
24	chr2:99347854-99347904	U87	brain:	n/a
25	chr2:99347987-99348037	AG10803	skin:	n/a
26	chr2:99342986-99343036	Caco-2	colon:	n/a
27	chr2:99347854-99347904	PANC-1	pancreas:	n/a
28	chr2:99351550-99351600	MCF-7	breast:	n/a
29	chr2:99351550-99351600	Jurkat	blood:	n/a
30	chr2:99347422-99347472	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:99347854-99347904	BE2_C	brain:	n/a
32	chr2:99347854-99347904	HCT-116	colon:	n/a
33	chr2:99347979-99348029	Jurkat	blood:	n/a
34	chr2:99347854-99347904	NH-A	brain:	n/a
35	chr2:99342685-99342735	GM12878	blood:	n/a
36	chr2:99347979-99348029	GM19239	blood:	n/a
37	chr2:99346902-99346952	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:99342685-99342735	HCPEpiC	choroid plexus:	n/a
39	chr2:99351550-99351600	T-47D	breast:	n/a
40	chr2:99347854-99347904	Hepatocyte	liver:	n/a
41	chr2:99348232-99348282	PFSK-1	brain:	n/a
42	chr2:99346635-99346685	SKMC	muscle:	n/a
43	chr2:99346818-99346868	HRCEpiC	kidney:	n/a
44	chr2:99347987-99348037	U87	brain:	n/a
45	chr2:99348176-99348226	ovcar-3	ovarian:	n/a
46	chr2:99347422-99347472	NHDF-neo	bronchial:	n/a
47	chr2:99346818-99346868	HCPEpiC	choroid plexus:	n/a
48	chr2:99348232-99348282	HUVEC	blood vessel:	n/a
49	chr2:99346635-99346685	Jurkat	blood:	n/a
50	chr2:99346635-99346685	AoSMC	blood vessel:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:99336480..99339286-chr2:99347871..99349769,2	MCF-7	breast:
2	chr2:99342228..99344879-chr2:99346177..99348874,2	K562	blood:
3	chr2:99345360..99347894-chr2:99396622..99399352,2	MCF-7	breast:
4	chr2:99338843..99341034-chr2:99341737..99344169,2	MCF-7	breast:
5	chr2:99344987..99348857-chr2:99353398..99358314,5	MCF-7	breast:
6	chr2:99221557..99223102-chr2:99346482..99348239,2	MCF-7	breast:
7	chr2:99352512..99355304-chr2:99377484..99380437,2	MCF-7	breast:
8	chr2:99334681..99338238-chr2:99344696..99347399,3	MCF-7	breast:
9	chr2:99345368..99349321-chr2:99385005..99390572,6	MCF-7	breast:
10	chr2:99329459..99332003-chr2:99335709..99337859,2	MCF-7	breast:
11	chr2:99342228..99344879-chr2:99346177..99348874,2	K562	blood:
12	chr2:99097067..99098913-chr2:99352317..99355051,2	MCF-7	breast:
13	chr2:99341666..99344183-chr2:99455107..99457899,2	MCF-7	breast:
14	chr2:99334922..99337052-chr2:99339872..99343548,3	MCF-7	breast:
15	chr2:99348346..99350092-chr2:99446085..99447956,2	MCF-7	breast:
16	chr2:99342514..99344879-chr2:99346177..99348798,2	K562	blood:
17	chr2:99316162..99318899-chr2:99339583..99342162,2	MCF-7	breast:
18	chr2:99332357..99333866-chr2:99344670..99347230,2	MCF-7	breast:
19	chr2:99336480..99339286-chr2:99347871..99349769,2	MCF-7	breast:
20	chr2:99344922..99348721-chr2:99382903..99389092,6	MCF-7	breast:
21	chr2:99343338..99345259-chr2:99346373..99348700,3	MCF-7	breast:
22	chr2:99352944..99355702-chr2:99450894..99453779,2	MCF-7	breast:
23	chr2:99329459..99332003-chr2:99335709..99337859,2	MCF-7	breast:
24	chr2:99346676..99348606-chr2:99349694..99353065,3	MCF-7	breast:
25	chr2:99343338..99345259-chr2:99346373..99348700,3	MCF-7	breast:
26	chr2:99342514..99344879-chr2:99346177..99348798,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC50-1	chr2:99347828-99348158	NONHSAT072721
2	lnc-UNC50-1	chr2:99348118-99348158	XLOC_001587

No data

Variant related genes	Relation type
MGAT4A	TF binding region
MGAT4A	CpG island
ENSG00000201070	chromatin interactions
ENSG00000183513	chromatin interactions
ENSG00000226791	chromatin interactions
ENSG00000238830	chromatin interactions
ENSG00000071073	chromatin interactions

Extended variants
information (count: 829 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554124819	chr2:99329117-99329118	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370769296	chr2:99329127-99329128	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374831484	chr2:99329135-99329136	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148091721	chr2:99329137-99329138	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185690530	chr2:99329167-99329168	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539141802	chr2:99329211-99329212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559132429	chr2:99329255-99329256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569251120	chr2:99329302-99329303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538268561	chr2:99329353-99329354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79407520	chr2:99329357-99329358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76932847	chr2:99329362-99329363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188589425	chr2:99329397-99329398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573897314	chr2:99329403-99329404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542485917	chr2:99329476-99329477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7599792	chr2:99329496-99329497	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs181320799	chr2:99329545-99329546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544794593	chr2:99329579-99329580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145705091	chr2:99329613-99329614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139508612	chr2:99329649-99329650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375642199	chr2:99329672-99329673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201508395	chr2:99329673-99329674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs28501671	chr2:99329676-99329677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530505970	chr2:99329866-99329867	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs544209812	chr2:99329921-99329922	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs4850883	chr2:99329925-99329926	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs11123748	chr2:99329929-99329930	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs186522112	chr2:99329939-99329940	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530423363	chr2:99330034-99330035	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs547273168	chr2:99330050-99330051	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs567159277	chr2:99330075-99330076	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs190881186	chr2:99330080-99330081	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs141979285	chr2:99330167-99330168	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs72825780	chr2:99330221-99330222	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs537920419	chr2:99330247-99330248	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs114459584	chr2:99330312-99330313	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs115110997	chr2:99330355-99330356	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs182758955	chr2:99330371-99330372	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs552890221	chr2:99330379-99330380	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs1877905	chr2:99330449-99330450	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs369658426	chr2:99330503-99330504	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs574325981	chr2:99330541-99330542	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs372277376	chr2:99330557-99330558	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs150694205	chr2:99330574-99330575	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs372289042	chr2:99330581-99330582	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs187269005	chr2:99330582-99330583	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs560947031	chr2:99330599-99330600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs140129174	chr2:99330612-99330613	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530997655	chr2:99330613-99330614	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190915925	chr2:99330614-99330615	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4295064	chr2:99330633-99330634	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
T-cell prolymphocytic leukemia	17713554	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99303200-99336400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr2:99316600-99336400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr2:99319200-99336800	Weak transcription	Spleen	Spleen
4	chr2:99321000-99336200	Weak transcription	Fetal Stomach	stomach
5	chr2:99321200-99335000	Weak transcription	Lung	lung
6	chr2:99321600-99336600	Weak transcription	Fetal Kidney	kidney
7	chr2:99322000-99332600	Weak transcription	Fetal Intestine Small	intestine
8	chr2:99322000-99334000	Weak transcription	Dnd41	blood
9	chr2:99322000-99336800	Weak transcription	Colonic Mucosa	Colon
10	chr2:99322200-99336200	Weak transcription	Fetal Intestine Large	intestine
11	chr2:99324200-99336600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr2:99325400-99331000	Enhancers	Primary B cells from peripheral blood	blood
13	chr2:99325400-99333400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr2:99325600-99329600	Enhancers	Fetal Thymus	thymus
15	chr2:99325600-99336800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr2:99325800-99334200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr2:99326400-99330200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr2:99326400-99336000	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr2:99326400-99336800	Weak transcription	Aorta	Aorta
20	chr2:99326400-99342600	Weak transcription	Adipose Nuclei	Adipose
21	chr2:99326400-99343600	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr2:99326400-99346400	Weak transcription	Fetal Muscle Leg	muscle
23	chr2:99326600-99330000	Weak transcription	Stomach Mucosa	stomach
24	chr2:99326600-99330800	Enhancers	Primary T cells fromperipheralblood	blood
25	chr2:99326600-99334200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr2:99326600-99336800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr2:99326600-99336800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr2:99326600-99336800	Weak transcription	Rectal Smooth Muscle	rectum
29	chr2:99326600-99340000	Weak transcription	Brain Angular Gyrus	brain
30	chr2:99326800-99330600	Weak transcription	HepG2	liver
31	chr2:99326800-99330800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:99326800-99332400	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr2:99326800-99335000	Weak transcription	Brain Substantia Nigra	brain
34	chr2:99326800-99336600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:99326800-99336600	Weak transcription	Brain Hippocampus Middle	brain
36	chr2:99326800-99336800	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr2:99326800-99337000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr2:99326800-99342600	Weak transcription	Liver	Liver
39	chr2:99326800-99343800	Weak transcription	Small Intestine	intestine
40	chr2:99327200-99330600	Weak transcription	Gastric	stomach
41	chr2:99327200-99336800	Weak transcription	Brain Anterior Caudate	brain
42	chr2:99327600-99329400	Enhancers	Thymus	Thymus
43	chr2:99327600-99330000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr2:99327600-99331200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr2:99327600-99333000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr2:99327600-99335000	Weak transcription	Right Ventricle	heart
47	chr2:99327800-99331400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr2:99327800-99334200	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr2:99327800-99336000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr2:99328000-99330200	Enhancers	Primary T cells from cord blood	blood

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