Variant report

Variant	esv1792289
Chromosome Location	chr2:63812148-63900292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1234)
CpG islands
(count:1834)
Chromatin interactive
region (count:61)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:63815326-63816983	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:63815231-63815343	K562	blood:	n/a	n/a
3	ARID3A	chr2:63814583-63814888	K562	blood:	n/a	n/a
4	ARID3A	chr2:63842267-63842522	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:63842248-63842400	K562	blood:	n/a	n/a
6	ARID3A	chr2:63841827-63841832	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:63823642-63824213	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:63818153-63818479	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:63815590-63816321	K562	blood:	n/a	n/a
10	ATF1	chr2:63813562-63813698	K562	blood:	n/a	n/a
11	ATF1	chr2:63815563-63816633	K562	blood:	n/a	n/a
12	ATF1	chr2:63842163-63842461	K562	blood:	n/a	n/a
13	ATF2	chr2:63815451-63816182	GM12878	blood:	n/a	n/a
14	ATF2	chr2:63815415-63816387	GM12878	blood:	n/a	n/a
15	ATF2	chr2:63840192-63842746	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr2:63815474-63816288	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:63815721-63816437	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr2:63840721-63842785	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr2:63815640-63816393	A549	lung:	n/a	n/a
20	ATF3	chr2:63815843-63816220	HepG2	liver:	n/a	n/a
21	ATF3	chr2:63815514-63816425	A549	lung:	n/a	n/a
22	ATF3	chr2:63815815-63816188	K562	blood:	n/a	n/a
23	ATF3	chr2:63815599-63816238	GM12878	blood:	n/a	n/a
24	BACH1	chr2:63815604-63816555	K562	blood:	n/a	n/a
25	BACH1	chr2:63815252-63816341	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr2:63840684-63840835	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr2:63820635-63820663	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr2:63882214-63882488	GM12878	blood:	n/a	chr2:63882342-63882353 chr2:63882343-63882353
29	BATF	chr2:63882223-63882452	GM12878	blood:	n/a	chr2:63882342-63882353 chr2:63882343-63882353
30	BCL11A	chr2:63841742-63842069	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr2:63841718-63842053	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr2:63815485-63816689	A549	lung:	n/a	n/a
33	BCL3	chr2:63815468-63816541	A549	lung:	n/a	n/a
34	BCLAF1	chr2:63815810-63816302	K562	blood:	n/a	n/a
35	BCLAF1	chr2:63815127-63816479	GM12878	blood:	n/a	n/a
36	BCLAF1	chr2:63818141-63818604	GM12878	blood:	n/a	chr2:63818161-63818170
37	BCLAF1	chr2:63815207-63816341	GM12878	blood:	n/a	n/a
38	BCLAF1	chr2:63815166-63816233	K562	blood:	n/a	n/a
39	BHLHE40	chr2:63815207-63816509	K562	blood:	n/a	n/a
40	BHLHE40	chr2:63840106-63840354	K562	blood:	n/a	n/a
41	BHLHE40	chr2:63815361-63816548	GM12878	blood:	n/a	n/a
42	BHLHE40	chr2:63815399-63816383	HepG2	liver:	n/a	n/a
43	BRCA1	chr2:63841457-63842982	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr2:63866840-63866997	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr2:63814772-63816581	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr2:63815628-63816519	HepG2	liver:	n/a	n/a
47	BRCA1	chr2:63815574-63816167	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr2:63817325-63817434	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr2:63815788-63816311	GM12878	blood:	n/a	n/a
50	CBX3	chr2:63859560-63859825	K562	blood:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:63849938-63849988	HCM	heart:	n/a
2	chr2:63816220-63816270	IMR90	lung:	fetal
3	chr2:63894458-63894508	SAEC	small airway:	n/a
4	chr2:63855097-63855147	H1-hESC	embryonic stem cell:	embryo
5	chr2:63849938-63849988	HCM	heart:	n/a
6	chr2:63816220-63816270	IMR90	lung:	fetal
7	chr2:63894458-63894508	SAEC	small airway:	n/a
8	chr2:63855097-63855147	H1-hESC	embryonic stem cell:	embryo
9	chr2:63855118-63855168	Hela-S3	cervix:	n/a
10	chr2:63816096-63816146	T-47D	breast:	n/a
11	chr2:63815760-63815810	NH-A	brain:	n/a
12	chr2:63849938-63849988	PrEC	prostate:	n/a
13	chr2:63846679-63846729	BE2_C	brain:	n/a
14	chr2:63815963-63816013	BJ	skin:	n/a
15	chr2:63888846-63888896	HEEpiC	esophagus:	n/a
16	chr2:63816052-63816102	PFSK-1	brain:	n/a
17	chr2:63850141-63850191	PANC-1	pancreas:	n/a
18	chr2:63815863-63815913	SK-N-SH_RA	brain:	n/a
19	chr2:63816047-63816097	NH-A	brain:	n/a
20	chr2:63843856-63843906	HEK293	kidney:	embryo
21	chr2:63820005-63820055	HCT-116	colon:	n/a
22	chr2:63850056-63850106	PANC-1	pancreas:	n/a
23	chr2:63816074-63816124	GM12878	blood:	n/a
24	chr2:63816220-63816270	Jurkat	blood:	n/a
25	chr2:63855048-63855098	CMK	blood:	n/a
26	chr2:63841200-63841250	ProgFib	skin:	n/a
27	chr2:63816052-63816102	SK-N-SH_RA	brain:	n/a
28	chr2:63816047-63816097	T-47D	breast:	n/a
29	chr2:63816074-63816124	HL-60	blood:	n/a
30	chr2:63866302-63866352	Hela-S3	cervix:	n/a
31	chr2:63815398-63815448	MCF-7	breast:	n/a
32	chr2:63829110-63829160	HNPCEpiC	eye:	n/a
33	chr2:63820005-63820055	NHBE	bronchial:	n/a
34	chr2:63815760-63815810	AG04450	lung:	fetal
35	chr2:63820005-63820055	GM06990	blood:	n/a
36	chr2:63820005-63820055	IMR90	lung:	fetal
37	chr2:63814964-63815014	Caco-2	colon:	n/a
38	chr2:63841200-63841250	GM12892	blood:	n/a
39	chr2:63843856-63843906	HIPEpiC	eye:	n/a
40	chr2:63841200-63841250	U87	brain:	n/a
41	chr2:63855097-63855147	ECC-1	luminal epithelium:	n/a
42	chr2:63816024-63816074	PFSK-1	brain:	n/a
43	chr2:63855048-63855098	BE2_C	brain:	n/a
44	chr2:63816096-63816146	RPTEC	kidney:	n/a
45	chr2:63816220-63816270	Caco-2	colon:	n/a
46	chr2:63841200-63841250	AG04450	lung:	fetal
47	chr2:63816024-63816074	NT2-D1	testis:	n/a
48	chr2:63855097-63855147	SK-N-MC	brain:	n/a
49	chr2:63816220-63816270	PANC-1	pancreas:	n/a
50	chr2:63816220-63816270	HepG2	liver:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:63823578..63825836-chr2:63839966..63841886,2	K562	blood:
2	chr2:63896309..63898337-chr2:63901828..63903559,2	K562	blood:
3	chr2:63815568..63817310-chr2:63819288..63820984,2	K562	blood:
4	chr2:63812159..63813845-chr2:63813874..63816684,2	MCF-7	breast:
5	chr2:63885934..63888803-chr2:63891795..63894476,2	MCF-7	breast:
6	chr2:63838300..63840634-chr2:63841674..63843707,2	K562	blood:
7	chr2:63825821..63829241-chr2:63832114..63835472,3	K562	blood:
8	chr2:63818700..63824856-chr2:63826464..63830770,7	K562	blood:
9	chr2:63807715..63810212-chr2:63810943..63813158,2	K562	blood:
10	chr2:63835463..63837099-chr2:63837397..63839181,2	K562	blood:
11	chr2:63825929..63827816-chr2:63834281..63836054,2	MCF-7	breast:
12	chr2:63815337..63817122-chr2:63899923..63902176,2	MCF-7	breast:
13	chr2:63818719..63820235-chr2:63820348..63821885,2	MCF-7	breast:
14	chr2:63814652..63820726-chr2:63822860..63830564,18	K562	blood:
15	chr2:63813715..63815657-chr2:63817128..63819220,2	MCF-7	breast:
16	chr2:63823771..63825836-chr2:63839190..63841466,2	K562	blood:
17	chr2:63821702..63823496-chr2:63825130..63826904,2	K562	blood:
18	chr2:63837894..63839908-chr2:63842107..63843778,2	MCF-7	breast:
19	chr2:63815935..63817710-chr2:63818424..63820016,3	MCF-7	breast:
20	chr2:63826813..63829662-chr2:63829983..63831966,2	K562	blood:
21	chr2:63816219..63818321-chr2:63826171..63829135,3	K562	blood:
22	chr2:63840506..63842686-chr2:63842776..63844510,2	MCF-7	breast:
23	chr2:63814544..63817562-chr2:63819288..63824360,10	K562	blood:
24	chr2:63814652..63820726-chr2:63822860..63830564,18	K562	blood:
25	chr2:63838300..63840634-chr2:63841674..63843707,2	K562	blood:
26	chr2:63815242..63817655-chr2:63832171..63835443,3	MCF-7	breast:
27	chr2:63886236..63889221-chr2:63894013..63896444,2	K562	blood:
28	chr2:63825183..63827204-chr2:64067010..64069226,2	MCF-7	breast:
29	chr2:63814544..63817562-chr2:63819288..63824360,10	K562	blood:
30	chr2:63837894..63839908-chr2:63842107..63843778,2	MCF-7	breast:
31	chr2:63822582..63825327-chr2:63828934..63831453,2	MCF-7	breast:
32	chr2:63798423..63800359-chr2:63810410..63812684,2	K562	blood:
33	chr2:63840506..63842686-chr2:63842776..63844510,2	MCF-7	breast:
34	chr2:63814966..63816928-chr2:63840140..63842095,2	MCF-7	breast:
35	chr2:63814719..63818163-chr2:63820081..63823220,6	MCF-7	breast:
36	chr2:63853331..63856276-chr2:63864737..63866577,2	K562	blood:
37	chr2:63816373..63818974-chr2:64066021..64069792,3	MCF-7	breast:
38	chr2:63814867..63817469-chr2:63922056..63924960,2	MCF-7	breast:
39	chr2:63814719..63818163-chr2:63820081..63823220,6	MCF-7	breast:
40	chr2:63821933..63822875-chr2:64115658..64116471,2	MCF-7	breast:
41	chr2:63853331..63856276-chr2:63864737..63866577,2	K562	blood:
42	chr2:63822280..63824856-chr2:63827175..63830502,4	K562	blood:
43	chr2:63821702..63823496-chr2:63825130..63826904,2	K562	blood:
44	chr2:63835075..63837932-chr2:63839225..63843249,3	K562	blood:
45	chr2:63886236..63889221-chr2:63894013..63896444,2	K562	blood:
46	chr2:63885934..63888803-chr2:63891795..63894476,2	MCF-7	breast:
47	chr2:63826813..63829662-chr2:63829983..63831966,2	K562	blood:
48	chr2:63835463..63837099-chr2:63837397..63839181,2	K562	blood:
49	chr2:63815123..63819073-chr2:63825061..63828288,3	MCF-7	breast:
50	chr2:63881623..63882123-chr7:2913394..2913983,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGP2-5	chr2:63817537-63818108	NONHSAT071063
2	lnc-UGP2-5	chr2:63816119-63816180	NONHSAT071063
3	lnc-VPS54-6	chr2:63880900-63881009	l_1845_chr2:63834528-63908444_heart
4	lnc-UGP2-5	chr2:63826304-63827186	NONHSAT071065
5	lnc-VPS54-6	chr2:63894257-63894345	l_1845_chr2:63834528-63908444_heart
6	lnc-VPS54-6	chr2:63881910-63882228	l_1845_chr2:63834528-63908444_heart
7	lnc-VPS54-6	chr2:63834529-63834608	l_1845_chr2:63834528-63908444_heart
8	lnc-VPS54-7	chr2:63815331-63815634	NONHSAT071061
9	lnc-UGP2-5	chr2:63824682-63824708	NONHSAT071065
10	lnc-WDPCP-3	chr2:63877793-63877972	NONHSAT071058

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MDH1	hsa-miR-26b-5p	chr2:63834201-63834222

Variant related genes	Relation type
MDH1	TF binding region
ENSG00000228305	TF binding region
RPS4XP5	TF binding region
WDPCP	TF binding region
MDH1	CpG island
ENSG00000228305	CpG island
RPS4XP5	CpG island
WDPCP	CpG island
ENSG00000014641	chromatin interactions
ENSG00000143951	chromatin interactions
ENSG00000169764	chromatin interactions
ENSG00000221085	chromatin interactions
ENSG00000158773	chromatin interactions

Extended variants
information (count: 2866 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2866 , 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	rs2028884	chr2:63812148-63812149	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs112441552	chr2:63812184-63812185	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs34669271	chr2:63812204-63812205	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557275170	chr2:63812261-63812262	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs545401986	chr2:63812301-63812302	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs552988474	chr2:63812341-63812342	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576998782	chr2:63812536-63812537	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs546019033	chr2:63812597-63812598	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538583193	chr2:63812615-63812616	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs557086392	chr2:63812682-63812683	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575370759	chr2:63812718-63812719	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs80158152	chr2:63812748-63812749	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369607696	chr2:63812766-63812767	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs76770860	chr2:63812779-63812780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559161279	chr2:63812910-63812911	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572561395	chr2:63812937-63812938	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143957321	chr2:63812969-63812970	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200888755	chr2:63812970-63812971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs75612223	chr2:63812986-63812987	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs397984825	chr2:63812988-63812989	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs528194203	chr2:63813119-63813120	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs541652155	chr2:63813129-63813130	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs112293948	chr2:63813138-63813139	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs541761617	chr2:63813167-63813168	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7596703	chr2:63813310-63813311	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs17618239	chr2:63813357-63813358	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186276385	chr2:63813427-63813428	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147391959	chr2:63813454-63813455	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs3754540	chr2:63813458-63813459	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs563875591	chr2:63813556-63813557	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190743915	chr2:63813593-63813594	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs531014334	chr2:63813608-63813609	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs570794247	chr2:63813613-63813614	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs183274271	chr2:63813617-63813618	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs186070941	chr2:63813629-63813630	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs578022387	chr2:63813660-63813661	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs528608604	chr2:63813673-63813674	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs546574421	chr2:63813729-63813730	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs571324879	chr2:63813788-63813789	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs72806040	chr2:63813799-63813800	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs538518110	chr2:63813829-63813830	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550604543	chr2:63813879-63813880	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145557863	chr2:63813882-63813883	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199816856	chr2:63813899-63813900	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554797700	chr2:63813912-63813913	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190580783	chr2:63813969-63813970	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2028885	chr2:63814007-63814008	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546839948	chr2:63814013-63814014	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566119700	chr2:63814043-63814044	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375710960	chr2:63814073-63814074	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:1835 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:63780200-63814800	Weak transcription	Psoas Muscle	Psoas
2	chr2:63801000-63814400	Weak transcription	Primary B cells from cord blood	blood
3	chr2:63803600-63813400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:63806000-63813600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:63806200-63813600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:63806200-63814000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:63806400-63813400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:63806400-63813400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr2:63808600-63813800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr2:63808600-63814200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr2:63808800-63813600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr2:63808800-63814800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr2:63809000-63813200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr2:63809000-63813600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:63809000-63813800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr2:63809000-63813800	Weak transcription	Brain Substantia Nigra	brain
17	chr2:63809000-63814200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:63809000-63814200	Weak transcription	Osteobl	bone
19	chr2:63809200-63813400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:63809200-63813600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:63809200-63813600	Weak transcription	Liver	Liver
22	chr2:63809200-63813600	Weak transcription	NHEK	skin
23	chr2:63809200-63813800	Weak transcription	Brain Anterior Caudate	brain
24	chr2:63809200-63813800	Weak transcription	Right Atrium	heart
25	chr2:63809200-63814000	Weak transcription	Brain Hippocampus Middle	brain
26	chr2:63809200-63814000	Weak transcription	NHDF-Ad	bronchial
27	chr2:63809200-63814200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr2:63809200-63814200	Weak transcription	Adipose Nuclei	Adipose
29	chr2:63809200-63814200	Weak transcription	Right Ventricle	heart
30	chr2:63809200-63814600	Weak transcription	Stomach Mucosa	stomach
31	chr2:63809200-63814800	Weak transcription	Left Ventricle	heart
32	chr2:63809400-63814200	Weak transcription	Colon Smooth Muscle	Colon
33	chr2:63809800-63813200	Weak transcription	GM12878-XiMat	blood
34	chr2:63809800-63813400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:63809800-63813800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:63809800-63814400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:63809800-63814800	Weak transcription	Thymus	Thymus
38	chr2:63810000-63813400	Weak transcription	Fetal Heart	heart
39	chr2:63810400-63814200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:63811200-63813600	Weak transcription	K562	blood
41	chr2:63811400-63813000	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr2:63811800-63814600	Weak transcription	Fetal Stomach	stomach
43	chr2:63812400-63813600	Enhancers	Dnd41	blood
44	chr2:63813000-63817800	Active TSS	H1 Cell Line	embryonic stem cell
45	chr2:63813200-63813400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr2:63813200-63813400	Active TSS	GM12878-XiMat	blood
47	chr2:63813200-63813600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr2:63813400-63813600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr2:63813400-63813600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:63813400-63813800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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