Variant report

Variant	nsv1004632
Chromosome Location	chr2:54469283-54590480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1083)
CpG islands
(count:1709)
Chromatin interactive
region (count:54)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1083 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:54557735-54558115	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:54488738-54489020	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:54557555-54557779	K562	blood:	n/a	n/a
4	ATF1	chr2:54535443-54535602	K562	blood:	n/a	n/a
5	ATF1	chr2:54568869-54569169	K562	blood:	n/a	n/a
6	ATF1	chr2:54491458-54491517	K562	blood:	n/a	n/a
7	ATF1	chr2:54563343-54563371	K562	blood:	n/a	n/a
8	ATF1	chr2:54501879-54502144	K562	blood:	n/a	n/a
9	ATF1	chr2:54482380-54482686	K562	blood:	n/a	n/a
10	ATF2	chr2:54499305-54499795	GM12878	blood:	n/a	n/a
11	ATF2	chr2:54501786-54502174	GM12878	blood:	n/a	n/a
12	ATF3	chr2:54501826-54502162	K562	blood:	n/a	n/a
13	ATF3	chr2:54482456-54482605	K562	blood:	n/a	n/a
14	BACH1	chr2:54557710-54558038	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr2:54486550-54486907	GM12878	blood:	n/a	n/a
16	BATF	chr2:54486493-54486929	GM12878	blood:	n/a	n/a
17	BCL3	chr2:54557590-54558332	A549	lung:	n/a	chr2:54557737-54557750 chr2:54557960-54557969
18	BHLHE40	chr2:54540387-54540509	K562	blood:	n/a	n/a
19	BHLHE40	chr2:54557684-54558363	K562	blood:	n/a	chr2:54557715-54557731
20	BHLHE40	chr2:54498562-54498577	GM12878	blood:	n/a	n/a
21	BRCA1	chr2:54557995-54558135	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr2:54557931-54558047	HepG2	liver:	n/a	n/a
23	CBX3	chr2:54483260-54483656	K562	blood:	n/a	n/a
24	CBX3	chr2:54483150-54483759	K562	blood:	n/a	n/a
25	CBX3	chr2:54557393-54558180	K562	blood:	n/a	n/a
26	CCNT2	chr2:54557570-54558141	K562	blood:	n/a	n/a
27	CEBPB	chr2:54501801-54502201	IMR90	lung:	n/a	chr2:54502006-54502017
28	CEBPB	chr2:54482440-54482590	K562	blood:	n/a	n/a
29	CEBPB	chr2:54489231-54489564	HepG2	liver:	n/a	chr2:54489390-54489401
30	CEBPB	chr2:54587608-54587908	IMR90	lung:	n/a	chr2:54587742-54587753
31	CEBPB	chr2:54534061-54534364	IMR90	lung:	n/a	chr2:54534227-54534240
32	CEBPB	chr2:54489290-54489459	HepG2	liver:	n/a	chr2:54489390-54489401
33	CEBPB	chr2:54501831-54502172	A549	lung:	n/a	chr2:54502006-54502017
34	CEBPB	chr2:54557932-54558132	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:54506513-54506737	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:54501839-54502192	K562	blood:	n/a	chr2:54502006-54502017
37	CEBPB	chr2:54501774-54502195	Hela-S3	cervix:	n/a	chr2:54502006-54502017
38	CEBPB	chr2:54513286-54513529	HepG2	liver:	n/a	chr2:54513425-54513436
39	CEBPB	chr2:54563221-54563917	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:54487244-54487489	A549	lung:	n/a	chr2:54487360-54487371
41	CEBPB	chr2:54501919-54502109	HepG2	liver:	n/a	chr2:54502006-54502017
42	CEBPB	chr2:54487241-54487487	HepG2	liver:	n/a	chr2:54487360-54487371
43	CEBPB	chr2:54527060-54527121	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:54501837-54502048	K562	blood:	n/a	chr2:54502006-54502017
45	CEBPB	chr2:54506562-54506738	A549	lung:	n/a	n/a
46	CEBPB	chr2:54587617-54587901	HepG2	liver:	n/a	chr2:54587742-54587753
47	CEBPB	chr2:54489334-54489439	Hela-S3	cervix:	n/a	chr2:54489390-54489401
48	CEBPB	chr2:54489219-54489559	IMR90	lung:	n/a	chr2:54489390-54489401
49	CEBPB	chr2:54501803-54502172	K562	blood:	n/a	chr2:54502006-54502017
50	CEBPB	chr2:54557906-54558078	Hela-S3	cervix:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:54481922-54481972	Hela-S3	cervix:	n/a
2	chr2:54481922-54481972	Hela-S3	cervix:	n/a
3	chr2:54555541-54555591	BE2_C	brain:	n/a
4	chr2:54557902-54557952	HAEpiC	amniotic membrane:	n/a
5	chr2:54517167-54517217	SAEC	small airway:	n/a
6	chr2:54555541-54555591	AG04449	skin:	fetal
7	chr2:54560557-54560607	K562	blood:	n/a
8	chr2:54557904-54557954	HCT-116	colon:	n/a
9	chr2:54483379-54483429	H1-hESC	embryonic stem cell:	embryo
10	chr2:54557902-54557952	MCF10A-Er-Src	breast:	n/a
11	chr2:54482475-54482525	GM19239	blood:	n/a
12	chr2:54483058-54483108	H1-hESC	embryonic stem cell:	embryo
13	chr2:54481922-54481972	BE2_C	brain:	n/a
14	chr2:54483817-54483867	HRE	kidney:	n/a
15	chr2:54483817-54483867	HCPEpiC	choroid plexus:	n/a
16	chr2:54558352-54558402	AG04450	lung:	fetal
17	chr2:54558352-54558402	HIPEpiC	eye:	n/a
18	chr2:54557836-54557886	K562	blood:	n/a
19	chr2:54483431-54483481	MCF10A-Er-Src	breast:	n/a
20	chr2:54555541-54555591	HEK293	kidney:	embryo
21	chr2:54481922-54481972	HCT-116	colon:	n/a
22	chr2:54483193-54483243	SAEC	small airway:	n/a
23	chr2:54483431-54483481	LNCaP	prostate:	n/a
24	chr2:54483433-54483483	SKMC	muscle:	n/a
25	chr2:54560557-54560607	ECC-1	luminal epithelium:	n/a
26	chr2:54483341-54483391	PrEC	prostate:	n/a
27	chr2:54557974-54558024	Jurkat	blood:	n/a
28	chr2:54483341-54483391	MCF-7	breast:	n/a
29	chr2:54557882-54557932	K562	blood:	n/a
30	chr2:54483433-54483483	GM12891	blood:	n/a
31	chr2:54557882-54557932	HCM	heart:	n/a
32	chr2:54483431-54483481	AG09319	gingival:	n/a
33	chr2:54485712-54485762	HRPEpiC	eye:	n/a
34	chr2:54482475-54482525	LNCaP	prostate:	n/a
35	chr2:54517382-54517432	PrEC	prostate:	n/a
36	chr2:54555541-54555591	K562	blood:	n/a
37	chr2:54557902-54557952	LNCaP	prostate:	n/a
38	chr2:54557974-54558024	AoSMC	blood vessel:	n/a
39	chr2:54483498-54483548	HRE	kidney:	n/a
40	chr2:54483431-54483481	Hepatocyte	liver:	n/a
41	chr2:54558089-54558139	AG04449	skin:	fetal
42	chr2:54483498-54483548	HNPCEpiC	eye:	n/a
43	chr2:54557882-54557932	H1-hESC	embryonic stem cell:	embryo
44	chr2:54557836-54557886	HCPEpiC	choroid plexus:	n/a
45	chr2:54483433-54483483	MCF-7	breast:	n/a
46	chr2:54558089-54558139	A549	lung:	n/a
47	chr2:54557902-54557952	BE2_C	brain:	n/a
48	chr2:54481922-54481972	PrEC	prostate:	n/a
49	chr2:54517167-54517217	HRE	kidney:	n/a
50	chr2:54482841-54482891	AG10803	skin:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:54503721..54505972-chr2:54523725..54525740,2	K562	blood:
2	chr2:54570432..54573126-chr2:54574195..54576367,2	K562	blood:
3	chr2:54570097..54573126-chr2:54573916..54576367,3	K562	blood:
4	chr2:54495606..54497945-chr2:54499369..54502319,2	K562	blood:
5	chr2:54516670..54519099-chr2:54522119..54523673,2	MCF-7	breast:
6	chr2:54587660..54591238-chr2:54594163..54597733,4	K562	blood:
7	chr2:54483388..54485294-chr2:54487468..54489310,2	K562	blood:
8	chr2:54340617..54344494-chr2:54480899..54484108,3	K562	blood:
9	chr2:54470373..54472757-chr2:54474538..54476431,2	K562	blood:
10	chr2:54501772..54502741-chr2:54515554..54516142,2	MCF-7	breast:
11	chr2:54342108..54344179-chr2:54478859..54480893,2	K562	blood:
12	chr2:54534452..54537396-chr2:54540353..54542646,2	MCF-7	breast:
13	chr2:54543376..54546512-chr2:54557012..54561316,4	MCF-7	breast:
14	chr2:54341443..54343043-chr2:54557751..54559883,2	MCF-7	breast:
15	chr2:54545854..54547406-chr2:54547534..54550529,2	MCF-7	breast:
16	chr2:54511470..54513165-chr2:54513322..54515700,2	K562	blood:
17	chr2:54467638..54470177-chr2:54473564..54475270,3	K562	blood:
18	chr2:54341887..54343531-chr2:54472985..54475968,2	K562	blood:
19	chr2:54501772..54502741-chr2:54515554..54516142,2	MCF-7	breast:
20	chr2:54483446..54484986-chr2:54498867..54501020,2	K562	blood:
21	chr2:54555822..54558489-chr2:54561441..54564836,3	MCF-7	breast:
22	chr2:54341307..54344135-chr2:54557168..54559182,2	K562	blood:
23	chr2:54482506..54484137-chr2:54492737..54494268,2	K562	blood:
24	chr2:54569839..54572791-chr2:54629016..54630836,2	K562	blood:
25	chr2:54501016..54503842-chr2:54504791..54507736,2	MCF-7	breast:
26	chr2:54560405..54562674-chr2:54570057..54572627,2	MCF-7	breast:
27	chr2:54578951..54582305-chr2:54585861..54589772,4	K562	blood:
28	chr2:54556162..54557934-chr2:54568229..54570513,2	K562	blood:
29	chr2:54470373..54472757-chr2:54474538..54476431,2	K562	blood:
30	chr2:53993157..53995066-chr2:54480511..54482787,2	K562	blood:
31	chr2:54501016..54503842-chr2:54504791..54507736,2	MCF-7	breast:
32	chr2:54483794..54487067-chr2:54487468..54489708,3	K562	blood:
33	chr2:54545854..54547406-chr2:54547534..54550529,2	MCF-7	breast:
34	chr2:54495606..54497945-chr2:54499369..54502319,2	K562	blood:
35	chr2:54466633..54468348-chr2:54481012..54483338,2	K562	blood:
36	chr2:54531334..54533448-chr2:54553590..54555791,2	K562	blood:
37	chr2:54516670..54519099-chr2:54522119..54523673,2	MCF-7	breast:
38	chr2:54467638..54470177-chr2:54473564..54475270,3	K562	blood:
39	chr2:54531334..54533448-chr2:54553590..54555791,2	K562	blood:
40	chr2:54552725..54555359-chr2:54555675..54557996,3	K562	blood:
41	chr2:54588749..54591238-chr2:54595941..54597733,2	K562	blood:
42	chr2:54560405..54562674-chr2:54570057..54572627,2	MCF-7	breast:
43	chr2:54587411..54590325-chr2:54591088..54593008,2	MCF-7	breast:
44	chr2:54503721..54505972-chr2:54523725..54525740,2	K562	blood:
45	chr2:54483446..54484986-chr2:54498867..54501020,2	K562	blood:
46	chr2:54511470..54513165-chr2:54513322..54515700,2	K562	blood:
47	chr2:54197613..54199597-chr2:54572061..54574613,2	K562	blood:
48	chr2:54534452..54537396-chr2:54540353..54542646,2	MCF-7	breast:
49	chr2:54570097..54573126-chr2:54573916..54576367,3	K562	blood:
50	chr2:54553431..54555359-chr2:54555675..54557996,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf73-1	chr2:54558124-54558138	NONHSAT070733
2	lnc-C2orf73-1	chr2:54587340-54587408	NONHSAT070733
3	lnc-C2orf73-1	chr2:54587981-54588079	NONHSAT070733

No data

Variant related genes	Relation type
C2orf73	TF binding region
TSPYL6	TF binding region
C2orf73	CpG island
TSPYL6	CpG island
ENSG00000177994	chromatin interactions
ENSG00000115239	chromatin interactions
ENSG00000178021	chromatin interactions
ENSG00000068878	chromatin interactions
ENSG00000143942	chromatin interactions
ENSG00000170634	chromatin interactions

Extended variants
information (count: 4648 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4648 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs843653	chr2:54469283-54469284	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538893562	chr2:54469392-54469393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558881568	chr2:54469422-54469423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572416815	chr2:54469448-54469449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541206471	chr2:54469457-54469458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554502493	chr2:54469563-54469564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543472657	chr2:54469591-54469592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574440233	chr2:54469614-54469615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187337636	chr2:54469666-54469667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563250297	chr2:54469701-54469702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs843652	chr2:54469703-54469704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs545436205	chr2:54469715-54469716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144122182	chr2:54469733-54469734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191655754	chr2:54469755-54469756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548727386	chr2:54469787-54469788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148700461	chr2:54469792-54469793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530985683	chr2:54469823-54469824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550803941	chr2:54469828-54469829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141367452	chr2:54469830-54469831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374400693	chr2:54469840-54469841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75018668	chr2:54469854-54469855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148469272	chr2:54469879-54469880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565964337	chr2:54469998-54469999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534932323	chr2:54470040-54470041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577501380	chr2:54470078-54470079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554722227	chr2:54470134-54470135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371522236	chr2:54470135-54470136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574551431	chr2:54470156-54470157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115628819	chr2:54470163-54470164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181704187	chr2:54470167-54470168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs843651	chr2:54470196-54470197	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs373777400	chr2:54470248-54470249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558935902	chr2:54470262-54470263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186351909	chr2:54470271-54470272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542182265	chr2:54470274-54470275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538714565	chr2:54470319-54470320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146235071	chr2:54470375-54470376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528662729	chr2:54470424-54470425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139309330	chr2:54470445-54470446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551184480	chr2:54470446-54470447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368141878	chr2:54470468-54470469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541977552	chr2:54470486-54470487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116455882	chr2:54470491-54470492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34931097	chr2:54470530-54470531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75516785	chr2:54470581-54470582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189940413	chr2:54470594-54470595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557087991	chr2:54470608-54470609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs843650	chr2:54470627-54470628	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534885799	chr2:54470630-54470631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549541358	chr2:54470662-54470663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
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
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54449800-54535200	Weak transcription	Primary T cells from cord blood	blood
2	chr2:54452800-54490200	Weak transcription	Primary B cells from cord blood	blood
3	chr2:54455800-54476000	Weak transcription	K562	blood
4	chr2:54456400-54487200	Weak transcription	Psoas Muscle	Psoas
5	chr2:54466200-54469400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr2:54466400-54469400	Enhancers	Adipose Nuclei	Adipose
7	chr2:54467800-54469400	Enhancers	Fetal Lung	lung
8	chr2:54468000-54470600	Weak transcription	Right Atrium	heart
9	chr2:54468200-54469600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:54468400-54469800	Weak transcription	Fetal Stomach	stomach
11	chr2:54468400-54474000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr2:54468400-54492200	Weak transcription	HSMMtube	muscle
13	chr2:54468600-54472400	Weak transcription	Osteobl	bone
14	chr2:54468600-54481600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr2:54468800-54471400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr2:54468800-54472600	Weak transcription	NHDF-Ad	bronchial
17	chr2:54468800-54474200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:54469400-54480800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:54470800-54471000	Enhancers	Right Atrium	heart
20	chr2:54472400-54473200	Enhancers	Osteobl	bone
21	chr2:54472800-54482400	Weak transcription	Fetal Stomach	stomach
22	chr2:54474000-54474600	Enhancers	Rectal Smooth Muscle	rectum
23	chr2:54474000-54474600	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr2:54474200-54474400	Weak transcription	Right Ventricle	heart
25	chr2:54474200-54474600	Enhancers	HepG2	liver
26	chr2:54474200-54474800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:54474200-54485600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr2:54474400-54474600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:54474400-54474600	Enhancers	Right Ventricle	heart
30	chr2:54474600-54478800	Weak transcription	HepG2	liver
31	chr2:54474600-54481800	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr2:54474600-54482600	Weak transcription	Right Ventricle	heart
33	chr2:54474600-54484200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr2:54476000-54476200	ZNF genes & repeats	K562	blood
35	chr2:54476200-54478800	Weak transcription	K562	blood
36	chr2:54477800-54482800	Weak transcription	Pancreas	Pancrea
37	chr2:54478200-54478600	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr2:54478800-54479200	Enhancers	HepG2	liver
39	chr2:54478800-54479400	ZNF genes & repeats	K562	blood
40	chr2:54479200-54487200	Weak transcription	HepG2	liver
41	chr2:54479200-54489200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:54479400-54479600	Weak transcription	K562	blood
43	chr2:54479600-54480800	Active TSS	K562	blood
44	chr2:54479600-54482600	Weak transcription	Liver	Liver
45	chr2:54479800-54489200	Weak transcription	Gastric	stomach
46	chr2:54480000-54481600	Weak transcription	Primary B cells from peripheral blood	blood
47	chr2:54480200-54482400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr2:54480400-54485400	Weak transcription	Fetal Lung	lung
49	chr2:54480600-54481000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:54480600-54481000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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