Variant report

Variant	nsv1011488
Chromosome Location	chr2:73852525-73909818
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:717)
CpG islands
(count:1100)
Chromatin interactive
region (count:16)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
3	ARID3A	chr2:73857942-73858125	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
6	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
7	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
8	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:73857107-73857303	K562	blood:	n/a	n/a
10	BATF	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
11	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
12	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
15	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
16	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
17	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
18	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
19	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
20	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
23	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
24	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
25	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
26	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
28	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
29	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
30	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
31	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
34	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
37	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
38	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
39	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
40	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
41	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
42	CTCF	chr2:73857960-73858250	GM12872	blood:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
43	CTCF	chr2:73907220-73907370	HFF	foreskin:	n/a	n/a
44	CTCF	chr2:73857870-73858091	MCF-7	breast:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
45	CTCF	chr2:73857685-73858214	A549	lung:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
46	CTCF	chr2:73907100-73907250	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr2:73907180-73907330	GM12868	blood:	n/a	n/a
48	CTCF	chr2:73879080-73879230	RPTEC	kidney:	n/a	n/a
49	CTCF	chr2:73907300-73907708	H1-hESC	embryonic stem cell:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
50	CTCF	chr2:73868740-73868890	HepG2	liver:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73871849-73871899	GM19239	blood:	n/a
2	chr2:73870294-73870344	SAEC	small airway:	n/a
3	chr2:73871849-73871899	GM19239	blood:	n/a
4	chr2:73870294-73870344	SAEC	small airway:	n/a
5	chr2:73871915-73871965	BE2_C	brain:	n/a
6	chr2:73871782-73871832	K562	blood:	n/a
7	chr2:73868919-73868969	SK-N-SH_RA	brain:	n/a
8	chr2:73871855-73871905	HCM	heart:	n/a
9	chr2:73867196-73867246	AG09309	skin:	n/a
10	chr2:73907327-73907377	AG10803	skin:	n/a
11	chr2:73871230-73871280	HCT-116	colon:	n/a
12	chr2:73867196-73867246	GM12892	blood:	n/a
13	chr2:73871942-73871992	K562	blood:	n/a
14	chr2:73871230-73871280	SAEC	small airway:	n/a
15	chr2:73868736-73868786	HIPEpiC	eye:	n/a
16	chr2:73869966-73870016	NHBE	bronchial:	n/a
17	chr2:73871309-73871359	SAEC	small airway:	n/a
18	chr2:73869666-73869716	HRE	kidney:	n/a
19	chr2:73869966-73870016	HCF	heart:	n/a
20	chr2:73871855-73871905	PFSK-1	brain:	n/a
21	chr2:73871855-73871905	AoSMC	blood vessel:	n/a
22	chr2:73868736-73868786	SK-N-SH	brain:	n/a
23	chr2:73870653-73870703	SAEC	small airway:	n/a
24	chr2:73868736-73868786	NHBE	bronchial:	n/a
25	chr2:73870105-73870155	HCF	heart:	n/a
26	chr2:73871230-73871280	HCPEpiC	choroid plexus:	n/a
27	chr2:73869966-73870016	HNPCEpiC	eye:	n/a
28	chr2:73871849-73871899	ovcar-3	ovarian:	n/a
29	chr2:73871849-73871899	RPTEC	kidney:	n/a
30	chr2:73868917-73868967	HCF	heart:	n/a
31	chr2:73867196-73867246	A549	lung:	n/a
32	chr2:73870294-73870344	MCF-7	breast:	n/a
33	chr2:73871849-73871899	GM12891	blood:	n/a
34	chr2:73868919-73868969	AoSMC	blood vessel:	n/a
35	chr2:73871782-73871832	PrEC	prostate:	n/a
36	chr2:73871849-73871899	HCF	heart:	n/a
37	chr2:73869966-73870016	NT2-D1	testis:	n/a
38	chr2:73867196-73867246	K562	blood:	n/a
39	chr2:73868917-73868967	LNCaP	prostate:	n/a
40	chr2:73871230-73871280	IMR90	lung:	fetal
41	chr2:73907327-73907377	HEEpiC	esophagus:	n/a
42	chr2:73871309-73871359	HCT-116	colon:	n/a
43	chr2:73870105-73870155	NT2-D1	testis:	n/a
44	chr2:73871855-73871905	LNCaP	prostate:	n/a
45	chr2:73871915-73871965	AG10803	skin:	n/a
46	chr2:73867196-73867246	SAEC	small airway:	n/a
47	chr2:73869666-73869716	Hela-S3	cervix:	n/a
48	chr2:73871849-73871899	NB4	blood:	n/a
49	chr2:73871855-73871905	U87	brain:	n/a
50	chr2:73871230-73871280	GM12892	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
2	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
3	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
4	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
5	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
6	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
7	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
8	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
9	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
10	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
11	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
12	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
13	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
14	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
15	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
16	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
2	lnc-ALMS1-2	chr2:73868076-73868755	NONHSAT071625
3	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
4	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
5	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
6	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
7	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683

No data

Variant related genes	Relation type
ALMS1P	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
NAT8	CpG island
ENSG00000144048	chromatin interactions
ENSG00000204872	chromatin interactions

Extended variants
information (count: 2087 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574454833	chr2:73852526-73852527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541868535	chr2:73852532-73852533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563324774	chr2:73852535-73852536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531096236	chr2:73852536-73852537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552875403	chr2:73852549-73852550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564474236	chr2:73852550-73852551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528670108	chr2:73852557-73852558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546654021	chr2:73852565-73852566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568237378	chr2:73852576-73852577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535579364	chr2:73852579-73852580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185902778	chr2:73852647-73852648	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386647345	chr2:73852648-73852649	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536941487	chr2:73852649-73852650	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115425992	chr2:73852650-73852651	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138283747	chr2:73852710-73852711	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369733155	chr2:73852713-73852714	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571973720	chr2:73852746-73852747	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192349240	chr2:73852764-73852765	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574562333	chr2:73852765-73852766	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541943479	chr2:73852777-73852778	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563129101	chr2:73852836-73852837	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575198202	chr2:73852840-73852841	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11281455	chr2:73852931-73852932	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567976042	chr2:73852935-73852936	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200675522	chr2:73852938-73852939	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60049316	chr2:73852945-73852946	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577165285	chr2:73852950-73852951	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558056852	chr2:73852992-73852993	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56963877	chr2:73853001-73853002	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183718515	chr2:73853010-73853011	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553563754	chr2:73853016-73853017	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186099687	chr2:73853029-73853030	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546765887	chr2:73853041-73853042	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11683970	chr2:73853057-73853058	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs529335206	chr2:73853160-73853161	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77768313	chr2:73853169-73853170	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551099551	chr2:73853187-73853188	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569112004	chr2:73853254-73853255	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148802028	chr2:73853259-73853260	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190469453	chr2:73853308-73853309	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570785683	chr2:73853309-73853310	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534944565	chr2:73853311-73853312	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553189570	chr2:73853355-73853356	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376081611	chr2:73853380-73853381	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535197341	chr2:73853445-73853446	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557026837	chr2:73853463-73853464	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575095387	chr2:73853477-73853478	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4241256	chr2:73853509-73853510	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs557534942	chr2:73853513-73853514	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573181998	chr2:73853565-73853566	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
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
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73830600-73854800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:73836400-73852600	Weak transcription	Ovary	ovary
3	chr2:73838400-73852600	Weak transcription	Right Ventricle	heart
4	chr2:73838600-73852600	Weak transcription	Pancreas	Pancrea
5	chr2:73842600-73852600	Weak transcription	Left Ventricle	heart
6	chr2:73844000-73854800	Weak transcription	Fetal Brain Female	brain
7	chr2:73851400-73853000	Weak transcription	GM12878-XiMat	blood
8	chr2:73852000-73852600	Enhancers	HepG2	liver
9	chr2:73852400-73852600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:73852400-73854000	Enhancers	Liver	Liver
11	chr2:73852400-73857400	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr2:73852600-73852800	Enhancers	Fetal Intestine Large	intestine
13	chr2:73852600-73852800	Enhancers	Left Ventricle	heart
14	chr2:73852600-73852800	Flanking Active TSS	HepG2	liver
15	chr2:73852600-73853000	Enhancers	Colonic Mucosa	Colon
16	chr2:73852600-73853200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr2:73852600-73853200	Enhancers	Duodenum Mucosa	Duodenum
18	chr2:73852600-73853200	Enhancers	Pancreas	Pancrea
19	chr2:73852600-73853200	Enhancers	Right Ventricle	heart
20	chr2:73852600-73853800	Enhancers	Ovary	ovary
21	chr2:73852600-73854000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr2:73852600-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:73852600-73854400	Enhancers	Primary hematopoietic stem cells	blood
24	chr2:73852600-73855000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr2:73852800-73853000	Enhancers	HepG2	liver
26	chr2:73852800-73853200	Enhancers	A549	lung
27	chr2:73852800-73853200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr2:73853000-73853200	Flanking Active TSS	HepG2	liver
29	chr2:73853000-73853400	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr2:73853000-73854000	Enhancers	GM12878-XiMat	blood
31	chr2:73853200-73853600	Enhancers	HepG2	liver
32	chr2:73853400-73853600	Enhancers	Fetal Intestine Large	intestine
33	chr2:73853800-73854000	Weak transcription	Ovary	ovary
34	chr2:73854000-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:73854000-73858000	Weak transcription	Liver	Liver
36	chr2:73854800-73855000	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr2:73855600-73857000	Enhancers	GM12878-XiMat	blood
38	chr2:73856600-73857000	Weak transcription	HSMMtube	muscle
39	chr2:73857000-73857200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
40	chr2:73857000-73857200	Active TSS	Primary B cells from cord blood	blood
41	chr2:73857000-73857200	Active TSS	NHLF	lung
42	chr2:73857000-73857400	Active TSS	GM12878-XiMat	blood
43	chr2:73857000-73857400	Active TSS	HSMM	muscle
44	chr2:73857000-73857400	ZNF genes & repeats	HSMMtube	muscle
45	chr2:73857400-73858800	Weak transcription	HSMMtube	muscle
46	chr2:73859800-73860400	Enhancers	Ovary	ovary
47	chr2:73860400-73867000	Weak transcription	Ovary	ovary
48	chr2:73863600-73863800	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr2:73863800-73864600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr2:73864200-73867400	Enhancers	Liver	Liver

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