Variant report

Variant	nsv582209
Chromosome Location	chr2:73857002-73907696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:660)
CpG islands
(count:1100)
Chromatin interactive
region (count:16)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:660 , 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	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
4	ARID3A	chr2:73857942-73858125	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:73867690-73868035	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	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
11	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
13	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
14	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
15	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
16	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
19	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
20	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
21	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
22	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
23	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
24	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
25	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
26	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
28	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
29	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
30	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
31	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
32	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
35	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
39	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
40	CTCF	chr2:73858080-73858230	GM12869	blood:	n/a	n/a
41	CTCF	chr2:73857700-73857850	AG09309	skin:	n/a	n/a
42	CTCF	chr2:73907480-73907630	Hela-S3	cervix:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
43	CTCF	chr2:73907400-73907550	AG04449	skin:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
44	CTCF	chr2:73907305-73907720	A549	lung:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
45	CTCF	chr2:73857840-73857990	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr2:73907279-73907654	HepG2	liver:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
47	CTCF	chr2:73874915-73875002	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:73857840-73857990	A549	lung:	n/a	n/a
49	CTCF	chr2:73857838-73858121	Fibrobl	skin:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
50	CTCF	chr2:73899297-73899322	GM10248	blood:	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	chr2:73907327-73907377	HIPEpiC	eye:	n/a
2	chr2:73868917-73868967	AoSMC	blood vessel:	n/a
3	chr2:73907327-73907377	HIPEpiC	eye:	n/a
4	chr2:73868917-73868967	AoSMC	blood vessel:	n/a
5	chr2:73869966-73870016	MCF10A-Er-Src	breast:	n/a
6	chr2:73907327-73907377	U87	brain:	n/a
7	chr2:73871849-73871899	SK-N-MC	brain:	n/a
8	chr2:73871782-73871832	PFSK-1	brain:	n/a
9	chr2:73871230-73871280	Hela-S3	cervix:	n/a
10	chr2:73871849-73871899	Caco-2	colon:	n/a
11	chr2:73870294-73870344	ovcar-3	ovarian:	n/a
12	chr2:73871942-73871992	GM19239	blood:	n/a
13	chr2:73870653-73870703	AG04449	skin:	fetal
14	chr2:73868736-73868786	IMR90	lung:	fetal
15	chr2:73870105-73870155	HRE	kidney:	n/a
16	chr2:73870294-73870344	MCF10A-Er-Src	breast:	n/a
17	chr2:73871849-73871899	NT2-D1	testis:	n/a
18	chr2:73871942-73871992	HCM	heart:	n/a
19	chr2:73869966-73870016	IMR90	lung:	fetal
20	chr2:73871309-73871359	HL-60	blood:	n/a
21	chr2:73870294-73870344	PANC-1	pancreas:	n/a
22	chr2:73868736-73868786	HUVEC	blood vessel:	n/a
23	chr2:73907327-73907377	T-47D	breast:	n/a
24	chr2:73871855-73871905	PrEC	prostate:	n/a
25	chr2:73871782-73871832	AG04450	lung:	fetal
26	chr2:73869666-73869716	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:73868919-73868969	AG09319	gingival:	n/a
28	chr2:73871855-73871905	HCPEpiC	choroid plexus:	n/a
29	chr2:73870105-73870155	HMEC	breast:	n/a
30	chr2:73870294-73870344	SAEC	small airway:	n/a
31	chr2:73869666-73869716	IMR90	lung:	fetal
32	chr2:73868736-73868786	MCF10A-Er-Src	breast:	n/a
33	chr2:73871309-73871359	K562	blood:	n/a
34	chr2:73870294-73870344	HMEC	breast:	n/a
35	chr2:73870294-73870344	HNPCEpiC	eye:	n/a
36	chr2:73869516-73869566	HCF	heart:	n/a
37	chr2:73868917-73868967	ovcar-3	ovarian:	n/a
38	chr2:73869966-73870016	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:73870294-73870344	NH-A	brain:	n/a
40	chr2:73871942-73871992	HEK293	kidney:	embryo
41	chr2:73868917-73868967	BE2_C	brain:	n/a
42	chr2:73870653-73870703	T-47D	breast:	n/a
43	chr2:73871915-73871965	HRCEpiC	kidney:	n/a
44	chr2:73870105-73870155	GM06990	blood:	n/a
45	chr2:73871942-73871992	SAEC	small airway:	n/a
46	chr2:73871309-73871359	AG09319	gingival:	n/a
47	chr2:73869966-73870016	PFSK-1	brain:	n/a
48	chr2:73871309-73871359	HNPCEpiC	eye:	n/a
49	chr2:73907327-73907377	HRPEpiC	eye:	n/a
50	chr2:73871855-73871905	HCM	heart:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 1763 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1763 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4852940	chr2:73857002-73857003	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201602504	chr2:73857066-73857067	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576122137	chr2:73857075-73857076	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs57809531	chr2:73857092-73857093	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150010907	chr2:73857094-73857095	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376048599	chr2:73857105-73857106	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374091161	chr2:73857133-73857134	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373629120	chr2:73857134-73857135	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62149813	chr2:73857135-73857136	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537264631	chr2:73857193-73857194	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568330029	chr2:73857233-73857234	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs576998998	chr2:73857248-73857249	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs10197233	chr2:73857270-73857271	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552690634	chr2:73857292-73857293	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs574379113	chr2:73857312-73857313	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs184399937	chr2:73857323-73857324	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs139873561	chr2:73857351-73857352	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs2947857	chr2:73857395-73857396	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs552523554	chr2:73857397-73857398	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs368425463	chr2:73857398-73857399	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs530986210	chr2:73857480-73857481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545967793	chr2:73857488-73857489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72075333	chr2:73857505-73857506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74790871	chr2:73857517-73857518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74415888	chr2:73857522-73857523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564378409	chr2:73857567-73857568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551041185	chr2:73857579-73857580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569448700	chr2:73857581-73857582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189865313	chr2:73857590-73857591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2969589	chr2:73857643-73857644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142038884	chr2:73857662-73857663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2860579	chr2:73857681-73857682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs192914012	chr2:73857689-73857690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548157659	chr2:73857696-73857697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569909203	chr2:73857733-73857734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537377084	chr2:73857750-73857751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555585206	chr2:73857785-73857786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139063402	chr2:73857791-73857792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570708057	chr2:73857802-73857803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534659120	chr2:73857863-73857864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184577391	chr2:73857872-73857873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62149814	chr2:73857951-73857952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189801855	chr2:73858038-73858039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4852941	chr2:73858040-73858041	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs556712516	chr2:73858054-73858055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28561721	chr2:73858064-73858065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181060919	chr2:73858067-73858068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62149815	chr2:73858085-73858086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10188074	chr2:73858120-73858121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs10187867	chr2:73858124-73858125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

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

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73852400-73857400	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr2:73854000-73858000	Weak transcription	Liver	Liver
3	chr2:73857000-73857200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
4	chr2:73857000-73857200	Active TSS	Primary B cells from cord blood	blood
5	chr2:73857000-73857200	Active TSS	NHLF	lung
6	chr2:73857000-73857400	Active TSS	GM12878-XiMat	blood
7	chr2:73857000-73857400	Active TSS	HSMM	muscle
8	chr2:73857000-73857400	ZNF genes & repeats	HSMMtube	muscle
9	chr2:73857400-73858800	Weak transcription	HSMMtube	muscle
10	chr2:73859800-73860400	Enhancers	Ovary	ovary
11	chr2:73860400-73867000	Weak transcription	Ovary	ovary
12	chr2:73863600-73863800	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr2:73863800-73864600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr2:73864200-73867400	Enhancers	Liver	Liver
15	chr2:73864400-73865000	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr2:73864400-73865400	Enhancers	Duodenum Mucosa	Duodenum
17	chr2:73864600-73865400	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr2:73864600-73865600	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr2:73865000-73865200	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr2:73865200-73865400	Enhancers	Stomach Smooth Muscle	stomach
21	chr2:73865200-73867600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr2:73865400-73868000	Weak transcription	Duodenum Mucosa	Duodenum
23	chr2:73865400-73868000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr2:73865600-73867200	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr2:73866200-73867200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:73866200-73870600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:73866400-73866600	Enhancers	Fetal Muscle Trunk	muscle
28	chr2:73866400-73866600	Enhancers	Right Atrium	heart
29	chr2:73866400-73866800	ZNF genes & repeats	Spleen	Spleen
30	chr2:73866400-73868800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr2:73866400-73871200	Enhancers	Fetal Lung	lung
32	chr2:73866600-73867600	Enhancers	HepG2	liver
33	chr2:73866800-73867800	Weak transcription	Spleen	Spleen
34	chr2:73867000-73867400	Enhancers	Placenta	Placenta
35	chr2:73867000-73868200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:73867000-73868600	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr2:73867000-73872200	Enhancers	Ovary	ovary
38	chr2:73867200-73869000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr2:73867200-73869800	Enhancers	Colonic Mucosa	Colon
40	chr2:73867400-73867800	Weak transcription	Placenta	Placenta
41	chr2:73867400-73868400	Enhancers	Brain Hippocampus Middle	brain
42	chr2:73867400-73868600	Enhancers	Adipose Nuclei	Adipose
43	chr2:73867400-73868600	Enhancers	Brain Cingulate Gyrus	brain
44	chr2:73867400-73869800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:73867400-73870200	Flanking Active TSS	Liver	Liver
46	chr2:73867400-73870200	Enhancers	Fetal Intestine Large	intestine
47	chr2:73867600-73867800	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr2:73867600-73868000	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr2:73867600-73868000	Flanking Active TSS	HepG2	liver
50	chr2:73867600-73868200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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