Variant report

Variant	nsv1006033
Chromosome Location	chr2:73840055-73900856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73857942-73858125	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
4	BACH1	chr2:73857107-73857303	K562	blood:	n/a	n/a
5	BATF	chr2:73851315-73851489	GM12878	blood:	n/a	chr2:73851419-73851430
6	BATF	chr2:73851278-73851536	GM12878	blood:	n/a	chr2:73851419-73851430
7	BATF	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
10	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
11	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
14	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
15	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:73841359-73841438	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
18	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
21	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
22	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
23	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
26	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
27	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
28	CTCF	chr2:73851794-73852065	MCF-7	breast:	n/a	n/a
29	CTCF	chr2:73847180-73847330	HCT-116	colon:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271
30	CTCF	chr2:73857960-73858110	GM06990	blood:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
31	CTCF	chr2:73847200-73847350	HBMEC	blood vessel:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271
32	CTCF	chr2:73851818-73852037	A549	lung:	n/a	n/a
33	CTCF	chr2:73851920-73852070	HVMF	connective:	n/a	n/a
34	CTCF	chr2:73847200-73847350	HRPEpiC	eye:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271
35	CTCF	chr2:73869620-73869646	HepG2	liver:	n/a	n/a
36	CTCF	chr2:73851808-73852013	A549	lung:	n/a	n/a
37	CTCF	chr2:73847144-73847344	GM13977	blood:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271
38	CTCF	chr2:73847160-73847310	BJ	skin:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271
39	CTCF	chr2:73879127-73879200	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:73858060-73858210	BE2_C	brain:	n/a	n/a
41	CTCF	chr2:73874906-73875001	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:73851748-73852223	A549	lung:	n/a	n/a
43	CTCF	chr2:73851814-73852011	LNCaP	prostate:	n/a	n/a
44	CTCF	chr2:73857840-73857990	GM12870	blood:	n/a	n/a
45	CTCF	chr2:73851840-73851990	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr2:73851860-73852010	GM12869	blood:	n/a	n/a
47	CTCF	chr2:73856078-73856102	GM13976	blood:	n/a	n/a
48	CTCF	chr2:73847200-73847350	GM12878	blood:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271
49	CTCF	chr2:73877571-73877588	GM13976	blood:	n/a	n/a
50	CTCF	chr2:73853840-73853892	MCF-7	breast:	n/a	chr2:73853868-73853886 chr2:73853870-73853891

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73868919-73868969	GM06990	blood:	n/a
2	chr2:73868736-73868786	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:73868736-73868786	PANC-1	pancreas:	n/a
4	chr2:73871855-73871905	HIPEpiC	eye:	n/a
5	chr2:73868919-73868969	GM06990	blood:	n/a
6	chr2:73868736-73868786	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:73868736-73868786	PANC-1	pancreas:	n/a
8	chr2:73871855-73871905	HIPEpiC	eye:	n/a
9	chr2:73871849-73871899	HIPEpiC	eye:	n/a
10	chr2:73867196-73867246	GM12878	blood:	n/a
11	chr2:73867196-73867246	K562	blood:	n/a
12	chr2:73868917-73868967	HNPCEpiC	eye:	n/a
13	chr2:73868917-73868967	A549	lung:	n/a
14	chr2:73868736-73868786	HepG2	liver:	n/a
15	chr2:73871942-73871992	PFSK-1	brain:	n/a
16	chr2:73868736-73868786	AG09319	gingival:	n/a
17	chr2:73869666-73869716	GM12891	blood:	n/a
18	chr2:73867196-73867246	HCF	heart:	n/a
19	chr2:73868917-73868967	PANC-1	pancreas:	n/a
20	chr2:73871942-73871992	HEEpiC	esophagus:	n/a
21	chr2:73867196-73867246	HUVEC	blood vessel:	n/a
22	chr2:73867196-73867246	AoSMC	blood vessel:	n/a
23	chr2:73870294-73870344	SK-N-SH_RA	brain:	n/a
24	chr2:73870105-73870155	BJ	skin:	n/a
25	chr2:73871915-73871965	CMK	blood:	n/a
26	chr2:73870105-73870155	CMK	blood:	n/a
27	chr2:73871849-73871899	GM12892	blood:	n/a
28	chr2:73871855-73871905	ovcar-3	ovarian:	n/a
29	chr2:73871942-73871992	AoSMC	blood vessel:	n/a
30	chr2:73871309-73871359	GM06990	blood:	n/a
31	chr2:73868919-73868969	HIPEpiC	eye:	n/a
32	chr2:73871782-73871832	NT2-D1	testis:	n/a
33	chr2:73868917-73868967	HL-60	blood:	n/a
34	chr2:73870294-73870344	BJ	skin:	n/a
35	chr2:73869966-73870016	SK-N-SH	brain:	n/a
36	chr2:73871855-73871905	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:73871230-73871280	PANC-1	pancreas:	n/a
38	chr2:73869666-73869716	T-47D	breast:	n/a
39	chr2:73869666-73869716	HCF	heart:	n/a
40	chr2:73868917-73868967	HEK293	kidney:	embryo
41	chr2:73871230-73871280	RPTEC	kidney:	n/a
42	chr2:73871230-73871280	GM06990	blood:	n/a
43	chr2:73871309-73871359	SK-N-SH_RA	brain:	n/a
44	chr2:73870294-73870344	SAEC	small airway:	n/a
45	chr2:73869516-73869566	HMEC	breast:	n/a
46	chr2:73869966-73870016	HIPEpiC	eye:	n/a
47	chr2:73868736-73868786	GM06990	blood:	n/a
48	chr2:73871230-73871280	Hela-S3	cervix:	n/a
49	chr2:73867196-73867246	HL-60	blood:	n/a
50	chr2:73869516-73869566	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:73839411..73842027-chr2:73845184..73847412,3	MCF-7	breast:
2	chr2:73842508..73845608-chr2:73846002..73848469,3	K562	blood:
3	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
4	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
5	chr2:73842404..73844324-chr2:73845193..73847014,2	MCF-7	breast:
6	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
7	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
8	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
9	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
10	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
11	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
12	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
13	chr2:73839411..73842027-chr2:73845184..73847412,3	MCF-7	breast:
14	chr2:73834970..73837319-chr2:73844095..73845745,2	K562	blood:
15	chr2:73842508..73845608-chr2:73846002..73848469,3	K562	blood:
16	chr2:73842404..73844324-chr2:73845193..73847014,2	MCF-7	breast:
17	chr2:73837883..73840443-chr2:74211046..74212867,2	MCF-7	breast:
18	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
19	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
20	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
21	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:

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

Variant related genes	Relation type
ALMS1P	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
NAT8	CpG island
ENSG00000204872	chromatin interactions
ENSG00000235499	chromatin interactions

Extended variants
information (count: 2210 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2210 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6745480	chr2:73840055-73840056	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544037909	chr2:73840117-73840118	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565340936	chr2:73840135-73840136	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532672734	chr2:73840144-73840145	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187732846	chr2:73840163-73840164	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544432739	chr2:73840264-73840265	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs559472152	chr2:73840293-73840294	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs193120331	chr2:73840320-73840321	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562854818	chr2:73840340-73840341	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545255463	chr2:73840369-73840370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184522773	chr2:73840370-73840371	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567554691	chr2:73840439-73840440	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188974906	chr2:73840455-73840456	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562825010	chr2:73840489-73840490	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192257490	chr2:73840500-73840501	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549587836	chr2:73840519-73840520	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571137225	chr2:73840545-73840546	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531932289	chr2:73840561-73840562	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375518678	chr2:73840573-73840574	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538332934	chr2:73840586-73840587	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184263611	chr2:73840623-73840624	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565540336	chr2:73840627-73840628	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189729754	chr2:73840630-73840631	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75140088	chr2:73840640-73840641	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12479158	chr2:73840664-73840665	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs544002809	chr2:73840721-73840722	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559171410	chr2:73840722-73840723	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200671101	chr2:73840811-73840812	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577546972	chr2:73840816-73840817	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541526759	chr2:73840880-73840881	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559844989	chr2:73840888-73840889	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529995454	chr2:73840899-73840900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574831619	chr2:73840924-73840925	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181153466	chr2:73840940-73840941	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560996794	chr2:73840962-73840963	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543730822	chr2:73840967-73840968	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35475318	chr2:73840984-73840985	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2421577	chr2:73840998-73840999	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs375353663	chr2:73841004-73841005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549699996	chr2:73841023-73841024	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369149761	chr2:73841045-73841046	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371360424	chr2:73841046-73841047	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571103224	chr2:73841059-73841060	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74926174	chr2:73841072-73841073	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547133339	chr2:73841111-73841112	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149491795	chr2:73841116-73841117	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535836468	chr2:73841185-73841186	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554568788	chr2:73841188-73841189	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569695035	chr2:73841231-73841232	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537723484	chr2:73841236-73841237	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73801000-73844000	Weak transcription	Fetal Kidney	kidney
2	chr2:73822600-73840800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:73823000-73844600	Weak transcription	Primary B cells from cord blood	blood
4	chr2:73826000-73841200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr2:73826200-73841400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:73827000-73840600	Weak transcription	NHLF	lung
7	chr2:73827800-73840400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr2:73829400-73845400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr2:73829600-73840200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr2:73829800-73840400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:73830000-73840800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr2:73830400-73843600	Weak transcription	Aorta	Aorta
13	chr2:73830600-73841200	Weak transcription	Liver	Liver
14	chr2:73830600-73843000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:73830600-73847600	Weak transcription	Spleen	Spleen
16	chr2:73830600-73854800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr2:73830800-73840800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr2:73831000-73842200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:73831200-73841200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr2:73836400-73844200	Weak transcription	Adipose Nuclei	Adipose
21	chr2:73836400-73852600	Weak transcription	Ovary	ovary
22	chr2:73837400-73845000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:73838000-73845200	Weak transcription	Brain Hippocampus Middle	brain
24	chr2:73838200-73843200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:73838400-73840200	Weak transcription	Fetal Muscle Trunk	muscle
26	chr2:73838400-73841800	Weak transcription	Left Ventricle	heart
27	chr2:73838400-73842200	Weak transcription	Brain Anterior Caudate	brain
28	chr2:73838400-73844200	Weak transcription	Fetal Lung	lung
29	chr2:73838400-73844200	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr2:73838400-73852600	Weak transcription	Right Ventricle	heart
31	chr2:73838600-73841000	Weak transcription	GM12878-XiMat	blood
32	chr2:73838600-73842200	Weak transcription	Duodenum Mucosa	Duodenum
33	chr2:73838600-73843800	Weak transcription	Lung	lung
34	chr2:73838600-73845200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:73838600-73845400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr2:73838600-73847400	Weak transcription	Brain Angular Gyrus	brain
37	chr2:73838600-73852600	Weak transcription	Pancreas	Pancrea
38	chr2:73838800-73840600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr2:73838800-73842000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr2:73838800-73842200	Weak transcription	Fetal Intestine Small	intestine
41	chr2:73838800-73843400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:73838800-73845800	Weak transcription	Fetal Stomach	stomach
43	chr2:73838800-73846600	Weak transcription	Fetal Muscle Leg	muscle
44	chr2:73838800-73849600	Weak transcription	Brain Germinal Matrix	brain
45	chr2:73839000-73842200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:73839200-73840400	Weak transcription	Fetal Thymus	thymus
47	chr2:73839200-73840800	Weak transcription	Fetal Brain Male	brain
48	chr2:73839200-73841800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr2:73839200-73842400	Weak transcription	Fetal Brain Female	brain
50	chr2:73839200-73844000	Strong transcription	Brain Inferior Temporal Lobe	brain

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