Variant report

Variant	nsv535969
Chromosome Location	chr2:148677122-148715921
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	chr2:148684448-148685625	HepG2	liver:	n/a	n/a
2	BHLHE40	chr2:148684660-148685068	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:148684676-148685032	A549	lung:	n/a	chr2:148684844-148684855
4	CEBPB	chr2:148697442-148697736	MCF-7	breast:	n/a	chr2:148697633-148697644
5	CEBPB	chr2:148684589-148685071	HepG2	liver:	n/a	chr2:148684844-148684855
6	CEBPB	chr2:148696927-148697156	MCF-7	breast:	n/a	chr2:148697048-148697059
7	CEBPB	chr2:148684629-148685086	HepG2	liver:	n/a	chr2:148684844-148684855
8	CEBPB	chr2:148696888-148697213	HepG2	liver:	n/a	chr2:148697048-148697059
9	CEBPB	chr2:148684637-148685029	HepG2	liver:	n/a	chr2:148684844-148684855
10	CEBPB	chr2:148684663-148684997	IMR90	lung:	n/a	chr2:148684844-148684855
11	CEBPB	chr2:148683830-148684193	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:148696853-148697203	MCF-7	breast:	n/a	chr2:148697048-148697059
13	CEBPB	chr2:148684498-148685409	HepG2	liver:	n/a	chr2:148684844-148684855
14	CEBPB	chr2:148691990-148692246	A549	lung:	n/a	n/a
15	CEBPB	chr2:148684622-148685028	MCF-7	breast:	n/a	chr2:148684844-148684855
16	CEBPB	chr2:148713810-148713855	HepG2	liver:	n/a	n/a
17	CEBPD	chr2:148684568-148685002	HepG2	liver:	n/a	n/a
18	CHD2	chr2:148684603-148685053	HepG2	liver:	n/a	n/a
19	CTCF	chr2:148695400-148695550	WERI-Rb-1	eye:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
20	CTCF	chr2:148697520-148697670	NHEK	skin:	n/a	n/a
21	CTCF	chr2:148695420-148695570	AG10803	skin:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
22	CTCF	chr2:148695480-148695630	BE2_C	brain:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
23	CTCF	chr2:148695400-148695550	GM12864	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
24	CTCF	chr2:148695384-148695596	MCF-7	breast:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
25	CTCF	chr2:148695374-148695545	T-47D	breast:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
26	CTCF	chr2:148695380-148695530	NHDF-neo	bronchial:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
27	CTCF	chr2:148695420-148695570	HPF	lung:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
28	CTCF	chr2:148695460-148695610	GM12873	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
29	CTCF	chr2:148695440-148695590	Caco-2	colon:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
30	CTCF	chr2:148695394-148695610	GM10248	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
31	CTCF	chr2:148695440-148695590	GM12865	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
32	CTCF	chr2:148695400-148695550	HCPEpiC	choroid plexus:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
33	CTCF	chr2:148695440-148695590	HA-sp	spinal cord:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
34	CTCF	chr2:148695400-148695550	HEEpiC	esophagus:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
35	CTCF	chr2:148695331-148695700	Spleen_OC	spleen:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
36	CTCF	chr2:148695420-148695570	Hela-S3	cervix:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
37	CTCF	chr2:148695383-148695619	HepG2	liver:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
38	CTCF	chr2:148695520-148695670	A549	lung:	n/a	n/a
39	CTCF	chr2:148695267-148695622	HepG2	liver:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
40	CTCF	chr2:148695757-148695823	Medullo	brain:	n/a	n/a
41	CTCF	chr2:148695420-148695570	AG04450	lung:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
42	CTCF	chr2:148695420-148695570	HPAF	blood vessel:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
43	CTCF	chr2:148703260-148703410	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr2:148695380-148695530	GM12868	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
45	CTCF	chr2:148695380-148695530	GM12867	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
46	CTCF	chr2:148695400-148695550	HepG2	liver:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
47	CTCF	chr2:148695480-148695630	HCM	heart:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
48	CTCF	chr2:148695420-148695570	GM12871	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
49	CTCF	chr2:148695362-148695610	HepG2	liver:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522
50	CTCF	chr2:148695372-148695609	GM13977	blood:	n/a	chr2:148695499-148695517 chr2:148695502-148695515 chr2:148695501-148695522

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:148687484-148687534	U87	brain:	n/a
2	chr2:148687484-148687534	H1-hESC	embryonic stem cell:	embryo
3	chr2:148687484-148687534	GM12878	blood:	n/a
4	chr2:148687484-148687534	HCT-116	colon:	n/a
5	chr2:148687484-148687534	GM12891	blood:	n/a
6	chr2:148687484-148687534	HNPCEpiC	eye:	n/a
7	chr2:148687484-148687534	PANC-1	pancreas:	n/a
8	chr2:148687484-148687534	HCPEpiC	choroid plexus:	n/a
9	chr2:148687484-148687534	BJ	skin:	n/a
10	chr2:148687484-148687534	MCF10A-Er-Src	breast:	n/a
11	chr2:148687484-148687534	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:148687484-148687534	HRPEpiC	eye:	n/a
13	chr2:148687484-148687534	NT2-D1	testis:	n/a
14	chr2:148687484-148687534	IMR90	lung:	fetal
15	chr2:148687484-148687534	HMEC	breast:	n/a
16	chr2:148687484-148687534	Hela-S3	cervix:	n/a
17	chr2:148687484-148687534	HEEpiC	esophagus:	n/a
18	chr2:148687484-148687534	GM06990	blood:	n/a
19	chr2:148687484-148687534	MCF-7	breast:	n/a
20	chr2:148687484-148687534	CMK	blood:	n/a
21	chr2:148687484-148687534	GM19239	blood:	n/a
22	chr2:148687484-148687534	HEK293	kidney:	embryo
23	chr2:148687484-148687534	LNCaP	prostate:	n/a
24	chr2:148687484-148687534	HCM	heart:	n/a
25	chr2:148687484-148687534	HepG2	liver:	n/a
26	chr2:148687484-148687534	NHBE	bronchial:	n/a
27	chr2:148687484-148687534	HRE	kidney:	n/a
28	chr2:148687484-148687534	SAEC	small airway:	n/a
29	chr2:148687484-148687534	AG04450	lung:	fetal
30	chr2:148687484-148687534	GM12892	blood:	n/a
31	chr2:148687484-148687534	A549	lung:	n/a
32	chr2:148687484-148687534	SK-N-SH	brain:	n/a
33	chr2:148687484-148687534	HAEpiC	amniotic membrane:	n/a
34	chr2:148687484-148687534	SK-N-SH_RA	brain:	n/a
35	chr2:148687484-148687534	HL-60	blood:	n/a
36	chr2:148687484-148687534	AG04449	skin:	fetal
37	chr2:148687484-148687534	HUVEC	blood vessel:	n/a
38	chr2:148687484-148687534	T-47D	breast:	n/a
39	chr2:148687484-148687534	AG10803	skin:	n/a
40	chr2:148687484-148687534	SK-N-MC	brain:	n/a
41	chr2:148687484-148687534	ProgFib	skin:	n/a
42	chr2:148687484-148687534	PFSK-1	brain:	n/a
43	chr2:148687484-148687534	K562	blood:	n/a
44	chr2:148687484-148687534	HCF	heart:	n/a
45	chr2:148687484-148687534	NHDF-neo	bronchial:	n/a
46	chr2:148687484-148687534	Hepatocyte	liver:	n/a
47	chr2:148687484-148687534	AG09309	skin:	n/a
48	chr2:148687484-148687534	ovcar-3	ovarian:	n/a
49	chr2:148687484-148687534	HRCEpiC	kidney:	n/a
50	chr2:148687484-148687534	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:148678040..148681031-chr2:148684341..148686999,2	MCF-7	breast:
2	chr2:148674607..148677009-chr2:148679440..148681399,2	K562	blood:
3	chr2:148679983..148681513-chr2:148684810..148687747,2	K562	blood:
4	chr2:148686945..148688969-chr2:148693419..148695079,2	MCF-7	breast:
5	chr2:148686777..148688417-chr2:148690685..148692251,2	MCF-7	breast:
6	chr2:148679983..148681513-chr2:148684810..148687747,2	K562	blood:
7	chr2:148674045..148677009-chr2:148679440..148682573,3	K562	blood:
8	chr2:148704147..148707130-chr2:149248171..149249711,2	K562	blood:
9	chr2:148686777..148688417-chr2:148690685..148692251,2	MCF-7	breast:
10	chr2:148686945..148688969-chr2:148693419..148695079,2	MCF-7	breast:
11	chr2:148679481..148681984-chr2:148684810..148687787,3	K562	blood:
12	chr2:148685824..148687356-chr2:149266124..149268743,2	K562	blood:
13	chr2:148678040..148681031-chr2:148684341..148686999,2	MCF-7	breast:
14	chr2:148679481..148681984-chr2:148684810..148687787,3	K562	blood:
15	chr2:148703238..148705482-chr2:148714226..148716736,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMADHC-12	chr2:148695546-148695782	NONHSAT074867
2	lnc-MMADHC-12	chr2:148695715-148695749	NONHSAT074866
3	lnc-MMADHC-12	chr2:148693882-148694584	NONHSAT074866
4	lnc-MMADHC-12	chr2:148695867-148696219	NONHSAT074867

No.	miRNA target gene	miRNA name	Chromosome Location
1	ACVR2A	hsa-miR-16-5p	chr2:148685345-148685351
2	ACVR2A	hsa-miR-192-5p	chr2:148686444-148686467
3	ACVR2A	hsa-miR-16-5p	chr2:148685592-148685615
4	ACVR2A	hsa-miR-186-5p	chr2:148687104-148687125
5	ACVR2A	hsa-miR-29b-3p	chr2:148687373-148687394
6	ACVR2A	hsa-miR-192-5p	chr2:148686627-148686647
7	ACVR2A	hsa-miR-192-5p	chr2:148686640-148686647
8	ACVR2A	hsa-miR-186-5p	chr2:148685890-148685918
9	ACVR2A	hsa-miR-16-5p	chr2:148685330-148685352

Variant related genes	Relation type
ACVR2A	TF binding region
ORC4	TF binding region
ENSG00000265049	TF binding region
ACVR2A	CpG island
ORC4	CpG island
ENSG00000265049	CpG island
ENSG00000115947	chromatin interactions

Extended variants
information (count: 1301 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1301 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143848637	chr2:148677125-148677126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs16828024	chr2:148677133-148677134	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs190890176	chr2:148677232-148677233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570561409	chr2:148677256-148677257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537903722	chr2:148677275-148677276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549874203	chr2:148677285-148677286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568647692	chr2:148677321-148677322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568216264	chr2:148677324-148677325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13388113	chr2:148677346-148677347	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs530414676	chr2:148677350-148677351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553965170	chr2:148677418-148677419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572234179	chr2:148677430-148677431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535458126	chr2:148677434-148677435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148640959	chr2:148677587-148677588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113105658	chr2:148677594-148677595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542110399	chr2:148677598-148677599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557738591	chr2:148677616-148677617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141226334	chr2:148677618-148677619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371979577	chr2:148677640-148677641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543507183	chr2:148677657-148677658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143208969	chr2:148677669-148677670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs16828025	chr2:148677681-148677682	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs367613736	chr2:148677713-148677714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140112453	chr2:148677754-148677755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560779394	chr2:148677755-148677756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375535810	chr2:148677760-148677761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372295463	chr2:148677770-148677771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376751852	chr2:148677791-148677792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369869413	chr2:148677817-148677818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149682383	chr2:148677836-148677837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111862877	chr2:148677842-148677843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201892566	chr2:148677862-148677863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200337943	chr2:148677898-148677899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183507950	chr2:148677926-148677927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145536659	chr2:148677949-148677950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564100734	chr2:148677957-148677958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113789278	chr2:148678041-148678042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549790254	chr2:148678073-148678074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187513657	chr2:148678082-148678083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190808518	chr2:148678091-148678092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547268352	chr2:148678105-148678106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557383437	chr2:148678106-148678107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183485264	chr2:148678127-148678128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572721799	chr2:148678144-148678145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188078118	chr2:148678160-148678161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533705507	chr2:148678186-148678187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192749672	chr2:148678200-148678201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111712953	chr2:148678207-148678208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573850104	chr2:148678217-148678218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555376996	chr2:148678227-148678228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	19904302	CNVD
Intellectual disability	19904302	CNVD
Microcephaly	19904302	CNVD
severe speech impairment	19904302	CNVD
Mental retardation	20152051	CNVD
2q23.1 microdeletion syndrome	18812405	CNVD
Mental retardation	19809484	CNVD
Autism	21981781	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD

Chromatin state (count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148637200-148752600	Weak transcription	Small Intestine	intestine
2	chr2:148646200-148684400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr2:148646600-148691000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr2:148647200-148719600	Weak transcription	Pancreas	Pancrea
5	chr2:148650200-148719600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:148651200-148691600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr2:148652800-148690000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr2:148652800-148693600	Weak transcription	Lung	lung
9	chr2:148653200-148692000	Weak transcription	Ovary	ovary
10	chr2:148653200-148719600	Weak transcription	Esophagus	oesophagus
11	chr2:148654000-148690000	Weak transcription	Primary T cells from cord blood	blood
12	chr2:148657800-148683000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr2:148658800-148741600	Weak transcription	Aorta	Aorta
14	chr2:148659600-148719800	Weak transcription	Gastric	stomach
15	chr2:148661600-148718200	Weak transcription	Fetal Intestine Small	intestine
16	chr2:148662000-148683800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr2:148663000-148692200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:148664600-148721200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:148664800-148693800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:148668600-148682400	Weak transcription	Psoas Muscle	Psoas
21	chr2:148668600-148683600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr2:148668600-148691800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr2:148668800-148683400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr2:148669200-148678000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr2:148670600-148690200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr2:148671200-148690200	Weak transcription	Placenta	Placenta
27	chr2:148671600-148690200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr2:148671800-148677800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:148671800-148679000	Weak transcription	NHDF-Ad	bronchial
30	chr2:148671800-148680200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:148671800-148683200	Weak transcription	Fetal Brain Male	brain
32	chr2:148671800-148683600	Weak transcription	Osteobl	bone
33	chr2:148671800-148687400	Weak transcription	NH-A	brain
34	chr2:148671800-148690200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr2:148671800-148691800	Weak transcription	NHLF	lung
36	chr2:148671800-148692000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:148671800-148698800	Weak transcription	NHEK	skin
38	chr2:148671800-148719600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:148672000-148678600	Weak transcription	Fetal Stomach	stomach
40	chr2:148672000-148683200	Weak transcription	HMEC	breast
41	chr2:148672000-148684600	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr2:148672000-148691400	Weak transcription	Brain Anterior Caudate	brain
43	chr2:148672000-148692000	Weak transcription	Brain Substantia Nigra	brain
44	chr2:148672000-148692800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr2:148672000-148693000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:148672200-148683200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:148672200-148683400	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr2:148672200-148683800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:148672200-148684000	Weak transcription	Fetal Brain Female	brain
50	chr2:148672200-148688400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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