Variant report

Variant	nsv548078
Chromosome Location	chr1:161941219-161980502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:227)
CpG islands
(count:610)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:161959048-161959325	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr1:161947826-161948196	K562	blood:	n/a	n/a
3	CBX3	chr1:161953758-161954091	K562	blood:	n/a	n/a
4	CEBPB	chr1:161960031-161960138	K562	blood:	n/a	chr1:161960083-161960094
5	CEBPB	chr1:161966371-161966373	A549	lung:	n/a	n/a
6	CEBPB	chr1:161959931-161960195	HepG2	liver:	n/a	chr1:161960083-161960094
7	CEBPB	chr1:161959986-161960196	A549	lung:	n/a	chr1:161960083-161960094
8	CEBPB	chr1:161959934-161960212	IMR90	lung:	n/a	chr1:161960083-161960094
9	CEBPB	chr1:161972975-161973418	IMR90	lung:	n/a	n/a
10	CTCF	chr1:161973100-161973250	AG10803	skin:	n/a	n/a
11	CTCF	chr1:161959052-161959206	K562	blood:	n/a	n/a
12	CTCF	chr1:161958980-161959235	K562	blood:	n/a	n/a
13	CTCF	chr1:161977400-161977550	HPF	lung:	n/a	n/a
14	CTCF	chr1:161951680-161951830	HMEC	breast:	n/a	n/a
15	CTCF	chr1:161947969-161948051	GM12892	blood:	n/a	n/a
16	CTCF	chr1:161977400-161977550	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr1:161977360-161977510	HepG2	liver:	n/a	n/a
18	CTCF	chr1:161972420-161972570	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr1:161972900-161973050	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr1:161959120-161959270	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr1:161980296-161980320	GM13976	blood:	n/a	n/a
22	CTCF	chr1:161955300-161955450	HepG2	liver:	n/a	chr1:161955363-161955376
23	CTCF	chr1:161973100-161973250	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr1:161963180-161963330	GM12866	blood:	n/a	n/a
25	CTCF	chr1:161973100-161973250	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr1:161959100-161959250	HFF	foreskin:	n/a	n/a
27	CTCF	chr1:161973600-161973750	HAc	cerebellar:	n/a	n/a
28	CTCF	chr1:161970800-161970827	GM13976	blood:	n/a	n/a
29	CTCF	chr1:161959040-161959190	GM12873	blood:	n/a	n/a
30	CTCF	chr1:161955340-161955490	WERI-Rb-1	eye:	n/a	chr1:161955472-161955480 chr1:161955363-161955376
31	CTCF	chr1:161959120-161959270	HEK293	kidney:	n/a	n/a
32	CTCF	chr1:161972840-161972990	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr1:161973100-161973250	HMF	breast:	n/a	n/a
34	CTCF	chr1:161973440-161973590	AG10803	skin:	n/a	n/a
35	CTCF	chr1:161951740-161951890	HMEC	breast:	n/a	n/a
36	CTCF	chr1:161947960-161948110	GM12866	blood:	n/a	n/a
37	CTCF	chr1:161973140-161973290	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr1:161965520-161965670	GM12866	blood:	n/a	n/a
39	CTCF	chr1:161977380-161977530	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr1:161959086-161959160	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:161951740-161951824	K562	blood:	n/a	n/a
42	CTCF	chr1:161973220-161973370	AG10803	skin:	n/a	n/a
43	CTCF	chr1:161959060-161959210	HMF	breast:	n/a	n/a
44	CTCF	chr1:161959060-161959210	HepG2	liver:	n/a	n/a
45	CTCF	chr1:161959000-161959150	AG09309	skin:	n/a	n/a
46	CTCF	chr1:161959020-161959170	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr1:161968600-161968750	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr1:161958700-161958850	RPTEC	kidney:	n/a	n/a
49	CTCF	chr1:161959078-161959148	NHEK	skin:	n/a	n/a
50	CTCF	chr1:161959020-161959170	AG10803	skin:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161953593-161953643	AG10803	skin:	n/a
2	chr1:161950791-161950841	HAEpiC	amniotic membrane:	n/a
3	chr1:161948059-161948109	MCF10A-Er-Src	breast:	n/a
4	chr1:161973909-161973959	AG04450	lung:	fetal
5	chr1:161965174-161965224	HIPEpiC	eye:	n/a
6	chr1:161953806-161953856	AG04450	lung:	fetal
7	chr1:161953982-161954032	NH-A	brain:	n/a
8	chr1:161953806-161953856	HMEC	breast:	n/a
9	chr1:161950791-161950841	SK-N-MC	brain:	n/a
10	chr1:161950791-161950841	HepG2	liver:	n/a
11	chr1:161948059-161948109	NB4	blood:	n/a
12	chr1:161973909-161973959	LNCaP	prostate:	n/a
13	chr1:161953593-161953643	Jurkat	blood:	n/a
14	chr1:161948059-161948109	HCPEpiC	choroid plexus:	n/a
15	chr1:161950791-161950841	AoSMC	blood vessel:	n/a
16	chr1:161948059-161948109	HRPEpiC	eye:	n/a
17	chr1:161953806-161953856	GM12878	blood:	n/a
18	chr1:161953806-161953856	SAEC	small airway:	n/a
19	chr1:161950791-161950841	BE2_C	brain:	n/a
20	chr1:161950791-161950841	HRCEpiC	kidney:	n/a
21	chr1:161953756-161953806	Jurkat	blood:	n/a
22	chr1:161953982-161954032	GM19239	blood:	n/a
23	chr1:161953982-161954032	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:161953982-161954032	U87	brain:	n/a
25	chr1:161973909-161973959	HUVEC	blood vessel:	n/a
26	chr1:161953756-161953806	PrEC	prostate:	n/a
27	chr1:161953982-161954032	HCPEpiC	choroid plexus:	n/a
28	chr1:161953593-161953643	HAEpiC	amniotic membrane:	n/a
29	chr1:161954657-161954707	HEEpiC	esophagus:	n/a
30	chr1:161956573-161956623	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:161954657-161954707	NB4	blood:	n/a
32	chr1:161956573-161956623	NHDF-neo	bronchial:	n/a
33	chr1:161953982-161954032	NHDF-neo	bronchial:	n/a
34	chr1:161956573-161956623	H1-hESC	embryonic stem cell:	embryo
35	chr1:161953982-161954032	GM12891	blood:	n/a
36	chr1:161953806-161953856	PFSK-1	brain:	n/a
37	chr1:161973909-161973959	PANC-1	pancreas:	n/a
38	chr1:161954657-161954707	MCF10A-Er-Src	breast:	n/a
39	chr1:161965174-161965224	HCM	heart:	n/a
40	chr1:161965174-161965224	ovcar-3	ovarian:	n/a
41	chr1:161954657-161954707	ovcar-3	ovarian:	n/a
42	chr1:161948059-161948109	PANC-1	pancreas:	n/a
43	chr1:161965174-161965224	T-47D	breast:	n/a
44	chr1:161953756-161953806	PANC-1	pancreas:	n/a
45	chr1:161965174-161965224	HAEpiC	amniotic membrane:	n/a
46	chr1:161950791-161950841	LNCaP	prostate:	n/a
47	chr1:161950791-161950841	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:161953982-161954032	GM12892	blood:	n/a
49	chr1:161965174-161965224	SK-N-MC	brain:	n/a
50	chr1:161965174-161965224	MCF10A-Er-Src	breast:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:161972369..161974094-chr1:161974684..161976262,2	K562	blood:
2	chr1:161951565..161953317-chr1:161954989..161957643,2	K562	blood:
3	chr1:161962621..161964963-chr1:161966345..161967912,3	K562	blood:
4	chr1:161942432..161944304-chr1:161946800..161948604,2	K562	blood:
5	chr1:161961819..161964553-chr1:161966173..161967912,3	K562	blood:
6	chr1:161962621..161964963-chr1:161966345..161967912,3	K562	blood:
7	chr1:161965187..161967166-chr1:161971567..161974146,3	MCF-7	breast:
8	chr1:161966226..161968937-chr1:161972125..161974541,2	K562	blood:
9	chr1:161942432..161944304-chr1:161946800..161948604,2	K562	blood:
10	chr1:161919306..161921320-chr1:161939267..161942009,2	MCF-7	breast:
11	chr1:161934236..161935963-chr1:161941588..161943984,2	K562	blood:
12	chr1:161967385..161969148-chr1:161971026..161972952,2	MCF-7	breast:
13	chr1:161951407..161954246-chr1:161954300..161956489,3	K562	blood:
14	chr1:161961819..161964553-chr1:161966173..161967912,3	K562	blood:
15	chr1:161978649..161980514-chr1:161983821..161985651,2	MCF-7	breast:
16	chr1:161946741..161950506-chr1:161953069..161956578,4	K562	blood:
17	chr1:161976766..161979689-chr1:161981047..161983365,4	K562	blood:
18	chr1:161972369..161974094-chr1:161974684..161976262,2	K562	blood:
19	chr1:161958606..161961453-chr1:161973614..161975628,2	MCF-7	breast:
20	chr1:161958606..161961453-chr1:161973614..161975628,2	MCF-7	breast:
21	chr1:161934463..161936874-chr1:161938543..161943088,4	K562	blood:
22	chr1:161965187..161967166-chr1:161971567..161974146,3	MCF-7	breast:
23	chr1:161951407..161954246-chr1:161954300..161956489,3	K562	blood:
24	chr1:161966226..161968937-chr1:161972125..161974541,2	K562	blood:
25	chr1:161967385..161969148-chr1:161971026..161972952,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	OLFML2B	hsa-miR-30b-5p	chr1:161953366-161953387

Variant related genes	Relation type
OLFML2B	TF binding region
OLFML2B	CpG island
ENSG00000162745	chromatin interactions

Extended variants
information (count: 1627 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1627 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2490431	chr1:161941219-161941220	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192044859	chr1:161941243-161941244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537237256	chr1:161941251-161941252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561534573	chr1:161941257-161941258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527513467	chr1:161941263-161941264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557004651	chr1:161941304-161941305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2490430	chr1:161941306-161941307	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs564430390	chr1:161941317-161941318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535885266	chr1:161941333-161941334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532759909	chr1:161941334-161941335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549762650	chr1:161941335-161941336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569724874	chr1:161941345-161941346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28505989	chr1:161941382-161941383	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs549141794	chr1:161941386-161941387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74560530	chr1:161941388-161941389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535241684	chr1:161941391-161941392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28628087	chr1:161941471-161941472	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs11582286	chr1:161941472-161941473	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs560501265	chr1:161941483-161941484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571917306	chr1:161941494-161941495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140912621	chr1:161941503-161941504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184859071	chr1:161941514-161941515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556929830	chr1:161941550-161941551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112790644	chr1:161941582-161941583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189342227	chr1:161941583-161941584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542694655	chr1:161941584-161941585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553076384	chr1:161941589-161941590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369195332	chr1:161941608-161941609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200156046	chr1:161941618-161941619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111798971	chr1:161941621-161941622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72709919	chr1:161941634-161941635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541380253	chr1:161941636-161941637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74691455	chr1:161941657-161941658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11582699	chr1:161941710-161941711	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs61809501	chr1:161941819-161941820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs577875444	chr1:161941831-161941832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111425247	chr1:161941870-161941871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192346551	chr1:161941872-161941873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374511174	chr1:161941907-161941908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563266574	chr1:161941912-161941913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138588324	chr1:161941918-161941919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549078854	chr1:161941945-161941946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149252166	chr1:161941980-161941981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530406149	chr1:161942032-161942033	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs560050064	chr1:161942107-161942108	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs184420719	chr1:161942142-161942143	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs79103253	chr1:161942143-161942144	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs143436643	chr1:161942175-161942176	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs148064123	chr1:161942196-161942197	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs567299783	chr1:161942198-161942199	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Cancer	17440070	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161902800-161943400	Weak transcription	Esophagus	oesophagus
2	chr1:161904800-161956600	Weak transcription	Fetal Brain Male	brain
3	chr1:161912600-161941600	Weak transcription	Fetal Kidney	kidney
4	chr1:161926200-161942200	Weak transcription	Right Ventricle	heart
5	chr1:161927000-161944000	Weak transcription	Colonic Mucosa	Colon
6	chr1:161928400-161941800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:161929000-161943800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:161929200-161944000	Weak transcription	Ovary	ovary
9	chr1:161931000-161943200	Weak transcription	Placenta	Placenta
10	chr1:161931200-161942400	Weak transcription	Spleen	Spleen
11	chr1:161931200-161943400	Weak transcription	Psoas Muscle	Psoas
12	chr1:161931400-161943400	Weak transcription	K562	blood
13	chr1:161931800-161942800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr1:161932400-161942200	Weak transcription	Colon Smooth Muscle	Colon
15	chr1:161932400-161955400	Weak transcription	Brain Substantia Nigra	brain
16	chr1:161932600-161943200	Weak transcription	Adipose Nuclei	Adipose
17	chr1:161932600-161943200	Weak transcription	Right Atrium	heart
18	chr1:161932600-161943800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr1:161932800-161943200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:161932800-161944000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:161933400-161941800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:161933600-161942000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:161933600-161953400	Weak transcription	HSMMtube	muscle
24	chr1:161937000-161942800	Weak transcription	Left Ventricle	heart
25	chr1:161937400-161941800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr1:161937400-161944000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:161937600-161941800	Weak transcription	Fetal Stomach	stomach
28	chr1:161937600-161954800	Weak transcription	Primary hematopoietic stem cells	blood
29	chr1:161938000-161942000	Weak transcription	Primary T cells from cord blood	blood
30	chr1:161938000-161942800	Weak transcription	Gastric	stomach
31	chr1:161938000-161944000	Weak transcription	Liver	Liver
32	chr1:161938000-161944000	Weak transcription	Pancreas	Pancrea
33	chr1:161939000-161943000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:161939200-161942000	Enhancers	Fetal Muscle Trunk	muscle
35	chr1:161939200-161946000	Enhancers	Fetal Muscle Leg	muscle
36	chr1:161939200-161956600	Weak transcription	Fetal Intestine Small	intestine
37	chr1:161940400-161941400	Enhancers	Brain Anterior Caudate	brain
38	chr1:161940400-161942400	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr1:161940600-161942200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr1:161940600-161944000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr1:161940800-161942000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:161940800-161942000	Weak transcription	Lung	lung
43	chr1:161940800-161944000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:161940800-161944000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:161940800-161952200	Weak transcription	Aorta	Aorta
46	chr1:161941200-161942600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr1:161941800-161942000	Enhancers	Fetal Kidney	kidney
48	chr1:161941800-161942000	Enhancers	Stomach Smooth Muscle	stomach
49	chr1:161941800-161942200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:161941800-161942600	Enhancers	Fetal Stomach	stomach

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