Variant report

Variant	nsv1001558
Chromosome Location	chr2:182590009-182732738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1883)
CpG islands
(count:305)
Chromatin interactive
region (count:171)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1883 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:182649211-182649514	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:182602874-182603074	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:182668865-182669104	K562	blood:	n/a	n/a
4	ARID3A	chr2:182607430-182608089	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:182668838-182669072	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:182655466-182656421	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:182656053-182656358	K562	blood:	n/a	n/a
8	ARID3A	chr2:182675458-182675957	K562	blood:	n/a	n/a
9	ARID3A	chr2:182652494-182652723	K562	blood:	n/a	n/a
10	ARID3A	chr2:182670092-182670712	K562	blood:	n/a	n/a
11	ARID3A	chr2:182693301-182693302	K562	blood:	n/a	n/a
12	ARID3A	chr2:182675519-182676053	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:182607616-182608095	K562	blood:	n/a	n/a
14	ATF1	chr2:182678804-182679193	K562	blood:	n/a	n/a
15	ATF1	chr2:182648713-182648938	K562	blood:	n/a	n/a
16	ATF1	chr2:182639384-182639518	K562	blood:	n/a	n/a
17	ATF1	chr2:182628838-182629182	K562	blood:	n/a	n/a
18	ATF1	chr2:182607606-182608194	K562	blood:	n/a	n/a
19	ATF1	chr2:182655392-182655728	K562	blood:	n/a	n/a
20	ATF1	chr2:182656035-182656390	K562	blood:	n/a	n/a
21	ATF1	chr2:182686904-182687016	K562	blood:	n/a	n/a
22	ATF1	chr2:182668816-182669123	K562	blood:	n/a	n/a
23	ATF1	chr2:182617145-182617291	K562	blood:	n/a	n/a
24	ATF1	chr2:182670096-182670827	K562	blood:	n/a	n/a
25	ATF1	chr2:182675451-182676042	K562	blood:	n/a	n/a
26	ATF1	chr2:182652211-182652809	K562	blood:	n/a	n/a
27	ATF1	chr2:182730242-182730355	K562	blood:	n/a	n/a
28	ATF1	chr2:182688073-182688124	K562	blood:	n/a	n/a
29	ATF1	chr2:182643948-182644563	K562	blood:	n/a	n/a
30	ATF1	chr2:182658786-182658888	K562	blood:	n/a	n/a
31	ATF2	chr2:182655883-182656380	GM12878	blood:	n/a	n/a
32	ATF2	chr2:182655973-182656374	GM12878	blood:	n/a	n/a
33	ATF3	chr2:182675409-182675865	A549	lung:	n/a	n/a
34	ATF3	chr2:182675448-182675801	K562	blood:	n/a	n/a
35	ATF3	chr2:182655918-182656403	A549	lung:	n/a	n/a
36	BATF	chr2:182639512-182639843	GM12878	blood:	n/a	n/a
37	BATF	chr2:182655968-182656406	GM12878	blood:	n/a	chr2:182656182-182656193
38	BCL11A	chr2:182656044-182656371	GM12878	blood:	n/a	chr2:182656082-182656091
39	BCL3	chr2:182655886-182656514	A549	lung:	n/a	chr2:182656082-182656091
40	BCL3	chr2:182655923-182656383	GM12878	blood:	n/a	chr2:182656082-182656091
41	BCL3	chr2:182675361-182675902	A549	lung:	n/a	chr2:182675697-182675706 chr2:182675696-182675705
42	BHLHE40	chr2:182655596-182656298	HepG2	liver:	n/a	n/a
43	BHLHE40	chr2:182727946-182728033	K562	blood:	n/a	n/a
44	BHLHE40	chr2:182628836-182629173	K562	blood:	n/a	n/a
45	BHLHE40	chr2:182675494-182676053	K562	blood:	n/a	n/a
46	BHLHE40	chr2:182654874-182655068	K562	blood:	n/a	n/a
47	BHLHE40	chr2:182670442-182670922	K562	blood:	n/a	n/a
48	BHLHE40	chr2:182678748-182679241	K562	blood:	n/a	n/a
49	BHLHE40	chr2:182644041-182644184	K562	blood:	n/a	n/a
50	BHLHE40	chr2:182668869-182669150	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:182676650-182676700	HCPEpiC	choroid plexus:	n/a
2	chr2:182656091-182656141	HIPEpiC	eye:	n/a
3	chr2:182656091-182656141	AG04449	skin:	fetal
4	chr2:182650931-182650981	CMK	blood:	n/a
5	chr2:182713409-182713459	Hela-S3	cervix:	n/a
6	chr2:182656091-182656141	HNPCEpiC	eye:	n/a
7	chr2:182644898-182644948	Hela-S3	cervix:	n/a
8	chr2:182676650-182676700	GM19239	blood:	n/a
9	chr2:182713409-182713459	MCF10A-Er-Src	breast:	n/a
10	chr2:182650931-182650981	HEEpiC	esophagus:	n/a
11	chr2:182713409-182713459	ProgFib	skin:	n/a
12	chr2:182656091-182656141	SK-N-MC	brain:	n/a
13	chr2:182644898-182644948	SK-N-MC	brain:	n/a
14	chr2:182650931-182650981	H1-hESC	embryonic stem cell:	embryo
15	chr2:182644898-182644948	HNPCEpiC	eye:	n/a
16	chr2:182650931-182650981	HEK293	kidney:	embryo
17	chr2:182650931-182650981	HRE	kidney:	n/a
18	chr2:182713409-182713459	GM12892	blood:	n/a
19	chr2:182676650-182676700	U87	brain:	n/a
20	chr2:182656091-182656141	HCT-116	colon:	n/a
21	chr2:182644898-182644948	SK-N-SH_RA	brain:	n/a
22	chr2:182650931-182650981	AG04450	lung:	fetal
23	chr2:182656091-182656141	HepG2	liver:	n/a
24	chr2:182676650-182676700	SK-N-SH	brain:	n/a
25	chr2:182650931-182650981	AoSMC	blood vessel:	n/a
26	chr2:182650931-182650981	HNPCEpiC	eye:	n/a
27	chr2:182656091-182656141	AoSMC	blood vessel:	n/a
28	chr2:182650931-182650981	NH-A	brain:	n/a
29	chr2:182676650-182676700	Jurkat	blood:	n/a
30	chr2:182713409-182713459	HEEpiC	esophagus:	n/a
31	chr2:182650931-182650981	AG04449	skin:	fetal
32	chr2:182676650-182676700	SAEC	small airway:	n/a
33	chr2:182676650-182676700	HRCEpiC	kidney:	n/a
34	chr2:182644898-182644948	HEK293	kidney:	embryo
35	chr2:182713409-182713459	HCM	heart:	n/a
36	chr2:182656091-182656141	NB4	blood:	n/a
37	chr2:182656091-182656141	LNCaP	prostate:	n/a
38	chr2:182644898-182644948	HMEC	breast:	n/a
39	chr2:182644898-182644948	PFSK-1	brain:	n/a
40	chr2:182713409-182713459	SK-N-SH	brain:	n/a
41	chr2:182650931-182650981	SK-N-SH_RA	brain:	n/a
42	chr2:182676650-182676700	GM12892	blood:	n/a
43	chr2:182713409-182713459	NB4	blood:	n/a
44	chr2:182713409-182713459	GM12891	blood:	n/a
45	chr2:182656091-182656141	AG09319	gingival:	n/a
46	chr2:182656091-182656141	H1-hESC	embryonic stem cell:	embryo
47	chr2:182713409-182713459	ovcar-3	ovarian:	n/a
48	chr2:182656091-182656141	HMEC	breast:	n/a
49	chr2:182644898-182644948	GM12891	blood:	n/a
50	chr2:182676650-182676700	MCF10A-Er-Src	breast:	n/a

(count:171 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr2:182590897..182592502-chr2:182592723..182595425,2	MCF-7	breast:
2	chr2:182627954..182630438-chr2:182634967..182637515,2	K562	blood:
3	chr2:182649909..182651915-chr2:182653150..182656385,3	MCF-7	breast:
4	chr2:182684155..182686496-chr2:182687932..182689511,2	MCF-7	breast:
5	chr2:182640621..182643492-chr2:182733143..182735326,2	K562	blood:
6	chr2:182615557..182618410-chr2:182759397..182761263,2	MCF-7	breast:
7	chr2:182646086..182659083-chr2:182754079..182762654,36	MCF-7	breast:
8	chr2:182687016..182689280-chr2:182756224..182758607,2	MCF-7	breast:
9	chr2:182637643..182640339-chr2:182643105..182646087,2	K562	blood:
10	chr2:182657640..182659735-chr2:182660701..182663303,2	K562	blood:
11	chr2:182677255..182678837-chr2:182768538..182770841,2	K562	blood:
12	chr2:181845007..181846793-chr2:182669919..182671758,2	K562	blood:
13	chr2:182607754..182610129-chr2:182643421..182645171,2	MCF-7	breast:
14	chr2:182607754..182610129-chr2:182643421..182645171,2	MCF-7	breast:
15	chr2:182617147..182619189-chr2:182727764..182729918,2	MCF-7	breast:
16	chr2:182702285..182703968-chr2:182722653..182724791,2	K562	blood:
17	chr2:182618952..182622731-chr2:182755843..182758799,3	MCF-7	breast:
18	chr2:182622812..182624319-chr2:182629170..182631069,2	K562	blood:
19	chr2:182683095..182685729-chr2:182754698..182757581,2	K562	blood:
20	chr2:182649357..182651111-chr2:182651745..182654044,2	MCF-7	breast:
21	chr2:182681410..182683561-chr2:182690955..182693010,2	MCF-7	breast:
22	chr2:182655375..182656915-chr2:182750868..182752797,2	MCF-7	breast:
23	chr2:182713642..182716430-chr2:182718168..182720643,2	K562	blood:
24	chr2:182685284..182687547-chr2:182730899..182732753,2	MCF-7	breast:
25	chr2:182716953..182719682-chr2:182723057..182725244,2	K562	blood:
26	chr2:182658638..182660215-chr2:182682406..182684395,2	MCF-7	breast:
27	chr2:182676782..182679506-chr2:182680066..182682576,2	K562	blood:
28	chr2:182708528..182710954-chr2:182712417..182715182,2	K562	blood:
29	chr2:182584946..182586497-chr2:182588246..182590571,2	K562	blood:
30	chr2:182722925..182725534-chr2:182728109..182731664,3	K562	blood:
31	chr2:182618261..182620386-chr2:182720885..182723855,2	MCF-7	breast:
32	chr2:182675680..182677290-chr2:182677371..182678893,2	MCF-7	breast:
33	chr2:182727750..182729370-chr2:182753560..182755515,2	MCF-7	breast:
34	chr2:182674418..182676903-chr2:182677977..182680829,2	K562	blood:
35	chr2:182641582..182643700-chr2:182645363..182647512,2	MCF-7	breast:
36	chr2:182607223..182607959-chr2:182768811..182769453,2	K562	blood:
37	chr2:182622819..182625911-chr2:182627931..182631069,3	K562	blood:
38	chr2:182618753..182621318-chr2:182622765..182624957,3	MCF-7	breast:
39	chr2:182641582..182643700-chr2:182645363..182647512,2	MCF-7	breast:
40	chr2:182621687..182624059-chr2:182624829..182627289,2	K562	blood:
41	chr2:182633341..182635444-chr2:182677151..182679786,2	MCF-7	breast:
42	chr2:182607324..182607987-chr2:182942180..182942981,3	MCF-7	breast:
43	chr2:182607273..182609890-chr2:182817856..182820250,2	MCF-7	breast:
44	chr2:182676782..182679506-chr2:182680066..182682576,2	K562	blood:
45	chr2:182607104..182609304-chr2:182780495..182782555,2	K562	blood:
46	chr2:182671198..182673524-chr2:182676933..182678703,2	K562	blood:
47	chr2:182695883..182698601-chr2:182754616..182756434,2	MCF-7	breast:
48	chr14:60987563..60988192-chr2:182606181..182606727,2	MCF-7	breast:
49	chr2:182649909..182651915-chr2:182653150..182656385,3	MCF-7	breast:
50	chr2:182605218..182608264-chr2:182780802..182783897,3	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6ATAC19P	TF binding region
RNU6ATAC19P	CpG island
ENSG00000170035	chromatin interactions
ENSG00000150722	chromatin interactions
ENSG00000138434	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000265129	chromatin interactions

Extended variants
information (count: 4610 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4610 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186448211	chr2:182591458-182591459	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs532839600	chr2:182591490-182591491	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374417876	chr2:182591506-182591507	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs552849542	chr2:182591509-182591510	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189683577	chr2:182591609-182591610	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs77676056	chr2:182591612-182591613	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs558729047	chr2:182591617-182591618	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs35292193	chr2:182591670-182591671	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs139509961	chr2:182591707-182591708	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs10540257	chr2:182591708-182591709	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs146933787	chr2:182591712-182591713	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs543162528	chr2:182591722-182591723	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs78367735	chr2:182591733-182591734	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs76386554	chr2:182591835-182591836	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs75985675	chr2:182591906-182591907	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553712270	chr2:182591934-182591935	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs533667076	chr2:182591966-182591967	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs78789969	chr2:182591991-182591992	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148650153	chr2:182591992-182591993	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs539323584	chr2:182591997-182591998	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs182259137	chr2:182592051-182592052	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs118155565	chr2:182592116-182592117	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186906845	chr2:182592151-182592152	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561783065	chr2:182592163-182592164	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs76065128	chr2:182592168-182592169	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs540765299	chr2:182592183-182592184	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs542035598	chr2:182592190-182592191	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs142114609	chr2:182592212-182592213	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532553939	chr2:182592243-182592244	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs75059721	chr2:182592383-182592384	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113396904	chr2:182592405-182592406	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs80098192	chr2:182592407-182592408	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531957650	chr2:182592408-182592409	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs62192065	chr2:182592456-182592457	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs71405464	chr2:182592461-182592462	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs548739823	chr2:182592489-182592490	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568347173	chr2:182592529-182592530	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528874284	chr2:182592534-182592535	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs527349266	chr2:182592594-182592595	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs528073781	chr2:182592611-182592612	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs200064065	chr2:182592612-182592613	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547916721	chr2:182592620-182592621	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547108417	chr2:182592639-182592640	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs567946111	chr2:182592711-182592712	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs536948692	chr2:182592754-182592755	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs570069652	chr2:182592755-182592756	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs2696356	chr2:182592756-182592757	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs145280176	chr2:182592781-182592782	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs192662246	chr2:182592805-182592806	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs76953095	chr2:182592830-182592831	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD

Chromatin state (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182596600-182596800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
2	chr2:182602800-182603200	Enhancers	Fetal Intestine Small	intestine
3	chr2:182603000-182603600	Enhancers	Duodenum Mucosa	Duodenum
4	chr2:182603200-182607200	Weak transcription	Fetal Intestine Small	intestine
5	chr2:182603600-182607400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr2:182605600-182606400	Enhancers	Sigmoid Colon	Sigmoid Colon
7	chr2:182605800-182606000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:182605800-182606400	Weak transcription	HSMMtube	muscle
9	chr2:182606000-182608400	Enhancers	HSMM	muscle
10	chr2:182606200-182606400	Enhancers	NH-A	brain
11	chr2:182606200-182606600	Enhancers	NHDF-Ad	bronchial
12	chr2:182606200-182607600	Enhancers	Fetal Heart	heart
13	chr2:182606200-182608600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr2:182606200-182608600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:182606200-182608600	Enhancers	Osteobl	bone
16	chr2:182606200-182608800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:182606200-182609000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr2:182606200-182609200	Enhancers	Hela-S3	cervix
19	chr2:182606400-182606600	Enhancers	HSMMtube	muscle
20	chr2:182606400-182607400	Weak transcription	NH-A	brain
21	chr2:182606600-182608000	Weak transcription	HSMMtube	muscle
22	chr2:182606600-182608600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:182607000-182607200	Enhancers	Liver	Liver
24	chr2:182607200-182607400	Enhancers	Fetal Intestine Small	intestine
25	chr2:182607200-182607800	Flanking Active TSS	Liver	Liver
26	chr2:182607200-182608800	Enhancers	NHLF	lung
27	chr2:182607400-182607800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr2:182607400-182608000	Weak transcription	Fetal Intestine Small	intestine
29	chr2:182607400-182608000	Enhancers	Fetal Kidney	kidney
30	chr2:182607400-182608200	Enhancers	Brain Anterior Caudate	brain
31	chr2:182607400-182608200	Enhancers	Brain Hippocampus Middle	brain
32	chr2:182607400-182608200	Enhancers	Duodenum Mucosa	Duodenum
33	chr2:182607400-182608200	Enhancers	Dnd41	blood
34	chr2:182607400-182608600	Enhancers	A549	lung
35	chr2:182607400-182608800	Enhancers	Stomach Mucosa	stomach
36	chr2:182607400-182608800	Enhancers	HepG2	liver
37	chr2:182607400-182608800	Enhancers	NH-A	brain
38	chr2:182607400-182609000	Enhancers	HMEC	breast
39	chr2:182607400-182609200	Enhancers	NHEK	skin
40	chr2:182607600-182608000	Active TSS	Brain Substantia Nigra	brain
41	chr2:182607600-182608000	Enhancers	Rectal Smooth Muscle	rectum
42	chr2:182607600-182608800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:182607800-182608200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr2:182607800-182608400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:182607800-182609200	Enhancers	Liver	Liver
46	chr2:182607800-182609200	Enhancers	HUVEC	blood vessel
47	chr2:182608000-182608200	Enhancers	Fetal Intestine Small	intestine
48	chr2:182608000-182608200	Enhancers	HSMMtube	muscle
49	chr2:182608000-182608400	Enhancers	Brain Angular Gyrus	brain
50	chr2:182608000-182608400	Enhancers	Brain Substantia Nigra	brain

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