Variant report

Variant	nsv1012275
Chromosome Location	chr2:149031668-149316793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1370)
CpG islands
(count:916)
Chromatin interactive
region (count:63)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:149168311-149168943	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:149266794-149267615	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:149303207-149303376	K562	blood:	n/a	n/a
4	ARID3A	chr2:149300675-149300926	K562	blood:	n/a	n/a
5	ATF1	chr2:149255682-149255825	K562	blood:	n/a	n/a
6	ATF1	chr2:149259144-149259478	K562	blood:	n/a	n/a
7	ATF1	chr2:149300674-149300961	K562	blood:	n/a	n/a
8	ATF1	chr2:149245658-149245668	K562	blood:	n/a	n/a
9	BACH1	chr2:149267136-149267373	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:149216849-149217127	GM12878	blood:	n/a	n/a
11	BATF	chr2:149266999-149267403	GM12878	blood:	n/a	n/a
12	BATF	chr2:149251826-149252044	GM12878	blood:	n/a	n/a
13	BCLAF1	chr2:149266979-149267394	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:149267085-149267339	K562	blood:	n/a	n/a
15	BHLHE40	chr2:149259096-149259591	K562	blood:	n/a	n/a
16	BHLHE40	chr2:149300051-149300930	K562	blood:	n/a	n/a
17	BHLHE40	chr2:149310469-149310500	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:149292421-149292571	K562	blood:	n/a	n/a
19	BHLHE40	chr2:149259165-149259472	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:149316237-149316437	HepG2	liver:	n/a	n/a
21	BHLHE40	chr2:149266777-149267353	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:149266822-149267351	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr2:149263078-149263081	HepG2	liver:	n/a	n/a
24	BRCA1	chr2:149266946-149267334	HepG2	liver:	n/a	n/a
25	BRCA1	chr2:149274889-149274953	HepG2	liver:	n/a	n/a
26	CBX3	chr2:149300591-149300997	K562	blood:	n/a	n/a
27	CBX3	chr2:149266747-149267315	K562	blood:	n/a	n/a
28	CBX3	chr2:149303004-149303422	K562	blood:	n/a	n/a
29	CBX3	chr2:149315677-149315992	K562	blood:	n/a	n/a
30	CCNT2	chr2:149300464-149300972	K562	blood:	n/a	n/a
31	CCNT2	chr2:149266925-149267366	K562	blood:	n/a	n/a
32	CCNT2	chr2:149259186-149259452	K562	blood:	n/a	n/a
33	CEBPB	chr2:149292359-149292789	K562	blood:	n/a	n/a
34	CEBPB	chr2:149118796-149118907	H1-hESC	embryonic stem cell:	n/a	chr2:149118869-149118880
35	CEBPB	chr2:149276685-149276885	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:149266946-149267371	K562	blood:	n/a	n/a
37	CEBPB	chr2:149148788-149149317	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:149292462-149292695	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:149313496-149313838	H1-hESC	embryonic stem cell:	n/a	chr2:149313661-149313670 chr2:149313659-149313670
40	CEBPB	chr2:149266786-149267374	Hela-S3	cervix:	n/a	chr2:149266792-149266805
41	CEBPB	chr2:149292443-149292692	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:149220160-149220369	A549	lung:	n/a	n/a
43	CEBPB	chr2:149108389-149108611	A549	lung:	n/a	chr2:149108533-149108546 chr2:149108534-149108545 chr2:149108533-149108546 chr2:149108533-149108544 chr2:149108533-149108546
44	CEBPB	chr2:149266885-149267397	MCF-7	breast:	n/a	n/a
45	CEBPB	chr2:149271562-149271670	A549	lung:	n/a	n/a
46	CEBPB	chr2:149168405-149168934	HepG2	liver:	n/a	chr2:149168769-149168780
47	CEBPB	chr2:149036791-149037095	IMR90	lung:	n/a	chr2:149036949-149036960
48	CEBPB	chr2:149292392-149292749	MCF-7	breast:	n/a	n/a
49	CEBPB	chr2:149168464-149168895	HepG2	liver:	n/a	chr2:149168769-149168780
50	CEBPB	chr2:149167050-149167142	H1-hESC	embryonic stem cell:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:149215642-149215692	SK-N-SH_RA	brain:	n/a
2	chr2:149215642-149215692	SK-N-SH_RA	brain:	n/a
3	chr2:149063092-149063142	LNCaP	prostate:	n/a
4	chr2:149312414-149312464	PFSK-1	brain:	n/a
5	chr2:149215884-149215934	PANC-1	pancreas:	n/a
6	chr2:149216409-149216459	K562	blood:	n/a
7	chr2:149215642-149215692	T-47D	breast:	n/a
8	chr2:149041060-149041110	HCM	heart:	n/a
9	chr2:149259371-149259421	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:149215642-149215692	HRPEpiC	eye:	n/a
11	chr2:149267116-149267166	GM12878	blood:	n/a
12	chr2:149216409-149216459	NT2-D1	testis:	n/a
13	chr2:149215884-149215934	ECC-1	luminal epithelium:	n/a
14	chr2:149215431-149215481	GM12892	blood:	n/a
15	chr2:149096527-149096577	HUVEC	blood vessel:	n/a
16	chr2:149310951-149311001	LNCaP	prostate:	n/a
17	chr2:149215535-149215585	GM06990	blood:	n/a
18	chr2:149215884-149215934	LNCaP	prostate:	n/a
19	chr2:149215642-149215692	Caco-2	colon:	n/a
20	chr2:149215535-149215585	SAEC	small airway:	n/a
21	chr2:149310951-149311001	ECC-1	luminal epithelium:	n/a
22	chr2:149215642-149215692	LNCaP	prostate:	n/a
23	chr2:149259371-149259421	AG09309	skin:	n/a
24	chr2:149270531-149270581	AG09309	skin:	n/a
25	chr2:149096527-149096577	IMR90	lung:	fetal
26	chr2:149041060-149041110	NB4	blood:	n/a
27	chr2:149270531-149270581	NH-A	brain:	n/a
28	chr2:149096527-149096577	HNPCEpiC	eye:	n/a
29	chr2:149215431-149215481	NB4	blood:	n/a
30	chr2:149282209-149282259	BE2_C	brain:	n/a
31	chr2:149215884-149215934	HL-60	blood:	n/a
32	chr2:149215884-149215934	HEK293	kidney:	embryo
33	chr2:149267116-149267166	HIPEpiC	eye:	n/a
34	chr2:149259371-149259421	H1-hESC	embryonic stem cell:	embryo
35	chr2:149215884-149215934	SK-N-SH	brain:	n/a
36	chr2:149215642-149215692	HL-60	blood:	n/a
37	chr2:149275796-149275846	HCPEpiC	choroid plexus:	n/a
38	chr2:149259371-149259421	AG04449	skin:	fetal
39	chr2:149310951-149311001	HCF	heart:	n/a
40	chr2:149215431-149215481	SK-N-SH_RA	brain:	n/a
41	chr2:149063092-149063142	T-47D	breast:	n/a
42	chr2:149215642-149215692	IMR90	lung:	fetal
43	chr2:149259371-149259421	ovcar-3	ovarian:	n/a
44	chr2:149267116-149267166	MCF-7	breast:	n/a
45	chr2:149275796-149275846	SK-N-MC	brain:	n/a
46	chr2:149259371-149259421	SKMC	muscle:	n/a
47	chr2:149215431-149215481	AoSMC	blood vessel:	n/a
48	chr2:149312414-149312464	Jurkat	blood:	n/a
49	chr2:149270531-149270581	AG10803	skin:	n/a
50	chr2:149282209-149282259	NT2-D1	testis:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:149287117..149288965-chr2:149289361..149291496,2	K562	blood:
2	chr2:149244268..149247294-chr2:149251555..149254307,3	K562	blood:
3	chr2:149224578..149227474-chr2:149227523..149230314,3	MCF-7	breast:
4	chr2:149239376..149241711-chr2:149247771..149249475,2	MCF-7	breast:
5	chr2:149277983..149279760-chr2:149282502..149284169,2	K562	blood:
6	chr2:149257990..149260894-chr2:149265586..149267154,2	K562	blood:
7	chr2:149315092..149315904-chr2:149364871..149365412,2	MCF-7	breast:
8	chr2:148925257..148925927-chr2:149266799..149267551,3	MCF-7	breast:
9	chr2:149308756..149311819-chr2:149312294..149315148,3	K562	blood:
10	chr2:149281731..149283651-chr2:149284269..149286431,2	K562	blood:
11	chr2:149244708..149247294-chr2:149251980..149254307,2	K562	blood:
12	chr2:149261445..149263712-chr2:149268921..149270599,2	MCF-7	breast:
13	chr2:149300100..149301867-chr2:149308613..149310548,2	MCF-7	breast:
14	chr2:149294626..149297219-chr2:149297327..149299085,2	K562	blood:
15	chr2:149281731..149283651-chr2:149284269..149286431,2	K562	blood:
16	chr2:149273481..149276815-chr2:149277336..149280531,3	MCF-7	breast:
17	chr2:148747086..148748063-chr2:149266705..149267668,7	MCF-7	breast:
18	chr2:148967081..148967666-chr2:149266757..149267493,2	MCF-7	breast:
19	chr2:149098190..149099193-chr8:103870990..103871561,3	MCF-7	breast:
20	chr2:149291312..149293367-chr2:149296532..149298461,2	K562	blood:
21	chr15:28276602..28277139-chr2:149188463..149189398,2	MCF-7	breast:
22	chr2:149257990..149260894-chr2:149265586..149267154,2	K562	blood:
23	chr2:149244708..149247294-chr2:149251980..149254307,2	K562	blood:
24	chr2:149294626..149297219-chr2:149297327..149299085,2	K562	blood:
25	chr2:148704147..148707130-chr2:149248171..149249711,2	K562	blood:
26	chr2:149300619..149303078-chr2:149303918..149306388,2	K562	blood:
27	chr2:149282589..149285549-chr2:149375360..149378026,2	MCF-7	breast:
28	chr2:149075837..149077502-chr2:149078187..149080957,2	K562	blood:
29	chr2:149294992..149296635-chr2:149307311..149309386,2	K562	blood:
30	chr2:149262235..149263751-chr2:149373469..149375065,2	K562	blood:
31	chr2:149257941..149260096-chr2:149261087..149264018,2	K562	blood:
32	chr2:149239376..149241711-chr2:149247771..149249475,2	MCF-7	breast:
33	chr2:149239006..149241977-chr2:149242411..149245032,2	K562	blood:
34	chr2:149294992..149296635-chr2:149307311..149309386,2	K562	blood:
35	chr2:149236787..149238551-chr2:149238732..149240365,2	MCF-7	breast:
36	chr2:148777185..148777981-chr2:149266660..149267608,2	MCF-7	breast:
37	chr2:149281538..149284330-chr2:149286609..149289120,3	K562	blood:
38	chr2:149134166..149136482-chr2:149845391..149847794,2	MCF-7	breast:
39	chr2:149273481..149276815-chr2:149277336..149280531,3	MCF-7	breast:
40	chr2:148685824..148687356-chr2:149266124..149268743,2	K562	blood:
41	chr2:149282393..149284860-chr2:149290355..149292370,2	K562	blood:
42	chr2:148695019..148695866-chr2:149266727..149267624,3	K562	blood:
43	chr2:149291312..149293367-chr2:149296532..149298461,2	K562	blood:
44	chr2:149235404..149238151-chr2:149241139..149243574,2	K562	blood:
45	chr2:149224535..149226528-chr2:149230831..149232542,2	MCF-7	breast:
46	chr2:148747289..148748018-chr2:149266484..149267635,9	MCF-7	breast:
47	chr2:149236787..149238551-chr2:149238732..149240365,2	MCF-7	breast:
48	chr2:149282393..149284860-chr2:149290355..149292370,2	K562	blood:
49	chr2:149300619..149303078-chr2:149303918..149306388,2	K562	blood:
50	chr2:149244268..149247294-chr2:149251555..149254307,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:149215772-149216066	NONHSAT074871
2	lnc-EPC2-1	chr2:149262047-149262433	expReg_chr2_10621_+
3	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074878
4	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074871
5	lnc-MBD5-1	chr2:149215772-149215927	NONHSAT074872
6	lnc-ORC4-3	chr2:149053225-149054248	NONHSAT074880
7	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074872
8	lnc-MBD5-1	chr2:149215772-149215886	NONHSAT074878

No data

Variant related genes	Relation type
MBD5	TF binding region
ENSG00000224007	TF binding region
MBD5	CpG island
ENSG00000224007	CpG island
ENSG00000135999	chromatin interactions
ENSG00000204406	chromatin interactions
ENSG00000115947	chromatin interactions
ENSG00000123560	chromatin interactions

Extended variants
information (count: 10038 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:10038 , 50 per page) page: 1 2 3 4 5 6 7 ... 201

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181857286	chr2:149031719-149031720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186483776	chr2:149031778-149031779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76346501	chr2:149031830-149031831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540556077	chr2:149031853-149031854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141106356	chr2:149031905-149031906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551172623	chr2:149031933-149031934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532021931	chr2:149031935-149031936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552482804	chr2:149031953-149031954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116200381	chr2:149031954-149031955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75951590	chr2:149031971-149031972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547846618	chr2:149032019-149032020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539504344	chr2:149032035-149032036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62182801	chr2:149032044-149032045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs190062736	chr2:149032127-149032128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571947782	chr2:149032148-149032149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4972344	chr2:149032151-149032152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs4972345	chr2:149032186-149032187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201348603	chr2:149032232-149032233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555377476	chr2:149032244-149032245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575694162	chr2:149032272-149032273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199569391	chr2:149032286-149032287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527817475	chr2:149032294-149032295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34560513	chr2:149032295-149032296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs28647742	chr2:149032299-149032300	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555075283	chr2:149032301-149032302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111276987	chr2:149032322-149032323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185178607	chr2:149032325-149032326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573834009	chr2:149032331-149032332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564924642	chr2:149032355-149032356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111860012	chr2:149032373-149032374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553551347	chr2:149032436-149032437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562516872	chr2:149032437-149032438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529611098	chr2:149032441-149032442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547883586	chr2:149032481-149032482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559774552	chr2:149032512-149032513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527375813	chr2:149032537-149032538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148918665	chr2:149032599-149032600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571728131	chr2:149032689-149032690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35044655	chr2:149032705-149032706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539353530	chr2:149032715-149032716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545782457	chr2:149032722-149032723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544123424	chr2:149032780-149032781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536605569	chr2:149032803-149032804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145634592	chr2:149032835-149032836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577143035	chr2:149032856-149032857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538847725	chr2:149032916-149032917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138371121	chr2:149032921-149032922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534013266	chr2:149032972-149032973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558749208	chr2:149033075-149033076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76086771	chr2:149033137-149033138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149012600-149043400	Weak transcription	Gastric	stomach
2	chr2:149012800-149096000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:149017200-149038000	Weak transcription	Primary B cells from cord blood	blood
4	chr2:149017400-149033600	Weak transcription	Pancreas	Pancrea
5	chr2:149017400-149037600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr2:149017400-149050600	Weak transcription	Thymus	Thymus
7	chr2:149017400-149062800	Weak transcription	Fetal Lung	lung
8	chr2:149017400-149070600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr2:149017600-149043400	Weak transcription	Fetal Stomach	stomach
10	chr2:149017600-149049000	Weak transcription	Duodenum Mucosa	Duodenum
11	chr2:149017600-149060800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr2:149023600-149039200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:149025800-149044600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:149026000-149045000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:149026000-149070400	Weak transcription	Fetal Intestine Small	intestine
16	chr2:149027000-149039200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr2:149027400-149032600	Weak transcription	Fetal Muscle Leg	muscle
18	chr2:149027600-149038000	Weak transcription	GM12878-XiMat	blood
19	chr2:149029400-149055400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr2:149029600-149036600	Weak transcription	Esophagus	oesophagus
21	chr2:149030200-149039200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr2:149031000-149041400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr2:149031200-149032200	Weak transcription	NH-A	brain
24	chr2:149031400-149033200	Weak transcription	Adipose Nuclei	Adipose
25	chr2:149031400-149036400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:149031400-149036800	Weak transcription	HepG2	liver
27	chr2:149031400-149039400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:149031400-149040400	Weak transcription	Aorta	Aorta
29	chr2:149031400-149042000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:149031400-149079000	Weak transcription	Left Ventricle	heart
31	chr2:149031600-149046200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:149031600-149055200	Weak transcription	Primary T cells from cord blood	blood
33	chr2:149033600-149033800	Enhancers	Pancreas	Pancrea
34	chr2:149036400-149036800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:149036600-149036800	Enhancers	Primary B cells from peripheral blood	blood
36	chr2:149036600-149036800	Enhancers	Esophagus	oesophagus
37	chr2:149036600-149037200	Enhancers	NHDF-Ad	bronchial
38	chr2:149036600-149038200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr2:149036600-149047000	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr2:149036800-149037200	Enhancers	HepG2	liver
41	chr2:149037200-149038400	Enhancers	Dnd41	blood
42	chr2:149037200-149039400	Weak transcription	NHDF-Ad	bronchial
43	chr2:149037200-149041200	Weak transcription	HepG2	liver
44	chr2:149037400-149037600	Enhancers	Primary B cells from peripheral blood	blood
45	chr2:149038000-149038200	Enhancers	GM12878-XiMat	blood
46	chr2:149038000-149038400	Enhancers	Primary B cells from cord blood	blood
47	chr2:149038400-149044800	Weak transcription	Primary B cells from cord blood	blood
48	chr2:149038800-149039600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:149039200-149039400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:149039200-149039400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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