Variant report

Variant	esv3361276
Chromosome Location	chr2:148756269-148781613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:897)
CpG islands
(count:672)
Chromatin interactive
region (count:21)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:897 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:148776453-148776679	K562	blood:	n/a	n/a
2	ARID3A	chr2:148777693-148778271	K562	blood:	n/a	n/a
3	ARID3A	chr2:148779891-148780131	K562	blood:	n/a	n/a
4	ARID3A	chr2:148780420-148780619	K562	blood:	n/a	n/a
5	ARID3A	chr2:148777639-148778741	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:148756715-148756858	K562	blood:	n/a	n/a
7	ARID3A	chr2:148778946-148779315	HepG2	liver:	n/a	n/a
8	ATF1	chr2:148778210-148778730	K562	blood:	n/a	n/a
9	ATF2	chr2:148778167-148779037	GM12878	blood:	n/a	n/a
10	ATF2	chr2:148777599-148779168	GM12878	blood:	n/a	n/a
11	ATF2	chr2:148777775-148778557	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr2:148778167-148778529	HepG2	liver:	n/a	chr2:148778471-148778480
13	ATF3	chr2:148777950-148778529	GM12878	blood:	n/a	chr2:148778471-148778480
14	BCL3	chr2:148778097-148778782	A549	lung:	n/a	chr2:148778394-148778403
15	BCLAF1	chr2:148778798-148779291	GM12878	blood:	n/a	n/a
16	BCLAF1	chr2:148777882-148779142	GM12878	blood:	n/a	chr2:148778394-148778403
17	BCLAF1	chr2:148777838-148778752	GM12878	blood:	n/a	chr2:148778394-148778403
18	BHLHE40	chr2:148778002-148779344	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:148777625-148779009	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:148777500-148779565	K562	blood:	n/a	n/a
21	BRCA1	chr2:148777945-148778567	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:148777798-148778676	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr2:148777938-148778665	GM12878	blood:	n/a	n/a
24	CBX3	chr2:148777781-148778727	K562	blood:	n/a	n/a
25	CCNT2	chr2:148777742-148778618	K562	blood:	n/a	chr2:148778341-148778350 chr2:148778471-148778480 chr2:148778557-148778566
26	CEBPB	chr2:148778000-148778770	GM12878	blood:	n/a	n/a
27	CEBPB	chr2:148757268-148757411	K562	blood:	n/a	n/a
28	CEBPB	chr2:148778396-148778585	GM12878	blood:	n/a	n/a
29	CEBPB	chr2:148777784-148778625	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:148777959-148778709	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:148777552-148778615	IMR90	lung:	n/a	n/a
32	CEBPD	chr2:148778004-148779143	HepG2	liver:	n/a	n/a
33	CEBPD	chr2:148778559-148778787	HepG2	liver:	n/a	n/a
34	CEBPD	chr2:148778106-148778739	K562	blood:	n/a	n/a
35	CHD1	chr2:148777851-148778180	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr2:148777993-148778235	GM12878	blood:	n/a	n/a
37	CHD1	chr2:148777546-148777623	GM12878	blood:	n/a	n/a
38	CHD1	chr2:148778439-148779323	GM12878	blood:	n/a	chr2:148778469-148778479 chr2:148778648-148778658
39	CHD2	chr2:148777818-148779600	Hela-S3	cervix:	n/a	chr2:148778339-148778349 chr2:148778469-148778479 chr2:148778648-148778658
40	CHD2	chr2:148777895-148779557	GM12878	blood:	n/a	chr2:148778339-148778349 chr2:148778469-148778479 chr2:148778648-148778658
41	CHD2	chr2:148777920-148779020	H1-hESC	embryonic stem cell:	n/a	chr2:148778339-148778349 chr2:148778469-148778479 chr2:148778648-148778658
42	CHD2	chr2:148777841-148778935	HepG2	liver:	n/a	chr2:148778339-148778349 chr2:148778469-148778479 chr2:148778648-148778658
43	CHD2	chr2:148777829-148779199	K562	blood:	n/a	chr2:148778339-148778349 chr2:148778469-148778479 chr2:148778648-148778658
44	CREB1	chr2:148777596-148779190	HepG2	liver:	n/a	n/a
45	CREB1	chr2:148778036-148778833	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr2:148778069-148778900	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr2:148778219-148778721	A549	lung:	n/a	n/a
48	CREB1	chr2:148778143-148778755	ECC-1	luminal epithelium:	n/a	n/a
49	CREB1	chr2:148777922-148778738	A549	lung:	n/a	n/a
50	CREB1	chr2:148777788-148778937	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:148778288-148778338	HCM	heart:	n/a
2	chr2:148778288-148778338	HCM	heart:	n/a
3	chr2:148779335-148779385	MCF10A-Er-Src	breast:	n/a
4	chr2:148779307-148779357	BJ	skin:	n/a
5	chr2:148778495-148778545	Caco-2	colon:	n/a
6	chr2:148778969-148779019	GM19239	blood:	n/a
7	chr2:148779307-148779357	H1-hESC	embryonic stem cell:	embryo
8	chr2:148779564-148779614	AG09309	skin:	n/a
9	chr2:148778495-148778545	HRCEpiC	kidney:	n/a
10	chr2:148778181-148778231	HCF	heart:	n/a
11	chr2:148758708-148758758	U87	brain:	n/a
12	chr2:148778495-148778545	GM12878	blood:	n/a
13	chr2:148758708-148758758	SK-N-MC	brain:	n/a
14	chr2:148779335-148779385	GM12892	blood:	n/a
15	chr2:148778969-148779019	PrEC	prostate:	n/a
16	chr2:148779307-148779357	ProgFib	skin:	n/a
17	chr2:148779307-148779357	HEEpiC	esophagus:	n/a
18	chr2:148779335-148779385	Hela-S3	cervix:	n/a
19	chr2:148777915-148777965	SAEC	small airway:	n/a
20	chr2:148778288-148778338	CMK	blood:	n/a
21	chr2:148778181-148778231	HCPEpiC	choroid plexus:	n/a
22	chr2:148778495-148778545	NB4	blood:	n/a
23	chr2:148779348-148779398	HRPEpiC	eye:	n/a
24	chr2:148779348-148779398	HUVEC	blood vessel:	n/a
25	chr2:148778181-148778231	HCM	heart:	n/a
26	chr2:148779564-148779614	GM19239	blood:	n/a
27	chr2:148778288-148778338	MCF10A-Er-Src	breast:	n/a
28	chr2:148779307-148779357	GM12891	blood:	n/a
29	chr2:148777915-148777965	HRE	kidney:	n/a
30	chr2:148777915-148777965	AoSMC	blood vessel:	n/a
31	chr2:148779335-148779385	BJ	skin:	n/a
32	chr2:148778495-148778545	NHDF-neo	bronchial:	n/a
33	chr2:148779564-148779614	SKMC	muscle:	n/a
34	chr2:148778969-148779019	HRE	kidney:	n/a
35	chr2:148779335-148779385	HEEpiC	esophagus:	n/a
36	chr2:148779683-148779733	HNPCEpiC	eye:	n/a
37	chr2:148779683-148779733	AG09319	gingival:	n/a
38	chr2:148778288-148778338	U87	brain:	n/a
39	chr2:148779683-148779733	HRE	kidney:	n/a
40	chr2:148779307-148779357	HEK293	kidney:	embryo
41	chr2:148758708-148758758	HAEpiC	amniotic membrane:	n/a
42	chr2:148779564-148779614	NT2-D1	testis:	n/a
43	chr2:148778969-148779019	NB4	blood:	n/a
44	chr2:148779307-148779357	SKMC	muscle:	n/a
45	chr2:148778495-148778545	PrEC	prostate:	n/a
46	chr2:148779335-148779385	SK-N-SH	brain:	n/a
47	chr2:148758708-148758758	HCT-116	colon:	n/a
48	chr2:148778181-148778231	IMR90	lung:	fetal
49	chr2:148778181-148778231	SK-N-SH	brain:	n/a
50	chr2:148778495-148778545	HPAEpiC	pulmonary alveolar:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:148765021..148767403-chr2:148770633..148772597,2	K562	blood:
2	chr2:148777810..148780521-chr2:149401501..149403816,2	MCF-7	breast:
3	chr2:148773879..148776006-chr2:148779968..148781591,2	MCF-7	breast:
4	chr2:148766857..148769068-chr2:148777403..148779388,2	K562	blood:
5	chr2:148777791..148778435-chr9:34611815..34612562,2	NB4	blood:
6	chr2:148777800..148778420-chr6:32821048..32821837,2	NB4	blood:
7	chr2:148773879..148776006-chr2:148779968..148781591,2	MCF-7	breast:
8	chr2:148765021..148767403-chr2:148770633..148772597,2	K562	blood:
9	chr2:148778374..148778927-chr5:41925178..41925893,2	Hela-S3	cervix:
10	chr2:148755309..148758512-chr2:148776445..148778931,3	MCF-7	breast:
11	chr2:148777185..148777981-chr2:149266660..149267608,2	MCF-7	breast:
12	chr2:148762432..148764977-chr2:148778675..148780305,2	MCF-7	breast:
13	chr2:148765218..148768390-chr2:148776521..148778728,3	MCF-7	breast:
14	chr2:148747119..148747979-chr2:148777459..148778023,2	MCF-7	breast:
15	chr2:148765519..148769720-chr2:148770172..148772833,3	K562	blood:
16	chr2:148765519..148769720-chr2:148770172..148772833,3	K562	blood:
17	chr2:148776962..148779896-chr2:148780492..148782888,3	MCF-7	breast:
18	chr2:148762250..148764768-chr2:148777590..148779447,2	MCF-7	breast:
19	chr14:31090963..31091593-chr2:148777702..148778439,2	Hela-S3	cervix:
20	chr2:148772919..148776158-chr2:148776634..148779455,3	MCF-7	breast:
21	chr1:145382244..145383020-chr2:148777927..148778778,2	HCT-116	colon:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:148778580-148778615	NONHSAT074871
2	lnc-MBD5-1	chr2:148779008-148779253	NONHSAT074874
3	lnc-MBD5-1	chr2:148778596-148778615	NONHSAT074872
4	lnc-MBD5-1	chr2:148779033-148779253	NONHSAT074875
5	lnc-MMADHC-10	chr2:148778202-148778295	NONHSAT074870
6	lnc-MBD5-1	chr2:148779162-148779253	NONHSAT074876
7	lnc-MBD5-1	chr2:148778807-148779253	NONHSAT074873

No data

Variant related genes	Relation type
ORC4	TF binding region
MBD5	TF binding region
ORC4	CpG island
MBD5	CpG island
ENSG00000204406	chromatin interactions
ENSG00000115947	chromatin interactions
ENSG00000168394	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000092108	chromatin interactions
ENSG00000151876	chromatin interactions
ENSG00000135999	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000164967	chromatin interactions

Extended variants
information (count: 911 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540928106	chr2:148756300-148756301	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs557277974	chr2:148756322-148756323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs532826006	chr2:148756323-148756324	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs138484818	chr2:148756374-148756375	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563276626	chr2:148756385-148756386	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543249765	chr2:148756453-148756454	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs180741878	chr2:148756466-148756467	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550371057	chr2:148756498-148756499	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544051079	chr2:148756502-148756503	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565224298	chr2:148756556-148756557	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs13022962	chr2:148756624-148756625	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs71413606	chr2:148756657-148756658	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12053401	chr2:148756668-148756669	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566062384	chr2:148756726-148756727	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs539476541	chr2:148756764-148756765	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs374795943	chr2:148756779-148756780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs558216734	chr2:148756822-148756823	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs141469519	chr2:148756829-148756830	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs537169638	chr2:148756845-148756846	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs555094093	chr2:148756882-148756883	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549003608	chr2:148756902-148756903	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs34268570	chr2:148756935-148756936	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs113355455	chr2:148756959-148756960	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs560137819	chr2:148756980-148756981	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186096341	chr2:148756989-148756990	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs541306275	chr2:148757124-148757125	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs13028348	chr2:148757144-148757145	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145161103	chr2:148757204-148757205	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544647635	chr2:148757218-148757219	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs17225249	chr2:148757250-148757251	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563318869	chr2:148757291-148757292	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs192206340	chr2:148757443-148757444	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374861806	chr2:148757470-148757471	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370049824	chr2:148757486-148757487	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549109417	chr2:148757490-148757491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561042011	chr2:148757496-148757497	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs531970393	chr2:148757499-148757500	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs562258579	chr2:148757522-148757523	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs184096874	chr2:148757563-148757564	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs548049268	chr2:148757586-148757587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs551444649	chr2:148757646-148757647	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs367668839	chr2:148757648-148757649	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs199929365	chr2:148757654-148757655	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533694755	chr2:148757655-148757656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs551457680	chr2:148757714-148757715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs73005186	chr2:148757731-148757732	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs74590630	chr2:148757734-148757735	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555479532	chr2:148757762-148757763	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs567118391	chr2:148757811-148757812	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs1994189	chr2:148757824-148757825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148694200-148777400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr2:148709400-148776800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:148721400-148763600	Weak transcription	Spleen	Spleen
4	chr2:148722800-148756400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr2:148728200-148773400	Weak transcription	K562	blood
6	chr2:148736000-148776800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr2:148736400-148765600	Weak transcription	A549	lung
8	chr2:148739000-148759800	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr2:148741200-148758000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr2:148741800-148757400	Weak transcription	Aorta	Aorta
11	chr2:148743600-148757800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr2:148743600-148757800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr2:148747400-148758600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr2:148748000-148771400	Weak transcription	Fetal Kidney	kidney
15	chr2:148748200-148756600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr2:148750800-148758000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:148750800-148764000	Weak transcription	Left Ventricle	heart
18	chr2:148751400-148758600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr2:148753400-148756400	Weak transcription	Fetal Muscle Leg	muscle
20	chr2:148753400-148756800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr2:148753400-148756800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:148753400-148757000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:148753400-148758400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:148753400-148760200	Weak transcription	Primary B cells from peripheral blood	blood
25	chr2:148753400-148763400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:148753400-148764400	Weak transcription	Primary B cells from cord blood	blood
27	chr2:148753400-148764600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr2:148753400-148765200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:148753400-148765800	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr2:148753400-148775800	Weak transcription	Thymus	Thymus
31	chr2:148753400-148776400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:148753400-148776400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr2:148753400-148777600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr2:148753600-148757200	Weak transcription	Fetal Thymus	thymus
35	chr2:148753600-148758200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr2:148753600-148763400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr2:148753600-148763400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:148753600-148763800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr2:148754000-148765000	Weak transcription	Fetal Intestine Large	intestine
40	chr2:148754600-148758200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr2:148754600-148764200	Weak transcription	HepG2	liver
42	chr2:148754800-148756600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr2:148754800-148757000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr2:148754800-148757000	Weak transcription	Fetal Lung	lung
45	chr2:148754800-148762200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr2:148755000-148756600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr2:148755000-148756800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr2:148755000-148758400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr2:148755000-148758400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:148755000-148764200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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