Variant report

Variant	nsv1000423
Chromosome Location	chr2:40143646-40245464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:244)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:40223765-40224372	K562	blood:	n/a	n/a
2	ATF1	chr2:40217162-40217725	K562	blood:	n/a	n/a
3	ATF1	chr2:40222613-40222712	K562	blood:	n/a	n/a
4	BACH1	chr2:40149983-40150021	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:40208471-40208655	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr2:40223784-40224393	HCT-116	colon:	n/a	n/a
7	CCNT2	chr2:40224014-40224213	K562	blood:	n/a	n/a
8	CEBPB	chr2:40218547-40218785	A549	lung:	n/a	chr2:40218674-40218685
9	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
10	CEBPB	chr2:40221391-40221660	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:40218529-40218785	HepG2	liver:	n/a	chr2:40218674-40218685
12	CEBPB	chr2:40187092-40187228	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:40187059-40187300	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:40218494-40218859	IMR90	lung:	n/a	chr2:40218674-40218685
15	CEBPB	chr2:40223752-40224243	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:40243703-40243880	A549	lung:	n/a	chr2:40243790-40243803 chr2:40243792-40243803
17	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
18	CEBPB	chr2:40223865-40224375	HCT-116	colon:	n/a	n/a
19	CEBPB	chr2:40218557-40218771	H1-hESC	embryonic stem cell:	n/a	chr2:40218674-40218685
20	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
21	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:40223859-40224267	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:40223962-40224177	A549	lung:	n/a	n/a
24	CEBPB	chr2:40223679-40224438	HCT-116	colon:	n/a	n/a
25	CEBPB	chr2:40194909-40195167	H1-hESC	embryonic stem cell:	n/a	chr2:40195008-40195019
26	CEBPB	chr2:40243495-40243987	IMR90	lung:	n/a	chr2:40243790-40243803 chr2:40243792-40243803
27	CEBPB	chr2:40144232-40144363	A549	lung:	n/a	n/a
28	CHD2	chr2:40223919-40224266	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr2:40216520-40216670	HMEC	breast:	n/a	n/a
30	CTCF	chr2:40187346-40187369	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr2:40228393-40228521	K562	blood:	n/a	n/a
32	CTCF	chr2:40191020-40191170	RPTEC	kidney:	n/a	n/a
33	CTCF	chr2:40190340-40190490	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr2:40232502-40232612	Fibrobl	skin:	n/a	n/a
35	CTCF	chr2:40191151-40191244	Gliobla	brain:	n/a	n/a
36	CTCF	chr2:40147227-40147330	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:40191040-40191190	NB4	blood:	n/a	n/a
38	CTCF	chr2:40190305-40190348	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:40191040-40191190	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr2:40190320-40190470	WI-38	lung:	n/a	n/a
41	CTCF	chr2:40235280-40235430	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr2:40190380-40190530	GM12869	blood:	n/a	n/a
43	CTCF	chr2:40235320-40235470	GM12871	blood:	n/a	n/a
44	CTCF	chr2:40147480-40147630	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr2:40190280-40190430	GM12868	blood:	n/a	n/a
46	CTCF	chr2:40228397-40228552	K562	blood:	n/a	n/a
47	CTCF	chr2:40191133-40191217	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr2:40147500-40147650	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr2:40191060-40191210	AG04449	skin:	n/a	n/a
50	CTCF	chr2:40190980-40191130	HFF	foreskin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40149258-40149308	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:40147801-40147851	U87	brain:	n/a
3	chr2:40165558-40165608	SK-N-SH_RA	brain:	n/a
4	chr2:40147801-40147851	SK-N-SH	brain:	n/a
5	chr2:40149258-40149308	K562	blood:	n/a
6	chr2:40165558-40165608	NH-A	brain:	n/a
7	chr2:40203342-40203392	BE2_C	brain:	n/a
8	chr2:40165558-40165608	H1-hESC	embryonic stem cell:	embryo
9	chr2:40149258-40149308	HCT-116	colon:	n/a
10	chr2:40147801-40147851	HAEpiC	amniotic membrane:	n/a
11	chr2:40165558-40165608	HepG2	liver:	n/a
12	chr2:40203342-40203392	CMK	blood:	n/a
13	chr2:40203342-40203392	HEEpiC	esophagus:	n/a
14	chr2:40203342-40203392	ECC-1	luminal epithelium:	n/a
15	chr2:40165558-40165608	Jurkat	blood:	n/a
16	chr2:40149258-40149308	SK-N-SH_RA	brain:	n/a
17	chr2:40147801-40147851	HCPEpiC	choroid plexus:	n/a
18	chr2:40165558-40165608	T-47D	breast:	n/a
19	chr2:40165558-40165608	HRCEpiC	kidney:	n/a
20	chr2:40203342-40203392	K562	blood:	n/a
21	chr2:40203342-40203392	HNPCEpiC	eye:	n/a
22	chr2:40149258-40149308	HL-60	blood:	n/a
23	chr2:40147801-40147851	ovcar-3	ovarian:	n/a
24	chr2:40149258-40149308	AG09309	skin:	n/a
25	chr2:40203342-40203392	HEK293	kidney:	embryo
26	chr2:40165558-40165608	ProgFib	skin:	n/a
27	chr2:40165558-40165608	NHBE	bronchial:	n/a
28	chr2:40203342-40203392	NHDF-neo	bronchial:	n/a
29	chr2:40149258-40149308	HepG2	liver:	n/a
30	chr2:40147801-40147851	AG04449	skin:	fetal
31	chr2:40149258-40149308	AoSMC	blood vessel:	n/a
32	chr2:40149258-40149308	HEEpiC	esophagus:	n/a
33	chr2:40165558-40165608	HCT-116	colon:	n/a
34	chr2:40165558-40165608	HMEC	breast:	n/a
35	chr2:40165558-40165608	HUVEC	blood vessel:	n/a
36	chr2:40147801-40147851	AoSMC	blood vessel:	n/a
37	chr2:40203342-40203392	NT2-D1	testis:	n/a
38	chr2:40147801-40147851	HRE	kidney:	n/a
39	chr2:40165558-40165608	AG04449	skin:	fetal
40	chr2:40147801-40147851	SKMC	muscle:	n/a
41	chr2:40149258-40149308	GM06990	blood:	n/a
42	chr2:40165558-40165608	GM06990	blood:	n/a
43	chr2:40165558-40165608	SAEC	small airway:	n/a
44	chr2:40203342-40203392	Caco-2	colon:	n/a
45	chr2:40165558-40165608	LNCaP	prostate:	n/a
46	chr2:40165558-40165608	NB4	blood:	n/a
47	chr2:40149258-40149308	HIPEpiC	eye:	n/a
48	chr2:40149258-40149308	Caco-2	colon:	n/a
49	chr2:40165558-40165608	AG09309	skin:	n/a
50	chr2:40147801-40147851	NHDF-neo	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:39991894..39993577-chr2:40151910..40153730,2	K562	blood:
2	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
3	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
4	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
5	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40149989-40150029	NONHSAT070261
2	lnc-TMEM178-2	chr2:40149990-40150029	NONHSAT070263
3	lnc-TMEM178-2	chr2:40185553-40185606	ucscGeneNc_uc002rrw_2
4	lnc-TMEM178-2	chr2:40144774-40144799	NONHSAT070261
5	lnc-TMEM178-2	chr2:40146833-40146923	ENSG00000227028.1
6	lnc-TMEM178-2	chr2:40149989-40150029	ENSG00000227028.1

No data

Variant related genes	Relation type
ENSG00000235653	TF binding region
SLC8A1-AS1	TF binding region
ENSG00000235653	CpG island
SLC8A1-AS1	CpG island
ENSG00000138050	chromatin interactions

Extended variants
information (count: 5776 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5776 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140879233	chr2:40143650-40143651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149758336	chr2:40143663-40143664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2215971	chr2:40143682-40143683	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs188739745	chr2:40143683-40143684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561687371	chr2:40143692-40143693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145437068	chr2:40143707-40143708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538380244	chr2:40143708-40143709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78895689	chr2:40143719-40143720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565412160	chr2:40143732-40143733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148827568	chr2:40143736-40143737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550743790	chr2:40143756-40143757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12712664	chr2:40143766-40143767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs200425252	chr2:40143774-40143775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374454588	chr2:40143790-40143791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181384840	chr2:40143801-40143802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146949340	chr2:40143846-40143847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80337094	chr2:40143849-40143850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566463324	chr2:40143851-40143852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527339521	chr2:40143860-40143861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551841885	chr2:40143924-40143925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368835755	chr2:40143929-40143930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62137224	chr2:40143953-40143954	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs185209072	chr2:40143985-40143986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34503564	chr2:40143986-40143987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566669103	chr2:40144004-40144005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114483379	chr2:40144007-40144008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569362069	chr2:40144033-40144034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536948175	chr2:40144044-40144045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555004079	chr2:40144045-40144046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534051811	chr2:40144094-40144095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190184945	chr2:40144096-40144097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78733357	chr2:40144153-40144154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559011188	chr2:40144207-40144208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200432503	chr2:40144208-40144209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201278473	chr2:40144212-40144213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs72932973	chr2:40144235-40144236	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182365764	chr2:40144266-40144267	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs115992430	chr2:40144275-40144276	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs529896758	chr2:40144336-40144337	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs187228337	chr2:40144344-40144345	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs62137248	chr2:40144401-40144402	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs568161168	chr2:40144406-40144407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527273168	chr2:40144478-40144479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551729135	chr2:40144485-40144486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570129606	chr2:40144514-40144515	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs531265777	chr2:40144550-40144551	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573100945	chr2:40144559-40144560	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs190915523	chr2:40144573-40144574	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs535445709	chr2:40144594-40144595	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs569424509	chr2:40144613-40144614	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40138400-40150400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr2:40138400-40150800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr2:40140600-40146800	Enhancers	Dnd41	blood
4	chr2:40141600-40144800	Weak transcription	Ovary	ovary
5	chr2:40141600-40145400	Weak transcription	HSMMtube	muscle
6	chr2:40141600-40164800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr2:40141800-40144400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:40141800-40145400	Weak transcription	HSMM	muscle
9	chr2:40141800-40146600	Weak transcription	Fetal Thymus	thymus
10	chr2:40141800-40146600	Weak transcription	Thymus	Thymus
11	chr2:40142000-40146400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr2:40142000-40147800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr2:40142200-40148000	Weak transcription	Fetal Stomach	stomach
14	chr2:40144400-40144800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:40144800-40146600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:40145200-40147800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr2:40145400-40146000	Enhancers	HSMMtube	muscle
18	chr2:40145400-40148200	Enhancers	HSMM	muscle
19	chr2:40146000-40146800	Weak transcription	HSMMtube	muscle
20	chr2:40146400-40147400	Enhancers	Muscle Satellite Cultured Cells	--
21	chr2:40146600-40147200	Enhancers	Fetal Thymus	thymus
22	chr2:40146600-40147400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:40146600-40149400	Enhancers	Thymus	Thymus
24	chr2:40146800-40147400	Enhancers	HSMMtube	muscle
25	chr2:40146800-40148000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr2:40146800-40148200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:40146800-40149600	Flanking Active TSS	Dnd41	blood
28	chr2:40147000-40148000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr2:40147000-40148200	Enhancers	Primary T cells from cord blood	blood
30	chr2:40147000-40167400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:40147200-40147400	Flanking Active TSS	Fetal Thymus	thymus
32	chr2:40147200-40147800	Enhancers	Fetal Muscle Trunk	muscle
33	chr2:40147200-40147800	Enhancers	Placenta Amnion	Placenta Amnion
34	chr2:40147400-40147600	Enhancers	Fetal Thymus	thymus
35	chr2:40147400-40147800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:40147400-40148000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:40147400-40148200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr2:40147600-40147800	Flanking Active TSS	Fetal Thymus	thymus
39	chr2:40147600-40148000	Enhancers	Primary B cells from cord blood	blood
40	chr2:40147600-40148000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:40147600-40148000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr2:40147800-40148000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:40147800-40148000	Enhancers	Fetal Thymus	thymus
44	chr2:40147800-40148000	Enhancers	Rectal Smooth Muscle	rectum
45	chr2:40148000-40148200	Enhancers	Fetal Stomach	stomach
46	chr2:40148000-40148200	Flanking Active TSS	Fetal Thymus	thymus
47	chr2:40148000-40148800	Weak transcription	Rectal Smooth Muscle	rectum
48	chr2:40148000-40150400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:40148000-40150600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr2:40148000-40153800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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