Variant report

Variant	nsv1003920
Chromosome Location	chr2:40141776-40245464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 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	chr2:40222613-40222712	K562	blood:	n/a	n/a
2	ATF1	chr2:40217162-40217725	K562	blood:	n/a	n/a
3	ATF1	chr2:40223765-40224372	K562	blood:	n/a	n/a
4	BACH1	chr2:40208471-40208655	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:40149983-40150021	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	chr2:40243703-40243880	A549	lung:	n/a	chr2:40243790-40243803 chr2:40243792-40243803
9	CEBPB	chr2:40223679-40224438	HCT-116	colon:	n/a	n/a
10	CEBPB	chr2:40187092-40187228	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:40221391-40221660	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:40223962-40224177	A549	lung:	n/a	n/a
13	CEBPB	chr2:40223865-40224375	HCT-116	colon:	n/a	n/a
14	CEBPB	chr2:40218494-40218859	IMR90	lung:	n/a	chr2:40218674-40218685
15	CEBPB	chr2:40223859-40224267	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
17	CEBPB	chr2:40194909-40195167	H1-hESC	embryonic stem cell:	n/a	chr2:40195008-40195019
18	CEBPB	chr2:40223752-40224243	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:40144232-40144363	A549	lung:	n/a	n/a
20	CEBPB	chr2:40218557-40218771	H1-hESC	embryonic stem cell:	n/a	chr2:40218674-40218685
21	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
22	CEBPB	chr2:40187059-40187300	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:40218547-40218785	A549	lung:	n/a	chr2:40218674-40218685
24	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
26	CEBPB	chr2:40218529-40218785	HepG2	liver:	n/a	chr2:40218674-40218685
27	CEBPB	chr2:40243495-40243987	IMR90	lung:	n/a	chr2:40243790-40243803 chr2:40243792-40243803
28	CHD1	chr2:40140686-40141899	IMR90	lung:	n/a	n/a
29	CHD2	chr2:40223919-40224266	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr2:40190220-40190370	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr2:40190380-40190530	GM12873	blood:	n/a	n/a
32	CTCF	chr2:40147416-40147732	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:40147280-40147430	HepG2	liver:	n/a	n/a
34	CTCF	chr2:40216640-40216790	HRE	kidney:	n/a	n/a
35	CTCF	chr2:40191146-40191249	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:40147466-40147628	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:40235280-40235430	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr2:40191174-40191232	HepG2	liver:	n/a	n/a
39	CTCF	chr2:40191133-40191217	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:40191060-40191210	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:40191040-40191190	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr2:40216520-40216670	HMEC	breast:	n/a	n/a
43	CTCF	chr2:40191060-40191210	AG04449	skin:	n/a	n/a
44	CTCF	chr2:40191156-40191225	NHEK	skin:	n/a	n/a
45	CTCF	chr2:40191169-40191216	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr2:40216540-40216690	NHEK	skin:	n/a	n/a
47	CTCF	chr2:40147500-40147650	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr2:40190252-40190334	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr2:40147481-40147618	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:40235240-40235390	GM12872	blood:	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	chr2:40147801-40147851	BJ	skin:	n/a
2	chr2:40165558-40165608	ECC-1	luminal epithelium:	n/a
3	chr2:40203342-40203392	GM12878	blood:	n/a
4	chr2:40165558-40165608	HRPEpiC	eye:	n/a
5	chr2:40149258-40149308	Hela-S3	cervix:	n/a
6	chr2:40149258-40149308	H1-hESC	embryonic stem cell:	embryo
7	chr2:40147801-40147851	PrEC	prostate:	n/a
8	chr2:40149258-40149308	SK-N-SH	brain:	n/a
9	chr2:40203342-40203392	Hepatocyte	liver:	n/a
10	chr2:40147801-40147851	HCPEpiC	choroid plexus:	n/a
11	chr2:40149258-40149308	NB4	blood:	n/a
12	chr2:40165558-40165608	GM19239	blood:	n/a
13	chr2:40165558-40165608	AoSMC	blood vessel:	n/a
14	chr2:40165558-40165608	HEK293	kidney:	embryo
15	chr2:40147801-40147851	NHDF-neo	bronchial:	n/a
16	chr2:40149258-40149308	HRE	kidney:	n/a
17	chr2:40149258-40149308	MCF10A-Er-Src	breast:	n/a
18	chr2:40165558-40165608	AG09319	gingival:	n/a
19	chr2:40149258-40149308	CMK	blood:	n/a
20	chr2:40147801-40147851	PANC-1	pancreas:	n/a
21	chr2:40203342-40203392	HMEC	breast:	n/a
22	chr2:40147801-40147851	Jurkat	blood:	n/a
23	chr2:40165558-40165608	Hela-S3	cervix:	n/a
24	chr2:40147801-40147851	HEEpiC	esophagus:	n/a
25	chr2:40165558-40165608	LNCaP	prostate:	n/a
26	chr2:40165558-40165608	MCF-7	breast:	n/a
27	chr2:40147801-40147851	SK-N-SH	brain:	n/a
28	chr2:40165558-40165608	HAEpiC	amniotic membrane:	n/a
29	chr2:40165558-40165608	SK-N-SH	brain:	n/a
30	chr2:40165558-40165608	GM06990	blood:	n/a
31	chr2:40149258-40149308	AG04449	skin:	fetal
32	chr2:40149258-40149308	SAEC	small airway:	n/a
33	chr2:40147801-40147851	AoSMC	blood vessel:	n/a
34	chr2:40165558-40165608	HIPEpiC	eye:	n/a
35	chr2:40149258-40149308	SK-N-MC	brain:	n/a
36	chr2:40149258-40149308	U87	brain:	n/a
37	chr2:40147801-40147851	HRCEpiC	kidney:	n/a
38	chr2:40147801-40147851	MCF10A-Er-Src	breast:	n/a
39	chr2:40203342-40203392	ProgFib	skin:	n/a
40	chr2:40147801-40147851	RPTEC	kidney:	n/a
41	chr2:40149258-40149308	IMR90	lung:	fetal
42	chr2:40149258-40149308	GM19239	blood:	n/a
43	chr2:40149258-40149308	HRPEpiC	eye:	n/a
44	chr2:40165558-40165608	NT2-D1	testis:	n/a
45	chr2:40149258-40149308	PANC-1	pancreas:	n/a
46	chr2:40203342-40203392	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:40165558-40165608	AG04449	skin:	fetal
48	chr2:40149258-40149308	GM12891	blood:	n/a
49	chr2:40147801-40147851	T-47D	breast:	n/a
50	chr2:40203342-40203392	RPTEC	kidney:	n/a

(count:6 , 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	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
4	chr2:40140915..40141986-chr2:40781509..40782393,3	MCF-7	breast:
5	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
6	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	chr2:40144774-40144799	NONHSAT070261
2	lnc-TMEM178-2	chr2:40185553-40185606	ucscGeneNc_uc002rrw_2
3	lnc-TMEM178-2	chr2:40149990-40150029	NONHSAT070263
4	lnc-TMEM178-2	chr2:40146833-40146923	ENSG00000227028.1
5	lnc-TMEM178-2	chr2:40149989-40150029	NONHSAT070261
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: 5883 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5883 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563414479	chr2:40141813-40141814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148717660	chr2:40141826-40141827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548397729	chr2:40141876-40141877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs72789143	chr2:40141894-40141895	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs562323546	chr2:40141895-40141896	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs182369531	chr2:40141957-40141958	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112310280	chr2:40141996-40141997	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs565935977	chr2:40141999-40142000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs115769106	chr2:40142029-40142030	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs2110676	chr2:40142050-40142051	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs569840528	chr2:40142054-40142055	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs59696471	chr2:40142104-40142105	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs555239737	chr2:40142118-40142119	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs567464681	chr2:40142124-40142125	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs546489139	chr2:40142133-40142134	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs553280234	chr2:40142134-40142135	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs187084176	chr2:40142145-40142146	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs545056311	chr2:40142163-40142164	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs190353859	chr2:40142165-40142166	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575375871	chr2:40142182-40142183	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs542753366	chr2:40142214-40142215	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs369369545	chr2:40142242-40142243	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs568373758	chr2:40142273-40142274	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs534035590	chr2:40142283-40142284	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs539641644	chr2:40142310-40142311	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs56191830	chr2:40142347-40142348	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs529536519	chr2:40142354-40142355	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs557809475	chr2:40142362-40142363	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs377618616	chr2:40142373-40142374	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs560027263	chr2:40142412-40142413	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs571388800	chr2:40142424-40142425	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs533131964	chr2:40142448-40142449	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551330371	chr2:40142456-40142457	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs182824018	chr2:40142457-40142458	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs530875273	chr2:40142458-40142459	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs57101947	chr2:40142478-40142479	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567347908	chr2:40142480-40142481	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs534737724	chr2:40142531-40142532	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs143653860	chr2:40142545-40142546	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs553296584	chr2:40142573-40142574	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs147344885	chr2:40142574-40142575	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs57938722	chr2:40142583-40142584	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs552978402	chr2:40142594-40142595	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs55913763	chr2:40142605-40142606	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs377117236	chr2:40142611-40142612	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs369646778	chr2:40142616-40142617	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs556955384	chr2:40142644-40142645	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs35044015	chr2:40142664-40142665	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs397870788	chr2:40142671-40142672	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs60496607	chr2:40142686-40142687	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:380 , 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	chr2:40140000-40141800	Enhancers	Fetal Thymus	thymus
4	chr2:40140600-40146800	Enhancers	Dnd41	blood
5	chr2:40141000-40141800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:40141000-40141800	Enhancers	Fetal Kidney	kidney
7	chr2:40141000-40141800	Enhancers	Thymus	Thymus
8	chr2:40141000-40141800	Enhancers	HSMM	muscle
9	chr2:40141000-40142000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:40141000-40142000	Enhancers	Rectal Smooth Muscle	rectum
11	chr2:40141000-40142200	Enhancers	Fetal Stomach	stomach
12	chr2:40141400-40141800	Weak transcription	Fetal Lung	lung
13	chr2:40141400-40143000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:40141600-40144800	Weak transcription	Ovary	ovary
15	chr2:40141600-40145400	Weak transcription	HSMMtube	muscle
16	chr2:40141600-40164800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:40141800-40142200	Enhancers	Fetal Lung	lung
18	chr2:40141800-40144400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:40141800-40145400	Weak transcription	HSMM	muscle
20	chr2:40141800-40146600	Weak transcription	Fetal Thymus	thymus
21	chr2:40141800-40146600	Weak transcription	Thymus	Thymus
22	chr2:40142000-40146400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr2:40142000-40147800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr2:40142200-40148000	Weak transcription	Fetal Stomach	stomach
25	chr2:40143000-40143200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr2:40144400-40144800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:40144800-40146600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:40145200-40147800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr2:40145400-40146000	Enhancers	HSMMtube	muscle
30	chr2:40145400-40148200	Enhancers	HSMM	muscle
31	chr2:40146000-40146800	Weak transcription	HSMMtube	muscle
32	chr2:40146400-40147400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr2:40146600-40147200	Enhancers	Fetal Thymus	thymus
34	chr2:40146600-40147400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:40146600-40149400	Enhancers	Thymus	Thymus
36	chr2:40146800-40147400	Enhancers	HSMMtube	muscle
37	chr2:40146800-40148000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:40146800-40148200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:40146800-40149600	Flanking Active TSS	Dnd41	blood
40	chr2:40147000-40148000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:40147000-40148200	Enhancers	Primary T cells from cord blood	blood
42	chr2:40147000-40167400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:40147200-40147400	Flanking Active TSS	Fetal Thymus	thymus
44	chr2:40147200-40147800	Enhancers	Fetal Muscle Trunk	muscle
45	chr2:40147200-40147800	Enhancers	Placenta Amnion	Placenta Amnion
46	chr2:40147400-40147600	Enhancers	Fetal Thymus	thymus
47	chr2:40147400-40147800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:40147400-40148000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr2:40147400-40148200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr2:40147600-40147800	Flanking Active TSS	Fetal Thymus	thymus

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