Variant report

Variant	nsv581497
Chromosome Location	chr2:40151882-40195548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:130)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:130 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
2	CEBPB	chr2:40187059-40187300	IMR90	lung:	n/a	n/a
3	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
4	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
5	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
6	CEBPB	chr2:40194909-40195167	H1-hESC	embryonic stem cell:	n/a	chr2:40195008-40195019
7	CEBPB	chr2:40187092-40187228	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr2:40191000-40191150	HAc	cerebellar:	n/a	n/a
9	CTCF	chr2:40187346-40187369	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr2:40190480-40190630	GM12868	blood:	n/a	n/a
11	CTCF	chr2:40190305-40190348	MCF-7	breast:	n/a	n/a
12	CTCF	chr2:40190320-40190470	WI-38	lung:	n/a	n/a
13	CTCF	chr2:40191040-40191190	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr2:40190420-40190570	GM12875	blood:	n/a	n/a
15	CTCF	chr2:40190380-40190530	GM12869	blood:	n/a	n/a
16	CTCF	chr2:40191020-40191170	RPTEC	kidney:	n/a	n/a
17	CTCF	chr2:40191116-40191231	GM12878	blood:	n/a	n/a
18	CTCF	chr2:40190252-40190334	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr2:40191208-40191273	GM20000	blood:	n/a	n/a
20	CTCF	chr2:40157840-40157990	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr2:40191040-40191190	NB4	blood:	n/a	n/a
22	CTCF	chr2:40191040-40191190	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr2:40191040-40191190	Caco-2	colon:	n/a	n/a
24	CTCF	chr2:40191133-40191217	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr2:40190340-40190490	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr2:40191156-40191225	NHEK	skin:	n/a	n/a
27	CTCF	chr2:40190220-40190370	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr2:40190980-40191130	HFF	foreskin:	n/a	n/a
29	CTCF	chr2:40191147-40191256	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:40191146-40191249	MCF-7	breast:	n/a	n/a
31	CTCF	chr2:40191169-40191216	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr2:40190280-40190430	HEK293	kidney:	n/a	n/a
33	CTCF	chr2:40191151-40191244	Gliobla	brain:	n/a	n/a
34	CTCF	chr2:40190340-40190490	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr2:40190440-40190590	GM12864	blood:	n/a	n/a
36	CTCF	chr2:40190300-40190450	BE2_C	brain:	n/a	n/a
37	CTCF	chr2:40191174-40191232	HepG2	liver:	n/a	n/a
38	CTCF	chr2:40191167-40191213	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:40190380-40190530	GM12873	blood:	n/a	n/a
40	CTCF	chr2:40191060-40191210	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:40191060-40191210	AG04449	skin:	n/a	n/a
42	CTCF	chr2:40190340-40190590	AG04450	lung:	n/a	n/a
43	CTCF	chr2:40190260-40190410	K562	blood:	n/a	n/a
44	CTCF	chr2:40190320-40190470	HCFaa	heart:	n/a	n/a
45	CTCF	chr2:40191020-40191170	GM12864	blood:	n/a	n/a
46	CTCF	chr2:40190280-40190430	GM12868	blood:	n/a	n/a
47	CTCF	chr2:40191103-40191247	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:40190340-40190490	HPAF	blood vessel:	n/a	n/a
49	EP300	chr2:40170130-40170528	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr2:40174274-40176745	SK-N-SH	brain:	n/a	chr2:40175516-40175530

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40165558-40165608	H1-hESC	embryonic stem cell:	embryo
2	chr2:40165558-40165608	HEK293	kidney:	embryo
3	chr2:40165558-40165608	AG10803	skin:	n/a
4	chr2:40165558-40165608	HCF	heart:	n/a
5	chr2:40165558-40165608	ProgFib	skin:	n/a
6	chr2:40165558-40165608	GM12878	blood:	n/a
7	chr2:40165558-40165608	PFSK-1	brain:	n/a
8	chr2:40165558-40165608	AG04450	lung:	fetal
9	chr2:40165558-40165608	Jurkat	blood:	n/a
10	chr2:40165558-40165608	NT2-D1	testis:	n/a
11	chr2:40165558-40165608	K562	blood:	n/a
12	chr2:40165558-40165608	SKMC	muscle:	n/a
13	chr2:40165558-40165608	SK-N-MC	brain:	n/a
14	chr2:40165558-40165608	T-47D	breast:	n/a
15	chr2:40165558-40165608	ovcar-3	ovarian:	n/a
16	chr2:40165558-40165608	MCF10A-Er-Src	breast:	n/a
17	chr2:40165558-40165608	GM19239	blood:	n/a
18	chr2:40165558-40165608	NH-A	brain:	n/a
19	chr2:40165558-40165608	Hela-S3	cervix:	n/a
20	chr2:40165558-40165608	NB4	blood:	n/a
21	chr2:40165558-40165608	SK-N-SH	brain:	n/a
22	chr2:40165558-40165608	AG09319	gingival:	n/a
23	chr2:40165558-40165608	A549	lung:	n/a
24	chr2:40165558-40165608	HL-60	blood:	n/a
25	chr2:40165558-40165608	RPTEC	kidney:	n/a
26	chr2:40165558-40165608	LNCaP	prostate:	n/a
27	chr2:40165558-40165608	U87	brain:	n/a
28	chr2:40165558-40165608	PrEC	prostate:	n/a
29	chr2:40165558-40165608	Caco-2	colon:	n/a
30	chr2:40165558-40165608	HCT-116	colon:	n/a
31	chr2:40165558-40165608	HRE	kidney:	n/a
32	chr2:40165558-40165608	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:40165558-40165608	BE2_C	brain:	n/a
34	chr2:40165558-40165608	AG09309	skin:	n/a
35	chr2:40165558-40165608	HAEpiC	amniotic membrane:	n/a
36	chr2:40165558-40165608	HepG2	liver:	n/a
37	chr2:40165558-40165608	IMR90	lung:	fetal
38	chr2:40165558-40165608	AG04449	skin:	fetal
39	chr2:40165558-40165608	HNPCEpiC	eye:	n/a
40	chr2:40165558-40165608	HRPEpiC	eye:	n/a
41	chr2:40165558-40165608	BJ	skin:	n/a
42	chr2:40165558-40165608	CMK	blood:	n/a
43	chr2:40165558-40165608	HUVEC	blood vessel:	n/a
44	chr2:40165558-40165608	SAEC	small airway:	n/a
45	chr2:40165558-40165608	NHDF-neo	bronchial:	n/a
46	chr2:40165558-40165608	HIPEpiC	eye:	n/a
47	chr2:40165558-40165608	SK-N-SH_RA	brain:	n/a
48	chr2:40165558-40165608	AoSMC	blood vessel:	n/a
49	chr2:40165558-40165608	GM12892	blood:	n/a
50	chr2:40165558-40165608	HRCEpiC	kidney:	n/a

(count:3 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40185553-40185606	ucscGeneNc_uc002rrw_2

No data

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

Extended variants
information (count: 2343 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2343 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7567740	chr2:40151882-40151883	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569898087	chr2:40151940-40151941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374671462	chr2:40151943-40151944	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369006427	chr2:40151974-40151975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs138179671	chr2:40151986-40151987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538894830	chr2:40152009-40152010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1476988	chr2:40152013-40152014	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs553138611	chr2:40152023-40152024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142783905	chr2:40152061-40152062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs186767205	chr2:40152073-40152074	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs143250985	chr2:40152080-40152081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371562874	chr2:40152128-40152129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543763877	chr2:40152145-40152146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566978955	chr2:40152154-40152155	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs527753512	chr2:40152162-40152163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549600961	chr2:40152190-40152191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529281852	chr2:40152246-40152247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547462214	chr2:40152253-40152254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191473448	chr2:40152255-40152256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112707486	chr2:40152259-40152260	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148320238	chr2:40152269-40152270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141488429	chr2:40152359-40152360	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs569751908	chr2:40152406-40152407	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150770785	chr2:40152408-40152409	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567904362	chr2:40152415-40152416	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549340219	chr2:40152419-40152420	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139667522	chr2:40152420-40152421	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576304831	chr2:40152429-40152430	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534632559	chr2:40152442-40152443	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377187966	chr2:40152480-40152481	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577635554	chr2:40152481-40152482	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541248846	chr2:40152508-40152509	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs183083180	chr2:40152538-40152539	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs370764117	chr2:40152549-40152550	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188035049	chr2:40152580-40152581	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543691154	chr2:40152601-40152602	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538432305	chr2:40152605-40152606	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574013754	chr2:40152630-40152631	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs540991801	chr2:40152631-40152632	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559330481	chr2:40152672-40152673	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs192976537	chr2:40152702-40152703	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201619758	chr2:40152707-40152708	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs76190595	chr2:40152708-40152709	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs201099862	chr2:40152712-40152713	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs202147701	chr2:40152715-40152716	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201444080	chr2:40152720-40152721	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs199891351	chr2:40152721-40152722	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112048904	chr2:40152723-40152724	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs112080118	chr2:40152725-40152726	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181578571	chr2:40152741-40152742	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Breast cancer	22522925	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40141600-40164800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:40147000-40167400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:40148000-40153800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:40148200-40152600	Enhancers	Fetal Thymus	thymus
5	chr2:40148200-40154000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:40149000-40156000	Weak transcription	HSMM	muscle
7	chr2:40150400-40152600	Enhancers	Thymus	Thymus
8	chr2:40150400-40153200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:40150800-40152400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:40151000-40152400	Enhancers	Dnd41	blood
11	chr2:40151200-40156600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:40151400-40153600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:40151600-40154000	Weak transcription	Fetal Stomach	stomach
14	chr2:40152000-40158800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:40152400-40152800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:40152400-40154400	Genic enhancers	Dnd41	blood
17	chr2:40152600-40155600	Weak transcription	Fetal Thymus	thymus
18	chr2:40152800-40156200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:40153200-40154200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:40153600-40154000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:40154000-40156400	Enhancers	Fetal Stomach	stomach
22	chr2:40154200-40154600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:40154400-40154800	Enhancers	Dnd41	blood
24	chr2:40154600-40156000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:40154800-40155000	Weak transcription	Dnd41	blood
26	chr2:40155000-40155600	Enhancers	Dnd41	blood
27	chr2:40155400-40156200	Enhancers	Ovary	ovary
28	chr2:40155600-40155800	Genic enhancers	Fetal Thymus	thymus
29	chr2:40155600-40155800	Genic enhancers	Dnd41	blood
30	chr2:40155600-40156200	Enhancers	Adipose Nuclei	Adipose
31	chr2:40155800-40156400	Strong transcription	Fetal Thymus	thymus
32	chr2:40155800-40157000	Strong transcription	Dnd41	blood
33	chr2:40156000-40156200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:40156000-40156600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:40156000-40156800	ZNF genes & repeats	HSMM	muscle
36	chr2:40156200-40156800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr2:40156200-40157600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:40156400-40157600	Weak transcription	Fetal Thymus	thymus
39	chr2:40156400-40160200	Weak transcription	Fetal Stomach	stomach
40	chr2:40156600-40156800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:40156800-40158600	Weak transcription	HSMM	muscle
42	chr2:40156800-40158800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:40157000-40159200	Genic enhancers	Dnd41	blood
44	chr2:40157600-40158000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:40157600-40158200	Enhancers	Thymus	Thymus
46	chr2:40157600-40158600	Enhancers	Fetal Thymus	thymus
47	chr2:40158600-40158800	Genic enhancers	Fetal Thymus	thymus
48	chr2:40158600-40159200	ZNF genes & repeats	HSMM	muscle
49	chr2:40158800-40159400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:40158800-40159400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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