Variant report

Variant	nsv1014718
Chromosome Location	chr2:134067133-134151633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:498)
CpG islands
(count:549)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:134097037-134097041	K562	blood:	n/a	n/a
2	BCL3	chr2:134084062-134084604	A549	lung:	n/a	chr2:134084326-134084335 chr2:134084327-134084336
3	BCL3	chr2:134104177-134104553	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:134119719-134119882	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:134069959-134070256	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:134081191-134081206	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr2:134102290-134102899	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr2:134119678-134120195	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr2:134084130-134084724	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr2:134103274-134103787	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:134147286-134147396	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:134084078-134084970	A549	lung:	n/a	n/a
13	CEBPB	chr2:134081859-134082203	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:134084072-134085004	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:134119668-134119880	A549	lung:	n/a	n/a
16	CEBPB	chr2:134102267-134102854	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:134119542-134119916	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:134134628-134134894	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:134119529-134120325	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:134104177-134104699	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:134103185-134103584	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:134069498-134070230	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:134120886-134121183	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:134095788-134096225	IMR90	lung:	n/a	chr2:134096054-134096065
25	CEBPB	chr2:134074709-134075358	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:134074848-134075050	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:134069908-134070215	A549	lung:	n/a	n/a
28	CEBPB	chr2:134092482-134092903	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:134084251-134084922	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:134119608-134119881	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:134081659-134082211	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:134104232-134104595	A549	lung:	n/a	n/a
33	CEBPB	chr2:134095890-134096128	Hela-S3	cervix:	n/a	chr2:134096054-134096065
34	CEBPB	chr2:134104155-134104720	IMR90	lung:	n/a	n/a
35	CHD2	chr2:134119196-134119209	GM12878	blood:	n/a	n/a
36	CHD2	chr2:134084103-134084638	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr2:134081477-134082104	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr2:134102392-134102835	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr2:134117528-134117539	GM12878	blood:	n/a	n/a
40	CREB1	chr2:134084098-134084570	A549	lung:	n/a	n/a
41	CREB1	chr2:134084237-134084570	A549	lung:	n/a	n/a
42	CTCF	chr2:134111944-134111980	A549	lung:	n/a	n/a
43	CTCF	chr2:134072440-134072590	AG04450	lung:	n/a	n/a
44	CTCF	chr2:134122260-134122410	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:134083480-134083630	A549	lung:	n/a	chr2:134083569-134083577
46	CTCF	chr2:134111920-134112070	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr2:134122120-134122410	GM12874	blood:	n/a	n/a
48	CTCF	chr2:134111540-134111690	GM12869	blood:	n/a	n/a
49	CTCF	chr2:134122343-134122486	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:134083540-134083690	Caco-2	colon:	n/a	chr2:134083569-134083577

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134135267-134135317	IMR90	lung:	fetal
2	chr2:134135267-134135317	SAEC	small airway:	n/a
3	chr2:134135267-134135317	BJ	skin:	n/a
4	chr2:134099762-134099812	HCF	heart:	n/a
5	chr2:134135267-134135317	HRCEpiC	kidney:	n/a
6	chr2:134068922-134068972	GM12892	blood:	n/a
7	chr2:134147854-134147904	HEEpiC	esophagus:	n/a
8	chr2:134075125-134075175	U87	brain:	n/a
9	chr2:134083495-134083545	HUVEC	blood vessel:	n/a
10	chr2:134068922-134068972	GM19239	blood:	n/a
11	chr2:134147854-134147904	AG09319	gingival:	n/a
12	chr2:134104516-134104566	HCM	heart:	n/a
13	chr2:134127568-134127618	CMK	blood:	n/a
14	chr2:134099762-134099812	BE2_C	brain:	n/a
15	chr2:134147854-134147904	HCM	heart:	n/a
16	chr2:134147854-134147904	HRE	kidney:	n/a
17	chr2:134099762-134099812	NT2-D1	testis:	n/a
18	chr2:134127568-134127618	HCPEpiC	choroid plexus:	n/a
19	chr2:134083495-134083545	AG04449	skin:	fetal
20	chr2:134104516-134104566	HCF	heart:	n/a
21	chr2:134135267-134135317	GM12891	blood:	n/a
22	chr2:134083495-134083545	Jurkat	blood:	n/a
23	chr2:134127568-134127618	AG09319	gingival:	n/a
24	chr2:134068922-134068972	AG04449	skin:	fetal
25	chr2:134104516-134104566	GM12878	blood:	n/a
26	chr2:134119805-134119855	Hepatocyte	liver:	n/a
27	chr2:134099762-134099812	RPTEC	kidney:	n/a
28	chr2:134068922-134068972	HL-60	blood:	n/a
29	chr2:134127568-134127618	MCF10A-Er-Src	breast:	n/a
30	chr2:134099762-134099812	Hepatocyte	liver:	n/a
31	chr2:134127568-134127618	HUVEC	blood vessel:	n/a
32	chr2:134099762-134099812	HepG2	liver:	n/a
33	chr2:134135267-134135317	T-47D	breast:	n/a
34	chr2:134119805-134119855	PANC-1	pancreas:	n/a
35	chr2:134075125-134075175	NHBE	bronchial:	n/a
36	chr2:134068922-134068972	A549	lung:	n/a
37	chr2:134147854-134147904	LNCaP	prostate:	n/a
38	chr2:134147854-134147904	HMEC	breast:	n/a
39	chr2:134104516-134104566	HIPEpiC	eye:	n/a
40	chr2:134104516-134104566	HRCEpiC	kidney:	n/a
41	chr2:134119805-134119855	HRE	kidney:	n/a
42	chr2:134147854-134147904	HCT-116	colon:	n/a
43	chr2:134104516-134104566	H1-hESC	embryonic stem cell:	embryo
44	chr2:134135267-134135317	NT2-D1	testis:	n/a
45	chr2:134068922-134068972	NHBE	bronchial:	n/a
46	chr2:134099762-134099812	LNCaP	prostate:	n/a
47	chr2:134068922-134068972	PANC-1	pancreas:	n/a
48	chr2:134135267-134135317	GM12892	blood:	n/a
49	chr2:134083495-134083545	HMEC	breast:	n/a
50	chr2:134135267-134135317	ProgFib	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:134086116..134088912-chr2:134093493..134094997,2	MCF-7	breast:
2	chr2:134088967..134089889-chr2:134250249..134251166,2	MCF-7	breast:
3	chr2:134072524..134074621-chr2:134077160..134080145,2	K562	blood:
4	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
5	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
6	chr2:134101590..134103181-chr2:134107237..134110074,2	K562	blood:
7	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
8	chr2:134147354..134149666-chr2:134150601..134153236,2	K562	blood:
9	chr2:134089010..134089877-chr2:134262426..134263057,3	MCF-7	breast:
10	chr2:134083491..134086031-chr2:134262913..134265457,2	MCF-7	breast:
11	chr2:134086116..134088912-chr2:134093493..134094997,2	MCF-7	breast:
12	chr2:134101590..134103181-chr2:134107237..134110074,2	K562	blood:
13	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
14	chr2:134089345..134089856-chr2:134262223..134263005,2	MCF-7	breast:
15	chr2:134072524..134074621-chr2:134077160..134080145,2	K562	blood:
16	chr2:134084453..134086561-chr2:134089070..134091697,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYPD1-4	chr2:134148681-134148970	NONHSAT074547

No data

Variant related genes	Relation type
RNU6-579P	TF binding region
RN7SKP154	TF binding region
RNU6-579P	CpG island
RN7SKP154	CpG island
ENSG00000222068	chromatin interactions
ENSG00000252688	chromatin interactions

Extended variants
information (count: 3119 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3119 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186731275	chr2:134067149-134067150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533721091	chr2:134067186-134067187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555618197	chr2:134067209-134067210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190004831	chr2:134067228-134067229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535949376	chr2:134067239-134067240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75560716	chr2:134067261-134067262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182666344	chr2:134067318-134067319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188070047	chr2:134067353-134067354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145021543	chr2:134067357-134067358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573495105	chr2:134067539-134067540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376195834	chr2:134067569-134067570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540384741	chr2:134067573-134067574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545506166	chr2:134067584-134067585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564039687	chr2:134067636-134067637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561949917	chr2:134067659-134067660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537733365	chr2:134067660-134067661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529493149	chr2:134067666-134067667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543896316	chr2:134067693-134067694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192727027	chr2:134067697-134067698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532771801	chr2:134067728-134067729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185133991	chr2:134067795-134067796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566616932	chr2:134067824-134067825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2033307	chr2:134067834-134067835	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs376588597	chr2:134067857-134067858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549342482	chr2:134067870-134067871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567457179	chr2:134067880-134067881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538069774	chr2:134067882-134067883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546668803	chr2:134067890-134067891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147549529	chr2:134067896-134067897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561761971	chr2:134067906-134067907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188500016	chr2:134067956-134067957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373159666	chr2:134067988-134067989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192441341	chr2:134067998-134067999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573412546	chr2:134068016-134068017	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149008895	chr2:134068017-134068018	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550735081	chr2:134068143-134068144	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368697798	chr2:134068156-134068157	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555680510	chr2:134068163-134068164	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569083505	chr2:134068178-134068179	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573881390	chr2:134068218-134068219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77175806	chr2:134068220-134068221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184851621	chr2:134068251-134068252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75056171	chr2:134068342-134068343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188149091	chr2:134068356-134068357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560089481	chr2:134068399-134068400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180686177	chr2:134068424-134068425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75923896	chr2:134068538-134068539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549280980	chr2:134068584-134068585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539690162	chr2:134068589-134068590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561191619	chr2:134068625-134068626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134057000-134067800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:134064400-134069000	Weak transcription	Hela-S3	cervix
3	chr2:134067000-134070000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:134067200-134067800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr2:134067400-134067800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:134067600-134068200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:134067800-134068000	Enhancers	NHEK	skin
8	chr2:134067800-134069800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr2:134067800-134072200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:134068000-134068200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:134068200-134070200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:134068200-134072000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:134069000-134070400	Enhancers	Hela-S3	cervix
14	chr2:134069200-134071800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:134069800-134070400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:134069800-134070800	Enhancers	Brain Substantia Nigra	brain
17	chr2:134070000-134070200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:134070000-134070400	Enhancers	NHEK	skin
19	chr2:134070000-134070800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:134070200-134070400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:134070200-134070800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:134070200-134071600	Enhancers	Brain Angular Gyrus	brain
23	chr2:134070200-134082200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:134070400-134072000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr2:134070400-134074200	Weak transcription	Hela-S3	cervix
26	chr2:134070400-134094600	Weak transcription	NHEK	skin
27	chr2:134070800-134074200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:134070800-134074400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:134071200-134081600	Weak transcription	Right Ventricle	heart
30	chr2:134071400-134071600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:134071600-134071800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:134071800-134072400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:134072000-134072600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr2:134072000-134076400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:134072200-134072600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:134074200-134075600	Enhancers	Fetal Stomach	stomach
37	chr2:134074200-134075800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:134074200-134076200	Enhancers	Hela-S3	cervix
39	chr2:134074600-134075200	Enhancers	Colon Smooth Muscle	Colon
40	chr2:134074600-134075200	Enhancers	Placenta Amnion	Placenta Amnion
41	chr2:134075800-134081000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:134076200-134081000	Weak transcription	Hela-S3	cervix
43	chr2:134076400-134078200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:134077000-134078000	Enhancers	Brain Germinal Matrix	brain
45	chr2:134078200-134079200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:134079200-134081000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:134080000-134080600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr2:134080600-134084600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr2:134081000-134084000	Enhancers	Hela-S3	cervix
50	chr2:134081000-134084200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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