Variant report

Variant	nsv1003964
Chromosome Location	chr2:134039363-134088319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:244)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:134084062-134084604	A549	lung:	n/a	chr2:134084326-134084335 chr2:134084327-134084336
2	BHLHE40	chr2:134069959-134070256	GM12878	blood:	n/a	n/a
3	BRCA1	chr2:134081191-134081206	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr2:134084130-134084724	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:134061949-134062267	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:134044066-134044190	K562	blood:	n/a	n/a
7	CEBPB	chr2:134043906-134044270	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:134043848-134044248	MCF-7	breast:	n/a	n/a
9	CEBPB	chr2:134069908-134070215	A549	lung:	n/a	n/a
10	CEBPB	chr2:134043889-134044238	A549	lung:	n/a	n/a
11	CEBPB	chr2:134045260-134045655	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:134043975-134044199	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:134054015-134054327	IMR90	lung:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
14	CEBPB	chr2:134064374-134064789	A549	lung:	n/a	chr2:134064375-134064388
15	CEBPB	chr2:134074709-134075358	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:134084072-134085004	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:134053980-134054421	Hela-S3	cervix:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
18	CEBPB	chr2:134081659-134082211	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:134043877-134044226	MCF-7	breast:	n/a	n/a
20	CEBPB	chr2:134069498-134070230	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:134081859-134082203	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:134043852-134044617	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:134061988-134062277	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:134084251-134084922	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:134084078-134084970	A549	lung:	n/a	n/a
26	CEBPB	chr2:134051161-134051752	IMR90	lung:	n/a	chr2:134051271-134051288
27	CEBPB	chr2:134043932-134044239	A549	lung:	n/a	n/a
28	CEBPB	chr2:134062013-134062244	A549	lung:	n/a	n/a
29	CEBPB	chr2:134043952-134044155	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:134062054-134062195	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:134074848-134075050	IMR90	lung:	n/a	n/a
32	CHD2	chr2:134081477-134082104	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr2:134084103-134084638	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr2:134084098-134084570	A549	lung:	n/a	n/a
35	CREB1	chr2:134084237-134084570	A549	lung:	n/a	n/a
36	CTCF	chr2:134072440-134072590	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr2:134044040-134044190	AG04450	lung:	n/a	chr2:134044135-134044144
38	CTCF	chr2:134072460-134072610	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr2:134044080-134044230	AG09309	skin:	n/a	chr2:134044135-134044144
40	CTCF	chr2:134072440-134072590	AG04450	lung:	n/a	n/a
41	CTCF	chr2:134044260-134044410	AG04450	lung:	n/a	n/a
42	CTCF	chr2:134052473-134052577	HUVEC	blood vessel:	n/a	chr2:134052511-134052521
43	CTCF	chr2:134044480-134044630	HPF	lung:	n/a	n/a
44	CTCF	chr2:134044100-134044250	AG04449	skin:	n/a	chr2:134044135-134044144
45	CTCF	chr2:134051340-134051490	AG04449	skin:	n/a	chr2:134051397-134051406
46	CTCF	chr2:134083520-134083627	Hela-S3	cervix:	n/a	chr2:134083569-134083577
47	CTCF	chr2:134087649-134087715	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr2:134044120-134044270	HCPEpiC	choroid plexus:	n/a	chr2:134044135-134044144
49	CTCF	chr2:134072460-134072610	HCFaa	heart:	n/a	n/a
50	CTCF	chr2:134084700-134084850	HCPEpiC	choroid plexus:	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	chr2:134083495-134083545	U87	brain:	n/a
2	chr2:134052012-134052062	HAEpiC	amniotic membrane:	n/a
3	chr2:134068922-134068972	GM19239	blood:	n/a
4	chr2:134068922-134068972	GM06990	blood:	n/a
5	chr2:134083495-134083545	RPTEC	kidney:	n/a
6	chr2:134083495-134083545	GM06990	blood:	n/a
7	chr2:134075125-134075175	HIPEpiC	eye:	n/a
8	chr2:134075125-134075175	GM12878	blood:	n/a
9	chr2:134075125-134075175	GM12891	blood:	n/a
10	chr2:134075125-134075175	AG04450	lung:	fetal
11	chr2:134083495-134083545	IMR90	lung:	fetal
12	chr2:134068922-134068972	HIPEpiC	eye:	n/a
13	chr2:134083495-134083545	ECC-1	luminal epithelium:	n/a
14	chr2:134068922-134068972	AG09309	skin:	n/a
15	chr2:134083495-134083545	SK-N-SH	brain:	n/a
16	chr2:134083495-134083545	H1-hESC	embryonic stem cell:	embryo
17	chr2:134052012-134052062	T-47D	breast:	n/a
18	chr2:134052012-134052062	HCPEpiC	choroid plexus:	n/a
19	chr2:134083495-134083545	A549	lung:	n/a
20	chr2:134075125-134075175	AoSMC	blood vessel:	n/a
21	chr2:134068922-134068972	H1-hESC	embryonic stem cell:	embryo
22	chr2:134052012-134052062	SAEC	small airway:	n/a
23	chr2:134083495-134083545	NHBE	bronchial:	n/a
24	chr2:134052012-134052062	GM19239	blood:	n/a
25	chr2:134068922-134068972	GM12878	blood:	n/a
26	chr2:134052012-134052062	HepG2	liver:	n/a
27	chr2:134052012-134052062	GM06990	blood:	n/a
28	chr2:134083495-134083545	HIPEpiC	eye:	n/a
29	chr2:134052012-134052062	GM12878	blood:	n/a
30	chr2:134052012-134052062	SK-N-SH_RA	brain:	n/a
31	chr2:134083495-134083545	GM12891	blood:	n/a
32	chr2:134068922-134068972	HEK293	kidney:	embryo
33	chr2:134068922-134068972	MCF10A-Er-Src	breast:	n/a
34	chr2:134083495-134083545	HCPEpiC	choroid plexus:	n/a
35	chr2:134075125-134075175	ProgFib	skin:	n/a
36	chr2:134075125-134075175	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:134075125-134075175	SK-N-SH	brain:	n/a
38	chr2:134052012-134052062	U87	brain:	n/a
39	chr2:134083495-134083545	SKMC	muscle:	n/a
40	chr2:134052012-134052062	AG09309	skin:	n/a
41	chr2:134083495-134083545	HCM	heart:	n/a
42	chr2:134083495-134083545	HCF	heart:	n/a
43	chr2:134052012-134052062	AG04449	skin:	fetal
44	chr2:134083495-134083545	Jurkat	blood:	n/a
45	chr2:134052012-134052062	NHDF-neo	bronchial:	n/a
46	chr2:134083495-134083545	HMEC	breast:	n/a
47	chr2:134052012-134052062	AG10803	skin:	n/a
48	chr2:134075125-134075175	HCM	heart:	n/a
49	chr2:134083495-134083545	HEEpiC	esophagus:	n/a
50	chr2:134075125-134075175	BJ	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:134084453..134086561-chr2:134089070..134091697,3	MCF-7	breast:
2	chr2:134086116..134088912-chr2:134093493..134094997,2	MCF-7	breast:
3	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
4	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
5	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
6	chr2:134072524..134074621-chr2:134077160..134080145,2	K562	blood:
7	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
8	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
9	chr2:134072524..134074621-chr2:134077160..134080145,2	K562	blood:
10	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
11	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
12	chr2:134083491..134086031-chr2:134262913..134265457,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-4	chr2:134042267-134042330	NR_110294
2	lnc-GPR39-4	chr2:134042267-134042334	ENSG00000226953

No data

Variant related genes	Relation type
RNU6-579P	TF binding region
RNU6-579P	CpG island
ENSG00000252688	chromatin interactions
KIF23	miRNA target sites

Extended variants
information (count: 1681 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1681 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6430407	chr2:134039363-134039364	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147847900	chr2:134039376-134039377	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537228197	chr2:134039380-134039381	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558499934	chr2:134039406-134039407	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148889141	chr2:134039423-134039424	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10185165	chr2:134039468-134039469	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs369625948	chr2:134039477-134039478	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578040073	chr2:134039557-134039558	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554098615	chr2:134039662-134039663	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs207462390	chr2:134039713-134039714	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558900735	chr2:134039756-134039757	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs61632923	chr2:134039814-134039815	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs199817546	chr2:134039842-134039843	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561235784	chr2:134039889-134039890	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6714262	chr2:134039905-134039906	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143552455	chr2:134039945-134039946	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185093953	chr2:134039981-134039982	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543971678	chr2:134040008-134040009	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565357438	chr2:134040071-134040072	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs16823190	chr2:134040149-134040150	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs554317608	chr2:134040180-134040181	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148023002	chr2:134040181-134040182	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141689950	chr2:134040200-134040201	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377186737	chr2:134040213-134040214	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144643180	chr2:134040216-134040217	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548243440	chr2:134040238-134040239	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569943974	chr2:134040267-134040268	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536967579	chr2:134040282-134040283	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190001760	chr2:134040285-134040286	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182585740	chr2:134040334-134040335	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539077577	chr2:134040350-134040351	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529316089	chr2:134040389-134040390	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553847375	chr2:134040397-134040398	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78628459	chr2:134040411-134040412	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572245163	chr2:134040449-134040450	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536228841	chr2:134040490-134040491	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554568565	chr2:134040508-134040509	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7577925	chr2:134040519-134040520	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
39	rs543775807	chr2:134040575-134040576	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373391605	chr2:134040577-134040578	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565435901	chr2:134040585-134040586	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138540460	chr2:134040661-134040662	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141511276	chr2:134040717-134040718	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369477552	chr2:134040727-134040728	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559476874	chr2:134040744-134040745	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529844915	chr2:134040797-134040798	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548181258	chr2:134040814-134040815	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563288553	chr2:134040850-134040851	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530795675	chr2:134040870-134040871	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552193725	chr2:134040894-134040895	Strong transcription 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
Breast cancer	22522925	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134028200-134042200	Weak transcription	Hela-S3	cervix
2	chr2:134036000-134043800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:134036200-134042000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:134038000-134042000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:134039200-134043800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:134040000-134040800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:134040200-134040400	Enhancers	NHDF-Ad	bronchial
8	chr2:134040200-134040800	Enhancers	Brain Substantia Nigra	brain
9	chr2:134040400-134040800	Enhancers	Brain Hippocampus Middle	brain
10	chr2:134040600-134042600	Weak transcription	NHDF-Ad	bronchial
11	chr2:134040800-134042200	Weak transcription	Brain Hippocampus Middle	brain
12	chr2:134040800-134042200	Weak transcription	Brain Substantia Nigra	brain
13	chr2:134040800-134045200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:134041800-134042800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr2:134042000-134042200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:134042000-134042800	Enhancers	Brain Cingulate Gyrus	brain
17	chr2:134042000-134046800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:134042200-134042400	Enhancers	Brain Substantia Nigra	brain
19	chr2:134042200-134042800	Enhancers	Brain Hippocampus Middle	brain
20	chr2:134042200-134046000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:134042200-134046400	Enhancers	Hela-S3	cervix
22	chr2:134042400-134042600	Enhancers	NHLF	lung
23	chr2:134042400-134042800	Enhancers	Fetal Muscle Leg	muscle
24	chr2:134042600-134043400	Enhancers	NHDF-Ad	bronchial
25	chr2:134042600-134043800	Weak transcription	NHLF	lung
26	chr2:134042800-134044000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr2:134042800-134051400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr2:134043400-134044200	Weak transcription	NHDF-Ad	bronchial
29	chr2:134043400-134046400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr2:134043800-134044400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr2:134043800-134044600	Enhancers	NHEK	skin
32	chr2:134043800-134046400	Enhancers	NHLF	lung
33	chr2:134043800-134046800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr2:134043800-134047400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:134044000-134045600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:134044000-134046000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:134044200-134046200	Enhancers	Osteobl	bone
38	chr2:134044200-134047200	Enhancers	NHDF-Ad	bronchial
39	chr2:134044400-134045400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:134044600-134050000	Weak transcription	NHEK	skin
41	chr2:134044800-134045200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:134045200-134046000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr2:134045400-134046000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr2:134046000-134051400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:134046000-134060600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:134046200-134050800	Weak transcription	Osteobl	bone
47	chr2:134046400-134050800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr2:134046400-134051200	Weak transcription	NHLF	lung
49	chr2:134046800-134051200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:134046800-134051200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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