Variant report

Variant	nsv1001064
Chromosome Location	chr2:127828941-127862257
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:50)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr2:127846603..127849237-chr2:127850068..127853450,3	K562	blood:
2	chr2:127820803..127824621-chr2:127824894..127830047,6	K562	blood:
3	chr2:127834701..127837421-chr2:127840734..127842424,2	MCF-7	breast:
4	chr2:127829702..127832406-chr2:127833096..127835380,2	K562	blood:
5	chr2:127843180..127845570-chr2:127848864..127852714,3	MCF-7	breast:
6	chr2:127834991..127836623-chr2:127840456..127842151,2	MCF-7	breast:
7	chr2:127818892..127820837-chr2:127828429..127830167,2	MCF-7	breast:
8	chr2:127844458..127846446-chr2:127850246..127851813,2	K562	blood:
9	chr2:127842254..127844330-chr2:127859021..127861716,3	MCF-7	breast:
10	chr2:127846603..127849237-chr2:127850068..127853450,3	K562	blood:
11	chr2:127846711..127850055-chr2:127853164..127855548,3	MCF-7	breast:
12	chr2:127822672..127825565-chr2:127830790..127832845,2	K562	blood:
13	chr2:127854702..127856656-chr2:127856950..127858701,2	MCF-7	breast:
14	chr2:127825651..127827427-chr2:127830304..127832432,2	MCF-7	breast:
15	chr2:127842780..127845072-chr2:127863578..127865079,2	K562	blood:
16	chr2:127823166..127825424-chr2:127856557..127859034,2	MCF-7	breast:
17	chr2:127822004..127823991-chr2:127859645..127861835,2	MCF-7	breast:
18	chr2:127829446..127832299-chr2:127837118..127839537,2	K562	blood:
19	chr2:127853140..127855394-chr2:127860485..127862176,2	MCF-7	breast:
20	chr2:127829446..127832299-chr2:127837118..127839537,2	K562	blood:
21	chr2:127834701..127837421-chr2:127840734..127842424,2	MCF-7	breast:
22	chr2:127846711..127850055-chr2:127853164..127855548,3	MCF-7	breast:
23	chr2:127853337..127855770-chr2:127871735..127873345,2	K562	blood:
24	chr2:127837291..127839948-chr2:127841422..127844629,3	K562	blood:
25	chr2:127841990..127844933-chr2:127856467..127858298,2	K562	blood:
26	chr2:127829702..127832406-chr2:127833096..127835380,2	K562	blood:
27	chr2:127837291..127839948-chr2:127841422..127844629,3	K562	blood:
28	chr2:127825324..127826896-chr2:127856890..127859750,2	MCF-7	breast:
29	chr2:127834991..127836623-chr2:127840456..127842151,2	MCF-7	breast:
30	chr2:127843180..127845570-chr2:127848864..127852714,3	MCF-7	breast:
31	chr2:127841990..127844933-chr2:127856467..127858298,2	K562	blood:
32	chr2:127840601..127843824-chr2:127844844..127848160,4	K562	blood:
33	chr2:127829694..127830341-chr2:127897153..127898129,2	MCF-7	breast:
34	chr2:127824897..127826990-chr2:127827722..127829890,2	K562	blood:
35	chr2:127825223..127826267-chr2:127857805..127858865,3	MCF-7	breast:
36	chr2:127854702..127856656-chr2:127856950..127858701,2	MCF-7	breast:
37	chr2:127853140..127855394-chr2:127860485..127862176,2	MCF-7	breast:
38	chr2:127837345..127839578-chr2:127840445..127843454,3	MCF-7	breast:
39	chr2:127857696..127862567-chr2:127862895..127866178,8	MCF-7	breast:
40	chr2:127840959..127842662-chr2:127845324..127846999,2	K562	blood:
41	chr2:127839430..127842816-chr2:127848432..127852029,4	MCF-7	breast:
42	chr2:127852372..127854342-chr2:127858358..127859956,2	MCF-7	breast:
43	chr2:127822717..127824541-chr2:127837362..127839026,2	MCF-7	breast:
44	chr2:127852372..127854342-chr2:127858358..127859956,2	MCF-7	breast:
45	chr2:127840601..127843824-chr2:127844844..127848160,4	K562	blood:
46	chr2:127837345..127839578-chr2:127840445..127843454,3	MCF-7	breast:
47	chr2:127844458..127846446-chr2:127850246..127851813,2	K562	blood:
48	chr2:127840959..127842662-chr2:127845324..127846999,2	K562	blood:
49	chr2:127842254..127844330-chr2:127859021..127861716,3	MCF-7	breast:
50	chr2:127839430..127842816-chr2:127848432..127852029,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP27C1-1	chr2:127861773-127862104	expReg_chr2_9105_-

No data

Variant related genes	Relation type
ENSG00000136717	chromatin interactions

Extended variants
information (count: 1440 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1440 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3820757	chr2:127828941-127828942	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564140546	chr2:127828967-127828968	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs80327618	chr2:127828998-127828999	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538627877	chr2:127829011-127829012	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs565460692	chr2:127829014-127829015	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575744245	chr2:127829036-127829037	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544409196	chr2:127829062-127829063	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560638274	chr2:127829207-127829208	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs529783723	chr2:127829212-127829213	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546174837	chr2:127829244-127829245	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559045710	chr2:127829258-127829259	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs3768857	chr2:127829282-127829283	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs142922248	chr2:127829304-127829305	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544443782	chr2:127829306-127829307	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188135316	chr2:127829332-127829333	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372296076	chr2:127829358-127829359	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569067102	chr2:127829369-127829370	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560874390	chr2:127829383-127829384	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77552350	chr2:127829396-127829397	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567742171	chr2:127829435-127829436	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111433960	chr2:127829436-127829437	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574686392	chr2:127829442-127829443	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536777442	chr2:127829490-127829491	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146156504	chr2:127829535-127829536	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540499050	chr2:127829566-127829567	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs74857591	chr2:127829589-127829590	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115175917	chr2:127829614-127829615	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559163112	chr2:127829624-127829625	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575572242	chr2:127829701-127829702	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs75836995	chr2:127829704-127829705	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561171922	chr2:127829729-127829730	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs532171950	chr2:127829730-127829731	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140157570	chr2:127829737-127829738	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539914820	chr2:127829758-127829759	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559996825	chr2:127829768-127829769	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112207767	chr2:127829771-127829772	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532094071	chr2:127829780-127829781	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551926182	chr2:127829794-127829795	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142455801	chr2:127829800-127829801	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs752780	chr2:127829801-127829802	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs150833590	chr2:127829831-127829832	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs180937337	chr2:127829874-127829875	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186338330	chr2:127829883-127829884	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533999122	chr2:127829907-127829908	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547024126	chr2:127829937-127829938	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs3754609	chr2:127829943-127829944	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs539011808	chr2:127829963-127829964	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375398827	chr2:127829964-127829965	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs575508992	chr2:127829965-127829966	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190942625	chr2:127829980-127829981	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1789 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127808600-127834200	Strong transcription	Primary T cells from cord blood	blood
2	chr2:127815200-127850800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:127816000-127829000	Weak transcription	Aorta	Aorta
4	chr2:127816600-127829600	Weak transcription	Brain Germinal Matrix	brain
5	chr2:127816800-127831200	Weak transcription	Fetal Brain Female	brain
6	chr2:127817200-127833800	Genic enhancers	Spleen	Spleen
7	chr2:127818400-127844400	Genic enhancers	Fetal Muscle Leg	muscle
8	chr2:127821200-127838600	Genic enhancers	Fetal Muscle Trunk	muscle
9	chr2:127821800-127829200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:127821800-127830000	Genic enhancers	Brain Substantia Nigra	brain
11	chr2:127821800-127830200	Genic enhancers	Brain Inferior Temporal Lobe	brain
12	chr2:127822000-127830200	Genic enhancers	Brain Cingulate Gyrus	brain
13	chr2:127822200-127829600	Genic enhancers	Brain Anterior Caudate	brain
14	chr2:127822800-127836600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:127822800-127836800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr2:127823000-127829800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr2:127823000-127832800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr2:127823200-127830600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr2:127823200-127831800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr2:127823200-127832600	Weak transcription	GM12878-XiMat	blood
21	chr2:127823200-127838200	Weak transcription	Left Ventricle	heart
22	chr2:127823400-127839200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr2:127823600-127838800	Weak transcription	Fetal Kidney	kidney
24	chr2:127824000-127838400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr2:127824800-127830000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr2:127824800-127830400	Genic enhancers	Brain Angular Gyrus	brain
27	chr2:127825000-127830400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr2:127825000-127831000	Strong transcription	Thymus	Thymus
29	chr2:127825200-127829000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:127825400-127832400	Weak transcription	Right Atrium	heart
31	chr2:127825600-127829400	Strong transcription	HSMMtube	muscle
32	chr2:127825600-127836600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr2:127825600-127840000	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr2:127825800-127830200	Weak transcription	HSMM	muscle
35	chr2:127825800-127830200	Weak transcription	NHDF-Ad	bronchial
36	chr2:127825800-127830600	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr2:127825800-127830600	Weak transcription	Fetal Heart	heart
38	chr2:127825800-127830800	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr2:127825800-127831000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr2:127825800-127832000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:127825800-127834600	Weak transcription	NHEK	skin
42	chr2:127825800-127835600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:127825800-127836600	Weak transcription	Pancreas	Pancrea
44	chr2:127825800-127836600	Weak transcription	Osteobl	bone
45	chr2:127825800-127838400	Weak transcription	HUVEC	blood vessel
46	chr2:127826000-127829800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr2:127826000-127830000	Strong transcription	Stomach Smooth Muscle	stomach
48	chr2:127826000-127830600	Strong transcription	Fetal Intestine Small	intestine
49	chr2:127826000-127830600	Strong transcription	Fetal Stomach	stomach
50	chr2:127826000-127830800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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