Variant report

Variant	nsv587481
Chromosome Location	chr21:40598721-40627020
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:114)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:114 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr21:40619331-40619461	HepG2	liver:	n/a	chr21:40619432-40619443
2	CEBPB	chr21:40616505-40616716	IMR90	lung:	n/a	n/a
3	CEBPB	chr21:40619429-40619504	K562	blood:	n/a	chr21:40619432-40619443
4	CEBPB	chr21:40616462-40616780	HepG2	liver:	n/a	n/a
5	CEBPB	chr21:40619402-40619462	IMR90	lung:	n/a	chr21:40619432-40619443
6	E2F4	chr21:40600667-40600867	MCF10A-Er-Src	breast:	n/a	n/a
7	E2F4	chr21:40605423-40605639	MCF10A-Er-Src	breast:	n/a	n/a
8	EP300	chr21:40603711-40603742	GM12878	blood:	n/a	n/a
9	GATA3	chr21:40624262-40624441	SH-SY5Y	brain:	n/a	n/a
10	GATA3	chr21:40610482-40610589	SH-SY5Y	brain:	n/a	n/a
11	IRF1	chr21:40626776-40626835	K562	blood:	n/a	n/a
12	IRF1	chr21:40614488-40614545	K562	blood:	n/a	n/a
13	IRF1	chr21:40601876-40601878	K562	blood:	n/a	n/a
14	MAFK	chr21:40617913-40618039	HepG2	liver:	n/a	n/a
15	MAZ	chr21:40602436-40602497	GM12878	blood:	n/a	n/a
16	MXI1	chr21:40616697-40616732	GM12878	blood:	n/a	n/a
17	MXI1	chr21:40599550-40599558	GM12878	blood:	n/a	n/a
18	MYC	chr21:40620489-40620511	MCF-7	breast:	n/a	n/a
19	MYC	chr21:40599966-40600071	H1-hESC	embryonic stem cell:	n/a	n/a
20	MYC	chr21:40600079-40600159	MCF-7	breast:	n/a	n/a
21	MYC	chr21:40607774-40607778	MCF-7	breast:	n/a	n/a
22	MYC	chr21:40607744-40607773	MCF-7	breast:	n/a	n/a
23	MYC	chr21:40620431-40620519	MCF-7	breast:	n/a	n/a
24	NFYB	chr21:40611668-40611888	GM12878	blood:	n/a	n/a
25	POLR2A	chr21:40620435-40620454	Gliobla	brain:	n/a	n/a
26	POLR2A	chr21:40606162-40606501	K562	blood:	n/a	n/a
27	POLR2A	chr21:40600815-40601168	K562	blood:	n/a	n/a
28	POLR2A	chr21:40607196-40607275	ProgFib	skin:	n/a	n/a
29	POLR2A	chr21:40602095-40602344	ProgFib	skin:	n/a	n/a
30	POLR2A	chr21:40608363-40608377	MCF-7	breast:	n/a	n/a
31	POLR2A	chr21:40601743-40601772	Gliobla	brain:	n/a	n/a
32	POLR2A	chr21:40602065-40603036	K562	blood:	n/a	n/a
33	POLR2A	chr21:40620340-40620466	MCF-7	breast:	n/a	n/a
34	POLR2A	chr21:40608310-40608325	MCF-7	breast:	n/a	n/a
35	POLR2A	chr21:40617575-40617723	MCF-7	breast:	n/a	n/a
36	POLR2A	chr21:40616561-40616765	K562	blood:	n/a	n/a
37	POLR2A	chr21:40620236-40620258	MCF-7	breast:	n/a	n/a
38	POLR2A	chr21:40599062-40599436	K562	blood:	n/a	n/a
39	POLR2A	chr21:40619585-40619854	K562	blood:	n/a	n/a
40	POLR2A	chr21:40598862-40598877	MCF-7	breast:	n/a	n/a
41	POLR2A	chr21:40618184-40618637	K562	blood:	n/a	n/a
42	POLR2A	chr21:40598817-40598832	MCF-7	breast:	n/a	n/a
43	POLR2A	chr21:40598910-40599070	MCF-7	breast:	n/a	n/a
44	POLR2A	chr21:40599971-40599992	MCF-7	breast:	n/a	n/a
45	POLR2A	chr21:40620509-40620513	MCF-7	breast:	n/a	n/a
46	POLR2A	chr21:40605835-40605848	A549	lung:	n/a	n/a
47	POLR2A	chr21:40607885-40608046	HepG2	liver:	n/a	n/a
48	POLR2A	chr21:40606896-40607079	ProgFib	skin:	n/a	n/a
49	POLR2A	chr21:40621147-40621190	MCF-7	breast:	n/a	n/a
50	POLR2A	chr21:40609250-40609276	GM12878	blood:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:40586470..40588300-chr21:40610304..40612724,2	K562	blood:
2	chr21:40602448..40605045-chr21:40605736..40607319,2	K562	blood:
3	chr21:40555075..40556681-chr21:40622988..40625845,2	K562	blood:
4	chr21:40597729..40601273-chr21:40623831..40625559,3	K562	blood:
5	chr21:40604603..40606220-chr21:40613422..40615728,2	K562	blood:
6	chr21:40604601..40607063-chr21:40608488..40609991,2	MCF-7	breast:
7	chr21:40579156..40581832-chr21:40603360..40605633,2	K562	blood:
8	chr21:40603008..40605391-chr21:40609514..40611568,2	MCF-7	breast:
9	chr21:40598000..40600070-chr21:40608365..40610635,2	K562	blood:
10	chr21:40624621..40626842-chr21:40719575..40722484,2	MCF-7	breast:
11	chr21:40598258..40599808-chr21:40617335..40620196,2	K562	blood:
12	chr21:40605137..40607837-chr21:40613025..40614570,2	MCF-7	breast:
13	chr21:40578990..40581803-chr21:40609609..40612432,2	K562	blood:
14	chr21:40608675..40611131-chr21:40611181..40613899,2	K562	blood:
15	chr21:40602289..40604074-chr21:40606998..40609550,3	MCF-7	breast:
16	chr21:40604601..40607063-chr21:40608488..40609991,2	MCF-7	breast:
17	chr21:40605137..40607837-chr21:40613025..40614570,2	MCF-7	breast:
18	chr21:40625733..40628275-chr21:40724083..40725744,2	MCF-7	breast:
19	chr21:40598000..40600070-chr21:40608365..40610635,2	K562	blood:
20	chr21:40592475..40595061-chr21:40604619..40606247,2	MCF-7	breast:
21	chr21:40626308..40628705-chr21:40634395..40637169,2	K562	blood:
22	chr21:40598258..40599808-chr21:40617335..40620196,2	K562	blood:
23	21:40614587-40619915..21:40757151-40764378	K562	blood:
24	chr21:40602604..40604323-chr21:40607724..40609289,2	K562	blood:
25	chr21:40608675..40611131-chr21:40611181..40613899,2	K562	blood:
26	chr21:40589600..40591908-chr21:40602305..40604047,2	K562	blood:
27	chr21:40617287..40619238-chr21:40626430..40628047,2	MCF-7	breast:
28	chr21:40597729..40601273-chr21:40623831..40625559,3	K562	blood:
29	chr21:40617287..40619238-chr21:40626430..40628047,2	MCF-7	breast:
30	chr21:40554651..40557222-chr21:40599686..40602201,3	K562	blood:
31	chr21:40618746..40621115-chr21:40683986..40686582,2	K562	blood:
32	chr21:40604603..40606220-chr21:40613422..40615728,2	K562	blood:
33	chr21:40553882..40556616-chr21:40598013..40600358,2	K562	blood:
34	chr21:40603008..40605391-chr21:40609514..40611568,2	MCF-7	breast:
35	chr21:40624517..40627116-chr21:40705623..40707478,3	MCF-7	breast:
36	chr21:40602448..40605045-chr21:40605736..40607319,2	K562	blood:
37	chr21:40552597..40556328-chr21:40608189..40610817,3	K562	blood:
38	chr21:40623160..40626100-chr21:40683274..40685842,2	MCF-7	breast:

No data

Variant related genes	Relation type
BRWD1	TF binding region
METTL21AP1	TF binding region
ENSG00000272991	chromatin interactions
ENSG00000185658	chromatin interactions
ENSG00000229623	chromatin interactions
ENSG00000205581	chromatin interactions
ENSG00000255568	chromatin interactions
ENSG00000237373	chromatin interactions
ENSG00000183527	chromatin interactions
ENSG00000182093	chromatin interactions

Extended variants
information (count: 1155 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7276914	chr21:40598721-40598722	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555616519	chr21:40598769-40598770	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs537276139	chr21:40598806-40598807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141223739	chr21:40598830-40598831	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576964118	chr21:40598841-40598842	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531149316	chr21:40598856-40598857	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs553335046	chr21:40598895-40598896	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185183591	chr21:40598915-40598916	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573917469	chr21:40598926-40598927	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146964249	chr21:40598936-40598937	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs541332717	chr21:40598945-40598946	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190825296	chr21:40598997-40598998	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs552460354	chr21:40599059-40599060	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541206868	chr21:40599060-40599061	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs371813225	chr21:40599075-40599076	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs8127969	chr21:40599126-40599127	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs182293745	chr21:40599134-40599135	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370975318	chr21:40599201-40599202	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543674113	chr21:40599224-40599225	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2183576	chr21:40599225-40599226	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs532250459	chr21:40599260-40599261	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551946633	chr21:40599283-40599284	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs11310553	chr21:40599303-40599304	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs565687155	chr21:40599313-40599314	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186945615	chr21:40599327-40599328	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs555185826	chr21:40599367-40599368	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141245570	chr21:40599369-40599370	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs10685999	chr21:40599370-40599371	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs375680217	chr21:40599374-40599375	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs537339830	chr21:40599387-40599388	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs546757758	chr21:40599415-40599416	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs557179024	chr21:40599420-40599421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370523551	chr21:40599489-40599490	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs568495629	chr21:40599510-40599511	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs4816618	chr21:40599529-40599530	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs539553785	chr21:40599627-40599628	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs553156382	chr21:40599648-40599649	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs2836948	chr21:40599677-40599678	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs535507783	chr21:40599693-40599694	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs34642583	chr21:40599698-40599699	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs2026266	chr21:40599720-40599721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs4816619	chr21:40599876-40599877	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs543696472	chr21:40599877-40599878	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs562028726	chr21:40599911-40599912	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs563485599	chr21:40599917-40599918	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577079504	chr21:40599963-40599964	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs529471674	chr21:40600015-40600016	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs147557512	chr21:40600057-40600058	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528175463	chr21:40600068-40600069	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs547918442	chr21:40600075-40600076	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Down syndrome	20877625	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21147910	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40556200-40602600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr21:40563000-40640600	Strong transcription	Placenta	Placenta
3	chr21:40563000-40643600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr21:40563400-40653400	Strong transcription	HUES64 Cell Line	embryonic stem cell
5	chr21:40563400-40660000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr21:40563600-40653600	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr21:40564600-40612600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr21:40565000-40654600	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr21:40565200-40653600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
10	chr21:40565400-40604200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr21:40565400-40612600	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr21:40565400-40653600	Strong transcription	Dnd41	blood
13	chr21:40565600-40615000	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr21:40566000-40653600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr21:40566400-40613200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr21:40569800-40607800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr21:40571400-40602400	Weak transcription	Fetal Brain Male	brain
18	chr21:40572000-40636800	Weak transcription	Psoas Muscle	Psoas
19	chr21:40573800-40631000	Weak transcription	Small Intestine	intestine
20	chr21:40577800-40598800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr21:40578000-40598800	Weak transcription	Gastric	stomach
22	chr21:40578000-40607600	Weak transcription	Aorta	Aorta
23	chr21:40578600-40608000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr21:40578800-40606600	Weak transcription	Brain Substantia Nigra	brain
25	chr21:40579000-40598800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr21:40580400-40606400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr21:40580600-40607600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr21:40580800-40607200	Weak transcription	Spleen	Spleen
29	chr21:40581400-40635400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr21:40581800-40607200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr21:40582200-40614200	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr21:40582600-40602000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr21:40582600-40622000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr21:40582800-40654000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr21:40583600-40606800	Weak transcription	NHLF	lung
36	chr21:40586600-40599200	Weak transcription	Hela-S3	cervix
37	chr21:40587800-40599800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr21:40588000-40599600	Weak transcription	Esophagus	oesophagus
39	chr21:40588000-40601800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr21:40588800-40607800	Weak transcription	Right Ventricle	heart
41	chr21:40589600-40598800	Weak transcription	Lung	lung
42	chr21:40590000-40605600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr21:40590200-40600400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr21:40590200-40607200	Weak transcription	NHEK	skin
45	chr21:40590200-40607600	Weak transcription	Brain Hippocampus Middle	brain
46	chr21:40590200-40608000	Weak transcription	Stomach Mucosa	stomach
47	chr21:40590400-40602000	Weak transcription	Fetal Kidney	kidney
48	chr21:40590400-40604600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr21:40590600-40602400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr21:40590600-40607400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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