Variant report

Variant	nsv914146
Chromosome Location	chr21:47838123-47858248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:1464)
Chromatin interactive
region (count:34)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 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	BACH1	chr21:47843931-47844247	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr21:47840574-47840684	K562	blood:	n/a	n/a
3	CEBPB	chr21:47855134-47855161	K562	blood:	n/a	n/a
4	CHD2	chr21:47854192-47854246	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr21:47840497-47840686	GM19239	blood:	n/a	n/a
6	CTCF	chr21:47841120-47841247	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr21:47841100-47841227	GM12892	blood:	n/a	n/a
8	CTCF	chr21:47840500-47840650	HRE	kidney:	n/a	n/a
9	CTCF	chr21:47840491-47840681	GM19238	blood:	n/a	n/a
10	CTCF	chr21:47840840-47840990	HA-sp	spinal cord:	n/a	n/a
11	CTCF	chr21:47841020-47841170	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr21:47841045-47841260	GM12891	blood:	n/a	n/a
13	CTCF	chr21:47840560-47840710	HEK293	kidney:	n/a	n/a
14	CTCF	chr21:47840513-47840657	Fibrobl	skin:	n/a	n/a
15	CTCF	chr21:47841125-47841158	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr21:47841060-47841210	K562	blood:	n/a	n/a
17	CTCF	chr21:47841143-47841219	LNCaP	prostate:	n/a	n/a
18	CTCF	chr21:47840440-47840590	AG09309	skin:	n/a	n/a
19	CTCF	chr21:47841120-47841270	MCF-7	breast:	n/a	chr21:47841250-47841263
20	CTCF	chr21:47840460-47840610	HepG2	liver:	n/a	n/a
21	CTCF	chr21:47841135-47841226	NHEK	skin:	n/a	n/a
22	CTCF	chr21:47840534-47840651	HepG2	liver:	n/a	n/a
23	CTCF	chr21:47841130-47841160	GM10266	blood:	n/a	n/a
24	CTCF	chr21:47840520-47840670	GM12864	blood:	n/a	n/a
25	CTCF	chr21:47841200-47841350	HFF-Myc	foreskin:	n/a	chr21:47841250-47841263 chr21:47841312-47841325
26	CTCF	chr21:47840480-47840630	HPF	lung:	n/a	n/a
27	CTCF	chr21:47840440-47840590	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr21:47844040-47844190	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr21:47841131-47841241	MCF-7	breast:	n/a	n/a
30	CTCF	chr21:47841084-47841261	MCF-7	breast:	n/a	n/a
31	CTCF	chr21:47841100-47841250	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr21:47840475-47840704	MCF-7	breast:	n/a	n/a
33	CTCF	chr21:47840560-47840710	K562	blood:	n/a	n/a
34	CTCF	chr21:47840484-47840597	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr21:47840510-47840651	K562	blood:	n/a	n/a
36	CTCF	chr21:47844020-47844170	HepG2	liver:	n/a	n/a
37	CTCF	chr21:47840469-47840689	MCF-7	breast:	n/a	n/a
38	CTCF	chr21:47841040-47841190	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr21:47840601-47840609	LNCaP	prostate:	n/a	n/a
40	CTCF	chr21:47840460-47840610	BE2_C	brain:	n/a	n/a
41	CTCF	chr21:47840480-47840630	AG04449	skin:	n/a	n/a
42	CTCF	chr21:47840500-47840650	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr21:47840497-47840674	A549	lung:	n/a	n/a
44	CTCF	chr21:47841094-47841249	A549	lung:	n/a	n/a
45	CTCF	chr21:47844040-47844190	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr21:47841085-47841263	MCF-7	breast:	n/a	chr21:47841250-47841263
47	CTCF	chr21:47841064-47841145	ProgFib	skin:	n/a	n/a
48	CTCF	chr21:47840557-47840623	GM10266	blood:	n/a	n/a
49	CTCF	chr21:47840540-47840690	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr21:47841140-47841290	HUVEC	blood vessel:	n/a	chr21:47841250-47841263

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47856140-47856190	BE2_C	brain:	n/a
2	chr21:47850317-47850367	HAEpiC	amniotic membrane:	n/a
3	chr21:47847919-47847969	AoSMC	blood vessel:	n/a
4	chr21:47851742-47851792	PrEC	prostate:	n/a
5	chr21:47844134-47844184	NHDF-neo	bronchial:	n/a
6	chr21:47855049-47855099	GM12892	blood:	n/a
7	chr21:47855893-47855943	AG09319	gingival:	n/a
8	chr21:47856215-47856265	SK-N-MC	brain:	n/a
9	chr21:47842207-47842257	NHBE	bronchial:	n/a
10	chr21:47849050-47849100	GM12878	blood:	n/a
11	chr21:47856020-47856070	HepG2	liver:	n/a
12	chr21:47851941-47851991	AG09309	skin:	n/a
13	chr21:47851941-47851991	HL-60	blood:	n/a
14	chr21:47845737-47845787	NHDF-neo	bronchial:	n/a
15	chr21:47856215-47856265	HIPEpiC	eye:	n/a
16	chr21:47856215-47856265	K562	blood:	n/a
17	chr21:47851545-47851595	U87	brain:	n/a
18	chr21:47845863-47845913	HRCEpiC	kidney:	n/a
19	chr21:47844134-47844184	AoSMC	blood vessel:	n/a
20	chr21:47845863-47845913	HEK293	kidney:	embryo
21	chr21:47851470-47851520	GM12878	blood:	n/a
22	chr21:47845863-47845913	HCPEpiC	choroid plexus:	n/a
23	chr21:47845788-47845838	AG04449	skin:	fetal
24	chr21:47855049-47855099	SK-N-SH	brain:	n/a
25	chr21:47856215-47856265	LNCaP	prostate:	n/a
26	chr21:47844012-47844062	ovcar-3	ovarian:	n/a
27	chr21:47856140-47856190	HCF	heart:	n/a
28	chr21:47851941-47851991	AG09319	gingival:	n/a
29	chr21:47846235-47846285	T-47D	breast:	n/a
30	chr21:47856020-47856070	HEK293	kidney:	embryo
31	chr21:47851742-47851792	A549	lung:	n/a
32	chr21:47848216-47848266	HCT-116	colon:	n/a
33	chr21:47847919-47847969	RPTEC	kidney:	n/a
34	chr21:47844134-47844184	HNPCEpiC	eye:	n/a
35	chr21:47844134-47844184	Jurkat	blood:	n/a
36	chr21:47851545-47851595	AG04450	lung:	fetal
37	chr21:47845788-47845838	PrEC	prostate:	n/a
38	chr21:47856020-47856070	Hela-S3	cervix:	n/a
39	chr21:47842207-47842257	HRE	kidney:	n/a
40	chr21:47851470-47851520	HL-60	blood:	n/a
41	chr21:47851742-47851792	IMR90	lung:	fetal
42	chr21:47851742-47851792	HPAEpiC	pulmonary alveolar:	n/a
43	chr21:47848216-47848266	HIPEpiC	eye:	n/a
44	chr21:47856020-47856070	HUVEC	blood vessel:	n/a
45	chr21:47851470-47851520	HCT-116	colon:	n/a
46	chr21:47844012-47844062	GM12878	blood:	n/a
47	chr21:47849050-47849100	H1-hESC	embryonic stem cell:	embryo
48	chr21:47842207-47842257	AG04449	skin:	fetal
49	chr21:47851941-47851991	U87	brain:	n/a
50	chr21:47842207-47842257	GM12892	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47649218..47651291-chr21:47846633..47848855,2	K562	blood:
2	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
3	chr21:47854363..47856833-chr21:47869358..47873122,3	MCF-7	breast:
4	chr21:47841259..47843546-chr21:47843811..47847040,4	K562	blood:
5	chr21:47845101..47846658-chr21:47877111..47880034,2	K562	blood:
6	chr21:47853352..47856633-chr21:47878140..47880096,4	MCF-7	breast:
7	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
8	chr21:47845265..47847081-chr21:47878915..47881102,2	K562	blood:
9	chr21:47842082..47844141-chr21:47845967..47848443,2	K562	blood:
10	chr21:47854459..47856094-chr21:47859695..47861438,2	K562	blood:
11	chr21:47746558..47749011-chr21:47851647..47853522,2	K562	blood:
12	chr21:47836799..47839696-chr21:47847990..47849925,2	K562	blood:
13	chr21:47857857..47859725-chr21:47876652..47878543,2	MCF-7	breast:
14	chr21:47844449..47847171-chr21:47854131..47855917,2	K562	blood:
15	chr21:47857607..47860157-chr21:47877897..47880411,2	MCF-7	breast:
16	chr21:47841235..47843966-chr21:47874444..47876872,2	K562	blood:
17	chr21:47842082..47844141-chr21:47845967..47848443,2	K562	blood:
18	chr21:47856273..47858659-chr21:47860032..47862884,2	K562	blood:
19	chr21:47839369..47841083-chr21:47878532..47880064,2	K562	blood:
20	chr21:47843264..47847636-chr21:47874814..47878644,6	K562	blood:
21	chr21:47841259..47843546-chr21:47843811..47847040,4	K562	blood:
22	chr21:47792720..47794427-chr21:47846612..47849567,2	K562	blood:
23	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
24	chr21:47857792..47859466-chr21:47861182..47863133,2	MCF-7	breast:
25	chr21:47838816..47841237-chr21:47842476..47844122,2	K562	blood:
26	chr21:47770994..47773091-chr21:47844111..47846045,2	K562	blood:
27	chr21:47844449..47847171-chr21:47854131..47855917,2	K562	blood:
28	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
29	chr21:47848467..47851272-chr21:47852866..47855440,2	K562	blood:
30	chr21:47856507..47858157-chr21:47860635..47863396,2	MCF-7	breast:
31	chr21:47843582..47848242-chr21:47854131..47857783,6	K562	blood:
32	chr21:47836799..47839696-chr21:47847990..47849925,2	K562	blood:
33	chr21:47839389..47841162-chr21:47847458..47849832,2	MCF-7	breast:
34	chr21:47742209..47744590-chr21:47846184..47848146,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C21orf58-3	chr21:47840467-47840948	NONHSAT083067

No data

Variant related genes	Relation type
PCNT	TF binding region
RPL18AP2	TF binding region
PCNT	CpG island
RPL18AP2	CpG island
ENSG00000160298	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000225043	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000215424	chromatin interactions

Extended variants
information (count: 1163 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1163 , 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	rs2839246	chr21:47838123-47838124	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148444313	chr21:47838129-47838130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537029143	chr21:47838130-47838131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143541917	chr21:47838149-47838150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61735813	chr21:47838153-47838154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201728927	chr21:47838173-47838174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369196091	chr21:47838178-47838179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35848602	chr21:47838182-47838183	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144612972	chr21:47838202-47838203	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138506849	chr21:47838207-47838208	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201161106	chr21:47838252-47838253	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553205944	chr21:47838284-47838285	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577873932	chr21:47838316-47838317	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546337623	chr21:47838322-47838323	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113445591	chr21:47838325-47838326	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531640177	chr21:47838326-47838327	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543784663	chr21:47838342-47838343	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562286408	chr21:47838357-47838358	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529588770	chr21:47838358-47838359	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560521637	chr21:47838362-47838363	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187395012	chr21:47838394-47838395	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559535311	chr21:47838419-47838420	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs60124276	chr21:47838421-47838422	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs58572600	chr21:47838443-47838444	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs73146772	chr21:47838477-47838478	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536685114	chr21:47838479-47838480	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146029093	chr21:47838495-47838496	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368959075	chr21:47838597-47838598	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369736286	chr21:47838604-47838605	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567103487	chr21:47838608-47838609	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534928606	chr21:47838627-47838628	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553271552	chr21:47838636-47838637	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577937212	chr21:47838657-47838658	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538817398	chr21:47838668-47838669	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534832409	chr21:47838671-47838672	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2268524	chr21:47838700-47838701	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs190499817	chr21:47838712-47838713	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184073859	chr21:47838716-47838717	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188957586	chr21:47838720-47838721	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs193039716	chr21:47838726-47838727	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115728365	chr21:47838737-47838738	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541347504	chr21:47838745-47838746	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559595985	chr21:47838746-47838747	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568964910	chr21:47838756-47838757	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35372646	chr21:47838771-47838772	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538102420	chr21:47838788-47838789	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533383578	chr21:47838796-47838797	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551547825	chr21:47838800-47838801	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182904246	chr21:47838860-47838861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs16979185	chr21:47838868-47838869	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47775600-47857600	Weak transcription	Stomach Mucosa	stomach
2	chr21:47789400-47842600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr21:47802200-47842600	Strong transcription	Dnd41	blood
4	chr21:47803200-47872400	Weak transcription	Fetal Kidney	kidney
5	chr21:47803600-47842600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr21:47804800-47843000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr21:47804800-47843000	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr21:47804800-47843400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr21:47809800-47842600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr21:47814400-47861000	Weak transcription	Fetal Brain Male	brain
11	chr21:47818400-47850200	Weak transcription	Small Intestine	intestine
12	chr21:47818600-47842600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr21:47820400-47851200	Weak transcription	NH-A	brain
14	chr21:47822800-47843000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr21:47823200-47850200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr21:47823400-47840000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr21:47827400-47866600	Strong transcription	Fetal Stomach	stomach
18	chr21:47827600-47842600	Strong transcription	Primary T cells from cord blood	blood
19	chr21:47827800-47842800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr21:47828000-47863200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr21:47828600-47872400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr21:47828800-47843200	Strong transcription	Fetal Muscle Leg	muscle
23	chr21:47829200-47843000	Strong transcription	Left Ventricle	heart
24	chr21:47829200-47843200	Strong transcription	Thymus	Thymus
25	chr21:47829400-47843200	Strong transcription	Fetal Muscle Trunk	muscle
26	chr21:47829400-47862600	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chr21:47829400-47867800	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr21:47829600-47842000	Strong transcription	Fetal Thymus	thymus
29	chr21:47829600-47842800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr21:47829600-47843000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr21:47829600-47843200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr21:47829600-47862800	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr21:47829600-47864000	Strong transcription	Fetal Intestine Small	intestine
34	chr21:47829800-47838600	Strong transcription	Spleen	Spleen
35	chr21:47829800-47842800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr21:47829800-47842800	Strong transcription	Right Ventricle	heart
37	chr21:47829800-47843000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr21:47830000-47842800	Strong transcription	Pancreas	Pancrea
39	chr21:47830000-47843200	Strong transcription	Adipose Nuclei	Adipose
40	chr21:47830000-47843400	Strong transcription	Stomach Smooth Muscle	stomach
41	chr21:47830200-47862800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr21:47830400-47842800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr21:47830400-47843200	Strong transcription	Placenta	Placenta
44	chr21:47830400-47862800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr21:47830600-47842200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr21:47830600-47843000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr21:47830800-47839800	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr21:47831000-47839000	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr21:47831000-47839000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr21:47831000-47839200	Weak transcription	Primary B cells from cord blood	blood

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