Variant report

Variant	nsv819608
Chromosome Location	chr21:47836122-47863025
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:1527)
Chromatin interactive
region (count:54)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:47862928-47863303	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr21:47843931-47844247	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr21:47840574-47840684	K562	blood:	n/a	n/a
4	CEBPB	chr21:47855134-47855161	K562	blood:	n/a	n/a
5	CEBPB	chr21:47837031-47837245	K562	blood:	n/a	n/a
6	CEBPB	chr21:47859695-47859943	HepG2	liver:	n/a	n/a
7	CHD2	chr21:47854192-47854246	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr21:47844120-47844270	GM12875	blood:	n/a	n/a
9	CTCF	chr21:47841084-47841261	MCF-7	breast:	n/a	n/a
10	CTCF	chr21:47840522-47840644	NHEK	skin:	n/a	n/a
11	CTCF	chr21:47841080-47841230	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr21:47841120-47841270	MCF-7	breast:	n/a	chr21:47841250-47841263
13	CTCF	chr21:47840460-47840610	GM06990	blood:	n/a	n/a
14	CTCF	chr21:47840500-47840650	BE2_C	brain:	n/a	n/a
15	CTCF	chr21:47844040-47844190	HEK293	kidney:	n/a	n/a
16	CTCF	chr21:47841100-47841250	GM12873	blood:	n/a	n/a
17	CTCF	chr21:47840445-47840748	GM12878	blood:	n/a	n/a
18	CTCF	chr21:47840540-47840690	GM06990	blood:	n/a	n/a
19	CTCF	chr21:47844100-47844250	GM12871	blood:	n/a	n/a
20	CTCF	chr21:47840473-47840725	MCF-7	breast:	n/a	n/a
21	CTCF	chr21:47841124-47841251	GM19238	blood:	n/a	n/a
22	CTCF	chr21:47841143-47841219	GM19240	blood:	n/a	n/a
23	CTCF	chr21:47841135-47841226	NHEK	skin:	n/a	n/a
24	CTCF	chr21:47840492-47840682	MCF-7	breast:	n/a	n/a
25	CTCF	chr21:47841141-47841197	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr21:47841126-47841263	K562	blood:	n/a	chr21:47841250-47841263
27	CTCF	chr21:47840513-47840657	Fibrobl	skin:	n/a	n/a
28	CTCF	chr21:47840480-47840630	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr21:47840548-47840667	ProgFib	skin:	n/a	n/a
30	CTCF	chr21:47840500-47840650	HCT-116	colon:	n/a	n/a
31	CTCF	chr21:47841040-47841190	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr21:47840440-47840590	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr21:47840500-47840650	MCF-7	breast:	n/a	n/a
34	CTCF	chr21:47841042-47841243	GM12878	blood:	n/a	n/a
35	CTCF	chr21:47841040-47841190	GM12875	blood:	n/a	n/a
36	CTCF	chr21:47840480-47840685	GM12891	blood:	n/a	n/a
37	CTCF	chr21:47840360-47840510	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr21:47840500-47840650	HRE	kidney:	n/a	n/a
39	CTCF	chr21:47840492-47840680	Gliobla	brain:	n/a	n/a
40	CTCF	chr21:47840460-47840610	BE2_C	brain:	n/a	n/a
41	CTCF	chr21:47840536-47840628	GM10248	blood:	n/a	n/a
42	CTCF	chr21:47841020-47841170	RPTEC	kidney:	n/a	n/a
43	CTCF	chr21:47840480-47840630	AG04449	skin:	n/a	n/a
44	CTCF	chr21:47840497-47840686	GM19239	blood:	n/a	n/a
45	CTCF	chr21:47840540-47840690	GM12864	blood:	n/a	n/a
46	CTCF	chr21:47840467-47840710	MCF-7	breast:	n/a	n/a
47	CTCF	chr21:47840440-47840590	AG09309	skin:	n/a	n/a
48	CTCF	chr21:47841100-47841250	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr21:47840469-47840689	MCF-7	breast:	n/a	n/a
50	CTCF	chr21:47841140-47841290	HUVEC	blood vessel:	n/a	chr21:47841250-47841263

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47851742-47851792	HUVEC	blood vessel:	n/a
2	chr21:47842207-47842257	AG09319	gingival:	n/a
3	chr21:47851742-47851792	HUVEC	blood vessel:	n/a
4	chr21:47842207-47842257	AG09319	gingival:	n/a
5	chr21:47851621-47851671	AG09319	gingival:	n/a
6	chr21:47850317-47850367	GM12878	blood:	n/a
7	chr21:47844012-47844062	U87	brain:	n/a
8	chr21:47846235-47846285	NT2-D1	testis:	n/a
9	chr21:47847919-47847969	AoSMC	blood vessel:	n/a
10	chr21:47856215-47856265	NHDF-neo	bronchial:	n/a
11	chr21:47855049-47855099	HRCEpiC	kidney:	n/a
12	chr21:47842207-47842257	ovcar-3	ovarian:	n/a
13	chr21:47856020-47856070	HL-60	blood:	n/a
14	chr21:47851941-47851991	T-47D	breast:	n/a
15	chr21:47846235-47846285	IMR90	lung:	fetal
16	chr21:47845610-47845660	HIPEpiC	eye:	n/a
17	chr21:47851470-47851520	HRE	kidney:	n/a
18	chr21:47856020-47856070	U87	brain:	n/a
19	chr21:47851621-47851671	MCF10A-Er-Src	breast:	n/a
20	chr21:47846235-47846285	PrEC	prostate:	n/a
21	chr21:47847919-47847969	HRE	kidney:	n/a
22	chr21:47859926-47859976	HAEpiC	amniotic membrane:	n/a
23	chr21:47855049-47855099	LNCaP	prostate:	n/a
24	chr21:47845788-47845838	GM12878	blood:	n/a
25	chr21:47847919-47847969	Caco-2	colon:	n/a
26	chr21:47850317-47850367	AG10803	skin:	n/a
27	chr21:47845863-47845913	Hepatocyte	liver:	n/a
28	chr21:47856020-47856070	IMR90	lung:	fetal
29	chr21:47859926-47859976	AG09319	gingival:	n/a
30	chr21:47842207-47842257	CMK	blood:	n/a
31	chr21:47855916-47855966	NT2-D1	testis:	n/a
32	chr21:47856140-47856190	MCF-7	breast:	n/a
33	chr21:47851621-47851671	SAEC	small airway:	n/a
34	chr21:47845610-47845660	HepG2	liver:	n/a
35	chr21:47849050-47849100	HNPCEpiC	eye:	n/a
36	chr21:47845788-47845838	HCM	heart:	n/a
37	chr21:47855893-47855943	HAEpiC	amniotic membrane:	n/a
38	chr21:47848216-47848266	ECC-1	luminal epithelium:	n/a
39	chr21:47855916-47855966	HEK293	kidney:	embryo
40	chr21:47844012-47844062	NT2-D1	testis:	n/a
41	chr21:47845610-47845660	HEK293	kidney:	embryo
42	chr21:47842207-47842257	HEK293	kidney:	embryo
43	chr21:47845610-47845660	AoSMC	blood vessel:	n/a
44	chr21:47845737-47845787	HCT-116	colon:	n/a
45	chr21:47856140-47856190	SK-N-MC	brain:	n/a
46	chr21:47845863-47845913	NHBE	bronchial:	n/a
47	chr21:47851545-47851595	GM06990	blood:	n/a
48	chr21:47851742-47851792	NH-A	brain:	n/a
49	chr21:47856140-47856190	AG10803	skin:	n/a
50	chr21:47855916-47855966	U87	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:47818533..47820839-chr21:47835124..47837401,2	K562	blood:
2	chr21:47649218..47651291-chr21:47846633..47848855,2	K562	blood:
3	chr21:47858571..47860642-chr21:47862519..47864961,2	MCF-7	breast:
4	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
5	chr21:47841259..47843546-chr21:47843811..47847040,4	K562	blood:
6	chr21:47842082..47844141-chr21:47845967..47848443,2	K562	blood:
7	chr21:47856507..47858157-chr21:47860635..47863396,2	MCF-7	breast:
8	chr21:47834319..47837549-chr21:47839408..47843063,3	K562	blood:
9	chr21:47830638..47832458-chr21:47836408..47838043,2	K562	blood:
10	chr21:47856273..47858659-chr21:47860032..47862884,2	K562	blood:
11	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
12	chr21:47857792..47859466-chr21:47861182..47863133,2	MCF-7	breast:
13	chr21:47843264..47847636-chr21:47874814..47878644,6	K562	blood:
14	chr21:47863005..47865990-chr21:47875934..47878581,2	MCF-7	breast:
15	chr21:47861367..47863286-chr21:48054038..48055974,2	K562	blood:
16	chr21:47848467..47851272-chr21:47852866..47855440,2	K562	blood:
17	chr21:47836799..47839696-chr21:47847990..47849925,2	K562	blood:
18	chr21:47845101..47846658-chr21:47877111..47880034,2	K562	blood:
19	chr21:47843582..47848242-chr21:47854131..47857783,6	K562	blood:
20	chr21:47848817..47851368-chr21:47861813..47863381,2	K562	blood:
21	chr21:47857607..47860157-chr21:47877897..47880411,2	MCF-7	breast:
22	chr21:47839389..47841162-chr21:47847458..47849832,2	MCF-7	breast:
23	chr21:47857792..47859466-chr21:47861182..47863133,2	MCF-7	breast:
24	chr21:47839369..47841083-chr21:47878532..47880064,2	K562	blood:
25	chr21:47858571..47860642-chr21:47862519..47864961,2	MCF-7	breast:
26	chr21:47862980..47864520-chr21:47866153..47868184,2	MCF-7	breast:
27	chr21:47857857..47859725-chr21:47876652..47878543,2	MCF-7	breast:
28	chr21:47828187..47830277-chr21:47834306..47836291,2	MCF-7	breast:
29	chr21:47829908..47831983-chr21:47862794..47864924,2	K562	blood:
30	chr21:47853352..47856633-chr21:47878140..47880096,4	MCF-7	breast:
31	chr21:47844449..47847171-chr21:47854131..47855917,2	K562	blood:
32	chr21:47844449..47847171-chr21:47854131..47855917,2	K562	blood:
33	chr21:47832440..47835140-chr21:47835369..47837767,2	MCF-7	breast:
34	chr21:47856273..47858659-chr21:47860032..47862884,2	K562	blood:
35	chr21:47833631..47836518-chr21:47877493..47879983,3	MCF-7	breast:
36	chr21:47770994..47773091-chr21:47844111..47846045,2	K562	blood:
37	chr21:47838816..47841237-chr21:47842476..47844122,2	K562	blood:
38	chr21:47856507..47858157-chr21:47860635..47863396,2	MCF-7	breast:
39	chr21:47858462..47860394-chr21:47879147..47880997,2	MCF-7	breast:
40	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
41	chr21:47862357..47865195-chr21:47870982..47877612,5	K562	blood:
42	chr21:47841259..47843546-chr21:47843811..47847040,4	K562	blood:
43	chr21:47845265..47847081-chr21:47878915..47881102,2	K562	blood:
44	chr21:47854459..47856094-chr21:47859695..47861438,2	K562	blood:
45	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
46	chr21:47836799..47839696-chr21:47847990..47849925,2	K562	blood:
47	chr21:47841235..47843966-chr21:47874444..47876872,2	K562	blood:
48	chr21:47742209..47744590-chr21:47846184..47848146,2	MCF-7	breast:
49	chr21:47842082..47844141-chr21:47845967..47848443,2	K562	blood:
50	chr21:47746558..47749011-chr21:47851647..47853522,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C21orf58-3	chr21:47840467-47840948	NONHSAT083067
2	lnc-DIP2A-1	chr21:47860907-47860997	NONHSAT083069
3	lnc-DIP2A-1	chr21:47862410-47863085	NONHSAT083069

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
ENSG00000160310	chromatin interactions
ENSG00000225043	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000215424	chromatin interactions

Extended variants
information (count: 1535 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1535 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839245	chr21:47836122-47836123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371054707	chr21:47836127-47836128	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs375610642	chr21:47836141-47836142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144430478	chr21:47836180-47836181	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs151082262	chr21:47836199-47836200	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35978208	chr21:47836206-47836207	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs368125717	chr21:47836213-47836214	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs60444527	chr21:47836216-47836217	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs145710874	chr21:47836236-47836237	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141594796	chr21:47836240-47836241	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370735505	chr21:47836242-47836243	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373849607	chr21:47836257-47836258	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs147033992	chr21:47836278-47836279	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs367739130	chr21:47836301-47836302	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs371302498	chr21:47836305-47836306	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs555273022	chr21:47836323-47836324	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs138227887	chr21:47836343-47836344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs375492793	chr21:47836351-47836352	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142252996	chr21:47836356-47836357	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs113105544	chr21:47836377-47836378	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs146006811	chr21:47836391-47836392	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1044998	chr21:47836395-47836396	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs199594027	chr21:47836397-47836398	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34151633	chr21:47836403-47836404	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs368565898	chr21:47836410-47836411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs150756913	chr21:47836411-47836412	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs372022297	chr21:47836417-47836418	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs375143479	chr21:47836418-47836419	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs369420036	chr21:47836422-47836423	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs137977081	chr21:47836425-47836426	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs57108405	chr21:47836426-47836427	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs9981448	chr21:47836448-47836449	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs144471022	chr21:47836466-47836467	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201503338	chr21:47836467-47836468	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144342729	chr21:47836477-47836478	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs527590016	chr21:47836480-47836481	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373358569	chr21:47836504-47836505	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552008852	chr21:47836509-47836510	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs35346764	chr21:47836547-47836548	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs142402562	chr21:47836554-47836555	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs199824488	chr21:47836561-47836562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs61735812	chr21:47836571-47836572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs200670600	chr21:47836575-47836576	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs141635334	chr21:47836593-47836594	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372687052	chr21:47836618-47836619	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145376230	chr21:47836624-47836625	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548287016	chr21:47836632-47836633	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182322703	chr21:47836633-47836634	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576146334	chr21:47836638-47836639	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs200610141	chr21:47836651-47836652	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	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:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr21:47829600-47837000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr21:47829600-47837200	Strong transcription	Lung	lung
30	chr21:47829600-47842000	Strong transcription	Fetal Thymus	thymus
31	chr21:47829600-47842800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr21:47829600-47843000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr21:47829600-47843200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr21:47829600-47862800	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr21:47829600-47864000	Strong transcription	Fetal Intestine Small	intestine
36	chr21:47829800-47836800	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr21:47829800-47838600	Strong transcription	Spleen	Spleen
38	chr21:47829800-47842800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr21:47829800-47842800	Strong transcription	Right Ventricle	heart
40	chr21:47829800-47843000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr21:47830000-47836800	Strong transcription	Brain Cingulate Gyrus	brain
42	chr21:47830000-47837200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr21:47830000-47837200	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr21:47830000-47842800	Strong transcription	Pancreas	Pancrea
45	chr21:47830000-47843200	Strong transcription	Adipose Nuclei	Adipose
46	chr21:47830000-47843400	Strong transcription	Stomach Smooth Muscle	stomach
47	chr21:47830200-47862800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr21:47830400-47842800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr21:47830400-47843200	Strong transcription	Placenta	Placenta
50	chr21:47830400-47862800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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