Variant report

Variant	nsv914084
Chromosome Location	chr21:47288453-47326666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:977)
Chromatin interactive
region (count:60)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47300411-47300587	HepG2	liver:	n/a	n/a
2	ATF1	chr21:47312104-47312255	K562	blood:	n/a	n/a
3	BACH1	chr21:47300042-47300646	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr21:47311523-47311813	GM12878	blood:	n/a	n/a
5	BHLHE40	chr21:47295046-47295376	HepG2	liver:	n/a	n/a
6	BHLHE40	chr21:47300397-47300678	K562	blood:	n/a	n/a
7	BHLHE40	chr21:47296636-47296655	K562	blood:	n/a	n/a
8	BHLHE40	chr21:47295064-47295332	K562	blood:	n/a	n/a
9	BHLHE40	chr21:47300363-47300708	HepG2	liver:	n/a	n/a
10	BHLHE40	chr21:47312164-47312380	K562	blood:	n/a	n/a
11	BHLHE40	chr21:47300411-47300694	GM12878	blood:	n/a	n/a
12	CCNT2	chr21:47295011-47295153	K562	blood:	n/a	n/a
13	CEBPB	chr21:47304830-47305050	HepG2	liver:	n/a	chr21:47304949-47304960
14	CEBPB	chr21:47304809-47304949	A549	lung:	n/a	n/a
15	CEBPB	chr21:47295092-47295422	HepG2	liver:	n/a	n/a
16	CEBPB	chr21:47294912-47295621	IMR90	lung:	n/a	n/a
17	CEBPB	chr21:47295180-47295381	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr21:47312410-47312571	K562	blood:	n/a	n/a
19	CHD2	chr21:47312425-47312441	HepG2	liver:	n/a	n/a
20	CTCF	chr21:47299817-47300992	SK-N-SH	brain:	n/a	n/a
21	CTCF	chr21:47300420-47300570	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr21:47300405-47300692	MCF-7	breast:	n/a	n/a
23	CTCF	chr21:47300440-47300590	GM12872	blood:	n/a	n/a
24	CTCF	chr21:47300403-47300633	GM10266	blood:	n/a	n/a
25	CTCF	chr21:47300420-47300570	HRE	kidney:	n/a	n/a
26	CTCF	chr21:47300440-47300590	GM12871	blood:	n/a	n/a
27	CTCF	chr21:47300400-47300550	BJ	skin:	n/a	n/a
28	CTCF	chr21:47300400-47300550	HCT-116	colon:	n/a	n/a
29	CTCF	chr21:47300387-47300664	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr21:47296700-47296850	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr21:47300420-47300570	GM12869	blood:	n/a	n/a
32	CTCF	chr21:47300380-47300530	HCM	heart:	n/a	n/a
33	CTCF	chr21:47300354-47300570	HepG2	liver:	n/a	n/a
34	CTCF	chr21:47300346-47300662	K562	blood:	n/a	n/a
35	CTCF	chr21:47300060-47300210	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr21:47299980-47300130	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr21:47314580-47314730	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr21:47300460-47300610	HPF	lung:	n/a	n/a
39	CTCF	chr21:47300215-47300695	MCF-7	breast:	n/a	n/a
40	CTCF	chr21:47300386-47300695	Fibrobl	skin:	n/a	n/a
41	CTCF	chr21:47300460-47300610	GM12875	blood:	n/a	n/a
42	CTCF	chr21:47300329-47300659	A549	lung:	n/a	n/a
43	CTCF	chr21:47300181-47300849	MCF-7	breast:	n/a	n/a
44	CTCF	chr21:47300420-47300570	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr21:47294677-47294760	GM12891	blood:	n/a	n/a
46	CTCF	chr21:47300460-47300610	NHEK	skin:	n/a	n/a
47	CTCF	chr21:47300420-47300570	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr21:47299923-47300867	K562	blood:	n/a	n/a
49	CTCF	chr21:47300380-47300530	NHEK	skin:	n/a	n/a
50	CTCF	chr21:47300420-47300570	HPAF	blood vessel:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47319304-47319354	SK-N-MC	brain:	n/a
2	chr21:47319304-47319354	SK-N-MC	brain:	n/a
3	chr21:47290548-47290598	HCPEpiC	choroid plexus:	n/a
4	chr21:47319304-47319354	HCM	heart:	n/a
5	chr21:47292253-47292303	AG04449	skin:	fetal
6	chr21:47319304-47319354	Hela-S3	cervix:	n/a
7	chr21:47294981-47295031	HPAEpiC	pulmonary alveolar:	n/a
8	chr21:47288721-47288771	HL-60	blood:	n/a
9	chr21:47319304-47319354	A549	lung:	n/a
10	chr21:47294739-47294789	SKMC	muscle:	n/a
11	chr21:47297840-47297890	HL-60	blood:	n/a
12	chr21:47297840-47297890	PFSK-1	brain:	n/a
13	chr21:47294762-47294812	HMEC	breast:	n/a
14	chr21:47317093-47317143	Jurkat	blood:	n/a
15	chr21:47288619-47288669	NHDF-neo	bronchial:	n/a
16	chr21:47290548-47290598	SK-N-SH	brain:	n/a
17	chr21:47292253-47292303	GM06990	blood:	n/a
18	chr21:47294981-47295031	K562	blood:	n/a
19	chr21:47322452-47322502	GM12892	blood:	n/a
20	chr21:47318899-47318949	IMR90	lung:	fetal
21	chr21:47288721-47288771	LNCaP	prostate:	n/a
22	chr21:47292253-47292303	HPAEpiC	pulmonary alveolar:	n/a
23	chr21:47288721-47288771	SK-N-SH	brain:	n/a
24	chr21:47292253-47292303	AG09319	gingival:	n/a
25	chr21:47288721-47288771	HCF	heart:	n/a
26	chr21:47288619-47288669	H1-hESC	embryonic stem cell:	embryo
27	chr21:47314725-47314775	T-47D	breast:	n/a
28	chr21:47314725-47314775	Jurkat	blood:	n/a
29	chr21:47322452-47322502	ProgFib	skin:	n/a
30	chr21:47294981-47295031	HEEpiC	esophagus:	n/a
31	chr21:47319304-47319354	K562	blood:	n/a
32	chr21:47317093-47317143	PANC-1	pancreas:	n/a
33	chr21:47288619-47288669	SK-N-MC	brain:	n/a
34	chr21:47295375-47295425	ProgFib	skin:	n/a
35	chr21:47318899-47318949	NB4	blood:	n/a
36	chr21:47294981-47295031	HRCEpiC	kidney:	n/a
37	chr21:47322452-47322502	RPTEC	kidney:	n/a
38	chr21:47294762-47294812	HNPCEpiC	eye:	n/a
39	chr21:47292253-47292303	HCPEpiC	choroid plexus:	n/a
40	chr21:47319304-47319354	H1-hESC	embryonic stem cell:	embryo
41	chr21:47294981-47295031	NB4	blood:	n/a
42	chr21:47288721-47288771	AG09319	gingival:	n/a
43	chr21:47318899-47318949	HNPCEpiC	eye:	n/a
44	chr21:47292253-47292303	PFSK-1	brain:	n/a
45	chr21:47294739-47294789	SK-N-SH	brain:	n/a
46	chr21:47314725-47314775	HCPEpiC	choroid plexus:	n/a
47	chr21:47295215-47295265	HL-60	blood:	n/a
48	chr21:47288438-47288488	HAEpiC	amniotic membrane:	n/a
49	chr21:47294739-47294789	NHDF-neo	bronchial:	n/a
50	chr21:47319304-47319354	BJ	skin:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:47267781..47268663-chr21:47299803..47300649,2	MCF-7	breast:
2	chr21:47325287..47328224-chr21:47334114..47336660,2	MCF-7	breast:
3	chr21:47286050..47288539-chr21:47292437..47294935,2	K562	blood:
4	chr21:47307528..47310993-chr21:47318183..47321905,4	K562	blood:
5	chr21:47286639..47289783-chr21:47334819..47337166,3	MCF-7	breast:
6	chr21:47295466..47298745-chr21:47300328..47303080,5	MCF-7	breast:
7	chr21:47292108..47294051-chr21:47294662..47296338,2	K562	blood:
8	chr21:47290679..47292853-chr21:47334808..47337713,2	MCF-7	breast:
9	chr21:47292095..47293643-chr21:47302560..47304735,2	K562	blood:
10	chr21:47300119..47302715-chr21:47341992..47344397,3	MCF-7	breast:
11	chr21:46806383..46806888-chr21:47288037..47288636,2	MCF-7	breast:
12	chr21:47311846..47315136-chr21:47319001..47321928,3	K562	blood:
13	chr21:47290546..47292380-chr21:47322273..47324632,2	MCF-7	breast:
14	chr21:47300028..47300909-chr21:47342650..47343811,5	MCF-7	breast:
15	chr21:47308979..47311967-chr21:47312189..47314453,2	MCF-7	breast:
16	chr21:47312796..47315650-chr21:47325639..47328184,2	MCF-7	breast:
17	chr21:47237629..47240751-chr21:47286627..47289424,3	MCF-7	breast:
18	chr21:47326297..47326825-chr21:47620902..47621507,2	MCF-7	breast:
19	chr21:47287743..47288527-chr21:47334754..47335348,2	MCF-7	breast:
20	chr21:47253579..47256281-chr21:47326370..47329354,2	K562	blood:
21	chr21:47282962..47285157-chr21:47294870..47296396,2	K562	blood:
22	chr21:46294382..46294995-chr21:47312113..47312613,2	Hela-S3	cervix:
23	chr21:47293178..47296152-chr21:47298575..47300607,2	K562	blood:
24	chr21:47290619..47293353-chr21:47296443..47298286,2	K562	blood:
25	chr21:47280971..47284906-chr21:47285301..47288996,5	K562	blood:
26	chr21:47299971..47300594-chr21:47342907..47343695,3	MCF-7	breast:
27	chr21:47280227..47282087-chr21:47299384..47301576,2	MCF-7	breast:
28	chr17:41381715..41383702-chr21:47312370..47313890,2	MCF-7	breast:
29	chr21:47240141..47240932-chr21:47300508..47301042,2	MCF-7	breast:
30	chr21:47326278..47326802-chr21:47335871..47336440,2	MCF-7	breast:
31	chr21:47304723..47306559-chr21:47309917..47311783,2	MCF-7	breast:
32	chr21:47324736..47327193-chr21:47327348..47329802,3	K562	blood:
33	chr21:47295466..47298745-chr21:47300328..47303080,5	MCF-7	breast:
34	chr21:47290546..47292380-chr21:47322273..47324632,2	MCF-7	breast:
35	chr21:47312057..47314177-chr21:47322993..47325323,2	MCF-7	breast:
36	chr21:47285455..47288368-chr21:47291495..47294082,2	MCF-7	breast:
37	chr21:47298754..47301234-chr21:47302328..47305027,3	K562	blood:
38	chr21:47292095..47293643-chr21:47302560..47304735,2	K562	blood:
39	chr21:47304723..47306559-chr21:47309917..47311783,2	MCF-7	breast:
40	chr21:47292108..47294051-chr21:47294662..47296338,2	K562	blood:
41	chr21:47322615..47325568-chr21:47331282..47333525,2	K562	blood:
42	chr21:47293178..47296152-chr21:47298575..47300607,2	K562	blood:
43	chr21:47308842..47311490-chr21:47321844..47323697,2	MCF-7	breast:
44	chr21:47277116..47279764-chr21:47286679..47288942,2	MCF-7	breast:
45	chr21:47298754..47301234-chr21:47302328..47305027,3	K562	blood:
46	chr21:47288031..47288840-chr21:47325915..47326785,5	MCF-7	breast:
47	chr21:47308842..47311490-chr21:47321844..47323697,2	MCF-7	breast:
48	chr21:47300090..47300627-chr21:47342032..47342538,2	MCF-7	breast:
49	chr21:47325937..47326745-chr21:47335899..47336761,2	MCF-7	breast:
50	chr21:47288031..47288840-chr21:47325915..47326785,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTCD-6	chr21:47318001-47318626	NONHSAT082999
2	lnc-FTCD-6	chr21:47318759-47318789	NONHSAT082999

No data

Variant related genes	Relation type
PCBP3	TF binding region
PCBP3	CpG island
ENSG00000188825	chromatin interactions
ENSG00000183570	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 1944 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1944 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839025	chr21:47288453-47288454	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76636709	chr21:47288466-47288467	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs549418428	chr21:47288469-47288470	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574118937	chr21:47288502-47288503	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs542808162	chr21:47288506-47288507	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567914403	chr21:47288543-47288544	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528806242	chr21:47288555-47288556	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2839026	chr21:47288665-47288666	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs113807006	chr21:47288671-47288672	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138656675	chr21:47288717-47288718	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571811459	chr21:47288742-47288743	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190605287	chr21:47288772-47288773	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557004092	chr21:47288821-47288822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149314420	chr21:47288843-47288844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568875855	chr21:47288863-47288864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2183599	chr21:47288873-47288874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554151595	chr21:47288938-47288939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368003533	chr21:47288973-47288974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62211893	chr21:47289032-47289033	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs183311964	chr21:47289039-47289040	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs371253228	chr21:47289040-47289041	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs558450418	chr21:47289087-47289088	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs576950982	chr21:47289152-47289153	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs113498624	chr21:47289311-47289312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563773446	chr21:47289358-47289359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530914430	chr21:47289359-47289360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543004989	chr21:47289369-47289370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs13050916	chr21:47289380-47289381	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs528545518	chr21:47289425-47289426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547293528	chr21:47289453-47289454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565475069	chr21:47289465-47289466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374202747	chr21:47289480-47289481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34760831	chr21:47289484-47289485	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs550916401	chr21:47289502-47289503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545311492	chr21:47289507-47289508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2839027	chr21:47289543-47289544	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148514620	chr21:47289553-47289554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547928304	chr21:47289625-47289626	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142760839	chr21:47289637-47289638	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533573910	chr21:47289674-47289675	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146103595	chr21:47289675-47289676	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2839028	chr21:47289683-47289684	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140054940	chr21:47289758-47289759	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367790400	chr21:47289767-47289768	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556096589	chr21:47289788-47289789	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370051950	chr21:47289856-47289857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116265077	chr21:47289864-47289865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4819160	chr21:47289870-47289871	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs77283134	chr21:47289872-47289873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35409950	chr21:47289897-47289898	Enhancers Weak transcription	n/a	n/a	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:853 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47266800-47300600	Weak transcription	Right Atrium	heart
2	chr21:47273200-47289400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr21:47273800-47299200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr21:47285600-47289400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr21:47285600-47289400	Weak transcription	NHDF-Ad	bronchial
6	chr21:47286000-47294000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr21:47286200-47288600	Enhancers	Spleen	Spleen
8	chr21:47286400-47289400	Weak transcription	HSMM	muscle
9	chr21:47286400-47289600	Weak transcription	HSMMtube	muscle
10	chr21:47286400-47294800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr21:47286600-47288600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr21:47286600-47289200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr21:47286600-47289400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr21:47286600-47289400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr21:47286600-47294800	Weak transcription	Fetal Thymus	thymus
16	chr21:47287000-47289400	Weak transcription	NH-A	brain
17	chr21:47287200-47289400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr21:47287400-47290400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr21:47287800-47288800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr21:47288000-47294800	Weak transcription	Thymus	Thymus
21	chr21:47288200-47292000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr21:47288400-47288800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
23	chr21:47288400-47288800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr21:47288400-47288800	Bivalent/Poised TSS	Osteobl	bone
25	chr21:47288400-47289600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr21:47288400-47289600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr21:47288600-47289400	Weak transcription	Spleen	Spleen
28	chr21:47288600-47292400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr21:47288800-47289800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr21:47289000-47289200	Bivalent Enhancer	Fetal Stomach	stomach
31	chr21:47289200-47290600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr21:47289200-47291600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr21:47289400-47289600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr21:47289400-47289600	Enhancers	Spleen	Spleen
35	chr21:47289400-47289800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr21:47289400-47289800	Enhancers	NHLF	lung
37	chr21:47289400-47290800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr21:47289400-47290800	Enhancers	HSMM	muscle
39	chr21:47289400-47290800	Enhancers	NH-A	brain
40	chr21:47289400-47290800	Enhancers	NHDF-Ad	bronchial
41	chr21:47289400-47290800	Enhancers	Osteobl	bone
42	chr21:47289400-47291200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr21:47289400-47291200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr21:47289600-47289800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr21:47289600-47289800	Enhancers	Placenta Amnion	Placenta Amnion
46	chr21:47289600-47289800	Genic enhancers	Spleen	Spleen
47	chr21:47289600-47289800	Enhancers	HSMMtube	muscle
48	chr21:47289600-47290400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr21:47289800-47290200	Weak transcription	HSMMtube	muscle
50	chr21:47289800-47290600	Weak transcription	Spleen	Spleen

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