Variant report

Variant	nsv1065227
Chromosome Location	chr21:47985655-48036224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:266)
CpG islands
(count:1039)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:266 , 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	ATF2	chr21:48028361-48029224	GM12878	blood:	n/a	n/a
2	ATF3	chr21:48017955-48018252	K562	blood:	n/a	chr21:48018068-48018088
3	BATF	chr21:48028473-48028947	GM12878	blood:	n/a	n/a
4	BATF	chr21:48028436-48029053	GM12878	blood:	n/a	n/a
5	BCLAF1	chr21:48025984-48026402	GM12878	blood:	n/a	n/a
6	BCLAF1	chr21:48028466-48029094	GM12878	blood:	n/a	n/a
7	CBX3	chr21:48017809-48018333	K562	blood:	n/a	n/a
8	CBX3	chr21:48014212-48014536	K562	blood:	n/a	n/a
9	CBX3	chr21:48017920-48018249	K562	blood:	n/a	n/a
10	CEBPB	chr21:47989029-47989304	A549	lung:	n/a	n/a
11	CEBPB	chr21:47989027-47989372	HepG2	liver:	n/a	n/a
12	CEBPB	chr21:48020264-48020558	K562	blood:	n/a	n/a
13	CEBPB	chr21:47988938-47989373	IMR90	lung:	n/a	n/a
14	CTCF	chr21:47988020-47988170	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr21:48018005-48018273	K562	blood:	n/a	chr21:48018186-48018199
16	CTCF	chr21:48007283-48007335	LNCaP	prostate:	n/a	n/a
17	CTCF	chr21:48018165-48018252	K562	blood:	n/a	chr21:48018186-48018199
18	CTCF	chr21:48015320-48015470	GM12866	blood:	n/a	n/a
19	CTCF	chr21:47988074-47988126	MCF-7	breast:	n/a	n/a
20	CTCF	chr21:48018080-48018230	K562	blood:	n/a	chr21:48018186-48018199
21	CTCF	chr21:48028680-48028830	GM12864	blood:	n/a	n/a
22	CTCF	chr21:48018020-48018170	K562	blood:	n/a	n/a
23	CTCF	chr21:48018060-48018210	Hela-S3	cervix:	n/a	chr21:48018186-48018199
24	CTCF	chr21:48018049-48018377	K562	blood:	n/a	chr21:48018186-48018199
25	CTCF	chr21:47988076-47988108	MCF-7	breast:	n/a	n/a
26	CTCF	chr21:48018100-48018250	GM12867	blood:	n/a	chr21:48018186-48018199
27	CTCF	chr21:47995160-47995310	MCF-7	breast:	n/a	n/a
28	CTCF	chr21:48028993-48029068	GM12878	blood:	n/a	n/a
29	CTCF	chr21:47988000-47988150	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr21:47987940-47988090	HL-60	blood:	n/a	n/a
31	CTCF	chr21:48002020-48002170	HepG2	liver:	n/a	n/a
32	CTCF	chr21:47988007-47988145	HepG2	liver:	n/a	n/a
33	CTCF	chr21:48028977-48029064	GM10266	blood:	n/a	n/a
34	CTCF	chr21:48018048-48018372	K562	blood:	n/a	chr21:48018186-48018199
35	CTCF	chr21:48028820-48028970	GM12873	blood:	n/a	n/a
36	CTCF	chr21:47988042-47988109	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr21:48008431-48008493	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr21:47988095-47988122	HepG2	liver:	n/a	n/a
39	EBF1	chr21:48025973-48026546	GM12878	blood:	n/a	n/a
40	EBF1	chr21:48026020-48026423	GM12878	blood:	n/a	n/a
41	EGR1	chr21:48024963-48025225	K562	blood:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
42	EGR1	chr21:48024950-48025231	K562	blood:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
43	EGR1	chr21:48024900-48025237	H1-hESC	embryonic stem cell:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
44	EGR1	chr21:48018016-48018248	K562	blood:	n/a	chr21:48018193-48018206
45	EGR1	chr21:48018008-48018258	K562	blood:	n/a	chr21:48018193-48018206
46	EGR1	chr21:48024866-48025287	ECC-1	luminal epithelium:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
47	ELF1	chr21:48017729-48017997	K562	blood:	n/a	chr21:48017927-48017938
48	ELF1	chr21:48017731-48018266	K562	blood:	n/a	chr21:48017927-48017938
49	ELF1	chr21:48026001-48026710	GM12878	blood:	n/a	chr21:48026169-48026182
50	ELF1	chr21:48018047-48018261	K562	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:48026298-48026348	HEEpiC	esophagus:	n/a
2	chr21:48018632-48018682	SK-N-SH	brain:	n/a
3	chr21:48026298-48026348	HEEpiC	esophagus:	n/a
4	chr21:48018632-48018682	SK-N-SH	brain:	n/a
5	chr21:48019296-48019346	MCF10A-Er-Src	breast:	n/a
6	chr21:48018632-48018682	MCF-7	breast:	n/a
7	chr21:48026298-48026348	NHBE	bronchial:	n/a
8	chr21:48015365-48015415	SK-N-SH_RA	brain:	n/a
9	chr21:48025100-48025150	H1-hESC	embryonic stem cell:	embryo
10	chr21:48015365-48015415	NHDF-neo	bronchial:	n/a
11	chr21:48025691-48025741	AG09319	gingival:	n/a
12	chr21:48022339-48022389	AG10803	skin:	n/a
13	chr21:48026181-48026231	PrEC	prostate:	n/a
14	chr21:48018790-48018840	AG10803	skin:	n/a
15	chr21:48025100-48025150	GM06990	blood:	n/a
16	chr21:48024639-48024689	H1-hESC	embryonic stem cell:	embryo
17	chr21:48025155-48025205	U87	brain:	n/a
18	chr21:48025691-48025741	ovcar-3	ovarian:	n/a
19	chr21:48018632-48018682	HEK293	kidney:	embryo
20	chr21:48015365-48015415	HIPEpiC	eye:	n/a
21	chr21:48026298-48026348	ProgFib	skin:	n/a
22	chr21:48017232-48017282	BE2_C	brain:	n/a
23	chr21:48026181-48026231	MCF10A-Er-Src	breast:	n/a
24	chr21:48018608-48018658	Jurkat	blood:	n/a
25	chr21:48025100-48025150	BJ	skin:	n/a
26	chr21:48024683-48024733	HRPEpiC	eye:	n/a
27	chr21:47987607-47987657	HCF	heart:	n/a
28	chr21:48018632-48018682	HRE	kidney:	n/a
29	chr21:48024683-48024733	HAEpiC	amniotic membrane:	n/a
30	chr21:48017232-48017282	Jurkat	blood:	n/a
31	chr21:48026043-48026093	HMEC	breast:	n/a
32	chr21:48017232-48017282	PrEC	prostate:	n/a
33	chr21:48017232-48017282	AG09319	gingival:	n/a
34	chr21:48021941-48021991	HCM	heart:	n/a
35	chr21:47987607-47987657	A549	lung:	n/a
36	chr21:48025155-48025205	SK-N-SH	brain:	n/a
37	chr21:48025100-48025150	Hela-S3	cervix:	n/a
38	chr21:48026043-48026093	H1-hESC	embryonic stem cell:	embryo
39	chr21:48017232-48017282	SAEC	small airway:	n/a
40	chr21:48026298-48026348	HMEC	breast:	n/a
41	chr21:48022339-48022389	HPAEpiC	pulmonary alveolar:	n/a
42	chr21:48024683-48024733	AoSMC	blood vessel:	n/a
43	chr21:48022339-48022389	HEK293	kidney:	embryo
44	chr21:48025100-48025150	HIPEpiC	eye:	n/a
45	chr21:48017232-48017282	Caco-2	colon:	n/a
46	chr21:48025691-48025741	H1-hESC	embryonic stem cell:	embryo
47	chr21:48026043-48026093	CMK	blood:	n/a
48	chr21:48025155-48025205	ECC-1	luminal epithelium:	n/a
49	chr21:48018632-48018682	H1-hESC	embryonic stem cell:	embryo
50	chr21:48018790-48018840	AoSMC	blood vessel:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47995242..47996902-chr21:48001318..48004298,2	K562	blood:
2	chr21:48028979..48030812-chr21:48051870..48054019,2	K562	blood:
3	chr21:47877021..47880570-chr21:47984512..47987705,4	K562	blood:
4	chr21:47986444..47988898-chr21:48015731..48017367,2	K562	blood:
5	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
6	chr21:47977884..47980372-chr21:47985950..47987706,2	K562	blood:
7	chr21:47872410..47874001-chr21:47987885..47990582,2	K562	blood:
8	chr21:48003128..48004642-chr21:48053741..48055698,2	MCF-7	breast:
9	chr21:48031009..48033882-chr21:48053845..48056552,2	MCF-7	breast:
10	chr21:48017941..48023722-chr21:48025363..48028133,5	K562	blood:
11	chr21:47984970..47986522-chr21:48008602..48011495,2	K562	blood:
12	chr21:48027694..48030453-chr21:48039157..48041006,2	MCF-7	breast:
13	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:
14	chr21:47973166..47976163-chr21:48002439..48005009,2	K562	blood:
15	chr21:48010670..48012334-chr21:48047542..48049804,2	K562	blood:
16	chr21:47920604..47922605-chr21:48015742..48017826,2	K562	blood:
17	chr21:48019242..48021637-chr21:48023777..48026826,3	MCF-7	breast:
18	chr21:48021540..48023901-chr21:48055495..48057109,2	MCF-7	breast:
19	chr21:48023339..48026982-chr21:48053855..48056881,6	MCF-7	breast:
20	chr21:48025522..48028149-chr21:48060514..48063166,2	MCF-7	breast:
21	chr21:48017805..48022026-chr21:48053687..48056894,4	K562	blood:
22	chr21:47990428..47992783-chr21:47994801..47997759,2	K562	blood:
23	chr21:48021498..48023722-chr21:48025363..48027869,3	K562	blood:
24	chr21:48005218..48007630-chr21:48055834..48057649,2	K562	blood:
25	chr21:47986444..47988898-chr21:48015731..48017367,2	K562	blood:
26	chr21:47990428..47992783-chr21:47994801..47997759,2	K562	blood:
27	chr21:47986038..47989683-chr21:48053926..48057221,4	MCF-7	breast:
28	chr21:48002194..48004914-chr21:48055144..48057333,3	MCF-7	breast:
29	chr21:48025603..48028303-chr21:48029330..48031658,3	MCF-7	breast:
30	chr21:48024575..48027546-chr21:48055306..48056858,2	K562	blood:
31	chr21:47971877..47975830-chr21:47983188..47986029,3	K562	blood:
32	chr21:47980753..47982887-chr21:48026648..48028879,2	MCF-7	breast:
33	chr21:47984970..47986522-chr21:48008602..48011495,2	K562	blood:
34	chr21:48025603..48028303-chr21:48029330..48031658,3	MCF-7	breast:
35	chr21:48016127..48018173-chr21:48020936..48022713,2	K562	blood:
36	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
37	chr21:47980561..47982874-chr21:47984744..47986654,2	MCF-7	breast:
38	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:
39	chr21:47982466..47985451-chr21:47987034..47988568,2	MCF-7	breast:
40	chr21:47995242..47996902-chr21:48001318..48004298,2	K562	blood:
41	chr21:48016127..48018173-chr21:48020936..48022713,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DIP2A	hsa-miR-125a-5p	chr21:47989806-47989829

Variant related genes	Relation type
S100B	TF binding region
S100B	CpG island
ENSG00000160305	chromatin interactions
ENSG00000160307	chromatin interactions
ENSG00000160310	chromatin interactions

Extended variants
information (count: 2034 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:2034 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2248636	chr21:47985655-47985656	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201956099	chr21:47985658-47985659	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370497841	chr21:47985668-47985669	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565228941	chr21:47985673-47985674	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs374347392	chr21:47985674-47985675	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376077244	chr21:47985682-47985683	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532677856	chr21:47985684-47985685	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112595846	chr21:47985685-47985686	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371547722	chr21:47985693-47985694	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs16979409	chr21:47985694-47985695	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs368468937	chr21:47985711-47985712	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371901616	chr21:47985714-47985715	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs374169205	chr21:47985789-47985790	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368045775	chr21:47985806-47985807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371625848	chr21:47985816-47985817	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182097185	chr21:47985824-47985825	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375900304	chr21:47985829-47985830	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200456358	chr21:47985830-47985831	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201440734	chr21:47985843-47985844	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537814460	chr21:47985919-47985920	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185423285	chr21:47985920-47985921	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs10641570	chr21:47985925-47985926	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367734476	chr21:47985961-47985962	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs151326350	chr21:47985968-47985969	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113362409	chr21:47985971-47985972	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2277827	chr21:47986001-47986002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs377601330	chr21:47986040-47986041	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570444987	chr21:47986050-47986051	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs189786617	chr21:47986054-47986055	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2839333	chr21:47986068-47986069	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs8133340	chr21:47986083-47986084	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs543310564	chr21:47986109-47986110	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs554951385	chr21:47986110-47986111	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573526173	chr21:47986114-47986115	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs540254590	chr21:47986116-47986117	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs117521527	chr21:47986131-47986132	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs532421038	chr21:47986148-47986149	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs376402726	chr21:47986168-47986169	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs16979410	chr21:47986182-47986183	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs369500297	chr21:47986210-47986211	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150097903	chr21:47986248-47986249	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2839334	chr21:47986269-47986270	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs2839335	chr21:47986283-47986284	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs138381902	chr21:47986316-47986317	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34998575	chr21:47986375-47986376	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551846932	chr21:47986413-47986414	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570431657	chr21:47986421-47986422	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs372870634	chr21:47986423-47986424	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373693484	chr21:47986449-47986450	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs377064083	chr21:47986476-47986477	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 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:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47943600-47990600	Strong transcription	Fetal Stomach	stomach
2	chr21:47947600-47989000	Strong transcription	Dnd41	blood
3	chr21:47947600-47991000	Strong transcription	Fetal Muscle Leg	muscle
4	chr21:47948400-47993600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr21:47948600-47993200	Strong transcription	Fetal Intestine Large	intestine
6	chr21:47949000-47988200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr21:47949000-47993600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr21:47949800-47991800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr21:47950000-47989200	Strong transcription	Skeletal Muscle Female	skeletal muscle
10	chr21:47950000-47991000	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr21:47950200-47993200	Strong transcription	Stomach Smooth Muscle	stomach
12	chr21:47953000-47988200	Strong transcription	Gastric	stomach
13	chr21:47953000-47988600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr21:47953200-47988400	Strong transcription	Fetal Intestine Small	intestine
15	chr21:47953200-47993000	Strong transcription	Osteobl	bone
16	chr21:47953400-47988000	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr21:47956200-48001800	Weak transcription	Stomach Mucosa	stomach
18	chr21:47961600-47992800	Strong transcription	Brain Hippocampus Middle	brain
19	chr21:47964600-47988400	Strong transcription	Brain Germinal Matrix	brain
20	chr21:47965200-47991200	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr21:47965800-47988600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr21:47965800-47993400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr21:47966200-47993400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr21:47966400-47987800	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr21:47966600-47988200	Strong transcription	Esophagus	oesophagus
26	chr21:47966800-47985800	Weak transcription	K562	blood
27	chr21:47967400-47994800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr21:47968600-47990800	Strong transcription	Fetal Brain Female	brain
29	chr21:47969400-47987600	Strong transcription	Aorta	Aorta
30	chr21:47969600-47988200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr21:47969600-47988400	Strong transcription	Colonic Mucosa	Colon
32	chr21:47969800-47989200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr21:47970200-47992400	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr21:47970400-47988200	Strong transcription	Placenta Amnion	Placenta Amnion
35	chr21:47970400-47993200	Strong transcription	Brain Cingulate Gyrus	brain
36	chr21:47971000-47989200	Strong transcription	Placenta	Placenta
37	chr21:47971600-47991600	Strong transcription	Brain Substantia Nigra	brain
38	chr21:47972000-47988800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr21:47973200-47993000	Strong transcription	Duodenum Mucosa	Duodenum
40	chr21:47973400-47993200	Strong transcription	Rectal Smooth Muscle	rectum
41	chr21:47973600-47989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr21:47973600-47990600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr21:47973600-47991600	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr21:47973600-47992600	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr21:47973800-47990600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr21:47974200-47988200	Strong transcription	NHLF	lung
47	chr21:47974200-47991200	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr21:47974400-47987800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
49	chr21:47975200-47992800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr21:47975600-47988600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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