Variant report

Variant	esv3359090
Chromosome Location	chr21:46519949-46522497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:136)
CpG islands
(count:184)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:136 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr21:46522460-46522610	HEEpiC	esophagus:	n/a	n/a
2	CTCF	chr21:46522480-46522630	HMEC	breast:	n/a	n/a
3	CTCF	chr21:46522444-46522812	HUVEC	blood vessel:	n/a	n/a
4	CTCF	chr21:46522440-46522590	HEK293	kidney:	n/a	n/a
5	CTCF	chr21:46522480-46522630	GM12867	blood:	n/a	n/a
6	CTCF	chr21:46522440-46522590	HEEpiC	esophagus:	n/a	n/a
7	CTCF	chr21:46522440-46522590	HPAF	blood vessel:	n/a	n/a
8	CTCF	chr21:46522440-46522590	AoAF	blood vessel:	n/a	n/a
9	CTCF	chr21:46522360-46522650	HCM	heart:	n/a	n/a
10	CTCF	chr21:46522422-46522832	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr21:46522440-46522590	GM12869	blood:	n/a	n/a
12	CTCF	chr21:46522480-46522630	GM12868	blood:	n/a	n/a
13	CTCF	chr21:46522424-46522820	MCF-7	breast:	n/a	n/a
14	CTCF	chr21:46522400-46522550	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr21:46522440-46522590	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr21:46522461-46522604	Gliobla	brain:	n/a	n/a
17	CTCF	chr21:46522480-46522630	GM06990	blood:	n/a	n/a
18	CTCF	chr21:46522480-46522630	HAc	cerebellar:	n/a	n/a
19	CTCF	chr21:46522460-46522610	NHEK	skin:	n/a	n/a
20	CTCF	chr21:46522300-46522914	MCF-7	breast:	n/a	n/a
21	CTCF	chr21:46522420-46522570	HRE	kidney:	n/a	n/a
22	CTCF	chr21:46522440-46522590	WI-38	lung:	n/a	n/a
23	CTCF	chr21:46522443-46522933	GM12878	blood:	n/a	n/a
24	CTCF	chr21:46522465-46522607	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr21:46522480-46522630	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr21:46522460-46522610	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr21:46522420-46522570	AG04450	lung:	n/a	n/a
28	CTCF	chr21:46522440-46522590	BE2_C	brain:	n/a	n/a
29	CTCF	chr21:46522460-46522610	BJ	skin:	n/a	n/a
30	CTCF	chr21:46522400-46522550	SAEC	small airway:	n/a	n/a
31	CTCF	chr21:46522460-46522610	AG04449	skin:	n/a	n/a
32	CTCF	chr21:46522446-46522548	NHEK	skin:	n/a	n/a
33	CTCF	chr21:46522480-46522630	GM12878	blood:	n/a	n/a
34	CTCF	chr21:46522453-46522587	MCF-7	breast:	n/a	n/a
35	CTCF	chr21:46522380-46522530	HepG2	liver:	n/a	n/a
36	CTCF	chr21:46522440-46522590	GM12868	blood:	n/a	n/a
37	CTCF	chr21:46522460-46522610	AG09319	gingival:	n/a	n/a
38	CTCF	chr21:46520040-46520190	GM12865	blood:	n/a	n/a
39	CTCF	chr21:46522440-46522590	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr21:46522460-46522610	GM12871	blood:	n/a	n/a
41	CTCF	chr21:46522240-46522390	AG04450	lung:	n/a	n/a
42	CTCF	chr21:46522400-46522550	A549	lung:	n/a	n/a
43	CTCF	chr21:46522458-46522575	ProgFib	skin:	n/a	n/a
44	CTCF	chr21:46522460-46522690	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr21:46522460-46522610	HCT-116	colon:	n/a	n/a
46	CTCF	chr21:46522400-46522550	GM12873	blood:	n/a	n/a
47	CTCF	chr21:46522460-46522610	HMEC	breast:	n/a	n/a
48	CTCF	chr21:46522459-46522829	K562	blood:	n/a	n/a
49	CTCF	chr21:46522484-46522551	GM10266	blood:	n/a	n/a
50	CTCF	chr21:46521975-46522976	A549	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:46521281-46521331	ECC-1	luminal epithelium:	n/a
2	chr21:46521281-46521331	ECC-1	luminal epithelium:	n/a
3	chr21:46521050-46521100	HEEpiC	esophagus:	n/a
4	chr21:46520883-46520933	RPTEC	kidney:	n/a
5	chr21:46521050-46521100	HCM	heart:	n/a
6	chr21:46521050-46521100	HRE	kidney:	n/a
7	chr21:46521050-46521100	A549	lung:	n/a
8	chr21:46521050-46521100	U87	brain:	n/a
9	chr21:46521281-46521331	NHBE	bronchial:	n/a
10	chr21:46521281-46521331	HEEpiC	esophagus:	n/a
11	chr21:46520883-46520933	HepG2	liver:	n/a
12	chr21:46521281-46521331	GM19239	blood:	n/a
13	chr21:46521050-46521100	LNCaP	prostate:	n/a
14	chr21:46521281-46521331	RPTEC	kidney:	n/a
15	chr21:46521281-46521331	NB4	blood:	n/a
16	chr21:46521281-46521331	HCF	heart:	n/a
17	chr21:46521281-46521331	GM06990	blood:	n/a
18	chr21:46521281-46521331	PFSK-1	brain:	n/a
19	chr21:46520883-46520933	SK-N-MC	brain:	n/a
20	chr21:46521050-46521100	K562	blood:	n/a
21	chr21:46520883-46520933	HUVEC	blood vessel:	n/a
22	chr21:46521050-46521100	ProgFib	skin:	n/a
23	chr21:46520883-46520933	AG04450	lung:	fetal
24	chr21:46521050-46521100	MCF10A-Er-Src	breast:	n/a
25	chr21:46521281-46521331	A549	lung:	n/a
26	chr21:46521050-46521100	AoSMC	blood vessel:	n/a
27	chr21:46521050-46521100	HIPEpiC	eye:	n/a
28	chr21:46521050-46521100	SK-N-SH	brain:	n/a
29	chr21:46520883-46520933	HRCEpiC	kidney:	n/a
30	chr21:46521281-46521331	SK-N-SH	brain:	n/a
31	chr21:46521281-46521331	GM12891	blood:	n/a
32	chr21:46520883-46520933	PFSK-1	brain:	n/a
33	chr21:46520883-46520933	GM06990	blood:	n/a
34	chr21:46521050-46521100	GM06990	blood:	n/a
35	chr21:46521050-46521100	BJ	skin:	n/a
36	chr21:46521281-46521331	HMEC	breast:	n/a
37	chr21:46521050-46521100	SK-N-MC	brain:	n/a
38	chr21:46520883-46520933	SK-N-SH_RA	brain:	n/a
39	chr21:46521050-46521100	H1-hESC	embryonic stem cell:	embryo
40	chr21:46521281-46521331	HRCEpiC	kidney:	n/a
41	chr21:46520883-46520933	T-47D	breast:	n/a
42	chr21:46520883-46520933	HCM	heart:	n/a
43	chr21:46520883-46520933	HL-60	blood:	n/a
44	chr21:46521050-46521100	HepG2	liver:	n/a
45	chr21:46520883-46520933	PANC-1	pancreas:	n/a
46	chr21:46520883-46520933	HPAEpiC	pulmonary alveolar:	n/a
47	chr21:46521050-46521100	Jurkat	blood:	n/a
48	chr21:46521281-46521331	Jurkat	blood:	n/a
49	chr21:46520883-46520933	A549	lung:	n/a
50	chr21:46521050-46521100	SKMC	muscle:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46514549..46517055-chr21:46520921..46524159,3	MCF-7	breast:
2	chr21:46515956..46522233-chr21:46528087..46531013,7	K562	blood:
3	chr21:46522238..46524278-chr21:46526397..46529123,2	MCF-7	breast:
4	chr21:46513014..46516027-chr21:46521774..46524473,3	MCF-7	breast:
5	chr21:46500190..46501705-chr21:46518779..46520799,2	K562	blood:
6	chr21:46421527..46423886-chr21:46518850..46521282,2	MCF-7	breast:
7	chr21:46493580..46496236-chr21:46521352..46523890,2	MCF-7	breast:
8	chr21:46493552..46495288-chr21:46521401..46524653,4	MCF-7	breast:
9	chr21:46492354..46499042-chr21:46517406..46531809,25	K562	blood:
10	chr21:46519046..46522635-chr21:46528087..46531462,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000268805	TF binding region
ENSG00000268805	CpG island
ENSG00000268856	chromatin interactions
ENSG00000235374	chromatin interactions
ENSG00000268805	chromatin interactions
ENSG00000197381	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541159479	chr21:46519950-46519951	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs542860095	chr21:46519989-46519990	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs369533093	chr21:46519990-46519991	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs183682877	chr21:46519994-46519995	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs559466869	chr21:46520003-46520004	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs80256955	chr21:46520024-46520025	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs554026161	chr21:46520054-46520055	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs572245952	chr21:46520071-46520072	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs138375541	chr21:46520145-46520146	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs75734900	chr21:46520243-46520244	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs576001212	chr21:46520271-46520272	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs114452303	chr21:46520294-46520295	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs186108054	chr21:46520374-46520375	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs149175040	chr21:46520377-46520378	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs541296440	chr21:46520388-46520389	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576025329	chr21:46520413-46520414	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs3178603	chr21:46520421-46520422	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs1055858	chr21:46520443-46520444	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs3171490	chr21:46520453-46520454	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190041854	chr21:46520458-46520459	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs79608741	chr21:46520492-46520493	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs143338785	chr21:46520528-46520529	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs549368512	chr21:46520582-46520583	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs568576862	chr21:46520588-46520589	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs535775665	chr21:46520596-46520597	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs182206371	chr21:46520601-46520602	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs376895688	chr21:46520605-46520606	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs565922613	chr21:46520662-46520663	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs148338353	chr21:46520663-46520664	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs557617189	chr21:46520677-46520678	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs576094605	chr21:46520724-46520725	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs116569216	chr21:46520731-46520732	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs554962872	chr21:46520755-46520756	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs573280846	chr21:46520796-46520797	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs187265611	chr21:46520827-46520828	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs17004733	chr21:46520840-46520841	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs577866773	chr21:46520973-46520974	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs545587397	chr21:46520975-46520976	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs563692038	chr21:46520985-46520986	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs531051860	chr21:46521014-46521015	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs549182023	chr21:46521020-46521021	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs374225304	chr21:46521051-46521052	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs141527411	chr21:46521054-46521055	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs528485120	chr21:46521166-46521167	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs547760348	chr21:46521200-46521201	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs191673967	chr21:46521208-46521209	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs539311750	chr21:46521220-46521221	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs551566244	chr21:46521230-46521231	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs569721514	chr21:46521237-46521238	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112934328	chr21:46521282-46521283	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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 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
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	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 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
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	17426248	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Williams-beuren syndrome	16826523	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:210 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46499000-46522200	Weak transcription	NHDF-Ad	bronchial
2	chr21:46500000-46522200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr21:46503000-46522200	Weak transcription	Brain Angular Gyrus	brain
4	chr21:46506600-46521400	Weak transcription	NHEK	skin
5	chr21:46509400-46524000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr21:46511800-46520200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr21:46512000-46521600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr21:46512200-46521800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr21:46512200-46522400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr21:46512200-46525600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr21:46512800-46520400	Enhancers	Fetal Muscle Leg	muscle
12	chr21:46513200-46529200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr21:46513400-46521600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr21:46513600-46520800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr21:46513600-46522200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr21:46513600-46522400	Weak transcription	Brain Hippocampus Middle	brain
17	chr21:46513600-46522600	Weak transcription	Aorta	Aorta
18	chr21:46513600-46522600	Weak transcription	Brain Anterior Caudate	brain
19	chr21:46513800-46520400	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr21:46513800-46522000	Weak transcription	Stomach Mucosa	stomach
21	chr21:46514200-46525000	Enhancers	Right Ventricle	heart
22	chr21:46514600-46522600	Weak transcription	Fetal Thymus	thymus
23	chr21:46514800-46522200	Weak transcription	Primary T cells from cord blood	blood
24	chr21:46514800-46523800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr21:46515000-46522200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr21:46515200-46521800	Weak transcription	Pancreas	Pancrea
27	chr21:46515200-46522000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr21:46515400-46522000	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr21:46515600-46522400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr21:46516200-46522200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr21:46516200-46524000	Weak transcription	Gastric	stomach
32	chr21:46516400-46520400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr21:46516400-46521600	Weak transcription	HMEC	breast
34	chr21:46516400-46525600	Weak transcription	K562	blood
35	chr21:46516400-46549400	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr21:46516600-46520200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr21:46516600-46520800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr21:46516600-46521600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr21:46516600-46522000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr21:46516600-46522600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr21:46516600-46522600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr21:46517400-46520400	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr21:46517400-46523800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr21:46517600-46520400	Enhancers	Colon Smooth Muscle	Colon
45	chr21:46517600-46520400	Enhancers	Fetal Lung	lung
46	chr21:46517600-46521400	Weak transcription	Adipose Nuclei	Adipose
47	chr21:46517600-46521400	Enhancers	Fetal Brain Male	brain
48	chr21:46518000-46520800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr21:46518200-46520200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr21:46518200-46522600	Weak transcription	Esophagus	oesophagus

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