Variant report

Variant	nsv979537
Chromosome Location	chr21:40714343-40716638
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr21:40715236-40715326	HepG2	liver:	n/a	n/a
2	CEBPB	chr21:40715241-40715649	K562	blood:	n/a	chr21:40715307-40715318
3	CEBPB	chr21:40715221-40715366	Hela-S3	cervix:	n/a	chr21:40715307-40715318
4	CEBPB	chr21:40715290-40715539	IMR90	lung:	n/a	chr21:40715307-40715318
5	CEBPB	chr21:40715178-40715521	HepG2	liver:	n/a	chr21:40715307-40715318
6	CTCF	chr21:40714365-40714598	T-47D	breast:	n/a	n/a
7	CTCF	chr21:40714788-40714899	Spleen_OC	spleen:	n/a	n/a
8	CTCF	chr21:40715300-40715450	GM12865	blood:	n/a	n/a
9	FOXA1	chr21:40715157-40715375	HepG2	liver:	n/a	n/a
10	POLR2A	chr21:40715279-40715321	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr21:40714216-40714808	GM12878	blood:	n/a	n/a
12	POLR2A	chr21:40714269-40714640	GM12878	blood:	n/a	n/a
13	POLR2A	chr21:40715191-40715623	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr21:40715134-40715712	GM12878	blood:	n/a	n/a
15	POLR2A	chr21:40715101-40715726	GM12878	blood:	n/a	n/a
16	POLR2A	chr21:40715105-40715917	K562	blood:	n/a	n/a
17	POLR2A	chr21:40715874-40715909	MCF-7	breast:	n/a	n/a
18	POLR2A	chr21:40715845-40715864	MCF-7	breast:	n/a	n/a
19	POLR2A	chr21:40714461-40714672	GM12891	blood:	n/a	n/a
20	POLR2A	chr21:40715162-40715656	HepG2	liver:	n/a	n/a
21	POLR2A	chr21:40714309-40714613	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr21:40714375-40714546	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr21:40715166-40715611	K562	blood:	n/a	n/a
24	POLR2A	chr21:40714362-40714662	GM12891	blood:	n/a	n/a
25	POLR2A	chr21:40715469-40715573	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr21:40715215-40715777	MCF-7	breast:	n/a	n/a
27	POLR2A	chr21:40715220-40715463	K562	blood:	n/a	n/a
28	POLR2A	chr21:40715371-40715431	HepG2	liver:	n/a	n/a
29	POLR2A	chr21:40714288-40714688	GM12892	blood:	n/a	n/a
30	POLR2A	chr21:40714109-40716057	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr21:40715120-40715980	GM12878	blood:	n/a	n/a
32	POLR2A	chr21:40715058-40715783	GM12892	blood:	n/a	n/a
33	POLR2A	chr21:40715104-40715650	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr21:40715193-40715634	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr21:40715107-40715632	K562	blood:	n/a	n/a
36	POLR2A	chr21:40715515-40715727	HepG2	liver:	n/a	n/a
37	POLR2A	chr21:40715347-40715392	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr21:40715135-40715455	PFSK-1	brain:	n/a	n/a
39	POLR2A	chr21:40716164-40723345	K562	blood:	n/a	n/a
40	POLR2A	chr21:40715075-40715756	SK-N-MC	brain:	n/a	n/a
41	POLR2A	chr21:40715314-40715370	HepG2	liver:	n/a	n/a
42	POLR2A	chr21:40714295-40714690	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr21:40716415-40718095	GM12878	blood:	n/a	n/a
44	POLR2A	chr21:40715158-40715491	K562	blood:	n/a	n/a
45	POLR2A	chr21:40715192-40715659	H1-hESC	embryonic stem cell:	n/a	n/a
46	SP1	chr21:40714312-40714562	H1-hESC	embryonic stem cell:	n/a	n/a
47	TBL1XR1	chr21:40715630-40715632	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:40714455-40714505	HNPCEpiC	eye:	n/a
2	chr21:40714455-40714505	Jurkat	blood:	n/a
3	chr21:40714455-40714505	AG04450	lung:	fetal
4	chr21:40714455-40714505	MCF-7	breast:	n/a
5	chr21:40714455-40714505	T-47D	breast:	n/a
6	chr21:40714455-40714505	HL-60	blood:	n/a
7	chr21:40714455-40714505	Caco-2	colon:	n/a
8	chr21:40714455-40714505	GM19239	blood:	n/a
9	chr21:40714455-40714505	IMR90	lung:	fetal
10	chr21:40714455-40714505	HEK293	kidney:	embryo
11	chr21:40714455-40714505	GM06990	blood:	n/a
12	chr21:40714455-40714505	HRCEpiC	kidney:	n/a
13	chr21:40714455-40714505	AG09309	skin:	n/a
14	chr21:40714455-40714505	AoSMC	blood vessel:	n/a
15	chr21:40714455-40714505	HPAEpiC	pulmonary alveolar:	n/a
16	chr21:40714455-40714505	HRPEpiC	eye:	n/a
17	chr21:40714455-40714505	H1-hESC	embryonic stem cell:	embryo
18	chr21:40714455-40714505	RPTEC	kidney:	n/a
19	chr21:40714455-40714505	Hela-S3	cervix:	n/a
20	chr21:40714455-40714505	NH-A	brain:	n/a
21	chr21:40714455-40714505	AG09319	gingival:	n/a
22	chr21:40714455-40714505	ProgFib	skin:	n/a
23	chr21:40714455-40714505	PFSK-1	brain:	n/a
24	chr21:40714455-40714505	Hepatocyte	liver:	n/a
25	chr21:40714455-40714505	BE2_C	brain:	n/a
26	chr21:40714455-40714505	NHBE	bronchial:	n/a
27	chr21:40714455-40714505	HCT-116	colon:	n/a
28	chr21:40714455-40714505	HEEpiC	esophagus:	n/a
29	chr21:40714455-40714505	HCPEpiC	choroid plexus:	n/a
30	chr21:40714455-40714505	HepG2	liver:	n/a
31	chr21:40714455-40714505	SK-N-SH	brain:	n/a
32	chr21:40714455-40714505	SK-N-SH_RA	brain:	n/a
33	chr21:40714455-40714505	GM12892	blood:	n/a
34	chr21:40714455-40714505	HCF	heart:	n/a
35	chr21:40714455-40714505	SAEC	small airway:	n/a
36	chr21:40714455-40714505	HMEC	breast:	n/a
37	chr21:40714455-40714505	HRE	kidney:	n/a
38	chr21:40714455-40714505	NT2-D1	testis:	n/a
39	chr21:40714455-40714505	PrEC	prostate:	n/a
40	chr21:40714455-40714505	AG04449	skin:	fetal
41	chr21:40714455-40714505	HUVEC	blood vessel:	n/a
42	chr21:40714455-40714505	NB4	blood:	n/a
43	chr21:40714455-40714505	SK-N-MC	brain:	n/a
44	chr21:40714455-40714505	A549	lung:	n/a
45	chr21:40714455-40714505	ovcar-3	ovarian:	n/a
46	chr21:40714455-40714505	PANC-1	pancreas:	n/a
47	chr21:40714455-40714505	U87	brain:	n/a
48	chr21:40714455-40714505	BJ	skin:	n/a
49	chr21:40714455-40714505	ECC-1	luminal epithelium:	n/a
50	chr21:40714455-40714505	K562	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:40681057..40687929-chr21:40707012..40715318,11	K562	blood:
2	chr21:40713610..40715714-chr21:40756121..40760531,5	K562	blood:
3	chr21:40691885..40693506-chr21:40712326..40714444,2	K562	blood:
4	chr21:40681596..40696529-chr21:40715399..40724266,46	K562	blood:
5	chr21:40716442..40724032-chr21:40756185..40762223,18	K562	blood:
6	chr21:40652004..40654564-chr21:40716456..40719134,2	MCF-7	breast:
7	chr21:40646616..40649505-chr21:40712893..40714626,2	K562	blood:
8	21:40712819-40717370..21:40748850-40752541	GM12878	blood:
9	chr21:40555173..40557304-chr21:40714737..40716613,2	K562	blood:
10	chr21:40716079..40725440-chr21:40756737..40764615,26	K562	blood:
11	chr21:40713943..40715737-chr21:40750711..40753188,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGN1-1	chr21:40714273-40714616	NONHSAT082168
2	lnc-HMGN1-1	chr21:40714244-40714584	NONHSAT082167
3	lnc-HMGN1-1	chr21:40714278-40714822	NONHSAT082169

No data

Variant related genes	Relation type
ENSG00000252915	TF binding region
ENSG00000252915	CpG island
ENSG00000238141	chromatin interactions
ENSG00000272991	chromatin interactions
ENSG00000227406	chromatin interactions
ENSG00000185658	chromatin interactions
ENSG00000183527	chromatin interactions
ENSG00000255568	chromatin interactions
ENSG00000182093	chromatin interactions

Extended variants
information (count: 124 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:124 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560136856	chr21:40714350-40714351	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
2	rs558338960	chr21:40714354-40714355	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
3	rs565670875	chr21:40714355-40714356	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
4	rs182875504	chr21:40714368-40714369	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
5	rs35148719	chr21:40714386-40714387	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
6	rs554882856	chr21:40714395-40714396	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
7	rs201008932	chr21:40714413-40714414	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
8	rs574787276	chr21:40714425-40714426	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
9	rs543636110	chr21:40714462-40714463	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
10	rs112580546	chr21:40714471-40714472	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
11	rs3167757	chr21:40714478-40714479	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs151188807	chr21:40714483-40714484	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
13	rs546281671	chr21:40714492-40714493	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
14	rs140317214	chr21:40714501-40714502	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
15	rs573230301	chr21:40714519-40714520	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
16	rs372138745	chr21:40714528-40714529	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
17	rs3199398	chr21:40714540-40714541	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
18	rs185679553	chr21:40714547-40714548	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
19	rs200707667	chr21:40714553-40714554	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
20	rs35306807	chr21:40714554-40714555	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
21	rs139878645	chr21:40714555-40714556	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
22	rs60176667	chr21:40714557-40714558	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
23	rs545777878	chr21:40714587-40714588	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs561197440	chr21:40714621-40714622	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs530002680	chr21:40714631-40714632	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
26	rs9977317	chr21:40714646-40714647	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
27	rs563492035	chr21:40714658-40714659	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
28	rs532158100	chr21:40714693-40714694	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
29	rs8134935	chr21:40714755-40714756	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
30	rs201702275	chr21:40714777-40714778	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
31	rs565627538	chr21:40714784-40714785	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
32	rs200365850	chr21:40714792-40714793	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
33	rs137926276	chr21:40714797-40714798	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
34	rs3988446	chr21:40714852-40714853	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs376888737	chr21:40714862-40714863	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs568448702	chr21:40714902-40714903	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs537370532	chr21:40714925-40714926	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs557186954	chr21:40714948-40714949	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs577378970	chr21:40714963-40714964	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs376820669	chr21:40715000-40715001	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs372081311	chr21:40715014-40715015	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs539637732	chr21:40715017-40715018	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs376373704	chr21:40715021-40715022	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs553480451	chr21:40715025-40715026	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs200281138	chr21:40715032-40715033	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs373249932	chr21:40715056-40715057	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs143824090	chr21:40715077-40715078	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs147235149	chr21:40715079-40715080	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs372501781	chr21:40715091-40715092	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs376492113	chr21:40715098-40715099	Strong transcription Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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 myeloid leukemia	20729466	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
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Down syndrome	20877625	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21147910	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40692400-40718400	Weak transcription	Right Atrium	heart
2	chr21:40704000-40719600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr21:40704400-40715000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr21:40704400-40715200	Weak transcription	Spleen	Spleen
5	chr21:40704600-40717200	Weak transcription	Right Ventricle	heart
6	chr21:40704600-40719600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr21:40704800-40715200	Weak transcription	Fetal Heart	heart
8	chr21:40708800-40715200	Weak transcription	Gastric	stomach
9	chr21:40710000-40715200	Weak transcription	Small Intestine	intestine
10	chr21:40710400-40715400	Weak transcription	Psoas Muscle	Psoas
11	chr21:40711600-40715400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr21:40711800-40715000	Weak transcription	NHLF	lung
13	chr21:40711800-40715200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr21:40711800-40715200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr21:40711800-40715200	Weak transcription	Brain Substantia Nigra	brain
16	chr21:40711800-40719600	Weak transcription	Pancreas	Pancrea
17	chr21:40712000-40715200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr21:40712000-40715200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr21:40712000-40715200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr21:40712000-40715200	Weak transcription	Aorta	Aorta
21	chr21:40712000-40717200	Strong transcription	Fetal Stomach	stomach
22	chr21:40712200-40716000	Strong transcription	Stomach Smooth Muscle	stomach
23	chr21:40712200-40716200	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr21:40712200-40718800	Strong transcription	Fetal Muscle Trunk	muscle
25	chr21:40712400-40715800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr21:40712600-40715200	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr21:40712600-40715400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr21:40712600-40716000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr21:40712600-40716400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr21:40712600-40716600	Strong transcription	Fetal Brain Female	brain
31	chr21:40712600-40716800	Strong transcription	Dnd41	blood
32	chr21:40712600-40717000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr21:40712600-40717000	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr21:40712600-40717000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr21:40712600-40717000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr21:40712600-40717000	Strong transcription	Duodenum Mucosa	Duodenum
37	chr21:40712600-40717200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr21:40712600-40717400	Strong transcription	Fetal Intestine Large	intestine
39	chr21:40712600-40717400	Strong transcription	Fetal Thymus	thymus
40	chr21:40712600-40717400	Strong transcription	Osteobl	bone
41	chr21:40712600-40717600	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr21:40712600-40717600	Strong transcription	Fetal Muscle Leg	muscle
43	chr21:40712600-40717600	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr21:40712600-40717600	Strong transcription	Thymus	Thymus
45	chr21:40712600-40718200	Strong transcription	HSMM	muscle
46	chr21:40712800-40715200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr21:40712800-40715800	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr21:40712800-40715800	Strong transcription	Brain Germinal Matrix	brain
49	chr21:40712800-40715800	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr21:40712800-40716000	Strong transcription	Brain Inferior Temporal Lobe	brain

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