Variant report

Variant	nsv828907
Chromosome Location	chr21:45755663-45757829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:62)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr21:45756438-45756462	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr21:45757366-45757638	K562	blood:	n/a	chr21:45757515-45757526
3	CEBPB	chr21:45757357-45757655	HepG2	liver:	n/a	chr21:45757515-45757526
4	CEBPB	chr21:45757374-45757628	IMR90	lung:	n/a	chr21:45757515-45757526
5	CHD1	chr21:45757748-45758570	IMR90	lung:	n/a	n/a
6	MXI1	chr21:45757518-45757541	GM12878	blood:	n/a	n/a
7	MXI1	chr21:45757667-45758645	SK-N-SH	brain:	n/a	n/a
8	POLR2A	chr21:45747288-45755768	HepG2	liver:	n/a	n/a
9	POLR2A	chr21:45755657-45756070	GM12878	blood:	n/a	n/a
10	POLR2A	chr21:45755622-45756209	GM12891	blood:	n/a	n/a
11	POLR2A	chr21:45755607-45756251	GM12892	blood:	n/a	n/a
12	POLR2A	chr21:45755466-45756100	GM12878	blood:	n/a	n/a
13	POLR2A	chr21:45755562-45755727	IMR90	lung:	n/a	n/a
14	POLR2A	chr21:45752217-45756651	GM12891	blood:	n/a	n/a
15	POLR2A	chr21:45755115-45756231	GM12878	blood:	n/a	n/a
16	POLR2A	chr21:45756350-45756458	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr21:45755334-45756079	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr21:45756163-45756622	HepG2	liver:	n/a	n/a
19	POLR2A	chr21:45755596-45756204	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr21:45755776-45756055	GM12891	blood:	n/a	n/a
21	POLR2A	chr21:45755743-45759333	K562	blood:	n/a	n/a
22	POLR2A	chr21:45752255-45756541	GM12891	blood:	n/a	n/a
23	POLR2A	chr21:45755463-45756235	GM12892	blood:	n/a	n/a
24	POLR2A	chr21:45755663-45755742	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr21:45755742-45756649	GM12878	blood:	n/a	n/a
26	POLR2A	chr21:45755613-45755942	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr21:45757215-45757295	HepG2	liver:	n/a	n/a
28	POLR2A	chr21:45752243-45755763	K562	blood:	n/a	n/a
29	POLR2A	chr21:45757168-45757648	IMR90	lung:	n/a	n/a
30	POLR2A	chr21:45754624-45755676	Hela-S3	cervix:	n/a	n/a
31	POU2F2	chr21:45755692-45756194	GM12891	blood:	n/a	n/a
32	RAD21	chr21:45757792-45758440	HepG2	liver:	n/a	n/a
33	RAD21	chr21:45757601-45758642	SK-N-SH	brain:	n/a	n/a
34	STAT3	chr21:45756472-45756640	MCF10A-Er-Src	breast:	n/a	n/a
35	USF2	chr21:45756211-45756244	Hela-S3	cervix:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45755740-45755790	HNPCEpiC	eye:	n/a
2	chr21:45755740-45755790	HNPCEpiC	eye:	n/a
3	chr21:45755740-45755790	ovcar-3	ovarian:	n/a
4	chr21:45755740-45755790	HRPEpiC	eye:	n/a
5	chr21:45755740-45755790	GM06990	blood:	n/a
6	chr21:45755740-45755790	HCT-116	colon:	n/a
7	chr21:45755740-45755790	ProgFib	skin:	n/a
8	chr21:45755740-45755790	SAEC	small airway:	n/a
9	chr21:45755740-45755790	HCM	heart:	n/a
10	chr21:45755740-45755790	HCPEpiC	choroid plexus:	n/a
11	chr21:45755740-45755790	HepG2	liver:	n/a
12	chr21:45755740-45755790	AG09319	gingival:	n/a
13	chr21:45755740-45755790	AG04449	skin:	fetal
14	chr21:45755740-45755790	LNCaP	prostate:	n/a
15	chr21:45755740-45755790	BE2_C	brain:	n/a
16	chr21:45755740-45755790	H1-hESC	embryonic stem cell:	embryo
17	chr21:45755740-45755790	HRE	kidney:	n/a
18	chr21:45755740-45755790	SKMC	muscle:	n/a
19	chr21:45755740-45755790	RPTEC	kidney:	n/a
20	chr21:45755740-45755790	PrEC	prostate:	n/a
21	chr21:45755740-45755790	PFSK-1	brain:	n/a
22	chr21:45755740-45755790	MCF-7	breast:	n/a
23	chr21:45755740-45755790	Caco-2	colon:	n/a
24	chr21:45755740-45755790	A549	lung:	n/a
25	chr21:45755740-45755790	PANC-1	pancreas:	n/a
26	chr21:45755740-45755790	HIPEpiC	eye:	n/a
27	chr21:45755740-45755790	Jurkat	blood:	n/a
28	chr21:45755740-45755790	NT2-D1	testis:	n/a
29	chr21:45755740-45755790	AG04450	lung:	fetal
30	chr21:45755740-45755790	ECC-1	luminal epithelium:	n/a
31	chr21:45755740-45755790	NHDF-neo	bronchial:	n/a
32	chr21:45755740-45755790	GM12878	blood:	n/a
33	chr21:45755740-45755790	Hepatocyte	liver:	n/a
34	chr21:45755740-45755790	AG10803	skin:	n/a
35	chr21:45755740-45755790	SK-N-SH_RA	brain:	n/a
36	chr21:45755740-45755790	HAEpiC	amniotic membrane:	n/a
37	chr21:45755740-45755790	IMR90	lung:	fetal
38	chr21:45755740-45755790	Hela-S3	cervix:	n/a
39	chr21:45755740-45755790	HRCEpiC	kidney:	n/a
40	chr21:45755740-45755790	U87	brain:	n/a
41	chr21:45755740-45755790	SK-N-SH	brain:	n/a
42	chr21:45755740-45755790	SK-N-MC	brain:	n/a
43	chr21:45755740-45755790	GM12892	blood:	n/a
44	chr21:45755740-45755790	MCF10A-Er-Src	breast:	n/a
45	chr21:45755740-45755790	HMEC	breast:	n/a
46	chr21:45755740-45755790	HEEpiC	esophagus:	n/a
47	chr21:45755740-45755790	CMK	blood:	n/a
48	chr21:45755740-45755790	K562	blood:	n/a
49	chr21:45755740-45755790	NHBE	bronchial:	n/a
50	chr21:45755740-45755790	AoSMC	blood vessel:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45525373..45527219-chr21:45757637..45759650,2	K562	blood:
2	chr21:45553139..45558622-chr21:45753607..45756462,4	K562	blood:
3	chr21:45561158..45563910-chr21:45754064..45756114,2	MCF-7	breast:
4	chr21:45552120..45555319-chr21:45756917..45761085,4	MCF-7	breast:
5	chr21:45757779..45764116-chr21:45768144..45773804,8	K562	blood:
6	chr21:45525933..45529754-chr21:45756924..45759975,4	MCF-7	breast:
7	chr21:45756335..45760049-chr21:45874026..45878349,7	MCF-7	breast:
8	chr21:45563311..45566975-chr21:45753410..45757143,4	K562	blood:
9	chr21:45604256..45606342-chr21:45755991..45757526,2	MCF-7	breast:
10	chr21:45553374..45555215-chr21:45757736..45759429,2	K562	blood:
11	chr21:45719852..45723806-chr21:45756512..45759776,5	MCF-7	breast:
12	chr21:45757587..45760440-chr21:45787714..45792009,6	MCF-7	breast:
13	chr21:45557797..45558562-chr21:45755481..45756116,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000232969	TF binding region
C21orf2	TF binding region
ENSG00000232969	CpG island
C21orf2	CpG island
ENSG00000142185	chromatin interactions
ENSG00000160233	chromatin interactions
ENSG00000241945	chromatin interactions
ENSG00000260256	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000229356	chromatin interactions

Extended variants
information (count: 127 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:127 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370014560	chr21:45755704-45755705	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs201127621	chr21:45755734-45755735	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs189695721	chr21:45755735-45755736	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs147855042	chr21:45755736-45755737	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs182333890	chr21:45755740-45755741	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562586179	chr21:45755743-45755744	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs139328963	chr21:45755752-45755753	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs112926736	chr21:45755753-45755754	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs376087157	chr21:45755758-45755759	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs111711465	chr21:45755768-45755769	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs548821694	chr21:45755791-45755792	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs62220411	chr21:45755808-45755809	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs373517822	chr21:45755812-45755813	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs191231691	chr21:45755814-45755815	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs552856457	chr21:45755828-45755829	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs75733226	chr21:45755857-45755858	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs76736548	chr21:45755858-45755859	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs550034375	chr21:45755863-45755864	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs76447640	chr21:45755864-45755865	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs74354449	chr21:45755866-45755867	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs112453644	chr21:45755911-45755912	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs61431795	chr21:45755914-45755915	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs561098269	chr21:45755950-45755951	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs59053694	chr21:45755962-45755963	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs112247441	chr21:45755963-45755964	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs528572740	chr21:45755975-45755976	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs554355758	chr21:45755980-45755981	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs71197893	chr21:45755984-45755985	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs13046339	chr21:45755990-45755991	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs67030350	chr21:45756015-45756016	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs143659446	chr21:45756027-45756028	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs183079367	chr21:45756042-45756043	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs576796801	chr21:45756054-45756055	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs544170863	chr21:45756068-45756069	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs66916924	chr21:45756069-45756070	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
36	rs148111961	chr21:45756096-45756097	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs541905436	chr21:45756101-45756102	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs188536480	chr21:45756138-45756139	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs532435036	chr21:45756160-45756161	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs527883972	chr21:45756163-45756164	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550917954	chr21:45756170-45756171	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs569079347	chr21:45756184-45756185	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs57970143	chr21:45756248-45756249	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73374021	chr21:45756267-45756268	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs554815129	chr21:45756308-45756309	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs57080308	chr21:45756318-45756319	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs531883168	chr21:45756321-45756322	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs4818710	chr21:45756344-45756345	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs533975602	chr21:45756390-45756391	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs192305710	chr21:45756395-45756396	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Hodgkin''s lymphoma	18641027	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
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	21364760	CNVD
Down syndrome	21154855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Williams-beuren syndrome	16826523	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45721000-45757600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr21:45725000-45758000	Weak transcription	Right Atrium	heart
3	chr21:45725800-45757400	Strong transcription	Thymus	Thymus
4	chr21:45726600-45757200	Strong transcription	Fetal Intestine Small	intestine
5	chr21:45731400-45757800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr21:45731400-45758000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr21:45731400-45758000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr21:45731400-45758000	Weak transcription	A549	lung
9	chr21:45731600-45756200	Weak transcription	Osteobl	bone
10	chr21:45731600-45758000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr21:45731800-45757600	Weak transcription	Fetal Kidney	kidney
12	chr21:45731800-45758000	Weak transcription	HSMM	muscle
13	chr21:45733400-45758000	Weak transcription	Psoas Muscle	Psoas
14	chr21:45734000-45758000	Weak transcription	HUVEC	blood vessel
15	chr21:45734200-45757800	Weak transcription	Hela-S3	cervix
16	chr21:45734400-45758000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr21:45736600-45757200	Strong transcription	Lung	lung
18	chr21:45738400-45756200	Weak transcription	HSMMtube	muscle
19	chr21:45740200-45758000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr21:45743000-45759000	Weak transcription	Primary B cells from cord blood	blood
21	chr21:45744200-45757800	Weak transcription	GM12878-XiMat	blood
22	chr21:45744600-45757800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr21:45744800-45756000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr21:45745200-45757000	Weak transcription	K562	blood
25	chr21:45745400-45756000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr21:45745400-45759000	Weak transcription	Small Intestine	intestine
27	chr21:45745600-45757800	Weak transcription	HMEC	breast
28	chr21:45745800-45757800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr21:45745800-45758200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr21:45746000-45757800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr21:45746200-45757800	Weak transcription	Stomach Mucosa	stomach
32	chr21:45746400-45756200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr21:45746400-45758000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr21:45746600-45758200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr21:45747000-45756200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr21:45747600-45756000	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr21:45747600-45758200	Weak transcription	Aorta	Aorta
38	chr21:45747800-45758000	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr21:45748000-45757800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr21:45748000-45758200	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr21:45748200-45757600	Weak transcription	Brain Angular Gyrus	brain
42	chr21:45748400-45756200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr21:45748400-45757800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr21:45749400-45756400	Strong transcription	Brain Hippocampus Middle	brain
45	chr21:45750000-45757400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr21:45750600-45758000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr21:45751600-45757400	Strong transcription	Primary T cells from cord blood	blood
48	chr21:45752200-45757400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr21:45752200-45757800	Weak transcription	Colon Smooth Muscle	Colon
50	chr21:45753200-45755800	Weak transcription	Left Ventricle	heart

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