Variant report

Variant	nsv587739
Chromosome Location	chr21:45628374-45640629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:0)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45638537-45638623	K562	blood:	n/a	n/a
2	ATF1	chr21:45638353-45638745	K562	blood:	n/a	n/a
3	ATF2	chr21:45632208-45632642	GM12878	blood:	n/a	n/a
4	ATF2	chr21:45634976-45635407	GM12878	blood:	n/a	n/a
5	ATF2	chr21:45631647-45632775	GM12878	blood:	n/a	n/a
6	ATF2	chr21:45639835-45640899	GM12878	blood:	n/a	n/a
7	ATF2	chr21:45638216-45638736	GM12878	blood:	n/a	n/a
8	BATF	chr21:45635423-45635665	GM12878	blood:	n/a	n/a
9	BATF	chr21:45635177-45635735	GM12878	blood:	n/a	n/a
10	BCL11A	chr21:45640590-45640939	GM12878	blood:	n/a	n/a
11	BCL3	chr21:45631471-45632171	GM12878	blood:	n/a	n/a
12	BCL3	chr21:45631415-45632600	GM12878	blood:	n/a	n/a
13	BCLAF1	chr21:45638339-45638846	GM12878	blood:	n/a	n/a
14	BCLAF1	chr21:45639813-45640874	GM12878	blood:	n/a	n/a
15	BCLAF1	chr21:45639703-45640268	GM12878	blood:	n/a	n/a
16	BCLAF1	chr21:45631717-45632370	GM12878	blood:	n/a	n/a
17	BCLAF1	chr21:45638337-45638932	GM12878	blood:	n/a	n/a
18	BCLAF1	chr21:45635123-45635688	GM12878	blood:	n/a	n/a
19	BCLAF1	chr21:45640318-45640949	GM12878	blood:	n/a	n/a
20	BCLAF1	chr21:45631987-45632771	GM12878	blood:	n/a	chr21:45632621-45632630
21	BHLHE40	chr21:45635413-45635420	GM12878	blood:	n/a	n/a
22	BHLHE40	chr21:45638327-45638777	K562	blood:	n/a	n/a
23	BHLHE40	chr21:45632226-45632563	GM12878	blood:	n/a	n/a
24	BHLHE40	chr21:45638323-45638771	GM12878	blood:	n/a	n/a
25	BHLHE40	chr21:45627566-45628378	K562	blood:	n/a	n/a
26	BRCA1	chr21:45631582-45632400	GM12878	blood:	n/a	n/a
27	BRCA1	chr21:45638147-45638309	GM12878	blood:	n/a	n/a
28	CEBPB	chr21:45631340-45632716	GM12878	blood:	n/a	chr21:45632695-45632706
29	CEBPB	chr21:45627914-45628489	IMR90	lung:	n/a	n/a
30	CEBPB	chr21:45636321-45636436	HepG2	liver:	n/a	n/a
31	CHD1	chr21:45635312-45635511	GM12878	blood:	n/a	n/a
32	CHD2	chr21:45631840-45632356	GM12878	blood:	n/a	n/a
33	CHD2	chr21:45628366-45628449	GM12878	blood:	n/a	n/a
34	CHD2	chr21:45639709-45639806	GM12878	blood:	n/a	n/a
35	CHD2	chr21:45640280-45640635	GM12878	blood:	n/a	n/a
36	CHD2	chr21:45639147-45639231	GM12878	blood:	n/a	n/a
37	CHD2	chr21:45638056-45638795	GM12878	blood:	n/a	n/a
38	CTCF	chr21:45640140-45640290	GM12864	blood:	n/a	n/a
39	CTCF	chr21:45640310-45640487	GM12878	blood:	n/a	n/a
40	CTCF	chr21:45640240-45640390	GM06990	blood:	n/a	n/a
41	CTCF	chr21:45640328-45640445	GM19240	blood:	n/a	n/a
42	CTCF	chr21:45628240-45628390	HEK293	kidney:	n/a	chr21:45628345-45628353
43	CTCF	chr21:45628240-45628390	GM12878	blood:	n/a	chr21:45628345-45628353
44	CTCF	chr21:45628360-45628510	GM12873	blood:	n/a	n/a
45	CTCF	chr21:45640374-45640456	GM10266	blood:	n/a	n/a
46	CTCF	chr21:45628360-45628510	HCFaa	heart:	n/a	n/a
47	CTCF	chr21:45628242-45628421	GM19239	blood:	n/a	chr21:45628345-45628353
48	CTCF	chr21:45628440-45628590	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr21:45628260-45628410	GM12871	blood:	n/a	chr21:45628345-45628353
50	CTCF	chr21:45628260-45628410	AG04449	skin:	n/a	chr21:45628345-45628353

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45625593..45629065-chr21:45717787..45720760,5	MCF-7	breast:
2	chr21:45631740..45633911-chr21:45635590..45640208,4	MCF-7	breast:
3	chr21:45628810..45630554-chr21:45636671..45638693,2	K562	blood:
4	chr21:45619816..45631884-chr21:45656529..45663802,30	MCF-7	breast:
5	chr21:45633493..45635981-chr21:45638938..45640638,2	MCF-7	breast:
6	chr21:45628810..45630554-chr21:45636671..45638693,2	K562	blood:
7	chr21:45631200..45631884-chr4:2306687..2307191,2	MCF-7	breast:
8	chr21:45626500..45630389-chr21:45636831..45640533,5	MCF-7	breast:
9	chr21:45638620..45641640-chr21:45644035..45648127,5	MCF-7	breast:
10	chr21:45590531..45598113-chr21:45625237..45630055,9	MCF-7	breast:
11	chr21:45636499..45639520-chr21:45653196..45656118,3	K562	blood:
12	chr21:45634893..45639040-chr21:45644730..45647153,4	K562	blood:
13	chr21:45621014..45624737-chr21:45625090..45629806,7	K562	blood:
14	chr21:45638024..45640421-chr21:45658228..45660769,4	MCF-7	breast:
15	chr21:45620311..45631567-chr21:45651002..45670824,52	MCF-7	breast:
16	chr21:45637599..45639295-chr21:45647938..45650241,2	MCF-7	breast:
17	chr21:45621014..45626357-chr21:45626432..45630019,5	K562	blood:
18	chr21:45631740..45633911-chr21:45635590..45640208,4	MCF-7	breast:
19	chr21:45571719..45574629-chr21:45639760..45641612,2	MCF-7	breast:
20	chr21:45621786..45624650-chr21:45632661..45635247,3	MCF-7	breast:
21	chr21:45633493..45635981-chr21:45638938..45640638,2	MCF-7	breast:
22	chr21:45638138..45641604-chr21:45643124..45645379,3	MCF-7	breast:
23	chr21:45626963..45630289-chr21:45630866..45636096,6	MCF-7	breast:
24	chr21:45555886..45558409-chr21:45626511..45629056,2	MCF-7	breast:
25	chr21:45633515..45635419-chr21:45641635..45644619,2	MCF-7	breast:
26	chr21:45634893..45639040-chr21:45644730..45647153,3	K562	blood:
27	chr21:45637874..45640737-chr21:45652531..45655334,2	MCF-7	breast:
28	chr21:45637636..45640956-chr21:45661307..45664168,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000232698	TF binding region
ENSG00000237604	chromatin interactions
ENSG00000232010	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000232124	chromatin interactions
ENSG00000267913	chromatin interactions
ENSG00000232698	chromatin interactions

Extended variants
information (count: 696 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2838523	chr21:45628374-45628375	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181551060	chr21:45628399-45628400	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs2838524	chr21:45628401-45628402	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs549855084	chr21:45628455-45628456	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs575967637	chr21:45628484-45628485	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs111819785	chr21:45628491-45628492	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs112832883	chr21:45628503-45628504	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs554712222	chr21:45628509-45628510	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs34560460	chr21:45628546-45628547	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs71322554	chr21:45628553-45628554	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs540408266	chr21:45628563-45628564	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs111614208	chr21:45628600-45628601	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs377050799	chr21:45628795-45628796	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs12481932	chr21:45628796-45628797	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs75499413	chr21:45628865-45628866	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs2838525	chr21:45628866-45628867	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs563253825	chr21:45628915-45628916	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs530672568	chr21:45628948-45628949	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs549258114	chr21:45628953-45628954	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs567193048	chr21:45628990-45628991	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs116682877	chr21:45628994-45628995	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs73381322	chr21:45629008-45629009	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs571327692	chr21:45629012-45629013	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs539241999	chr21:45629016-45629017	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs553846404	chr21:45629029-45629030	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs565665375	chr21:45629059-45629060	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs529134902	chr21:45629085-45629086	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs536582755	chr21:45629091-45629092	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs555227848	chr21:45629101-45629102	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs376122830	chr21:45629116-45629117	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs58911644	chr21:45629121-45629122	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs7277413	chr21:45629157-45629158	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs374468955	chr21:45629195-45629196	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs558642843	chr21:45629197-45629198	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs576886771	chr21:45629237-45629238	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs112841346	chr21:45629262-45629263	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs368612309	chr21:45629345-45629346	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs2838526	chr21:45629368-45629369	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs530724942	chr21:45629387-45629388	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs149291673	chr21:45629435-45629436	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs144566190	chr21:45629470-45629471	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs373690053	chr21:45629473-45629474	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs186028342	chr21:45629498-45629499	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs546532721	chr21:45629535-45629536	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs34521677	chr21:45629554-45629555	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs3804030	chr21:45629565-45629566	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs7277916	chr21:45629593-45629594	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs148479405	chr21:45629597-45629598	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs569505865	chr21:45629598-45629599	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs536832782	chr21:45629602-45629603	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45622800-45629800	Enhancers	Placenta	Placenta
2	chr21:45623000-45629400	Enhancers	K562	blood
3	chr21:45623000-45629800	Enhancers	Fetal Muscle Leg	muscle
4	chr21:45624200-45628800	Enhancers	Fetal Stomach	stomach
5	chr21:45624600-45629200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr21:45625200-45629600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr21:45625400-45628400	Enhancers	Small Intestine	intestine
8	chr21:45625400-45628800	Enhancers	NHLF	lung
9	chr21:45625400-45629000	Enhancers	Fetal Thymus	thymus
10	chr21:45625400-45629400	Enhancers	Placenta Amnion	Placenta Amnion
11	chr21:45625400-45630200	Enhancers	Primary hematopoietic stem cells	blood
12	chr21:45625800-45628800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr21:45625800-45629200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr21:45625800-45629600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr21:45626000-45628400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr21:45626000-45628400	Enhancers	Fetal Intestine Large	intestine
17	chr21:45626000-45628400	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr21:45626000-45628600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr21:45626000-45628600	Enhancers	Fetal Intestine Small	intestine
20	chr21:45626000-45628600	Enhancers	Pancreas	Pancrea
21	chr21:45626000-45628800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr21:45626000-45628800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr21:45626000-45628800	Enhancers	Lung	lung
24	chr21:45626000-45628800	Enhancers	Spleen	Spleen
25	chr21:45626000-45629000	Enhancers	Adipose Nuclei	Adipose
26	chr21:45626000-45629000	Flanking Active TSS	GM12878-XiMat	blood
27	chr21:45626000-45629200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
28	chr21:45626000-45629400	Enhancers	Esophagus	oesophagus
29	chr21:45626200-45628600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr21:45626200-45628600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr21:45626200-45628800	Enhancers	Left Ventricle	heart
32	chr21:45626200-45629000	Enhancers	Right Ventricle	heart
33	chr21:45626200-45629000	Enhancers	NHEK	skin
34	chr21:45626400-45628600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr21:45626400-45628800	Enhancers	Fetal Kidney	kidney
36	chr21:45626600-45628400	Enhancers	Thymus	Thymus
37	chr21:45626600-45629800	Enhancers	HUVEC	blood vessel
38	chr21:45626800-45628600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr21:45626800-45628600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr21:45626800-45628600	Enhancers	Right Atrium	heart
41	chr21:45626800-45629000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr21:45626800-45629000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr21:45626800-45629200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr21:45626800-45630600	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr21:45627000-45628400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr21:45627000-45628600	Enhancers	Liver	Liver
47	chr21:45627000-45629000	Enhancers	Brain Substantia Nigra	brain
48	chr21:45627000-45629000	Enhancers	HMEC	breast
49	chr21:45627000-45629200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr21:45627000-45629200	Enhancers	Stomach Mucosa	stomach

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