Variant report

Variant	nsv913951
Chromosome Location	chr21:45985068-46012524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:549)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:46003779-46003798	HepG2	liver:	n/a	n/a
2	ATF1	chr21:45989043-45989370	K562	blood:	n/a	n/a
3	ATF1	chr21:46001857-46002317	K562	blood:	n/a	n/a
4	ATF1	chr21:45993004-45993077	K562	blood:	n/a	n/a
5	BATF	chr21:46003684-46003988	GM12878	blood:	n/a	chr21:46003842-46003853
6	BATF	chr21:46003684-46003941	GM12878	blood:	n/a	chr21:46003842-46003853
7	BATF	chr21:45984834-45985416	GM12878	blood:	n/a	n/a
8	BATF	chr21:45984861-45985442	GM12878	blood:	n/a	n/a
9	BCL11A	chr21:45985180-45985430	GM12878	blood:	n/a	n/a
10	BCLAF1	chr21:46003696-46003953	GM12878	blood:	n/a	n/a
11	BHLHE40	chr21:46001901-46002243	K562	blood:	n/a	n/a
12	BHLHE40	chr21:46003254-46003447	K562	blood:	n/a	n/a
13	BHLHE40	chr21:46003715-46003915	GM12878	blood:	n/a	n/a
14	BHLHE40	chr21:45993089-45993414	HepG2	liver:	n/a	n/a
15	BHLHE40	chr21:45988860-45989389	K562	blood:	n/a	chr21:45988914-45988930
16	BHLHE40	chr21:45993089-45993220	K562	blood:	n/a	n/a
17	BHLHE40	chr21:46003781-46003870	HepG2	liver:	n/a	n/a
18	CBX3	chr21:45989069-45989379	K562	blood:	n/a	n/a
19	CBX3	chr21:45989101-45989409	K562	blood:	n/a	n/a
20	CCNT2	chr21:46001980-46002156	K562	blood:	n/a	n/a
21	CEBPB	chr21:45992071-45992108	HepG2	liver:	n/a	n/a
22	CEBPB	chr21:45992028-45992129	K562	blood:	n/a	chr21:45992102-45992113
23	CEBPB	chr21:45994898-45995082	HepG2	liver:	n/a	n/a
24	CEBPB	chr21:45992965-45993094	HepG2	liver:	n/a	n/a
25	CHD2	chr21:45994914-45995251	HepG2	liver:	n/a	chr21:45995063-45995073
26	CREB1	chr21:45985166-45985492	GM12878	blood:	n/a	n/a
27	CREB1	chr21:46003637-46004073	GM12878	blood:	n/a	n/a
28	CREB1	chr21:46003590-46003944	GM12878	blood:	n/a	n/a
29	CREB1	chr21:45989022-45989466	K562	blood:	n/a	n/a
30	CTCF	chr21:46011660-46011810	NHEK	skin:	n/a	n/a
31	CTCF	chr21:45994360-45994510	K562	blood:	n/a	n/a
32	CTCF	chr21:45999973-45999977	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr21:46000140-46000290	MCF-7	breast:	n/a	n/a
34	CTCF	chr21:45994326-45994557	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr21:45995160-45995310	A549	lung:	n/a	n/a
36	CTCF	chr21:45994360-45994510	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr21:45994546-45994631	Fibrobl	skin:	n/a	n/a
38	CTCF	chr21:45994500-45994650	HEK293	kidney:	n/a	n/a
39	CTCF	chr21:45994360-45994510	NHEK	skin:	n/a	n/a
40	CTCF	chr21:45994300-45994450	GM12874	blood:	n/a	n/a
41	CTCF	chr21:46011804-46011986	LNCaP	prostate:	n/a	n/a
42	CTCF	chr21:46003778-46003834	ProgFib	skin:	n/a	n/a
43	CTCF	chr21:45994160-45994220	GM13977	blood:	n/a	n/a
44	CTCF	chr21:45996300-45996321	LNCaP	prostate:	n/a	n/a
45	CTCF	chr21:45994300-45994450	GM12875	blood:	n/a	n/a
46	CTCF	chr21:45994380-45994530	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr21:45994400-45994550	GM12866	blood:	n/a	n/a
48	CTCF	chr21:45993986-45994189	Lung_OC	lung:	n/a	n/a
49	CTCF	chr21:45994506-45994514	A549	lung:	n/a	n/a
50	CTCF	chr21:45994300-45994450	GM12872	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45992152-45992202	SK-N-SH	brain:	n/a
2	chr21:45992414-45992464	AG04449	skin:	fetal
3	chr21:45994842-45994892	GM12892	blood:	n/a
4	chr21:46012520-46012570	BJ	skin:	n/a
5	chr21:46011329-46011379	U87	brain:	n/a
6	chr21:46001928-46001978	GM06990	blood:	n/a
7	chr21:45994842-45994892	HRPEpiC	eye:	n/a
8	chr21:45992414-45992464	ovcar-3	ovarian:	n/a
9	chr21:45999571-45999621	GM12891	blood:	n/a
10	chr21:45993280-45993330	NB4	blood:	n/a
11	chr21:45992414-45992464	HIPEpiC	eye:	n/a
12	chr21:46011329-46011379	AoSMC	blood vessel:	n/a
13	chr21:45994842-45994892	AG09319	gingival:	n/a
14	chr21:45999571-45999621	A549	lung:	n/a
15	chr21:45992152-45992202	HAEpiC	amniotic membrane:	n/a
16	chr21:45992414-45992464	PANC-1	pancreas:	n/a
17	chr21:45999571-45999621	Hela-S3	cervix:	n/a
18	chr21:45999571-45999621	AG09319	gingival:	n/a
19	chr21:45992152-45992202	GM12892	blood:	n/a
20	chr21:45993280-45993330	MCF10A-Er-Src	breast:	n/a
21	chr21:45994842-45994892	Caco-2	colon:	n/a
22	chr21:46012520-46012570	A549	lung:	n/a
23	chr21:45994842-45994892	Hepatocyte	liver:	n/a
24	chr21:46001680-46001730	GM12891	blood:	n/a
25	chr21:45992152-45992202	GM06990	blood:	n/a
26	chr21:46001680-46001730	AG10803	skin:	n/a
27	chr21:45993280-45993330	HCM	heart:	n/a
28	chr21:45992414-45992464	SK-N-SH	brain:	n/a
29	chr21:46001680-46001730	AG09319	gingival:	n/a
30	chr21:45992414-45992464	HepG2	liver:	n/a
31	chr21:46001928-46001978	HCM	heart:	n/a
32	chr21:45999571-45999621	HMEC	breast:	n/a
33	chr21:46012520-46012570	NT2-D1	testis:	n/a
34	chr21:46001928-46001978	Jurkat	blood:	n/a
35	chr21:46012520-46012570	NH-A	brain:	n/a
36	chr21:45999571-45999621	NH-A	brain:	n/a
37	chr21:45999571-45999621	HIPEpiC	eye:	n/a
38	chr21:45994842-45994892	SK-N-SH_RA	brain:	n/a
39	chr21:46012520-46012570	HNPCEpiC	eye:	n/a
40	chr21:45992414-45992464	AG04450	lung:	fetal
41	chr21:45993280-45993330	ProgFib	skin:	n/a
42	chr21:46001928-46001978	NHDF-neo	bronchial:	n/a
43	chr21:45992414-45992464	NB4	blood:	n/a
44	chr21:46001928-46001978	U87	brain:	n/a
45	chr21:45992152-45992202	HRPEpiC	eye:	n/a
46	chr21:45992152-45992202	HCM	heart:	n/a
47	chr21:46012520-46012570	HPAEpiC	pulmonary alveolar:	n/a
48	chr21:46001680-46001730	GM12878	blood:	n/a
49	chr21:45993280-45993330	HEEpiC	esophagus:	n/a
50	chr21:45992414-45992464	GM06990	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45971316..45974046-chr21:45988116..45989981,2	MCF-7	breast:
2	chr21:45997782..46000332-chr21:46014593..46016862,2	MCF-7	breast:
3	chr21:45987563..45989403-chr21:45990992..45992920,2	MCF-7	breast:
4	chr21:45987378..45989214-chr21:45998869..46000795,2	MCF-7	breast:
5	chr21:45979063..45980801-chr21:45987415..45990235,2	MCF-7	breast:
6	chr21:45989841..45993258-chr21:45994452..45997591,3	MCF-7	breast:
7	chr21:46001819..46004380-chr21:46009202..46011051,3	K562	blood:
8	chr21:45996027..45998365-chr21:45999932..46001503,2	MCF-7	breast:
9	chr21:45947897..45950026-chr21:45993818..45996487,2	MCF-7	breast:
10	chr21:45987563..45989403-chr21:45990992..45992920,2	MCF-7	breast:
11	chr21:45989841..45993258-chr21:45994452..45997591,3	MCF-7	breast:
12	chr21:46004403..46006273-chr21:46126860..46128813,2	MCF-7	breast:
13	chr21:46001819..46004380-chr21:46009202..46011051,3	K562	blood:
14	chr21:46010036..46012728-chr21:46031362..46034012,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTAP10-4-1	chr21:45994970-45995428	NONHSAT082869
2	lnc-KRTAP10-5-1	chr21:45999254-45999677	NONHSAT082870
3	lnc-KRTAP10-4-1	chr21:45997192-45997328	NONHSAT082869
4	lnc-KRTAP10-4-1	chr21:45995808-45995960	NONHSAT082869

No data

Variant related genes	Relation type
TSPEAR	TF binding region
KRTAP10-5	TF binding region
KRTAP10-6	TF binding region
KRTAP10-4	TF binding region
TSPEAR	CpG island
KRTAP10-5	CpG island
KRTAP10-6	CpG island
KRTAP10-4	CpG island
ENSG00000241123	chromatin interactions
ENSG00000205445	chromatin interactions
ENSG00000187766	chromatin interactions

Extended variants
information (count: 1613 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188725307	chr21:45985099-45985100	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs140733466	chr21:45985110-45985111	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs143245918	chr21:45985121-45985122	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs587734221	chr21:45985228-45985229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587613796	chr21:45985243-45985244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138841374	chr21:45985263-45985264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs233324	chr21:45985337-45985338	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs587672795	chr21:45985338-45985339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587705231	chr21:45985364-45985365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs57153975	chr21:45985376-45985377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587713744	chr21:45985449-45985450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146361629	chr21:45985477-45985478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs587755319	chr21:45985486-45985487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139729453	chr21:45985508-45985509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587761062	chr21:45985515-45985516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs233325	chr21:45985558-45985559	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs143037531	chr21:45985640-45985641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587602568	chr21:45985686-45985687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150701005	chr21:45985715-45985716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587706405	chr21:45985783-45985784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139999448	chr21:45985837-45985838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192028582	chr21:45985859-45985860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371011182	chr21:45985879-45985880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184626356	chr21:45985883-45985884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149871517	chr21:45985884-45985885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587673983	chr21:45985999-45986000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587725948	chr21:45986021-45986022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144896542	chr21:45986033-45986034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587721561	chr21:45986084-45986085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373009423	chr21:45986092-45986093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587649237	chr21:45986103-45986104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190305660	chr21:45986203-45986204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9974682	chr21:45986342-45986343	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs233326	chr21:45986351-45986352	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs80087886	chr21:45986396-45986397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115660372	chr21:45986458-45986459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76688524	chr21:45986474-45986475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587759904	chr21:45986475-45986476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587650786	chr21:45986506-45986507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587706261	chr21:45986520-45986521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587606321	chr21:45986600-45986601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140360935	chr21:45986636-45986637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182518463	chr21:45986651-45986652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185907256	chr21:45986659-45986660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73233049	chr21:45986672-45986673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73233050	chr21:45986677-45986678	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189634574	chr21:45986848-45986849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs199985117	chr21:45986876-45986877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587729184	chr21:45986883-45986884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144350697	chr21:45986892-45986893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45978400-45994400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr21:45979400-45987800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr21:45984400-45985600	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr21:45984400-45985600	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr21:45984400-45985800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr21:45984600-45985200	Active TSS	GM12878-XiMat	blood
7	chr21:45984600-45985400	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr21:45984600-45985600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr21:45984600-45985600	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr21:45985000-45985200	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr21:45985000-45985400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr21:45985000-45985600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr21:45985000-45987200	Enhancers	Primary B cells from peripheral blood	blood
14	chr21:45985200-45985600	Enhancers	GM12878-XiMat	blood
15	chr21:45985200-45986800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr21:45985200-45987400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr21:45985600-45986200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr21:45987000-45989600	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr21:45987800-45989400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr21:45988200-45989400	Enhancers	Fetal Muscle Leg	muscle
21	chr21:45988200-45989800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr21:45988400-45988800	Weak transcription	Gastric	stomach
23	chr21:45988800-45989000	ZNF genes & repeats	Gastric	stomach
24	chr21:45989000-45994200	Weak transcription	Gastric	stomach
25	chr21:45989400-45991200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr21:45991200-45991600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr21:45991200-45992200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr21:45991400-45991800	Bivalent Enhancer	HepG2	liver
29	chr21:45991600-45992000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr21:45991800-45994400	Enhancers	HepG2	liver
31	chr21:45992000-45992800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr21:45992200-45994400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr21:45992600-45994000	Enhancers	Stomach Mucosa	stomach
34	chr21:45992800-45993000	Bivalent Enhancer	Osteobl	bone
35	chr21:45992800-45993200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr21:45993200-45993400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr21:45993200-45993400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr21:45993200-45993400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
39	chr21:45993200-45993600	Enhancers	Fetal Brain Male	brain
40	chr21:45993400-45994200	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr21:45993400-45994400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr21:45994200-45994400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
43	chr21:45994200-45994400	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr21:45994200-45994600	Flanking Active TSS	Colonic Mucosa	Colon
45	chr21:45994200-45994600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr21:45994200-45994800	Enhancers	Esophagus	oesophagus
47	chr21:45994200-45995000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr21:45994200-45995000	Bivalent Enhancer	Fetal Muscle Leg	muscle
49	chr21:45994200-45995000	Enhancers	Gastric	stomach
50	chr21:45994200-45995600	Enhancers	Liver	Liver

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