Variant report

Variant	nsv914003
Chromosome Location	chr21:46670874-46695039
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:463)
CpG islands
(count:1344)
Chromatin interactive
region (count:41)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:463 , 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	chr21:46676990-46677206	K562	blood:	n/a	n/a
2	ATF3	chr21:46675311-46675580	GM12878	blood:	n/a	n/a
3	ATF3	chr21:46675278-46675584	K562	blood:	n/a	n/a
4	BACH1	chr21:46676892-46676955	K562	blood:	n/a	n/a
5	BATF	chr21:46686667-46686864	GM12878	blood:	n/a	n/a
6	BHLHE40	chr21:46675345-46675594	GM12878	blood:	n/a	n/a
7	BHLHE40	chr21:46675292-46675623	K562	blood:	n/a	n/a
8	BHLHE40	chr21:46676789-46677338	K562	blood:	n/a	n/a
9	BHLHE40	chr21:46678360-46678702	K562	blood:	n/a	n/a
10	BHLHE40	chr21:46686651-46686835	GM12878	blood:	n/a	n/a
11	BHLHE40	chr21:46678366-46678676	HepG2	liver:	n/a	n/a
12	BHLHE40	chr21:46675319-46675588	HepG2	liver:	n/a	n/a
13	CBX3	chr21:46676751-46677224	K562	blood:	n/a	n/a
14	CCNT2	chr21:46676659-46677313	K562	blood:	n/a	chr21:46677014-46677034
15	CCNT2	chr21:46686029-46686137	K562	blood:	n/a	n/a
16	CCNT2	chr21:46675308-46675567	K562	blood:	n/a	n/a
17	CEBPB	chr21:46676773-46677204	K562	blood:	n/a	n/a
18	CEBPB	chr21:46670836-46671145	K562	blood:	n/a	chr21:46671003-46671014
19	CEBPB	chr21:46670863-46671075	H1-hESC	embryonic stem cell:	n/a	chr21:46671003-46671014
20	CEBPB	chr21:46670952-46671102	A549	lung:	n/a	chr21:46671003-46671014
21	CEBPB	chr21:46670881-46671169	MCF-7	breast:	n/a	chr21:46671003-46671014
22	CEBPB	chr21:46676950-46677138	K562	blood:	n/a	n/a
23	CEBPB	chr21:46670920-46671049	HepG2	liver:	n/a	chr21:46671003-46671014
24	CEBPB	chr21:46670887-46671120	IMR90	lung:	n/a	chr21:46671003-46671014
25	CEBPB	chr21:46670828-46671176	HepG2	liver:	n/a	chr21:46671003-46671014
26	CEBPD	chr21:46676807-46677247	K562	blood:	n/a	n/a
27	CEBPD	chr21:46676701-46677306	K562	blood:	n/a	n/a
28	CHD2	chr21:46676832-46677120	K562	blood:	n/a	n/a
29	CTCF	chr21:46690199-46690487	Gliobla	brain:	n/a	n/a
30	CTCF	chr21:46690240-46690390	HCM	heart:	n/a	n/a
31	CTCF	chr21:46690180-46690330	HAc	cerebellar:	n/a	n/a
32	CTCF	chr21:46690336-46690344	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr21:46690260-46690410	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr21:46690220-46690370	GM12865	blood:	n/a	n/a
35	CTCF	chr21:46690260-46690410	HPF	lung:	n/a	n/a
36	CTCF	chr21:46690301-46690377	GM12892	blood:	n/a	n/a
37	CTCF	chr21:46690278-46690438	LNCaP	prostate:	n/a	n/a
38	CTCF	chr21:46690280-46690430	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr21:46690235-46690466	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr21:46690290-46690414	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr21:46690200-46690350	AG10803	skin:	n/a	n/a
42	CTCF	chr21:46690260-46690410	A549	lung:	n/a	n/a
43	CTCF	chr21:46690240-46690390	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr21:46690223-46690399	GM12878	blood:	n/a	n/a
45	CTCF	chr21:46690240-46690390	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr21:46690260-46690410	HCM	heart:	n/a	n/a
47	CTCF	chr21:46690280-46690430	GM12864	blood:	n/a	n/a
48	CTCF	chr21:46690260-46690410	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr21:46690290-46690414	GM19240	blood:	n/a	n/a
50	CTCF	chr21:46690240-46690390	GM12872	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:46677879-46677929	HepG2	liver:	n/a
2	chr21:46694944-46694994	HNPCEpiC	eye:	n/a
3	chr21:46677879-46677929	HepG2	liver:	n/a
4	chr21:46694944-46694994	HNPCEpiC	eye:	n/a
5	chr21:46684377-46684427	IMR90	lung:	fetal
6	chr21:46694944-46694994	K562	blood:	n/a
7	chr21:46677879-46677929	NB4	blood:	n/a
8	chr21:46687249-46687299	AG04449	skin:	fetal
9	chr21:46677854-46677904	NB4	blood:	n/a
10	chr21:46686908-46686958	NHBE	bronchial:	n/a
11	chr21:46690014-46690064	SK-N-SH_RA	brain:	n/a
12	chr21:46684377-46684427	HMEC	breast:	n/a
13	chr21:46685287-46685337	HCT-116	colon:	n/a
14	chr21:46694944-46694994	LNCaP	prostate:	n/a
15	chr21:46686990-46687040	HMEC	breast:	n/a
16	chr21:46675571-46675621	U87	brain:	n/a
17	chr21:46677750-46677800	HEK293	kidney:	embryo
18	chr21:46677854-46677904	HCPEpiC	choroid plexus:	n/a
19	chr21:46681294-46681344	NB4	blood:	n/a
20	chr21:46675571-46675621	T-47D	breast:	n/a
21	chr21:46687659-46687709	HL-60	blood:	n/a
22	chr21:46675571-46675621	HRCEpiC	kidney:	n/a
23	chr21:46685512-46685562	HRCEpiC	kidney:	n/a
24	chr21:46677482-46677532	HCPEpiC	choroid plexus:	n/a
25	chr21:46685512-46685562	HCT-116	colon:	n/a
26	chr21:46677854-46677904	Jurkat	blood:	n/a
27	chr21:46675571-46675621	NB4	blood:	n/a
28	chr21:46687249-46687299	AoSMC	blood vessel:	n/a
29	chr21:46681294-46681344	AoSMC	blood vessel:	n/a
30	chr21:46675622-46675672	AG10803	skin:	n/a
31	chr21:46684377-46684427	NHBE	bronchial:	n/a
32	chr21:46675622-46675672	SK-N-MC	brain:	n/a
33	chr21:46675770-46675820	AG10803	skin:	n/a
34	chr21:46690014-46690064	HepG2	liver:	n/a
35	chr21:46685154-46685204	PANC-1	pancreas:	n/a
36	chr21:46681294-46681344	HMEC	breast:	n/a
37	chr21:46675622-46675672	SK-N-SH_RA	brain:	n/a
38	chr21:46677879-46677929	PrEC	prostate:	n/a
39	chr21:46681294-46681344	AG04450	lung:	fetal
40	chr21:46677750-46677800	SK-N-SH_RA	brain:	n/a
41	chr21:46677750-46677800	HepG2	liver:	n/a
42	chr21:46686908-46686958	HEEpiC	esophagus:	n/a
43	chr21:46681294-46681344	BJ	skin:	n/a
44	chr21:46685154-46685204	CMK	blood:	n/a
45	chr21:46678524-46678574	NHBE	bronchial:	n/a
46	chr21:46687659-46687709	Caco-2	colon:	n/a
47	chr21:46694944-46694994	HRE	kidney:	n/a
48	chr21:46684377-46684427	HNPCEpiC	eye:	n/a
49	chr21:46690014-46690064	GM12892	blood:	n/a
50	chr21:46686908-46686958	NT2-D1	testis:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46672166..46673879-chr21:46677164..46679113,2	K562	blood:
2	chr21:46673750..46676059-chr21:46688475..46690450,2	MCF-7	breast:
3	chr21:46677096..46679104-chr21:46679185..46682740,7	K562	blood:
4	chr21:46493414..46496701-chr21:46675649..46680419,4	K562	blood:
5	chr21:46683847..46685633-chr4:13362055..13364820,2	MCF-7	breast:
6	chr21:46689820..46691425-chr21:46707957..46710383,2	K562	blood:
7	chr21:46664716..46666767-chr21:46668227..46671842,4	K562	blood:
8	chr21:46649193..46651949-chr21:46675292..46677661,2	K562	blood:
9	chr21:46560131..46560865-chr21:46690017..46690870,2	MCF-7	breast:
10	chr21:46677096..46679104-chr21:46679185..46682740,7	K562	blood:
11	chr21:46645128..46646956-chr21:46675006..46677594,2	MCF-7	breast:
12	chr21:46671702..46674861-chr21:46675485..46679113,5	K562	blood:
13	chr21:46675852..46678920-chr21:46700237..46703123,3	MCF-7	breast:
14	chr21:46675057..46677884-chr21:47243864..47245535,2	MCF-7	breast:
15	chr21:46671702..46674861-chr21:46675485..46679113,5	K562	blood:
16	chr21:46677076..46679332-chr21:46681439..46683653,2	MCF-7	breast:
17	chr21:46692010..46694662-chr21:46699455..46702810,3	K562	blood:
18	chr21:46651731..46653403-chr21:46671567..46674343,2	MCF-7	breast:
19	chr21:46653586..46657139-chr21:46668984..46671071,3	K562	blood:
20	chr21:46692010..46694631-chr21:46699455..46701835,2	K562	blood:
21	chr21:46492783..46494831-chr21:46669105..46671961,2	K562	blood:
22	chr21:46660126..46662433-chr21:46678344..46680642,2	K562	blood:
23	chr21:46694513..46697207-chr21:46719469..46721206,2	K562	blood:
24	chr21:46675525..46679390-chr21:46682642..46685767,4	MCF-7	breast:
25	chr21:46689925..46691815-chr21:46705952..46709457,3	K562	blood:
26	chr21:46664721..46667302-chr21:46670973..46673031,2	MCF-7	breast:
27	chr21:46675036..46676875-chr21:46680682..46682536,2	MCF-7	breast:
28	chr21:46561382..46564170-chr21:46683644..46686214,2	MCF-7	breast:
29	chr21:46586605..46588915-chr21:46675140..46677229,2	K562	blood:
30	chr21:46563443..46566343-chr21:46679834..46682718,2	K562	blood:
31	chr21:46677076..46679332-chr21:46681439..46683653,2	MCF-7	breast:
32	chr21:46572711..46575083-chr21:46683577..46685513,2	K562	blood:
33	chr21:46676803..46681179-chr21:46705386..46709769,5	MCF-7	breast:
34	chr21:46687855..46689998-chr21:46706272..46708765,2	MCF-7	breast:
35	chr21:46672166..46673879-chr21:46677164..46679113,2	K562	blood:
36	chr21:46675525..46679390-chr21:46682642..46685767,4	MCF-7	breast:
37	chr21:46677419..46679156-chr21:46838210..46839952,2	MCF-7	breast:
38	chr21:46684872..46686636-chr21:46690367..46692168,2	K562	blood:
39	chr21:46671592..46674476-chr21:46821725..46823483,2	MCF-7	breast:
40	chr21:46679461..46682130-chr21:46702747..46705388,2	MCF-7	breast:
41	chr21:46675036..46676875-chr21:46680682..46682536,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADARB1-2	chr21:46678366-46678645	XLOC_013979
2	lnc-ADARB1-2	chr21:46676826-46677182	ENSG00000182586.3

No data

Variant related genes	Relation type
POFUT2	TF binding region
POFUT2	CpG island
ENSG00000197381	chromatin interactions
ENSG00000268856	chromatin interactions
ENSG00000186866	chromatin interactions
ENSG00000215447	chromatin interactions
ENSG00000182586	chromatin interactions
ENSG00000235374	chromatin interactions

Extended variants
information (count: 1230 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1230 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2838846	chr21:46670874-46670875	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7275450	chr21:46670893-46670894	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574054271	chr21:46670931-46670932	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs184009531	chr21:46670941-46670942	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs2838847	chr21:46670958-46670959	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs112407875	chr21:46670965-46670966	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs545656328	chr21:46670976-46670977	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs563929424	chr21:46670982-46670983	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs1006778	chr21:46670989-46670990	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs2838848	chr21:46671017-46671018	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs2838849	chr21:46671027-46671028	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs139607684	chr21:46671050-46671051	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs549848601	chr21:46671067-46671068	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs546354713	chr21:46671069-46671070	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs78738700	chr21:46671075-46671076	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs532166689	chr21:46671093-46671094	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs145121340	chr21:46671127-46671128	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs568764138	chr21:46671147-46671148	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs57404120	chr21:46671160-46671161	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs397774908	chr21:46671161-46671162	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs536177938	chr21:46671178-46671179	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs7275870	chr21:46671214-46671215	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs74990715	chr21:46671215-46671216	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs7275874	chr21:46671223-46671224	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs553191072	chr21:46671230-46671231	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs578150597	chr21:46671233-46671234	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs187712141	chr21:46671282-46671283	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs7283915	chr21:46671288-46671289	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs575971750	chr21:46671300-46671301	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs116612594	chr21:46671301-46671302	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs7279604	chr21:46671309-46671310	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs572745314	chr21:46671360-46671361	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs36049371	chr21:46671406-46671407	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs191351452	chr21:46671420-46671421	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs150992468	chr21:46671430-46671431	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs2838850	chr21:46671445-46671446	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs550333691	chr21:46671452-46671453	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs182115574	chr21:46671493-46671494	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs529936661	chr21:46671564-46671565	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs548168410	chr21:46671572-46671573	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs187031978	chr21:46671587-46671588	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs2838851	chr21:46671602-46671603	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs568635183	chr21:46671606-46671607	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs8131143	chr21:46671646-46671647	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs116404174	chr21:46671650-46671651	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539148031	chr21:46671665-46671666	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs557524277	chr21:46671666-46671667	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs569330499	chr21:46671671-46671672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs150171333	chr21:46671688-46671689	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs536896865	chr21:46671689-46671690	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:982 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46669000-46672600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr21:46669000-46683400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr21:46669200-46672800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr21:46669200-46674600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr21:46669200-46677000	Weak transcription	Left Ventricle	heart
6	chr21:46669200-46706600	Weak transcription	Right Atrium	heart
7	chr21:46669400-46671000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr21:46669400-46671600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr21:46669400-46673200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr21:46669400-46673200	Weak transcription	Osteobl	bone
11	chr21:46670600-46671000	Enhancers	Colon Smooth Muscle	Colon
12	chr21:46670800-46671200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
13	chr21:46670800-46676200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr21:46671000-46671200	Enhancers	Rectal Smooth Muscle	rectum
15	chr21:46671000-46671600	Weak transcription	Colon Smooth Muscle	Colon
16	chr21:46671000-46672800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr21:46671200-46683000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr21:46671600-46671800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr21:46671600-46671800	Enhancers	Colon Smooth Muscle	Colon
20	chr21:46671600-46673400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr21:46671800-46672400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr21:46671800-46673000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr21:46672600-46673800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr21:46672600-46673800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr21:46672800-46673200	Enhancers	HSMMtube	muscle
26	chr21:46672800-46673400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr21:46672800-46673400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr21:46672800-46673800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr21:46672800-46673800	Enhancers	NH-A	brain
30	chr21:46673000-46673200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr21:46673000-46673200	Flanking Bivalent TSS/Enh	Hela-S3	cervix
32	chr21:46673000-46673400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr21:46673000-46673600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr21:46673000-46673600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr21:46673000-46673600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr21:46673000-46673600	Enhancers	Colon Smooth Muscle	Colon
37	chr21:46673000-46673600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr21:46673000-46673800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr21:46673000-46673800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr21:46673000-46673800	Enhancers	HSMM	muscle
41	chr21:46673000-46674400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr21:46673200-46673400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr21:46673200-46673400	Bivalent Enhancer	Placenta	Placenta
44	chr21:46673200-46673400	Bivalent Enhancer	Hela-S3	cervix
45	chr21:46673200-46673400	Bivalent Enhancer	HepG2	liver
46	chr21:46673200-46673400	Bivalent Enhancer	NHLF	lung
47	chr21:46673200-46673600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr21:46673200-46673600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr21:46673200-46673600	Enhancers	Osteobl	bone
50	chr21:46673200-46673800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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