Variant report

Variant	nsv895378
Chromosome Location	chr10:50801342-50955649
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1630)
CpG islands
(count:3847)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1630 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:50802598-50802899	K562	blood:	n/a	n/a
2	ATF3	chr10:50887396-50887744	H1-hESC	embryonic stem cell:	n/a	chr10:50887595-50887615 chr10:50887595-50887604
3	ATF3	chr10:50887442-50887695	K562	blood:	n/a	chr10:50887595-50887615 chr10:50887595-50887604
4	ATF3	chr10:50887389-50887778	H1-hESC	embryonic stem cell:	n/a	chr10:50887595-50887615 chr10:50887595-50887604
5	BACH1	chr10:50891044-50891267	K562	blood:	n/a	n/a
6	BACH1	chr10:50819285-50819539	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:50818924-50819042	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:50818288-50818355	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:50827761-50827855	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:50943326-50943356	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:50821165-50821429	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:50898059-50898816	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:50815079-50815303	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr10:50887334-50887920	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr10:50898345-50898505	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr10:50946090-50946405	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:50810021-50810128	K562	blood:	n/a	n/a
18	BHLHE40	chr10:50801191-50801396	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:50802683-50802901	K562	blood:	n/a	n/a
20	BHLHE40	chr10:50887496-50887751	GM12878	blood:	n/a	chr10:50887514-50887530 chr10:50887594-50887603 chr10:50887596-50887605 chr10:50887595-50887604 chr10:50887593-50887606 chr10:50887595-50887604 chr10:50887589-50887610
21	BHLHE40	chr10:50887359-50887793	K562	blood:	n/a	chr10:50887514-50887530 chr10:50887594-50887603 chr10:50887596-50887605 chr10:50887595-50887604 chr10:50887593-50887606 chr10:50887595-50887604 chr10:50887589-50887610
22	BRCA1	chr10:50815248-50815321	HepG2	liver:	n/a	n/a
23	BRCA1	chr10:50835996-50836004	HepG2	liver:	n/a	n/a
24	BRCA1	chr10:50802766-50803071	HepG2	liver:	n/a	n/a
25	BRCA1	chr10:50801101-50801550	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr10:50814962-50815285	K562	blood:	n/a	n/a
27	CBX3	chr10:50887316-50887870	K562	blood:	n/a	n/a
28	CBX3	chr10:50887396-50887667	K562	blood:	n/a	n/a
29	CCNT2	chr10:50887452-50887816	K562	blood:	n/a	chr10:50887637-50887646
30	CEBPB	chr10:50801631-50801890	HepG2	liver:	n/a	n/a
31	CEBPB	chr10:50894687-50894983	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr10:50867047-50867170	K562	blood:	n/a	n/a
33	CEBPB	chr10:50801715-50801807	K562	blood:	n/a	n/a
34	CEBPB	chr10:50809667-50810221	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr10:50807023-50807308	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr10:50841039-50841309	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr10:50855055-50855316	HepG2	liver:	n/a	chr10:50855178-50855195 chr10:50855181-50855194
38	CEBPB	chr10:50887921-50888100	K562	blood:	n/a	chr10:50887970-50887981
39	CEBPB	chr10:50848510-50848713	K562	blood:	n/a	chr10:50848618-50848629
40	CEBPB	chr10:50848578-50848778	HepG2	liver:	n/a	chr10:50848618-50848629
41	CEBPB	chr10:50850109-50850150	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:50848473-50848673	H1-hESC	embryonic stem cell:	n/a	chr10:50848618-50848629
43	CEBPB	chr10:50853943-50854217	Hela-S3	cervix:	n/a	chr10:50854051-50854062 chr10:50854051-50854062
44	CEBPB	chr10:50816413-50816417	K562	blood:	n/a	n/a
45	CEBPB	chr10:50887907-50888094	A549	lung:	n/a	chr10:50887970-50887981
46	CEBPB	chr10:50887493-50887661	K562	blood:	n/a	n/a
47	CEBPB	chr10:50892798-50892932	K562	blood:	n/a	n/a
48	CEBPB	chr10:50816441-50816632	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr10:50887829-50888143	HepG2	liver:	n/a	chr10:50887970-50887981
50	CEBPB	chr10:50942650-50943054	MCF-7	breast:	n/a	n/a

(count:3847 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:50887578-50887628	Jurkat	blood:	n/a
2	chr10:50816262-50816312	HIPEpiC	eye:	n/a
3	chr10:50887049-50887099	HL-60	blood:	n/a
4	chr10:50822606-50822656	HEEpiC	esophagus:	n/a
5	chr10:50887578-50887628	Jurkat	blood:	n/a
6	chr10:50816262-50816312	HIPEpiC	eye:	n/a
7	chr10:50887049-50887099	HL-60	blood:	n/a
8	chr10:50822606-50822656	HEEpiC	esophagus:	n/a
9	chr10:50887058-50887108	AG09309	skin:	n/a
10	chr10:50818153-50818203	BJ	skin:	n/a
11	chr10:50816262-50816312	HEEpiC	esophagus:	n/a
12	chr10:50817804-50817854	BE2_C	brain:	n/a
13	chr10:50887568-50887618	GM19239	blood:	n/a
14	chr10:50817213-50817263	NHBE	bronchial:	n/a
15	chr10:50818299-50818349	GM06990	blood:	n/a
16	chr10:50942972-50943022	HMEC	breast:	n/a
17	chr10:50857556-50857606	Hepatocyte	liver:	n/a
18	chr10:50887632-50887682	T-47D	breast:	n/a
19	chr10:50887578-50887628	CMK	blood:	n/a
20	chr10:50857556-50857606	GM12891	blood:	n/a
21	chr10:50817104-50817154	Hela-S3	cervix:	n/a
22	chr10:50818652-50818702	HepG2	liver:	n/a
23	chr10:50817096-50817146	ProgFib	skin:	n/a
24	chr10:50822175-50822225	H1-hESC	embryonic stem cell:	embryo
25	chr10:50887472-50887522	GM12891	blood:	n/a
26	chr10:50887472-50887522	BJ	skin:	n/a
27	chr10:50887488-50887538	AG09319	gingival:	n/a
28	chr10:50818707-50818757	HRPEpiC	eye:	n/a
29	chr10:50863136-50863186	AG04449	skin:	fetal
30	chr10:50816963-50817013	GM06990	blood:	n/a
31	chr10:50820803-50820853	AoSMC	blood vessel:	n/a
32	chr10:50820803-50820853	GM12892	blood:	n/a
33	chr10:50815015-50815065	RPTEC	kidney:	n/a
34	chr10:50819500-50819550	MCF-7	breast:	n/a
35	chr10:50821031-50821081	HepG2	liver:	n/a
36	chr10:50817651-50817701	GM12878	blood:	n/a
37	chr10:50902733-50902783	HMEC	breast:	n/a
38	chr10:50816963-50817013	Caco-2	colon:	n/a
39	chr10:50857556-50857606	A549	lung:	n/a
40	chr10:50822752-50822802	BE2_C	brain:	n/a
41	chr10:50890136-50890186	GM06990	blood:	n/a
42	chr10:50816058-50816108	HUVEC	blood vessel:	n/a
43	chr10:50887632-50887682	GM06990	blood:	n/a
44	chr10:50821031-50821081	ECC-1	luminal epithelium:	n/a
45	chr10:50887566-50887616	GM06990	blood:	n/a
46	chr10:50822158-50822208	AG10803	skin:	n/a
47	chr10:50887616-50887666	A549	lung:	n/a
48	chr10:50916667-50916717	MCF10A-Er-Src	breast:	n/a
49	chr10:50886878-50886928	HRCEpiC	kidney:	n/a
50	chr10:50817810-50817860	HRPEpiC	eye:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:50802140..50803292-chr10:50991595..50992439,4	MCF-7	breast:
2	chr10:50746012..50749014-chr10:50799370..50802016,3	MCF-7	breast:
3	chr10:50817979..50819560-chr10:50821869..50824788,2	K562	blood:
4	chr10:50849505..50851359-chr10:50859501..50862354,2	K562	blood:
5	chr10:50825488..50827089-chr10:50860500..50862659,2	MCF-7	breast:
6	chr10:50814065..50816075-chr10:50831042..50833228,2	K562	blood:
7	chr10:50817275..50819669-chr10:50821869..50826020,4	K562	blood:
8	chr10:50820607..50822869-chr10:50825214..50827220,2	MCF-7	breast:
9	chr10:50719950..50720567-chr10:50801233..50801768,2	K562	blood:
10	chr10:50801763..50803293-chr10:50810457..50812694,2	K562	blood:
11	chr10:50800816..50801717-chr10:50991472..50992349,4	MCF-7	breast:
12	chr10:50801155..50801773-chr10:50810806..50811622,2	MCF-7	breast:
13	chr10:50849505..50851359-chr10:50859501..50862354,2	K562	blood:
14	chr10:50828397..50830202-chr10:50831455..50833344,2	K562	blood:
15	chr10:50817275..50819669-chr10:50821869..50826020,4	K562	blood:
16	chr10:50801245..50801840-chr10:50953036..50953570,2	MCF-7	breast:
17	chr10:50802656..50803582-chr10:50810996..50811794,2	K562	blood:
18	chr10:50833978..50837174-chr10:50837215..50839127,3	K562	blood:
19	chr10:50865610..50868131-chr10:50870738..50873167,2	K562	blood:
20	chr10:50815088..50816772-chr10:50825663..50828109,2	K562	blood:
21	chr10:50829861..50831911-chr10:50834667..50836429,2	MCF-7	breast:
22	chr10:50868130..50870327-chr10:50874133..50876599,2	K562	blood:
23	chr10:50801763..50803293-chr10:50810457..50812694,2	K562	blood:
24	chr10:50829861..50831911-chr10:50834667..50836429,2	MCF-7	breast:
25	chr10:50828397..50830202-chr10:50831455..50833344,2	K562	blood:
26	chr10:50815088..50816772-chr10:50825663..50828109,2	K562	blood:
27	chr10:50835151..50837782-chr10:50840451..50842242,2	K562	blood:
28	chr10:50865610..50868131-chr10:50870738..50873167,2	K562	blood:
29	chr10:50864973..50867492-chr10:50869627..50872109,2	MCF-7	breast:
30	chr10:50814065..50816075-chr10:50831042..50833228,2	K562	blood:
31	chr10:50812639..50815273-chr10:50822744..50824617,2	MCF-7	breast:
32	chr10:50953927..50957241-chr10:50965194..50969750,5	K562	blood:
33	chr10:50825488..50827089-chr10:50860500..50862659,2	MCF-7	breast:
34	chr10:50835151..50837782-chr10:50840451..50842242,2	K562	blood:
35	chr10:50814760..50816913-chr10:50829962..50832640,2	MCF-7	breast:
36	chr10:50801243..50801878-chr10:50826995..50827951,3	K562	blood:
37	chr10:50809370..50811659-chr10:52048315..52050149,2	K562	blood:
38	chr10:50829978..50831621-chr10:50840399..50842582,2	MCF-7	breast:
39	chr10:50833978..50837174-chr10:50837215..50839127,3	K562	blood:
40	chr10:50801243..50801878-chr10:50826995..50827951,3	K562	blood:
41	chr10:50954773..50957241-chr10:50965884..50969750,3	K562	blood:
42	chr10:50864973..50867492-chr10:50869627..50872109,2	MCF-7	breast:
43	chr10:50813090..50816091-chr10:50817397..50820029,4	K562	blood:
44	chr10:50802714..50803240-chr10:52035391..52036038,2	K562	blood:
45	chr10:50868130..50870327-chr10:50874133..50876599,2	K562	blood:
46	chr10:50801155..50801773-chr10:50810806..50811622,2	MCF-7	breast:
47	chr10:50799877..50800776-chr10:50814007..50814522,2	K562	blood:
48	chr10:50799759..50802460-chr10:50816992..50818492,2	MCF-7	breast:
49	chr10:50802656..50803582-chr10:50810996..50811794,2	K562	blood:
50	chr10:50814760..50816913-chr10:50829962..50832640,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC18A3-1	chr10:50824548-50824648	NONHSAT013316
2	lnc-SLC18A3-1	chr10:50827771-50827841	NONHSAT013316
3	lnc-SLC18A3-1	chr10:50821165-50821248	NONHSAT013316

No data

Variant related genes	Relation type
CHAT	TF binding region
SLC18A3	TF binding region
OGDHL	TF binding region
C10orf53	TF binding region
CHAT	CpG island
SLC18A3	CpG island
OGDHL	CpG island
C10orf53	CpG island
ENSG00000225830	chromatin interactions
ENSG00000187714	chromatin interactions
ENSG00000258838	chromatin interactions
ENSG00000070748	chromatin interactions
ENSG00000197444	chromatin interactions

Extended variants
information (count: 5382 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:5382 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1917804	chr10:50801342-50801343	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
2	rs564155938	chr10:50801346-50801347	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs553359042	chr10:50801347-50801348	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs539612647	chr10:50801365-50801366	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs11595012	chr10:50801368-50801369	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549811285	chr10:50801417-50801418	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs536671315	chr10:50801445-50801446	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs558415619	chr10:50801475-50801476	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs191306885	chr10:50801477-50801478	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs575090508	chr10:50801480-50801481	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs529757869	chr10:50801482-50801483	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs542202650	chr10:50801526-50801527	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs369502479	chr10:50801583-50801584	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs535924813	chr10:50801602-50801603	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs75497825	chr10:50801618-50801619	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs182580161	chr10:50801627-50801628	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs575428548	chr10:50801651-50801652	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs547638839	chr10:50801668-50801669	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs565850188	chr10:50801675-50801676	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs150281733	chr10:50801700-50801701	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs564592413	chr10:50801785-50801786	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs539553140	chr10:50801792-50801793	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs531804416	chr10:50801794-50801795	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs543847402	chr10:50801826-50801827	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs34147823	chr10:50801827-50801828	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs185016343	chr10:50801833-50801834	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs529285644	chr10:50801853-50801854	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs547415493	chr10:50801879-50801880	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs4838390	chr10:50801887-50801888	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533010042	chr10:50801899-50801900	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs551135254	chr10:50801922-50801923	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs569430227	chr10:50801934-50801935	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs536710955	chr10:50801943-50801944	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs370196439	chr10:50801958-50801959	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs138950503	chr10:50802013-50802014	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs75005207	chr10:50802022-50802023	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs189900642	chr10:50802023-50802024	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs79882076	chr10:50802053-50802054	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145822496	chr10:50802138-50802139	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs138388828	chr10:50802182-50802183	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs576613843	chr10:50802188-50802189	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs74877711	chr10:50802220-50802221	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562202852	chr10:50802229-50802230	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs183205175	chr10:50802305-50802306	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541396537	chr10:50802332-50802333	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs56775828	chr10:50802373-50802374	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs535727795	chr10:50802412-50802413	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs145963692	chr10:50802419-50802420	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs527990984	chr10:50802430-50802431	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs199950058	chr10:50802431-50802432	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
XY gonadal dysgenesis	20685758	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD

Chromatin state (count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50799800-50802800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:50800600-50801600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr10:50800600-50801800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:50800600-50801800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr10:50800800-50801600	Enhancers	NHEK	skin
6	chr10:50800800-50801800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:50800800-50801800	Enhancers	HMEC	breast
8	chr10:50800800-50803000	Enhancers	Hela-S3	cervix
9	chr10:50801000-50801400	Enhancers	Osteobl	bone
10	chr10:50801000-50801600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr10:50801000-50801600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr10:50801000-50801600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr10:50801200-50801600	Enhancers	Primary B cells from peripheral blood	blood
14	chr10:50801200-50801600	Enhancers	Liver	Liver
15	chr10:50801200-50801600	Enhancers	Brain Anterior Caudate	brain
16	chr10:50801200-50801600	Enhancers	K562	blood
17	chr10:50801200-50803600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr10:50801400-50801600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr10:50801400-50802800	Weak transcription	Osteobl	bone
20	chr10:50801600-50802600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr10:50801600-50802600	Weak transcription	NHEK	skin
22	chr10:50801600-50802800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr10:50801600-50802800	Weak transcription	Primary B cells from peripheral blood	blood
24	chr10:50801600-50803800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr10:50801600-50806800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr10:50801800-50802400	Weak transcription	K562	blood
27	chr10:50801800-50802800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr10:50801800-50802800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr10:50801800-50802800	Weak transcription	HMEC	breast
30	chr10:50801800-50803800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr10:50801800-50803800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr10:50802600-50803000	Enhancers	NHEK	skin
33	chr10:50802600-50803200	Enhancers	Placenta Amnion	Placenta Amnion
34	chr10:50802800-50803000	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr10:50802800-50803000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
36	chr10:50802800-50803000	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr10:50802800-50803000	Enhancers	Primary B cells from peripheral blood	blood
38	chr10:50802800-50803000	Enhancers	Muscle Satellite Cultured Cells	--
39	chr10:50802800-50803000	Enhancers	Brain Anterior Caudate	brain
40	chr10:50802800-50803000	Active TSS	HepG2	liver
41	chr10:50802800-50803000	Flanking Active TSS	HSMM	muscle
42	chr10:50802800-50803000	Enhancers	K562	blood
43	chr10:50802800-50803200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
44	chr10:50802800-50803200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr10:50802800-50803200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr10:50802800-50803200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr10:50802800-50803200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr10:50802800-50803200	Enhancers	Esophagus	oesophagus
49	chr10:50802800-50803200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr10:50802800-50803200	Enhancers	Osteobl	bone

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