Variant report

Variant	nsv906874
Chromosome Location	chr16:70677785-70740707
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2469)
CpG islands
(count:3178)
Chromatin interactive
region (count:128)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:2469 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70729555-70729873	K562	blood:	n/a	n/a
2	ARID3A	chr16:70687569-70688101	K562	blood:	n/a	n/a
3	ARID3A	chr16:70687628-70687944	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:70690613-70690765	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:70723501-70723726	HepG2	liver:	n/a	n/a
6	ATF1	chr16:70687709-70688084	K562	blood:	n/a	n/a
7	ATF2	chr16:70727915-70728403	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr16:70719798-70720136	K562	blood:	n/a	chr16:70720000-70720009 chr16:70719988-70720008
9	ATF3	chr16:70687616-70688014	K562	blood:	n/a	n/a
10	ATF3	chr16:70719875-70720111	HepG2	liver:	n/a	chr16:70720000-70720009 chr16:70719988-70720008
11	BACH1	chr16:70728018-70728457	H1-hESC	embryonic stem cell:	n/a	chr16:70728171-70728185
12	BACH1	chr16:70719312-70719513	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr16:70729711-70729940	K562	blood:	n/a	n/a
14	BACH1	chr16:70710538-70710648	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr16:70696002-70696021	K562	blood:	n/a	n/a
16	BACH1	chr16:70719910-70720474	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr16:70713819-70714151	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr16:70727687-70728702	A549	lung:	n/a	n/a
19	BCL3	chr16:70719867-70720618	A549	lung:	n/a	chr16:70720296-70720305 chr16:70720004-70720013 chr16:70720001-70720010 chr16:70720041-70720054
20	BCL3	chr16:70696017-70696559	K562	blood:	n/a	n/a
21	BCL3	chr16:70695304-70695694	A549	lung:	n/a	n/a
22	BCL3	chr16:70719910-70720275	GM12878	blood:	n/a	chr16:70720004-70720013 chr16:70720001-70720010 chr16:70720041-70720054
23	BHLHE40	chr16:70720928-70721497	K562	blood:	n/a	n/a
24	BHLHE40	chr16:70719789-70720182	K562	blood:	n/a	n/a
25	BHLHE40	chr16:70729308-70729987	K562	blood:	n/a	n/a
26	BHLHE40	chr16:70723501-70723740	HepG2	liver:	n/a	n/a
27	BHLHE40	chr16:70687678-70688281	K562	blood:	n/a	n/a
28	BHLHE40	chr16:70719828-70721453	HepG2	liver:	n/a	n/a
29	BHLHE40	chr16:70680190-70680410	HepG2	liver:	n/a	chr16:70680317-70680326 chr16:70680314-70680327 chr16:70680310-70680331
30	BHLHE40	chr16:70680201-70680401	K562	blood:	n/a	chr16:70680317-70680326 chr16:70680314-70680327 chr16:70680310-70680331
31	BHLHE40	chr16:70690577-70691176	HepG2	liver:	n/a	n/a
32	BRCA1	chr16:70716261-70716421	HepG2	liver:	n/a	n/a
33	BRCA1	chr16:70687630-70688061	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr16:70715668-70716034	HepG2	liver:	n/a	n/a
35	BRCA1	chr16:70723666-70723763	HepG2	liver:	n/a	n/a
36	BRCA1	chr16:70717199-70717278	HepG2	liver:	n/a	n/a
37	BRCA1	chr16:70719326-70719329	HepG2	liver:	n/a	n/a
38	BRCA1	chr16:70716747-70716841	HepG2	liver:	n/a	n/a
39	CBX3	chr16:70702761-70703016	K562	blood:	n/a	n/a
40	CBX3	chr16:70719896-70720161	K562	blood:	n/a	n/a
41	CBX3	chr16:70687637-70688163	K562	blood:	n/a	n/a
42	CBX3	chr16:70729269-70730023	K562	blood:	n/a	n/a
43	CCNT2	chr16:70687686-70688061	K562	blood:	n/a	n/a
44	CCNT2	chr16:70713996-70714229	K562	blood:	n/a	n/a
45	CCNT2	chr16:70719419-70720258	K562	blood:	n/a	n/a
46	CCNT2	chr16:70729500-70730051	K562	blood:	n/a	chr16:70729780-70729800
47	CEBPB	chr16:70726451-70726571	K562	blood:	n/a	n/a
48	CEBPB	chr16:70713940-70714038	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr16:70710563-70710716	A549	lung:	n/a	chr16:70710700-70710713
50	CEBPB	chr16:70730765-70731305	MCF-7	breast:	n/a	n/a

(count:3178 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70700420-70700470	HPAEpiC	pulmonary alveolar:	n/a
2	chr16:70680817-70680867	NHDF-neo	bronchial:	n/a
3	chr16:70720817-70720867	HCPEpiC	choroid plexus:	n/a
4	chr16:70721696-70721746	CMK	blood:	n/a
5	chr16:70714606-70714656	SKMC	muscle:	n/a
6	chr16:70728425-70728475	SAEC	small airway:	n/a
7	chr16:70700420-70700470	HPAEpiC	pulmonary alveolar:	n/a
8	chr16:70680817-70680867	NHDF-neo	bronchial:	n/a
9	chr16:70720817-70720867	HCPEpiC	choroid plexus:	n/a
10	chr16:70721696-70721746	CMK	blood:	n/a
11	chr16:70714606-70714656	SKMC	muscle:	n/a
12	chr16:70728425-70728475	SAEC	small airway:	n/a
13	chr16:70714357-70714407	AG09309	skin:	n/a
14	chr16:70733772-70733822	NB4	blood:	n/a
15	chr16:70720133-70720183	SK-N-SH_RA	brain:	n/a
16	chr16:70700420-70700470	HL-60	blood:	n/a
17	chr16:70688171-70688221	NHDF-neo	bronchial:	n/a
18	chr16:70698146-70698196	NHDF-neo	bronchial:	n/a
19	chr16:70680108-70680158	NH-A	brain:	n/a
20	chr16:70714606-70714656	HCF	heart:	n/a
21	chr16:70720314-70720364	HRPEpiC	eye:	n/a
22	chr16:70736032-70736082	HEK293	kidney:	embryo
23	chr16:70720083-70720133	RPTEC	kidney:	n/a
24	chr16:70680104-70680154	U87	brain:	n/a
25	chr16:70720133-70720183	Hepatocyte	liver:	n/a
26	chr16:70717902-70717952	SAEC	small airway:	n/a
27	chr16:70709930-70709980	Hepatocyte	liver:	n/a
28	chr16:70720817-70720867	HCT-116	colon:	n/a
29	chr16:70680631-70680681	AG04449	skin:	fetal
30	chr16:70700420-70700470	HepG2	liver:	n/a
31	chr16:70733234-70733284	HNPCEpiC	eye:	n/a
32	chr16:70719667-70719717	Hepatocyte	liver:	n/a
33	chr16:70680817-70680867	RPTEC	kidney:	n/a
34	chr16:70713203-70713253	Hepatocyte	liver:	n/a
35	chr16:70714357-70714407	HPAEpiC	pulmonary alveolar:	n/a
36	chr16:70680631-70680681	AG09319	gingival:	n/a
37	chr16:70720817-70720867	NH-A	brain:	n/a
38	chr16:70698362-70698412	HMEC	breast:	n/a
39	chr16:70698053-70698103	GM12892	blood:	n/a
40	chr16:70700420-70700470	LNCaP	prostate:	n/a
41	chr16:70714378-70714428	Jurkat	blood:	n/a
42	chr16:70698831-70698881	NHBE	bronchial:	n/a
43	chr16:70733234-70733284	NH-A	brain:	n/a
44	chr16:70720083-70720133	GM19239	blood:	n/a
45	chr16:70697712-70697762	GM12891	blood:	n/a
46	chr16:70713933-70713983	HAEpiC	amniotic membrane:	n/a
47	chr16:70680320-70680370	BJ	skin:	n/a
48	chr16:70680320-70680370	NH-A	brain:	n/a
49	chr16:70720817-70720867	HIPEpiC	eye:	n/a
50	chr16:70679178-70679228	HAEpiC	amniotic membrane:	n/a

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:70700778..70704017-chr16:70704220..70706631,3	K562	blood:
2	chr16:70611435..70614345-chr16:70688186..70690575,2	K562	blood:
3	chr16:70721359..70722001-chr16:70804625..70805130,2	NB4	blood:
4	chr16:70686356..70687984-chr16:70719406..70721233,2	K562	blood:
5	chr16:70708118..70709797-chr16:70771075..70773341,2	MCF-7	breast:
6	chr16:70731234..70732060-chr16:70804672..70805218,2	MCF-7	breast:
7	chr16:70681076..70682967-chr16:70686271..70687994,2	K562	blood:
8	chr16:70735376..70737642-chr16:70737721..70740521,2	K562	blood:
9	chr16:70700082..70702033-chr16:70779098..70781687,2	MCF-7	breast:
10	chr16:70557413..70558963-chr16:70714996..70717937,3	MCF-7	breast:
11	chr16:70695734..70697501-chr16:70719641..70721197,2	MCF-7	breast:
12	chr16:70684913..70687861-chr16:70697213..70699784,2	MCF-7	breast:
13	chr16:70694604..70697183-chr16:70727406..70729893,2	K562	blood:
14	chr16:70555993..70558227-chr16:70687892..70690787,2	K562	blood:
15	chr16:70704267..70706050-chr16:70717985..70719949,2	MCF-7	breast:
16	chr16:70680910..70683567-chr16:70688856..70691172,2	K562	blood:
17	chr16:70412847..70415449-chr16:70713492..70715384,2	MCF-7	breast:
18	chr16:70413470..70415352-chr16:70682126..70684373,2	MCF-7	breast:
19	chr16:70702333..70704559-chr16:70708648..70711646,3	MCF-7	breast:
20	chr16:70731581..70732230-chr16:70771694..70772666,3	MCF-7	breast:
21	chr16:70704267..70706050-chr16:70717985..70719949,2	MCF-7	breast:
22	chr16:70708575..70710347-chr16:70756383..70757936,2	K562	blood:
23	chr16:70726776..70729774-chr16:70778926..70781727,2	K562	blood:
24	chr16:70555634..70562342-chr16:70718026..70723686,6	MCF-7	breast:
25	chr16:70693052..70694903-chr16:70718583..70720776,2	K562	blood:
26	chr16:70408756..70411643-chr16:70690769..70692311,2	MCF-7	breast:
27	chr16:70685129..70687949-chr16:70714245..70716905,2	K562	blood:
28	chr16:70728939..70732766-chr16:70778342..70782420,7	MCF-7	breast:
29	chr16:70718434..70719938-chr16:70760026..70761921,2	K562	blood:
30	chr16:70688760..70693483-chr16:70698297..70703877,5	K562	blood:
31	chr1:28974074..28976735-chr16:70718527..70720954,2	K562	blood:
32	chr16:70725942..70727688-chr16:70759419..70762080,2	K562	blood:
33	chr16:70718149..70722046-chr16:70735012..70737866,4	K562	blood:
34	chr16:70714365..70716642-chr16:70800502..70803105,2	K562	blood:
35	chr16:70706397..70707963-chr16:70716501..70718128,2	K562	blood:
36	chr16:70696392..70700109-chr16:70707157..70709688,3	K562	blood:
37	chr16:70562753..70563960-chr16:70687318..70688116,3	MCF-7	breast:
38	chr16:70717596..70719954-chr16:70769240..70771432,3	K562	blood:
39	chr16:70731044..70733238-chr16:70775632..70778039,2	MCF-7	breast:
40	chr16:70736848..70738799-chr16:70767007..70768655,2	MCF-7	breast:
41	chr16:70696273..70698842-chr16:70700749..70702411,2	MCF-7	breast:
42	chr16:70739967..70742335-chr16:70770927..70772720,2	MCF-7	breast:
43	chr16:70715424..70721545-chr16:70778213..70783786,16	MCF-7	breast:
44	chr16:70557802..70559378-chr16:70727499..70729855,2	MCF-7	breast:
45	chr16:70414936..70416804-chr16:70716789..70719608,2	MCF-7	breast:
46	chr16:70737857..70741498-chr16:70742534..70745125,3	K562	blood:
47	chr16:70729613..70734171-chr16:70734566..70738930,4	K562	blood:
48	chr16:70301218..70302071-chr16:70687403..70688222,2	K562	blood:
49	chr16:70696392..70700109-chr16:70707157..70709688,3	K562	blood:
50	chr16:70681046..70683051-chr16:70685956..70688661,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTSS1L-1	chr16:70695093-70695583	NONHSAT143439
2	lnc-SF3B3-2	chr16:70690505-70690582	NONHSAT143438
3	lnc-SF3B3-2	chr16:70690866-70691260	NONHSAT143438
4	lnc-SF3B3-2	chr16:70680776-70680878	NONHSAT143438

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MTSS1L	hsa-miR-101-3p	chr16:70695114-70695139
2	MTSS1L	hsa-miR-93-5p	chr16:70697456-70697450
3	MTSS1L	hsa-miR-101-3p	chr16:70695120-70695113
4	MTSS1L	hsa-miR-186-5p	chr16:70695404-70695428
5	MTSS1L	hsa-miR-186-5p	chr16:70695410-70695404

Variant related genes	Relation type
MTSS1L	TF binding region
VAC14	TF binding region
IL34	TF binding region
ENSG00000268927	TF binding region
MTSS1L	CpG island
VAC14	CpG island
IL34	CpG island
ENSG00000268927	CpG island
ENSG00000090861	chromatin interactions
ENSG00000260156	chromatin interactions
ENSG00000262136	chromatin interactions
ENSG00000221514	chromatin interactions
ENSG00000132613	chromatin interactions
ENSG00000181019	chromatin interactions
ENSG00000168872	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000260111	chromatin interactions
ENSG00000262890	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000268927	chromatin interactions
ENSG00000214353	chromatin interactions
ENSG00000261777	chromatin interactions
ENSG00000103043	chromatin interactions
ENSG00000157368	chromatin interactions
ENSG00000103051	chromatin interactions

Extended variants
information (count: 3237 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3237 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6499330	chr16:70677785-70677786	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559905885	chr16:70677835-70677836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541209220	chr16:70677842-70677843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374462660	chr16:70677850-70677851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs140051352	chr16:70677856-70677857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs8060584	chr16:70677864-70677865	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143703235	chr16:70677866-70677867	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs151290668	chr16:70677889-70677890	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544628902	chr16:70677900-70677901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550029701	chr16:70677909-70677910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568197631	chr16:70677910-70677911	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375132737	chr16:70677937-70677938	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190061535	chr16:70677958-70677959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553523885	chr16:70677963-70677964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112691047	chr16:70677972-70677973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539136218	chr16:70677985-70677986	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557377140	chr16:70677996-70677997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150463086	chr16:70678028-70678029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181752758	chr16:70678063-70678064	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565656570	chr16:70678077-70678078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145400464	chr16:70678093-70678094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114862657	chr16:70678117-70678118	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372719369	chr16:70678125-70678126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541644856	chr16:70678149-70678150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185670246	chr16:70678211-70678212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559944453	chr16:70678215-70678216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533508039	chr16:70678221-70678222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113378377	chr16:70678230-70678231	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs551903137	chr16:70678251-70678252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563704851	chr16:70678260-70678261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs77412645	chr16:70678263-70678264	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549073732	chr16:70678272-70678273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142665437	chr16:70678288-70678289	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs373332466	chr16:70678297-70678298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs113129713	chr16:70678303-70678304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs146930917	chr16:70678317-70678318	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188858885	chr16:70678344-70678345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs137913432	chr16:70678407-70678408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78666893	chr16:70678449-70678450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs180783895	chr16:70678484-70678485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs374310525	chr16:70678495-70678496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576017658	chr16:70678524-70678525	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs57738457	chr16:70678533-70678534	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs574975980	chr16:70678539-70678540	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs76077819	chr16:70678563-70678564	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs74685786	chr16:70678581-70678582	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544040162	chr16:70678599-70678600	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs557544152	chr16:70678603-70678604	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199713334	chr16:70678604-70678605	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs147719208	chr16:70678609-70678610	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	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
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:2965 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70666000-70679000	Weak transcription	Spleen	Spleen
2	chr16:70669400-70679000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr16:70669600-70679000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:70669600-70679400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr16:70669600-70687800	Weak transcription	Right Atrium	heart
6	chr16:70670600-70680000	Weak transcription	Fetal Intestine Small	intestine
7	chr16:70673600-70680200	Weak transcription	Brain Anterior Caudate	brain
8	chr16:70673600-70680200	Weak transcription	HSMMtube	muscle
9	chr16:70673600-70683200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr16:70673600-70684000	Weak transcription	Esophagus	oesophagus
11	chr16:70673800-70680200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr16:70673800-70680200	Weak transcription	Fetal Stomach	stomach
13	chr16:70673800-70682800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr16:70674000-70680200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr16:70674000-70680200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr16:70674200-70680200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr16:70674200-70680600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr16:70675200-70679000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr16:70678000-70681200	Weak transcription	Fetal Intestine Large	intestine
20	chr16:70678800-70679600	Bivalent Enhancer	Fetal Brain Male	brain
21	chr16:70679000-70679600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr16:70679000-70679600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr16:70679000-70680200	Enhancers	Spleen	Spleen
24	chr16:70679000-70680600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr16:70679200-70679400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr16:70679400-70679600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr16:70679400-70680000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr16:70679400-70680000	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr16:70679600-70680200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr16:70679600-70681000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr16:70679600-70681400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr16:70679800-70681200	Enhancers	Placenta	Placenta
33	chr16:70679800-70682400	Enhancers	Fetal Brain Male	brain
34	chr16:70680000-70680200	Weak transcription	Brain Cingulate Gyrus	brain
35	chr16:70680000-70680200	Weak transcription	Brain Hippocampus Middle	brain
36	chr16:70680000-70680200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr16:70680000-70680200	Enhancers	Fetal Brain Female	brain
38	chr16:70680000-70680200	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr16:70680000-70680400	Enhancers	Fetal Muscle Trunk	muscle
40	chr16:70680000-70681000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr16:70680000-70681000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr16:70680000-70682000	Enhancers	Fetal Muscle Leg	muscle
43	chr16:70680000-70687200	Strong transcription	Fetal Intestine Small	intestine
44	chr16:70680200-70680400	Flanking Active TSS	Brain Cingulate Gyrus	brain
45	chr16:70680200-70680400	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr16:70680200-70680400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
47	chr16:70680200-70680400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr16:70680200-70680400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr16:70680200-70680400	Flanking Active TSS	Stomach Smooth Muscle	stomach
50	chr16:70680200-70680400	Flanking Active TSS	Spleen	Spleen

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