Variant report

Variant	nsv981568
Chromosome Location	chr7:105222012-105223485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105221547-105222227	HepG2	liver:	n/a	n/a
2	ATF3	chr7:105221673-105222264	H1-hESC	embryonic stem cell:	n/a	chr7:105221987-105221996 chr7:105221976-105221996
3	ATF3	chr7:105221713-105222176	H1-hESC	embryonic stem cell:	n/a	chr7:105221987-105221996 chr7:105221976-105221996
4	BHLHE40	chr7:105221793-105222193	HepG2	liver:	n/a	chr7:105221986-105221995 chr7:105221987-105221996 chr7:105221981-105222002 chr7:105221988-105221997 chr7:105221987-105221996 chr7:105221985-105221998
5	BHLHE40	chr7:105221446-105222148	GM12878	blood:	n/a	chr7:105221986-105221995 chr7:105221987-105221996 chr7:105221981-105222002 chr7:105221988-105221997 chr7:105221987-105221996 chr7:105221985-105221998
6	BHLHE40	chr7:105221632-105222173	A549	lung:	n/a	chr7:105221986-105221995 chr7:105221987-105221996 chr7:105221981-105222002 chr7:105221988-105221997 chr7:105221987-105221996 chr7:105221985-105221998
7	CEBPB	chr7:105221807-105222312	H1-hESC	embryonic stem cell:	n/a	chr7:105222256-105222269 chr7:105222257-105222268 chr7:105222256-105222267
8	CEBPB	chr7:105221969-105222421	HepG2	liver:	n/a	chr7:105222256-105222269 chr7:105222257-105222268 chr7:105222256-105222267
9	CEBPB	chr7:105221428-105222427	A549	lung:	n/a	chr7:105222256-105222269 chr7:105222257-105222268 chr7:105222256-105222267
10	CEBPB	chr7:105221985-105222522	A549	lung:	n/a	chr7:105222256-105222269 chr7:105222257-105222268 chr7:105222256-105222267
11	CHD2	chr7:105221639-105222206	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr7:105221682-105222190	A549	lung:	n/a	n/a
13	CREB1	chr7:105221509-105222342	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr7:105221689-105222303	HepG2	liver:	n/a	n/a
15	CREB1	chr7:105221654-105222296	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr7:105221764-105222339	HepG2	liver:	n/a	n/a
17	CTCF	chr7:105222986-105222988	GM10266	blood:	n/a	n/a
18	CTCF	chr7:105221920-105222070	GM12872	blood:	n/a	n/a
19	CTCF	chr7:105221920-105222070	AG04449	skin:	n/a	n/a
20	CTCF	chr7:105222564-105222617	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr7:105221880-105222030	GM12865	blood:	n/a	n/a
22	CTCF	chr7:105222994-105223061	GM10266	blood:	n/a	n/a
23	CTCF	chr7:105222080-105222230	SAEC	small airway:	n/a	n/a
24	E2F6	chr7:105221478-105222274	A549	lung:	n/a	n/a
25	EP300	chr7:105221823-105222166	HepG2	liver:	n/a	n/a
26	GATA2	chr7:105221526-105222262	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr7:105221748-105222170	MCF-7	breast:	n/a	n/a
28	GTF2F1	chr7:105221677-105222178	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUND	chr7:105221476-105222192	H1-hESC	embryonic stem cell:	n/a	n/a
30	MAX	chr7:105221508-105222285	H1-hESC	embryonic stem cell:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
31	MAX	chr7:105221489-105222258	A549	lung:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
32	MAX	chr7:105221505-105222289	MCF-7	breast:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
33	MAX	chr7:105221533-105222201	A549	lung:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
34	MAX	chr7:105221953-105222041	GM12878	blood:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221985-105221998
35	MAX	chr7:105220418-105222344	HCT-116	colon:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
36	MAX	chr7:105221380-105222362	A549	lung:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
37	MAX	chr7:105221521-105222330	MCF-7	breast:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
38	MAX	chr7:105221534-105222295	SK-N-SH	brain:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
39	MAX	chr7:105221509-105222273	H1-hESC	embryonic stem cell:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
40	MAX	chr7:105221528-105222308	SK-N-SH	brain:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
41	MAX	chr7:105221571-105222191	H1-hESC	embryonic stem cell:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221697-105221706 chr7:105221987-105221996 chr7:105221696-105221707 chr7:105221985-105221998
42	MAX	chr7:105221814-105222202	HepG2	liver:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221985-105221998
43	MXI1	chr7:105221514-105222160	H1-hESC	embryonic stem cell:	n/a	chr7:105221986-105221995
44	MXI1	chr7:105221724-105222196	HepG2	liver:	n/a	chr7:105221986-105221995
45	MXI1	chr7:105221469-105222273	IMR90	lung:	n/a	chr7:105221986-105221995
46	MXI1	chr7:105220901-105222488	SK-N-SH	brain:	n/a	chr7:105221986-105221995
47	MYBL2	chr7:105221773-105222266	HepG2	liver:	n/a	n/a
48	MYC	chr7:105221930-105222018	MCF-7	breast:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221985-105221998
49	MYC	chr7:105222063-105222114	MCF-7	breast:	n/a	n/a
50	MYC	chr7:105221930-105222116	MCF-7	breast:	n/a	chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221987-105221996 chr7:105221985-105221998

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105223119-105223169	PANC-1	pancreas:	n/a
2	chr7:105223119-105223169	PANC-1	pancreas:	n/a
3	chr7:105221991-105222041	HRCEpiC	kidney:	n/a
4	chr7:105222048-105222098	A549	lung:	n/a
5	chr7:105221998-105222048	BJ	skin:	n/a
6	chr7:105223119-105223169	PrEC	prostate:	n/a
7	chr7:105222945-105222995	Hela-S3	cervix:	n/a
8	chr7:105222180-105222230	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:105222019-105222069	HUVEC	blood vessel:	n/a
10	chr7:105222019-105222069	HRE	kidney:	n/a
11	chr7:105222180-105222230	NT2-D1	testis:	n/a
12	chr7:105222945-105222995	HIPEpiC	eye:	n/a
13	chr7:105222180-105222230	BE2_C	brain:	n/a
14	chr7:105222048-105222098	NHBE	bronchial:	n/a
15	chr7:105221998-105222048	SK-N-SH_RA	brain:	n/a
16	chr7:105222048-105222098	Hepatocyte	liver:	n/a
17	chr7:105222945-105222995	GM12892	blood:	n/a
18	chr7:105222945-105222995	PrEC	prostate:	n/a
19	chr7:105223119-105223169	AG09309	skin:	n/a
20	chr7:105223119-105223169	HCF	heart:	n/a
21	chr7:105222699-105222749	A549	lung:	n/a
22	chr7:105222945-105222995	HRCEpiC	kidney:	n/a
23	chr7:105222180-105222230	H1-hESC	embryonic stem cell:	embryo
24	chr7:105222019-105222069	GM12878	blood:	n/a
25	chr7:105221998-105222048	HepG2	liver:	n/a
26	chr7:105222024-105222074	GM12891	blood:	n/a
27	chr7:105222019-105222069	HepG2	liver:	n/a
28	chr7:105221985-105222035	HRPEpiC	eye:	n/a
29	chr7:105222699-105222749	SAEC	small airway:	n/a
30	chr7:105222180-105222230	NH-A	brain:	n/a
31	chr7:105221991-105222041	HCF	heart:	n/a
32	chr7:105223119-105223169	A549	lung:	n/a
33	chr7:105222019-105222069	HRPEpiC	eye:	n/a
34	chr7:105221991-105222041	Caco-2	colon:	n/a
35	chr7:105222699-105222749	ovcar-3	ovarian:	n/a
36	chr7:105222945-105222995	HEEpiC	esophagus:	n/a
37	chr7:105222699-105222749	HCM	heart:	n/a
38	chr7:105222019-105222069	HAEpiC	amniotic membrane:	n/a
39	chr7:105221998-105222048	GM06990	blood:	n/a
40	chr7:105222945-105222995	SAEC	small airway:	n/a
41	chr7:105221998-105222048	AG04450	lung:	fetal
42	chr7:105221991-105222041	NH-A	brain:	n/a
43	chr7:105221985-105222035	IMR90	lung:	fetal
44	chr7:105222048-105222098	HMEC	breast:	n/a
45	chr7:105221998-105222048	NHDF-neo	bronchial:	n/a
46	chr7:105221998-105222048	AG09309	skin:	n/a
47	chr7:105222019-105222069	HNPCEpiC	eye:	n/a
48	chr7:105222048-105222098	Jurkat	blood:	n/a
49	chr7:105222019-105222069	GM19239	blood:	n/a
50	chr7:105223119-105223169	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:105171405..105173628-chr7:105221272..105223628,2	MCF-7	breast:
2	chr7:105159598..105163989-chr7:105219696..105223115,7	MCF-7	breast:
3	chr19:5690148..5691832-chr7:105220231..105223207,2	K562	blood:

Variant related genes	Relation type
EFCAB10	TF binding region
EFCAB10	CpG island
ENSG00000130255	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000135249	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556758741	chr7:105222016-105222017	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs549619179	chr7:105222049-105222050	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs574615971	chr7:105222121-105222122	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs561717083	chr7:105222146-105222147	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs530629159	chr7:105222233-105222234	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs183403081	chr7:105222262-105222263	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs570424244	chr7:105222274-105222275	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs372498709	chr7:105222295-105222296	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs186747114	chr7:105222346-105222347	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs370287994	chr7:105222374-105222375	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs148922582	chr7:105222424-105222425	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs116979167	chr7:105222451-105222452	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	disease
13	rs372036509	chr7:105222471-105222472	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs555153443	chr7:105222475-105222476	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs200859242	chr7:105222476-105222477	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs75393038	chr7:105222483-105222484	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs138281073	chr7:105222487-105222488	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs372136417	chr7:105222503-105222504	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs577956939	chr7:105222529-105222530	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs540282227	chr7:105222534-105222535	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs191595716	chr7:105222552-105222553	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs58194204	chr7:105222581-105222582	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs574387987	chr7:105222591-105222592	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs543200268	chr7:105222594-105222595	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs571996984	chr7:105222598-105222599	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs183779819	chr7:105222613-105222614	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs370830145	chr7:105222697-105222698	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs564043430	chr7:105222699-105222700	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs189299389	chr7:105222714-105222715	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs57492756	chr7:105222738-105222739	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs532913787	chr7:105222814-105222815	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs546282779	chr7:105222815-105222816	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs113397505	chr7:105222835-105222836	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs529143296	chr7:105222836-105222837	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs548915495	chr7:105222841-105222842	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs568690562	chr7:105222889-105222890	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs537681511	chr7:105222901-105222902	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs558200463	chr7:105222907-105222908	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs561532843	chr7:105222928-105222929	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs571668634	chr7:105222940-105222941	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs534147610	chr7:105222952-105222953	Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs568110111	chr7:105222997-105222998	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs376021525	chr7:105223051-105223052	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs534222833	chr7:105223066-105223067	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs1706922	chr7:105223071-105223072	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530164820	chr7:105223074-105223075	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs1721504	chr7:105223081-105223082	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs114270872	chr7:105223093-105223094	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs556922673	chr7:105223110-105223111	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs576694552	chr7:105223119-105223120	Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105220600-105222400	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr7:105221200-105222200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr7:105221200-105222200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:105221400-105222200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:105221400-105222200	Active TSS	Brain Anterior Caudate	brain
6	chr7:105221400-105222200	Active TSS	Brain Substantia Nigra	brain
7	chr7:105221400-105222400	Active TSS	H9 Cell Line	embryonic stem cell
8	chr7:105221400-105222400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:105221400-105222400	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr7:105221400-105222400	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr7:105221400-105222400	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr7:105221400-105222400	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr7:105221400-105222400	Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr7:105221400-105222400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:105221400-105222400	Active TSS	Brain Angular Gyrus	brain
16	chr7:105221400-105222400	Active TSS	Brain Germinal Matrix	brain
17	chr7:105221600-105222200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:105221600-105222200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr7:105221600-105222200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:105221600-105222200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:105221600-105222200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:105221600-105222200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:105221600-105222200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr7:105221600-105222200	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr7:105221600-105222200	Active TSS	Primary T cells from cord blood	blood
26	chr7:105221600-105222200	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr7:105221600-105222200	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
28	chr7:105221600-105222200	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
29	chr7:105221600-105222200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:105221600-105222200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
31	chr7:105221600-105222200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
32	chr7:105221600-105222200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
33	chr7:105221600-105222200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:105221600-105222200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:105221600-105222200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:105221600-105222200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr7:105221600-105222200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:105221600-105222200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr7:105221600-105222200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:105221600-105222200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:105221600-105222200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:105221600-105222200	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
43	chr7:105221600-105222200	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr7:105221600-105222200	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr7:105221600-105222200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr7:105221600-105222200	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr7:105221600-105222200	ZNF genes & repeats	Esophagus	oesophagus
48	chr7:105221600-105222200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
49	chr7:105221600-105222200	Flanking Active TSS	Fetal Intestine Small	intestine
50	chr7:105221600-105222200	Active TSS	Fetal Kidney	kidney

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