Variant report

Variant	esv3379760
Chromosome Location	chr7:5012976-5014924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:679)
CpG islands
(count:671)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5013448-5013655	K562	blood:	n/a	n/a
2	ARID3A	chr7:5013472-5013773	HepG2	liver:	n/a	n/a
3	ATF1	chr7:5013441-5013824	K562	blood:	n/a	n/a
4	ATF2	chr7:5013463-5013903	GM12878	blood:	n/a	n/a
5	ATF2	chr7:5013248-5013806	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr7:5013348-5013704	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr7:5013503-5013709	K562	blood:	n/a	n/a
8	ATF3	chr7:5013460-5013859	A549	lung:	n/a	n/a
9	ATF3	chr7:5013393-5013842	A549	lung:	n/a	n/a
10	BACH1	chr7:5013568-5014066	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr7:5013318-5013901	A549	lung:	n/a	n/a
12	BCL3	chr7:5013460-5013850	A549	lung:	n/a	n/a
13	BCLAF1	chr7:5013287-5013900	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:5013230-5013900	K562	blood:	n/a	n/a
15	BCLAF1	chr7:5013225-5014244	GM12878	blood:	n/a	chr7:5014075-5014088 chr7:5014083-5014092
16	BHLHE40	chr7:5013471-5014331	K562	blood:	n/a	chr7:5013793-5013809 chr7:5014073-5014089
17	BHLHE40	chr7:5013437-5014320	GM12878	blood:	n/a	chr7:5013793-5013809 chr7:5014073-5014089
18	BRCA1	chr7:5013468-5013824	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:5014090-5014228	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:5013609-5013803	HepG2	liver:	n/a	n/a
21	CBX3	chr7:5013182-5014155	HCT-116	colon:	n/a	n/a
22	CBX3	chr7:5013163-5013772	K562	blood:	n/a	n/a
23	CBX3	chr7:5013157-5014292	K562	blood:	n/a	n/a
24	CCNT2	chr7:5013526-5014282	K562	blood:	n/a	n/a
25	CEBPB	chr7:5013257-5013641	K562	blood:	n/a	n/a
26	CEBPB	chr7:5013255-5013821	GM12878	blood:	n/a	n/a
27	CEBPB	chr7:5014266-5014468	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:5013461-5013809	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:5013500-5013672	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPD	chr7:5013568-5013902	HepG2	liver:	n/a	n/a
31	CHD1	chr7:5013580-5013694	GM12878	blood:	n/a	n/a
32	CHD1	chr7:5014049-5014196	GM12878	blood:	n/a	chr7:5014128-5014138
33	CHD2	chr7:5013596-5014366	K562	blood:	n/a	chr7:5014128-5014138
34	CHD2	chr7:5013511-5013757	HepG2	liver:	n/a	n/a
35	CHD2	chr7:5013432-5013737	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr7:5013957-5014370	HepG2	liver:	n/a	chr7:5014128-5014138
37	CHD2	chr7:5013431-5014382	GM12878	blood:	n/a	chr7:5014128-5014138
38	CHD2	chr7:5013456-5014230	Hela-S3	cervix:	n/a	chr7:5014128-5014138
39	CREB1	chr7:5013278-5014082	HepG2	liver:	n/a	n/a
40	CREB1	chr7:5013385-5014328	A549	lung:	n/a	n/a
41	CREB1	chr7:5013421-5013900	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr7:5013401-5013947	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr7:5013400-5014076	GM12878	blood:	n/a	n/a
44	CREB1	chr7:5013459-5013747	A549	lung:	n/a	n/a
45	CTCF	chr7:5013364-5013856	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:5013480-5013630	HEK293	kidney:	n/a	n/a
47	CTCF	chr7:5013303-5013835	K562	blood:	n/a	n/a
48	CTCF	chr7:5013369-5013751	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr7:5013262-5013832	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:5013580-5013730	MCF-7	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5013468-5013518	HepG2	liver:	n/a
2	chr7:5014415-5014465	AG04450	lung:	fetal
3	chr7:5013509-5013559	CMK	blood:	n/a
4	chr7:5014435-5014485	NT2-D1	testis:	n/a
5	chr7:5013509-5013559	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:5014008-5014058	HMEC	breast:	n/a
7	chr7:5013639-5013689	GM12892	blood:	n/a
8	chr7:5013468-5013518	NH-A	brain:	n/a
9	chr7:5013509-5013559	ECC-1	luminal epithelium:	n/a
10	chr7:5013641-5013691	ProgFib	skin:	n/a
11	chr7:5014435-5014485	HepG2	liver:	n/a
12	chr7:5013451-5013501	AoSMC	blood vessel:	n/a
13	chr7:5013639-5013689	HRCEpiC	kidney:	n/a
14	chr7:5014008-5014058	HL-60	blood:	n/a
15	chr7:5013468-5013518	HRE	kidney:	n/a
16	chr7:5014415-5014465	HRPEpiC	eye:	n/a
17	chr7:5013490-5013540	NH-A	brain:	n/a
18	chr7:5013509-5013559	NB4	blood:	n/a
19	chr7:5013524-5013574	GM12891	blood:	n/a
20	chr7:5013641-5013691	CMK	blood:	n/a
21	chr7:5013641-5013691	H1-hESC	embryonic stem cell:	embryo
22	chr7:5013524-5013574	HCT-116	colon:	n/a
23	chr7:5014435-5014485	MCF-7	breast:	n/a
24	chr7:5013509-5013559	AG04450	lung:	fetal
25	chr7:5013536-5013586	HIPEpiC	eye:	n/a
26	chr7:5014008-5014058	Hepatocyte	liver:	n/a
27	chr7:5013641-5013691	GM19239	blood:	n/a
28	chr7:5013490-5013540	Hepatocyte	liver:	n/a
29	chr7:5013524-5013574	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:5013509-5013559	GM19239	blood:	n/a
31	chr7:5013468-5013518	GM12891	blood:	n/a
32	chr7:5014008-5014058	GM12892	blood:	n/a
33	chr7:5013639-5013689	T-47D	breast:	n/a
34	chr7:5013641-5013691	GM12878	blood:	n/a
35	chr7:5013524-5013574	H1-hESC	embryonic stem cell:	embryo
36	chr7:5014008-5014058	HEEpiC	esophagus:	n/a
37	chr7:5013536-5013586	AG10803	skin:	n/a
38	chr7:5013490-5013540	SKMC	muscle:	n/a
39	chr7:5013524-5013574	AG04450	lung:	fetal
40	chr7:5013451-5013501	A549	lung:	n/a
41	chr7:5013639-5013689	HRE	kidney:	n/a
42	chr7:5013490-5013540	T-47D	breast:	n/a
43	chr7:5014008-5014058	SKMC	muscle:	n/a
44	chr7:5013490-5013540	HRPEpiC	eye:	n/a
45	chr7:5013468-5013518	PANC-1	pancreas:	n/a
46	chr7:5014435-5014485	GM12878	blood:	n/a
47	chr7:5014008-5014058	HepG2	liver:	n/a
48	chr7:5013468-5013518	SAEC	small airway:	n/a
49	chr7:5014435-5014485	HL-60	blood:	n/a
50	chr7:5013451-5013501	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:5012217..5014206-chr7:5819722..5821650,2	MCF-7	breast:
2	chr7:5012931..5013720-chr7:5820910..5821674,3	MCF-7	breast:
3	chr7:5012695..5014428-chr7:5820890..5822170,10	MCF-7	breast:
4	chr7:5013631..5016563-chr7:5022027..5023765,2	K562	blood:
5	chr7:4923091..4923826-chr7:5013336..5013934,3	K562	blood:
6	chr7:5013249..5014674-chr7:5819932..5821408,8	Hela-S3	cervix:
7	chr7:5012983..5015694-chr7:5819277..5821133,2	K562	blood:
8	chr7:5013311..5013911-chr7:5820908..5821412,3	HCT-116	colon:
9	chr7:5012537..5014887-chr7:5022005..5024140,2	K562	blood:
10	chr7:5013565..5014445-chr7:5820432..5821785,4	K562	blood:
11	chr7:5012957..5014985-chr7:5085347..5086905,2	MCF-7	breast:
12	chr7:5012284..5014483-chr7:5819277..5821280,2	K562	blood:
13	chr7:5012944..5014466-chr7:5819776..5821589,2	MCF-7	breast:
14	chr1:144533720..144534707-chr7:5013377..5013986,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
RNF216P1	TF binding region
RNF216P1	CpG island
ENSG00000201699	chromatin interactions
ENSG00000196204	chromatin interactions
ENSG00000157927	chromatin interactions
ENSG00000272968	chromatin interactions
ENSG00000146587	chromatin interactions
ENSG00000011275	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186527911	chr7:5012997-5012998	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs575340053	chr7:5013015-5013016	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs139433268	chr7:5013019-5013020	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs554747525	chr7:5013038-5013039	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs112309986	chr7:5013101-5013102	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs191210855	chr7:5013102-5013103	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs2942565	chr7:5013116-5013117	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368384034	chr7:5013137-5013138	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs532277182	chr7:5013155-5013156	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs112004983	chr7:5013163-5013164	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs562525912	chr7:5013199-5013200	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs530074959	chr7:5013201-5013202	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs184797833	chr7:5013252-5013253	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs117592580	chr7:5013293-5013294	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
15	rs559488574	chr7:5013295-5013296	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs386709664	chr7:5013298-5013299	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs117290715	chr7:5013299-5013300	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
18	rs548127402	chr7:5013310-5013311	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs190619064	chr7:5013369-5013370	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs538135612	chr7:5013382-5013383	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs563979305	chr7:5013406-5013407	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs371303781	chr7:5013452-5013453	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs556932485	chr7:5013459-5013460	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs192982947	chr7:5013460-5013461	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs536205667	chr7:5013462-5013463	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs554614134	chr7:5013517-5013518	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs371894983	chr7:5013524-5013525	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs572816907	chr7:5013535-5013536	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs6944061	chr7:5013545-5013546	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs75067994	chr7:5013568-5013569	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs185117401	chr7:5013584-5013585	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs544089675	chr7:5013629-5013630	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs6978215	chr7:5013688-5013689	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs370721661	chr7:5013701-5013702	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs541783519	chr7:5013714-5013715	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs377487680	chr7:5013818-5013819	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs560552378	chr7:5013819-5013820	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs189585781	chr7:5013837-5013838	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs552668749	chr7:5013844-5013845	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs564506960	chr7:5013848-5013849	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs6957907	chr7:5013879-5013880	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs199724821	chr7:5013881-5013882	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs550494424	chr7:5013883-5013884	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs71529315	chr7:5013886-5013887	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	mRNA abundance
45	rs536170399	chr7:5013890-5013891	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs145540911	chr7:5013955-5013956	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	mRNA abundance
47	rs566491374	chr7:5013958-5013959	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs371056952	chr7:5014017-5014018	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs34218981	chr7:5014019-5014020	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs576958362	chr7:5014048-5014049	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4999200-5013400	Weak transcription	Right Atrium	heart
2	chr7:5011400-5013200	Weak transcription	K562	blood
3	chr7:5011400-5013600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:5012800-5013200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:5012800-5014800	Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr7:5013000-5013200	Enhancers	Colon Smooth Muscle	Colon
7	chr7:5013200-5013400	Enhancers	Primary T cells fromperipheralblood	blood
8	chr7:5013200-5013400	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr7:5013200-5013400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr7:5013200-5013400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:5013200-5013400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr7:5013200-5013400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:5013200-5013400	Enhancers	Adipose Nuclei	Adipose
14	chr7:5013200-5013400	Enhancers	Liver	Liver
15	chr7:5013200-5013400	Active TSS	Brain Germinal Matrix	brain
16	chr7:5013200-5013400	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr7:5013200-5013400	Enhancers	Stomach Mucosa	stomach
18	chr7:5013200-5013600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:5013200-5013600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr7:5013200-5013600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:5013200-5013600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:5013200-5013600	Flanking Active TSS	Colon Smooth Muscle	Colon
23	chr7:5013200-5013600	Flanking Active TSS	Dnd41	blood
24	chr7:5013200-5013800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:5013200-5014200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:5013200-5014400	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr7:5013200-5014400	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr7:5013200-5014600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:5013200-5014600	Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr7:5013200-5014600	Active TSS	HSMMtube	muscle
31	chr7:5013200-5014800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:5013200-5014800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr7:5013200-5014800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:5013200-5014800	Active TSS	Colonic Mucosa	Colon
35	chr7:5013200-5014800	Active TSS	Duodenum Mucosa	Duodenum
36	chr7:5013200-5014800	Active TSS	Fetal Stomach	stomach
37	chr7:5013200-5014800	Active TSS	HUVEC	blood vessel
38	chr7:5013200-5014800	Active TSS	NHDF-Ad	bronchial
39	chr7:5013200-5015000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:5013200-5015000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr7:5013200-5015000	Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr7:5013200-5015000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:5013200-5015000	Active TSS	Muscle Satellite Cultured Cells	--
44	chr7:5013200-5015000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:5013200-5015000	Active TSS	Brain Angular Gyrus	brain
46	chr7:5013200-5015000	Active TSS	Brain Anterior Caudate	brain
47	chr7:5013200-5015000	Active TSS	Brain Cingulate Gyrus	brain
48	chr7:5013200-5015000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr7:5013200-5015000	Active TSS	Fetal Brain Female	brain
50	chr7:5013200-5015000	Active TSS	Pancreatic Islets	Pancreatic Islet

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