Variant report

Variant	nsv970915
Chromosome Location	chr7:100846996-100852070
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:245)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:100847712-100847829	HepG2	liver:	n/a	n/a
2	CEBPB	chr7:100847636-100847943	K562	blood:	n/a	n/a
3	CEBPB	chr7:100847644-100847844	K562	blood:	n/a	n/a
4	CEBPB	chr7:100847639-100847931	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr7:100847658-100847833	K562	blood:	n/a	n/a
6	CTCF	chr7:100847580-100847730	NB4	blood:	n/a	n/a
7	CTCF	chr7:100847700-100847850	HCM	heart:	n/a	n/a
8	CTCF	chr7:100847720-100847870	HCFaa	heart:	n/a	n/a
9	CTCF	chr7:100847797-100847821	K562	blood:	n/a	n/a
10	CTCF	chr7:100847720-100847870	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr7:100847640-100847790	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:100847740-100847890	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr7:100847820-100847970	NB4	blood:	n/a	n/a
14	CTCF	chr7:100847207-100847229	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr7:100847780-100847930	BJ	skin:	n/a	n/a
16	CTCF	chr7:100847700-100847850	AG09319	gingival:	n/a	n/a
17	CTCF	chr7:100847680-100847830	AG09309	skin:	n/a	n/a
18	CTCF	chr7:100847720-100847870	AG10803	skin:	n/a	n/a
19	CTCF	chr7:100847680-100847830	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr7:100847760-100847910	MCF-7	breast:	n/a	n/a
21	CTCF	chr7:100847780-100847930	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr7:100847700-100847850	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr7:100847740-100847890	HL-60	blood:	n/a	n/a
24	CTCF	chr7:100847800-100847950	AG09319	gingival:	n/a	n/a
25	CTCFL	chr7:100847771-100847867	K562	blood:	n/a	n/a
26	EBF1	chr7:100847091-100847336	GM12878	blood:	n/a	n/a
27	EGR1	chr7:100849941-100850155	K562	blood:	n/a	chr7:100850027-100850041 chr7:100850027-100850040 chr7:100850029-100850039 chr7:100850023-100850045 chr7:100850028-100850039 chr7:100850027-100850040 chr7:100850029-100850039 chr7:100850028-100850039 chr7:100850030-100850039
28	GABPA	chr7:100847464-100847919	HL-60	blood:	n/a	n/a
29	HEY1	chr7:100849735-100850214	HepG2	liver:	n/a	n/a
30	HEY1	chr7:100850716-100851428	HepG2	liver:	n/a	n/a
31	HEY1	chr7:100849295-100849633	HepG2	liver:	n/a	n/a
32	MAX	chr7:100847655-100847884	NB4	blood:	n/a	n/a
33	MYC	chr7:100847647-100847907	NB4	blood:	n/a	n/a
34	NRF1	chr7:100847150-100847332	GM12878	blood:	n/a	n/a
35	PAX5	chr7:100847009-100847262	GM12878	blood:	n/a	n/a
36	POLR2A	chr7:100851005-100851162	K562	blood:	n/a	n/a
37	POLR2A	chr7:100850781-100851001	K562	blood:	n/a	n/a
38	POLR2A	chr7:100850418-100851631	HepG2	liver:	n/a	n/a
39	POLR2A	chr7:100847341-100856339	HepG2	liver:	n/a	n/a
40	POLR2A	chr7:100850575-100850736	HepG2	liver:	n/a	n/a
41	POLR2A	chr7:100848377-100849546	PFSK-1	brain:	n/a	n/a
42	POLR2A	chr7:100851984-100852430	HepG2	liver:	n/a	n/a
43	POLR2A	chr7:100848187-100848198	K562	blood:	n/a	n/a
44	POLR2A	chr7:100851884-100851898	K562	blood:	n/a	n/a
45	POLR2A	chr7:100849547-100849549	ProgFib	skin:	n/a	n/a
46	POLR2A	chr7:100850786-100851064	HepG2	liver:	n/a	n/a
47	POLR2A	chr7:100849556-100849625	ProgFib	skin:	n/a	n/a
48	POLR2A	chr7:100848680-100848865	K562	blood:	n/a	n/a
49	POLR2A	chr7:100850682-100850696	K562	blood:	n/a	n/a
50	POLR2A	chr7:100851324-100851336	K562	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100849825-100849875	GM19239	blood:	n/a
2	chr7:100849825-100849875	GM19239	blood:	n/a
3	chr7:100849501-100849551	SK-N-SH	brain:	n/a
4	chr7:100850157-100850207	AG10803	skin:	n/a
5	chr7:100849825-100849875	AG09319	gingival:	n/a
6	chr7:100849501-100849551	AG09319	gingival:	n/a
7	chr7:100850157-100850207	SK-N-MC	brain:	n/a
8	chr7:100849607-100849657	A549	lung:	n/a
9	chr7:100849825-100849875	ovcar-3	ovarian:	n/a
10	chr7:100849607-100849657	Hepatocyte	liver:	n/a
11	chr7:100849825-100849875	HMEC	breast:	n/a
12	chr7:100849607-100849657	HCT-116	colon:	n/a
13	chr7:100849825-100849875	NH-A	brain:	n/a
14	chr7:100850157-100850207	NT2-D1	testis:	n/a
15	chr7:100849501-100849551	GM19239	blood:	n/a
16	chr7:100849607-100849657	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:100849501-100849551	ProgFib	skin:	n/a
18	chr7:100850157-100850207	MCF-7	breast:	n/a
19	chr7:100849825-100849875	AG04449	skin:	fetal
20	chr7:100849607-100849657	Jurkat	blood:	n/a
21	chr7:100850157-100850207	IMR90	lung:	fetal
22	chr7:100850157-100850207	HCPEpiC	choroid plexus:	n/a
23	chr7:100849607-100849657	HUVEC	blood vessel:	n/a
24	chr7:100850157-100850207	Hela-S3	cervix:	n/a
25	chr7:100849501-100849551	Hepatocyte	liver:	n/a
26	chr7:100850157-100850207	ovcar-3	ovarian:	n/a
27	chr7:100849825-100849875	NB4	blood:	n/a
28	chr7:100849501-100849551	NH-A	brain:	n/a
29	chr7:100849825-100849875	CMK	blood:	n/a
30	chr7:100849607-100849657	HCPEpiC	choroid plexus:	n/a
31	chr7:100849607-100849657	NHBE	bronchial:	n/a
32	chr7:100850157-100850207	HIPEpiC	eye:	n/a
33	chr7:100850157-100850207	HepG2	liver:	n/a
34	chr7:100850157-100850207	HUVEC	blood vessel:	n/a
35	chr7:100849607-100849657	H1-hESC	embryonic stem cell:	embryo
36	chr7:100849607-100849657	LNCaP	prostate:	n/a
37	chr7:100849825-100849875	AG04450	lung:	fetal
38	chr7:100849825-100849875	U87	brain:	n/a
39	chr7:100850157-100850207	CMK	blood:	n/a
40	chr7:100849825-100849875	K562	blood:	n/a
41	chr7:100849825-100849875	PFSK-1	brain:	n/a
42	chr7:100849825-100849875	SKMC	muscle:	n/a
43	chr7:100849825-100849875	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:100849501-100849551	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:100849825-100849875	T-47D	breast:	n/a
46	chr7:100849825-100849875	Hela-S3	cervix:	n/a
47	chr7:100849607-100849657	AG09309	skin:	n/a
48	chr7:100849501-100849551	RPTEC	kidney:	n/a
49	chr7:100849501-100849551	NB4	blood:	n/a
50	chr7:100849501-100849551	PrEC	prostate:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100843889..100849523-chr7:100857776..100861352,9	MCF-7	breast:
2	chr7:100846063..100847917-chr7:100849711..100851294,2	K562	blood:
3	chr7:100781461..100784552-chr7:100848282..100850837,3	K562	blood:
4	chr7:100850699..100858131-chr7:100858977..100863722,10	K562	blood:
5	chr7:100845269..100846779-chr7:100848748..100850891,2	MCF-7	breast:
6	chr7:100843556..100846193-chr7:100851130..100853588,2	MCF-7	breast:
7	chr7:100846805..100850556-chr7:100852421..100856995,5	K562	blood:
8	chr7:100845614..100849082-chr7:100852501..100856274,3	K562	blood:
9	chr7:100845358..100847563-chr7:100848809..100851294,2	K562	blood:
10	chr7:100851245..100853294-chr7:100875735..100877488,2	MCF-7	breast:
11	chr7:100848095..100852084-chr7:100860123..100862131,3	MCF-7	breast:
12	chr7:100849449..100852061-chr7:100853988..100855543,2	MCF-7	breast:
13	chr7:100847669..100852607-chr7:100855025..100859313,4	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PLOD3	hsa-miR-124-3p	chr7:100849526-100849520
2	PLOD3	hsa-miR-124-3p	chr7:100849520-100849539

Variant related genes	Relation type
ENSG00000213394	TF binding region
MOGAT3	TF binding region
DGAT2L7P	TF binding region
ENSG00000213394	CpG island
MOGAT3	CpG island
DGAT2L7P	CpG island
ENSG00000106397	chromatin interactions
ENSG00000106400	chromatin interactions
ENSG00000205267	chromatin interactions
ENSG00000213394	chromatin interactions
ENSG00000106384	chromatin interactions

Extended variants
information (count: 342 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370417232	chr7:100847004-100847005	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs533544930	chr7:100847065-100847066	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs551617364	chr7:100847139-100847140	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs376104966	chr7:100847196-100847197	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs566960761	chr7:100847222-100847223	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs181913737	chr7:100847225-100847226	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs549400078	chr7:100847247-100847248	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs567625012	chr7:100847296-100847297	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs373101208	chr7:100847314-100847315	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs535402001	chr7:100847315-100847316	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs573407013	chr7:100847348-100847349	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs567885558	chr7:100847372-100847373	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs56196736	chr7:100847388-100847389	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs73185918	chr7:100847398-100847399	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568985226	chr7:100847428-100847429	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs539606905	chr7:100847435-100847436	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs557473771	chr7:100847478-100847479	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs186152920	chr7:100847480-100847481	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs532322787	chr7:100847489-100847490	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs539896397	chr7:100847495-100847496	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs554956660	chr7:100847506-100847507	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs59549594	chr7:100847519-100847520	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs544604693	chr7:100847542-100847543	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs563177770	chr7:100847576-100847577	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs115764981	chr7:100847662-100847663	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs545613707	chr7:100847665-100847666	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs148405548	chr7:100847707-100847708	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs527797213	chr7:100847732-100847733	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs141762620	chr7:100847770-100847771	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs567685806	chr7:100847771-100847772	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs563539634	chr7:100847775-100847776	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs550639037	chr7:100847779-100847780	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs569125887	chr7:100847801-100847802	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs539303742	chr7:100847820-100847821	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs189734191	chr7:100847822-100847823	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs180721809	chr7:100847823-100847824	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs55633440	chr7:100847837-100847838	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs547300960	chr7:100847849-100847850	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs533660850	chr7:100847859-100847860	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs79433236	chr7:100847863-100847864	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs372371261	chr7:100847867-100847868	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs530851516	chr7:100847871-100847872	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs544185445	chr7:100847885-100847886	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs28621921	chr7:100847887-100847888	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs200802548	chr7:100847918-100847919	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs59632369	chr7:100847924-100847925	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs545674973	chr7:100847966-100847967	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs372778769	chr7:100847973-100847974	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs112466316	chr7:100848025-100848026	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs139972715	chr7:100848046-100848047	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Gastric cancer	24379144	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
Prostate cancer	16461572	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
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19214233	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100844600-100853600	Weak transcription	A549	lung
2	chr7:100844600-100856800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:100844600-100859000	Weak transcription	Hela-S3	cervix
4	chr7:100845000-100847800	Enhancers	Spleen	Spleen
5	chr7:100845400-100847200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr7:100845400-100847600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
7	chr7:100845600-100849000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr7:100845600-100849400	Weak transcription	Lung	lung
9	chr7:100845800-100847000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:100845800-100847000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:100845800-100849200	Weak transcription	Liver	Liver
12	chr7:100845800-100849400	Weak transcription	Pancreas	Pancrea
13	chr7:100845800-100849600	Weak transcription	Gastric	stomach
14	chr7:100845800-100852000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:100845800-100859600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:100846000-100849000	Weak transcription	Right Ventricle	heart
17	chr7:100846000-100849400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:100846000-100852000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr7:100846200-100847000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
20	chr7:100846200-100847000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
21	chr7:100846200-100847400	Enhancers	Primary B cells from peripheral blood	blood
22	chr7:100846200-100849200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr7:100846400-100847800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:100846400-100847800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr7:100846400-100849200	Weak transcription	Duodenum Mucosa	Duodenum
26	chr7:100846400-100849400	Weak transcription	Colonic Mucosa	Colon
27	chr7:100846400-100849400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr7:100846400-100851200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr7:100846600-100847000	Enhancers	Primary B cells from cord blood	blood
30	chr7:100846600-100847000	Enhancers	HepG2	liver
31	chr7:100846600-100847400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr7:100846600-100847400	Bivalent Enhancer	Adipose Nuclei	Adipose
33	chr7:100846600-100848400	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr7:100846600-100849200	Weak transcription	Colon Smooth Muscle	Colon
35	chr7:100846600-100849400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr7:100846600-100849400	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr7:100846600-100853000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr7:100846600-100853400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr7:100846600-100858200	Weak transcription	NHDF-Ad	bronchial
40	chr7:100846800-100847000	Bivalent Enhancer	Primary T cells from cord blood	blood
41	chr7:100846800-100847000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr7:100846800-100847000	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr7:100846800-100847000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:100846800-100847000	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr7:100846800-100847000	Enhancers	Left Ventricle	heart
46	chr7:100846800-100847000	Enhancers	GM12878-XiMat	blood
47	chr7:100846800-100847200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
48	chr7:100846800-100847200	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr7:100846800-100847400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:100846800-100847800	Enhancers	Primary T helper cells PMA-I stimulated	--

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