Variant report

Variant	nsv1031405
Chromosome Location	chr7:112431403-112476756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:172)
CpG islands
(count:183)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:172 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:112438984-112439353	K562	blood:	n/a	n/a
2	ARID3A	chr7:112431765-112432278	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:112434541-112434790	K562	blood:	n/a	n/a
4	ATF1	chr7:112434525-112434784	K562	blood:	n/a	n/a
5	ATF1	chr7:112438902-112439403	K562	blood:	n/a	n/a
6	BACH1	chr7:112460008-112460010	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:112470316-112470356	K562	blood:	n/a	n/a
8	BATF	chr7:112473188-112473388	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:112474845-112474879	K562	blood:	n/a	n/a
10	BHLHE40	chr7:112438964-112439324	K562	blood:	n/a	n/a
11	BHLHE40	chr7:112433913-112433959	K562	blood:	n/a	n/a
12	CBX3	chr7:112434186-112434880	K562	blood:	n/a	n/a
13	CCNT2	chr7:112438951-112439251	K562	blood:	n/a	n/a
14	CEBPB	chr7:112445960-112446247	A549	lung:	n/a	chr7:112446082-112446093 chr7:112446080-112446091 chr7:112446082-112446091
15	CEBPB	chr7:112445990-112446241	HepG2	liver:	n/a	chr7:112446082-112446093 chr7:112446080-112446091 chr7:112446082-112446091
16	CEBPB	chr7:112473138-112473370	K562	blood:	n/a	chr7:112473235-112473246
17	CEBPB	chr7:112433661-112434400	HCT-116	colon:	n/a	n/a
18	CEBPB	chr7:112473083-112473430	MCF-7	breast:	n/a	chr7:112473235-112473246
19	CEBPB	chr7:112449716-112449880	HepG2	liver:	n/a	chr7:112449746-112449757
20	CEBPB	chr7:112433976-112434123	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:112431500-112431853	HepG2	liver:	n/a	chr7:112431663-112431676
22	CEBPB	chr7:112446002-112446259	IMR90	lung:	n/a	chr7:112446082-112446093 chr7:112446080-112446091 chr7:112446082-112446091
23	CEBPB	chr7:112473139-112473362	HepG2	liver:	n/a	chr7:112473235-112473246
24	CEBPB	chr7:112443862-112444034	HepG2	liver:	n/a	chr7:112443957-112443968
25	CEBPB	chr7:112473142-112473402	A549	lung:	n/a	chr7:112473235-112473246
26	CEBPB	chr7:112433914-112434189	K562	blood:	n/a	n/a
27	CEBPB	chr7:112439115-112439210	K562	blood:	n/a	n/a
28	CEBPB	chr7:112442550-112442808	HepG2	liver:	n/a	chr7:112442702-112442713
29	CEBPB	chr7:112433826-112434387	HCT-116	colon:	n/a	n/a
30	CEBPB	chr7:112433918-112434218	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr7:112463660-112463915	GM12878	blood:	n/a	n/a
32	CTCF	chr7:112449880-112450030	GM12872	blood:	n/a	n/a
33	CUX1	chr7:112438996-112439287	K562	blood:	n/a	n/a
34	CUX1	chr7:112434531-112434692	K562	blood:	n/a	n/a
35	E2F4	chr7:112465164-112465168	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr7:112463657-112463930	GM12878	blood:	n/a	n/a
37	ELF1	chr7:112434434-112434841	K562	blood:	n/a	n/a
38	EP300	chr7:112433966-112434781	K562	blood:	n/a	n/a
39	EP300	chr7:112431554-112431733	HepG2	liver:	n/a	n/a
40	EP300	chr7:112438894-112439313	K562	blood:	n/a	n/a
41	FAM48A	chr7:112462023-112462126	GM12878	blood:	n/a	n/a
42	FAM48A	chr7:112450688-112450802	GM12878	blood:	n/a	n/a
43	FOS	chr7:112434606-112434806	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr7:112434101-112434105	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr7:112434526-112434844	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr7:112434547-112434806	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr7:112434089-112434108	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr7:112461373-112461608	MCF10A-Er-Src	breast:	n/a	n/a
49	FOXA1	chr7:112446245-112446437	T-47D	breast:	n/a	n/a
50	FOXA1	chr7:112431448-112432164	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112431576-112431626	HCPEpiC	choroid plexus:	n/a
2	chr7:112459177-112459227	GM12891	blood:	n/a
3	chr7:112459177-112459227	AG04449	skin:	fetal
4	chr7:112431576-112431626	HIPEpiC	eye:	n/a
5	chr7:112459177-112459227	SK-N-MC	brain:	n/a
6	chr7:112459177-112459227	AG09309	skin:	n/a
7	chr7:112431576-112431626	MCF-7	breast:	n/a
8	chr7:112431576-112431626	HCM	heart:	n/a
9	chr7:112431576-112431626	SK-N-SH	brain:	n/a
10	chr7:112434498-112434548	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:112434498-112434548	PrEC	prostate:	n/a
12	chr7:112434498-112434548	U87	brain:	n/a
13	chr7:112459177-112459227	GM12892	blood:	n/a
14	chr7:112459177-112459227	A549	lung:	n/a
15	chr7:112459177-112459227	K562	blood:	n/a
16	chr7:112459177-112459227	Hepatocyte	liver:	n/a
17	chr7:112434498-112434548	H1-hESC	embryonic stem cell:	embryo
18	chr7:112431576-112431626	HNPCEpiC	eye:	n/a
19	chr7:112459177-112459227	HCM	heart:	n/a
20	chr7:112459177-112459227	IMR90	lung:	fetal
21	chr7:112431576-112431626	HCF	heart:	n/a
22	chr7:112459177-112459227	H1-hESC	embryonic stem cell:	embryo
23	chr7:112431576-112431626	NHBE	bronchial:	n/a
24	chr7:112434498-112434548	ovcar-3	ovarian:	n/a
25	chr7:112434498-112434548	AG04449	skin:	fetal
26	chr7:112434498-112434548	AG04450	lung:	fetal
27	chr7:112434498-112434548	NHBE	bronchial:	n/a
28	chr7:112434498-112434548	SK-N-SH	brain:	n/a
29	chr7:112434498-112434548	MCF10A-Er-Src	breast:	n/a
30	chr7:112459177-112459227	SAEC	small airway:	n/a
31	chr7:112459177-112459227	Jurkat	blood:	n/a
32	chr7:112459177-112459227	HIPEpiC	eye:	n/a
33	chr7:112434498-112434548	PFSK-1	brain:	n/a
34	chr7:112459177-112459227	PrEC	prostate:	n/a
35	chr7:112431576-112431626	RPTEC	kidney:	n/a
36	chr7:112459177-112459227	HRCEpiC	kidney:	n/a
37	chr7:112459177-112459227	SKMC	muscle:	n/a
38	chr7:112431576-112431626	NT2-D1	testis:	n/a
39	chr7:112434498-112434548	AG09309	skin:	n/a
40	chr7:112434498-112434548	NHDF-neo	bronchial:	n/a
41	chr7:112431576-112431626	HMEC	breast:	n/a
42	chr7:112459177-112459227	GM06990	blood:	n/a
43	chr7:112434498-112434548	SKMC	muscle:	n/a
44	chr7:112431576-112431626	GM12878	blood:	n/a
45	chr7:112434498-112434548	GM19239	blood:	n/a
46	chr7:112434498-112434548	HRCEpiC	kidney:	n/a
47	chr7:112431576-112431626	HEEpiC	esophagus:	n/a
48	chr7:112431576-112431626	HRCEpiC	kidney:	n/a
49	chr7:112431576-112431626	AG09319	gingival:	n/a
50	chr7:112431576-112431626	ovcar-3	ovarian:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:112464327..112467031-chr7:112469420..112472125,2	K562	blood:
2	chr7:112429949..112431702-chr7:112439578..112441274,2	MCF-7	breast:
3	chr7:112442436..112445188-chr7:112575668..112578638,2	K562	blood:
4	chr7:112460967..112462582-chr7:112467318..112468834,2	MCF-7	breast:
5	chr7:112431532..112434194-chr7:112463729..112466329,2	K562	blood:
6	chr7:112088410..112092985-chr7:112428999..112431698,4	K562	blood:
7	chr7:112429306..112431701-chr7:112443388..112445678,2	MCF-7	breast:
8	chr7:112439935..112445178-chr7:112445414..112449539,5	K562	blood:
9	chr7:112430477..112433385-chr7:112446391..112449066,2	K562	blood:
10	chr7:112460967..112462582-chr7:112467318..112468834,2	MCF-7	breast:
11	chr7:112464327..112467031-chr7:112469420..112472125,2	K562	blood:
12	chr7:112428959..112431266-chr7:112462884..112465767,2	K562	blood:
13	chr7:112431532..112434194-chr7:112463729..112466329,2	K562	blood:
14	chr7:112457341..112459401-chr7:112460833..112463216,2	K562	blood:
15	chr7:112089239..112091876-chr7:112428390..112433191,6	K562	blood:
16	chr7:112440427..112442573-chr7:112447288..112451136,3	K562	blood:
17	chr7:112469172..112470968-chr7:112479580..112481135,2	K562	blood:
18	chr7:112445350..112448501-chr7:112449970..112452849,3	K562	blood:
19	chr7:112399378..112401790-chr7:112440568..112442211,2	K562	blood:
20	chr7:112429019..112430745-chr7:112433310..112435464,2	MCF-7	breast:
21	chr7:112445350..112448501-chr7:112449970..112452849,3	K562	blood:
22	chr7:112421571..112428519-chr7:112428661..112431818,11	MCF-7	breast:
23	chr7:112432334..112434564-chr7:112518600..112520396,2	K562	blood:
24	chr7:112457341..112459401-chr7:112460833..112463216,2	K562	blood:
25	chr7:112439935..112445178-chr7:112445414..112449539,5	K562	blood:
26	chr7:112420290..112422919-chr7:112432152..112433977,2	MCF-7	breast:
27	chr7:112421681..112427261-chr7:112427948..112432124,6	MCF-7	breast:
28	chr7:112469510..112471987-chr7:112486621..112488702,2	K562	blood:
29	chr7:112429386..112431628-chr7:112438433..112441266,2	MCF-7	breast:
30	chr7:112440427..112442573-chr7:112447288..112451136,3	K562	blood:
31	chr7:112427720..112431505-chr7:112447113..112451957,4	K562	blood:

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	C7orf60	hsa-miR-186-5p	chr7:112460090-112460113
2	C7orf60	hsa-miR-130b-3p	chr7:112460487-112460481
3	C7orf60	hsa-miR-130b-3p	chr7:112460947-112460941
4	C7orf60	hsa-let-7a-5p	chr7:112460505-112460499
5	C7orf60	hsa-miR-130b-3p	chr7:112461411-112461432
6	C7orf60	hsa-miR-186-5p	chr7:112461232-112461253
7	C7orf60	hsa-miR-130b-3p	chr7:112460481-112460502
8	C7orf60	hsa-miR-130b-3p	chr7:112460941-112460966
9	C7orf60	hsa-miR-130b-3p	chr7:112459535-112459557
10	C7orf60	hsa-miR-186-5p	chr7:112461629-112461648
11	C7orf60	hsa-let-7a-5p	chr7:112460500-112460523
12	C7orf60	hsa-miR-130b-3p	chr7:112461417-112461411

Variant related genes	Relation type
TMEM168	TF binding region
TMEM168	CpG island
ENSG00000146802	chromatin interactions
ENSG00000006652	chromatin interactions

Extended variants
information (count: 1524 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543715824	chr7:112431429-112431430	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs555333092	chr7:112431461-112431462	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs573827192	chr7:112431498-112431499	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs147752811	chr7:112431522-112431523	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs550902252	chr7:112431524-112431525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs142521929	chr7:112431551-112431552	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs544795942	chr7:112431560-112431561	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs533232951	chr7:112431581-112431582	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs28428168	chr7:112431665-112431666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs563360517	chr7:112431761-112431762	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs530774254	chr7:112431765-112431766	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549652374	chr7:112431768-112431769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs567857539	chr7:112431802-112431803	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs528722039	chr7:112431806-112431807	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs547197901	chr7:112431814-112431815	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs368248644	chr7:112431849-112431850	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs562902805	chr7:112431864-112431865	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs572673892	chr7:112431867-112431868	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs139419616	chr7:112431871-112431872	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs565807660	chr7:112431891-112431892	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs539561161	chr7:112431927-112431928	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs561514076	chr7:112431958-112431959	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs188501827	chr7:112431962-112431963	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs569678498	chr7:112431972-112431973	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs528858616	chr7:112431992-112431993	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs6972330	chr7:112432019-112432020	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs193065155	chr7:112432170-112432171	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146703955	chr7:112432174-112432175	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs530157399	chr7:112432195-112432196	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573839935	chr7:112432209-112432210	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs541250406	chr7:112432225-112432226	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552773055	chr7:112432238-112432239	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577385322	chr7:112432299-112432300	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs545109876	chr7:112432301-112432302	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563397947	chr7:112432302-112432303	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs73205173	chr7:112432320-112432321	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530977570	chr7:112432336-112432337	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542644502	chr7:112432344-112432345	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561657620	chr7:112432366-112432367	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs528757503	chr7:112432387-112432388	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115426629	chr7:112432390-112432391	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs1718957	chr7:112432401-112432402	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs532712608	chr7:112432497-112432498	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551503963	chr7:112432534-112432535	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs569642156	chr7:112432584-112432585	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184083042	chr7:112432606-112432607	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs564304947	chr7:112432637-112432638	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567227439	chr7:112432754-112432755	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187725254	chr7:112432758-112432759	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs139267969	chr7:112432784-112432785	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112430400-112433000	Active TSS	HepG2	liver
2	chr7:112430800-112440400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:112431000-112431600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr7:112431000-112431600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:112431000-112431600	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr7:112431000-112431600	Weak transcription	Pancreas	Pancrea
7	chr7:112431000-112431600	Enhancers	GM12878-XiMat	blood
8	chr7:112431000-112431800	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:112431000-112432000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:112431000-112432000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:112431000-112432000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:112431000-112432400	Weak transcription	K562	blood
13	chr7:112431200-112432200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr7:112431200-112433600	Weak transcription	Primary B cells from cord blood	blood
15	chr7:112431400-112431600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:112431400-112431800	ZNF genes & repeats	Esophagus	oesophagus
17	chr7:112431400-112431800	Flanking Active TSS	NHEK	skin
18	chr7:112431600-112431800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:112431600-112431800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr7:112431600-112431800	Enhancers	Pancreas	Pancrea
21	chr7:112431800-112432000	Weak transcription	Esophagus	oesophagus
22	chr7:112431800-112432800	Active TSS	NHEK	skin
23	chr7:112432000-112432200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:112432000-112432200	Enhancers	Esophagus	oesophagus
25	chr7:112432000-112432400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:112432200-112432400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:112432200-112432600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:112432400-112432600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr7:112432400-112434800	Enhancers	K562	blood
30	chr7:112432600-112432800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:112432800-112434000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr7:112432800-112434400	Enhancers	NHEK	skin
33	chr7:112434000-112434200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:112434800-112438400	Weak transcription	K562	blood
35	chr7:112438400-112440800	Enhancers	Fetal Heart	heart
36	chr7:112438400-112440800	Enhancers	K562	blood
37	chr7:112438400-112441800	Enhancers	Fetal Lung	lung
38	chr7:112438800-112439200	Active TSS	Fetal Brain Male	brain
39	chr7:112438800-112439400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:112438800-112439600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:112438800-112439600	Enhancers	Ovary	ovary
42	chr7:112439000-112441000	Enhancers	Fetal Stomach	stomach
43	chr7:112440400-112440600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:112440400-112441000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:112440600-112441200	Enhancers	Fetal Muscle Leg	muscle
46	chr7:112441000-112442400	Weak transcription	Fetal Stomach	stomach
47	chr7:112441000-112443000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:112441800-112442800	Enhancers	Lung	lung
49	chr7:112442400-112442600	ZNF genes & repeats	Fetal Stomach	stomach
50	chr7:112442600-112443000	Weak transcription	Fetal Stomach	stomach

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