Variant report

Variant	nsv889118
Chromosome Location	chr7:120683751-120800837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2068)
CpG islands
(count:611)
Chromatin interactive
region (count:211)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:120719020-120719586	K562	blood:	n/a	n/a
2	ARID3A	chr7:120778432-120778625	K562	blood:	n/a	n/a
3	ARID3A	chr7:120683006-120683949	K562	blood:	n/a	n/a
4	ARID3A	chr7:120724896-120725031	K562	blood:	n/a	n/a
5	ARID3A	chr7:120747983-120748273	K562	blood:	n/a	n/a
6	ARID3A	chr7:120715862-120717615	K562	blood:	n/a	n/a
7	ARID3A	chr7:120711748-120712087	K562	blood:	n/a	n/a
8	ARID3A	chr7:120735693-120736439	K562	blood:	n/a	chr7:120736063-120736079
9	ARID3A	chr7:120714923-120715159	K562	blood:	n/a	n/a
10	ARID3A	chr7:120686842-120687556	K562	blood:	n/a	n/a
11	ARID3A	chr7:120724859-120725121	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:120723039-120723664	K562	blood:	n/a	n/a
13	ARID3A	chr7:120719901-120720326	K562	blood:	n/a	n/a
14	ARID3A	chr7:120689326-120689898	K562	blood:	n/a	n/a
15	ARID3A	chr7:120800023-120800487	K562	blood:	n/a	n/a
16	ARID3A	chr7:120720624-120722162	K562	blood:	n/a	n/a
17	ARID3A	chr7:120684739-120686576	K562	blood:	n/a	n/a
18	ARID3A	chr7:120709160-120709188	K562	blood:	n/a	n/a
19	ARID3A	chr7:120709444-120709898	K562	blood:	n/a	n/a
20	ARID3A	chr7:120695431-120695493	K562	blood:	n/a	n/a
21	ARID3A	chr7:120721437-120721773	HepG2	liver:	n/a	n/a
22	ATF1	chr7:120778322-120778731	K562	blood:	n/a	n/a
23	ATF1	chr7:120689365-120689889	K562	blood:	n/a	n/a
24	ATF1	chr7:120687065-120687405	K562	blood:	n/a	n/a
25	ATF1	chr7:120721397-120721954	K562	blood:	n/a	n/a
26	ATF1	chr7:120799677-120800576	K562	blood:	n/a	n/a
27	ATF1	chr7:120716345-120716834	K562	blood:	n/a	n/a
28	ATF1	chr7:120741816-120741840	K562	blood:	n/a	n/a
29	ATF2	chr7:120778230-120778840	GM12878	blood:	n/a	n/a
30	ATF2	chr7:120778277-120778721	GM12878	blood:	n/a	n/a
31	ATF3	chr7:120687007-120687368	K562	blood:	n/a	n/a
32	ATF3	chr7:120800134-120800510	K562	blood:	n/a	n/a
33	ATF3	chr7:120715926-120716892	K562	blood:	n/a	n/a
34	ATF3	chr7:120723078-120723515	K562	blood:	n/a	n/a
35	ATF3	chr7:120716978-120717420	K562	blood:	n/a	n/a
36	ATF3	chr7:120778265-120778713	K562	blood:	n/a	n/a
37	BACH1	chr7:120724172-120724174	K562	blood:	n/a	n/a
38	BACH1	chr7:120716017-120716863	K562	blood:	n/a	chr7:120716591-120716605
39	BACH1	chr7:120779259-120779282	K562	blood:	n/a	n/a
40	BACH1	chr7:120736364-120736379	K562	blood:	n/a	n/a
41	BACH1	chr7:120771434-120771460	K562	blood:	n/a	n/a
42	BACH1	chr7:120698149-120698173	K562	blood:	n/a	n/a
43	BACH1	chr7:120722246-120722371	K562	blood:	n/a	n/a
44	BACH1	chr7:120705589-120705605	K562	blood:	n/a	n/a
45	BACH1	chr7:120723323-120723346	K562	blood:	n/a	n/a
46	BACH1	chr7:120689433-120689761	K562	blood:	n/a	n/a
47	BCL3	chr7:120716255-120716969	K562	blood:	n/a	n/a
48	BCLAF1	chr7:120716170-120717427	K562	blood:	n/a	n/a
49	BCLAF1	chr7:120716200-120717203	K562	blood:	n/a	n/a
50	BCLAF1	chr7:120720782-120722254	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:120701117-120701167	SKMC	muscle:	n/a
2	chr7:120701117-120701167	SKMC	muscle:	n/a
3	chr7:120721606-120721656	HCF	heart:	n/a
4	chr7:120689323-120689373	PFSK-1	brain:	n/a
5	chr7:120701117-120701167	NHDF-neo	bronchial:	n/a
6	chr7:120716340-120716390	ProgFib	skin:	n/a
7	chr7:120704511-120704561	U87	brain:	n/a
8	chr7:120702049-120702099	HEK293	kidney:	embryo
9	chr7:120716340-120716390	ovcar-3	ovarian:	n/a
10	chr7:120701829-120701879	IMR90	lung:	fetal
11	chr7:120716269-120716319	MCF10A-Er-Src	breast:	n/a
12	chr7:120721606-120721656	SK-N-MC	brain:	n/a
13	chr7:120721606-120721656	HepG2	liver:	n/a
14	chr7:120704511-120704561	AoSMC	blood vessel:	n/a
15	chr7:120702049-120702099	SK-N-SH	brain:	n/a
16	chr7:120742600-120742650	NT2-D1	testis:	n/a
17	chr7:120689323-120689373	GM12892	blood:	n/a
18	chr7:120701829-120701879	SK-N-SH	brain:	n/a
19	chr7:120716340-120716390	HIPEpiC	eye:	n/a
20	chr7:120689323-120689373	A549	lung:	n/a
21	chr7:120701117-120701167	GM12891	blood:	n/a
22	chr7:120716340-120716390	GM12891	blood:	n/a
23	chr7:120689323-120689373	GM12878	blood:	n/a
24	chr7:120702049-120702099	Jurkat	blood:	n/a
25	chr7:120701829-120701879	A549	lung:	n/a
26	chr7:120689323-120689373	AG09309	skin:	n/a
27	chr7:120716269-120716319	GM12878	blood:	n/a
28	chr7:120716340-120716390	MCF10A-Er-Src	breast:	n/a
29	chr7:120701117-120701167	SAEC	small airway:	n/a
30	chr7:120725046-120725096	MCF10A-Er-Src	breast:	n/a
31	chr7:120716340-120716390	NB4	blood:	n/a
32	chr7:120704511-120704561	ovcar-3	ovarian:	n/a
33	chr7:120725046-120725096	CMK	blood:	n/a
34	chr7:120716269-120716319	Caco-2	colon:	n/a
35	chr7:120716269-120716319	ovcar-3	ovarian:	n/a
36	chr7:120704511-120704561	HCT-116	colon:	n/a
37	chr7:120725046-120725096	HIPEpiC	eye:	n/a
38	chr7:120701829-120701879	NHDF-neo	bronchial:	n/a
39	chr7:120704511-120704561	K562	blood:	n/a
40	chr7:120716340-120716390	BE2_C	brain:	n/a
41	chr7:120701117-120701167	U87	brain:	n/a
42	chr7:120716269-120716319	HMEC	breast:	n/a
43	chr7:120702049-120702099	HEEpiC	esophagus:	n/a
44	chr7:120701829-120701879	RPTEC	kidney:	n/a
45	chr7:120716269-120716319	HepG2	liver:	n/a
46	chr7:120689323-120689373	K562	blood:	n/a
47	chr7:120725046-120725096	HMEC	breast:	n/a
48	chr7:120725046-120725096	BJ	skin:	n/a
49	chr7:120725046-120725096	HCM	heart:	n/a
50	chr7:120701117-120701167	HPAEpiC	pulmonary alveolar:	n/a

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:120776773..120780025-chr7:120780036..120783879,5	K562	blood:
2	chr7:120788426..120790789-chr7:120791125..120793163,2	K562	blood:
3	chr7:120629478..120632230-chr7:120728269..120729776,2	K562	blood:
4	chr7:120635913..120636486-chr7:120747716..120748711,2	K562	blood:
5	chr7:120773227..120776221-chr7:120776532..120780949,5	K562	blood:
6	chr7:120778509..120781370-chr7:120785067..120788347,3	K562	blood:
7	chr7:120762968..120765297-chr7:120774508..120778182,3	K562	blood:
8	chr7:120697778..120699427-chr7:120715523..120718079,2	K562	blood:
9	chr7:120750275..120752757-chr7:120754885..120757852,3	K562	blood:
10	chr7:120590034..120592222-chr7:120792128..120794840,3	K562	blood:
11	chr7:120627648..120628254-chr7:120721307..120722315,3	MCF-7	breast:
12	chr7:120698569..120700981-chr7:120701062..120703872,2	K562	blood:
13	chr7:120748117..120751439-chr7:120760191..120762453,3	K562	blood:
14	chr7:120695659..120698795-chr7:120708123..120711912,4	K562	blood:
15	chr7:120766585..120767374-chr7:121187327..121188280,3	MCF-7	breast:
16	chr7:120688120..120689909-chr7:120713674..120716576,3	K562	blood:
17	chr7:120627757..120628266-chr7:120734232..120734768,2	K562	blood:
18	chr7:120617320..120619610-chr7:120694736..120697163,2	K562	blood:
19	chr7:120661476..120663248-chr7:120721625..120723394,2	K562	blood:
20	chr7:120682952..120685567-chr7:120708911..120710433,2	K562	blood:
21	chr7:120742066..120745673-chr7:120758680..120764316,5	K562	blood:
22	chr7:120695659..120698795-chr7:120708123..120711912,4	K562	blood:
23	chr7:120682952..120685567-chr7:120708911..120710433,2	K562	blood:
24	chr7:120684359..120686005-chr7:120688473..120690743,2	MCF-7	breast:
25	chr7:120732885..120735517-chr7:120747045..120751097,5	K562	blood:
26	chr7:120795773..120797824-chr7:120798929..120800429,2	K562	blood:
27	chr7:120688105..120689645-chr7:120709795..120712085,2	K562	blood:
28	chr7:120589647..120592092-chr7:120755972..120758448,2	K562	blood:
29	chr7:120674087..120676521-chr7:120718031..120719674,2	K562	blood:
30	chr7:120677155..120680507-chr7:120717086..120719349,5	K562	blood:
31	chr7:120651629..120654433-chr7:120773346..120775726,2	K562	blood:
32	chr7:120685095..120691151-chr7:120712234..120720635,10	K562	blood:
33	chr7:120684341..120686164-chr7:120720780..120722996,2	K562	blood:
34	chr7:120589600..120593889-chr7:120719099..120726294,8	K562	blood:
35	chr7:120742066..120743891-chr7:120758680..120761342,2	K562	blood:
36	chr7:120734442..120735992-chr7:120738253..120740799,2	K562	blood:
37	chr7:120673687..120675615-chr7:120719879..120722056,2	K562	blood:
38	chr7:120658657..120661112-chr7:120743405..120745049,2	K562	blood:
39	chr7:120718771..120721283-chr7:120791408..120793421,2	K562	blood:
40	chr7:120765203..120766976-chr7:120768801..120771594,2	K562	blood:
41	chr7:120739132..120740761-chr7:120746818..120749642,2	K562	blood:
42	chr7:120745612..120749676-chr7:120751128..120754629,5	K562	blood:
43	chr7:120775298..120777729-chr7:120784980..120787236,2	K562	blood:
44	chr7:120770037..120772769-chr7:120796157..120798436,2	K562	blood:
45	chr7:120590626..120592952-chr7:120680967..120683892,2	K562	blood:
46	chr7:120590369..120591908-chr7:120749449..120751566,2	K562	blood:
47	chr7:120718771..120721283-chr7:120791408..120793421,2	K562	blood:
48	chr2:38977053..38978639-chr7:120723003..120724994,2	K562	blood:
49	chr7:120739132..120740761-chr7:120746818..120749642,2	K562	blood:
50	chr7:120627349..120628383-chr7:120747676..120749167,11	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ING3-5	chr7:120690445-120690496	NONHSAT122999
2	lnc-ING3-6	chr7:120702382-120702597	expReg_chr7_8599_+
3	lnc-ING3-5	chr7:120686941-120687047	NONHSAT122999

No data

Variant related genes	Relation type
HMGN1P18	TF binding region
CPED1	TF binding region
RNA5SP241	TF binding region
HMGN1P18	CpG island
CPED1	CpG island
RNA5SP241	CpG island
ENSG00000071243	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000106034	chromatin interactions
ENSG00000196937	chromatin interactions
ENSG00000202225	chromatin interactions
ENSG00000212628	chromatin interactions
ENSG00000234927	chromatin interactions

Extended variants
information (count: 4301 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:4301 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4730988	chr7:120683751-120683752	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535930549	chr7:120683808-120683809	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs532759510	chr7:120683836-120683837	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs190734335	chr7:120683877-120683878	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs573076907	chr7:120683906-120683907	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192414164	chr7:120683907-120683908	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534951476	chr7:120683916-120683917	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559219610	chr7:120683964-120683965	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114387022	chr7:120683967-120683968	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183830612	chr7:120684044-120684045	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149725505	chr7:120684104-120684105	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561228334	chr7:120684105-120684106	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188101387	chr7:120684106-120684107	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540728443	chr7:120684156-120684157	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs180873904	chr7:120684158-120684159	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528302650	chr7:120684159-120684160	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186730115	chr7:120684174-120684175	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10263726	chr7:120684208-120684209	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189503798	chr7:120684243-120684244	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530675200	chr7:120684250-120684251	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182091813	chr7:120684322-120684323	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566917225	chr7:120684370-120684371	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs535968776	chr7:120684384-120684385	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs369023029	chr7:120684385-120684386	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112266919	chr7:120684390-120684391	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs77601171	chr7:120684395-120684396	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531731538	chr7:120684417-120684418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76342960	chr7:120684449-120684450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575906242	chr7:120684473-120684474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144564320	chr7:120684476-120684477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539381950	chr7:120684555-120684556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs56087715	chr7:120684576-120684577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371414755	chr7:120684701-120684702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376113123	chr7:120684702-120684703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs79110420	chr7:120684704-120684705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370569289	chr7:120684705-120684706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78338191	chr7:120684716-120684717	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs58884492	chr7:120684723-120684724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368415783	chr7:120684724-120684725	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371438054	chr7:120684725-120684726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375758925	chr7:120684727-120684728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540765436	chr7:120684756-120684757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148452117	chr7:120684768-120684769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371661856	chr7:120684779-120684780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577220303	chr7:120684810-120684811	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545197162	chr7:120684897-120684898	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568447394	chr7:120684940-120684941	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527744610	chr7:120684968-120684969	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192349235	chr7:120684983-120684984	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566520683	chr7:120685016-120685017	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	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
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120673200-120685200	Weak transcription	Left Ventricle	heart
2	chr7:120673400-120689200	Weak transcription	HSMMtube	muscle
3	chr7:120673800-120694200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr7:120679200-120685200	Weak transcription	Aorta	Aorta
5	chr7:120680600-120685200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:120681600-120684400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr7:120681800-120684200	Transcr. at gene 5' and 3'	K562	blood
8	chr7:120682000-120683800	Enhancers	Ovary	ovary
9	chr7:120682000-120685200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr7:120682000-120687000	Weak transcription	Colon Smooth Muscle	Colon
11	chr7:120682000-120689200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:120682000-120689400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:120682000-120689400	Weak transcription	Osteobl	bone
14	chr7:120682200-120687000	Weak transcription	Adipose Nuclei	Adipose
15	chr7:120682200-120687000	Weak transcription	NHDF-Ad	bronchial
16	chr7:120682200-120687600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:120682200-120695800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr7:120682400-120685600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:120682400-120687000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:120682400-120687000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:120682400-120688000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr7:120682400-120719600	Weak transcription	Fetal Lung	lung
23	chr7:120682600-120685400	Weak transcription	Hela-S3	cervix
24	chr7:120682600-120692000	Weak transcription	Fetal Stomach	stomach
25	chr7:120682800-120700800	Weak transcription	Fetal Kidney	kidney
26	chr7:120683000-120684200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr7:120683000-120686800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr7:120683200-120687000	Weak transcription	HSMM	muscle
29	chr7:120683200-120689400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr7:120683200-120689400	Weak transcription	Right Ventricle	heart
31	chr7:120683400-120684200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr7:120683600-120683800	Enhancers	Psoas Muscle	Psoas
33	chr7:120683600-120683800	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr7:120683600-120684400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:120683600-120684400	Enhancers	NHLF	lung
36	chr7:120683600-120687200	Enhancers	Liver	Liver
37	chr7:120683800-120684000	Enhancers	Small Intestine	intestine
38	chr7:120683800-120684400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:120683800-120689400	Weak transcription	Ovary	ovary
40	chr7:120683800-120689400	Weak transcription	Psoas Muscle	Psoas
41	chr7:120683800-120690800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:120684000-120684200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:120684000-120684400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:120684000-120684400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr7:120684000-120694000	Weak transcription	Small Intestine	intestine
46	chr7:120684200-120684400	Flanking Active TSS	K562	blood
47	chr7:120684200-120685200	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr7:120684200-120687000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr7:120684200-120687200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:120684200-120689400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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