Variant report

Variant	nsv1051032
Chromosome Location	chr11:57290124-57363064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2256)
CpG islands
(count:2197)
Chromatin interactive
region (count:83)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2256 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:57294365-57294882	K562	blood:	n/a	n/a
2	ARID3A	chr11:57314781-57314826	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:57298030-57298828	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:57336838-57337029	K562	blood:	n/a	n/a
5	ARID3A	chr11:57320050-57320231	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:57298071-57299806	K562	blood:	n/a	n/a
7	ARID3A	chr11:57335854-57335901	K562	blood:	n/a	n/a
8	ATF1	chr11:57298084-57299030	K562	blood:	n/a	n/a
9	ATF2	chr11:57297975-57298687	GM12878	blood:	n/a	n/a
10	ATF2	chr11:57335317-57335794	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr11:57294455-57294992	GM12878	blood:	n/a	n/a
12	ATF2	chr11:57297961-57298857	GM12878	blood:	n/a	n/a
13	ATF2	chr11:57335531-57336062	GM12878	blood:	n/a	n/a
14	ATF2	chr11:57335581-57336051	GM12878	blood:	n/a	n/a
15	ATF3	chr11:57299578-57299831	K562	blood:	n/a	n/a
16	ATF3	chr11:57294579-57294999	K562	blood:	n/a	n/a
17	ATF3	chr11:57297994-57298651	A549	lung:	n/a	n/a
18	ATF3	chr11:57298142-57298641	A549	lung:	n/a	n/a
19	BACH1	chr11:57298402-57298857	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:57336897-57337145	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:57298602-57298902	K562	blood:	n/a	n/a
22	BACH1	chr11:57335363-57335910	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr11:57314651-57314930	GM12878	blood:	n/a	chr11:57314767-57314778 chr11:57314768-57314778
24	BATF	chr11:57314523-57314976	GM12878	blood:	n/a	chr11:57314767-57314778 chr11:57314768-57314778
25	BATF	chr11:57335646-57335939	GM12878	blood:	n/a	n/a
26	BCL3	chr11:57297517-57298779	A549	lung:	n/a	n/a
27	BCL3	chr11:57294459-57295031	A549	lung:	n/a	n/a
28	BCL3	chr11:57294272-57295054	A549	lung:	n/a	n/a
29	BCL3	chr11:57322048-57322351	GM12878	blood:	n/a	n/a
30	BCL3	chr11:57297974-57298657	A549	lung:	n/a	n/a
31	BCLAF1	chr11:57298032-57298928	K562	blood:	n/a	n/a
32	BCLAF1	chr11:57335549-57335981	GM12878	blood:	n/a	chr11:57335823-57335831 chr11:57335942-57335951
33	BCLAF1	chr11:57335533-57336054	GM12878	blood:	n/a	chr11:57335823-57335831 chr11:57335942-57335951
34	BCLAF1	chr11:57297996-57298695	GM12878	blood:	n/a	n/a
35	BCLAF1	chr11:57297627-57298871	GM12878	blood:	n/a	n/a
36	BCLAF1	chr11:57297761-57298635	K562	blood:	n/a	n/a
37	BHLHE40	chr11:57294659-57294967	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:57315295-57315918	GM12878	blood:	n/a	n/a
39	BHLHE40	chr11:57337023-57337058	K562	blood:	n/a	n/a
40	BHLHE40	chr11:57298080-57298995	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:57314669-57314869	GM12878	blood:	n/a	n/a
42	BHLHE40	chr11:57298061-57299022	K562	blood:	n/a	n/a
43	BHLHE40	chr11:57333607-57333901	K562	blood:	n/a	n/a
44	BHLHE40	chr11:57335303-57335961	K562	blood:	n/a	chr11:57335454-57335470
45	BHLHE40	chr11:57333556-57333963	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:57294652-57294952	K562	blood:	n/a	n/a
47	BRCA1	chr11:57297949-57298526	GM12878	blood:	n/a	n/a
48	BRCA1	chr11:57298051-57298923	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr11:57294592-57294996	K562	blood:	n/a	n/a
50	CBX3	chr11:57314560-57314945	K562	blood:	n/a	n/a

(count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:57336941-57336991	H1-hESC	embryonic stem cell:	embryo
2	chr11:57336941-57336991	H1-hESC	embryonic stem cell:	embryo
3	chr11:57335585-57335635	GM12891	blood:	n/a
4	chr11:57298594-57298644	AG09319	gingival:	n/a
5	chr11:57317706-57317756	Hepatocyte	liver:	n/a
6	chr11:57298081-57298131	MCF10A-Er-Src	breast:	n/a
7	chr11:57335730-57335780	NB4	blood:	n/a
8	chr11:57308609-57308659	SK-N-SH	brain:	n/a
9	chr11:57317706-57317756	HIPEpiC	eye:	n/a
10	chr11:57335675-57335725	ovcar-3	ovarian:	n/a
11	chr11:57333612-57333662	GM12891	blood:	n/a
12	chr11:57304885-57304935	HCPEpiC	choroid plexus:	n/a
13	chr11:57335454-57335504	SK-N-MC	brain:	n/a
14	chr11:57319872-57319922	LNCaP	prostate:	n/a
15	chr11:57298301-57298351	AG09319	gingival:	n/a
16	chr11:57335356-57335406	HIPEpiC	eye:	n/a
17	chr11:57313734-57313784	PFSK-1	brain:	n/a
18	chr11:57298543-57298593	HNPCEpiC	eye:	n/a
19	chr11:57317706-57317756	GM12891	blood:	n/a
20	chr11:57298301-57298351	AG04449	skin:	fetal
21	chr11:57335551-57335601	HepG2	liver:	n/a
22	chr11:57308609-57308659	RPTEC	kidney:	n/a
23	chr11:57335585-57335635	LNCaP	prostate:	n/a
24	chr11:57332013-57332063	GM12891	blood:	n/a
25	chr11:57335150-57335200	LNCaP	prostate:	n/a
26	chr11:57298252-57298302	HRE	kidney:	n/a
27	chr11:57335454-57335504	A549	lung:	n/a
28	chr11:57333612-57333662	NHBE	bronchial:	n/a
29	chr11:57296133-57296183	Caco-2	colon:	n/a
30	chr11:57298081-57298131	HMEC	breast:	n/a
31	chr11:57313734-57313784	HCM	heart:	n/a
32	chr11:57298349-57298399	PFSK-1	brain:	n/a
33	chr11:57335675-57335725	H1-hESC	embryonic stem cell:	embryo
34	chr11:57308952-57309002	HRPEpiC	eye:	n/a
35	chr11:57336941-57336991	NT2-D1	testis:	n/a
36	chr11:57336941-57336991	HIPEpiC	eye:	n/a
37	chr11:57310571-57310621	LNCaP	prostate:	n/a
38	chr11:57298301-57298351	HRCEpiC	kidney:	n/a
39	chr11:57304885-57304935	NH-A	brain:	n/a
40	chr11:57335140-57335190	HEK293	kidney:	embryo
41	chr11:57304885-57304935	AG04449	skin:	fetal
42	chr11:57317706-57317756	HRE	kidney:	n/a
43	chr11:57335551-57335601	HUVEC	blood vessel:	n/a
44	chr11:57335585-57335635	PrEC	prostate:	n/a
45	chr11:57298349-57298399	GM19239	blood:	n/a
46	chr11:57298252-57298302	SK-N-MC	brain:	n/a
47	chr11:57296305-57296355	SK-N-SH_RA	brain:	n/a
48	chr11:57313734-57313784	ProgFib	skin:	n/a
49	chr11:57308609-57308659	LNCaP	prostate:	n/a
50	chr11:57335585-57335635	SKMC	muscle:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:57294877..57297638-chr11:57477867..57480575,2	K562	blood:
2	chr11:57335355..57336298-chr11:57408531..57409635,7	K562	blood:
3	chr11:57299281..57301007-chr11:57311388..57313824,2	K562	blood:
4	chr11:57296541..57298189-chr11:57320767..57323633,2	K562	blood:
5	chr11:57299281..57301007-chr11:57311388..57313824,2	K562	blood:
6	chr11:57226847..57229273-chr11:57333715..57336392,3	K562	blood:
7	chr11:57340284..57342621-chr11:57408042..57409998,2	K562	blood:
8	chr11:57335649..57336286-chr11:57413903..57414633,2	MCF-7	breast:
9	chr11:57358699..57361621-chr11:57412591..57415066,2	K562	blood:
10	chr11:57112463..57114876-chr11:57292592..57294764,2	K562	blood:
11	chr11:57261958..57264952-chr11:57292189..57295088,2	K562	blood:
12	chr11:57280118..57282048-chr11:57295886..57298266,2	MCF-7	breast:
13	chr11:57328509..57330286-chr11:57332816..57335358,2	K562	blood:
14	chr11:57260501..57261553-chr11:57294214..57295258,6	MCF-7	breast:
15	chr11:57258981..57259832-chr11:57294341..57295266,3	K562	blood:
16	chr11:57335324..57336323-chr11:57408291..57409695,14	MCF-7	breast:
17	chr11:57258861..57259534-chr11:57294323..57294936,2	MCF-7	breast:
18	chr11:57327395..57330441-chr11:57334291..57337676,3	K562	blood:
19	chr11:57297015..57298977-chr11:58345779..58348496,3	K562	blood:
20	chr11:57333866..57335515-chr11:57412954..57415220,2	MCF-7	breast:
21	chr11:57296719..57299374-chr11:57308110..57310728,2	K562	blood:
22	chr11:57325867..57327995-chr11:57414658..57417368,2	K562	blood:
23	chr11:57224304..57226625-chr11:57294106..57296478,4	K562	blood:
24	chr11:57258661..57259261-chr11:57328962..57329548,2	MCF-7	breast:
25	chr11:57260557..57261860-chr11:57294319..57295311,12	MCF-7	breast:
26	chr11:57260987..57261534-chr11:57294341..57295268,4	K562	blood:
27	chr11:57224499..57227061-chr11:57335779..57338545,2	K562	blood:
28	chr11:57327644..57330005-chr11:57333922..57337612,3	MCF-7	breast:
29	chr11:57225860..57226373-chr11:57294312..57294844,2	MCF-7	breast:
30	chr11:57279377..57284601-chr11:57296598..57300992,7	K562	blood:
31	chr11:57293312..57295959-chr11:57408961..57411007,2	MCF-7	breast:
32	chr11:57229455..57232112-chr11:57299211..57300946,2	K562	blood:
33	chr11:57296719..57299374-chr11:57308110..57310728,2	K562	blood:
34	chr11:57224656..57225281-chr11:57329063..57329842,2	K562	blood:
35	chr11:57297426..57300384-chr11:57328449..57331684,3	K562	blood:
36	chr11:57333149..57335001-chr11:57423752..57425633,2	MCF-7	breast:
37	chr11:57259469..57263127-chr11:57289484..57293312,4	K562	blood:
38	chr11:57224518..57225774-chr11:57293864..57295277,11	K562	blood:
39	chr11:57225517..57229165-chr11:57295790..57298188,3	K562	blood:
40	chr11:57327395..57330441-chr11:57334291..57337676,3	K562	blood:
41	chr11:57308278..57310197-chr11:57313267..57314907,2	K562	blood:
42	chr11:57334543..57336941-chr11:57357836..57360654,2	K562	blood:
43	chr11:57312168..57315118-chr11:57412878..57415826,2	K562	blood:
44	chr11:57225876..57227114-chr11:57294349..57295273,7	K562	blood:
45	chr11:57296819..57301795-chr11:57434465..57437903,4	K562	blood:
46	chr11:57116975..57117493-chr11:57294361..57294888,2	MCF-7	breast:
47	chr11:57280468..57282716-chr11:57310708..57312251,2	K562	blood:
48	chr11:57336503..57337044-chr11:57408560..57409853,3	MCF-7	breast:
49	chr11:57298175..57301007-chr11:57311281..57313824,2	K562	blood:
50	chr11:57279697..57283964-chr11:57296063..57300992,5	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERPING1-2	chr11:57316055-57316469	expReg_chr11_4539_+
2	lnc-SMTNL1-1	chr11:57299739-57299980	expReg_chr11_4488_+
3	lnc-TIMM10-1	chr11:57309889-57309993	NONHSAT021419
4	lnc-SERPING1-3	chr11:57312033-57312260	expReg_chr11_4527_+
5	lnc-TIMM10-1	chr11:57298645-57299056	NONHSAT021419

No data

Variant related genes	Relation type
SMTNL1	TF binding region
UBE2L6	TF binding region
TIMM10	TF binding region
SERPING1	TF binding region
RPS4XP13	TF binding region
SMTNL1	CpG island
UBE2L6	CpG island
TIMM10	CpG island
SERPING1	CpG island
RPS4XP13	CpG island
ENSG00000214872	chromatin interactions
ENSG00000134809	chromatin interactions
ENSG00000254462	chromatin interactions
ENSG00000208009	chromatin interactions
ENSG00000149131	chromatin interactions
ENSG00000156603	chromatin interactions
ENSG00000156587	chromatin interactions
ENSG00000186907	chromatin interactions
ENSG00000166793	chromatin interactions
ENSG00000156599	chromatin interactions
ENSG00000149150	chromatin interactions
ENSG00000213593	chromatin interactions
ENSG00000186660	chromatin interactions
ENSG00000254979	chromatin interactions
ENSG00000172409	chromatin interactions
ENSG00000254602	chromatin interactions
ENSG00000134802	chromatin interactions
ENSG00000255073	chromatin interactions

Extended variants
information (count: 2617 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2617 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545018880	chr11:57290133-57290134	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs560088842	chr11:57290174-57290175	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs148382954	chr11:57290195-57290196	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs77362863	chr11:57290272-57290273	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs143283946	chr11:57290313-57290314	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561216602	chr11:57290327-57290328	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531980547	chr11:57290341-57290342	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561890605	chr11:57290343-57290344	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540581910	chr11:57290363-57290364	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549114776	chr11:57290366-57290367	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546599688	chr11:57290370-57290371	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs369585022	chr11:57290386-57290387	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs199537343	chr11:57290393-57290394	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs550060977	chr11:57290471-57290472	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs571983909	chr11:57290508-57290509	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs58516757	chr11:57290540-57290541	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs548086923	chr11:57290574-57290575	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565714040	chr11:57290589-57290590	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs535858247	chr11:57290594-57290595	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs554693530	chr11:57290598-57290599	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576005349	chr11:57290719-57290720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182029789	chr11:57290723-57290724	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs376515809	chr11:57290808-57290809	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187328731	chr11:57290910-57290911	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190102306	chr11:57290944-57290945	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs4939148	chr11:57290961-57290962	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs116647571	chr11:57291046-57291047	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572148650	chr11:57291147-57291148	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs559591104	chr11:57291153-57291154	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs114037787	chr11:57291168-57291169	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182070431	chr11:57291190-57291191	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs186604710	chr11:57291236-57291237	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs550369965	chr11:57291249-57291250	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs565505990	chr11:57291283-57291284	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532737314	chr11:57291313-57291314	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs36112164	chr11:57291332-57291333	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs56825161	chr11:57291333-57291334	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs59961603	chr11:57291336-57291337	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs566370875	chr11:57291348-57291349	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs61192177	chr11:57291350-57291351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs59892068	chr11:57291363-57291364	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs182515433	chr11:57291396-57291397	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113802717	chr11:57291397-57291398	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs34096044	chr11:57291400-57291401	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs569749350	chr11:57291418-57291419	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs536721604	chr11:57291424-57291425	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs558211586	chr11:57291552-57291553	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs375250618	chr11:57291583-57291584	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs534500375	chr11:57291614-57291615	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs185505509	chr11:57291644-57291645	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Breast cancer	21509527	CNVD
Angio-oedema	21790735	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2483 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57283400-57297400	Weak transcription	Gastric	stomach
2	chr11:57283600-57292200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:57283600-57292400	Weak transcription	Aorta	Aorta
4	chr11:57283600-57295200	Weak transcription	Lung	lung
5	chr11:57283600-57296000	Weak transcription	Spleen	Spleen
6	chr11:57283600-57296200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:57283800-57291200	Weak transcription	Adipose Nuclei	Adipose
8	chr11:57283800-57292200	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:57283800-57292200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr11:57283800-57292200	Weak transcription	Brain Substantia Nigra	brain
11	chr11:57283800-57292200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr11:57283800-57292400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:57283800-57292400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr11:57283800-57292400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:57283800-57293800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr11:57283800-57293800	Weak transcription	HUVEC	blood vessel
17	chr11:57283800-57294400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr11:57283800-57294400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr11:57283800-57294600	Weak transcription	Primary T cells from cord blood	blood
20	chr11:57283800-57295000	Weak transcription	NHLF	lung
21	chr11:57283800-57295000	Weak transcription	Osteobl	bone
22	chr11:57283800-57295200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:57283800-57295200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr11:57283800-57295200	Weak transcription	Brain Anterior Caudate	brain
25	chr11:57283800-57295200	Weak transcription	Fetal Intestine Small	intestine
26	chr11:57283800-57295200	Weak transcription	Fetal Muscle Leg	muscle
27	chr11:57283800-57295800	Weak transcription	Fetal Intestine Large	intestine
28	chr11:57283800-57296000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:57283800-57296000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr11:57283800-57296000	Weak transcription	Left Ventricle	heart
31	chr11:57283800-57296200	Weak transcription	HSMM	muscle
32	chr11:57283800-57296400	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr11:57283800-57296600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:57283800-57296600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:57283800-57297000	Weak transcription	Brain Angular Gyrus	brain
36	chr11:57283800-57297200	Weak transcription	Fetal Lung	lung
37	chr11:57283800-57297200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr11:57283800-57297200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr11:57283800-57297200	Weak transcription	Right Atrium	heart
40	chr11:57283800-57297200	Weak transcription	NH-A	brain
41	chr11:57283800-57297400	Weak transcription	Colonic Mucosa	Colon
42	chr11:57283800-57297400	Weak transcription	HSMMtube	muscle
43	chr11:57284000-57292200	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr11:57284000-57292200	Weak transcription	A549	lung
45	chr11:57284000-57292400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr11:57284000-57294000	Weak transcription	GM12878-XiMat	blood
47	chr11:57284000-57294200	Weak transcription	Primary B cells from peripheral blood	blood
48	chr11:57284000-57294600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr11:57284000-57295800	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr11:57284000-57296000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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