Variant report

Variant	nsv832117
Chromosome Location	chr11:34639008-34831199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3006)
CpG islands
(count:916)
Chromatin interactive
region (count:130)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34830689-34831538	K562	blood:	n/a	n/a
2	ARID3A	chr11:34804472-34804673	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:34689665-34690249	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:34673150-34674076	K562	blood:	n/a	n/a
5	ARID3A	chr11:34675333-34678461	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:34664524-34664676	K562	blood:	n/a	n/a
7	ARID3A	chr11:34812201-34812444	K562	blood:	n/a	n/a
8	ARID3A	chr11:34812906-34812934	K562	blood:	n/a	n/a
9	ARID3A	chr11:34655611-34656115	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:34707057-34707061	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:34706908-34707346	K562	blood:	n/a	n/a
12	ARID3A	chr11:34640475-34640903	K562	blood:	n/a	n/a
13	ARID3A	chr11:34804939-34806559	HepG2	liver:	n/a	chr11:34806400-34806416
14	ARID3A	chr11:34667925-34667948	K562	blood:	n/a	n/a
15	ARID3A	chr11:34661875-34662144	HepG2	liver:	n/a	n/a
16	ARID3A	chr11:34686478-34687268	HepG2	liver:	n/a	n/a
17	ARID3A	chr11:34827457-34827921	K562	blood:	n/a	n/a
18	ARID3A	chr11:34828529-34828710	K562	blood:	n/a	n/a
19	ARID3A	chr11:34748846-34749059	K562	blood:	n/a	n/a
20	ATF1	chr11:34687084-34687254	K562	blood:	n/a	n/a
21	ATF1	chr11:34706870-34707207	K562	blood:	n/a	n/a
22	ATF1	chr11:34827473-34827813	K562	blood:	n/a	n/a
23	ATF1	chr11:34640574-34640880	K562	blood:	n/a	n/a
24	ATF1	chr11:34831188-34831517	K562	blood:	n/a	n/a
25	ATF1	chr11:34779809-34780240	K562	blood:	n/a	n/a
26	ATF1	chr11:34805606-34805830	K562	blood:	n/a	n/a
27	ATF1	chr11:34673739-34674051	K562	blood:	n/a	n/a
28	ATF1	chr11:34675550-34675863	K562	blood:	n/a	n/a
29	ATF1	chr11:34748782-34749093	K562	blood:	n/a	n/a
30	ATF2	chr11:34671847-34672599	GM12878	blood:	n/a	n/a
31	ATF2	chr11:34673623-34674581	GM12878	blood:	n/a	n/a
32	ATF2	chr11:34671884-34672577	GM12878	blood:	n/a	n/a
33	ATF2	chr11:34644852-34645273	GM12878	blood:	n/a	n/a
34	ATF2	chr11:34706715-34707242	GM12878	blood:	n/a	n/a
35	ATF2	chr11:34655408-34656051	GM12878	blood:	n/a	n/a
36	ATF2	chr11:34706739-34707148	GM12878	blood:	n/a	n/a
37	ATF3	chr11:34706580-34707376	HCT-116	colon:	n/a	n/a
38	ATF3	chr11:34661628-34662235	A549	lung:	n/a	n/a
39	ATF3	chr11:34675433-34676137	A549	lung:	n/a	n/a
40	ATF3	chr11:34706702-34707206	K562	blood:	n/a	n/a
41	ATF3	chr11:34676265-34676876	A549	lung:	n/a	n/a
42	ATF3	chr11:34675408-34676126	A549	lung:	n/a	n/a
43	ATF3	chr11:34830633-34831620	K562	blood:	n/a	n/a
44	ATF3	chr11:34706685-34707409	A549	lung:	n/a	n/a
45	ATF3	chr11:34673654-34674049	K562	blood:	n/a	n/a
46	ATF3	chr11:34706711-34707373	A549	lung:	n/a	n/a
47	ATF3	chr11:34676387-34677171	A549	lung:	n/a	n/a
48	ATF3	chr11:34706701-34707439	HCT-116	colon:	n/a	n/a
49	ATF3	chr11:34661411-34662279	A549	lung:	n/a	n/a
50	BACH1	chr11:34816262-34816669	H1-hESC	embryonic stem cell:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34642885-34642935	AG10803	skin:	n/a
2	chr11:34642885-34642935	AG10803	skin:	n/a
3	chr11:34642303-34642353	IMR90	lung:	fetal
4	chr11:34681375-34681425	GM06990	blood:	n/a
5	chr11:34642885-34642935	GM12891	blood:	n/a
6	chr11:34642885-34642935	SKMC	muscle:	n/a
7	chr11:34702946-34702996	Hela-S3	cervix:	n/a
8	chr11:34681375-34681425	SKMC	muscle:	n/a
9	chr11:34675402-34675452	MCF-7	breast:	n/a
10	chr11:34642885-34642935	HEK293	kidney:	embryo
11	chr11:34642463-34642513	HNPCEpiC	eye:	n/a
12	chr11:34642885-34642935	HRE	kidney:	n/a
13	chr11:34702946-34702996	HNPCEpiC	eye:	n/a
14	chr11:34672025-34672075	GM12892	blood:	n/a
15	chr11:34666060-34666110	H1-hESC	embryonic stem cell:	embryo
16	chr11:34701819-34701869	HCPEpiC	choroid plexus:	n/a
17	chr11:34675402-34675452	T-47D	breast:	n/a
18	chr11:34642463-34642513	HRPEpiC	eye:	n/a
19	chr11:34675402-34675452	HMEC	breast:	n/a
20	chr11:34641925-34641975	NB4	blood:	n/a
21	chr11:34642885-34642935	BE2_C	brain:	n/a
22	chr11:34642463-34642513	ovcar-3	ovarian:	n/a
23	chr11:34672025-34672075	ovcar-3	ovarian:	n/a
24	chr11:34676683-34676733	HCPEpiC	choroid plexus:	n/a
25	chr11:34681375-34681425	HCF	heart:	n/a
26	chr11:34702946-34702996	K562	blood:	n/a
27	chr11:34672025-34672075	HEEpiC	esophagus:	n/a
28	chr11:34676683-34676733	LNCaP	prostate:	n/a
29	chr11:34641925-34641975	IMR90	lung:	fetal
30	chr11:34675402-34675452	IMR90	lung:	fetal
31	chr11:34666060-34666110	ECC-1	luminal epithelium:	n/a
32	chr11:34702946-34702996	AoSMC	blood vessel:	n/a
33	chr11:34642303-34642353	ProgFib	skin:	n/a
34	chr11:34701819-34701869	SK-N-SH_RA	brain:	n/a
35	chr11:34642303-34642353	AG09319	gingival:	n/a
36	chr11:34642463-34642513	GM06990	blood:	n/a
37	chr11:34814081-34814131	HRE	kidney:	n/a
38	chr11:34771918-34771968	HIPEpiC	eye:	n/a
39	chr11:34666060-34666110	HCF	heart:	n/a
40	chr11:34676683-34676733	K562	blood:	n/a
41	chr11:34642885-34642935	SK-N-SH	brain:	n/a
42	chr11:34779084-34779134	H1-hESC	embryonic stem cell:	embryo
43	chr11:34672025-34672075	HRCEpiC	kidney:	n/a
44	chr11:34779084-34779134	LNCaP	prostate:	n/a
45	chr11:34779084-34779134	HCT-116	colon:	n/a
46	chr11:34654233-34654283	HEK293	kidney:	embryo
47	chr11:34771918-34771968	PFSK-1	brain:	n/a
48	chr11:34642885-34642935	HL-60	blood:	n/a
49	chr11:34779084-34779134	BE2_C	brain:	n/a
50	chr11:34702946-34702996	SKMC	muscle:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:34652609..34656733-chr11:34661493..34664204,6	MCF-7	breast:
2	chr11:34675426..34678725-chr11:34681137..34686486,6	MCF-7	breast:
3	chr11:34676055..34678665-chr11:34685926..34687942,2	MCF-7	breast:
4	chr11:34643086..34644601-chr11:34653927..34655826,2	K562	blood:
5	chr11:34667165..34669347-chr11:34670992..34673618,3	K562	blood:
6	chr11:34656114..34658130-chr11:34661592..34663186,2	K562	blood:
7	chr11:34777504..34779332-chr11:34816777..34819047,2	MCF-7	breast:
8	chr11:34608499..34609105-chr11:34675652..34676481,2	MCF-7	breast:
9	chr11:34807272..34809273-chr11:34809643..34812382,3	K562	blood:
10	chr11:34624693..34626791-chr11:34672431..34674013,2	K562	blood:
11	chr11:34670807..34672858-chr11:34677571..34680304,2	K562	blood:
12	chr11:34737373..34739523-chr11:34745601..34747414,2	K562	blood:
13	chr11:34819205..34826551-chr11:34829823..34835499,8	K562	blood:
14	chr11:34679939..34683842-chr11:34684452..34687073,3	MCF-7	breast:
15	chr11:34671248..34673590-chr11:34674140..34675712,2	MCF-7	breast:
16	chr11:34805559..34807304-chr11:34808633..34811203,2	K562	blood:
17	chr11:34669421..34671173-chr11:34672153..34673980,2	MCF-7	breast:
18	chr11:34637828..34640376-chr11:34674188..34675830,2	K562	blood:
19	chr11:34646456..34649204-chr11:34658693..34661498,2	K562	blood:
20	chr11:34642302..34644592-chr11:34647851..34649607,2	K562	blood:
21	chr11:34804567..34805318-chr11:34844825..34845441,2	MCF-7	breast:
22	chr11:34679021..34681559-chr11:34682485..34684482,3	K562	blood:
23	chr11:34673700..34675383-chr11:34678871..34681043,2	K562	blood:
24	chr11:34652119..34655863-chr11:34659054..34663383,5	MCF-7	breast:
25	chr11:34641972..34644254-chr11:34644762..34647514,2	MCF-7	breast:
26	chr11:34802267..34806129-chr11:34812467..34815224,3	K562	blood:
27	chr11:34679021..34681559-chr11:34682485..34684482,3	K562	blood:
28	chr11:34642981..34644601-chr11:34653348..34655427,2	K562	blood:
29	chr11:34741790..34743892-chr11:34746421..34748174,2	K562	blood:
30	chr11:34830057..34832042-chr11:34848126..34850634,2	K562	blood:
31	chr11:34820151..34822976-chr11:34824163..34828080,3	K562	blood:
32	chr11:34686232..34690169-chr11:34690691..34694222,3	K562	blood:
33	chr11:34673816..34675543-chr11:34675726..34677757,2	K562	blood:
34	chr11:34653892..34655575-chr11:34674253..34677029,2	MCF-7	breast:
35	chr11:34736912..34738637-chr11:34937479..34939117,2	MCF-7	breast:
36	chr11:34814107..34816684-chr11:34826234..34828652,3	K562	blood:
37	chr11:34823667..34825703-chr11:34832026..34833847,2	K562	blood:
38	chr11:34667165..34669347-chr11:34670992..34673618,3	K562	blood:
39	chr11:34819205..34826551-chr11:34829823..34835499,8	K562	blood:
40	chr11:34569575..34572188-chr11:34654026..34656831,2	MCF-7	breast:
41	chr11:34646456..34649204-chr11:34658693..34661498,2	K562	blood:
42	chr11:34639668..34642067-chr11:34645120..34646701,2	K562	blood:
43	chr11:34683526..34685341-chr11:34687454..34689901,2	K562	blood:
44	chr11:34660366..34662512-chr11:34808028..34810446,2	MCF-7	breast:
45	chr11:34683526..34685341-chr11:34687454..34689901,2	K562	blood:
46	chr11:34831080..34832844-chr11:34868501..34870661,2	K562	blood:
47	chr11:34683754..34686000-chr11:34698951..34701034,2	MCF-7	breast:
48	chr11:34671534..34674106-chr11:34677263..34680105,2	K562	blood:
49	chr11:34621214..34622751-chr11:34769844..34772782,2	MCF-7	breast:
50	chr11:34637761..34639405-chr11:34642097..34644790,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELF5-3	chr11:34736818-34736842	NONHSAT018762
2	lnc-EHF-4	chr11:34731147-34731708	NONHSAT018761
3	lnc-ELF5-3	chr11:34736903-34737435	NONHSAT018762
4	lnc-ELF5-3	chr11:34736767-34736787	NONHSAT018762
5	lnc-ELF5-3	chr11:34736881-34736897	NONHSAT018762
6	lnc-EHF-5	chr11:34764453-34764746	NONHSAT018763

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EHF	hsa-miR-335-5p	chr11:34680781-34680805
2	EHF	hsa-miR-335-5p	chr11:34681304-34681326

Variant related genes	Relation type
EHF	TF binding region
ENSG00000271369	TF binding region
ENSG00000270491	TF binding region
EHF	CpG island
ENSG00000271369	CpG island
ENSG00000270491	CpG island
ENSG00000110435	chromatin interactions
ENSG00000135373	chromatin interactions
ENSG00000149089	chromatin interactions

Extended variants
information (count: 7083 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:7083 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537496255	chr11:34639180-34639181	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs2167906	chr11:34639284-34639285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7926672	chr11:34639376-34639377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs182465276	chr11:34639382-34639383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs149095797	chr11:34639392-34639393	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368416338	chr11:34639420-34639421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372148285	chr11:34639441-34639442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569583666	chr11:34639459-34639460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs572280356	chr11:34639471-34639472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs286928	chr11:34639500-34639501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs561213760	chr11:34639567-34639568	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs529937413	chr11:34639605-34639606	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs143182381	chr11:34639616-34639617	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs563114850	chr11:34639741-34639742	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532102702	chr11:34639748-34639749	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs551869555	chr11:34639750-34639751	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs573270940	chr11:34639777-34639778	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs373528783	chr11:34639791-34639792	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200768291	chr11:34639811-34639812	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7927246	chr11:34639817-34639818	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs548368195	chr11:34639835-34639836	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs7942038	chr11:34639838-34639839	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186890427	chr11:34639890-34639891	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs367573424	chr11:34639893-34639894	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs141448018	chr11:34639916-34639917	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs540412378	chr11:34639920-34639921	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576155559	chr11:34640013-34640014	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559013509	chr11:34640052-34640053	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191782874	chr11:34640065-34640066	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184128597	chr11:34640123-34640124	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201374484	chr11:34640130-34640131	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs72410826	chr11:34640134-34640135	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs200086581	chr11:34640138-34640139	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540471921	chr11:34640141-34640142	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs66815923	chr11:34640181-34640182	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs200965445	chr11:34640184-34640185	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs55721438	chr11:34640188-34640189	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs199797908	chr11:34640191-34640192	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs371259469	chr11:34640192-34640193	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs3834927	chr11:34640206-34640207	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs189501183	chr11:34640270-34640271	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs16925885	chr11:34640278-34640279	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs11032786	chr11:34640304-34640305	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs577917542	chr11:34640308-34640309	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs574702802	chr11:34640323-34640324	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs2421644	chr11:34640335-34640336	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs563561572	chr11:34640373-34640374	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532019711	chr11:34640381-34640382	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573857998	chr11:34640408-34640409	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375970695	chr11:34640425-34640426	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2213 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34608400-34643600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:34625400-34642800	Weak transcription	Gastric	stomach
3	chr11:34634000-34643200	Weak transcription	Lung	lung
4	chr11:34635000-34643400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:34635200-34642000	Weak transcription	Esophagus	oesophagus
6	chr11:34636200-34639600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:34636200-34641000	Weak transcription	Fetal Intestine Small	intestine
8	chr11:34636200-34644000	Enhancers	K562	blood
9	chr11:34636400-34641800	Weak transcription	Fetal Intestine Large	intestine
10	chr11:34636600-34640800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:34636600-34641400	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr11:34636800-34640800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr11:34637200-34641600	Weak transcription	Primary B cells from peripheral blood	blood
14	chr11:34637400-34641000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr11:34637400-34641200	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr11:34637600-34639800	Enhancers	Right Ventricle	heart
17	chr11:34637600-34640400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr11:34637800-34642000	Enhancers	Stomach Mucosa	stomach
19	chr11:34637800-34649200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr11:34638000-34639800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr11:34638400-34639200	Enhancers	Duodenum Mucosa	Duodenum
22	chr11:34638600-34639200	Enhancers	Right Atrium	heart
23	chr11:34638600-34640000	Enhancers	Pancreas	Pancrea
24	chr11:34639000-34641200	Enhancers	Fetal Heart	heart
25	chr11:34639000-34641400	Weak transcription	NHEK	skin
26	chr11:34639000-34641600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:34639200-34639600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr11:34639200-34639600	Weak transcription	Right Atrium	heart
29	chr11:34639600-34639800	Enhancers	Duodenum Mucosa	Duodenum
30	chr11:34639600-34639800	Enhancers	Left Ventricle	heart
31	chr11:34639600-34639800	Enhancers	Right Atrium	heart
32	chr11:34639600-34640000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:34639800-34641000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr11:34639800-34653800	Weak transcription	Right Atrium	heart
35	chr11:34640000-34640400	Weak transcription	Pancreas	Pancrea
36	chr11:34640000-34643200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:34640400-34641800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr11:34640400-34642000	Enhancers	Pancreas	Pancrea
39	chr11:34640400-34643200	Enhancers	Placenta	Placenta
40	chr11:34640800-34641200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:34640800-34641800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:34641000-34641400	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr11:34641000-34641600	Enhancers	Duodenum Mucosa	Duodenum
44	chr11:34641000-34642000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr11:34641000-34642800	Enhancers	Fetal Intestine Small	intestine
46	chr11:34641000-34643400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr11:34641200-34642400	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr11:34641400-34641800	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr11:34641400-34642000	Enhancers	NHEK	skin
50	chr11:34641400-34642200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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