Variant report

Variant	esv1807609
Chromosome Location	chr11:45915859-45940195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1470)
CpG islands
(count:2200)
Chromatin interactive
region (count:39)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45921040-45921116	K562	blood:	n/a	n/a
2	ARID3A	chr11:45939422-45939874	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:45939775-45940079	K562	blood:	n/a	n/a
4	ARID3A	chr11:45921441-45921541	K562	blood:	n/a	n/a
5	ATF1	chr11:45921213-45921587	K562	blood:	n/a	n/a
6	ATF2	chr11:45939137-45939942	GM12878	blood:	n/a	n/a
7	ATF2	chr11:45939276-45939783	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr11:45921305-45921598	GM12878	blood:	n/a	n/a
9	ATF2	chr11:45939175-45939642	GM12878	blood:	n/a	n/a
10	ATF2	chr11:45939644-45939943	GM12878	blood:	n/a	n/a
11	ATF2	chr11:45920836-45921630	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:45920751-45921633	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr11:45921230-45921547	K562	blood:	n/a	chr11:45921401-45921414
14	ATF3	chr11:45921288-45921589	A549	lung:	n/a	chr11:45921401-45921414
15	ATF3	chr11:45921322-45921627	A549	lung:	n/a	chr11:45921401-45921414
16	ATF3	chr11:45939190-45939620	A549	lung:	n/a	chr11:45939582-45939590
17	ATF3	chr11:45921125-45921680	K562	blood:	n/a	chr11:45921401-45921414
18	ATF3	chr11:45939259-45939963	A549	lung:	n/a	chr11:45939582-45939590
19	ATF3	chr11:45921190-45921495	H1-hESC	embryonic stem cell:	n/a	chr11:45921401-45921414
20	ATF3	chr11:45921233-45921578	H1-hESC	embryonic stem cell:	n/a	chr11:45921401-45921414
21	BCL3	chr11:45939029-45939668	A549	lung:	n/a	n/a
22	BCL3	chr11:45929347-45929593	GM12878	blood:	n/a	n/a
23	BCL3	chr11:45939139-45940098	A549	lung:	n/a	n/a
24	BCLAF1	chr11:45939160-45940001	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:45918145-45918150	K562	blood:	n/a	n/a
26	BHLHE40	chr11:45938963-45940020	K562	blood:	n/a	n/a
27	BHLHE40	chr11:45921330-45921680	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:45921011-45921713	K562	blood:	n/a	n/a
29	BHLHE40	chr11:45926202-45926402	K562	blood:	n/a	n/a
30	BHLHE40	chr11:45921277-45921714	HepG2	liver:	n/a	n/a
31	BHLHE40	chr11:45938839-45939950	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:45921317-45921651	A549	lung:	n/a	n/a
33	BHLHE40	chr11:45934755-45934884	GM12878	blood:	n/a	n/a
34	BRCA1	chr11:45939286-45939620	HepG2	liver:	n/a	n/a
35	BRCA1	chr11:45921421-45921517	HepG2	liver:	n/a	n/a
36	BRCA1	chr11:45921019-45921643	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr11:45939990-45940329	HepG2	liver:	n/a	n/a
38	BRCA1	chr11:45939254-45940668	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr11:45921456-45921558	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr11:45921343-45921624	K562	blood:	n/a	n/a
41	CBX3	chr11:45920816-45921195	K562	blood:	n/a	n/a
42	CBX3	chr11:45939214-45939929	K562	blood:	n/a	n/a
43	CBX3	chr11:45925969-45926532	K562	blood:	n/a	n/a
44	CCNT2	chr11:45938994-45940528	K562	blood:	n/a	n/a
45	CCNT2	chr11:45921094-45921773	K562	blood:	n/a	chr11:45921190-45921199 chr11:45921299-45921308
46	CCNT2	chr11:45926160-45926402	K562	blood:	n/a	n/a
47	CCNT2	chr11:45929515-45929778	K562	blood:	n/a	n/a
48	CEBPB	chr11:45938966-45940565	Hela-S3	cervix:	n/a	chr11:45940408-45940416
49	CEBPB	chr11:45939323-45939515	GM12878	blood:	n/a	n/a
50	CEBPB	chr11:45939176-45939858	MCF-7	breast:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45929519-45929569	RPTEC	kidney:	n/a
2	chr11:45939543-45939593	HepG2	liver:	n/a
3	chr11:45940058-45940108	SK-N-SH	brain:	n/a
4	chr11:45921557-45921607	NB4	blood:	n/a
5	chr11:45929519-45929569	RPTEC	kidney:	n/a
6	chr11:45939543-45939593	HepG2	liver:	n/a
7	chr11:45940058-45940108	SK-N-SH	brain:	n/a
8	chr11:45921557-45921607	NB4	blood:	n/a
9	chr11:45915823-45915873	GM06990	blood:	n/a
10	chr11:45924507-45924557	H1-hESC	embryonic stem cell:	embryo
11	chr11:45938923-45938973	PFSK-1	brain:	n/a
12	chr11:45924191-45924241	HMEC	breast:	n/a
13	chr11:45921134-45921184	A549	lung:	n/a
14	chr11:45937020-45937070	ECC-1	luminal epithelium:	n/a
15	chr11:45928841-45928891	HEK293	kidney:	embryo
16	chr11:45923319-45923369	AG09309	skin:	n/a
17	chr11:45923319-45923369	HIPEpiC	eye:	n/a
18	chr11:45939723-45939773	AG09319	gingival:	n/a
19	chr11:45937020-45937070	HIPEpiC	eye:	n/a
20	chr11:45922184-45922234	HL-60	blood:	n/a
21	chr11:45928937-45928987	Jurkat	blood:	n/a
22	chr11:45929541-45929591	AG09319	gingival:	n/a
23	chr11:45924507-45924557	GM12878	blood:	n/a
24	chr11:45922184-45922234	PFSK-1	brain:	n/a
25	chr11:45928841-45928891	NT2-D1	testis:	n/a
26	chr11:45928898-45928948	Hela-S3	cervix:	n/a
27	chr11:45928937-45928987	SK-N-SH_RA	brain:	n/a
28	chr11:45921388-45921438	AG09309	skin:	n/a
29	chr11:45928370-45928420	ovcar-3	ovarian:	n/a
30	chr11:45939458-45939508	Hepatocyte	liver:	n/a
31	chr11:45926170-45926220	SK-N-SH	brain:	n/a
32	chr11:45924624-45924674	H1-hESC	embryonic stem cell:	embryo
33	chr11:45924434-45924484	HEK293	kidney:	embryo
34	chr11:45937020-45937070	GM12891	blood:	n/a
35	chr11:45921134-45921184	PrEC	prostate:	n/a
36	chr11:45918197-45918247	AG09319	gingival:	n/a
37	chr11:45931715-45931765	Hela-S3	cervix:	n/a
38	chr11:45915823-45915873	HL-60	blood:	n/a
39	chr11:45937020-45937070	H1-hESC	embryonic stem cell:	embryo
40	chr11:45924434-45924484	LNCaP	prostate:	n/a
41	chr11:45918197-45918247	IMR90	lung:	fetal
42	chr11:45929519-45929569	NH-A	brain:	n/a
43	chr11:45923319-45923369	BJ	skin:	n/a
44	chr11:45939723-45939773	HNPCEpiC	eye:	n/a
45	chr11:45928854-45928904	MCF10A-Er-Src	breast:	n/a
46	chr11:45940039-45940089	RPTEC	kidney:	n/a
47	chr11:45939543-45939593	LNCaP	prostate:	n/a
48	chr11:45928805-45928855	AG09309	skin:	n/a
49	chr11:45923319-45923369	HCT-116	colon:	n/a
50	chr11:45918197-45918247	Caco-2	colon:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45937934..45940310-chr17:56708373..56710113,2	MCF-7	breast:
2	chr11:45867027..45870378-chr11:45924400..45927960,4	K562	blood:
3	chr11:45898608..45900937-chr11:45921279..45922958,2	MCF-7	breast:
4	chr11:45904999..45908778-chr11:45926674..45929138,4	MCF-7	breast:
5	chr1:198127987..198130106-chr11:45920994..45922551,2	MCF-7	breast:
6	chr11:45915026..45916740-chr11:45938253..45939770,2	MCF-7	breast:
7	chr11:45939411..45941074-chr11:46142423..46143961,2	MCF-7	breast:
8	chr11:45939300..45941780-chr11:46259462..46260979,2	K562	blood:
9	chr11:45907546..45909448-chr11:45934193..45936568,2	MCF-7	breast:
10	chr11:45925111..45927750-chr11:45943585..45946023,2	K562	blood:
11	chr11:45937002..45939512-chr11:45985947..45988260,2	MCF-7	breast:
12	chr11:45868894..45870500-chr11:45937119..45938981,2	K562	blood:
13	chr11:45911137..45915484-chr11:45918170..45921125,3	MCF-7	breast:
14	chr11:45825326..45828118-chr11:45934084..45936499,2	K562	blood:
15	chr11:45868914..45870628-chr11:45938803..45941080,3	MCF-7	breast:
16	chr11:45826170..45827093-chr11:45939119..45939790,2	NB4	blood:
17	chr11:45880127..45882891-chr11:45927875..45929936,2	K562	blood:
18	chr11:45918493..45920124-chr11:45923045..45924721,2	MCF-7	breast:
19	chr11:45906755..45908288-chr11:45937921..45939853,2	MCF-7	breast:
20	chr11:45920093..45922965-chr11:46143378..46145105,2	K562	blood:
21	chr11:45868921..45870450-chr11:45919310..45922192,2	K562	blood:
22	chr11:45919268..45921220-chr11:46000248..46001826,2	MCF-7	breast:
23	chr11:45889972..45892712-chr11:45915582..45918547,2	K562	blood:
24	chr11:45918756..45920830-chr11:46147616..46150404,2	K562	blood:
25	chr11:45897697..45900039-chr11:45919922..45922515,2	K562	blood:
26	chr11:45921817..45923409-chr11:45925394..45927956,2	K562	blood:
27	chr11:45904574..45907083-chr11:45920026..45922634,2	MCF-7	breast:
28	chr11:45920062..45922983-chr11:45935210..45941830,10	K562	blood:
29	chr11:45824638..45826704-chr11:45938955..45940480,2	MCF-7	breast:
30	chr11:45911458..45913124-chr11:45919086..45920633,2	MCF-7	breast:
31	chr11:45928634..45930948-chr12:122237013..122238884,2	MCF-7	breast:
32	chr11:45924750..45927395-chr11:45942360..45945085,3	K562	blood:
33	chr11:45897449..45899197-chr11:45919922..45922462,2	K562	blood:
34	chr11:45915081..45916599-chr11:46391904..46393436,2	K562	blood:
35	chr11:45938612..45941036-chr11:46368136..46369719,2	K562	blood:
36	chr11:45904585..45907305-chr11:45939491..45941669,2	K562	blood:
37	chr11:45921817..45923409-chr11:45925394..45927956,2	K562	blood:
38	chr11:45939172..45939872-chr2:113032560..113033279,2	HCT-116	colon:
39	chr11:45890873..45893526-chr11:45930539..45932384,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf94-1	chr11:45927960-45928012	ENSG00000255498.1
2	lnc-C11orf94-1	chr11:45927492-45927847	ENSG00000255498.1
3	lnc-C11orf94-2	chr11:45926604-45926823	expReg_chr11_3331_-

No data

Variant related genes	Relation type
MAPK8IP1	TF binding region
ENSG00000255498	TF binding region
GYLTL1B	TF binding region
PEX16	TF binding region
C11orf94	TF binding region
MAPK8IP1	CpG island
ENSG00000255498	CpG island
GYLTL1B	CpG island
PEX16	CpG island
C11orf94	CpG island
ENSG00000165905	chromatin interactions
ENSG00000135365	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000181830	chromatin interactions
ENSG00000121653	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000254639	chromatin interactions
ENSG00000188177	chromatin interactions
ENSG00000121671	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 1129 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369941609	chr11:45915941-45915942	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs550271586	chr11:45915943-45915944	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs143011859	chr11:45915947-45915948	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs548625644	chr11:45915989-45915990	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs189803213	chr11:45916006-45916007	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs534133444	chr11:45916017-45916018	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs78697786	chr11:45916021-45916022	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs148728239	chr11:45916023-45916024	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs565407110	chr11:45916032-45916033	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs142271868	chr11:45916087-45916088	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs529731005	chr11:45916112-45916113	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs183567732	chr11:45916167-45916168	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs546720652	chr11:45916222-45916223	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs372453871	chr11:45916239-45916240	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs554603728	chr11:45916245-45916246	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs151282909	chr11:45916286-45916287	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs35563946	chr11:45916302-45916303	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs539982212	chr11:45916319-45916320	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs559703923	chr11:45916343-45916344	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs139939559	chr11:45916345-45916346	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs546053104	chr11:45916368-45916369	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs562652512	chr11:45916385-45916386	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs35389927	chr11:45916436-45916437	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs145256794	chr11:45916440-45916441	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs568306602	chr11:45916500-45916501	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs375192424	chr11:45916514-45916515	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs147602520	chr11:45916567-45916568	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs118033599	chr11:45916586-45916587	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs539470491	chr11:45916624-45916625	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs186294304	chr11:45916632-45916633	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369836939	chr11:45916639-45916640	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs373035668	chr11:45916641-45916642	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs570257147	chr11:45916656-45916657	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs190683563	chr11:45916664-45916665	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs150176995	chr11:45916736-45916737	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs114270191	chr11:45916747-45916748	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs192153982	chr11:45916756-45916757	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs7114162	chr11:45916781-45916782	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145619626	chr11:45916793-45916794	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs73468356	chr11:45916809-45916810	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs148831112	chr11:45916852-45916853	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545488044	chr11:45916937-45916938	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562753120	chr11:45916941-45916942	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs531503085	chr11:45916958-45916959	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143438037	chr11:45916997-45916998	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561849379	chr11:45916998-45916999	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527509897	chr11:45917100-45917101	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182923418	chr11:45917113-45917114	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12281986	chr11:45917166-45917167	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376278110	chr11:45917186-45917187	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45907600-45920800	Weak transcription	Right Atrium	heart
2	chr11:45908400-45916200	Weak transcription	Brain Anterior Caudate	brain
3	chr11:45908600-45917600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr11:45910000-45917400	Weak transcription	Fetal Brain Female	brain
5	chr11:45912800-45916200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr11:45912800-45916400	Weak transcription	Fetal Brain Male	brain
7	chr11:45913400-45916200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr11:45913400-45916200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr11:45914000-45916200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:45914000-45920400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:45914600-45916400	Weak transcription	Brain Germinal Matrix	brain
12	chr11:45915000-45916000	Weak transcription	Brain Angular Gyrus	brain
13	chr11:45915000-45916000	Weak transcription	Brain Hippocampus Middle	brain
14	chr11:45915000-45917600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:45915200-45917200	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr11:45915200-45917400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:45915200-45917400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr11:45915200-45917600	Weak transcription	Brain Substantia Nigra	brain
19	chr11:45915200-45918000	Weak transcription	Liver	Liver
20	chr11:45915400-45916000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:45915400-45917400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:45915400-45917600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr11:45915400-45917600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:45915400-45917600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr11:45915400-45917600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr11:45915600-45917600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr11:45915600-45917600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr11:45915800-45917600	Enhancers	Fetal Muscle Leg	muscle
29	chr11:45916000-45916400	Enhancers	Brain Angular Gyrus	brain
30	chr11:45916000-45916600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr11:45916000-45916600	Enhancers	Fetal Muscle Trunk	muscle
32	chr11:45916000-45917800	Enhancers	Brain Hippocampus Middle	brain
33	chr11:45916200-45916600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr11:45916200-45916800	Enhancers	Brain Anterior Caudate	brain
35	chr11:45916200-45917400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:45916200-45918000	Enhancers	Brain Cingulate Gyrus	brain
37	chr11:45916200-45918000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr11:45916400-45916600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
39	chr11:45916400-45916600	Genic enhancers	Brain Germinal Matrix	brain
40	chr11:45916400-45917400	Weak transcription	Brain Angular Gyrus	brain
41	chr11:45916400-45918600	Enhancers	Fetal Brain Male	brain
42	chr11:45916600-45917400	Weak transcription	Brain Germinal Matrix	brain
43	chr11:45916600-45917600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr11:45916600-45917600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr11:45916600-45920200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:45916800-45917400	Weak transcription	Brain Anterior Caudate	brain
47	chr11:45917200-45919400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr11:45917400-45917600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr11:45917400-45917600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:45917400-45917600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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