Variant report

Variant	esv3339891
Chromosome Location	chr11:66088976-66093674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:62)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:66091637-66091868	GM12878	blood:	n/a	chr11:66091759-66091769 chr11:66091758-66091769
2	BHLHE40	chr11:66092702-66092984	K562	blood:	n/a	n/a
3	CHD2	chr11:66092152-66092545	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr11:66089800-66089950	GM12865	blood:	n/a	n/a
5	CTCF	chr11:66089840-66089990	AoAF	blood vessel:	n/a	n/a
6	CTCF	chr11:66092827-66092907	GM19239	blood:	n/a	n/a
7	CTCF	chr11:66089845-66090084	HepG2	liver:	n/a	n/a
8	CTCF	chr11:66089860-66090010	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr11:66089840-66089990	NHLF	lung:	n/a	n/a
10	CTCF	chr11:66089860-66090010	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr11:66089820-66089970	WI-38	lung:	n/a	n/a
12	CTCF	chr11:66089820-66089970	GM12872	blood:	n/a	n/a
13	CTCF	chr11:66089863-66089945	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr11:66089920-66090070	AG10803	skin:	n/a	n/a
15	CTCF	chr11:66089817-66090057	K562	blood:	n/a	n/a
16	CTCF	chr11:66089900-66090050	MCF-7	breast:	n/a	n/a
17	CTCF	chr11:66089820-66089970	AG04449	skin:	n/a	n/a
18	CTCF	chr11:66089840-66089990	GM12872	blood:	n/a	n/a
19	CTCF	chr11:66089883-66090014	Medullo	brain:	n/a	n/a
20	CTCF	chr11:66089940-66090090	AG04450	lung:	n/a	n/a
21	CTCF	chr11:66089960-66090110	HVMF	connective:	n/a	n/a
22	CTCF	chr11:66089879-66089973	Fibrobl	skin:	n/a	n/a
23	CTCF	chr11:66089820-66089970	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr11:66089960-66090110	NB4	blood:	n/a	n/a
25	CTCF	chr11:66089934-66089955	Lung_OC	lung:	n/a	n/a
26	CTCF	chr11:66089800-66089950	GM12875	blood:	n/a	n/a
27	CTCF	chr11:66089880-66090030	HPF	lung:	n/a	n/a
28	CTCF	chr11:66089860-66090010	AG04449	skin:	n/a	n/a
29	CTCF	chr11:66089840-66089990	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr11:66089840-66089990	GM12873	blood:	n/a	n/a
31	CTCF	chr11:66089840-66089990	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr11:66089705-66090108	K562	blood:	n/a	n/a
33	CTCF	chr11:66089820-66089970	HMF	breast:	n/a	n/a
34	CTCF	chr11:66089920-66090070	AG09309	skin:	n/a	n/a
35	CTCF	chr11:66089915-66089941	GM12892	blood:	n/a	n/a
36	CTCF	chr11:66089820-66089970	GM12864	blood:	n/a	n/a
37	CTCF	chr11:66090080-66090230	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr11:66089763-66090134	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr11:66089869-66089967	MCF-7	breast:	n/a	n/a
40	CTCF	chr11:66089900-66090050	AG09319	gingival:	n/a	n/a
41	CTCF	chr11:66089655-66090053	K562	blood:	n/a	n/a
42	CTCF	chr11:66089840-66089990	HFF	foreskin:	n/a	n/a
43	CTCF	chr11:66089810-66090031	IMR90	lung:	n/a	n/a
44	CTCF	chr11:66089840-66089990	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr11:66089800-66089950	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr11:66089900-66090050	GM12866	blood:	n/a	n/a
47	CTCF	chr11:66089880-66090030	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr11:66089900-66090050	BE2_C	brain:	n/a	n/a
49	CTCF	chr11:66089740-66089890	HCM	heart:	n/a	n/a
50	CTCF	chr11:66089744-66090129	H1-hESC	embryonic stem cell:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:66092918-66092968	SK-N-SH_RA	brain:	n/a
2	chr11:66092918-66092968	SK-N-SH_RA	brain:	n/a
3	chr11:66092918-66092968	SAEC	small airway:	n/a
4	chr11:66092918-66092968	Hepatocyte	liver:	n/a
5	chr11:66092918-66092968	HCF	heart:	n/a
6	chr11:66092918-66092968	AoSMC	blood vessel:	n/a
7	chr11:66092918-66092968	K562	blood:	n/a
8	chr11:66092918-66092968	AG09309	skin:	n/a
9	chr11:66092918-66092968	PFSK-1	brain:	n/a
10	chr11:66092918-66092968	HCM	heart:	n/a
11	chr11:66092918-66092968	LNCaP	prostate:	n/a
12	chr11:66092918-66092968	AG09319	gingival:	n/a
13	chr11:66092918-66092968	Jurkat	blood:	n/a
14	chr11:66092918-66092968	PrEC	prostate:	n/a
15	chr11:66092918-66092968	MCF-7	breast:	n/a
16	chr11:66092918-66092968	SKMC	muscle:	n/a
17	chr11:66092918-66092968	GM19239	blood:	n/a
18	chr11:66092918-66092968	SK-N-MC	brain:	n/a
19	chr11:66092918-66092968	HCPEpiC	choroid plexus:	n/a
20	chr11:66092918-66092968	ovcar-3	ovarian:	n/a
21	chr11:66092918-66092968	PANC-1	pancreas:	n/a
22	chr11:66092918-66092968	AG04449	skin:	fetal
23	chr11:66092918-66092968	HUVEC	blood vessel:	n/a
24	chr11:66092918-66092968	NT2-D1	testis:	n/a
25	chr11:66092918-66092968	Caco-2	colon:	n/a
26	chr11:66092918-66092968	GM06990	blood:	n/a
27	chr11:66092918-66092968	SK-N-SH	brain:	n/a
28	chr11:66092918-66092968	AG10803	skin:	n/a
29	chr11:66092918-66092968	IMR90	lung:	fetal
30	chr11:66092918-66092968	HRE	kidney:	n/a
31	chr11:66092918-66092968	ECC-1	luminal epithelium:	n/a
32	chr11:66092918-66092968	GM12892	blood:	n/a
33	chr11:66092918-66092968	HL-60	blood:	n/a
34	chr11:66092918-66092968	HRPEpiC	eye:	n/a
35	chr11:66092918-66092968	BJ	skin:	n/a
36	chr11:66092918-66092968	NHBE	bronchial:	n/a
37	chr11:66092918-66092968	BE2_C	brain:	n/a
38	chr11:66092918-66092968	HCT-116	colon:	n/a
39	chr11:66092918-66092968	AG04450	lung:	fetal
40	chr11:66092918-66092968	ProgFib	skin:	n/a
41	chr11:66092918-66092968	HEK293	kidney:	embryo
42	chr11:66092918-66092968	NB4	blood:	n/a
43	chr11:66092918-66092968	T-47D	breast:	n/a
44	chr11:66092918-66092968	HRCEpiC	kidney:	n/a
45	chr11:66092918-66092968	H1-hESC	embryonic stem cell:	embryo
46	chr11:66092918-66092968	GM12891	blood:	n/a
47	chr11:66092918-66092968	RPTEC	kidney:	n/a
48	chr11:66092918-66092968	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:66092918-66092968	MCF10A-Er-Src	breast:	n/a
50	chr11:66092918-66092968	HAEpiC	amniotic membrane:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66055517..66058444-chr11:66093639..66096253,2	K562	blood:
2	chr11:66083687..66088090-chr11:66090957..66094133,5	K562	blood:
3	chr11:66089326..66092230-chr11:66092519..66097068,6	K562	blood:
4	chr11:66079025..66079721-chr11:66089471..66090121,2	K562	blood:
5	chr11:65990260..65990801-chr11:66089476..66090019,2	K562	blood:
6	chr11:66089278..66092280-chr11:66092886..66097368,7	K562	blood:
7	chr11:66091883..66093491-chr11:66094338..66095923,2	MCF-7	breast:
8	chr11:66052087..66053610-chr11:66091121..66094110,2	MCF-7	breast:
9	chr11:66076960..66082217-chr11:66092441..66098354,9	K562	blood:
10	chr11:66054084..66058324-chr11:66093357..66097768,5	K562	blood:
11	chr11:66055159..66056762-chr11:66090994..66093285,2	K562	blood:
12	chr11:66089278..66092280-chr11:66092886..66097368,7	K562	blood:
13	chr11:66044842..66048035-chr11:66092705..66097892,5	K562	blood:
14	chr11:66089326..66092230-chr11:66092519..66097068,6	K562	blood:
15	chr11:66084338..66086031-chr11:66092947..66095134,2	K562	blood:
16	chr11:66092468..66094191-chr11:66107437..66109172,2	K562	blood:
17	chr11:66092528..66094950-chr11:66110471..66113392,3	K562	blood:
18	chr11:66080788..66082813-chr11:66088055..66089641,2	K562	blood:
19	chr11:66054081..66055900-chr11:66092894..66095581,2	MCF-7	breast:
20	chr11:66054004..66059089-chr11:66088488..66094920,9	MCF-7	breast:
21	chr11:66079702..66081226-chr11:66092137..66094285,2	MCF-7	breast:
22	chr11:66079319..66080867-chr11:66093163..66095729,2	MCF-7	breast:
23	chr11:66090714..66092332-chr20:48939411..48940911,2	MCF-7	breast:

No data

Variant related genes	Relation type
CD248	TF binding region
CD248	CpG island
ENSG00000174744	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000254452	chromatin interactions
ENSG00000174871	chromatin interactions
ENSG00000174807	chromatin interactions
ENSG00000245156	chromatin interactions
ENSG00000254458	chromatin interactions

Extended variants
information (count: 156 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:156 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71036284	chr11:66088978-66088979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs200486393	chr11:66088980-66088981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201781225	chr11:66088981-66088982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143610693	chr11:66088989-66088990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531454176	chr11:66089000-66089001	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs190218203	chr11:66089082-66089083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549120722	chr11:66089097-66089098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs150738684	chr11:66089125-66089126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531526544	chr11:66089129-66089130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs78472894	chr11:66089144-66089145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs137953638	chr11:66089162-66089163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533775859	chr11:66089309-66089310	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553446315	chr11:66089324-66089325	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370973918	chr11:66089389-66089390	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536204398	chr11:66089447-66089448	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549700421	chr11:66089476-66089477	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547061895	chr11:66089497-66089498	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373054529	chr11:66089510-66089511	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576016972	chr11:66089532-66089533	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376501201	chr11:66089566-66089567	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558529692	chr11:66089567-66089568	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs578216228	chr11:66089738-66089739	Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs36034820	chr11:66089761-66089762	Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs191953351	chr11:66089766-66089767	Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540834649	chr11:66089768-66089769	Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560532704	chr11:66089774-66089775	Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574068232	chr11:66089788-66089789	Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184605918	chr11:66089805-66089806	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs562715594	chr11:66089806-66089807	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531763045	chr11:66089818-66089819	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112317593	chr11:66089845-66089846	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564880527	chr11:66089870-66089871	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs527435827	chr11:66089883-66089884	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs373916031	chr11:66089891-66089892	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188576372	chr11:66089924-66089925	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567319763	chr11:66089935-66089936	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535986264	chr11:66089963-66089964	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549883228	chr11:66089965-66089966	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs10219183	chr11:66090032-66090033	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs538675610	chr11:66090056-66090057	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565697633	chr11:66090138-66090139	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558448281	chr11:66090141-66090142	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370342499	chr11:66090179-66090180	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534358391	chr11:66090228-66090229	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1190621	chr11:66090307-66090308	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs574202503	chr11:66090331-66090332	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549511327	chr11:66090335-66090336	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566052905	chr11:66090385-66090386	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs140136089	chr11:66090452-66090453	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs1190622	chr11:66090468-66090469	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66084600-66103200	Weak transcription	Small Intestine	intestine
2	chr11:66085800-66089200	Weak transcription	Right Atrium	heart
3	chr11:66086000-66089000	Weak transcription	Fetal Brain Female	brain
4	chr11:66086200-66089200	Weak transcription	Colon Smooth Muscle	Colon
5	chr11:66086200-66090600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:66086200-66091800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:66086200-66092000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr11:66086200-66095400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr11:66086400-66092200	Weak transcription	Lung	lung
10	chr11:66086400-66092400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr11:66086400-66092600	Weak transcription	Colonic Mucosa	Colon
12	chr11:66086600-66090000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:66086600-66091800	Weak transcription	HSMM	muscle
14	chr11:66086600-66092600	Weak transcription	Right Ventricle	heart
15	chr11:66086600-66093600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:66086600-66095000	Weak transcription	Duodenum Mucosa	Duodenum
17	chr11:66086800-66089000	Weak transcription	NHDF-Ad	bronchial
18	chr11:66086800-66089200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr11:66086800-66089200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr11:66086800-66089200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr11:66086800-66089200	Weak transcription	NHLF	lung
22	chr11:66086800-66089200	Weak transcription	Osteobl	bone
23	chr11:66086800-66089400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr11:66086800-66090000	Weak transcription	Fetal Stomach	stomach
25	chr11:66086800-66091000	Weak transcription	Spleen	Spleen
26	chr11:66086800-66091600	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr11:66086800-66091800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr11:66086800-66091800	Weak transcription	Fetal Lung	lung
29	chr11:66086800-66091800	Weak transcription	Hela-S3	cervix
30	chr11:66086800-66092200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr11:66086800-66092400	Weak transcription	Fetal Intestine Large	intestine
32	chr11:66086800-66093200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr11:66086800-66093600	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr11:66086800-66093600	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr11:66087000-66089000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:66087000-66089000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:66087000-66089000	Weak transcription	Adipose Nuclei	Adipose
38	chr11:66087000-66089000	Weak transcription	Fetal Muscle Leg	muscle
39	chr11:66087000-66089400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:66087000-66090400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr11:66087000-66091600	Weak transcription	Esophagus	oesophagus
42	chr11:66087200-66089000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr11:66087200-66089000	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr11:66087200-66089000	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr11:66087200-66089000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr11:66087200-66089000	Weak transcription	Fetal Thymus	thymus
47	chr11:66087200-66090000	Weak transcription	Thymus	Thymus
48	chr11:66087200-66091800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr11:66087200-66093400	Weak transcription	Fetal Intestine Small	intestine
50	chr11:66087600-66089000	Weak transcription	Primary T cells fromperipheralblood	blood

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