Variant report

Variant	esv2756165
Chromosome Location	chr11:34914137-34942836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:854)
CpG islands
(count:1404)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34937595-34937654	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34938026-34938300	HepG2	liver:	n/a	n/a
3	ATF1	chr11:34938972-34939307	K562	blood:	n/a	n/a
4	ATF2	chr11:34937331-34938461	GM12878	blood:	n/a	n/a
5	ATF3	chr11:34937943-34938123	K562	blood:	n/a	chr11:34938069-34938078
6	ATF3	chr11:34929799-34930110	K562	blood:	n/a	n/a
7	BACH1	chr11:34929700-34929782	K562	blood:	n/a	n/a
8	BACH1	chr11:34929538-34930075	H1-hESC	embryonic stem cell:	n/a	chr11:34929943-34929957
9	BATF	chr11:34929853-34930086	GM12878	blood:	n/a	chr11:34929946-34929957
10	BCL3	chr11:34937631-34938491	A549	lung:	n/a	chr11:34937662-34937675 chr11:34937706-34937719 chr11:34938167-34938180 chr11:34938070-34938079
11	BCLAF1	chr11:34937505-34938414	GM12878	blood:	n/a	chr11:34937662-34937675 chr11:34937706-34937719 chr11:34938167-34938180 chr11:34938070-34938079
12	BHLHE40	chr11:34937154-34938341	K562	blood:	n/a	chr11:34937703-34937719
13	BHLHE40	chr11:34937479-34938347	HepG2	liver:	n/a	chr11:34937703-34937719
14	BHLHE40	chr11:34937544-34938374	GM12878	blood:	n/a	chr11:34937703-34937719
15	BRCA1	chr11:34938188-34938367	HepG2	liver:	n/a	n/a
16	BRCA1	chr11:34937408-34938225	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr11:34920613-34920873	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr11:34937774-34937854	HepG2	liver:	n/a	n/a
19	BRCA1	chr11:34938700-34938727	GM12878	blood:	n/a	n/a
20	BRCA1	chr11:34938224-34938340	GM12878	blood:	n/a	n/a
21	CBX3	chr11:34937599-34938382	K562	blood:	n/a	n/a
22	CCNT2	chr11:34937180-34938821	K562	blood:	n/a	chr11:34937763-34937772 chr11:34938069-34938078
23	CEBPB	chr11:34928015-34928209	HepG2	liver:	n/a	chr11:34928076-34928087
24	CEBPB	chr11:34931435-34931781	HepG2	liver:	n/a	chr11:34931690-34931701
25	CEBPB	chr11:34931589-34931846	K562	blood:	n/a	chr11:34931690-34931701
26	CEBPB	chr11:34921467-34921725	K562	blood:	n/a	chr11:34921564-34921575
27	CEBPB	chr11:34931492-34931921	MCF-7	breast:	n/a	chr11:34931690-34931701
28	CEBPB	chr11:34928016-34928212	IMR90	lung:	n/a	chr11:34928076-34928087
29	CEBPB	chr11:34938078-34938226	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:34927973-34928162	A549	lung:	n/a	chr11:34928076-34928087
31	CEBPB	chr11:34918324-34918454	HepG2	liver:	n/a	chr11:34918349-34918360
32	CEBPB	chr11:34931538-34931864	Hela-S3	cervix:	n/a	chr11:34931690-34931701
33	CEBPB	chr11:34924848-34924975	HepG2	liver:	n/a	n/a
34	CEBPB	chr11:34931527-34931869	IMR90	lung:	n/a	chr11:34931690-34931701
35	CEBPB	chr11:34921547-34921595	HepG2	liver:	n/a	chr11:34921564-34921575
36	CEBPB	chr11:34928039-34928228	K562	blood:	n/a	chr11:34928076-34928087
37	CEBPB	chr11:34938119-34938278	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:34931572-34931817	HepG2	liver:	n/a	chr11:34931690-34931701
39	CEBPB	chr11:34921297-34921703	A549	lung:	n/a	chr11:34921564-34921575
40	CEBPB	chr11:34937699-34937923	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:34931509-34931891	HepG2	liver:	n/a	chr11:34931690-34931701
42	CEBPB	chr11:34931512-34931857	K562	blood:	n/a	chr11:34931690-34931701
43	CEBPB	chr11:34931522-34931867	A549	lung:	n/a	chr11:34931690-34931701
44	CEBPB	chr11:34931502-34931890	HepG2	liver:	n/a	chr11:34931690-34931701
45	CEBPD	chr11:34937404-34938005	HepG2	liver:	n/a	n/a
46	CEBPD	chr11:34938015-34938390	HepG2	liver:	n/a	n/a
47	CEBPD	chr11:34937568-34938487	K562	blood:	n/a	n/a
48	CEBPD	chr11:34931572-34931809	HepG2	liver:	n/a	n/a
49	CEBPD	chr11:34938061-34938371	HepG2	liver:	n/a	n/a
50	CEBPD	chr11:34937661-34938385	K562	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34937559-34937609	Jurkat	blood:	n/a
2	chr11:34937559-34937609	Jurkat	blood:	n/a
3	chr11:34934680-34934730	Caco-2	colon:	n/a
4	chr11:34937484-34937534	HRE	kidney:	n/a
5	chr11:34937778-34937828	HepG2	liver:	n/a
6	chr11:34937341-34937391	AG09319	gingival:	n/a
7	chr11:34937933-34937983	K562	blood:	n/a
8	chr11:34937992-34938042	AG10803	skin:	n/a
9	chr11:34938234-34938284	HRCEpiC	kidney:	n/a
10	chr11:34937958-34938008	HEK293	kidney:	embryo
11	chr11:34937484-34937534	AG04450	lung:	fetal
12	chr11:34936781-34936831	MCF10A-Er-Src	breast:	n/a
13	chr11:34937933-34937983	PANC-1	pancreas:	n/a
14	chr11:34938348-34938398	HAEpiC	amniotic membrane:	n/a
15	chr11:34940794-34940844	BJ	skin:	n/a
16	chr11:34937484-34937534	Hepatocyte	liver:	n/a
17	chr11:34937564-34937614	SK-N-MC	brain:	n/a
18	chr11:34934680-34934730	SK-N-SH	brain:	n/a
19	chr11:34936862-34936912	GM12878	blood:	n/a
20	chr11:34937573-34937623	HUVEC	blood vessel:	n/a
21	chr11:34938348-34938398	HL-60	blood:	n/a
22	chr11:34937778-34937828	SKMC	muscle:	n/a
23	chr11:34940794-34940844	AG09319	gingival:	n/a
24	chr11:34937647-34937697	SAEC	small airway:	n/a
25	chr11:34937647-34937697	AoSMC	blood vessel:	n/a
26	chr11:34938348-34938398	PrEC	prostate:	n/a
27	chr11:34937958-34938008	HEEpiC	esophagus:	n/a
28	chr11:34937958-34938008	MCF-7	breast:	n/a
29	chr11:34936862-34936912	HAEpiC	amniotic membrane:	n/a
30	chr11:34938143-34938193	IMR90	lung:	fetal
31	chr11:34938348-34938398	NT2-D1	testis:	n/a
32	chr11:34937341-34937391	PrEC	prostate:	n/a
33	chr11:34937778-34937828	HCF	heart:	n/a
34	chr11:34937559-34937609	NH-A	brain:	n/a
35	chr11:34938507-34938557	SAEC	small airway:	n/a
36	chr11:34937933-34937983	U87	brain:	n/a
37	chr11:34938348-34938398	AG09309	skin:	n/a
38	chr11:34938011-34938061	SKMC	muscle:	n/a
39	chr11:34937933-34937983	Hela-S3	cervix:	n/a
40	chr11:34937992-34938042	K562	blood:	n/a
41	chr11:34938112-34938162	HEK293	kidney:	embryo
42	chr11:34938112-34938162	PFSK-1	brain:	n/a
43	chr11:34937665-34937715	HEEpiC	esophagus:	n/a
44	chr11:34937778-34937828	HRE	kidney:	n/a
45	chr11:34934680-34934730	GM19239	blood:	n/a
46	chr11:34938507-34938557	BJ	skin:	n/a
47	chr11:34936781-34936831	NT2-D1	testis:	n/a
48	chr11:34938014-34938064	NB4	blood:	n/a
49	chr11:34929792-34929842	HCM	heart:	n/a
50	chr11:34937559-34937609	ovcar-3	ovarian:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:34605985..34608292-chr11:34938833..34941617,2	K562	blood:
2	chr11:34923966..34926335-chr11:34931824..34933676,2	K562	blood:
3	chr11:34938030..34938538-chr11:82996860..82997460,2	Hela-S3	cervix:
4	chr11:34928494..34930891-chr11:34936071..34939196,3	MCF-7	breast:
5	chr11:34932335..34935204-chr11:34935436..34938565,3	MCF-7	breast:
6	chr11:34905872..34908385-chr11:34915875..34918496,2	K562	blood:
7	chr11:34937322..34938942-chr11:35639938..35642002,2	MCF-7	breast:
8	chr11:34932295..34934736-chr11:34941620..34944045,2	MCF-7	breast:
9	chr11:34928718..34934554-chr11:34935181..34939232,15	MCF-7	breast:
10	chr11:34923546..34926678-chr11:34933429..34938581,5	MCF-7	breast:
11	chr11:34940522..34942447-chr11:34942724..34944906,2	K562	blood:
12	chr11:34534104..34535140-chr11:34920268..34920796,4	K562	blood:
13	chr11:34919773..34921558-chr11:34929230..34931688,2	K562	blood:
14	chr11:34942697..34945540-chr11:34950429..34952948,3	K562	blood:
15	chr11:34588812..34589630-chr11:34920341..34921212,2	K562	blood:
16	chr11:34937697..34938489-chr19:2475911..2476465,2	Hela-S3	cervix:
17	chr11:34921303..34922935-chr11:34924601..34927346,2	MCF-7	breast:
18	chr11:34937942..34938533-chr7:22893673..22894331,2	Hela-S3	cervix:
19	chr11:34921303..34922935-chr11:34924601..34927346,2	MCF-7	breast:
20	chr11:34927454..34929735-chr11:34930952..34932783,2	K562	blood:
21	chr11:34938207..34939863-chr11:35260000..35262264,2	K562	blood:
22	chr11:34932295..34934736-chr11:34941620..34944045,2	MCF-7	breast:
23	chr1:148241501..148242022-chr11:34938412..34939404,2	Hela-S3	cervix:
24	chr11:34937272..34938502-chr11:118134559..118135201,3	Hela-S3	cervix:
25	chr11:34930292..34932707-chr11:35355903..35358489,2	K562	blood:
26	chr11:34937866..34938405-chr16:87425618..87426289,2	HCT-116	colon:
27	chr11:34936821..34938525-chr17:38476825..38479359,2	MCF-7	breast:
28	chr11:34927454..34929735-chr11:34930952..34932783,2	K562	blood:
29	chr11:34919773..34921558-chr11:34929230..34931688,2	K562	blood:
30	chr11:34938300..34939878-chr11:34967011..34969816,2	MCF-7	breast:
31	chr11:34940522..34942447-chr11:34942724..34944906,2	K562	blood:
32	chr11:34591227..34593757-chr11:34936738..34938685,2	MCF-7	breast:
33	chr11:34923966..34926335-chr11:34931824..34933676,2	K562	blood:
34	chr11:34937811..34940525-chr11:34962659..34964952,2	MCF-7	breast:
35	chr11:34926486..34928206-chr11:36379103..36382037,2	K562	blood:
36	chr11:34607165..34608016-chr11:34920268..34920858,2	K562	blood:
37	chr11:34891442..34894035-chr11:34912560..34915333,2	K562	blood:
38	chr11:34941386..34944859-chr11:34946221..34949330,3	K562	blood:

No data

Variant related genes	Relation type
PDHX	TF binding region
APIP	TF binding region
PDHX	CpG island
APIP	CpG island
ENSG00000137500	chromatin interactions
ENSG00000103264	chromatin interactions
ENSG00000099860	chromatin interactions
ENSG00000179431	chromatin interactions
ENSG00000228649	chromatin interactions
ENSG00000251862	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000255234	chromatin interactions
ENSG00000149089	chromatin interactions
ENSG00000255427	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000149573	chromatin interactions
ENSG00000131759	chromatin interactions

Extended variants
information (count: 1179 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2915223	chr11:34914137-34914138	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554614293	chr11:34914141-34914142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529810738	chr11:34914341-34914342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375046262	chr11:34914342-34914343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2915222	chr11:34914360-34914361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs533547956	chr11:34914390-34914391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563296227	chr11:34914440-34914441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2915221	chr11:34914480-34914481	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs576846554	chr11:34914605-34914606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145001086	chr11:34914618-34914619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2915220	chr11:34914650-34914651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs184612242	chr11:34914686-34914687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548817455	chr11:34914687-34914688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76266273	chr11:34914713-34914714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537555683	chr11:34914731-34914732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563513060	chr11:34914749-34914750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140359320	chr11:34914769-34914770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189993930	chr11:34914878-34914879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541176635	chr11:34914900-34914901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs180792757	chr11:34914960-34914961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2986422	chr11:34915006-34915007	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs144414317	chr11:34915050-34915051	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561156296	chr11:34915067-34915068	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs59184525	chr11:34915071-34915072	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs543510436	chr11:34915074-34915075	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs563278910	chr11:34915091-34915092	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2163373	chr11:34915132-34915133	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs183968419	chr11:34915141-34915142	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs145590502	chr11:34915153-34915154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs552228175	chr11:34915164-34915165	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs148874323	chr11:34915273-34915274	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528818294	chr11:34915312-34915313	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189421333	chr11:34915316-34915317	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143620942	chr11:34915324-34915325	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537287814	chr11:34915330-34915331	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181793744	chr11:34915341-34915342	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368847311	chr11:34915365-34915366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2986423	chr11:34915370-34915371	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs539434182	chr11:34915372-34915373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552963553	chr11:34915383-34915384	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552798798	chr11:34915413-34915414	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2986424	chr11:34915446-34915447	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs554424821	chr11:34915473-34915474	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574565331	chr11:34915480-34915481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77336834	chr11:34915513-34915514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563373738	chr11:34915520-34915521	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151004289	chr11:34915555-34915556	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs16926365	chr11:34915650-34915651	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs559395204	chr11:34915659-34915660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78865569	chr11:34915744-34915745	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34882000-34919800	Weak transcription	Left Ventricle	heart
2	chr11:34891200-34919200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:34893000-34921400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:34895000-34921200	Weak transcription	Right Ventricle	heart
5	chr11:34897000-34919200	Weak transcription	Fetal Stomach	stomach
6	chr11:34897600-34919200	Weak transcription	Fetal Heart	heart
7	chr11:34898200-34926800	Weak transcription	HSMMtube	muscle
8	chr11:34899000-34917400	Weak transcription	HSMM	muscle
9	chr11:34900000-34918200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr11:34900200-34917200	Weak transcription	HUVEC	blood vessel
11	chr11:34900200-34921000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:34901400-34917400	Weak transcription	Fetal Kidney	kidney
13	chr11:34901400-34920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:34901600-34918200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr11:34901800-34916800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr11:34901800-34917000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:34902000-34921600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr11:34902200-34915600	Weak transcription	Colon Smooth Muscle	Colon
19	chr11:34903600-34919200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:34903800-34914200	Weak transcription	Fetal Brain Male	brain
21	chr11:34904000-34918600	Weak transcription	NHDF-Ad	bronchial
22	chr11:34904800-34915600	Weak transcription	GM12878-XiMat	blood
23	chr11:34905000-34917800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:34905200-34915200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:34905200-34915400	Weak transcription	Fetal Brain Female	brain
26	chr11:34905200-34917800	Weak transcription	Primary B cells from peripheral blood	blood
27	chr11:34906200-34916200	Weak transcription	Primary T cells from cord blood	blood
28	chr11:34907200-34918200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:34907400-34917800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:34907800-34918000	Weak transcription	Fetal Intestine Large	intestine
31	chr11:34908400-34921200	Weak transcription	Aorta	Aorta
32	chr11:34908600-34917800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr11:34908800-34915600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:34908800-34921000	Weak transcription	Ovary	ovary
35	chr11:34909000-34915000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:34909200-34919200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr11:34909400-34918200	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr11:34909600-34918200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr11:34909800-34921600	Weak transcription	Stomach Mucosa	stomach
40	chr11:34910000-34915800	Weak transcription	Fetal Muscle Leg	muscle
41	chr11:34910000-34918200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr11:34910200-34914200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr11:34910200-34915400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr11:34910200-34916200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr11:34910200-34917600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:34910200-34917800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr11:34910200-34918000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr11:34910200-34918000	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr11:34910200-34918400	Weak transcription	Fetal Lung	lung
50	chr11:34910200-34919400	Weak transcription	Thymus	Thymus

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