Variant report

Variant	esv3462630
Chromosome Location	chr11:74022904-74029002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:368)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr11:74027858-74028188	K562	blood:	n/a	n/a
2	CEBPB	chr11:74023429-74023756	HepG2	liver:	n/a	chr11:74023581-74023592
3	CEBPB	chr11:74023438-74023800	MCF-7	breast:	n/a	chr11:74023581-74023592
4	CEBPB	chr11:74023466-74023693	HepG2	liver:	n/a	chr11:74023581-74023592
5	CEBPB	chr11:74023394-74023814	Hela-S3	cervix:	n/a	chr11:74023581-74023592
6	CEBPB	chr11:74023398-74023778	HepG2	liver:	n/a	chr11:74023581-74023592
7	CEBPB	chr11:74023396-74023801	A549	lung:	n/a	chr11:74023581-74023592
8	CEBPB	chr11:74023406-74023802	IMR90	lung:	n/a	chr11:74023581-74023592
9	CEBPB	chr11:74023386-74023824	A549	lung:	n/a	chr11:74023581-74023592
10	CEBPB	chr11:74023423-74023752	K562	blood:	n/a	chr11:74023581-74023592
11	CEBPB	chr11:74023395-74023856	A549	lung:	n/a	chr11:74023816-74023829 chr11:74023581-74023592
12	CEBPB	chr11:74023456-74023744	H1-hESC	embryonic stem cell:	n/a	chr11:74023581-74023592
13	E2F4	chr11:74028188-74028348	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F6	chr11:74022365-74023218	A549	lung:	n/a	chr11:74022708-74022719
15	E2F6	chr11:74022375-74023155	A549	lung:	n/a	chr11:74022708-74022719
16	E2F6	chr11:74022328-74023269	K562	blood:	n/a	chr11:74022708-74022719
17	E2F6	chr11:74022449-74023378	H1-hESC	embryonic stem cell:	n/a	chr11:74022708-74022719
18	E2F6	chr11:74022487-74023326	H1-hESC	embryonic stem cell:	n/a	chr11:74022708-74022719
19	E2F6	chr11:74022840-74023016	K562	blood:	n/a	n/a
20	EP300	chr11:74023527-74023727	Hela-S3	cervix:	n/a	n/a
21	FOS	chr11:74023421-74023615	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr11:74023390-74023660	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr11:74023426-74023662	MCF10A-Er-Src	breast:	n/a	n/a
24	FOXA1	chr11:74023296-74023641	HepG2	liver:	n/a	chr11:74023534-74023549
25	FOXA1	chr11:74023312-74023660	HepG2	liver:	n/a	chr11:74023534-74023549
26	FOXA1	chr11:74023384-74023784	HepG2	liver:	n/a	chr11:74023534-74023549
27	FOXA1	chr11:74023309-74023699	HepG2	liver:	n/a	chr11:74023534-74023549
28	FOXA2	chr11:74023426-74023763	A549	lung:	n/a	n/a
29	FOXA2	chr11:74023401-74023662	HepG2	liver:	n/a	n/a
30	FOXA2	chr11:74023306-74023762	A549	lung:	n/a	n/a
31	GATA3	chr11:74027870-74028540	SK-N-SH	brain:	n/a	n/a
32	KAP1	chr11:74027796-74028173	K562	blood:	n/a	n/a
33	MAX	chr11:74022404-74023200	A549	lung:	n/a	n/a
34	MAX	chr11:74022413-74023234	ECC-1	luminal epithelium:	n/a	n/a
35	MAX	chr11:74022637-74023036	A549	lung:	n/a	n/a
36	MAX	chr11:74022433-74023021	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAX	chr11:74022458-74023204	HCT-116	colon:	n/a	n/a
38	MAX	chr11:74021742-74023285	A549	lung:	n/a	n/a
39	MAX	chr11:74022308-74023011	K562	blood:	n/a	n/a
40	MAX	chr11:74022708-74022934	K562	blood:	n/a	n/a
41	MAX	chr11:74022796-74023159	H1-hESC	embryonic stem cell:	n/a	n/a
42	MAX	chr11:74022376-74023200	HCT-116	colon:	n/a	n/a
43	MAX	chr11:74022504-74022905	K562	blood:	n/a	n/a
44	MAX	chr11:74022310-74023127	MCF-7	breast:	n/a	n/a
45	MAX	chr11:74022351-74023124	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr11:74022451-74023083	SK-N-SH	brain:	n/a	n/a
47	MAX	chr11:74022226-74023132	ECC-1	luminal epithelium:	n/a	n/a
48	MAZ	chr11:74022376-74022960	K562	blood:	n/a	n/a
49	MAZ	chr11:74023636-74023640	Hela-S3	cervix:	n/a	n/a
50	MXI1	chr11:74023577-74023608	HepG2	liver:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:74022882-74022932	HCT-116	colon:	n/a
2	chr11:74022875-74022925	SK-N-SH	brain:	n/a
3	chr11:74022882-74022932	HCT-116	colon:	n/a
4	chr11:74022875-74022925	SK-N-SH	brain:	n/a
5	chr11:74022882-74022932	GM06990	blood:	n/a
6	chr11:74022882-74022932	Jurkat	blood:	n/a
7	chr11:74022875-74022925	IMR90	lung:	fetal
8	chr11:74026371-74026421	AG09309	skin:	n/a
9	chr11:74022910-74022960	PANC-1	pancreas:	n/a
10	chr11:74023050-74023100	Hepatocyte	liver:	n/a
11	chr11:74026371-74026421	PFSK-1	brain:	n/a
12	chr11:74022910-74022960	Caco-2	colon:	n/a
13	chr11:74023050-74023100	AG10803	skin:	n/a
14	chr11:74022930-74022980	HEK293	kidney:	embryo
15	chr11:74026371-74026421	GM12891	blood:	n/a
16	chr11:74022882-74022932	BE2_C	brain:	n/a
17	chr11:74023050-74023100	ProgFib	skin:	n/a
18	chr11:74022875-74022925	HAEpiC	amniotic membrane:	n/a
19	chr11:74022930-74022980	RPTEC	kidney:	n/a
20	chr11:74022910-74022960	GM06990	blood:	n/a
21	chr11:74022882-74022932	H1-hESC	embryonic stem cell:	embryo
22	chr11:74022875-74022925	SKMC	muscle:	n/a
23	chr11:74026371-74026421	HEEpiC	esophagus:	n/a
24	chr11:74026371-74026421	ProgFib	skin:	n/a
25	chr11:74022930-74022980	HCF	heart:	n/a
26	chr11:74022930-74022980	MCF10A-Er-Src	breast:	n/a
27	chr11:74022875-74022925	T-47D	breast:	n/a
28	chr11:74022882-74022932	SKMC	muscle:	n/a
29	chr11:74022910-74022960	AG09309	skin:	n/a
30	chr11:74023050-74023100	NB4	blood:	n/a
31	chr11:74023050-74023100	HRE	kidney:	n/a
32	chr11:74023050-74023100	ECC-1	luminal epithelium:	n/a
33	chr11:74022910-74022960	HEEpiC	esophagus:	n/a
34	chr11:74023050-74023100	HCPEpiC	choroid plexus:	n/a
35	chr11:74022882-74022932	AG09319	gingival:	n/a
36	chr11:74022930-74022980	NH-A	brain:	n/a
37	chr11:74026371-74026421	HNPCEpiC	eye:	n/a
38	chr11:74022882-74022932	Hepatocyte	liver:	n/a
39	chr11:74022930-74022980	HNPCEpiC	eye:	n/a
40	chr11:74022882-74022932	HRE	kidney:	n/a
41	chr11:74022882-74022932	Caco-2	colon:	n/a
42	chr11:74022882-74022932	HEEpiC	esophagus:	n/a
43	chr11:74023050-74023100	PANC-1	pancreas:	n/a
44	chr11:74023050-74023100	RPTEC	kidney:	n/a
45	chr11:74022930-74022980	IMR90	lung:	fetal
46	chr11:74022910-74022960	GM12892	blood:	n/a
47	chr11:74022910-74022960	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:74023050-74023100	HCT-116	colon:	n/a
49	chr11:74026371-74026421	HIPEpiC	eye:	n/a
50	chr11:74022882-74022932	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:74020783..74024598-chr11:74028105..74031169,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPME1-1	chr11:74022870-74022991	ENSG00000246211
2	lnc-PPME1-1	chr11:74023164-74023264	ENSG00000246211

No data

Variant related genes	Relation type
P4HA3	TF binding region
P4HA3	CpG island
ENSG00000246211	chromatin interactions
ENSG00000149380	chromatin interactions
HNRNPA2B1	miRNA target sites

Extended variants
information (count: 193 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:193 , 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	rs554529858	chr11:74022909-74022910	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs368218910	chr11:74022953-74022954	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs80073258	chr11:74022961-74022962	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs542596871	chr11:74023051-74023052	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs559293311	chr11:74023104-74023105	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs77060670	chr11:74023182-74023183	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs567783886	chr11:74023186-74023187	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs192326542	chr11:74023197-74023198	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs372105505	chr11:74023236-74023237	Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs185517671	chr11:74023311-74023312	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148180733	chr11:74023367-74023368	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs560433421	chr11:74023407-74023408	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs143335923	chr11:74023428-74023429	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs147104631	chr11:74023446-74023447	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs189419191	chr11:74023457-74023458	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs558310618	chr11:74023537-74023538	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs182063717	chr11:74023695-74023696	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs7947911	chr11:74023751-74023752	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534333812	chr11:74023778-74023779	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558022928	chr11:74023857-74023858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577907133	chr11:74023860-74023861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536829890	chr11:74023866-74023867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556774104	chr11:74023871-74023872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556474930	chr11:74023895-74023896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577605962	chr11:74023907-74023908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184484826	chr11:74023967-74023968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376336283	chr11:74023977-74023978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78724004	chr11:74023994-74023995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559601574	chr11:74024003-74024004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553885717	chr11:74024012-74024013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573181009	chr11:74024014-74024015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545116727	chr11:74024015-74024016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189142438	chr11:74024110-74024111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531141082	chr11:74024116-74024117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551310077	chr11:74024130-74024131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143972874	chr11:74024135-74024136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74816809	chr11:74024181-74024182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572078458	chr11:74024203-74024204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549062061	chr11:74024232-74024233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs752577	chr11:74024240-74024241	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs670974	chr11:74024257-74024258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs371787851	chr11:74024284-74024285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181184824	chr11:74024286-74024287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186366897	chr11:74024302-74024303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539369898	chr11:74024341-74024342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116638505	chr11:74024350-74024351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573460032	chr11:74024399-74024400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34641911	chr11:74024406-74024407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536081605	chr11:74024441-74024442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553429234	chr11:74024442-74024443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74021600-74023000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:74021800-74023000	Active TSS	HSMM	muscle
3	chr11:74021800-74023200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr11:74021800-74023200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:74022000-74023000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:74022000-74023000	Active TSS	Cortex derived primary cultured neurospheres	brain
7	chr11:74022000-74023000	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr11:74022000-74023200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
9	chr11:74022000-74023200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:74022200-74023000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:74022200-74023000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
12	chr11:74022200-74023000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:74022200-74023000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:74022200-74023000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:74022200-74023000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
16	chr11:74022200-74023000	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
17	chr11:74022200-74023000	Flanking Active TSS	Right Ventricle	heart
18	chr11:74022200-74023000	Bivalent/Poised TSS	Thymus	Thymus
19	chr11:74022200-74023000	ZNF genes & repeats	Spleen	Spleen
20	chr11:74022200-74023000	Flanking Active TSS	HMEC	breast
21	chr11:74022200-74023200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
22	chr11:74022200-74023200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
23	chr11:74022200-74023200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr11:74022200-74023200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
25	chr11:74022200-74023200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr11:74022200-74023200	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr11:74022400-74023000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
28	chr11:74022400-74023000	Enhancers	Primary B cells from peripheral blood	blood
29	chr11:74022400-74023000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr11:74022400-74023000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr11:74022400-74023000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:74022400-74023000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr11:74022400-74023000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
34	chr11:74022400-74023000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
35	chr11:74022400-74023000	Flanking Active TSS	Colonic Mucosa	Colon
36	chr11:74022400-74023000	Active TSS	Duodenum Mucosa	Duodenum
37	chr11:74022400-74023000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
38	chr11:74022400-74023000	Active TSS	Rectal Smooth Muscle	rectum
39	chr11:74022400-74023000	Active TSS	Right Atrium	heart
40	chr11:74022400-74023000	Bivalent Enhancer	Stomach Mucosa	stomach
41	chr11:74022400-74023000	Active TSS	K562	blood
42	chr11:74022400-74023000	Active TSS	NHDF-Ad	bronchial
43	chr11:74022400-74023200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr11:74022400-74023200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr11:74022400-74023200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:74022400-74023200	Active TSS	Primary T cells from cord blood	blood
47	chr11:74022400-74023200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
48	chr11:74022400-74023200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr11:74022600-74023000	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
50	chr11:74022600-74023000	Active TSS	Liver	Liver

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