Variant report

Variant	esv3496471
Chromosome Location	chr11:65641426-65644524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr11:65641113-65641434	K562	blood:	n/a	chr11:65641272-65641292 chr11:65641160-65641180
2	BCL3	chr11:65640885-65641455	GM12878	blood:	n/a	n/a
3	BCL3	chr11:65640862-65641506	A549	lung:	n/a	n/a
4	BCL3	chr11:65640736-65641544	A549	lung:	n/a	n/a
5	BCLAF1	chr11:65640997-65641508	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:65640916-65641449	K562	blood:	n/a	n/a
7	BHLHE40	chr11:65640936-65641500	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:65640860-65641489	GM12878	blood:	n/a	n/a
9	CBX3	chr11:65640800-65641482	K562	blood:	n/a	n/a
10	CREB1	chr11:65640863-65641442	H1-hESC	embryonic stem cell:	n/a	n/a
11	CREB1	chr11:65640798-65641502	GM12878	blood:	n/a	n/a
12	CREB1	chr11:65640690-65641503	HepG2	liver:	n/a	n/a
13	CREB1	chr11:65640836-65641464	A549	lung:	n/a	n/a
14	CTCF	chr11:65641635-65641662	Kidney_OC	kidney:	n/a	n/a
15	E2F6	chr11:65640772-65641484	A549	lung:	n/a	chr11:65641183-65641190 chr11:65641183-65641190 chr11:65641179-65641191 chr11:65641183-65641190 chr11:65641173-65641183 chr11:65641180-65641191
16	E2F6	chr11:65640973-65641435	H1-hESC	embryonic stem cell:	n/a	chr11:65641183-65641190 chr11:65641183-65641190 chr11:65641179-65641191 chr11:65641183-65641190 chr11:65641173-65641183 chr11:65641180-65641191
17	EBF1	chr11:65640856-65641438	GM12878	blood:	n/a	chr11:65641280-65641289
18	EBF1	chr11:65640776-65641452	GM12878	blood:	n/a	chr11:65641280-65641289
19	EBF1	chr11:65640884-65641437	GM12878	blood:	n/a	chr11:65641280-65641289
20	EGR1	chr11:65640627-65641522	HCT-116	colon:	n/a	chr11:65641076-65641089 chr11:65641092-65641102 chr11:65640929-65640942 chr11:65641090-65641104 chr11:65641073-65641087
21	EGR1	chr11:65640635-65641509	HCT-116	colon:	n/a	chr11:65641076-65641089 chr11:65641092-65641102 chr11:65640929-65640942 chr11:65641090-65641104 chr11:65641073-65641087
22	EGR1	chr11:65640810-65641444	MCF-7	breast:	n/a	chr11:65641076-65641089 chr11:65641092-65641102 chr11:65640929-65640942 chr11:65641090-65641104 chr11:65641073-65641087
23	ELF1	chr11:65640566-65641513	GM12878	blood:	n/a	chr11:65641078-65641087
24	ELF1	chr11:65640760-65641438	MCF-7	breast:	n/a	chr11:65641078-65641087
25	ELF1	chr11:65640700-65641481	MCF-7	breast:	n/a	chr11:65641078-65641087
26	FOXA1	chr11:65641041-65641473	HepG2	liver:	n/a	n/a
27	FOXM1	chr11:65641018-65641590	GM12878	blood:	n/a	n/a
28	FOXP2	chr11:65640888-65641430	PFSK-1	brain:	n/a	n/a
29	GABPA	chr11:65640637-65641436	MCF-7	breast:	n/a	n/a
30	GABPA	chr11:65640738-65641451	K562	blood:	n/a	n/a
31	GTF3C2	chr11:65641400-65641981	Hela-S3	cervix:	n/a	n/a
32	HCFC1	chr11:65640375-65641466	Hela-S3	cervix:	n/a	n/a
33	HEY1	chr11:65640771-65641450	HepG2	liver:	n/a	n/a
34	HEY1	chr11:65640807-65641426	K562	blood:	n/a	n/a
35	JUN	chr11:65640385-65641486	K562	blood:	n/a	n/a
36	JUND	chr11:65641007-65641499	A549	lung:	n/a	n/a
37	MAX	chr11:65640846-65641494	K562	blood:	n/a	n/a
38	MAX	chr11:65640713-65641471	HepG2	liver:	n/a	n/a
39	MAX	chr11:65640856-65641460	K562	blood:	n/a	n/a
40	MAX	chr11:65640847-65641550	MCF-7	breast:	n/a	n/a
41	MAX	chr11:65640683-65641461	ECC-1	luminal epithelium:	n/a	n/a
42	MAX	chr11:65640848-65641523	A549	lung:	n/a	n/a
43	MAX	chr11:65640968-65641441	HepG2	liver:	n/a	n/a
44	MAX	chr11:65640856-65641520	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr11:65640681-65641543	HCT-116	colon:	n/a	n/a
46	MAX	chr11:65640680-65641537	A549	lung:	n/a	n/a
47	MAX	chr11:65640814-65641457	SK-N-SH	brain:	n/a	n/a
48	MAX	chr11:65640808-65641490	MCF-7	breast:	n/a	n/a
49	MAX	chr11:65640832-65641466	ECC-1	luminal epithelium:	n/a	n/a
50	MAX	chr11:65640909-65641452	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65643970-65644020	PFSK-1	brain:	n/a
2	chr11:65641445-65641495	K562	blood:	n/a
3	chr11:65643970-65644020	PFSK-1	brain:	n/a
4	chr11:65641445-65641495	K562	blood:	n/a
5	chr11:65643970-65644020	ECC-1	luminal epithelium:	n/a
6	chr11:65641445-65641495	HRCEpiC	kidney:	n/a
7	chr11:65641445-65641495	PrEC	prostate:	n/a
8	chr11:65641445-65641495	PANC-1	pancreas:	n/a
9	chr11:65643970-65644020	IMR90	lung:	fetal
10	chr11:65643970-65644020	BJ	skin:	n/a
11	chr11:65641445-65641495	AG04450	lung:	fetal
12	chr11:65643970-65644020	AG09319	gingival:	n/a
13	chr11:65641445-65641495	GM12892	blood:	n/a
14	chr11:65643970-65644020	MCF10A-Er-Src	breast:	n/a
15	chr11:65641445-65641495	Hepatocyte	liver:	n/a
16	chr11:65643970-65644020	SK-N-SH_RA	brain:	n/a
17	chr11:65643970-65644020	HCF	heart:	n/a
18	chr11:65641445-65641495	MCF-7	breast:	n/a
19	chr11:65643970-65644020	T-47D	breast:	n/a
20	chr11:65643970-65644020	RPTEC	kidney:	n/a
21	chr11:65641445-65641495	A549	lung:	n/a
22	chr11:65641445-65641495	HNPCEpiC	eye:	n/a
23	chr11:65641445-65641495	HL-60	blood:	n/a
24	chr11:65643970-65644020	AG04449	skin:	fetal
25	chr11:65641445-65641495	RPTEC	kidney:	n/a
26	chr11:65643970-65644020	HEEpiC	esophagus:	n/a
27	chr11:65641445-65641495	NH-A	brain:	n/a
28	chr11:65643970-65644020	HMEC	breast:	n/a
29	chr11:65643970-65644020	GM12891	blood:	n/a
30	chr11:65643970-65644020	HNPCEpiC	eye:	n/a
31	chr11:65641445-65641495	HCF	heart:	n/a
32	chr11:65641445-65641495	PFSK-1	brain:	n/a
33	chr11:65641445-65641495	ECC-1	luminal epithelium:	n/a
34	chr11:65641445-65641495	MCF10A-Er-Src	breast:	n/a
35	chr11:65641445-65641495	HepG2	liver:	n/a
36	chr11:65643970-65644020	PrEC	prostate:	n/a
37	chr11:65643970-65644020	SAEC	small airway:	n/a
38	chr11:65643970-65644020	GM06990	blood:	n/a
39	chr11:65641445-65641495	BJ	skin:	n/a
40	chr11:65643970-65644020	SK-N-SH	brain:	n/a
41	chr11:65643970-65644020	LNCaP	prostate:	n/a
42	chr11:65641445-65641495	NT2-D1	testis:	n/a
43	chr11:65641445-65641495	HUVEC	blood vessel:	n/a
44	chr11:65641445-65641495	LNCaP	prostate:	n/a
45	chr11:65643970-65644020	HRE	kidney:	n/a
46	chr11:65641445-65641495	SK-N-SH_RA	brain:	n/a
47	chr11:65643970-65644020	ProgFib	skin:	n/a
48	chr11:65643970-65644020	NH-A	brain:	n/a
49	chr11:65643970-65644020	HepG2	liver:	n/a
50	chr11:65643970-65644020	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65642046..65643611-chr7:5563687..5566581,2	K562	blood:
2	chr11:65638895..65641565-chr11:65834356..65837225,2	K562	blood:
3	chr11:65639484..65641571-chr8:144697740..144699528,2	MCF-7	breast:
4	chr11:65640551..65642134-chr11:65685115..65687811,2	MCF-7	breast:
5	chr11:65482061..65486231-chr11:65638918..65641829,3	K562	blood:
6	chr11:65547235..65549033-chr11:65639667..65642031,2	K562	blood:

Variant related genes	Relation type
CTSW	TF binding region
EFEMP2	TF binding region
CTSW	CpG island
EFEMP2	CpG island
ENSG00000172977	chromatin interactions
ENSG00000175573	chromatin interactions
ENSG00000175827	chromatin interactions
ENSG00000255038	chromatin interactions
ENSG00000104522	chromatin interactions
ENSG00000254470	chromatin interactions
ENSG00000175550	chromatin interactions

Extended variants
information (count: 89 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112971520	chr11:65641496-65641497	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs561912491	chr11:65641507-65641508	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs7122843	chr11:65641518-65641519	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs111897528	chr11:65641549-65641550	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs370913748	chr11:65641555-65641556	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs192208819	chr11:65641580-65641581	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs200059608	chr11:65641618-65641619	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs550608473	chr11:65641622-65641623	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs201234364	chr11:65641637-65641638	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs570689821	chr11:65641666-65641667	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs559940769	chr11:65641710-65641711	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs528695918	chr11:65641716-65641717	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs532808092	chr11:65641745-65641746	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs184629882	chr11:65641748-65641749	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs566114957	chr11:65641809-65641810	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs188264239	chr11:65641888-65641889	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs625652	chr11:65641931-65641932	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs571755452	chr11:65641963-65641964	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs192161370	chr11:65641997-65641998	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs368839015	chr11:65642051-65642052	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537618618	chr11:65642075-65642076	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs116997238	chr11:65642094-65642095	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577494922	chr11:65642128-65642129	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs543447546	chr11:65642228-65642229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546507169	chr11:65642229-65642230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553446839	chr11:65642237-65642238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368708858	chr11:65642387-65642388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34017216	chr11:65642389-65642390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573273386	chr11:65642399-65642400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs398016444	chr11:65642408-65642409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11227333	chr11:65642417-65642418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs562169872	chr11:65642455-65642456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184642699	chr11:65642456-65642457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189311292	chr11:65642464-65642465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564102144	chr11:65642626-65642627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533291763	chr11:65642637-65642638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546480323	chr11:65642674-65642675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150181376	chr11:65642931-65642932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114735548	chr11:65643113-65643114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181966278	chr11:65643190-65643191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542406424	chr11:65643238-65643239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568907457	chr11:65643258-65643259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537522336	chr11:65643264-65643265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184278066	chr11:65643300-65643301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570949974	chr11:65643324-65643325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540184836	chr11:65643340-65643341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs688721	chr11:65643366-65643367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553658172	chr11:65643388-65643389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188808611	chr11:65643425-65643426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573285767	chr11:65643443-65643444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Pituitary adenoma	18645599	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
Prostate cancer	18779856	CNVD
Cancer	17160897	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:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65639200-65641600	Active TSS	Brain Substantia Nigra	brain
2	chr11:65639400-65641600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:65639400-65641600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:65639400-65641600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:65639400-65641600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:65639400-65641600	Active TSS	Brain Angular Gyrus	brain
7	chr11:65639400-65641600	Active TSS	Right Atrium	heart
8	chr11:65639400-65641600	Active TSS	HSMM	muscle
9	chr11:65639400-65641600	Active TSS	NHDF-Ad	bronchial
10	chr11:65639600-65641600	Active TSS	H9 Cell Line	embryonic stem cell
11	chr11:65639600-65641600	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr11:65639600-65641600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:65639600-65641600	Active TSS	Colon Smooth Muscle	Colon
14	chr11:65639600-65641600	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr11:65639600-65641600	Active TSS	Left Ventricle	heart
16	chr11:65639600-65641600	Active TSS	Ovary	ovary
17	chr11:65639600-65641800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:65639800-65641600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:65639800-65641600	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr11:65639800-65641600	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr11:65639800-65641600	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr11:65639800-65641600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr11:65639800-65641600	Active TSS	Psoas Muscle	Psoas
24	chr11:65640000-65641600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:65640000-65641600	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr11:65640200-65641600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr11:65640200-65641600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:65640400-65641600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr11:65640400-65641600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
30	chr11:65640400-65641600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr11:65640400-65641600	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr11:65640400-65641600	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr11:65640400-65641600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
34	chr11:65640400-65641600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr11:65640400-65641600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:65640400-65641600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr11:65640400-65641600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr11:65640400-65641600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr11:65640400-65641600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
40	chr11:65640400-65641600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:65640400-65641600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:65640400-65641600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr11:65640400-65641600	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr11:65640400-65641600	Flanking Active TSS	Colonic Mucosa	Colon
45	chr11:65640400-65641600	Flanking Active TSS	Fetal Muscle Leg	muscle
46	chr11:65640400-65641600	Flanking Active TSS	Placenta	Placenta
47	chr11:65640400-65641600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
48	chr11:65640400-65641600	Flanking Active TSS	Dnd41	blood
49	chr11:65640400-65641600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr11:65640400-65641800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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