Variant report

Variant	esv3442487
Chromosome Location	chr11:65683409-65683711
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	ARID3A	chr11:65683303-65683516	HepG2	liver:	n/a	n/a
2	ATF3	chr11:65683057-65683801	A549	lung:	n/a	chr11:65683544-65683564
3	ATF3	chr11:65683091-65683648	A549	lung:	n/a	chr11:65683544-65683564
4	BACH1	chr11:65683332-65683454	K562	blood:	n/a	n/a
5	BACH1	chr11:65683118-65683486	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr11:65682080-65684051	A549	lung:	n/a	n/a
7	BCL3	chr11:65682784-65683972	A549	lung:	n/a	n/a
8	BHLHE40	chr11:65683307-65683502	HepG2	liver:	n/a	n/a
9	BHLHE40	chr11:65683200-65683765	A549	lung:	n/a	n/a
10	BHLHE40	chr11:65683170-65683650	K562	blood:	n/a	n/a
11	BHLHE40	chr11:65683196-65683697	HepG2	liver:	n/a	n/a
12	BRCA1	chr11:65683205-65683509	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr11:65683140-65683455	K562	blood:	n/a	n/a
14	CCNT2	chr11:65683222-65683536	K562	blood:	n/a	n/a
15	CEBPB	chr11:65683090-65683897	A549	lung:	n/a	n/a
16	CEBPB	chr11:65683277-65683653	IMR90	lung:	n/a	n/a
17	CEBPB	chr11:65683345-65683455	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:65683177-65683621	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr11:65683113-65683698	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr11:65683479-65683519	HepG2	liver:	n/a	n/a
21	CREB1	chr11:65682988-65683666	A549	lung:	n/a	n/a
22	CTCF	chr11:65683380-65683530	AG04449	skin:	n/a	n/a
23	E2F4	chr11:65683381-65683518	MCF10A-Er-Src	breast:	n/a	n/a
24	ELF1	chr11:65683090-65683796	A549	lung:	n/a	n/a
25	ELK1	chr11:65683183-65683550	Hela-S3	cervix:	n/a	n/a
26	ELK4	chr11:65683232-65683470	Hela-S3	cervix:	n/a	n/a
27	EP300	chr11:65682871-65683892	SK-N-SH	brain:	n/a	chr11:65683301-65683310
28	EP300	chr11:65682927-65683798	SK-N-SH	brain:	n/a	chr11:65683301-65683310
29	EP300	chr11:65683157-65683546	HepG2	liver:	n/a	chr11:65683301-65683310
30	EP300	chr11:65682580-65684199	A549	lung:	n/a	chr11:65683301-65683310
31	EP300	chr11:65683081-65683625	ECC-1	luminal epithelium:	n/a	chr11:65683301-65683310
32	EP300	chr11:65683236-65683527	HepG2	liver:	n/a	chr11:65683301-65683310
33	EP300	chr11:65683140-65683517	SK-N-SH_RA	brain:	n/a	chr11:65683301-65683310
34	EP300	chr11:65683203-65683527	SK-N-SH_RA	brain:	n/a	chr11:65683301-65683310
35	EP300	chr11:65682579-65684195	A549	lung:	n/a	chr11:65683301-65683310
36	EP300	chr11:65683198-65683526	Hela-S3	cervix:	n/a	chr11:65683301-65683310
37	EP300	chr11:65682510-65683806	ECC-1	luminal epithelium:	n/a	chr11:65683301-65683310
38	ETS1	chr11:65683063-65683618	A549	lung:	n/a	n/a
39	FOS	chr11:65683155-65683571	MCF10A-Er-Src	breast:	n/a	chr11:65683383-65683394 chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
40	FOS	chr11:65683126-65684015	MCF10A-Er-Src	breast:	n/a	chr11:65683383-65683394 chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
41	FOS	chr11:65683115-65683599	MCF10A-Er-Src	breast:	n/a	chr11:65683383-65683394 chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
42	FOS	chr11:65683155-65683560	MCF10A-Er-Src	breast:	n/a	chr11:65683383-65683394 chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
43	FOS	chr11:65683153-65683585	Hela-S3	cervix:	n/a	chr11:65683383-65683394 chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
44	FOS	chr11:65683044-65683613	HUVEC	blood vessel:	n/a	chr11:65683383-65683394 chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
45	FOSL1	chr11:65682695-65683890	HCT-116	colon:	n/a	chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683383-65683394 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
46	FOSL1	chr11:65683125-65683507	K562	blood:	n/a	chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683383-65683394 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
47	FOSL1	chr11:65682758-65684162	HCT-116	colon:	n/a	chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683383-65683394 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
48	FOSL1	chr11:65683258-65683480	K562	blood:	n/a	chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683383-65683394 chr11:65683301-65683309 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
49	FOSL2	chr11:65682992-65683739	A549	lung:	n/a	chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683382-65683393 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310
50	FOSL2	chr11:65682798-65684134	A549	lung:	n/a	chr11:65683299-65683311 chr11:65683301-65683309 chr11:65683301-65683309 chr11:65683382-65683393 chr11:65683300-65683311 chr11:65683301-65683308 chr11:65683384-65683394 chr11:65683300-65683310

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65683543-65683593	AoSMC	blood vessel:	n/a
2	chr11:65683543-65683593	HNPCEpiC	eye:	n/a
3	chr11:65683543-65683593	BE2_C	brain:	n/a
4	chr11:65683543-65683593	AG04450	lung:	fetal
5	chr11:65683543-65683593	HRPEpiC	eye:	n/a
6	chr11:65683543-65683593	HUVEC	blood vessel:	n/a
7	chr11:65683543-65683593	NH-A	brain:	n/a
8	chr11:65683543-65683593	SK-N-MC	brain:	n/a
9	chr11:65683543-65683593	Hela-S3	cervix:	n/a
10	chr11:65683543-65683593	GM12892	blood:	n/a
11	chr11:65683543-65683593	HEK293	kidney:	embryo
12	chr11:65683543-65683593	HCT-116	colon:	n/a
13	chr11:65683543-65683593	ProgFib	skin:	n/a
14	chr11:65683543-65683593	HIPEpiC	eye:	n/a
15	chr11:65683543-65683593	AG04449	skin:	fetal
16	chr11:65683543-65683593	ovcar-3	ovarian:	n/a
17	chr11:65683543-65683593	BJ	skin:	n/a
18	chr11:65683543-65683593	GM19239	blood:	n/a
19	chr11:65683543-65683593	AG09319	gingival:	n/a
20	chr11:65683543-65683593	AG10803	skin:	n/a
21	chr11:65683543-65683593	K562	blood:	n/a
22	chr11:65683543-65683593	PANC-1	pancreas:	n/a
23	chr11:65683543-65683593	A549	lung:	n/a
24	chr11:65683543-65683593	HCM	heart:	n/a
25	chr11:65683543-65683593	HRE	kidney:	n/a
26	chr11:65683543-65683593	LNCaP	prostate:	n/a
27	chr11:65683543-65683593	CMK	blood:	n/a
28	chr11:65683543-65683593	PFSK-1	brain:	n/a
29	chr11:65683543-65683593	SK-N-SH	brain:	n/a
30	chr11:65683543-65683593	GM12878	blood:	n/a
31	chr11:65683543-65683593	SKMC	muscle:	n/a
32	chr11:65683543-65683593	RPTEC	kidney:	n/a
33	chr11:65683543-65683593	NHBE	bronchial:	n/a
34	chr11:65683543-65683593	IMR90	lung:	fetal
35	chr11:65683543-65683593	SK-N-SH_RA	brain:	n/a
36	chr11:65683543-65683593	HL-60	blood:	n/a
37	chr11:65683543-65683593	AG09309	skin:	n/a
38	chr11:65683543-65683593	H1-hESC	embryonic stem cell:	embryo
39	chr11:65683543-65683593	Jurkat	blood:	n/a
40	chr11:65683543-65683593	ECC-1	luminal epithelium:	n/a
41	chr11:65683543-65683593	HRCEpiC	kidney:	n/a
42	chr11:65683543-65683593	MCF-7	breast:	n/a
43	chr11:65683543-65683593	GM12891	blood:	n/a
44	chr11:65683543-65683593	HMEC	breast:	n/a
45	chr11:65683543-65683593	NB4	blood:	n/a
46	chr11:65683543-65683593	Caco-2	colon:	n/a
47	chr11:65683543-65683593	MCF10A-Er-Src	breast:	n/a
48	chr11:65683543-65683593	HepG2	liver:	n/a
49	chr11:65683543-65683593	HCPEpiC	choroid plexus:	n/a
50	chr11:65683543-65683593	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65622510..65630779-chr11:65675126..65689187,23	MCF-7	breast:
2	chr11:65650579..65663306-chr11:65677153..65690311,39	MCF-7	breast:
3	chr11:65681117..65683931-chr9:19374587..19377457,2	K562	blood:
4	chr11:65681469..65683579-chr11:65785097..65787781,2	MCF-7	breast:
5	chr11:65683165..65691632-chr11:65723620..65730701,28	MCF-7	breast:
6	chr11:65682118..65684018-chr11:65775122..65778045,2	MCF-7	breast:
7	chr11:65485702..65488169-chr11:65683105..65685418,2	MCF-7	breast:
8	chr11:65663912..65665764-chr11:65680753..65683444,3	MCF-7	breast:
9	chr11:65624095..65629782-chr11:65682347..65689302,13	MCF-7	breast:
10	chr11:65485621..65487776-chr11:65682434..65684591,2	K562	blood:
11	chr11:65683260..65685556-chr11:65700127..65702595,2	MCF-7	breast:
12	chr11:65682614..65684925-chr11:65768572..65770745,2	MCF-7	breast:
13	chr11:65652289..65653954-chr11:65682790..65684539,2	MCF-7	breast:
14	chr11:65682062..65683635-chr11:65735954..65737652,2	MCF-7	breast:

Variant related genes	Relation type
DRAP1	TF binding region
DRAP1	CpG island
ENSG00000175376	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000273226	chromatin interactions
ENSG00000175467	chromatin interactions
ENSG00000172977	chromatin interactions
ENSG00000175602	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000172922	chromatin interactions
ENSG00000175334	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000172500	chromatin interactions

Extended variants
information (count: 10 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372684657	chr11:65683447-65683448	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs531460024	chr11:65683475-65683476	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs551522010	chr11:65683503-65683504	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs9326359	chr11:65683513-65683514	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs677029	chr11:65683531-65683532	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs181984943	chr11:65683537-65683538	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs553531397	chr11:65683557-65683558	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs138886412	chr11:65683607-65683608	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs184757360	chr11:65683665-65683666	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs111457584	chr11:65683678-65683679	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	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:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65676400-65683600	Enhancers	NHDF-Ad	bronchial
2	chr11:65676400-65683800	Weak transcription	Primary T cells from cord blood	blood
3	chr11:65677800-65684000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:65679400-65685200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:65679600-65684400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:65679600-65684400	Enhancers	Placenta	Placenta
7	chr11:65680000-65684400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:65680000-65684600	Weak transcription	Fetal Lung	lung
9	chr11:65681600-65683800	Weak transcription	GM12878-XiMat	blood
10	chr11:65681600-65685400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr11:65681800-65684800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr11:65682000-65683800	Weak transcription	Fetal Intestine Large	intestine
13	chr11:65682000-65684800	Enhancers	Esophagus	oesophagus
14	chr11:65682000-65685200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:65682000-65685400	Enhancers	Placenta Amnion	Placenta Amnion
16	chr11:65682200-65683600	Genic enhancers	NHLF	lung
17	chr11:65682200-65684000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:65682200-65684000	Enhancers	Fetal Muscle Trunk	muscle
19	chr11:65682200-65684200	Flanking Active TSS	HSMMtube	muscle
20	chr11:65682200-65684200	Flanking Active TSS	NHEK	skin
21	chr11:65682200-65684400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:65682200-65684400	Enhancers	Primary B cells from peripheral blood	blood
23	chr11:65682200-65684400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:65682200-65684800	Enhancers	Ovary	ovary
25	chr11:65682200-65684800	Enhancers	Psoas Muscle	Psoas
26	chr11:65682200-65684800	Enhancers	Right Ventricle	heart
27	chr11:65682200-65685000	Genic enhancers	Fetal Stomach	stomach
28	chr11:65682200-65685000	Enhancers	Pancreas	Pancrea
29	chr11:65682200-65685200	Enhancers	Left Ventricle	heart
30	chr11:65682200-65685800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:65682400-65683600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr11:65682400-65683600	Enhancers	Colonic Mucosa	Colon
33	chr11:65682400-65684000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr11:65682400-65684200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:65682400-65684200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr11:65682400-65684200	Enhancers	Fetal Muscle Leg	muscle
37	chr11:65682400-65684200	Enhancers	Right Atrium	heart
38	chr11:65682400-65684400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:65682400-65684400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:65682400-65684400	Enhancers	Spleen	Spleen
41	chr11:65682400-65684600	Enhancers	Lung	lung
42	chr11:65682400-65684800	Enhancers	Duodenum Mucosa	Duodenum
43	chr11:65682400-65685200	Enhancers	Brain Cingulate Gyrus	brain
44	chr11:65682400-65685200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr11:65682600-65683800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr11:65682600-65683800	Flanking Active TSS	Colon Smooth Muscle	Colon
47	chr11:65682600-65683800	Strong transcription	Thymus	Thymus
48	chr11:65682600-65684000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:65682600-65684200	Strong transcription	Fetal Intestine Small	intestine
50	chr11:65682600-65684200	Flanking Active TSS	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links