Variant report

Variant	esv11709
Chromosome Location	chr11:18138662-18200717
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:1041)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18193081-18193472	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:18194351-18194592	HepG2	liver:	n/a	n/a
3	BHLHE40	chr11:18166100-18166164	GM12878	blood:	n/a	n/a
4	CBX3	chr11:18165709-18166352	HCT-116	colon:	n/a	n/a
5	CEBPB	chr11:18153079-18153202	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:18193077-18193257	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr11:18152988-18153271	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:18152991-18153228	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr11:18153094-18153283	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:18153050-18153193	K562	blood:	n/a	n/a
11	CEBPB	chr11:18143006-18143270	HepG2	liver:	n/a	chr11:18143125-18143136
12	CEBPB	chr11:18152968-18153327	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:18152983-18153256	A549	lung:	n/a	n/a
14	CEBPB	chr11:18143062-18143194	HepG2	liver:	n/a	chr11:18143125-18143136
15	CEBPD	chr11:18142831-18143084	HepG2	liver:	n/a	n/a
16	CHD2	chr11:18157025-18157031	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr11:18169620-18169896	K562	blood:	n/a	n/a
18	CREB1	chr11:18192998-18193199	A549	lung:	n/a	n/a
19	CTCF	chr11:18166660-18166810	HPF	lung:	n/a	n/a
20	CTCF	chr11:18193040-18193190	HAc	cerebellar:	n/a	chr11:18193103-18193112
21	CTCF	chr11:18192660-18192810	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr11:18166660-18166810	A549	lung:	n/a	n/a
23	CTCF	chr11:18193040-18193190	MCF-7	breast:	n/a	chr11:18193103-18193112
24	CTCF	chr11:18193040-18193190	HCPEpiC	choroid plexus:	n/a	chr11:18193103-18193112
25	CTCF	chr11:18193000-18193150	HPAF	blood vessel:	n/a	chr11:18193103-18193112
26	CTCF	chr11:18193020-18193170	NHDF-neo	bronchial:	n/a	chr11:18193103-18193112
27	CTCF	chr11:18193005-18193215	HUVEC	blood vessel:	n/a	chr11:18193103-18193112
28	CTCF	chr11:18166660-18166810	AG04450	lung:	n/a	n/a
29	CTCF	chr11:18193060-18193210	HCM	heart:	n/a	chr11:18193103-18193112
30	CTCF	chr11:18193040-18193190	BE2_C	brain:	n/a	chr11:18193103-18193112
31	CTCF	chr11:18193040-18193190	K562	blood:	n/a	chr11:18193103-18193112
32	CTCF	chr11:18166660-18166810	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr11:18193040-18193190	GM12874	blood:	n/a	chr11:18193103-18193112
34	CTCF	chr11:18193080-18193230	GM12865	blood:	n/a	chr11:18193103-18193112
35	CTCF	chr11:18166640-18166790	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr11:18193040-18193190	GM12865	blood:	n/a	chr11:18193103-18193112
37	CTCF	chr11:18193040-18193190	HEK293	kidney:	n/a	chr11:18193103-18193112
38	CTCF	chr11:18166719-18166820	K562	blood:	n/a	n/a
39	CTCF	chr11:18166703-18166827	Gliobla	brain:	n/a	n/a
40	CTCF	chr11:18193040-18193190	HEEpiC	esophagus:	n/a	chr11:18193103-18193112
41	CTCF	chr11:18166660-18166810	GM12878	blood:	n/a	n/a
42	CTCF	chr11:18166740-18166890	GM12864	blood:	n/a	n/a
43	CTCF	chr11:18193060-18193210	GM12878	blood:	n/a	chr11:18193103-18193112
44	CTCF	chr11:18193040-18193190	HCT-116	colon:	n/a	chr11:18193103-18193112
45	CTCF	chr11:18166439-18167039	SK-N-SH	brain:	n/a	n/a
46	CTCF	chr11:18166700-18166850	GM12874	blood:	n/a	n/a
47	CTCF	chr11:18193020-18193170	HCM	heart:	n/a	chr11:18193103-18193112
48	CTCF	chr11:18193020-18193170	HL-60	blood:	n/a	chr11:18193103-18193112
49	CTCF	chr11:18192837-18193395	MCF-7	breast:	n/a	chr11:18193103-18193112
50	CTCF	chr11:18166600-18166750	NHLF	lung:	n/a	n/a

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18157405-18157455	HepG2	liver:	n/a
2	chr11:18139019-18139069	ProgFib	skin:	n/a
3	chr11:18194904-18194954	MCF10A-Er-Src	breast:	n/a
4	chr11:18141625-18141675	PANC-1	pancreas:	n/a
5	chr11:18157405-18157455	HepG2	liver:	n/a
6	chr11:18139019-18139069	ProgFib	skin:	n/a
7	chr11:18194904-18194954	MCF10A-Er-Src	breast:	n/a
8	chr11:18141625-18141675	PANC-1	pancreas:	n/a
9	chr11:18159842-18159892	Jurkat	blood:	n/a
10	chr11:18193422-18193472	RPTEC	kidney:	n/a
11	chr11:18139019-18139069	HEEpiC	esophagus:	n/a
12	chr11:18141625-18141675	GM12891	blood:	n/a
13	chr11:18193674-18193724	NT2-D1	testis:	n/a
14	chr11:18193360-18193410	HEEpiC	esophagus:	n/a
15	chr11:18157898-18157948	AG09319	gingival:	n/a
16	chr11:18157898-18157948	AG10803	skin:	n/a
17	chr11:18195086-18195136	AG04450	lung:	fetal
18	chr11:18195086-18195136	HRPEpiC	eye:	n/a
19	chr11:18158918-18158968	NB4	blood:	n/a
20	chr11:18158980-18159030	U87	brain:	n/a
21	chr11:18195086-18195136	HCT-116	colon:	n/a
22	chr11:18172905-18172955	HIPEpiC	eye:	n/a
23	chr11:18141625-18141675	HCPEpiC	choroid plexus:	n/a
24	chr11:18157898-18157948	HCF	heart:	n/a
25	chr11:18193422-18193472	CMK	blood:	n/a
26	chr11:18141625-18141675	LNCaP	prostate:	n/a
27	chr11:18157898-18157948	U87	brain:	n/a
28	chr11:18193360-18193410	HAEpiC	amniotic membrane:	n/a
29	chr11:18157898-18157948	HEK293	kidney:	embryo
30	chr11:18194904-18194954	HCF	heart:	n/a
31	chr11:18193674-18193724	AoSMC	blood vessel:	n/a
32	chr11:18194514-18194564	SK-N-MC	brain:	n/a
33	chr11:18193360-18193410	T-47D	breast:	n/a
34	chr11:18159842-18159892	SK-N-SH_RA	brain:	n/a
35	chr11:18158980-18159030	H1-hESC	embryonic stem cell:	embryo
36	chr11:18193674-18193724	NH-A	brain:	n/a
37	chr11:18172905-18172955	AoSMC	blood vessel:	n/a
38	chr11:18158918-18158968	ovcar-3	ovarian:	n/a
39	chr11:18139019-18139069	HCF	heart:	n/a
40	chr11:18172905-18172955	MCF10A-Er-Src	breast:	n/a
41	chr11:18172905-18172955	LNCaP	prostate:	n/a
42	chr11:18158850-18158900	ECC-1	luminal epithelium:	n/a
43	chr11:18194514-18194564	SK-N-SH_RA	brain:	n/a
44	chr11:18194904-18194954	HRE	kidney:	n/a
45	chr11:18193674-18193724	HNPCEpiC	eye:	n/a
46	chr11:18157405-18157455	HCT-116	colon:	n/a
47	chr11:18195086-18195136	HUVEC	blood vessel:	n/a
48	chr11:18193360-18193410	PFSK-1	brain:	n/a
49	chr11:18158850-18158900	H1-hESC	embryonic stem cell:	embryo
50	chr11:18158980-18159030	AG09309	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18158132..18160556-chr11:18162021..18163694,2	K562	blood:
2	chr11:18127466..18129015-chr11:18138742..18140750,2	K562	blood:
3	chr11:18192847..18193418-chr11:18785532..18786067,2	MCF-7	breast:
4	chr11:18192633..18193561-chr11:18225013..18225969,5	MCF-7	breast:
5	chr11:18173467..18175393-chr11:18177019..18179182,2	MCF-7	breast:
6	chr11:18192652..18193394-chr11:18672481..18673351,2	K562	blood:
7	chr11:18137193..18137763-chr11:18192627..18193399,2	MCF-7	breast:
8	chr11:18152566..18154757-chr11:18415660..18417661,2	K562	blood:
9	chr11:18137092..18139128-chr11:18156082..18158829,2	K562	blood:
10	chr11:18158132..18160556-chr11:18162021..18163694,2	K562	blood:
11	chr11:18193078..18193637-chr11:18785527..18786047,2	K562	blood:
12	chr11:18013193..18013909-chr11:18166278..18166794,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRGPRX3-2	chr11:18174824-18175802	NONHSAT018264

No data

Variant related genes	Relation type
MRGPRX3	TF binding region
ENSG00000221037	TF binding region
MRGPRX4	TF binding region
SAA3P	TF binding region
ENSG00000254857	TF binding region
MRGPRX3	CpG island
ENSG00000221037	CpG island
MRGPRX4	CpG island
SAA3P	CpG island
ENSG00000254857	CpG island
ENSG00000166787	chromatin interactions
ENSG00000254857	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000255254	chromatin interactions
ENSG00000166788	chromatin interactions

Extended variants
information (count: 1606 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1606 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2468847	chr11:18138666-18138667	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2468846	chr11:18138684-18138685	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs34232320	chr11:18138706-18138707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576736246	chr11:18138823-18138824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537449056	chr11:18138837-18138838	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs142681429	chr11:18138860-18138861	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs574496544	chr11:18138863-18138864	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs542807005	chr11:18138870-18138871	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs554778851	chr11:18138871-18138872	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs367569116	chr11:18138879-18138880	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs573181777	chr11:18138911-18138912	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs10741736	chr11:18138935-18138936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs565456739	chr11:18138994-18138995	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186852970	chr11:18139000-18139001	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544283651	chr11:18139005-18139006	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191372214	chr11:18139007-18139008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562759944	chr11:18139059-18139060	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs2445154	chr11:18139115-18139116	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs553323790	chr11:18139156-18139157	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2445153	chr11:18139165-18139166	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs183512126	chr11:18139167-18139168	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566642808	chr11:18139185-18139186	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs377396325	chr11:18139207-18139208	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs578105534	chr11:18139224-18139225	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112524668	chr11:18139236-18139237	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538827762	chr11:18139242-18139243	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs80169981	chr11:18139252-18139253	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs78880048	chr11:18139257-18139258	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs555929161	chr11:18139274-18139275	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs5790018	chr11:18139276-18139277	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs57920488	chr11:18139281-18139282	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs189460214	chr11:18139287-18139288	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs535203860	chr11:18139296-18139297	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs553474812	chr11:18139301-18139302	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs368629768	chr11:18139335-18139336	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs193060392	chr11:18139400-18139401	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559159054	chr11:18139407-18139408	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577507478	chr11:18139445-18139446	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185485180	chr11:18139446-18139447	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs562769798	chr11:18139447-18139448	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs189961946	chr11:18139463-18139464	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372092731	chr11:18139464-18139465	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs542307261	chr11:18139487-18139488	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560574652	chr11:18139488-18139489	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs144036011	chr11:18139544-18139545	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs552132163	chr11:18139580-18139581	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs181639644	chr11:18139600-18139601	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs113305803	chr11:18139755-18139756	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555192787	chr11:18139764-18139765	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs549730220	chr11:18139765-18139766	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18129000-18139000	Weak transcription	Right Atrium	heart
2	chr11:18136600-18141600	Enhancers	HepG2	liver
3	chr11:18136800-18139800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:18136800-18141600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:18137400-18141600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:18138200-18140200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:18138400-18139200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:18139000-18139600	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr11:18139200-18139600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:18139200-18140000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr11:18141600-18142800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:18141600-18143600	Weak transcription	HepG2	liver
13	chr11:18141600-18143800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr11:18142800-18144200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr11:18143600-18144200	Enhancers	HepG2	liver
16	chr11:18143800-18144000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr11:18150200-18150400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:18150400-18156200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:18151800-18154200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:18152400-18154600	Enhancers	HepG2	liver
21	chr11:18153800-18154000	Enhancers	HMEC	breast
22	chr11:18153800-18154600	Enhancers	NHEK	skin
23	chr11:18153800-18155000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:18153800-18155600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr11:18154000-18154200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr11:18154000-18154600	Flanking Active TSS	HMEC	breast
27	chr11:18154200-18154400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr11:18154200-18156800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr11:18154400-18154600	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr11:18154400-18155000	Enhancers	Esophagus	oesophagus
31	chr11:18154600-18155400	Enhancers	HMEC	breast
32	chr11:18154600-18155600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
33	chr11:18154600-18156000	Weak transcription	NHEK	skin
34	chr11:18155000-18156000	Weak transcription	Esophagus	oesophagus
35	chr11:18155600-18156400	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr11:18156000-18156200	Enhancers	NHEK	skin
37	chr11:18156200-18156400	Enhancers	Esophagus	oesophagus
38	chr11:18156200-18156600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr11:18156200-18156800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr11:18156200-18157000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr11:18156200-18157400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr11:18156200-18157400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr11:18156400-18157000	Enhancers	H9 Cell Line	embryonic stem cell
44	chr11:18156400-18157000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr11:18156400-18161200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr11:18156600-18157000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr11:18156800-18157200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:18156800-18157400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr11:18156800-18157400	Enhancers	HepG2	liver
50	chr11:18157200-18165600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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