Variant report

Variant	nsv8787
Chromosome Location	chr11:8954949-8959098
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:206)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:206 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:8956401-8956711	K562	blood:	n/a	n/a
2	ATF2	chr11:8958641-8959164	GM12878	blood:	n/a	n/a
3	ATF2	chr11:8958557-8959209	GM12878	blood:	n/a	n/a
4	BATF	chr11:8958632-8959155	GM12878	blood:	n/a	n/a
5	BCL3	chr11:8958622-8959086	GM12878	blood:	n/a	n/a
6	BCL3	chr11:8958736-8959033	GM12878	blood:	n/a	n/a
7	BCLAF1	chr11:8958629-8959151	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:8955589-8955598	K562	blood:	n/a	n/a
9	BHLHE40	chr11:8958705-8959053	GM12878	blood:	n/a	n/a
10	CEBPB	chr11:8956314-8956816	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:8956342-8956936	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr11:8956363-8956769	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr11:8955599-8955693	Fibrobl	skin:	n/a	n/a
14	CTCF	chr11:8955720-8955870	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr11:8955508-8955781	IMR90	lung:	n/a	n/a
16	CTCF	chr11:8955640-8955790	GM06990	blood:	n/a	n/a
17	CTCF	chr11:8955560-8955710	NHLF	lung:	n/a	n/a
18	CTCF	chr11:8955639-8955677	GM10266	blood:	n/a	n/a
19	CTCF	chr11:8955614-8955684	GM19240	blood:	n/a	n/a
20	CTCF	chr11:8955620-8955770	GM12864	blood:	n/a	n/a
21	CTCF	chr11:8955580-8955730	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr11:8955580-8955730	Caco-2	colon:	n/a	n/a
23	CTCF	chr11:8955600-8955750	GM12865	blood:	n/a	n/a
24	CTCF	chr11:8955560-8955710	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr11:8955600-8955750	AG04450	lung:	n/a	n/a
26	CTCF	chr11:8955560-8955710	HCT-116	colon:	n/a	n/a
27	CTCF	chr11:8955580-8955730	HCT-116	colon:	n/a	n/a
28	CTCF	chr11:8955400-8955550	HFF	foreskin:	n/a	n/a
29	CTCF	chr11:8955580-8955730	RPTEC	kidney:	n/a	n/a
30	CTCF	chr11:8955440-8955590	GM12873	blood:	n/a	n/a
31	CTCF	chr11:8955621-8955663	Medullo	brain:	n/a	n/a
32	CTCF	chr11:8955560-8955710	Caco-2	colon:	n/a	n/a
33	CTCF	chr11:8955600-8955750	GM12873	blood:	n/a	n/a
34	CTCF	chr11:8955580-8955730	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr11:8955586-8955719	GM12892	blood:	n/a	n/a
36	CTCF	chr11:8955580-8955730	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr11:8955560-8955710	GM12874	blood:	n/a	n/a
38	CTCF	chr11:8955500-8955650	WI-38	lung:	n/a	n/a
39	CTCF	chr11:8955540-8955690	GM12875	blood:	n/a	n/a
40	CTCF	chr11:8955620-8955770	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:8955540-8955690	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr11:8955525-8955875	K562	blood:	n/a	n/a
43	CTCF	chr11:8955600-8955750	HVMF	connective:	n/a	n/a
44	CTCF	chr11:8955600-8955750	HAc	cerebellar:	n/a	n/a
45	CTCF	chr11:8955580-8955730	A549	lung:	n/a	n/a
46	CTCF	chr11:8955560-8955710	K562	blood:	n/a	n/a
47	CTCF	chr11:8955500-8955650	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr11:8955600-8955750	SAEC	small airway:	n/a	n/a
49	CTCF	chr11:8955600-8955750	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr11:8955640-8955790	HPAF	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:8955878-8955928	ECC-1	luminal epithelium:	n/a
2	chr11:8955878-8955928	NT2-D1	testis:	n/a
3	chr11:8955884-8955934	AG04449	skin:	fetal
4	chr11:8955878-8955928	BJ	skin:	n/a
5	chr11:8955884-8955934	IMR90	lung:	fetal
6	chr11:8955878-8955928	PFSK-1	brain:	n/a
7	chr11:8955884-8955934	GM19239	blood:	n/a
8	chr11:8955884-8955934	Jurkat	blood:	n/a
9	chr11:8955878-8955928	Hepatocyte	liver:	n/a
10	chr11:8955884-8955934	HEK293	kidney:	embryo
11	chr11:8955878-8955928	AG04450	lung:	fetal
12	chr11:8955878-8955928	HUVEC	blood vessel:	n/a
13	chr11:8955878-8955928	AG04449	skin:	fetal
14	chr11:8955884-8955934	NHDF-neo	bronchial:	n/a
15	chr11:8955878-8955928	HAEpiC	amniotic membrane:	n/a
16	chr11:8955884-8955934	AG09319	gingival:	n/a
17	chr11:8955878-8955928	HRPEpiC	eye:	n/a
18	chr11:8955884-8955934	HepG2	liver:	n/a
19	chr11:8955884-8955934	SK-N-SH_RA	brain:	n/a
20	chr11:8955884-8955934	HRE	kidney:	n/a
21	chr11:8955878-8955928	PANC-1	pancreas:	n/a
22	chr11:8955878-8955928	HepG2	liver:	n/a
23	chr11:8955884-8955934	AG09309	skin:	n/a
24	chr11:8955884-8955934	SK-N-SH	brain:	n/a
25	chr11:8955884-8955934	MCF10A-Er-Src	breast:	n/a
26	chr11:8955878-8955928	Caco-2	colon:	n/a
27	chr11:8955878-8955928	SK-N-MC	brain:	n/a
28	chr11:8955878-8955928	HL-60	blood:	n/a
29	chr11:8955884-8955934	H1-hESC	embryonic stem cell:	embryo
30	chr11:8955884-8955934	ovcar-3	ovarian:	n/a
31	chr11:8955884-8955934	Hepatocyte	liver:	n/a
32	chr11:8955878-8955928	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:8955884-8955934	HIPEpiC	eye:	n/a
34	chr11:8955884-8955934	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:8955884-8955934	HCPEpiC	choroid plexus:	n/a
36	chr11:8955878-8955928	MCF-7	breast:	n/a
37	chr11:8955878-8955928	HCF	heart:	n/a
38	chr11:8955878-8955928	HIPEpiC	eye:	n/a
39	chr11:8955884-8955934	HCT-116	colon:	n/a
40	chr11:8955884-8955934	HNPCEpiC	eye:	n/a
41	chr11:8955878-8955928	HRCEpiC	kidney:	n/a
42	chr11:8955878-8955928	GM12892	blood:	n/a
43	chr11:8955884-8955934	RPTEC	kidney:	n/a
44	chr11:8955884-8955934	SKMC	muscle:	n/a
45	chr11:8955878-8955928	H1-hESC	embryonic stem cell:	embryo
46	chr11:8955884-8955934	AoSMC	blood vessel:	n/a
47	chr11:8955884-8955934	A549	lung:	n/a
48	chr11:8955884-8955934	PrEC	prostate:	n/a
49	chr11:8955884-8955934	HAEpiC	amniotic membrane:	n/a
50	chr11:8955878-8955928	SAEC	small airway:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:8955484..8958608-chr11:8984431..8986354,3	K562	blood:
2	chr11:8955859..8958646-chr11:8984465..8986441,3	MCF-7	breast:
3	chr11:8957976..8959649-chr11:8961738..8963442,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKIP1-6	chr11:8956716-8957048	NONHSAT017892
2	lnc-AKIP1-6	chr11:8958467-8958768	NONHSAT017892

No data

Variant related genes	Relation type
C11orf16	TF binding region
C11orf16	CpG island
ENSG00000254860	chromatin interactions
ENSG00000175348	chromatin interactions

Extended variants
information (count: 171 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:171 , 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	rs569011633	chr11:8954997-8954998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552184535	chr11:8955044-8955045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537759538	chr11:8955065-8955066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140160733	chr11:8955080-8955081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181655266	chr11:8955106-8955107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371539697	chr11:8955113-8955114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540067403	chr11:8955182-8955183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553573882	chr11:8955210-8955211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370977118	chr11:8955211-8955212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542257628	chr11:8955260-8955261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1109305	chr11:8955272-8955273	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs531867144	chr11:8955286-8955287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150299291	chr11:8955348-8955349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185434419	chr11:8955351-8955352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530480112	chr11:8955366-8955367	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs118188275	chr11:8955408-8955409	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs548042530	chr11:8955440-8955441	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs568006943	chr11:8955452-8955453	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs1109304	chr11:8955455-8955456	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs190258768	chr11:8955487-8955488	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs75720253	chr11:8955492-8955493	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs2653584	chr11:8955496-8955497	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs537720159	chr11:8955584-8955585	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs551242342	chr11:8955588-8955589	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs571244855	chr11:8955589-8955590	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs533731597	chr11:8955599-8955600	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs182485735	chr11:8955770-8955771	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs573606158	chr11:8955780-8955781	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs538766462	chr11:8955802-8955803	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs185767251	chr11:8955835-8955836	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs2742509	chr11:8955854-8955855	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs576126016	chr11:8955879-8955880	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs35639384	chr11:8955906-8955907	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs545049951	chr11:8955908-8955909	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs189887033	chr11:8955911-8955912	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs535643343	chr11:8955912-8955913	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs181046910	chr11:8955921-8955922	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs541640402	chr11:8955951-8955952	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561541124	chr11:8955979-8955980	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs572354143	chr11:8956018-8956019	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs185695625	chr11:8956026-8956027	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs530105672	chr11:8956047-8956048	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs550270822	chr11:8956078-8956079	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs367860381	chr11:8956103-8956104	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs137857523	chr11:8956110-8956111	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs35335581	chr11:8956124-8956125	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs190375851	chr11:8956135-8956136	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs544626193	chr11:8956137-8956138	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs2742508	chr11:8956185-8956186	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs2742507	chr11:8956265-8956266	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8941200-8956200	Weak transcription	K562	blood
2	chr11:8942400-8959000	Weak transcription	Fetal Kidney	kidney
3	chr11:8943800-8969200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr11:8944200-8956400	Weak transcription	HUVEC	blood vessel
5	chr11:8944600-8985000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:8944800-8956400	Weak transcription	Fetal Intestine Large	intestine
7	chr11:8945000-8955000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr11:8945000-8956200	Weak transcription	NH-A	brain
9	chr11:8945200-8956200	Weak transcription	A549	lung
10	chr11:8945800-8974000	Weak transcription	Colon Smooth Muscle	Colon
11	chr11:8946400-8956200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:8947000-8968800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr11:8947000-8977000	Weak transcription	Aorta	Aorta
14	chr11:8947200-8956400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:8947400-8956200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:8947400-8969000	Weak transcription	Thymus	Thymus
17	chr11:8947600-8956200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr11:8947600-8956400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr11:8947600-8969000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr11:8948000-8955600	Weak transcription	NHLF	lung
21	chr11:8948200-8969000	Weak transcription	Fetal Brain Female	brain
22	chr11:8948600-8969200	Weak transcription	Gastric	stomach
23	chr11:8948600-8969200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr11:8951000-8956200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr11:8951200-8956200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:8951200-8974400	Weak transcription	HepG2	liver
27	chr11:8952600-8955200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:8952600-8956200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr11:8952600-8957200	Weak transcription	Spleen	Spleen
30	chr11:8952600-8975800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:8952800-8955200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:8952800-8956200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:8952800-8956200	Weak transcription	HSMM	muscle
34	chr11:8952800-8956200	Weak transcription	Osteobl	bone
35	chr11:8952800-8968600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:8953000-8956200	Weak transcription	NHDF-Ad	bronchial
37	chr11:8953000-8956400	Weak transcription	HSMMtube	muscle
38	chr11:8953400-8955600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr11:8953600-8955400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:8953600-8955800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr11:8953600-8955800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr11:8953800-8955400	Enhancers	Fetal Muscle Trunk	muscle
43	chr11:8954000-8955000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr11:8954000-8955000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr11:8954000-8956400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr11:8954200-8955200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr11:8954200-8956000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr11:8954400-8955200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr11:8954400-8984400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr11:8954600-8955000	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links