Variant report

Variant	nsv897009
Chromosome Location	chr11:15166201-15181614
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	CEBPB	chr11:15166029-15166287	HepG2	liver:	n/a	chr11:15166188-15166199 chr11:15166187-15166198
2	CEBPB	chr11:15171686-15171977	A549	lung:	n/a	chr11:15171832-15171843
3	CEBPB	chr11:15171677-15171889	H1-hESC	embryonic stem cell:	n/a	chr11:15171832-15171843
4	CEBPB	chr11:15171662-15171989	K562	blood:	n/a	chr11:15171832-15171843
5	CEBPB	chr11:15171652-15172010	HepG2	liver:	n/a	chr11:15171832-15171843
6	CEBPB	chr11:15171670-15171995	IMR90	lung:	n/a	chr11:15171832-15171843
7	CTCF	chr11:15180728-15180894	MCF-7	breast:	n/a	chr11:15180842-15180850
8	CTCF	chr11:15180820-15180970	BE2_C	brain:	n/a	chr11:15180842-15180850
9	CTCF	chr11:15180734-15180903	MCF-7	breast:	n/a	chr11:15180842-15180850
10	CTCF	chr11:15180820-15180970	GM12869	blood:	n/a	chr11:15180842-15180850
11	CTCF	chr11:15180840-15180990	WI-38	lung:	n/a	chr11:15180842-15180850
12	CTCF	chr11:15180648-15180887	K562	blood:	n/a	chr11:15180842-15180850
13	CTCF	chr11:15180710-15181003	GM12878	blood:	n/a	chr11:15180842-15180850
14	CTCF	chr11:15180736-15180975	Spleen_OC	spleen:	n/a	chr11:15180842-15180850
15	CTCF	chr11:15180780-15180930	HEEpiC	esophagus:	n/a	chr11:15180842-15180850
16	CTCF	chr11:15180780-15180930	AG10803	skin:	n/a	chr11:15180842-15180850
17	CTCF	chr11:15180780-15180930	GM06990	blood:	n/a	chr11:15180842-15180850
18	CTCF	chr11:15180760-15180910	AG04449	skin:	n/a	chr11:15180842-15180850
19	CTCF	chr11:15181080-15181230	AG04449	skin:	n/a	n/a
20	CTCF	chr11:15180780-15180930	GM12865	blood:	n/a	chr11:15180842-15180850
21	CTCF	chr11:15180601-15181046	IMR90	lung:	n/a	chr11:15180842-15180850 chr11:15180618-15180631
22	CTCF	chr11:15180780-15180930	HPAF	blood vessel:	n/a	chr11:15180842-15180850
23	CTCF	chr11:15180800-15180950	HA-sp	spinal cord:	n/a	chr11:15180842-15180850
24	CTCF	chr11:15180780-15180930	HUVEC	blood vessel:	n/a	chr11:15180842-15180850
25	CTCF	chr11:15180760-15180910	MCF-7	breast:	n/a	chr11:15180842-15180850
26	CTCF	chr11:15180780-15180930	GM12875	blood:	n/a	chr11:15180842-15180850
27	CTCF	chr11:15180760-15180910	HCM	heart:	n/a	chr11:15180842-15180850
28	CTCF	chr11:15180737-15180915	A549	lung:	n/a	chr11:15180842-15180850
29	CTCF	chr11:15180780-15180930	HAc	cerebellar:	n/a	chr11:15180842-15180850
30	CTCF	chr11:15180780-15180930	HCPEpiC	choroid plexus:	n/a	chr11:15180842-15180850
31	CTCF	chr11:15180740-15180960	GM10266	blood:	n/a	chr11:15180842-15180850
32	CTCF	chr11:15180800-15180950	HL-60	blood:	n/a	chr11:15180842-15180850
33	CTCF	chr11:15180760-15180910	SK-N-SH_RA	brain:	n/a	chr11:15180842-15180850
34	CTCF	chr11:15180780-15180930	HRPEpiC	eye:	n/a	chr11:15180842-15180850
35	CTCF	chr11:15180800-15180950	GM12873	blood:	n/a	chr11:15180842-15180850
36	CTCF	chr11:15180706-15180921	GM12892	blood:	n/a	chr11:15180842-15180850
37	CTCF	chr11:15180767-15180919	GM19239	blood:	n/a	chr11:15180842-15180850
38	CTCF	chr11:15180840-15180990	GM12878	blood:	n/a	chr11:15180842-15180850
39	CTCF	chr11:15180709-15180923	GM19238	blood:	n/a	chr11:15180842-15180850
40	CTCF	chr11:15180712-15181007	K562	blood:	n/a	chr11:15180842-15180850
41	CTCF	chr11:15180760-15180910	NHEK	skin:	n/a	chr11:15180842-15180850
42	CTCF	chr11:15180740-15180890	GM12801	blood:	n/a	chr11:15180842-15180850
43	CTCF	chr11:15180668-15181033	K562	blood:	n/a	chr11:15180842-15180850
44	CTCF	chr11:15180800-15180950	AoAF	blood vessel:	n/a	chr11:15180842-15180850
45	CTCF	chr11:15180610-15181118	HCT-116	colon:	n/a	chr11:15180842-15180850 chr11:15180618-15180631
46	CTCF	chr11:15180727-15180943	Fibrobl	skin:	n/a	chr11:15180842-15180850
47	CTCF	chr11:15180780-15180930	GM12870	blood:	n/a	chr11:15180842-15180850
48	CTCF	chr11:15180590-15181073	MCF-7	breast:	n/a	chr11:15180842-15180850 chr11:15180618-15180631
49	CTCF	chr11:15180744-15180940	HepG2	liver:	n/a	chr11:15180842-15180850
50	CTCF	chr11:15180740-15180890	GM12867	blood:	n/a	chr11:15180842-15180850

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:15180922-15180972	HMEC	breast:	n/a
2	chr11:15180922-15180972	SKMC	muscle:	n/a
3	chr11:15169792-15169842	HCM	heart:	n/a
4	chr11:15169792-15169842	ECC-1	luminal epithelium:	n/a
5	chr11:15180922-15180972	HepG2	liver:	n/a
6	chr11:15169792-15169842	AG04449	skin:	fetal
7	chr11:15169792-15169842	HL-60	blood:	n/a
8	chr11:15180922-15180972	NHBE	bronchial:	n/a
9	chr11:15180922-15180972	AG09309	skin:	n/a
10	chr11:15180922-15180972	HEEpiC	esophagus:	n/a
11	chr11:15180922-15180972	A549	lung:	n/a
12	chr11:15169792-15169842	SK-N-SH	brain:	n/a
13	chr11:15180922-15180972	PFSK-1	brain:	n/a
14	chr11:15169792-15169842	LNCaP	prostate:	n/a
15	chr11:15180922-15180972	GM06990	blood:	n/a
16	chr11:15180922-15180972	AG10803	skin:	n/a
17	chr11:15180922-15180972	HUVEC	blood vessel:	n/a
18	chr11:15169792-15169842	NH-A	brain:	n/a
19	chr11:15180922-15180972	NB4	blood:	n/a
20	chr11:15169792-15169842	NHBE	bronchial:	n/a
21	chr11:15169792-15169842	HCT-116	colon:	n/a
22	chr11:15169792-15169842	BJ	skin:	n/a
23	chr11:15180922-15180972	HCM	heart:	n/a
24	chr11:15169792-15169842	SK-N-SH_RA	brain:	n/a
25	chr11:15169792-15169842	SKMC	muscle:	n/a
26	chr11:15180922-15180972	GM19239	blood:	n/a
27	chr11:15169792-15169842	NHDF-neo	bronchial:	n/a
28	chr11:15169792-15169842	AG04450	lung:	fetal
29	chr11:15180922-15180972	HCF	heart:	n/a
30	chr11:15180922-15180972	IMR90	lung:	fetal
31	chr11:15169792-15169842	GM12892	blood:	n/a
32	chr11:15180922-15180972	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:15169792-15169842	AG09309	skin:	n/a
34	chr11:15180922-15180972	AG04450	lung:	fetal
35	chr11:15169792-15169842	HNPCEpiC	eye:	n/a
36	chr11:15180922-15180972	HIPEpiC	eye:	n/a
37	chr11:15180922-15180972	NH-A	brain:	n/a
38	chr11:15180922-15180972	SAEC	small airway:	n/a
39	chr11:15169792-15169842	U87	brain:	n/a
40	chr11:15180922-15180972	HCT-116	colon:	n/a
41	chr11:15169792-15169842	CMK	blood:	n/a
42	chr11:15180922-15180972	HL-60	blood:	n/a
43	chr11:15169792-15169842	PANC-1	pancreas:	n/a
44	chr11:15169792-15169842	HUVEC	blood vessel:	n/a
45	chr11:15180922-15180972	NT2-D1	testis:	n/a
46	chr11:15180922-15180972	ovcar-3	ovarian:	n/a
47	chr11:15180922-15180972	PrEC	prostate:	n/a
48	chr11:15180922-15180972	HEK293	kidney:	embryo
49	chr11:15169792-15169842	HCPEpiC	choroid plexus:	n/a
50	chr11:15169792-15169842	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:15096186..15096707-chr11:15180542..15181331,2	MCF-7	breast:
2	chr11:15170324..15172702-chr11:15174630..15177617,2	K562	blood:
3	chr11:15122380..15123325-chr11:15180400..15181564,9	MCF-7	breast:
4	chr11:15174454..15176169-chr11:15182316..15184921,2	K562	blood:
5	chr11:15122445..15123286-chr11:15180348..15181279,4	MCF-7	breast:
6	chr11:15162720..15165648-chr11:15176899..15178406,2	K562	blood:

Variant related genes	Relation type
INSC	TF binding region
INSC	CpG island
ENSG00000188487	chromatin interactions

Extended variants
information (count: 627 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12226609	chr11:15166201-15166202	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574863107	chr11:15166208-15166209	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs111298701	chr11:15166241-15166242	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs540677242	chr11:15166267-15166268	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs537476290	chr11:15166305-15166306	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs78441666	chr11:15166313-15166314	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs543745920	chr11:15166324-15166325	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs187166726	chr11:15166348-15166349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554292178	chr11:15166349-15166350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537959891	chr11:15166360-15166361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373612822	chr11:15166361-15166362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34924065	chr11:15166363-15166364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78808538	chr11:15166371-15166372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558895624	chr11:15166382-15166383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566220835	chr11:15166392-15166393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139539376	chr11:15166452-15166453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544737673	chr11:15166495-15166496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577257169	chr11:15166504-15166505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149695724	chr11:15166529-15166530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531011999	chr11:15166544-15166545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145496929	chr11:15166566-15166567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140348155	chr11:15166575-15166576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75975118	chr11:15166626-15166627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547018101	chr11:15166675-15166676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571625043	chr11:15166718-15166719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529633598	chr11:15166777-15166778	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs550793455	chr11:15166782-15166783	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs569859581	chr11:15166788-15166789	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs34025225	chr11:15166803-15166804	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs543308397	chr11:15166817-15166818	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533613105	chr11:15166819-15166820	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs536828518	chr11:15166865-15166866	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs555505487	chr11:15166895-15166896	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563108961	chr11:15166967-15166968	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs191274489	chr11:15166988-15166989	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs144087622	chr11:15167007-15167008	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs184469919	chr11:15167039-15167040	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs116603767	chr11:15167047-15167048	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs76322194	chr11:15167167-15167168	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141110567	chr11:15167275-15167276	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs34782327	chr11:15167298-15167299	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs373694494	chr11:15167345-15167346	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs143258084	chr11:15167350-15167351	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs542871750	chr11:15167392-15167393	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs190581951	chr11:15167401-15167402	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs551897777	chr11:15167414-15167415	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs117338709	chr11:15167441-15167442	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs527739570	chr11:15167459-15167460	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs148301019	chr11:15167478-15167479	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs547496674	chr11:15167487-15167488	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Myelofibrosis	22110671	CNVD
Cancer	24489367	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Neuroblastoma	19435921	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15149600-15166600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:15161600-15172600	Weak transcription	Pancreas	Pancrea
3	chr11:15164800-15167400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:15164800-15168000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr11:15165200-15167800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:15165200-15167800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:15165200-15168000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr11:15165200-15169400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:15165400-15167000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr11:15165800-15167600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:15166000-15166400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:15166000-15167600	Enhancers	Liver	Liver
13	chr11:15166200-15166400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:15166200-15168000	Enhancers	Fetal Intestine Large	intestine
15	chr11:15166200-15168400	Enhancers	Colonic Mucosa	Colon
16	chr11:15166400-15168200	Enhancers	Stomach Mucosa	stomach
17	chr11:15166400-15168800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:15166400-15170200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr11:15166400-15170200	Enhancers	Osteobl	bone
20	chr11:15166400-15170400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:15166600-15167600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr11:15166600-15169000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:15166800-15167200	Enhancers	Fetal Intestine Small	intestine
24	chr11:15166800-15167600	Enhancers	Duodenum Mucosa	Duodenum
25	chr11:15166800-15167800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr11:15166800-15168000	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr11:15166800-15168400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr11:15167000-15167200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr11:15167000-15167600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr11:15167000-15167600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:15167000-15167800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr11:15167200-15167400	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr11:15167200-15167600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr11:15167200-15168400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:15167200-15169000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:15167200-15169000	Enhancers	NHDF-Ad	bronchial
37	chr11:15167200-15182800	Weak transcription	Fetal Intestine Small	intestine
38	chr11:15167400-15167600	Enhancers	Brain Substantia Nigra	brain
39	chr11:15167400-15167600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr11:15167400-15168200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:15167400-15168800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:15167600-15168600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr11:15167600-15168800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:15167600-15170400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr11:15167600-15171400	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr11:15167800-15168200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:15167800-15168400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr11:15167800-15168400	Enhancers	NH-A	brain
49	chr11:15167800-15169000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr11:15167800-15180000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links