Variant report

Variant	nsv1036474
Chromosome Location	chr11:15181521-15209506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:62 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:15201733-15201966	GM12878	blood:	n/a	n/a
2	BATF	chr11:15201769-15202026	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:15206534-15206918	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:15206616-15206916	A549	lung:	n/a	n/a
5	CEBPB	chr11:15184725-15185053	IMR90	lung:	n/a	n/a
6	CEBPB	chr11:15206613-15206932	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:15206592-15206844	HepG2	liver:	n/a	n/a
8	CHD2	chr11:15182007-15182113	GM12878	blood:	n/a	n/a
9	CTCF	chr11:15181520-15181670	GM12865	blood:	n/a	n/a
10	CTCF	chr11:15182440-15182590	NHDF-neo	bronchial:	n/a	n/a
11	CTCF	chr11:15204619-15204685	Spleen_OC	spleen:	n/a	n/a
12	E2F4	chr11:15197521-15197758	MCF10A-Er-Src	breast:	n/a	chr11:15197694-15197703 chr11:15197654-15197666
13	E2F4	chr11:15183338-15183475	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr11:15185598-15185830	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr11:15193583-15193728	MCF10A-Er-Src	breast:	n/a	chr11:15193713-15193723 chr11:15193714-15193722 chr11:15193713-15193723 chr11:15193712-15193724
16	FOS	chr11:15206586-15206964	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr11:15206544-15206943	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr11:15206612-15206953	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr11:15206581-15206968	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr11:15191383-15192411	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr11:15191756-15191938	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr11:15196062-15196300	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr11:15196018-15196387	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr11:15196038-15196335	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr11:15196023-15196381	MCF10A-Er-Src	breast:	n/a	n/a
26	FOXA1	chr11:15187530-15187674	T-47D	breast:	n/a	n/a
27	GATA2	chr11:15193475-15193811	SH-SY5Y	brain:	n/a	chr11:15193712-15193721
28	GATA3	chr11:15200440-15200992	SK-N-SH	brain:	n/a	n/a
29	GATA3	chr11:15193365-15193851	SH-SY5Y	brain:	n/a	chr11:15193712-15193721
30	KAP1	chr11:15191821-15192123	U2OS	brain:	n/a	n/a
31	MAFK	chr11:15209119-15209486	IMR90	lung:	n/a	chr11:15209271-15209291
32	MAFK	chr11:15207281-15207372	HepG2	liver:	n/a	n/a
33	MAFK	chr11:15209115-15209372	HepG2	liver:	n/a	chr11:15209271-15209291
34	MAX	chr11:15195794-15195851	NB4	blood:	n/a	n/a
35	MAZ	chr11:15199948-15199951	Hela-S3	cervix:	n/a	n/a
36	MAZ	chr11:15188865-15188878	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr11:15187756-15187939	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr11:15193533-15194048	H1-neurons	neurons:	n/a	n/a
39	POLR2A	chr11:15208152-15208349	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr11:15196148-15196210	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr11:15197520-15197564	A549	lung:	n/a	n/a
42	POLR2A	chr11:15184437-15184472	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr11:15197575-15197602	A549	lung:	n/a	n/a
44	POLR2A	chr11:15197464-15197498	A549	lung:	n/a	n/a
45	POLR2A	chr11:15190116-15190171	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr11:15192693-15192820	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr11:15206624-15206658	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr11:15194970-15195059	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr11:15182515-15182699	MCF10A-Er-Src	breast:	n/a	n/a
50	SPI1	chr11:15181744-15182029	HL-60	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:15200692-15200742	HIPEpiC	eye:	n/a
2	chr11:15200692-15200742	GM12878	blood:	n/a
3	chr11:15200692-15200742	Hela-S3	cervix:	n/a
4	chr11:15200692-15200742	HUVEC	blood vessel:	n/a
5	chr11:15200692-15200742	HCPEpiC	choroid plexus:	n/a
6	chr11:15200692-15200742	HAEpiC	amniotic membrane:	n/a
7	chr11:15200692-15200742	SKMC	muscle:	n/a
8	chr11:15200692-15200742	NHBE	bronchial:	n/a
9	chr11:15200692-15200742	SK-N-MC	brain:	n/a
10	chr11:15200692-15200742	SK-N-SH_RA	brain:	n/a
11	chr11:15200692-15200742	GM06990	blood:	n/a
12	chr11:15200692-15200742	CMK	blood:	n/a
13	chr11:15200692-15200742	T-47D	breast:	n/a
14	chr11:15200692-15200742	ECC-1	luminal epithelium:	n/a
15	chr11:15200692-15200742	AG04449	skin:	fetal
16	chr11:15200692-15200742	GM12892	blood:	n/a
17	chr11:15200692-15200742	Jurkat	blood:	n/a
18	chr11:15200692-15200742	HL-60	blood:	n/a
19	chr11:15200692-15200742	SK-N-SH	brain:	n/a
20	chr11:15200692-15200742	PrEC	prostate:	n/a
21	chr11:15200692-15200742	AG09309	skin:	n/a
22	chr11:15200692-15200742	AG10803	skin:	n/a
23	chr11:15200692-15200742	H1-hESC	embryonic stem cell:	embryo
24	chr11:15200692-15200742	HNPCEpiC	eye:	n/a
25	chr11:15200692-15200742	HCT-116	colon:	n/a
26	chr11:15200692-15200742	ProgFib	skin:	n/a
27	chr11:15200692-15200742	HEK293	kidney:	embryo
28	chr11:15200692-15200742	U87	brain:	n/a
29	chr11:15200692-15200742	K562	blood:	n/a
30	chr11:15200692-15200742	HCF	heart:	n/a
31	chr11:15200692-15200742	AoSMC	blood vessel:	n/a
32	chr11:15200692-15200742	PFSK-1	brain:	n/a
33	chr11:15200692-15200742	MCF10A-Er-Src	breast:	n/a
34	chr11:15200692-15200742	BE2_C	brain:	n/a
35	chr11:15200692-15200742	HEEpiC	esophagus:	n/a
36	chr11:15200692-15200742	MCF-7	breast:	n/a
37	chr11:15200692-15200742	IMR90	lung:	fetal
38	chr11:15200692-15200742	HCM	heart:	n/a
39	chr11:15200692-15200742	RPTEC	kidney:	n/a
40	chr11:15200692-15200742	HRCEpiC	kidney:	n/a
41	chr11:15200692-15200742	HRPEpiC	eye:	n/a
42	chr11:15200692-15200742	NHDF-neo	bronchial:	n/a
43	chr11:15200692-15200742	ovcar-3	ovarian:	n/a
44	chr11:15200692-15200742	HepG2	liver:	n/a
45	chr11:15200692-15200742	AG04450	lung:	fetal
46	chr11:15200692-15200742	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:15200692-15200742	GM19239	blood:	n/a
48	chr11:15200692-15200742	NH-A	brain:	n/a
49	chr11:15200692-15200742	SAEC	small airway:	n/a
50	chr11:15200692-15200742	A549	lung:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:15186678..15192407-chr11:15194914..15199255,7	K562	blood:
2	chr11:15174454..15176169-chr11:15182316..15184921,2	K562	blood:
3	chr11:15208080..15209726-chr11:15210862..15213085,2	K562	blood:
4	chr11:15203716..15205826-chr11:15210080..15213068,2	K562	blood:
5	chr11:15122380..15123325-chr11:15180400..15181564,9	MCF-7	breast:
6	chr11:15186678..15192407-chr11:15194914..15199255,7	K562	blood:
7	chr11:15201953..15202711-chrX:99179927..99180588,2	MCF-7	breast:

No data

Variant related genes	Relation type
INSC	TF binding region
INSC	CpG island

Extended variants
information (count: 1133 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1133 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7109292	chr11:15181521-15181522	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553986685	chr11:15181522-15181523	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572459441	chr11:15181530-15181531	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs56391143	chr11:15181535-15181536	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147227404	chr11:15181544-15181545	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12293568	chr11:15181589-15181590	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1714344	chr11:15181614-15181615	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs111456677	chr11:15181648-15181649	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562551460	chr11:15181650-15181651	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200763957	chr11:15181652-15181653	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1792571	chr11:15181696-15181697	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs539633889	chr11:15181706-15181707	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1792570	chr11:15181708-15181709	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs1714343	chr11:15181718-15181719	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs553238107	chr11:15181782-15181783	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140585857	chr11:15181785-15181786	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1792555	chr11:15181791-15181792	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs114615029	chr11:15181795-15181796	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183943056	chr11:15181819-15181820	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550055784	chr11:15181824-15181825	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568699871	chr11:15181841-15181842	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79814533	chr11:15181859-15181860	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535487576	chr11:15181895-15181896	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144662731	chr11:15181908-15181909	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566059116	chr11:15181915-15181916	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144672763	chr11:15181937-15181938	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558816483	chr11:15181948-15181949	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374999052	chr11:15181965-15181966	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142872410	chr11:15182017-15182018	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556192986	chr11:15182144-15182145	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75881439	chr11:15182158-15182159	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541481206	chr11:15182204-15182205	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560059906	chr11:15182225-15182226	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151055346	chr11:15182281-15182282	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12275048	chr11:15182292-15182293	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs564382756	chr11:15182304-15182305	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575696275	chr11:15182346-15182347	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531776412	chr11:15182442-15182443	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543951411	chr11:15182460-15182461	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4370917	chr11:15182465-15182466	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562269962	chr11:15182472-15182473	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4612784	chr11:15182577-15182578	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188544809	chr11:15182592-15182593	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1109326	chr11:15182597-15182598	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs1109327	chr11:15182662-15182663	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533514003	chr11:15182683-15182684	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551896673	chr11:15182709-15182710	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368911208	chr11:15182719-15182720	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141357682	chr11:15182726-15182727	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1109328	chr11:15182729-15182730	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15167200-15182800	Weak transcription	Fetal Intestine Small	intestine
2	chr11:15178200-15183600	Enhancers	NHLF	lung
3	chr11:15179200-15183000	Weak transcription	Fetal Stomach	stomach
4	chr11:15179600-15181800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:15180200-15181600	Weak transcription	Fetal Lung	lung
6	chr11:15180400-15184400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:15180800-15181800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:15180800-15182000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr11:15180800-15182200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:15180800-15182800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:15180800-15191400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr11:15181400-15184400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:15181600-15185200	Enhancers	Fetal Lung	lung
14	chr11:15181800-15182000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:15181800-15182400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr11:15182200-15187000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:15182400-15182600	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr11:15182400-15182800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr11:15182800-15183400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:15182800-15183600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr11:15183000-15183200	Enhancers	Fetal Stomach	stomach
22	chr11:15183200-15183600	Weak transcription	Fetal Stomach	stomach
23	chr11:15183400-15185200	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr11:15183400-15191200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:15183600-15184000	Enhancers	Fetal Stomach	stomach
26	chr11:15183600-15191400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:15184400-15185200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:15184400-15190600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr11:15184600-15185400	Enhancers	Primary B cells from cord blood	blood
30	chr11:15184800-15186200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr11:15184800-15188400	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr11:15185200-15185600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr11:15185600-15188800	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr11:15186200-15187800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr11:15187000-15188800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:15187400-15188600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:15187600-15188400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:15187800-15188400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr11:15188400-15191400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr11:15188800-15191400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:15188800-15195400	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr11:15190600-15190800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:15190800-15191200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr11:15191000-15201000	Weak transcription	Aorta	Aorta
45	chr11:15191200-15192200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr11:15191200-15194200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:15191400-15192000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:15191400-15192200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:15191400-15192200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr11:15191400-15192200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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