Variant report

Variant	nsv818799
Chromosome Location	chr11:15930472-15946803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 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	CEBPB	chr11:15933169-15933533	IMR90	lung:	n/a	n/a
2	CTCF	chr11:15944880-15945030	WERI-Rb-1	eye:	n/a	chr11:15944935-15944948
3	CTCF	chr11:15944800-15944950	HMEC	breast:	n/a	chr11:15944935-15944948
4	CTCF	chr11:15944900-15945050	SK-N-SH_RA	brain:	n/a	chr11:15944935-15944948
5	CTCF	chr11:15944900-15945050	HEEpiC	esophagus:	n/a	chr11:15944935-15944948
6	CTCF	chr11:15944715-15944987	K562	blood:	n/a	chr11:15944935-15944948
7	CTCF	chr11:15944880-15945030	HBMEC	blood vessel:	n/a	chr11:15944935-15944948
8	CTCF	chr11:15940060-15940210	NHEK	skin:	n/a	chr11:15940078-15940086
9	CTCF	chr11:15934900-15935050	HRPEpiC	eye:	n/a	n/a
10	CTCF	chr11:15939888-15939970	Pancreas_OC	pancreas:	n/a	chr11:15939915-15939928
11	CTCF	chr11:15935000-15935150	AG09319	gingival:	n/a	n/a
12	CTCF	chr11:15944787-15945016	K562	blood:	n/a	chr11:15944935-15944948
13	CTCF	chr11:15944786-15945169	K562	blood:	n/a	chr11:15944935-15944948
14	CTCF	chr11:15944900-15945050	SAEC	small airway:	n/a	chr11:15944935-15944948
15	CTCF	chr11:15934920-15935070	BE2_C	brain:	n/a	n/a
16	CTCF	chr11:15934920-15935070	Caco-2	colon:	n/a	n/a
17	CTCF	chr11:15944831-15945064	H1-hESC	embryonic stem cell:	n/a	chr11:15944935-15944948
18	CTCF	chr11:15934909-15935087	NHEK	skin:	n/a	n/a
19	CTCF	chr11:15934980-15935130	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr11:15944780-15944930	BE2_C	brain:	n/a	n/a
21	CTCF	chr11:15944840-15944990	AG04449	skin:	n/a	chr11:15944935-15944948
22	CTCF	chr11:15939916-15939936	K562	blood:	n/a	n/a
23	CTCF	chr11:15934900-15935050	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr11:15944892-15945013	ProgFib	skin:	n/a	chr11:15944935-15944948
25	CTCF	chr11:15944900-15945050	HVMF	connective:	n/a	chr11:15944935-15944948
26	CTCF	chr11:15934880-15935030	AG04449	skin:	n/a	n/a
27	CTCF	chr11:15944820-15944970	HPF	lung:	n/a	chr11:15944935-15944948
28	CTCF	chr11:15944806-15945033	GM12878	blood:	n/a	chr11:15944935-15944948
29	CTCF	chr11:15934880-15935030	MCF-7	breast:	n/a	n/a
30	CTCF	chr11:15935140-15935290	GM12872	blood:	n/a	n/a
31	CTCF	chr11:15935040-15935190	HAc	cerebellar:	n/a	n/a
32	CTCF	chr11:15944900-15945050	BE2_C	brain:	n/a	chr11:15944935-15944948
33	CTCF	chr11:15934967-15935010	MCF-7	breast:	n/a	n/a
34	CTCF	chr11:15934980-15935130	RPTEC	kidney:	n/a	n/a
35	CTCF	chr11:15939854-15939965	LNCaP	prostate:	n/a	chr11:15939915-15939928
36	CTCF	chr11:15934980-15935130	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr11:15934953-15934995	GM12878	blood:	n/a	n/a
38	CTCF	chr11:15944932-15945006	HepG2	liver:	n/a	chr11:15944935-15944948
39	CTCF	chr11:15934961-15935063	MCF-7	breast:	n/a	n/a
40	CTCF	chr11:15944840-15944990	SAEC	small airway:	n/a	chr11:15944935-15944948
41	CTCF	chr11:15934960-15935110	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr11:15939760-15939910	NHEK	skin:	n/a	n/a
43	CTCF	chr11:15944838-15945056	MCF-7	breast:	n/a	chr11:15944935-15944948
44	CTCF	chr11:15934932-15935044	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:15934890-15935160	K562	blood:	n/a	n/a
46	CTCF	chr11:15934848-15935174	IMR90	lung:	n/a	n/a
47	CTCF	chr11:15934933-15935079	K562	blood:	n/a	n/a
48	CTCF	chr11:15944757-15945112	H1-hESC	embryonic stem cell:	n/a	chr11:15944935-15944948
49	CTCF	chr11:15944734-15945149	MCF-7	breast:	n/a	chr11:15944935-15944948
50	CTCF	chr11:15939862-15939977	NHEK	skin:	n/a	chr11:15939915-15939928

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:15933403-15933453	SK-N-MC	brain:	n/a
2	chr11:15933403-15933453	T-47D	breast:	n/a
3	chr11:15933403-15933453	Jurkat	blood:	n/a
4	chr11:15933403-15933453	BJ	skin:	n/a
5	chr11:15933403-15933453	GM19239	blood:	n/a
6	chr11:15933403-15933453	IMR90	lung:	fetal
7	chr11:15933403-15933453	PFSK-1	brain:	n/a
8	chr11:15933403-15933453	Caco-2	colon:	n/a
9	chr11:15933403-15933453	HCPEpiC	choroid plexus:	n/a
10	chr11:15933403-15933453	SAEC	small airway:	n/a
11	chr11:15933403-15933453	Hepatocyte	liver:	n/a
12	chr11:15933403-15933453	HRPEpiC	eye:	n/a
13	chr11:15933403-15933453	AG09309	skin:	n/a
14	chr11:15933403-15933453	GM12878	blood:	n/a
15	chr11:15933403-15933453	SK-N-SH	brain:	n/a
16	chr11:15933403-15933453	AG04450	lung:	fetal
17	chr11:15933403-15933453	HL-60	blood:	n/a
18	chr11:15933403-15933453	NHBE	bronchial:	n/a
19	chr11:15933403-15933453	GM06990	blood:	n/a
20	chr11:15933403-15933453	HRE	kidney:	n/a
21	chr11:15933403-15933453	HAEpiC	amniotic membrane:	n/a
22	chr11:15933403-15933453	NT2-D1	testis:	n/a
23	chr11:15933403-15933453	GM12891	blood:	n/a
24	chr11:15933403-15933453	NHDF-neo	bronchial:	n/a
25	chr11:15933403-15933453	HUVEC	blood vessel:	n/a
26	chr11:15933403-15933453	HNPCEpiC	eye:	n/a
27	chr11:15933403-15933453	GM12892	blood:	n/a
28	chr11:15933403-15933453	PANC-1	pancreas:	n/a
29	chr11:15933403-15933453	ECC-1	luminal epithelium:	n/a
30	chr11:15933403-15933453	HEK293	kidney:	embryo
31	chr11:15933403-15933453	RPTEC	kidney:	n/a
32	chr11:15933403-15933453	AG09319	gingival:	n/a
33	chr11:15933403-15933453	Hela-S3	cervix:	n/a
34	chr11:15933403-15933453	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:15933403-15933453	HCF	heart:	n/a
36	chr11:15933403-15933453	AG04449	skin:	fetal
37	chr11:15933403-15933453	AG10803	skin:	n/a
38	chr11:15933403-15933453	SK-N-SH_RA	brain:	n/a
39	chr11:15933403-15933453	AoSMC	blood vessel:	n/a
40	chr11:15933403-15933453	MCF10A-Er-Src	breast:	n/a
41	chr11:15933403-15933453	MCF-7	breast:	n/a
42	chr11:15933403-15933453	SKMC	muscle:	n/a
43	chr11:15933403-15933453	A549	lung:	n/a
44	chr11:15933403-15933453	PrEC	prostate:	n/a
45	chr11:15933403-15933453	HRCEpiC	kidney:	n/a
46	chr11:15933403-15933453	NH-A	brain:	n/a
47	chr11:15933403-15933453	ovcar-3	ovarian:	n/a
48	chr11:15933403-15933453	LNCaP	prostate:	n/a
49	chr11:15933403-15933453	K562	blood:	n/a
50	chr11:15933403-15933453	H1-hESC	embryonic stem cell:	embryo

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:15924300..15926457-chr11:15932975..15935932,2	K562	blood:
2	chr11:15905811..15907638-chr11:15937488..15939318,2	K562	blood:
3	chr11:15932707..15934813-chr11:15985160..15987558,2	MCF-7	breast:
4	chr11:15927726..15929606-chr11:15934881..15937502,2	K562	blood:
5	chr11:15873733..15874420-chr11:15944016..15945522,4	MCF-7	breast:
6	chr11:15944097..15946118-chr11:15948040..15950175,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INSC-3	chr11:15933277-15933430	XLOC_009075
2	lnc-INSC-3	chr11:15932503-15932616	ENSG00000254661
3	lnc-INSC-3	chr11:15933328-15933430	ENSG00000254661
4	lnc-INSC-3	chr11:15933329-15933430	NONHSAT018165
5	lnc-SOX6-1	chr11:15933334-15933620	XLOC_009382
6	lnc-INSC-3	chr11:15933323-15933430	ENSG00000254661
7	lnc-INSC-3	chr11:15939848-15940087	ENSG00000254661
8	lnc-INSC-3	chr11:15932495-15932692	ENSG00000254661
9	lnc-SOX6-1	chr11:15932520-15932618	XLOC_009382
10	lnc-INSC-3	chr11:15944830-15944928	ENSG00000254661
11	lnc-INSC-3	chr11:15944830-15945453	NONHSAT018165
12	lnc-INSC-3	chr11:15944830-15944928	XLOC_009075

No data

Variant related genes	Relation type
ENSG00000254661	TF binding region
ENSG00000254661	CpG island
RLIM	miRNA target sites
RLF	miRNA target sites

Extended variants
information (count: 643 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:643 , 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	rs10832529	chr11:15930472-15930473	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149957072	chr11:15930562-15930563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181281730	chr11:15930568-15930569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549937523	chr11:15930668-15930669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80102773	chr11:15930677-15930678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529348116	chr11:15930737-15930738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547478123	chr11:15930755-15930756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566064091	chr11:15930759-15930760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74951944	chr11:15930778-15930779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552477768	chr11:15930825-15930826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547156132	chr11:15930883-15930884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570730586	chr11:15930891-15930892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11023773	chr11:15930944-15930945	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185018322	chr11:15930945-15930946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60922416	chr11:15930970-15930971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189870191	chr11:15931008-15931009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553526656	chr11:15931022-15931023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571990667	chr11:15931040-15931041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113167451	chr11:15931116-15931117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546118755	chr11:15931149-15931150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564464188	chr11:15931150-15931151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs80105763	chr11:15931162-15931163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61882853	chr11:15931182-15931183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74341600	chr11:15931204-15931205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183223098	chr11:15931238-15931239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577405926	chr11:15931270-15931271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546035686	chr11:15931280-15931281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147649054	chr11:15931352-15931353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs386751030	chr11:15931465-15931466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75749774	chr11:15931466-15931467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs59382041	chr11:15931515-15931516	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs386751031	chr11:15931569-15931570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs116649131	chr11:15931570-15931571	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs11023774	chr11:15931588-15931589	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs368450809	chr11:15931631-15931632	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs538088163	chr11:15931672-15931673	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556615083	chr11:15931673-15931674	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs111256812	chr11:15931683-15931684	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs76608833	chr11:15931691-15931692	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs66658380	chr11:15931692-15931693	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs35716934	chr11:15931693-15931694	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs555469736	chr11:15931738-15931739	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs11023775	chr11:15931747-15931748	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs535230357	chr11:15931759-15931760	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs12797842	chr11:15931802-15931803	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs145986691	chr11:15931852-15931853	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs73430961	chr11:15931881-15931882	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539064646	chr11:15931883-15931884	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs368914028	chr11:15931885-15931886	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs576331418	chr11:15931925-15931926	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15919800-15934400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr11:15923600-15931600	Weak transcription	Fetal Heart	heart
3	chr11:15923600-15933200	Weak transcription	Right Atrium	heart
4	chr11:15923800-15933200	Weak transcription	Right Ventricle	heart
5	chr11:15924000-15932000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:15928000-15933200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr11:15928400-15931800	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr11:15928400-15932000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr11:15928400-15933200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr11:15928600-15941800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:15929000-15933000	Weak transcription	Spleen	Spleen
12	chr11:15929200-15932200	Weak transcription	Pancreas	Pancrea
13	chr11:15929400-15932000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr11:15930200-15930600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr11:15930600-15932000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:15931400-15934200	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr11:15931600-15932000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:15931600-15935800	Enhancers	Fetal Heart	heart
19	chr11:15931800-15932400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:15931800-15934000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr11:15932000-15932200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:15932000-15932200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:15932000-15933600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr11:15932000-15933800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr11:15932000-15933800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:15932000-15935200	Enhancers	Fetal Muscle Leg	muscle
27	chr11:15932000-15935600	Enhancers	Fetal Muscle Trunk	muscle
28	chr11:15932200-15932400	Enhancers	Pancreas	Pancrea
29	chr11:15932200-15932600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:15932200-15932600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr11:15932200-15933400	Enhancers	Placenta	Placenta
32	chr11:15932200-15933400	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr11:15932400-15932800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:15932600-15933800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr11:15932600-15933800	Enhancers	Fetal Lung	lung
36	chr11:15932600-15935000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:15932800-15933600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr11:15932800-15935000	Enhancers	Fetal Stomach	stomach
39	chr11:15933000-15933200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:15933000-15933200	Enhancers	HSMMtube	muscle
41	chr11:15933000-15933600	Enhancers	Left Ventricle	heart
42	chr11:15933000-15933600	Enhancers	Lung	lung
43	chr11:15933000-15933800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr11:15933000-15934000	Enhancers	Brain Germinal Matrix	brain
45	chr11:15933000-15934000	Enhancers	Spleen	Spleen
46	chr11:15933000-15934400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:15933200-15933600	Enhancers	Fetal Brain Female	brain
48	chr11:15933200-15933600	Enhancers	Stomach Smooth Muscle	stomach
49	chr11:15933200-15933600	Enhancers	Osteobl	bone
50	chr11:15933200-15933800	Enhancers	Primary hematopoietic stem cells	blood

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