Variant report

Variant	nsv870005
Chromosome Location	chr12:9624859-9735356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:219)
CpG islands
(count:245)
Chromatin interactive
region (count:0)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:219 , 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	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
2	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
3	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
4	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
5	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
6	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
7	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
8	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
10	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
11	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
12	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
13	CTCF	chr12:9709315-9709383	LNCaP	prostate:	n/a	n/a
14	CTCF	chr12:9664977-9665006	GM10248	blood:	n/a	n/a
15	CTCF	chr12:9691647-9691785	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:9719543-9719625	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr12:9665444-9665629	K562	blood:	n/a	n/a
18	CTCF	chr12:9725642-9725709	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr12:9632112-9632186	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:9695807-9695847	GM13976	blood:	n/a	n/a
21	CTCF	chr12:9665294-9665647	A549	lung:	n/a	n/a
22	CTCF	chr12:9724378-9724451	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr12:9665360-9665510	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr12:9723300-9723450	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr12:9665432-9665541	GM19239	blood:	n/a	n/a
26	CTCF	chr12:9665404-9665570	NHEK	skin:	n/a	n/a
27	CTCF	chr12:9723279-9723384	GM19238	blood:	n/a	n/a
28	CTCF	chr12:9665431-9665574	Medullo	brain:	n/a	n/a
29	CTCF	chr12:9691655-9691786	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:9665477-9665516	GM13977	blood:	n/a	n/a
31	CTCF	chr12:9726760-9726829	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr12:9730389-9730511	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr12:9669822-9669862	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr12:9665360-9665590	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:9665380-9665578	K562	blood:	n/a	n/a
36	CTCF	chr12:9665294-9665690	A549	lung:	n/a	n/a
37	CTCF	chr12:9697887-9697942	GM13977	blood:	n/a	n/a
38	CTCF	chr12:9665377-9665602	K562	blood:	n/a	n/a
39	CTCF	chr12:9665376-9665490	HepG2	liver:	n/a	n/a
40	CTCF	chr12:9665374-9665581	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:9695857-9695928	GM13976	blood:	n/a	n/a
42	CTCF	chr12:9634822-9634891	GM12891	blood:	n/a	n/a
43	CTCF	chr12:9695383-9695441	GM20000	blood:	n/a	n/a
44	CTCF	chr12:9665402-9665599	LNCaP	prostate:	n/a	n/a
45	CTCF	chr12:9665305-9665671	A549	lung:	n/a	n/a
46	CTCF	chr12:9665390-9665555	ProgFib	skin:	n/a	n/a
47	CTCF	chr12:9703380-9703388	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr12:9730978-9731104	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr12:9665360-9665510	HMF	breast:	n/a	n/a
50	CTCF	chr12:9665352-9665595	Hela-S3	cervix:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9723402-9723452	HEK293	kidney:	embryo
2	chr12:9723402-9723452	HEK293	kidney:	embryo
3	chr12:9723402-9723452	GM06990	blood:	n/a
4	chr12:9722091-9722141	HepG2	liver:	n/a
5	chr12:9722091-9722141	HNPCEpiC	eye:	n/a
6	chr12:9723402-9723452	NHBE	bronchial:	n/a
7	chr12:9723402-9723452	NH-A	brain:	n/a
8	chr12:9720090-9720140	NH-A	brain:	n/a
9	chr12:9722091-9722141	SAEC	small airway:	n/a
10	chr12:9722091-9722141	PANC-1	pancreas:	n/a
11	chr12:9720090-9720140	HCF	heart:	n/a
12	chr12:9723402-9723452	GM12878	blood:	n/a
13	chr12:9720554-9720604	HCM	heart:	n/a
14	chr12:9723402-9723452	ovcar-3	ovarian:	n/a
15	chr12:9720090-9720140	GM12878	blood:	n/a
16	chr12:9720554-9720604	HCF	heart:	n/a
17	chr12:9720554-9720604	Caco-2	colon:	n/a
18	chr12:9720090-9720140	HRPEpiC	eye:	n/a
19	chr12:9720090-9720140	ovcar-3	ovarian:	n/a
20	chr12:9723402-9723452	Hela-S3	cervix:	n/a
21	chr12:9723402-9723452	AG04449	skin:	fetal
22	chr12:9722091-9722141	HEK293	kidney:	embryo
23	chr12:9723402-9723452	AoSMC	blood vessel:	n/a
24	chr12:9720090-9720140	NHBE	bronchial:	n/a
25	chr12:9720554-9720604	GM06990	blood:	n/a
26	chr12:9723402-9723452	BJ	skin:	n/a
27	chr12:9723402-9723452	HEEpiC	esophagus:	n/a
28	chr12:9720090-9720140	PrEC	prostate:	n/a
29	chr12:9720554-9720604	HCT-116	colon:	n/a
30	chr12:9723402-9723452	HUVEC	blood vessel:	n/a
31	chr12:9723402-9723452	AG09319	gingival:	n/a
32	chr12:9720090-9720140	A549	lung:	n/a
33	chr12:9720090-9720140	BE2_C	brain:	n/a
34	chr12:9720554-9720604	GM12878	blood:	n/a
35	chr12:9722091-9722141	NB4	blood:	n/a
36	chr12:9722091-9722141	NHDF-neo	bronchial:	n/a
37	chr12:9720090-9720140	K562	blood:	n/a
38	chr12:9720090-9720140	SK-N-MC	brain:	n/a
39	chr12:9720090-9720140	T-47D	breast:	n/a
40	chr12:9722091-9722141	MCF-7	breast:	n/a
41	chr12:9723402-9723452	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:9723402-9723452	AG04450	lung:	fetal
43	chr12:9723402-9723452	HCF	heart:	n/a
44	chr12:9722091-9722141	U87	brain:	n/a
45	chr12:9720554-9720604	A549	lung:	n/a
46	chr12:9720554-9720604	AG09309	skin:	n/a
47	chr12:9720554-9720604	H1-hESC	embryonic stem cell:	embryo
48	chr12:9723402-9723452	GM12891	blood:	n/a
49	chr12:9720090-9720140	CMK	blood:	n/a
50	chr12:9720554-9720604	SKMC	muscle:	n/a

No data

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRB1-2	chr12:9691704-9691933	l_603_chr12:9690762-9691933_testes
2	lnc-KLRB1-2	chr12:9690763-9691239	l_603_chr12:9690762-9691933_testes
3	lnc-CLEC2D-9	chr12:9728714-9728863	NONHSAT026830
4	lnc-CLEC2D-9	chr12:9728239-9728313	NONHSAT026830
5	lnc-CLEC2D-9	chr12:9723357-9723488	NONHSAT026830
6	lnc-CLEC2D-9	chr12:9725599-9725666	NONHSAT026830
7	lnc-CLEC2D-9	chr12:9725984-9726130	NONHSAT026830
8	lnc-CLEC2D-9	chr12:9724057-9724169	NONHSAT026830
9	lnc-CLEC2D-9	chr12:9727443-9727545	NONHSAT026830

No data

Variant related genes	Relation type
ENSG00000266633	TF binding region
ENSG00000256975	TF binding region
ENSG00000214776	TF binding region
ENSG00000266633	CpG island
ENSG00000256975	CpG island
ENSG00000214776	CpG island

Extended variants
information (count: 2176 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2176 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55762675	chr12:9624906-9624907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368100485	chr12:9625009-9625010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537997326	chr12:9625211-9625212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187146324	chr12:9625229-9625230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554773848	chr12:9625230-9625231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146860271	chr12:9625274-9625275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190241504	chr12:9625320-9625321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10743739	chr12:9625331-9625332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs182827714	chr12:9625351-9625352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374399046	chr12:9625499-9625500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150348676	chr12:9625559-9625560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138240027	chr12:9625609-9625610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187115806	chr12:9625643-9625644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189970511	chr12:9625669-9625670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71450678	chr12:9625684-9625685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10743741	chr12:9625685-9625686	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142956940	chr12:9625713-9625714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115635787	chr12:9625757-9625758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539760890	chr12:9625782-9625783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370920886	chr12:9625784-9625785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556414646	chr12:9625809-9625810	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7313401	chr12:9625814-9625815	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs182713788	chr12:9625836-9625837	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116901417	chr12:9625850-9625851	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12296952	chr12:9625887-9625888	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574450464	chr12:9625945-9625946	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139106793	chr12:9626201-9626202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140814654	chr12:9626311-9626312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11051176	chr12:9626490-9626491	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs116597904	chr12:9626519-9626520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10843863	chr12:9626574-9626575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10771784	chr12:9626678-9626679	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs367798091	chr12:9626685-9626686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535321427	chr12:9626722-9626723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs58471109	chr12:9626723-9626724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11051179	chr12:9626724-9626725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188847127	chr12:9626767-9626768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10734795	chr12:9626772-9626773	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs193214891	chr12:9626831-9626832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183445633	chr12:9626833-9626834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10771785	chr12:9626847-9626848	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs10771786	chr12:9626863-9626864	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs371037024	chr12:9626885-9626886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188847728	chr12:9626895-9626896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10734796	chr12:9626908-9626909	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs548364182	chr12:9626983-9626984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142129583	chr12:9626997-9626998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568489584	chr12:9627045-9627046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147454552	chr12:9627156-9627157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547452058	chr12:9627199-9627200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9608800-9642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:9621800-9625800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:9622000-9625800	Weak transcription	Fetal Lung	lung
4	chr12:9623200-9653000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr12:9623600-9630200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr12:9624600-9625800	Weak transcription	Placenta	Placenta
7	chr12:9625800-9626000	Enhancers	Placenta	Placenta
8	chr12:9625800-9627000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:9627000-9627400	Enhancers	NHEK	skin
10	chr12:9627000-9663400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:9630200-9630400	Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr12:9638400-9640200	Weak transcription	Fetal Thymus	thymus
13	chr12:9640200-9640600	Enhancers	Fetal Thymus	thymus
14	chr12:9655400-9656000	Enhancers	Dnd41	blood
15	chr12:9657000-9664800	Weak transcription	Fetal Lung	lung
16	chr12:9659400-9662200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:9661800-9663000	Enhancers	Hela-S3	cervix
18	chr12:9662000-9662800	Enhancers	HMEC	breast
19	chr12:9662000-9663400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:9662200-9662600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:9662200-9663000	Enhancers	NHEK	skin
22	chr12:9662200-9663400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:9662400-9662800	Enhancers	HUVEC	blood vessel
24	chr12:9662400-9663000	Enhancers	Osteobl	bone
25	chr12:9662400-9663400	Enhancers	Fetal Heart	heart
26	chr12:9662600-9663000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:9662600-9663200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr12:9662600-9663200	Enhancers	Primary B cells from cord blood	blood
29	chr12:9662600-9664400	Enhancers	Fetal Thymus	thymus
30	chr12:9663000-9663600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr12:9663000-9664200	Enhancers	Thymus	Thymus
32	chr12:9663400-9663600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:9663400-9667200	Weak transcription	Fetal Heart	heart
34	chr12:9663600-9664000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:9664000-9664200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:9664200-9702200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:9665000-9667800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr12:9667200-9668000	Enhancers	Fetal Heart	heart
39	chr12:9667800-9668600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr12:9667800-9668800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr12:9668200-9668800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr12:9668800-9679600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr12:9679600-9680000	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr12:9686000-9703600	Weak transcription	Hela-S3	cervix
45	chr12:9703600-9705600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:9704000-9721800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:9705600-9706400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:9706400-9735000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:9717000-9717400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr12:9721200-9722400	Weak transcription	Thymus	Thymus

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