Variant report

Variant	nsv898749
Chromosome Location	chr12:9623616-9740839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9740655-9741170	K562	blood:	n/a	n/a
2	ATF1	chr12:9740572-9740926	K562	blood:	n/a	n/a
3	BACH1	chr12:9740595-9741065	K562	blood:	n/a	n/a
4	BACH1	chr12:9740652-9740897	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
6	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
7	CCNT2	chr12:9740427-9741071	K562	blood:	n/a	n/a
8	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
9	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
11	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
12	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
13	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
14	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
15	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
16	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
17	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr12:9665444-9665629	K562	blood:	n/a	n/a
19	CTCF	chr12:9665360-9665510	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr12:9665600-9665750	RPTEC	kidney:	n/a	n/a
21	CTCF	chr12:9665477-9665516	GM13977	blood:	n/a	n/a
22	CTCF	chr12:9665432-9665541	GM19239	blood:	n/a	n/a
23	CTCF	chr12:9703380-9703388	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr12:9665380-9665578	K562	blood:	n/a	n/a
25	CTCF	chr12:9723279-9723384	GM19238	blood:	n/a	n/a
26	CTCF	chr12:9726760-9726829	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr12:9669822-9669862	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr12:9634822-9634891	GM12891	blood:	n/a	n/a
29	CTCF	chr12:9665305-9665671	A549	lung:	n/a	n/a
30	CTCF	chr12:9665459-9665498	Fibrobl	skin:	n/a	n/a
31	CTCF	chr12:9665390-9665555	ProgFib	skin:	n/a	n/a
32	CTCF	chr12:9730398-9730556	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr12:9665404-9665570	NHEK	skin:	n/a	n/a
34	CTCF	chr12:9630516-9630628	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr12:9695383-9695441	GM20000	blood:	n/a	n/a
36	CTCF	chr12:9665862-9665881	GM13977	blood:	n/a	n/a
37	CTCF	chr12:9709315-9709383	LNCaP	prostate:	n/a	n/a
38	CTCF	chr12:9634643-9634716	GM19239	blood:	n/a	n/a
39	CTCF	chr12:9691717-9691734	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr12:9665349-9665783	A549	lung:	n/a	n/a
41	CTCF	chr12:9665377-9665602	K562	blood:	n/a	n/a
42	CTCF	chr12:9730978-9731104	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr12:9664977-9665006	GM10248	blood:	n/a	n/a
44	CTCF	chr12:9665406-9665624	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr12:9730389-9730511	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr12:9695807-9695847	GM13976	blood:	n/a	n/a
47	CTCF	chr12:9665360-9665558	A549	lung:	n/a	n/a
48	CTCF	chr12:9665315-9665625	A549	lung:	n/a	n/a
49	CTCF	chr12:9632112-9632186	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:9665402-9665599	LNCaP	prostate:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9723402-9723452	LNCaP	prostate:	n/a
2	chr12:9720554-9720604	NHBE	bronchial:	n/a
3	chr12:9720090-9720140	HRCEpiC	kidney:	n/a
4	chr12:9720554-9720604	BJ	skin:	n/a
5	chr12:9720090-9720140	Jurkat	blood:	n/a
6	chr12:9722091-9722141	H1-hESC	embryonic stem cell:	embryo
7	chr12:9720554-9720604	A549	lung:	n/a
8	chr12:9720554-9720604	T-47D	breast:	n/a
9	chr12:9723402-9723452	NHDF-neo	bronchial:	n/a
10	chr12:9720554-9720604	AG04450	lung:	fetal
11	chr12:9722091-9722141	A549	lung:	n/a
12	chr12:9722091-9722141	AG04449	skin:	fetal
13	chr12:9723402-9723452	NT2-D1	testis:	n/a
14	chr12:9723402-9723452	ProgFib	skin:	n/a
15	chr12:9722091-9722141	ECC-1	luminal epithelium:	n/a
16	chr12:9723402-9723452	AG09319	gingival:	n/a
17	chr12:9722091-9722141	HAEpiC	amniotic membrane:	n/a
18	chr12:9720090-9720140	GM19239	blood:	n/a
19	chr12:9720090-9720140	SK-N-SH_RA	brain:	n/a
20	chr12:9722091-9722141	HEK293	kidney:	embryo
21	chr12:9720554-9720604	K562	blood:	n/a
22	chr12:9722091-9722141	HMEC	breast:	n/a
23	chr12:9723402-9723452	SK-N-MC	brain:	n/a
24	chr12:9720090-9720140	SK-N-MC	brain:	n/a
25	chr12:9723402-9723452	HNPCEpiC	eye:	n/a
26	chr12:9720554-9720604	BE2_C	brain:	n/a
27	chr12:9720554-9720604	AoSMC	blood vessel:	n/a
28	chr12:9723402-9723452	HL-60	blood:	n/a
29	chr12:9722091-9722141	NH-A	brain:	n/a
30	chr12:9723402-9723452	HCF	heart:	n/a
31	chr12:9720554-9720604	HCM	heart:	n/a
32	chr12:9723402-9723452	HIPEpiC	eye:	n/a
33	chr12:9720090-9720140	HRE	kidney:	n/a
34	chr12:9723402-9723452	CMK	blood:	n/a
35	chr12:9720554-9720604	HIPEpiC	eye:	n/a
36	chr12:9722091-9722141	GM12892	blood:	n/a
37	chr12:9720090-9720140	NHDF-neo	bronchial:	n/a
38	chr12:9722091-9722141	MCF-7	breast:	n/a
39	chr12:9720554-9720604	U87	brain:	n/a
40	chr12:9720554-9720604	HEK293	kidney:	embryo
41	chr12:9720090-9720140	PFSK-1	brain:	n/a
42	chr12:9720090-9720140	HUVEC	blood vessel:	n/a
43	chr12:9723402-9723452	HMEC	breast:	n/a
44	chr12:9720554-9720604	GM12878	blood:	n/a
45	chr12:9720554-9720604	NHDF-neo	bronchial:	n/a
46	chr12:9722091-9722141	Caco-2	colon:	n/a
47	chr12:9722091-9722141	HCM	heart:	n/a
48	chr12:9723402-9723452	GM12892	blood:	n/a
49	chr12:9723402-9723452	HRE	kidney:	n/a
50	chr12:9720554-9720604	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9739995..9741756-chr12:9800822..9803051,2	K562	blood:
2	chr12:9740551..9742492-chr12:9759137..9760711,2	K562	blood:

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

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

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
ENSG00000111796	chromatin interactions

Extended variants
information (count: 2392 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2392 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10743737	chr12:9623616-9623617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150296700	chr12:9623684-9623685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7138356	chr12:9623783-9623784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112881185	chr12:9623803-9623804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185417455	chr12:9623816-9623817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10743738	chr12:9623841-9623842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs2536676	chr12:9623963-9623964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2536675	chr12:9623964-9623965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189527202	chr12:9623974-9623975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142649610	chr12:9623992-9623993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562727396	chr12:9624005-9624006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs55655311	chr12:9624045-9624046	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs369240827	chr12:9624095-9624096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181349185	chr12:9624127-9624128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs55978742	chr12:9624146-9624147	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146334994	chr12:9624157-9624158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560994059	chr12:9624223-9624224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10843860	chr12:9624242-9624243	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs373617244	chr12:9624251-9624252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3953616	chr12:9624259-9624260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376001712	chr12:9624263-9624264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566402210	chr12:9624327-9624328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12578736	chr12:9624357-9624358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183994476	chr12:9624372-9624373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187990192	chr12:9624421-9624422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140021858	chr12:9624462-9624463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs28533282	chr12:9624541-9624542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs180905923	chr12:9624581-9624582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs71447586	chr12:9624693-9624694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4015223	chr12:9624710-9624711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs147949331	chr12:9624721-9624722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11051164	chr12:9624724-9624725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs192418874	chr12:9624728-9624729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140092789	chr12:9624758-9624759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181680779	chr12:9624816-9624817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2191962	chr12:9624844-9624845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs55762675	chr12:9624906-9624907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368100485	chr12:9625009-9625010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537997326	chr12:9625211-9625212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187146324	chr12:9625229-9625230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554773848	chr12:9625230-9625231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146860271	chr12:9625274-9625275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190241504	chr12:9625320-9625321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10743739	chr12:9625331-9625332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs182827714	chr12:9625351-9625352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374399046	chr12:9625499-9625500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150348676	chr12:9625559-9625560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138240027	chr12:9625609-9625610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187115806	chr12:9625643-9625644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189970511	chr12:9625669-9625670	Weak transcription	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:76 , 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	chr12:9622000-9624000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:9622000-9625800	Weak transcription	Fetal Lung	lung
5	chr12:9623200-9653000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:9623600-9630200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:9624000-9624400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:9624000-9624400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:9624000-9624600	Enhancers	Placenta	Placenta
10	chr12:9624600-9625800	Weak transcription	Placenta	Placenta
11	chr12:9625800-9626000	Enhancers	Placenta	Placenta
12	chr12:9625800-9627000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:9627000-9627400	Enhancers	NHEK	skin
14	chr12:9627000-9663400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:9630200-9630400	Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr12:9638400-9640200	Weak transcription	Fetal Thymus	thymus
17	chr12:9640200-9640600	Enhancers	Fetal Thymus	thymus
18	chr12:9655400-9656000	Enhancers	Dnd41	blood
19	chr12:9657000-9664800	Weak transcription	Fetal Lung	lung
20	chr12:9659400-9662200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:9661800-9663000	Enhancers	Hela-S3	cervix
22	chr12:9662000-9662800	Enhancers	HMEC	breast
23	chr12:9662000-9663400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:9662200-9662600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:9662200-9663000	Enhancers	NHEK	skin
26	chr12:9662200-9663400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:9662400-9662800	Enhancers	HUVEC	blood vessel
28	chr12:9662400-9663000	Enhancers	Osteobl	bone
29	chr12:9662400-9663400	Enhancers	Fetal Heart	heart
30	chr12:9662600-9663000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:9662600-9663200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:9662600-9663200	Enhancers	Primary B cells from cord blood	blood
33	chr12:9662600-9664400	Enhancers	Fetal Thymus	thymus
34	chr12:9663000-9663600	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr12:9663000-9664200	Enhancers	Thymus	Thymus
36	chr12:9663400-9663600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:9663400-9667200	Weak transcription	Fetal Heart	heart
38	chr12:9663600-9664000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:9664000-9664200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:9664200-9702200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:9665000-9667800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr12:9667200-9668000	Enhancers	Fetal Heart	heart
43	chr12:9667800-9668600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr12:9667800-9668800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr12:9668200-9668800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr12:9668800-9679600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr12:9679600-9680000	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr12:9686000-9703600	Weak transcription	Hela-S3	cervix
49	chr12:9703600-9705600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:9704000-9721800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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