Variant report

Variant	nsv983274
Chromosome Location	chr12:9436590-9439756
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	ATF1	chr12:9436462-9436639	K562	blood:	n/a	n/a
2	BATF	chr12:9437291-9437995	GM12878	blood:	n/a	n/a
3	BATF	chr12:9436520-9437233	GM12878	blood:	n/a	n/a
4	BATF	chr12:9437518-9437975	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:9436547-9436721	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:9436213-9436749	GM12878	blood:	n/a	chr12:9436247-9436260 chr12:9436252-9436261 chr12:9436523-9436532
7	BCL11A	chr12:9437585-9438094	GM12878	blood:	n/a	chr12:9438052-9438061
8	BCL11A	chr12:9437489-9438007	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:9436867-9437442	GM12878	blood:	n/a	chr12:9436944-9436953
10	BCL11A	chr12:9436944-9437125	GM12878	blood:	n/a	chr12:9436944-9436953
11	BHLHE40	chr12:9436092-9436639	K562	blood:	n/a	n/a
12	CEBPB	chr12:9436587-9437294	GM12878	blood:	n/a	n/a
13	CEBPD	chr12:9436229-9436895	K562	blood:	n/a	n/a
14	CHD2	chr12:9436206-9436653	GM12878	blood:	n/a	n/a
15	CTCF	chr12:9436980-9437130	HEEpiC	esophagus:	n/a	chr12:9437084-9437097
16	CTCF	chr12:9437078-9437085	GM13977	blood:	n/a	n/a
17	CTCF	chr12:9437057-9437114	MCF-7	breast:	n/a	chr12:9437084-9437097
18	CTCF	chr12:9436980-9437130	GM12868	blood:	n/a	chr12:9437084-9437097
19	CTCF	chr12:9436960-9437110	GM12864	blood:	n/a	chr12:9437084-9437097
20	CTCF	chr12:9437020-9437170	Hela-S3	cervix:	n/a	chr12:9437084-9437097
21	CTCF	chr12:9437000-9437150	GM12871	blood:	n/a	chr12:9437084-9437097
22	CTCF	chr12:9436960-9437110	GM12873	blood:	n/a	chr12:9437084-9437097
23	CTCF	chr12:9436980-9437130	SAEC	small airway:	n/a	chr12:9437084-9437097
24	CTCF	chr12:9436960-9437110	SAEC	small airway:	n/a	chr12:9437084-9437097
25	CTCF	chr12:9437040-9437190	HMEC	breast:	n/a	chr12:9437084-9437097
26	CTCF	chr12:9437080-9437230	GM12878	blood:	n/a	chr12:9437084-9437097
27	CTCF	chr12:9437100-9437250	Caco-2	colon:	n/a	n/a
28	CTCF	chr12:9437000-9437150	GM12867	blood:	n/a	chr12:9437084-9437097
29	CTCF	chr12:9437099-9437120	GM13977	blood:	n/a	n/a
30	CTCF	chr12:9436980-9437130	HCPEpiC	choroid plexus:	n/a	chr12:9437084-9437097
31	CTCF	chr12:9437054-9437074	GM13977	blood:	n/a	n/a
32	CTCF	chr12:9437000-9437150	GM12870	blood:	n/a	chr12:9437084-9437097
33	CTCF	chr12:9437061-9437111	GM12892	blood:	n/a	chr12:9437084-9437097
34	CTCF	chr12:9437080-9437230	RPTEC	kidney:	n/a	chr12:9437084-9437097
35	CTCF	chr12:9437000-9437150	GM12872	blood:	n/a	chr12:9437084-9437097
36	CTCF	chr12:9437060-9437210	Hela-S3	cervix:	n/a	chr12:9437084-9437097
37	CTCF	chr12:9436840-9436990	GM12872	blood:	n/a	n/a
38	CTCF	chr12:9436980-9437130	GM12865	blood:	n/a	chr12:9437084-9437097
39	CTCF	chr12:9437077-9437138	GM10266	blood:	n/a	chr12:9437084-9437097
40	CTCF	chr12:9437017-9437150	MCF-7	breast:	n/a	chr12:9437084-9437097
41	CTCF	chr12:9437120-9437270	AG09319	gingival:	n/a	n/a
42	CTCF	chr12:9437000-9437150	GM12873	blood:	n/a	chr12:9437084-9437097
43	CTCF	chr12:9437100-9437250	HepG2	liver:	n/a	n/a
44	CTCF	chr12:9437027-9437138	GM19239	blood:	n/a	chr12:9437084-9437097
45	CTCF	chr12:9437000-9437150	SK-N-SH_RA	brain:	n/a	chr12:9437084-9437097
46	CTCF	chr12:9436960-9437110	WERI-Rb-1	eye:	n/a	chr12:9437084-9437097
47	CTCF	chr12:9437040-9437190	HRE	kidney:	n/a	chr12:9437084-9437097
48	CTCF	chr12:9437073-9437181	GM10248	blood:	n/a	chr12:9437084-9437097
49	CTCF	chr12:9436969-9437157	K562	blood:	n/a	chr12:9437084-9437097
50	CTCF	chr12:9437031-9437154	H1-hESC	embryonic stem cell:	n/a	chr12:9437084-9437097

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9436616-9436666	HRE	kidney:	n/a
2	chr12:9436621-9436671	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:9436621-9436671	ProgFib	skin:	n/a
4	chr12:9437009-9437059	HEK293	kidney:	embryo
5	chr12:9436616-9436666	T-47D	breast:	n/a
6	chr12:9436621-9436671	U87	brain:	n/a
7	chr12:9436616-9436666	ECC-1	luminal epithelium:	n/a
8	chr12:9437009-9437059	ECC-1	luminal epithelium:	n/a
9	chr12:9436616-9436666	HAEpiC	amniotic membrane:	n/a
10	chr12:9437009-9437059	HPAEpiC	pulmonary alveolar:	n/a
11	chr12:9436621-9436671	CMK	blood:	n/a
12	chr12:9436616-9436666	GM06990	blood:	n/a
13	chr12:9436616-9436666	HRPEpiC	eye:	n/a
14	chr12:9436616-9436666	PANC-1	pancreas:	n/a
15	chr12:9436621-9436671	HCM	heart:	n/a
16	chr12:9437009-9437059	NB4	blood:	n/a
17	chr12:9436621-9436671	GM12892	blood:	n/a
18	chr12:9436621-9436671	NT2-D1	testis:	n/a
19	chr12:9436616-9436666	HRCEpiC	kidney:	n/a
20	chr12:9436621-9436671	NH-A	brain:	n/a
21	chr12:9436621-9436671	SKMC	muscle:	n/a
22	chr12:9436621-9436671	LNCaP	prostate:	n/a
23	chr12:9436616-9436666	SAEC	small airway:	n/a
24	chr12:9437009-9437059	GM19239	blood:	n/a
25	chr12:9436616-9436666	NHBE	bronchial:	n/a
26	chr12:9437009-9437059	HUVEC	blood vessel:	n/a
27	chr12:9436616-9436666	HIPEpiC	eye:	n/a
28	chr12:9436616-9436666	HPAEpiC	pulmonary alveolar:	n/a
29	chr12:9436616-9436666	AG09309	skin:	n/a
30	chr12:9436616-9436666	Hela-S3	cervix:	n/a
31	chr12:9436621-9436671	ECC-1	luminal epithelium:	n/a
32	chr12:9437009-9437059	MCF-7	breast:	n/a
33	chr12:9436616-9436666	SK-N-SH	brain:	n/a
34	chr12:9436616-9436666	K562	blood:	n/a
35	chr12:9436616-9436666	PFSK-1	brain:	n/a
36	chr12:9436621-9436671	AG04450	lung:	fetal
37	chr12:9436616-9436666	RPTEC	kidney:	n/a
38	chr12:9437009-9437059	HL-60	blood:	n/a
39	chr12:9437009-9437059	Caco-2	colon:	n/a
40	chr12:9436616-9436666	BE2_C	brain:	n/a
41	chr12:9436616-9436666	GM12891	blood:	n/a
42	chr12:9436616-9436666	SK-N-MC	brain:	n/a
43	chr12:9437009-9437059	Jurkat	blood:	n/a
44	chr12:9436621-9436671	HNPCEpiC	eye:	n/a
45	chr12:9436621-9436671	BJ	skin:	n/a
46	chr12:9436621-9436671	PANC-1	pancreas:	n/a
47	chr12:9437009-9437059	PrEC	prostate:	n/a
48	chr12:9437009-9437059	AG09309	skin:	n/a
49	chr12:9436621-9436671	RPTEC	kidney:	n/a
50	chr12:9436621-9436671	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:
2	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:
3	chr12:9436030..9436711-chr12:9600583..9601103,2	HCT-116	colon:
4	chr12:9436150..9437103-chr12:9600374..9601086,2	Hela-S3	cervix:
5	chr12:9436222..9437012-chr17:48045663..48046428,2	NB4	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRG1-6	chr12:9436616-9436729	NONHSAT026397
2	lnc-KLRG1-3	chr12:9438394-9438514	l_599_chr12:9406531-9439851_testes
3	lnc-KLRG1-3	chr12:9439608-9439851	l_599_chr12:9406531-9439851_testes

Variant related genes	Relation type
ENSG00000212440	TF binding region
ENSG00000212440	CpG island
ENSG00000108813	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000214826	chromatin interactions

Extended variants
information (count: 54 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:54 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78176743	chr12:9436617-9436618	Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs3864913	chr12:9436619-9436620	Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs2433011	chr12:9436635-9436636	Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs141108594	chr12:9436705-9436706	Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs202099377	chr12:9436760-9436761	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374500669	chr12:9436866-9436867	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2429869	chr12:9436875-9436876	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535131507	chr12:9436991-9436992	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs2433010	chr12:9437006-9437007	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181161050	chr12:9437042-9437043	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs3882943	chr12:9437043-9437044	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs397833764	chr12:9437155-9437156	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs61916195	chr12:9437216-9437217	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs397833763	chr12:9437217-9437218	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs28712430	chr12:9437221-9437222	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs2553176	chr12:9437259-9437260	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs61916197	chr12:9437336-9437337	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs374627795	chr12:9437386-9437387	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs3874120	chr12:9437428-9437429	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs113334835	chr12:9437482-9437483	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2553174	chr12:9437570-9437571	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12425975	chr12:9437614-9437615	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs2536741	chr12:9437694-9437695	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs201548374	chr12:9437707-9437708	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs199994668	chr12:9437749-9437750	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs200853700	chr12:9437755-9437756	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs370643083	chr12:9437778-9437779	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs201658681	chr12:9437826-9437827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374308131	chr12:9437946-9437947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368663004	chr12:9438014-9438015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370798814	chr12:9438066-9438067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2553170	chr12:9438094-9438095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2553166	chr12:9438490-9438491	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs200119573	chr12:9438565-9438566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201220005	chr12:9438658-9438659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61916199	chr12:9438722-9438723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2433009	chr12:9438929-9438930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113787381	chr12:9438953-9438954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201703850	chr12:9439222-9439223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61916200	chr12:9439257-9439258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200340789	chr12:9439294-9439295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542882702	chr12:9439351-9439352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553164058	chr12:9439395-9439396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573062621	chr12:9439399-9439400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144848791	chr12:9439404-9439405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs61916202	chr12:9439435-9439436	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs2433008	chr12:9439461-9439462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4316594	chr12:9439553-9439554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4516053	chr12:9439635-9439636	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs199502360	chr12:9439670-9439671	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9435400-9437800	Active TSS	A549	lung
2	chr12:9435400-9464000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:9435600-9437800	Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr12:9435600-9437800	Active TSS	GM12878-XiMat	blood
5	chr12:9435800-9436600	Active TSS	Primary T killer memory cells from peripheral blood	blood
6	chr12:9435800-9437000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:9435800-9437000	Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr12:9435800-9437000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:9435800-9437000	Active TSS	Brain Anterior Caudate	brain
10	chr12:9435800-9437000	Active TSS	Brain Inferior Temporal Lobe	brain
11	chr12:9435800-9437000	Active TSS	Stomach Smooth Muscle	stomach
12	chr12:9435800-9437200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr12:9435800-9437200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr12:9435800-9437200	Active TSS	Brain Substantia Nigra	brain
15	chr12:9435800-9437200	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr12:9435800-9437200	Active TSS	NHDF-Ad	bronchial
17	chr12:9435800-9437400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:9435800-9437400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr12:9435800-9437400	Active TSS	Fetal Brain Female	brain
20	chr12:9435800-9437600	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr12:9435800-9437600	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr12:9435800-9437800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:9435800-9437800	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr12:9435800-9437800	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr12:9435800-9437800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:9435800-9437800	Active TSS	K562	blood
27	chr12:9436000-9436600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
28	chr12:9436000-9436800	Active TSS	Placenta	Placenta
29	chr12:9436000-9437000	Active TSS	Primary monocytes fromperipheralblood	blood
30	chr12:9436000-9437000	Active TSS	Primary B cells from cord blood	blood
31	chr12:9436000-9437000	Active TSS	Primary B cells from peripheral blood	blood
32	chr12:9436000-9437000	Active TSS	Primary T cells fromperipheralblood	blood
33	chr12:9436000-9437000	Active TSS	Primary hematopoietic stem cells	blood
34	chr12:9436000-9437000	Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr12:9436000-9437000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
36	chr12:9436000-9437000	Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr12:9436000-9437000	Active TSS	Adipose Nuclei	Adipose
38	chr12:9436000-9437000	Active TSS	Brain Angular Gyrus	brain
39	chr12:9436000-9437000	Active TSS	Brain Cingulate Gyrus	brain
40	chr12:9436000-9437000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr12:9436000-9437000	Active TSS	Fetal Intestine Small	intestine
42	chr12:9436000-9437000	Active TSS	Fetal Stomach	stomach
43	chr12:9436000-9437000	Active TSS	Ovary	ovary
44	chr12:9436000-9437000	Active TSS	Rectal Mucosa Donor 31	rectum
45	chr12:9436000-9437000	Active TSS	Right Atrium	heart
46	chr12:9436000-9437000	Active TSS	HUVEC	blood vessel
47	chr12:9436000-9437000	Active TSS	NHEK	skin
48	chr12:9436000-9437200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr12:9436000-9437200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr12:9436000-9437200	Active TSS	Primary T helper naive cells fromperipheralblood	blood

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