Variant report

Variant	nsv1042682
Chromosome Location	chr12:9617083-9713662
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	ARID3A	chr12:9621679-9621874	HepG2	liver:	n/a	n/a
2	BATF	chr12:9623145-9623344	GM12878	blood:	n/a	n/a
3	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
4	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
5	BHLHE40	chr12:9621680-9621866	K562	blood:	n/a	n/a
6	BRCA1	chr12:9621725-9621746	GM12878	blood:	n/a	n/a
7	CEBPB	chr12:9621557-9621862	HepG2	liver:	n/a	n/a
8	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
9	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
10	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
11	CEBPB	chr12:9621719-9621810	K562	blood:	n/a	n/a
12	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
13	CEBPB	chr12:9621651-9621793	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
15	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
16	CEBPB	chr12:9621705-9621858	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
19	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr12:9665459-9665498	Fibrobl	skin:	n/a	n/a
21	CTCF	chr12:9620820-9620970	HEEpiC	esophagus:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
22	CTCF	chr12:9665359-9665586	Gliobla	brain:	n/a	n/a
23	CTCF	chr12:9695807-9695847	GM13976	blood:	n/a	n/a
24	CTCF	chr12:9621700-9621850	GM12866	blood:	n/a	n/a
25	CTCF	chr12:9621611-9621891	HepG2	liver:	n/a	n/a
26	CTCF	chr12:9703380-9703388	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr12:9621715-9621836	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr12:9621700-9621850	GM12872	blood:	n/a	n/a
29	CTCF	chr12:9621720-9621870	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr12:9620798-9621051	GM12878	blood:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
31	CTCF	chr12:9621780-9621930	HRE	kidney:	n/a	chr12:9621901-9621914
32	CTCF	chr12:9621671-9621932	GM12891	blood:	n/a	chr12:9621901-9621914
33	CTCF	chr12:9620828-9620990	Lung_OC	lung:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
34	CTCF	chr12:9621760-9621910	WI-38	lung:	n/a	n/a
35	CTCF	chr12:9621734-9621904	GM10248	blood:	n/a	n/a
36	CTCF	chr12:9621672-9621919	A549	lung:	n/a	chr12:9621901-9621914
37	CTCF	chr12:9620940-9621090	RPTEC	kidney:	n/a	n/a
38	CTCF	chr12:9665404-9665570	NHEK	skin:	n/a	n/a
39	CTCF	chr12:9621720-9621870	GM12870	blood:	n/a	n/a
40	CTCF	chr12:9620330-9620410	GM10266	blood:	n/a	n/a
41	CTCF	chr12:9621651-9621900	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr12:9620820-9620970	AG10803	skin:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
43	CTCF	chr12:9621720-9621870	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr12:9621720-9621870	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr12:9620800-9620950	HRPEpiC	eye:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
46	CTCF	chr12:9621720-9621870	GM12864	blood:	n/a	n/a
47	CTCF	chr12:9621692-9621894	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr12:9620806-9620990	Spleen_OC	spleen:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
49	CTCF	chr12:9621720-9621870	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr12:9621713-9621876	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9618783-9618833	PFSK-1	brain:	n/a
2	chr12:9618783-9618833	HepG2	liver:	n/a
3	chr12:9618783-9618833	NB4	blood:	n/a
4	chr12:9618783-9618833	CMK	blood:	n/a
5	chr12:9618783-9618833	BE2_C	brain:	n/a
6	chr12:9618783-9618833	H1-hESC	embryonic stem cell:	embryo
7	chr12:9618783-9618833	HRCEpiC	kidney:	n/a
8	chr12:9618783-9618833	GM06990	blood:	n/a
9	chr12:9618783-9618833	SK-N-MC	brain:	n/a
10	chr12:9618783-9618833	AG10803	skin:	n/a
11	chr12:9618783-9618833	HRPEpiC	eye:	n/a
12	chr12:9618783-9618833	GM12892	blood:	n/a
13	chr12:9618783-9618833	AG04449	skin:	fetal
14	chr12:9618783-9618833	Hela-S3	cervix:	n/a
15	chr12:9618783-9618833	HMEC	breast:	n/a
16	chr12:9618783-9618833	HCPEpiC	choroid plexus:	n/a
17	chr12:9618783-9618833	HAEpiC	amniotic membrane:	n/a
18	chr12:9618783-9618833	HL-60	blood:	n/a
19	chr12:9618783-9618833	SAEC	small airway:	n/a
20	chr12:9618783-9618833	GM12878	blood:	n/a
21	chr12:9618783-9618833	SK-N-SH	brain:	n/a
22	chr12:9618783-9618833	AoSMC	blood vessel:	n/a
23	chr12:9618783-9618833	K562	blood:	n/a
24	chr12:9618783-9618833	PANC-1	pancreas:	n/a
25	chr12:9618783-9618833	LNCaP	prostate:	n/a
26	chr12:9618783-9618833	RPTEC	kidney:	n/a
27	chr12:9618783-9618833	T-47D	breast:	n/a
28	chr12:9618783-9618833	HCM	heart:	n/a
29	chr12:9618783-9618833	HUVEC	blood vessel:	n/a
30	chr12:9618783-9618833	BJ	skin:	n/a
31	chr12:9618783-9618833	HEK293	kidney:	embryo
32	chr12:9618783-9618833	Hepatocyte	liver:	n/a
33	chr12:9618783-9618833	GM12891	blood:	n/a
34	chr12:9618783-9618833	HPAEpiC	pulmonary alveolar:	n/a
35	chr12:9618783-9618833	HRE	kidney:	n/a
36	chr12:9618783-9618833	NH-A	brain:	n/a
37	chr12:9618783-9618833	A549	lung:	n/a
38	chr12:9618783-9618833	HCF	heart:	n/a
39	chr12:9618783-9618833	IMR90	lung:	fetal
40	chr12:9618783-9618833	Caco-2	colon:	n/a
41	chr12:9618783-9618833	NHDF-neo	bronchial:	n/a
42	chr12:9618783-9618833	MCF-7	breast:	n/a
43	chr12:9618783-9618833	SK-N-SH_RA	brain:	n/a
44	chr12:9618783-9618833	AG09319	gingival:	n/a
45	chr12:9618783-9618833	ProgFib	skin:	n/a
46	chr12:9618783-9618833	HCT-116	colon:	n/a
47	chr12:9618783-9618833	PrEC	prostate:	n/a
48	chr12:9618783-9618833	Jurkat	blood:	n/a
49	chr12:9618783-9618833	GM19239	blood:	n/a
50	chr12:9618783-9618833	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
2	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:
3	chr12:9530894..9532008-chr12:9621312..9622244,4	MCF-7	breast:

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

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: 1867 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1867 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7966062	chr12:9617083-9617084	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375905678	chr12:9617110-9617111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11051107	chr12:9617122-9617123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
4	rs147633448	chr12:9617202-9617203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11051110	chr12:9617261-9617262	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs193157540	chr12:9617290-9617291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182807833	chr12:9617353-9617354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11051112	chr12:9617461-9617462	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs142476720	chr12:9617475-9617476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532379995	chr12:9617479-9617480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138061392	chr12:9617495-9617496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377321391	chr12:9617676-9617677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559840436	chr12:9617693-9617694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143938382	chr12:9617732-9617733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7300782	chr12:9617798-9617799	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs116012372	chr12:9617805-9617806	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375899184	chr12:9617806-9617807	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188328529	chr12:9617821-9617822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367754262	chr12:9617861-9617862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10609263	chr12:9617877-9617878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4763376	chr12:9617905-9617906	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs192216983	chr12:9617913-9617914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374787935	chr12:9617932-9617933	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2536693	chr12:9617948-9617949	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143762905	chr12:9618019-9618020	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs148231533	chr12:9618035-9618036	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs141196650	chr12:9618051-9618052	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs2536692	chr12:9618059-9618060	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs4764071	chr12:9618116-9618117	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
30	rs183898821	chr12:9618161-9618162	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs143382423	chr12:9618536-9618537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546873528	chr12:9618541-9618542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187840428	chr12:9618592-9618593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192670179	chr12:9618626-9618627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71234757	chr12:9618627-9618628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2536690	chr12:9618649-9618650	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs2536689	chr12:9618651-9618652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2536688	chr12:9618691-9618692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116943402	chr12:9618695-9618696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375577373	chr12:9618790-9618791	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs11829861	chr12:9618801-9618802	Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs61047753	chr12:9618842-9618843	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs60997310	chr12:9618854-9618855	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs397951257	chr12:9618855-9618856	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs3867148	chr12:9618930-9618931	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570931187	chr12:9618979-9618980	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184533923	chr12:9619007-9619008	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs536600090	chr12:9619044-9619045	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs16916227	chr12:9619074-9619075	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs2536687	chr12:9619077-9619078	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9607200-9623000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:9608800-9642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:9610200-9621000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:9611200-9621400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:9615200-9621600	Weak transcription	Fetal Muscle Leg	muscle
6	chr12:9615400-9622600	Weak transcription	Primary B cells from peripheral blood	blood
7	chr12:9617000-9618800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:9617400-9621600	Weak transcription	Fetal Lung	lung
9	chr12:9617600-9618200	Enhancers	GM12878-XiMat	blood
10	chr12:9617800-9622800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr12:9618200-9622600	Weak transcription	GM12878-XiMat	blood
12	chr12:9618800-9621000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:9619600-9621600	Enhancers	Fetal Heart	heart
14	chr12:9619600-9623600	Enhancers	Fetal Thymus	thymus
15	chr12:9620800-9621200	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr12:9620800-9623600	Enhancers	Primary T cells from cord blood	blood
17	chr12:9620800-9623600	Enhancers	Primary T cells fromperipheralblood	blood
18	chr12:9621000-9621200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr12:9621000-9621400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:9621000-9621600	Enhancers	HSMMtube	muscle
21	chr12:9621000-9621800	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr12:9621000-9621800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr12:9621000-9621800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:9621000-9621800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr12:9621000-9622000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:9621000-9622000	Enhancers	HepG2	liver
27	chr12:9621000-9622200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr12:9621000-9623600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:9621200-9621400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr12:9621200-9621800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr12:9621200-9621800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr12:9621400-9621600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr12:9621400-9621800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr12:9621400-9621800	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr12:9621400-9622000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:9621400-9622000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:9621400-9622400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr12:9621400-9623600	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr12:9621600-9621800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr12:9621600-9621800	Enhancers	Fetal Muscle Leg	muscle
41	chr12:9621600-9621800	Enhancers	Thymus	Thymus
42	chr12:9621600-9622000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr12:9621600-9622000	Enhancers	Liver	Liver
44	chr12:9621600-9622000	Enhancers	Fetal Lung	lung
45	chr12:9621600-9622000	Enhancers	Dnd41	blood
46	chr12:9621800-9622600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr12:9621800-9622800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr12:9621800-9623000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr12:9621800-9623000	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr12:9621800-9623000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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