Variant report

Variant	esv1800244
Chromosome Location	chr12:8214261-8224464
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	chr12:8218663-8219299	K562	blood:	n/a	n/a
2	ARID3A	chr12:8223247-8223270	K562	blood:	n/a	n/a
3	ARID3A	chr12:8219892-8220025	K562	blood:	n/a	n/a
4	ATF1	chr12:8218747-8219252	K562	blood:	n/a	n/a
5	ATF3	chr12:8218859-8219211	K562	blood:	n/a	n/a
6	BACH1	chr12:8216821-8216976	K562	blood:	n/a	n/a
7	BATF	chr12:8218866-8219202	GM12878	blood:	n/a	chr12:8219082-8219092 chr12:8219081-8219092
8	BATF	chr12:8218912-8219211	GM12878	blood:	n/a	chr12:8219082-8219092 chr12:8219081-8219092
9	BHLHE40	chr12:8218960-8219156	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:8218097-8218116	K562	blood:	n/a	n/a
11	BHLHE40	chr12:8218933-8219206	K562	blood:	n/a	n/a
12	CBX3	chr12:8218747-8219249	K562	blood:	n/a	n/a
13	CCNT2	chr12:8218733-8219208	K562	blood:	n/a	n/a
14	CHD2	chr12:8218880-8219025	K562	blood:	n/a	n/a
15	CTCF	chr12:8218929-8219063	K562	blood:	n/a	n/a
16	CUX1	chr12:8219570-8219730	K562	blood:	n/a	n/a
17	CUX1	chr12:8223099-8223484	K562	blood:	n/a	n/a
18	CUX1	chr12:8218481-8219215	K562	blood:	n/a	n/a
19	EGR1	chr12:8223187-8223428	K562	blood:	n/a	chr12:8223301-8223314
20	ELF1	chr12:8218893-8219136	K562	blood:	n/a	n/a
21	ELF1	chr12:8218780-8219181	K562	blood:	n/a	n/a
22	ELF1	chr12:8218812-8219198	GM12878	blood:	n/a	n/a
23	ELF1	chr12:8218776-8219304	SK-N-SH	brain:	n/a	n/a
24	EP300	chr12:8218989-8219233	GM12878	blood:	n/a	chr12:8219080-8219089 chr12:8218991-8219005
25	EP300	chr12:8223221-8223262	K562	blood:	n/a	n/a
26	EP300	chr12:8218468-8219219	K562	blood:	n/a	chr12:8219080-8219089 chr12:8218991-8219005
27	EP300	chr12:8218958-8219294	GM12878	blood:	n/a	chr12:8219080-8219089 chr12:8218991-8219005
28	EP300	chr12:8219031-8219095	GM12878	blood:	n/a	chr12:8219080-8219089
29	FOS	chr12:8218922-8219254	MCF10A-Er-Src	breast:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219079-8219090 chr12:8219074-8219086
30	FOS	chr12:8218888-8219307	MCF10A-Er-Src	breast:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219079-8219090 chr12:8219074-8219086
31	FOS	chr12:8218888-8219238	MCF10A-Er-Src	breast:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219079-8219090 chr12:8219074-8219086
32	FOS	chr12:8218692-8219297	HUVEC	blood vessel:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219079-8219090 chr12:8219074-8219086
33	FOSL2	chr12:8218810-8219348	SK-N-SH	brain:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219074-8219086
34	GATA2	chr12:8218645-8219384	HUVEC	blood vessel:	n/a	n/a
35	HCFC1	chr12:8218961-8219245	K562	blood:	n/a	n/a
36	HEY1	chr12:8218779-8218997	K562	blood:	n/a	n/a
37	HMGN3	chr12:8218652-8219206	K562	blood:	n/a	n/a
38	IRF1	chr12:8216771-8217032	K562	blood:	n/a	n/a
39	IRF1	chr12:8222633-8222934	K562	blood:	n/a	n/a
40	IRF1	chr12:8216791-8217038	K562	blood:	n/a	n/a
41	IRF1	chr12:8218616-8219271	K562	blood:	n/a	chr12:8219227-8219241
42	JUN	chr12:8218790-8219249	K562	blood:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219074-8219086
43	JUN	chr12:8218522-8219429	K562	blood:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219074-8219086
44	JUN	chr12:8218698-8219536	K562	blood:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219074-8219086
45	JUN	chr12:8218837-8219244	HUVEC	blood vessel:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219074-8219086
46	JUND	chr12:8223225-8223329	K562	blood:	n/a	n/a
47	JUND	chr12:8218638-8219548	K562	blood:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219074-8219086
48	JUND	chr12:8218762-8219388	SK-N-SH	brain:	n/a	chr12:8219080-8219090 chr12:8219080-8219089 chr12:8219080-8219090 chr12:8219082-8219089 chr12:8219074-8219086
49	KAP1	chr12:8218738-8219213	U2OS	brain:	n/a	chr12:8218989-8218997 chr12:8219082-8219091
50	KAP1	chr12:8218481-8219182	K562	blood:	n/a	chr12:8218989-8218997 chr12:8219082-8219091

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8220002-8220052	Hepatocyte	liver:	n/a
2	chr12:8218922-8218972	PrEC	prostate:	n/a
3	chr12:8220002-8220052	CMK	blood:	n/a
4	chr12:8219020-8219070	GM06990	blood:	n/a
5	chr12:8218922-8218972	SAEC	small airway:	n/a
6	chr12:8216109-8216159	SK-N-SH_RA	brain:	n/a
7	chr12:8219358-8219408	AoSMC	blood vessel:	n/a
8	chr12:8219358-8219408	AG09309	skin:	n/a
9	chr12:8219020-8219070	NH-A	brain:	n/a
10	chr12:8218922-8218972	HRE	kidney:	n/a
11	chr12:8218922-8218972	HepG2	liver:	n/a
12	chr12:8219020-8219070	BJ	skin:	n/a
13	chr12:8218922-8218972	Hela-S3	cervix:	n/a
14	chr12:8218922-8218972	HL-60	blood:	n/a
15	chr12:8218922-8218972	GM06990	blood:	n/a
16	chr12:8219020-8219070	SKMC	muscle:	n/a
17	chr12:8218922-8218972	MCF10A-Er-Src	breast:	n/a
18	chr12:8219358-8219408	AG04450	lung:	fetal
19	chr12:8218922-8218972	Caco-2	colon:	n/a
20	chr12:8219358-8219408	A549	lung:	n/a
21	chr12:8218922-8218972	NB4	blood:	n/a
22	chr12:8216109-8216159	HepG2	liver:	n/a
23	chr12:8220002-8220052	ProgFib	skin:	n/a
24	chr12:8219020-8219070	HCF	heart:	n/a
25	chr12:8219358-8219408	IMR90	lung:	fetal
26	chr12:8219020-8219070	HCM	heart:	n/a
27	chr12:8219020-8219070	ovcar-3	ovarian:	n/a
28	chr12:8219358-8219408	U87	brain:	n/a
29	chr12:8219020-8219070	GM12878	blood:	n/a
30	chr12:8218922-8218972	SKMC	muscle:	n/a
31	chr12:8219358-8219408	SK-N-SH_RA	brain:	n/a
32	chr12:8219020-8219070	AG09309	skin:	n/a
33	chr12:8219020-8219070	HAEpiC	amniotic membrane:	n/a
34	chr12:8218922-8218972	AG09319	gingival:	n/a
35	chr12:8219020-8219070	NB4	blood:	n/a
36	chr12:8220002-8220052	Hela-S3	cervix:	n/a
37	chr12:8219358-8219408	ECC-1	luminal epithelium:	n/a
38	chr12:8219020-8219070	K562	blood:	n/a
39	chr12:8218922-8218972	AoSMC	blood vessel:	n/a
40	chr12:8220002-8220052	HRPEpiC	eye:	n/a
41	chr12:8220002-8220052	K562	blood:	n/a
42	chr12:8216109-8216159	PANC-1	pancreas:	n/a
43	chr12:8219020-8219070	H1-hESC	embryonic stem cell:	embryo
44	chr12:8216109-8216159	NB4	blood:	n/a
45	chr12:8219020-8219070	HNPCEpiC	eye:	n/a
46	chr12:8220002-8220052	SK-N-SH	brain:	n/a
47	chr12:8219020-8219070	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:8220002-8220052	BJ	skin:	n/a
49	chr12:8219358-8219408	MCF10A-Er-Src	breast:	n/a
50	chr12:8218922-8218972	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:8223318..8224960-chr12:8230452..8232757,2	K562	blood:
2	chr12:8194960..8197695-chr12:8212666..8215370,2	K562	blood:
3	chr12:8211948..8215026-chr12:8217388..8219244,3	K562	blood:
4	chr12:8221669..8224292-chr12:8233219..8235745,2	MCF-7	breast:
5	chr12:8220893..8223462-chr12:8227865..8229975,2	K562	blood:
6	chr12:8218395..8221034-chr12:8223986..8225652,2	K562	blood:
7	chr12:8220956..8223794-chr12:8232037..8234849,3	K562	blood:
8	chr12:8217345..8219129-chr12:8233768..8236260,3	K562	blood:

Variant related genes	Relation type
C3AR1	TF binding region
C3AR1	CpG island
ENSG00000171860	chromatin interactions
ENSG00000089818	chromatin interactions

Extended variants
information (count: 229 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:229 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11567802	chr12:8214261-8214262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552217253	chr12:8214362-8214363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374184035	chr12:8214454-8214455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183176572	chr12:8214661-8214662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187967044	chr12:8214676-8214677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191423168	chr12:8214838-8214839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2110070	chr12:8214856-8214857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs531292824	chr12:8214890-8214891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs372823333	chr12:8214940-8214941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539917552	chr12:8214979-8214980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149460418	chr12:8215115-8215116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11567801	chr12:8215116-8215117	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182375543	chr12:8215195-8215196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187920677	chr12:8215271-8215272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78381356	chr12:8215333-8215334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148278380	chr12:8215336-8215337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112626788	chr12:8215505-8215506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184653135	chr12:8215506-8215507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368317759	chr12:8215540-8215541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs71451936	chr12:8215570-8215571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141239031	chr12:8215604-8215605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11567800	chr12:8215623-8215624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs28470705	chr12:8215672-8215673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11567799	chr12:8215702-8215703	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs28410785	chr12:8215711-8215712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10846447	chr12:8215754-8215755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11567798	chr12:8215769-8215770	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs375766628	chr12:8215773-8215774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192091452	chr12:8215795-8215796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11567797	chr12:8215799-8215800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11567796	chr12:8215803-8215804	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs11567795	chr12:8215807-8215808	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs369070201	chr12:8216133-8216134	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs11567794	chr12:8216136-8216137	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs11567793	chr12:8216157-8216158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs11567792	chr12:8216168-8216169	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs181449849	chr12:8216266-8216267	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs554159783	chr12:8216289-8216290	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs11567791	chr12:8216308-8216309	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs55687531	chr12:8216310-8216311	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs184204198	chr12:8216415-8216416	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs11567790	chr12:8216416-8216417	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1966409	chr12:8216576-8216577	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs200004880	chr12:8216681-8216682	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs372128078	chr12:8216690-8216691	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs539277419	chr12:8216806-8216807	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7956636	chr12:8216854-8216855	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374384318	chr12:8216872-8216873	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11567789	chr12:8216873-8216874	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72135277	chr12:8216874-8216875	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8203000-8218800	Weak transcription	HMEC	breast
2	chr12:8203400-8217400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr12:8205600-8218800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:8205600-8218800	Weak transcription	Hela-S3	cervix
5	chr12:8206000-8221600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr12:8206200-8217200	Weak transcription	K562	blood
7	chr12:8206200-8218800	Weak transcription	NH-A	brain
8	chr12:8206600-8216800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr12:8206800-8218400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr12:8207600-8215400	Weak transcription	Colonic Mucosa	Colon
11	chr12:8207600-8217200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:8207600-8217800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr12:8207600-8218800	Weak transcription	NHDF-Ad	bronchial
14	chr12:8207800-8217000	Weak transcription	Placenta	Placenta
15	chr12:8207800-8218000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr12:8207800-8218400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr12:8207800-8221400	Weak transcription	Brain Substantia Nigra	brain
18	chr12:8208000-8217400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr12:8208000-8217400	Weak transcription	Duodenum Mucosa	Duodenum
20	chr12:8208000-8218400	Weak transcription	GM12878-XiMat	blood
21	chr12:8208000-8218800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:8208000-8218800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:8208000-8218800	Weak transcription	Thymus	Thymus
24	chr12:8208200-8216400	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr12:8208200-8218400	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr12:8208200-8218800	Weak transcription	Fetal Thymus	thymus
27	chr12:8208400-8216400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:8208400-8216600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr12:8208400-8216800	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr12:8208400-8217400	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr12:8208400-8217400	Weak transcription	Fetal Muscle Leg	muscle
32	chr12:8208400-8217400	Weak transcription	Left Ventricle	heart
33	chr12:8208400-8217600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr12:8208400-8218200	Weak transcription	Dnd41	blood
35	chr12:8208400-8218400	Weak transcription	Liver	Liver
36	chr12:8208400-8218400	Weak transcription	Brain Hippocampus Middle	brain
37	chr12:8208400-8218600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr12:8208400-8218800	Weak transcription	Primary B cells from peripheral blood	blood
39	chr12:8208400-8218800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr12:8208400-8218800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:8208400-8218800	Weak transcription	HSMMtube	muscle
42	chr12:8208600-8217400	Weak transcription	Primary T cells from cord blood	blood
43	chr12:8208600-8219600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr12:8208600-8233800	Weak transcription	Aorta	Aorta
45	chr12:8210600-8218600	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr12:8210600-8218800	Weak transcription	Osteobl	bone
47	chr12:8211000-8218600	Weak transcription	NHEK	skin
48	chr12:8211200-8217400	Weak transcription	Primary B cells from cord blood	blood
49	chr12:8211200-8218400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:8211200-8218800	Weak transcription	NHLF	lung

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