Variant report

Variant	nsv8907
Chromosome Location	chr12:9564662-9575213
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:237)
CpG islands
(count:245)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:237 , 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	chr12:9574493-9574708	GM12878	blood:	n/a	n/a
2	BCL11A	chr12:9564505-9564797	GM12878	blood:	n/a	n/a
3	CTCF	chr12:9569276-9569366	GM13976	blood:	n/a	n/a
4	CTCF	chr12:9564875-9565007	GM19238	blood:	n/a	n/a
5	CTCF	chr12:9564895-9565004	GM12878	blood:	n/a	n/a
6	CTCF	chr12:9564884-9565025	GM19239	blood:	n/a	n/a
7	CTCF	chr12:9564891-9565000	A549	lung:	n/a	n/a
8	CTCF	chr12:9564939-9564974	GM12891	blood:	n/a	n/a
9	CTCF	chr12:9564888-9565004	MCF-7	breast:	n/a	n/a
10	CTCF	chr12:9564865-9565009	K562	blood:	n/a	n/a
11	CTCF	chr12:9569018-9569050	GM20000	blood:	n/a	n/a
12	CTCF	chr12:9573096-9573215	Lung_OC	lung:	n/a	n/a
13	CTCF	chr12:9571174-9571189	MCF-7	breast:	n/a	n/a
14	CTCF	chr12:9564896-9565031	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr12:9574373-9574453	GM12892	blood:	n/a	n/a
16	CTCF	chr12:9564877-9565006	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:9575168-9575296	GM10248	blood:	n/a	n/a
18	CTCF	chr12:9564942-9565007	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr12:9564889-9564998	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:9566834-9566892	GM13976	blood:	n/a	n/a
21	CTCF	chr12:9564893-9565003	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:9570603-9570657	GM13976	blood:	n/a	n/a
23	CTCF	chr12:9564891-9565003	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:9564955-9564994	NHEK	skin:	n/a	n/a
25	CTCF	chr12:9573212-9573231	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr12:9572556-9572580	GM10248	blood:	n/a	n/a
27	CTCF	chr12:9568917-9568998	Lung_OC	lung:	n/a	n/a
28	CTCF	chr12:9571200-9571280	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:9564927-9564999	GM19240	blood:	n/a	n/a
30	CTCF	chr12:9564877-9565011	GM12892	blood:	n/a	n/a
31	EBF1	chr12:9568820-9569199	GM12878	blood:	n/a	n/a
32	EGR1	chr12:9564605-9564769	GM12878	blood:	n/a	chr12:9564650-9564664
33	EP300	chr12:9564842-9565723	SK-N-SH	brain:	n/a	n/a
34	FOSL2	chr12:9570481-9570818	HepG2	liver:	n/a	n/a
35	FOSL2	chr12:9570908-9571436	HepG2	liver:	n/a	n/a
36	FOSL2	chr12:9570963-9571293	HepG2	liver:	n/a	n/a
37	FOSL2	chr12:9567289-9567717	HepG2	liver:	n/a	chr12:9567422-9567434
38	FOSL2	chr12:9568782-9569231	HepG2	liver:	n/a	chr12:9569127-9569137 chr12:9569127-9569137 chr12:9569127-9569137
39	FOSL2	chr12:9565420-9565663	HepG2	liver:	n/a	n/a
40	FOXA1	chr12:9570909-9571427	HepG2	liver:	n/a	n/a
41	GABPA	chr12:9570487-9570698	Hela-S3	cervix:	n/a	n/a
42	HEY1	chr12:9570914-9571429	HepG2	liver:	n/a	n/a
43	HEY1	chr12:9570970-9571383	HepG2	liver:	n/a	n/a
44	JUND	chr12:9571056-9571388	HepG2	liver:	n/a	n/a
45	JUND	chr12:9570539-9570728	HepG2	liver:	n/a	n/a
46	JUND	chr12:9571147-9571267	HepG2	liver:	n/a	n/a
47	MAX	chr12:9564441-9564760	GM12878	blood:	n/a	n/a
48	MYC	chr12:9571111-9571252	MCF-7	breast:	n/a	n/a
49	MYC	chr12:9571057-9571198	HepG2	liver:	n/a	n/a
50	MYC	chr12:9566336-9566351	HepG2	liver:	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	chr12:9573914-9573964	ECC-1	luminal epithelium:	n/a
2	chr12:9573914-9573964	ECC-1	luminal epithelium:	n/a
3	chr12:9573914-9573964	RPTEC	kidney:	n/a
4	chr12:9573914-9573964	HUVEC	blood vessel:	n/a
5	chr12:9568315-9568365	HCPEpiC	choroid plexus:	n/a
6	chr12:9571130-9571180	SK-N-SH	brain:	n/a
7	chr12:9569744-9569794	AoSMC	blood vessel:	n/a
8	chr12:9569744-9569794	SK-N-SH	brain:	n/a
9	chr12:9568315-9568365	RPTEC	kidney:	n/a
10	chr12:9571130-9571180	NB4	blood:	n/a
11	chr12:9573914-9573964	PFSK-1	brain:	n/a
12	chr12:9568315-9568365	ProgFib	skin:	n/a
13	chr12:9568315-9568365	HRCEpiC	kidney:	n/a
14	chr12:9573914-9573964	AG10803	skin:	n/a
15	chr12:9573914-9573964	HAEpiC	amniotic membrane:	n/a
16	chr12:9569744-9569794	NB4	blood:	n/a
17	chr12:9568315-9568365	PrEC	prostate:	n/a
18	chr12:9568315-9568365	MCF-7	breast:	n/a
19	chr12:9573914-9573964	GM06990	blood:	n/a
20	chr12:9573914-9573964	SK-N-MC	brain:	n/a
21	chr12:9571130-9571180	HRE	kidney:	n/a
22	chr12:9569744-9569794	U87	brain:	n/a
23	chr12:9573914-9573964	AG04449	skin:	fetal
24	chr12:9569744-9569794	HUVEC	blood vessel:	n/a
25	chr12:9571130-9571180	PrEC	prostate:	n/a
26	chr12:9568315-9568365	SAEC	small airway:	n/a
27	chr12:9569744-9569794	AG04450	lung:	fetal
28	chr12:9573914-9573964	HRPEpiC	eye:	n/a
29	chr12:9568315-9568365	GM12878	blood:	n/a
30	chr12:9569744-9569794	GM19239	blood:	n/a
31	chr12:9571130-9571180	Hepatocyte	liver:	n/a
32	chr12:9569744-9569794	HCF	heart:	n/a
33	chr12:9571130-9571180	GM19239	blood:	n/a
34	chr12:9568315-9568365	U87	brain:	n/a
35	chr12:9571130-9571180	AG04450	lung:	fetal
36	chr12:9571130-9571180	HRCEpiC	kidney:	n/a
37	chr12:9573914-9573964	PANC-1	pancreas:	n/a
38	chr12:9568315-9568365	AG09319	gingival:	n/a
39	chr12:9568315-9568365	NHDF-neo	bronchial:	n/a
40	chr12:9568315-9568365	GM06990	blood:	n/a
41	chr12:9573914-9573964	A549	lung:	n/a
42	chr12:9569744-9569794	NHBE	bronchial:	n/a
43	chr12:9573914-9573964	HRE	kidney:	n/a
44	chr12:9573914-9573964	Hela-S3	cervix:	n/a
45	chr12:9573914-9573964	BE2_C	brain:	n/a
46	chr12:9573914-9573964	LNCaP	prostate:	n/a
47	chr12:9568315-9568365	HepG2	liver:	n/a
48	chr12:9569744-9569794	GM12891	blood:	n/a
49	chr12:9568315-9568365	PFSK-1	brain:	n/a
50	chr12:9573914-9573964	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9471764..9473665-chr12:9564371..9566160,2	MCF-7	breast:
2	chr12:9471846..9472542-chr12:9564639..9565202,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PZP-12	chr12:9566315-9566384	NONHSAT026823
2	lnc-PZP-12	chr12:9565722-9566143	NONHSAT026825
3	lnc-PZP-12	chr12:9565722-9566137	NONHSAT026823
4	lnc-PZP-12	chr12:9567399-9567447	NONHSAT026817
5	lnc-PZP-12	chr12:9564668-9564845	NONHSAT026825

No data

Variant related genes	Relation type
ENSG00000256673	TF binding region
ENSG00000256673	CpG island

Extended variants
information (count: 317 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182251844	chr12:9564671-9564672	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
2	rs113021273	chr12:9564704-9564705	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs74062840	chr12:9564705-9564706	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs10843720	chr12:9564727-9564728	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186150681	chr12:9564737-9564738	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs145662627	chr12:9564749-9564750	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs569736061	chr12:9564768-9564769	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs181482566	chr12:9564778-9564779	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
9	rs191005698	chr12:9564795-9564796	Weak transcription Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs74062841	chr12:9564826-9564827	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs74062842	chr12:9564861-9564862	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs182834714	chr12:9564908-9564909	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544525619	chr12:9564937-9564938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368408011	chr12:9565044-9565045	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs555465081	chr12:9565158-9565159	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs147353598	chr12:9565205-9565206	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386760181	chr12:9565206-9565207	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12296667	chr12:9565208-9565209	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs150582255	chr12:9565257-9565258	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188540284	chr12:9565293-9565294	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370589452	chr12:9565303-9565304	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117707113	chr12:9565400-9565401	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192912045	chr12:9565404-9565405	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111352058	chr12:9565534-9565535	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201355602	chr12:9565552-9565553	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182796829	chr12:9565555-9565556	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145202058	chr12:9565636-9565637	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116470785	chr12:9565642-9565643	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188307454	chr12:9565680-9565681	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568492967	chr12:9565732-9565733	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs55638494	chr12:9565753-9565754	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs557564451	chr12:9565756-9565757	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs191300056	chr12:9565817-9565818	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs148385680	chr12:9565823-9565824	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs183888066	chr12:9565837-9565838	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs189398648	chr12:9565900-9565901	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs537072521	chr12:9565920-9565921	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs7312968	chr12:9565979-9565980	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543214492	chr12:9566122-9566123	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs59453560	chr12:9566138-9566139	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs56091587	chr12:9566200-9566201	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs56878978	chr12:9566247-9566248	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192635799	chr12:9566254-9566255	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10843723	chr12:9566302-9566303	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs71447570	chr12:9566340-9566341	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs549823872	chr12:9566371-9566372	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs569906932	chr12:9566412-9566413	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7967859	chr12:9566465-9566466	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150736580	chr12:9566521-9566522	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548730490	chr12:9566531-9566532	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
early-passage human iPS cells	21368824	CNVD
Obesity	21131291	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Cancer	21272361	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9544800-9593200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:9545400-9573800	Weak transcription	Fetal Intestine Small	intestine
3	chr12:9545400-9575600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:9557600-9572200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr12:9557800-9571400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:9558800-9566600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr12:9559000-9565800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:9559200-9571000	Weak transcription	Thymus	Thymus
9	chr12:9559200-9599600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr12:9559600-9576600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:9559800-9565600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:9559800-9566000	Weak transcription	Lung	lung
13	chr12:9559800-9572000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:9559800-9573800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr12:9559800-9574000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr12:9559800-9577800	Weak transcription	A549	lung
17	chr12:9560000-9569600	Weak transcription	Fetal Stomach	stomach
18	chr12:9560000-9572000	Weak transcription	Fetal Muscle Leg	muscle
19	chr12:9560000-9576400	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr12:9560000-9584000	Weak transcription	Right Ventricle	heart
21	chr12:9560000-9599800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr12:9560200-9599600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr12:9560400-9599600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr12:9560400-9599600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr12:9563800-9565200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:9563800-9565200	Enhancers	Primary B cells from peripheral blood	blood
27	chr12:9564000-9564800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:9564000-9565000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:9564000-9565000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:9564000-9565200	Enhancers	Primary B cells from cord blood	blood
31	chr12:9564000-9565400	Enhancers	GM12878-XiMat	blood
32	chr12:9564200-9564800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr12:9564200-9564800	Enhancers	NHEK	skin
34	chr12:9564200-9565000	Strong transcription	Dnd41	blood
35	chr12:9564200-9584600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:9564400-9564800	Enhancers	Fetal Lung	lung
37	chr12:9564400-9565000	Enhancers	HepG2	liver
38	chr12:9564400-9566000	Enhancers	Brain Germinal Matrix	brain
39	chr12:9564400-9566800	Enhancers	Fetal Thymus	thymus
40	chr12:9564600-9564800	Flanking Active TSS	Primary T cells from cord blood	blood
41	chr12:9564600-9564800	Enhancers	Primary T cells fromperipheralblood	blood
42	chr12:9564600-9565000	Enhancers	Esophagus	oesophagus
43	chr12:9564600-9567200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr12:9564800-9565000	Enhancers	Primary T cells from cord blood	blood
45	chr12:9564800-9565000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr12:9564800-9565600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr12:9564800-9565600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr12:9564800-9573800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:9564800-9578000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr12:9564800-9586000	Weak transcription	Fetal Lung	lung

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