Variant report

Variant	nsv909395
Chromosome Location	chr18:12057195-12078224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:399)
CpG islands
(count:733)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr18:12076645-12076788	K562	blood:	n/a	n/a
2	CEBPB	chr18:12067920-12068124	HepG2	liver:	n/a	n/a
3	CEBPB	chr18:12069057-12069324	K562	blood:	n/a	n/a
4	CEBPB	chr18:12069020-12069213	IMR90	lung:	n/a	n/a
5	CEBPB	chr18:12067926-12068149	K562	blood:	n/a	n/a
6	CREB1	chr18:12076434-12076834	A549	lung:	n/a	n/a
7	CTCF	chr18:12068580-12068730	GM12870	blood:	n/a	n/a
8	CTCF	chr18:12074852-12074996	Gliobla	brain:	n/a	n/a
9	CTCF	chr18:12068476-12068627	Pancreas_OC	pancreas:	n/a	n/a
10	CTCF	chr18:12074860-12075010	GM12872	blood:	n/a	n/a
11	CTCF	chr18:12074860-12075010	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr18:12068437-12068606	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr18:12057760-12057920	GM12878	blood:	n/a	n/a
14	CTCF	chr18:12057740-12057890	HEK293	kidney:	n/a	n/a
15	CTCF	chr18:12057760-12057910	GM12867	blood:	n/a	n/a
16	CTCF	chr18:12068460-12068610	GM12864	blood:	n/a	n/a
17	CTCF	chr18:12057649-12058004	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr18:12057680-12057830	A549	lung:	n/a	n/a
19	CTCF	chr18:12057700-12057932	K562	blood:	n/a	n/a
20	CTCF	chr18:12074840-12074990	HAc	cerebellar:	n/a	n/a
21	CTCF	chr18:12074860-12075010	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr18:12068420-12068570	HCM	heart:	n/a	n/a
23	CTCF	chr18:12074880-12075030	SAEC	small airway:	n/a	n/a
24	CTCF	chr18:12057800-12057950	GM12873	blood:	n/a	n/a
25	CTCF	chr18:12057780-12057930	GM12873	blood:	n/a	n/a
26	CTCF	chr18:12074860-12075010	AG04449	skin:	n/a	n/a
27	CTCF	chr18:12074880-12074950	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr18:12074920-12075070	NHEK	skin:	n/a	n/a
29	CTCF	chr18:12074860-12075010	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr18:12068400-12068550	HVMF	connective:	n/a	n/a
31	CTCF	chr18:12057742-12057941	HepG2	liver:	n/a	n/a
32	CTCF	chr18:12068420-12068570	HCT-116	colon:	n/a	n/a
33	CTCF	chr18:12074940-12075090	HVMF	connective:	n/a	n/a
34	CTCF	chr18:12064512-12064580	MCF-7	breast:	n/a	n/a
35	CTCF	chr18:12057760-12057910	GM06990	blood:	n/a	n/a
36	CTCF	chr18:12064578-12064639	ProgFib	skin:	n/a	n/a
37	CTCF	chr18:12068480-12068630	HCM	heart:	n/a	n/a
38	CTCF	chr18:12074840-12074990	GM12865	blood:	n/a	n/a
39	CTCF	chr18:12074877-12074982	MCF-7	breast:	n/a	n/a
40	CTCF	chr18:12074840-12074990	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr18:12074880-12075030	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr18:12057729-12057925	GM12891	blood:	n/a	n/a
43	CTCF	chr18:12068552-12068593	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr18:12057740-12057890	HVMF	connective:	n/a	n/a
45	CTCF	chr18:12057740-12057890	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr18:12068400-12068550	HCT-116	colon:	n/a	n/a
47	CTCF	chr18:12060258-12060397	Gliobla	brain:	n/a	n/a
48	CTCF	chr18:12074880-12075030	GM12875	blood:	n/a	n/a
49	CTCF	chr18:12057783-12057875	GM13977	blood:	n/a	n/a
50	CTCF	chr18:12057700-12057850	GM12872	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12076435-12076485	GM19239	blood:	n/a
2	chr18:12076435-12076485	GM19239	blood:	n/a
3	chr18:12064388-12064438	AG04450	lung:	fetal
4	chr18:12076476-12076526	HCF	heart:	n/a
5	chr18:12076365-12076415	IMR90	lung:	fetal
6	chr18:12077147-12077197	IMR90	lung:	fetal
7	chr18:12068884-12068934	CMK	blood:	n/a
8	chr18:12076365-12076415	A549	lung:	n/a
9	chr18:12076365-12076415	GM12892	blood:	n/a
10	chr18:12076435-12076485	SK-N-MC	brain:	n/a
11	chr18:12068363-12068413	ProgFib	skin:	n/a
12	chr18:12064388-12064438	HepG2	liver:	n/a
13	chr18:12072395-12072445	H1-hESC	embryonic stem cell:	embryo
14	chr18:12067067-12067117	NH-A	brain:	n/a
15	chr18:12076435-12076485	HCPEpiC	choroid plexus:	n/a
16	chr18:12064388-12064438	SK-N-SH	brain:	n/a
17	chr18:12076365-12076415	Caco-2	colon:	n/a
18	chr18:12072395-12072445	HIPEpiC	eye:	n/a
19	chr18:12073455-12073505	GM12878	blood:	n/a
20	chr18:12072395-12072445	AoSMC	blood vessel:	n/a
21	chr18:12076476-12076526	NHDF-neo	bronchial:	n/a
22	chr18:12077147-12077197	Jurkat	blood:	n/a
23	chr18:12077147-12077197	HepG2	liver:	n/a
24	chr18:12073455-12073505	HCF	heart:	n/a
25	chr18:12077147-12077197	AG04450	lung:	fetal
26	chr18:12068099-12068149	LNCaP	prostate:	n/a
27	chr18:12064388-12064438	HMEC	breast:	n/a
28	chr18:12077147-12077197	HCM	heart:	n/a
29	chr18:12073455-12073505	SK-N-SH_RA	brain:	n/a
30	chr18:12073455-12073505	AG10803	skin:	n/a
31	chr18:12068065-12068115	GM06990	blood:	n/a
32	chr18:12067067-12067117	AG09309	skin:	n/a
33	chr18:12073455-12073505	HCPEpiC	choroid plexus:	n/a
34	chr18:12077147-12077197	HRPEpiC	eye:	n/a
35	chr18:12073455-12073505	GM19239	blood:	n/a
36	chr18:12067067-12067117	HEK293	kidney:	embryo
37	chr18:12072395-12072445	NH-A	brain:	n/a
38	chr18:12068065-12068115	HRCEpiC	kidney:	n/a
39	chr18:12068099-12068149	GM12878	blood:	n/a
40	chr18:12068099-12068149	PFSK-1	brain:	n/a
41	chr18:12068884-12068934	NHDF-neo	bronchial:	n/a
42	chr18:12076476-12076526	NH-A	brain:	n/a
43	chr18:12072395-12072445	MCF-7	breast:	n/a
44	chr18:12076365-12076415	PFSK-1	brain:	n/a
45	chr18:12067067-12067117	K562	blood:	n/a
46	chr18:12076435-12076485	PANC-1	pancreas:	n/a
47	chr18:12076435-12076485	K562	blood:	n/a
48	chr18:12076365-12076415	HCM	heart:	n/a
49	chr18:12077147-12077197	HCF	heart:	n/a
50	chr18:12068363-12068413	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:12067124..12068647-chr19:18543710..18545740,2	K562	blood:
2	chr18:12076450..12076959-chr4:22517248..22517778,2	HCT-116	colon:
3	chr18:12063010..12065990-chr19:13351067..13352603,2	MCF-7	breast:
4	chr18:12067124..12068644-chr19:18543710..18545856,2	K562	blood:
5	chr18:12057151..12059400-chr18:12062481..12064510,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD62-1	chr18:12074792-12075074	XLOC_012628
2	lnc-ANKRD62-1	chr18:12073319-12073537	XLOC_012628

No data

Variant related genes	Relation type
ENSG00000267722	TF binding region
ENSG00000256616	TF binding region
ENSG00000267533	TF binding region
ENSG00000212712	TF binding region
ENSG00000267722	CpG island
ENSG00000256616	CpG island
ENSG00000267533	CpG island
ENSG00000212712	CpG island
ENSG00000212712	chromatin interactions
ENSG00000152990	chromatin interactions
ENSG00000130511	chromatin interactions

Extended variants
information (count: 944 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9959517	chr18:12057195-12057196	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571439078	chr18:12057201-12057202	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs538841530	chr18:12057202-12057203	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs557928956	chr18:12057239-12057240	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs573287355	chr18:12057254-12057255	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs533935362	chr18:12057268-12057269	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs531253322	chr18:12057282-12057283	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs555380702	chr18:12057309-12057310	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs573981222	chr18:12057347-12057348	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs374455994	chr18:12057348-12057349	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs544534706	chr18:12057367-12057368	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs562868758	chr18:12057378-12057379	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs575315511	chr18:12057379-12057380	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs9959781	chr18:12057389-12057390	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs189661116	chr18:12057400-12057401	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9959774	chr18:12057403-12057404	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs527429249	chr18:12057409-12057410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370308283	chr18:12057422-12057423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548990939	chr18:12057451-12057452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115577825	chr18:12057455-12057456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181498192	chr18:12057492-12057493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375315532	chr18:12057498-12057499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185795660	chr18:12057550-12057551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538405640	chr18:12057568-12057569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547613748	chr18:12057576-12057577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528287937	chr18:12057577-12057578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9960082	chr18:12057635-12057636	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs555321749	chr18:12057670-12057671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573331433	chr18:12057671-12057672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200165173	chr18:12057693-12057694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573671754	chr18:12057706-12057707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565910244	chr18:12057720-12057721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73406519	chr18:12057731-12057732	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs141694675	chr18:12057744-12057745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548033250	chr18:12057750-12057751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565370007	chr18:12057751-12057752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs578199717	chr18:12057808-12057809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9960429	chr18:12057809-12057810	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs73947225	chr18:12057812-12057813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572032165	chr18:12057844-12057845	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs190659293	chr18:12057845-12057846	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs9960443	chr18:12057854-12057855	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs531291613	chr18:12057875-12057876	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs181863284	chr18:12057878-12057879	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs565027489	chr18:12057882-12057883	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs7237877	chr18:12057904-12057905	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs150101724	chr18:12057910-12057911	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs138386103	chr18:12057913-12057914	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs7236715	chr18:12057923-12057924	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs372950568	chr18:12057936-12057937	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12049000-12060000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:12054200-12063400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:12055600-12076400	Weak transcription	Right Atrium	heart
4	chr18:12056400-12061600	Weak transcription	Spleen	Spleen
5	chr18:12056800-12057200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr18:12056800-12057200	Enhancers	Fetal Stomach	stomach
7	chr18:12056800-12057400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr18:12057400-12058000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr18:12058000-12059400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr18:12059400-12059800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr18:12059400-12059800	Enhancers	Lung	lung
12	chr18:12059800-12060200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr18:12059800-12060800	Enhancers	A549	lung
14	chr18:12060000-12060200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr18:12060000-12060600	Active TSS	Brain Angular Gyrus	brain
16	chr18:12060000-12060800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr18:12060000-12060800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr18:12060200-12061000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr18:12060800-12064400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr18:12061000-12062200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr18:12061600-12062000	Active TSS	Spleen	Spleen
22	chr18:12061800-12062000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr18:12062000-12064400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr18:12062000-12064400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr18:12062200-12064400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr18:12063000-12063200	Enhancers	Right Ventricle	heart
27	chr18:12063600-12064000	Enhancers	Fetal Muscle Trunk	muscle
28	chr18:12064400-12064600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr18:12064400-12064600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
30	chr18:12064400-12064800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr18:12064400-12064800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr18:12064400-12064800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr18:12064600-12064800	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr18:12064600-12067000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr18:12064800-12065000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr18:12064800-12065400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr18:12065800-12066000	Enhancers	H9 Cell Line	embryonic stem cell
38	chr18:12066000-12076400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr18:12067000-12068600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr18:12067400-12068400	Enhancers	Fetal Muscle Trunk	muscle
41	chr18:12068000-12068600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr18:12068200-12068600	Active TSS	Pancreas	Pancrea
43	chr18:12068200-12068800	Active TSS	HUVEC	blood vessel
44	chr18:12068200-12069000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr18:12068600-12069200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr18:12068600-12076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr18:12068800-12069000	Bivalent/Poised TSS	Osteobl	bone
48	chr18:12068800-12069200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr18:12068800-12069200	Enhancers	Fetal Lung	lung
50	chr18:12068800-12069200	Flanking Active TSS	HUVEC	blood vessel

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