Variant report

Variant	esv3338945
Chromosome Location	chr18:12419177-12422125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:510)
CpG islands
(count:306)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:12421215-12421460	HepG2	liver:	n/a	n/a
2	BACH1	chr18:12421133-12421470	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:12419896-12420532	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr18:12420274-12420589	GM12878	blood:	n/a	chr18:12420275-12420291 chr18:12420498-12420514
5	BHLHE40	chr18:12420897-12421455	HepG2	liver:	n/a	n/a
6	BHLHE40	chr18:12420957-12421323	GM12878	blood:	n/a	n/a
7	BRCA1	chr18:12421213-12421326	HepG2	liver:	n/a	n/a
8	BRCA1	chr18:12420233-12420411	HepG2	liver:	n/a	n/a
9	BRCA1	chr18:12420393-12420404	GM12878	blood:	n/a	n/a
10	BRCA1	chr18:12421140-12421360	H1-hESC	embryonic stem cell:	n/a	n/a
11	CCNT2	chr18:12420365-12420500	K562	blood:	n/a	n/a
12	CEBPB	chr18:12419833-12420174	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr18:12419910-12420249	HepG2	liver:	n/a	n/a
14	CEBPD	chr18:12420920-12421405	HepG2	liver:	n/a	n/a
15	CEBPD	chr18:12420264-12420519	HepG2	liver:	n/a	n/a
16	CHD1	chr18:12420958-12421341	GM12878	blood:	n/a	n/a
17	CHD1	chr18:12420951-12421704	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr18:12420026-12420374	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr18:12420310-12420471	GM12878	blood:	n/a	n/a
20	CHD2	chr18:12420304-12420532	GM12878	blood:	n/a	n/a
21	CHD2	chr18:12420969-12421099	HepG2	liver:	n/a	n/a
22	CHD2	chr18:12419890-12420560	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr18:12420158-12420501	HepG2	liver:	n/a	n/a
24	CHD2	chr18:12420864-12421173	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr18:12420970-12421204	GM12878	blood:	n/a	n/a
26	CHD2	chr18:12419978-12420459	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr18:12419920-12420070	AG04450	lung:	n/a	n/a
28	CTCF	chr18:12420000-12420150	AG04449	skin:	n/a	n/a
29	CTCF	chr18:12420280-12420430	AG10803	skin:	n/a	n/a
30	CTCF	chr18:12420020-12420170	AG09309	skin:	n/a	n/a
31	CTCF	chr18:12420320-12420470	GM12870	blood:	n/a	n/a
32	CTCF	chr18:12419980-12420130	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr18:12420200-12420350	HAc	cerebellar:	n/a	n/a
34	CTCF	chr18:12420080-12420230	GM12864	blood:	n/a	n/a
35	CTCF	chr18:12420120-12420270	HCT-116	colon:	n/a	n/a
36	CTCF	chr18:12420280-12420430	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr18:12420280-12420430	GM12864	blood:	n/a	n/a
38	CTCF	chr18:12420306-12420508	MCF-7	breast:	n/a	n/a
39	CTCF	chr18:12421851-12421977	GM12891	blood:	n/a	n/a
40	CTCF	chr18:12421820-12421970	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr18:12419940-12420090	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr18:12420340-12420490	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr18:12420336-12420473	MCF-7	breast:	n/a	n/a
44	CTCF	chr18:12420260-12420410	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr18:12420380-12420530	NHEK	skin:	n/a	n/a
46	CTCF	chr18:12421840-12421990	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr18:12419940-12420090	BJ	skin:	n/a	n/a
48	CTCF	chr18:12419980-12420130	HMEC	breast:	n/a	n/a
49	CTCF	chr18:12420100-12420250	HVMF	connective:	n/a	n/a
50	CTCF	chr18:12420320-12420470	HCFaa	heart:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12420136-12420186	ovcar-3	ovarian:	n/a
2	chr18:12420136-12420186	ovcar-3	ovarian:	n/a
3	chr18:12420136-12420186	NB4	blood:	n/a
4	chr18:12420082-12420132	HL-60	blood:	n/a
5	chr18:12420136-12420186	HPAEpiC	pulmonary alveolar:	n/a
6	chr18:12420862-12420912	HCPEpiC	choroid plexus:	n/a
7	chr18:12420082-12420132	SKMC	muscle:	n/a
8	chr18:12420412-12420462	NH-A	brain:	n/a
9	chr18:12420136-12420186	AoSMC	blood vessel:	n/a
10	chr18:12421072-12421122	PrEC	prostate:	n/a
11	chr18:12420082-12420132	SK-N-SH	brain:	n/a
12	chr18:12421072-12421122	H1-hESC	embryonic stem cell:	embryo
13	chr18:12420862-12420912	U87	brain:	n/a
14	chr18:12420412-12420462	AG10803	skin:	n/a
15	chr18:12420862-12420912	AG10803	skin:	n/a
16	chr18:12420082-12420132	AG04449	skin:	fetal
17	chr18:12420412-12420462	A549	lung:	n/a
18	chr18:12420082-12420132	HRE	kidney:	n/a
19	chr18:12421072-12421122	GM06990	blood:	n/a
20	chr18:12421072-12421122	GM12892	blood:	n/a
21	chr18:12420136-12420186	HRCEpiC	kidney:	n/a
22	chr18:12421072-12421122	HepG2	liver:	n/a
23	chr18:12421072-12421122	BE2_C	brain:	n/a
24	chr18:12421072-12421122	HEEpiC	esophagus:	n/a
25	chr18:12421072-12421122	T-47D	breast:	n/a
26	chr18:12421072-12421122	HCPEpiC	choroid plexus:	n/a
27	chr18:12420082-12420132	T-47D	breast:	n/a
28	chr18:12420412-12420462	CMK	blood:	n/a
29	chr18:12421072-12421122	A549	lung:	n/a
30	chr18:12420136-12420186	PrEC	prostate:	n/a
31	chr18:12421072-12421122	NH-A	brain:	n/a
32	chr18:12420136-12420186	HepG2	liver:	n/a
33	chr18:12420136-12420186	U87	brain:	n/a
34	chr18:12421072-12421122	Jurkat	blood:	n/a
35	chr18:12420082-12420132	GM12891	blood:	n/a
36	chr18:12420082-12420132	GM12892	blood:	n/a
37	chr18:12421072-12421122	HL-60	blood:	n/a
38	chr18:12420412-12420462	Caco-2	colon:	n/a
39	chr18:12420136-12420186	CMK	blood:	n/a
40	chr18:12420136-12420186	HIPEpiC	eye:	n/a
41	chr18:12420412-12420462	SKMC	muscle:	n/a
42	chr18:12420082-12420132	Caco-2	colon:	n/a
43	chr18:12420082-12420132	ECC-1	luminal epithelium:	n/a
44	chr18:12420136-12420186	SK-N-MC	brain:	n/a
45	chr18:12420862-12420912	SK-N-MC	brain:	n/a
46	chr18:12420412-12420462	RPTEC	kidney:	n/a
47	chr18:12420412-12420462	ovcar-3	ovarian:	n/a
48	chr18:12420862-12420912	Jurkat	blood:	n/a
49	chr18:12420412-12420462	NB4	blood:	n/a
50	chr18:12420136-12420186	K562	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12422115..12425082-chr18:12427051..12428777,2	K562	blood:
2	chr18:12375743..12378274-chr18:12418543..12422031,3	MCF-7	breast:
3	chr18:12421209..12423248-chr18:12437108..12438890,2	MCF-7	breast:
4	chr18:12418687..12420720-chr18:12430201..12431737,2	MCF-7	breast:
5	chr18:12407594..12413164-chr18:12414407..12422412,12	MCF-7	breast:
6	chr18:12406749..12409861-chr18:12418820..12421803,8	MCF-7	breast:
7	chr18:12418519..12420831-chr18:12657213..12660140,3	MCF-7	breast:
8	chr18:12418998..12421842-chr18:12658407..12660489,3	MCF-7	breast:

No data

Variant related genes	Relation type
SLMO1	TF binding region
SLMO1	CpG island
ENSG00000215527	chromatin interactions
ENSG00000128789	chromatin interactions
ENSG00000141385	chromatin interactions
ENSG00000141391	chromatin interactions
ENSG00000267199	chromatin interactions
ENSG00000256786	chromatin interactions
ENSG00000134278	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148091530	chr18:12419210-12419211	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs34481458	chr18:12419235-12419236	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs12957046	chr18:12419240-12419241	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs572246735	chr18:12419247-12419248	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs376215038	chr18:12419250-12419251	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs371337096	chr18:12419272-12419273	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs182869445	chr18:12419273-12419274	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs560098601	chr18:12419312-12419313	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs560633338	chr18:12419324-12419325	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs71172083	chr18:12419325-12419326	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs187175345	chr18:12419353-12419354	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs541264475	chr18:12419395-12419396	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs140039458	chr18:12419402-12419403	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs568245739	chr18:12419411-12419412	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs535541126	chr18:12419417-12419418	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs550606141	chr18:12419450-12419451	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs569184327	chr18:12419504-12419505	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs539752221	chr18:12419510-12419511	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs558393152	chr18:12419523-12419524	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs370609110	chr18:12419558-12419559	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs559650585	chr18:12419608-12419609	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs572771587	chr18:12419609-12419610	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs534422954	chr18:12419664-12419665	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs1785660	chr18:12419676-12419677	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573820530	chr18:12419705-12419706	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs544321473	chr18:12419720-12419721	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs140036572	chr18:12419735-12419736	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs191927139	chr18:12419739-12419740	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs1785326	chr18:12419776-12419777	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs527562278	chr18:12419796-12419797	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs563866233	chr18:12419805-12419806	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs373918995	chr18:12419806-12419807	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs184481869	chr18:12419821-12419822	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs1785327	chr18:12419846-12419847	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs529347499	chr18:12419885-12419886	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs148844725	chr18:12419894-12419895	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs531309827	chr18:12419922-12419923	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs569171147	chr18:12419946-12419947	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs539791850	chr18:12419961-12419962	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs532750688	chr18:12419964-12419965	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs551463634	chr18:12420000-12420001	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs75944517	chr18:12420013-12420014	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs112860307	chr18:12420067-12420068	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs187617064	chr18:12420132-12420133	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs567814905	chr18:12420142-12420143	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs193168355	chr18:12420146-12420147	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs139385267	chr18:12420147-12420148	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs556189895	chr18:12420164-12420165	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs386801359	chr18:12420183-12420184	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs370628635	chr18:12420184-12420185	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12408600-12419600	Weak transcription	Thymus	Thymus
2	chr18:12408800-12419800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr18:12408800-12419800	Weak transcription	Pancreas	Pancrea
4	chr18:12409000-12419600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr18:12409000-12419800	Weak transcription	Colonic Mucosa	Colon
6	chr18:12409000-12419800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr18:12409000-12419800	Weak transcription	Fetal Kidney	kidney
8	chr18:12409000-12419800	Weak transcription	Fetal Thymus	thymus
9	chr18:12409800-12419800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr18:12410200-12419800	Weak transcription	NH-A	brain
11	chr18:12410400-12419800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr18:12410400-12419800	Weak transcription	Right Ventricle	heart
13	chr18:12410400-12430400	Weak transcription	A549	lung
14	chr18:12411800-12419800	Weak transcription	NHEK	skin
15	chr18:12414400-12419600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr18:12416000-12419600	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr18:12416000-12419800	Weak transcription	Esophagus	oesophagus
18	chr18:12416000-12419800	Weak transcription	Stomach Mucosa	stomach
19	chr18:12416000-12419800	Weak transcription	NHLF	lung
20	chr18:12416000-12420000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr18:12416200-12419800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr18:12416200-12419800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr18:12416200-12419800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr18:12416200-12419800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr18:12416200-12419800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr18:12416200-12419800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr18:12416200-12419800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr18:12416200-12419800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr18:12416200-12419800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr18:12416200-12419800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr18:12416200-12419800	Weak transcription	Fetal Intestine Small	intestine
32	chr18:12416200-12419800	Weak transcription	Ovary	ovary
33	chr18:12416200-12419800	Weak transcription	Right Atrium	heart
34	chr18:12416200-12420000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr18:12416200-12420000	Weak transcription	Aorta	Aorta
36	chr18:12416200-12420000	Weak transcription	Fetal Heart	heart
37	chr18:12416200-12420000	Weak transcription	Left Ventricle	heart
38	chr18:12416200-12420000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr18:12416200-12420000	Weak transcription	Spleen	Spleen
40	chr18:12416400-12419800	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr18:12416400-12419800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr18:12416400-12419800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr18:12416400-12419800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr18:12416400-12419800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr18:12416400-12419800	Weak transcription	Adipose Nuclei	Adipose
46	chr18:12416400-12419800	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr18:12416400-12419800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr18:12416400-12419800	Weak transcription	Stomach Smooth Muscle	stomach
49	chr18:12416400-12419800	Weak transcription	HUVEC	blood vessel
50	chr18:12416400-12419800	Weak transcription	Osteobl	bone

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