Variant report

Variant	nsv9610
Chromosome Location	chr18:12417586-12424527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:714)
CpG islands
(count:429)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr18:12419896-12420532	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:12421133-12421470	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr18:12423048-12423161	K562	blood:	n/a	n/a
5	BHLHE40	chr18:12420274-12420589	GM12878	blood:	n/a	chr18:12420275-12420291 chr18:12420498-12420514
6	BHLHE40	chr18:12420897-12421455	HepG2	liver:	n/a	n/a
7	BHLHE40	chr18:12420957-12421323	GM12878	blood:	n/a	n/a
8	BRCA1	chr18:12421213-12421326	HepG2	liver:	n/a	n/a
9	BRCA1	chr18:12420233-12420411	HepG2	liver:	n/a	n/a
10	BRCA1	chr18:12423079-12423102	HepG2	liver:	n/a	n/a
11	BRCA1	chr18:12420393-12420404	GM12878	blood:	n/a	n/a
12	BRCA1	chr18:12421140-12421360	H1-hESC	embryonic stem cell:	n/a	n/a
13	CCNT2	chr18:12420365-12420500	K562	blood:	n/a	n/a
14	CEBPB	chr18:12419833-12420174	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr18:12420264-12420519	HepG2	liver:	n/a	n/a
16	CEBPD	chr18:12420920-12421405	HepG2	liver:	n/a	n/a
17	CEBPD	chr18:12419910-12420249	HepG2	liver:	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	CHD1	chr18:12420951-12421704	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr18:12420958-12421341	GM12878	blood:	n/a	n/a
22	CHD2	chr18:12420970-12421204	GM12878	blood:	n/a	n/a
23	CHD2	chr18:12419978-12420459	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr18:12419890-12420560	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr18:12420864-12421173	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr18:12420969-12421099	HepG2	liver:	n/a	n/a
27	CHD2	chr18:12420158-12420501	HepG2	liver:	n/a	n/a
28	CHD2	chr18:12420304-12420532	GM12878	blood:	n/a	n/a
29	CTCF	chr18:12422810-12423467	HCT-116	colon:	n/a	chr18:12422848-12422866 chr18:12423444-12423453 chr18:12423159-12423175
30	CTCF	chr18:12420380-12420530	NHEK	skin:	n/a	n/a
31	CTCF	chr18:12421820-12421970	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr18:12422844-12423361	A549	lung:	n/a	chr18:12422848-12422866 chr18:12423159-12423175
33	CTCF	chr18:12419940-12420170	NHEK	skin:	n/a	n/a
34	CTCF	chr18:12422855-12423274	MCF-7	breast:	n/a	chr18:12423159-12423175
35	CTCF	chr18:12422617-12423509	MCF-7	breast:	n/a	chr18:12422848-12422866 chr18:12423444-12423453 chr18:12423159-12423175
36	CTCF	chr18:12423980-12424130	SAEC	small airway:	n/a	chr18:12424026-12424034 chr18:12424021-12424034
37	CTCF	chr18:12423080-12423230	GM12872	blood:	n/a	chr18:12423159-12423175
38	CTCF	chr18:12422980-12423130	NHEK	skin:	n/a	n/a
39	CTCF	chr18:12423805-12424282	MCF-7	breast:	n/a	chr18:12424026-12424034 chr18:12424021-12424034
40	CTCF	chr18:12423936-12424056	MCF-7	breast:	n/a	chr18:12424026-12424034 chr18:12424021-12424034
41	CTCF	chr18:12422976-12423239	ECC-1	luminal epithelium:	n/a	chr18:12423159-12423175
42	CTCF	chr18:12422891-12423266	MCF-7	breast:	n/a	chr18:12423159-12423175
43	CTCF	chr18:12421320-12421470	HepG2	liver:	n/a	chr18:12421367-12421375
44	CTCF	chr18:12423000-12423150	GM12869	blood:	n/a	n/a
45	CTCF	chr18:12421903-12421964	GM19240	blood:	n/a	n/a
46	CTCF	chr18:12423000-12423150	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr18:12419960-12420110	Caco-2	colon:	n/a	n/a
48	CTCF	chr18:12420240-12420390	SAEC	small airway:	n/a	n/a
49	CTCF	chr18:12420340-12420490	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr18:12420040-12420190	SAEC	small airway:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12421072-12421122	HIPEpiC	eye:	n/a
2	chr18:12421072-12421122	SK-N-MC	brain:	n/a
3	chr18:12421072-12421122	HIPEpiC	eye:	n/a
4	chr18:12421072-12421122	SK-N-MC	brain:	n/a
5	chr18:12420082-12420132	Hela-S3	cervix:	n/a
6	chr18:12420136-12420186	CMK	blood:	n/a
7	chr18:12420862-12420912	PANC-1	pancreas:	n/a
8	chr18:12421072-12421122	GM12878	blood:	n/a
9	chr18:12418005-12418055	GM12891	blood:	n/a
10	chr18:12423766-12423816	BE2_C	brain:	n/a
11	chr18:12423766-12423816	HRE	kidney:	n/a
12	chr18:12420136-12420186	GM19239	blood:	n/a
13	chr18:12418005-12418055	IMR90	lung:	fetal
14	chr18:12420136-12420186	SAEC	small airway:	n/a
15	chr18:12420862-12420912	PrEC	prostate:	n/a
16	chr18:12420136-12420186	NT2-D1	testis:	n/a
17	chr18:12421072-12421122	NH-A	brain:	n/a
18	chr18:12420412-12420462	MCF10A-Er-Src	breast:	n/a
19	chr18:12420412-12420462	NH-A	brain:	n/a
20	chr18:12421072-12421122	HepG2	liver:	n/a
21	chr18:12418005-12418055	NHDF-neo	bronchial:	n/a
22	chr18:12421072-12421122	HNPCEpiC	eye:	n/a
23	chr18:12420862-12420912	PFSK-1	brain:	n/a
24	chr18:12420412-12420462	HCPEpiC	choroid plexus:	n/a
25	chr18:12420412-12420462	HepG2	liver:	n/a
26	chr18:12418005-12418055	HepG2	liver:	n/a
27	chr18:12421072-12421122	AoSMC	blood vessel:	n/a
28	chr18:12420412-12420462	HRE	kidney:	n/a
29	chr18:12418005-12418055	Hepatocyte	liver:	n/a
30	chr18:12418005-12418055	SAEC	small airway:	n/a
31	chr18:12420082-12420132	LNCaP	prostate:	n/a
32	chr18:12418005-12418055	NH-A	brain:	n/a
33	chr18:12423766-12423816	HMEC	breast:	n/a
34	chr18:12420862-12420912	NH-A	brain:	n/a
35	chr18:12420136-12420186	SK-N-SH	brain:	n/a
36	chr18:12418005-12418055	A549	lung:	n/a
37	chr18:12420136-12420186	HRE	kidney:	n/a
38	chr18:12421072-12421122	HEEpiC	esophagus:	n/a
39	chr18:12418005-12418055	AG09319	gingival:	n/a
40	chr18:12420862-12420912	IMR90	lung:	fetal
41	chr18:12418005-12418055	Hela-S3	cervix:	n/a
42	chr18:12423766-12423816	HAEpiC	amniotic membrane:	n/a
43	chr18:12420862-12420912	ovcar-3	ovarian:	n/a
44	chr18:12421072-12421122	AG10803	skin:	n/a
45	chr18:12420082-12420132	HEK293	kidney:	embryo
46	chr18:12423766-12423816	NT2-D1	testis:	n/a
47	chr18:12420412-12420462	IMR90	lung:	fetal
48	chr18:12420082-12420132	U87	brain:	n/a
49	chr18:12418005-12418055	SK-N-SH_RA	brain:	n/a
50	chr18:12420082-12420132	HCPEpiC	choroid plexus:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12393796..12395269-chr18:12422174..12423544,7	MCF-7	breast:
2	chr18:12418519..12420831-chr18:12657213..12660140,3	MCF-7	breast:
3	chr18:12393173..12395442-chr18:12422638..12423834,17	MCF-7	breast:
4	chr18:12407594..12413164-chr18:12414407..12422412,12	MCF-7	breast:
5	chr18:12396027..12396913-chr18:12422599..12423644,3	MCF-7	breast:
6	chr18:12396537..12397287-chr18:12423683..12424400,2	MCF-7	breast:
7	chr18:12418998..12421842-chr18:12658407..12660489,3	MCF-7	breast:
8	chr18:12422525..12425509-chr18:12660961..12663016,2	MCF-7	breast:
9	chr18:12423062..12423996-chr18:12659741..12660319,3	MCF-7	breast:
10	chr18:12375250..12378013-chr18:12414688..12417638,3	MCF-7	breast:
11	chr18:12423021..12425076-chr18:12425258..12426812,2	K562	blood:
12	chr18:12407282..12409335-chr18:12423368..12426046,2	MCF-7	breast:
13	chr18:12419727..12422689-chr18:12423004..12425928,2	K562	blood:
14	chr18:12422648..12423634-chr18:12659546..12660559,6	MCF-7	breast:
15	chr18:12421209..12423248-chr18:12437108..12438890,2	MCF-7	breast:
16	chr18:12395766..12397047-chr18:12422358..12424257,19	MCF-7	breast:
17	chr18:12375743..12378274-chr18:12418543..12422031,3	MCF-7	breast:
18	chr18:12422115..12425082-chr18:12427051..12428777,2	K562	blood:
19	chr18:12406749..12409861-chr18:12418820..12421803,8	MCF-7	breast:
20	chr18:12423760..12426090-chr18:12656515..12659098,3	MCF-7	breast:
21	chr18:12391302..12392306-chr18:12422603..12423519,6	MCF-7	breast:
22	chr18:12418687..12420720-chr18:12430201..12431737,2	MCF-7	breast:

No data

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

Extended variants
information (count: 287 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114771722	chr18:12417609-12417610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs559958	chr18:12417654-12417655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs564156466	chr18:12417658-12417659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531464176	chr18:12417695-12417696	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531271995	chr18:12417727-12417728	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs557911605	chr18:12417741-12417742	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs570892611	chr18:12417769-12417770	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs549731787	chr18:12417792-12417793	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs535109126	chr18:12417800-12417801	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs140056629	chr18:12417873-12417874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs503307	chr18:12417905-12417906	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs502525	chr18:12417955-12417956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552900047	chr18:12417977-12417978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190288018	chr18:12418026-12418027	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546109895	chr18:12418027-12418028	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535394519	chr18:12418046-12418047	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181513418	chr18:12418070-12418071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs138102220	chr18:12418116-12418117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540280945	chr18:12418133-12418134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561672957	chr18:12418166-12418167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547709988	chr18:12418193-12418194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs185995107	chr18:12418248-12418249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs569203170	chr18:12418252-12418253	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146327883	chr18:12418266-12418267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201826971	chr18:12418309-12418310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565975750	chr18:12418326-12418327	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113515035	chr18:12418342-12418343	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs551328971	chr18:12418357-12418358	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs11665408	chr18:12418373-12418374	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs144818526	chr18:12418383-12418384	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs138637404	chr18:12418389-12418390	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376219643	chr18:12418477-12418478	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534811031	chr18:12418496-12418497	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs529500298	chr18:12418582-12418583	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs553012662	chr18:12418619-12418620	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs190801582	chr18:12418643-12418644	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs510878	chr18:12418665-12418666	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs556917211	chr18:12418675-12418676	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs71351478	chr18:12418735-12418736	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs183741569	chr18:12418761-12418762	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs575887594	chr18:12418766-12418767	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs540120320	chr18:12418803-12418804	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs142041466	chr18:12418806-12418807	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs62095750	chr18:12418808-12418809	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs573342548	chr18:12418884-12418885	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs189123380	chr18:12419048-12419049	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs12232560	chr18:12419060-12419061	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs190623597	chr18:12419104-12419105	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs35617867	chr18:12419165-12419166	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs35420599	chr18:12419167-12419168	Weak transcription Enhancers	Chromatin interactive region	6 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:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12408600-12419600	Weak transcription	Thymus	Thymus
2	chr18:12408800-12417800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr18:12408800-12419800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr18:12408800-12419800	Weak transcription	Pancreas	Pancrea
5	chr18:12409000-12417600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr18:12409000-12419600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr18:12409000-12419800	Weak transcription	Colonic Mucosa	Colon
8	chr18:12409000-12419800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr18:12409000-12419800	Weak transcription	Fetal Kidney	kidney
10	chr18:12409000-12419800	Weak transcription	Fetal Thymus	thymus
11	chr18:12409200-12418400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr18:12409800-12418000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr18:12409800-12419800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr18:12410200-12419800	Weak transcription	NH-A	brain
15	chr18:12410400-12419800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr18:12410400-12419800	Weak transcription	Right Ventricle	heart
17	chr18:12410400-12430400	Weak transcription	A549	lung
18	chr18:12410600-12417600	Weak transcription	HMEC	breast
19	chr18:12411800-12419800	Weak transcription	NHEK	skin
20	chr18:12414400-12419600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr18:12416000-12417600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr18:12416000-12419600	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr18:12416000-12419800	Weak transcription	Esophagus	oesophagus
24	chr18:12416000-12419800	Weak transcription	Stomach Mucosa	stomach
25	chr18:12416000-12419800	Weak transcription	NHLF	lung
26	chr18:12416000-12420000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr18:12416200-12417600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr18:12416200-12417600	Weak transcription	Fetal Brain Female	brain
29	chr18:12416200-12417600	Weak transcription	Fetal Stomach	stomach
30	chr18:12416200-12417600	Weak transcription	HepG2	liver
31	chr18:12416200-12417800	Weak transcription	Fetal Lung	lung
32	chr18:12416200-12418400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr18:12416200-12418400	Weak transcription	GM12878-XiMat	blood
34	chr18:12416200-12419800	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr18:12416200-12419800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr18:12416200-12419800	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr18:12416200-12419800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr18:12416200-12419800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr18:12416200-12419800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr18:12416200-12419800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:12416200-12419800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr18:12416200-12419800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr18:12416200-12419800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr18:12416200-12419800	Weak transcription	Fetal Intestine Small	intestine
45	chr18:12416200-12419800	Weak transcription	Ovary	ovary
46	chr18:12416200-12419800	Weak transcription	Right Atrium	heart
47	chr18:12416200-12420000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr18:12416200-12420000	Weak transcription	Aorta	Aorta
49	chr18:12416200-12420000	Weak transcription	Fetal Heart	heart
50	chr18:12416200-12420000	Weak transcription	Left Ventricle	heart

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