Variant report

Variant	nsv519557
Chromosome Location	chr18:12417905-12431506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:764)
CpG islands
(count:671)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	BCL3	chr18:12430406-12431190	GM12878	blood:	n/a	n/a
5	BCL3	chr18:12430339-12431103	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:12420957-12421323	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:12420274-12420589	GM12878	blood:	n/a	chr18:12420275-12420291 chr18:12420498-12420514
8	BHLHE40	chr18:12420897-12421455	HepG2	liver:	n/a	n/a
9	BHLHE40	chr18:12423048-12423161	K562	blood:	n/a	n/a
10	BRCA1	chr18:12421213-12421326	HepG2	liver:	n/a	n/a
11	BRCA1	chr18:12420393-12420404	GM12878	blood:	n/a	n/a
12	BRCA1	chr18:12420233-12420411	HepG2	liver:	n/a	n/a
13	BRCA1	chr18:12421140-12421360	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr18:12423079-12423102	HepG2	liver:	n/a	n/a
15	CCNT2	chr18:12420365-12420500	K562	blood:	n/a	n/a
16	CEBPB	chr18:12419833-12420174	Hela-S3	cervix:	n/a	n/a
17	CEBPD	chr18:12420920-12421405	HepG2	liver:	n/a	n/a
18	CEBPD	chr18:12420264-12420519	HepG2	liver:	n/a	n/a
19	CEBPD	chr18:12419910-12420249	HepG2	liver:	n/a	n/a
20	CHD1	chr18:12420951-12421704	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr18:12420026-12420374	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr18:12420310-12420471	GM12878	blood:	n/a	n/a
23	CHD1	chr18:12420958-12421341	GM12878	blood:	n/a	n/a
24	CHD2	chr18:12420969-12421099	HepG2	liver:	n/a	n/a
25	CHD2	chr18:12420864-12421173	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr18:12419978-12420459	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr18:12419890-12420560	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr18:12420304-12420532	GM12878	blood:	n/a	n/a
29	CHD2	chr18:12420970-12421204	GM12878	blood:	n/a	n/a
30	CHD2	chr18:12420158-12420501	HepG2	liver:	n/a	n/a
31	CTCF	chr18:12420340-12420490	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr18:12420220-12420370	GM12867	blood:	n/a	n/a
33	CTCF	chr18:12420284-12420471	IMR90	lung:	n/a	n/a
34	CTCF	chr18:12420340-12420490	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr18:12420363-12420472	MCF-7	breast:	n/a	n/a
36	CTCF	chr18:12422980-12423130	MCF-7	breast:	n/a	n/a
37	CTCF	chr18:12421800-12421950	GM12867	blood:	n/a	n/a
38	CTCF	chr18:12421782-12421982	GM12878	blood:	n/a	n/a
39	CTCF	chr18:12422937-12423260	MCF-7	breast:	n/a	chr18:12423159-12423175
40	CTCF	chr18:12422960-12423110	GM12878	blood:	n/a	n/a
41	CTCF	chr18:12422987-12423225	GM12878	blood:	n/a	chr18:12423159-12423175
42	CTCF	chr18:12422980-12423130	NHEK	skin:	n/a	n/a
43	CTCF	chr18:12423020-12423170	GM12873	blood:	n/a	n/a
44	CTCF	chr18:12419960-12420110	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr18:12420280-12420430	GM12864	blood:	n/a	n/a
46	CTCF	chr18:12422952-12423274	GM12891	blood:	n/a	chr18:12423159-12423175
47	CTCF	chr18:12422901-12423173	T-47D	breast:	n/a	n/a
48	CTCF	chr18:12421800-12421950	GM12872	blood:	n/a	n/a
49	CTCF	chr18:12423000-12423150	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr18:12421880-12422030	HRPEpiC	eye:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12420082-12420132	HCM	heart:	n/a
2	chr18:12423766-12423816	NHDF-neo	bronchial:	n/a
3	chr18:12429120-12429170	GM12892	blood:	n/a
4	chr18:12429989-12430039	HIPEpiC	eye:	n/a
5	chr18:12421072-12421122	AG04450	lung:	fetal
6	chr18:12421072-12421122	ECC-1	luminal epithelium:	n/a
7	chr18:12421072-12421122	AG04449	skin:	fetal
8	chr18:12420136-12420186	PrEC	prostate:	n/a
9	chr18:12429989-12430039	K562	blood:	n/a
10	chr18:12420136-12420186	HEK293	kidney:	embryo
11	chr18:12431241-12431291	HRCEpiC	kidney:	n/a
12	chr18:12420082-12420132	BJ	skin:	n/a
13	chr18:12429989-12430039	LNCaP	prostate:	n/a
14	chr18:12431241-12431291	CMK	blood:	n/a
15	chr18:12421072-12421122	RPTEC	kidney:	n/a
16	chr18:12420412-12420462	Jurkat	blood:	n/a
17	chr18:12429120-12429170	HNPCEpiC	eye:	n/a
18	chr18:12420862-12420912	HNPCEpiC	eye:	n/a
19	chr18:12431241-12431291	NHDF-neo	bronchial:	n/a
20	chr18:12431241-12431291	AG04449	skin:	fetal
21	chr18:12418005-12418055	GM12878	blood:	n/a
22	chr18:12420412-12420462	AG09309	skin:	n/a
23	chr18:12421072-12421122	H1-hESC	embryonic stem cell:	embryo
24	chr18:12431464-12431514	ECC-1	luminal epithelium:	n/a
25	chr18:12420082-12420132	Jurkat	blood:	n/a
26	chr18:12420412-12420462	NH-A	brain:	n/a
27	chr18:12431241-12431291	AoSMC	blood vessel:	n/a
28	chr18:12420082-12420132	HRCEpiC	kidney:	n/a
29	chr18:12421072-12421122	PrEC	prostate:	n/a
30	chr18:12431241-12431291	AG04450	lung:	fetal
31	chr18:12420412-12420462	HPAEpiC	pulmonary alveolar:	n/a
32	chr18:12420412-12420462	MCF-7	breast:	n/a
33	chr18:12431464-12431514	U87	brain:	n/a
34	chr18:12421072-12421122	Caco-2	colon:	n/a
35	chr18:12420412-12420462	Hepatocyte	liver:	n/a
36	chr18:12420136-12420186	SKMC	muscle:	n/a
37	chr18:12418005-12418055	T-47D	breast:	n/a
38	chr18:12429120-12429170	SKMC	muscle:	n/a
39	chr18:12420862-12420912	PFSK-1	brain:	n/a
40	chr18:12431241-12431291	GM06990	blood:	n/a
41	chr18:12431464-12431514	NH-A	brain:	n/a
42	chr18:12420136-12420186	HAEpiC	amniotic membrane:	n/a
43	chr18:12431241-12431291	PANC-1	pancreas:	n/a
44	chr18:12429989-12430039	GM06990	blood:	n/a
45	chr18:12429989-12430039	BE2_C	brain:	n/a
46	chr18:12431464-12431514	HUVEC	blood vessel:	n/a
47	chr18:12418005-12418055	SK-N-SH_RA	brain:	n/a
48	chr18:12420136-12420186	HIPEpiC	eye:	n/a
49	chr18:12420862-12420912	NHBE	bronchial:	n/a
50	chr18:12420412-12420462	GM12891	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12422648..12423634-chr18:12659546..12660559,6	MCF-7	breast:
2	chr18:12396537..12397287-chr18:12423683..12424400,2	MCF-7	breast:
3	chr18:12422115..12425082-chr18:12427051..12428777,2	K562	blood:
4	chr18:12421209..12423248-chr18:12437108..12438890,2	MCF-7	breast:
5	chr18:12391302..12392306-chr18:12422603..12423519,6	MCF-7	breast:
6	chr18:12422115..12425082-chr18:12427051..12428777,2	K562	blood:
7	chr18:12419727..12422689-chr18:12423004..12425928,2	K562	blood:
8	chr18:12423021..12425076-chr18:12425258..12426812,2	K562	blood:
9	chr18:12395766..12397047-chr18:12422358..12424257,19	MCF-7	breast:
10	chr18:12418687..12420720-chr18:12430201..12431737,2	MCF-7	breast:
11	chr18:12396027..12396913-chr18:12422599..12423644,3	MCF-7	breast:
12	chr18:12407594..12413164-chr18:12414407..12422412,12	MCF-7	breast:
13	chr18:12427958..12434396-chr18:12436312..12440619,6	K562	blood:
14	chr18:12407282..12409335-chr18:12423368..12426046,2	MCF-7	breast:
15	chr18:12418519..12420831-chr18:12657213..12660140,3	MCF-7	breast:
16	chr18:12423062..12423996-chr18:12659741..12660319,3	MCF-7	breast:
17	chr18:12423021..12425076-chr18:12425258..12426812,2	K562	blood:
18	chr18:12423760..12426090-chr18:12656515..12659098,3	MCF-7	breast:
19	chr18:12422525..12425509-chr18:12660961..12663016,2	MCF-7	breast:
20	chr18:12375743..12378274-chr18:12418543..12422031,3	MCF-7	breast:
21	chr18:12393173..12395442-chr18:12422638..12423834,17	MCF-7	breast:
22	chr18:12393796..12395269-chr18:12422174..12423544,7	MCF-7	breast:
23	chr18:12418687..12420720-chr18:12430201..12431737,2	MCF-7	breast:
24	chr18:12418998..12421842-chr18:12658407..12660489,3	MCF-7	breast:
25	chr18:12427173..12429276-chr18:12453042..12455618,2	K562	blood:
26	chr18:12406749..12409861-chr18:12418820..12421803,8	MCF-7	breast:
27	chr18:12428003..12430631-chr18:12490469..12492690,2	K562	blood:

No data

Variant related genes	Relation type
SLMO1	TF binding region
ENSG00000267108	TF binding region
ENSG00000256786	TF binding region
SLMO1	CpG island
ENSG00000267108	CpG island
ENSG00000256786	CpG island
ENSG00000215527	chromatin interactions
ENSG00000141385	chromatin interactions
ENSG00000134278	chromatin interactions
ENSG00000141391	chromatin interactions
ENSG00000267199	chromatin interactions
ENSG00000256786	chromatin interactions
ENSG00000128789	chromatin interactions

Extended variants
information (count: 661 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs503307	chr18:12417905-12417906	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs502525	chr18:12417955-12417956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552900047	chr18:12417977-12417978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs190288018	chr18:12418026-12418027	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546109895	chr18:12418027-12418028	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535394519	chr18:12418046-12418047	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs181513418	chr18:12418070-12418071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138102220	chr18:12418116-12418117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540280945	chr18:12418133-12418134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561672957	chr18:12418166-12418167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547709988	chr18:12418193-12418194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185995107	chr18:12418248-12418249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569203170	chr18:12418252-12418253	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs146327883	chr18:12418266-12418267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201826971	chr18:12418309-12418310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs565975750	chr18:12418326-12418327	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs113515035	chr18:12418342-12418343	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs551328971	chr18:12418357-12418358	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs11665408	chr18:12418373-12418374	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs144818526	chr18:12418383-12418384	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs138637404	chr18:12418389-12418390	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs376219643	chr18:12418477-12418478	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534811031	chr18:12418496-12418497	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs529500298	chr18:12418582-12418583	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs553012662	chr18:12418619-12418620	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs190801582	chr18:12418643-12418644	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs510878	chr18:12418665-12418666	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556917211	chr18:12418675-12418676	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs71351478	chr18:12418735-12418736	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs183741569	chr18:12418761-12418762	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs575887594	chr18:12418766-12418767	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs540120320	chr18:12418803-12418804	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs142041466	chr18:12418806-12418807	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs62095750	chr18:12418808-12418809	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs573342548	chr18:12418884-12418885	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs189123380	chr18:12419048-12419049	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs12232560	chr18:12419060-12419061	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs190623597	chr18:12419104-12419105	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs35617867	chr18:12419165-12419166	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs35420599	chr18:12419167-12419168	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs397859044	chr18:12419175-12419176	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs148091530	chr18:12419210-12419211	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs34481458	chr18:12419235-12419236	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs12957046	chr18:12419240-12419241	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs572246735	chr18:12419247-12419248	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs376215038	chr18:12419250-12419251	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs371337096	chr18:12419272-12419273	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs182869445	chr18:12419273-12419274	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs560098601	chr18:12419312-12419313	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs560633338	chr18:12419324-12419325	Weak transcription	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:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr18:12409200-12418400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr18:12409800-12418000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr18:12409800-12419800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr18:12410200-12419800	Weak transcription	NH-A	brain
13	chr18:12410400-12419800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr18:12410400-12419800	Weak transcription	Right Ventricle	heart
15	chr18:12410400-12430400	Weak transcription	A549	lung
16	chr18:12411800-12419800	Weak transcription	NHEK	skin
17	chr18:12414400-12419600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr18:12416000-12419600	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr18:12416000-12419800	Weak transcription	Esophagus	oesophagus
20	chr18:12416000-12419800	Weak transcription	Stomach Mucosa	stomach
21	chr18:12416000-12419800	Weak transcription	NHLF	lung
22	chr18:12416000-12420000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr18:12416200-12418400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr18:12416200-12418400	Weak transcription	GM12878-XiMat	blood
25	chr18:12416200-12419800	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr18:12416200-12419800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr18:12416200-12419800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr18:12416200-12419800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr18:12416200-12419800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr18:12416200-12419800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr18:12416200-12419800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr18:12416200-12419800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr18:12416200-12419800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr18:12416200-12419800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr18:12416200-12419800	Weak transcription	Fetal Intestine Small	intestine
36	chr18:12416200-12419800	Weak transcription	Ovary	ovary
37	chr18:12416200-12419800	Weak transcription	Right Atrium	heart
38	chr18:12416200-12420000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr18:12416200-12420000	Weak transcription	Aorta	Aorta
40	chr18:12416200-12420000	Weak transcription	Fetal Heart	heart
41	chr18:12416200-12420000	Weak transcription	Left Ventricle	heart
42	chr18:12416200-12420000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr18:12416200-12420000	Weak transcription	Spleen	Spleen
44	chr18:12416400-12418400	Weak transcription	Fetal Brain Male	brain
45	chr18:12416400-12419800	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr18:12416400-12419800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr18:12416400-12419800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr18:12416400-12419800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr18:12416400-12419800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr18:12416400-12419800	Weak transcription	Adipose Nuclei	Adipose

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