Variant report

Variant	nsv1063292
Chromosome Location	chr18:43295094-43317005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:43302931-43303205	K562	blood:	n/a	n/a
2	ARID3A	chr18:43303637-43303722	K562	blood:	n/a	n/a
3	BCL3	chr18:43302423-43302775	GM12878	blood:	n/a	n/a
4	BHLHE40	chr18:43302947-43303229	K562	blood:	n/a	n/a
5	BRCA1	chr18:43313658-43313754	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr18:43302921-43303230	K562	blood:	n/a	n/a
7	CEBPB	chr18:43301690-43301823	A549	lung:	n/a	chr18:43301739-43301750 chr18:43301741-43301750 chr18:43301741-43301750 chr18:43301741-43301750 chr18:43301740-43301751 chr18:43301741-43301750
8	CEBPB	chr18:43302943-43303174	K562	blood:	n/a	n/a
9	CEBPB	chr18:43314487-43314842	IMR90	lung:	n/a	chr18:43314655-43314666
10	CEBPB	chr18:43314483-43314800	A549	lung:	n/a	chr18:43314655-43314666
11	CEBPB	chr18:43314485-43314836	K562	blood:	n/a	chr18:43314655-43314666
12	CEBPB	chr18:43311109-43311576	A549	lung:	n/a	n/a
13	CEBPB	chr18:43314479-43314844	HepG2	liver:	n/a	chr18:43314655-43314666
14	CEBPB	chr18:43314530-43314762	MCF-7	breast:	n/a	chr18:43314655-43314666
15	CEBPB	chr18:43295364-43295575	IMR90	lung:	n/a	n/a
16	CEBPB	chr18:43311803-43311926	IMR90	lung:	n/a	chr18:43311868-43311879
17	CEBPB	chr18:43314519-43314792	H1-hESC	embryonic stem cell:	n/a	chr18:43314655-43314666
18	CEBPB	chr18:43302934-43303212	K562	blood:	n/a	n/a
19	CEBPB	chr18:43301586-43301918	HepG2	liver:	n/a	chr18:43301739-43301750 chr18:43301859-43301870 chr18:43301741-43301750 chr18:43301741-43301750 chr18:43301858-43301875 chr18:43301741-43301750 chr18:43301740-43301751 chr18:43301741-43301750
20	CEBPB	chr18:43301572-43301902	IMR90	lung:	n/a	chr18:43301739-43301750 chr18:43301859-43301870 chr18:43301741-43301750 chr18:43301741-43301750 chr18:43301858-43301875 chr18:43301741-43301750 chr18:43301740-43301751 chr18:43301741-43301750
21	CEBPB	chr18:43314596-43314697	Hela-S3	cervix:	n/a	chr18:43314655-43314666
22	CEBPB	chr18:43297437-43297538	A549	lung:	n/a	n/a
23	CEBPD	chr18:43302883-43303289	K562	blood:	n/a	n/a
24	CEBPD	chr18:43302823-43303244	K562	blood:	n/a	n/a
25	CTCF	chr18:43302980-43303130	GM06990	blood:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
26	CTCF	chr18:43313481-43313763	K562	blood:	n/a	chr18:43313665-43313686
27	CTCF	chr18:43303040-43303190	HFF	foreskin:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
28	CTCF	chr18:43313618-43313763	GM12891	blood:	n/a	chr18:43313665-43313686
29	CTCF	chr18:43302980-43303130	GM12865	blood:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
30	CTCF	chr18:43313589-43313776	MCF-7	breast:	n/a	chr18:43313665-43313686
31	CTCF	chr18:43313560-43313710	WERI-Rb-1	eye:	n/a	chr18:43313665-43313686
32	CTCF	chr18:43302980-43303130	GM12867	blood:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
33	CTCF	chr18:43303000-43303150	GM06990	blood:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
34	CTCF	chr18:43302890-43303179	LNCaP	prostate:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
35	CTCF	chr18:43302920-43303070	NHEK	skin:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
36	CTCF	chr18:43303000-43303150	HAc	cerebellar:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
37	CTCF	chr18:43313560-43313710	GM12871	blood:	n/a	chr18:43313665-43313686
38	CTCF	chr18:43313600-43313750	MCF-7	breast:	n/a	chr18:43313665-43313686
39	CTCF	chr18:43302915-43303167	LNCaP	prostate:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
40	CTCF	chr18:43302898-43303195	A549	lung:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
41	CTCF	chr18:43313620-43313770	HepG2	liver:	n/a	chr18:43313665-43313686
42	CTCF	chr18:43302907-43303170	HepG2	liver:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
43	CTCF	chr18:43303000-43303150	NHDF-neo	bronchial:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
44	CTCF	chr18:43302847-43303193	K562	blood:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
45	CTCF	chr18:43302947-43303160	HepG2	liver:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
46	CTCF	chr18:43302874-43303185	MCF-7	breast:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
47	CTCF	chr18:43313600-43313750	Caco-2	colon:	n/a	chr18:43313665-43313686
48	CTCF	chr18:43302960-43303110	GM12874	blood:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
49	CTCF	chr18:43302940-43303090	GM12868	blood:	n/a	chr18:43303048-43303061 chr18:43303045-43303063
50	CTCF	chr18:43313580-43313730	GM12873	blood:	n/a	chr18:43313665-43313686

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:43305617-43305667	ProgFib	skin:	n/a
2	chr18:43305617-43305667	ProgFib	skin:	n/a
3	chr18:43305540-43305590	HNPCEpiC	eye:	n/a
4	chr18:43305784-43305834	HCM	heart:	n/a
5	chr18:43304007-43304057	NT2-D1	testis:	n/a
6	chr18:43305784-43305834	SKMC	muscle:	n/a
7	chr18:43304452-43304502	AG09319	gingival:	n/a
8	chr18:43306919-43306969	AG09309	skin:	n/a
9	chr18:43304007-43304057	AG09309	skin:	n/a
10	chr18:43306919-43306969	Jurkat	blood:	n/a
11	chr18:43304079-43304129	BJ	skin:	n/a
12	chr18:43304452-43304502	HRE	kidney:	n/a
13	chr18:43302872-43302922	GM12891	blood:	n/a
14	chr18:43302872-43302922	SK-N-SH_RA	brain:	n/a
15	chr18:43304007-43304057	SK-N-SH	brain:	n/a
16	chr18:43305540-43305590	AoSMC	blood vessel:	n/a
17	chr18:43303777-43303827	HRE	kidney:	n/a
18	chr18:43305784-43305834	SK-N-SH_RA	brain:	n/a
19	chr18:43305540-43305590	NB4	blood:	n/a
20	chr18:43305617-43305667	A549	lung:	n/a
21	chr18:43306919-43306969	SK-N-MC	brain:	n/a
22	chr18:43302987-43303037	SK-N-MC	brain:	n/a
23	chr18:43303777-43303827	H1-hESC	embryonic stem cell:	embryo
24	chr18:43302987-43303037	H1-hESC	embryonic stem cell:	embryo
25	chr18:43304452-43304502	Hepatocyte	liver:	n/a
26	chr18:43305540-43305590	GM12878	blood:	n/a
27	chr18:43302987-43303037	SK-N-SH	brain:	n/a
28	chr18:43304452-43304502	HCT-116	colon:	n/a
29	chr18:43303777-43303827	SK-N-SH_RA	brain:	n/a
30	chr18:43304079-43304129	AG09309	skin:	n/a
31	chr18:43305617-43305667	HEEpiC	esophagus:	n/a
32	chr18:43302872-43302922	GM06990	blood:	n/a
33	chr18:43304079-43304129	AG09319	gingival:	n/a
34	chr18:43302872-43302922	BJ	skin:	n/a
35	chr18:43305540-43305590	Caco-2	colon:	n/a
36	chr18:43302872-43302922	HIPEpiC	eye:	n/a
37	chr18:43303777-43303827	NHBE	bronchial:	n/a
38	chr18:43306919-43306969	PANC-1	pancreas:	n/a
39	chr18:43304452-43304502	IMR90	lung:	fetal
40	chr18:43306919-43306969	ProgFib	skin:	n/a
41	chr18:43302987-43303037	NH-A	brain:	n/a
42	chr18:43302872-43302922	NH-A	brain:	n/a
43	chr18:43306919-43306969	HL-60	blood:	n/a
44	chr18:43305617-43305667	HPAEpiC	pulmonary alveolar:	n/a
45	chr18:43303777-43303827	AoSMC	blood vessel:	n/a
46	chr18:43304007-43304057	AG04449	skin:	fetal
47	chr18:43305784-43305834	AG09319	gingival:	n/a
48	chr18:43305784-43305834	AG04450	lung:	fetal
49	chr18:43305784-43305834	GM19239	blood:	n/a
50	chr18:43304007-43304057	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:43298152..43299670-chr18:43422427..43424275,2	MCF-7	breast:
2	chr18:43302589..43303496-chr18:43419127..43419988,3	MCF-7	breast:
3	chr18:43313147..43313738-chr18:43419137..43419763,2	MCF-7	breast:
4	chr18:43313599..43315940-chr18:43318137..43319930,2	MCF-7	breast:
5	chr18:43302652..43303528-chr18:43429652..43430244,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPG5-5	chr18:43311293-43311620	ENSG00000267193.1

Variant related genes	Relation type
SLC14A1	TF binding region
SLC14A1	CpG island
ENSG00000141469	chromatin interactions

Extended variants
information (count: 967 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16978459	chr18:43295094-43295095	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535729205	chr18:43295140-43295141	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs877788	chr18:43295148-43295149	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs554502184	chr18:43295200-43295201	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568854898	chr18:43295208-43295209	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117266964	chr18:43295218-43295219	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544500728	chr18:43295237-43295238	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537771417	chr18:43295241-43295242	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs877787	chr18:43295247-43295248	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs142750575	chr18:43295321-43295322	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs28410141	chr18:43295327-43295328	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs877786	chr18:43295347-43295348	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs542133231	chr18:43295410-43295411	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563613369	chr18:43295416-43295417	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183930373	chr18:43295434-43295435	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528186959	chr18:43295444-43295445	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114484655	chr18:43295461-43295462	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79817314	chr18:43295466-43295467	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188425944	chr18:43295525-43295526	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563216589	chr18:43295572-43295573	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528556413	chr18:43295591-43295592	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531775303	chr18:43295620-43295621	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548750068	chr18:43295621-43295622	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546850304	chr18:43295724-43295725	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551417541	chr18:43295770-43295771	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146050688	chr18:43295787-43295788	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529068558	chr18:43295817-43295818	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550894808	chr18:43295844-43295845	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370238573	chr18:43295912-43295913	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140035263	chr18:43295929-43295930	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539461711	chr18:43295949-43295950	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551089891	chr18:43295971-43295972	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs193186489	chr18:43295987-43295988	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374606289	chr18:43295999-43296000	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533627144	chr18:43296027-43296028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370428091	chr18:43296030-43296031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561975559	chr18:43296040-43296041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564834518	chr18:43296041-43296042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529739901	chr18:43296100-43296101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114998710	chr18:43296170-43296171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530706300	chr18:43296181-43296182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574715447	chr18:43296248-43296249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535607679	chr18:43296272-43296273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs16978460	chr18:43296286-43296287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs8083365	chr18:43296304-43296305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141802503	chr18:43296313-43296314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11659324	chr18:43296314-43296315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573154362	chr18:43296343-43296344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540749078	chr18:43296348-43296349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562115685	chr18:43296356-43296357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Breast cancer	21509527	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43290200-43323000	Weak transcription	Primary B cells from cord blood	blood
2	chr18:43291000-43295200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr18:43292800-43311200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr18:43293200-43295400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr18:43293400-43307000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr18:43293600-43298800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr18:43293600-43302200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr18:43293800-43295200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr18:43293800-43295400	Weak transcription	A549	lung
10	chr18:43293800-43295600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr18:43293800-43298800	Weak transcription	NH-A	brain
12	chr18:43294000-43296000	Strong transcription	Primary T cells from cord blood	blood
13	chr18:43294400-43295600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr18:43295200-43295600	Enhancers	Brain Anterior Caudate	brain
15	chr18:43295200-43295800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr18:43295200-43296000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr18:43295400-43295600	Weak transcription	Spleen	Spleen
18	chr18:43295400-43295800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr18:43295400-43296000	Enhancers	Primary B cells from peripheral blood	blood
20	chr18:43295400-43296000	Enhancers	A549	lung
21	chr18:43295600-43295800	Enhancers	Spleen	Spleen
22	chr18:43295600-43302000	Weak transcription	Brain Anterior Caudate	brain
23	chr18:43295800-43296000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr18:43295800-43296000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr18:43295800-43298800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr18:43295800-43298800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr18:43296000-43298600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr18:43296000-43311200	Weak transcription	A549	lung
29	chr18:43296000-43319400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr18:43296000-43325600	Weak transcription	Primary T cells from cord blood	blood
31	chr18:43296200-43304000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr18:43298600-43299200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr18:43298600-43299200	Enhancers	HSMM	muscle
34	chr18:43298600-43299200	Enhancers	HSMMtube	muscle
35	chr18:43298600-43299400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr18:43298600-43299600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr18:43298600-43299600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr18:43298600-43299600	Enhancers	NHLF	lung
39	chr18:43298600-43299600	Enhancers	Osteobl	bone
40	chr18:43298600-43301800	Weak transcription	Fetal Intestine Small	intestine
41	chr18:43298800-43299200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr18:43298800-43299400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr18:43298800-43299400	Enhancers	HMEC	breast
44	chr18:43298800-43299400	Enhancers	NH-A	brain
45	chr18:43298800-43299600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr18:43298800-43299600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr18:43299000-43299400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr18:43299000-43299400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr18:43299400-43300400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr18:43299400-43302200	Weak transcription	HMEC	breast

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