Variant report

Variant	esv3412252
Chromosome Location	chr18:44684003-44711534
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:734)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44702625-44702867	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:44710998-44711426	K562	blood:	n/a	n/a
3	ARID3A	chr18:44684883-44685040	K562	blood:	n/a	n/a
4	ATF1	chr18:44711025-44711419	K562	blood:	n/a	n/a
5	ATF3	chr18:44711077-44711260	K562	blood:	n/a	n/a
6	ATF3	chr18:44684823-44685126	K562	blood:	n/a	n/a
7	BACH1	chr18:44702353-44702791	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr18:44710880-44711366	K562	blood:	n/a	n/a
9	BATF	chr18:44689575-44690016	GM12878	blood:	n/a	n/a
10	BATF	chr18:44689580-44689951	GM12878	blood:	n/a	n/a
11	BCL11A	chr18:44689553-44689930	GM12878	blood:	n/a	n/a
12	BCLAF1	chr18:44702454-44702973	GM12878	blood:	n/a	chr18:44702689-44702698
13	BCLAF1	chr18:44689560-44690104	GM12878	blood:	n/a	n/a
14	BHLHE40	chr18:44702530-44702867	K562	blood:	n/a	n/a
15	BHLHE40	chr18:44690225-44690288	GM12878	blood:	n/a	n/a
16	BHLHE40	chr18:44711098-44711434	HepG2	liver:	n/a	n/a
17	BHLHE40	chr18:44710938-44711538	K562	blood:	n/a	n/a
18	BRCA1	chr18:44702684-44702798	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr18:44702702-44702922	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr18:44710933-44711468	K562	blood:	n/a	n/a
21	CBX3	chr18:44684698-44685113	K562	blood:	n/a	n/a
22	CBX3	chr18:44710960-44711379	HCT-116	colon:	n/a	n/a
23	CBX3	chr18:44711025-44711366	K562	blood:	n/a	n/a
24	CBX3	chr18:44711005-44711446	HCT-116	colon:	n/a	n/a
25	CCNT2	chr18:44702484-44702876	K562	blood:	n/a	n/a
26	CCNT2	chr18:44711051-44711370	K562	blood:	n/a	n/a
27	CEBPB	chr18:44702330-44703039	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr18:44702630-44702977	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr18:44700961-44701085	H1-hESC	embryonic stem cell:	n/a	chr18:44700990-44701001
30	CEBPB	chr18:44711075-44711357	HepG2	liver:	n/a	chr18:44711217-44711228
31	CEBPB	chr18:44711008-44711370	K562	blood:	n/a	chr18:44711217-44711228
32	CEBPB	chr18:44701703-44702014	IMR90	lung:	n/a	chr18:44701890-44701901
33	CEBPB	chr18:44711076-44711345	K562	blood:	n/a	chr18:44711217-44711228
34	CEBPB	chr18:44684821-44685045	K562	blood:	n/a	n/a
35	CEBPB	chr18:44701098-44702095	Hela-S3	cervix:	n/a	chr18:44701890-44701901
36	CEBPB	chr18:44701685-44701987	A549	lung:	n/a	chr18:44701890-44701901
37	CEBPB	chr18:44702660-44703013	A549	lung:	n/a	n/a
38	CEBPB	chr18:44684768-44685183	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr18:44701770-44702005	HepG2	liver:	n/a	chr18:44701890-44701901
40	CEBPB	chr18:44702606-44703027	HepG2	liver:	n/a	n/a
41	CEBPB	chr18:44702616-44702985	MCF-7	breast:	n/a	n/a
42	CEBPB	chr18:44687729-44687737	K562	blood:	n/a	n/a
43	CEBPB	chr18:44701736-44701995	K562	blood:	n/a	chr18:44701890-44701901
44	CEBPB	chr18:44700948-44701079	HepG2	liver:	n/a	chr18:44700990-44701001
45	CEBPB	chr18:44711019-44711407	K562	blood:	n/a	chr18:44711217-44711228
46	CEBPB	chr18:44702689-44703007	K562	blood:	n/a	n/a
47	CEBPB	chr18:44705901-44705975	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr18:44701754-44702155	H1-hESC	embryonic stem cell:	n/a	chr18:44701890-44701901
49	CEBPB	chr18:44702584-44702995	IMR90	lung:	n/a	n/a
50	CEBPB	chr18:44702454-44703016	HepG2	liver:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44702545-44702595	Caco-2	colon:	n/a
2	chr18:44702766-44702816	K562	blood:	n/a
3	chr18:44702545-44702595	Caco-2	colon:	n/a
4	chr18:44702766-44702816	K562	blood:	n/a
5	chr18:44702545-44702595	RPTEC	kidney:	n/a
6	chr18:44702797-44702847	BE2_C	brain:	n/a
7	chr18:44703596-44703646	HNPCEpiC	eye:	n/a
8	chr18:44699437-44699487	SKMC	muscle:	n/a
9	chr18:44702603-44702653	GM12892	blood:	n/a
10	chr18:44702896-44702946	HRPEpiC	eye:	n/a
11	chr18:44706583-44706633	GM06990	blood:	n/a
12	chr18:44702797-44702847	AG09309	skin:	n/a
13	chr18:44702766-44702816	RPTEC	kidney:	n/a
14	chr18:44702603-44702653	HRE	kidney:	n/a
15	chr18:44706583-44706633	Hepatocyte	liver:	n/a
16	chr18:44702735-44702785	Jurkat	blood:	n/a
17	chr18:44702603-44702653	Hepatocyte	liver:	n/a
18	chr18:44702797-44702847	Jurkat	blood:	n/a
19	chr18:44702839-44702889	GM06990	blood:	n/a
20	chr18:44702735-44702785	MCF-7	breast:	n/a
21	chr18:44702839-44702889	HPAEpiC	pulmonary alveolar:	n/a
22	chr18:44702735-44702785	RPTEC	kidney:	n/a
23	chr18:44702545-44702595	HRCEpiC	kidney:	n/a
24	chr18:44702757-44702807	RPTEC	kidney:	n/a
25	chr18:44702766-44702816	NHBE	bronchial:	n/a
26	chr18:44702797-44702847	HMEC	breast:	n/a
27	chr18:44703596-44703646	GM19239	blood:	n/a
28	chr18:44702652-44702702	HRCEpiC	kidney:	n/a
29	chr18:44702766-44702816	Caco-2	colon:	n/a
30	chr18:44702757-44702807	HIPEpiC	eye:	n/a
31	chr18:44702797-44702847	ECC-1	luminal epithelium:	n/a
32	chr18:44702603-44702653	HAEpiC	amniotic membrane:	n/a
33	chr18:44706583-44706633	CMK	blood:	n/a
34	chr18:44702545-44702595	HepG2	liver:	n/a
35	chr18:44702797-44702847	NT2-D1	testis:	n/a
36	chr18:44702545-44702595	HEK293	kidney:	embryo
37	chr18:44703596-44703646	GM12892	blood:	n/a
38	chr18:44706583-44706633	HRPEpiC	eye:	n/a
39	chr18:44702757-44702807	HRPEpiC	eye:	n/a
40	chr18:44702735-44702785	LNCaP	prostate:	n/a
41	chr18:44702896-44702946	MCF10A-Er-Src	breast:	n/a
42	chr18:44699437-44699487	ovcar-3	ovarian:	n/a
43	chr18:44702735-44702785	CMK	blood:	n/a
44	chr18:44702839-44702889	Jurkat	blood:	n/a
45	chr18:44702766-44702816	PFSK-1	brain:	n/a
46	chr18:44702735-44702785	NH-A	brain:	n/a
47	chr18:44702735-44702785	U87	brain:	n/a
48	chr18:44702896-44702946	GM19239	blood:	n/a
49	chr18:44702839-44702889	HAEpiC	amniotic membrane:	n/a
50	chr18:44702757-44702807	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr18:44676773..44678330-chr18:44690150..44692924,2	K562	blood:
2	chr18:44669254..44671555-chr18:44682680..44684488,2	K562	blood:
3	chr18:44673432..44675834-chr18:44691617..44693277,2	MCF-7	breast:
4	chr18:44675848..44678361-chr18:44699497..44704011,6	MCF-7	breast:
5	chr18:44674746..44679194-chr18:44680542..44685924,9	K562	blood:
6	chr18:44675372..44679287-chr18:44700113..44704114,10	MCF-7	breast:
7	chr18:44693298..44695901-chr18:44700902..44702609,2	K562	blood:
8	chr18:44687727..44690082-chr18:44690575..44692828,2	K562	blood:
9	chr18:44495357..44497403-chr18:44700842..44702618,2	MCF-7	breast:
10	chr18:44695853..44698494-chr18:44701006..44702709,2	MCF-7	breast:
11	chr18:44676902..44678518-chr18:44699803..44701757,2	K562	blood:
12	chr18:44687665..44690240-chr18:44700822..44702824,2	MCF-7	breast:
13	chr18:44675406..44678402-chr18:44700257..44702641,2	K562	blood:
14	chr18:44676287..44678007-chr18:44686109..44688856,2	MCF-7	breast:
15	chr18:44675609..44678059-chr18:44682172..44686072,5	MCF-7	breast:
16	chr18:44693298..44695901-chr18:44700902..44702609,2	K562	blood:
17	chr18:44676158..44678571-chr18:44705279..44707685,2	MCF-7	breast:
18	chr18:44687727..44690082-chr18:44690575..44692828,2	K562	blood:
19	chr18:44675461..44681646-chr18:44682135..44691602,15	MCF-7	breast:
20	chr18:44685820..44687618-chr18:44709763..44711914,2	K562	blood:
21	chr18:44701224..44703839-chr18:44708863..44711758,3	MCF-7	breast:
22	chr18:44685820..44687618-chr18:44709763..44711914,2	K562	blood:

No data

Variant related genes	Relation type
IER3IP1	TF binding region
ENSG00000267228	TF binding region
IER3IP1	CpG island
ENSG00000267228	CpG island
ENSG00000078043	chromatin interactions
ENSG00000267228	chromatin interactions
ENSG00000167220	chromatin interactions
ENSG00000134049	chromatin interactions

Extended variants
information (count: 851 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570986357	chr18:44684072-44684073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376607189	chr18:44684090-44684091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532736487	chr18:44684155-44684156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112483860	chr18:44684190-44684191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs151115502	chr18:44684307-44684308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533738622	chr18:44684353-44684354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190364378	chr18:44684363-44684364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567207202	chr18:44684370-44684371	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536449350	chr18:44684390-44684391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs77615793	chr18:44684464-44684465	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192855130	chr18:44684509-44684510	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184149850	chr18:44684513-44684514	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188508355	chr18:44684530-44684531	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372896696	chr18:44684537-44684538	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540987254	chr18:44684552-44684553	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs561436897	chr18:44684556-44684557	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574884379	chr18:44684563-44684564	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181051042	chr18:44684577-44684578	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs563765759	chr18:44684593-44684594	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532733200	chr18:44684684-44684685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558416059	chr18:44684722-44684723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552924061	chr18:44684766-44684767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141364634	chr18:44684780-44684781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145090656	chr18:44684836-44684837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs547370314	chr18:44684853-44684854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138884580	chr18:44684861-44684862	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536002297	chr18:44684862-44684863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113027807	chr18:44684874-44684875	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs185086535	chr18:44684921-44684922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs189038462	chr18:44684950-44684951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558437837	chr18:44684954-44684955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372015319	chr18:44684991-44684992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553145150	chr18:44685012-44685013	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs375356910	chr18:44685024-44685025	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572996117	chr18:44685037-44685038	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534603187	chr18:44685094-44685095	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545222684	chr18:44685152-44685153	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574761761	chr18:44685196-44685197	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369007987	chr18:44685201-44685202	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs182540345	chr18:44685204-44685205	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563773343	chr18:44685339-44685340	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577526668	chr18:44685350-44685351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs56963764	chr18:44685378-44685379	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546376283	chr18:44685390-44685391	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150405595	chr18:44685393-44685394	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs575793421	chr18:44685414-44685415	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528840920	chr18:44685419-44685420	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs80135187	chr18:44685421-44685422	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs78010471	chr18:44685422-44685423	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs542500346	chr18:44685424-44685425	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	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
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
Ependymoma	20639864	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44677600-44685400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr18:44677600-44700200	Weak transcription	Aorta	Aorta
3	chr18:44677800-44684800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr18:44677800-44685600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr18:44677800-44686400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr18:44677800-44686600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr18:44677800-44686600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr18:44677800-44689800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr18:44677800-44693400	Weak transcription	Gastric	stomach
10	chr18:44677800-44698200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr18:44677800-44699000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr18:44677800-44700400	Weak transcription	Spleen	Spleen
13	chr18:44677800-44701000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr18:44677800-44701000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr18:44677800-44701000	Weak transcription	A549	lung
16	chr18:44677800-44701800	Weak transcription	Esophagus	oesophagus
17	chr18:44678000-44684400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr18:44678000-44687000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr18:44678000-44689200	Weak transcription	GM12878-XiMat	blood
20	chr18:44678000-44699600	Weak transcription	Colon Smooth Muscle	Colon
21	chr18:44678000-44700400	Weak transcription	Small Intestine	intestine
22	chr18:44678000-44700800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr18:44678000-44701000	Weak transcription	Fetal Stomach	stomach
24	chr18:44678200-44684200	Weak transcription	Fetal Brain Male	brain
25	chr18:44678200-44685400	Weak transcription	Hela-S3	cervix
26	chr18:44678200-44685600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr18:44678200-44689200	Weak transcription	NHEK	skin
28	chr18:44678200-44689800	Weak transcription	HSMMtube	muscle
29	chr18:44678200-44690800	Weak transcription	Fetal Intestine Small	intestine
30	chr18:44678200-44692400	Weak transcription	Thymus	Thymus
31	chr18:44678200-44692600	Weak transcription	NHLF	lung
32	chr18:44678200-44700200	Weak transcription	Brain Angular Gyrus	brain
33	chr18:44678200-44700800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr18:44678200-44701000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr18:44678200-44701200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr18:44678200-44701200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr18:44678400-44685800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr18:44678400-44689800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr18:44678400-44690000	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr18:44678400-44692200	Weak transcription	Right Ventricle	heart
41	chr18:44678400-44695400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr18:44678400-44700000	Weak transcription	Psoas Muscle	Psoas
43	chr18:44678400-44700800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr18:44678400-44700800	Weak transcription	Lung	lung
45	chr18:44678600-44684200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr18:44678600-44691200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr18:44678600-44699000	Weak transcription	Dnd41	blood
48	chr18:44680800-44686400	Weak transcription	Fetal Lung	lung
49	chr18:44681200-44684800	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr18:44681200-44687600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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