Variant report

Variant	nsv909594
Chromosome Location	chr18:44279892-44400621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:701)
CpG islands
(count:855)
Chromatin interactive
region (count:11)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:701 , 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	chr18:44291594-44291809	K562	blood:	n/a	n/a
2	ARID3A	chr18:44343741-44343800	HepG2	liver:	n/a	n/a
3	ATF1	chr18:44291355-44291752	K562	blood:	n/a	n/a
4	ATF2	chr18:44291349-44291738	GM12878	blood:	n/a	n/a
5	ATF2	chr18:44291343-44291737	GM12878	blood:	n/a	n/a
6	ATF3	chr18:44291373-44291757	K562	blood:	n/a	n/a
7	BACH1	chr18:44287055-44287212	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr18:44335079-44335249	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr18:44291404-44291604	K562	blood:	n/a	n/a
10	BACH1	chr18:44336050-44336250	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr18:44294139-44294257	HepG2	liver:	n/a	n/a
12	BHLHE40	chr18:44367638-44367984	GM12878	blood:	n/a	n/a
13	BHLHE40	chr18:44291404-44291771	K562	blood:	n/a	n/a
14	BHLHE40	chr18:44299297-44299305	K562	blood:	n/a	n/a
15	BHLHE40	chr18:44334478-44334576	GM12878	blood:	n/a	n/a
16	BRCA1	chr18:44318689-44318719	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr18:44291375-44291672	K562	blood:	n/a	n/a
18	CCNT2	chr18:44291435-44291748	K562	blood:	n/a	n/a
19	CEBPB	chr18:44376035-44376269	IMR90	lung:	n/a	n/a
20	CEBPB	chr18:44298913-44299496	HCT-116	colon:	n/a	n/a
21	CEBPB	chr18:44346904-44347188	K562	blood:	n/a	n/a
22	CEBPB	chr18:44376072-44376263	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr18:44299061-44299279	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr18:44331573-44331857	HepG2	liver:	n/a	chr18:44331721-44331732
25	CEBPB	chr18:44369682-44369880	HepG2	liver:	n/a	chr18:44369709-44369720
26	CEBPB	chr18:44380339-44380513	HepG2	liver:	n/a	chr18:44380462-44380473
27	CEBPB	chr18:44376072-44376254	A549	lung:	n/a	n/a
28	CEBPB	chr18:44298198-44298374	K562	blood:	n/a	n/a
29	CEBPB	chr18:44307201-44307385	HepG2	liver:	n/a	n/a
30	CEBPB	chr18:44291467-44291759	K562	blood:	n/a	n/a
31	CEBPB	chr18:44298091-44298404	IMR90	lung:	n/a	n/a
32	CEBPB	chr18:44291358-44291613	K562	blood:	n/a	n/a
33	CEBPD	chr18:44291321-44291792	K562	blood:	n/a	n/a
34	CEBPD	chr18:44291359-44291881	K562	blood:	n/a	n/a
35	CHD1	chr18:44336734-44336908	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr18:44334253-44334329	GM12878	blood:	n/a	n/a
37	CHD2	chr18:44291380-44291723	GM12878	blood:	n/a	n/a
38	CHD2	chr18:44291348-44291684	K562	blood:	n/a	n/a
39	CHD2	chr18:44336861-44337128	H1-hESC	embryonic stem cell:	n/a	chr18:44337023-44337033
40	CTBP2	chr18:44336144-44337128	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr18:44337460-44338259	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr18:44350860-44351010	HAc	cerebellar:	n/a	n/a
43	CTCF	chr18:44302520-44302670	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr18:44373500-44373650	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr18:44352340-44352490	HL-60	blood:	n/a	n/a
46	CTCF	chr18:44352420-44352570	Hela-S3	cervix:	n/a	chr18:44352478-44352499
47	CTCF	chr18:44373587-44373926	K562	blood:	n/a	chr18:44373713-44373720
48	CTCF	chr18:44352615-44352658	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr18:44373660-44373810	HPAF	blood vessel:	n/a	chr18:44373713-44373720
50	CTCF	chr18:44373640-44373790	AG04450	lung:	n/a	chr18:44373713-44373720

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44334713-44334763	HL-60	blood:	n/a
2	chr18:44334713-44334763	HL-60	blood:	n/a
3	chr18:44334713-44334763	ovcar-3	ovarian:	n/a
4	chr18:44337922-44337972	PANC-1	pancreas:	n/a
5	chr18:44392124-44392174	GM12891	blood:	n/a
6	chr18:44334713-44334763	AG10803	skin:	n/a
7	chr18:44339513-44339563	HEEpiC	esophagus:	n/a
8	chr18:44338147-44338197	AG09319	gingival:	n/a
9	chr18:44337099-44337149	HRE	kidney:	n/a
10	chr18:44333130-44333180	AG09319	gingival:	n/a
11	chr18:44337099-44337149	H1-hESC	embryonic stem cell:	embryo
12	chr18:44335109-44335159	HNPCEpiC	eye:	n/a
13	chr18:44337922-44337972	AG04449	skin:	fetal
14	chr18:44339513-44339563	HMEC	breast:	n/a
15	chr18:44339513-44339563	PANC-1	pancreas:	n/a
16	chr18:44335109-44335159	T-47D	breast:	n/a
17	chr18:44337664-44337714	HRE	kidney:	n/a
18	chr18:44340177-44340227	Hela-S3	cervix:	n/a
19	chr18:44335109-44335159	ProgFib	skin:	n/a
20	chr18:44337853-44337903	GM12878	blood:	n/a
21	chr18:44338099-44338149	HNPCEpiC	eye:	n/a
22	chr18:44337664-44337714	AG09319	gingival:	n/a
23	chr18:44333130-44333180	AG10803	skin:	n/a
24	chr18:44339513-44339563	H1-hESC	embryonic stem cell:	embryo
25	chr18:44338147-44338197	HepG2	liver:	n/a
26	chr18:44337664-44337714	HCPEpiC	choroid plexus:	n/a
27	chr18:44334713-44334763	MCF10A-Er-Src	breast:	n/a
28	chr18:44337910-44337960	HPAEpiC	pulmonary alveolar:	n/a
29	chr18:44336399-44336449	A549	lung:	n/a
30	chr18:44337664-44337714	GM19239	blood:	n/a
31	chr18:44337099-44337149	MCF-7	breast:	n/a
32	chr18:44338099-44338149	HCT-116	colon:	n/a
33	chr18:44338147-44338197	BE2_C	brain:	n/a
34	chr18:44337853-44337903	HCF	heart:	n/a
35	chr18:44337099-44337149	Caco-2	colon:	n/a
36	chr18:44333130-44333180	NHBE	bronchial:	n/a
37	chr18:44336399-44336449	HAEpiC	amniotic membrane:	n/a
38	chr18:44337099-44337149	HL-60	blood:	n/a
39	chr18:44337099-44337149	GM19239	blood:	n/a
40	chr18:44337664-44337714	Jurkat	blood:	n/a
41	chr18:44334713-44334763	U87	brain:	n/a
42	chr18:44338099-44338149	ovcar-3	ovarian:	n/a
43	chr18:44337099-44337149	HPAEpiC	pulmonary alveolar:	n/a
44	chr18:44333130-44333180	K562	blood:	n/a
45	chr18:44335109-44335159	AG10803	skin:	n/a
46	chr18:44334713-44334763	RPTEC	kidney:	n/a
47	chr18:44336399-44336449	HIPEpiC	eye:	n/a
48	chr18:44338147-44338197	HCF	heart:	n/a
49	chr18:44337664-44337714	A549	lung:	n/a
50	chr18:44337910-44337960	SK-N-SH	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:44295920..44298422-chr18:44298971..44300843,2	K562	blood:
2	chr18:44290160..44292978-chr18:44295020..44296704,2	K562	blood:
3	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
4	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:
5	chr18:44274609..44276484-chr18:44283280..44285724,2	K562	blood:
6	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:
7	chr18:44290160..44292978-chr18:44295020..44296704,2	K562	blood:
8	chr18:44339087..44341037-chr18:44341994..44343919,2	K562	blood:
9	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
10	chr18:44295920..44298422-chr18:44298971..44300843,2	K562	blood:
11	chr18:44287477..44289570-chr18:44301088..44303006,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIAS2-1	chr18:44383187-44383857	ENSG00000267167.1
2	lnc-KATNAL2-1	chr18:44336896-44336994	ENSG00000270112.2
3	lnc-KATNAL2-1	chr18:44339972-44340204	XLOC_012667
4	lnc-KATNAL2-1	chr18:44338415-44338422	XLOC_012667
5	lnc-KATNAL2-1	chr18:44336450-44336587	ENSG00000270112.2
6	lnc-KATNAL2-1	chr18:44337689-44338426	NONHSAT059140
7	lnc-KATNAL2-1	chr18:44339774-44340307	ENSG00000270112.2
8	lnc-KATNAL2-1	chr18:44336746-44337039	ENSG00000270112.2
9	lnc-KATNAL2-10	chr18:44302938-44303186	NONHSAT059136
10	lnc-KATNAL2-1	chr18:44339687-44344371	NONHSAT059142
11	lnc-KATNAL2-1	chr18:44338764-44339028	NONHSAT059140
12	lnc-KATNAL2-7	chr18:44383140-44387340	NONHSAT059143

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PIAS2	hsa-miR-26b-5p	chr18:44392379-44392395

Variant related genes	Relation type
ENSG00000270112	TF binding region
ST8SIA5	TF binding region
ENSG00000240983	TF binding region
ENSG00000267167	TF binding region
ENSG00000270112	CpG island
ST8SIA5	CpG island
ENSG00000240983	CpG island
ENSG00000267167	CpG island
ENSG00000240983	chromatin interactions
ENSG00000101638	chromatin interactions

Extended variants
information (count: 4365 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4365 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs650329	chr18:44279892-44279893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78271214	chr18:44279895-44279896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549369237	chr18:44279940-44279941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116710938	chr18:44279947-44279948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199833105	chr18:44279950-44279951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569573753	chr18:44279966-44279967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529165793	chr18:44279967-44279968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368409516	chr18:44280052-44280053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561037519	chr18:44280062-44280063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529918787	chr18:44280063-44280064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35624372	chr18:44280121-44280122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543700103	chr18:44280127-44280128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372748724	chr18:44280137-44280138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144277842	chr18:44280230-44280231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532349929	chr18:44280268-44280269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552522115	chr18:44280277-44280278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183872195	chr18:44280297-44280298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529395298	chr18:44280300-44280301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549488940	chr18:44280386-44280387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187480234	chr18:44280427-44280428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535100392	chr18:44280465-44280466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557170729	chr18:44280480-44280481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148724397	chr18:44280518-44280519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190449118	chr18:44280521-44280522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558008685	chr18:44280571-44280572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1038005	chr18:44280609-44280610	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs71364560	chr18:44280643-44280644	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs535311206	chr18:44280665-44280666	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs182765461	chr18:44280678-44280679	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs557403904	chr18:44280681-44280682	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs574626172	chr18:44280688-44280689	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs187092892	chr18:44280715-44280716	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs563365326	chr18:44280718-44280719	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs376731402	chr18:44280757-44280758	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs532421386	chr18:44280760-44280761	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs545794279	chr18:44280788-44280789	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs559669623	chr18:44280818-44280819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114321300	chr18:44280867-44280868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141396912	chr18:44281002-44281003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192539895	chr18:44281012-44281013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530943589	chr18:44281035-44281036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551140671	chr18:44281075-44281076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570974498	chr18:44281076-44281077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150800836	chr18:44281078-44281079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2469901	chr18:44281093-44281094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58301061	chr18:44281122-44281123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2943795	chr18:44281126-44281127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2927375	chr18:44281129-44281130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553395875	chr18:44281258-44281259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2447526	chr18:44281265-44281266	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

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
small cell lung cancer	17426248	CNVD
Prostate cancer	22341455	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1204 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44253000-44291400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr18:44258200-44280000	Weak transcription	HSMMtube	muscle
3	chr18:44260800-44286600	Weak transcription	Brain Germinal Matrix	brain
4	chr18:44273200-44288000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr18:44276600-44286600	Weak transcription	Left Ventricle	heart
6	chr18:44277000-44282200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr18:44277000-44282200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr18:44277000-44282400	Weak transcription	Psoas Muscle	Psoas
9	chr18:44278400-44280600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr18:44279600-44285200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr18:44280000-44280200	Enhancers	HSMMtube	muscle
12	chr18:44280600-44280800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr18:44280600-44281000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr18:44280600-44286600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr18:44280600-44286600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr18:44281000-44283800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr18:44282200-44283000	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr18:44282200-44283200	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr18:44282400-44285800	Enhancers	Psoas Muscle	Psoas
20	chr18:44283000-44285200	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr18:44283200-44284800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr18:44283800-44287600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr18:44284800-44287000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr18:44284800-44288600	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr18:44285000-44285400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr18:44285200-44285600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr18:44285200-44285800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr18:44285200-44287000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr18:44285200-44291600	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr18:44285400-44286000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr18:44285400-44286000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr18:44285400-44287400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr18:44285600-44286800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr18:44285600-44287200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr18:44285800-44290000	Weak transcription	Psoas Muscle	Psoas
36	chr18:44286000-44286400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr18:44286000-44287000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr18:44286200-44286800	Enhancers	Brain Substantia Nigra	brain
39	chr18:44286400-44287200	Enhancers	Brain Angular Gyrus	brain
40	chr18:44286400-44288000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr18:44286600-44286800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr18:44286600-44286800	Enhancers	Brain Hippocampus Middle	brain
43	chr18:44286600-44286800	Enhancers	Left Ventricle	heart
44	chr18:44286600-44287200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr18:44286600-44287200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr18:44286600-44287200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr18:44286600-44287200	Enhancers	Fetal Heart	heart
48	chr18:44286600-44287600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr18:44286600-44288000	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr18:44286600-44288400	Enhancers	Brain Germinal Matrix	brain

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