Variant report

Variant	nsv909293
Chromosome Location	chr18:572336-603871
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	chr18:572540-572852	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:597008-597221	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:577622-577755	HepG2	liver:	n/a	n/a
4	ATF1	chr18:596993-597072	K562	blood:	n/a	n/a
5	ATF2	chr18:596947-597269	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:574849-575169	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr18:597008-597243	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr18:596915-597242	K562	blood:	n/a	n/a
9	BHLHE40	chr18:596967-597251	HepG2	liver:	n/a	n/a
10	BHLHE40	chr18:597007-597159	GM12878	blood:	n/a	n/a
11	BRCA1	chr18:597067-597178	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr18:596938-597263	K562	blood:	n/a	n/a
13	CBX3	chr18:580040-580662	K562	blood:	n/a	n/a
14	CCNT2	chr18:580269-580459	K562	blood:	n/a	n/a
15	CCNT2	chr18:596910-597210	K562	blood:	n/a	n/a
16	CEBPB	chr18:577631-577852	HepG2	liver:	n/a	n/a
17	CEBPB	chr18:577670-577824	HepG2	liver:	n/a	n/a
18	CEBPB	chr18:597013-597205	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr18:574971-575160	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr18:581236-581482	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr18:597199-597220	HepG2	liver:	n/a	n/a
22	CHD2	chr18:597022-597364	H1-hESC	embryonic stem cell:	n/a	chr18:597160-597170
23	CREB1	chr18:596912-597403	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr18:596917-597297	K562	blood:	n/a	n/a
25	CREB1	chr18:596916-597280	ECC-1	luminal epithelium:	n/a	n/a
26	CREB1	chr18:596492-597372	HepG2	liver:	n/a	n/a
27	CREB1	chr18:596679-597183	A549	lung:	n/a	n/a
28	CREB1	chr18:596938-597287	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr18:596588-596880	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr18:597020-597170	HEEpiC	esophagus:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
31	CTCF	chr18:597019-597190	HUVEC	blood vessel:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
32	CTCF	chr18:596841-597263	K562	blood:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
33	CTCF	chr18:596951-597221	MCF-7	breast:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
34	CTCF	chr18:597080-597230	AG10803	skin:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104
35	CTCF	chr18:596939-597230	HepG2	liver:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
36	CTCF	chr18:596975-597205	MCF-7	breast:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
37	CTCF	chr18:596900-597272	GM12878	blood:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
38	CTCF	chr18:596963-597198	A549	lung:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
39	CTCF	chr18:598400-598550	BJ	skin:	n/a	n/a
40	CTCF	chr18:597000-597150	HCFaa	heart:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
41	CTCF	chr18:597000-597150	HCPEpiC	choroid plexus:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
42	CTCF	chr18:596960-597110	WERI-Rb-1	eye:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
43	CTCF	chr18:597020-597170	BE2_C	brain:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
44	CTCF	chr18:597040-597190	NHEK	skin:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
45	CTCF	chr18:597000-597150	GM12870	blood:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
46	CTCF	chr18:597020-597170	GM12873	blood:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
47	CTCF	chr18:596980-597130	GM12875	blood:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
48	CTCF	chr18:596968-597224	K562	blood:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
49	CTCF	chr18:596989-597187	GM10266	blood:	n/a	chr18:597089-597102 chr18:597089-597098 chr18:597088-597109 chr18:597086-597104 chr18:597070-597083
50	CTCF	chr18:580221-580533	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:580228-580278	MCF10A-Er-Src	breast:	n/a
2	chr18:580188-580238	HNPCEpiC	eye:	n/a
3	chr18:580209-580259	AG09309	skin:	n/a
4	chr18:580228-580278	MCF-7	breast:	n/a
5	chr18:580209-580259	NH-A	brain:	n/a
6	chr18:580244-580294	HCPEpiC	choroid plexus:	n/a
7	chr18:580435-580485	NB4	blood:	n/a
8	chr18:596759-596809	GM06990	blood:	n/a
9	chr18:580435-580485	SKMC	muscle:	n/a
10	chr18:580188-580238	AG04450	lung:	fetal
11	chr18:597075-597125	HCM	heart:	n/a
12	chr18:580702-580752	Jurkat	blood:	n/a
13	chr18:579237-579287	AG04450	lung:	fetal
14	chr18:580244-580294	AG09319	gingival:	n/a
15	chr18:577110-577160	NB4	blood:	n/a
16	chr18:579237-579287	HRCEpiC	kidney:	n/a
17	chr18:579237-579287	NHBE	bronchial:	n/a
18	chr18:580209-580259	GM12878	blood:	n/a
19	chr18:577110-577160	HUVEC	blood vessel:	n/a
20	chr18:596703-596753	PFSK-1	brain:	n/a
21	chr18:581171-581221	HRPEpiC	eye:	n/a
22	chr18:581171-581221	K562	blood:	n/a
23	chr18:597111-597161	GM12891	blood:	n/a
24	chr18:580209-580259	Jurkat	blood:	n/a
25	chr18:583805-583855	MCF10A-Er-Src	breast:	n/a
26	chr18:596757-596807	NHBE	bronchial:	n/a
27	chr18:580334-580384	NH-A	brain:	n/a
28	chr18:596713-596763	GM12891	blood:	n/a
29	chr18:580244-580294	HUVEC	blood vessel:	n/a
30	chr18:580258-580308	SAEC	small airway:	n/a
31	chr18:580209-580259	Hela-S3	cervix:	n/a
32	chr18:583805-583855	HEEpiC	esophagus:	n/a
33	chr18:580435-580485	PrEC	prostate:	n/a
34	chr18:579713-579763	HCM	heart:	n/a
35	chr18:580702-580752	NT2-D1	testis:	n/a
36	chr18:577110-577160	GM19239	blood:	n/a
37	chr18:580258-580308	CMK	blood:	n/a
38	chr18:579237-579287	U87	brain:	n/a
39	chr18:580228-580278	HEK293	kidney:	embryo
40	chr18:580435-580485	HEEpiC	esophagus:	n/a
41	chr18:579237-579287	GM12892	blood:	n/a
42	chr18:580244-580294	NT2-D1	testis:	n/a
43	chr18:580188-580238	HEK293	kidney:	embryo
44	chr18:596757-596807	HPAEpiC	pulmonary alveolar:	n/a
45	chr18:577110-577160	Hepatocyte	liver:	n/a
46	chr18:580209-580259	HL-60	blood:	n/a
47	chr18:596757-596807	T-47D	breast:	n/a
48	chr18:580209-580259	HNPCEpiC	eye:	n/a
49	chr18:580244-580294	HCT-116	colon:	n/a
50	chr18:596703-596753	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:597037..597571-chr18:612004..612507,2	K562	blood:
2	chr18:603691..606447-chr18:810738..812347,2	K562	blood:
3	chr12:6960313..6962763-chr18:595597..598209,2	MCF-7	breast:
4	chr18:590838..593015-chr18:596280..598090,2	MCF-7	breast:
5	chr18:570210..572740-chr18:576690..579289,2	K562	blood:
6	chr18:577506..581309-chr18:585130..588053,4	K562	blood:
7	chr18:570210..572740-chr18:576690..579289,2	K562	blood:
8	chr18:596672..598254-chr18:601606..603609,2	MCF-7	breast:
9	chr18:582101..583884-chr18:584335..585947,2	MCF-7	breast:
10	chr18:574055..576248-chr18:594242..596141,2	K562	blood:
11	chr18:513812..515978-chr18:595645..597205,2	MCF-7	breast:
12	chr18:583208..586140-chr18:590268..592916,3	MCF-7	breast:
13	chr18:577506..581309-chr18:585130..588053,4	K562	blood:
14	chr18:582101..583884-chr18:584335..585947,2	MCF-7	breast:
15	chr18:598315..601493-chr18:602058..605759,5	K562	blood:
16	chr18:581007..582847-chr18:587987..590964,2	MCF-7	breast:
17	chr18:588087..590665-chr18:658985..661981,2	K562	blood:
18	chr18:596672..598254-chr18:601606..603609,2	MCF-7	breast:
19	chr18:583208..586140-chr18:590268..592916,3	MCF-7	breast:
20	chr18:569366..571710-chr18:576690..578191,2	K562	blood:
21	chr18:581007..582847-chr18:587987..590964,2	MCF-7	breast:
22	chr18:574055..576248-chr18:594242..596141,2	K562	blood:
23	chr18:599119..600795-chr18:610361..612404,2	K562	blood:
24	chr18:596793..597621-chr18:616099..617012,5	K562	blood:
25	chr18:499620..501884-chr18:596147..598528,2	K562	blood:
26	chr18:598315..601493-chr18:602058..605759,5	K562	blood:
27	chr18:596612..597183-chr18:616160..617004,2	MCF-7	breast:
28	chr18:266563..269513-chr18:596555..599263,2	K562	blood:
29	chr18:600276..602735-chr18:648496..651246,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLUL1-2	chr18:597002-597129	NONHSAT056848
2	lnc-CLUL1-2	chr18:596998-597129	NONHSAT056847
3	lnc-C18orf56-2	chr18:586517-586850	NONHSAT056846

Variant related genes	Relation type
RN7SKP146	TF binding region
CETN1	TF binding region
ENSG00000239158	TF binding region
CLUL1	TF binding region
RN7SKP146	CpG island
CETN1	CpG island
ENSG00000239158	CpG island
CLUL1	CpG island
ENSG00000263884	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000266456	chromatin interactions
ENSG00000177143	chromatin interactions
ENSG00000111665	chromatin interactions
ENSG00000111667	chromatin interactions
ENSG00000176105	chromatin interactions
ENSG00000264265	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000158270	chromatin interactions
ENSG00000222174	chromatin interactions
ENSG00000239158	chromatin interactions

Extended variants
information (count: 1319 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1319 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs595879	chr18:572336-572337	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148497187	chr18:572368-572369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190290502	chr18:572370-572371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144203423	chr18:572382-572383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182840494	chr18:572406-572407	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs115634170	chr18:572458-572459	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs187967264	chr18:572484-572485	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs117462712	chr18:572487-572488	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs146560480	chr18:572524-572525	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs372752105	chr18:572525-572526	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs555856643	chr18:572544-572545	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs116572807	chr18:572563-572564	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs56300733	chr18:572576-572577	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs11404070	chr18:572580-572581	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs397796796	chr18:572585-572586	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs57666352	chr18:572591-572592	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs115120303	chr18:572776-572777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540933377	chr18:572810-572811	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs141103440	chr18:572821-572822	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs115555358	chr18:572822-572823	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs144916978	chr18:572841-572842	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs593589	chr18:572859-572860	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs529890155	chr18:572969-572970	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs67002643	chr18:572995-572996	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs115943560	chr18:573079-573080	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs544959678	chr18:573125-573126	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs377626835	chr18:573183-573184	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs190696122	chr18:573185-573186	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs12969481	chr18:573269-573270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs114011702	chr18:573404-573405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555817894	chr18:573460-573461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151189105	chr18:573467-573468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs671408	chr18:573472-573473	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184188055	chr18:573476-573477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573389558	chr18:573508-573509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3016823	chr18:573546-573547	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs539349	chr18:573550-573551	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577291929	chr18:573634-573635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73362444	chr18:573672-573673	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs140323455	chr18:573718-573719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530174039	chr18:573762-573763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs517189	chr18:573765-573766	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs560041269	chr18:573784-573785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527503053	chr18:573860-573861	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs372328133	chr18:573872-573873	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552018742	chr18:574099-574100	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs558108104	chr18:574149-574150	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs571903051	chr18:574151-574152	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs375744824	chr18:574189-574190	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs187731583	chr18:574209-574210	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	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
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
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Bladder cancer	21909424	CNVD
Schizophrenia	21346763	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:565800-573000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr18:565800-582000	Weak transcription	Right Atrium	heart
3	chr18:568200-572600	Weak transcription	Fetal Stomach	stomach
4	chr18:570000-572400	Enhancers	HepG2	liver
5	chr18:571800-575800	Enhancers	Fetal Kidney	kidney
6	chr18:572000-574600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr18:572000-576200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr18:572200-573200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr18:572200-574200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr18:572200-575400	Enhancers	Fetal Lung	lung
11	chr18:572200-575800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr18:572200-576000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr18:572200-576000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr18:572200-576000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr18:572200-581600	Enhancers	Fetal Muscle Leg	muscle
16	chr18:572400-572600	Flanking Active TSS	HepG2	liver
17	chr18:572400-576200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr18:572600-572800	Enhancers	HepG2	liver
19	chr18:572600-574600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr18:572600-575800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr18:572600-578400	Enhancers	Fetal Stomach	stomach
22	chr18:572800-573000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr18:572800-573400	Flanking Active TSS	HepG2	liver
24	chr18:572800-575600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr18:573000-574200	Enhancers	Fetal Muscle Trunk	muscle
26	chr18:573000-574600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr18:573000-576000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr18:573000-576000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr18:573200-574800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr18:573200-575000	Enhancers	Aorta	Aorta
31	chr18:573400-573800	Enhancers	HepG2	liver
32	chr18:573600-573800	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr18:573600-573800	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr18:573800-574000	Flanking Active TSS	HepG2	liver
35	chr18:573800-575600	Enhancers	Adipose Nuclei	Adipose
36	chr18:573800-577800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr18:574000-574600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr18:574000-575000	Enhancers	HepG2	liver
39	chr18:574200-575400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr18:574200-575600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr18:574200-576000	Weak transcription	Fetal Muscle Trunk	muscle
42	chr18:574600-575000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr18:574600-575000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr18:574600-575400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr18:574600-575800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr18:574800-575000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr18:574800-575200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr18:574800-575200	Enhancers	Brain Cingulate Gyrus	brain
49	chr18:575000-575200	Enhancers	Rectal Smooth Muscle	rectum
50	chr18:575000-575200	Enhancers	Skeletal Muscle Male	skeletal muscle

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