Variant report

Variant	nsv2204
Chromosome Location	chr18:11499825-11544209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:852)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:11500265-11501942	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:11519203-11519408	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:11512685-11512993	HepG2	liver:	n/a	n/a
4	ATF2	chr18:11511325-11511711	GM12878	blood:	n/a	n/a
5	ATF2	chr18:11511354-11511912	GM12878	blood:	n/a	n/a
6	ATF3	chr18:11519178-11519339	K562	blood:	n/a	n/a
7	ATF3	chr18:11519029-11519344	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr18:11500458-11500756	GM12878	blood:	n/a	n/a
9	BHLHE40	chr18:11500447-11501074	HepG2	liver:	n/a	n/a
10	BHLHE40	chr18:11532341-11532541	HepG2	liver:	n/a	n/a
11	BHLHE40	chr18:11519095-11519341	K562	blood:	n/a	n/a
12	BHLHE40	chr18:11533514-11533708	K562	blood:	n/a	n/a
13	BHLHE40	chr18:11511453-11512073	GM12878	blood:	n/a	n/a
14	BRCA1	chr18:11500423-11500877	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr18:11519100-11519333	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr18:11500467-11500505	HepG2	liver:	n/a	n/a
17	BRCA1	chr18:11506874-11507253	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr18:11500325-11500942	HCT-116	colon:	n/a	n/a
19	CBX3	chr18:11500362-11500760	HCT-116	colon:	n/a	n/a
20	CBX3	chr18:11544117-11544406	K562	blood:	n/a	n/a
21	CBX3	chr18:11544082-11544485	HCT-116	colon:	n/a	n/a
22	CBX3	chr18:11544140-11544504	HCT-116	colon:	n/a	n/a
23	CBX3	chr18:11544142-11544394	K562	blood:	n/a	n/a
24	CEBPB	chr18:11500892-11501483	HepG2	liver:	n/a	chr18:11501301-11501312
25	CEBPB	chr18:11500483-11500776	IMR90	lung:	n/a	n/a
26	CEBPB	chr18:11501211-11501419	A549	lung:	n/a	chr18:11501301-11501312
27	CEBPB	chr18:11500382-11500973	HCT-116	colon:	n/a	n/a
28	CEBPB	chr18:11519104-11519317	HepG2	liver:	n/a	n/a
29	CEBPB	chr18:11512219-11512921	Hela-S3	cervix:	n/a	chr18:11512377-11512388
30	CEBPB	chr18:11500303-11500912	HCT-116	colon:	n/a	n/a
31	CEBPB	chr18:11500188-11500838	Hela-S3	cervix:	n/a	n/a
32	CEBPZ	chr18:11512737-11512842	HepG2	liver:	n/a	n/a
33	CHD2	chr18:11500495-11501017	HepG2	liver:	n/a	n/a
34	CHD2	chr18:11519046-11519067	GM12878	blood:	n/a	n/a
35	CHD2	chr18:11500363-11500823	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr18:11511491-11511849	GM12878	blood:	n/a	n/a
37	CHD2	chr18:11512741-11512930	HepG2	liver:	n/a	n/a
38	CHD2	chr18:11519138-11519370	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr18:11500541-11500743	A549	lung:	n/a	n/a
40	CTCF	chr18:11533956-11534076	HepG2	liver:	n/a	chr18:11534006-11534024
41	CTCF	chr18:11512733-11512925	T-47D	breast:	n/a	n/a
42	CTCF	chr18:11534129-11534220	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr18:11519200-11519350	SK-N-SH_RA	brain:	n/a	chr18:11519267-11519283 chr18:11519261-11519282 chr18:11519266-11519284 chr18:11519271-11519279 chr18:11519268-11519281
44	CTCF	chr18:11512767-11512920	GM10266	blood:	n/a	n/a
45	CTCF	chr18:11512720-11512870	GM12874	blood:	n/a	n/a
46	CTCF	chr18:11519220-11519370	SAEC	small airway:	n/a	chr18:11519267-11519283 chr18:11519261-11519282 chr18:11519266-11519284 chr18:11519271-11519279 chr18:11519268-11519281
47	CTCF	chr18:11533930-11534086	Fibrobl	skin:	n/a	chr18:11534006-11534024
48	CTCF	chr18:11512660-11512810	HFF	foreskin:	n/a	n/a
49	CTCF	chr18:11519240-11519390	GM12872	blood:	n/a	chr18:11519267-11519283 chr18:11519261-11519282 chr18:11519266-11519284 chr18:11519271-11519279 chr18:11519268-11519281
50	CTCF	chr18:11519220-11519370	AG04449	skin:	n/a	chr18:11519267-11519283 chr18:11519261-11519282 chr18:11519266-11519284 chr18:11519271-11519279 chr18:11519268-11519281

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11519034-11519084	HEEpiC	esophagus:	n/a
2	chr18:11519034-11519084	Hela-S3	cervix:	n/a
3	chr18:11519034-11519084	Jurkat	blood:	n/a
4	chr18:11519034-11519084	GM12891	blood:	n/a
5	chr18:11519034-11519084	K562	blood:	n/a
6	chr18:11519034-11519084	MCF10A-Er-Src	breast:	n/a
7	chr18:11519034-11519084	GM12892	blood:	n/a
8	chr18:11519034-11519084	NB4	blood:	n/a
9	chr18:11519034-11519084	BJ	skin:	n/a
10	chr18:11519034-11519084	HNPCEpiC	eye:	n/a
11	chr18:11519034-11519084	GM19239	blood:	n/a
12	chr18:11519034-11519084	SK-N-MC	brain:	n/a
13	chr18:11519034-11519084	A549	lung:	n/a
14	chr18:11519034-11519084	AG04450	lung:	fetal
15	chr18:11519034-11519084	BE2_C	brain:	n/a
16	chr18:11519034-11519084	AoSMC	blood vessel:	n/a
17	chr18:11519034-11519084	AG04449	skin:	fetal
18	chr18:11519034-11519084	MCF-7	breast:	n/a
19	chr18:11519034-11519084	U87	brain:	n/a
20	chr18:11519034-11519084	NHDF-neo	bronchial:	n/a
21	chr18:11519034-11519084	HCM	heart:	n/a
22	chr18:11519034-11519084	AG09309	skin:	n/a
23	chr18:11519034-11519084	GM12878	blood:	n/a
24	chr18:11519034-11519084	PrEC	prostate:	n/a
25	chr18:11519034-11519084	ECC-1	luminal epithelium:	n/a
26	chr18:11519034-11519084	LNCaP	prostate:	n/a
27	chr18:11519034-11519084	PANC-1	pancreas:	n/a
28	chr18:11519034-11519084	GM06990	blood:	n/a
29	chr18:11519034-11519084	HCT-116	colon:	n/a
30	chr18:11519034-11519084	IMR90	lung:	fetal
31	chr18:11519034-11519084	NH-A	brain:	n/a
32	chr18:11519034-11519084	HCF	heart:	n/a
33	chr18:11519034-11519084	Hepatocyte	liver:	n/a
34	chr18:11519034-11519084	HepG2	liver:	n/a
35	chr18:11519034-11519084	HRCEpiC	kidney:	n/a
36	chr18:11519034-11519084	HEK293	kidney:	embryo
37	chr18:11519034-11519084	HRPEpiC	eye:	n/a
38	chr18:11519034-11519084	HPAEpiC	pulmonary alveolar:	n/a
39	chr18:11519034-11519084	HRE	kidney:	n/a
40	chr18:11519034-11519084	NT2-D1	testis:	n/a
41	chr18:11519034-11519084	HAEpiC	amniotic membrane:	n/a
42	chr18:11519034-11519084	CMK	blood:	n/a
43	chr18:11519034-11519084	SKMC	muscle:	n/a
44	chr18:11519034-11519084	SK-N-SH_RA	brain:	n/a
45	chr18:11519034-11519084	HL-60	blood:	n/a
46	chr18:11519034-11519084	AG09319	gingival:	n/a
47	chr18:11519034-11519084	HUVEC	blood vessel:	n/a
48	chr18:11519034-11519084	SK-N-SH	brain:	n/a
49	chr18:11519034-11519084	ovcar-3	ovarian:	n/a
50	chr18:11519034-11519084	HCPEpiC	choroid plexus:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:11518713..11519703-chr18:11552996..11553743,6	MCF-7	breast:
2	chr18:11513286..11515221-chr18:11517194..11519674,2	K562	blood:
3	chr18:11518909..11519601-chr18:11549107..11549874,2	MCF-7	breast:
4	chr18:11268822..11269508-chr18:11500370..11501110,2	MCF-7	breast:
5	chr18:11513286..11515221-chr18:11517194..11519674,2	K562	blood:
6	chr18:11309816..11310769-chr18:11512438..11513268,3	MCF-7	breast:
7	chr18:11494387..11496981-chr18:11498491..11500808,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC35G4-1	chr18:11506756-11506946	NONHSAT057308
2	lnc-SLC35G4-1	chr18:11506755-11506982	NONHSAT057314
3	lnc-SLC35G4-1	chr18:11503733-11503935	XLOC_012626
4	lnc-SLC35G4-1	chr18:11504827-11505056	XLOC_012626
5	lnc-SLC35G4-1	chr18:11505775-11505923	XLOC_012626
6	lnc-SLC35G4-1	chr18:11506531-11506635	NONHSAT057308
7	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
8	lnc-SLC35G4-1	chr18:11503733-11503883	ENSG00000267252.1
9	lnc-SLC35G4-1	chr18:11506756-11506982	XLOC_012626
10	lnc-SLC35G4-1	chr18:11506756-11506975	ENSG00000267252.1
11	lnc-SLC35G4-1	chr18:11506756-11506979	XLOC_012626
12	lnc-SLC35G4-1	chr18:11506756-11506967	ENSG00000267252.1
13	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
14	lnc-SLC35G4-1	chr18:11503733-11503883	ENSG00000267252.1
15	lnc-SLC35G4-1	chr18:11506756-11506979	XLOC_012626
16	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
17	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
18	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
19	lnc-SLC35G4-1	chr18:11505502-11506635	NONHSAT057314
20	lnc-SLC35G4-1	chr18:11506756-11506982	XLOC_012626
21	lnc-SLC35G4-1	chr18:11505778-11505923	ENSG00000267252.1
22	lnc-SLC35G4-1	chr18:11506756-11506982	ENSG00000267252.1
23	lnc-SLC35G4-1	chr18:11504827-11505058	ENSG00000267252.1
24	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
25	lnc-SLC35G4-1	chr18:11505503-11506635	XLOC_012626

No data

Variant related genes	Relation type
ENSG00000267252	TF binding region
ENSG00000267252	CpG island
TMF1	miRNA target sites
NUP153	miRNA target sites
TMEM9B	miRNA target sites
SLC30A7	miRNA target sites

Extended variants
information (count: 1899 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1899 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7226952	chr18:11499839-11499840	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188149370	chr18:11499841-11499842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577927862	chr18:11499992-11499993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191448301	chr18:11499997-11499998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560342225	chr18:11499998-11499999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375395706	chr18:11500000-11500001	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs572226831	chr18:11500017-11500018	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs545989830	chr18:11500026-11500027	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs543290050	chr18:11500039-11500040	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183838373	chr18:11500050-11500051	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs532072105	chr18:11500067-11500068	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs188561161	chr18:11500070-11500071	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs541068158	chr18:11500102-11500103	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs114842125	chr18:11500111-11500112	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs9963650	chr18:11500118-11500119	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547474940	chr18:11500119-11500120	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs565688031	chr18:11500161-11500162	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs535934953	chr18:11500166-11500167	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs543380627	chr18:11500167-11500168	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs181565230	chr18:11500197-11500198	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs554374379	chr18:11500268-11500269	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs569488974	chr18:11500276-11500277	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs151239582	chr18:11500283-11500284	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs140457809	chr18:11500324-11500325	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs75018498	chr18:11500344-11500345	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs545025621	chr18:11500347-11500348	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs190122850	chr18:11500370-11500371	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs572607248	chr18:11500398-11500399	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs182293287	chr18:11500423-11500424	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs114909262	chr18:11500444-11500445	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs76137202	chr18:11500445-11500446	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs544106327	chr18:11500459-11500460	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs565394315	chr18:11500506-11500507	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs4796926	chr18:11500610-11500611	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547120945	chr18:11500642-11500643	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs35597967	chr18:11500662-11500663	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs150477386	chr18:11500665-11500666	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189803509	chr18:11500666-11500667	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs549924940	chr18:11500679-11500680	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs549592505	chr18:11500699-11500700	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs10623305	chr18:11500700-11500701	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs569528778	chr18:11500708-11500709	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs397939575	chr18:11500711-11500712	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs78254359	chr18:11500712-11500713	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs111243299	chr18:11500718-11500719	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552446873	chr18:11500815-11500816	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs570702865	chr18:11500935-11500936	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs116306793	chr18:11500973-11500974	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs553907080	chr18:11500988-11500989	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs9954648	chr18:11501034-11501035	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
abnormal development	18461090	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	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11493800-11502400	Enhancers	HSMM	muscle
2	chr18:11493800-11502600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr18:11493800-11502600	Enhancers	NHDF-Ad	bronchial
4	chr18:11494800-11500000	Enhancers	HepG2	liver
5	chr18:11495600-11502000	Enhancers	Hela-S3	cervix
6	chr18:11496200-11501400	Enhancers	Osteobl	bone
7	chr18:11496400-11502800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr18:11496800-11502400	Enhancers	NHLF	lung
9	chr18:11497200-11501600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr18:11497400-11501400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr18:11497600-11502600	Enhancers	HMEC	breast
12	chr18:11498400-11501000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr18:11498600-11501600	Enhancers	HUVEC	blood vessel
14	chr18:11498600-11502600	Enhancers	HSMMtube	muscle
15	chr18:11498800-11500200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr18:11499400-11500000	Enhancers	A549	lung
17	chr18:11499400-11500400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr18:11499600-11501200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr18:11499600-11501600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr18:11499600-11501800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr18:11499600-11501800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr18:11499600-11502800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr18:11499800-11500200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr18:11499800-11500200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr18:11499800-11500200	Enhancers	NH-A	brain
26	chr18:11499800-11500800	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr18:11499800-11501000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr18:11499800-11501200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr18:11499800-11501600	Enhancers	NHEK	skin
30	chr18:11500000-11500200	Enhancers	GM12878-XiMat	blood
31	chr18:11500000-11500400	Flanking Active TSS	A549	lung
32	chr18:11500000-11500400	Flanking Active TSS	HepG2	liver
33	chr18:11500000-11500800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr18:11500000-11501000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr18:11500200-11500600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr18:11500200-11500600	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr18:11500200-11500600	Flanking Active TSS	GM12878-XiMat	blood
38	chr18:11500200-11500600	Flanking Active TSS	NH-A	brain
39	chr18:11500200-11500800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr18:11500200-11501200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr18:11500200-11501800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr18:11500200-11502200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr18:11500200-11506600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr18:11500400-11501000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr18:11500400-11501200	Active TSS	A549	lung
46	chr18:11500400-11501200	Enhancers	HepG2	liver
47	chr18:11500400-11501400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr18:11500600-11501000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr18:11500600-11502600	Enhancers	NH-A	brain
50	chr18:11500800-11501200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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