Variant report

Variant	nsv833600
Chromosome Location	chr18:24473894-24681019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1120)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:24641618-24642040	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:24597977-24598176	HepG2	liver:	n/a	n/a
3	ATF1	chr18:24610955-24610984	K562	blood:	n/a	n/a
4	ATF1	chr18:24680024-24680135	K562	blood:	n/a	n/a
5	ATF1	chr18:24663203-24663207	K562	blood:	n/a	n/a
6	ATF1	chr18:24668979-24668983	K562	blood:	n/a	n/a
7	ATF2	chr18:24653235-24653878	GM12878	blood:	n/a	n/a
8	ATF2	chr18:24558928-24559377	GM12878	blood:	n/a	n/a
9	ATF2	chr18:24653219-24653861	GM12878	blood:	n/a	n/a
10	ATF2	chr18:24558816-24559341	GM12878	blood:	n/a	n/a
11	BATF	chr18:24653243-24653721	GM12878	blood:	n/a	chr18:24653467-24653480
12	BATF	chr18:24558684-24558944	GM12878	blood:	n/a	n/a
13	BCL11A	chr18:24536886-24537213	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr18:24558970-24559271	GM12878	blood:	n/a	n/a
15	BCL11A	chr18:24536879-24537112	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr18:24653240-24653552	GM12878	blood:	n/a	chr18:24653410-24653419
17	BCL11A	chr18:24653235-24653781	GM12878	blood:	n/a	chr18:24653410-24653419
18	BCL3	chr18:24653281-24653600	GM12878	blood:	n/a	chr18:24653410-24653419
19	BCLAF1	chr18:24585578-24585881	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:24653404-24653604	GM12878	blood:	n/a	n/a
21	BHLHE40	chr18:24597908-24598105	GM12878	blood:	n/a	n/a
22	BHLHE40	chr18:24641394-24642038	HepG2	liver:	n/a	n/a
23	BHLHE40	chr18:24557899-24558066	GM12878	blood:	n/a	n/a
24	BHLHE40	chr18:24658700-24658716	K562	blood:	n/a	n/a
25	BHLHE40	chr18:24641514-24641793	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:24558451-24559307	GM12878	blood:	n/a	n/a
27	CCNT2	chr18:24647874-24648076	K562	blood:	n/a	n/a
28	CCNT2	chr18:24604223-24604391	K562	blood:	n/a	n/a
29	CCNT2	chr18:24622103-24622165	K562	blood:	n/a	n/a
30	CEBPB	chr18:24641567-24641771	IMR90	lung:	n/a	chr18:24641584-24641595
31	CEBPB	chr18:24560487-24560519	HepG2	liver:	n/a	n/a
32	CEBPB	chr18:24655604-24655822	HepG2	liver:	n/a	chr18:24655747-24655758
33	CEBPB	chr18:24628882-24629128	HepG2	liver:	n/a	chr18:24629051-24629064
34	CEBPB	chr18:24578945-24579262	HepG2	liver:	n/a	chr18:24579111-24579122 chr18:24579110-24579123 chr18:24579110-24579121 chr18:24579112-24579121
35	CEBPB	chr18:24655686-24655886	A549	lung:	n/a	chr18:24655747-24655758
36	CEBPB	chr18:24602546-24602660	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr18:24538150-24538297	HepG2	liver:	n/a	chr18:24538231-24538242
38	CEBPB	chr18:24666103-24666319	HepG2	liver:	n/a	chr18:24666146-24666157
39	CEBPB	chr18:24655594-24655848	IMR90	lung:	n/a	chr18:24655747-24655758
40	CEBPB	chr18:24619394-24619687	HepG2	liver:	n/a	chr18:24619509-24619520 chr18:24619552-24619563
41	CEBPB	chr18:24609335-24609465	HepG2	liver:	n/a	chr18:24609384-24609395
42	CEBPB	chr18:24638078-24638138	A549	lung:	n/a	chr18:24638125-24638134 chr18:24638125-24638134 chr18:24638125-24638134
43	CEBPB	chr18:24637983-24638298	HepG2	liver:	n/a	chr18:24638125-24638134 chr18:24638125-24638134 chr18:24638125-24638134
44	CEBPB	chr18:24638007-24638289	H1-hESC	embryonic stem cell:	n/a	chr18:24638125-24638134 chr18:24638125-24638134 chr18:24638125-24638134
45	CEBPB	chr18:24641413-24642030	HepG2	liver:	n/a	chr18:24641584-24641595
46	CEBPB	chr18:24619435-24619659	IMR90	lung:	n/a	chr18:24619509-24619520 chr18:24619552-24619563
47	CEBPB	chr18:24578936-24579257	IMR90	lung:	n/a	chr18:24579111-24579122 chr18:24579110-24579123 chr18:24579110-24579121 chr18:24579112-24579121
48	CEBPB	chr18:24641407-24642057	HepG2	liver:	n/a	chr18:24641584-24641595
49	CEBPB	chr18:24543836-24544029	IMR90	lung:	n/a	chr18:24543940-24543951
50	CEBPB	chr18:24648788-24648866	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:24537063-24537113	SAEC	small airway:	n/a
2	chr18:24537063-24537113	HL-60	blood:	n/a
3	chr18:24537063-24537113	ECC-1	luminal epithelium:	n/a
4	chr18:24537063-24537113	NHBE	bronchial:	n/a
5	chr18:24537063-24537113	HCF	heart:	n/a
6	chr18:24537063-24537113	HepG2	liver:	n/a
7	chr18:24537063-24537113	HPAEpiC	pulmonary alveolar:	n/a
8	chr18:24537063-24537113	HRCEpiC	kidney:	n/a
9	chr18:24537063-24537113	RPTEC	kidney:	n/a
10	chr18:24537063-24537113	GM12891	blood:	n/a
11	chr18:24537063-24537113	PrEC	prostate:	n/a
12	chr18:24537063-24537113	MCF10A-Er-Src	breast:	n/a
13	chr18:24537063-24537113	Jurkat	blood:	n/a
14	chr18:24537063-24537113	Hepatocyte	liver:	n/a
15	chr18:24537063-24537113	AG09319	gingival:	n/a
16	chr18:24537063-24537113	NB4	blood:	n/a
17	chr18:24537063-24537113	HRE	kidney:	n/a
18	chr18:24537063-24537113	H1-hESC	embryonic stem cell:	embryo
19	chr18:24537063-24537113	HCM	heart:	n/a
20	chr18:24537063-24537113	ProgFib	skin:	n/a
21	chr18:24537063-24537113	MCF-7	breast:	n/a
22	chr18:24537063-24537113	SKMC	muscle:	n/a
23	chr18:24537063-24537113	Caco-2	colon:	n/a
24	chr18:24537063-24537113	SK-N-SH	brain:	n/a
25	chr18:24537063-24537113	HNPCEpiC	eye:	n/a
26	chr18:24537063-24537113	HCT-116	colon:	n/a
27	chr18:24537063-24537113	SK-N-MC	brain:	n/a
28	chr18:24537063-24537113	HIPEpiC	eye:	n/a
29	chr18:24537063-24537113	Hela-S3	cervix:	n/a
30	chr18:24537063-24537113	U87	brain:	n/a
31	chr18:24537063-24537113	ovcar-3	ovarian:	n/a
32	chr18:24537063-24537113	GM12892	blood:	n/a
33	chr18:24537063-24537113	AG04450	lung:	fetal
34	chr18:24537063-24537113	GM06990	blood:	n/a
35	chr18:24537063-24537113	IMR90	lung:	fetal
36	chr18:24537063-24537113	HUVEC	blood vessel:	n/a
37	chr18:24537063-24537113	AG09309	skin:	n/a
38	chr18:24537063-24537113	NT2-D1	testis:	n/a
39	chr18:24537063-24537113	AoSMC	blood vessel:	n/a
40	chr18:24537063-24537113	HMEC	breast:	n/a
41	chr18:24537063-24537113	HRPEpiC	eye:	n/a
42	chr18:24537063-24537113	CMK	blood:	n/a
43	chr18:24537063-24537113	AG10803	skin:	n/a
44	chr18:24537063-24537113	T-47D	breast:	n/a
45	chr18:24537063-24537113	HCPEpiC	choroid plexus:	n/a
46	chr18:24537063-24537113	A549	lung:	n/a
47	chr18:24537063-24537113	AG04449	skin:	fetal
48	chr18:24537063-24537113	BJ	skin:	n/a
49	chr18:24537063-24537113	NH-A	brain:	n/a
50	chr18:24537063-24537113	NHDF-neo	bronchial:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:24510517..24511026-chr4:22608675..22609202,2	MCF-7	breast:
2	chr18:24590450..24592639-chr18:24595397..24598206,2	K562	blood:
3	chr18:24574463..24577146-chr18:24577247..24578836,2	K562	blood:
4	chr18:24574463..24577146-chr18:24577247..24578836,2	K562	blood:
5	chr18:24654215..24656527-chr18:24658995..24661475,2	K562	blood:
6	chr18:24598911..24600419-chr18:24602103..24604133,2	K562	blood:
7	chr17:57915136..57916681-chr18:24622286..24624382,2	MCF-7	breast:
8	chr18:24563994..24566667-chr18:24568829..24570336,2	K562	blood:
9	chr18:24563994..24566667-chr18:24568829..24570336,2	K562	blood:
10	chr18:24392717..24393537-chr18:24585343..24586051,3	MCF-7	breast:
11	chr18:24510025..24511017-chr4:22608413..22609080,2	MCF-7	breast:
12	chr18:24564837..24566667-chr18:24568829..24570386,2	K562	blood:
13	chr18:24598911..24600419-chr18:24602103..24604133,2	K562	blood:
14	chr18:24590450..24592639-chr18:24595397..24598206,2	K562	blood:
15	chr18:24622509..24625016-chr18:24625239..24626896,2	MCF-7	breast:
16	chr18:24385096..24386862-chr18:24541525..24543667,2	MCF-7	breast:
17	chr18:24622509..24625016-chr18:24625239..24626896,2	MCF-7	breast:
18	chr18:24392703..24393679-chr18:24542716..24543961,5	MCF-7	breast:
19	chr18:24392850..24393920-chr18:24583781..24585072,6	MCF-7	breast:
20	chr18:24597605..24598649-chr18:24878090..24879048,4	MCF-7	breast:
21	chr18:24392758..24393709-chr18:24584107..24584615,2	MCF-7	breast:
22	chr18:24598008..24598574-chr18:25195967..25196583,2	MCF-7	breast:
23	chr18:24558208..24560365-chr18:24586834..24589687,2	K562	blood:
24	chr18:24587162..24589841-chr18:24735427..24737669,2	K562	blood:
25	chr18:24564837..24566667-chr18:24568829..24570386,2	K562	blood:
26	chr18:24558208..24560365-chr18:24586834..24589687,2	K562	blood:
27	chr18:24654215..24656527-chr18:24658995..24661475,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAF4B-4	chr18:24510634-24510721	ENSG00000260372.2
2	lnc-AQP4-3	chr18:24532165-24532522	NONHSAT058769
3	lnc-TAF4B-4	chr18:24512957-24513086	NONHSAT058768
4	lnc-TAF4B-4	chr18:24514244-24515910	ENSG00000260372.2
5	lnc-TAF4B-4	chr18:24510624-24510787	NONHSAT058768
6	lnc-TAF4B-4	chr18:24513580-24513713	ENSG00000260372.2
7	lnc-TAF4B-4	chr18:24505781-24505826	ENSG00000260372.2
8	lnc-TAF4B-4	chr18:24505781-24505826	ENSG00000260372.2
9	lnc-TAF4B-4	chr18:24504724-24504809	ENSG00000260372.2
10	lnc-CHST9-1	chr18:24487309-24490289	NONHSAT058767
11	lnc-TAF4B-4	chr18:24512957-24513049	ENSG00000260372.2
12	lnc-TAF4B-4	chr18:24513580-24513672	NONHSAT058768
13	lnc-TAF4B-4	chr18:24512957-24513086	ENSG00000260372.2
14	lnc-TAF4B-4	chr18:24505781-24505826	ENSG00000260372.2
15	lnc-CHST9-1	chr18:24490298-24490602	NONHSAT058767
16	lnc-TAF4B-4	chr18:24504724-24504809	ENSG00000260372.2
17	lnc-TAF4B-4	chr18:24510634-24510787	ENSG00000260372.2
18	lnc-TAF4B-4	chr18:24504724-24504809	ENSG00000260372.2
19	lnc-TAF4B-4	chr18:24504724-24504809	ENSG00000260372.2
20	lnc-TAF4B-4	chr18:24510634-24510787	ENSG00000260372.2

No data

Variant related genes	Relation type
ENSG00000266549	TF binding region
ENSG00000266549	CpG island
ENSG00000251516	chromatin interactions
ENSG00000062716	chromatin interactions

Extended variants
information (count: 7519 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:7519 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558468500	chr18:24473926-24473927	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs576711857	chr18:24473979-24473980	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs163060	chr18:24474009-24474010	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs114312240	chr18:24474075-24474076	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs71353409	chr18:24474111-24474112	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542269791	chr18:24474121-24474122	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs560525094	chr18:24474137-24474138	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs527939383	chr18:24474178-24474179	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs12963431	chr18:24474185-24474186	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs564801735	chr18:24474187-24474188	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs550465437	chr18:24474217-24474218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375147852	chr18:24474237-24474238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550324669	chr18:24474255-24474256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs163059	chr18:24474267-24474268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529760639	chr18:24474270-24474271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548220870	chr18:24474315-24474316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554745693	chr18:24474316-24474317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566460975	chr18:24474323-24474324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566226619	chr18:24474366-24474367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533773470	chr18:24474386-24474387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558309636	chr18:24474418-24474419	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570437197	chr18:24474438-24474439	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs538110116	chr18:24474451-24474452	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs190666486	chr18:24474469-24474470	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs182898979	chr18:24474499-24474500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs574730852	chr18:24474513-24474514	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs113207299	chr18:24474558-24474559	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs377040281	chr18:24474578-24474579	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs78525312	chr18:24474606-24474607	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554350580	chr18:24474632-24474633	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs572552587	chr18:24474636-24474637	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs546444141	chr18:24474679-24474680	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs9962406	chr18:24474680-24474681	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs564640708	chr18:24474701-24474702	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs185776135	chr18:24474706-24474707	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs544052130	chr18:24474711-24474712	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs190159890	chr18:24474828-24474829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529740611	chr18:24474973-24474974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547867506	chr18:24475014-24475015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559843621	chr18:24475082-24475083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72883992	chr18:24475181-24475182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577424285	chr18:24475210-24475211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544891259	chr18:24475223-24475224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556476077	chr18:24475227-24475228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575014942	chr18:24475229-24475230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568258809	chr18:24475250-24475251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7241492	chr18:24475251-24475252	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs557866349	chr18:24475260-24475261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182418483	chr18:24475263-24475264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147907731	chr18:24475296-24475297	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Esophageal squamous carcinoma	18350619	CNVD
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
Glioblastoma multiforme	21922591	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
Lung cancer	18438408	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
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
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	19651600	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24473800-24474000	Enhancers	H9 Cell Line	embryonic stem cell
2	chr18:24473800-24474200	Active TSS	Skeletal Muscle Female	skeletal muscle
3	chr18:24473800-24474600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr18:24473800-24474800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:24473800-24475400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr18:24473800-24475600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr18:24473800-24475600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr18:24473800-24476000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr18:24474000-24474400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr18:24474000-24474800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr18:24474000-24475600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr18:24474200-24475200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr18:24474400-24474800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr18:24474400-24475600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr18:24474600-24474800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr18:24474600-24475400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr18:24474800-24475200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr18:24474800-24476000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr18:24475200-24475600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr18:24475200-24475600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr18:24475400-24475600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr18:24476000-24483000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr18:24479200-24479600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr18:24479200-24479600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr18:24479600-24480800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr18:24481000-24481200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr18:24483200-24483400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
28	chr18:24484000-24484400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr18:24486200-24486400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr18:24486400-24488600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr18:24488000-24488200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr18:24488200-24492600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr18:24488400-24489600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr18:24488400-24501200	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr18:24488600-24490600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr18:24489000-24490400	Enhancers	Stomach Smooth Muscle	stomach
37	chr18:24489200-24490600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr18:24489400-24491200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr18:24489600-24489800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr18:24489600-24490000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr18:24489600-24490200	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr18:24489600-24491200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr18:24489600-24492000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr18:24489800-24490000	Enhancers	Brain Anterior Caudate	brain
45	chr18:24489800-24490200	Enhancers	Ovary	ovary
46	chr18:24489800-24490400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr18:24489800-24490400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr18:24489800-24490400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr18:24489800-24490400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr18:24489800-24490600	Enhancers	H9 Cell Line	embryonic stem cell

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