Variant report

Variant	nsv960221
Chromosome Location	chr18:14948300-14977956
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	ATF1	chr18:14971054-14971139	K562	blood:	n/a	n/a
2	CEBPB	chr18:14974278-14974509	HepG2	liver:	n/a	chr18:14974416-14974427 chr18:14974350-14974361
3	CTCF	chr18:14977840-14977990	HEK293	kidney:	n/a	n/a
4	CTCF	chr18:14976839-14976972	SK-N-SH_RA	brain:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
5	CTCF	chr18:14976853-14977028	ProgFib	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
6	CTCF	chr18:14963406-14963543	MCF-7	breast:	n/a	n/a
7	CTCF	chr18:14976843-14977018	HUVEC	blood vessel:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
8	CTCF	chr18:14976820-14976970	HCFaa	heart:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
9	CTCF	chr18:14976836-14977036	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
10	CTCF	chr18:14976740-14976890	NHLF	lung:	n/a	n/a
11	CTCF	chr18:14976820-14976970	HAc	cerebellar:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
12	CTCF	chr18:14976795-14977091	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
13	CTCF	chr18:14976860-14977010	AG09309	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
14	CTCF	chr18:14976817-14977041	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
15	CTCF	chr18:14968815-14968817	GM10266	blood:	n/a	n/a
16	CTCF	chr18:14976840-14976990	HRE	kidney:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
17	CTCF	chr18:14976860-14977010	NB4	blood:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
18	CTCF	chr18:14976840-14976990	AG04449	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
19	CTCF	chr18:14976897-14976964	GM12891	blood:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
20	CTCF	chr18:14976870-14976976	Fibrobl	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
21	CTCF	chr18:14976860-14977010	RPTEC	kidney:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
22	CTCF	chr18:14976860-14977010	HA-sp	spinal cord:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
23	CTCF	chr18:14963426-14963535	MCF-7	breast:	n/a	n/a
24	CTCF	chr18:14976840-14976990	HEK293	kidney:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
25	CTCF	chr18:14965760-14965910	GM12871	blood:	n/a	n/a
26	CTCF	chr18:14976890-14976981	HepG2	liver:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
27	CTCF	chr18:14976820-14976970	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
28	CTCF	chr18:14976800-14976950	HMEC	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
29	CTCF	chr18:14976820-14976970	AG10803	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
30	CTCF	chr18:14963416-14963540	MCF-7	breast:	n/a	n/a
31	CTCF	chr18:14976840-14976990	RPTEC	kidney:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
32	CTCF	chr18:14976811-14977049	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
33	CTCF	chr18:14976795-14977060	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
34	CTCF	chr18:14976820-14976970	SAEC	small airway:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
35	CTCF	chr18:14976833-14977054	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
36	CTCF	chr18:14976820-14976970	AoAF	blood vessel:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
37	CTCF	chr18:14976840-14976990	HBMEC	blood vessel:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
38	CTCF	chr18:14976800-14976950	SAEC	small airway:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
39	CTCF	chr18:14976820-14976970	HUVEC	blood vessel:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
40	CTCF	chr18:14976831-14977042	Gliobla	brain:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
41	CTCF	chr18:14976820-14976970	HepG2	liver:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
42	CTCF	chr18:14976820-14976970	SK-N-SH_RA	brain:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
43	CTCF	chr18:14976820-14976970	HRE	kidney:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
44	CTCF	chr18:14976893-14976967	Hela-S3	cervix:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
45	CTCF	chr18:14976843-14977021	H1-hESC	embryonic stem cell:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
46	CTCF	chr18:14976848-14977015	K562	blood:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
47	CTCF	chr18:14976820-14976970	AG04449	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
48	CTCF	chr18:14976819-14977049	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
49	CTCF	chr18:14976880-14977030	HMEC	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
50	CTCF	chr18:14976820-14976970	HBMEC	blood vessel:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938

No.	Distal block	Cell Line	Cell type
1	chr18:14955184..14958029-chr18:14978854..14981375,2	MCF-7	breast:
2	chr18:14952155..14952955-chr7:115149293..115150054,2	MCF-7	breast:
3	chr18:14970038..14971592-chr18:14972164..14974948,2	MCF-7	breast:
4	chr18:14944732..14947248-chr18:14957647..14959908,2	MCF-7	breast:
5	chr18:14940976..14942480-chr18:14946479..14948653,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD30B-4	chr18:14972355-14973738	ENSG00000266554.1
2	lnc-POTEC-3	chr18:14969877-14970467	ENSG00000264301.1
3	lnc-ANKRD30B-4	chr18:14971496-14971885	ENSG00000266554.1
4	lnc-ANKRD30B-4	chr18:14972377-14973769	ENSG00000266554.1
5	lnc-POTEC-3	chr18:14969000-14969571	ENSG00000264301.1
6	lnc-POTEC-3	chr18:14969675-14969756	ENSG00000264301.1
7	lnc-ANKRD30B-4	chr18:14965616-14965809	ENSG00000266554.1
8	lnc-POTEC-3	chr18:14969605-14969777	ENSG00000264301.1
9	lnc-ANKRD30B-4	chr18:14972355-14973755	NR_104164
10	lnc-ANKRD30B-4	chr18:14962069-14962282	ENSG00000266554.1
11	lnc-ANKRD30B-4	chr18:14962069-14962282	NR_104164
12	lnc-ANKRD30B-4	chr18:14965616-14965809	NR_104164

Variant related genes	Relation type
ENSG00000264301	TF binding region
ENSG00000266554	TF binding region
ENSG00000263821	TF binding region
ENSG00000266554	chromatin interactions
ENSG00000264301	chromatin interactions

Extended variants
information (count: 1048 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1048 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544917265	chr18:14948454-14948455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556634449	chr18:14948474-14948475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181987802	chr18:14948502-14948503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140821740	chr18:14948571-14948572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12954059	chr18:14948622-14948623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145205906	chr18:14948641-14948642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112061863	chr18:14948714-14948715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569273524	chr18:14948726-14948727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538192070	chr18:14948731-14948732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140596291	chr18:14948779-14948780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571709214	chr18:14948844-14948845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574871265	chr18:14948878-14948879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374181635	chr18:14948879-14948880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569914494	chr18:14948985-14948986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs786045	chr18:14949001-14949002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs73961135	chr18:14949020-14949021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs386801517	chr18:14949025-14949026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs786044	chr18:14949027-14949028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376098506	chr18:14949037-14949038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186098602	chr18:14949041-14949042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140135957	chr18:14949088-14949089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368372174	chr18:14949089-14949090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543946194	chr18:14949164-14949165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149880219	chr18:14949171-14949172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535221198	chr18:14949240-14949241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553565049	chr18:14949310-14949311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199973516	chr18:14949311-14949312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532790559	chr18:14949330-14949331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372243603	chr18:14949339-14949340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375337195	chr18:14949346-14949347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540117822	chr18:14949366-14949367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560029877	chr18:14949403-14949404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571873666	chr18:14949427-14949428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529055439	chr18:14949428-14949429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539134398	chr18:14949438-14949439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190627280	chr18:14949446-14949447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140925529	chr18:14949499-14949500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557850207	chr18:14949521-14949522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551933679	chr18:14949533-14949534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183431967	chr18:14949563-14949564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534201506	chr18:14949575-14949576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs8093953	chr18:14949581-14949582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs567870456	chr18:14949673-14949674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs786043	chr18:14949675-14949676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs556473911	chr18:14949689-14949690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555243120	chr18:14949807-14949808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576626994	chr18:14949820-14949821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537523414	chr18:14949855-14949856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117502625	chr18:14949912-14949913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149001394	chr18:14949930-14949931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
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
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
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	17122850	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Schizophrenia	23813976	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14947200-14953200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr18:14950000-14950400	Enhancers	Spleen	Spleen
3	chr18:14953200-14953600	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr18:14957000-14961800	Weak transcription	Osteobl	bone
5	chr18:14961600-14962400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr18:14961800-14962400	Enhancers	Osteobl	bone
7	chr18:14961800-14963000	Enhancers	HUVEC	blood vessel
8	chr18:14962400-14967800	Weak transcription	Osteobl	bone
9	chr18:14962600-14962800	Active TSS	Spleen	Spleen
10	chr18:14962800-14963000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr18:14962800-14963000	Enhancers	Spleen	Spleen
12	chr18:14963000-14963200	Flanking Active TSS	Spleen	Spleen
13	chr18:14963200-14974000	Weak transcription	Spleen	Spleen
14	chr18:14963800-14964000	Enhancers	Gastric	stomach
15	chr18:14964000-14965800	Weak transcription	Gastric	stomach
16	chr18:14964400-14965200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr18:14965800-14966000	Enhancers	Gastric	stomach
18	chr18:14967800-14968600	Enhancers	Osteobl	bone
19	chr18:14968600-14970400	Flanking Active TSS	Osteobl	bone
20	chr18:14968600-14971000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr18:14969000-14969200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr18:14969200-14969600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr18:14969200-14972600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr18:14969400-14972600	Enhancers	NHDF-Ad	bronchial
25	chr18:14969600-14971000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr18:14969800-14970400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr18:14970000-14971200	Enhancers	HUVEC	blood vessel
28	chr18:14970000-14972800	Enhancers	HSMM	muscle
29	chr18:14970200-14972400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr18:14970200-14972600	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr18:14970400-14971000	Enhancers	Osteobl	bone
32	chr18:14970400-14974800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:14970600-14971200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr18:14970600-14972600	Enhancers	HMEC	breast
35	chr18:14970600-14972600	Enhancers	HSMMtube	muscle
36	chr18:14970800-14972200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr18:14971000-14971800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
38	chr18:14971000-14972200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr18:14971000-14972200	Flanking Active TSS	Osteobl	bone
40	chr18:14971200-14971400	Flanking Active TSS	HUVEC	blood vessel
41	chr18:14971200-14972200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr18:14971200-14972600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr18:14971400-14971800	Enhancers	HUVEC	blood vessel
44	chr18:14971800-14972200	Flanking Active TSS	HUVEC	blood vessel
45	chr18:14971800-14972600	Enhancers	Lung	lung
46	chr18:14971800-14977800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr18:14972000-14972400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr18:14972200-14972800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr18:14972200-14977400	Enhancers	HUVEC	blood vessel
50	chr18:14972200-14977800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links