Variant report

Variant	esv34611
Chromosome Location	chr18:6741970-6838290
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	chr18:6835362-6835608	HepG2	liver:	n/a	n/a
2	ATF1	chr18:6836325-6836793	K562	blood:	n/a	n/a
3	ATF1	chr18:6767665-6767865	K562	blood:	n/a	n/a
4	ATF2	chr18:6752312-6752936	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr18:6752364-6752981	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr18:6836359-6836675	K562	blood:	n/a	n/a
7	BACH1	chr18:6746406-6746521	K562	blood:	n/a	n/a
8	BCL11A	chr18:6752560-6752887	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr18:6752509-6752888	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr18:6781274-6781391	K562	blood:	n/a	n/a
11	BHLHE40	chr18:6836478-6836689	K562	blood:	n/a	n/a
12	BHLHE40	chr18:6745702-6745827	K562	blood:	n/a	n/a
13	CEBPB	chr18:6752226-6752903	H1-hESC	embryonic stem cell:	n/a	chr18:6752407-6752420 chr18:6752407-6752418
14	CEBPB	chr18:6752300-6752561	HepG2	liver:	n/a	chr18:6752407-6752420 chr18:6752407-6752418
15	CEBPB	chr18:6837950-6838252	K562	blood:	n/a	chr18:6838112-6838123 chr18:6838082-6838095 chr18:6838084-6838093 chr18:6838084-6838093 chr18:6838082-6838095 chr18:6838084-6838095 chr18:6838084-6838093 chr18:6838082-6838093 chr18:6838084-6838093
16	CEBPB	chr18:6835386-6835693	Hela-S3	cervix:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
17	CEBPB	chr18:6835416-6835634	A549	lung:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
18	CEBPB	chr18:6785541-6785707	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr18:6837948-6838264	HepG2	liver:	n/a	chr18:6838112-6838123 chr18:6838082-6838095 chr18:6838084-6838093 chr18:6838084-6838093 chr18:6838082-6838095 chr18:6838084-6838095 chr18:6838084-6838093 chr18:6838082-6838093 chr18:6838084-6838093
20	CEBPB	chr18:6835350-6835719	HepG2	liver:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
21	CEBPB	chr18:6837936-6838263	IMR90	lung:	n/a	chr18:6838112-6838123 chr18:6838082-6838095 chr18:6838084-6838093 chr18:6838084-6838093 chr18:6838082-6838095 chr18:6838084-6838095 chr18:6838084-6838093 chr18:6838082-6838093 chr18:6838084-6838093
22	CEBPB	chr18:6821409-6821614	HepG2	liver:	n/a	n/a
23	CEBPB	chr18:6798225-6798259	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr18:6752287-6752514	Hela-S3	cervix:	n/a	chr18:6752407-6752420 chr18:6752407-6752418
25	CEBPB	chr18:6830942-6831227	IMR90	lung:	n/a	n/a
26	CEBPB	chr18:6752226-6752836	IMR90	lung:	n/a	chr18:6752407-6752420 chr18:6752407-6752418
27	CEBPB	chr18:6835343-6835732	IMR90	lung:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
28	CEBPB	chr18:6752271-6752584	K562	blood:	n/a	chr18:6752407-6752420 chr18:6752407-6752418
29	CEBPB	chr18:6758765-6758954	HepG2	liver:	n/a	n/a
30	CEBPB	chr18:6831031-6831149	K562	blood:	n/a	n/a
31	CEBPB	chr18:6821359-6821719	IMR90	lung:	n/a	n/a
32	CEBPB	chr18:6835398-6835674	K562	blood:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
33	CEBPB	chr18:6836363-6836585	K562	blood:	n/a	n/a
34	CEBPB	chr18:6798199-6798398	K562	blood:	n/a	n/a
35	CEBPB	chr18:6837943-6838254	A549	lung:	n/a	chr18:6838112-6838123 chr18:6838082-6838095 chr18:6838084-6838093 chr18:6838084-6838093 chr18:6838082-6838095 chr18:6838084-6838095 chr18:6838084-6838093 chr18:6838082-6838093 chr18:6838084-6838093
36	CHD2	chr18:6752499-6752981	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr18:6752393-6753027	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTBP2	chr18:6752502-6752876	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr18:6762491-6762520	Lung_OC	lung:	n/a	n/a
40	CTCF	chr18:6778633-6778818	K562	blood:	n/a	n/a
41	CTCF	chr18:6770032-6770120	LNCaP	prostate:	n/a	chr18:6770064-6770085
42	CTCF	chr18:6776194-6776416	IMR90	lung:	n/a	n/a
43	CTCF	chr18:6778640-6778790	HEK293	kidney:	n/a	n/a
44	CTCF	chr18:6770032-6770059	LNCaP	prostate:	n/a	n/a
45	CTCF	chr18:6817037-6817132	GM10248	blood:	n/a	n/a
46	CTCF	chr18:6776220-6776370	HPF	lung:	n/a	n/a
47	CTCF	chr18:6817025-6817135	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr18:6750328-6750385	Lung_OC	lung:	n/a	n/a
49	CTCF	chr18:6778697-6778756	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr18:6836241-6836305	Fibrobl	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:6835382-6835432	SAEC	small airway:	n/a
2	chr18:6835382-6835432	GM19239	blood:	n/a
3	chr18:6834653-6834703	ProgFib	skin:	n/a
4	chr18:6834653-6834703	NHBE	bronchial:	n/a
5	chr18:6833417-6833467	MCF-7	breast:	n/a
6	chr18:6835382-6835432	BJ	skin:	n/a
7	chr18:6834653-6834703	HCPEpiC	choroid plexus:	n/a
8	chr18:6834653-6834703	H1-hESC	embryonic stem cell:	embryo
9	chr18:6835382-6835432	HEEpiC	esophagus:	n/a
10	chr18:6835382-6835432	HCT-116	colon:	n/a
11	chr18:6835382-6835432	HAEpiC	amniotic membrane:	n/a
12	chr18:6833417-6833467	AG09319	gingival:	n/a
13	chr18:6833417-6833467	PANC-1	pancreas:	n/a
14	chr18:6834653-6834703	SK-N-MC	brain:	n/a
15	chr18:6834653-6834703	PFSK-1	brain:	n/a
16	chr18:6835382-6835432	NT2-D1	testis:	n/a
17	chr18:6833417-6833467	HCF	heart:	n/a
18	chr18:6834653-6834703	GM12878	blood:	n/a
19	chr18:6834653-6834703	AG10803	skin:	n/a
20	chr18:6834653-6834703	HCT-116	colon:	n/a
21	chr18:6835382-6835432	ovcar-3	ovarian:	n/a
22	chr18:6833417-6833467	HUVEC	blood vessel:	n/a
23	chr18:6834653-6834703	NT2-D1	testis:	n/a
24	chr18:6833417-6833467	HL-60	blood:	n/a
25	chr18:6833417-6833467	AG04449	skin:	fetal
26	chr18:6834653-6834703	ovcar-3	ovarian:	n/a
27	chr18:6833417-6833467	HCM	heart:	n/a
28	chr18:6834653-6834703	GM12891	blood:	n/a
29	chr18:6833417-6833467	HepG2	liver:	n/a
30	chr18:6833417-6833467	HMEC	breast:	n/a
31	chr18:6833417-6833467	IMR90	lung:	fetal
32	chr18:6833417-6833467	Hepatocyte	liver:	n/a
33	chr18:6833417-6833467	PrEC	prostate:	n/a
34	chr18:6835382-6835432	HCPEpiC	choroid plexus:	n/a
35	chr18:6835382-6835432	CMK	blood:	n/a
36	chr18:6834653-6834703	CMK	blood:	n/a
37	chr18:6833417-6833467	HNPCEpiC	eye:	n/a
38	chr18:6834653-6834703	AoSMC	blood vessel:	n/a
39	chr18:6833417-6833467	SK-N-MC	brain:	n/a
40	chr18:6835382-6835432	MCF10A-Er-Src	breast:	n/a
41	chr18:6835382-6835432	HEK293	kidney:	embryo
42	chr18:6833417-6833467	HAEpiC	amniotic membrane:	n/a
43	chr18:6834653-6834703	Hela-S3	cervix:	n/a
44	chr18:6835382-6835432	GM12891	blood:	n/a
45	chr18:6833417-6833467	MCF10A-Er-Src	breast:	n/a
46	chr18:6835382-6835432	AoSMC	blood vessel:	n/a
47	chr18:6834653-6834703	SK-N-SH_RA	brain:	n/a
48	chr18:6835382-6835432	Caco-2	colon:	n/a
49	chr18:6834653-6834703	HCM	heart:	n/a
50	chr18:6835382-6835432	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr18:6743142..6745780-chr18:6746474..6749078,2	K562	blood:
2	chr18:6743142..6744914-chr18:6746474..6748281,2	K562	blood:
3	chr18:6685911..6687499-chr18:6763330..6765130,2	K562	blood:
4	chr18:6743142..6744914-chr18:6746474..6748281,2	K562	blood:
5	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:
6	chr18:6731530..6734164-chr18:6740298..6742070,2	K562	blood:
7	chr18:6742579..6744550-chr18:6848151..6850631,2	K562	blood:
8	chr18:6743142..6745780-chr18:6746474..6749078,2	K562	blood:
9	chr18:6770718..6772411-chr18:6775406..6777040,2	K562	blood:
10	chr18:6770718..6772411-chr18:6775406..6777040,2	K562	blood:
11	chr18:6780742..6782495-chr18:6812998..6814877,2	K562	blood:
12	chr18:6780742..6782495-chr18:6812998..6814877,2	K562	blood:
13	chr18:6834903..6836491-chr18:6842166..6845111,2	K562	blood:
14	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC30-3	chr18:6778921-6779022	XLOC_012619
2	lnc-LRRC30-3	chr18:6774030-6774233	XLOC_012619

Variant related genes	Relation type
ARHGAP28	TF binding region
ARHGAP28	CpG island

Extended variants
information (count: 3548 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3548 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7505383	chr18:6741974-6741975	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138589097	chr18:6741975-6741976	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs562538906	chr18:6742011-6742012	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs531410650	chr18:6742062-6742063	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs541593414	chr18:6742081-6742082	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs184817600	chr18:6742098-6742099	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs57136505	chr18:6742115-6742116	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs533931241	chr18:6742148-6742149	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs200431199	chr18:6742162-6742163	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs554288921	chr18:6742168-6742169	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs370307970	chr18:6742169-6742170	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs77506881	chr18:6742182-6742183	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs559467508	chr18:6742249-6742250	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547227268	chr18:6742256-6742257	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566835883	chr18:6742275-6742276	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189634221	chr18:6742306-6742307	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552175820	chr18:6742317-6742318	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568939151	chr18:6742336-6742337	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372932468	chr18:6742344-6742345	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7506085	chr18:6742357-6742358	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554806506	chr18:6742376-6742377	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370336120	chr18:6742385-6742386	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143623823	chr18:6742399-6742400	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533755012	chr18:6742420-6742421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79235672	chr18:6742449-6742450	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72882571	chr18:6742459-6742460	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs568403078	chr18:6742464-6742465	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546145270	chr18:6742465-6742466	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138210708	chr18:6742515-6742516	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576146109	chr18:6742554-6742555	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116473869	chr18:6742555-6742556	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs71360047	chr18:6742574-6742575	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530276115	chr18:6742608-6742609	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540488332	chr18:6742611-6742612	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560386174	chr18:6742660-6742661	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75413529	chr18:6742689-6742690	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377396109	chr18:6742690-6742691	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113945223	chr18:6742761-6742762	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4365369	chr18:6742845-6742846	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181558392	chr18:6742850-6742851	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs539484371	chr18:6742896-6742897	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs11873962	chr18:6742958-6742959	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs142791700	chr18:6742960-6742961	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs568477596	chr18:6742978-6742979	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs117071390	chr18:6743011-6743012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4586535	chr18:6743016-6743017	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs570690576	chr18:6743045-6743046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370932858	chr18:6743046-6743047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369742403	chr18:6743091-6743092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534920611	chr18:6743136-6743137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
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
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
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	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
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Breast cancer	17133270	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:6730200-6747800	Weak transcription	Left Ventricle	heart
2	chr18:6731800-6743800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr18:6735000-6743800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr18:6736000-6745600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr18:6736000-6761400	Weak transcription	Spleen	Spleen
6	chr18:6738800-6743000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr18:6739200-6747600	Weak transcription	Fetal Heart	heart
8	chr18:6740000-6743000	Enhancers	NHDF-Ad	bronchial
9	chr18:6740200-6742200	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr18:6740200-6742600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr18:6740200-6742600	Enhancers	NHLF	lung
12	chr18:6740200-6742800	Enhancers	HUVEC	blood vessel
13	chr18:6740200-6743200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr18:6740200-6743200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr18:6740200-6743400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr18:6740400-6742200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr18:6740600-6742000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr18:6740600-6742200	Enhancers	Fetal Stomach	stomach
19	chr18:6740600-6742200	Enhancers	HMEC	breast
20	chr18:6740800-6742000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr18:6740800-6742000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr18:6740800-6742000	Enhancers	Colon Smooth Muscle	Colon
23	chr18:6740800-6742200	Enhancers	Hela-S3	cervix
24	chr18:6740800-6743000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr18:6740800-6744400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr18:6741000-6742200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr18:6741000-6742200	Weak transcription	Ovary	ovary
28	chr18:6741000-6743000	Enhancers	Fetal Muscle Leg	muscle
29	chr18:6741000-6743000	Enhancers	HSMM	muscle
30	chr18:6741000-6747200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr18:6741000-6751200	Weak transcription	Placenta	Placenta
32	chr18:6741200-6742400	Enhancers	Osteobl	bone
33	chr18:6741200-6751600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr18:6741400-6742600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr18:6741400-6743400	Enhancers	HSMMtube	muscle
36	chr18:6741400-6746600	Weak transcription	Fetal Brain Male	brain
37	chr18:6741400-6747800	Weak transcription	Right Atrium	heart
38	chr18:6741600-6742000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr18:6741600-6742000	Enhancers	Fetal Lung	lung
40	chr18:6741600-6742000	Weak transcription	Psoas Muscle	Psoas
41	chr18:6741600-6742200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr18:6741600-6742200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr18:6741600-6742200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr18:6741600-6744200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr18:6741600-6751400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr18:6741600-6751800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr18:6741600-6761400	Weak transcription	Pancreas	Pancrea
48	chr18:6741800-6742200	Flanking Active TSS	NH-A	brain
49	chr18:6741800-6745200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr18:6741800-6747200	Weak transcription	Fetal Kidney	kidney

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