Variant report

Variant	nsv569206
Chromosome Location	chr15:39048231-39098349
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	CEBPB	chr15:39088804-39089137	H1-hESC	embryonic stem cell:	n/a	chr15:39088888-39088899
2	CEBPB	chr15:39073448-39073762	HepG2	liver:	n/a	chr15:39073591-39073600 chr15:39073589-39073600 chr15:39073590-39073601 chr15:39073591-39073600 chr15:39073591-39073600 chr15:39073591-39073600
3	CEBPB	chr15:39088842-39089069	A549	lung:	n/a	chr15:39088888-39088899
4	CEBPB	chr15:39073412-39073783	IMR90	lung:	n/a	chr15:39073591-39073600 chr15:39073589-39073600 chr15:39073590-39073601 chr15:39073591-39073600 chr15:39073591-39073600 chr15:39073591-39073600
5	CEBPB	chr15:39073554-39073631	Hela-S3	cervix:	n/a	chr15:39073591-39073600 chr15:39073589-39073600 chr15:39073590-39073601 chr15:39073591-39073600 chr15:39073591-39073600 chr15:39073591-39073600
6	CEBPB	chr15:39073539-39073709	K562	blood:	n/a	chr15:39073591-39073600 chr15:39073589-39073600 chr15:39073590-39073601 chr15:39073591-39073600 chr15:39073591-39073600 chr15:39073591-39073600
7	CEBPB	chr15:39088848-39089038	HepG2	liver:	n/a	chr15:39088888-39088899
8	CEBPB	chr15:39073446-39073728	A549	lung:	n/a	chr15:39073591-39073600 chr15:39073589-39073600 chr15:39073590-39073601 chr15:39073591-39073600 chr15:39073591-39073600 chr15:39073591-39073600
9	CTCF	chr15:39061308-39061424	GM19238	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
10	CTCF	chr15:39061258-39061451	K562	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
11	CTCF	chr15:39088920-39089070	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr15:39061240-39061390	HEEpiC	esophagus:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
13	CTCF	chr15:39061240-39061390	HEK293	kidney:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
14	CTCF	chr15:39061277-39061446	H1-hESC	embryonic stem cell:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
15	CTCF	chr15:39061240-39061390	GM12875	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
16	CTCF	chr15:39061340-39061490	SAEC	small airway:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
17	CTCF	chr15:39061285-39061392	SK-N-SH_RA	brain:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
18	CTCF	chr15:39061220-39061370	Caco-2	colon:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
19	CTCF	chr15:39061280-39061430	NHLF	lung:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
20	CTCF	chr15:39061273-39061449	NHEK	skin:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
21	CTCF	chr15:39061289-39061434	GM12892	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
22	CTCF	chr15:39061360-39061510	HVMF	connective:	n/a	n/a
23	CTCF	chr15:39061120-39061390	A549	lung:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
24	CTCF	chr15:39061240-39061390	GM12865	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
25	CTCF	chr15:39061300-39061450	NB4	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
26	CTCF	chr15:39061300-39061450	HBMEC	blood vessel:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
27	CTCF	chr15:39061163-39061579	IMR90	lung:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
28	CTCF	chr15:39074976-39075063	Lung_OC	lung:	n/a	n/a
29	CTCF	chr15:39061240-39061390	Caco-2	colon:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
30	CTCF	chr15:39061279-39061434	GM12878	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
31	CTCF	chr15:39061220-39061370	GM12869	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
32	CTCF	chr15:39061310-39061406	GM19239	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
33	CTCF	chr15:39061248-39061460	Gliobla	brain:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
34	CTCF	chr15:39061280-39061430	NHEK	skin:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
35	CTCF	chr15:39061280-39061430	HCPEpiC	choroid plexus:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
36	CTCF	chr15:39061260-39061410	RPTEC	kidney:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
37	CTCF	chr15:39061260-39061410	AoAF	blood vessel:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
38	CTCF	chr15:39088920-39089070	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr15:39061260-39061410	BE2_C	brain:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
40	CTCF	chr15:39061320-39061470	NHDF-neo	bronchial:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
41	CTCF	chr15:39061240-39061390	HFF	foreskin:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
42	CTCF	chr15:39061279-39061450	MCF-7	breast:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
43	CTCF	chr15:39061280-39061430	AG09319	gingival:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
44	CTCF	chr15:39061260-39061410	AG10803	skin:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
45	CTCF	chr15:39061232-39061426	HepG2	liver:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
46	CTCF	chr15:39088845-39089106	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr15:39061280-39061430	AoAF	blood vessel:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
48	CTCF	chr15:39061300-39061450	NHDF-neo	bronchial:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
49	CTCF	chr15:39061227-39061475	MCF-7	breast:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369
50	CTCF	chr15:39061280-39061430	K562	blood:	n/a	chr15:39061349-39061362 chr15:39061346-39061364 chr15:39061348-39061369

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:39050013-39050063	H1-hESC	embryonic stem cell:	embryo
2	chr15:39050013-39050063	HCM	heart:	n/a
3	chr15:39050013-39050063	GM06990	blood:	n/a
4	chr15:39050013-39050063	T-47D	breast:	n/a
5	chr15:39050013-39050063	Jurkat	blood:	n/a
6	chr15:39050013-39050063	HMEC	breast:	n/a
7	chr15:39050013-39050063	ECC-1	luminal epithelium:	n/a
8	chr15:39050013-39050063	AoSMC	blood vessel:	n/a
9	chr15:39050013-39050063	HL-60	blood:	n/a
10	chr15:39050013-39050063	MCF10A-Er-Src	breast:	n/a
11	chr15:39050013-39050063	GM12892	blood:	n/a
12	chr15:39050013-39050063	PANC-1	pancreas:	n/a
13	chr15:39050013-39050063	HRE	kidney:	n/a
14	chr15:39050013-39050063	AG10803	skin:	n/a
15	chr15:39050013-39050063	PFSK-1	brain:	n/a
16	chr15:39050013-39050063	MCF-7	breast:	n/a
17	chr15:39050013-39050063	HCT-116	colon:	n/a
18	chr15:39050013-39050063	HEEpiC	esophagus:	n/a
19	chr15:39050013-39050063	AG09309	skin:	n/a
20	chr15:39050013-39050063	SK-N-SH_RA	brain:	n/a
21	chr15:39050013-39050063	HCPEpiC	choroid plexus:	n/a
22	chr15:39050013-39050063	Hepatocyte	liver:	n/a
23	chr15:39050013-39050063	GM19239	blood:	n/a
24	chr15:39050013-39050063	K562	blood:	n/a
25	chr15:39050013-39050063	AG04449	skin:	fetal
26	chr15:39050013-39050063	SKMC	muscle:	n/a
27	chr15:39050013-39050063	NB4	blood:	n/a
28	chr15:39050013-39050063	HEK293	kidney:	embryo
29	chr15:39050013-39050063	SAEC	small airway:	n/a
30	chr15:39050013-39050063	GM12878	blood:	n/a
31	chr15:39050013-39050063	ovcar-3	ovarian:	n/a
32	chr15:39050013-39050063	HepG2	liver:	n/a
33	chr15:39050013-39050063	LNCaP	prostate:	n/a
34	chr15:39050013-39050063	SK-N-MC	brain:	n/a
35	chr15:39050013-39050063	HUVEC	blood vessel:	n/a
36	chr15:39050013-39050063	A549	lung:	n/a
37	chr15:39050013-39050063	AG09319	gingival:	n/a
38	chr15:39050013-39050063	BE2_C	brain:	n/a
39	chr15:39050013-39050063	U87	brain:	n/a
40	chr15:39050013-39050063	BJ	skin:	n/a
41	chr15:39050013-39050063	SK-N-SH	brain:	n/a
42	chr15:39050013-39050063	Caco-2	colon:	n/a
43	chr15:39050013-39050063	HRCEpiC	kidney:	n/a
44	chr15:39050013-39050063	HNPCEpiC	eye:	n/a
45	chr15:39050013-39050063	PrEC	prostate:	n/a
46	chr15:39050013-39050063	RPTEC	kidney:	n/a
47	chr15:39050013-39050063	Hela-S3	cervix:	n/a
48	chr15:39050013-39050063	IMR90	lung:	fetal
49	chr15:39050013-39050063	ProgFib	skin:	n/a
50	chr15:39050013-39050063	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:39085713..39088566-chr15:39372910..39375619,2	MCF-7	breast:
2	chr15:39060876..39061871-chr15:39109578..39110390,2	MCF-7	breast:
3	chr1:76081387..76081887-chr15:39080643..39081147,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP1-2	chr15:39049095-39049147	ENSG00000259731.1
2	lnc-RASGRP1-2	chr15:39051237-39051614	ENSG00000259731.1
3	lnc-RASGRP1-1	chr15:39048612-39048732	XLOC_011433
4	lnc-RASGRP1-1	chr15:39049397-39049710	XLOC_011433
5	lnc-RASGRP1-2	chr15:39050963-39051141	ENSG00000259731.1
6	lnc-RASGRP1-1	chr15:39048612-39048732	XLOC_011433
7	lnc-C15orf53-3	chr15:39080325-39080381	NONHSAT041722
8	lnc-RASGRP1-1	chr15:39049397-39049571	XLOC_011433
9	lnc-RASGRP1-2	chr15:39048755-39048965	ENSG00000259731.1
10	lnc-C15orf53-3	chr15:39073218-39073381	NONHSAT041722

Variant related genes	Relation type
ENSG00000259731	TF binding region
ENSG00000259731	CpG island
LRRC8C	miRNA target sites
LRRFIP1	miRNA target sites

Extended variants
information (count: 819 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4461048	chr15:39048231-39048232	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77253678	chr15:39048274-39048275	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538537510	chr15:39048311-39048312	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2912371	chr15:39048325-39048326	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115210350	chr15:39048336-39048337	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543747666	chr15:39048365-39048366	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367838915	chr15:39048368-39048369	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371623961	chr15:39048380-39048381	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs8033016	chr15:39048381-39048382	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs8038263	chr15:39048396-39048397	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537100023	chr15:39048428-39048429	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs59320522	chr15:39048498-39048499	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149825643	chr15:39048507-39048508	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61415249	chr15:39048518-39048519	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2958268	chr15:39048533-39048534	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs576228323	chr15:39048541-39048542	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs8037289	chr15:39048558-39048559	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74318753	chr15:39048567-39048568	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61557749	chr15:39048606-39048607	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs573529145	chr15:39048638-39048639	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs529827906	chr15:39048642-39048643	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs144770856	chr15:39048652-39048653	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs187647295	chr15:39048653-39048654	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs551045179	chr15:39048659-39048660	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs563320744	chr15:39048660-39048661	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs547833129	chr15:39048662-39048663	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs139767181	chr15:39048692-39048693	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs144538960	chr15:39048719-39048720	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs140647541	chr15:39048737-39048738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568664948	chr15:39048747-39048748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs397811895	chr15:39048749-39048750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35732613	chr15:39048750-39048751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140843995	chr15:39048792-39048793	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs193090427	chr15:39048798-39048799	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs565993112	chr15:39048800-39048801	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs28527363	chr15:39048907-39048908	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs80084958	chr15:39048913-39048914	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs550632686	chr15:39048914-39048915	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs184154788	chr15:39048918-39048919	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs374172835	chr15:39048950-39048951	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs187557000	chr15:39049005-39049006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552871236	chr15:39049086-39049087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs202128740	chr15:39049090-39049091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs397817180	chr15:39049092-39049093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540787357	chr15:39049098-39049099	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs552754767	chr15:39049118-39049119	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs527941543	chr15:39049137-39049138	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs2929654	chr15:39049241-39049242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563124867	chr15:39049278-39049279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371743460	chr15:39049304-39049305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39046400-39049400	Weak transcription	Fetal Kidney	kidney
2	chr15:39047200-39048600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr15:39047600-39052400	Enhancers	HUVEC	blood vessel
4	chr15:39048000-39048600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr15:39048000-39048600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr15:39048000-39048600	Enhancers	Fetal Muscle Leg	muscle
7	chr15:39048200-39048400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:39048200-39049000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:39048200-39052600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr15:39048400-39052800	Enhancers	Osteobl	bone
11	chr15:39048600-39050400	Weak transcription	Fetal Muscle Leg	muscle
12	chr15:39049000-39050400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:39049400-39050000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr15:39049400-39051800	Enhancers	Fetal Kidney	kidney
15	chr15:39049600-39051000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr15:39049600-39051000	Enhancers	NHDF-Ad	bronchial
17	chr15:39049600-39052800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr15:39049800-39050600	Enhancers	NHLF	lung
19	chr15:39049800-39050800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr15:39049800-39050800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:39049800-39050800	Enhancers	Hela-S3	cervix
22	chr15:39049800-39050800	Enhancers	HSMMtube	muscle
23	chr15:39049800-39051000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr15:39049800-39051000	Enhancers	NH-A	brain
25	chr15:39050000-39050200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
26	chr15:39050000-39050600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:39050000-39050800	Enhancers	Fetal Heart	heart
28	chr15:39050000-39050800	Enhancers	A549	lung
29	chr15:39050000-39051000	Enhancers	HSMM	muscle
30	chr15:39050200-39050400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr15:39050200-39050400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr15:39050200-39050800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:39050400-39050600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr15:39050400-39050600	Enhancers	Right Ventricle	heart
35	chr15:39050400-39050800	Enhancers	Fetal Muscle Leg	muscle
36	chr15:39050400-39051000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:39050600-39051200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr15:39051000-39051600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr15:39051000-39052200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr15:39051600-39051800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr15:39051800-39052600	Weak transcription	Fetal Kidney	kidney
42	chr15:39052200-39052400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:39052600-39052800	Enhancers	Fetal Kidney	kidney
44	chr15:39054400-39054800	Enhancers	Fetal Brain Male	brain
45	chr15:39061000-39062000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr15:39061200-39061800	Enhancers	Fetal Stomach	stomach
47	chr15:39061200-39061800	Enhancers	Osteobl	bone
48	chr15:39061200-39062000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr15:39061400-39061800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr15:39061400-39061800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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