Variant report

Variant	esv1842687
Chromosome Location	chr15:77307260-77332606
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1077)
CpG islands
(count:854)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77324454-77324600	HepG2	liver:	n/a	n/a
2	ATF2	chr15:77314226-77314800	GM12878	blood:	n/a	n/a
3	ATF2	chr15:77316619-77316962	GM12878	blood:	n/a	n/a
4	ATF2	chr15:77314306-77314560	GM12878	blood:	n/a	n/a
5	BACH1	chr15:77320425-77320611	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr15:77312280-77312501	GM12878	blood:	n/a	n/a
7	BCL3	chr15:77325651-77326184	A549	lung:	n/a	n/a
8	BCL3	chr15:77319696-77320041	GM12878	blood:	n/a	n/a
9	BCL3	chr15:77326777-77327284	A549	lung:	n/a	n/a
10	BCL3	chr15:77325266-77325980	A549	lung:	n/a	n/a
11	BCL3	chr15:77326463-77328028	A549	lung:	n/a	n/a
12	BCL3	chr15:77327427-77328043	A549	lung:	n/a	n/a
13	BCL3	chr15:77319746-77319961	GM12878	blood:	n/a	n/a
14	BCLAF1	chr15:77306496-77307260	GM12878	blood:	n/a	n/a
15	BHLHE40	chr15:77323768-77323927	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:77320463-77320709	K562	blood:	n/a	chr15:77320651-77320667
17	BHLHE40	chr15:77312372-77312424	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:77315646-77315869	K562	blood:	n/a	n/a
19	BHLHE40	chr15:77316652-77316796	K562	blood:	n/a	n/a
20	BHLHE40	chr15:77327273-77327720	K562	blood:	n/a	chr15:77327366-77327387 chr15:77327372-77327381 chr15:77327370-77327383 chr15:77327371-77327380 chr15:77327372-77327381
21	BHLHE40	chr15:77319308-77319431	K562	blood:	n/a	n/a
22	BHLHE40	chr15:77320006-77320083	K562	blood:	n/a	n/a
23	BHLHE40	chr15:77319232-77319473	HepG2	liver:	n/a	n/a
24	BRCA1	chr15:77316763-77316878	Hela-S3	cervix:	n/a	n/a
25	CCNT2	chr15:77320595-77320914	K562	blood:	n/a	n/a
26	CEBPB	chr15:77330718-77330925	Hela-S3	cervix:	n/a	chr15:77330791-77330804
27	CEBPB	chr15:77312536-77312661	K562	blood:	n/a	chr15:77312579-77312590
28	CEBPB	chr15:77324292-77324502	HepG2	liver:	n/a	n/a
29	CEBPB	chr15:77314436-77314701	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:77312427-77312735	HepG2	liver:	n/a	chr15:77312579-77312590
31	CEBPB	chr15:77316733-77316956	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:77312440-77312720	A549	lung:	n/a	chr15:77312579-77312590
33	CEBPD	chr15:77324291-77324757	HepG2	liver:	n/a	n/a
34	CHD1	chr15:77311660-77311805	GM12878	blood:	n/a	n/a
35	CHD2	chr15:77326498-77326592	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr15:77306140-77307358	GM12878	blood:	n/a	n/a
37	CHD2	chr15:77311888-77312640	GM12878	blood:	n/a	n/a
38	CHD2	chr15:77323767-77324050	GM12878	blood:	n/a	n/a
39	CHD2	chr15:77327544-77327607	HepG2	liver:	n/a	n/a
40	CHD2	chr15:77316658-77316664	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr15:77316743-77316928	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr15:77320794-77320880	K562	blood:	n/a	n/a
43	CHD2	chr15:77329799-77329867	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr15:77324707-77324888	HepG2	liver:	n/a	n/a
45	CHD2	chr15:77316800-77316802	HepG2	liver:	n/a	n/a
46	CHD2	chr15:77316213-77316223	HepG2	liver:	n/a	n/a
47	CHD2	chr15:77313388-77313599	GM12878	blood:	n/a	n/a
48	CHD2	chr15:77327460-77327662	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr15:77323823-77323943	HepG2	liver:	n/a	n/a
50	CHD2	chr15:77327435-77327673	Hela-S3	cervix:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77320261-77320311	GM19239	blood:	n/a
2	chr15:77324758-77324808	HRE	kidney:	n/a
3	chr15:77324758-77324808	NHDF-neo	bronchial:	n/a
4	chr15:77320211-77320261	Hela-S3	cervix:	n/a
5	chr15:77320384-77320434	AG04449	skin:	fetal
6	chr15:77320672-77320722	AoSMC	blood vessel:	n/a
7	chr15:77324526-77324576	SKMC	muscle:	n/a
8	chr15:77327887-77327937	GM12878	blood:	n/a
9	chr15:77323565-77323615	SK-N-MC	brain:	n/a
10	chr15:77326735-77326785	GM12891	blood:	n/a
11	chr15:77327887-77327937	MCF10A-Er-Src	breast:	n/a
12	chr15:77320384-77320434	ProgFib	skin:	n/a
13	chr15:77320261-77320311	GM12891	blood:	n/a
14	chr15:77320787-77320837	HRE	kidney:	n/a
15	chr15:77320261-77320311	BJ	skin:	n/a
16	chr15:77314406-77314456	HEEpiC	esophagus:	n/a
17	chr15:77314406-77314456	Hepatocyte	liver:	n/a
18	chr15:77320211-77320261	HUVEC	blood vessel:	n/a
19	chr15:77324607-77324657	AG04450	lung:	fetal
20	chr15:77324526-77324576	GM12892	blood:	n/a
21	chr15:77317370-77317420	HIPEpiC	eye:	n/a
22	chr15:77320384-77320434	AG10803	skin:	n/a
23	chr15:77320384-77320434	HMEC	breast:	n/a
24	chr15:77320672-77320722	GM06990	blood:	n/a
25	chr15:77317370-77317420	GM12878	blood:	n/a
26	chr15:77320787-77320837	HCPEpiC	choroid plexus:	n/a
27	chr15:77324607-77324657	K562	blood:	n/a
28	chr15:77326735-77326785	GM06990	blood:	n/a
29	chr15:77324607-77324657	HRCEpiC	kidney:	n/a
30	chr15:77314406-77314456	HCT-116	colon:	n/a
31	chr15:77314406-77314456	HL-60	blood:	n/a
32	chr15:77324526-77324576	HIPEpiC	eye:	n/a
33	chr15:77324607-77324657	NHBE	bronchial:	n/a
34	chr15:77317370-77317420	LNCaP	prostate:	n/a
35	chr15:77320384-77320434	PrEC	prostate:	n/a
36	chr15:77320261-77320311	HUVEC	blood vessel:	n/a
37	chr15:77320672-77320722	HUVEC	blood vessel:	n/a
38	chr15:77314406-77314456	PANC-1	pancreas:	n/a
39	chr15:77320261-77320311	NHDF-neo	bronchial:	n/a
40	chr15:77320787-77320837	U87	brain:	n/a
41	chr15:77326735-77326785	SK-N-MC	brain:	n/a
42	chr15:77324751-77324801	HPAEpiC	pulmonary alveolar:	n/a
43	chr15:77323565-77323615	NB4	blood:	n/a
44	chr15:77324751-77324801	ECC-1	luminal epithelium:	n/a
45	chr15:77320672-77320722	Hepatocyte	liver:	n/a
46	chr15:77320672-77320722	K562	blood:	n/a
47	chr15:77320211-77320261	AG04449	skin:	fetal
48	chr15:77326735-77326785	HNPCEpiC	eye:	n/a
49	chr15:77320261-77320311	HAEpiC	amniotic membrane:	n/a
50	chr15:77314406-77314456	ProgFib	skin:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:77332598..77335104-chr15:77338074..77339723,2	MCF-7	breast:
2	chr15:77316407..77317258-chr15:77399611..77400626,4	MCF-7	breast:
3	chr15:77315639..77319825-chr15:77322811..77328362,7	MCF-7	breast:
4	chr15:77316409..77317242-chr15:77835418..77836097,2	MCF-7	breast:
5	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
6	chr15:77316659..77317287-chr15:77410867..77411851,3	MCF-7	breast:
7	chr15:77320639..77324428-chr15:77362244..77364696,3	K562	blood:
8	chr15:77325493..77328166-chr15:77329882..77331634,3	MCF-7	breast:
9	chr15:77316331..77317283-chr15:77835334..77836400,5	K562	blood:
10	chr15:77265408..77266372-chr15:77316053..77316927,2	MCF-7	breast:
11	chr15:77316351..77317289-chr15:77788854..77789825,3	K562	blood:
12	chr15:77328280..77330879-chr15:77355103..77356921,2	K562	blood:
13	chr15:77305426..77307546-chr15:77319169..77320927,2	K562	blood:
14	chr15:77320466..77323005-chr15:77324460..77327682,3	MCF-7	breast:
15	chr15:77320466..77323005-chr15:77324460..77327682,3	MCF-7	breast:
16	chr15:77327656..77330194-chr15:77332164..77335172,3	K562	blood:
17	chr15:77311951..77316312-chr15:77325010..77329080,4	K562	blood:
18	chr15:77327656..77329511-chr15:77332033..77335172,3	K562	blood:

No data

Variant related genes	Relation type
PSTPIP1	TF binding region
ENSG00000259652	TF binding region
PSTPIP1	CpG island
ENSG00000259652	CpG island
ENSG00000140368	chromatin interactions
ENSG00000140391	chromatin interactions

Extended variants
information (count: 1297 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17465692	chr15:77307260-77307261	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs72742446	chr15:77307271-77307272	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs113807864	chr15:77307297-77307298	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs556579932	chr15:77307316-77307317	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs188791228	chr15:77307326-77307327	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs62007173	chr15:77307347-77307348	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs146236077	chr15:77307389-77307390	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs11072639	chr15:77307401-77307402	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs568670467	chr15:77307431-77307432	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs149513523	chr15:77307440-77307441	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs375469954	chr15:77307591-77307592	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs376044745	chr15:77307616-77307617	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs558898543	chr15:77307618-77307619	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs536111717	chr15:77307622-77307623	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs80227391	chr15:77307628-77307629	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs569467801	chr15:77307668-77307669	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs539635591	chr15:77307696-77307697	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs16968616	chr15:77307728-77307729	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148104406	chr15:77307731-77307732	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs17465755	chr15:77307752-77307753	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs115573927	chr15:77307758-77307759	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs573872239	chr15:77307768-77307769	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs192673278	chr15:77307777-77307778	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs141956863	chr15:77307829-77307830	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs79941195	chr15:77307840-77307841	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs545222701	chr15:77307841-77307842	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs374876117	chr15:77307852-77307853	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs4886508	chr15:77307910-77307911	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs547032830	chr15:77307926-77307927	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs562086519	chr15:77307927-77307928	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs62007205	chr15:77307955-77307956	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551296934	chr15:77307961-77307962	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs572242536	chr15:77308033-77308034	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs539647104	chr15:77308043-77308044	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs563458003	chr15:77308051-77308052	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs62007206	chr15:77308059-77308060	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs566243222	chr15:77308077-77308078	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs182512082	chr15:77308089-77308090	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533612498	chr15:77308090-77308091	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs555145672	chr15:77308146-77308147	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs116992402	chr15:77308152-77308153	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs35988555	chr15:77308205-77308206	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs537436588	chr15:77308216-77308217	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs556470201	chr15:77308229-77308230	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs140185335	chr15:77308234-77308235	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs187207524	chr15:77308251-77308252	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs78138579	chr15:77308255-77308256	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs536508173	chr15:77308261-77308262	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191291154	chr15:77308276-77308277	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs559297012	chr15:77308300-77308301	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77289200-77311200	Weak transcription	Aorta	Aorta
2	chr15:77289400-77310000	Weak transcription	Colon Smooth Muscle	Colon
3	chr15:77302800-77307600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:77303000-77307400	Enhancers	Spleen	Spleen
5	chr15:77303000-77319600	Weak transcription	Pancreas	Pancrea
6	chr15:77304400-77309000	Enhancers	Primary B cells from peripheral blood	blood
7	chr15:77304600-77310600	Enhancers	Primary B cells from cord blood	blood
8	chr15:77304800-77312600	Enhancers	Fetal Thymus	thymus
9	chr15:77305000-77307800	Enhancers	Thymus	Thymus
10	chr15:77305000-77310200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr15:77305200-77307600	Enhancers	Esophagus	oesophagus
12	chr15:77305200-77309000	Enhancers	Primary hematopoietic stem cells	blood
13	chr15:77305200-77309000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr15:77305400-77308400	Weak transcription	Stomach Smooth Muscle	stomach
15	chr15:77305600-77308800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr15:77305600-77309000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr15:77305800-77307400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr15:77305800-77307600	Enhancers	Duodenum Mucosa	Duodenum
19	chr15:77305800-77308800	Enhancers	Adipose Nuclei	Adipose
20	chr15:77306000-77311400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr15:77306200-77308800	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr15:77306200-77309600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr15:77306200-77310200	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr15:77306400-77309200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr15:77306600-77307400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
26	chr15:77306600-77307800	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr15:77306600-77308000	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr15:77306600-77308600	Enhancers	Placenta	Placenta
29	chr15:77306600-77310200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr15:77306600-77314000	Weak transcription	NHEK	skin
31	chr15:77306600-77316800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr15:77306800-77308200	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr15:77306800-77309000	Enhancers	Right Ventricle	heart
34	chr15:77306800-77309400	Enhancers	Primary T cells from cord blood	blood
35	chr15:77306800-77311200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr15:77307000-77309000	Enhancers	GM12878-XiMat	blood
37	chr15:77307000-77309400	Enhancers	Primary T cells fromperipheralblood	blood
38	chr15:77307200-77307400	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr15:77307200-77307600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr15:77307200-77307600	Enhancers	Brain Substantia Nigra	brain
41	chr15:77307200-77308400	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr15:77307200-77308600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr15:77307200-77309000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr15:77307200-77310000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr15:77307200-77310400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr15:77307200-77310400	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr15:77307400-77308400	Weak transcription	Spleen	Spleen
48	chr15:77307400-77309200	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr15:77307400-77309800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr15:77307400-77322400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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