Variant report

Variant	esv2763105
Chromosome Location	chr15:72975344-72978616
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:537)
CpG islands
(count:367)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:72977887-72979352	K562	blood:	n/a	n/a
2	ARID3A	chr15:72977748-72978617	HepG2	liver:	n/a	n/a
3	ATF1	chr15:72978281-72978674	K562	blood:	n/a	n/a
4	ATF2	chr15:72978208-72978729	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:72978238-72978649	GM12878	blood:	n/a	n/a
6	ATF2	chr15:72978221-72978651	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr15:72978018-72978873	A549	lung:	n/a	n/a
8	BACH1	chr15:72978252-72979073	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr15:72978144-72979170	A549	lung:	n/a	chr15:72978619-72978632
10	BCL3	chr15:72977600-72979096	A549	lung:	n/a	chr15:72978619-72978632 chr15:72978101-72978108 chr15:72977714-72977722
11	BCLAF1	chr15:72978200-72978897	GM12878	blood:	n/a	chr15:72978619-72978632
12	BHLHE40	chr15:72978207-72979046	K562	blood:	n/a	n/a
13	BHLHE40	chr15:72978239-72978665	HepG2	liver:	n/a	n/a
14	BHLHE40	chr15:72978251-72978969	GM12878	blood:	n/a	n/a
15	BRCA1	chr15:72978199-72979374	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr15:72978311-72978828	GM12878	blood:	n/a	n/a
17	BRCA1	chr15:72978186-72978643	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr15:72978033-72978724	K562	blood:	n/a	n/a
19	CCNT2	chr15:72978116-72978800	K562	blood:	n/a	n/a
20	CEBPB	chr15:72978233-72978645	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPD	chr15:72978401-72978873	HepG2	liver:	n/a	n/a
22	CEBPD	chr15:72978271-72978769	K562	blood:	n/a	n/a
23	CHD1	chr15:72977911-72979183	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr15:72978057-72979015	GM12878	blood:	n/a	n/a
25	CHD2	chr15:72978390-72978779	K562	blood:	n/a	n/a
26	CHD2	chr15:72978037-72978749	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr15:72978125-72979142	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr15:72978230-72978951	GM12878	blood:	n/a	n/a
29	CHD2	chr15:72978318-72978791	HepG2	liver:	n/a	n/a
30	CREB1	chr15:72978052-72979034	HepG2	liver:	n/a	n/a
31	CREB1	chr15:72978102-72978827	A549	lung:	n/a	n/a
32	CREB1	chr15:72978191-72978906	GM12878	blood:	n/a	n/a
33	CREB1	chr15:72978233-72978774	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr15:72978318-72978716	A549	lung:	n/a	n/a
35	CTCF	chr15:72978585-72978624	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr15:72978080-72978230	HRE	kidney:	n/a	n/a
37	CTCF	chr15:72977960-72978110	HRPEpiC	eye:	n/a	chr15:72978054-72978063
38	CTCF	chr15:72977040-72977190	HepG2	liver:	n/a	n/a
39	CTCF	chr15:72977920-72978070	AG04450	lung:	n/a	chr15:72978054-72978063
40	CTCF	chr15:72978587-72978588	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr15:72978040-72978190	Caco-2	colon:	n/a	chr15:72978054-72978063
42	CTCF	chr15:72978020-72978170	RPTEC	kidney:	n/a	chr15:72978054-72978063
43	CTCF	chr15:72978180-72978330	SAEC	small airway:	n/a	n/a
44	CTCF	chr15:72977914-72978479	K562	blood:	n/a	chr15:72978054-72978063
45	CTCF	chr15:72977880-72978030	Caco-2	colon:	n/a	n/a
46	CTCF	chr15:72978060-72978210	AG10803	skin:	n/a	n/a
47	CTCF	chr15:72978200-72978350	HCM	heart:	n/a	n/a
48	CTCF	chr15:72978286-72978287	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr15:72978120-72978270	BE2_C	brain:	n/a	n/a
50	CTCF	chr15:72977940-72978090	HEEpiC	esophagus:	n/a	chr15:72978054-72978063

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72978361-72978411	HNPCEpiC	eye:	n/a
2	chr15:72978361-72978411	HNPCEpiC	eye:	n/a
3	chr15:72975894-72975944	Hela-S3	cervix:	n/a
4	chr15:72975894-72975944	AoSMC	blood vessel:	n/a
5	chr15:72978371-72978421	AG04449	skin:	fetal
6	chr15:72978165-72978215	AG04450	lung:	fetal
7	chr15:72978361-72978411	NH-A	brain:	n/a
8	chr15:72978371-72978421	HL-60	blood:	n/a
9	chr15:72978165-72978215	HepG2	liver:	n/a
10	chr15:72978040-72978090	SAEC	small airway:	n/a
11	chr15:72978361-72978411	HCPEpiC	choroid plexus:	n/a
12	chr15:72978361-72978411	Hela-S3	cervix:	n/a
13	chr15:72978371-72978421	RPTEC	kidney:	n/a
14	chr15:72978040-72978090	AG09309	skin:	n/a
15	chr15:72978165-72978215	HCPEpiC	choroid plexus:	n/a
16	chr15:72975894-72975944	PFSK-1	brain:	n/a
17	chr15:72978040-72978090	ECC-1	luminal epithelium:	n/a
18	chr15:72978371-72978421	HRE	kidney:	n/a
19	chr15:72975894-72975944	GM12892	blood:	n/a
20	chr15:72975894-72975944	A549	lung:	n/a
21	chr15:72978040-72978090	NHDF-neo	bronchial:	n/a
22	chr15:72978165-72978215	RPTEC	kidney:	n/a
23	chr15:72978040-72978090	GM19239	blood:	n/a
24	chr15:72978040-72978090	GM06990	blood:	n/a
25	chr15:72975894-72975944	AG09309	skin:	n/a
26	chr15:72978371-72978421	NH-A	brain:	n/a
27	chr15:72978040-72978090	Jurkat	blood:	n/a
28	chr15:72977851-72977901	SK-N-SH	brain:	n/a
29	chr15:72978165-72978215	HRPEpiC	eye:	n/a
30	chr15:72977851-72977901	SK-N-SH_RA	brain:	n/a
31	chr15:72978371-72978421	NT2-D1	testis:	n/a
32	chr15:72978165-72978215	NH-A	brain:	n/a
33	chr15:72975894-72975944	H1-hESC	embryonic stem cell:	embryo
34	chr15:72978371-72978421	HCT-116	colon:	n/a
35	chr15:72975894-72975944	Hepatocyte	liver:	n/a
36	chr15:72975894-72975944	HNPCEpiC	eye:	n/a
37	chr15:72975894-72975944	HEEpiC	esophagus:	n/a
38	chr15:72975894-72975944	HCF	heart:	n/a
39	chr15:72975894-72975944	SK-N-SH	brain:	n/a
40	chr15:72975894-72975944	SK-N-SH_RA	brain:	n/a
41	chr15:72977851-72977901	NB4	blood:	n/a
42	chr15:72978361-72978411	HPAEpiC	pulmonary alveolar:	n/a
43	chr15:72978165-72978215	Hepatocyte	liver:	n/a
44	chr15:72978165-72978215	SK-N-MC	brain:	n/a
45	chr15:72978040-72978090	GM12878	blood:	n/a
46	chr15:72978361-72978411	HRCEpiC	kidney:	n/a
47	chr15:72978371-72978421	AG09319	gingival:	n/a
48	chr15:72978040-72978090	HRE	kidney:	n/a
49	chr15:72975894-72975944	T-47D	breast:	n/a
50	chr15:72978165-72978215	Jurkat	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:72978405..72979084-chr15:73076020..73076684,2	Hela-S3	cervix:
2	chr1:225965472..225966023-chr15:72978001..72978969,2	Hela-S3	cervix:
3	chr15:72971779..72975423-chr15:72976170..72980827,7	K562	blood:
4	chr15:72978250..72978999-chr17:62502049..62502770,2	NB4	blood:
5	chr15:72977449..72978326-chrX:48659259..48660248,2	Hela-S3	cervix:
6	chr12:112846958..112847755-chr15:72978300..72979259,2	Hela-S3	cervix:
7	chr15:72977264..72978956-chr15:73075083..73076901,2	MCF-7	breast:
8	chr15:72971779..72975423-chr15:72976170..72980827,7	K562	blood:
9	chr15:72972683..72975253-chr15:72975906..72977855,2	MCF-7	breast:
10	chr10:112257437..112258408-chr15:72978244..72979060,2	Hela-S3	cervix:
11	chr15:72521683..72524680-chr15:72976957..72979803,2	K562	blood:
12	chr15:72976932..72978751-chr15:73073825..73076141,2	MCF-7	breast:
13	chr15:72521996..72524543-chr15:72977386..72979463,3	MCF-7	breast:
14	chr1:153507658..153508549-chr15:72977999..72978681,2	Hela-S3	cervix:
15	chr15:41055462..41056415-chr15:72977930..72978582,2	Hela-S3	cervix:
16	chr15:72562851..72564645-chr15:72977653..72979663,2	K562	blood:
17	chr15:72978470..72980550-chr15:73014196..73015991,2	K562	blood:
18	chr15:72973101..72975344-chr15:72976692..72980792,4	MCF-7	breast:
19	chr15:72512307..72515184-chr15:72976836..72978920,2	MCF-7	breast:
20	chr15:72973101..72975344-chr15:72976692..72980792,4	MCF-7	breast:
21	chr15:72978281..72979189-chr16:89119223..89119876,2	NB4	blood:
22	chr15:72972671..72974749-chr15:72976443..72978214,2	K562	blood:
23	chr15:72764850..72767674-chr15:72977020..72979928,5	K562	blood:
24	chr15:72978333..72978951-chrX:119077217..119077919,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
BBS4	TF binding region
ENSG00000261281	TF binding region
HIGD2B	TF binding region
BBS4	CpG island
ENSG00000261281	CpG island
HIGD2B	CpG island
ENSG00000258890	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000137817	chromatin interactions
ENSG00000101882	chromatin interactions
ENSG00000175202	chromatin interactions
ENSG00000140463	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000256982	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000261281	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000159322	chromatin interactions
ENSG00000138166	chromatin interactions
ENSG00000094631	chromatin interactions
ENSG00000260898	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000137880	chromatin interactions
ENSG00000089009	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568298664	chr15:72975347-72975348	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs537252471	chr15:72975356-72975357	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs545965212	chr15:72975359-72975360	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs372128105	chr15:72975368-72975369	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs564261517	chr15:72975394-72975395	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs7182789	chr15:72975443-72975444	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs17753627	chr15:72975502-72975503	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs533996291	chr15:72975504-72975505	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs190105294	chr15:72975510-72975511	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs118027190	chr15:72975587-72975588	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs183454643	chr15:72975591-72975592	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs569312719	chr15:72975610-72975611	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs533394641	chr15:72975642-72975643	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs551948858	chr15:72975664-72975665	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs567023962	chr15:72975679-72975680	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs114885420	chr15:72975687-72975688	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs556063596	chr15:72975708-72975709	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs11329719	chr15:72975780-72975781	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs79355859	chr15:72975794-72975795	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs75883781	chr15:72975796-72975797	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs568086784	chr15:72975848-72975849	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs1991288	chr15:72975909-72975910	Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs556816603	chr15:72975976-72975977	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs558992823	chr15:72976013-72976014	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575286784	chr15:72976074-72976075	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs60405894	chr15:72976075-72976076	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs557934120	chr15:72976115-72976116	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572658833	chr15:72976122-72976123	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs8026286	chr15:72976126-72976127	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs561619649	chr15:72976131-72976132	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs529277726	chr15:72976168-72976169	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs188509330	chr15:72976206-72976207	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs60280180	chr15:72976240-72976241	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs398027907	chr15:72976254-72976255	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140752767	chr15:72976303-72976304	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs373997438	chr15:72976312-72976313	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs533470156	chr15:72976336-72976337	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs192020301	chr15:72976376-72976377	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs567086733	chr15:72976405-72976406	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527861063	chr15:72976419-72976420	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549727324	chr15:72976441-72976442	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567947071	chr15:72976454-72976455	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs8026559	chr15:72976511-72976512	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs76317157	chr15:72976521-72976522	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
45	rs373497166	chr15:72976566-72976567	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs568711051	chr15:72976577-72976578	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539527932	chr15:72976649-72976650	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11856110	chr15:72976650-72976651	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs368755228	chr15:72976660-72976661	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75927241	chr15:72976667-72976668	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72963800-72977600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:72973200-72977400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr15:72973600-72977600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr15:72975400-72975600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr15:72975600-72977400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr15:72975600-72977400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr15:72976400-72976600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr15:72977000-72977800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr15:72977400-72977600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr15:72977400-72977600	Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr15:72977400-72977600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr15:72977400-72977600	Enhancers	Primary hematopoietic stem cells	blood
13	chr15:72977400-72977600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr15:72977400-72977600	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr15:72977400-72977600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr15:72977400-72977600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr15:72977400-72977600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr15:72977400-72977600	Enhancers	Brain Germinal Matrix	brain
19	chr15:72977400-72977600	Enhancers	Brain Hippocampus Middle	brain
20	chr15:72977400-72977600	Enhancers	Colon Smooth Muscle	Colon
21	chr15:72977400-72977600	Enhancers	Fetal Intestine Small	intestine
22	chr15:72977400-72977600	Enhancers	Fetal Kidney	kidney
23	chr15:72977400-72977600	Active TSS	Rectal Mucosa Donor 29	rectum
24	chr15:72977400-72977600	Enhancers	Hela-S3	cervix
25	chr15:72977400-72977800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:72977400-72977800	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr15:72977400-72977800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr15:72977400-72977800	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr15:72977400-72978000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr15:72977400-72978000	Active TSS	HepG2	liver
31	chr15:72977400-72978000	Flanking Active TSS	NHEK	skin
32	chr15:72977400-72978200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr15:72977400-72978200	Flanking Active TSS	Liver	Liver
34	chr15:72977400-72978400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr15:72977400-72978400	Flanking Active TSS	Dnd41	blood
36	chr15:72977400-72979400	Active TSS	GM12878-XiMat	blood
37	chr15:72977400-72979600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr15:72977400-72979600	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr15:72977400-72979800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr15:72977400-72980000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:72977400-72980200	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr15:72977600-72977800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr15:72977600-72977800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr15:72977600-72977800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr15:72977600-72977800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr15:72977600-72977800	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr15:72977600-72977800	Enhancers	Primary B cells from peripheral blood	blood
48	chr15:72977600-72977800	Enhancers	Primary T cells fromperipheralblood	blood
49	chr15:72977600-72977800	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr15:72977600-72977800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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