Variant report

Variant	esv1000067
Chromosome Location	chr15:79291602-79300177
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	chr15:79299529-79299871	K562	blood:	n/a	n/a
2	ARID3A	chr15:79299472-79299822	HepG2	liver:	n/a	n/a
3	ATF1	chr15:79296813-79297099	K562	blood:	n/a	n/a
4	ATF1	chr15:79299484-79299801	K562	blood:	n/a	n/a
5	ATF2	chr15:79296546-79297258	GM12878	blood:	n/a	n/a
6	ATF2	chr15:79296649-79297255	GM12878	blood:	n/a	n/a
7	ATF3	chr15:79296798-79297131	K562	blood:	n/a	n/a
8	ATF3	chr15:79296849-79297071	K562	blood:	n/a	n/a
9	ATF3	chr15:79299501-79299720	K562	blood:	n/a	n/a
10	BATF	chr15:79296631-79297227	GM12878	blood:	n/a	chr15:79296942-79296953
11	BATF	chr15:79296775-79297183	GM12878	blood:	n/a	chr15:79296942-79296953
12	BCL11A	chr15:79296722-79297127	GM12878	blood:	n/a	chr15:79296747-79296756
13	BCL11A	chr15:79296607-79297191	GM12878	blood:	n/a	chr15:79296747-79296756
14	BCLAF1	chr15:79296595-79297341	GM12878	blood:	n/a	chr15:79296747-79296756
15	BHLHE40	chr15:79299442-79299726	K562	blood:	n/a	n/a
16	BHLHE40	chr15:79296907-79297002	K562	blood:	n/a	n/a
17	BHLHE40	chr15:79296555-79297233	GM12878	blood:	n/a	n/a
18	CBX3	chr15:79299454-79299845	K562	blood:	n/a	n/a
19	CBX3	chr15:79296679-79297099	K562	blood:	n/a	n/a
20	CEBPB	chr15:79299525-79299874	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:79299447-79299963	A549	lung:	n/a	n/a
22	CEBPB	chr15:79299416-79299867	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:79299500-79299913	K562	blood:	n/a	n/a
24	CEBPB	chr15:79296593-79297344	GM12878	blood:	n/a	n/a
25	CEBPB	chr15:79299529-79299893	MCF-7	breast:	n/a	n/a
26	CEBPB	chr15:79299579-79299717	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:79299528-79299893	A549	lung:	n/a	n/a
28	CEBPB	chr15:79299464-79299839	K562	blood:	n/a	n/a
29	CEBPB	chr15:79299491-79299828	MCF-7	breast:	n/a	n/a
30	CEBPB	chr15:79299500-79299886	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr15:79296788-79297179	GM12878	blood:	n/a	n/a
32	CHD1	chr15:79296589-79297469	GM12878	blood:	n/a	chr15:79296856-79296866
33	CHD2	chr15:79296819-79297122	Hela-S3	cervix:	n/a	chr15:79296856-79296866
34	CHD2	chr15:79299373-79299670	GM12878	blood:	n/a	n/a
35	CHD2	chr15:79296491-79297310	GM12878	blood:	n/a	chr15:79296856-79296866
36	CREB1	chr15:79299390-79299704	A549	lung:	n/a	n/a
37	CREB1	chr15:79296600-79297298	GM12878	blood:	n/a	n/a
38	CTCF	chr15:79299600-79299750	HPF	lung:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
39	CTCF	chr15:79299427-79299843	GM12878	blood:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
40	CTCF	chr15:79299560-79299710	GM12873	blood:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
41	CTCF	chr15:79299557-79299749	GM13977	blood:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
42	CTCF	chr15:79295093-79295222	Gliobla	brain:	n/a	chr15:79295145-79295166 chr15:79295150-79295168 chr15:79295152-79295165
43	CTCF	chr15:79299488-79299770	HepG2	liver:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
44	CTCF	chr15:79299495-79299770	GM10248	blood:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
45	CTCF	chr15:79299532-79299740	MCF-7	breast:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
46	CTCF	chr15:79299540-79299690	MCF-7	breast:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
47	CTCF	chr15:79299520-79299670	HEK293	kidney:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663
48	CTCF	chr15:79295098-79295207	NHEK	skin:	n/a	chr15:79295145-79295166 chr15:79295150-79295168 chr15:79295152-79295165
49	CTCF	chr15:79295100-79295250	NB4	blood:	n/a	chr15:79295145-79295166 chr15:79295150-79295168 chr15:79295152-79295165
50	CTCF	chr15:79299454-79299836	IMR90	lung:	n/a	chr15:79299649-79299659 chr15:79299641-79299662 chr15:79299646-79299664 chr15:79299648-79299661 chr15:79299647-79299663

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:79298659-79298709	HAEpiC	amniotic membrane:	n/a
2	chr15:79297159-79297209	HRE	kidney:	n/a
3	chr15:79298606-79298656	SK-N-MC	brain:	n/a
4	chr15:79298209-79298259	SK-N-MC	brain:	n/a
5	chr15:79296585-79296635	U87	brain:	n/a
6	chr15:79298637-79298687	HRCEpiC	kidney:	n/a
7	chr15:79297159-79297209	AG10803	skin:	n/a
8	chr15:79298651-79298701	HRE	kidney:	n/a
9	chr15:79298396-79298446	GM06990	blood:	n/a
10	chr15:79298637-79298687	A549	lung:	n/a
11	chr15:79296424-79296474	MCF10A-Er-Src	breast:	n/a
12	chr15:79298651-79298701	ProgFib	skin:	n/a
13	chr15:79296424-79296474	GM19239	blood:	n/a
14	chr15:79296585-79296635	ovcar-3	ovarian:	n/a
15	chr15:79298651-79298701	PANC-1	pancreas:	n/a
16	chr15:79298769-79298819	GM19239	blood:	n/a
17	chr15:79298769-79298819	HUVEC	blood vessel:	n/a
18	chr15:79297159-79297209	SAEC	small airway:	n/a
19	chr15:79296446-79296496	HL-60	blood:	n/a
20	chr15:79298384-79298434	SAEC	small airway:	n/a
21	chr15:79298769-79298819	A549	lung:	n/a
22	chr15:79297159-79297209	PrEC	prostate:	n/a
23	chr15:79298691-79298741	HUVEC	blood vessel:	n/a
24	chr15:79296377-79296427	GM19239	blood:	n/a
25	chr15:79298209-79298259	U87	brain:	n/a
26	chr15:79296446-79296496	Hela-S3	cervix:	n/a
27	chr15:79298651-79298701	K562	blood:	n/a
28	chr15:79298769-79298819	LNCaP	prostate:	n/a
29	chr15:79296446-79296496	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:79298234-79298284	A549	lung:	n/a
31	chr15:79298396-79298446	CMK	blood:	n/a
32	chr15:79298678-79298728	SAEC	small airway:	n/a
33	chr15:79298659-79298709	ovcar-3	ovarian:	n/a
34	chr15:79298637-79298687	HPAEpiC	pulmonary alveolar:	n/a
35	chr15:79296446-79296496	GM12891	blood:	n/a
36	chr15:79298637-79298687	HRE	kidney:	n/a
37	chr15:79298678-79298728	T-47D	breast:	n/a
38	chr15:79296446-79296496	CMK	blood:	n/a
39	chr15:79297210-79297260	A549	lung:	n/a
40	chr15:79296585-79296635	RPTEC	kidney:	n/a
41	chr15:79297159-79297209	HPAEpiC	pulmonary alveolar:	n/a
42	chr15:79296585-79296635	GM12892	blood:	n/a
43	chr15:79298651-79298701	GM12891	blood:	n/a
44	chr15:79296446-79296496	BE2_C	brain:	n/a
45	chr15:79298659-79298709	PrEC	prostate:	n/a
46	chr15:79296585-79296635	AG10803	skin:	n/a
47	chr15:79298209-79298259	HCT-116	colon:	n/a
48	chr15:79298659-79298709	AG04450	lung:	fetal
49	chr15:79298604-79298654	HRCEpiC	kidney:	n/a
50	chr15:79298606-79298656	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:79213555..79216067-chr15:79295400..79297888,2	K562	blood:
2	chr15:79221775..79223364-chr15:79294791..79297170,2	MCF-7	breast:
3	chr15:79274591..79277278-chr15:79290967..79292503,2	K562	blood:
4	chr15:79237353..79240243-chr15:79292172..79293938,2	K562	blood:
5	chr15:79286840..79288798-chr15:79290749..79294640,3	MCF-7	breast:
6	chr15:79289665..79292067-chr15:79295332..79297530,2	MCF-7	breast:
7	chr15:79278181..79281070-chr15:79299396..79302014,2	K562	blood:
8	chr15:79287783..79290330-chr15:79294942..79296932,2	MCF-7	breast:
9	chr15:79289154..79291802-chr15:79293548..79295310,2	MCF-7	breast:
10	chr15:79206034..79206939-chr15:79295471..79296333,2	MCF-7	breast:
11	chr15:79220482..79222111-chr15:79292818..79294616,2	MCF-7	breast:

Variant related genes	Relation type
RASGRF1	TF binding region
RASGRF1	CpG island
ENSG00000103811	chromatin interactions
ENSG00000058335	chromatin interactions

Extended variants
information (count: 378 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531697940	chr15:79291604-79291605	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545524385	chr15:79291605-79291606	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565335062	chr15:79291607-79291608	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527895512	chr15:79291621-79291622	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111808869	chr15:79291624-79291625	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74027003	chr15:79291625-79291626	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560135049	chr15:79291647-79291648	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561266600	chr15:79291678-79291679	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117115587	chr15:79291682-79291683	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548552286	chr15:79291693-79291694	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79125187	chr15:79291713-79291714	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117432329	chr15:79291729-79291730	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551456450	chr15:79291761-79291762	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192386706	chr15:79291787-79291788	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184392321	chr15:79291853-79291854	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554082716	chr15:79291914-79291915	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12900315	chr15:79291937-79291938	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs188505476	chr15:79291952-79291953	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369867508	chr15:79291969-79291970	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192716144	chr15:79292008-79292009	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57004337	chr15:79292009-79292010	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545126880	chr15:79292022-79292023	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565393517	chr15:79292028-79292029	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370929987	chr15:79292050-79292051	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs376306169	chr15:79292059-79292060	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs370960086	chr15:79292063-79292064	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs76100557	chr15:79292102-79292103	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs143525438	chr15:79292136-79292137	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs373938270	chr15:79292145-79292146	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs112402687	chr15:79292146-79292147	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs141767671	chr15:79292149-79292150	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs199661393	chr15:79292172-79292173	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs144903599	chr15:79292173-79292174	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs138773007	chr15:79292196-79292197	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376020482	chr15:79292202-79292203	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs184880194	chr15:79292215-79292216	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs141523460	chr15:79292223-79292224	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs576164632	chr15:79292288-79292289	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs12591384	chr15:79292289-79292290	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562296475	chr15:79292330-79292331	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs531344727	chr15:79292338-79292339	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368999623	chr15:79292340-79292341	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147265933	chr15:79292349-79292350	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529643112	chr15:79292388-79292389	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189342790	chr15:79292391-79292392	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547600792	chr15:79292417-79292418	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557250956	chr15:79292424-79292425	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs536549379	chr15:79292458-79292459	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556426651	chr15:79292463-79292464	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138825442	chr15:79292475-79292476	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
Breast cancer	17133270	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79276400-79309200	Weak transcription	Right Atrium	heart
2	chr15:79281800-79296000	Weak transcription	Primary B cells from cord blood	blood
3	chr15:79281800-79296600	Weak transcription	Esophagus	oesophagus
4	chr15:79281800-79296600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr15:79283000-79295000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr15:79285600-79294400	Weak transcription	HSMM	muscle
7	chr15:79285800-79294600	Weak transcription	Brain Angular Gyrus	brain
8	chr15:79285800-79298400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr15:79287200-79325800	Weak transcription	Brain Hippocampus Middle	brain
10	chr15:79288000-79293600	Strong transcription	Pancreatic Islets	Pancreatic Islet
11	chr15:79288400-79295400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:79289000-79296600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr15:79289200-79292000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr15:79289400-79291800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:79289400-79292000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr15:79289400-79292400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:79289400-79293200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr15:79289400-79297000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr15:79289600-79295000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr15:79289600-79295000	Weak transcription	HMEC	breast
21	chr15:79289600-79295200	Weak transcription	NH-A	brain
22	chr15:79290200-79292800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr15:79290400-79292600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr15:79290400-79293400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr15:79290400-79295000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:79290800-79291800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr15:79290800-79294400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr15:79290800-79294800	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr15:79290800-79334800	Weak transcription	Brain Substantia Nigra	brain
30	chr15:79291000-79293600	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr15:79291000-79294600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr15:79291000-79296200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:79291200-79294600	Weak transcription	HSMMtube	muscle
34	chr15:79291200-79295000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:79291200-79295800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr15:79291400-79294800	Weak transcription	Spleen	Spleen
37	chr15:79291400-79295200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr15:79291400-79296600	Weak transcription	Lung	lung
39	chr15:79291600-79292200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:79291600-79292800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr15:79291600-79293800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr15:79291600-79295200	Weak transcription	GM12878-XiMat	blood
43	chr15:79291600-79296000	Weak transcription	HepG2	liver
44	chr15:79291800-79292600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr15:79291800-79293400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr15:79292000-79292400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr15:79292000-79292400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr15:79292000-79293600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr15:79292200-79295600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr15:79292400-79292600	Enhancers	H9 Cell Line	embryonic stem cell

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