Variant report

Variant	esv3312334
Chromosome Location	chr15:79162451-79167158
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:967)
CpG islands
(count:794)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:79165832-79166648	K562	blood:	n/a	chr15:79165909-79165924
2	ARID3A	chr15:79164988-79165116	K562	blood:	n/a	n/a
3	ARID3A	chr15:79163866-79164240	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:79164926-79166553	HepG2	liver:	n/a	chr15:79165909-79165924
5	ARID3A	chr15:79165446-79165490	K562	blood:	n/a	n/a
6	ARID3A	chr15:79167155-79167523	K562	blood:	n/a	n/a
7	ATF1	chr15:79164480-79166460	K562	blood:	n/a	n/a
8	ATF2	chr15:79165241-79166353	GM12878	blood:	n/a	n/a
9	ATF2	chr15:79165754-79166483	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr15:79165789-79166470	GM12878	blood:	n/a	n/a
11	ATF2	chr15:79165742-79166439	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr15:79164940-79165230	GM12878	blood:	n/a	n/a
13	ATF3	chr15:79165021-79165265	GM12878	blood:	n/a	chr15:79165209-79165222
14	ATF3	chr15:79164957-79165282	K562	blood:	n/a	chr15:79165209-79165222
15	ATF3	chr15:79165723-79166185	A549	lung:	n/a	n/a
16	ATF3	chr15:79164881-79165277	HepG2	liver:	n/a	chr15:79165209-79165222
17	ATF3	chr15:79164982-79165279	HepG2	liver:	n/a	chr15:79165209-79165222
18	ATF3	chr15:79165040-79165332	H1-hESC	embryonic stem cell:	n/a	chr15:79165209-79165222
19	ATF3	chr15:79165013-79165353	K562	blood:	n/a	chr15:79165209-79165222
20	ATF3	chr15:79165703-79166614	A549	lung:	n/a	chr15:79166276-79166286
21	ATF3	chr15:79164990-79165202	GM12878	blood:	n/a	n/a
22	BACH1	chr15:79165924-79165976	K562	blood:	n/a	n/a
23	BACH1	chr15:79164777-79165066	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr15:79165879-79166131	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr15:79165400-79165703	GM12878	blood:	n/a	n/a
26	BCL3	chr15:79165556-79166726	A549	lung:	n/a	chr15:79165787-79165800 chr15:79165754-79165763 chr15:79165753-79165766
27	BCL3	chr15:79165234-79166692	A549	lung:	n/a	chr15:79165787-79165800 chr15:79165482-79165491 chr15:79165754-79165763 chr15:79165753-79165766
28	BCL3	chr15:79165408-79166140	GM12878	blood:	n/a	chr15:79165787-79165800 chr15:79165482-79165491 chr15:79165754-79165763 chr15:79165753-79165766
29	BCLAF1	chr15:79165271-79166304	GM12878	blood:	n/a	chr15:79165787-79165800 chr15:79165482-79165491 chr15:79165754-79165763 chr15:79165753-79165766
30	BCLAF1	chr15:79165691-79166323	GM12878	blood:	n/a	chr15:79165787-79165800 chr15:79165754-79165763 chr15:79165753-79165766
31	BHLHE40	chr15:79163392-79163480	HepG2	liver:	n/a	n/a
32	BHLHE40	chr15:79165061-79166083	HepG2	liver:	n/a	n/a
33	BHLHE40	chr15:79164871-79166586	GM12878	blood:	n/a	chr15:79165006-79165022
34	BHLHE40	chr15:79164461-79166359	K562	blood:	n/a	chr15:79165006-79165022
35	BRCA1	chr15:79164511-79165256	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr15:79165766-79166622	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr15:79165000-79166867	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr15:79165811-79166052	GM12878	blood:	n/a	n/a
39	BRCA1	chr15:79164735-79165285	HepG2	liver:	n/a	n/a
40	BRCA1	chr15:79165922-79165965	HepG2	liver:	n/a	n/a
41	CBX3	chr15:79165898-79166163	K562	blood:	n/a	n/a
42	CBX3	chr15:79165480-79166323	K562	blood:	n/a	n/a
43	CCNT2	chr15:79164936-79166199	K562	blood:	n/a	chr15:79165037-79165046 chr15:79165042-79165051 chr15:79165762-79165771
44	CEBPB	chr15:79165852-79166132	HepG2	liver:	n/a	n/a
45	CEBPB	chr15:79165557-79166132	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr15:79164807-79166611	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:79165881-79166796	GM12878	blood:	n/a	n/a
48	CEBPB	chr15:79165856-79166289	K562	blood:	n/a	n/a
49	CEBPB	chr15:79165836-79166555	K562	blood:	n/a	n/a
50	CEBPB	chr15:79165651-79166752	A549	lung:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:79166157-79166207	PrEC	prostate:	n/a
2	chr15:79166157-79166207	PrEC	prostate:	n/a
3	chr15:79164806-79164856	HCT-116	colon:	n/a
4	chr15:79165343-79165393	NB4	blood:	n/a
5	chr15:79165638-79165688	SK-N-SH	brain:	n/a
6	chr15:79164806-79164856	SK-N-SH_RA	brain:	n/a
7	chr15:79165343-79165393	HCM	heart:	n/a
8	chr15:79164980-79165030	K562	blood:	n/a
9	chr15:79164980-79165030	H1-hESC	embryonic stem cell:	embryo
10	chr15:79164714-79164764	SK-N-MC	brain:	n/a
11	chr15:79164980-79165030	AG04449	skin:	fetal
12	chr15:79164541-79164591	HCT-116	colon:	n/a
13	chr15:79165367-79165417	AoSMC	blood vessel:	n/a
14	chr15:79164980-79165030	LNCaP	prostate:	n/a
15	chr15:79164980-79165030	SK-N-SH_RA	brain:	n/a
16	chr15:79165973-79166023	GM12891	blood:	n/a
17	chr15:79164806-79164856	PFSK-1	brain:	n/a
18	chr15:79162671-79162721	LNCaP	prostate:	n/a
19	chr15:79164980-79165030	HCF	heart:	n/a
20	chr15:79165638-79165688	PANC-1	pancreas:	n/a
21	chr15:79164714-79164764	U87	brain:	n/a
22	chr15:79164806-79164856	ProgFib	skin:	n/a
23	chr15:79165379-79165429	U87	brain:	n/a
24	chr15:79164980-79165030	T-47D	breast:	n/a
25	chr15:79162671-79162721	AG04449	skin:	fetal
26	chr15:79165343-79165393	K562	blood:	n/a
27	chr15:79162671-79162721	AG09309	skin:	n/a
28	chr15:79165638-79165688	Hela-S3	cervix:	n/a
29	chr15:79165367-79165417	H1-hESC	embryonic stem cell:	embryo
30	chr15:79164806-79164856	K562	blood:	n/a
31	chr15:79165343-79165393	LNCaP	prostate:	n/a
32	chr15:79165225-79165275	HRE	kidney:	n/a
33	chr15:79164980-79165030	MCF-7	breast:	n/a
34	chr15:79164100-79164150	AG09319	gingival:	n/a
35	chr15:79165638-79165688	HNPCEpiC	eye:	n/a
36	chr15:79162671-79162721	GM12891	blood:	n/a
37	chr15:79166157-79166207	MCF-7	breast:	n/a
38	chr15:79164714-79164764	AG09319	gingival:	n/a
39	chr15:79165367-79165417	HMEC	breast:	n/a
40	chr15:79165379-79165429	MCF10A-Er-Src	breast:	n/a
41	chr15:79164714-79164764	AG09309	skin:	n/a
42	chr15:79165225-79165275	HRPEpiC	eye:	n/a
43	chr15:79165379-79165429	BJ	skin:	n/a
44	chr15:79164100-79164150	HMEC	breast:	n/a
45	chr15:79165973-79166023	GM12892	blood:	n/a
46	chr15:79164980-79165030	GM06990	blood:	n/a
47	chr15:79165638-79165688	Hepatocyte	liver:	n/a
48	chr15:79165638-79165688	MCF10A-Er-Src	breast:	n/a
49	chr15:79164714-79164764	SK-N-SH	brain:	n/a
50	chr15:79162671-79162721	SK-N-SH_RA	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:79164137..79170280-chr15:79189650..79200289,14	K562	blood:
2	chr15:79164853..79165697-chr16:89988493..89989100,2	Hela-S3	cervix:
3	chr15:79164147..79167807-chr15:79181870..79184969,5	MCF-7	breast:
4	chr1:54303745..54304370-chr15:79165446..79166154,2	Hela-S3	cervix:
5	chr15:79165172..79166048-chr3:149095199..149095871,2	Hela-S3	cervix:
6	chr15:79165092..79167959-chr15:79271269..79275481,5	MCF-7	breast:
7	chr15:79147722..79157046-chr15:79163022..79167664,11	K562	blood:
8	chr15:79165078..79165962-chr5:43483693..43484397,2	Hela-S3	cervix:
9	chr15:79164114..79167612-chr15:79169909..79172320,4	MCF-7	breast:
10	chr15:79102834..79106085-chr15:79164025..79165931,3	MCF-7	breast:
11	chr15:79149764..79156555-chr15:79163462..79168215,14	K562	blood:
12	chr15:79166291..79168090-chr15:79212016..79214147,2	K562	blood:
13	chr15:79155412..79157094-chr15:79165344..79167511,2	MCF-7	breast:
14	chr15:79164841..79165710-chr6:34204367..34204927,2	HCT-116	colon:
15	chr15:79165233..79165946-chr4:108910433..108911395,2	Hela-S3	cervix:
16	chr15:79166327..79167939-chr15:79173370..79175440,2	MCF-7	breast:
17	chr15:79164120..79166028-chr15:79235714..79238649,2	K562	blood:
18	chr1:11159486..11160014-chr15:79165519..79166035,2	Hela-S3	cervix:
19	chr15:79164120..79166260-chr15:79235714..79238649,3	K562	blood:
20	chr15:79155360..79158242-chr15:79163713..79165870,2	MCF-7	breast:
21	chr15:79160634..79162512-chr15:79167187..79168992,2	K562	blood:
22	chr13:20437135..20437902-chr15:79164969..79165733,2	NB4	blood:

No data

Variant related genes	Relation type
MORF4L1	TF binding region
MORF4L1	CpG island
ENSG00000151881	chromatin interactions
ENSG00000136378	chromatin interactions
ENSG00000103811	chromatin interactions
ENSG00000058804	chromatin interactions
ENSG00000132950	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000185787	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000252061	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000171824	chromatin interactions
ENSG00000138796	chromatin interactions
ENSG00000058335	chromatin interactions
ENSG00000230337	chromatin interactions
ENSG00000169908	chromatin interactions
ENSG00000240541	chromatin interactions
ENSG00000243711	chromatin interactions

Extended variants
information (count: 235 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:235 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566170060	chr15:79162461-79162462	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs528752438	chr15:79162468-79162469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs139791864	chr15:79162498-79162499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566879833	chr15:79162537-79162538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559673906	chr15:79162565-79162566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535845490	chr15:79162569-79162570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375511968	chr15:79162588-79162589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35836211	chr15:79162623-79162624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569726472	chr15:79162656-79162657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538392576	chr15:79162662-79162663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11633850	chr15:79162680-79162681	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs146205027	chr15:79162701-79162702	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs111464320	chr15:79162738-79162739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62011055	chr15:79162757-79162758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs552786233	chr15:79162781-79162782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117235023	chr15:79162807-79162808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554914200	chr15:79162846-79162847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574830697	chr15:79162854-79162855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543828966	chr15:79162858-79162859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142611473	chr15:79162866-79162867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532616701	chr15:79162898-79162899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188644388	chr15:79162919-79162920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374198615	chr15:79162931-79162932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368693457	chr15:79162945-79162946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559861239	chr15:79162952-79162953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200341385	chr15:79162955-79162956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35313054	chr15:79162975-79162976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528686083	chr15:79163017-79163018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7171615	chr15:79163022-79163023	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs192786503	chr15:79163054-79163055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184235796	chr15:79163080-79163081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564695454	chr15:79163110-79163111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568457508	chr15:79163113-79163114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs139623507	chr15:79163171-79163172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569581056	chr15:79163174-79163175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74737430	chr15:79163284-79163285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538698373	chr15:79163304-79163305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs74545338	chr15:79163331-79163332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs569637497	chr15:79163373-79163374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570355301	chr15:79163374-79163375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189352742	chr15:79163394-79163395	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147670825	chr15:79163399-79163400	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554843648	chr15:79163409-79163410	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs561701117	chr15:79163509-79163510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182193026	chr15:79163532-79163533	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537371040	chr15:79163544-79163545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs142326031	chr15:79163549-79163550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146601578	chr15:79163556-79163557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs73477663	chr15:79163565-79163566	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4778738	chr15:79163602-79163603	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

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

Chromatin state (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79153000-79163200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr15:79153200-79163200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr15:79153200-79164600	Weak transcription	A549	lung
4	chr15:79156800-79164400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr15:79157200-79163400	Weak transcription	HepG2	liver
6	chr15:79161000-79164400	Weak transcription	Adipose Nuclei	Adipose
7	chr15:79161400-79163800	Weak transcription	Placenta	Placenta
8	chr15:79161400-79164600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr15:79161800-79164600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:79163000-79163800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr15:79163200-79163400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:79163200-79163400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr15:79163200-79163400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr15:79163200-79163400	Enhancers	Hela-S3	cervix
15	chr15:79163200-79164000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr15:79163200-79164400	Enhancers	K562	blood
17	chr15:79163400-79163800	Enhancers	HepG2	liver
18	chr15:79163400-79164000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:79163400-79164400	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr15:79163400-79164400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr15:79163400-79164400	Weak transcription	Hela-S3	cervix
22	chr15:79163600-79163800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:79163800-79164000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr15:79163800-79164400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:79163800-79164600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr15:79163800-79164600	Enhancers	Placenta	Placenta
27	chr15:79163800-79165000	Flanking Active TSS	HepG2	liver
28	chr15:79164000-79164200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr15:79164000-79164200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr15:79164000-79164200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr15:79164000-79164200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr15:79164000-79164200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:79164000-79164200	Enhancers	Brain Germinal Matrix	brain
34	chr15:79164000-79164200	Enhancers	Fetal Intestine Small	intestine
35	chr15:79164000-79164400	Enhancers	Aorta	Aorta
36	chr15:79164000-79164400	Enhancers	Fetal Brain Male	brain
37	chr15:79164000-79164400	Enhancers	Fetal Muscle Trunk	muscle
38	chr15:79164000-79164600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr15:79164000-79164600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:79164000-79167800	Active TSS	Fetal Intestine Large	intestine
41	chr15:79164000-79169200	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr15:79164200-79164400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr15:79164200-79164400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr15:79164200-79164400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr15:79164200-79164400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:79164200-79164400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr15:79164200-79164400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr15:79164200-79164400	Active TSS	Primary hematopoietic stem cells	blood
49	chr15:79164200-79164400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr15:79164200-79164400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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