Variant report

Variant	esv3426665
Chromosome Location	chr15:99862575-99866059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:187)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:187 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:99864437-99864834	K562	blood:	n/a	n/a
2	ATF2	chr15:99864341-99864893	GM12878	blood:	n/a	n/a
3	ATF2	chr15:99864284-99864957	GM12878	blood:	n/a	n/a
4	ATF3	chr15:99864139-99865019	HCT-116	colon:	n/a	n/a
5	ATF3	chr15:99863947-99864628	A549	lung:	n/a	n/a
6	ATF3	chr15:99864085-99864956	A549	lung:	n/a	n/a
7	BATF	chr15:99864228-99864489	GM12878	blood:	n/a	chr15:99864364-99864375
8	BCL3	chr15:99863946-99865300	A549	lung:	n/a	n/a
9	BCL3	chr15:99864031-99864882	A549	lung:	n/a	n/a
10	BCLAF1	chr15:99864343-99864871	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:99864143-99864788	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr15:99864037-99864951	HCT-116	colon:	n/a	n/a
13	CEBPB	chr15:99864265-99865017	A549	lung:	n/a	n/a
14	CEBPB	chr15:99864118-99864877	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr15:99864148-99864668	A549	lung:	n/a	n/a
16	CEBPB	chr15:99864782-99864978	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:99864160-99865034	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr15:99864072-99865043	HCT-116	colon:	n/a	n/a
19	CEBPB	chr15:99864191-99864670	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr15:99864258-99864999	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:99863929-99864905	A549	lung:	n/a	n/a
22	CEBPB	chr15:99864066-99865036	HCT-116	colon:	n/a	n/a
23	CHD2	chr15:99864230-99864758	Hela-S3	cervix:	n/a	n/a
24	CREB1	chr15:99864249-99864899	GM12878	blood:	n/a	n/a
25	CTCF	chr15:99862480-99862630	A549	lung:	n/a	n/a
26	CTCF	chr15:99863340-99863490	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr15:99862964-99863027	A549	lung:	n/a	n/a
28	E2F4	chr15:99864233-99865141	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr15:99863273-99863473	MCF10A-Er-Src	breast:	n/a	n/a
30	EGR1	chr15:99864095-99865063	HCT-116	colon:	n/a	chr15:99864712-99864726
31	EGR1	chr15:99864615-99864761	GM12878	blood:	n/a	chr15:99864712-99864726
32	EGR1	chr15:99864209-99864863	ECC-1	luminal epithelium:	n/a	chr15:99864712-99864726
33	EGR1	chr15:99864623-99864761	GM12878	blood:	n/a	chr15:99864712-99864726
34	EGR1	chr15:99864267-99865016	HCT-116	colon:	n/a	chr15:99864712-99864726
35	EGR1	chr15:99864534-99864848	ECC-1	luminal epithelium:	n/a	chr15:99864712-99864726
36	EP300	chr15:99863966-99865304	A549	lung:	n/a	chr15:99865125-99865132 chr15:99864949-99864959 chr15:99864940-99864950
37	EP300	chr15:99864052-99864958	ECC-1	luminal epithelium:	n/a	chr15:99864940-99864950
38	EP300	chr15:99864125-99865220	Hela-S3	cervix:	n/a	chr15:99865125-99865132 chr15:99864949-99864959 chr15:99864940-99864950
39	EP300	chr15:99862822-99863200	HepG2	liver:	n/a	n/a
40	EP300	chr15:99864298-99864473	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr15:99863826-99865396	A549	lung:	n/a	chr15:99865125-99865132 chr15:99864949-99864959 chr15:99864940-99864950
42	EP300	chr15:99864156-99864855	SK-N-SH	brain:	n/a	n/a
43	EP300	chr15:99863972-99865091	ECC-1	luminal epithelium:	n/a	chr15:99864949-99864959 chr15:99864940-99864950
44	ESR1	chr15:99864129-99864860	ECC-1	luminal epithelium:	n/a	n/a
45	ESR1	chr15:99864050-99864815	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr15:99864212-99864831	ECC-1	luminal epithelium:	n/a	n/a
47	ESR1	chr15:99864095-99864827	ECC-1	luminal epithelium:	n/a	n/a
48	FOS	chr15:99864157-99864871	MCF10A-Er-Src	breast:	n/a	chr15:99864424-99864435 chr15:99864366-99864377
49	FOS	chr15:99863330-99863530	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr15:99863254-99863561	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99864059-99864109	HAEpiC	amniotic membrane:	n/a
2	chr15:99864059-99864109	PANC-1	pancreas:	n/a
3	chr15:99864059-99864109	HRCEpiC	kidney:	n/a
4	chr15:99864059-99864109	SAEC	small airway:	n/a
5	chr15:99864059-99864109	SK-N-SH_RA	brain:	n/a
6	chr15:99864059-99864109	ovcar-3	ovarian:	n/a
7	chr15:99864059-99864109	SK-N-SH	brain:	n/a
8	chr15:99864059-99864109	HL-60	blood:	n/a
9	chr15:99864059-99864109	GM12892	blood:	n/a
10	chr15:99864059-99864109	HCF	heart:	n/a
11	chr15:99864059-99864109	AoSMC	blood vessel:	n/a
12	chr15:99864059-99864109	BE2_C	brain:	n/a
13	chr15:99864059-99864109	Caco-2	colon:	n/a
14	chr15:99864059-99864109	NB4	blood:	n/a
15	chr15:99864059-99864109	NT2-D1	testis:	n/a
16	chr15:99864059-99864109	ECC-1	luminal epithelium:	n/a
17	chr15:99864059-99864109	ProgFib	skin:	n/a
18	chr15:99864059-99864109	HEEpiC	esophagus:	n/a
19	chr15:99864059-99864109	HNPCEpiC	eye:	n/a
20	chr15:99864059-99864109	PFSK-1	brain:	n/a
21	chr15:99864059-99864109	SK-N-MC	brain:	n/a
22	chr15:99864059-99864109	CMK	blood:	n/a
23	chr15:99864059-99864109	GM19239	blood:	n/a
24	chr15:99864059-99864109	AG04449	skin:	fetal
25	chr15:99864059-99864109	HCPEpiC	choroid plexus:	n/a
26	chr15:99864059-99864109	K562	blood:	n/a
27	chr15:99864059-99864109	SKMC	muscle:	n/a
28	chr15:99864059-99864109	NHDF-neo	bronchial:	n/a
29	chr15:99864059-99864109	PrEC	prostate:	n/a
30	chr15:99864059-99864109	A549	lung:	n/a
31	chr15:99864059-99864109	GM12878	blood:	n/a
32	chr15:99864059-99864109	T-47D	breast:	n/a
33	chr15:99864059-99864109	NHBE	bronchial:	n/a
34	chr15:99864059-99864109	U87	brain:	n/a
35	chr15:99864059-99864109	AG10803	skin:	n/a
36	chr15:99864059-99864109	NH-A	brain:	n/a
37	chr15:99864059-99864109	MCF10A-Er-Src	breast:	n/a
38	chr15:99864059-99864109	HPAEpiC	pulmonary alveolar:	n/a
39	chr15:99864059-99864109	AG04450	lung:	fetal
40	chr15:99864059-99864109	HCT-116	colon:	n/a
41	chr15:99864059-99864109	HEK293	kidney:	embryo
42	chr15:99864059-99864109	HRPEpiC	eye:	n/a
43	chr15:99864059-99864109	MCF-7	breast:	n/a
44	chr15:99864059-99864109	Hela-S3	cervix:	n/a
45	chr15:99864059-99864109	AG09319	gingival:	n/a
46	chr15:99864059-99864109	GM12891	blood:	n/a
47	chr15:99864059-99864109	GM06990	blood:	n/a
48	chr15:99864059-99864109	Hepatocyte	liver:	n/a
49	chr15:99864059-99864109	HCM	heart:	n/a
50	chr15:99864059-99864109	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:99856389..99859314-chr15:99863031..99866195,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000268730	TF binding region
LRRC28	TF binding region
ENSG00000268730	CpG island
LRRC28	CpG island

Extended variants
information (count: 115 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558620463	chr15:99862628-99862629	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs576973976	chr15:99862647-99862648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541130675	chr15:99862662-99862663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563276495	chr15:99862668-99862669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182351553	chr15:99862673-99862674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111878414	chr15:99862675-99862676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112557335	chr15:99862703-99862704	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs561269927	chr15:99862710-99862711	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs530575549	chr15:99862712-99862713	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs185042862	chr15:99862726-99862727	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs542249540	chr15:99862881-99862882	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs192067834	chr15:99862888-99862889	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs183965330	chr15:99862897-99862898	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs532201086	chr15:99862919-99862920	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs547481476	chr15:99862943-99862944	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs188668199	chr15:99863012-99863013	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs530342464	chr15:99863079-99863080	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs191945204	chr15:99863094-99863095	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs140367080	chr15:99863108-99863109	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs537046872	chr15:99863156-99863157	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs370448221	chr15:99863157-99863158	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs552108460	chr15:99863219-99863220	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs570522572	chr15:99863225-99863226	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs531641479	chr15:99863231-99863232	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs534774345	chr15:99863322-99863323	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs77556127	chr15:99863376-99863377	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs547600367	chr15:99863386-99863387	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs572127607	chr15:99863460-99863461	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs536485796	chr15:99863467-99863468	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs554563605	chr15:99863502-99863503	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs183258600	chr15:99863512-99863513	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs543746971	chr15:99863560-99863561	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs564946363	chr15:99863564-99863565	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs187187609	chr15:99863609-99863610	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs8024982	chr15:99863613-99863614	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs35362785	chr15:99863626-99863627	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs551702157	chr15:99863645-99863646	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs570002524	chr15:99863664-99863665	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs367831811	chr15:99863668-99863669	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs537484213	chr15:99863716-99863717	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs114940467	chr15:99863825-99863826	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs191780352	chr15:99863844-99863845	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs563546009	chr15:99863849-99863850	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs183952724	chr15:99863875-99863876	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs186739198	chr15:99863890-99863891	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs570486385	chr15:99863923-99863924	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs549088100	chr15:99863978-99863979	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs111257251	chr15:99864057-99864058	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs547171355	chr15:99864059-99864060	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
50	rs79552925	chr15:99864060-99864061	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99793000-99866600	Weak transcription	Gastric	stomach
2	chr15:99833200-99875800	Weak transcription	Thymus	Thymus
3	chr15:99835200-99864200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:99847400-99877200	Weak transcription	Ovary	ovary
5	chr15:99850400-99863800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:99853000-99876000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr15:99853200-99875400	Weak transcription	Fetal Thymus	thymus
8	chr15:99853600-99875800	Weak transcription	Fetal Intestine Large	intestine
9	chr15:99854200-99864200	Weak transcription	Left Ventricle	heart
10	chr15:99854400-99863600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:99854400-99864000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr15:99854400-99876000	Weak transcription	Dnd41	blood
13	chr15:99858600-99876600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr15:99859400-99906600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr15:99860400-99864400	Enhancers	HMEC	breast
16	chr15:99860400-99864800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr15:99860600-99863200	Enhancers	Liver	Liver
18	chr15:99860600-99864000	Enhancers	Osteobl	bone
19	chr15:99860600-99864200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr15:99860600-99865000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:99860600-99867200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr15:99860600-99867200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr15:99860600-99869200	Enhancers	HepG2	liver
24	chr15:99860800-99863800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:99861000-99862800	Weak transcription	Hela-S3	cervix
26	chr15:99861000-99863000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr15:99861000-99863000	Weak transcription	HSMMtube	muscle
28	chr15:99861000-99864000	Weak transcription	HUVEC	blood vessel
29	chr15:99861000-99864200	Weak transcription	Aorta	Aorta
30	chr15:99861000-99865600	Weak transcription	Psoas Muscle	Psoas
31	chr15:99861200-99863000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr15:99861200-99863200	Weak transcription	Fetal Heart	heart
33	chr15:99861400-99863000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr15:99861400-99863400	Weak transcription	NHLF	lung
35	chr15:99861600-99862800	Enhancers	A549	lung
36	chr15:99861800-99876600	Weak transcription	Primary T cells from cord blood	blood
37	chr15:99862000-99863000	Weak transcription	NH-A	brain
38	chr15:99862400-99862800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr15:99862400-99862800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr15:99862400-99863200	Enhancers	Right Ventricle	heart
41	chr15:99862400-99864400	Enhancers	NHEK	skin
42	chr15:99862600-99863400	Weak transcription	NHDF-Ad	bronchial
43	chr15:99862800-99863200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr15:99862800-99864000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr15:99862800-99864000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr15:99862800-99864200	Enhancers	Hela-S3	cervix
47	chr15:99862800-99865400	Flanking Active TSS	A549	lung
48	chr15:99863000-99863200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr15:99863000-99863200	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr15:99863000-99864000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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