Variant report

Variant	esv3332853
Chromosome Location	chr15:75538752-75607377
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	chr15:75566765-75567085	HepG2	liver:	n/a	n/a
2	ATF1	chr15:75600620-75600665	K562	blood:	n/a	n/a
3	BATF	chr15:75566750-75567078	GM12878	blood:	n/a	n/a
4	BATF	chr15:75591658-75591928	GM12878	blood:	n/a	n/a
5	BATF	chr15:75571142-75571340	GM12878	blood:	n/a	n/a
6	BCL11A	chr15:75560181-75560352	GM12878	blood:	n/a	n/a
7	BCL11A	chr15:75553856-75554029	GM12878	blood:	n/a	n/a
8	BCL11A	chr15:75575109-75575293	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:75584457-75584628	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:75571092-75571384	GM12878	blood:	n/a	chr15:75571302-75571309
11	BCL11A	chr15:75550815-75550962	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:75578133-75578306	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:75600364-75600620	HepG2	liver:	n/a	n/a
14	BHLHE40	chr15:75600281-75600726	K562	blood:	n/a	n/a
15	BRCA1	chr15:75600364-75600683	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr15:75591275-75591876	K562	blood:	n/a	n/a
17	CEBPB	chr15:75600378-75600664	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr15:75602157-75602380	HepG2	liver:	n/a	chr15:75602273-75602284
19	CEBPB	chr15:75602115-75602365	HepG2	liver:	n/a	chr15:75602273-75602284
20	CHD2	chr15:75600440-75600690	Hela-S3	cervix:	n/a	n/a
21	CREB1	chr15:75600437-75600670	A549	lung:	n/a	n/a
22	CTCF	chr15:75600520-75600670	HepG2	liver:	n/a	chr15:75600584-75600592 chr15:75600585-75600593
23	CTCF	chr15:75566620-75566770	GM12870	blood:	n/a	n/a
24	CTCF	chr15:75567197-75567315	GM13977	blood:	n/a	n/a
25	CTCF	chr15:75566920-75567070	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr15:75591346-75591455	HepG2	liver:	n/a	n/a
27	CTCF	chr15:75544500-75544650	A549	lung:	n/a	n/a
28	CTCF	chr15:75566920-75567070	HCFaa	heart:	n/a	n/a
29	CTCF	chr15:75605140-75605290	HEK293	kidney:	n/a	n/a
30	CTCF	chr15:75566721-75567173	A549	lung:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
31	CTCF	chr15:75560316-75560347	Lung_OC	lung:	n/a	n/a
32	CTCF	chr15:75600540-75600690	RPTEC	kidney:	n/a	chr15:75600584-75600592 chr15:75600585-75600593
33	CTCF	chr15:75591366-75591866	NHEK	skin:	n/a	chr15:75591467-75591488 chr15:75591478-75591487 chr15:75591745-75591766 chr15:75591751-75591767 chr15:75591473-75591489 chr15:75591756-75591765 chr15:75591750-75591768 chr15:75591472-75591490 chr15:75591752-75591765
34	CTCF	chr15:75591640-75591790	HA-sp	spinal cord:	n/a	chr15:75591745-75591766 chr15:75591751-75591767 chr15:75591756-75591765 chr15:75591750-75591768 chr15:75591752-75591765
35	CTCF	chr15:75600459-75600720	GM12878	blood:	n/a	chr15:75600584-75600592 chr15:75600585-75600593
36	CTCF	chr15:75566900-75567050	SK-N-SH_RA	brain:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566903-75566921
37	CTCF	chr15:75566920-75567210	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr15:75591740-75591890	GM12872	blood:	n/a	chr15:75591745-75591766 chr15:75591751-75591767 chr15:75591756-75591765 chr15:75591750-75591768 chr15:75591752-75591765
39	CTCF	chr15:75567040-75567190	GM06990	blood:	n/a	n/a
40	CTCF	chr15:75591336-75591889	GM12878	blood:	n/a	chr15:75591467-75591488 chr15:75591478-75591487 chr15:75591745-75591766 chr15:75591751-75591767 chr15:75591473-75591489 chr15:75591756-75591765 chr15:75591750-75591768 chr15:75591472-75591490 chr15:75591752-75591765
41	CTCF	chr15:75566920-75567070	GM12864	blood:	n/a	n/a
42	CTCF	chr15:75600540-75600690	MCF-7	breast:	n/a	chr15:75600584-75600592 chr15:75600585-75600593
43	CTCF	chr15:75600520-75600670	GM12873	blood:	n/a	chr15:75600584-75600592 chr15:75600585-75600593
44	CTCF	chr15:75560116-75560472	K562	blood:	n/a	n/a
45	CTCF	chr15:75566697-75567137	K562	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
46	CTCF	chr15:75566840-75566990	GM12864	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
47	CTCF	chr15:75566920-75567070	HL-60	blood:	n/a	n/a
48	CTCF	chr15:75591640-75591790	GM12871	blood:	n/a	chr15:75591745-75591766 chr15:75591751-75591767 chr15:75591756-75591765 chr15:75591750-75591768 chr15:75591752-75591765
49	CTCF	chr15:75600520-75600670	GM12874	blood:	n/a	chr15:75600584-75600592 chr15:75600585-75600593
50	CTCF	chr15:75591620-75591770	RPTEC	kidney:	n/a	chr15:75591745-75591766 chr15:75591751-75591767 chr15:75591756-75591765 chr15:75591750-75591768 chr15:75591752-75591765

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75595395-75595445	HepG2	liver:	n/a
2	chr15:75595395-75595445	HepG2	liver:	n/a
3	chr15:75595395-75595445	AoSMC	blood vessel:	n/a
4	chr15:75586717-75586767	AoSMC	blood vessel:	n/a
5	chr15:75596660-75596710	HNPCEpiC	eye:	n/a
6	chr15:75596489-75596539	H1-hESC	embryonic stem cell:	embryo
7	chr15:75596489-75596539	T-47D	breast:	n/a
8	chr15:75596489-75596539	CMK	blood:	n/a
9	chr15:75595395-75595445	HCM	heart:	n/a
10	chr15:75596660-75596710	PrEC	prostate:	n/a
11	chr15:75586717-75586767	NHDF-neo	bronchial:	n/a
12	chr15:75575161-75575211	HRE	kidney:	n/a
13	chr15:75586717-75586767	Caco-2	colon:	n/a
14	chr15:75596660-75596710	HCF	heart:	n/a
15	chr15:75596489-75596539	Hepatocyte	liver:	n/a
16	chr15:75596660-75596710	NHDF-neo	bronchial:	n/a
17	chr15:75587027-75587077	MCF-7	breast:	n/a
18	chr15:75551123-75551173	ovcar-3	ovarian:	n/a
19	chr15:75575161-75575211	U87	brain:	n/a
20	chr15:75586717-75586767	SKMC	muscle:	n/a
21	chr15:75596660-75596710	AG09309	skin:	n/a
22	chr15:75551123-75551173	Caco-2	colon:	n/a
23	chr15:75596489-75596539	GM12892	blood:	n/a
24	chr15:75586717-75586767	HCT-116	colon:	n/a
25	chr15:75551123-75551173	GM19239	blood:	n/a
26	chr15:75596660-75596710	SK-N-SH	brain:	n/a
27	chr15:75551123-75551173	NB4	blood:	n/a
28	chr15:75596660-75596710	HL-60	blood:	n/a
29	chr15:75587027-75587077	HRCEpiC	kidney:	n/a
30	chr15:75586717-75586767	ovcar-3	ovarian:	n/a
31	chr15:75586717-75586767	GM06990	blood:	n/a
32	chr15:75595395-75595445	AG04450	lung:	fetal
33	chr15:75596489-75596539	MCF10A-Er-Src	breast:	n/a
34	chr15:75596660-75596710	GM19239	blood:	n/a
35	chr15:75596489-75596539	K562	blood:	n/a
36	chr15:75587027-75587077	SK-N-MC	brain:	n/a
37	chr15:75587027-75587077	NHDF-neo	bronchial:	n/a
38	chr15:75575161-75575211	AoSMC	blood vessel:	n/a
39	chr15:75596660-75596710	K562	blood:	n/a
40	chr15:75596489-75596539	ovcar-3	ovarian:	n/a
41	chr15:75587027-75587077	AG09309	skin:	n/a
42	chr15:75595395-75595445	HCF	heart:	n/a
43	chr15:75551123-75551173	HMEC	breast:	n/a
44	chr15:75596660-75596710	AG04450	lung:	fetal
45	chr15:75586717-75586767	BJ	skin:	n/a
46	chr15:75596489-75596539	NT2-D1	testis:	n/a
47	chr15:75551123-75551173	NHBE	bronchial:	n/a
48	chr15:75551123-75551173	GM06990	blood:	n/a
49	chr15:75551123-75551173	RPTEC	kidney:	n/a
50	chr15:75587027-75587077	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:75321592..75322142-chr15:75566565..75567153,2	MCF-7	breast:
2	chr15:75321381..75322163-chr15:75591397..75591903,2	MCF-7	breast:
3	chr15:75505897..75507685-chr15:75540087..75541728,2	MCF-7	breast:
4	chr15:75533027..75534734-chr15:75536293..75539167,2	MCF-7	breast:
5	chr15:75321298..75321970-chr15:75600164..75600664,2	K562	blood:
6	chr15:74600289..74600861-chr15:75566666..75567634,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAN2C1-9	chr15:75564454-75564996	ncRnaDb_ncrna_FR096405_1
2	lnc-GOLGA6D-1	chr15:75590842-75591336	NONHSAT047304
3	lnc-GOLGA6D-3	chr15:75560749-75561024	NONHSAT047302
4	lnc-MAN2C1-8	chr15:75594785-75595005	NONHSAT047305
5	lnc-MAN2C1-8	chr15:75593983-75594076	NONHSAT047305
6	lnc-GOLGA6C-1	chr15:75585025-75585300	NONHSAT047303

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA6A	hsa-miR-192-5p	chr15:75562833-75562852

Variant related genes	Relation type
RN7SL327P	TF binding region
GOLGA6D	TF binding region
ENSG00000260104	TF binding region
GOLGA6C	TF binding region
NIFKP4	TF binding region
RN7SL489P	TF binding region
DNM1P34	TF binding region
RN7SL327P	CpG island
GOLGA6D	CpG island
ENSG00000260104	CpG island
GOLGA6C	CpG island
NIFKP4	CpG island
RN7SL489P	CpG island
DNM1P34	CpG island

Extended variants
information (count: 1145 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556695135	chr15:75538777-75538778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376313381	chr15:75538791-75538792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559609265	chr15:75538793-75538794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147393066	chr15:75538818-75538819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370102613	chr15:75538826-75538827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150595417	chr15:75538851-75538852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543006036	chr15:75538895-75538896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561874260	chr15:75538929-75538930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573864698	chr15:75538933-75538934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544108492	chr15:75538955-75538956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562697770	chr15:75538980-75538981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192727684	chr15:75538982-75538983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2899789	chr15:75539008-75539009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551512269	chr15:75539024-75539025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560284192	chr15:75539072-75539073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12591234	chr15:75539073-75539074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548946745	chr15:75539106-75539107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144196136	chr15:75539137-75539138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530556036	chr15:75539208-75539209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538551891	chr15:75539397-75539398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146560519	chr15:75539456-75539457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554996669	chr15:75539500-75539501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370138966	chr15:75539507-75539508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184252470	chr15:75539516-75539517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538801935	chr15:75539522-75539523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553895747	chr15:75539547-75539548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572199843	chr15:75539604-75539605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189250047	chr15:75539611-75539612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558578233	chr15:75539640-75539641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182239344	chr15:75539675-75539676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549943758	chr15:75539696-75539697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576331864	chr15:75539717-75539718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544513499	chr15:75539737-75539738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562734500	chr15:75539871-75539872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577957054	chr15:75539924-75539925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs8032189	chr15:75539944-75539945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200430311	chr15:75539975-75539976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560321394	chr15:75539987-75539988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527356572	chr15:75539997-75539998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143705225	chr15:75540006-75540007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560953335	chr15:75540007-75540008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569952634	chr15:75540008-75540009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145794737	chr15:75540014-75540015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550451795	chr15:75540015-75540016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571604775	chr15:75540036-75540037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112957412	chr15:75540196-75540197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552545857	chr15:75540226-75540227	Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566383566	chr15:75540267-75540268	Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184634887	chr15:75540402-75540403	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189445857	chr15:75540409-75540410	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	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
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital diaphragmatic hernia	21525063	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75538000-75545400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:75540000-75540200	Enhancers	H9 Cell Line	embryonic stem cell
3	chr15:75540000-75540400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:75540000-75541600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr15:75540200-75540400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:75540200-75542200	Enhancers	Fetal Intestine Small	intestine
7	chr15:75540200-75544600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr15:75540400-75540600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:75540400-75542200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr15:75540400-75542400	Enhancers	Fetal Intestine Large	intestine
11	chr15:75540600-75540800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:75540600-75542200	Bivalent Enhancer	HepG2	liver
13	chr15:75541600-75541800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr15:75541600-75542600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr15:75541800-75542000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr15:75541800-75542400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr15:75541800-75542400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr15:75541800-75542400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr15:75542000-75542400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr15:75542000-75542400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:75542000-75542400	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr15:75542200-75542400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr15:75542400-75544600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr15:75542400-75544600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr15:75542400-75545400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr15:75542600-75544600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr15:75544600-75544800	Enhancers	H9 Cell Line	embryonic stem cell
28	chr15:75544600-75544800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr15:75544600-75546200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr15:75544600-75547000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr15:75544800-75545200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr15:75544800-75545400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr15:75545200-75545600	Enhancers	H9 Cell Line	embryonic stem cell
34	chr15:75545400-75545800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:75545400-75546200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr15:75545400-75546200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr15:75545400-75546200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr15:75545600-75546200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr15:75545600-75546200	Enhancers	HepG2	liver
40	chr15:75545600-75546400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr15:75546000-75546400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr15:75566200-75567200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr15:75566400-75568000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:75566600-75567200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr15:75566600-75567200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr15:75566800-75567200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr15:75566800-75567400	Enhancers	Liver	Liver
48	chr15:75567000-75567200	Enhancers	Spleen	Spleen
49	chr15:75567000-75567200	Bivalent Enhancer	HepG2	liver
50	chr15:75567000-75567400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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