Variant report

Variant	nsv900724
Chromosome Location	chr13:85612388-85726019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr13:85669014-85669111	GM12878	blood:	n/a	n/a
2	CEBPB	chr13:85645107-85645368	Hela-S3	cervix:	n/a	chr13:85645332-85645343
3	CEBPB	chr13:85646691-85646960	HepG2	liver:	n/a	n/a
4	CEBPB	chr13:85645141-85645432	HepG2	liver:	n/a	chr13:85645332-85645343
5	CEBPB	chr13:85692248-85692429	K562	blood:	n/a	n/a
6	CEBPB	chr13:85692255-85692467	IMR90	lung:	n/a	n/a
7	CTCF	chr13:85643020-85643170	HRE	kidney:	n/a	n/a
8	CTCF	chr13:85634612-85634648	Lung_OC	lung:	n/a	n/a
9	CTCF	chr13:85680580-85680730	AG04449	skin:	n/a	n/a
10	CTCF	chr13:85706120-85706270	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr13:85692540-85692690	AG04450	lung:	n/a	n/a
12	CTCF	chr13:85624600-85624750	MCF-7	breast:	n/a	n/a
13	CTCF	chr13:85624540-85624690	BE2_C	brain:	n/a	n/a
14	CTCF	chr13:85692620-85692770	HPF	lung:	n/a	n/a
15	CTCF	chr13:85624600-85624750	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr13:85624520-85624749	MCF-7	breast:	n/a	n/a
17	CTCF	chr13:85624546-85624707	MCF-7	breast:	n/a	n/a
18	CUX1	chr13:85613027-85613183	K562	blood:	n/a	n/a
19	E2F4	chr13:85630665-85630817	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr13:85668091-85668291	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr13:85620331-85620613	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr13:85714352-85714513	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr13:85713480-85713554	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr13:85692842-85692853	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr13:85637348-85637382	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr13:85625808-85626008	GM12878	blood:	n/a	chr13:85625835-85625846
27	EP300	chr13:85670169-85670397	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr13:85711338-85712377	SK-N-SH	brain:	n/a	chr13:85711470-85711484
29	EP300	chr13:85614333-85614723	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr13:85614261-85615578	SK-N-SH	brain:	n/a	n/a
31	EP300	chr13:85670159-85670363	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr13:85614375-85614679	SK-N-SH_RA	brain:	n/a	n/a
33	FOS	chr13:85667917-85668341	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr13:85667980-85668353	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr13:85649109-85649403	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr13:85649165-85649370	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr13:85620522-85620759	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr13:85667944-85668398	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr13:85714281-85714669	MCF10A-Er-Src	breast:	n/a	chr13:85714473-85714483 chr13:85714473-85714483 chr13:85714474-85714482 chr13:85714474-85714482 chr13:85714475-85714482
40	FOS	chr13:85667878-85668383	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr13:85714321-85714632	MCF10A-Er-Src	breast:	n/a	chr13:85714473-85714483 chr13:85714473-85714483 chr13:85714474-85714482 chr13:85714474-85714482 chr13:85714475-85714482
42	FOS	chr13:85720390-85720419	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr13:85714305-85714668	MCF10A-Er-Src	breast:	n/a	chr13:85714473-85714483 chr13:85714473-85714483 chr13:85714474-85714482 chr13:85714474-85714482 chr13:85714475-85714482
44	FOS	chr13:85633131-85633232	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr13:85714286-85714669	MCF10A-Er-Src	breast:	n/a	chr13:85714473-85714483 chr13:85714473-85714483 chr13:85714474-85714482 chr13:85714474-85714482 chr13:85714475-85714482
46	FOXA2	chr13:85697536-85698015	A549	lung:	n/a	n/a
47	FOXA2	chr13:85697477-85697986	A549	lung:	n/a	n/a
48	FOXP2	chr13:85715630-85715867	SK-N-MC	brain:	n/a	n/a
49	FOXP2	chr13:85668083-85668290	PFSK-1	brain:	n/a	n/a
50	FOXP2	chr13:85716387-85716680	SK-N-MC	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:85715101-85715151	HAEpiC	amniotic membrane:	n/a
2	chr13:85697598-85697648	HL-60	blood:	n/a
3	chr13:85715101-85715151	NB4	blood:	n/a
4	chr13:85697598-85697648	HCT-116	colon:	n/a
5	chr13:85697598-85697648	LNCaP	prostate:	n/a
6	chr13:85697598-85697648	ECC-1	luminal epithelium:	n/a
7	chr13:85715101-85715151	SKMC	muscle:	n/a
8	chr13:85715101-85715151	HEK293	kidney:	embryo
9	chr13:85715101-85715151	GM06990	blood:	n/a
10	chr13:85697598-85697648	T-47D	breast:	n/a
11	chr13:85715101-85715151	HNPCEpiC	eye:	n/a
12	chr13:85697598-85697648	Caco-2	colon:	n/a
13	chr13:85697598-85697648	PANC-1	pancreas:	n/a
14	chr13:85697598-85697648	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:85697598-85697648	HEK293	kidney:	embryo
16	chr13:85715101-85715151	HepG2	liver:	n/a
17	chr13:85697598-85697648	NH-A	brain:	n/a
18	chr13:85715101-85715151	PANC-1	pancreas:	n/a
19	chr13:85697598-85697648	HCPEpiC	choroid plexus:	n/a
20	chr13:85715101-85715151	Jurkat	blood:	n/a
21	chr13:85697598-85697648	GM19239	blood:	n/a
22	chr13:85715101-85715151	U87	brain:	n/a
23	chr13:85697598-85697648	HMEC	breast:	n/a
24	chr13:85697598-85697648	NB4	blood:	n/a
25	chr13:85697598-85697648	GM12891	blood:	n/a
26	chr13:85697598-85697648	HepG2	liver:	n/a
27	chr13:85715101-85715151	ovcar-3	ovarian:	n/a
28	chr13:85715101-85715151	HMEC	breast:	n/a
29	chr13:85715101-85715151	A549	lung:	n/a
30	chr13:85697598-85697648	PFSK-1	brain:	n/a
31	chr13:85697598-85697648	H1-hESC	embryonic stem cell:	embryo
32	chr13:85715101-85715151	MCF-7	breast:	n/a
33	chr13:85697598-85697648	SK-N-MC	brain:	n/a
34	chr13:85715101-85715151	ECC-1	luminal epithelium:	n/a
35	chr13:85697598-85697648	SAEC	small airway:	n/a
36	chr13:85697598-85697648	HRE	kidney:	n/a
37	chr13:85715101-85715151	HRE	kidney:	n/a
38	chr13:85715101-85715151	AG10803	skin:	n/a
39	chr13:85715101-85715151	LNCaP	prostate:	n/a
40	chr13:85697598-85697648	NT2-D1	testis:	n/a
41	chr13:85715101-85715151	GM12878	blood:	n/a
42	chr13:85715101-85715151	IMR90	lung:	fetal
43	chr13:85715101-85715151	NT2-D1	testis:	n/a
44	chr13:85715101-85715151	SAEC	small airway:	n/a
45	chr13:85715101-85715151	GM12891	blood:	n/a
46	chr13:85697598-85697648	MCF10A-Er-Src	breast:	n/a
47	chr13:85697598-85697648	HAEpiC	amniotic membrane:	n/a
48	chr13:85697598-85697648	GM06990	blood:	n/a
49	chr13:85715101-85715151	AG09309	skin:	n/a
50	chr13:85715101-85715151	NHBE	bronchial:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:85665406..85665957-chr9:85236784..85237385,2	MCF-7	breast:
2	chr13:85624379..85624909-chr13:86373073..86373588,2	MCF-7	breast:
3	chr12:102083101..102085803-chr13:85724711..85727561,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-3	chr13:85691327-85691464	XLOC_010679
2	lnc-SLITRK6-3	chr13:85685979-85687120	XLOC_010679
3	lnc-SLITRK6-3	chr13:85722163-85722284	XLOC_010679
4	lnc-SLITRK6-4	chr13:85639222-85639353	ENSG00000226370
5	lnc-SLITRK6-3	chr13:85691327-85691458	XLOC_010679
6	lnc-SLITRK6-3	chr13:85722163-85722284	XLOC_010679
7	lnc-SLITRK6-4	chr13:85650938-85651117	ENSG00000226370
8	lnc-SLITRK6-3	chr13:85686774-85687120	XLOC_010679
9	lnc-SLITRK6-3	chr13:85718789-85719009	XLOC_010679
10	lnc-SLITRK6-4	chr13:85642135-85642163	ENSG00000226370
11	lnc-SLITRK6-4	chr13:85649179-85649279	ENSG00000226370
12	lnc-SLITRK6-4	chr13:85652897-85653055	ENSG00000226370

No data

Variant related genes	Relation type
LINC00375	TF binding region
LINC00375	CpG island

Extended variants
information (count: 1607 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1607 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9319110	chr13:85612388-85612389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367721847	chr13:85612441-85612442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76421264	chr13:85612480-85612481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556386055	chr13:85612487-85612488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77296077	chr13:85612488-85612489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112323849	chr13:85612503-85612504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560639343	chr13:85612510-85612511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371510745	chr13:85612550-85612551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572770209	chr13:85612577-85612578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9593969	chr13:85612591-85612592	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs564959812	chr13:85612618-85612619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9593970	chr13:85612619-85612620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs9593971	chr13:85612641-85612642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs142365682	chr13:85612670-85612671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529860657	chr13:85612672-85612673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535393023	chr13:85612716-85612717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190352600	chr13:85612717-85612718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9575717	chr13:85612721-85612722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534181850	chr13:85612760-85612761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550127448	chr13:85612763-85612764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536257566	chr13:85612782-85612783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79712151	chr13:85612796-85612797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552192187	chr13:85612817-85612818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182917889	chr13:85612848-85612849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9602633	chr13:85612867-85612868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7992697	chr13:85612883-85612884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574942121	chr13:85612920-85612921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151269887	chr13:85612925-85612926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554425823	chr13:85612937-85612938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201353128	chr13:85612969-85612970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188819108	chr13:85612979-85612980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540226221	chr13:85612983-85612984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9575718	chr13:85613018-85613019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs576913767	chr13:85613029-85613030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544286675	chr13:85613047-85613048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79307795	chr13:85613064-85613065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529875111	chr13:85613124-85613125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141586428	chr13:85613140-85613141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560385399	chr13:85613165-85613166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369507261	chr13:85613166-85613167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576101051	chr13:85613181-85613182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552055740	chr13:85613192-85613193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570472153	chr13:85613213-85613214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111842906	chr13:85613222-85613223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543154229	chr13:85613241-85613242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549835508	chr13:85613257-85613258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58674304	chr13:85613287-85613288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs58210939	chr13:85613304-85613305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs554114009	chr13:85613337-85613338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566363074	chr13:85613387-85613388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	19490664	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:85608600-85615600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:85615600-85616200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:85627000-85627200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr13:85627200-85628600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr13:85628600-85629400	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr13:85629400-85631800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr13:85631800-85632000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr13:85642000-85642800	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr13:85642000-85643200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr13:85643000-85643400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:85643000-85643600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr13:85650400-85651200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr13:85651200-85654800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr13:85651400-85652000	Enhancers	Fetal Lung	lung
15	chr13:85654400-85654800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:85654800-85655600	Enhancers	Fetal Heart	heart
17	chr13:85654800-85655800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr13:85665600-85666800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr13:85665600-85666800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr13:85665800-85667200	Enhancers	NHEK	skin
21	chr13:85667200-85667600	Weak transcription	NHEK	skin
22	chr13:85667600-85668600	Enhancers	NHEK	skin
23	chr13:85667800-85668200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:85668000-85668600	Enhancers	HMEC	breast
25	chr13:85670200-85670400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:85670600-85671600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:85671600-85672400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr13:85676600-85677200	Active TSS	Aorta	Aorta
29	chr13:85680600-85681200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:85682000-85683400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr13:85682400-85682800	Enhancers	NHEK	skin
32	chr13:85682400-85683200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr13:85682400-85683200	Enhancers	Esophagus	oesophagus
34	chr13:85682400-85683400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr13:85682400-85683600	Enhancers	HMEC	breast
36	chr13:85682600-85682800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr13:85682600-85683000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr13:85682600-85683400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr13:85682800-85683000	Flanking Active TSS	NHEK	skin
40	chr13:85683000-85683400	ZNF genes & repeats	NHEK	skin
41	chr13:85697400-85698000	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr13:85697600-85698000	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr13:85711200-85712000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr13:85711600-85712200	Enhancers	Fetal Heart	heart
45	chr13:85711600-85712200	Enhancers	NHEK	skin
46	chr13:85711800-85712000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr13:85711800-85712200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr13:85711800-85712600	Enhancers	HMEC	breast
49	chr13:85712000-85714000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr13:85712200-85713800	Weak transcription	NHEK	skin

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