Variant report

Variant	nsv456050
Chromosome Location	chr13:85880422-85952325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:427)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 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	ARID3A	chr13:85947684-85947808	HepG2	liver:	n/a	n/a
2	BHLHE40	chr13:85933207-85933215	GM12878	blood:	n/a	n/a
3	CEBPB	chr13:85903432-85903667	HepG2	liver:	n/a	chr13:85903579-85903590
4	CEBPB	chr13:85892817-85892995	HepG2	liver:	n/a	chr13:85892866-85892877
5	CEBPB	chr13:85927994-85928181	HepG2	liver:	n/a	chr13:85928083-85928092 chr13:85928083-85928094 chr13:85928083-85928092 chr13:85928081-85928094 chr13:85928081-85928094 chr13:85928083-85928092 chr13:85928081-85928094 chr13:85928083-85928092 chr13:85928081-85928092 chr13:85928083-85928094
6	CTCF	chr13:85952000-85952150	HMEC	breast:	n/a	n/a
7	CTCF	chr13:85922000-85922150	AG10803	skin:	n/a	n/a
8	CTCF	chr13:85939105-85939164	Gliobla	brain:	n/a	n/a
9	CTCF	chr13:85952040-85952190	NHEK	skin:	n/a	n/a
10	CTCF	chr13:85925115-85925144	GM20000	blood:	n/a	n/a
11	CTCF	chr13:85900947-85900982	Lung_OC	lung:	n/a	n/a
12	E2F4	chr13:85920604-85920640	MCF10A-Er-Src	breast:	n/a	n/a
13	EBF1	chr13:85890890-85890903	GM12878	blood:	n/a	n/a
14	EP300	chr13:85941725-85942567	SK-N-SH	brain:	n/a	n/a
15	EP300	chr13:85887850-85888194	SK-N-SH_RA	brain:	n/a	chr13:85887961-85887971
16	EP300	chr13:85947428-85947892	HepG2	liver:	n/a	chr13:85947661-85947671
17	EP300	chr13:85945439-85945719	HepG2	liver:	n/a	n/a
18	EP300	chr13:85945461-85945662	HepG2	liver:	n/a	n/a
19	EP300	chr13:85941975-85942518	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr13:85941968-85942460	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr13:85941729-85942534	SK-N-SH	brain:	n/a	n/a
22	EP300	chr13:85887865-85888305	SK-N-SH_RA	brain:	n/a	chr13:85887961-85887971
23	FOS	chr13:85951955-85952326	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr13:85925527-85925822	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr13:85951973-85952334	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr13:85903416-85903671	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr13:85887887-85888293	MCF10A-Er-Src	breast:	n/a	chr13:85888113-85888124
28	FOS	chr13:85925544-85925846	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr13:85951973-85952313	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr13:85903433-85903749	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr13:85903428-85903637	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr13:85903517-85903662	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr13:85887832-85888349	HUVEC	blood vessel:	n/a	chr13:85888113-85888124
34	FOS	chr13:85925534-85925784	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr13:85887935-85888264	MCF10A-Er-Src	breast:	n/a	chr13:85888113-85888124
36	FOS	chr13:85951974-85952307	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr13:85887933-85888266	MCF10A-Er-Src	breast:	n/a	chr13:85888113-85888124
38	FOS	chr13:85887888-85888306	MCF10A-Er-Src	breast:	n/a	chr13:85888113-85888124
39	FOSL1	chr13:85887835-85888296	HCT-116	colon:	n/a	n/a
40	FOSL2	chr13:85941899-85942447	SK-N-SH	brain:	n/a	n/a
41	FOSL2	chr13:85887840-85888347	SK-N-SH	brain:	n/a	n/a
42	FOXA1	chr13:85947414-85947805	A549	lung:	n/a	n/a
43	FOXA1	chr13:85945356-85945687	HepG2	liver:	n/a	chr13:85945563-85945575
44	FOXA1	chr13:85947452-85947810	HepG2	liver:	n/a	n/a
45	FOXA1	chr13:85947470-85947897	HepG2	liver:	n/a	n/a
46	FOXA1	chr13:85947495-85947703	T-47D	breast:	n/a	n/a
47	FOXA1	chr13:85947367-85947820	HepG2	liver:	n/a	n/a
48	FOXA1	chr13:85945339-85945786	HepG2	liver:	n/a	chr13:85945563-85945575
49	FOXA1	chr13:85945390-85945757	HepG2	liver:	n/a	chr13:85945563-85945575
50	FOXA1	chr13:85945293-85945798	HepG2	liver:	n/a	chr13:85945563-85945575

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:85937957-85938007	HCT-116	colon:	n/a
2	chr13:85937957-85938007	PrEC	prostate:	n/a
3	chr13:85937788-85937838	GM12891	blood:	n/a
4	chr13:85937730-85937780	NH-A	brain:	n/a
5	chr13:85937926-85937976	HepG2	liver:	n/a
6	chr13:85937788-85937838	IMR90	lung:	fetal
7	chr13:85915140-85915190	MCF10A-Er-Src	breast:	n/a
8	chr13:85937730-85937780	HNPCEpiC	eye:	n/a
9	chr13:85937730-85937780	ECC-1	luminal epithelium:	n/a
10	chr13:85937926-85937976	U87	brain:	n/a
11	chr13:85937957-85938007	BJ	skin:	n/a
12	chr13:85937788-85937838	U87	brain:	n/a
13	chr13:85937957-85938007	HEEpiC	esophagus:	n/a
14	chr13:85937518-85937568	NB4	blood:	n/a
15	chr13:85937788-85937838	SK-N-SH	brain:	n/a
16	chr13:85937788-85937838	HRE	kidney:	n/a
17	chr13:85915140-85915190	SAEC	small airway:	n/a
18	chr13:85937788-85937838	SKMC	muscle:	n/a
19	chr13:85937518-85937568	AG09319	gingival:	n/a
20	chr13:85937788-85937838	BE2_C	brain:	n/a
21	chr13:85915140-85915190	NB4	blood:	n/a
22	chr13:85937518-85937568	ECC-1	luminal epithelium:	n/a
23	chr13:85937788-85937838	PFSK-1	brain:	n/a
24	chr13:85937788-85937838	NT2-D1	testis:	n/a
25	chr13:85937861-85937911	HCM	heart:	n/a
26	chr13:85937926-85937976	MCF10A-Er-Src	breast:	n/a
27	chr13:85937957-85938007	MCF10A-Er-Src	breast:	n/a
28	chr13:85937926-85937976	HAEpiC	amniotic membrane:	n/a
29	chr13:85915140-85915190	HRE	kidney:	n/a
30	chr13:85937518-85937568	AoSMC	blood vessel:	n/a
31	chr13:85937861-85937911	NHBE	bronchial:	n/a
32	chr13:85937861-85937911	HepG2	liver:	n/a
33	chr13:85937730-85937780	HPAEpiC	pulmonary alveolar:	n/a
34	chr13:85937730-85937780	Hepatocyte	liver:	n/a
35	chr13:85937730-85937780	ovcar-3	ovarian:	n/a
36	chr13:85937730-85937780	HRCEpiC	kidney:	n/a
37	chr13:85937518-85937568	Hepatocyte	liver:	n/a
38	chr13:85937518-85937568	K562	blood:	n/a
39	chr13:85937926-85937976	PANC-1	pancreas:	n/a
40	chr13:85937926-85937976	A549	lung:	n/a
41	chr13:85937518-85937568	HCM	heart:	n/a
42	chr13:85915140-85915190	A549	lung:	n/a
43	chr13:85937788-85937838	LNCaP	prostate:	n/a
44	chr13:85937957-85938007	HRE	kidney:	n/a
45	chr13:85915140-85915190	PANC-1	pancreas:	n/a
46	chr13:85937926-85937976	Caco-2	colon:	n/a
47	chr13:85937518-85937568	Jurkat	blood:	n/a
48	chr13:85937730-85937780	HMEC	breast:	n/a
49	chr13:85937788-85937838	HCT-116	colon:	n/a
50	chr13:85937518-85937568	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:85919914..85922732-chr13:85924658..85927029,2	K562	blood:
2	chr13:85919914..85922732-chr13:85924658..85927029,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-11	chr13:85937736-85938230	XLOC_010460
2	lnc-SLITRK5-11	chr13:85937736-85938230	ENSG00000226317.2
3	lnc-SLITRK5-11	chr13:85937738-85938230	NONHSAT034564
4	lnc-SLITRK5-11	chr13:85937981-85938230	XLOC_010460

No data

Variant related genes	Relation type
LINC00351	TF binding region
LINC00351	CpG island
PDE3B	miRNA target sites

Extended variants
information (count: 852 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541936267	chr13:85883652-85883653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs557204363	chr13:85883657-85883658	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs1412029	chr13:85883666-85883667	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs530528778	chr13:85883671-85883672	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs186414041	chr13:85883680-85883681	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs191177900	chr13:85883698-85883699	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs182958021	chr13:85883738-85883739	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs564440060	chr13:85883759-85883760	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs187593888	chr13:85883770-85883771	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs550204872	chr13:85883792-85883793	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs1175964	chr13:85883801-85883802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs529827206	chr13:85883820-85883821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547962600	chr13:85883851-85883852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566528711	chr13:85883852-85883853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4911062	chr13:85883880-85883881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs558738684	chr13:85883938-85883939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570800230	chr13:85883981-85883982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4911063	chr13:85884000-85884001	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556621953	chr13:85884011-85884012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35128400	chr13:85884032-85884033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10537380	chr13:85884093-85884094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374581403	chr13:85884096-85884097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74799736	chr13:85884110-85884111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4911064	chr13:85884117-85884118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553994864	chr13:85884121-85884122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572453385	chr13:85884136-85884137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191040755	chr13:85884139-85884140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545994238	chr13:85884166-85884167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564333811	chr13:85884308-85884309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1984044	chr13:85884371-85884372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs9531754	chr13:85884407-85884408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543688911	chr13:85884481-85884482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78947300	chr13:85884502-85884503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183306003	chr13:85884525-85884526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529674759	chr13:85884539-85884540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557019955	chr13:85884557-85884558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566448114	chr13:85884565-85884566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566979415	chr13:85884634-85884635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs202053792	chr13:85884635-85884636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527370800	chr13:85884646-85884647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200730336	chr13:85884652-85884653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs137863028	chr13:85884657-85884658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542583569	chr13:85884658-85884659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202096495	chr13:85884661-85884662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs66597786	chr13:85884663-85884664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200215052	chr13:85884664-85884665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72637013	chr13:85884673-85884674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570637674	chr13:85884724-85884725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139081183	chr13:85884763-85884764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75765806	chr13:85884778-85884779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:85883600-85883800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr13:85883800-85887600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:85884200-85887600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr13:85885800-85887400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr13:85886200-85886400	Enhancers	Brain Substantia Nigra	brain
6	chr13:85887400-85887800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:85887400-85888200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr13:85887600-85888400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr13:85887600-85888400	Enhancers	HUVEC	blood vessel
10	chr13:85887600-85888600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr13:85887600-85888800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr13:85887600-85889000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr13:85887800-85888400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:85887800-85888400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr13:85887800-85888400	Enhancers	NHEK	skin
16	chr13:85888000-85888400	Enhancers	Brain Cingulate Gyrus	brain
17	chr13:85888000-85888400	Enhancers	Brain Substantia Nigra	brain
18	chr13:85888000-85888600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr13:85888000-85889200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:85888200-85888600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr13:85888200-85889200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr13:85888200-85889200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr13:85888400-85888800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr13:85888400-85890800	Weak transcription	HUVEC	blood vessel
25	chr13:85888600-85889000	Enhancers	Brain Substantia Nigra	brain
26	chr13:85888800-85889200	Enhancers	Brain Cingulate Gyrus	brain
27	chr13:85888800-85890600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr13:85889200-85890200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr13:85890400-85890600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr13:85890600-85891000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr13:85890600-85891000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr13:85890600-85891000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr13:85890800-85891200	Active TSS	Fetal Muscle Leg	muscle
34	chr13:85890800-85891200	Enhancers	HUVEC	blood vessel
35	chr13:85891000-85895400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr13:85895400-85895800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr13:85911800-85912000	Bivalent Enhancer	Liver	Liver
38	chr13:85915600-85915800	Enhancers	HSMM	muscle
39	chr13:85915600-85916000	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr13:85931200-85933600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr13:85940400-85940600	Enhancers	NH-A	brain
42	chr13:85940600-85941600	Weak transcription	NH-A	brain
43	chr13:85940800-85942600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr13:85941000-85941800	Enhancers	A549	lung
45	chr13:85941400-85943000	Enhancers	Dnd41	blood
46	chr13:85941600-85942000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr13:85941600-85942400	Enhancers	NH-A	brain
48	chr13:85945000-85948000	Enhancers	HepG2	liver
49	chr13:85952000-85952400	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links