Variant report

Variant	nsv974118
Chromosome Location	chr13:96346708-96351488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr13:96348516-96348806	GM12878	blood:	n/a	n/a
2	CEBPB	chr13:96350308-96350657	Hela-S3	cervix:	n/a	chr13:96350467-96350478
3	CEBPB	chr13:96350322-96350667	HepG2	liver:	n/a	chr13:96350467-96350478
4	CEBPB	chr13:96350298-96350626	K562	blood:	n/a	chr13:96350467-96350478
5	CEBPB	chr13:96350303-96350649	H1-hESC	embryonic stem cell:	n/a	chr13:96350467-96350478
6	CEBPB	chr13:96350253-96350748	MCF-7	breast:	n/a	chr13:96350467-96350478
7	CEBPB	chr13:96350285-96350663	HepG2	liver:	n/a	chr13:96350467-96350478
8	CEBPB	chr13:96350213-96350602	MCF-7	breast:	n/a	chr13:96350467-96350478
9	CEBPB	chr13:96350295-96350646	IMR90	lung:	n/a	chr13:96350467-96350478
10	CEBPB	chr13:96350334-96350593	ECC-1	luminal epithelium:	n/a	chr13:96350467-96350478
11	CEBPB	chr13:96350416-96350574	HepG2	liver:	n/a	chr13:96350467-96350478
12	CEBPB	chr13:96350282-96350634	A549	lung:	n/a	chr13:96350467-96350478
13	CEBPB	chr13:96350289-96350665	K562	blood:	n/a	chr13:96350467-96350478
14	CTCF	chr13:96350424-96350550	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr13:96350420-96350570	RPTEC	kidney:	n/a	n/a
16	CTCF	chr13:96350400-96350550	GM12873	blood:	n/a	n/a
17	CTCF	chr13:96350420-96350570	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr13:96350360-96350510	GM12864	blood:	n/a	n/a
19	CTCF	chr13:96350420-96350570	BJ	skin:	n/a	n/a
20	CTCF	chr13:96350440-96350590	GM12870	blood:	n/a	n/a
21	CTCF	chr13:96350740-96350890	GM12865	blood:	n/a	n/a
22	CTCF	chr13:96350460-96350610	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr13:96350400-96350550	GM12875	blood:	n/a	n/a
24	CTCF	chr13:96350360-96350510	GM06990	blood:	n/a	n/a
25	CTCF	chr13:96350400-96350550	HEK293	kidney:	n/a	n/a
26	CTCF	chr13:96350400-96350550	HCM	heart:	n/a	n/a
27	CTCF	chr13:96350400-96350550	SAEC	small airway:	n/a	n/a
28	CTCF	chr13:96350460-96350610	HRE	kidney:	n/a	n/a
29	CTCF	chr13:96350680-96350830	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr13:96350380-96350530	GM12872	blood:	n/a	n/a
31	CTCF	chr13:96350420-96350570	GM12868	blood:	n/a	n/a
32	CTCF	chr13:96350400-96350550	HMEC	breast:	n/a	n/a
33	CTCF	chr13:96350400-96350550	AG09319	gingival:	n/a	n/a
34	CTCF	chr13:96350420-96350570	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr13:96350440-96350590	MCF-7	breast:	n/a	n/a
36	CTCF	chr13:96350360-96350510	GM12874	blood:	n/a	n/a
37	CTCF	chr13:96350460-96350610	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr13:96350400-96350550	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr13:96350380-96350530	AG10803	skin:	n/a	n/a
40	CTCF	chr13:96350440-96350590	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr13:96350420-96350570	GM12870	blood:	n/a	n/a
42	CTCF	chr13:96350720-96350870	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr13:96350375-96350568	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr13:96350380-96350530	GM12865	blood:	n/a	n/a
45	CTCF	chr13:96350380-96350530	AG04450	lung:	n/a	n/a
46	CTCF	chr13:96350440-96350590	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr13:96350420-96350570	HMEC	breast:	n/a	n/a
48	CTCF	chr13:96350460-96350610	GM12867	blood:	n/a	n/a
49	CTCF	chr13:96350329-96350658	IMR90	lung:	n/a	n/a
50	CTCF	chr13:96350430-96350560	GM12878	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:96345027..96347672-chr13:96350101..96351866,2	K562	blood:
2	chr13:96329213..96330784-chr13:96346091..96348298,2	MCF-7	breast:
3	chr13:96328787..96332431-chr13:96349403..96351175,3	K562	blood:
4	chr13:96327018..96329777-chr13:96348435..96352062,3	MCF-7	breast:
5	chr13:96327692..96330287-chr13:96346205..96350903,4	K562	blood:
6	chr13:96349364..96351436-chr13:96453335..96455358,2	MCF-7	breast:
7	chr13:96347421..96350839-chr13:96352908..96355509,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DZIP1-5	chr13:96346237-96346749	NONHSAT034771

No data

Variant related genes	Relation type
MTND6P18	TF binding region
MTCYBP3	TF binding region
ENSG00000227714	chromatin interactions
ENSG00000232373	chromatin interactions
ENSG00000102580	chromatin interactions
ENSG00000247400	chromatin interactions

Extended variants
information (count: 165 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:165 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189928489	chr13:96346734-96346735	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs532569352	chr13:96346784-96346785	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs140879703	chr13:96346794-96346795	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546047353	chr13:96346875-96346876	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs17879147	chr13:96346936-96346937	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs527898095	chr13:96346937-96346938	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541591946	chr13:96346939-96346940	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs180735873	chr13:96346963-96346964	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145135890	chr13:96346992-96346993	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186120770	chr13:96346993-96346994	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569576952	chr13:96346994-96346995	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs528829543	chr13:96347044-96347045	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs190199613	chr13:96347046-96347047	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs17878928	chr13:96347077-96347078	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs565594847	chr13:96347091-96347092	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs17878616	chr13:96347095-96347096	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557711102	chr13:96347114-96347115	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571407307	chr13:96347124-96347125	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562858255	chr13:96347164-96347165	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs9561932	chr13:96347177-96347178	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs556594907	chr13:96347250-96347251	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576522267	chr13:96347274-96347275	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs17886940	chr13:96347304-96347305	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12870185	chr13:96347321-96347322	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs556098446	chr13:96347324-96347325	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs376530634	chr13:96347365-96347366	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs144946325	chr13:96347411-96347412	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs186428327	chr13:96347517-96347518	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190443017	chr13:96347548-96347549	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs17885445	chr13:96347570-96347571	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs564558873	chr13:96347602-96347603	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527827371	chr13:96347625-96347626	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs17882474	chr13:96347636-96347637	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs17884908	chr13:96347667-96347668	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs182988682	chr13:96347668-96347669	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543173979	chr13:96347676-96347677	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563359615	chr13:96347682-96347683	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528866374	chr13:96347693-96347694	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548520313	chr13:96347708-96347709	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs149044071	chr13:96347719-96347720	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs566626675	chr13:96347727-96347728	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs17882010	chr13:96347748-96347749	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs371119877	chr13:96347774-96347775	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551634202	chr13:96347777-96347778	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186249199	chr13:96347811-96347812	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs191492412	chr13:96347812-96347813	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550017688	chr13:96347881-96347882	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs17879910	chr13:96347889-96347890	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535949784	chr13:96347896-96347897	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs555838524	chr13:96347908-96347909	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	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
Metanephric adenoma	20802469	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96331400-96350600	Weak transcription	Aorta	Aorta
2	chr13:96331400-96362200	Weak transcription	HSMM	muscle
3	chr13:96332000-96348000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr13:96332400-96360400	Weak transcription	NHDF-Ad	bronchial
5	chr13:96332600-96350200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr13:96337400-96347600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr13:96337400-96350400	Weak transcription	Lung	lung
8	chr13:96337600-96347200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr13:96337600-96347800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:96337600-96348400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:96337600-96350400	Weak transcription	Pancreas	Pancrea
12	chr13:96337600-96350400	Weak transcription	Right Ventricle	heart
13	chr13:96337600-96350400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr13:96337600-96350400	Weak transcription	Small Intestine	intestine
15	chr13:96337600-96356000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr13:96337600-96358800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr13:96337600-96360800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr13:96337600-96362200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr13:96337600-96364200	Weak transcription	Ovary	ovary
20	chr13:96341000-96350600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr13:96341200-96350400	Weak transcription	Psoas Muscle	Psoas
22	chr13:96341200-96350400	Weak transcription	Right Atrium	heart
23	chr13:96342000-96350400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr13:96342000-96350400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr13:96342000-96350600	Weak transcription	Liver	Liver
26	chr13:96342200-96349200	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr13:96343400-96347000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr13:96344200-96348200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:96345000-96352600	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr13:96345200-96362200	Weak transcription	Duodenum Mucosa	Duodenum
31	chr13:96345800-96347800	Weak transcription	Fetal Lung	lung
32	chr13:96346000-96347000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:96346400-96346800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr13:96346400-96348600	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr13:96346400-96350200	Weak transcription	Fetal Heart	heart
36	chr13:96346600-96350000	ZNF genes & repeats	GM12878-XiMat	blood
37	chr13:96346600-96350600	Weak transcription	Brain Anterior Caudate	brain
38	chr13:96346800-96348600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr13:96346800-96349600	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr13:96347000-96347400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
41	chr13:96347000-96348600	ZNF genes & repeats	Primary T cells from cord blood	blood
42	chr13:96347000-96348600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr13:96347000-96349200	Weak transcription	Adipose Nuclei	Adipose
44	chr13:96347000-96351000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr13:96347000-96377600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr13:96347200-96348200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr13:96347200-96349000	ZNF genes & repeats	Primary B cells from cord blood	blood
48	chr13:96347400-96350400	Weak transcription	HSMMtube	muscle
49	chr13:96347600-96348200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr13:96347600-96348800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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