Variant report

Variant	nsv461597
Chromosome Location	chr4:102968082-103016878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:103007318-103007577	HepG2	liver:	n/a	chr4:103007450-103007461
2	CEBPB	chr4:102969012-102969231	HepG2	liver:	n/a	chr4:102969164-102969175 chr4:102969113-102969126 chr4:102969113-102969126 chr4:102969113-102969124 chr4:102969113-102969124 chr4:102969114-102969125
3	CEBPB	chr4:103007377-103007553	A549	lung:	n/a	chr4:103007450-103007461
4	CEBPB	chr4:103007322-103007591	IMR90	lung:	n/a	chr4:103007450-103007461
5	CEBPB	chr4:102997869-102998165	A549	lung:	n/a	n/a
6	CTCF	chr4:102977040-102977190	HRPEpiC	eye:	n/a	n/a
7	CTCF	chr4:102976980-102977130	RPTEC	kidney:	n/a	n/a
8	CTCF	chr4:102977240-102977390	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr4:102977320-102977470	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr4:102977040-102977190	HMF	breast:	n/a	n/a
11	CTCF	chr4:102976980-102977130	AG04450	lung:	n/a	n/a
12	CTCF	chr4:102977080-102977230	HVMF	connective:	n/a	n/a
13	CTCF	chr4:102977088-102977234	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr4:102977060-102977210	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr4:102977100-102977250	SAEC	small airway:	n/a	n/a
16	CTCF	chr4:102973299-102973366	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:102977060-102977210	SAEC	small airway:	n/a	n/a
18	CTCF	chr4:102977220-102977370	HCFaa	heart:	n/a	n/a
19	CTCF	chr4:102977180-102977330	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr4:102977080-102977230	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr4:102977060-102977210	GM12864	blood:	n/a	n/a
22	CTCF	chr4:102977333-102977359	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr4:102977040-102977190	GM12871	blood:	n/a	n/a
24	CTCF	chr4:102977060-102977210	HEK293	kidney:	n/a	n/a
25	CTCF	chr4:102977040-102977190	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr4:102977060-102977210	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr4:102977320-102977470	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr4:102977060-102977210	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr4:102976980-102977130	GM12864	blood:	n/a	n/a
30	CTCF	chr4:102977200-102977350	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr4:102977040-102977190	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr4:103014580-103014730	GM12870	blood:	n/a	n/a
33	CTCF	chr4:102977100-102977250	NHEK	skin:	n/a	n/a
34	CTCF	chr4:102977240-102977390	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr4:102977180-102977330	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr4:102977120-102977350	NHEK	skin:	n/a	n/a
37	CTCF	chr4:103006381-103006456	GM10266	blood:	n/a	n/a
38	CTCF	chr4:102977120-102977270	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:102977220-102977370	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr4:102977100-102977250	HMEC	breast:	n/a	n/a
41	CTCF	chr4:102977080-102977230	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr4:102977000-102977150	AG09319	gingival:	n/a	n/a
43	CTCF	chr4:102977020-102977170	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr4:102977080-102977230	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr4:102977180-102977330	HCT-116	colon:	n/a	n/a
46	CTCF	chr4:102977200-102977350	RPTEC	kidney:	n/a	n/a
47	CTCF	chr4:102977080-102977230	GM12873	blood:	n/a	n/a
48	CTCF	chr4:102977060-102977210	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr4:102977120-102977270	HCT-116	colon:	n/a	n/a
50	CTCF	chr4:102977060-102977210	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102995477-102995527	CMK	blood:	n/a
2	chr4:102995477-102995527	RPTEC	kidney:	n/a
3	chr4:102995477-102995527	K562	blood:	n/a
4	chr4:102995477-102995527	ECC-1	luminal epithelium:	n/a
5	chr4:102995477-102995527	HEEpiC	esophagus:	n/a
6	chr4:102995477-102995527	AG04449	skin:	fetal
7	chr4:102995477-102995527	PANC-1	pancreas:	n/a
8	chr4:102995477-102995527	A549	lung:	n/a
9	chr4:102995477-102995527	AG04450	lung:	fetal
10	chr4:102995477-102995527	NB4	blood:	n/a
11	chr4:102995477-102995527	AG09309	skin:	n/a
12	chr4:102995477-102995527	Hela-S3	cervix:	n/a
13	chr4:102995477-102995527	HCPEpiC	choroid plexus:	n/a
14	chr4:102995477-102995527	SKMC	muscle:	n/a
15	chr4:102995477-102995527	SK-N-MC	brain:	n/a
16	chr4:102995477-102995527	SK-N-SH_RA	brain:	n/a
17	chr4:102995477-102995527	BJ	skin:	n/a
18	chr4:102995477-102995527	PFSK-1	brain:	n/a
19	chr4:102995477-102995527	HCT-116	colon:	n/a
20	chr4:102995477-102995527	MCF-7	breast:	n/a
21	chr4:102995477-102995527	HCF	heart:	n/a
22	chr4:102995477-102995527	HEK293	kidney:	embryo
23	chr4:102995477-102995527	GM12891	blood:	n/a
24	chr4:102995477-102995527	BE2_C	brain:	n/a
25	chr4:102995477-102995527	ovcar-3	ovarian:	n/a
26	chr4:102995477-102995527	HMEC	breast:	n/a
27	chr4:102995477-102995527	HUVEC	blood vessel:	n/a
28	chr4:102995477-102995527	HRE	kidney:	n/a
29	chr4:102995477-102995527	AG09319	gingival:	n/a
30	chr4:102995477-102995527	HRPEpiC	eye:	n/a
31	chr4:102995477-102995527	NH-A	brain:	n/a
32	chr4:102995477-102995527	T-47D	breast:	n/a
33	chr4:102995477-102995527	U87	brain:	n/a
34	chr4:102995477-102995527	HNPCEpiC	eye:	n/a
35	chr4:102995477-102995527	NHBE	bronchial:	n/a
36	chr4:102995477-102995527	AoSMC	blood vessel:	n/a
37	chr4:102995477-102995527	HIPEpiC	eye:	n/a
38	chr4:102995477-102995527	PrEC	prostate:	n/a
39	chr4:102995477-102995527	HL-60	blood:	n/a
40	chr4:102995477-102995527	HepG2	liver:	n/a
41	chr4:102995477-102995527	AG10803	skin:	n/a
42	chr4:102995477-102995527	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:102995477-102995527	GM06990	blood:	n/a
44	chr4:102995477-102995527	Hepatocyte	liver:	n/a
45	chr4:102995477-102995527	Jurkat	blood:	n/a
46	chr4:102995477-102995527	SAEC	small airway:	n/a
47	chr4:102995477-102995527	NT2-D1	testis:	n/a
48	chr4:102995477-102995527	HRCEpiC	kidney:	n/a
49	chr4:102995477-102995527	HAEpiC	amniotic membrane:	n/a
50	chr4:102995477-102995527	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:102983408..102985207-chr4:102988825..102991000,2	MCF-7	breast:
2	chr4:102983408..102985207-chr4:102988825..102991000,2	MCF-7	breast:
3	chr4:102984591..102987150-chr4:102995563..102997735,2	MCF-7	breast:
4	chr4:102984591..102987150-chr4:102995563..102997735,2	MCF-7	breast:
5	chr4:103006830..103008574-chr4:103015934..103018544,2	K562	blood:
6	chr17:56735383..56737967-chr4:102987580..102990239,2	MCF-7	breast:
7	chr4:103006830..103008574-chr4:103015934..103018544,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NFKB1-5	chr4:102995162-102995377	NONHSAT097576
2	lnc-NFKB1-5	chr4:102994841-102994905	NONHSAT097576
3	lnc-NFKB1-5	chr4:102992432-102992461	NONHSAT097576
4	lnc-NFKB1-5	chr4:102982573-102984295	NONHSAT097576
5	lnc-NFKB1-5	chr4:102993502-102993557	NONHSAT097576

No data

Variant related genes	Relation type
BANK1	TF binding region
BANK1	CpG island
ENSG00000202077	chromatin interactions

Extended variants
information (count: 1145 )
Associated
traits (count: 77 )

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	rs2850395	chr4:102968082-102968083	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115119117	chr4:102968085-102968086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190481974	chr4:102968121-102968122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537973330	chr4:102968213-102968214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78591044	chr4:102968255-102968256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565261080	chr4:102968262-102968263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs71597116	chr4:102968271-102968272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76122686	chr4:102968303-102968304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377620404	chr4:102968324-102968325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554156219	chr4:102968354-102968355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78200954	chr4:102968371-102968372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143515217	chr4:102968432-102968433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545774876	chr4:102968433-102968434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183418421	chr4:102968442-102968443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2850396	chr4:102968448-102968449	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547880671	chr4:102968487-102968488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115989222	chr4:102968533-102968534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563076133	chr4:102968537-102968538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530277406	chr4:102968541-102968542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17211449	chr4:102968557-102968558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111570785	chr4:102968588-102968589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11326096	chr4:102968590-102968591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560375957	chr4:102968605-102968606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571827598	chr4:102968628-102968629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527983911	chr4:102968631-102968632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570292265	chr4:102968658-102968659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552518140	chr4:102968694-102968695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375019230	chr4:102968695-102968696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187076427	chr4:102968714-102968715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114413831	chr4:102968748-102968749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550032220	chr4:102968828-102968829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568240096	chr4:102968906-102968907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535689196	chr4:102968907-102968908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554018071	chr4:102968919-102968920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60836428	chr4:102968932-102968933	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191116717	chr4:102968947-102968948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551911594	chr4:102968983-102968984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557721613	chr4:102969023-102969024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564117482	chr4:102969047-102969048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575981981	chr4:102969124-102969125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183324382	chr4:102969169-102969170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534426912	chr4:102969182-102969183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555212964	chr4:102969188-102969189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573414830	chr4:102969264-102969265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527476562	chr4:102969340-102969341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187499498	chr4:102969348-102969349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191284718	chr4:102969412-102969413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183087994	chr4:102969422-102969423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564481571	chr4:102969430-102969431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531653839	chr4:102969484-102969485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102951800-102979200	Strong transcription	Primary B cells from peripheral blood	blood
2	chr4:102958400-102983600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:102967600-102976000	Strong transcription	Primary B cells from cord blood	blood
4	chr4:102970800-102971600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:102971600-102990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:102973800-102974600	Enhancers	Primary T cells from cord blood	blood
7	chr4:102975200-102975800	Enhancers	Colon Smooth Muscle	Colon
8	chr4:102975800-102980200	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:102976000-102977400	Weak transcription	Primary B cells from cord blood	blood
10	chr4:102977400-102987200	Strong transcription	Primary B cells from cord blood	blood
11	chr4:102978200-102978600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:102978200-102978600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
13	chr4:102979200-102980000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr4:102980000-102980800	Enhancers	Aorta	Aorta
15	chr4:102980000-102981400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:102980000-102998400	Strong transcription	Primary B cells from peripheral blood	blood
17	chr4:102980200-102981400	Enhancers	Colon Smooth Muscle	Colon
18	chr4:102980400-102981400	Enhancers	A549	lung
19	chr4:102983600-102984400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:102984400-102999000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:102984800-102994400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr4:102985800-102986400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:102985800-102986600	Enhancers	NHEK	skin
24	chr4:102986000-102986400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:102986000-102986600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:102986000-102986800	Enhancers	HMEC	breast
27	chr4:102986600-102986800	Flanking Active TSS	NHEK	skin
28	chr4:102987200-102989600	Weak transcription	Primary B cells from cord blood	blood
29	chr4:102989600-102998800	Strong transcription	Primary B cells from cord blood	blood
30	chr4:102989800-103001000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr4:102990400-102990800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:102997400-102998600	Enhancers	A549	lung
33	chr4:102997600-102998200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:102997600-102998200	Enhancers	NHEK	skin
35	chr4:102998000-102998600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:102998400-103000600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr4:102998800-103001200	Weak transcription	Primary B cells from cord blood	blood
38	chr4:103010800-103011200	Enhancers	Muscle Satellite Cultured Cells	--

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