Variant report

Variant	nsv1009302
Chromosome Location	chr4:102335072-102410893
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:175)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:175 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:102339134-102339737	GM12878	blood:	n/a	n/a
2	ATF2	chr4:102340441-102340905	GM12878	blood:	n/a	n/a
3	ATF2	chr4:102339234-102339683	GM12878	blood:	n/a	n/a
4	BATF	chr4:102341861-102342125	GM12878	blood:	n/a	n/a
5	BATF	chr4:102339267-102339612	GM12878	blood:	n/a	n/a
6	BATF	chr4:102339200-102339646	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:102339259-102339562	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:102339255-102339648	GM12878	blood:	n/a	n/a
9	BCLAF1	chr4:102339132-102339714	GM12878	blood:	n/a	n/a
10	BCLAF1	chr4:102340390-102340904	GM12878	blood:	n/a	chr4:102340518-102340527
11	BHLHE40	chr4:102339219-102339605	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:102340516-102340716	GM12878	blood:	n/a	n/a
13	CEBPB	chr4:102339203-102339354	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:102342549-102342988	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr4:102339246-102339518	GM12878	blood:	n/a	n/a
16	CEBPB	chr4:102347376-102347451	HepG2	liver:	n/a	n/a
17	CHD1	chr4:102397490-102397495	GM12878	blood:	n/a	n/a
18	CHD1	chr4:102356854-102356870	GM12878	blood:	n/a	n/a
19	CHD2	chr4:102340571-102340815	GM12878	blood:	n/a	n/a
20	CHD2	chr4:102339232-102339588	GM12878	blood:	n/a	n/a
21	CTCF	chr4:102338360-102338510	GM12867	blood:	n/a	n/a
22	CTCF	chr4:102358875-102358963	Medullo	brain:	n/a	n/a
23	CTCF	chr4:102358904-102358955	GM13977	blood:	n/a	n/a
24	CTCF	chr4:102358774-102359104	GM12878	blood:	n/a	n/a
25	CTCF	chr4:102339920-102340070	GM12878	blood:	n/a	n/a
26	CTCF	chr4:102358914-102358947	Lung_OC	lung:	n/a	n/a
27	CTCF	chr4:102346647-102346701	GM13976	blood:	n/a	n/a
28	CTCF	chr4:102365161-102365226	GM20000	blood:	n/a	n/a
29	CTCF	chr4:102358868-102358975	GM12878	blood:	n/a	n/a
30	CTCF	chr4:102358875-102359013	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr4:102392340-102392382	Spleen_OC	spleen:	n/a	n/a
32	CUX1	chr4:102339104-102339411	GM12878	blood:	n/a	n/a
33	CUX1	chr4:102341996-102342024	GM12878	blood:	n/a	n/a
34	CUX1	chr4:102397426-102397469	K562	blood:	n/a	n/a
35	CUX1	chr4:102358502-102358742	GM12878	blood:	n/a	n/a
36	E2F4	chr4:102342404-102342595	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr4:102363507-102363511	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr4:102410522-102410576	MCF10A-Er-Src	breast:	n/a	n/a
39	EBF1	chr4:102339301-102339485	GM12878	blood:	n/a	n/a
40	ELK1	chr4:102340512-102340654	GM12878	blood:	n/a	n/a
41	EP300	chr4:102372135-102372480	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr4:102340546-102340828	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr4:102342433-102343006	ECC-1	luminal epithelium:	n/a	n/a
44	EP300	chr4:102340500-102340818	GM12878	blood:	n/a	chr4:102340518-102340527
45	EP300	chr4:102339201-102340042	GM12878	blood:	n/a	n/a
46	EP300	chr4:102339283-102339530	GM12878	blood:	n/a	n/a
47	EP300	chr4:102339155-102339862	GM12878	blood:	n/a	n/a
48	EP300	chr4:102340253-102340893	GM12878	blood:	n/a	chr4:102340518-102340527
49	EP300	chr4:102372087-102372428	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr4:102340285-102340313	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102340691-102340741	HRE	kidney:	n/a
2	chr4:102341105-102341155	Hela-S3	cervix:	n/a
3	chr4:102341105-102341155	BJ	skin:	n/a
4	chr4:102340823-102340873	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:102340823-102340873	Caco-2	colon:	n/a
6	chr4:102340691-102340741	GM06990	blood:	n/a
7	chr4:102340823-102340873	MCF10A-Er-Src	breast:	n/a
8	chr4:102341105-102341155	AG09309	skin:	n/a
9	chr4:102340691-102340741	NHDF-neo	bronchial:	n/a
10	chr4:102340823-102340873	BE2_C	brain:	n/a
11	chr4:102341105-102341155	HCPEpiC	choroid plexus:	n/a
12	chr4:102341105-102341155	Caco-2	colon:	n/a
13	chr4:102341105-102341155	AG10803	skin:	n/a
14	chr4:102340691-102340741	NT2-D1	testis:	n/a
15	chr4:102341105-102341155	NT2-D1	testis:	n/a
16	chr4:102340691-102340741	Hepatocyte	liver:	n/a
17	chr4:102340691-102340741	HRPEpiC	eye:	n/a
18	chr4:102341105-102341155	T-47D	breast:	n/a
19	chr4:102340691-102340741	RPTEC	kidney:	n/a
20	chr4:102340823-102340873	HL-60	blood:	n/a
21	chr4:102341105-102341155	PrEC	prostate:	n/a
22	chr4:102341105-102341155	AG04450	lung:	fetal
23	chr4:102341105-102341155	ProgFib	skin:	n/a
24	chr4:102340823-102340873	ovcar-3	ovarian:	n/a
25	chr4:102340691-102340741	CMK	blood:	n/a
26	chr4:102340691-102340741	AG09309	skin:	n/a
27	chr4:102340823-102340873	HepG2	liver:	n/a
28	chr4:102341105-102341155	Hepatocyte	liver:	n/a
29	chr4:102341105-102341155	GM12892	blood:	n/a
30	chr4:102340823-102340873	Hela-S3	cervix:	n/a
31	chr4:102340691-102340741	GM12891	blood:	n/a
32	chr4:102341105-102341155	NHBE	bronchial:	n/a
33	chr4:102340691-102340741	HIPEpiC	eye:	n/a
34	chr4:102340823-102340873	U87	brain:	n/a
35	chr4:102340823-102340873	ProgFib	skin:	n/a
36	chr4:102340823-102340873	AoSMC	blood vessel:	n/a
37	chr4:102340691-102340741	HepG2	liver:	n/a
38	chr4:102340823-102340873	RPTEC	kidney:	n/a
39	chr4:102340823-102340873	SK-N-SH_RA	brain:	n/a
40	chr4:102341105-102341155	GM12891	blood:	n/a
41	chr4:102340691-102340741	HAEpiC	amniotic membrane:	n/a
42	chr4:102340691-102340741	SK-N-SH	brain:	n/a
43	chr4:102340691-102340741	MCF10A-Er-Src	breast:	n/a
44	chr4:102341105-102341155	PFSK-1	brain:	n/a
45	chr4:102341105-102341155	HCM	heart:	n/a
46	chr4:102340691-102340741	NH-A	brain:	n/a
47	chr4:102341105-102341155	CMK	blood:	n/a
48	chr4:102340823-102340873	GM12891	blood:	n/a
49	chr4:102340823-102340873	PANC-1	pancreas:	n/a
50	chr4:102340691-102340741	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:101657397..101659960-chr4:102360000..102362694,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BANK1-1	chr4:102348718-102348797	NONHSAT097572
2	lnc-BANK1-1	chr4:102341171-102341254	NONHSAT097572
3	lnc-BANK1-1	chr4:102343790-102343815	NONHSAT097572

No data

Variant related genes	Relation type
BANK1	TF binding region
BANK1	CpG island

Extended variants
information (count: 1297 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550504604	chr4:102335076-102335077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs193152432	chr4:102335079-102335080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548864164	chr4:102335115-102335116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567253015	chr4:102335126-102335127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183243405	chr4:102335158-102335159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566123142	chr4:102335159-102335160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28503426	chr4:102335168-102335169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs114082860	chr4:102335202-102335203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575644012	chr4:102335213-102335214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542968750	chr4:102335238-102335239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568791358	chr4:102335239-102335240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555267696	chr4:102335243-102335244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114734038	chr4:102335254-102335255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535443846	chr4:102335263-102335264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540911869	chr4:102335333-102335334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559526778	chr4:102335335-102335336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532981012	chr4:102335351-102335352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546320189	chr4:102335357-102335358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189100086	chr4:102335400-102335401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146737866	chr4:102335509-102335510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116165703	chr4:102335576-102335577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140343345	chr4:102335653-102335654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs72918879	chr4:102335679-102335680	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs537496799	chr4:102335695-102335696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569158791	chr4:102335699-102335700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547749361	chr4:102335704-102335705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114005005	chr4:102335714-102335715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539633788	chr4:102335736-102335737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192367193	chr4:102335747-102335748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569386591	chr4:102335770-102335771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113405064	chr4:102335816-102335817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201553162	chr4:102335819-102335820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58285648	chr4:102335820-102335821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116671897	chr4:102335821-102335822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35105187	chr4:102335830-102335831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558008880	chr4:102335842-102335843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573381111	chr4:102335992-102335993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112674441	chr4:102335993-102335994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77230126	chr4:102336016-102336017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573280605	chr4:102336024-102336025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10007821	chr4:102336044-102336045	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs10007902	chr4:102336118-102336119	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs577379270	chr4:102336175-102336176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183708127	chr4:102336194-102336195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373629814	chr4:102336201-102336202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533983258	chr4:102336215-102336216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79032439	chr4:102336231-102336232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538730364	chr4:102336237-102336238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542613164	chr4:102336241-102336242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10708625	chr4:102336242-102336243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Hirschsprung''s Disease	21712996	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
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102332800-102336400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr4:102333400-102336400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr4:102333800-102335200	Weak transcription	A549	lung
4	chr4:102335200-102336000	Enhancers	A549	lung
5	chr4:102335200-102337200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:102335400-102336400	Enhancers	HUVEC	blood vessel
7	chr4:102335800-102336000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr4:102335800-102337800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr4:102336200-102336800	Enhancers	Primary T cells from cord blood	blood
10	chr4:102336200-102337800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:102336400-102336600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
12	chr4:102336400-102336600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr4:102336400-102337600	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr4:102336400-102339600	Weak transcription	HUVEC	blood vessel
15	chr4:102336400-102340200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr4:102336400-102341600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr4:102336600-102336800	Enhancers	Adipose Nuclei	Adipose
18	chr4:102336800-102340400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr4:102336800-102341400	Weak transcription	Adipose Nuclei	Adipose
20	chr4:102337000-102337600	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr4:102337200-102337800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:102337200-102337800	Enhancers	Right Ventricle	heart
23	chr4:102337200-102338400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
24	chr4:102337200-102338800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr4:102337200-102339200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:102337600-102338000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:102337600-102338400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
28	chr4:102337600-102338600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
29	chr4:102337600-102338600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
30	chr4:102337600-102338800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
31	chr4:102337600-102340600	Enhancers	Dnd41	blood
32	chr4:102337800-102338000	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr4:102337800-102338200	Weak transcription	Right Ventricle	heart
34	chr4:102337800-102338800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
35	chr4:102337800-102339400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr4:102337800-102341400	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr4:102337800-102341600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr4:102338000-102338400	Enhancers	Primary T cells from cord blood	blood
39	chr4:102338000-102338600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:102338000-102338600	Enhancers	Colonic Mucosa	Colon
41	chr4:102338000-102338800	Bivalent Enhancer	Fetal Thymus	thymus
42	chr4:102338000-102339200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr4:102338000-102339200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:102338000-102342400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:102338200-102338400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
46	chr4:102338200-102338400	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr4:102338200-102338600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
48	chr4:102338200-102338600	Enhancers	Right Ventricle	heart
49	chr4:102338200-102338800	Enhancers	Thymus	Thymus
50	chr4:102338200-102341800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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