Variant report

Variant	esv16226
Chromosome Location	chr4:119552399-119584340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:155)
CpG islands
(count:367)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:155 , 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	chr4:119580936-119581135	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:119583224-119583485	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:119576461-119576486	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:119582224-119582465	HepG2	liver:	n/a	n/a
5	CEBPB	chr4:119566666-119567031	K562	blood:	n/a	n/a
6	CEBPB	chr4:119575027-119575397	K562	blood:	n/a	n/a
7	CEBPB	chr4:119563765-119563790	HepG2	liver:	n/a	chr4:119563768-119563779 chr4:119563767-119563780
8	CEBPD	chr4:119570052-119570409	K562	blood:	n/a	n/a
9	CEBPD	chr4:119574979-119575474	K562	blood:	n/a	n/a
10	CTCF	chr4:119552420-119552570	MCF-7	breast:	n/a	n/a
11	CTCF	chr4:119556320-119556553	K562	blood:	n/a	chr4:119556484-119556497
12	CTCF	chr4:119554627-119554944	K562	blood:	n/a	n/a
13	CTCF	chr4:119552340-119552490	WERI-Rb-1	eye:	n/a	chr4:119552363-119552376
14	CTCF	chr4:119575049-119575379	K562	blood:	n/a	chr4:119575211-119575232
15	CTCF	chr4:119571229-119571274	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr4:119552340-119552490	SK-N-SH_RA	brain:	n/a	chr4:119552363-119552376
17	CTCF	chr4:119551772-119552562	K562	blood:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552043-119552061 chr4:119552363-119552376 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
18	CTCF	chr4:119575082-119575277	K562	blood:	n/a	chr4:119575211-119575232
19	CTCF	chr4:119556298-119556561	K562	blood:	n/a	chr4:119556484-119556497
20	CTCF	chr4:119551866-119552441	K562	blood:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552043-119552061 chr4:119552363-119552376 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
21	CTCF	chr4:119556321-119556513	K562	blood:	n/a	chr4:119556484-119556497
22	CTCF	chr4:119570085-119570134	Medullo	brain:	n/a	n/a
23	EBF1	chr4:119583491-119583871	GM12878	blood:	n/a	n/a
24	EP300	chr4:119583262-119583517	GM12878	blood:	n/a	n/a
25	EP300	chr4:119583811-119584104	GM12878	blood:	n/a	chr4:119583926-119583933
26	EP300	chr4:119580895-119581113	GM12878	blood:	n/a	n/a
27	EP300	chr4:119582447-119582722	GM12878	blood:	n/a	n/a
28	FOSL2	chr4:119559112-119559408	HepG2	liver:	n/a	n/a
29	FOSL2	chr4:119553243-119553653	HepG2	liver:	n/a	n/a
30	FOSL2	chr4:119580909-119581126	HepG2	liver:	n/a	n/a
31	FOSL2	chr4:119558490-119558822	HepG2	liver:	n/a	n/a
32	FOSL2	chr4:119557170-119557609	HepG2	liver:	n/a	n/a
33	FOSL2	chr4:119554007-119554631	HepG2	liver:	n/a	n/a
34	FOSL2	chr4:119558080-119558486	HepG2	liver:	n/a	n/a
35	FOSL2	chr4:119583617-119584124	HepG2	liver:	n/a	n/a
36	FOSL2	chr4:119581693-119581954	HepG2	liver:	n/a	n/a
37	FOSL2	chr4:119582208-119582989	HepG2	liver:	n/a	chr4:119582484-119582495
38	FOSL2	chr4:119583844-119584062	HepG2	liver:	n/a	n/a
39	FOSL2	chr4:119582139-119582882	HepG2	liver:	n/a	chr4:119582484-119582495
40	FOXA1	chr4:119582248-119582872	HepG2	liver:	n/a	n/a
41	FOXA1	chr4:119583761-119584090	HepG2	liver:	n/a	n/a
42	GABPA	chr4:119582385-119582674	Hela-S3	cervix:	n/a	n/a
43	GABPA	chr4:119553648-119553762	Hela-S3	cervix:	n/a	n/a
44	GATA2	chr4:119582024-119582725	K562	blood:	n/a	n/a
45	GATA2	chr4:119583535-119584406	K562	blood:	n/a	n/a
46	GATA2	chr4:119581303-119581606	K562	blood:	n/a	n/a
47	GATA2	chr4:119583192-119583448	K562	blood:	n/a	n/a
48	GATA2	chr4:119570006-119570373	K562	blood:	n/a	chr4:119570212-119570222
49	GATA2	chr4:119580410-119581141	K562	blood:	n/a	n/a
50	GATA2	chr4:119574926-119575220	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119554219-119554269	NT2-D1	testis:	n/a
2	chr4:119554219-119554269	NT2-D1	testis:	n/a
3	chr4:119554219-119554269	AG10803	skin:	n/a
4	chr4:119555556-119555606	BE2_C	brain:	n/a
5	chr4:119557464-119557514	HNPCEpiC	eye:	n/a
6	chr4:119556601-119556651	GM12892	blood:	n/a
7	chr4:119556601-119556651	MCF-7	breast:	n/a
8	chr4:119557464-119557514	SK-N-MC	brain:	n/a
9	chr4:119556601-119556651	HNPCEpiC	eye:	n/a
10	chr4:119554219-119554269	HMEC	breast:	n/a
11	chr4:119557464-119557514	Hela-S3	cervix:	n/a
12	chr4:119557464-119557514	BJ	skin:	n/a
13	chr4:119557464-119557514	ECC-1	luminal epithelium:	n/a
14	chr4:119556601-119556651	Hela-S3	cervix:	n/a
15	chr4:119555395-119555445	U87	brain:	n/a
16	chr4:119555556-119555606	HepG2	liver:	n/a
17	chr4:119553015-119553065	PFSK-1	brain:	n/a
18	chr4:119554219-119554269	ovcar-3	ovarian:	n/a
19	chr4:119555395-119555445	HEK293	kidney:	embryo
20	chr4:119556601-119556651	HCPEpiC	choroid plexus:	n/a
21	chr4:119557464-119557514	HRPEpiC	eye:	n/a
22	chr4:119554219-119554269	HAEpiC	amniotic membrane:	n/a
23	chr4:119555556-119555606	HCPEpiC	choroid plexus:	n/a
24	chr4:119553015-119553065	BJ	skin:	n/a
25	chr4:119556601-119556651	AoSMC	blood vessel:	n/a
26	chr4:119554219-119554269	A549	lung:	n/a
27	chr4:119554219-119554269	IMR90	lung:	fetal
28	chr4:119555395-119555445	AG04449	skin:	fetal
29	chr4:119557464-119557514	CMK	blood:	n/a
30	chr4:119555556-119555606	A549	lung:	n/a
31	chr4:119554219-119554269	HepG2	liver:	n/a
32	chr4:119554219-119554269	GM19239	blood:	n/a
33	chr4:119554219-119554269	NHBE	bronchial:	n/a
34	chr4:119555556-119555606	GM12891	blood:	n/a
35	chr4:119555395-119555445	HCPEpiC	choroid plexus:	n/a
36	chr4:119553015-119553065	Jurkat	blood:	n/a
37	chr4:119555395-119555445	T-47D	breast:	n/a
38	chr4:119555556-119555606	HCT-116	colon:	n/a
39	chr4:119555556-119555606	NHDF-neo	bronchial:	n/a
40	chr4:119555556-119555606	PrEC	prostate:	n/a
41	chr4:119557464-119557514	HUVEC	blood vessel:	n/a
42	chr4:119555556-119555606	HCM	heart:	n/a
43	chr4:119553015-119553065	MCF10A-Er-Src	breast:	n/a
44	chr4:119555556-119555606	ProgFib	skin:	n/a
45	chr4:119556601-119556651	H1-hESC	embryonic stem cell:	embryo
46	chr4:119553015-119553065	IMR90	lung:	fetal
47	chr4:119555556-119555606	SK-N-SH_RA	brain:	n/a
48	chr4:119554219-119554269	K562	blood:	n/a
49	chr4:119553015-119553065	SAEC	small airway:	n/a
50	chr4:119557464-119557514	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:119200131..119202202-chr4:119563480..119565428,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEC24D-1	chr4:119584229-119584309	XLOC_004053

No data

Variant related genes	Relation type
ENSG00000251155	TF binding region
CICP16	TF binding region
ENSG00000225892	TF binding region
ENSG00000251155	CpG island
CICP16	CpG island
ENSG00000225892	CpG island
ENSG00000269893	chromatin interactions

Extended variants
information (count: 562 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551929678	chr4:119552399-119552400	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs562906459	chr4:119552402-119552403	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs571763402	chr4:119552405-119552406	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs534234625	chr4:119552426-119552427	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs547768596	chr4:119552435-119552436	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs9760578	chr4:119552436-119552437	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs551834655	chr4:119552447-119552448	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs536511766	chr4:119552486-119552487	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs191354773	chr4:119552510-119552511	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs576589625	chr4:119552537-119552538	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs565526835	chr4:119552554-119552555	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs534069370	chr4:119552558-119552559	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538832065	chr4:119552564-119552565	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs72489558	chr4:119552579-119552580	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79233181	chr4:119552603-119552604	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139057991	chr4:119552606-119552607	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557470011	chr4:119552610-119552611	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577314200	chr4:119552617-119552618	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539844033	chr4:119552628-119552629	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559852535	chr4:119552645-119552646	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181403429	chr4:119552648-119552649	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186078356	chr4:119552676-119552677	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542527533	chr4:119552678-119552679	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562777169	chr4:119552719-119552720	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531568560	chr4:119552723-119552724	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527889246	chr4:119552725-119552726	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551601539	chr4:119552734-119552735	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565383720	chr4:119552758-119552759	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527747474	chr4:119552797-119552798	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547787296	chr4:119552804-119552805	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567525811	chr4:119552806-119552807	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139350225	chr4:119552820-119552821	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs67276048	chr4:119552849-119552850	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs534338537	chr4:119552852-119552853	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538891883	chr4:119552911-119552912	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558677902	chr4:119552933-119552934	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373339882	chr4:119552935-119552936	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533606619	chr4:119552937-119552938	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139367429	chr4:119552940-119552941	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539663932	chr4:119552943-119552944	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573581981	chr4:119552955-119552956	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559905619	chr4:119552961-119552962	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556233791	chr4:119552968-119552969	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576360812	chr4:119552971-119552972	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183066824	chr4:119553021-119553022	Weak transcription Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs145044690	chr4:119553022-119553023	Weak transcription Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs527809554	chr4:119553030-119553031	Weak transcription Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs3956493	chr4:119553076-119553077	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4001265	chr4:119553091-119553092	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148693152	chr4:119553098-119553099	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119513400-119554000	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:119513400-119554800	Weak transcription	Ovary	ovary
3	chr4:119513400-119557200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr4:119513600-119552400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:119513600-119552400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr4:119513600-119552400	Weak transcription	Fetal Brain Female	brain
7	chr4:119513600-119552400	Weak transcription	Lung	lung
8	chr4:119513600-119552400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr4:119513600-119554000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:119513600-119555800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr4:119513600-119559200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr4:119513800-119552400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:119513800-119555000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr4:119513800-119556000	Weak transcription	Fetal Lung	lung
15	chr4:119518400-119552600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr4:119518800-119557000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:119519400-119552400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr4:119519600-119552400	Weak transcription	Brain Angular Gyrus	brain
19	chr4:119519800-119552600	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr4:119519800-119559000	Weak transcription	Brain Hippocampus Middle	brain
21	chr4:119520600-119552400	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr4:119520800-119552400	Weak transcription	Right Ventricle	heart
23	chr4:119521200-119552400	Weak transcription	Placenta	Placenta
24	chr4:119526000-119556200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr4:119527600-119552400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr4:119527800-119555800	Weak transcription	Primary B cells from peripheral blood	blood
27	chr4:119528200-119552400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:119528800-119558000	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr4:119538600-119555200	Weak transcription	Brain Germinal Matrix	brain
30	chr4:119542000-119557200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr4:119542600-119554400	Weak transcription	Rectal Smooth Muscle	rectum
32	chr4:119544600-119554600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:119545400-119552400	Weak transcription	Brain Substantia Nigra	brain
34	chr4:119546800-119552400	Weak transcription	Primary T cells from cord blood	blood
35	chr4:119547400-119555600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:119547600-119552400	Weak transcription	Aorta	Aorta
37	chr4:119547800-119552800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr4:119548600-119552800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:119548800-119554600	Strong transcription	Liver	Liver
40	chr4:119549000-119554800	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:119549000-119554800	Weak transcription	NH-A	brain
42	chr4:119549000-119556000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:119549200-119553600	Strong transcription	Fetal Muscle Leg	muscle
44	chr4:119549200-119555800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:119549200-119555800	Strong transcription	Spleen	Spleen
46	chr4:119549200-119557800	Strong transcription	Fetal Stomach	stomach
47	chr4:119549400-119553000	Strong transcription	Fetal Intestine Large	intestine
48	chr4:119549400-119556600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr4:119549600-119557600	Strong transcription	Fetal Intestine Small	intestine
50	chr4:119550000-119555800	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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