Variant report

Variant	nsv595687
Chromosome Location	chr4:150070596-150178533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:329)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr4:150085578-150085819	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:150089964-150090273	H1-hESC	embryonic stem cell:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
3	CEBPB	chr4:150109374-150109673	HepG2	liver:	n/a	chr4:150109488-150109499
4	CEBPB	chr4:150081486-150081932	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr4:150103753-150104034	HepG2	liver:	n/a	chr4:150103910-150103923 chr4:150103911-150103922 chr4:150103912-150103921
6	CEBPB	chr4:150130695-150130739	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:150130637-150130875	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:150089802-150090171	IMR90	lung:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
9	CEBPB	chr4:150089819-150090159	HepG2	liver:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
10	CEBPB	chr4:150155028-150155228	IMR90	lung:	n/a	n/a
11	CHD2	chr4:150126306-150126345	HepG2	liver:	n/a	n/a
12	CTCF	chr4:150075116-150075162	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr4:150085605-150085770	ProgFib	skin:	n/a	n/a
14	CTCF	chr4:150112340-150112490	AG09309	skin:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
15	CTCF	chr4:150093720-150093870	AG04450	lung:	n/a	n/a
16	CTCF	chr4:150085560-150085710	HAc	cerebellar:	n/a	n/a
17	CTCF	chr4:150085600-150085750	AG04449	skin:	n/a	n/a
18	CTCF	chr4:150112340-150112490	AG09319	gingival:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
19	CTCF	chr4:150085560-150085710	HPF	lung:	n/a	n/a
20	CTCF	chr4:150112300-150112450	AG10803	skin:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
21	CTCF	chr4:150085560-150085710	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr4:150085540-150085690	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr4:150112389-150112451	LNCaP	prostate:	n/a	chr4:150112392-150112405 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
24	CTCF	chr4:150085520-150085670	AG09309	skin:	n/a	n/a
25	CTCF	chr4:150085640-150085790	BJ	skin:	n/a	n/a
26	CTCF	chr4:150085640-150085790	AG10803	skin:	n/a	n/a
27	CTCF	chr4:150085560-150085710	AG09319	gingival:	n/a	n/a
28	CTCF	chr4:150075020-150075170	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:150085640-150085790	WI-38	lung:	n/a	n/a
30	CTCF	chr4:150074900-150075050	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:150085580-150085730	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr4:150101652-150101695	LNCaP	prostate:	n/a	n/a
33	CTCF	chr4:150150785-150150835	LNCaP	prostate:	n/a	n/a
34	CTCF	chr4:150168871-150168892	Lung_OC	lung:	n/a	n/a
35	CTCF	chr4:150074989-150075254	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:150107916-150107950	K562	blood:	n/a	n/a
37	CTCF	chr4:150112375-150112463	ProgFib	skin:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
38	CTCF	chr4:150075122-150075141	HepG2	liver:	n/a	n/a
39	CTCF	chr4:150085540-150085690	HMF	breast:	n/a	n/a
40	CTCF	chr4:150085580-150085730	AG10803	skin:	n/a	n/a
41	CTCF	chr4:150085560-150085710	AG04449	skin:	n/a	n/a
42	CTCF	chr4:150088080-150088230	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr4:150085540-150085690	AG04450	lung:	n/a	n/a
44	CTCF	chr4:150085520-150085670	HMF	breast:	n/a	n/a
45	CTCF	chr4:150085540-150085690	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr4:150085592-150085787	Gliobla	brain:	n/a	n/a
47	CTCF	chr4:150085620-150085770	BJ	skin:	n/a	n/a
48	CTCF	chr4:150085580-150085730	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr4:150112140-150112290	AG09319	gingival:	n/a	n/a
50	CTCF	chr4:150085620-150085770	HCPEpiC	choroid plexus:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:150085703-150085753	HCF	heart:	n/a
2	chr4:150085703-150085753	NH-A	brain:	n/a
3	chr4:150085703-150085753	MCF-7	breast:	n/a
4	chr4:150087191-150087241	NHDF-neo	bronchial:	n/a
5	chr4:150087191-150087241	AG04450	lung:	fetal
6	chr4:150085703-150085753	HRPEpiC	eye:	n/a
7	chr4:150085703-150085753	NHBE	bronchial:	n/a
8	chr4:150087191-150087241	SKMC	muscle:	n/a
9	chr4:150085703-150085753	GM12891	blood:	n/a
10	chr4:150085703-150085753	GM12892	blood:	n/a
11	chr4:150087191-150087241	GM12878	blood:	n/a
12	chr4:150085703-150085753	RPTEC	kidney:	n/a
13	chr4:150087191-150087241	NHBE	bronchial:	n/a
14	chr4:150087191-150087241	HAEpiC	amniotic membrane:	n/a
15	chr4:150085703-150085753	HCPEpiC	choroid plexus:	n/a
16	chr4:150087191-150087241	HCM	heart:	n/a
17	chr4:150087191-150087241	HUVEC	blood vessel:	n/a
18	chr4:150085703-150085753	SKMC	muscle:	n/a
19	chr4:150085703-150085753	GM06990	blood:	n/a
20	chr4:150087191-150087241	HRCEpiC	kidney:	n/a
21	chr4:150087191-150087241	LNCaP	prostate:	n/a
22	chr4:150085703-150085753	H1-hESC	embryonic stem cell:	embryo
23	chr4:150085703-150085753	MCF10A-Er-Src	breast:	n/a
24	chr4:150085703-150085753	HRE	kidney:	n/a
25	chr4:150087191-150087241	AoSMC	blood vessel:	n/a
26	chr4:150085703-150085753	HUVEC	blood vessel:	n/a
27	chr4:150085703-150085753	HEK293	kidney:	embryo
28	chr4:150085703-150085753	U87	brain:	n/a
29	chr4:150085703-150085753	NT2-D1	testis:	n/a
30	chr4:150087191-150087241	RPTEC	kidney:	n/a
31	chr4:150085703-150085753	T-47D	breast:	n/a
32	chr4:150087191-150087241	AG04449	skin:	fetal
33	chr4:150087191-150087241	NT2-D1	testis:	n/a
34	chr4:150087191-150087241	AG10803	skin:	n/a
35	chr4:150085703-150085753	SK-N-MC	brain:	n/a
36	chr4:150087191-150087241	BJ	skin:	n/a
37	chr4:150085703-150085753	AoSMC	blood vessel:	n/a
38	chr4:150085703-150085753	AG09319	gingival:	n/a
39	chr4:150087191-150087241	Caco-2	colon:	n/a
40	chr4:150087191-150087241	T-47D	breast:	n/a
41	chr4:150085703-150085753	PFSK-1	brain:	n/a
42	chr4:150087191-150087241	MCF-7	breast:	n/a
43	chr4:150087191-150087241	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:150087191-150087241	Hela-S3	cervix:	n/a
45	chr4:150085703-150085753	LNCaP	prostate:	n/a
46	chr4:150087191-150087241	HIPEpiC	eye:	n/a
47	chr4:150085703-150085753	HAEpiC	amniotic membrane:	n/a
48	chr4:150085703-150085753	Hela-S3	cervix:	n/a
49	chr4:150087191-150087241	Hepatocyte	liver:	n/a
50	chr4:150087191-150087241	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:150074768..150075429-chr4:150185153..150186021,2	MCF-7	breast:
2	chr4:150107886..150110536-chr4:150111462..150113624,2	K562	blood:
3	chr4:150107886..150110536-chr4:150111462..150113624,2	K562	blood:
4	chr4:150063409..150066191-chr4:150071536..150073450,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCLK2-3	chr4:150126059-150126366	NONHSAT098714
2	lnc-NR3C2-4	chr4:150070701-150070932	XLOC_004120
3	lnc-DCLK2-3	chr4:150139117-150139172	NONHSAT098714
4	lnc-DCLK2-3	chr4:150177156-150177247	NONHSAT098714
5	lnc-DCLK2-3	chr4:150076604-150076877	NONHSAT098714
6	lnc-DCLK2-3	chr4:150135596-150135683	NONHSAT098714
7	lnc-NR3C2-4	chr4:150070701-150070929	XLOC_004120
8	lnc-NR3C2-9	chr4:150175507-150175629	NONHSAT098715
9	lnc-NR3C2-4	chr4:150071377-150071438	XLOC_004120
10	lnc-DCLK2-3	chr4:150075447-150075771	NONHSAT098714
11	lnc-DCLK2-3	chr4:150177385-150177550	NONHSAT098714
12	lnc-DCLK2-3	chr4:150125045-150125304	NONHSAT098714
13	lnc-DCLK2-3	chr4:150137555-150137729	NONHSAT098714
14	lnc-DCLK2-3	chr4:150123515-150123708	NONHSAT098714
15	lnc-DCLK2-3	chr4:150135803-150136039	NONHSAT098714

No data

Variant related genes	Relation type
ENSG00000248210	TF binding region
ENSG00000250252	TF binding region
ENSG00000248210	CpG island
ENSG00000250252	CpG island

Extended variants
information (count: 1420 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1420 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550917630	chr4:150070776-150070777	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs76690497	chr4:150070905-150070906	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs528374506	chr4:150074908-150074909	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs548412395	chr4:150074983-150074984	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs538228599	chr4:150075014-150075015	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs561723956	chr4:150075034-150075035	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs28716105	chr4:150075092-150075093	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs28701608	chr4:150075125-150075126	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs76687771	chr4:150075136-150075137	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs28410739	chr4:150075143-150075144	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552128982	chr4:150075149-150075150	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs28723415	chr4:150075154-150075155	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs28378847	chr4:150075178-150075179	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs374802013	chr4:150075207-150075208	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs28474774	chr4:150075216-150075217	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs115056158	chr4:150075222-150075223	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs537626608	chr4:150075239-150075240	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs77164034	chr4:150075258-150075259	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs137981981	chr4:150075282-150075283	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs28654818	chr4:150075284-150075285	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs553001812	chr4:150075287-150075288	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs563467613	chr4:150075466-150075467	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs532465845	chr4:150075493-150075494	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs73857574	chr4:150075506-150075507	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs149240874	chr4:150075511-150075512	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs57054897	chr4:150075569-150075570	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs373761953	chr4:150075609-150075610	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs548626775	chr4:150075610-150075611	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs568705966	chr4:150075630-150075631	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs75680645	chr4:150075643-150075644	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs144404505	chr4:150075661-150075662	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs570609507	chr4:150075671-150075672	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs539530857	chr4:150075715-150075716	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs28441660	chr4:150075716-150075717	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs572771728	chr4:150075718-150075719	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs374383299	chr4:150075753-150075754	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs1371003	chr4:150076661-150076662	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs551084017	chr4:150076668-150076669	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs60065159	chr4:150076688-150076689	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs112137431	chr4:150076694-150076695	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs113056770	chr4:150076718-150076719	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs573268772	chr4:150076743-150076744	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs11732984	chr4:150076761-150076762	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs567415228	chr4:150078606-150078607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536474054	chr4:150078611-150078612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556082171	chr4:150078622-150078623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564845538	chr4:150078638-150078639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569413072	chr4:150078655-150078656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538350718	chr4:150078662-150078663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558233888	chr4:150078667-150078668	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
Intellectual disability	22102821	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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150078600-150080800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:150079400-150080200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:150079400-150081000	Enhancers	NHLF	lung
4	chr4:150079400-150083000	Enhancers	NHDF-Ad	bronchial
5	chr4:150079800-150080600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:150080200-150080400	Enhancers	HSMM	muscle
7	chr4:150080200-150080600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr4:150080400-150080600	Enhancers	Osteobl	bone
9	chr4:150080400-150081800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:150080400-150081800	Weak transcription	HSMM	muscle
11	chr4:150080600-150081600	Weak transcription	Osteobl	bone
12	chr4:150080600-150082000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:150080600-150085200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:150080800-150082200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:150081000-150084200	Weak transcription	NHLF	lung
16	chr4:150081400-150083600	Enhancers	Fetal Heart	heart
17	chr4:150081600-150083000	Enhancers	Osteobl	bone
18	chr4:150081600-150083200	Enhancers	HSMMtube	muscle
19	chr4:150081800-150082200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:150081800-150083200	Enhancers	HSMM	muscle
21	chr4:150082000-150083400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr4:150082200-150083400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:150082200-150085000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:150082400-150082600	Enhancers	Left Ventricle	heart
25	chr4:150082400-150082800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr4:150082400-150082800	Enhancers	Adipose Nuclei	Adipose
27	chr4:150083000-150084200	Weak transcription	NHDF-Ad	bronchial
28	chr4:150083000-150084400	Weak transcription	Osteobl	bone
29	chr4:150083200-150084400	Weak transcription	HSMM	muscle
30	chr4:150083200-150085600	Weak transcription	HSMMtube	muscle
31	chr4:150083400-150084400	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr4:150083400-150092200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:150083600-150085200	Weak transcription	Fetal Heart	heart
34	chr4:150084200-150084600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:150084200-150086200	Enhancers	NHDF-Ad	bronchial
36	chr4:150084200-150086400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr4:150084200-150086600	Enhancers	NHLF	lung
38	chr4:150084400-150084600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:150084400-150084600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr4:150084400-150084600	Enhancers	HSMM	muscle
41	chr4:150084400-150085200	Enhancers	NH-A	brain
42	chr4:150084400-150085200	Enhancers	Osteobl	bone
43	chr4:150084400-150085400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:150084400-150086000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:150084400-150086200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr4:150084400-150086400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:150084400-150086400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:150084400-150086600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:150084400-150087800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:150084400-150088400	Enhancers	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links