Variant report

Variant	nsv1018566
Chromosome Location	chr4:144284927-144298930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:470)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:144293283-144294071	GM12878	blood:	n/a	n/a
2	ATF2	chr4:144298593-144299412	GM12878	blood:	n/a	n/a
3	ATF2	chr4:144293374-144294131	GM12878	blood:	n/a	n/a
4	ATF2	chr4:144298635-144299351	GM12878	blood:	n/a	n/a
5	ATF2	chr4:144297148-144297630	GM12878	blood:	n/a	n/a
6	BATF	chr4:144293442-144294070	GM12878	blood:	n/a	chr4:144293727-144293738
7	BATF	chr4:144297351-144297543	GM12878	blood:	n/a	n/a
8	BATF	chr4:144293469-144293997	GM12878	blood:	n/a	chr4:144293727-144293738
9	BCL11A	chr4:144293593-144293987	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:144298783-144299242	GM12878	blood:	n/a	chr4:144299002-144299011 chr4:144298844-144298853
11	BCL11A	chr4:144293420-144294104	GM12878	blood:	n/a	n/a
12	BCL3	chr4:144298720-144299294	GM12878	blood:	n/a	chr4:144299002-144299011 chr4:144298844-144298853
13	BCL3	chr4:144293534-144294035	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:144293417-144294065	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:144298700-144299448	GM12878	blood:	n/a	chr4:144299002-144299011 chr4:144298844-144298853
16	BCLAF1	chr4:144293238-144294109	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:144293281-144294215	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:144298356-144299297	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:144295414-144295437	K562	blood:	n/a	n/a
20	CEBPB	chr4:144291986-144292321	A549	lung:	n/a	chr4:144292145-144292156
21	CEBPB	chr4:144292998-144294244	GM12878	blood:	n/a	n/a
22	CEBPB	chr4:144291985-144292186	HepG2	liver:	n/a	chr4:144292145-144292156
23	CEBPB	chr4:144298704-144299319	GM12878	blood:	n/a	n/a
24	CEBPB	chr4:144291964-144292167	IMR90	lung:	n/a	chr4:144292145-144292156
25	CEBPB	chr4:144291988-144292177	K562	blood:	n/a	chr4:144292145-144292156
26	CEBPD	chr4:144296427-144296920	K562	blood:	n/a	n/a
27	CEBPD	chr4:144296528-144296937	K562	blood:	n/a	n/a
28	CHD1	chr4:144298552-144299492	GM12878	blood:	n/a	n/a
29	CHD1	chr4:144293294-144294050	GM12878	blood:	n/a	n/a
30	CHD1	chr4:144297544-144297881	GM12878	blood:	n/a	n/a
31	CHD2	chr4:144293364-144294164	GM12878	blood:	n/a	n/a
32	CHD2	chr4:144298791-144299720	GM12878	blood:	n/a	n/a
33	CREB1	chr4:144298594-144299403	GM12878	blood:	n/a	n/a
34	CREB1	chr4:144293375-144294035	GM12878	blood:	n/a	n/a
35	CTCF	chr4:144296920-144297070	HMEC	breast:	n/a	n/a
36	CTCF	chr4:144296520-144296670	HEK293	kidney:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
37	CTCF	chr4:144296816-144297187	IMR90	lung:	n/a	n/a
38	CTCF	chr4:144296840-144296990	HCT-116	colon:	n/a	n/a
39	CTCF	chr4:144296901-144297075	K562	blood:	n/a	n/a
40	CTCF	chr4:144296897-144297095	Medullo	brain:	n/a	n/a
41	CTCF	chr4:144296867-144297128	Fibrobl	skin:	n/a	n/a
42	CTCF	chr4:144296557-144296665	Hela-S3	cervix:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
43	CTCF	chr4:144296920-144297070	GM06990	blood:	n/a	n/a
44	CTCF	chr4:144296900-144297050	HPF	lung:	n/a	n/a
45	CTCF	chr4:144296890-144297133	GM12891	blood:	n/a	n/a
46	CTCF	chr4:144296794-144297217	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:144296500-144296650	AoAF	blood vessel:	n/a	chr4:144296581-144296591 chr4:144296578-144296596 chr4:144296573-144296594 chr4:144296584-144296593 chr4:144296579-144296595
48	CTCF	chr4:144296900-144297050	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:144296580-144296730	HMF	breast:	n/a	chr4:144296581-144296591 chr4:144296584-144296593
50	CTCF	chr4:144296903-144297104	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:144297236-144297286	GM12891	blood:	n/a
2	chr4:144297236-144297286	MCF10A-Er-Src	breast:	n/a
3	chr4:144297236-144297286	AG04450	lung:	fetal
4	chr4:144297236-144297286	HL-60	blood:	n/a
5	chr4:144297236-144297286	RPTEC	kidney:	n/a
6	chr4:144297236-144297286	HepG2	liver:	n/a
7	chr4:144297236-144297286	HRPEpiC	eye:	n/a
8	chr4:144297236-144297286	GM06990	blood:	n/a
9	chr4:144297236-144297286	Hela-S3	cervix:	n/a
10	chr4:144297236-144297286	ProgFib	skin:	n/a
11	chr4:144297236-144297286	PANC-1	pancreas:	n/a
12	chr4:144297236-144297286	AG09319	gingival:	n/a
13	chr4:144297236-144297286	PFSK-1	brain:	n/a
14	chr4:144297236-144297286	SAEC	small airway:	n/a
15	chr4:144297236-144297286	AG09309	skin:	n/a
16	chr4:144297236-144297286	ovcar-3	ovarian:	n/a
17	chr4:144297236-144297286	Hepatocyte	liver:	n/a
18	chr4:144297236-144297286	AG04449	skin:	fetal
19	chr4:144297236-144297286	NT2-D1	testis:	n/a
20	chr4:144297236-144297286	HEK293	kidney:	embryo
21	chr4:144297236-144297286	K562	blood:	n/a
22	chr4:144297236-144297286	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:144297236-144297286	HRCEpiC	kidney:	n/a
24	chr4:144297236-144297286	BJ	skin:	n/a
25	chr4:144297236-144297286	MCF-7	breast:	n/a
26	chr4:144297236-144297286	GM19239	blood:	n/a
27	chr4:144297236-144297286	HAEpiC	amniotic membrane:	n/a
28	chr4:144297236-144297286	HCM	heart:	n/a
29	chr4:144297236-144297286	SK-N-MC	brain:	n/a
30	chr4:144297236-144297286	PrEC	prostate:	n/a
31	chr4:144297236-144297286	H1-hESC	embryonic stem cell:	embryo
32	chr4:144297236-144297286	Caco-2	colon:	n/a
33	chr4:144297236-144297286	NB4	blood:	n/a
34	chr4:144297236-144297286	LNCaP	prostate:	n/a
35	chr4:144297236-144297286	HUVEC	blood vessel:	n/a
36	chr4:144297236-144297286	HCF	heart:	n/a
37	chr4:144297236-144297286	SK-N-SH_RA	brain:	n/a
38	chr4:144297236-144297286	AG10803	skin:	n/a
39	chr4:144297236-144297286	AoSMC	blood vessel:	n/a
40	chr4:144297236-144297286	A549	lung:	n/a
41	chr4:144297236-144297286	U87	brain:	n/a
42	chr4:144297236-144297286	CMK	blood:	n/a
43	chr4:144297236-144297286	HCT-116	colon:	n/a
44	chr4:144297236-144297286	HRE	kidney:	n/a
45	chr4:144297236-144297286	GM12892	blood:	n/a
46	chr4:144297236-144297286	SK-N-SH	brain:	n/a
47	chr4:144297236-144297286	HNPCEpiC	eye:	n/a
48	chr4:144297236-144297286	NHDF-neo	bronchial:	n/a
49	chr4:144297236-144297286	BE2_C	brain:	n/a
50	chr4:144297236-144297286	HEEpiC	esophagus:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:144296798..144297742-chr4:144403694..144404468,2	MCF-7	breast:
2	chr4:144290996..144292995-chr4:144295055..144297084,2	MCF-7	breast:
3	chr4:144254627..144258395-chr4:144297952..144301828,4	K562	blood:
4	chr4:144274310..144276106-chr4:144283049..144285599,2	MCF-7	breast:
5	chr4:144295435..144296093-chr5:75459165..75460000,2	MCF-7	breast:
6	chr4:144284857..144287398-chr4:144288484..144291385,2	K562	blood:
7	chr4:144289833..144291469-chr4:144294402..144296058,2	K562	blood:
8	chr4:144257678..144260213-chr4:144284163..144287062,2	MCF-7	breast:
9	chr4:144284857..144287398-chr4:144288484..144291385,2	K562	blood:
10	chr4:144289833..144292177-chr4:144294492..144296058,2	K562	blood:
11	chr4:144289833..144291469-chr4:144294402..144296058,2	K562	blood:
12	chr4:144294005..144295749-chr4:144303829..144305469,2	K562	blood:
13	chr4:144280022..144283375-chr4:144285064..144288406,3	K562	blood:
14	chr4:144283863..144286903-chr4:144287176..144291126,4	K562	blood:
15	chr4:144292852..144297100-chr4:144298409..144302941,5	K562	blood:
16	chr4:144256664..144258280-chr4:144293930..144296084,2	MCF-7	breast:
17	chr4:144292852..144297100-chr4:144298409..144302941,5	K562	blood:
18	chr4:144290996..144292995-chr4:144295055..144297084,2	MCF-7	breast:
19	chr4:144289833..144292177-chr4:144294492..144296058,2	K562	blood:
20	chr4:144257935..144259880-chr4:144296110..144298167,2	MCF-7	breast:
21	chr4:144296980..144297503-chr4:144403654..144404586,2	MCF-7	breast:
22	chr4:144279254..144282177-chr4:144295139..144296728,2	MCF-7	breast:
23	chr4:144283863..144286903-chr4:144287176..144291126,4	K562	blood:

No data

Variant related genes	Relation type
GAB1	TF binding region
GAB1	CpG island
ENSG00000109458	chromatin interactions
ENSG00000178972	chromatin interactions

Extended variants
information (count: 503 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528513020	chr4:144284971-144284972	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs138266321	chr4:144284983-144284984	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs575522170	chr4:144285025-144285026	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532340667	chr4:144285039-144285040	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs377159009	chr4:144285041-144285042	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs568365116	chr4:144285068-144285069	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs535252147	chr4:144285075-144285076	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550846024	chr4:144285151-144285152	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs28989214	chr4:144285159-144285160	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs557106894	chr4:144285171-144285172	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569123002	chr4:144285179-144285180	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs28989215	chr4:144285200-144285201	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs28989216	chr4:144285205-144285206	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375932274	chr4:144285336-144285337	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs76330519	chr4:144285341-144285342	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs77304786	chr4:144285344-144285345	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs572470529	chr4:144285389-144285390	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs539846109	chr4:144285434-144285435	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553211166	chr4:144285438-144285439	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs138830124	chr4:144285443-144285444	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs542206546	chr4:144285446-144285447	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs573910315	chr4:144285519-144285520	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563887938	chr4:144285531-144285532	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs28989217	chr4:144285545-144285546	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546246724	chr4:144285600-144285601	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs17017677	chr4:144285606-144285607	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs528446578	chr4:144285627-144285628	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs3805254	chr4:144285683-144285684	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs28989218	chr4:144285700-144285701	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs529181916	chr4:144285748-144285749	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs550629033	chr4:144285796-144285797	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561695747	chr4:144285803-144285804	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs148116827	chr4:144285814-144285815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551033081	chr4:144285821-144285822	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566240912	chr4:144285832-144285833	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533682184	chr4:144285836-144285837	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554940424	chr4:144285840-144285841	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs62337516	chr4:144285873-144285874	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186708923	chr4:144285882-144285883	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191130685	chr4:144285895-144285896	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs575767248	chr4:144285912-144285913	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs141888507	chr4:144285917-144285918	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564529208	chr4:144285927-144285928	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs573362041	chr4:144285951-144285952	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575548797	chr4:144285952-144285953	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs375299332	chr4:144285953-144285954	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs117220286	chr4:144285956-144285957	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562092569	chr4:144285984-144285985	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529304852	chr4:144285993-144285994	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs367953855	chr4:144286018-144286019	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:144272800-144299800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr4:144276400-144286000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:144277200-144290400	Weak transcription	Pancreas	Pancrea
4	chr4:144277400-144296800	Weak transcription	HSMMtube	muscle
5	chr4:144278200-144285400	Enhancers	Fetal Heart	heart
6	chr4:144279800-144286000	Enhancers	Brain Cingulate Gyrus	brain
7	chr4:144280200-144285400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr4:144280400-144285600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:144280800-144286000	Enhancers	Brain Hippocampus Middle	brain
10	chr4:144281200-144285200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:144281200-144285400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr4:144281200-144285400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:144281200-144290000	Weak transcription	Fetal Stomach	stomach
14	chr4:144281200-144296800	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:144281400-144296800	Weak transcription	Fetal Kidney	kidney
16	chr4:144281800-144286000	Enhancers	Brain Substantia Nigra	brain
17	chr4:144281800-144293400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:144282000-144291200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:144282200-144285600	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr4:144282400-144285400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr4:144282600-144285000	Enhancers	Small Intestine	intestine
22	chr4:144282600-144285200	Enhancers	Left Ventricle	heart
23	chr4:144282600-144286000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr4:144282800-144285400	Enhancers	Aorta	Aorta
25	chr4:144282800-144290600	Weak transcription	Fetal Lung	lung
26	chr4:144283000-144285000	Weak transcription	Esophagus	oesophagus
27	chr4:144283000-144285800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:144283000-144286400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:144283000-144290600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr4:144283000-144290800	Weak transcription	Primary B cells from cord blood	blood
31	chr4:144283000-144290800	Weak transcription	Gastric	stomach
32	chr4:144283000-144291200	Weak transcription	Ovary	ovary
33	chr4:144283000-144293400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:144283000-144295400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr4:144283000-144302200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:144283200-144293400	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr4:144283400-144285000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:144283800-144285000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr4:144283800-144285200	Enhancers	Psoas Muscle	Psoas
40	chr4:144283800-144285200	Enhancers	Right Atrium	heart
41	chr4:144284000-144286000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:144284000-144293600	Weak transcription	Spleen	Spleen
43	chr4:144284000-144296600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr4:144284000-144296600	Weak transcription	Fetal Thymus	thymus
45	chr4:144284200-144285400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr4:144284200-144286400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:144284200-144287000	Weak transcription	Brain Anterior Caudate	brain
48	chr4:144284200-144295600	Weak transcription	Duodenum Mucosa	Duodenum
49	chr4:144284400-144285400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr4:144284400-144285400	Weak transcription	Colon Smooth Muscle	Colon

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