Variant report

Variant	nsv880168
Chromosome Location	chr4:141826780-141900370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:306)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:141851945-141852158	GM12878	blood:	n/a	n/a
2	CEBPB	chr4:141873863-141874222	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr4:141873925-141874164	HepG2	liver:	n/a	n/a
4	CEBPB	chr4:141874055-141874080	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:141846665-141846919	A549	lung:	n/a	chr4:141846784-141846795 chr4:141846873-141846881
6	CEBPB	chr4:141884470-141884625	A549	lung:	n/a	n/a
7	CEBPB	chr4:141873872-141874221	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:141834731-141834994	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:141889561-141889832	IMR90	lung:	n/a	chr4:141889702-141889715 chr4:141889703-141889714
10	CEBPB	chr4:141889599-141889822	HepG2	liver:	n/a	chr4:141889702-141889715 chr4:141889703-141889714
11	CEBPB	chr4:141873908-141874139	A549	lung:	n/a	n/a
12	CEBPB	chr4:141846656-141846937	IMR90	lung:	n/a	chr4:141846784-141846795 chr4:141846873-141846881
13	CEBPB	chr4:141889576-141889770	H1-hESC	embryonic stem cell:	n/a	chr4:141889702-141889715 chr4:141889703-141889714
14	CEBPB	chr4:141836176-141836307	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:141884482-141884601	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:141846619-141846961	HepG2	liver:	n/a	chr4:141846784-141846795 chr4:141846873-141846881
17	CEBPB	chr4:141846749-141846819	K562	blood:	n/a	chr4:141846784-141846795
18	CTBP2	chr4:141846040-141846553	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr4:141846240-141846390	BE2_C	brain:	n/a	n/a
20	CTCF	chr4:141884480-141884630	HCFaa	heart:	n/a	n/a
21	CTCF	chr4:141884460-141884610	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr4:141884500-141884650	AG04449	skin:	n/a	n/a
23	CTCF	chr4:141884531-141884593	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:141877747-141877784	GM10248	blood:	n/a	n/a
25	CTCF	chr4:141884400-141884550	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr4:141831848-141831904	Fibrobl	skin:	n/a	n/a
27	CTCF	chr4:141884520-141884670	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr4:141884460-141884610	HPF	lung:	n/a	n/a
29	CTCF	chr4:141877420-141877570	AG09319	gingival:	n/a	n/a
30	CTCF	chr4:141868741-141868801	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:141884506-141884624	Medullo	brain:	n/a	n/a
32	CTCF	chr4:141881040-141881092	GM13976	blood:	n/a	n/a
33	CTCF	chr4:141884460-141884610	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr4:141846140-141846290	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr4:141884447-141884628	IMR90	lung:	n/a	n/a
36	CTCF	chr4:141884504-141884633	LNCaP	prostate:	n/a	n/a
37	CTCF	chr4:141846320-141846470	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr4:141884440-141884590	HMF	breast:	n/a	n/a
39	CTCF	chr4:141846204-141846254	LNCaP	prostate:	n/a	n/a
40	CTCF	chr4:141884460-141884610	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr4:141884500-141884650	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr4:141884506-141884609	LNCaP	prostate:	n/a	n/a
43	CTCF	chr4:141884480-141884630	HMF	breast:	n/a	n/a
44	CTCF	chr4:141884480-141884630	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr4:141846120-141846270	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr4:141884520-141884670	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:141884500-141884650	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:141846300-141846450	BE2_C	brain:	n/a	n/a
49	CTCF	chr4:141884500-141884650	BE2_C	brain:	n/a	n/a
50	CTCF	chr4:141846164-141846329	Medullo	brain:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:141859672-141859722	CMK	blood:	n/a
2	chr4:141859672-141859722	CMK	blood:	n/a
3	chr4:141859472-141859522	Hepatocyte	liver:	n/a
4	chr4:141865108-141865158	A549	lung:	n/a
5	chr4:141859672-141859722	PrEC	prostate:	n/a
6	chr4:141865108-141865158	ovcar-3	ovarian:	n/a
7	chr4:141846078-141846128	SK-N-SH	brain:	n/a
8	chr4:141877033-141877083	HEK293	kidney:	embryo
9	chr4:141865108-141865158	SAEC	small airway:	n/a
10	chr4:141859472-141859522	K562	blood:	n/a
11	chr4:141859472-141859522	HCT-116	colon:	n/a
12	chr4:141865108-141865158	HCM	heart:	n/a
13	chr4:141846078-141846128	AG09309	skin:	n/a
14	chr4:141859472-141859522	PANC-1	pancreas:	n/a
15	chr4:141859672-141859722	HAEpiC	amniotic membrane:	n/a
16	chr4:141859472-141859522	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:141877033-141877083	SK-N-SH	brain:	n/a
18	chr4:141877033-141877083	SK-N-SH_RA	brain:	n/a
19	chr4:141846078-141846128	A549	lung:	n/a
20	chr4:141846078-141846128	IMR90	lung:	fetal
21	chr4:141846078-141846128	PrEC	prostate:	n/a
22	chr4:141865108-141865158	BJ	skin:	n/a
23	chr4:141859672-141859722	AG09309	skin:	n/a
24	chr4:141865108-141865158	HCT-116	colon:	n/a
25	chr4:141859672-141859722	RPTEC	kidney:	n/a
26	chr4:141859672-141859722	SK-N-SH	brain:	n/a
27	chr4:141846078-141846128	MCF10A-Er-Src	breast:	n/a
28	chr4:141846078-141846128	HAEpiC	amniotic membrane:	n/a
29	chr4:141865108-141865158	HAEpiC	amniotic membrane:	n/a
30	chr4:141859472-141859522	HepG2	liver:	n/a
31	chr4:141859472-141859522	HCM	heart:	n/a
32	chr4:141859672-141859722	GM12891	blood:	n/a
33	chr4:141846078-141846128	NH-A	brain:	n/a
34	chr4:141865108-141865158	NH-A	brain:	n/a
35	chr4:141859672-141859722	NB4	blood:	n/a
36	chr4:141859672-141859722	PANC-1	pancreas:	n/a
37	chr4:141877033-141877083	Hepatocyte	liver:	n/a
38	chr4:141859472-141859522	ProgFib	skin:	n/a
39	chr4:141846078-141846128	SK-N-SH_RA	brain:	n/a
40	chr4:141859672-141859722	SAEC	small airway:	n/a
41	chr4:141877033-141877083	NHBE	bronchial:	n/a
42	chr4:141859472-141859522	SAEC	small airway:	n/a
43	chr4:141859472-141859522	ECC-1	luminal epithelium:	n/a
44	chr4:141846078-141846128	NHDF-neo	bronchial:	n/a
45	chr4:141865108-141865158	HIPEpiC	eye:	n/a
46	chr4:141859472-141859522	GM12891	blood:	n/a
47	chr4:141865108-141865158	Jurkat	blood:	n/a
48	chr4:141859472-141859522	NB4	blood:	n/a
49	chr4:141846078-141846128	AG10803	skin:	n/a
50	chr4:141877033-141877083	Caco-2	colon:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:141865472..141867411-chr4:142030563..142032115,2	MCF-7	breast:
2	chr4:141864985..141866884-chr4:141889124..141891392,2	K562	blood:
3	chr4:141857760..141859447-chr4:141874857..141876675,2	K562	blood:
4	chr4:141870898..141873805-chr4:142207109..142209928,2	K562	blood:
5	chr4:141888929..141891016-chr4:141891201..141893150,2	K562	blood:
6	chr4:141782326..141783157-chr4:141884203..141884946,4	MCF-7	breast:
7	chr4:141866516..141868304-chr4:141870029..141871688,2	K562	blood:
8	chr4:141864985..141866884-chr4:141889124..141891392,2	K562	blood:
9	chr4:141857760..141859447-chr4:141874857..141876675,2	K562	blood:
10	chr4:141858527..141861200-chr4:141868423..141870294,2	K562	blood:
11	chr4:141866516..141868304-chr4:141870029..141871688,2	K562	blood:
12	chr4:141858527..141861200-chr4:141868423..141870294,2	K562	blood:

No data

Variant related genes	Relation type
RNF150	TF binding region
RNF150	CpG island
ENSG00000170153	chromatin interactions

Extended variants
information (count: 2957 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2957 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1030356	chr4:141826780-141826781	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2059496	chr4:141826795-141826796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs79550770	chr4:141826806-141826807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150630289	chr4:141826821-141826822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573362242	chr4:141826846-141826847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560978944	chr4:141826851-141826852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6148696	chr4:141826877-141826878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs3217282	chr4:141826886-141826887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368367751	chr4:141826906-141826907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115112544	chr4:141826922-141826923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562318051	chr4:141826959-141826960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577779045	chr4:141826964-141826965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139699405	chr4:141827002-141827003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184960462	chr4:141827107-141827108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527622814	chr4:141827109-141827110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376014025	chr4:141827152-141827153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2059497	chr4:141827155-141827156	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs565405130	chr4:141827191-141827192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2059498	chr4:141827222-141827223	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs189767459	chr4:141827309-141827310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149790667	chr4:141827330-141827331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550802303	chr4:141827341-141827342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551999795	chr4:141827379-141827380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146816580	chr4:141827407-141827408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183084509	chr4:141827411-141827412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs71608412	chr4:141827488-141827489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554897293	chr4:141827493-141827494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573325810	chr4:141827519-141827520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189057805	chr4:141827550-141827551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569106090	chr4:141827562-141827563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140319634	chr4:141827574-141827575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116328692	chr4:141827597-141827598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35164406	chr4:141827599-141827600	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs569702659	chr4:141827606-141827607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7685273	chr4:141827659-141827660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs374323573	chr4:141827662-141827663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193148269	chr4:141827679-141827680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534631872	chr4:141827745-141827746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562027533	chr4:141827840-141827841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543590109	chr4:141827898-141827899	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183626998	chr4:141827902-141827903	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376189668	chr4:141827911-141827912	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188507977	chr4:141827936-141827937	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs984839	chr4:141827937-141827938	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs533509172	chr4:141827945-141827946	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372919365	chr4:141828001-141828002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191701128	chr4:141828010-141828011	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184236846	chr4:141828016-141828017	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186638660	chr4:141828108-141828109	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549285401	chr4:141828124-141828125	Weak transcription Strong transcription Enhancers	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
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
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:141789600-141831600	Weak transcription	Aorta	Aorta
2	chr4:141816200-141851400	Weak transcription	Brain Anterior Caudate	brain
3	chr4:141816400-141831600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:141817800-141831800	Weak transcription	Pancreas	Pancrea
5	chr4:141822800-141826800	Enhancers	Fetal Brain Male	brain
6	chr4:141823000-141827000	Enhancers	Fetal Lung	lung
7	chr4:141823200-141827200	Enhancers	Fetal Muscle Leg	muscle
8	chr4:141823200-141829000	Enhancers	Fetal Stomach	stomach
9	chr4:141823200-141855800	Weak transcription	Osteobl	bone
10	chr4:141823600-141831600	Weak transcription	Fetal Brain Female	brain
11	chr4:141824000-141827200	Enhancers	Fetal Heart	heart
12	chr4:141824200-141827800	Weak transcription	Psoas Muscle	Psoas
13	chr4:141824600-141826800	Enhancers	Colon Smooth Muscle	Colon
14	chr4:141824800-141827800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr4:141825200-141831800	Weak transcription	Fetal Intestine Small	intestine
16	chr4:141825400-141827000	Enhancers	Stomach Smooth Muscle	stomach
17	chr4:141825400-141827800	Weak transcription	Ovary	ovary
18	chr4:141825400-141827800	Weak transcription	Spleen	Spleen
19	chr4:141825400-141831600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:141825400-141831600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:141825400-141831600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr4:141825400-141831600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr4:141825400-141831600	Weak transcription	Right Ventricle	heart
24	chr4:141825400-141831800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:141825800-141828000	Weak transcription	Rectal Smooth Muscle	rectum
26	chr4:141825800-141828000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr4:141825800-141847200	Weak transcription	Fetal Kidney	kidney
28	chr4:141826000-141834000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:141826200-141826800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr4:141826400-141827800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:141826400-141831800	Weak transcription	Adipose Nuclei	Adipose
32	chr4:141826600-141826800	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr4:141826600-141827000	Enhancers	Left Ventricle	heart
34	chr4:141826600-141835000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:141826600-141836600	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr4:141826800-141828200	Weak transcription	Colon Smooth Muscle	Colon
37	chr4:141826800-141828400	Weak transcription	Fetal Brain Male	brain
38	chr4:141826800-141831600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr4:141826800-141833800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr4:141827000-141827800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr4:141827000-141828000	Weak transcription	Left Ventricle	heart
42	chr4:141827000-141828400	Weak transcription	Fetal Lung	lung
43	chr4:141827200-141827600	Weak transcription	Fetal Heart	heart
44	chr4:141827200-141831800	Weak transcription	Fetal Muscle Leg	muscle
45	chr4:141827600-141829600	Enhancers	Fetal Heart	heart
46	chr4:141827800-141828200	Enhancers	Spleen	Spleen
47	chr4:141827800-141828400	Enhancers	Right Atrium	heart
48	chr4:141827800-141828800	Enhancers	Psoas Muscle	Psoas
49	chr4:141827800-141829000	Enhancers	Ovary	ovary
50	chr4:141827800-141829000	Enhancers	Stomach Smooth Muscle	stomach

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