Variant report

Variant	nsv879006
Chromosome Location	chr4:47525054-47555196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:314 , 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	ATF2	chr4:47533593-47534069	GM12878	blood:	n/a	n/a
2	ATF2	chr4:47533555-47534185	GM12878	blood:	n/a	n/a
3	BCL11A	chr4:47533703-47533967	GM12878	blood:	n/a	n/a
4	BCLAF1	chr4:47533624-47534189	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:47527356-47528014	HCT-116	colon:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
6	CEBPB	chr4:47544669-47545142	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:47527422-47527929	A549	lung:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
8	CEBPB	chr4:47527577-47527852	HepG2	liver:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
9	CEBPB	chr4:47545252-47545559	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:47533357-47534135	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:47527570-47527844	ECC-1	luminal epithelium:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
12	CEBPB	chr4:47530031-47530346	IMR90	lung:	n/a	chr4:47530167-47530178
13	CEBPB	chr4:47553708-47554054	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:47545335-47545535	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:47527625-47527834	K562	blood:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
16	CEBPB	chr4:47527576-47527839	A549	lung:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
17	CEBPB	chr4:47527416-47528072	HCT-116	colon:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
18	CEBPB	chr4:47527375-47528010	IMR90	lung:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
19	CEBPB	chr4:47530098-47530188	K562	blood:	n/a	chr4:47530167-47530178
20	CEBPB	chr4:47527525-47527820	A549	lung:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
21	CEBPB	chr4:47545379-47545386	K562	blood:	n/a	n/a
22	CEBPB	chr4:47530124-47530327	HepG2	liver:	n/a	chr4:47530167-47530178
23	CEBPB	chr4:47544711-47545047	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:47527272-47528046	Hela-S3	cervix:	n/a	chr4:47527702-47527715 chr4:47527703-47527714
25	CEBPB	chr4:47533306-47533630	Hela-S3	cervix:	n/a	n/a
26	CHD1	chr4:47533181-47534326	IMR90	lung:	n/a	n/a
27	CHD1	chr4:47533633-47534067	GM12878	blood:	n/a	n/a
28	CHD2	chr4:47527271-47527820	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr4:47533363-47533600	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr4:47533656-47534084	GM12878	blood:	n/a	n/a
31	CTCF	chr4:47533820-47533970	AG10803	skin:	n/a	n/a
32	CTCF	chr4:47533920-47534070	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr4:47532541-47532631	Fibrobl	skin:	n/a	n/a
34	CTCF	chr4:47533700-47533850	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr4:47551887-47551919	ProgFib	skin:	n/a	n/a
36	CUX1	chr4:47528564-47528570	GM12878	blood:	n/a	n/a
37	CUX1	chr4:47535294-47535322	GM12878	blood:	n/a	n/a
38	CUX1	chr4:47535653-47536406	GM12878	blood:	n/a	n/a
39	E2F4	chr4:47528621-47528860	MCF10A-Er-Src	breast:	n/a	n/a
40	EBF1	chr4:47533724-47534012	GM12878	blood:	n/a	n/a
41	EBF1	chr4:47533722-47534296	GM12878	blood:	n/a	n/a
42	EBF1	chr4:47536079-47536374	GM12878	blood:	n/a	n/a
43	EGR1	chr4:47527332-47527912	HCT-116	colon:	n/a	n/a
44	EGR1	chr4:47527447-47527878	HCT-116	colon:	n/a	n/a
45	EP300	chr4:47533315-47533600	Hela-S3	cervix:	n/a	n/a
46	EP300	chr4:47535804-47536093	GM12878	blood:	n/a	n/a
47	EP300	chr4:47553662-47553960	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr4:47527258-47527891	Hela-S3	cervix:	n/a	chr4:47527700-47527714 chr4:47527338-47527347
49	EP300	chr4:47533332-47533761	ECC-1	luminal epithelium:	n/a	n/a
50	EP300	chr4:47527206-47528062	SK-N-SH	brain:	n/a	chr4:47527700-47527714 chr4:47527338-47527347

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:47533905-47533955	GM12891	blood:	n/a
2	chr4:47533905-47533955	SK-N-MC	brain:	n/a
3	chr4:47533905-47533955	NB4	blood:	n/a
4	chr4:47533905-47533955	HUVEC	blood vessel:	n/a
5	chr4:47533905-47533955	HAEpiC	amniotic membrane:	n/a
6	chr4:47533905-47533955	BJ	skin:	n/a
7	chr4:47533905-47533955	K562	blood:	n/a
8	chr4:47533905-47533955	AG04450	lung:	fetal
9	chr4:47533905-47533955	BE2_C	brain:	n/a
10	chr4:47533905-47533955	NT2-D1	testis:	n/a
11	chr4:47533905-47533955	PrEC	prostate:	n/a
12	chr4:47533905-47533955	HRCEpiC	kidney:	n/a
13	chr4:47533905-47533955	LNCaP	prostate:	n/a
14	chr4:47533905-47533955	Jurkat	blood:	n/a
15	chr4:47533905-47533955	CMK	blood:	n/a
16	chr4:47533905-47533955	AG04449	skin:	fetal
17	chr4:47533905-47533955	GM12892	blood:	n/a
18	chr4:47533905-47533955	HMEC	breast:	n/a
19	chr4:47533905-47533955	T-47D	breast:	n/a
20	chr4:47533905-47533955	H1-hESC	embryonic stem cell:	embryo
21	chr4:47533905-47533955	HL-60	blood:	n/a
22	chr4:47533905-47533955	SK-N-SH	brain:	n/a
23	chr4:47533905-47533955	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:47533905-47533955	AoSMC	blood vessel:	n/a
25	chr4:47533905-47533955	PFSK-1	brain:	n/a
26	chr4:47533905-47533955	HIPEpiC	eye:	n/a
27	chr4:47533905-47533955	HRPEpiC	eye:	n/a
28	chr4:47533905-47533955	SAEC	small airway:	n/a
29	chr4:47533905-47533955	Caco-2	colon:	n/a
30	chr4:47533905-47533955	GM19239	blood:	n/a
31	chr4:47533905-47533955	AG09319	gingival:	n/a
32	chr4:47533905-47533955	NHBE	bronchial:	n/a
33	chr4:47533905-47533955	MCF-7	breast:	n/a
34	chr4:47533905-47533955	AG09309	skin:	n/a
35	chr4:47533905-47533955	MCF10A-Er-Src	breast:	n/a
36	chr4:47533905-47533955	HCPEpiC	choroid plexus:	n/a
37	chr4:47533905-47533955	ovcar-3	ovarian:	n/a
38	chr4:47533905-47533955	GM06990	blood:	n/a
39	chr4:47533905-47533955	GM12878	blood:	n/a
40	chr4:47533905-47533955	NH-A	brain:	n/a
41	chr4:47533905-47533955	Hepatocyte	liver:	n/a
42	chr4:47533905-47533955	SKMC	muscle:	n/a
43	chr4:47533905-47533955	RPTEC	kidney:	n/a
44	chr4:47533905-47533955	U87	brain:	n/a
45	chr4:47533905-47533955	HCF	heart:	n/a
46	chr4:47533905-47533955	Hela-S3	cervix:	n/a
47	chr4:47533905-47533955	HRE	kidney:	n/a
48	chr4:47533905-47533955	IMR90	lung:	fetal
49	chr4:47533905-47533955	HCT-116	colon:	n/a
50	chr4:47533905-47533955	ProgFib	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:47533452..47535756-chr4:47565106..47567780,2	K562	blood:
2	chr4:47536442..47538388-chr4:47538970..47540735,2	K562	blood:
3	chr4:47551527..47553990-chr4:47565795..47567988,3	K562	blood:
4	chr4:47523458..47525968-chr4:47532454..47534503,2	K562	blood:
5	chr4:47551465..47554055-chr4:47561436..47564386,2	K562	blood:
6	chr1:36983678..36984348-chr4:47541449..47542413,2	MCF-7	breast:
7	chr4:47523458..47525968-chr4:47532454..47534503,2	K562	blood:
8	chr4:47536442..47538388-chr4:47538970..47540735,2	K562	blood:
9	chr4:47551527..47553990-chr4:47565971..47567988,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATP10D	hsa-miR-192-5p	chr4:47548938-47548960

Variant related genes	Relation type
ATP10D	TF binding region
ATP10D	CpG island
ENSG00000248254	chromatin interactions

Extended variants
information (count: 1177 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1177 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7683838	chr4:47525054-47525055	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367712180	chr4:47525062-47525063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371308151	chr4:47525065-47525066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200556408	chr4:47525087-47525088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114311534	chr4:47525088-47525089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182993483	chr4:47525093-47525094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371624169	chr4:47525102-47525103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376532237	chr4:47525104-47525105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187325459	chr4:47525125-47525126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369447775	chr4:47525128-47525129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372769135	chr4:47525173-47525174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200306183	chr4:47525178-47525179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192815760	chr4:47525216-47525217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559976209	chr4:47525217-47525218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554858774	chr4:47525245-47525246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552322089	chr4:47525258-47525259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113184821	chr4:47525259-47525260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368313783	chr4:47525264-47525265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573444591	chr4:47525366-47525367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74504545	chr4:47525457-47525458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567617589	chr4:47525465-47525466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532679925	chr4:47525480-47525481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183315255	chr4:47525496-47525497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187853879	chr4:47525534-47525535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535141015	chr4:47525563-47525564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536605757	chr4:47525603-47525604	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548912929	chr4:47525605-47525606	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192761032	chr4:47525622-47525623	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567123200	chr4:47525668-47525669	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6842769	chr4:47525681-47525682	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs559143130	chr4:47525689-47525690	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577358950	chr4:47525724-47525725	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6837743	chr4:47525750-47525751	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs569125978	chr4:47525771-47525772	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184233700	chr4:47525789-47525790	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189601404	chr4:47525798-47525799	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376056847	chr4:47525822-47525823	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370869184	chr4:47525823-47525824	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544073201	chr4:47525824-47525825	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114551615	chr4:47525839-47525840	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192490506	chr4:47525865-47525866	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141828352	chr4:47525943-47525944	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184712655	chr4:47526022-47526023	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139076594	chr4:47526090-47526091	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564351146	chr4:47526105-47526106	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531359035	chr4:47526135-47526136	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551103475	chr4:47526173-47526174	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189082840	chr4:47526175-47526176	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10213210	chr4:47526194-47526195	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530136781	chr4:47526234-47526235	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19214233	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47488000-47533800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:47488800-47559800	Weak transcription	Right Ventricle	heart
3	chr4:47489200-47533600	Weak transcription	Esophagus	oesophagus
4	chr4:47501000-47527600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr4:47502200-47533000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:47507800-47526400	Weak transcription	NHDF-Ad	bronchial
7	chr4:47507800-47527800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr4:47510000-47526000	Weak transcription	Pancreas	Pancrea
9	chr4:47512200-47536800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr4:47512400-47530200	Weak transcription	Fetal Brain Male	brain
11	chr4:47512400-47577200	Weak transcription	Small Intestine	intestine
12	chr4:47512800-47532600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:47513000-47527600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr4:47513600-47533200	Weak transcription	Brain Substantia Nigra	brain
15	chr4:47513800-47530600	Weak transcription	Fetal Heart	heart
16	chr4:47513800-47534000	Weak transcription	Brain Hippocampus Middle	brain
17	chr4:47514000-47531400	Weak transcription	Brain Anterior Caudate	brain
18	chr4:47514000-47551000	Weak transcription	Gastric	stomach
19	chr4:47514200-47533800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr4:47515800-47527800	Weak transcription	Aorta	Aorta
21	chr4:47515800-47530000	Weak transcription	Primary T cells from cord blood	blood
22	chr4:47515800-47531200	Weak transcription	Colon Smooth Muscle	Colon
23	chr4:47515800-47533800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr4:47515800-47533800	Weak transcription	Lung	lung
25	chr4:47516000-47525600	Weak transcription	NHLF	lung
26	chr4:47516000-47527400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr4:47516000-47529600	Weak transcription	Fetal Muscle Leg	muscle
28	chr4:47516000-47534000	Weak transcription	Stomach Mucosa	stomach
29	chr4:47516200-47525800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr4:47516200-47526200	Weak transcription	Fetal Lung	lung
31	chr4:47516200-47527800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr4:47516400-47547800	Weak transcription	Ovary	ovary
33	chr4:47516400-47548200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr4:47516600-47527800	Weak transcription	Fetal Intestine Large	intestine
35	chr4:47517800-47528800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr4:47518000-47525600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr4:47518000-47526400	Weak transcription	NHEK	skin
38	chr4:47518000-47527200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:47518000-47527800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:47518000-47544800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr4:47519400-47525400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr4:47520400-47533600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr4:47521600-47526000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr4:47521800-47532800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr4:47521800-47533200	Weak transcription	Spleen	Spleen
46	chr4:47522000-47525800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:47522000-47526000	Weak transcription	HUVEC	blood vessel
48	chr4:47522000-47526400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:47522000-47531000	Strong transcription	Placenta	Placenta
50	chr4:47522000-47533000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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