Variant report

Variant	esv1847399
Chromosome Location	chr4:166259587-166284836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:166261743-166261910	K562	blood:	n/a	n/a
2	ARID3A	chr4:166281588-166281860	K562	blood:	n/a	n/a
3	ARID3A	chr4:166264413-166265310	K562	blood:	n/a	n/a
4	ARID3A	chr4:166264658-166265444	HepG2	liver:	n/a	n/a
5	ATF3	chr4:166281577-166281862	K562	blood:	n/a	n/a
6	BACH1	chr4:166272882-166273046	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:166272820-166273110	GM12878	blood:	n/a	chr4:166273004-166273015
8	BCL3	chr4:166264834-166265531	GM12878	blood:	n/a	n/a
9	BCLAF1	chr4:166264853-166265454	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:166269417-166269467	K562	blood:	n/a	n/a
11	BHLHE40	chr4:166264999-166265335	K562	blood:	n/a	n/a
12	BRCA1	chr4:166276799-166276964	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr4:166261525-166261836	K562	blood:	n/a	n/a
14	CCNT2	chr4:166263897-166265414	K562	blood:	n/a	n/a
15	CCNT2	chr4:166263319-166263404	K562	blood:	n/a	n/a
16	CEBPB	chr4:166280833-166280926	A549	lung:	n/a	chr4:166280856-166280868
17	CEBPB	chr4:166269072-166269397	HepG2	liver:	n/a	chr4:166269226-166269237 chr4:166269224-166269235 chr4:166269226-166269235
18	CEBPB	chr4:166270121-166270321	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:166269098-166269391	Hela-S3	cervix:	n/a	chr4:166269226-166269237 chr4:166269224-166269235 chr4:166269226-166269235
20	CEBPB	chr4:166270061-166270407	K562	blood:	n/a	n/a
21	CEBPB	chr4:166269051-166269408	IMR90	lung:	n/a	chr4:166269226-166269237 chr4:166269224-166269235 chr4:166269226-166269235
22	CEBPB	chr4:166276939-166277427	HepG2	liver:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
23	CEBPB	chr4:166274966-166275131	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:166281538-166281900	K562	blood:	n/a	chr4:166281704-166281717
25	CEBPB	chr4:166277053-166277443	MCF-7	breast:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
26	CEBPB	chr4:166269052-166269411	K562	blood:	n/a	chr4:166269226-166269237 chr4:166269224-166269235 chr4:166269226-166269235
27	CEBPB	chr4:166270060-166270402	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:166276917-166277358	K562	blood:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
29	CEBPB	chr4:166281528-166281852	K562	blood:	n/a	chr4:166281704-166281717
30	CEBPB	chr4:166282166-166282473	K562	blood:	n/a	chr4:166282316-166282327
31	CEBPB	chr4:166276946-166277432	K562	blood:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
32	CEBPB	chr4:166274925-166275076	K562	blood:	n/a	n/a
33	CEBPB	chr4:166282242-166282493	A549	lung:	n/a	chr4:166282316-166282327
34	CEBPB	chr4:166276984-166277433	H1-hESC	embryonic stem cell:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
35	CEBPB	chr4:166277079-166277356	A549	lung:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
36	CEBPB	chr4:166282179-166282433	HepG2	liver:	n/a	chr4:166282316-166282327
37	CEBPB	chr4:166269052-166269373	A549	lung:	n/a	chr4:166269226-166269237 chr4:166269224-166269235 chr4:166269226-166269235
38	CEBPB	chr4:166276976-166277451	Hela-S3	cervix:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
39	CEBPB	chr4:166280658-166281047	Hela-S3	cervix:	n/a	chr4:166280856-166280868 chr4:166280790-166280803
40	CEBPB	chr4:166281553-166281862	IMR90	lung:	n/a	chr4:166281704-166281717
41	CEBPB	chr4:166282155-166282481	IMR90	lung:	n/a	chr4:166282316-166282327
42	CEBPB	chr4:166276979-166277394	IMR90	lung:	n/a	chr4:166277257-166277268 chr4:166277107-166277120 chr4:166277256-166277267 chr4:166277107-166277120 chr4:166277109-166277120
43	CEBPB	chr4:166270060-166270395	Hela-S3	cervix:	n/a	n/a
44	CEBPD	chr4:166269769-166270249	K562	blood:	n/a	n/a
45	CHD2	chr4:166264358-166265360	K562	blood:	n/a	n/a
46	CHD2	chr4:166264656-166265350	HepG2	liver:	n/a	n/a
47	CHD2	chr4:166277254-166277409	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr4:166277200-166277350	HUVEC	blood vessel:	n/a	chr4:166277275-166277293 chr4:166277278-166277291 chr4:166277277-166277298
49	CTCF	chr4:166264942-166265217	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:166264940-166265090	HL-60	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:166262631..166267437-chr4:166267990..166271315,4	K562	blood:
2	chr4:166248172..166250457-chr4:166265165..166267668,2	MCF-7	breast:
3	chr4:166253639..166255171-chr4:166261974..166264196,2	K562	blood:
4	chr4:166276597..166279121-chr4:166279967..166282162,2	K562	blood:
5	chr4:166262631..166267437-chr4:166267990..166271315,4	K562	blood:
6	chr4:166247031..166249903-chr4:166268462..166270625,2	K562	blood:
7	chr4:166284247..166286679-chr4:166288539..166290783,2	K562	blood:
8	chr4:166052186..166053056-chr4:166264613..166265364,4	MCF-7	breast:
9	chr4:166052311..166053023-chr4:166265996..166266912,2	MCF-7	breast:
10	chr4:166260940..166262583-chr4:166265474..166268224,2	K562	blood:
11	chr4:166279563..166282339-chr4:166287037..166289622,2	MCF-7	breast:
12	chr4:166276683..166277608-chr4:166385622..166387104,5	MCF-7	breast:
13	chr4:166051363..166053095-chr4:166265302..166266870,2	MCF-7	breast:
14	chr4:166052208..166052989-chr4:166267211..166267831,3	MCF-7	breast:
15	chr4:166260940..166262583-chr4:166265474..166268224,2	K562	blood:
16	chr4:166277287..166279356-chr4:166299374..166301924,3	MCF-7	breast:
17	chr4:166265012..166266616-chr4:166301468..166303091,2	K562	blood:
18	chr4:166279128..166280930-chr4:166292985..166295203,2	K562	blood:
19	chr4:166276597..166279121-chr4:166279967..166282162,2	K562	blood:
20	chr4:166052342..166053351-chr4:166266832..166267864,6	MCF-7	breast:
21	chr4:166254481..166256226-chr4:166260007..166262078,2	K562	blood:
22	chr4:166052131..166053206-chr4:166263833..166265852,12	MCF-7	breast:
23	chr4:166249129..166252121-chr4:166265324..166266921,2	K562	blood:
24	chr4:166251079..166252856-chr4:166258884..166260563,2	MCF-7	breast:
25	chr4:166034224..166034823-chr4:166264610..166265422,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location
1	SC4MOL	hsa-miR-26b-5p	chr4:166264061-166264068
2	SC4MOL	hsa-let-7e-5p	chr4:166263721-166263743
3	SC4MOL	hsa-miR-19a-3p	chr4:166264167-166264188
4	SC4MOL	hsa-miR-335-5p	chr4:166264178-166264200
5	SC4MOL	hsa-miR-26b-5p	chr4:166264049-166264068
6	SC4MOL	hsa-miR-19a-3p	chr4:166264181-166264187

Variant related genes	Relation type
CPE	TF binding region
ENSG00000052802	chromatin interactions
ENSG00000109472	chromatin interactions

Extended variants
information (count: 1005 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1005 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17046253	chr4:166259643-166259644	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192814912	chr4:166259715-166259716	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17046259	chr4:166259719-166259720	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs184224508	chr4:166259733-166259734	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549282037	chr4:166259739-166259740	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542993632	chr4:166259756-166259757	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375675952	chr4:166259795-166259796	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369080275	chr4:166259799-166259800	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372815904	chr4:166259944-166259945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112787177	chr4:166259945-166259946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369726198	chr4:166259957-166259958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376852737	chr4:166259964-166259965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371223310	chr4:166259971-166259972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549896595	chr4:166260017-166260018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188560110	chr4:166260045-166260046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561533905	chr4:166260058-166260059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544020676	chr4:166260070-166260071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528917436	chr4:166260100-166260101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143699913	chr4:166260157-166260158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191526199	chr4:166260160-166260161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183717274	chr4:166260163-166260164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115263689	chr4:166260186-166260187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566623167	chr4:166260189-166260190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539988336	chr4:166260190-166260191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534118567	chr4:166260218-166260219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs28697162	chr4:166260236-166260237	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555225594	chr4:166260281-166260282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377206997	chr4:166260287-166260288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140349521	chr4:166260298-166260299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145409252	chr4:166260343-166260344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545039281	chr4:166260367-166260368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28622225	chr4:166260369-166260370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572603836	chr4:166260371-166260372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568325761	chr4:166260413-166260414	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62352297	chr4:166260414-166260415	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531832613	chr4:166260416-166260417	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150875061	chr4:166260420-166260421	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562277779	chr4:166260520-166260521	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532881693	chr4:166260521-166260522	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140832901	chr4:166260546-166260547	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190546444	chr4:166260550-166260551	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527579957	chr4:166260552-166260553	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553966947	chr4:166260579-166260580	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74347892	chr4:166260586-166260587	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115796803	chr4:166260592-166260593	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6829944	chr4:166260601-166260602	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556408157	chr4:166260617-166260618	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182387161	chr4:166260651-166260652	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6830103	chr4:166260657-166260658	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs536240461	chr4:166260667-166260668	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166249600-166266600	Weak transcription	Left Ventricle	heart
2	chr4:166249800-166262400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr4:166249800-166262600	Weak transcription	Thymus	Thymus
4	chr4:166250000-166264600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr4:166250200-166259800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr4:166250200-166260400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr4:166250200-166260800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr4:166250200-166262600	Weak transcription	Spleen	Spleen
9	chr4:166250200-166262800	Weak transcription	Right Ventricle	heart
10	chr4:166250200-166263800	Weak transcription	Colon Smooth Muscle	Colon
11	chr4:166250200-166265000	Weak transcription	Psoas Muscle	Psoas
12	chr4:166250200-166265200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:166250400-166259600	Weak transcription	Fetal Kidney	kidney
14	chr4:166250400-166260800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr4:166250400-166260800	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr4:166250400-166262600	Weak transcription	Aorta	Aorta
17	chr4:166250600-166259800	Weak transcription	Adipose Nuclei	Adipose
18	chr4:166250600-166259800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr4:166250600-166263200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr4:166250600-166265400	Weak transcription	Colonic Mucosa	Colon
21	chr4:166250600-166266800	Weak transcription	A549	lung
22	chr4:166252000-166259600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr4:166252200-166260200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:166252200-166269200	Weak transcription	Stomach Mucosa	stomach
25	chr4:166252200-166269400	Weak transcription	Gastric	stomach
26	chr4:166252400-166260400	Weak transcription	Esophagus	oesophagus
27	chr4:166252400-166260400	Weak transcription	Ovary	ovary
28	chr4:166252600-166260200	Weak transcription	Fetal Intestine Small	intestine
29	chr4:166252800-166259600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr4:166253200-166260200	Weak transcription	Fetal Stomach	stomach
31	chr4:166253400-166260200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:166253400-166263000	Weak transcription	Pancreas	Pancrea
33	chr4:166253400-166272600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:166253600-166265400	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:166253800-166259600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr4:166253800-166260200	Weak transcription	Lung	lung
37	chr4:166253800-166265200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:166253800-166266600	Weak transcription	Small Intestine	intestine
39	chr4:166254000-166259600	Weak transcription	Fetal Lung	lung
40	chr4:166254000-166260200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr4:166254000-166260400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr4:166254000-166260400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr4:166254000-166264600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr4:166254000-166264800	Weak transcription	Hela-S3	cervix
45	chr4:166254000-166265200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:166254000-166265200	Strong transcription	NHDF-Ad	bronchial
47	chr4:166254000-166269400	Weak transcription	Fetal Heart	heart
48	chr4:166254200-166261200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr4:166254200-166264200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr4:166254200-166265200	Strong transcription	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links