Variant report

Variant	nsv1064282
Chromosome Location	chr18:45369857-45404768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:272)
CpG islands
(count:0)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:45397603-45397941	HepG2	liver:	n/a	chr18:45397770-45397786
2	BACH1	chr18:45391890-45391917	K562	blood:	n/a	n/a
3	BATF	chr18:45379443-45379821	GM12878	blood:	n/a	n/a
4	BATF	chr18:45379570-45379813	GM12878	blood:	n/a	n/a
5	BCL11A	chr18:45379557-45379920	GM12878	blood:	n/a	n/a
6	BCL11A	chr18:45379518-45379810	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:45379541-45379905	HepG2	liver:	n/a	n/a
8	CEBPB	chr18:45397656-45397855	HepG2	liver:	n/a	chr18:45397738-45397749
9	CEBPB	chr18:45390754-45391063	HepG2	liver:	n/a	n/a
10	CEBPB	chr18:45379586-45379786	K562	blood:	n/a	n/a
11	CEBPB	chr18:45389601-45389752	A549	lung:	n/a	n/a
12	CEBPB	chr18:45370495-45370786	HepG2	liver:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
13	CEBPB	chr18:45390790-45391041	A549	lung:	n/a	n/a
14	CEBPB	chr18:45370562-45370782	A549	lung:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
15	CEBPB	chr18:45370478-45370783	IMR90	lung:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
16	CEBPB	chr18:45370450-45370801	K562	blood:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
17	CEBPB	chr18:45390727-45391043	IMR90	lung:	n/a	n/a
18	CEBPD	chr18:45379393-45379959	K562	blood:	n/a	n/a
19	CHD1	chr18:45380009-45380040	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr18:45403280-45403430	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr18:45397176-45397227	Medullo	brain:	n/a	n/a
22	CTCF	chr18:45372789-45372882	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr18:45391448-45391521	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr18:45391400-45391550	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr18:45397000-45397150	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr18:45403240-45403390	GM12864	blood:	n/a	n/a
27	CTCF	chr18:45397147-45397225	GM12878	blood:	n/a	n/a
28	CTCF	chr18:45397074-45397282	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr18:45403320-45403470	GM12874	blood:	n/a	n/a
30	CTCF	chr18:45391418-45391544	HepG2	liver:	n/a	n/a
31	CTCF	chr18:45397866-45397900	Fibrobl	skin:	n/a	n/a
32	CTCF	chr18:45391466-45391531	Medullo	brain:	n/a	n/a
33	CTCF	chr18:45403300-45403450	HCFaa	heart:	n/a	n/a
34	CTCF	chr18:45399007-45399037	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr18:45403334-45403434	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr18:45403260-45403410	AG04449	skin:	n/a	n/a
37	CTCF	chr18:45403352-45403411	Medullo	brain:	n/a	n/a
38	CTCF	chr18:45397120-45397270	NHEK	skin:	n/a	n/a
39	CTCF	chr18:45403320-45403470	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr18:45397097-45397248	GM12878	blood:	n/a	n/a
41	CTCF	chr18:45403240-45403390	GM12867	blood:	n/a	n/a
42	CTCF	chr18:45374240-45374390	HCM	heart:	n/a	n/a
43	CTCF	chr18:45403240-45403390	HCM	heart:	n/a	n/a
44	CTCF	chr18:45391431-45391563	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr18:45403300-45403423	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr18:45391482-45391517	LNCaP	prostate:	n/a	n/a
47	CTCF	chr18:45403340-45403490	HMF	breast:	n/a	n/a
48	CTCF	chr18:45397120-45397270	HEK293	kidney:	n/a	n/a
49	CTCF	chr18:45391441-45391530	K562	blood:	n/a	n/a
50	CTCF	chr18:45391400-45391550	HMEC	breast:	n/a	n/a

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:45401120..45404562-chr18:45404621..45407593,3	K562	blood:
2	chr18:45393055..45395642-chr18:45402481..45404020,2	MCF-7	breast:
3	chr16:2732028..2732807-chr18:45399145..45399845,2	Hela-S3	cervix:
4	chr18:45379137..45382377-chr18:45391896..45394821,3	K562	blood:
5	chr18:45400689..45404562-chr18:45404621..45407103,3	K562	blood:
6	chr18:45370062..45371817-chr18:45453252..45455227,2	MCF-7	breast:
7	chr18:45396878..45399642-chr18:45401844..45403752,2	MCF-7	breast:
8	chr18:45402056..45405449-chr18:45544846..45548415,3	MCF-7	breast:
9	chr18:45401120..45404562-chr18:45404621..45407593,3	K562	blood:
10	chr18:45367507..45370509-chr18:45371769..45374946,4	K562	blood:
11	chr18:45388105..45390269-chr18:45393560..45395389,2	K562	blood:
12	chr18:45388105..45390269-chr18:45393560..45395389,2	K562	blood:
13	chr18:45403717..45406207-chr18:45456494..45458562,2	K562	blood:
14	chr17:57916192..57918375-chr18:45387752..45390655,2	MCF-7	breast:
15	chr18:45390223..45391741-chr18:45457289..45459666,2	MCF-7	breast:
16	chr18:45391818..45394321-chr18:45399787..45402085,2	MCF-7	breast:
17	chr18:45402129..45404983-chr18:45456603..45459042,2	MCF-7	breast:
18	chr18:45368468..45370509-chr18:45372236..45375671,3	K562	blood:
19	chr18:45372242..45375198-chr18:45455382..45457471,2	K562	blood:
20	chr18:45391818..45394321-chr18:45399787..45402085,2	MCF-7	breast:
21	chr18:45400689..45404562-chr18:45404621..45407103,3	K562	blood:
22	chr18:45367507..45370509-chr18:45371769..45374946,4	K562	blood:
23	chr18:45396878..45399642-chr18:45401844..45403752,2	MCF-7	breast:
24	chr18:45393055..45395642-chr18:45402481..45404020,2	MCF-7	breast:
25	chr18:45368468..45370509-chr18:45372236..45375671,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB7C-5	chr18:45396844-45396935	NONHSAT059175
2	lnc-ZBTB7C-4	chr18:45404666-45404867	ENSG00000269365.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SMAD2	hsa-miR-200a-3p	chr18:45371474-45371494

Variant related genes	Relation type
ENSG00000267541	TF binding region
ENSG00000175387	chromatin interactions
ENSG00000167977	chromatin interactions
ENSG00000267541	chromatin interactions

Extended variants
information (count: 1427 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1427 , 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	rs1792684	chr18:45369857-45369858	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552229488	chr18:45369902-45369903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138985297	chr18:45369920-45369921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534733062	chr18:45369927-45369928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547849181	chr18:45369932-45369933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190136834	chr18:45369956-45369957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537303173	chr18:45369999-45370000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557334729	chr18:45370041-45370042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367955342	chr18:45370058-45370059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539678593	chr18:45370122-45370123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553147440	chr18:45370145-45370146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs16958530	chr18:45370165-45370166	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533106363	chr18:45370173-45370174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542310334	chr18:45370259-45370260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182718491	chr18:45370310-45370311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372139136	chr18:45370324-45370325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200373587	chr18:45370335-45370336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57746325	chr18:45370336-45370337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575273785	chr18:45370379-45370380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546201632	chr18:45370425-45370426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9304357	chr18:45370466-45370467	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs145847169	chr18:45370470-45370471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148986116	chr18:45370481-45370482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187342570	chr18:45370504-45370505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546847231	chr18:45370529-45370530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560761372	chr18:45370593-45370594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528127255	chr18:45370678-45370679	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147096063	chr18:45370706-45370707	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115129173	chr18:45370750-45370751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73953610	chr18:45370752-45370753	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550876532	chr18:45370767-45370768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576568586	chr18:45370805-45370806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542398303	chr18:45370837-45370838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539766159	chr18:45370877-45370878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147715873	chr18:45370954-45370955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566666273	chr18:45371008-45371009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535566729	chr18:45371020-45371021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142480543	chr18:45371078-45371079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575214634	chr18:45371083-45371084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74477905	chr18:45371086-45371087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368702265	chr18:45371092-45371093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529716513	chr18:45371150-45371151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577891889	chr18:45371192-45371193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116901228	chr18:45371231-45371232	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560440432	chr18:45371291-45371292	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529532503	chr18:45371349-45371350	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541558766	chr18:45371402-45371403	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192240283	chr18:45371410-45371411	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559741606	chr18:45371421-45371422	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148299845	chr18:45371436-45371437	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Asthma	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45342200-45384200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:45344000-45373000	Weak transcription	Pancreas	Pancrea
3	chr18:45345400-45400200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr18:45347600-45381800	Weak transcription	Right Ventricle	heart
5	chr18:45351000-45374600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr18:45353000-45381200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr18:45354600-45381800	Weak transcription	Fetal Intestine Small	intestine
8	chr18:45354800-45370800	Weak transcription	Fetal Brain Male	brain
9	chr18:45355600-45375600	Strong transcription	Hela-S3	cervix
10	chr18:45355600-45375800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr18:45355600-45376200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr18:45356000-45378000	Weak transcription	Small Intestine	intestine
13	chr18:45356200-45377800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr18:45356200-45384000	Weak transcription	Spleen	Spleen
15	chr18:45356600-45376200	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr18:45357200-45370000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr18:45357200-45373200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr18:45358600-45376400	Strong transcription	Dnd41	blood
19	chr18:45358800-45382400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr18:45359000-45374400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr18:45359800-45370000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr18:45359800-45375600	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr18:45359800-45375600	Strong transcription	Fetal Thymus	thymus
24	chr18:45360000-45373200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr18:45360000-45375400	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr18:45360000-45375600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr18:45361400-45375600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr18:45361400-45375600	Strong transcription	A549	lung
29	chr18:45361400-45376000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr18:45362400-45373000	Strong transcription	Placenta	Placenta
31	chr18:45362400-45375200	Strong transcription	Primary B cells from cord blood	blood
32	chr18:45362400-45375600	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr18:45362600-45371800	Strong transcription	Liver	Liver
34	chr18:45362600-45372400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr18:45362600-45375600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr18:45363000-45370000	Strong transcription	Primary T cells from cord blood	blood
37	chr18:45363000-45375800	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr18:45363200-45371000	Weak transcription	HMEC	breast
39	chr18:45363400-45373600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:45363800-45375600	Strong transcription	H1 Cell Line	embryonic stem cell
41	chr18:45363800-45375600	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr18:45363800-45376400	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr18:45364000-45370000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr18:45364000-45372200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr18:45364000-45375400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr18:45364200-45370000	Strong transcription	Primary B cells from peripheral blood	blood
47	chr18:45364400-45375600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr18:45364600-45375600	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr18:45364600-45376200	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr18:45364800-45371200	Strong transcription	Rectal Mucosa Donor 29	rectum

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