Variant report

Variant	nsv1063859
Chromosome Location	chr18:45372027-45404492
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:265)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:265 , 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	chr18:45379570-45379813	GM12878	blood:	n/a	n/a
4	BATF	chr18:45379443-45379821	GM12878	blood:	n/a	n/a
5	BCL11A	chr18:45379518-45379810	GM12878	blood:	n/a	n/a
6	BCL11A	chr18:45379557-45379920	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:45379541-45379905	HepG2	liver:	n/a	n/a
8	CEBPB	chr18:45389601-45389752	A549	lung:	n/a	n/a
9	CEBPB	chr18:45390754-45391063	HepG2	liver:	n/a	n/a
10	CEBPB	chr18:45390727-45391043	IMR90	lung:	n/a	n/a
11	CEBPB	chr18:45379586-45379786	K562	blood:	n/a	n/a
12	CEBPB	chr18:45397656-45397855	HepG2	liver:	n/a	chr18:45397738-45397749
13	CEBPB	chr18:45390790-45391041	A549	lung:	n/a	n/a
14	CEBPD	chr18:45379393-45379959	K562	blood:	n/a	n/a
15	CHD1	chr18:45380009-45380040	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr18:45403240-45403390	GM12864	blood:	n/a	n/a
17	CTCF	chr18:45403240-45403390	HCM	heart:	n/a	n/a
18	CTCF	chr18:45391448-45391521	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr18:45403260-45403410	HPF	lung:	n/a	n/a
20	CTCF	chr18:45391400-45391550	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr18:45403352-45403411	Medullo	brain:	n/a	n/a
22	CTCF	chr18:45403260-45403410	AG04449	skin:	n/a	n/a
23	CTCF	chr18:45403300-45403450	GM06990	blood:	n/a	n/a
24	CTCF	chr18:45397147-45397238	K562	blood:	n/a	n/a
25	CTCF	chr18:45397160-45397310	HMEC	breast:	n/a	n/a
26	CTCF	chr18:45403300-45403450	HCFaa	heart:	n/a	n/a
27	CTCF	chr18:45397120-45397270	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr18:45391400-45391550	HMEC	breast:	n/a	n/a
29	CTCF	chr18:45397120-45397270	NHEK	skin:	n/a	n/a
30	CTCF	chr18:45391452-45391621	GM12878	blood:	n/a	n/a
31	CTCF	chr18:45403296-45403298	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr18:45403334-45403434	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr18:45372789-45372882	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr18:45397102-45397279	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr18:45403280-45403430	HEK293	kidney:	n/a	n/a
36	CTCF	chr18:45403320-45403470	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr18:45379570-45379796	K562	blood:	n/a	n/a
38	CTCF	chr18:45397080-45397230	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr18:45403340-45403490	HMF	breast:	n/a	n/a
40	CTCF	chr18:45403320-45403470	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr18:45391431-45391563	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr18:45403260-45403410	A549	lung:	n/a	n/a
43	CTCF	chr18:45403280-45403430	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr18:45397097-45397248	GM12878	blood:	n/a	n/a
45	CTCF	chr18:45397147-45397225	GM12878	blood:	n/a	n/a
46	CTCF	chr18:45395363-45395424	Lung_OC	lung:	n/a	n/a
47	CTCF	chr18:45397100-45397250	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr18:45397866-45397900	Fibrobl	skin:	n/a	n/a
49	CTCF	chr18:45391492-45391566	Lung_OC	lung:	n/a	n/a
50	CTCF	chr18:45403240-45403390	SK-N-SH_RA	brain:	n/a	n/a

No data

(count:20 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB7C-5	chr18:45396844-45396935	NONHSAT059175

No data

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

Extended variants
information (count: 1335 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202199806	chr18:45372059-45372060	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140112787	chr18:45372137-45372138	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189675475	chr18:45372189-45372190	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150380700	chr18:45372200-45372201	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546554852	chr18:45372226-45372227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560432746	chr18:45372229-45372230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529192911	chr18:45372233-45372234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568602666	chr18:45372242-45372243	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111335519	chr18:45372255-45372256	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs80038261	chr18:45372289-45372290	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537909481	chr18:45372293-45372294	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs546595155	chr18:45372325-45372326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571548469	chr18:45372331-45372332	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534304512	chr18:45372411-45372412	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12604595	chr18:45372415-45372416	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534227911	chr18:45372439-45372440	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs138072584	chr18:45372476-45372477	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574245521	chr18:45372489-45372490	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536948551	chr18:45372503-45372504	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113563294	chr18:45372537-45372538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs956861	chr18:45372545-45372546	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs956860	chr18:45372547-45372548	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191777365	chr18:45372576-45372577	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184312132	chr18:45372582-45372583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371943024	chr18:45372625-45372626	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189002454	chr18:45372742-45372743	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537982263	chr18:45372750-45372751	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554279272	chr18:45372795-45372796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577548226	chr18:45372811-45372812	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34457374	chr18:45372832-45372833	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373252067	chr18:45372933-45372934	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs57673669	chr18:45372936-45372937	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs60662746	chr18:45372953-45372954	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs117274061	chr18:45372959-45372960	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529142157	chr18:45372973-45372974	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs535102865	chr18:45372981-45372982	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs79515383	chr18:45373000-45373001	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs117614763	chr18:45373006-45373007	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142648214	chr18:45373008-45373009	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs539779381	chr18:45373019-45373020	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566504462	chr18:45373064-45373065	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115173432	chr18:45373065-45373066	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs146011629	chr18:45373104-45373105	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181681007	chr18:45373152-45373153	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs567561824	chr18:45373164-45373165	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187253926	chr18:45373166-45373167	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556940931	chr18:45373189-45373190	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576686397	chr18:45373202-45373203	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35353787	chr18:45373267-45373268	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539268907	chr18:45373299-45373300	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	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:1200 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr18:45355600-45375600	Strong transcription	Hela-S3	cervix
9	chr18:45355600-45375800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
10	chr18:45355600-45376200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr18:45356000-45378000	Weak transcription	Small Intestine	intestine
12	chr18:45356200-45377800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr18:45356200-45384000	Weak transcription	Spleen	Spleen
14	chr18:45356600-45376200	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr18:45357200-45373200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr18:45358600-45376400	Strong transcription	Dnd41	blood
17	chr18:45358800-45382400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr18:45359000-45374400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr18:45359800-45375600	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr18:45359800-45375600	Strong transcription	Fetal Thymus	thymus
21	chr18:45360000-45373200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr18:45360000-45375400	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr18:45360000-45375600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr18:45361400-45375600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr18:45361400-45375600	Strong transcription	A549	lung
26	chr18:45361400-45376000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr18:45362400-45373000	Strong transcription	Placenta	Placenta
28	chr18:45362400-45375200	Strong transcription	Primary B cells from cord blood	blood
29	chr18:45362400-45375600	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr18:45362600-45372400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr18:45362600-45375600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr18:45363000-45375800	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr18:45363400-45373600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr18:45363800-45375600	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr18:45363800-45375600	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr18:45363800-45376400	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr18:45364000-45372200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr18:45364000-45375400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr18:45364400-45375600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
40	chr18:45364600-45375600	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr18:45364600-45376200	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr18:45364800-45372400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr18:45364800-45372600	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr18:45365000-45373200	Strong transcription	Fetal Lung	lung
45	chr18:45365000-45373400	Strong transcription	Adipose Nuclei	Adipose
46	chr18:45365200-45373600	Strong transcription	Duodenum Mucosa	Duodenum
47	chr18:45365200-45375800	Strong transcription	Primary hematopoietic stem cells	blood
48	chr18:45365400-45372400	Strong transcription	HepG2	liver
49	chr18:45365400-45375000	Strong transcription	GM12878-XiMat	blood
50	chr18:45365600-45373600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood

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