Variant report

Variant	nsv543687
Chromosome Location	chr18:39691269-39808287
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:900)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:44)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:900 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:39751178-39751423	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:39693941-39694141	K562	blood:	n/a	n/a
3	ARID3A	chr18:39693801-39694659	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:39739204-39739442	HepG2	liver:	n/a	chr18:39739276-39739292
5	ARID3A	chr18:39772671-39773280	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:39748155-39749256	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:39692657-39693205	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:39721483-39721683	HepG2	liver:	n/a	n/a
9	ATF2	chr18:39767923-39768305	GM12878	blood:	n/a	n/a
10	BACH1	chr18:39763737-39764096	H1-hESC	embryonic stem cell:	n/a	chr18:39763920-39763934
11	BATF	chr18:39772309-39772479	GM12878	blood:	n/a	n/a
12	BATF	chr18:39767884-39768290	GM12878	blood:	n/a	n/a
13	BATF	chr18:39694341-39694593	GM12878	blood:	n/a	n/a
14	BATF	chr18:39756655-39756883	GM12878	blood:	n/a	n/a
15	BCL11A	chr18:39767875-39768269	GM12878	blood:	n/a	n/a
16	BCL11A	chr18:39781152-39781461	GM12878	blood:	n/a	n/a
17	BCL11A	chr18:39770691-39770876	GM12878	blood:	n/a	n/a
18	BCL11A	chr18:39693887-39694158	GM12878	blood:	n/a	n/a
19	BCL11A	chr18:39770644-39770908	GM12878	blood:	n/a	n/a
20	BCL11A	chr18:39767938-39768307	GM12878	blood:	n/a	n/a
21	BHLHE40	chr18:39770695-39770944	GM12878	blood:	n/a	n/a
22	BHLHE40	chr18:39781246-39781446	GM12878	blood:	n/a	n/a
23	BHLHE40	chr18:39756693-39756906	GM12878	blood:	n/a	n/a
24	BHLHE40	chr18:39692743-39693176	HepG2	liver:	n/a	n/a
25	BHLHE40	chr18:39694015-39694627	GM12878	blood:	n/a	n/a
26	BHLHE40	chr18:39717225-39717263	GM12878	blood:	n/a	n/a
27	BHLHE40	chr18:39767925-39768326	GM12878	blood:	n/a	n/a
28	BRCA1	chr18:39802055-39802094	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr18:39765105-39765439	HepG2	liver:	n/a	chr18:39765263-39765272 chr18:39765261-39765274 chr18:39765263-39765274 chr18:39765263-39765272 chr18:39765261-39765272 chr18:39765263-39765272 chr18:39765263-39765272
30	CEBPB	chr18:39750942-39751500	HepG2	liver:	n/a	chr18:39751342-39751353
31	CEBPB	chr18:39802637-39802858	H1-hESC	embryonic stem cell:	n/a	chr18:39802720-39802731
32	CEBPB	chr18:39753625-39753888	HepG2	liver:	n/a	chr18:39753687-39753698
33	CEBPB	chr18:39721479-39721734	HepG2	liver:	n/a	n/a
34	CEBPB	chr18:39772756-39773149	A549	lung:	n/a	chr18:39772945-39772956
35	CEBPB	chr18:39802553-39802893	IMR90	lung:	n/a	chr18:39802720-39802731
36	CEBPB	chr18:39693851-39694550	IMR90	lung:	n/a	chr18:39694042-39694053
37	CEBPB	chr18:39802552-39802896	HepG2	liver:	n/a	chr18:39802720-39802731
38	CEBPB	chr18:39775810-39776051	HepG2	liver:	n/a	chr18:39775912-39775923
39	CEBPB	chr18:39765115-39765395	IMR90	lung:	n/a	chr18:39765263-39765272 chr18:39765261-39765274 chr18:39765263-39765274 chr18:39765263-39765272 chr18:39765261-39765272 chr18:39765263-39765272 chr18:39765263-39765272
40	CEBPB	chr18:39693929-39694143	HepG2	liver:	n/a	chr18:39694042-39694053
41	CEBPB	chr18:39748421-39748779	HepG2	liver:	n/a	n/a
42	CEBPB	chr18:39802581-39802845	A549	lung:	n/a	chr18:39802720-39802731
43	CEBPB	chr18:39772729-39773151	Hela-S3	cervix:	n/a	chr18:39772945-39772956
44	CEBPB	chr18:39727070-39727242	HepG2	liver:	n/a	n/a
45	CEBPB	chr18:39697809-39698139	HepG2	liver:	n/a	chr18:39697953-39697964
46	CEBPB	chr18:39697904-39698025	H1-hESC	embryonic stem cell:	n/a	chr18:39697953-39697964
47	CEBPB	chr18:39802648-39802812	Hela-S3	cervix:	n/a	chr18:39802720-39802731
48	CEBPB	chr18:39756563-39756928	HepG2	liver:	n/a	n/a
49	CEBPB	chr18:39756673-39756835	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr18:39693866-39694191	K562	blood:	n/a	chr18:39694042-39694053

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:39694318..39694934-chr18:40851655..40852415,2	MCF-7	breast:

(count:44 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIT2-1	chr18:39805927-39805980	XLOC_012829
2	lnc-PIK3C3-5	chr18:39766633-39766727	NONHSAT059064
3	lnc-PIK3C3-5	chr18:39805929-39806072	NONHSAT059064
4	lnc-PIK3C3-5	chr18:39766633-39766727	ENSG00000267586.2
5	lnc-PIK3C3-5	chr18:39792329-39792491	NONHSAT059065
6	lnc-PIK3C3-5	chr18:39766635-39766727	ENSG00000267586.2
7	lnc-PIK3C3-5	chr18:39792329-39792491	ENSG00000267586.2
8	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
9	lnc-RIT2-1	chr18:39766366-39766725	XLOC_012829
10	lnc-PIK3C3-5	chr18:39766668-39766727	ENSG00000267586.2
11	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
12	lnc-PIK3C3-5	chr18:39739247-39739441	ENSG00000267586.2
13	lnc-PIK3C3-5	chr18:39766132-39766356	ENSG00000267586.2
14	lnc-PIK3C3-5	chr18:39805929-39806072	NONHSAT059068
15	lnc-PIK3C3-5	chr18:39792329-39792491	ENSG00000267586.2
16	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
17	lnc-PIK3C3-5	chr18:39766635-39766727	ENSG00000267586.2
18	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
19	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
20	lnc-PIK3C3-5	chr18:39805929-39806069	ENSG00000267586.2
21	lnc-PIK3C3-5	chr18:39766633-39766727	ENSG00000267586.2
22	lnc-PIK3C3-5	chr18:39766657-39766727	ENSG00000267586.2
23	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
24	lnc-PIK3C3-5	chr18:39766633-39766727	NONHSAT059066
25	lnc-PIK3C3-5	chr18:39766654-39766727	ENSG00000267586.2
26	lnc-PIK3C3-5	chr18:39805929-39806072	NONHSAT059066
27	lnc-PIK3C3-5	chr18:39792329-39792491	NONHSAT059064
28	lnc-PIK3C3-5	chr18:39805929-39806072	NONHSAT059065
29	lnc-PIK3C3-5	chr18:39792329-39792491	ENSG00000267586.2
30	lnc-PIK3C3-5	chr18:39792329-39792491	ENSG00000267586.2
31	lnc-PIK3C3-5	chr18:39792329-39792491	ENSG00000267586.2
32	lnc-PIK3C3-5	chr18:39766633-39766727	NONHSAT059068
33	lnc-PIK3C3-5	chr18:39766641-39766727	ENSG00000267586.2
34	lnc-PIK3C3-5	chr18:39766635-39766727	ENSG00000267586.2
35	lnc-PIK3C3-5	chr18:39792329-39792491	NONHSAT059068
36	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
37	lnc-PIK3C3-5	chr18:39792329-39792491	NONHSAT059066
38	lnc-PIK3C3-5	chr18:39766650-39766727	ENSG00000267586.2
39	lnc-PIK3C3-5	chr18:39792329-39792491	ENSG00000267586.2
40	lnc-PIK3C3-5	chr18:39766633-39766727	NONHSAT059065
41	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
42	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
43	lnc-PIK3C3-5	chr18:39805929-39806072	ENSG00000267586.2
44	lnc-PIK3C3-5	chr18:39792329-39792491	ENSG00000267586.2

No data

Variant related genes	Relation type
LINC00907	TF binding region
ENSG00000132872	chromatin interactions
AKAP12	miRNA target sites
GJA1	miRNA target sites

Extended variants
information (count: 1967 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1967 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541768849	chr18:39691275-39691276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560737928	chr18:39691285-39691286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182887317	chr18:39691349-39691350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7229086	chr18:39691350-39691351	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs13380922	chr18:39691384-39691385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374135214	chr18:39691393-39691394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76383286	chr18:39691426-39691427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528651148	chr18:39691430-39691431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546835479	chr18:39691431-39691432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528060817	chr18:39691456-39691457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188253734	chr18:39691485-39691486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541389280	chr18:39691547-39691548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529549124	chr18:39691587-39691588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374019448	chr18:39691623-39691624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77520405	chr18:39691642-39691643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569203648	chr18:39691655-39691656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116492552	chr18:39691666-39691667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533608293	chr18:39691695-39691696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs8085708	chr18:39691777-39691778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs557647570	chr18:39691805-39691806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567019804	chr18:39691818-39691819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534292068	chr18:39691844-39691845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112573533	chr18:39691862-39691863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs36012779	chr18:39691899-39691900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574561945	chr18:39691922-39691923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542080293	chr18:39691929-39691930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557002718	chr18:39691939-39691940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113493086	chr18:39691953-39691954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193268414	chr18:39691963-39691964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141340926	chr18:39691995-39691996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528126753	chr18:39691996-39691997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531038471	chr18:39692023-39692024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185494650	chr18:39692025-39692026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs479052	chr18:39692031-39692032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187974104	chr18:39692055-39692056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370259619	chr18:39692077-39692078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549425717	chr18:39692086-39692087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551231446	chr18:39692090-39692091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115805126	chr18:39692091-39692092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375598052	chr18:39692110-39692111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551755202	chr18:39692125-39692126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566883301	chr18:39692129-39692130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534253324	chr18:39692151-39692152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555602983	chr18:39692171-39692172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373646125	chr18:39692220-39692221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535324153	chr18:39692221-39692222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557211291	chr18:39692259-39692260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567578111	chr18:39692321-39692322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534999620	chr18:39692359-39692360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553031503	chr18:39692361-39692362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Hepatocellular carcinoma	16750200	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	16774939	CNVD
Colorectal cancer	21297112	CNVD
Cancer	21183584	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Pancreatic cancer	21811587	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39688200-39692400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr18:39689400-39692200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr18:39691200-39693800	Enhancers	HepG2	liver
4	chr18:39692200-39695600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:39692400-39693000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr18:39692600-39694800	Enhancers	Fetal Intestine Small	intestine
7	chr18:39692800-39694000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr18:39692800-39694800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr18:39693000-39694200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr18:39693000-39695000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr18:39693200-39693400	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr18:39693200-39693800	Enhancers	GM12878-XiMat	blood
13	chr18:39693200-39694000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr18:39693200-39694000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr18:39693200-39694200	Enhancers	Primary hematopoietic stem cells	blood
16	chr18:39693200-39694400	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr18:39693200-39694400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr18:39693200-39694800	Enhancers	Dnd41	blood
19	chr18:39693400-39694000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr18:39693400-39694200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr18:39693400-39694200	Enhancers	K562	blood
22	chr18:39693400-39694400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr18:39693400-39694600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr18:39693400-39694600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr18:39693400-39694800	Enhancers	Colon Smooth Muscle	Colon
26	chr18:39693400-39694800	Enhancers	Fetal Intestine Large	intestine
27	chr18:39693400-39694800	Enhancers	Osteobl	bone
28	chr18:39693600-39693800	Enhancers	Fetal Brain Female	brain
29	chr18:39693600-39693800	Enhancers	HSMMtube	muscle
30	chr18:39693600-39694600	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr18:39693600-39694800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr18:39693800-39694000	Flanking Active TSS	HSMMtube	muscle
33	chr18:39693800-39694200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr18:39693800-39694200	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr18:39693800-39694200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr18:39693800-39694200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr18:39693800-39694200	Enhancers	Duodenum Mucosa	Duodenum
38	chr18:39693800-39694200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr18:39693800-39694200	Flanking Active TSS	GM12878-XiMat	blood
40	chr18:39693800-39694400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr18:39693800-39694400	Enhancers	Primary B cells from peripheral blood	blood
42	chr18:39693800-39694400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr18:39693800-39694400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr18:39693800-39694400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr18:39693800-39694400	Enhancers	Brain Angular Gyrus	brain
46	chr18:39693800-39694400	Enhancers	Brain Cingulate Gyrus	brain
47	chr18:39693800-39694400	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr18:39693800-39694400	Enhancers	Stomach Smooth Muscle	stomach
49	chr18:39693800-39694400	Enhancers	A549	lung
50	chr18:39693800-39694400	Flanking Active TSS	HepG2	liver

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