Variant report

Variant	esv3388554
Chromosome Location	chr19:45424146-45430075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:244)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:45428702-45429030	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:45424155-45424271	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:45427454-45427972	HepG2	liver:	n/a	n/a
4	BHLHE40	chr19:45428627-45429047	HepG2	liver:	n/a	n/a
5	BHLHE40	chr19:45427445-45427908	HepG2	liver:	n/a	n/a
6	BRCA1	chr19:45427503-45427772	HepG2	liver:	n/a	n/a
7	CEBPB	chr19:45428637-45428963	HepG2	liver:	n/a	chr19:45428766-45428777
8	CEBPB	chr19:45428659-45428929	A549	lung:	n/a	chr19:45428766-45428777
9	CEBPB	chr19:45428605-45429317	HepG2	liver:	n/a	chr19:45428766-45428777
10	CEBPB	chr19:45429140-45429308	K562	blood:	n/a	n/a
11	CEBPB	chr19:45427391-45427865	HepG2	liver:	n/a	n/a
12	CEBPB	chr19:45427499-45427849	HepG2	liver:	n/a	n/a
13	CEBPB	chr19:45428640-45428910	K562	blood:	n/a	chr19:45428766-45428777
14	CEBPB	chr19:45428625-45428871	H1-hESC	embryonic stem cell:	n/a	chr19:45428766-45428777
15	CEBPB	chr19:45427547-45427779	HepG2	liver:	n/a	n/a
16	CEBPB	chr19:45428612-45429310	IMR90	lung:	n/a	chr19:45428766-45428777
17	CEBPB	chr19:45428608-45429316	HepG2	liver:	n/a	chr19:45428766-45428777
18	CEBPB	chr19:45428525-45429014	HepG2	liver:	n/a	chr19:45428766-45428777
19	CEBPB	chr19:45429037-45429280	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:45429128-45429295	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPD	chr19:45427480-45427942	HepG2	liver:	n/a	n/a
22	CEBPD	chr19:45428486-45429103	HepG2	liver:	n/a	chr19:45428765-45428776 chr19:45428803-45428814
23	CEBPD	chr19:45428576-45428995	HepG2	liver:	n/a	chr19:45428765-45428776 chr19:45428803-45428814
24	CEBPD	chr19:45427489-45427791	HepG2	liver:	n/a	n/a
25	CHD2	chr19:45428668-45428990	HepG2	liver:	n/a	n/a
26	CHD2	chr19:45427392-45427887	HepG2	liver:	n/a	n/a
27	CTCF	chr19:45428420-45428570	HBMEC	blood vessel:	n/a	n/a
28	EGR1	chr19:45428146-45428444	K562	blood:	n/a	n/a
29	EGR1	chr19:45429742-45430066	K562	blood:	n/a	chr19:45429902-45429926 chr19:45430009-45430022 chr19:45430008-45430023 chr19:45430007-45430017 chr19:45430009-45430022 chr19:45430010-45430020
30	ELF1	chr19:45428547-45428983	HepG2	liver:	n/a	n/a
31	ELF1	chr19:45427483-45427860	HepG2	liver:	n/a	n/a
32	ELF1	chr19:45428504-45429084	HepG2	liver:	n/a	n/a
33	EP300	chr19:45427335-45427998	HepG2	liver:	n/a	n/a
34	EP300	chr19:45427337-45427921	A549	lung:	n/a	n/a
35	EP300	chr19:45428617-45429066	HepG2	liver:	n/a	chr19:45428763-45428777
36	EP300	chr19:45427235-45428000	HepG2	liver:	n/a	n/a
37	EP300	chr19:45427367-45427929	HepG2	liver:	n/a	n/a
38	EP300	chr19:45428397-45429135	HepG2	liver:	n/a	chr19:45428763-45428777
39	EP300	chr19:45428473-45429129	HepG2	liver:	n/a	chr19:45428763-45428777
40	FOSL2	chr19:45428510-45429069	HepG2	liver:	n/a	n/a
41	FOSL2	chr19:45427366-45427957	HepG2	liver:	n/a	chr19:45427503-45427513 chr19:45427503-45427513
42	FOSL2	chr19:45428484-45429176	HepG2	liver:	n/a	n/a
43	FOSL2	chr19:45427306-45427949	HepG2	liver:	n/a	chr19:45427503-45427513 chr19:45427346-45427357 chr19:45427503-45427513
44	FOXA1	chr19:45427546-45427713	T-47D	breast:	n/a	n/a
45	FOXA1	chr19:45427423-45427962	HepG2	liver:	n/a	n/a
46	FOXA1	chr19:45427282-45427941	HepG2	liver:	n/a	n/a
47	FOXA1	chr19:45428504-45429084	HepG2	liver:	n/a	n/a
48	FOXA1	chr19:45427308-45427972	HepG2	liver:	n/a	n/a
49	FOXA1	chr19:45428528-45429110	HepG2	liver:	n/a	n/a
50	FOXA1	chr19:45428516-45429058	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45428924-45428974	AG09309	skin:	n/a
2	chr19:45429910-45429960	PANC-1	pancreas:	n/a
3	chr19:45429870-45429920	SAEC	small airway:	n/a
4	chr19:45429870-45429920	HCT-116	colon:	n/a
5	chr19:45429771-45429821	AG04450	lung:	fetal
6	chr19:45429771-45429821	NHDF-neo	bronchial:	n/a
7	chr19:45429910-45429960	GM06990	blood:	n/a
8	chr19:45429771-45429821	Hela-S3	cervix:	n/a
9	chr19:45428924-45428974	NHBE	bronchial:	n/a
10	chr19:45428924-45428974	HCT-116	colon:	n/a
11	chr19:45428924-45428974	HCPEpiC	choroid plexus:	n/a
12	chr19:45429870-45429920	Hela-S3	cervix:	n/a
13	chr19:45429870-45429920	HEEpiC	esophagus:	n/a
14	chr19:45428924-45428974	HIPEpiC	eye:	n/a
15	chr19:45428924-45428974	MCF-7	breast:	n/a
16	chr19:45429771-45429821	HUVEC	blood vessel:	n/a
17	chr19:45429910-45429960	HIPEpiC	eye:	n/a
18	chr19:45429910-45429960	A549	lung:	n/a
19	chr19:45428924-45428974	HEEpiC	esophagus:	n/a
20	chr19:45428924-45428974	ECC-1	luminal epithelium:	n/a
21	chr19:45429771-45429821	HRE	kidney:	n/a
22	chr19:45428924-45428974	ProgFib	skin:	n/a
23	chr19:45429771-45429821	NB4	blood:	n/a
24	chr19:45429870-45429920	A549	lung:	n/a
25	chr19:45429910-45429960	H1-hESC	embryonic stem cell:	embryo
26	chr19:45429910-45429960	AG04449	skin:	fetal
27	chr19:45429910-45429960	T-47D	breast:	n/a
28	chr19:45429910-45429960	BE2_C	brain:	n/a
29	chr19:45429910-45429960	GM12878	blood:	n/a
30	chr19:45429771-45429821	ProgFib	skin:	n/a
31	chr19:45429870-45429920	SKMC	muscle:	n/a
32	chr19:45428924-45428974	RPTEC	kidney:	n/a
33	chr19:45428924-45428974	HUVEC	blood vessel:	n/a
34	chr19:45429870-45429920	BJ	skin:	n/a
35	chr19:45428924-45428974	SK-N-SH	brain:	n/a
36	chr19:45429870-45429920	ovcar-3	ovarian:	n/a
37	chr19:45429771-45429821	K562	blood:	n/a
38	chr19:45429870-45429920	HCM	heart:	n/a
39	chr19:45429771-45429821	ovcar-3	ovarian:	n/a
40	chr19:45429870-45429920	NB4	blood:	n/a
41	chr19:45429870-45429920	PrEC	prostate:	n/a
42	chr19:45429771-45429821	SKMC	muscle:	n/a
43	chr19:45429870-45429920	Jurkat	blood:	n/a
44	chr19:45429870-45429920	Hepatocyte	liver:	n/a
45	chr19:45429870-45429920	AG09319	gingival:	n/a
46	chr19:45428924-45428974	T-47D	breast:	n/a
47	chr19:45429910-45429960	NT2-D1	testis:	n/a
48	chr19:45429910-45429960	NH-A	brain:	n/a
49	chr19:45429910-45429960	HCPEpiC	choroid plexus:	n/a
50	chr19:45428924-45428974	GM12892	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:45428887..45430724-chr19:45458504..45460514,2	MCF-7	breast:
2	chr19:45407631..45409490-chr19:45429549..45431974,2	K562	blood:
3	chr19:45409319..45412903-chr19:45425106..45429142,3	K562	blood:
4	chr19:45407631..45409490-chr19:45429198..45431974,3	K562	blood:
5	chr19:45425754..45427401-chr19:45457007..45459341,2	MCF-7	breast:
6	chr19:45420587..45422636-chr19:45425873..45427506,2	K562	blood:
7	chr19:45428614..45431090-chr19:45445301..45448167,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011481.1-1	chr19:45430060-45430290	NONHSAT066736
2	lnc-AC011481.1-1	chr19:45430060-45430089	NONHSAT066737
3	lnc-AC011481.1-1	chr19:45430060-45430290	NONHSAT066738

No data

Variant related genes	Relation type
APOC1P1	TF binding region
APOC1P1	CpG island
ENSG00000130203	chromatin interactions
ENSG00000104853	chromatin interactions
ENSG00000267114	chromatin interactions
ENSG00000267467	chromatin interactions
ENSG00000224916	chromatin interactions

Extended variants
information (count: 242 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:242 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142677003	chr19:45424237-45424238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540916196	chr19:45424268-45424269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs151017799	chr19:45424291-45424292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560231226	chr19:45424339-45424340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374461848	chr19:45424340-45424341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574151443	chr19:45424350-45424351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368340812	chr19:45424351-45424352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs56369833	chr19:45424352-45424353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562952649	chr19:45424353-45424354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531686685	chr19:45424366-45424367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551399712	chr19:45424382-45424383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566009937	chr19:45424446-45424447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533085345	chr19:45424481-45424482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546844448	chr19:45424500-45424501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs157592	chr19:45424514-45424515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535597135	chr19:45424567-45424568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371653372	chr19:45424576-45424577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551643023	chr19:45424617-45424618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs157593	chr19:45424624-45424625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569020444	chr19:45424660-45424661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537931200	chr19:45424661-45424662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183026989	chr19:45424683-45424684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367691441	chr19:45424691-45424692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557824290	chr19:45424742-45424743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10420046	chr19:45424783-45424784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534520467	chr19:45424785-45424786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376236690	chr19:45424816-45424817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201675797	chr19:45424817-45424818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560840278	chr19:45424847-45424848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569749742	chr19:45424863-45424864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554413648	chr19:45424880-45424881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574153005	chr19:45424900-45424901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543250404	chr19:45424901-45424902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556467872	chr19:45424945-45424946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576162310	chr19:45424973-45424974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545076529	chr19:45424988-45424989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564958573	chr19:45424996-45424997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527644601	chr19:45424997-45424998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540167417	chr19:45425002-45425003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7257728	chr19:45425011-45425012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199769815	chr19:45425022-45425023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188535946	chr19:45425066-45425067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548816456	chr19:45425087-45425088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569059888	chr19:45425101-45425102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193163858	chr19:45425133-45425134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs7257018	chr19:45425141-45425142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185367012	chr19:45425142-45425143	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149782856	chr19:45425171-45425172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs157594	chr19:45425175-45425176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190712692	chr19:45425178-45425179	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Adrenocortical carcinoma	18281524	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Muscular dystrophy	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	17440070	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45418800-45427400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr19:45418800-45427600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr19:45418800-45427600	Weak transcription	Spleen	Spleen
4	chr19:45418800-45430000	Weak transcription	Right Atrium	heart
5	chr19:45419000-45429800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr19:45419600-45425400	Weak transcription	Placenta	Placenta
7	chr19:45422400-45424200	Enhancers	Liver	Liver
8	chr19:45422800-45424400	Enhancers	HepG2	liver
9	chr19:45423000-45427200	Weak transcription	A549	lung
10	chr19:45423200-45427400	Weak transcription	K562	blood
11	chr19:45423400-45424400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr19:45423600-45425000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr19:45423600-45430000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr19:45424000-45424400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr19:45424200-45425800	Weak transcription	Liver	Liver
16	chr19:45424400-45425400	Weak transcription	HepG2	liver
17	chr19:45424400-45427000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr19:45424400-45427600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr19:45425400-45427200	Enhancers	HepG2	liver
20	chr19:45425400-45431800	Enhancers	Placenta	Placenta
21	chr19:45425800-45427400	Enhancers	Liver	Liver
22	chr19:45427000-45431400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr19:45427200-45428400	Enhancers	A549	lung
24	chr19:45427200-45429200	Flanking Active TSS	HepG2	liver
25	chr19:45427200-45430200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr19:45427200-45431400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr19:45427200-45431400	Enhancers	Fetal Lung	lung
28	chr19:45427200-45431600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr19:45427400-45427600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr19:45427400-45427600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr19:45427400-45427600	Flanking Active TSS	Liver	Liver
32	chr19:45427400-45427600	Enhancers	Brain Angular Gyrus	brain
33	chr19:45427400-45427600	Enhancers	Fetal Intestine Small	intestine
34	chr19:45427400-45427600	Enhancers	Right Ventricle	heart
35	chr19:45427400-45427600	Bivalent Enhancer	Osteobl	bone
36	chr19:45427400-45427800	Enhancers	Gastric	stomach
37	chr19:45427400-45427800	Enhancers	Pancreas	Pancrea
38	chr19:45427400-45427800	Enhancers	K562	blood
39	chr19:45427400-45428000	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr19:45427400-45428400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:45427400-45428600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr19:45427400-45428600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr19:45427400-45429000	Enhancers	Fetal Muscle Trunk	muscle
44	chr19:45427400-45429200	Enhancers	Muscle Satellite Cultured Cells	--
45	chr19:45427400-45429200	Enhancers	Ovary	ovary
46	chr19:45427400-45429400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr19:45427400-45430000	Enhancers	Brain Anterior Caudate	brain
48	chr19:45427400-45430000	Enhancers	Brain Cingulate Gyrus	brain
49	chr19:45427400-45430000	Enhancers	HSMM	muscle
50	chr19:45427400-45430200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links