Variant report

Variant	esv3413514
Chromosome Location	chr19:45418155-45430302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:500)
CpG islands
(count:427)
Chromatin interactive
region (count:10)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:45424155-45424271	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:45428702-45429030	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:45427454-45427972	HepG2	liver:	n/a	n/a
4	ATF1	chr19:45418230-45418608	K562	blood:	n/a	n/a
5	ATF1	chr19:45430291-45430704	K562	blood:	n/a	n/a
6	BACH1	chr19:45418375-45418688	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr19:45417463-45418281	A549	lung:	n/a	n/a
8	BHLHE40	chr19:45418258-45418564	K562	blood:	n/a	n/a
9	BHLHE40	chr19:45427445-45427908	HepG2	liver:	n/a	n/a
10	BHLHE40	chr19:45418258-45418552	HepG2	liver:	n/a	n/a
11	BHLHE40	chr19:45418290-45418569	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:45428627-45429047	HepG2	liver:	n/a	n/a
13	BRCA1	chr19:45418296-45418483	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr19:45427503-45427772	HepG2	liver:	n/a	n/a
15	CBX3	chr19:45417739-45418578	K562	blood:	n/a	n/a
16	CBX3	chr19:45422679-45423180	K562	blood:	n/a	n/a
17	CEBPB	chr19:45418170-45418494	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr19:45423333-45423553	IMR90	lung:	n/a	chr19:45423390-45423401
19	CEBPB	chr19:45423316-45423491	MCF-7	breast:	n/a	chr19:45423390-45423401
20	CEBPB	chr19:45427499-45427849	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:45423229-45423569	K562	blood:	n/a	chr19:45423390-45423401
22	CEBPB	chr19:45429128-45429295	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr19:45428605-45429317	HepG2	liver:	n/a	chr19:45428766-45428777
24	CEBPB	chr19:45418195-45418494	A549	lung:	n/a	n/a
25	CEBPB	chr19:45428637-45428963	HepG2	liver:	n/a	chr19:45428766-45428777
26	CEBPB	chr19:45418230-45418441	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:45418243-45418452	HepG2	liver:	n/a	n/a
28	CEBPB	chr19:45423304-45423493	ECC-1	luminal epithelium:	n/a	chr19:45423390-45423401
29	CEBPB	chr19:45423241-45423568	HepG2	liver:	n/a	chr19:45423390-45423401
30	CEBPB	chr19:45428659-45428929	A549	lung:	n/a	chr19:45428766-45428777
31	CEBPB	chr19:45427547-45427779	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:45429037-45429280	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:45428625-45428871	H1-hESC	embryonic stem cell:	n/a	chr19:45428766-45428777
34	CEBPB	chr19:45423389-45423410	A549	lung:	n/a	chr19:45423390-45423401
35	CEBPB	chr19:45418235-45418619	A549	lung:	n/a	n/a
36	CEBPB	chr19:45429140-45429308	K562	blood:	n/a	n/a
37	CEBPB	chr19:45428608-45429316	HepG2	liver:	n/a	chr19:45428766-45428777
38	CEBPB	chr19:45418178-45418520	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:45418165-45418513	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:45423189-45423505	HepG2	liver:	n/a	chr19:45423390-45423401
41	CEBPB	chr19:45428612-45429310	IMR90	lung:	n/a	chr19:45428766-45428777
42	CEBPB	chr19:45423242-45423463	HepG2	liver:	n/a	chr19:45423390-45423401
43	CEBPB	chr19:45427391-45427865	HepG2	liver:	n/a	n/a
44	CEBPB	chr19:45428640-45428910	K562	blood:	n/a	chr19:45428766-45428777
45	CEBPB	chr19:45428525-45429014	HepG2	liver:	n/a	chr19:45428766-45428777
46	CEBPB	chr19:45418146-45418516	K562	blood:	n/a	n/a
47	CEBPD	chr19:45428486-45429103	HepG2	liver:	n/a	chr19:45428765-45428776 chr19:45428803-45428814
48	CEBPD	chr19:45427480-45427942	HepG2	liver:	n/a	n/a
49	CEBPD	chr19:45427489-45427791	HepG2	liver:	n/a	n/a
50	CEBPD	chr19:45428576-45428995	HepG2	liver:	n/a	chr19:45428765-45428776 chr19:45428803-45428814

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45422541-45422591	BJ	skin:	n/a
2	chr19:45430113-45430163	ProgFib	skin:	n/a
3	chr19:45429870-45429920	MCF-7	breast:	n/a
4	chr19:45429910-45429960	MCF-7	breast:	n/a
5	chr19:45429771-45429821	NHDF-neo	bronchial:	n/a
6	chr19:45429910-45429960	NHBE	bronchial:	n/a
7	chr19:45429771-45429821	HCF	heart:	n/a
8	chr19:45422541-45422591	GM06990	blood:	n/a
9	chr19:45429771-45429821	AG10803	skin:	n/a
10	chr19:45428924-45428974	HAEpiC	amniotic membrane:	n/a
11	chr19:45430113-45430163	HUVEC	blood vessel:	n/a
12	chr19:45430113-45430163	AG04449	skin:	fetal
13	chr19:45429910-45429960	HCPEpiC	choroid plexus:	n/a
14	chr19:45429910-45429960	HEEpiC	esophagus:	n/a
15	chr19:45429910-45429960	AG04450	lung:	fetal
16	chr19:45430113-45430163	CMK	blood:	n/a
17	chr19:45429870-45429920	SK-N-SH	brain:	n/a
18	chr19:45430113-45430163	HPAEpiC	pulmonary alveolar:	n/a
19	chr19:45428924-45428974	CMK	blood:	n/a
20	chr19:45422541-45422591	NHBE	bronchial:	n/a
21	chr19:45429910-45429960	ECC-1	luminal epithelium:	n/a
22	chr19:45429910-45429960	SAEC	small airway:	n/a
23	chr19:45422541-45422591	Hela-S3	cervix:	n/a
24	chr19:45429870-45429920	ProgFib	skin:	n/a
25	chr19:45429870-45429920	Caco-2	colon:	n/a
26	chr19:45418417-45418467	IMR90	lung:	fetal
27	chr19:45430113-45430163	AG09309	skin:	n/a
28	chr19:45418417-45418467	SK-N-MC	brain:	n/a
29	chr19:45429910-45429960	SK-N-SH_RA	brain:	n/a
30	chr19:45422541-45422591	GM12891	blood:	n/a
31	chr19:45428924-45428974	HCPEpiC	choroid plexus:	n/a
32	chr19:45429771-45429821	NH-A	brain:	n/a
33	chr19:45429910-45429960	HCF	heart:	n/a
34	chr19:45422541-45422591	PANC-1	pancreas:	n/a
35	chr19:45422541-45422591	HNPCEpiC	eye:	n/a
36	chr19:45429870-45429920	GM12878	blood:	n/a
37	chr19:45430113-45430163	SKMC	muscle:	n/a
38	chr19:45429771-45429821	H1-hESC	embryonic stem cell:	embryo
39	chr19:45429771-45429821	HEK293	kidney:	embryo
40	chr19:45429910-45429960	GM12878	blood:	n/a
41	chr19:45428924-45428974	PANC-1	pancreas:	n/a
42	chr19:45428924-45428974	MCF10A-Er-Src	breast:	n/a
43	chr19:45430113-45430163	HCM	heart:	n/a
44	chr19:45430113-45430163	Hela-S3	cervix:	n/a
45	chr19:45429910-45429960	LNCaP	prostate:	n/a
46	chr19:45430113-45430163	NHDF-neo	bronchial:	n/a
47	chr19:45429771-45429821	HMEC	breast:	n/a
48	chr19:45429870-45429920	A549	lung:	n/a
49	chr19:45429771-45429821	HepG2	liver:	n/a
50	chr19:45430113-45430163	HAEpiC	amniotic membrane:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:45425754..45427401-chr19:45457007..45459341,2	MCF-7	breast:
2	chr19:45407631..45409490-chr19:45429549..45431974,2	K562	blood:
3	chr19:45409319..45412903-chr19:45425106..45429142,3	K562	blood:
4	chr19:45420587..45422636-chr19:45425873..45427506,2	K562	blood:
5	chr19:45428614..45431090-chr19:45445301..45448167,2	K562	blood:
6	chr19:45428887..45430724-chr19:45458504..45460514,2	MCF-7	breast:
7	chr19:45416225..45418303-chr19:45596248..45598636,2	K562	blood:
8	chr19:45420587..45422636-chr19:45425873..45427506,2	K562	blood:
9	chr19:45407631..45409490-chr19:45429198..45431974,3	K562	blood:
10	chr19:45391987..45395479-chr19:45416556..45421203,6	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011481.1-1	chr19:45430060-45430089	NONHSAT066737
2	lnc-AC011481.1-1	chr19:45430060-45430290	NONHSAT066736
3	lnc-AC011481.1-1	chr19:45430213-45430290	NONHSAT066737
4	lnc-APOC1-1	chr19:45417929-45418206	NONHSAT066734
5	lnc-AC011481.1-1	chr19:45430213-45430290	NONHSAT066739
6	lnc-AC011481.1-1	chr19:45430077-45430086	NONHSAT066739
7	lnc-APOC1-1	chr19:45422430-45422606	NONHSAT066734
8	lnc-AC011481.1-1	chr19:45430060-45430290	NONHSAT066738

No data

Variant related genes	Relation type
APOC1P1	TF binding region
APOC1P1	CpG island
ENSG00000267282	chromatin interactions
ENSG00000267114	chromatin interactions
ENSG00000104853	chromatin interactions
ENSG00000267467	chromatin interactions
ENSG00000130203	chromatin interactions
ENSG00000224916	chromatin interactions
ENSG00000130204	chromatin interactions
ENSG00000104866	chromatin interactions

Extended variants
information (count: 508 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145422421	chr19:45418155-45418156	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs147697738	chr19:45418162-45418163	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs371532131	chr19:45418165-45418166	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs5111	chr19:45418166-45418167	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs12721047	chr19:45418169-45418170	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs375842464	chr19:45418172-45418173	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs542891315	chr19:45418176-45418177	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs142470704	chr19:45418177-45418178	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs72654453	chr19:45418196-45418197	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs72654454	chr19:45418209-45418210	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs111873720	chr19:45418229-45418230	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs12721048	chr19:45418237-45418238	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs45575140	chr19:45418251-45418252	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs376302246	chr19:45418334-45418335	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs138954121	chr19:45418359-45418360	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs576548559	chr19:45418374-45418375	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs545184380	chr19:45418386-45418387	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs564995337	chr19:45418391-45418392	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs5114	chr19:45418446-45418447	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs547436084	chr19:45418457-45418458	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs186062339	chr19:45418466-45418467	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529210785	chr19:45418479-45418480	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs12691088	chr19:45418486-45418487	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs568979138	chr19:45418562-45418563	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs433391	chr19:45418564-45418565	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs12709881	chr19:45418604-45418605	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551511928	chr19:45418641-45418642	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs571317930	chr19:45418647-45418648	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576138812	chr19:45418690-45418691	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs5115	chr19:45418753-45418754	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs5116	chr19:45418777-45418778	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs533862500	chr19:45418782-45418783	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs5117	chr19:45418790-45418791	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573656427	chr19:45418800-45418801	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs5118	chr19:45418844-45418845	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs181324013	chr19:45418846-45418847	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs536562430	chr19:45418886-45418887	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556781141	chr19:45418946-45418947	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs3826688	chr19:45418961-45418962	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs8107634	chr19:45418988-45418989	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs8107841	chr19:45418995-45418996	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs8107549	chr19:45418999-45419000	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs368575738	chr19:45419096-45419097	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs5119	chr19:45419107-45419108	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs77882010	chr19:45419168-45419169	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545536296	chr19:45419185-45419186	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs185495905	chr19:45419216-45419217	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs371220643	chr19:45419272-45419273	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs375780016	chr19:45419318-45419319	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544207008	chr19:45419319-45419320	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45416400-45418200	Weak transcription	HSMMtube	muscle
2	chr19:45417200-45418800	Active TSS	HepG2	liver
3	chr19:45417400-45418200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr19:45417400-45418200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr19:45417400-45418200	Flanking Active TSS	Brain Hippocampus Middle	brain
6	chr19:45417400-45418200	Enhancers	Fetal Heart	heart
7	chr19:45417400-45418200	Enhancers	Lung	lung
8	chr19:45417400-45418200	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr19:45417400-45418200	Flanking Active TSS	K562	blood
10	chr19:45417400-45418400	Enhancers	Fetal Brain Male	brain
11	chr19:45417400-45418600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr19:45417400-45418600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr19:45417400-45418800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr19:45417400-45419000	Active TSS	H9 Cell Line	embryonic stem cell
15	chr19:45417400-45419000	Active TSS	Brain Germinal Matrix	brain
16	chr19:45417400-45419000	Active TSS	Fetal Brain Female	brain
17	chr19:45417400-45419200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr19:45417600-45418200	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr19:45417600-45418200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
20	chr19:45417600-45418200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr19:45417600-45418200	Flanking Active TSS	Fetal Intestine Small	intestine
22	chr19:45417600-45418200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
23	chr19:45417600-45418400	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr19:45417600-45418400	Flanking Active TSS	Colonic Mucosa	Colon
25	chr19:45417600-45418600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr19:45417600-45418600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr19:45417600-45418600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr19:45417600-45418800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr19:45417600-45418800	Active TSS	Right Ventricle	heart
30	chr19:45417600-45419000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr19:45417600-45419000	Active TSS	Brain Anterior Caudate	brain
32	chr19:45417600-45419000	Active TSS	Osteobl	bone
33	chr19:45417800-45418200	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
34	chr19:45417800-45418200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr19:45417800-45418400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
36	chr19:45417800-45418400	Flanking Active TSS	Fetal Intestine Large	intestine
37	chr19:45417800-45418400	Active TSS	Stomach Smooth Muscle	stomach
38	chr19:45417800-45418600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr19:45417800-45418600	Flanking Active TSS	Primary hematopoietic stem cells	blood
40	chr19:45417800-45418600	Active TSS	Psoas Muscle	Psoas
41	chr19:45417800-45418600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr19:45417800-45418600	Active TSS	NHDF-Ad	bronchial
43	chr19:45417800-45418800	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr19:45417800-45418800	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr19:45417800-45418800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr19:45417800-45418800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:45417800-45418800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr19:45417800-45418800	Active TSS	Colon Smooth Muscle	Colon
49	chr19:45417800-45418800	Flanking Active TSS	Placenta	Placenta
50	chr19:45417800-45418800	Active TSS	Ovary	ovary

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