Variant report

Variant	esv996035
Chromosome Location	chr19:41881445-41887549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:371)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41882235-41882563	HepG2	liver:	n/a	n/a
2	ATF2	chr19:41884257-41884636	GM12878	blood:	n/a	n/a
3	ATF3	chr19:41881994-41882483	A549	lung:	n/a	n/a
4	BACH1	chr19:41882646-41882650	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:41884322-41884571	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr19:41881874-41883724	A549	lung:	n/a	chr19:41882570-41882579
7	BCL3	chr19:41881822-41883679	A549	lung:	n/a	chr19:41882570-41882579
8	BCLAF1	chr19:41884318-41884809	GM12878	blood:	n/a	chr19:41884535-41884544
9	BHLHE40	chr19:41884272-41884647	GM12878	blood:	n/a	n/a
10	BRCA1	chr19:41884329-41884343	HepG2	liver:	n/a	n/a
11	CBX3	chr19:41885981-41886597	HCT-116	colon:	n/a	n/a
12	CEBPB	chr19:41881510-41881807	HepG2	liver:	n/a	chr19:41881667-41881678
13	CEBPB	chr19:41881539-41881782	H1-hESC	embryonic stem cell:	n/a	chr19:41881667-41881678
14	CEBPB	chr19:41882169-41882599	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr19:41882070-41882645	MCF-7	breast:	n/a	n/a
16	CEBPB	chr19:41884812-41884839	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:41882165-41882569	IMR90	lung:	n/a	n/a
18	CEBPB	chr19:41882174-41882563	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr19:41882100-41882753	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr19:41882169-41882518	K562	blood:	n/a	n/a
21	CEBPB	chr19:41882189-41882544	K562	blood:	n/a	n/a
22	CEBPB	chr19:41882279-41882458	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:41881419-41881875	A549	lung:	n/a	chr19:41881667-41881678
24	CEBPB	chr19:41882245-41882457	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:41882133-41882585	MCF-7	breast:	n/a	n/a
26	CEBPB	chr19:41882172-41882561	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:41881615-41881726	IMR90	lung:	n/a	chr19:41881667-41881678
28	CEBPB	chr19:41882080-41882586	A549	lung:	n/a	n/a
29	CEBPB	chr19:41882149-41882560	A549	lung:	n/a	n/a
30	CEBPB	chr19:41881563-41881762	A549	lung:	n/a	chr19:41881667-41881678
31	CEBPB	chr19:41882016-41882792	A549	lung:	n/a	n/a
32	CEBPB	chr19:41882155-41882595	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:41881535-41881738	K562	blood:	n/a	chr19:41881667-41881678
34	CEBPB	chr19:41882171-41882563	HepG2	liver:	n/a	n/a
35	CEBPD	chr19:41882216-41882794	HepG2	liver:	n/a	n/a
36	CEBPD	chr19:41882162-41882501	HepG2	liver:	n/a	n/a
37	CHD1	chr19:41884263-41884281	GM12878	blood:	n/a	n/a
38	CHD2	chr19:41882175-41882705	HepG2	liver:	n/a	n/a
39	CHD2	chr19:41884376-41884479	HepG2	liver:	n/a	n/a
40	CHD2	chr19:41882543-41882553	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr19:41884303-41884637	GM12878	blood:	n/a	n/a
42	CREB1	chr19:41882272-41883236	A549	lung:	n/a	n/a
43	CTCF	chr19:41884340-41884490	GM06990	blood:	n/a	n/a
44	CTCF	chr19:41884320-41884470	GM12869	blood:	n/a	n/a
45	CTCF	chr19:41884320-41884470	GM12875	blood:	n/a	n/a
46	CTCF	chr19:41884240-41884390	NHLF	lung:	n/a	n/a
47	CTCF	chr19:41884320-41884470	HepG2	liver:	n/a	n/a
48	CTCF	chr19:41884300-41884450	GM06990	blood:	n/a	n/a
49	CTCF	chr19:41884280-41884430	HCFaa	heart:	n/a	n/a
50	CTCF	chr19:41884440-41884590	HFF-Myc	foreskin:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41882232-41882282	Hepatocyte	liver:	n/a
2	chr19:41882232-41882282	Hepatocyte	liver:	n/a
3	chr19:41882234-41882284	BE2_C	brain:	n/a
4	chr19:41882253-41882303	ovcar-3	ovarian:	n/a
5	chr19:41886265-41886315	ovcar-3	ovarian:	n/a
6	chr19:41882253-41882303	SKMC	muscle:	n/a
7	chr19:41886265-41886315	Caco-2	colon:	n/a
8	chr19:41882253-41882303	GM12878	blood:	n/a
9	chr19:41882232-41882282	NHBE	bronchial:	n/a
10	chr19:41886265-41886315	RPTEC	kidney:	n/a
11	chr19:41882327-41882377	AG09309	skin:	n/a
12	chr19:41882741-41882791	HAEpiC	amniotic membrane:	n/a
13	chr19:41882642-41882692	HEK293	kidney:	embryo
14	chr19:41882327-41882377	Caco-2	colon:	n/a
15	chr19:41882253-41882303	HEEpiC	esophagus:	n/a
16	chr19:41882642-41882692	MCF-7	breast:	n/a
17	chr19:41882741-41882791	A549	lung:	n/a
18	chr19:41882253-41882303	HMEC	breast:	n/a
19	chr19:41882642-41882692	A549	lung:	n/a
20	chr19:41883891-41883941	GM12892	blood:	n/a
21	chr19:41886265-41886315	AG09309	skin:	n/a
22	chr19:41883891-41883941	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:41883891-41883941	NHBE	bronchial:	n/a
24	chr19:41883891-41883941	HCF	heart:	n/a
25	chr19:41882253-41882303	SK-N-MC	brain:	n/a
26	chr19:41882741-41882791	AG04450	lung:	fetal
27	chr19:41882253-41882303	IMR90	lung:	fetal
28	chr19:41882253-41882303	HRCEpiC	kidney:	n/a
29	chr19:41882234-41882284	HEK293	kidney:	embryo
30	chr19:41882234-41882284	SAEC	small airway:	n/a
31	chr19:41886265-41886315	MCF10A-Er-Src	breast:	n/a
32	chr19:41882253-41882303	GM06990	blood:	n/a
33	chr19:41886265-41886315	HRE	kidney:	n/a
34	chr19:41886265-41886315	AG09319	gingival:	n/a
35	chr19:41882232-41882282	ProgFib	skin:	n/a
36	chr19:41882642-41882692	HCPEpiC	choroid plexus:	n/a
37	chr19:41882642-41882692	RPTEC	kidney:	n/a
38	chr19:41882232-41882282	GM12892	blood:	n/a
39	chr19:41882232-41882282	K562	blood:	n/a
40	chr19:41883891-41883941	NHDF-neo	bronchial:	n/a
41	chr19:41882234-41882284	HepG2	liver:	n/a
42	chr19:41882232-41882282	HL-60	blood:	n/a
43	chr19:41883891-41883941	HEEpiC	esophagus:	n/a
44	chr19:41882642-41882692	BE2_C	brain:	n/a
45	chr19:41882642-41882692	PFSK-1	brain:	n/a
46	chr19:41882642-41882692	SK-N-SH_RA	brain:	n/a
47	chr19:41886265-41886315	AoSMC	blood vessel:	n/a
48	chr19:41883891-41883941	PFSK-1	brain:	n/a
49	chr19:41882253-41882303	AG10803	skin:	n/a
50	chr19:41883891-41883941	T-47D	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41878956..41881468-chr19:41882311..41885014,3	K562	blood:
2	chr19:41883523..41885589-chr19:41888415..41890497,2	K562	blood:
3	chr19:41880830..41883046-chr19:41887103..41889706,2	MCF-7	breast:
4	chr19:41880830..41883046-chr19:41887103..41889706,2	MCF-7	breast:
5	chr19:41858284..41860006-chr19:41877759..41881473,3	K562	blood:
6	chr19:41846876..41849699-chr19:41880679..41882557,2	K562	blood:
7	chr19:41886073..41888188-chr19:41891478..41893284,2	K562	blood:
8	chr19:41882074..41885616-chr19:41888544..41893640,5	K562	blood:
9	chr19:41869640..41871954-chr19:41878739..41881491,2	MCF-7	breast:
10	chr19:41869853..41871782-chr19:41881681..41884054,2	K562	blood:
11	chr19:41872814..41874606-chr19:41878668..41881645,2	MCF-7	breast:
12	chr19:41878619..41881645-chr19:41882135..41886243,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000255730	TF binding region
TMEM91	TF binding region
BCKDHA	TF binding region
ENSG00000255730	CpG island
TMEM91	CpG island
BCKDHA	CpG island
ENSG00000142046	chromatin interactions
ENSG00000105329	chromatin interactions
ENSG00000248098	chromatin interactions
ENSG00000255730	chromatin interactions
ENSG00000123810	chromatin interactions

Extended variants
information (count: 229 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:229 , 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	rs567876169	chr19:41881447-41881448	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs373577383	chr19:41881521-41881522	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs11670739	chr19:41881545-41881546	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs529098721	chr19:41881552-41881553	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs185696998	chr19:41881644-41881645	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs538581344	chr19:41881669-41881670	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs373935887	chr19:41881703-41881704	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs111892267	chr19:41881732-41881733	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs571991636	chr19:41881735-41881736	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs190540310	chr19:41881742-41881743	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs560829573	chr19:41881749-41881750	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs576055638	chr19:41881834-41881835	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs181892996	chr19:41881899-41881900	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs563105172	chr19:41881951-41881952	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs536755133	chr19:41881981-41881982	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs376830132	chr19:41882008-41882009	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs545758847	chr19:41882011-41882012	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs186917004	chr19:41882017-41882018	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs535104213	chr19:41882025-41882026	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs57948035	chr19:41882045-41882046	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs527691874	chr19:41882048-41882049	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs113260546	chr19:41882071-41882072	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs60180822	chr19:41882072-41882073	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs148925726	chr19:41882082-41882083	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs397780504	chr19:41882087-41882088	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs549323338	chr19:41882096-41882097	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs567674840	chr19:41882097-41882098	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs531718515	chr19:41882102-41882103	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs35698602	chr19:41882149-41882150	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs386809356	chr19:41882179-41882180	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs549845861	chr19:41882193-41882194	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs557399842	chr19:41882208-41882209	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs190269851	chr19:41882294-41882295	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs543191928	chr19:41882323-41882324	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs561216641	chr19:41882336-41882337	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs565926243	chr19:41882341-41882342	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs531369098	chr19:41882365-41882366	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs535885871	chr19:41882371-41882372	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs529120748	chr19:41882378-41882379	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs148125442	chr19:41882416-41882417	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs75484256	chr19:41882428-41882429	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs571159572	chr19:41882459-41882460	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs540846128	chr19:41882504-41882505	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs112245822	chr19:41882577-41882578	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs547027885	chr19:41882587-41882588	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs566904899	chr19:41882589-41882590	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs185397361	chr19:41882598-41882599	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs560635232	chr19:41882603-41882604	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs527955635	chr19:41882609-41882610	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs542926978	chr19:41882613-41882614	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41870600-41882000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr19:41870800-41882000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr19:41871000-41881800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr19:41871000-41882000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr19:41871000-41882000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr19:41871000-41882000	Weak transcription	Primary T cells from cord blood	blood
7	chr19:41871200-41881800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr19:41871200-41882000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr19:41871200-41882000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:41871200-41882000	Weak transcription	Thymus	Thymus
11	chr19:41871200-41882200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr19:41871200-41884000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr19:41871200-41888600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:41871400-41882000	Weak transcription	Liver	Liver
15	chr19:41871400-41888400	Weak transcription	Dnd41	blood
16	chr19:41872600-41881600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr19:41872600-41882200	Weak transcription	Fetal Thymus	thymus
18	chr19:41873800-41882000	Weak transcription	Spleen	Spleen
19	chr19:41874200-41881800	Weak transcription	Primary B cells from peripheral blood	blood
20	chr19:41874200-41881800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr19:41874200-41882000	Weak transcription	Stomach Mucosa	stomach
22	chr19:41874200-41882200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr19:41874400-41882200	Weak transcription	Small Intestine	intestine
24	chr19:41874400-41882200	Weak transcription	HSMM	muscle
25	chr19:41874800-41881600	Weak transcription	Primary B cells from cord blood	blood
26	chr19:41874800-41882000	Weak transcription	Esophagus	oesophagus
27	chr19:41875000-41882000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr19:41875000-41882000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr19:41875200-41881800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr19:41875400-41881800	Weak transcription	Fetal Intestine Large	intestine
31	chr19:41875400-41882800	Weak transcription	K562	blood
32	chr19:41875400-41883000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr19:41876000-41881600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr19:41876200-41881600	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr19:41877400-41881800	Weak transcription	Fetal Kidney	kidney
36	chr19:41878800-41882000	Enhancers	Fetal Brain Female	brain
37	chr19:41879000-41882000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr19:41879600-41881600	Enhancers	Fetal Muscle Trunk	muscle
39	chr19:41879600-41882000	Enhancers	Fetal Brain Male	brain
40	chr19:41879600-41882000	Enhancers	Fetal Muscle Leg	muscle
41	chr19:41879800-41882000	Enhancers	Fetal Stomach	stomach
42	chr19:41879800-41882200	Enhancers	Brain Hippocampus Middle	brain
43	chr19:41880200-41881800	Weak transcription	Lung	lung
44	chr19:41880200-41881800	Weak transcription	NHEK	skin
45	chr19:41880200-41882000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr19:41880200-41882000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:41880200-41882000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr19:41880200-41882000	Weak transcription	Fetal Intestine Small	intestine
49	chr19:41880200-41882000	Weak transcription	Gastric	stomach
50	chr19:41880200-41882000	Weak transcription	Rectal Mucosa Donor 31	rectum

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