Variant report

Variant	esv3389051
Chromosome Location	chr19:40696662-40698860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:671)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40696496-40696900	HepG2	liver:	n/a	n/a
2	ATF1	chr19:40697129-40697494	K562	blood:	n/a	n/a
3	ATF2	chr19:40696306-40696953	GM12878	blood:	n/a	n/a
4	ATF3	chr19:40696835-40697440	K562	blood:	n/a	chr19:40697328-40697348
5	ATF3	chr19:40697207-40697451	H1-hESC	embryonic stem cell:	n/a	chr19:40697328-40697348
6	ATF3	chr19:40696773-40697281	A549	lung:	n/a	n/a
7	ATF3	chr19:40697148-40697419	HepG2	liver:	n/a	chr19:40697328-40697348
8	ATF3	chr19:40697053-40697456	GM12878	blood:	n/a	chr19:40697328-40697348
9	BCL3	chr19:40698520-40699332	A549	lung:	n/a	n/a
10	BCL3	chr19:40696378-40697420	A549	lung:	n/a	chr19:40697314-40697323 chr19:40697229-40697242 chr19:40697343-40697356 chr19:40697309-40697322 chr19:40697313-40697326 chr19:40697317-40697326 chr19:40697379-40697392 chr19:40697312-40697325
11	BCLAF1	chr19:40696348-40696956	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:40696447-40697465	GM12878	blood:	n/a	chr19:40697365-40697381 chr19:40696884-40696900 chr19:40697373-40697389
13	BHLHE40	chr19:40696952-40697383	K562	blood:	n/a	chr19:40697365-40697381
14	BRCA1	chr19:40696938-40697062	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr19:40697272-40697307	HepG2	liver:	n/a	n/a
16	BRCA1	chr19:40697197-40697397	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr19:40696556-40697135	GM12878	blood:	n/a	n/a
18	CBX3	chr19:40698651-40699048	K562	blood:	n/a	n/a
19	CBX3	chr19:40696394-40696997	K562	blood:	n/a	n/a
20	CCNT2	chr19:40696754-40697548	K562	blood:	n/a	chr19:40697383-40697392
21	CCNT2	chr19:40697818-40698093	K562	blood:	n/a	chr19:40697929-40697938 chr19:40697923-40697932
22	CEBPB	chr19:40696418-40697288	A549	lung:	n/a	n/a
23	CEBPB	chr19:40696420-40696984	Hela-S3	cervix:	n/a	n/a
24	CEBPD	chr19:40697801-40698053	HepG2	liver:	n/a	n/a
25	CHD1	chr19:40696592-40697278	GM12878	blood:	n/a	n/a
26	CHD1	chr19:40697874-40698028	GM12878	blood:	n/a	n/a
27	CHD1	chr19:40696999-40697009	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr19:40697785-40697973	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr19:40696852-40697014	HepG2	liver:	n/a	n/a
30	CHD2	chr19:40696866-40697252	K562	blood:	n/a	n/a
31	CHD2	chr19:40697822-40698021	GM12878	blood:	n/a	n/a
32	CHD2	chr19:40697217-40697229	HepG2	liver:	n/a	n/a
33	CHD2	chr19:40696516-40697505	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr19:40696575-40697447	GM12878	blood:	n/a	n/a
35	CREB1	chr19:40697057-40697445	ECC-1	luminal epithelium:	n/a	n/a
36	CREB1	chr19:40697059-40697457	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr19:40696431-40697455	HepG2	liver:	n/a	n/a
38	CREB1	chr19:40696878-40697616	K562	blood:	n/a	n/a
39	CREB1	chr19:40697047-40697437	ECC-1	luminal epithelium:	n/a	n/a
40	CREB1	chr19:40696999-40697599	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr19:40696814-40697442	K562	blood:	n/a	n/a
42	CREB1	chr19:40696363-40697843	GM12878	blood:	n/a	n/a
43	CREB1	chr19:40696550-40697662	HepG2	liver:	n/a	n/a
44	CREB1	chr19:40697126-40697519	A549	lung:	n/a	n/a
45	CREB1	chr19:40696650-40698092	A549	lung:	n/a	n/a
46	CTCF	chr19:40697740-40697890	HCFaa	heart:	n/a	chr19:40697793-40697806
47	CTCF	chr19:40697665-40697954	K562	blood:	n/a	chr19:40697793-40697806
48	CTCF	chr19:40697760-40697910	BE2_C	brain:	n/a	chr19:40697793-40697806
49	CTCF	chr19:40697740-40697890	SK-N-SH_RA	brain:	n/a	chr19:40697793-40697806
50	CTCF	chr19:40697700-40697850	HPF	lung:	n/a	chr19:40697793-40697806

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40697797-40697847	AG09309	skin:	n/a
2	chr19:40697394-40697444	GM06990	blood:	n/a
3	chr19:40697398-40697448	MCF-7	breast:	n/a
4	chr19:40698192-40698242	HEK293	kidney:	embryo
5	chr19:40698551-40698601	HRE	kidney:	n/a
6	chr19:40696613-40696663	IMR90	lung:	fetal
7	chr19:40698551-40698601	GM12891	blood:	n/a
8	chr19:40697394-40697444	NH-A	brain:	n/a
9	chr19:40697797-40697847	HCF	heart:	n/a
10	chr19:40697804-40697854	HCF	heart:	n/a
11	chr19:40697398-40697448	ProgFib	skin:	n/a
12	chr19:40697425-40697475	GM12891	blood:	n/a
13	chr19:40697394-40697444	AoSMC	blood vessel:	n/a
14	chr19:40697059-40697109	PrEC	prostate:	n/a
15	chr19:40697804-40697854	K562	blood:	n/a
16	chr19:40697059-40697109	U87	brain:	n/a
17	chr19:40698192-40698242	AG10803	skin:	n/a
18	chr19:40697394-40697444	HUVEC	blood vessel:	n/a
19	chr19:40697398-40697448	RPTEC	kidney:	n/a
20	chr19:40697601-40697651	HEEpiC	esophagus:	n/a
21	chr19:40697425-40697475	K562	blood:	n/a
22	chr19:40698551-40698601	SAEC	small airway:	n/a
23	chr19:40697601-40697651	HCM	heart:	n/a
24	chr19:40697797-40697847	HPAEpiC	pulmonary alveolar:	n/a
25	chr19:40696613-40696663	HCT-116	colon:	n/a
26	chr19:40698551-40698601	AG10803	skin:	n/a
27	chr19:40698551-40698601	BE2_C	brain:	n/a
28	chr19:40697256-40697306	HEK293	kidney:	embryo
29	chr19:40697059-40697109	BE2_C	brain:	n/a
30	chr19:40697797-40697847	PrEC	prostate:	n/a
31	chr19:40697804-40697854	AoSMC	blood vessel:	n/a
32	chr19:40697797-40697847	HRPEpiC	eye:	n/a
33	chr19:40697797-40697847	GM19239	blood:	n/a
34	chr19:40697601-40697651	GM12891	blood:	n/a
35	chr19:40696613-40696663	HIPEpiC	eye:	n/a
36	chr19:40697601-40697651	NH-A	brain:	n/a
37	chr19:40698192-40698242	HRE	kidney:	n/a
38	chr19:40697394-40697444	AG09319	gingival:	n/a
39	chr19:40697797-40697847	RPTEC	kidney:	n/a
40	chr19:40697601-40697651	T-47D	breast:	n/a
41	chr19:40697398-40697448	BJ	skin:	n/a
42	chr19:40697394-40697444	PFSK-1	brain:	n/a
43	chr19:40698192-40698242	GM12892	blood:	n/a
44	chr19:40696613-40696663	HMEC	breast:	n/a
45	chr19:40697601-40697651	GM12892	blood:	n/a
46	chr19:40697256-40697306	HRCEpiC	kidney:	n/a
47	chr19:40697059-40697109	NT2-D1	testis:	n/a
48	chr19:40697804-40697854	GM19239	blood:	n/a
49	chr19:40697256-40697306	SK-N-MC	brain:	n/a
50	chr19:40697256-40697306	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:40688598..40690270-chr19:40694622..40697425,2	K562	blood:
2	chr19:40696492..40699360-chr19:41104510..41106083,2	MCF-7	breast:
3	chr19:40684807..40686349-chr19:40694812..40696838,2	K562	blood:
4	chr19:40695427..40698103-chr19:41080992..41083965,2	K562	blood:
5	chr19:40688006..40692388-chr19:40694622..40697525,4	K562	blood:
6	chr19:40696418..40698830-chr19:40709554..40711978,2	K562	blood:
7	chr19:40695407..40698481-chr19:40788292..40792778,5	K562	blood:
8	chr13:111367593..111368509-chr19:40696817..40697667,2	HCT-116	colon:
9	chr19:40697008..40699890-chr19:40723055..40726049,3	MCF-7	breast:
10	chr19:40476601..40478274-chr19:40696597..40698505,2	MCF-7	breast:

No data

Variant related genes	Relation type
MAP3K10	TF binding region
MAP3K10	CpG island
ENSG00000130758	chromatin interactions
ENSG00000221051	chromatin interactions
ENSG00000013275	chromatin interactions
ENSG00000090006	chromatin interactions
ENSG00000105221	chromatin interactions
ENSG00000160410	chromatin interactions
ENSG00000174521	chromatin interactions
ENSG00000207631	chromatin interactions
ENSG00000153487	chromatin interactions

Extended variants
information (count: 52 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531858331	chr19:40696707-40696708	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs540217642	chr19:40696722-40696723	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs561753542	chr19:40696774-40696775	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs111977112	chr19:40696879-40696880	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs529507289	chr19:40696895-40696896	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs550078240	chr19:40696909-40696910	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs568340389	chr19:40696946-40696947	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs376838048	chr19:40696979-40696980	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs369682233	chr19:40697002-40697003	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs569234753	chr19:40697005-40697006	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs117408195	chr19:40697026-40697027	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs339526	chr19:40697061-40697062	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs566440131	chr19:40697094-40697095	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs533897049	chr19:40697111-40697112	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs555028879	chr19:40697126-40697127	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs182412324	chr19:40697156-40697157	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs537869832	chr19:40697180-40697181	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs556483626	chr19:40697218-40697219	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs578029804	chr19:40697228-40697229	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs544875736	chr19:40697336-40697337	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs553938645	chr19:40697351-40697352	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs186641061	chr19:40697371-40697372	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	mRNA abundance
23	rs192014184	chr19:40697372-40697373	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs200824781	chr19:40697610-40697611	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs561716797	chr19:40697674-40697675	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs529225807	chr19:40697815-40697816	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs376665121	chr19:40697817-40697818	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs544233148	chr19:40697857-40697858	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs201467895	chr19:40697932-40697933	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs377356617	chr19:40697996-40697997	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs370034354	chr19:40697998-40697999	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs374398619	chr19:40698100-40698101	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs3746007	chr19:40698118-40698119	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs200853191	chr19:40698172-40698173	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs374135624	chr19:40698179-40698180	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs539939105	chr19:40698211-40698212	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs139116041	chr19:40698232-40698233	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs55987909	chr19:40698235-40698236	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs143046006	chr19:40698254-40698255	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs369104373	chr19:40698317-40698318	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs1046744	chr19:40698328-40698329	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs199866647	chr19:40698365-40698366	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs558754842	chr19:40698415-40698416	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs200025571	chr19:40698433-40698434	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs36102209	chr19:40698441-40698442	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs149643657	chr19:40698480-40698481	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs144372418	chr19:40698506-40698507	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs373849251	chr19:40698587-40698588	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs202035880	chr19:40698641-40698642	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs140903126	chr19:40698713-40698714	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Lung cancer	21569311	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
Anaplastic thyroid cancer	18753363	CNVD
Pleomorphic liposarcoma	18784837	CNVD

Chromatin state (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40695800-40698000	Active TSS	GM12878-XiMat	blood
2	chr19:40695800-40698600	Active TSS	Osteobl	bone
3	chr19:40696000-40698400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:40696000-40698400	Active TSS	Brain Angular Gyrus	brain
5	chr19:40696200-40696800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr19:40696200-40696800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr19:40696200-40696800	Active TSS	Colonic Mucosa	Colon
8	chr19:40696200-40697000	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr19:40696200-40697800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr19:40696200-40698000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:40696200-40698000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr19:40696200-40698000	Active TSS	Brain Anterior Caudate	brain
13	chr19:40696200-40698000	Active TSS	Brain Hippocampus Middle	brain
14	chr19:40696200-40698000	Active TSS	Psoas Muscle	Psoas
15	chr19:40696200-40698000	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr19:40696200-40698200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr19:40696400-40696800	Flanking Active TSS	Primary B cells from peripheral blood	blood
18	chr19:40696400-40696800	Flanking Active TSS	Primary T cells from cord blood	blood
19	chr19:40696400-40696800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
20	chr19:40696400-40696800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr19:40696400-40696800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr19:40696400-40696800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr19:40696400-40696800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr19:40696400-40696800	Flanking Active TSS	A549	lung
25	chr19:40696400-40696800	Flanking Active TSS	Hela-S3	cervix
26	chr19:40696400-40696800	Flanking Active TSS	NHEK	skin
27	chr19:40696400-40697000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
28	chr19:40696400-40697000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr19:40696400-40697000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
30	chr19:40696400-40697000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
31	chr19:40696400-40697000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr19:40696400-40697000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:40696400-40697000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr19:40696400-40697000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr19:40696400-40697000	Flanking Active TSS	Dnd41	blood
36	chr19:40696400-40697000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr19:40696400-40697200	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr19:40696400-40697200	Active TSS	Fetal Heart	heart
39	chr19:40696400-40697200	Flanking Active TSS	Placenta	Placenta
40	chr19:40696400-40697400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
41	chr19:40696400-40697800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr19:40696400-40697800	Active TSS	Liver	Liver
43	chr19:40696400-40697800	Active TSS	Right Ventricle	heart
44	chr19:40696400-40697800	Active TSS	Stomach Smooth Muscle	stomach
45	chr19:40696400-40698000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr19:40696400-40698000	Active TSS	Brain Cingulate Gyrus	brain
47	chr19:40696400-40698000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr19:40696400-40698000	Active TSS	Duodenum Mucosa	Duodenum
49	chr19:40696400-40698000	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr19:40696400-40698000	Active TSS	Fetal Muscle Leg	muscle

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