Variant report

Variant	esv3440429
Chromosome Location	chr1:10269390-10271938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:907)
CpG islands
(count:732)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:907 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10270329-10270704	K562	blood:	n/a	n/a
2	ARID3A	chr1:10271526-10272346	HepG2	liver:	n/a	chr1:10272272-10272288
3	ARID3A	chr1:10269733-10270729	HepG2	liver:	n/a	n/a
4	ATF1	chr1:10269976-10270734	K562	blood:	n/a	n/a
5	ATF2	chr1:10270383-10270766	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:10269733-10270280	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:10269759-10270603	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:10270311-10270367	K562	blood:	n/a	n/a
9	BACH1	chr1:10269766-10270771	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr1:10269930-10270563	A549	lung:	n/a	chr1:10270436-10270449
11	BCLAF1	chr1:10270105-10270612	GM12878	blood:	n/a	chr1:10270436-10270449
12	BHLHE40	chr1:10269929-10270756	K562	blood:	n/a	chr1:10270524-10270540 chr1:10270686-10270702
13	BHLHE40	chr1:10271182-10271453	K562	blood:	n/a	chr1:10271229-10271245
14	BHLHE40	chr1:10270026-10270624	GM12878	blood:	n/a	chr1:10270524-10270540
15	BRCA1	chr1:10271383-10271834	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr1:10269930-10270631	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr1:10269986-10270757	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr1:10270316-10270635	GM12878	blood:	n/a	n/a
19	BRCA1	chr1:10270334-10270708	HepG2	liver:	n/a	n/a
20	CBX3	chr1:10270001-10270756	K562	blood:	n/a	n/a
21	CBX3	chr1:10271310-10272140	K562	blood:	n/a	n/a
22	CCNT2	chr1:10269990-10271679	K562	blood:	n/a	chr1:10270977-10270986 chr1:10271088-10271097
23	CEBPB	chr1:10271494-10272292	IMR90	lung:	n/a	chr1:10271774-10271787
24	CEBPB	chr1:10271591-10271725	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:10271499-10271896	HepG2	liver:	n/a	chr1:10271774-10271787
26	CEBPB	chr1:10271505-10271878	K562	blood:	n/a	chr1:10271774-10271787
27	CEBPB	chr1:10269906-10270653	Hela-S3	cervix:	n/a	chr1:10270469-10270477
28	CEBPB	chr1:10270564-10270660	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:10271516-10271897	ECC-1	luminal epithelium:	n/a	chr1:10271774-10271787
30	CEBPB	chr1:10271456-10271955	ECC-1	luminal epithelium:	n/a	chr1:10271774-10271787
31	CEBPB	chr1:10271298-10272180	Hela-S3	cervix:	n/a	chr1:10271774-10271787
32	CEBPD	chr1:10270536-10270723	HepG2	liver:	n/a	n/a
33	CEBPD	chr1:10270103-10270780	HepG2	liver:	n/a	n/a
34	CHD1	chr1:10271094-10271667	GM12878	blood:	n/a	n/a
35	CHD1	chr1:10269843-10270760	GM12878	blood:	n/a	n/a
36	CHD1	chr1:10269586-10270414	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr1:10270756-10270769	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:10270045-10270780	K562	blood:	n/a	n/a
39	CHD2	chr1:10271343-10271883	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr1:10271274-10271801	K562	blood:	n/a	n/a
41	CHD2	chr1:10271131-10272062	GM12878	blood:	n/a	n/a
42	CHD2	chr1:10269930-10270756	GM12878	blood:	n/a	n/a
43	CHD2	chr1:10269740-10270820	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr1:10269851-10270707	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr1:10269945-10270807	HepG2	liver:	n/a	n/a
46	CHD2	chr1:10271499-10272121	HepG2	liver:	n/a	n/a
47	CREB1	chr1:10270211-10270766	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr1:10270123-10270914	HepG2	liver:	n/a	n/a
49	CREB1	chr1:10270239-10270715	A549	lung:	n/a	n/a
50	CREB1	chr1:10270095-10270941	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10270641-10270691	Caco-2	colon:	n/a
2	chr1:10271724-10271774	AG04450	lung:	fetal
3	chr1:10271217-10271267	ProgFib	skin:	n/a
4	chr1:10269828-10269878	PrEC	prostate:	n/a
5	chr1:10270439-10270489	CMK	blood:	n/a
6	chr1:10271191-10271241	AG09319	gingival:	n/a
7	chr1:10269828-10269878	HUVEC	blood vessel:	n/a
8	chr1:10271191-10271241	AoSMC	blood vessel:	n/a
9	chr1:10271724-10271774	SK-N-SH	brain:	n/a
10	chr1:10270641-10270691	AoSMC	blood vessel:	n/a
11	chr1:10270641-10270691	HAEpiC	amniotic membrane:	n/a
12	chr1:10270712-10270762	HAEpiC	amniotic membrane:	n/a
13	chr1:10270521-10270571	AoSMC	blood vessel:	n/a
14	chr1:10271217-10271267	HRCEpiC	kidney:	n/a
15	chr1:10270658-10270708	IMR90	lung:	fetal
16	chr1:10270712-10270762	Caco-2	colon:	n/a
17	chr1:10270521-10270571	CMK	blood:	n/a
18	chr1:10270641-10270691	HMEC	breast:	n/a
19	chr1:10270641-10270691	HNPCEpiC	eye:	n/a
20	chr1:10270641-10270691	Hela-S3	cervix:	n/a
21	chr1:10270515-10270565	PANC-1	pancreas:	n/a
22	chr1:10271217-10271267	HCF	heart:	n/a
23	chr1:10270515-10270565	Hepatocyte	liver:	n/a
24	chr1:10270641-10270691	HEEpiC	esophagus:	n/a
25	chr1:10270521-10270571	AG04450	lung:	fetal
26	chr1:10270439-10270489	HepG2	liver:	n/a
27	chr1:10271724-10271774	HepG2	liver:	n/a
28	chr1:10271217-10271267	T-47D	breast:	n/a
29	chr1:10270712-10270762	MCF-7	breast:	n/a
30	chr1:10271217-10271267	SK-N-SH_RA	brain:	n/a
31	chr1:10270439-10270489	Hepatocyte	liver:	n/a
32	chr1:10270658-10270708	HL-60	blood:	n/a
33	chr1:10269828-10269878	IMR90	lung:	fetal
34	chr1:10270641-10270691	T-47D	breast:	n/a
35	chr1:10270658-10270708	Jurkat	blood:	n/a
36	chr1:10271217-10271267	Jurkat	blood:	n/a
37	chr1:10270515-10270565	K562	blood:	n/a
38	chr1:10270641-10270691	ProgFib	skin:	n/a
39	chr1:10271724-10271774	T-47D	breast:	n/a
40	chr1:10270515-10270565	SK-N-MC	brain:	n/a
41	chr1:10270658-10270708	AoSMC	blood vessel:	n/a
42	chr1:10271724-10271774	MCF10A-Er-Src	breast:	n/a
43	chr1:10271724-10271774	HEEpiC	esophagus:	n/a
44	chr1:10269828-10269878	BE2_C	brain:	n/a
45	chr1:10269828-10269878	HL-60	blood:	n/a
46	chr1:10271217-10271267	K562	blood:	n/a
47	chr1:10269828-10269878	T-47D	breast:	n/a
48	chr1:10270439-10270489	ProgFib	skin:	n/a
49	chr1:10270521-10270571	HNPCEpiC	eye:	n/a
50	chr1:10270515-10270565	U87	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10270721..10271416-chr17:6917944..6918783,2	Hela-S3	cervix:
2	chr1:10269993..10270712-chr1:10488254..10488767,2	K562	blood:
3	chr1:10271685..10272582-chr12:62033319..62034137,2	MCF-7	breast:
4	chr1:10269768..10272241-chr11:62606834..62608360,2	MCF-7	breast:
5	chr1:10269869..10270448-chr12:64845349..64846337,2	Hela-S3	cervix:
6	chr1:10270305..10270868-chr12:99038434..99039063,2	Hela-S3	cervix:
7	chr1:10269508..10272201-chr1:10459062..10462119,3	K562	blood:
8	chr1:10269636..10272138-chr1:10457591..10460138,4	K562	blood:
9	chr1:10269968..10270783-chr1:86046649..86047447,2	Hela-S3	cervix:
10	chr1:10270585..10272249-chr1:10490197..10491890,2	K562	blood:
11	chr1:10269235..10270735-chr17:41462941..41466799,3	K562	blood:

No data

Variant related genes	Relation type
KIF1B	TF binding region
KIF1B	CpG island
ENSG00000175279	chromatin interactions
ENSG00000251503	chromatin interactions
ENSG00000120868	chromatin interactions
ENSG00000166130	chromatin interactions
ENSG00000183735	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000142871	chromatin interactions
ENSG00000142657	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000258315	chromatin interactions

Extended variants
information (count: 77 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:77 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530680092	chr1:10269469-10269470	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs551942231	chr1:10269484-10269485	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565021469	chr1:10269499-10269500	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs189539435	chr1:10269529-10269530	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs573206721	chr1:10269627-10269628	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535508664	chr1:10269632-10269633	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs77659689	chr1:10269688-10269689	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs371128958	chr1:10269692-10269693	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs535731496	chr1:10269705-10269706	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78535522	chr1:10269743-10269744	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs568912576	chr1:10269792-10269793	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs114252518	chr1:10269805-10269806	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs558747572	chr1:10269832-10269833	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs147538325	chr1:10269859-10269860	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs534723579	chr1:10269893-10269894	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs546211783	chr1:10269916-10269917	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs552930965	chr1:10269958-10269959	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs574831486	chr1:10270014-10270015	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs542116810	chr1:10270019-10270020	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs557536462	chr1:10270023-10270024	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs112209859	chr1:10270071-10270072	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs530885242	chr1:10270125-10270126	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs142933780	chr1:10270161-10270162	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs116787047	chr1:10270164-10270165	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs540266314	chr1:10270171-10270172	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs561659086	chr1:10270189-10270190	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs529204955	chr1:10270219-10270220	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs181074995	chr1:10270235-10270236	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs569047963	chr1:10270249-10270250	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs532954416	chr1:10270276-10270277	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs576628320	chr1:10270300-10270301	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs570888825	chr1:10270338-10270339	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs534782162	chr1:10270354-10270355	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs552994362	chr1:10270371-10270372	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs543418640	chr1:10270373-10270374	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs3828081	chr1:10270386-10270387	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs183620260	chr1:10270391-10270392	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs116570550	chr1:10270402-10270403	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs559622355	chr1:10270427-10270428	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs557627286	chr1:10270433-10270434	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs550705843	chr1:10270448-10270449	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs558316944	chr1:10270479-10270480	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs61784580	chr1:10270496-10270497	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs6695456	chr1:10270526-10270527	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561676701	chr1:10270636-10270637	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs528859522	chr1:10270657-10270658	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs140167753	chr1:10270716-10270717	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs544517259	chr1:10270727-10270728	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs149705989	chr1:10270756-10270757	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs533237549	chr1:10270774-10270775	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10250000-10269800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:10262000-10269400	Weak transcription	Fetal Brain Male	brain
3	chr1:10264600-10269400	Weak transcription	HSMMtube	muscle
4	chr1:10265400-10269400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr1:10265400-10269400	Weak transcription	HepG2	liver
6	chr1:10265400-10269600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:10268200-10269400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr1:10268600-10269600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr1:10268600-10270400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr1:10268800-10269800	Enhancers	Primary B cells from peripheral blood	blood
11	chr1:10269000-10269600	Enhancers	Colon Smooth Muscle	Colon
12	chr1:10269000-10269800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr1:10269000-10269800	Enhancers	Fetal Muscle Trunk	muscle
14	chr1:10269200-10269400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:10269200-10269400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:10269200-10269400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:10269200-10269400	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr1:10269200-10269400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:10269200-10269400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:10269200-10269400	Enhancers	Fetal Brain Female	brain
21	chr1:10269200-10269400	Enhancers	Rectal Smooth Muscle	rectum
22	chr1:10269200-10269400	Enhancers	A549	lung
23	chr1:10269200-10269400	Enhancers	GM12878-XiMat	blood
24	chr1:10269200-10269600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:10269200-10269600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr1:10269200-10269600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr1:10269200-10269600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:10269200-10269600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr1:10269200-10269600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
30	chr1:10269200-10269600	Enhancers	Stomach Smooth Muscle	stomach
31	chr1:10269200-10269800	Active TSS	Primary hematopoietic stem cells	blood
32	chr1:10269400-10269600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:10269400-10269600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr1:10269400-10269600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr1:10269400-10269600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:10269400-10269600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr1:10269400-10269600	Bivalent Enhancer	Primary B cells from cord blood	blood
38	chr1:10269400-10269600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:10269400-10269600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:10269400-10269600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:10269400-10269600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:10269400-10269600	Enhancers	Adipose Nuclei	Adipose
43	chr1:10269400-10269600	Enhancers	Brain Anterior Caudate	brain
44	chr1:10269400-10269600	Enhancers	Brain Cingulate Gyrus	brain
45	chr1:10269400-10269600	Enhancers	Brain Germinal Matrix	brain
46	chr1:10269400-10269600	Enhancers	Fetal Brain Male	brain
47	chr1:10269400-10269600	Enhancers	Fetal Intestine Large	intestine
48	chr1:10269400-10269600	Enhancers	Fetal Intestine Small	intestine
49	chr1:10269400-10269600	Enhancers	Fetal Stomach	stomach
50	chr1:10269400-10269600	Flanking Active TSS	GM12878-XiMat	blood

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