Variant report

Variant	nsv893617
Chromosome Location	chr9:101585992-101634716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1012)
CpG islands
(count:61)
Chromatin interactive
region (count:87)
LncRNA
region (count:59)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:101613357-101614467	K562	blood:	n/a	chr9:101613614-101613630
2	ARID3A	chr9:101610765-101611153	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:101624343-101624344	K562	blood:	n/a	n/a
4	ARID3A	chr9:101595329-101595794	K562	blood:	n/a	n/a
5	ARID3A	chr9:101629830-101630391	K562	blood:	n/a	n/a
6	ARID3A	chr9:101623258-101623565	K562	blood:	n/a	n/a
7	ARID3A	chr9:101619269-101619548	K562	blood:	n/a	n/a
8	ARID3A	chr9:101610787-101611263	K562	blood:	n/a	n/a
9	ATF1	chr9:101610782-101611491	K562	blood:	n/a	n/a
10	ATF1	chr9:101619505-101619734	K562	blood:	n/a	n/a
11	ATF1	chr9:101613867-101614504	K562	blood:	n/a	n/a
12	ATF1	chr9:101629565-101630442	K562	blood:	n/a	n/a
13	ATF3	chr9:101630029-101630284	K562	blood:	n/a	n/a
14	ATF3	chr9:101613968-101614306	K562	blood:	n/a	n/a
15	ATF3	chr9:101629897-101630410	K562	blood:	n/a	n/a
16	BACH1	chr9:101614006-101614168	K562	blood:	n/a	n/a
17	BACH1	chr9:101623297-101623422	H1-hESC	embryonic stem cell:	n/a	n/a
18	BHLHE40	chr9:101633224-101633569	K562	blood:	n/a	n/a
19	BHLHE40	chr9:101610733-101611086	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:101623244-101623475	K562	blood:	n/a	n/a
21	BHLHE40	chr9:101610759-101611314	K562	blood:	n/a	n/a
22	BHLHE40	chr9:101613397-101613461	K562	blood:	n/a	n/a
23	BHLHE40	chr9:101629400-101630458	K562	blood:	n/a	n/a
24	BHLHE40	chr9:101595226-101595967	K562	blood:	n/a	n/a
25	BRCA1	chr9:101617625-101617628	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr9:101610847-101611422	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr9:101613920-101614547	K562	blood:	n/a	n/a
28	CBX3	chr9:101631363-101631839	K562	blood:	n/a	n/a
29	CBX3	chr9:101629915-101630356	K562	blood:	n/a	n/a
30	CBX3	chr9:101586455-101586981	K562	blood:	n/a	n/a
31	CBX3	chr9:101595307-101595947	K562	blood:	n/a	n/a
32	CBX3	chr9:101629954-101630516	K562	blood:	n/a	n/a
33	CBX3	chr9:101617913-101618191	K562	blood:	n/a	n/a
34	CBX3	chr9:101631298-101631731	K562	blood:	n/a	n/a
35	CBX3	chr9:101595145-101596431	K562	blood:	n/a	n/a
36	CBX3	chr9:101617828-101618238	K562	blood:	n/a	n/a
37	CBX3	chr9:101610495-101611288	HCT-116	colon:	n/a	n/a
38	CCNT2	chr9:101610792-101611353	K562	blood:	n/a	n/a
39	CCNT2	chr9:101595381-101595927	K562	blood:	n/a	n/a
40	CCNT2	chr9:101629992-101630369	K562	blood:	n/a	n/a
41	CEBPB	chr9:101623048-101623377	A549	lung:	n/a	n/a
42	CEBPB	chr9:101624426-101624915	IMR90	lung:	n/a	chr9:101624617-101624628
43	CEBPB	chr9:101610786-101611173	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:101629852-101630407	Hela-S3	cervix:	n/a	chr9:101630159-101630172 chr9:101630159-101630170
45	CEBPB	chr9:101624460-101624802	K562	blood:	n/a	chr9:101624617-101624628
46	CEBPB	chr9:101623062-101623377	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:101626584-101626865	K562	blood:	n/a	chr9:101626714-101626727 chr9:101626714-101626725
48	CEBPB	chr9:101593320-101593584	K562	blood:	n/a	chr9:101593440-101593453 chr9:101593440-101593451
49	CEBPB	chr9:101626622-101626778	K562	blood:	n/a	chr9:101626714-101626727 chr9:101626714-101626725
50	CEBPB	chr9:101629816-101630518	HCT-116	colon:	n/a	chr9:101630159-101630172 chr9:101630159-101630170

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:101594150-101594200	GM12891	blood:	n/a
2	chr9:101594150-101594200	PANC-1	pancreas:	n/a
3	chr9:101594150-101594200	SK-N-SH	brain:	n/a
4	chr9:101594150-101594200	HEK293	kidney:	embryo
5	chr9:101594150-101594200	GM12892	blood:	n/a
6	chr9:101594150-101594200	GM19239	blood:	n/a
7	chr9:101594150-101594200	AG09309	skin:	n/a
8	chr9:101594150-101594200	HAEpiC	amniotic membrane:	n/a
9	chr9:101594150-101594200	HRCEpiC	kidney:	n/a
10	chr9:101594150-101594200	MCF-7	breast:	n/a
11	chr9:101594150-101594200	MCF10A-Er-Src	breast:	n/a
12	chr9:101594150-101594200	HRE	kidney:	n/a
13	chr9:101594150-101594200	HIPEpiC	eye:	n/a
14	chr9:101594150-101594200	HCPEpiC	choroid plexus:	n/a
15	chr9:101594150-101594200	ovcar-3	ovarian:	n/a
16	chr9:101594150-101594200	HRPEpiC	eye:	n/a
17	chr9:101594150-101594200	SKMC	muscle:	n/a
18	chr9:101594150-101594200	NB4	blood:	n/a
19	chr9:101594150-101594200	HEEpiC	esophagus:	n/a
20	chr9:101594150-101594200	CMK	blood:	n/a
21	chr9:101594150-101594200	AG04450	lung:	fetal
22	chr9:101594150-101594200	AG10803	skin:	n/a
23	chr9:101594150-101594200	BE2_C	brain:	n/a
24	chr9:101594150-101594200	NHBE	bronchial:	n/a
25	chr9:101594150-101594200	ECC-1	luminal epithelium:	n/a
26	chr9:101594150-101594200	H1-hESC	embryonic stem cell:	embryo
27	chr9:101594150-101594200	AoSMC	blood vessel:	n/a
28	chr9:101594150-101594200	HPAEpiC	pulmonary alveolar:	n/a
29	chr9:101594150-101594200	A549	lung:	n/a
30	chr9:101594150-101594200	Hepatocyte	liver:	n/a
31	chr9:101594150-101594200	AG04449	skin:	fetal
32	chr9:101594150-101594200	PrEC	prostate:	n/a
33	chr9:101594150-101594200	LNCaP	prostate:	n/a
34	chr9:101594150-101594200	GM12878	blood:	n/a
35	chr9:101594150-101594200	BJ	skin:	n/a
36	chr9:101594150-101594200	PFSK-1	brain:	n/a
37	chr9:101594150-101594200	HMEC	breast:	n/a
38	chr9:101594150-101594200	HCF	heart:	n/a
39	chr9:101594150-101594200	GM06990	blood:	n/a
40	chr9:101594150-101594200	IMR90	lung:	fetal
41	chr9:101594150-101594200	HCT-116	colon:	n/a
42	chr9:101594150-101594200	SAEC	small airway:	n/a
43	chr9:101594150-101594200	NH-A	brain:	n/a
44	chr9:101594150-101594200	HUVEC	blood vessel:	n/a
45	chr9:101594150-101594200	NHDF-neo	bronchial:	n/a
46	chr9:101594150-101594200	Hela-S3	cervix:	n/a
47	chr9:101594150-101594200	HNPCEpiC	eye:	n/a
48	chr9:101594150-101594200	HepG2	liver:	n/a
49	chr9:101594150-101594200	SK-N-MC	brain:	n/a
50	chr9:101594150-101594200	HCM	heart:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:101622903..101624002-chr9:101736884..101738046,3	MCF-7	breast:
2	chr9:101613008..101615141-chr9:101615540..101618315,3	K562	blood:
3	chr9:101622672..101623296-chr9:101946632..101947533,2	MCF-7	breast:
4	chr9:101590538..101592139-chr9:101593190..101595343,2	K562	blood:
5	chr9:101594094..101597495-chr9:101837008..101839345,3	K562	blood:
6	chr9:101555276..101559481-chr9:101592543..101597638,8	K562	blood:
7	chr9:101595306..101598484-chr9:101600696..101602900,3	MCF-7	breast:
8	chr9:101608339..101609840-chr9:101709573..101711689,2	K562	blood:
9	chr9:101587717..101590652-chr9:101598442..101600978,2	K562	blood:
10	chr9:101568546..101571235-chr9:101609367..101611059,3	MCF-7	breast:
11	chr9:101569167..101574169-chr9:101584327..101589428,7	K562	blood:
12	chr9:101583330..101586949-chr9:101590792..101593415,3	MCF-7	breast:
13	chr9:101587154..101591377-chr9:101593024..101595541,4	K562	blood:
14	chr9:101614852..101617810-chr9:101836306..101838522,2	K562	blood:
15	chr9:101606847..101608387-chr9:101617500..101619533,2	K562	blood:
16	chr9:101593411..101597126-chr9:101612510..101614474,3	K562	blood:
17	chr9:101581569..101586454-chr9:101592165..101596926,7	K562	blood:
18	chr9:101622816..101623807-chr9:101760819..101761758,4	K562	blood:
19	chr9:101589019..101591816-chr9:101593283..101595363,3	MCF-7	breast:
20	chr9:101579352..101582875-chr9:101585039..101587415,4	K562	blood:
21	chr9:101551244..101553592-chr9:101594494..101597222,2	K562	blood:
22	chr9:101568220..101570784-chr9:101592023..101594699,3	K562	blood:
23	chr9:101613892..101617810-chr9:101836029..101839366,3	K562	blood:
24	chr9:101601345..101603678-chr9:101836999..101839273,2	K562	blood:
25	chr9:101557527..101559121-chr9:101593365..101595947,2	MCF-7	breast:
26	chr9:101598174..101601137-chr9:101612213..101615543,3	K562	blood:
27	chr9:101602137..101603976-chr9:101608820..101610859,2	K562	blood:
28	chr9:101598592..101601247-chr9:101835043..101836842,2	K562	blood:
29	chr9:101613008..101615141-chr9:101615540..101618315,3	K562	blood:
30	chr9:101613389..101615613-chr9:101644197..101646621,2	K562	blood:
31	chr9:101627906..101629623-chr9:101640903..101642469,2	MCF-7	breast:
32	chr9:101631572..101634031-chr9:101638975..101641818,3	MCF-7	breast:
33	chr9:101581569..101586454-chr9:101592165..101596926,7	K562	blood:
34	chr9:101594248..101597008-chr9:101735799..101737374,2	K562	blood:
35	chr9:101583304..101585662-chr9:101606150..101607939,2	K562	blood:
36	chr9:101606847..101608387-chr9:101617500..101619533,2	K562	blood:
37	chr9:101587717..101590652-chr9:101598442..101600978,2	K562	blood:
38	chr9:101602137..101603976-chr9:101608820..101610859,2	K562	blood:
39	chr9:101595508..101597827-chr9:101735693..101737299,2	K562	blood:
40	chr9:101595893..101597634-chr9:101606763..101609498,3	K562	blood:
41	chr9:101570303..101574512-chr9:101580563..101586059,9	K562	blood:
42	chr9:101622815..101623852-chr9:101760749..101761771,5	MCF-7	breast:
43	chr9:101574925..101576845-chr9:101603404..101606201,2	K562	blood:
44	chr9:101594868..101597972-chr9:101638974..101641912,3	K562	blood:
45	chr9:101616947..101619322-chr9:101629462..101631343,2	K562	blood:
46	chr9:101608179..101610561-chr9:101756787..101758772,2	K562	blood:
47	chr9:101623095..101624060-chr9:101737038..101737804,3	MCF-7	breast:
48	chr9:101616947..101619322-chr9:101629462..101631343,2	K562	blood:
49	chr9:101594752..101596934-chr9:101836815..101838508,2	K562	blood:
50	chr9:101625807..101630456-chr9:101833733..101838551,4	K562	blood:

(count:59 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKS6-1	chr9:101632263-101632346	ENSG00000267026.1
2	lnc-ANKS6-1	chr9:101631273-101631699	ENSG00000267026.1
3	lnc-ANKS6-2	chr9:101606305-101606765	l_3822_chr9:101387877-101520361_testes
4	lnc-ANKS6-2	chr9:101607851-101608288	l_3822_chr9:101387877-101520361_testes
5	lnc-ANKS6-1	chr9:101634471-101634545	ENSG00000267026.1
6	lnc-ANKS6-1	chr9:101634471-101634545	ENSG00000267026.1
7	lnc-ANKS6-1	chr9:101624521-101624794	ENSG00000267026.1
8	lnc-ANKS6-1	chr9:101631273-101631739	ENSG00000267026.1
9	lnc-ANKS6-2	chr9:101621924-101622020	l_3822_chr9:101387877-101520361_testes
10	lnc-ANKS6-1	chr9:101611210-101611895	ENSG00000267026.1
11	lnc-ANKS6-1	chr9:101631397-101631772	ENSG00000267026.1
12	lnc-ANKS6-1	chr9:101633173-101633266	ENSG00000267026.1
13	lnc-ANKS6-1	chr9:101632247-101632346	ENSG00000267026.1
14	lnc-ANKS6-1	chr9:101631869-101631965	ENSG00000267026.1
15	lnc-ANKS6-1	chr9:101634471-101634560	ENSG00000238264.1
16	lnc-ANKS6-1	chr9:101609511-101609773	ENSG00000238264.1
17	lnc-ANKS6-1	chr9:101631447-101631772	ENSG00000267026.1
18	lnc-ANKS6-1	chr9:101634471-101634542	ENSG00000267026.1
19	lnc-ANKS6-1	chr9:101634471-101634544	ENSG00000267026.1
20	lnc-ANKS6-1	chr9:101631664-101631772	ENSG00000267026.1
21	lnc-ANKS6-1	chr9:101631284-101631772	ENSG00000267026.1
22	lnc-ANKS6-1	chr9:101628967-101629134	ENSG00000267026.1
23	lnc-ANKS6-1	chr9:101631619-101631739	ENSG00000267026.1
24	lnc-ANKS6-1	chr9:101631869-101631965	ENSG00000267026.1
25	lnc-ANKS6-1	chr9:101634471-101634545	ENSG00000267026.1
26	lnc-ANKS6-1	chr9:101632715-101633053	ENSG00000267026.1
27	lnc-ANKS6-1	chr9:101631344-101631965	ENSG00000267026.1
28	lnc-ANKS6-1	chr9:101633642-101633678	ENSG00000267026.1
29	lnc-ANKS6-1	chr9:101631277-101631739	ENSG00000267026.1
30	lnc-ANKS6-1	chr9:101634471-101634545	ENSG00000267026.1
31	lnc-ANKS6-1	chr9:101629321-101629392	ENSG00000267026.1
32	lnc-ANKS6-1	chr9:101632715-101633053	ENSG00000267026.1
33	lnc-ANKS6-1	chr9:101631273-101631739	ENSG00000267026.1
34	lnc-ANKS6-1	chr9:101631869-101631965	ENSG00000267026.1
35	lnc-ANKS6-1	chr9:101632631-101633266	ENSG00000267026.1
36	lnc-ANKS6-1	chr9:101634471-101634545	ENSG00000267026.1
37	lnc-ANKS6-1	chr9:101634471-101634697	ENSG00000267026.1
38	lnc-ANKS6-1	chr9:101634471-101634697	ENSG00000267026.1
39	lnc-ANKS6-1	chr9:101634471-101634545	ENSG00000267026.1
40	lnc-COL15A1-3	chr9:101611234-101611916	NONHSAT133608
41	lnc-ANKS6-1	chr9:101634345-101634545	ENSG00000267026.1
42	lnc-COL15A1-3	chr9:101611054-101611142	NONHSAT133608
43	lnc-ANKS6-1	chr9:101634471-101634545	ENSG00000267026.1
44	lnc-ANKS6-1	chr9:101634471-101634697	ENSG00000267026.1
45	lnc-ANKS6-1	chr9:101632715-101633053	ENSG00000267026.1
46	lnc-ANKS6-1	chr9:101632715-101633053	ENSG00000267026.1
47	lnc-GALNT12-1	chr9:101624161-101624449	NONHSAT133609
48	lnc-ANKS6-1	chr9:101634240-101634545	ENSG00000267026.1
49	lnc-ANKS6-1	chr9:101633173-101633266	ENSG00000267026.1
50	lnc-ANKS6-1	chr9:101632247-101632346	ENSG00000267026.1

No data

Variant related genes	Relation type
GALNT12	TF binding region
ENSG00000267026	TF binding region
GALNT12	CpG island
ENSG00000267026	CpG island
ENSG00000106799	chromatin interactions
ENSG00000119403	chromatin interactions
ENSG00000267026	chromatin interactions
ENSG00000119514	chromatin interactions
ENSG00000165138	chromatin interactions

Extended variants
information (count: 1994 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1994 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2295925	chr9:101585992-101585993	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10987851	chr9:101586028-101586029	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs568395126	chr9:101586100-101586101	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112056674	chr9:101586104-101586105	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537218021	chr9:101586136-101586137	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550813440	chr9:101586165-101586166	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs151056926	chr9:101586189-101586190	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539554722	chr9:101586220-101586221	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs75631276	chr9:101586232-101586233	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571491148	chr9:101586236-101586237	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535877680	chr9:101586297-101586298	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185014870	chr9:101586319-101586320	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575554323	chr9:101586382-101586383	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372171464	chr9:101586570-101586571	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544364803	chr9:101586635-101586636	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564348571	chr9:101586653-101586654	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576823946	chr9:101586657-101586658	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs189341941	chr9:101586698-101586699	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559438430	chr9:101586704-101586705	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199682949	chr9:101586735-101586736	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567938834	chr9:101586745-101586746	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528057817	chr9:101586829-101586830	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149768791	chr9:101586856-101586857	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561933039	chr9:101586879-101586880	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200611920	chr9:101586891-101586892	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530838019	chr9:101586924-101586925	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs182031241	chr9:101587018-101587019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186223317	chr9:101587125-101587126	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs367676883	chr9:101587138-101587139	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7043234	chr9:101587162-101587163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs566984588	chr9:101587202-101587203	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535430409	chr9:101587224-101587225	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188285467	chr9:101587239-101587240	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs180786077	chr9:101587243-101587244	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538152447	chr9:101587255-101587256	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs145098010	chr9:101587282-101587283	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555155040	chr9:101587312-101587313	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34385986	chr9:101587318-101587319	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142233577	chr9:101587327-101587328	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371572213	chr9:101587353-101587354	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572913362	chr9:101587383-101587384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs375123581	chr9:101587387-101587388	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186647582	chr9:101587394-101587395	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561672636	chr9:101587409-101587410	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35160816	chr9:101587468-101587469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs75786121	chr9:101587481-101587482	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191038692	chr9:101587488-101587489	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183705578	chr9:101587499-101587500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs74586206	chr9:101587511-101587512	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185902321	chr9:101587512-101587513	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	17363583	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:945 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101571000-101586600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:101572600-101586600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr9:101572800-101589200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr9:101573000-101586600	Weak transcription	Esophagus	oesophagus
5	chr9:101573000-101612800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr9:101573800-101586000	Weak transcription	Fetal Intestine Large	intestine
7	chr9:101576000-101605000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr9:101577800-101610600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr9:101578000-101596800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr9:101579200-101610800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:101581400-101586600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr9:101581400-101586600	Weak transcription	Colonic Mucosa	Colon
13	chr9:101581600-101586200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr9:101581600-101591000	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr9:101581800-101592400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr9:101582000-101588800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr9:101582000-101610600	Weak transcription	Aorta	Aorta
18	chr9:101583800-101588800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr9:101583800-101589600	Weak transcription	Colon Smooth Muscle	Colon
20	chr9:101583800-101599600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr9:101583800-101610600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr9:101584400-101587200	Strong transcription	Fetal Intestine Small	intestine
23	chr9:101584400-101602000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr9:101584600-101586200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:101584800-101602600	Strong transcription	Fetal Stomach	stomach
26	chr9:101585000-101591000	Strong transcription	Duodenum Mucosa	Duodenum
27	chr9:101585000-101610600	Weak transcription	Brain Angular Gyrus	brain
28	chr9:101585000-101611000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr9:101585200-101586000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr9:101585200-101586800	Enhancers	Stomach Mucosa	stomach
31	chr9:101585200-101589000	Weak transcription	Thymus	Thymus
32	chr9:101585200-101598800	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr9:101585400-101586800	Strong transcription	Stomach Smooth Muscle	stomach
34	chr9:101585400-101589200	Weak transcription	Pancreas	Pancrea
35	chr9:101585600-101586800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:101585600-101586800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:101585800-101586200	Weak transcription	K562	blood
38	chr9:101585800-101587000	Genic enhancers	Gastric	stomach
39	chr9:101585800-101587200	Strong transcription	Primary T cells from cord blood	blood
40	chr9:101585800-101587200	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr9:101586000-101586600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
42	chr9:101586000-101586800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr9:101586000-101586800	ZNF genes & repeats	Fetal Intestine Large	intestine
44	chr9:101586000-101610400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr9:101586200-101586800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:101586200-101586800	ZNF genes & repeats	K562	blood
47	chr9:101586200-101587000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr9:101586200-101588400	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr9:101586400-101587000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr9:101586600-101586800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell

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