Variant report

Variant	nsv615213
Chromosome Location	chr9:115905850-115936903
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:890)
CpG islands
(count:611)
Chromatin interactive
region (count:58)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115905739-115905943	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115913003-115913279	HepG2	liver:	n/a	n/a
3	ATF3	chr9:115913083-115913325	H1-hESC	embryonic stem cell:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
4	ATF3	chr9:115913051-115913311	GM12878	blood:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
5	ATF3	chr9:115913054-115913384	HepG2	liver:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
6	ATF3	chr9:115912933-115913396	GM12878	blood:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
7	ATF3	chr9:115912920-115913440	H1-hESC	embryonic stem cell:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
8	ATF3	chr9:115912959-115913376	K562	blood:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
9	BHLHE40	chr9:115913008-115913338	HepG2	liver:	n/a	n/a
10	BHLHE40	chr9:115913003-115913242	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:115912975-115913573	K562	blood:	n/a	chr9:115913445-115913461
12	BRCA1	chr9:115913056-115913256	GM12878	blood:	n/a	n/a
13	BRCA1	chr9:115913045-115913342	HepG2	liver:	n/a	n/a
14	BRCA1	chr9:115913018-115913389	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr9:115913176-115913376	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr9:115912885-115913315	K562	blood:	n/a	n/a
17	CCNT2	chr9:115912978-115913789	K562	blood:	n/a	chr9:115913503-115913512 chr9:115913670-115913679
18	CEBPB	chr9:115912928-115913110	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:115920925-115921096	K562	blood:	n/a	n/a
20	CEBPB	chr9:115915259-115915400	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:115920838-115921075	A549	lung:	n/a	n/a
22	CEBPB	chr9:115917243-115917493	K562	blood:	n/a	chr9:115917387-115917398
23	CEBPB	chr9:115917227-115917560	HepG2	liver:	n/a	chr9:115917387-115917398
24	CEBPB	chr9:115920873-115921139	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:115917219-115917570	IMR90	lung:	n/a	chr9:115917387-115917398
26	CEBPB	chr9:115905520-115905886	HepG2	liver:	n/a	chr9:115905698-115905709
27	CEBPB	chr9:115927116-115927463	K562	blood:	n/a	n/a
28	CEBPB	chr9:115927047-115927536	IMR90	lung:	n/a	n/a
29	CEBPB	chr9:115905556-115905870	K562	blood:	n/a	chr9:115905698-115905709
30	CEBPB	chr9:115920836-115921093	Hela-S3	cervix:	n/a	n/a
31	CEBPD	chr9:115913159-115913528	HepG2	liver:	n/a	n/a
32	CHD1	chr9:115913352-115913393	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr9:115912971-115913479	H1-hESC	embryonic stem cell:	n/a	chr9:115913126-115913136 chr9:115913219-115913229
34	CHD2	chr9:115912981-115913630	Hela-S3	cervix:	n/a	chr9:115913126-115913136 chr9:115913219-115913229
35	CHD2	chr9:115913005-115913515	GM12878	blood:	n/a	chr9:115913126-115913136 chr9:115913219-115913229
36	CHD2	chr9:115913015-115913443	HepG2	liver:	n/a	chr9:115913126-115913136 chr9:115913219-115913229
37	CHD2	chr9:115911805-115911894	HepG2	liver:	n/a	n/a
38	CHD2	chr9:115919866-115919920	HepG2	liver:	n/a	n/a
39	CHD2	chr9:115913022-115913645	K562	blood:	n/a	chr9:115913126-115913136 chr9:115913219-115913229
40	CREB1	chr9:115912950-115913547	K562	blood:	n/a	n/a
41	CREB1	chr9:115912975-115913445	A549	lung:	n/a	n/a
42	CREB1	chr9:115912892-115913715	HepG2	liver:	n/a	n/a
43	CREB1	chr9:115912942-115913516	GM12878	blood:	n/a	n/a
44	CREB1	chr9:115912975-115913543	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr9:115912871-115913437	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:115911469-115911642	HepG2	liver:	n/a	chr9:115911573-115911582
47	CTCF	chr9:115915133-115915151	GM10248	blood:	n/a	n/a
48	CTCF	chr9:115905740-115905890	HCT-116	colon:	n/a	n/a
49	CTCF	chr9:115913000-115913150	GM12873	blood:	n/a	n/a
50	CTCF	chr9:115919279-115919422	MCF-7	breast:	n/a	chr9:115919331-115919347 chr9:115919332-115919353 chr9:115919330-115919348

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115915001-115915051	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:115915001-115915051	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:115913052-115913102	GM12892	blood:	n/a
4	chr9:115910751-115910801	GM12878	blood:	n/a
5	chr9:115912974-115913024	GM12878	blood:	n/a
6	chr9:115910751-115910801	GM06990	blood:	n/a
7	chr9:115912974-115913024	HMEC	breast:	n/a
8	chr9:115913781-115913831	HepG2	liver:	n/a
9	chr9:115912974-115913024	AG09319	gingival:	n/a
10	chr9:115910751-115910801	NT2-D1	testis:	n/a
11	chr9:115912974-115913024	HRPEpiC	eye:	n/a
12	chr9:115913783-115913833	HEK293	kidney:	embryo
13	chr9:115915892-115915942	HepG2	liver:	n/a
14	chr9:115913515-115913565	HEEpiC	esophagus:	n/a
15	chr9:115913515-115913565	HAEpiC	amniotic membrane:	n/a
16	chr9:115915001-115915051	HCM	heart:	n/a
17	chr9:115913783-115913833	HRPEpiC	eye:	n/a
18	chr9:115912047-115912097	HRE	kidney:	n/a
19	chr9:115913052-115913102	ProgFib	skin:	n/a
20	chr9:115912974-115913024	AG04449	skin:	fetal
21	chr9:115915892-115915942	NHDF-neo	bronchial:	n/a
22	chr9:115913515-115913565	K562	blood:	n/a
23	chr9:115913783-115913833	CMK	blood:	n/a
24	chr9:115912974-115913024	HEK293	kidney:	embryo
25	chr9:115912047-115912097	HEEpiC	esophagus:	n/a
26	chr9:115926922-115926972	SK-N-SH	brain:	n/a
27	chr9:115913781-115913831	NHBE	bronchial:	n/a
28	chr9:115913052-115913102	NB4	blood:	n/a
29	chr9:115915001-115915051	PANC-1	pancreas:	n/a
30	chr9:115915001-115915051	NB4	blood:	n/a
31	chr9:115926922-115926972	GM19239	blood:	n/a
32	chr9:115913781-115913831	PrEC	prostate:	n/a
33	chr9:115913515-115913565	MCF-7	breast:	n/a
34	chr9:115913781-115913831	HAEpiC	amniotic membrane:	n/a
35	chr9:115913781-115913831	AG04449	skin:	fetal
36	chr9:115913052-115913102	U87	brain:	n/a
37	chr9:115913783-115913833	GM12892	blood:	n/a
38	chr9:115913052-115913102	Hela-S3	cervix:	n/a
39	chr9:115913781-115913831	HCM	heart:	n/a
40	chr9:115912974-115913024	AG09309	skin:	n/a
41	chr9:115913052-115913102	AoSMC	blood vessel:	n/a
42	chr9:115910751-115910801	NHBE	bronchial:	n/a
43	chr9:115913783-115913833	HL-60	blood:	n/a
44	chr9:115915001-115915051	SK-N-SH_RA	brain:	n/a
45	chr9:115912974-115913024	AG04450	lung:	fetal
46	chr9:115912974-115913024	SK-N-MC	brain:	n/a
47	chr9:115912974-115913024	IMR90	lung:	fetal
48	chr9:115915892-115915942	HEEpiC	esophagus:	n/a
49	chr9:115915001-115915051	SKMC	muscle:	n/a
50	chr9:115912047-115912097	GM12892	blood:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:115928135..115929979-chr9:115931425..115934458,3	MCF-7	breast:
2	chr9:115872624..115875532-chr9:115912017..115913734,2	MCF-7	breast:
3	chr9:115904166..115905985-chr9:115907508..115909495,2	K562	blood:
4	chr9:115932248..115934923-chr9:115939803..115942130,2	MCF-7	breast:
5	chr9:115913111..115914699-chr9:115915133..115916997,2	K562	blood:
6	chr9:115905644..115908349-chr9:115914691..115916468,2	K562	blood:
7	chr9:115892442..115895400-chr9:115904212..115906056,3	MCF-7	breast:
8	chr9:115929834..115932137-chr9:115938047..115940360,2	MCF-7	breast:
9	chr9:115875175..115875677-chr9:115914252..115914851,2	MCF-7	breast:
10	chr9:115916182..115918262-chr9:115925062..115927268,3	MCF-7	breast:
11	chr9:115916286..115919484-chr9:115921664..115924647,3	K562	blood:
12	chr9:115930657..115933062-chr9:115933610..115935378,2	MCF-7	breast:
13	chr9:115887611..115890231-chr9:115913519..115916345,2	MCF-7	breast:
14	chr9:115875142..115875676-chr9:115912672..115913501,2	MCF-7	breast:
15	chr9:115899892..115901950-chr9:115925051..115926804,2	MCF-7	breast:
16	chr9:115873465..115874103-chr9:115925243..115926162,2	MCF-7	breast:
17	chr2:38145180..38147484-chr9:115926725..115928562,2	MCF-7	breast:
18	chr9:115904438..115911145-chr9:115911174..115916685,7	K562	blood:
19	chr9:115905644..115908349-chr9:115914691..115916468,2	K562	blood:
20	chr9:115924412..115926824-chr9:115928011..115930786,2	MCF-7	breast:
21	chr7:100183524..100184078-chr9:115926719..115927469,2	NB4	blood:
22	chr9:115919736..115921795-chr9:115923893..115926255,3	MCF-7	breast:
23	chr17:59470592..59472862-chr9:115912081..115913641,2	MCF-7	breast:
24	chr9:115912624..115913401-chr9:116037240..116038163,3	K562	blood:
25	chr9:115935268..115937947-chr9:115939386..115941079,2	K562	blood:
26	chr9:115934999..115936781-chr9:115940096..115941741,2	MCF-7	breast:
27	chr9:115913338..115915206-chr9:115920921..115923373,3	K562	blood:
28	chr9:115930029..115932056-chr9:115932264..115933880,2	MCF-7	breast:
29	chr9:115917061..115918640-chr9:115927400..115929607,2	MCF-7	breast:
30	chr9:115916182..115918262-chr9:115925062..115927268,3	MCF-7	breast:
31	chr9:115873156..115875899-chr9:115915858..115921312,4	MCF-7	breast:
32	chr9:115919736..115921795-chr9:115923893..115926255,3	MCF-7	breast:
33	chr9:115930303..115932387-chr9:115934929..115937094,2	K562	blood:
34	chr9:115887976..115889749-chr9:115910119..115911972,2	MCF-7	breast:
35	chr9:115912871..115915332-chr9:115935674..115937488,2	K562	blood:
36	chr9:115930657..115933062-chr9:115933610..115935378,2	MCF-7	breast:
37	chr9:115929480..115931440-chr9:115950780..115952442,2	MCF-7	breast:
38	chr9:115900227..115901850-chr9:115926488..115929015,2	MCF-7	breast:
39	chr9:115913327..115916086-chr9:115970304..115972231,2	MCF-7	breast:
40	chr9:115913631..115915237-chr9:115923889..115925758,2	K562	blood:
41	chr9:115913232..115915242-chr9:115917477..115919096,2	K562	blood:
42	chr9:115930029..115932056-chr9:115932264..115933880,2	MCF-7	breast:
43	chr9:115882894..115884462-chr9:115915677..115917990,2	MCF-7	breast:
44	chr9:115913338..115915206-chr9:115920921..115923373,3	K562	blood:
45	chr9:115904166..115905985-chr9:115907508..115909495,2	K562	blood:
46	chr9:115905880..115908127-chr9:115911738..115913287,2	K562	blood:
47	chr9:115916286..115919484-chr9:115921664..115924647,3	K562	blood:
48	chr9:115935810..115938271-chr9:115941276..115943911,2	K562	blood:
49	chr9:115881515..115883241-chr9:115913395..115914943,2	MCF-7	breast:
50	chr9:115913631..115915237-chr9:115923889..115925758,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKBP15-1	chr9:115923286-115924232	NONHSAT134322
2	lnc-SLC31A1-3	chr9:115925030-115925194	NONHSAT134321
3	lnc-SLC31A1-4	chr9:115913931-115914596	NONHSAT134319
4	lnc-SLC31A1-3	chr9:115920002-115920073	NONHSAT134321
5	lnc-SLC31A1-3	chr9:115923790-115923978	NONHSAT134321
6	lnc-SLC31A1-4	chr9:115913256-115913360	NONHSAT134319

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC31A2	hsa-miR-124-3p	chr9:115925588-115925607
2	SLC31A2	hsa-miR-124-3p	chr9:115925600-115925607
3	FKBP15	hsa-miR-192-5p	chr9:115927845-115927865

Variant related genes	Relation type
SLC31A2	TF binding region
SLC31A2	CpG island
ENSG00000136867	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000106336	chromatin interactions
ENSG00000225684	chromatin interactions
ENSG00000077454	chromatin interactions
ENSG00000136875	chromatin interactions
ENSG00000231528	chromatin interactions
ENSG00000119321	chromatin interactions
ENSG00000176386	chromatin interactions

Extended variants
information (count: 1183 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1183 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12115536	chr9:115905850-115905851	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532374343	chr9:115905875-115905876	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552650712	chr9:115905901-115905902	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs569051588	chr9:115906068-115906069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs151181484	chr9:115906080-115906081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140185005	chr9:115906090-115906091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111355722	chr9:115906125-115906126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536565501	chr9:115906154-115906155	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs553764817	chr9:115906173-115906174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145788286	chr9:115906219-115906220	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs77549041	chr9:115906300-115906301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs539481890	chr9:115906329-115906330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147104653	chr9:115906370-115906371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572939120	chr9:115906408-115906409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181459465	chr9:115906458-115906459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554109746	chr9:115906461-115906462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs4332199	chr9:115906465-115906466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs185898041	chr9:115906561-115906562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372396563	chr9:115906562-115906563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10981646	chr9:115906634-115906635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575208937	chr9:115906640-115906641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143327943	chr9:115906644-115906645	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372475468	chr9:115906645-115906646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149408787	chr9:115906647-115906648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200808790	chr9:115906651-115906652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113872926	chr9:115906666-115906667	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs202191369	chr9:115906674-115906675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376948008	chr9:115906676-115906677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs78434763	chr9:115906677-115906678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs138259931	chr9:115906688-115906689	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs199794592	chr9:115906696-115906697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573905560	chr9:115906751-115906752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560575821	chr9:115906756-115906757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs532832912	chr9:115906777-115906778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138528822	chr9:115906813-115906814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143887369	chr9:115906814-115906815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs12337704	chr9:115906815-115906816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371746990	chr9:115906834-115906835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542138635	chr9:115906875-115906876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183270673	chr9:115906887-115906888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369453237	chr9:115906901-115906902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529805813	chr9:115906913-115906914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs200918006	chr9:115906928-115906929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547860162	chr9:115906930-115906931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546883617	chr9:115906931-115906932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566691819	chr9:115906935-115906936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538918089	chr9:115906939-115906940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148327969	chr9:115906947-115906948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10759625	chr9:115906951-115906952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs150777705	chr9:115906957-115906958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1246 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115899000-115906400	Enhancers	Brain Anterior Caudate	brain
2	chr9:115899000-115913000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:115900600-115913000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:115902800-115912600	Weak transcription	Brain Angular Gyrus	brain
5	chr9:115903400-115906400	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr9:115903400-115912600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr9:115904400-115906400	Enhancers	Brain Substantia Nigra	brain
8	chr9:115904800-115907000	Enhancers	Brain Hippocampus Middle	brain
9	chr9:115905000-115907400	Enhancers	Placenta	Placenta
10	chr9:115905400-115906400	Enhancers	Placenta Amnion	Placenta Amnion
11	chr9:115905400-115906400	Enhancers	HepG2	liver
12	chr9:115905800-115906000	Flanking Active TSS	Brain Cingulate Gyrus	brain
13	chr9:115906000-115906400	Enhancers	Brain Cingulate Gyrus	brain
14	chr9:115906400-115909400	Weak transcription	Brain Substantia Nigra	brain
15	chr9:115906400-115909600	Weak transcription	Brain Anterior Caudate	brain
16	chr9:115906400-115909600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr9:115906400-115909600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr9:115907000-115909600	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:115907400-115909200	Weak transcription	Placenta	Placenta
20	chr9:115909200-115912000	Enhancers	Placenta	Placenta
21	chr9:115909400-115910600	Enhancers	HepG2	liver
22	chr9:115909400-115911000	Enhancers	Brain Substantia Nigra	brain
23	chr9:115909600-115910000	Enhancers	Brain Anterior Caudate	brain
24	chr9:115909600-115910000	Enhancers	Brain Cingulate Gyrus	brain
25	chr9:115909600-115910000	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr9:115909600-115912600	Enhancers	Brain Hippocampus Middle	brain
27	chr9:115910000-115912400	Weak transcription	Brain Anterior Caudate	brain
28	chr9:115910000-115912400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr9:115910000-115912800	Enhancers	Liver	Liver
30	chr9:115910000-115912800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr9:115910600-115911000	Flanking Active TSS	HepG2	liver
32	chr9:115910600-115912800	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr9:115910800-115911000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr9:115911000-115911800	Weak transcription	Brain Substantia Nigra	brain
35	chr9:115911000-115912000	Enhancers	Spleen	Spleen
36	chr9:115911000-115912000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr9:115911000-115912800	Enhancers	HepG2	liver
38	chr9:115911600-115912200	Enhancers	K562	blood
39	chr9:115911800-115912000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr9:115911800-115912800	Enhancers	Brain Substantia Nigra	brain
41	chr9:115912000-115912600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr9:115912000-115912800	Weak transcription	Placenta	Placenta
43	chr9:115912000-115913000	Weak transcription	Spleen	Spleen
44	chr9:115912200-115912600	Weak transcription	K562	blood
45	chr9:115912400-115912600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:115912400-115912600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr9:115912400-115912600	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr9:115912400-115912600	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr9:115912400-115912600	Enhancers	Dnd41	blood
50	chr9:115912400-115912800	Enhancers	Primary B cells from peripheral blood	blood

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