Variant report

Variant	nsv491807
Chromosome Location	chr9:18243672-19009770
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4593)
CpG islands
(count:1221)
Chromatin interactive
region (count:69)
LncRNA
region (count:9)
Mature miRNA
region (count: 2)
miRNA target
sites (count:5)

(count:4593 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:18452384-18452493	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:18669020-18669356	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:18705112-18705234	K562	blood:	n/a	n/a
4	ARID3A	chr9:18456661-18457094	HepG2	liver:	n/a	chr9:18456664-18456680
5	ARID3A	chr9:18622195-18622391	HepG2	liver:	n/a	n/a
6	ATF2	chr9:18379104-18379511	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:18366112-18366540	GM12878	blood:	n/a	n/a
8	ATF2	chr9:18768932-18769740	GM12878	blood:	n/a	n/a
9	ATF2	chr9:18768817-18769760	GM12878	blood:	n/a	n/a
10	ATF3	chr9:18393238-18393764	HCT-116	colon:	n/a	n/a
11	ATF3	chr9:18393270-18393654	HCT-116	colon:	n/a	n/a
12	ATF3	chr9:18393257-18393736	A549	lung:	n/a	n/a
13	BACH1	chr9:18379220-18379436	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:18606813-18606827	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:18821759-18822288	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:18708496-18708726	H1-hESC	embryonic stem cell:	n/a	chr9:18708633-18708647
17	BATF	chr9:18890372-18890733	GM12878	blood:	n/a	chr9:18890552-18890563
18	BATF	chr9:18768943-18769625	GM12878	blood:	n/a	n/a
19	BATF	chr9:18890434-18890714	GM12878	blood:	n/a	chr9:18890552-18890563
20	BATF	chr9:18834825-18835133	GM12878	blood:	n/a	n/a
21	BATF	chr9:18834786-18835105	GM12878	blood:	n/a	n/a
22	BATF	chr9:18768878-18769670	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:18768959-18769211	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:18908260-18908440	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:18768921-18769607	GM12878	blood:	n/a	n/a
26	BCL3	chr9:18887784-18888212	GM12878	blood:	n/a	n/a
27	BCL3	chr9:18887844-18888106	GM12878	blood:	n/a	n/a
28	BCL3	chr9:18393211-18393726	A549	lung:	n/a	n/a
29	BCL3	chr9:18768916-18769623	GM12878	blood:	n/a	n/a
30	BCL3	chr9:18393172-18393686	A549	lung:	n/a	n/a
31	BHLHE40	chr9:18768912-18769756	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:18847612-18847839	HepG2	liver:	n/a	n/a
33	BHLHE40	chr9:18834809-18835097	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:18366277-18366484	GM12878	blood:	n/a	n/a
35	BHLHE40	chr9:18791280-18791295	K562	blood:	n/a	n/a
36	BRCA1	chr9:18574188-18574199	GM12878	blood:	n/a	n/a
37	BRCA1	chr9:18393063-18394411	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr9:18821746-18822028	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr9:18459902-18460682	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr9:18437528-18438248	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr9:18331838-18332335	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr9:18443194-18443410	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr9:18658837-18659489	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr9:18393227-18393748	HCT-116	colon:	n/a	n/a
45	CCNT2	chr9:18404527-18404747	K562	blood:	n/a	n/a
46	CEBPB	chr9:18631140-18631424	IMR90	lung:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
47	CEBPB	chr9:18896500-18896851	HepG2	liver:	n/a	chr9:18896668-18896679
48	CEBPB	chr9:18631227-18631419	K562	blood:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
49	CEBPB	chr9:18756477-18756591	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:18442516-18442940	Hela-S3	cervix:	n/a	chr9:18442652-18442663 chr9:18442654-18442665

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18976715-18976765	AoSMC	blood vessel:	n/a
2	chr9:18976715-18976765	AoSMC	blood vessel:	n/a
3	chr9:18437917-18437967	HRE	kidney:	n/a
4	chr9:18473902-18473952	K562	blood:	n/a
5	chr9:18776340-18776390	HNPCEpiC	eye:	n/a
6	chr9:18825658-18825708	HEK293	kidney:	embryo
7	chr9:18793879-18793929	PFSK-1	brain:	n/a
8	chr9:18706865-18706915	NH-A	brain:	n/a
9	chr9:18770966-18771016	HCT-116	colon:	n/a
10	chr9:18862115-18862165	HCPEpiC	choroid plexus:	n/a
11	chr9:18622331-18622381	HL-60	blood:	n/a
12	chr9:18770966-18771016	SKMC	muscle:	n/a
13	chr9:18622331-18622381	K562	blood:	n/a
14	chr9:18706865-18706915	PFSK-1	brain:	n/a
15	chr9:18605667-18605717	NT2-D1	testis:	n/a
16	chr9:18777555-18777605	ProgFib	skin:	n/a
17	chr9:18706865-18706915	HEK293	kidney:	embryo
18	chr9:18605667-18605717	GM06990	blood:	n/a
19	chr9:18978650-18978700	SAEC	small airway:	n/a
20	chr9:18862115-18862165	T-47D	breast:	n/a
21	chr9:18474243-18474293	T-47D	breast:	n/a
22	chr9:18777555-18777605	Caco-2	colon:	n/a
23	chr9:18727406-18727456	HMEC	breast:	n/a
24	chr9:18770966-18771016	SK-N-MC	brain:	n/a
25	chr9:18474243-18474293	HEEpiC	esophagus:	n/a
26	chr9:18622331-18622381	CMK	blood:	n/a
27	chr9:18793879-18793929	A549	lung:	n/a
28	chr9:18770966-18771016	GM12892	blood:	n/a
29	chr9:18793879-18793929	IMR90	lung:	fetal
30	chr9:18490009-18490059	K562	blood:	n/a
31	chr9:18622331-18622381	AG04449	skin:	fetal
32	chr9:18474243-18474293	SKMC	muscle:	n/a
33	chr9:18474243-18474293	HNPCEpiC	eye:	n/a
34	chr9:18473902-18473952	ECC-1	luminal epithelium:	n/a
35	chr9:18777683-18777733	HEEpiC	esophagus:	n/a
36	chr9:18770966-18771016	Jurkat	blood:	n/a
37	chr9:18793879-18793929	HepG2	liver:	n/a
38	chr9:18909891-18909941	HRPEpiC	eye:	n/a
39	chr9:18474243-18474293	HCT-116	colon:	n/a
40	chr9:18474243-18474293	PrEC	prostate:	n/a
41	chr9:18777683-18777733	A549	lung:	n/a
42	chr9:18437917-18437967	GM12891	blood:	n/a
43	chr9:18976715-18976765	HPAEpiC	pulmonary alveolar:	n/a
44	chr9:18862115-18862165	HAEpiC	amniotic membrane:	n/a
45	chr9:18777683-18777733	Jurkat	blood:	n/a
46	chr9:18770966-18771016	NH-A	brain:	n/a
47	chr9:18862115-18862165	HRCEpiC	kidney:	n/a
48	chr9:18770966-18771016	HRE	kidney:	n/a
49	chr9:18437917-18437967	HCPEpiC	choroid plexus:	n/a
50	chr9:18777683-18777733	MCF10A-Er-Src	breast:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:18975628..18978246-chr9:18981249..18983402,2	K562	blood:
2	chr9:18254775..18255482-chr9:18823832..18824683,3	MCF-7	breast:
3	chr9:18255104..18255666-chr9:18823787..18824360,2	MCF-7	breast:
4	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
5	chr9:18762802..18765724-chr9:18766149..18769161,3	K562	blood:
6	chr9:18906548..18908118-chr9:18909861..18912820,2	K562	blood:
7	chr9:18908849..18913182-chr9:18913314..18916525,3	K562	blood:
8	chr9:18824289..18824965-chr9:19028543..19029149,2	MCF-7	breast:
9	chr9:18769799..18772875-chr9:18776003..18779587,3	K562	blood:
10	chr9:18254776..18255758-chr9:18790832..18791755,3	MCF-7	breast:
11	chr9:18377972..18379506-chr9:18518837..18521140,2	K562	blood:
12	chr9:18745157..18747160-chr9:18747921..18750231,2	MCF-7	breast:
13	chr9:18943902..18945642-chr9:18949010..18951609,3	K562	blood:
14	chr9:18826203..18828034-chr9:18832223..18834749,2	MCF-7	breast:
15	chr9:18254805..18255425-chr9:18442379..18443060,2	MCF-7	breast:
16	chr9:18254776..18255758-chr9:18790832..18791755,3	MCF-7	breast:
17	chr9:18930120..18933009-chr9:19409759..19411895,3	K562	blood:
18	chr2:126575127..126575844-chr9:18665491..18666183,2	MCF-7	breast:
19	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
20	chr9:18943902..18945642-chr9:18949010..18951609,3	K562	blood:
21	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
22	chr9:18377972..18379506-chr9:18518837..18521140,2	K562	blood:
23	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
24	chr9:18254973..18255762-chr9:19028514..19029097,2	MCF-7	breast:
25	chr9:18930120..18932657-chr9:19409759..19411895,2	K562	blood:
26	chr9:18762802..18765724-chr9:18766149..18769161,3	K562	blood:
27	chr9:18552353..18554750-chr9:18819699..18822182,2	MCF-7	breast:
28	chr9:18770497..18772251-chr9:18783540..18785289,2	K562	blood:
29	chr1:149223814..149224438-chr9:18512987..18513487,3	MCF-7	breast:
30	chr9:18552353..18554750-chr9:18819699..18822182,2	MCF-7	breast:
31	chr9:18926118..18927929-chr9:18928691..18930681,2	K562	blood:
32	chr9:18906548..18908118-chr9:18909861..18912820,2	K562	blood:
33	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
34	chr8:61562599..61565494-chr9:18702295..18704681,2	MCF-7	breast:
35	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
36	chr17:59322960..59323509-chr9:18863651..18864333,2	MCF-7	breast:
37	chr9:18733967..18736858-chr9:18739933..18741976,3	MCF-7	breast:
38	chr9:18722180..18723810-chr9:18726997..18728852,2	K562	blood:
39	chr9:18255104..18255666-chr9:18823787..18824360,2	MCF-7	breast:
40	chr10:103812339..103814566-chr9:18385028..18387430,2	MCF-7	breast:
41	chr9:18920619..18922521-chr9:18924227..18925910,2	K562	blood:
42	chr9:18917515..18919753-chr9:18924648..18926162,2	K562	blood:
43	chr9:18255224..18255738-chr9:19028566..19029077,2	K562	blood:
44	chr21:39358274..39359037-chr9:18704805..18705621,2	MCF-7	breast:
45	chr13:100230633..100231487-chr9:18324433..18324983,2	MCF-7	breast:
46	chr9:18926118..18927929-chr9:18928691..18930681,2	K562	blood:
47	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
48	chr9:18254805..18255425-chr9:18442379..18443060,2	MCF-7	breast:
49	chr9:18254620..18255832-chr9:18825877..18827696,5	MCF-7	breast:
50	chr9:18436804..18438586-chr9:18439890..18441991,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM154A-2	chr9:18360595-18360693	XLOC_007653
2	lnc-FAM154A-3	chr9:18717972-18718524	NONHSAT130313
3	lnc-ADAMTSL1-1	chr9:18288533-18288954	NONHSAT130306
4	lnc-FAM154A-2	chr9:18362081-18362218	XLOC_007653
5	lnc-ADAMTSL1-1	chr9:18283558-18283630	NONHSAT130306
6	lnc-RRAGA-3	chr9:18651145-18651448	NONHSAT130312
7	lnc-ADAMTSL1-1	chr9:18290279-18290518	NONHSAT130306
8	lnc-FAM154A-4	chr9:18350595-18350693	NONHSAT130307
9	lnc-FAM154A-4	chr9:18352081-18352218	NONHSAT130307

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3152-3p	chr9:18573348-18573369	MIMAT0015025
hsa-miR-3152-5p	chr9:18573314-18573335	MIMAT0019207

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ADAMTSL1	hsa-miR-25-3p	chr9:18681336-18681357
2	ADAMTSL1	hsa-miR-25-3p	chr9:18681248-18681269
3	ADAMTSL1	hsa-miR-132-3p	chr9:18684803-18684824
4	ADAMTSL1	hsa-miR-25-3p	chr9:18910328-18910349
5	ADAMTSL1	hsa-miR-25-3p	chr9:18910342-18910349

Variant related genes	Relation type
RN7SKP258	TF binding region
ADAMTSL1	TF binding region
MIR3152	TF binding region
ENSG00000227167	TF binding region
ENSG00000223211	TF binding region
ENSG00000236857	TF binding region
RN7SKP258	CpG island
ADAMTSL1	CpG island
MIR3152	CpG island
ENSG00000227167	CpG island
ENSG00000223211	CpG island
ENSG00000236857	CpG island
ENSG00000206737	chromatin interactions
ENSG00000178031	chromatin interactions
CPPED1	miRNA target sites
CRAMP1L	miRNA target sites

Extended variants
information (count: 34742 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:34742 , 50 per page) page: 1 2 3 4 5 6 7 ... 695

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573488554	chr9:18243679-18243680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10963534	chr9:18243696-18243697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs180947805	chr9:18243765-18243766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540390210	chr9:18243767-18243768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534405668	chr9:18243774-18243775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560466907	chr9:18243796-18243797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34583454	chr9:18243841-18243842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573537827	chr9:18243850-18243851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574534747	chr9:18243869-18243870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544158547	chr9:18243881-18243882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114963685	chr9:18243898-18243899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12335943	chr9:18243905-18243906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533206197	chr9:18243910-18243911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554690788	chr9:18243941-18243942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186298447	chr9:18243951-18243952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113904152	chr9:18243955-18243956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189627292	chr9:18243983-18243984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11788211	chr9:18244002-18244003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs79762362	chr9:18244019-18244020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367627837	chr9:18244021-18244022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs202059598	chr9:18244086-18244087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs5896778	chr9:18244097-18244098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397755814	chr9:18244107-18244108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377563238	chr9:18244108-18244109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370199055	chr9:18244109-18244110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374449777	chr9:18244110-18244111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201157126	chr9:18244111-18244112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs202182082	chr9:18244112-18244113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546668309	chr9:18244121-18244122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs5896779	chr9:18244122-18244123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34712376	chr9:18244126-18244127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568574559	chr9:18244134-18244135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535592481	chr9:18244140-18244141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540264012	chr9:18244142-18244143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550926146	chr9:18244208-18244209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114069577	chr9:18244268-18244269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540086636	chr9:18244269-18244270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558531517	chr9:18244318-18244319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567046523	chr9:18244352-18244353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534427285	chr9:18244395-18244396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556008564	chr9:18244431-18244432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573649702	chr9:18244455-18244456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146255075	chr9:18244466-18244467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181819132	chr9:18244483-18244484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577606122	chr9:18244515-18244516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544898342	chr9:18244528-18244529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560044402	chr9:18244569-18244570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186284504	chr9:18244584-18244585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542381246	chr9:18244624-18244625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567859901	chr9:18244629-18244630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Ovarian cancer	19835627	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Chordoma	21215367	CNVD
Autism	20841430	CNVD
Medullary thyroid carcinoma	18765511	CNVD

Chromatin state (count:6651 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18225800-18260600	Weak transcription	Aorta	Aorta
2	chr9:18245000-18245600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:18245400-18247000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:18250000-18250600	Enhancers	Osteobl	bone
5	chr9:18250200-18250600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:18250200-18250600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:18250200-18250600	Enhancers	Fetal Heart	heart
8	chr9:18250200-18250600	Enhancers	NH-A	brain
9	chr9:18250200-18250800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:18250200-18250800	Enhancers	NHDF-Ad	bronchial
11	chr9:18250400-18250800	Enhancers	NHEK	skin
12	chr9:18250600-18255400	Weak transcription	Fetal Heart	heart
13	chr9:18250600-18255400	Weak transcription	Osteobl	bone
14	chr9:18250600-18255800	Weak transcription	NH-A	brain
15	chr9:18250800-18255400	Weak transcription	NHDF-Ad	bronchial
16	chr9:18250800-18255600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:18255000-18255200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr9:18255200-18255400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
19	chr9:18255200-18255600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:18255200-18255600	Enhancers	Brain Hippocampus Middle	brain
21	chr9:18255200-18256000	Enhancers	Fetal Stomach	stomach
22	chr9:18255200-18256400	Enhancers	Fetal Kidney	kidney
23	chr9:18255200-18256600	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr9:18255200-18260400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr9:18255400-18255600	Enhancers	Fetal Brain Male	brain
26	chr9:18255400-18256000	Enhancers	Muscle Satellite Cultured Cells	--
27	chr9:18255400-18256000	Enhancers	HUVEC	blood vessel
28	chr9:18255400-18256200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr9:18255400-18256200	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr9:18255400-18256600	Enhancers	Colon Smooth Muscle	Colon
31	chr9:18255400-18256600	Enhancers	NHLF	lung
32	chr9:18255400-18256800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:18255400-18256800	Enhancers	Fetal Heart	heart
34	chr9:18255400-18256800	Enhancers	Osteobl	bone
35	chr9:18255400-18257000	Enhancers	NHDF-Ad	bronchial
36	chr9:18255600-18256000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr9:18255600-18256000	Enhancers	Fetal Thymus	thymus
38	chr9:18255600-18256800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr9:18255600-18257000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:18255600-18260000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:18255800-18256200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:18255800-18256400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr9:18255800-18256600	Enhancers	NH-A	brain
44	chr9:18256000-18256400	Enhancers	Lung	lung
45	chr9:18256000-18260400	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr9:18256000-18260400	Weak transcription	Fetal Stomach	stomach
47	chr9:18256200-18256600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr9:18256200-18256600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr9:18256200-18256800	Enhancers	Fetal Lung	lung
50	chr9:18256200-18256800	Enhancers	Right Atrium	heart

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