Variant report

Variant	nsv1051731
Chromosome Location	chr9:98154815-98201115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:918)
CpG islands
(count:61)
Chromatin interactive
region (count:99)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:918 , 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	chr9:98179585-98179652	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:98172142-98172572	K562	blood:	n/a	n/a
3	ARID3A	chr9:98188935-98189067	K562	blood:	n/a	n/a
4	ARID3A	chr9:98197027-98197901	K562	blood:	n/a	n/a
5	ARID3A	chr9:98189197-98189232	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:98196428-98196812	K562	blood:	n/a	n/a
7	ATF1	chr9:98196461-98197544	K562	blood:	n/a	n/a
8	ATF1	chr9:98173937-98174262	K562	blood:	n/a	n/a
9	ATF1	chr9:98172271-98172575	K562	blood:	n/a	n/a
10	ATF2	chr9:98189088-98189467	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr9:98196421-98196831	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr9:98172168-98172633	K562	blood:	n/a	n/a
13	ATF3	chr9:98172134-98172799	HCT-116	colon:	n/a	n/a
14	BACH1	chr9:98172285-98172530	H1-hESC	embryonic stem cell:	n/a	chr9:98172410-98172424
15	BACH1	chr9:98196479-98196925	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:98196487-98197214	K562	blood:	n/a	n/a
17	BATF	chr9:98189698-98189964	GM12878	blood:	n/a	n/a
18	BATF	chr9:98189652-98190008	GM12878	blood:	n/a	n/a
19	BCL3	chr9:98188561-98189508	A549	lung:	n/a	n/a
20	BCLAF1	chr9:98188940-98189514	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:98173765-98174268	K562	blood:	n/a	n/a
22	BHLHE40	chr9:98189121-98189488	A549	lung:	n/a	n/a
23	BHLHE40	chr9:98188530-98189598	K562	blood:	n/a	n/a
24	BHLHE40	chr9:98161467-98161541	K562	blood:	n/a	n/a
25	BHLHE40	chr9:98196468-98197755	K562	blood:	n/a	n/a
26	BHLHE40	chr9:98192263-98192617	HepG2	liver:	n/a	n/a
27	BHLHE40	chr9:98188909-98189492	HepG2	liver:	n/a	n/a
28	BHLHE40	chr9:98188988-98189344	GM12878	blood:	n/a	n/a
29	BRCA1	chr9:98188855-98189387	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr9:98184909-98185257	K562	blood:	n/a	n/a
31	CBX3	chr9:98196328-98197371	K562	blood:	n/a	n/a
32	CBX3	chr9:98192442-98192998	K562	blood:	n/a	n/a
33	CBX3	chr9:98189125-98189542	K562	blood:	n/a	n/a
34	CBX3	chr9:98192532-98192911	K562	blood:	n/a	n/a
35	CBX3	chr9:98173783-98174354	K562	blood:	n/a	n/a
36	CBX3	chr9:98184921-98185341	K562	blood:	n/a	n/a
37	CBX3	chr9:98188729-98189770	HCT-116	colon:	n/a	n/a
38	CBX3	chr9:98188867-98189694	HCT-116	colon:	n/a	n/a
39	CBX3	chr9:98184863-98185356	HCT-116	colon:	n/a	n/a
40	CBX3	chr9:98196315-98197072	HCT-116	colon:	n/a	n/a
41	CBX3	chr9:98188870-98189580	K562	blood:	n/a	n/a
42	CBX3	chr9:98196473-98196807	K562	blood:	n/a	n/a
43	CCNT2	chr9:98173898-98174261	K562	blood:	n/a	n/a
44	CCNT2	chr9:98188856-98189479	K562	blood:	n/a	n/a
45	CCNT2	chr9:98196467-98197541	K562	blood:	n/a	n/a
46	CEBPB	chr9:98199868-98200224	K562	blood:	n/a	n/a
47	CEBPB	chr9:98188971-98189649	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:98188868-98189027	K562	blood:	n/a	n/a
49	CEBPB	chr9:98189613-98189685	A549	lung:	n/a	n/a
50	CEBPB	chr9:98172257-98172614	MCF-7	breast:	n/a	chr9:98172446-98172457 chr9:98172400-98172413 chr9:98172401-98172412

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:98173099-98173149	K562	blood:	n/a
2	chr9:98173099-98173149	NHDF-neo	bronchial:	n/a
3	chr9:98173099-98173149	HUVEC	blood vessel:	n/a
4	chr9:98173099-98173149	HAEpiC	amniotic membrane:	n/a
5	chr9:98173099-98173149	LNCaP	prostate:	n/a
6	chr9:98173099-98173149	U87	brain:	n/a
7	chr9:98173099-98173149	SK-N-MC	brain:	n/a
8	chr9:98173099-98173149	ProgFib	skin:	n/a
9	chr9:98173099-98173149	HepG2	liver:	n/a
10	chr9:98173099-98173149	HPAEpiC	pulmonary alveolar:	n/a
11	chr9:98173099-98173149	CMK	blood:	n/a
12	chr9:98173099-98173149	BJ	skin:	n/a
13	chr9:98173099-98173149	AG10803	skin:	n/a
14	chr9:98173099-98173149	SAEC	small airway:	n/a
15	chr9:98173099-98173149	SK-N-SH_RA	brain:	n/a
16	chr9:98173099-98173149	GM12878	blood:	n/a
17	chr9:98173099-98173149	HRPEpiC	eye:	n/a
18	chr9:98173099-98173149	HCPEpiC	choroid plexus:	n/a
19	chr9:98173099-98173149	NT2-D1	testis:	n/a
20	chr9:98173099-98173149	NH-A	brain:	n/a
21	chr9:98173099-98173149	AG09309	skin:	n/a
22	chr9:98173099-98173149	HMEC	breast:	n/a
23	chr9:98173099-98173149	HEK293	kidney:	embryo
24	chr9:98173099-98173149	H1-hESC	embryonic stem cell:	embryo
25	chr9:98173099-98173149	HIPEpiC	eye:	n/a
26	chr9:98173099-98173149	AG04450	lung:	fetal
27	chr9:98173099-98173149	AG04449	skin:	fetal
28	chr9:98173099-98173149	Jurkat	blood:	n/a
29	chr9:98173099-98173149	HCT-116	colon:	n/a
30	chr9:98173099-98173149	HNPCEpiC	eye:	n/a
31	chr9:98173099-98173149	PANC-1	pancreas:	n/a
32	chr9:98173099-98173149	PrEC	prostate:	n/a
33	chr9:98173099-98173149	NB4	blood:	n/a
34	chr9:98173099-98173149	AG09319	gingival:	n/a
35	chr9:98173099-98173149	HCM	heart:	n/a
36	chr9:98173099-98173149	ovcar-3	ovarian:	n/a
37	chr9:98173099-98173149	Hela-S3	cervix:	n/a
38	chr9:98173099-98173149	A549	lung:	n/a
39	chr9:98173099-98173149	PFSK-1	brain:	n/a
40	chr9:98173099-98173149	GM06990	blood:	n/a
41	chr9:98173099-98173149	NHBE	bronchial:	n/a
42	chr9:98173099-98173149	HCF	heart:	n/a
43	chr9:98173099-98173149	MCF-7	breast:	n/a
44	chr9:98173099-98173149	Caco-2	colon:	n/a
45	chr9:98173099-98173149	BE2_C	brain:	n/a
46	chr9:98173099-98173149	ECC-1	luminal epithelium:	n/a
47	chr9:98173099-98173149	GM19239	blood:	n/a
48	chr9:98173099-98173149	IMR90	lung:	fetal
49	chr9:98173099-98173149	GM12892	blood:	n/a
50	chr9:98173099-98173149	SKMC	muscle:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:98187946..98190669-chr9:98199281..98201947,3	MCF-7	breast:
2	chr9:98176993..98179487-chr9:98191596..98193512,2	MCF-7	breast:
3	chr9:98198490..98200651-chr9:98245045..98247507,2	K562	blood:
4	chr9:98194162..98198925-chr9:98199539..98203355,6	K562	blood:
5	chr9:98187259..98193172-chr9:98208629..98217669,12	MCF-7	breast:
6	chr9:98182926..98184668-chr9:98252213..98254652,2	K562	blood:
7	chr9:98179149..98181138-chr9:98267525..98270206,2	K562	blood:
8	chr9:98144872..98147433-chr9:98200358..98201911,2	K562	blood:
9	chr9:98172180..98174810-chr9:98179006..98181290,3	MCF-7	breast:
10	chr9:98188670..98189479-chr9:98637800..98638512,2	Hela-S3	cervix:
11	chr9:98199109..98200665-chr9:98217953..98219861,2	K562	blood:
12	chr9:98186276..98191956-chr9:98269234..98276633,9	K562	blood:
13	chr9:98079206..98081701-chr9:98186785..98188899,2	K562	blood:
14	chr9:98172380..98174560-chr9:98273339..98275804,2	K562	blood:
15	chr9:98184189..98187188-chr9:98271024..98273730,2	K562	blood:
16	chr9:98188569..98190136-chr9:98266994..98268557,2	MCF-7	breast:
17	chr9:98193214..98197304-chr9:98277800..98280363,5	K562	blood:
18	chr9:98078552..98082181-chr9:98188850..98192317,4	MCF-7	breast:
19	chr9:98169863..98171382-chr9:98172486..98174897,2	K562	blood:
20	chr12:52445014..52445648-chr9:98188994..98189705,2	Hela-S3	cervix:
21	chr9:98171854..98174072-chr9:98176315..98178311,2	MCF-7	breast:
22	chr9:98176993..98179487-chr9:98191596..98193512,2	MCF-7	breast:
23	chr9:98187644..98190286-chr9:98266151..98268622,2	K562	blood:
24	chr9:98173730..98177988-chr9:98187520..98191004,5	K562	blood:
25	chr9:98162269..98164911-chr9:98170422..98173133,2	K562	blood:
26	chr9:98172180..98174810-chr9:98179006..98181290,3	MCF-7	breast:
27	chr9:98180365..98181885-chr9:98188558..98190074,2	K562	blood:
28	chr9:98195063..98197090-chr9:98200998..98203192,2	K562	blood:
29	chr9:98173730..98177988-chr9:98187520..98191004,5	K562	blood:
30	chr9:98170943..98174116-chr9:98263782..98265821,3	K562	blood:
31	chr9:98195217..98198103-chr9:98267041..98269977,4	K562	blood:
32	chr9:98170943..98172976-chr9:98263782..98265543,2	K562	blood:
33	chr9:98167871..98172268-chr9:98186784..98190412,5	MCF-7	breast:
34	chr9:98175278..98177936-chr9:98179160..98180755,2	K562	blood:
35	chr9:98172552..98175777-chr9:98180826..98183716,4	K562	blood:
36	chr9:98184923..98187907-chr9:98195296..98197240,2	K562	blood:
37	chr9:98170885..98173194-chr9:98189275..98191495,2	K562	blood:
38	chr9:98195063..98197090-chr9:98200998..98203192,2	K562	blood:
39	chr9:98162269..98164911-chr9:98170422..98173133,2	K562	blood:
40	chr9:98199420..98202939-chr9:98265831..98269665,3	MCF-7	breast:
41	chr9:98167948..98170232-chr9:98170329..98172486,2	K562	blood:
42	chr9:98155426..98158383-chr9:98173646..98175890,2	MCF-7	breast:
43	chr9:98200946..98203462-chr9:98205677..98208531,4	K562	blood:
44	chr4:84456903..84457679-chr9:98188999..98189686,2	HCT-116	colon:
45	chr9:98077890..98080706-chr9:98186785..98188874,2	K562	blood:
46	chr9:98171235..98175849-chr9:98186797..98190089,10	MCF-7	breast:
47	chr9:98197131..98198876-chr9:98214885..98216623,2	K562	blood:
48	chr9:98194162..98198925-chr9:98199539..98203355,6	K562	blood:
49	chr9:98174229..98176138-chr9:98194675..98196475,2	K562	blood:
50	chr9:98178048..98179712-chr9:98187198..98189751,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf3-5	chr9:98159485-98159579	NONHSAT133364
2	lnc-PTCH1-5	chr9:98169272-98169944	ENSG00000271384.1
3	lnc-C9orf3-5	chr9:98153011-98158004	NONHSAT133364
4	lnc-PTCH1-1	chr9:98189006-98189163	NONHSAT133367
5	lnc-PTCH1-1	chr9:98173738-98173970	NONHSAT133365
6	lnc-PTCH1-1	chr9:98170781-98173959	NONHSAT133367
7	lnc-C9orf3-5	chr9:98158699-98158743	NONHSAT133364
8	lnc-PTCH1-1	chr9:98159446-98159565	NONHSAT133365

No data

Variant related genes	Relation type
MT1P1	TF binding region
ENSG00000237857	TF binding region
ENSG00000271384	TF binding region
MT1P1	CpG island
ENSG00000237857	CpG island
ENSG00000271384	CpG island
ENSG00000138678	chromatin interactions
ENSG00000137203	chromatin interactions
ENSG00000185267	chromatin interactions
ENSG00000187522	chromatin interactions
ENSG00000271659	chromatin interactions
ENSG00000185920	chromatin interactions
ENSG00000213761	chromatin interactions
ENSG00000271155	chromatin interactions
ENSG00000175611	chromatin interactions
ENSG00000146143	chromatin interactions
ENSG00000182150	chromatin interactions
ENSG00000158169	chromatin interactions
ENSG00000271384	chromatin interactions
ENSG00000237857	chromatin interactions
ENSG00000123358	chromatin interactions

Extended variants
information (count: 1724 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1724 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs419574	chr9:98154815-98154816	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145198520	chr9:98154817-98154818	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs141181658	chr9:98154835-98154836	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs143717006	chr9:98154869-98154870	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs376410579	chr9:98154903-98154904	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs370830955	chr9:98154919-98154920	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs78989693	chr9:98154921-98154922	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs533811865	chr9:98154924-98154925	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs570767875	chr9:98154945-98154946	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs555683551	chr9:98154985-98154986	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs375054802	chr9:98154999-98155000	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs115455446	chr9:98155010-98155011	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs146809567	chr9:98155029-98155030	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs562555277	chr9:98155038-98155039	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs11792812	chr9:98155056-98155057	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs575650900	chr9:98155064-98155065	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs531780666	chr9:98155110-98155111	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs10993534	chr9:98155124-98155125	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs544427380	chr9:98155141-98155142	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs564285033	chr9:98155147-98155148	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs75269234	chr9:98155195-98155196	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs568803474	chr9:98155229-98155230	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs187187855	chr9:98155231-98155232	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs546627235	chr9:98155265-98155266	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs191685794	chr9:98155322-98155323	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs539322480	chr9:98155338-98155339	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs183853823	chr9:98155352-98155353	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs554004016	chr9:98155402-98155403	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs141045819	chr9:98155409-98155410	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs551120255	chr9:98155419-98155420	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs375019799	chr9:98155426-98155427	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs539493151	chr9:98155453-98155454	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs551499534	chr9:98155565-98155566	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs566605010	chr9:98155656-98155657	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs189395658	chr9:98155697-98155698	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs111461668	chr9:98155706-98155707	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs148285398	chr9:98155709-98155710	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs555088728	chr9:98155744-98155745	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs140395450	chr9:98155750-98155751	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs77483457	chr9:98155769-98155770	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs573715186	chr9:98155774-98155775	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs577756402	chr9:98155794-98155795	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs74426229	chr9:98155800-98155801	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs77141263	chr9:98155831-98155832	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs562527135	chr9:98155837-98155838	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs376222951	chr9:98155843-98155844	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs150365967	chr9:98155861-98155862	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs12348774	chr9:98155862-98155863	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs554091748	chr9:98155943-98155944	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs566513022	chr9:98155945-98155946	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98144000-98172400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:98146600-98168400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr9:98150600-98173600	Weak transcription	Fetal Intestine Small	intestine
4	chr9:98152400-98161600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:98160400-98188400	Weak transcription	Pancreas	Pancrea
6	chr9:98161200-98162200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr9:98161400-98162000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:98161400-98162000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr9:98161400-98162000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:98161400-98162000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:98161400-98162000	Enhancers	Adipose Nuclei	Adipose
12	chr9:98161400-98162000	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr9:98161400-98162000	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr9:98161400-98162200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:98161400-98162200	Enhancers	Fetal Muscle Leg	muscle
16	chr9:98161600-98161800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr9:98161600-98162000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:98161600-98162000	Enhancers	Fetal Muscle Trunk	muscle
19	chr9:98161600-98162200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:98161600-98162200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr9:98161600-98162200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:98161800-98172200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr9:98162200-98163600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:98166600-98169400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:98167800-98169600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr9:98168000-98168400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr9:98168000-98170000	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr9:98168200-98168400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:98168200-98168800	Enhancers	Adipose Nuclei	Adipose
30	chr9:98168200-98168800	Enhancers	Hela-S3	cervix
31	chr9:98168200-98169800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr9:98168200-98169800	Enhancers	Fetal Lung	lung
33	chr9:98168200-98170000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr9:98168400-98168600	Enhancers	A549	lung
35	chr9:98168400-98169000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr9:98168400-98169000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr9:98168400-98169600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:98168400-98169800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:98168400-98169800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr9:98168400-98170000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr9:98168400-98170400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr9:98168600-98169800	Enhancers	Brain Germinal Matrix	brain
43	chr9:98168600-98172200	Weak transcription	A549	lung
44	chr9:98168800-98171600	Weak transcription	Hela-S3	cervix
45	chr9:98169000-98169200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr9:98169000-98169800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr9:98169000-98172400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr9:98169200-98169600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:98169200-98171200	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr9:98169400-98169600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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