Variant report

Variant	nsv894113
Chromosome Location	chr9:136538798-136586367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:729)
CpG islands
(count:1041)
Chromatin interactive
region (count:64)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:136579985-136580313	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:136563925-136564017	K562	blood:	n/a	n/a
3	ARID3A	chr9:136581322-136581601	HepG2	liver:	n/a	n/a
4	ATF2	chr9:136574386-136574739	GM12878	blood:	n/a	n/a
5	BACH1	chr9:136580868-136581317	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:136557810-136558010	K562	blood:	n/a	chr9:136557867-136557888 chr9:136557872-136557881 chr9:136557871-136557884
7	BRCA1	chr9:136581078-136581211	HepG2	liver:	n/a	n/a
8	CEBPB	chr9:136572235-136572251	A549	lung:	n/a	n/a
9	CEBPB	chr9:136551248-136551498	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:136561795-136562031	IMR90	lung:	n/a	n/a
11	CEBPB	chr9:136579965-136580217	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:136579934-136580364	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:136551247-136551530	K562	blood:	n/a	n/a
14	CEBPB	chr9:136551294-136551490	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr9:136551217-136551457	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:136579836-136580275	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:136572038-136572467	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:136579928-136580332	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:136564648-136564840	HepG2	liver:	n/a	chr9:136564797-136564808
20	CEBPB	chr9:136579921-136580319	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:136572141-136572280	HepG2	liver:	n/a	n/a
22	CEBPD	chr9:136578521-136578790	HepG2	liver:	n/a	n/a
23	CEBPD	chr9:136579918-136580181	HepG2	liver:	n/a	n/a
24	CEBPD	chr9:136581418-136581795	HepG2	liver:	n/a	n/a
25	CEBPD	chr9:136579997-136580284	HepG2	liver:	n/a	n/a
26	CHD2	chr9:136580056-136580345	HepG2	liver:	n/a	n/a
27	CTCF	chr9:136580968-136581277	MCF-7	breast:	n/a	n/a
28	CTCF	chr9:136549060-136549210	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr9:136580964-136581459	MCF-7	breast:	n/a	chr9:136580967-136580985
30	CTCF	chr9:136581040-136581190	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr9:136581000-136581150	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr9:136580911-136581220	HepG2	liver:	n/a	chr9:136580967-136580985
33	CTCF	chr9:136578970-136579104	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:136545400-136545550	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr9:136545466-136545544	K562	blood:	n/a	n/a
36	CTCF	chr9:136576680-136576830	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr9:136574361-136574447	A549	lung:	n/a	n/a
38	CTCF	chr9:136580980-136581130	GM12874	blood:	n/a	n/a
39	CTCF	chr9:136581060-136581210	HCT-116	colon:	n/a	n/a
40	CTCF	chr9:136581040-136581190	GM12875	blood:	n/a	n/a
41	CTCF	chr9:136581020-136581170	RPTEC	kidney:	n/a	n/a
42	CTCF	chr9:136549100-136549370	HCM	heart:	n/a	chr9:136549198-136549211
43	CTCF	chr9:136549020-136549170	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr9:136580980-136581130	GM12865	blood:	n/a	n/a
45	CTCF	chr9:136581020-136581170	GM12872	blood:	n/a	n/a
46	CTCF	chr9:136581020-136581170	NHEK	skin:	n/a	n/a
47	CTCF	chr9:136549120-136549270	BJ	skin:	n/a	chr9:136549198-136549211
48	CTCF	chr9:136580989-136581242	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr9:136578920-136579070	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr9:136581032-136581183	GM13976	blood:	n/a	n/a

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136567339-136567389	HNPCEpiC	eye:	n/a
2	chr9:136567739-136567789	AG09309	skin:	n/a
3	chr9:136567064-136567114	HCPEpiC	choroid plexus:	n/a
4	chr9:136539392-136539442	AG04449	skin:	fetal
5	chr9:136567339-136567389	HNPCEpiC	eye:	n/a
6	chr9:136567739-136567789	AG09309	skin:	n/a
7	chr9:136567064-136567114	HCPEpiC	choroid plexus:	n/a
8	chr9:136539392-136539442	AG04449	skin:	fetal
9	chr9:136547862-136547912	NT2-D1	testis:	n/a
10	chr9:136545056-136545106	PrEC	prostate:	n/a
11	chr9:136547862-136547912	HL-60	blood:	n/a
12	chr9:136556337-136556387	AoSMC	blood vessel:	n/a
13	chr9:136567339-136567389	PFSK-1	brain:	n/a
14	chr9:136566991-136567041	NB4	blood:	n/a
15	chr9:136539392-136539442	HIPEpiC	eye:	n/a
16	chr9:136565608-136565658	AG04449	skin:	fetal
17	chr9:136562840-136562890	HIPEpiC	eye:	n/a
18	chr9:136569664-136569714	LNCaP	prostate:	n/a
19	chr9:136556337-136556387	IMR90	lung:	fetal
20	chr9:136539392-136539442	H1-hESC	embryonic stem cell:	embryo
21	chr9:136567739-136567789	HL-60	blood:	n/a
22	chr9:136569664-136569714	SK-N-MC	brain:	n/a
23	chr9:136573518-136573568	PrEC	prostate:	n/a
24	chr9:136567064-136567114	GM12891	blood:	n/a
25	chr9:136567064-136567114	HepG2	liver:	n/a
26	chr9:136567739-136567789	A549	lung:	n/a
27	chr9:136545056-136545106	PFSK-1	brain:	n/a
28	chr9:136581211-136581261	SK-N-SH_RA	brain:	n/a
29	chr9:136547862-136547912	HCT-116	colon:	n/a
30	chr9:136567064-136567114	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:136573518-136573568	HEEpiC	esophagus:	n/a
32	chr9:136562840-136562890	NB4	blood:	n/a
33	chr9:136567739-136567789	ProgFib	skin:	n/a
34	chr9:136565608-136565658	ProgFib	skin:	n/a
35	chr9:136565608-136565658	AG10803	skin:	n/a
36	chr9:136562840-136562890	HCF	heart:	n/a
37	chr9:136567064-136567114	BJ	skin:	n/a
38	chr9:136567339-136567389	AG04449	skin:	fetal
39	chr9:136567739-136567789	HepG2	liver:	n/a
40	chr9:136567739-136567789	AG09319	gingival:	n/a
41	chr9:136569664-136569714	GM19239	blood:	n/a
42	chr9:136567064-136567114	NHBE	bronchial:	n/a
43	chr9:136573518-136573568	HCM	heart:	n/a
44	chr9:136567064-136567114	AoSMC	blood vessel:	n/a
45	chr9:136581211-136581261	HRPEpiC	eye:	n/a
46	chr9:136556337-136556387	SKMC	muscle:	n/a
47	chr9:136565608-136565658	HNPCEpiC	eye:	n/a
48	chr9:136573518-136573568	HIPEpiC	eye:	n/a
49	chr9:136581211-136581261	AoSMC	blood vessel:	n/a
50	chr9:136562840-136562890	CMK	blood:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:136566342..136568091-chr9:136574335..136575910,2	K562	blood:
2	chr9:136536158..136538637-chr9:136540445..136542494,2	K562	blood:
3	chr9:136398236..136398863-chr9:136573868..136574473,2	MCF-7	breast:
4	chr9:136558023..136560608-chr9:136564719..136567845,3	MCF-7	breast:
5	chr9:136575619..136578440-chr9:136578792..136581710,2	K562	blood:
6	chr9:136397639..136398833-chr9:136580643..136581791,10	MCF-7	breast:
7	chr9:136562168..136564427-chr9:136565551..136567295,2	K562	blood:
8	chr9:136533491..136538951-chr9:136540367..136544630,5	MCF-7	breast:
9	chr9:136457926..136458783-chr9:136580652..136581261,2	MCF-7	breast:
10	chr9:136562168..136564427-chr9:136565551..136567295,2	K562	blood:
11	chr9:136213643..136215369-chr9:136571224..136574187,2	MCF-7	breast:
12	chr9:136556867..136559389-chr9:136579580..136582803,3	MCF-7	breast:
13	chr9:136556867..136559389-chr9:136579580..136582803,3	MCF-7	breast:
14	chr9:136530487..136533087-chr9:136574041..136576943,2	MCF-7	breast:
15	chr9:136571721..136574254-chr9:136575200..136579195,4	K562	blood:
16	chr9:136558023..136560608-chr9:136564719..136567845,3	MCF-7	breast:
17	chr22:50714348..50715426-chr9:136539069..136540069,7	MCF-7	breast:
18	chr9:136551308..136553495-chr9:136555046..136558031,3	MCF-7	breast:
19	chr9:136541535..136543901-chr9:136557001..136558944,2	K562	blood:
20	chr9:136553976..136556938-chr9:136571128..136573086,2	MCF-7	breast:
21	chr9:136571721..136574254-chr9:136575200..136579195,4	K562	blood:
22	chr9:136547609..136549609-chr9:136554134..136556211,2	MCF-7	breast:
23	chr9:136582872..136585372-chr9:136587573..136590477,2	MCF-7	breast:
24	chr9:136545056..136547450-chr9:136550910..136552726,2	K562	blood:
25	chr9:136541535..136544211-chr9:136557001..136558713,2	K562	blood:
26	chr9:136396895..136399641-chr9:136573286..136575991,2	K562	blood:
27	chr9:136531219..136533253-chr9:136536385..136539171,2	K562	blood:
28	chr9:136547327..136548989-chr9:136894094..136896056,2	MCF-7	breast:
29	chr9:136573704..136576391-chr9:136578401..136581568,3	MCF-7	breast:
30	chr9:136569675..136574254-chr9:136574982..136578726,4	K562	blood:
31	chr9:136551308..136553495-chr9:136555046..136558031,3	MCF-7	breast:
32	chr9:136397924..136398838-chr9:136580700..136581803,6	MCF-7	breast:
33	chr9:136562276..136565149-chr9:136581460..136583950,2	MCF-7	breast:
34	chr9:136584513..136587440-chr9:136590928..136593741,2	K562	blood:
35	chr9:136401564..136404417-chr9:136570647..136572781,2	K562	blood:
36	chr9:136541535..136543901-chr9:136557001..136558944,2	K562	blood:
37	chr9:136562276..136565149-chr9:136581460..136583950,2	MCF-7	breast:
38	chr9:136566342..136568091-chr9:136574335..136575910,2	K562	blood:
39	chr9:136546579..136549426-chr9:136551457..136554920,3	K562	blood:
40	chr9:136547609..136549609-chr9:136554134..136556211,2	MCF-7	breast:
41	chr9:136454458..136455161-chr9:136580969..136581838,2	MCF-7	breast:
42	chr9:136531862..136534344-chr9:136553283..136554796,2	K562	blood:
43	chr9:136510698..136512936-chr9:136554635..136557267,2	MCF-7	breast:
44	chr9:136533491..136538951-chr9:136540367..136544630,5	MCF-7	breast:
45	chr9:136560902..136563128-chr9:136576018..136578776,2	MCF-7	breast:
46	chr9:136420115..136422179-chr9:136562100..136563900,2	MCF-7	breast:
47	chr9:136553976..136556938-chr9:136571128..136573086,2	MCF-7	breast:
48	chr9:136573704..136576391-chr9:136578401..136581568,3	MCF-7	breast:
49	chr9:136556489..136558847-chr9:136922082..136923657,2	K562	blood:
50	chr9:136560902..136563128-chr9:136576018..136578776,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VAV2-3	chr9:136576587-136576911	NONHSAT135338
2	lnc-VAV2-4	chr9:136552132-136552287	NONHSAT135336
3	lnc-DBH-4	chr9:136585389-136585564	NONHSAT135339
4	lnc-VAV2-4	chr9:136552891-136553109	NONHSAT135336
5	lnc-DBH-4	chr9:136584405-136584508	NONHSAT135339
6	lnc-DBH-3	chr9:136548433-136550559	NONHSAT135337
7	lnc-VAV2-3	chr9:136558849-136558951	NONHSAT135338

No data

Variant related genes	Relation type
SARDH	TF binding region
SARDH	CpG island
ENSG00000197859	chromatin interactions
ENSG00000235106	chromatin interactions
ENSG00000148297	chromatin interactions
ENSG00000123453	chromatin interactions
ENSG00000148303	chromatin interactions

Extended variants
information (count: 2351 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2351 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs129934	chr9:136538798-136538799	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543689563	chr9:136538812-136538813	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75239212	chr9:136538830-136538831	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs145090005	chr9:136538842-136538843	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35054983	chr9:136538917-136538918	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191444091	chr9:136538927-136538928	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538913644	chr9:136538939-136538940	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533314641	chr9:136538949-136538950	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371717507	chr9:136538951-136538952	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs149034624	chr9:136538954-136538955	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532946257	chr9:136538959-136538960	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143004561	chr9:136538978-136538979	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs60193008	chr9:136538986-136538987	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs374921110	chr9:136539011-136539012	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549670169	chr9:136539020-136539021	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543510624	chr9:136539032-136539033	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115111919	chr9:136539045-136539046	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569694291	chr9:136539074-136539075	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113495971	chr9:136539097-136539098	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs369665488	chr9:136539100-136539101	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557327090	chr9:136539109-136539110	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs138600988	chr9:136539134-136539135	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189343732	chr9:136539146-136539147	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181327920	chr9:136539161-136539162	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569215792	chr9:136539167-136539168	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536971846	chr9:136539168-136539169	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140272370	chr9:136539178-136539179	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs573511295	chr9:136539183-136539184	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs376119469	chr9:136539202-136539203	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs145322793	chr9:136539215-136539216	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs376633253	chr9:136539237-136539238	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs186335835	chr9:136539288-136539289	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs138441014	chr9:136539348-136539349	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs189075839	chr9:136539364-136539365	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs535238401	chr9:136539380-136539381	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs563159556	chr9:136539389-136539390	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs141939767	chr9:136539392-136539393	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs373324510	chr9:136539414-136539415	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs561517830	chr9:136539418-136539419	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs528789911	chr9:136539441-136539442	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs181584645	chr9:136539442-136539443	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs565462424	chr9:136539458-136539459	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs150704878	chr9:136539478-136539479	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs551028062	chr9:136539481-136539482	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs569175056	chr9:136539488-136539489	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs370215963	chr9:136539501-136539502	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs375370208	chr9:136539506-136539507	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs377541513	chr9:136539529-136539530	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs186555064	chr9:136539552-136539553	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs190959234	chr9:136539553-136539554	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	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
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136524400-136541200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr9:136524800-136542800	Weak transcription	Right Atrium	heart
3	chr9:136524800-136555600	Weak transcription	HSMM	muscle
4	chr9:136525000-136556800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr9:136528400-136540800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr9:136528600-136544200	Weak transcription	Ovary	ovary
7	chr9:136530800-136561000	Weak transcription	Gastric	stomach
8	chr9:136532000-136543600	Weak transcription	Lung	lung
9	chr9:136533200-136539600	Weak transcription	Thymus	Thymus
10	chr9:136534400-136539400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:136534400-136540400	Strong transcription	Liver	Liver
12	chr9:136534600-136540000	Strong transcription	Primary T cells from cord blood	blood
13	chr9:136534800-136539000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr9:136535000-136538800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr9:136535000-136541800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr9:136535200-136540200	Weak transcription	Fetal Intestine Small	intestine
17	chr9:136536200-136539400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:136536400-136540600	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr9:136537600-136539600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr9:136537600-136539800	Genic enhancers	Primary T cells fromperipheralblood	blood
21	chr9:136538000-136539000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr9:136538000-136539200	Enhancers	Fetal Heart	heart
23	chr9:136538000-136540000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr9:136538200-136538800	Weak transcription	HepG2	liver
25	chr9:136538200-136539000	Bivalent Enhancer	Fetal Stomach	stomach
26	chr9:136538200-136539000	Weak transcription	Fetal Thymus	thymus
27	chr9:136538200-136539600	Enhancers	Fetal Muscle Leg	muscle
28	chr9:136538400-136538800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:136538400-136538800	Weak transcription	Spleen	Spleen
30	chr9:136538400-136539000	Enhancers	Fetal Lung	lung
31	chr9:136538400-136539200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:136538400-136539200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:136538400-136548200	Weak transcription	Pancreas	Pancrea
34	chr9:136538600-136538800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:136538600-136541600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:136538600-136544600	Weak transcription	Right Ventricle	heart
37	chr9:136538600-136549000	Weak transcription	Fetal Brain Female	brain
38	chr9:136538800-136539000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:136538800-136539200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
40	chr9:136538800-136539200	Enhancers	Spleen	Spleen
41	chr9:136538800-136539600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr9:136538800-136539800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr9:136538800-136540000	Strong transcription	HepG2	liver
44	chr9:136539000-136539400	Bivalent Enhancer	Placenta	Placenta
45	chr9:136539000-136539600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr9:136539000-136539800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr9:136539000-136540000	Enhancers	Fetal Thymus	thymus
48	chr9:136539000-136540200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr9:136539000-136543800	Weak transcription	Fetal Lung	lung
50	chr9:136539200-136541200	Weak transcription	Spleen	Spleen

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