Variant report

Variant	nsv466393
Chromosome Location	chr9:71453443-71704827
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3324)
CpG islands
(count:1405)
Chromatin interactive
region (count:163)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3324 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71642563-71642873	K562	blood:	n/a	n/a
2	ARID3A	chr9:71614594-71614886	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:71634748-71635103	K562	blood:	n/a	n/a
4	ARID3A	chr9:71460000-71460212	K562	blood:	n/a	n/a
5	ARID3A	chr9:71584469-71584970	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:71701730-71702036	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:71598080-71598400	K562	blood:	n/a	n/a
8	ARID3A	chr9:71635426-71635919	K562	blood:	n/a	n/a
9	ARID3A	chr9:71584464-71585376	K562	blood:	n/a	n/a
10	ARID3A	chr9:71631852-71631872	K562	blood:	n/a	n/a
11	ARID3A	chr9:71650444-71651128	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:71542080-71542315	K562	blood:	n/a	n/a
13	ARID3A	chr9:71650526-71650743	K562	blood:	n/a	n/a
14	ARID3A	chr9:71651502-71651839	K562	blood:	n/a	n/a
15	ARID3A	chr9:71576402-71576900	K562	blood:	n/a	n/a
16	ATF1	chr9:71634756-71635094	K562	blood:	n/a	n/a
17	ATF1	chr9:71613777-71614153	K562	blood:	n/a	n/a
18	ATF1	chr9:71584518-71584727	K562	blood:	n/a	n/a
19	ATF1	chr9:71576511-71576777	K562	blood:	n/a	n/a
20	ATF1	chr9:71542195-71542403	K562	blood:	n/a	n/a
21	ATF1	chr9:71590616-71590989	K562	blood:	n/a	n/a
22	ATF1	chr9:71635543-71635967	K562	blood:	n/a	n/a
23	ATF1	chr9:71642591-71642873	K562	blood:	n/a	n/a
24	ATF1	chr9:71598096-71598406	K562	blood:	n/a	n/a
25	ATF2	chr9:71562782-71563303	GM12878	blood:	n/a	n/a
26	ATF2	chr9:71548349-71548993	GM12878	blood:	n/a	n/a
27	ATF2	chr9:71581505-71582024	GM12878	blood:	n/a	n/a
28	ATF2	chr9:71650325-71650801	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr9:71561786-71562440	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr9:71532495-71533061	GM12878	blood:	n/a	n/a
31	ATF2	chr9:71532395-71533134	GM12878	blood:	n/a	n/a
32	ATF2	chr9:71590432-71591070	GM12878	blood:	n/a	n/a
33	ATF2	chr9:71510851-71511392	GM12878	blood:	n/a	n/a
34	ATF2	chr9:71650422-71650822	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr9:71581453-71582017	GM12878	blood:	n/a	n/a
36	ATF2	chr9:71486796-71487469	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr9:71590514-71590994	GM12878	blood:	n/a	n/a
38	ATF2	chr9:71589185-71589864	GM12878	blood:	n/a	n/a
39	ATF2	chr9:71548216-71549106	GM12878	blood:	n/a	n/a
40	ATF2	chr9:71486910-71487495	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr9:71589241-71589855	GM12878	blood:	n/a	n/a
42	ATF2	chr9:71566854-71567581	GM12878	blood:	n/a	n/a
43	ATF2	chr9:71596689-71597229	GM12878	blood:	n/a	n/a
44	ATF3	chr9:71650292-71651027	A549	lung:	n/a	n/a
45	BACH1	chr9:71470643-71470787	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr9:71486897-71487488	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr9:71650535-71650996	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr9:71634639-71634975	K562	blood:	n/a	n/a
49	BACH1	chr9:71565650-71565999	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr9:71581550-71581855	GM12878	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71627667-71627717	CMK	blood:	n/a
2	chr9:71651331-71651381	HEK293	kidney:	embryo
3	chr9:71627667-71627717	CMK	blood:	n/a
4	chr9:71651331-71651381	HEK293	kidney:	embryo
5	chr9:71652532-71652582	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:71623401-71623451	GM12878	blood:	n/a
7	chr9:71651331-71651381	PFSK-1	brain:	n/a
8	chr9:71627667-71627717	HMEC	breast:	n/a
9	chr9:71654823-71654873	Caco-2	colon:	n/a
10	chr9:71691305-71691355	H1-hESC	embryonic stem cell:	embryo
11	chr9:71652532-71652582	HEK293	kidney:	embryo
12	chr9:71627524-71627574	HMEC	breast:	n/a
13	chr9:71651175-71651225	HRE	kidney:	n/a
14	chr9:71651331-71651381	SK-N-MC	brain:	n/a
15	chr9:71669714-71669764	NB4	blood:	n/a
16	chr9:71650237-71650287	AG04450	lung:	fetal
17	chr9:71652532-71652582	HIPEpiC	eye:	n/a
18	chr9:71627524-71627574	AG09309	skin:	n/a
19	chr9:71650237-71650287	BE2_C	brain:	n/a
20	chr9:71682302-71682352	K562	blood:	n/a
21	chr9:71627667-71627717	AG09309	skin:	n/a
22	chr9:71654823-71654873	Jurkat	blood:	n/a
23	chr9:71685390-71685440	Caco-2	colon:	n/a
24	chr9:71650719-71650769	SK-N-SH	brain:	n/a
25	chr9:71627667-71627717	ovcar-3	ovarian:	n/a
26	chr9:71631514-71631564	ProgFib	skin:	n/a
27	chr9:71691305-71691355	SK-N-SH	brain:	n/a
28	chr9:71691305-71691355	ProgFib	skin:	n/a
29	chr9:71661107-71661157	Caco-2	colon:	n/a
30	chr9:71629130-71629180	IMR90	lung:	fetal
31	chr9:71589563-71589613	AoSMC	blood vessel:	n/a
32	chr9:71669714-71669764	HCT-116	colon:	n/a
33	chr9:71682105-71682155	SKMC	muscle:	n/a
34	chr9:71652532-71652582	HAEpiC	amniotic membrane:	n/a
35	chr9:71682105-71682155	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:71683936-71683986	HMEC	breast:	n/a
37	chr9:71661107-71661157	HPAEpiC	pulmonary alveolar:	n/a
38	chr9:71652532-71652582	MCF10A-Er-Src	breast:	n/a
39	chr9:71661107-71661157	AG09309	skin:	n/a
40	chr9:71628906-71628956	GM06990	blood:	n/a
41	chr9:71654823-71654873	AG04450	lung:	fetal
42	chr9:71627667-71627717	PrEC	prostate:	n/a
43	chr9:71629130-71629180	HRE	kidney:	n/a
44	chr9:71650237-71650287	HEK293	kidney:	embryo
45	chr9:71650331-71650381	ECC-1	luminal epithelium:	n/a
46	chr9:71650331-71650381	BJ	skin:	n/a
47	chr9:71661107-71661157	AG04450	lung:	fetal
48	chr9:71627524-71627574	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:71627524-71627574	HRPEpiC	eye:	n/a
50	chr9:71651331-71651381	SK-N-SH_RA	brain:	n/a

(count:163 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr9:71472846..71475720-chr9:71476283..71478210,2	K562	blood:
2	chr9:71474756..71477086-chr9:71501374..71504122,2	K562	blood:
3	chr9:71651712..71654573-chr9:71656499..71659593,3	K562	blood:
4	chr9:71587606..71589215-chr9:71606682..71608603,2	MCF-7	breast:
5	chr9:71600704..71602578-chr9:71603137..71605557,2	K562	blood:
6	chr9:71319203..71320145-chr9:71614622..71615180,2	MCF-7	breast:
7	chr9:71680760..71683108-chr9:71693749..71695954,2	K562	blood:
8	chr9:71393142..71395397-chr9:71613352..71615098,2	K562	blood:
9	chr9:71688887..71691252-chr9:71735697..71737532,2	MCF-7	breast:
10	chr9:71576569..71578561-chr9:71582492..71584226,2	MCF-7	breast:
11	chr9:71199108..71199619-chr9:71642191..71643182,2	K562	blood:
12	chr9:71513862..71516503-chr9:71520061..71522924,2	MCF-7	breast:
13	chr9:71671307..71672957-chr9:71675793..71678189,2	MCF-7	breast:
14	chr9:71655862..71658846-chr9:71661896..71664645,2	MCF-7	breast:
15	chr9:71639276..71640998-chr9:71649555..71652246,2	MCF-7	breast:
16	chr9:71509323..71512196-chr9:71514082..71515973,2	K562	blood:
17	chr9:71477461..71479791-chr9:71480861..71483693,2	MCF-7	breast:
18	chr9:71477100..71479785-chr9:71480744..71483651,2	K562	blood:
19	chr9:71614613..71617089-chr9:71618925..71621633,2	K562	blood:
20	chr9:71392487..71395427-chr9:71649569..71651600,2	K562	blood:
21	chr9:71650420..71652084-chr9:71654261..71655791,2	MCF-7	breast:
22	chr9:71646520..71648758-chr9:71649618..71651156,2	MCF-7	breast:
23	chr9:71642300..71643929-chr9:71644528..71647295,2	MCF-7	breast:
24	chr9:71568407..71571024-chr9:71572381..71575201,2	K562	blood:
25	chr9:71699941..71701534-chr9:71703830..71705802,2	MCF-7	breast:
26	chr9:71622551..71625318-chr9:71628981..71631159,4	K562	blood:
27	chr9:71700139..71702820-chr9:71819428..71821529,2	MCF-7	breast:
28	chr9:71199122..71199719-chr9:71614348..71615097,4	MCF-7	breast:
29	chr9:71483920..71486082-chr9:71487169..71489754,2	K562	blood:
30	chr9:71472846..71475720-chr9:71476283..71478210,2	K562	blood:
31	chr9:71451909..71453715-chr9:71457092..71459544,2	K562	blood:
32	chr9:71199440..71199949-chr9:71642261..71643160,3	MCF-7	breast:
33	chr9:71577956..71581283-chr9:71582183..71585440,6	K562	blood:
34	chr9:71577984..71579536-chr9:71582505..71585285,2	K562	blood:
35	chr9:71658862..71661009-chr9:71818957..71821038,2	K562	blood:
36	chr9:71674276..71676864-chr9:71678272..71680734,2	MCF-7	breast:
37	chr9:71481298..71483718-chr9:71491074..71493993,2	MCF-7	breast:
38	chr9:71465582..71467985-chr9:71469828..71471360,2	MCF-7	breast:
39	chr9:71634014..71636921-chr9:71638059..71641027,2	K562	blood:
40	chr9:71637586..71639711-chr9:71650641..71653127,2	K562	blood:
41	chr9:71704008..71706268-chr9:71714594..71717470,2	MCF-7	breast:
42	chr9:71572197..71575075-chr9:71576543..71579524,4	K562	blood:
43	chr9:71674276..71676864-chr9:71678272..71680734,2	MCF-7	breast:
44	chr9:71525845..71528360-chr9:71529223..71531031,2	MCF-7	breast:
45	chr9:71459672..71460600-chr9:71642433..71642935,2	K562	blood:
46	chr9:71594449..71596709-chr9:71598735..71600800,2	K562	blood:
47	chr9:71627843..71630592-chr9:71632071..71633725,3	K562	blood:
48	chr9:71545273..71547947-chr9:71556049..71558568,2	MCF-7	breast:
49	chr9:71672508..71675484-chr9:71734022..71736530,5	MCF-7	breast:
50	chr9:71598980..71601285-chr9:71602200..71604374,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACG-1	chr9:71570856-71572127	NONHSAT131759
2	lnc-PRKACG-3	chr9:71458083-71458191	ENSG00000236733.1
3	lnc-PRKACG-4	chr9:71625289-71625403	ucscGeneNc_uc004ahk_2
4	lnc-PRKACG-1	chr9:71568004-71569861	ENSG00000249652
5	lnc-PRKACG-1	chr9:71590580-71590757	ENSG00000249652
6	lnc-PRKACG-4	chr9:71624143-71625000	ucscGeneNc_uc004ahk_2
7	lnc-PRKACG-1	chr9:71590580-71590735	NONHSAT131759
8	lnc-PRKACG-1	chr9:71571942-71572127	ENSG00000249652
9	lnc-PRKACG-5	chr9:71563250-71563521	expReg_chr9_3063_-

No data

Variant related genes	Relation type
PRKACG	TF binding region
ENSG00000236733	TF binding region
FXN	TF binding region
RNU6-820P	TF binding region
PRKACG	CpG island
ENSG00000236733	CpG island
FXN	CpG island
RNU6-820P	CpG island
ENSG00000187866	chromatin interactions
ENSG00000165059	chromatin interactions
ENSG00000107242	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000236733	chromatin interactions
ENSG00000165060	chromatin interactions
NFIB	miRNA target sites
TRIP12	miRNA target sites
SMAD7	miRNA target sites

Extended variants
information (count: 9184 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:9184 , 50 per page) page: 1 2 3 4 5 6 7 ... 184

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4745321	chr9:71453443-71453444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576800121	chr9:71453482-71453483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79115342	chr9:71453553-71453554	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs553207138	chr9:71453585-71453586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575078467	chr9:71453602-71453603	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542052793	chr9:71453631-71453632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563947126	chr9:71453671-71453672	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs80340859	chr9:71453704-71453705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545912304	chr9:71453792-71453793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563009614	chr9:71453936-71453937	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs67147762	chr9:71453939-71453940	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10448322	chr9:71453998-71453999	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs144528255	chr9:71454025-71454026	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564807798	chr9:71454039-71454040	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561962362	chr9:71454049-71454050	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529230764	chr9:71454071-71454072	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145388476	chr9:71454075-71454076	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185465509	chr9:71454079-71454080	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149194049	chr9:71454092-71454093	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111775042	chr9:71454216-71454217	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570619149	chr9:71454229-71454230	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12378600	chr9:71454245-71454246	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376073497	chr9:71454253-71454254	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552994404	chr9:71454265-71454266	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142378148	chr9:71454279-71454280	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536179460	chr9:71454301-71454302	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35213945	chr9:71454305-71454306	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7871676	chr9:71454316-71454317	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs7865800	chr9:71454346-71454347	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs141273000	chr9:71454350-71454351	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114917097	chr9:71454363-71454364	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548660037	chr9:71454407-71454408	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375071449	chr9:71454427-71454428	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573023033	chr9:71454446-71454447	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540225902	chr9:71454509-71454510	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191350457	chr9:71454530-71454531	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74597576	chr9:71454546-71454547	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs80309194	chr9:71454632-71454633	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200418526	chr9:71454661-71454662	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113632240	chr9:71454680-71454681	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533105988	chr9:71454681-71454682	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146953534	chr9:71454813-71454814	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185970228	chr9:71454816-71454817	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11143975	chr9:71454879-71454880	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374593608	chr9:71454940-71454941	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533674982	chr9:71454942-71454943	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11143976	chr9:71454944-71454945	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs535503789	chr9:71454967-71454968	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs137936785	chr9:71454985-71454986	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141932968	chr9:71455029-71455030	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:4625 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71435800-71464800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:71438000-71491200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:71439200-71456000	Weak transcription	GM12878-XiMat	blood
4	chr9:71440600-71466600	Weak transcription	Gastric	stomach
5	chr9:71441000-71478600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr9:71441600-71459800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr9:71443600-71458600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr9:71443600-71459000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:71445600-71454400	Weak transcription	Fetal Intestine Large	intestine
10	chr9:71445600-71458600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr9:71448200-71485600	Weak transcription	Stomach Mucosa	stomach
12	chr9:71448800-71455800	Weak transcription	Aorta	Aorta
13	chr9:71449200-71459200	Weak transcription	Primary B cells from cord blood	blood
14	chr9:71449800-71456800	Weak transcription	Fetal Intestine Small	intestine
15	chr9:71450400-71453800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:71451600-71455000	Enhancers	Fetal Heart	heart
17	chr9:71452000-71458400	Weak transcription	Spleen	Spleen
18	chr9:71452200-71454200	Weak transcription	Left Ventricle	heart
19	chr9:71452200-71456400	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr9:71452200-71456800	Weak transcription	Right Atrium	heart
21	chr9:71452200-71456800	Weak transcription	Right Ventricle	heart
22	chr9:71452200-71458000	Weak transcription	Lung	lung
23	chr9:71453200-71454400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr9:71453200-71456000	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr9:71453400-71454600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr9:71453800-71458600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:71454200-71454800	Enhancers	Left Ventricle	heart
28	chr9:71454400-71455600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr9:71454400-71456000	Strong transcription	Fetal Intestine Large	intestine
30	chr9:71454600-71455800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr9:71454800-71456800	Weak transcription	Left Ventricle	heart
32	chr9:71455000-71455400	Weak transcription	Fetal Heart	heart
33	chr9:71455400-71455800	Enhancers	Fetal Heart	heart
34	chr9:71455600-71456800	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr9:71455800-71456000	Enhancers	Aorta	Aorta
36	chr9:71455800-71456200	Flanking Active TSS	Fetal Heart	heart
37	chr9:71455800-71457200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr9:71455800-71459400	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr9:71456000-71456200	Enhancers	Fetal Stomach	stomach
40	chr9:71456000-71456800	Weak transcription	Aorta	Aorta
41	chr9:71456000-71457800	Weak transcription	Fetal Intestine Large	intestine
42	chr9:71456000-71458000	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr9:71456000-71458000	Enhancers	GM12878-XiMat	blood
44	chr9:71456200-71456600	Enhancers	Fetal Heart	heart
45	chr9:71456400-71457200	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr9:71456600-71457000	Flanking Active TSS	Fetal Heart	heart
47	chr9:71456800-71457000	Enhancers	Fetal Stomach	stomach
48	chr9:71456800-71457200	Enhancers	Brain Hippocampus Middle	brain
49	chr9:71456800-71457200	Enhancers	Fetal Muscle Trunk	muscle
50	chr9:71456800-71457200	Enhancers	Fetal Muscle Leg	muscle

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