Variant report

Variant	esv3693040
Chromosome Location	chr9:115381164-115578065
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3228)
CpG islands
(count:854)
Chromatin interactive
region (count:213)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3228 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115509251-115509790	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115480786-115481091	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:115480237-115480501	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:115512832-115512868	K562	blood:	n/a	n/a
5	ARID3A	chr9:115480303-115480518	K562	blood:	n/a	n/a
6	ARID3A	chr9:115526787-115526979	K562	blood:	n/a	n/a
7	ARID3A	chr9:115494056-115494755	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:115512431-115512988	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:115527085-115527557	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:115479963-115479990	K562	blood:	n/a	n/a
11	ATF1	chr9:115479899-115480664	K562	blood:	n/a	n/a
12	ATF1	chr9:115546849-115547018	K562	blood:	n/a	n/a
13	ATF1	chr9:115492920-115493063	K562	blood:	n/a	n/a
14	ATF2	chr9:115534041-115534389	GM12878	blood:	n/a	n/a
15	ATF2	chr9:115480059-115480571	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr9:115571491-115572271	GM12878	blood:	n/a	n/a
17	ATF2	chr9:115546485-115546980	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr9:115546557-115547024	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr9:115533877-115534620	GM12878	blood:	n/a	n/a
20	ATF2	chr9:115461429-115461926	GM12878	blood:	n/a	n/a
21	ATF2	chr9:115479969-115480608	GM12878	blood:	n/a	n/a
22	ATF2	chr9:115479964-115480574	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr9:115461473-115461858	GM12878	blood:	n/a	n/a
24	ATF2	chr9:115571553-115572322	GM12878	blood:	n/a	n/a
25	ATF2	chr9:115536387-115537342	GM12878	blood:	n/a	n/a
26	ATF3	chr9:115512764-115513021	K562	blood:	n/a	n/a
27	ATF3	chr9:115513811-115514038	K562	blood:	n/a	chr9:115513959-115513968
28	BACH1	chr9:115480800-115481000	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr9:115480689-115480847	K562	blood:	n/a	n/a
30	BACH1	chr9:115391691-115391696	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:115555648-115555803	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr9:115383915-115383962	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr9:115513425-115513999	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr9:115571596-115572164	GM12878	blood:	n/a	chr9:115571860-115571871
35	BATF	chr9:115555592-115555842	GM12878	blood:	n/a	n/a
36	BATF	chr9:115477422-115477655	GM12878	blood:	n/a	n/a
37	BATF	chr9:115477441-115477621	GM12878	blood:	n/a	n/a
38	BATF	chr9:115481594-115481937	GM12878	blood:	n/a	n/a
39	BATF	chr9:115481521-115481962	GM12878	blood:	n/a	n/a
40	BATF	chr9:115571549-115572196	GM12878	blood:	n/a	chr9:115571860-115571871
41	BATF	chr9:115450305-115450695	GM12878	blood:	n/a	chr9:115450534-115450545 chr9:115450535-115450545
42	BCL11A	chr9:115571550-115572162	GM12878	blood:	n/a	n/a
43	BCL11A	chr9:115571502-115572209	GM12878	blood:	n/a	n/a
44	BCL3	chr9:115461526-115461832	GM12878	blood:	n/a	n/a
45	BCL3	chr9:115571588-115572096	GM12878	blood:	n/a	n/a
46	BCLAF1	chr9:115555367-115555922	GM12878	blood:	n/a	n/a
47	BCLAF1	chr9:115461422-115462143	GM12878	blood:	n/a	n/a
48	BCLAF1	chr9:115479865-115480402	GM12878	blood:	n/a	n/a
49	BCLAF1	chr9:115512540-115513253	GM12878	blood:	n/a	chr9:115513227-115513236 chr9:115513036-115513049 chr9:115513132-115513145
50	BCLAF1	chr9:115571497-115572306	GM12878	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115509770-115509820	HepG2	liver:	n/a
2	chr9:115509770-115509820	GM12891	blood:	n/a
3	chr9:115512612-115512662	HAEpiC	amniotic membrane:	n/a
4	chr9:115480539-115480589	SAEC	small airway:	n/a
5	chr9:115513820-115513870	NHBE	bronchial:	n/a
6	chr9:115513756-115513806	NH-A	brain:	n/a
7	chr9:115512612-115512662	U87	brain:	n/a
8	chr9:115513820-115513870	GM06990	blood:	n/a
9	chr9:115480324-115480374	HRE	kidney:	n/a
10	chr9:115509770-115509820	AG10803	skin:	n/a
11	chr9:115480060-115480110	HAEpiC	amniotic membrane:	n/a
12	chr9:115513525-115513575	Jurkat	blood:	n/a
13	chr9:115480630-115480680	A549	lung:	n/a
14	chr9:115513482-115513532	HCF	heart:	n/a
15	chr9:115513056-115513106	SKMC	muscle:	n/a
16	chr9:115513056-115513106	AoSMC	blood vessel:	n/a
17	chr9:115513756-115513806	HCT-116	colon:	n/a
18	chr9:115513820-115513870	SK-N-MC	brain:	n/a
19	chr9:115512612-115512662	HEEpiC	esophagus:	n/a
20	chr9:115480625-115480675	GM06990	blood:	n/a
21	chr9:115513820-115513870	LNCaP	prostate:	n/a
22	chr9:115480539-115480589	HCT-116	colon:	n/a
23	chr9:115513525-115513575	AG09319	gingival:	n/a
24	chr9:115509770-115509820	HEEpiC	esophagus:	n/a
25	chr9:115512530-115512580	HRE	kidney:	n/a
26	chr9:115481039-115481089	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:115480625-115480675	K562	blood:	n/a
28	chr9:115480625-115480675	LNCaP	prostate:	n/a
29	chr9:115512530-115512580	RPTEC	kidney:	n/a
30	chr9:115481039-115481089	HAEpiC	amniotic membrane:	n/a
31	chr9:115513482-115513532	HCT-116	colon:	n/a
32	chr9:115512530-115512580	Hepatocyte	liver:	n/a
33	chr9:115481039-115481089	NB4	blood:	n/a
34	chr9:115512530-115512580	GM12891	blood:	n/a
35	chr9:115480630-115480680	SAEC	small airway:	n/a
36	chr9:115481039-115481089	HEEpiC	esophagus:	n/a
37	chr9:115512612-115512662	PANC-1	pancreas:	n/a
38	chr9:115513525-115513575	HIPEpiC	eye:	n/a
39	chr9:115480060-115480110	HRCEpiC	kidney:	n/a
40	chr9:115480539-115480589	SK-N-SH_RA	brain:	n/a
41	chr9:115513482-115513532	MCF10A-Er-Src	breast:	n/a
42	chr9:115480060-115480110	ECC-1	luminal epithelium:	n/a
43	chr9:115480630-115480680	HCPEpiC	choroid plexus:	n/a
44	chr9:115513056-115513106	SK-N-SH_RA	brain:	n/a
45	chr9:115480060-115480110	MCF-7	breast:	n/a
46	chr9:115480539-115480589	PFSK-1	brain:	n/a
47	chr9:115513756-115513806	HCPEpiC	choroid plexus:	n/a
48	chr9:115513820-115513870	NHDF-neo	bronchial:	n/a
49	chr9:115480625-115480675	GM12878	blood:	n/a
50	chr9:115513056-115513106	SAEC	small airway:	n/a

(count:213 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr9:115503540..115508214-chr9:115510505..115515257,6	MCF-7	breast:
2	chr9:115248998..115250713-chr9:115421666..115423998,2	MCF-7	breast:
3	chr9:115465512..115468135-chr9:115469344..115471975,2	MCF-7	breast:
4	chr9:115565460..115568341-chr9:115568700..115570833,2	MCF-7	breast:
5	chr9:115374076..115376330-chr9:115394723..115396428,2	K562	blood:
6	chr9:115511729..115513827-chr9:115524619..115527032,2	K562	blood:
7	chr9:115465064..115467730-chr9:115468816..115472137,3	K562	blood:
8	chr9:115512086..115514376-chr9:115549215..115552051,3	MCF-7	breast:
9	chr9:115425089..115427194-chr9:115429213..115432033,2	K562	blood:
10	chr9:115505189..115506150-chr9:115555231..115556122,11	MCF-7	breast:
11	chr9:115398901..115401113-chr9:115401178..115403996,2	K562	blood:
12	chr9:115447768..115450470-chr9:115455814..115458350,2	MCF-7	breast:
13	chr9:115503663..115506191-chr9:115515083..115517470,2	K562	blood:
14	chr9:114848920..114849575-chr9:115467847..115468664,2	MCF-7	breast:
15	chr9:115469893..115474595-chr9:115477865..115481972,7	K562	blood:
16	chr9:115549006..115551974-chr9:115557854..115560441,2	K562	blood:
17	chr9:115498256..115499821-chr9:115502701..115504658,2	MCF-7	breast:
18	chr9:115384018..115386931-chr9:115389351..115391854,2	K562	blood:
19	chr9:115505232..115509202-chr9:115509878..115514316,6	K562	blood:
20	chr9:115425694..115427398-chr9:115429129..115432033,2	K562	blood:
21	chr9:115431402..115433363-chr9:115441682..115443542,2	K562	blood:
22	chr9:115449599..115451431-chr9:115473540..115475115,2	K562	blood:
23	chr9:115421461..115423373-chr9:115424758..115428380,4	K562	blood:
24	chr9:115478146..115483068-chr9:115509233..115514262,7	K562	blood:
25	chr9:115498256..115499821-chr9:115502701..115504658,2	MCF-7	breast:
26	chr9:115512668..115515460-chr9:115534425..115536617,2	K562	blood:
27	chr9:115224285..115224817-chr9:115427888..115428611,2	MCF-7	breast:
28	chr9:115380523..115382087-chr9:115395680..115398625,2	K562	blood:
29	chr9:115401662..115403762-chr9:115408579..115410766,2	K562	blood:
30	chr9:115512422..115514539-chr9:115533926..115536411,4	MCF-7	breast:
31	chr9:115568430..115571071-chr9:115577497..115580948,3	MCF-7	breast:
32	chr9:115465332..115466995-chr9:115480196..115481737,2	K562	blood:
33	chr9:115204852..115206161-chr9:115427327..115428280,9	MCF-7	breast:
34	chr9:115505276..115505895-chr9:115555411..115556004,2	MCF-7	breast:
35	chr9:115491320..115493108-chr9:115519478..115521653,2	MCF-7	breast:
36	chr9:115465512..115468135-chr9:115469344..115471975,2	MCF-7	breast:
37	chr9:115512404..115513313-chr9:115551025..115551948,2	MCF-7	breast:
38	chr9:115549478..115551812-chr9:115554338..115556959,2	MCF-7	breast:
39	chr9:115383838..115387286-chr9:115392608..115396534,4	K562	blood:
40	chr9:115571216..115573226-chr9:115575838..115578800,2	K562	blood:
41	chr9:115552552..115554676-chr9:115556505..115559633,3	MCF-7	breast:
42	chr9:115449599..115451431-chr9:115473540..115475115,2	K562	blood:
43	chr9:115537609..115539652-chr9:115540859..115543192,2	K562	blood:
44	chr9:115205537..115206125-chr9:115473120..115473635,2	MCF-7	breast:
45	chr9:115485448..115488278-chr9:115512375..115514169,2	MCF-7	breast:
46	chr9:115473485..115475875-chr9:115478661..115482867,3	MCF-7	breast:
47	chr9:115533346..115535894-chr9:115545369..115547662,2	MCF-7	breast:
48	chr9:115235092..115237289-chr9:115391747..115394330,2	K562	blood:
49	chr9:115505276..115505895-chr9:115555411..115556004,2	MCF-7	breast:
50	chr9:115542323..115543892-chr9:115545474..115547035,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf80-1	chr9:115505051-115505514	XLOC_007830
2	lnc-SNX30-2	chr9:115390750-115391983	NONHSAT134020
3	lnc-C9orf80-1	chr9:115511182-115511550	XLOC_007830
4	lnc-SLC46A2-4	chr9:115478741-115478821	NONHSAT134023
5	lnc-C9orf80-1	chr9:115511360-115512795	XLOC_007830
6	lnc-KIAA1958-1	chr9:115454118-115454181	NONHSAT134022
7	lnc-SLC46A2-4	chr9:115480267-115480397	NONHSAT134023
8	lnc-KIAA1958-1	chr9:115453057-115453265	NONHSAT134022
9	lnc-C9orf80-1	chr9:115512686-115512736	XLOC_007830
10	lnc-KIAA1958-1	chr9:115484007-115484956	NONHSAT134022
11	lnc-SLC46A2-4	chr9:115456314-115456513	NONHSAT134023

No data

Variant related genes	Relation type
ENSG00000226609	TF binding region
INIP	TF binding region
SNX30	TF binding region
ENSG00000226609	CpG island
INIP	CpG island
SNX30	CpG island
ENSG00000148158	chromatin interactions
ENSG00000230185	chromatin interactions
ENSG00000150760	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000148153	chromatin interactions
ENSG00000119471	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000271631	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000173473	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000165185	chromatin interactions
SETD8	miRNA target sites

Extended variants
information (count: 7226 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:7226 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3780687	chr9:115381164-115381165	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149946235	chr9:115381191-115381192	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562542332	chr9:115381206-115381207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373267558	chr9:115381266-115381267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537118908	chr9:115381302-115381303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557190137	chr9:115381330-115381331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576145631	chr9:115381375-115381376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181989895	chr9:115381413-115381414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184216389	chr9:115381468-115381469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572358810	chr9:115381549-115381550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541369142	chr9:115381551-115381552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146423730	chr9:115381557-115381558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140847943	chr9:115381560-115381561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117295800	chr9:115381569-115381570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563241266	chr9:115381582-115381583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529032809	chr9:115381599-115381600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144599034	chr9:115381611-115381612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189025480	chr9:115381633-115381634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181103207	chr9:115381638-115381639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146705246	chr9:115381674-115381675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377341208	chr9:115381714-115381715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537056701	chr9:115381799-115381800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551005479	chr9:115381856-115381857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186385040	chr9:115381891-115381892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536791642	chr9:115381925-115381926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs148844642	chr9:115381945-115381946	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565908209	chr9:115381994-115381995	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs553298768	chr9:115382124-115382125	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs578187741	chr9:115382156-115382157	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs545104791	chr9:115382196-115382197	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs16917136	chr9:115382208-115382209	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs577666738	chr9:115382296-115382297	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77718726	chr9:115382335-115382336	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs556958818	chr9:115382350-115382351	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs148340508	chr9:115382400-115382401	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377723885	chr9:115382425-115382426	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs557299138	chr9:115382444-115382445	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542736078	chr9:115382503-115382504	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs141577937	chr9:115382533-115382534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148989296	chr9:115382553-115382554	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs191587944	chr9:115382562-115382563	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545255018	chr9:115382567-115382568	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs565239605	chr9:115382593-115382594	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531154395	chr9:115382594-115382595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs180852779	chr9:115382657-115382658	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs185429342	chr9:115382682-115382683	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs73543150	chr9:115382711-115382712	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs527362932	chr9:115382777-115382778	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs114163684	chr9:115382790-115382791	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs575519360	chr9:115382798-115382799	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4621 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115346400-115385000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:115368600-115391600	Weak transcription	Brain Hippocampus Middle	brain
3	chr9:115374600-115382200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:115377200-115381400	Weak transcription	Right Atrium	heart
5	chr9:115378000-115383400	Weak transcription	GM12878-XiMat	blood
6	chr9:115378400-115382400	Weak transcription	A549	lung
7	chr9:115378400-115386600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr9:115378600-115382800	Weak transcription	Fetal Kidney	kidney
9	chr9:115379000-115391400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:115379000-115410200	Weak transcription	HSMMtube	muscle
11	chr9:115379200-115381200	Strong transcription	HepG2	liver
12	chr9:115379400-115381200	Strong transcription	Dnd41	blood
13	chr9:115379400-115386400	Weak transcription	Brain Anterior Caudate	brain
14	chr9:115379600-115382200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr9:115379800-115381200	Strong transcription	Primary B cells from cord blood	blood
16	chr9:115379800-115384000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr9:115379800-115386600	Weak transcription	Brain Substantia Nigra	brain
18	chr9:115380000-115381200	Genic enhancers	HUES64 Cell Line	embryonic stem cell
19	chr9:115380000-115381200	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr9:115380000-115381200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:115380000-115381200	Strong transcription	Liver	Liver
22	chr9:115380000-115381200	Strong transcription	Fetal Intestine Large	intestine
23	chr9:115380000-115381200	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr9:115380000-115382400	Weak transcription	Fetal Brain Female	brain
25	chr9:115380000-115383400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr9:115380000-115385800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr9:115380000-115392000	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr9:115380200-115381200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:115380200-115381200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:115380200-115381200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
31	chr9:115380200-115381200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr9:115380200-115381200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:115380200-115381200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr9:115380200-115381200	Strong transcription	Esophagus	oesophagus
35	chr9:115380200-115381200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr9:115380200-115381200	Strong transcription	Fetal Intestine Small	intestine
37	chr9:115380200-115381200	Strong transcription	Fetal Muscle Trunk	muscle
38	chr9:115380200-115381200	Strong transcription	Fetal Muscle Leg	muscle
39	chr9:115380200-115381200	Strong transcription	Fetal Stomach	stomach
40	chr9:115380200-115381200	Strong transcription	Pancreas	Pancrea
41	chr9:115380200-115381200	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr9:115380200-115381200	Strong transcription	Thymus	Thymus
43	chr9:115380200-115381200	Strong transcription	K562	blood
44	chr9:115380400-115381200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr9:115380600-115381200	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr9:115380600-115381200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr9:115380600-115381200	Strong transcription	Duodenum Mucosa	Duodenum
48	chr9:115380600-115381200	ZNF genes & repeats	Lung	lung
49	chr9:115380600-115381200	Strong transcription	NHDF-Ad	bronchial
50	chr9:115380600-115382000	Weak transcription	Fetal Lung	lung

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