Variant report

Variant	nsv515899
Chromosome Location	chr9:115359049-115593870
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3600)
CpG islands
(count:855)
Chromatin interactive
region (count:255)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3600 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115480786-115481091	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115480303-115480518	K562	blood:	n/a	n/a
3	ARID3A	chr9:115479963-115479990	K562	blood:	n/a	n/a
4	ARID3A	chr9:115494056-115494755	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:115509251-115509790	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:115526787-115526979	K562	blood:	n/a	n/a
7	ARID3A	chr9:115512832-115512868	K562	blood:	n/a	n/a
8	ARID3A	chr9:115527085-115527557	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:115480237-115480501	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:115512431-115512988	HepG2	liver:	n/a	n/a
11	ATF1	chr9:115546849-115547018	K562	blood:	n/a	n/a
12	ATF1	chr9:115376140-115376239	K562	blood:	n/a	n/a
13	ATF1	chr9:115492920-115493063	K562	blood:	n/a	n/a
14	ATF1	chr9:115479899-115480664	K562	blood:	n/a	n/a
15	ATF2	chr9:115534041-115534389	GM12878	blood:	n/a	n/a
16	ATF2	chr9:115546485-115546980	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr9:115461473-115461858	GM12878	blood:	n/a	n/a
18	ATF2	chr9:115479964-115480574	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr9:115536387-115537342	GM12878	blood:	n/a	n/a
20	ATF2	chr9:115533877-115534620	GM12878	blood:	n/a	n/a
21	ATF2	chr9:115571553-115572322	GM12878	blood:	n/a	n/a
22	ATF2	chr9:115367668-115368275	GM12878	blood:	n/a	n/a
23	ATF2	chr9:115571491-115572271	GM12878	blood:	n/a	n/a
24	ATF2	chr9:115546557-115547024	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr9:115479969-115480608	GM12878	blood:	n/a	n/a
26	ATF2	chr9:115461429-115461926	GM12878	blood:	n/a	n/a
27	ATF2	chr9:115480059-115480571	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr9:115512764-115513021	K562	blood:	n/a	n/a
29	ATF3	chr9:115513811-115514038	K562	blood:	n/a	chr9:115513959-115513968
30	BACH1	chr9:115555648-115555803	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:115513425-115513999	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	chr9:115480800-115481000	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr9:115391691-115391696	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr9:115480689-115480847	K562	blood:	n/a	n/a
36	BATF	chr9:115571596-115572164	GM12878	blood:	n/a	chr9:115571860-115571871
37	BATF	chr9:115367791-115368112	GM12878	blood:	n/a	n/a
38	BATF	chr9:115481521-115481962	GM12878	blood:	n/a	n/a
39	BATF	chr9:115555592-115555842	GM12878	blood:	n/a	n/a
40	BATF	chr9:115450305-115450695	GM12878	blood:	n/a	chr9:115450534-115450545 chr9:115450535-115450545
41	BATF	chr9:115477441-115477621	GM12878	blood:	n/a	n/a
42	BATF	chr9:115477422-115477655	GM12878	blood:	n/a	n/a
43	BATF	chr9:115367729-115368181	GM12878	blood:	n/a	n/a
44	BATF	chr9:115571549-115572196	GM12878	blood:	n/a	chr9:115571860-115571871
45	BATF	chr9:115481594-115481937	GM12878	blood:	n/a	n/a
46	BCL11A	chr9:115367758-115368144	GM12878	blood:	n/a	n/a
47	BCL11A	chr9:115571550-115572162	GM12878	blood:	n/a	n/a
48	BCL11A	chr9:115571502-115572209	GM12878	blood:	n/a	n/a
49	BCL3	chr9:115571588-115572096	GM12878	blood:	n/a	n/a
50	BCL3	chr9:115461526-115461832	GM12878	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115480324-115480374	ovcar-3	ovarian:	n/a
2	chr9:115480324-115480374	ovcar-3	ovarian:	n/a
3	chr9:115513756-115513806	PrEC	prostate:	n/a
4	chr9:115513756-115513806	K562	blood:	n/a
5	chr9:115480060-115480110	NB4	blood:	n/a
6	chr9:115512612-115512662	AG09309	skin:	n/a
7	chr9:115513056-115513106	GM06990	blood:	n/a
8	chr9:115481039-115481089	IMR90	lung:	fetal
9	chr9:115480625-115480675	HepG2	liver:	n/a
10	chr9:115480630-115480680	HEEpiC	esophagus:	n/a
11	chr9:115513482-115513532	HL-60	blood:	n/a
12	chr9:115513482-115513532	LNCaP	prostate:	n/a
13	chr9:115480625-115480675	HRCEpiC	kidney:	n/a
14	chr9:115509770-115509820	SKMC	muscle:	n/a
15	chr9:115480625-115480675	HRE	kidney:	n/a
16	chr9:115480630-115480680	H1-hESC	embryonic stem cell:	embryo
17	chr9:115481039-115481089	T-47D	breast:	n/a
18	chr9:115480625-115480675	NHBE	bronchial:	n/a
19	chr9:115480539-115480589	MCF-7	breast:	n/a
20	chr9:115480324-115480374	HMEC	breast:	n/a
21	chr9:115480324-115480374	HUVEC	blood vessel:	n/a
22	chr9:115513056-115513106	SK-N-MC	brain:	n/a
23	chr9:115512612-115512662	RPTEC	kidney:	n/a
24	chr9:115512530-115512580	RPTEC	kidney:	n/a
25	chr9:115480324-115480374	ProgFib	skin:	n/a
26	chr9:115513482-115513532	AG09309	skin:	n/a
27	chr9:115480060-115480110	SK-N-SH_RA	brain:	n/a
28	chr9:115513820-115513870	NT2-D1	testis:	n/a
29	chr9:115481039-115481089	NHDF-neo	bronchial:	n/a
30	chr9:115513820-115513870	HAEpiC	amniotic membrane:	n/a
31	chr9:115512612-115512662	Jurkat	blood:	n/a
32	chr9:115512612-115512662	SK-N-MC	brain:	n/a
33	chr9:115480630-115480680	SK-N-SH_RA	brain:	n/a
34	chr9:115513056-115513106	AG04450	lung:	fetal
35	chr9:115513482-115513532	A549	lung:	n/a
36	chr9:115480324-115480374	HRE	kidney:	n/a
37	chr9:115480060-115480110	HCPEpiC	choroid plexus:	n/a
38	chr9:115513482-115513532	RPTEC	kidney:	n/a
39	chr9:115513756-115513806	GM12878	blood:	n/a
40	chr9:115513482-115513532	NHDF-neo	bronchial:	n/a
41	chr9:115512612-115512662	NH-A	brain:	n/a
42	chr9:115480625-115480675	SKMC	muscle:	n/a
43	chr9:115513820-115513870	MCF-7	breast:	n/a
44	chr9:115513820-115513870	NH-A	brain:	n/a
45	chr9:115509770-115509820	AoSMC	blood vessel:	n/a
46	chr9:115513482-115513532	AG04450	lung:	fetal
47	chr9:115512612-115512662	SK-N-SH_RA	brain:	n/a
48	chr9:115480630-115480680	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:115513482-115513532	AG10803	skin:	n/a
50	chr9:115512612-115512662	NB4	blood:	n/a

(count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr9:115529521..115533265-chr9:115533546..115536712,4	K562	blood:
2	chr9:115348712..115350635-chr9:115364212..115367112,2	K562	blood:
3	chr9:115512316..115514216-chr9:115529153..115530836,3	MCF-7	breast:
4	chr9:115537609..115539652-chr9:115540859..115543192,2	K562	blood:
5	chr9:115093683..115097222-chr9:115479226..115482201,3	K562	blood:
6	chr10:128593848..128594420-chr9:115480055..115480808,2	HCT-116	colon:
7	chr9:115204840..115206554-chr9:115427326..115428723,8	MCF-7	breast:
8	chr9:115356821..115358756-chr9:115361387..115363697,2	K562	blood:
9	chr9:115371233..115374134-chr9:115375827..115377994,2	K562	blood:
10	chr9:115586128..115587696-chr9:115592074..115593808,2	MCF-7	breast:
11	chr9:115361340..115364791-chr9:115372850..115375456,3	K562	blood:
12	chr9:115446137..115448834-chr9:115451791..115453700,3	K562	blood:
13	chr9:115383838..115387286-chr9:115392608..115396534,4	K562	blood:
14	chr9:115372923..115374938-chr9:115378723..115381486,2	MCF-7	breast:
15	chr9:115247555..115250048-chr9:115510709..115513501,2	K562	blood:
16	chr9:115369992..115372791-chr9:115372880..115374738,2	K562	blood:
17	chr9:115512086..115514376-chr9:115549215..115552051,3	MCF-7	breast:
18	chr1:171750400..171751284-chr9:115512246..115512858,2	Hela-S3	cervix:
19	chr9:115358060..115360047-chr9:115363749..115366289,2	K562	blood:
20	chr9:115363911..115365862-chr9:115389104..115390742,2	K562	blood:
21	chr9:115533906..115536575-chr9:115567141..115568722,2	MCF-7	breast:
22	chr9:115513040..115515459-chr9:115588123..115591278,3	MCF-7	breast:
23	chr9:115549478..115551812-chr9:115554338..115556959,2	MCF-7	breast:
24	chr9:115542323..115543892-chr9:115545474..115547035,2	K562	blood:
25	chr9:115511487..115514115-chr9:115544583..115546972,6	MCF-7	breast:
26	chr9:115361340..115364791-chr9:115372850..115375456,3	K562	blood:
27	chr9:115439423..115442262-chr9:115442382..115444578,2	MCF-7	breast:
28	chr9:115465332..115466995-chr9:115480196..115481737,2	K562	blood:
29	chr9:115500108..115502596-chr9:115512247..115514612,3	MCF-7	breast:
30	chr12:51476737..51477475-chr9:115512516..115513185,2	Hela-S3	cervix:
31	chr9:115476889..115478492-chr9:115480105..115481755,2	MCF-7	breast:
32	chr9:115555096..115556091-chr9:115581952..115582779,4	MCF-7	breast:
33	chr9:115205537..115206125-chr9:115473120..115473635,2	MCF-7	breast:
34	chr9:115545454..115548524-chr9:115549503..115552233,3	MCF-7	breast:
35	chr9:115574660..115576391-chr9:115583184..115586176,2	K562	blood:
36	chr9:115475870..115478172-chr9:115478861..115481812,2	K562	blood:
37	chr9:115534861..115537925-chr9:115540163..115544235,3	MCF-7	breast:
38	chr9:115545740..115547705-chr9:115549522..115552424,3	K562	blood:
39	chr9:115520162..115522782-chr9:115581748..115584081,2	MCF-7	breast:
40	chr9:115571216..115573226-chr9:115575838..115578800,2	K562	blood:
41	chr9:115574660..115576391-chr9:115583184..115586176,2	K562	blood:
42	chr9:115505313..115506170-chr9:115581939..115582872,6	MCF-7	breast:
43	chr9:115383838..115387286-chr9:115392608..115396534,4	K562	blood:
44	chr9:115496362..115497969-chr9:115509483..115511853,2	K562	blood:
45	chr9:115555372..115556213-chr9:115581844..115582573,3	MCF-7	breast:
46	chr9:115439423..115442262-chr9:115442382..115444578,2	MCF-7	breast:
47	chr9:115421830..115423698-chr9:115425235..115427164,2	K562	blood:
48	chr9:115512668..115515460-chr9:115534425..115536617,2	K562	blood:
49	chr9:115520162..115522782-chr9:115581748..115584081,2	MCF-7	breast:
50	chr9:115503663..115506191-chr9:115515083..115517470,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC46A2-4	chr9:115480267-115480397	NONHSAT134023
2	lnc-C9orf80-1	chr9:115512686-115512736	XLOC_007830
3	lnc-KIAA1958-1	chr9:115454118-115454181	NONHSAT134022
4	lnc-KIAA1958-1	chr9:115453057-115453265	NONHSAT134022
5	lnc-C9orf80-1	chr9:115505051-115505514	XLOC_007830
6	lnc-KIAA1958-1	chr9:115484007-115484956	NONHSAT134022
7	lnc-C9orf80-1	chr9:115511360-115512795	XLOC_007830
8	lnc-SLC46A2-4	chr9:115478741-115478821	NONHSAT134023
9	lnc-SNX30-2	chr9:115390750-115391983	NONHSAT134020
10	lnc-C9orf80-1	chr9:115511182-115511550	XLOC_007830
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
ENSG00000150760	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000148158	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000173473	chromatin interactions
ENSG00000148153	chromatin interactions
ENSG00000271631	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000119471	chromatin interactions
ENSG00000230185	chromatin interactions
ENSG00000165185	chromatin interactions
SETD8	miRNA target sites

Extended variants
information (count: 8527 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:8527 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2676624	chr9:115359049-115359050	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567768816	chr9:115359077-115359078	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530110929	chr9:115359097-115359098	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186596207	chr9:115359109-115359110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566517753	chr9:115359162-115359163	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549440950	chr9:115359179-115359180	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs538991089	chr9:115359180-115359181	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs200141715	chr9:115359302-115359303	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs398011905	chr9:115359305-115359306	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs56737604	chr9:115359306-115359307	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147932725	chr9:115359378-115359379	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567206234	chr9:115359440-115359441	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs554839041	chr9:115359463-115359464	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs148968871	chr9:115359504-115359505	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs542731186	chr9:115359519-115359520	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553046722	chr9:115359563-115359564	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs572873031	chr9:115359587-115359588	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs544631546	chr9:115359628-115359629	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142918774	chr9:115359657-115359658	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs114658368	chr9:115359696-115359697	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370963136	chr9:115359751-115359752	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs115651892	chr9:115359799-115359800	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs564428587	chr9:115359868-115359869	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534473136	chr9:115359923-115359924	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373573477	chr9:115359938-115359939	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544423233	chr9:115360091-115360092	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs560732540	chr9:115360145-115360146	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs578236438	chr9:115360146-115360147	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371107278	chr9:115360148-115360149	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs530173362	chr9:115360218-115360219	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs559839032	chr9:115360223-115360224	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs191341864	chr9:115360237-115360238	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs566577355	chr9:115360246-115360247	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs532376826	chr9:115360252-115360253	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs151125751	chr9:115360267-115360268	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs569553970	chr9:115360275-115360276	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs374376119	chr9:115360290-115360291	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs538137553	chr9:115360336-115360337	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528342225	chr9:115360354-115360355	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs141086923	chr9:115360356-115360357	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs145011616	chr9:115360463-115360464	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs536402073	chr9:115360477-115360478	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs138795854	chr9:115360486-115360487	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570838764	chr9:115360487-115360488	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2806315	chr9:115360505-115360506	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs556619457	chr9:115360511-115360512	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370838471	chr9:115360520-115360521	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538645581	chr9:115360557-115360558	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs558240860	chr9:115360570-115360571	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs575527989	chr9:115360606-115360607	Weak transcription Enhancers	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:5223 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115337600-115363800	Weak transcription	Fetal Stomach	stomach
2	chr9:115337600-115380200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:115337800-115377800	Weak transcription	Dnd41	blood
4	chr9:115338400-115379800	Weak transcription	Primary B cells from cord blood	blood
5	chr9:115344400-115360600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:115344400-115363200	Weak transcription	Aorta	Aorta
7	chr9:115344400-115380200	Weak transcription	Gastric	stomach
8	chr9:115345200-115361000	Weak transcription	Fetal Intestine Small	intestine
9	chr9:115345600-115360400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr9:115345600-115369600	Weak transcription	Fetal Intestine Large	intestine
11	chr9:115346400-115385000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr9:115346800-115377800	Weak transcription	HepG2	liver
13	chr9:115352600-115359400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr9:115352600-115360600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr9:115353000-115359800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr9:115356400-115360200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:115356800-115359800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:115357200-115359200	Weak transcription	GM12878-XiMat	blood
19	chr9:115358200-115380000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr9:115359000-115360000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:115359000-115360000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr9:115359000-115361000	Enhancers	Brain Germinal Matrix	brain
23	chr9:115359200-115359400	Enhancers	GM12878-XiMat	blood
24	chr9:115359200-115359600	Enhancers	Brain Hippocampus Middle	brain
25	chr9:115359200-115359800	Enhancers	Brain Angular Gyrus	brain
26	chr9:115359200-115360600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr9:115359400-115359800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr9:115359400-115359800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr9:115359400-115360000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr9:115359400-115360000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:115359400-115360000	Enhancers	Brain Anterior Caudate	brain
32	chr9:115359400-115360000	Flanking Active TSS	GM12878-XiMat	blood
33	chr9:115359400-115360000	Enhancers	HMEC	breast
34	chr9:115359400-115360600	Enhancers	NHEK	skin
35	chr9:115359600-115360000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr9:115359600-115360000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr9:115359600-115360000	Enhancers	Brain Cingulate Gyrus	brain
38	chr9:115359600-115360200	Enhancers	Ovary	ovary
39	chr9:115359600-115368200	Weak transcription	Brain Hippocampus Middle	brain
40	chr9:115359800-115360000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr9:115359800-115360600	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr9:115359800-115360600	Enhancers	Brain Substantia Nigra	brain
43	chr9:115359800-115380400	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr9:115360000-115360400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr9:115360000-115360400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr9:115360000-115360600	Enhancers	GM12878-XiMat	blood
47	chr9:115360000-115362200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr9:115360200-115360600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:115360200-115360600	Weak transcription	Ovary	ovary
50	chr9:115360400-115360600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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