Variant report

Variant	nsv614934
Chromosome Location	chr9:100482976-100550253
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:665)
CpG islands
(count:244)
Chromatin interactive
region (count:81)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:100522217-100522716	HepG2	liver:	n/a	n/a
2	ATF1	chr9:100507670-100507870	K562	blood:	n/a	n/a
3	ATF1	chr9:100536068-100536427	K562	blood:	n/a	n/a
4	ATF3	chr9:100499783-100500073	K562	blood:	n/a	n/a
5	BACH1	chr9:100503546-100504031	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr9:100533100-100533466	GM12878	blood:	n/a	n/a
7	BCL3	chr9:100533177-100533483	GM12878	blood:	n/a	n/a
8	BCL3	chr9:100531930-100532150	GM12878	blood:	n/a	n/a
9	BCL3	chr9:100531952-100532178	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:100506356-100506671	K562	blood:	n/a	n/a
11	BHLHE40	chr9:100528999-100529205	K562	blood:	n/a	n/a
12	BRCA1	chr9:100514223-100514234	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr9:100541894-100542246	K562	blood:	n/a	n/a
14	CBX3	chr9:100504852-100505222	K562	blood:	n/a	n/a
15	CBX3	chr9:100537770-100538025	K562	blood:	n/a	n/a
16	CBX3	chr9:100541948-100542223	K562	blood:	n/a	n/a
17	CCNT2	chr9:100503632-100504021	K562	blood:	n/a	chr9:100503895-100503915
18	CEBPB	chr9:100548697-100548970	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:100548695-100548976	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:100522215-100522730	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:100523349-100523429	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr9:100522230-100522721	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:100500451-100500621	A549	lung:	n/a	n/a
24	CEBPB	chr9:100522362-100522557	A549	lung:	n/a	n/a
25	CEBPB	chr9:100515809-100515923	H1-hESC	embryonic stem cell:	n/a	chr9:100515829-100515840
26	CEBPB	chr9:100501427-100501617	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:100531272-100531462	K562	blood:	n/a	chr9:100531395-100531406
28	CEBPB	chr9:100515690-100516012	K562	blood:	n/a	chr9:100515829-100515840
29	CEBPB	chr9:100515665-100516004	IMR90	lung:	n/a	chr9:100515829-100515840
30	CEBPB	chr9:100498341-100498367	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:100515682-100515988	A549	lung:	n/a	chr9:100515829-100515840
32	CEBPB	chr9:100531225-100531440	IMR90	lung:	n/a	chr9:100531395-100531406
33	CEBPB	chr9:100522269-100522551	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:100548756-100548956	K562	blood:	n/a	n/a
35	CEBPB	chr9:100530841-100530904	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:100515672-100516005	HepG2	liver:	n/a	chr9:100515829-100515840
37	CEBPB	chr9:100498246-100498392	K562	blood:	n/a	n/a
38	CEBPB	chr9:100531089-100531703	Hela-S3	cervix:	n/a	chr9:100531395-100531406
39	CEBPB	chr9:100498299-100498393	A549	lung:	n/a	n/a
40	CEBPB	chr9:100494668-100494762	HepG2	liver:	n/a	chr9:100494719-100494730
41	CEBPB	chr9:100528374-100528749	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr9:100530859-100530860	A549	lung:	n/a	n/a
43	CEBPB	chr9:100500492-100500608	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:100522225-100522691	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:100531365-100531723	HepG2	liver:	n/a	chr9:100531395-100531406
46	CEBPD	chr9:100522078-100522324	HepG2	liver:	n/a	n/a
47	CHD2	chr9:100506463-100506544	HepG2	liver:	n/a	n/a
48	CHD2	chr9:100503249-100504075	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr9:100499787-100499994	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr9:100506368-100506568	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:100510201-100510251	HRPEpiC	eye:	n/a
2	chr9:100510201-100510251	HMEC	breast:	n/a
3	chr9:100504065-100504115	A549	lung:	n/a
4	chr9:100502850-100502900	CMK	blood:	n/a
5	chr9:100504065-100504115	RPTEC	kidney:	n/a
6	chr9:100502742-100502792	HCPEpiC	choroid plexus:	n/a
7	chr9:100510201-100510251	HNPCEpiC	eye:	n/a
8	chr9:100510201-100510251	NHDF-neo	bronchial:	n/a
9	chr9:100502850-100502900	HepG2	liver:	n/a
10	chr9:100510201-100510251	AoSMC	blood vessel:	n/a
11	chr9:100510201-100510251	SK-N-SH_RA	brain:	n/a
12	chr9:100504065-100504115	HAEpiC	amniotic membrane:	n/a
13	chr9:100502742-100502792	GM12878	blood:	n/a
14	chr9:100504065-100504115	BJ	skin:	n/a
15	chr9:100504065-100504115	SKMC	muscle:	n/a
16	chr9:100502850-100502900	GM12878	blood:	n/a
17	chr9:100504065-100504115	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:100502850-100502900	GM12891	blood:	n/a
19	chr9:100510201-100510251	HUVEC	blood vessel:	n/a
20	chr9:100502850-100502900	HRE	kidney:	n/a
21	chr9:100510201-100510251	AG09319	gingival:	n/a
22	chr9:100502742-100502792	BE2_C	brain:	n/a
23	chr9:100502742-100502792	AG09309	skin:	n/a
24	chr9:100504065-100504115	CMK	blood:	n/a
25	chr9:100502742-100502792	SK-N-MC	brain:	n/a
26	chr9:100502742-100502792	SK-N-SH_RA	brain:	n/a
27	chr9:100504065-100504115	AG09319	gingival:	n/a
28	chr9:100502742-100502792	NT2-D1	testis:	n/a
29	chr9:100502742-100502792	NHBE	bronchial:	n/a
30	chr9:100502850-100502900	RPTEC	kidney:	n/a
31	chr9:100502742-100502792	BJ	skin:	n/a
32	chr9:100502742-100502792	HRE	kidney:	n/a
33	chr9:100510201-100510251	HPAEpiC	pulmonary alveolar:	n/a
34	chr9:100502850-100502900	MCF10A-Er-Src	breast:	n/a
35	chr9:100510201-100510251	Hela-S3	cervix:	n/a
36	chr9:100504065-100504115	HRPEpiC	eye:	n/a
37	chr9:100502742-100502792	HepG2	liver:	n/a
38	chr9:100502850-100502900	K562	blood:	n/a
39	chr9:100502850-100502900	HUVEC	blood vessel:	n/a
40	chr9:100510201-100510251	A549	lung:	n/a
41	chr9:100504065-100504115	HEK293	kidney:	embryo
42	chr9:100510201-100510251	BJ	skin:	n/a
43	chr9:100510201-100510251	SKMC	muscle:	n/a
44	chr9:100502742-100502792	LNCaP	prostate:	n/a
45	chr9:100502742-100502792	GM12892	blood:	n/a
46	chr9:100502742-100502792	MCF-7	breast:	n/a
47	chr9:100504065-100504115	GM06990	blood:	n/a
48	chr9:100502742-100502792	PANC-1	pancreas:	n/a
49	chr9:100502742-100502792	IMR90	lung:	fetal
50	chr9:100504065-100504115	PrEC	prostate:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:100490724..100492306-chr9:100494376..100496011,2	K562	blood:
2	chr9:100511988..100512975-chr9:100652311..100652871,4	MCF-7	breast:
3	chr20:47360676..47363617-chr9:100509407..100511558,2	MCF-7	breast:
4	chr9:100531338..100533176-chr9:100533250..100535001,2	K562	blood:
5	chr9:100491615..100493759-chr9:100496731..100498823,2	K562	blood:
6	chr9:100490447..100493759-chr9:100496731..100499744,4	K562	blood:
7	chr9:100532701..100535323-chr9:100542602..100545758,3	MCF-7	breast:
8	chr12:122517991..122518971-chr9:100536663..100537421,2	Hela-S3	cervix:
9	chr9:100508324..100510279-chr9:100516593..100518821,3	K562	blood:
10	chr9:100501919..100504802-chr9:100515954..100517460,2	K562	blood:
11	chr9:100455758..100458745-chr9:100534997..100536831,2	K562	blood:
12	chr9:100490724..100492306-chr9:100494376..100496011,2	K562	blood:
13	chr9:100514901..100517878-chr9:100521505..100523332,2	K562	blood:
14	chr9:100501919..100504802-chr9:100515954..100517460,2	K562	blood:
15	chr9:100519613..100522363-chr9:100523340..100525819,2	K562	blood:
16	chr9:100471241..100474154-chr9:100481493..100483041,2	K562	blood:
17	chr9:100530381..100532814-chr9:100532881..100535803,2	MCF-7	breast:
18	chr9:100503142..100505275-chr9:100512495..100514714,2	MCF-7	breast:
19	chr9:100510873..100512697-chr9:100522952..100525566,2	MCF-7	breast:
20	chr9:100503142..100505275-chr9:100512495..100514714,2	MCF-7	breast:
21	chr9:100481943..100484213-chr9:100684517..100686414,2	MCF-7	breast:
22	chr9:100503377..100504989-chr9:100510733..100512469,2	MCF-7	breast:
23	chr9:100496207..100499449-chr9:100501174..100504756,3	MCF-7	breast:
24	chr9:100501080..100504475-chr9:100513042..100515549,3	K562	blood:
25	chr9:100476626..100478474-chr9:100481765..100484991,3	MCF-7	breast:
26	chr9:100394686..100396632-chr9:100483638..100486483,2	MCF-7	breast:
27	chr9:100528937..100530582-chr9:100549177..100551177,2	K562	blood:
28	chr9:100480674..100483581-chr9:100484932..100487285,2	K562	blood:
29	chr9:100477106..100478683-chr9:100480479..100483251,2	MCF-7	breast:
30	chr9:100513670..100516311-chr9:100564353..100566639,2	MCF-7	breast:
31	chr9:100483705..100485989-chr9:100486600..100490449,4	K562	blood:
32	chr9:100512417..100513062-chr9:100654481..100655001,2	MCF-7	breast:
33	chr9:100475449..100479903-chr9:100484059..100486391,3	MCF-7	breast:
34	chr9:100521393..100523336-chr9:100532827..100534532,2	MCF-7	breast:
35	chr9:100510873..100512697-chr9:100522952..100525566,2	MCF-7	breast:
36	chr9:100459040..100460602-chr9:100535693..100538522,2	MCF-7	breast:
37	chr9:100519613..100522363-chr9:100523340..100525819,2	K562	blood:
38	chr9:100530381..100532814-chr9:100532881..100535803,2	MCF-7	breast:
39	chr9:100478863..100481337-chr9:100486347..100488581,2	MCF-7	breast:
40	chr9:100529991..100532148-chr9:100565472..100567018,2	MCF-7	breast:
41	chr9:100513746..100515614-chr9:100528271..100531174,2	K562	blood:
42	chr9:100501560..100504087-chr9:100522833..100525239,2	K562	blood:
43	chr9:100491615..100493759-chr9:100496731..100498823,2	K562	blood:
44	chr9:100532701..100535323-chr9:100542602..100545758,3	MCF-7	breast:
45	chr9:100483705..100485989-chr9:100486600..100490449,4	K562	blood:
46	chr9:100548531..100552481-chr9:100563456..100568278,5	MCF-7	breast:
47	chr9:100501080..100504475-chr9:100513042..100515549,3	K562	blood:
48	chr9:100490447..100493759-chr9:100496731..100499744,4	K562	blood:
49	chr9:100514901..100517878-chr9:100521505..100523332,2	K562	blood:
50	chr9:100532556..100536215-chr9:100536880..100540277,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NCBP1-1	chr9:100505490-100505852	NONHSAT133532
2	lnc-NCBP1-1	chr9:100505868-100507217	NONHSAT133532
3	lnc-NCBP1-1	chr9:100505490-100507217	ENSG00000260677.1

No data

Variant related genes	Relation type
ENSG00000260677	TF binding region
ENSG00000260677	CpG island
ENSG00000136937	chromatin interactions
ENSG00000136932	chromatin interactions
ENSG00000214417	chromatin interactions
ENSG00000136938	chromatin interactions
ENSG00000136925	chromatin interactions
ENSG00000136936	chromatin interactions

Extended variants
information (count: 2359 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2359 , 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	rs953199	chr9:100482976-100482977	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78512686	chr9:100482995-100482996	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142235919	chr9:100483008-100483009	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537531419	chr9:100483016-100483017	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549413814	chr9:100483025-100483026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571177385	chr9:100483055-100483056	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189674588	chr9:100483069-100483070	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2668796	chr9:100483138-100483139	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs182349738	chr9:100483188-100483189	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs368801695	chr9:100483189-100483190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547036294	chr9:100483243-100483244	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs150767716	chr9:100483246-100483247	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs186924351	chr9:100483269-100483270	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs57898891	chr9:100483283-100483284	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs139171141	chr9:100483292-100483293	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376477681	chr9:100483307-100483308	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs191822828	chr9:100483333-100483334	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs77730198	chr9:100483351-100483352	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs11794042	chr9:100483370-100483371	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs527569628	chr9:100483387-100483388	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548798581	chr9:100483408-100483409	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560738749	chr9:100483447-100483448	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs145236246	chr9:100483450-100483451	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571221265	chr9:100483487-100483488	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs147577998	chr9:100483497-100483498	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs571170825	chr9:100483516-100483517	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs532104969	chr9:100483526-100483527	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547059489	chr9:100483566-100483567	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs567190356	chr9:100483663-100483664	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs534488664	chr9:100483667-100483668	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs113605332	chr9:100483714-100483715	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs183316904	chr9:100483740-100483741	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs113035822	chr9:100483780-100483781	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs188253338	chr9:100483812-100483813	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs78926591	chr9:100483827-100483828	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs368903104	chr9:100483840-100483841	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs577976243	chr9:100483861-100483862	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs533265360	chr9:100483901-100483902	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs114106225	chr9:100483903-100483904	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs2668795	chr9:100483916-100483917	Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs572344895	chr9:100483935-100483936	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs542467412	chr9:100484035-100484036	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs560758750	chr9:100484063-100484064	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs531369222	chr9:100484066-100484067	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs193155840	chr9:100484092-100484093	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs565021985	chr9:100484127-100484128	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs532095302	chr9:100484144-100484145	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs11792527	chr9:100484180-100484181	Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs565538608	chr9:100484210-100484211	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs527992588	chr9:100484318-100484319	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100482600-100483000	ZNF genes & repeats	HSMMtube	muscle
2	chr9:100483000-100483400	Weak transcription	HSMMtube	muscle
3	chr9:100483400-100485000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:100483400-100485000	Enhancers	HSMMtube	muscle
5	chr9:100483600-100484000	Enhancers	HSMM	muscle
6	chr9:100484200-100485000	Enhancers	HepG2	liver
7	chr9:100486000-100486600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr9:100486200-100486800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:100486800-100490600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:100488200-100488400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr9:100489800-100490800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:100490600-100491000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:100490600-100491000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:100491000-100503200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:100492600-100492800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:100492600-100493000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:100492800-100503200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:100493000-100503000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:100495000-100495800	Enhancers	Fetal Intestine Large	intestine
20	chr9:100495200-100496000	Enhancers	Fetal Intestine Small	intestine
21	chr9:100495400-100495800	Enhancers	HepG2	liver
22	chr9:100495800-100496200	Weak transcription	HepG2	liver
23	chr9:100495800-100502600	Weak transcription	Fetal Intestine Large	intestine
24	chr9:100496200-100496800	Enhancers	HepG2	liver
25	chr9:100497000-100497800	Enhancers	Esophagus	oesophagus
26	chr9:100497400-100497600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr9:100499400-100499600	Flanking Active TSS	K562	blood
28	chr9:100499600-100500200	Active TSS	K562	blood
29	chr9:100499600-100500400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:100499600-100500400	Enhancers	Hela-S3	cervix
31	chr9:100499800-100500000	Bivalent Enhancer	Placenta	Placenta
32	chr9:100499800-100500200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr9:100500000-100500200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr9:100500000-100500200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr9:100500000-100500200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
36	chr9:100500200-100500400	Flanking Active TSS	K562	blood
37	chr9:100500200-100503000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr9:100500400-100503000	Weak transcription	K562	blood
39	chr9:100501400-100501600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr9:100501400-100503400	Enhancers	Esophagus	oesophagus
41	chr9:100502000-100502200	Enhancers	Gastric	stomach
42	chr9:100502200-100503200	Weak transcription	Gastric	stomach
43	chr9:100502400-100503000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr9:100502600-100503200	Enhancers	Fetal Intestine Large	intestine
45	chr9:100502600-100503200	Enhancers	Fetal Intestine Small	intestine
46	chr9:100502800-100503000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr9:100502800-100503000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
48	chr9:100502800-100503000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr9:100502800-100503000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr9:100502800-100503200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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