Variant report

Variant	esv1794590
Chromosome Location	chr2:112005278-112369881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4107)
CpG islands
(count:305)
Chromatin interactive
region (count:9)
LncRNA
region (count:88)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4107 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
2	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
3	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:112221794-112221988	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:112286629-112286892	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
7	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
8	ARID3A	chr2:112279969-112280556	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
10	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
11	ATF1	chr2:112251003-112251203	K562	blood:	n/a	n/a
12	ATF1	chr2:112252616-112252812	K562	blood:	n/a	n/a
13	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
14	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
15	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
16	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
17	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
18	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
19	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
20	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
21	ATF2	chr2:112236677-112236938	GM12878	blood:	n/a	n/a
22	ATF3	chr2:112292952-112293475	HepG2	liver:	n/a	chr2:112293252-112293272 chr2:112293263-112293272
23	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
24	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
25	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
26	BACH1	chr2:112251425-112251440	K562	blood:	n/a	n/a
27	BATF	chr2:112267135-112267389	GM12878	blood:	n/a	n/a
28	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a
29	BATF	chr2:112327815-112328182	GM12878	blood:	n/a	n/a
30	BATF	chr2:112240605-112241034	GM12878	blood:	n/a	chr2:112240788-112240798
31	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
32	BATF	chr2:112209363-112210356	GM12878	blood:	n/a	n/a
33	BATF	chr2:112236428-112237126	GM12878	blood:	n/a	n/a
34	BATF	chr2:112285289-112285637	GM12878	blood:	n/a	n/a
35	BATF	chr2:112303521-112304031	GM12878	blood:	n/a	chr2:112303735-112303744
36	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
37	BATF	chr2:112237987-112238183	GM12878	blood:	n/a	n/a
38	BATF	chr2:112195786-112196106	GM12878	blood:	n/a	n/a
39	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
40	BATF	chr2:112220893-112221142	GM12878	blood:	n/a	n/a
41	BATF	chr2:112221408-112221914	GM12878	blood:	n/a	n/a
42	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
43	BATF	chr2:112248607-112249357	GM12878	blood:	n/a	n/a
44	BATF	chr2:112195321-112195643	GM12878	blood:	n/a	chr2:112195574-112195583
45	BATF	chr2:112221520-112221892	GM12878	blood:	n/a	n/a
46	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
47	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
48	BATF	chr2:112248667-112249139	GM12878	blood:	n/a	n/a
49	BATF	chr2:112049811-112050042	GM12878	blood:	n/a	n/a
50	BATF	chr2:112250737-112250940	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124118-112124168	ovcar-3	ovarian:	n/a
2	chr2:112280286-112280336	HepG2	liver:	n/a
3	chr2:112252254-112252304	HRPEpiC	eye:	n/a
4	chr2:112124380-112124430	MCF-7	breast:	n/a
5	chr2:112252254-112252304	HCT-116	colon:	n/a
6	chr2:112280286-112280336	LNCaP	prostate:	n/a
7	chr2:112124118-112124168	Jurkat	blood:	n/a
8	chr2:112124380-112124430	HRPEpiC	eye:	n/a
9	chr2:112293267-112293317	GM19239	blood:	n/a
10	chr2:112252254-112252304	NB4	blood:	n/a
11	chr2:112293267-112293317	SK-N-SH_RA	brain:	n/a
12	chr2:112280286-112280336	ovcar-3	ovarian:	n/a
13	chr2:112124118-112124168	CMK	blood:	n/a
14	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
15	chr2:112124380-112124430	HUVEC	blood vessel:	n/a
16	chr2:112252254-112252304	SAEC	small airway:	n/a
17	chr2:112124380-112124430	IMR90	lung:	fetal
18	chr2:112252254-112252304	NT2-D1	testis:	n/a
19	chr2:112124380-112124430	AoSMC	blood vessel:	n/a
20	chr2:112124380-112124430	Caco-2	colon:	n/a
21	chr2:112124380-112124430	K562	blood:	n/a
22	chr2:112280286-112280336	HRCEpiC	kidney:	n/a
23	chr2:112280286-112280336	A549	lung:	n/a
24	chr2:112293267-112293317	Jurkat	blood:	n/a
25	chr2:112280286-112280336	HEK293	kidney:	embryo
26	chr2:112124380-112124430	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:112280286-112280336	AG10803	skin:	n/a
28	chr2:112252254-112252304	SK-N-MC	brain:	n/a
29	chr2:112293267-112293317	Caco-2	colon:	n/a
30	chr2:112124380-112124430	RPTEC	kidney:	n/a
31	chr2:112293267-112293317	AG09309	skin:	n/a
32	chr2:112293267-112293317	ovcar-3	ovarian:	n/a
33	chr2:112280286-112280336	Caco-2	colon:	n/a
34	chr2:112280286-112280336	HRE	kidney:	n/a
35	chr2:112280286-112280336	NT2-D1	testis:	n/a
36	chr2:112280286-112280336	GM19239	blood:	n/a
37	chr2:112252254-112252304	PrEC	prostate:	n/a
38	chr2:112124380-112124430	NB4	blood:	n/a
39	chr2:112124380-112124430	GM12891	blood:	n/a
40	chr2:112293267-112293317	HAEpiC	amniotic membrane:	n/a
41	chr2:112252254-112252304	AG10803	skin:	n/a
42	chr2:112280286-112280336	T-47D	breast:	n/a
43	chr2:112124380-112124430	ovcar-3	ovarian:	n/a
44	chr2:112124380-112124430	BE2_C	brain:	n/a
45	chr2:112124380-112124430	Hepatocyte	liver:	n/a
46	chr2:112293267-112293317	IMR90	lung:	fetal
47	chr2:112293267-112293317	CMK	blood:	n/a
48	chr2:112124118-112124168	HAEpiC	amniotic membrane:	n/a
49	chr2:112280286-112280336	HL-60	blood:	n/a
50	chr2:112124380-112124430	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:
2	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:
3	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:
4	chr2:111877393..111879713-chr2:112235053..112237981,2	K562	blood:
5	chr2:111878764..111880387-chr2:112231090..112233888,2	MCF-7	breast:
6	chr2:111877705..111880008-chr2:112211679..112213711,2	MCF-7	breast:
7	chr2:111996763..111999930-chr2:112002314..112005967,4	K562	blood:
8	chr2:112239413..112241217-chr2:112461159..112463413,2	MCF-7	breast:
9	chr2:111970999..111973382-chr2:112004350..112006635,2	MCF-7	breast:

(count:88 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112252462-112252610	ENSG00000172965.6
2	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
3	lnc-AC108463.1-3	chr2:112227215-112227564	ENSG00000172965.6
4	lnc-AC108463.1-3	chr2:112252462-112252597	ENSG00000172965.6
5	lnc-ANAPC1-3	chr2:112315990-112317514	NONHSAT073659
6	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
7	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
8	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
9	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
10	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
11	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
12	lnc-AC108463.1-3	chr2:112005725-112005818	ENSG00000172965.6
13	lnc-AC108463.1-3	chr2:112227180-112227564	ENSG00000172965.6
14	lnc-AC108463.1-2	chr2:112252134-112252388	ENSG00000224959
15	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
16	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
17	lnc-BCL2L11-3	chr2:112248850-112249239	XLOC_001625
18	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
19	lnc-BCL2L11-3	chr2:112268201-112268567	XLOC_001625
20	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
22	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
23	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073640
24	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073654
25	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
26	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073656
27	lnc-AC108463.1-3	chr2:112033908-112033997	ENSG00000172965.6
28	lnc-AC108463.1-3	chr2:112199085-112199198	ENSG00000172965.6
29	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
30	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
31	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
32	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
33	lnc-MERTK-1	chr2:112365418-112365592	XLOC_001626
34	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073656
35	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
36	lnc-AC108463.1-3	chr2:112252462-112252540	NONHSAT073639
37	lnc-BCL2L11-2	chr2:112037022-112037457	XLOC_001624
38	lnc-AC108463.1-3	chr2:112227095-112227564	ENSG00000172965.6
39	lnc-BCL2L11-2	chr2:112022860-112023040	XLOC_001624
40	lnc-MERTK-1	chr2:112369479-112370095	XLOC_001626
41	lnc-AC108463.1-3	chr2:112252462-112252602	ENSG00000172965.6
42	lnc-AC108463.1-4	chr2:112024419-112025062	NONHSAT073632
43	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
44	lnc-MERTK-1	chr2:112365277-112365592	NONHSAT073660
45	lnc-AC108463.1-3	chr2:112005725-112005818	NONHSAT073622
46	lnc-AC108463.1-3	chr2:112005725-112005822	NONHSAT073620
47	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
48	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
49	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
50	lnc-AC108463.1-3	chr2:112227364-112227376	NONHSAT073639

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
ENSG00000270190	TF binding region
ENSG00000240350	TF binding region
ENSG00000224959	TF binding region
ENSG00000225744	TF binding region
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000229118	TF binding region
ENSG00000271635	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
ENSG00000270190	CpG island
ENSG00000240350	CpG island
ENSG00000224959	CpG island
ENSG00000225744	CpG island
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000229118	CpG island
ENSG00000271635	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions
KLHL24	miRNA target sites
ASCC3	miRNA target sites
ITSN2	miRNA target sites

Extended variants
information (count: 9034 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:9034 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536930391	chr2:112005324-112005325	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143715445	chr2:112005343-112005344	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550713626	chr2:112005362-112005363	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13017148	chr2:112005393-112005394	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540212008	chr2:112005413-112005414	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560432369	chr2:112005414-112005415	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545538236	chr2:112005484-112005485	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79768304	chr2:112005488-112005489	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577287377	chr2:112005511-112005512	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539866179	chr2:112005512-112005513	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116458229	chr2:112005527-112005528	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148078005	chr2:112005594-112005595	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542552435	chr2:112005631-112005632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562753020	chr2:112005675-112005676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180724324	chr2:112005683-112005684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551519617	chr2:112005685-112005686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565398187	chr2:112005813-112005814	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs186364586	chr2:112005888-112005889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189246977	chr2:112005899-112005900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567656204	chr2:112005934-112005935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2879937	chr2:112005953-112005954	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181660552	chr2:112005955-112005956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550210597	chr2:112005961-112005962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4595974	chr2:112006019-112006020	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs370649651	chr2:112006033-112006034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13431174	chr2:112006059-112006060	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186727172	chr2:112006062-112006063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377623179	chr2:112006124-112006125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577348760	chr2:112006161-112006162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143856545	chr2:112006195-112006196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564023852	chr2:112006198-112006199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573302926	chr2:112006212-112006213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191629714	chr2:112006224-112006225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542566149	chr2:112006236-112006237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs938096	chr2:112006339-112006340	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548243410	chr2:112006397-112006398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559173618	chr2:112006428-112006429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565056341	chr2:112006448-112006449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527827903	chr2:112006460-112006461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572533722	chr2:112006497-112006498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568136313	chr2:112006509-112006510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147004349	chr2:112006520-112006521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183032153	chr2:112006523-112006524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80152494	chr2:112006594-112006595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371929523	chr2:112006613-112006614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186359855	chr2:112006676-112006677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570277611	chr2:112006680-112006681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539299999	chr2:112006899-112006900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116771222	chr2:112006915-112006916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565929943	chr2:112006919-112006920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3024 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111954800-112006800	Weak transcription	HUVEC	blood vessel
2	chr2:111975200-112008200	Weak transcription	Pancreas	Pancrea
3	chr2:111977600-112011400	Weak transcription	A549	lung
4	chr2:111985800-112009600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr2:111993200-112008200	Weak transcription	Aorta	Aorta
6	chr2:111993200-112008200	Weak transcription	Lung	lung
7	chr2:111994000-112006800	Weak transcription	Adipose Nuclei	Adipose
8	chr2:111994000-112009600	Weak transcription	Left Ventricle	heart
9	chr2:111994400-112006600	Weak transcription	Right Ventricle	heart
10	chr2:111995600-112006200	Weak transcription	Gastric	stomach
11	chr2:111996400-112006600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr2:111996400-112009000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:111997000-112008200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:112002600-112008200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr2:112003400-112006600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr2:112003400-112006800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:112003800-112005600	Genic enhancers	HSMMtube	muscle
18	chr2:112004000-112005600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:112004000-112005600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr2:112004000-112005600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr2:112004000-112005800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:112004000-112006200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:112004000-112006200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr2:112004000-112006600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr2:112004000-112006600	Strong transcription	K562	blood
26	chr2:112004000-112006800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:112004000-112006800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:112004200-112005600	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr2:112004200-112006200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr2:112004400-112005800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:112004400-112006400	Strong transcription	NHEK	skin
32	chr2:112004400-112006600	Strong transcription	Dnd41	blood
33	chr2:112004600-112006400	Strong transcription	NH-A	brain
34	chr2:112004600-112006800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr2:112004600-112007600	Weak transcription	Ovary	ovary
36	chr2:112004600-112009200	Weak transcription	Fetal Muscle Leg	muscle
37	chr2:112005000-112005600	Genic enhancers	NHDF-Ad	bronchial
38	chr2:112005000-112006000	Strong transcription	NHLF	lung
39	chr2:112005200-112006000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:112005200-112006200	Strong transcription	HSMM	muscle
41	chr2:112005200-112006200	Strong transcription	Osteobl	bone
42	chr2:112005200-112007800	Weak transcription	HepG2	liver
43	chr2:112005200-112009000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:112005600-112007200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:112005600-112007800	Weak transcription	HSMMtube	muscle
46	chr2:112005600-112008200	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr2:112005600-112008200	Weak transcription	NHDF-Ad	bronchial
48	chr2:112005600-112008600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:112005600-112009000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr2:112005600-112015800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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