Variant report

Variant	nsv591853
Chromosome Location	chr3:138100539-138194435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1555)
CpG islands
(count:2077)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1555 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138119682-138119990	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:138161260-138161463	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:138117981-138118405	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:138129663-138129710	K562	blood:	n/a	n/a
5	ARID3A	chr3:138161304-138161671	K562	blood:	n/a	n/a
6	ATF1	chr3:138161267-138161641	K562	blood:	n/a	n/a
7	ATF3	chr3:138109096-138109544	A549	lung:	n/a	n/a
8	ATF3	chr3:138109014-138109666	HCT-116	colon:	n/a	n/a
9	BACH1	chr3:138153468-138153646	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:138153892-138154114	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:138127504-138128011	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:138129506-138129569	K562	blood:	n/a	n/a
13	BATF	chr3:138107966-138108138	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:138129486-138129880	K562	blood:	n/a	n/a
15	BHLHE40	chr3:138102722-138102828	K562	blood:	n/a	n/a
16	BHLHE40	chr3:138152952-138153745	HepG2	liver:	n/a	n/a
17	BHLHE40	chr3:138131603-138131866	K562	blood:	n/a	n/a
18	BHLHE40	chr3:138118065-138118395	HepG2	liver:	n/a	n/a
19	BHLHE40	chr3:138161357-138161658	K562	blood:	n/a	n/a
20	BHLHE40	chr3:138153048-138153470	HepG2	liver:	n/a	n/a
21	BHLHE40	chr3:138118625-138118951	HepG2	liver:	n/a	n/a
22	BHLHE40	chr3:138174985-138175101	K562	blood:	n/a	n/a
23	BHLHE40	chr3:138153202-138153422	HepG2	liver:	n/a	n/a
24	BHLHE40	chr3:138136381-138136766	HepG2	liver:	n/a	n/a
25	BHLHE40	chr3:138117959-138119029	HepG2	liver:	n/a	n/a
26	BRCA1	chr3:138109188-138109450	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr3:138136412-138136698	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr3:138136385-138136736	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr3:138108940-138109663	HCT-116	colon:	n/a	n/a
30	CBX3	chr3:138136382-138136707	K562	blood:	n/a	n/a
31	CBX3	chr3:138104995-138105351	HCT-116	colon:	n/a	n/a
32	CBX3	chr3:138129493-138129788	K562	blood:	n/a	n/a
33	CCNT2	chr3:138148699-138148899	K562	blood:	n/a	n/a
34	CCNT2	chr3:138161413-138161817	K562	blood:	n/a	n/a
35	CEBPB	chr3:138100836-138101136	K562	blood:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
36	CEBPB	chr3:138100904-138101174	A549	lung:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
37	CEBPB	chr3:138100795-138101202	HepG2	liver:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
38	CEBPB	chr3:138109232-138109558	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr3:138100783-138101235	A549	lung:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
40	CEBPB	chr3:138100811-138101182	Hela-S3	cervix:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
41	CEBPB	chr3:138154578-138154778	H1-hESC	embryonic stem cell:	n/a	chr3:138154664-138154677 chr3:138154666-138154677 chr3:138154666-138154677 chr3:138154664-138154675
42	CEBPB	chr3:138159452-138159734	A549	lung:	n/a	chr3:138159591-138159602 chr3:138159590-138159603 chr3:138159590-138159603 chr3:138159590-138159601
43	CEBPB	chr3:138100799-138101186	HepG2	liver:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
44	CEBPB	chr3:138108958-138109547	A549	lung:	n/a	n/a
45	CEBPB	chr3:138100733-138101154	ECC-1	luminal epithelium:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
46	CEBPB	chr3:138159432-138159720	K562	blood:	n/a	chr3:138159591-138159602 chr3:138159590-138159603 chr3:138159590-138159603 chr3:138159590-138159601
47	CEBPB	chr3:138159519-138159743	Hela-S3	cervix:	n/a	chr3:138159591-138159602 chr3:138159590-138159603 chr3:138159590-138159603 chr3:138159590-138159601
48	CEBPB	chr3:138119716-138120054	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:138143923-138144251	IMR90	lung:	n/a	n/a
50	CEBPB	chr3:138100750-138101178	MCF-7	breast:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998

(count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138153372-138153422	ovcar-3	ovarian:	n/a
2	chr3:138152837-138152887	HEEpiC	esophagus:	n/a
3	chr3:138160066-138160116	GM12891	blood:	n/a
4	chr3:138153372-138153422	ovcar-3	ovarian:	n/a
5	chr3:138152837-138152887	HEEpiC	esophagus:	n/a
6	chr3:138160066-138160116	GM12891	blood:	n/a
7	chr3:138167430-138167480	GM19239	blood:	n/a
8	chr3:138153763-138153813	HUVEC	blood vessel:	n/a
9	chr3:138160066-138160116	Hela-S3	cervix:	n/a
10	chr3:138101310-138101360	ovcar-3	ovarian:	n/a
11	chr3:138153278-138153328	HepG2	liver:	n/a
12	chr3:138153278-138153328	GM06990	blood:	n/a
13	chr3:138154278-138154328	HMEC	breast:	n/a
14	chr3:138109298-138109348	HIPEpiC	eye:	n/a
15	chr3:138136952-138137002	NB4	blood:	n/a
16	chr3:138153381-138153431	AG10803	skin:	n/a
17	chr3:138154620-138154670	ovcar-3	ovarian:	n/a
18	chr3:138101415-138101465	GM12878	blood:	n/a
19	chr3:138170939-138170989	BJ	skin:	n/a
20	chr3:138172124-138172174	Jurkat	blood:	n/a
21	chr3:138170552-138170602	ProgFib	skin:	n/a
22	chr3:138153168-138153218	BE2_C	brain:	n/a
23	chr3:138153357-138153407	SKMC	muscle:	n/a
24	chr3:138154754-138154804	ECC-1	luminal epithelium:	n/a
25	chr3:138169728-138169778	HCF	heart:	n/a
26	chr3:138170705-138170755	NHDF-neo	bronchial:	n/a
27	chr3:138115973-138116023	A549	lung:	n/a
28	chr3:138152837-138152887	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:138153127-138153177	HNPCEpiC	eye:	n/a
30	chr3:138153278-138153328	ProgFib	skin:	n/a
31	chr3:138128339-138128389	GM12892	blood:	n/a
32	chr3:138170766-138170816	RPTEC	kidney:	n/a
33	chr3:138160066-138160116	HEEpiC	esophagus:	n/a
34	chr3:138169728-138169778	LNCaP	prostate:	n/a
35	chr3:138160066-138160116	AG09319	gingival:	n/a
36	chr3:138136952-138137002	HRE	kidney:	n/a
37	chr3:138121287-138121337	HEK293	kidney:	embryo
38	chr3:138101310-138101360	HCF	heart:	n/a
39	chr3:138174025-138174075	HNPCEpiC	eye:	n/a
40	chr3:138170939-138170989	H1-hESC	embryonic stem cell:	embryo
41	chr3:138160066-138160116	SK-N-MC	brain:	n/a
42	chr3:138153372-138153422	HAEpiC	amniotic membrane:	n/a
43	chr3:138174025-138174075	AG09319	gingival:	n/a
44	chr3:138153170-138153220	NHDF-neo	bronchial:	n/a
45	chr3:138169728-138169778	AG10803	skin:	n/a
46	chr3:138154278-138154328	AG09309	skin:	n/a
47	chr3:138101415-138101465	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:138152837-138152887	T-47D	breast:	n/a
49	chr3:138154278-138154328	HCM	heart:	n/a
50	chr3:138121287-138121337	K562	blood:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:138186020..138187574-chr3:138189253..138191029,2	K562	blood:
2	chr3:138169355..138171117-chr3:138172389..138174530,2	MCF-7	breast:
3	chr3:138069326..138072318-chr3:138105183..138106708,2	K562	blood:
4	chr3:138152067..138153775-chr3:138169983..138172416,2	MCF-7	breast:
5	chr3:138147884..138150331-chr3:138154238..138156616,2	K562	blood:
6	chr3:137905080..137907634-chr3:138135260..138137806,2	MCF-7	breast:
7	chr3:138159991..138162907-chr3:138171980..138174435,2	MCF-7	breast:
8	chr3:138186886..138189284-chr3:138191772..138193552,2	K562	blood:
9	chr3:138108137..138110673-chr3:138113889..138116211,2	K562	blood:
10	chr3:138136501..138137088-chr3:138634470..138634998,2	K562	blood:
11	chr3:138150985..138152959-chr3:138153482..138156074,2	MCF-7	breast:
12	chr3:138108024..138110952-chr3:138113271..138115084,3	MCF-7	breast:
13	chr3:138152375..138158526-chr3:138160154..138163422,8	MCF-7	breast:
14	chr3:138108137..138110673-chr3:138113889..138116211,2	K562	blood:
15	chr3:138147884..138150331-chr3:138154238..138156616,2	K562	blood:
16	chr1:109618765..109621666-chr3:138122913..138124560,2	MCF-7	breast:
17	chr3:138065940..138068792-chr3:138150528..138153476,2	K562	blood:
18	chr3:138135853..138136964-chr3:138178372..138179276,3	MCF-7	breast:
19	chr3:138194164..138195969-chr3:138327251..138329519,2	MCF-7	breast:
20	chr3:138051070..138051808-chr3:138136099..138136657,2	MCF-7	breast:
21	chr3:138136439..138137007-chr3:138313354..138314017,2	MCF-7	breast:
22	chr3:138051022..138051610-chr3:138144950..138145530,2	MCF-7	breast:
23	chr3:138148704..138150264-chr3:138152661..138154776,2	MCF-7	breast:
24	chr3:138136047..138137057-chr3:138178340..138179089,3	MCF-7	breast:
25	chr3:138153249..138157225-chr3:138162199..138165931,3	K562	blood:
26	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
27	chr3:138049031..138051913-chr3:138117150..138118923,2	MCF-7	breast:
28	chr3:138136047..138137057-chr3:138178340..138179089,3	MCF-7	breast:
29	chr3:138159991..138162907-chr3:138171980..138174435,2	MCF-7	breast:
30	chr3:138136460..138136987-chr3:138144957..138145493,2	MCF-7	breast:
31	chr3:138134087..138136316-chr3:138150846..138153488,2	MCF-7	breast:
32	chr3:138079655..138082250-chr3:138142327..138144870,2	K562	blood:
33	chr3:138066927..138067654-chr3:138136135..138137134,2	MCF-7	breast:
34	chr3:138153677..138156615-chr3:138182530..138184739,2	MCF-7	breast:
35	chr3:138136384..138136956-chr3:139280690..139281277,2	K562	blood:
36	chr3:138130760..138133096-chr3:138134779..138137650,2	MCF-7	breast:
37	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
38	chr3:138143800..138147354-chr3:138150796..138153111,3	MCF-7	breast:
39	chr3:138094416..138096515-chr3:138105748..138108016,2	MCF-7	breast:
40	chr3:138151622..138154032-chr3:138155099..138156633,2	K562	blood:
41	chr3:138150985..138152959-chr3:138153482..138156074,2	MCF-7	breast:
42	chr3:138112036..138114862-chr3:138120590..138122113,2	K562	blood:
43	chr3:138186886..138189284-chr3:138191772..138193552,2	K562	blood:
44	chr3:138185730..138189738-chr3:138190908..138194397,4	MCF-7	breast:
45	chr3:138173174..138174919-chr3:138181076..138182864,2	MCF-7	breast:
46	chr3:138185730..138189738-chr3:138190908..138194397,4	MCF-7	breast:
47	chr3:138135853..138136964-chr3:138178372..138179276,3	MCF-7	breast:
48	chr3:138169355..138171117-chr3:138172389..138174530,2	MCF-7	breast:
49	chr3:138153677..138156615-chr3:138182530..138184739,2	MCF-7	breast:
50	chr3:138099681..138102999-chr3:138104936..138107535,3	MCF-7	breast:

No data

Variant related genes	Relation type
MRAS	TF binding region
ESYT3	TF binding region
MRAS	CpG island
ESYT3	CpG island
ENSG00000158186	chromatin interactions
ENSG00000158234	chromatin interactions
ENSG00000114107	chromatin interactions
ENSG00000114098	chromatin interactions
ENSG00000158220	chromatin interactions

Extended variants
information (count: 3411 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3411 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1720819	chr3:138100539-138100540	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573843724	chr3:138100607-138100608	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9860895	chr3:138100630-138100631	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113595841	chr3:138100638-138100639	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79084753	chr3:138100647-138100648	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529707494	chr3:138100653-138100654	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549485472	chr3:138100678-138100679	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542866727	chr3:138100718-138100719	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552140855	chr3:138100796-138100797	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs180785581	chr3:138100797-138100798	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538033262	chr3:138100808-138100809	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551586717	chr3:138100813-138100814	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13079209	chr3:138100850-138100851	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575963366	chr3:138100972-138100973	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534516890	chr3:138101071-138101072	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs183674887	chr3:138101086-138101087	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs142299635	chr3:138101112-138101113	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs74889986	chr3:138101180-138101181	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs556681252	chr3:138101191-138101192	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs576640114	chr3:138101202-138101203	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs189459264	chr3:138101242-138101243	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs77690929	chr3:138101246-138101247	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs565119463	chr3:138101296-138101297	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs375557354	chr3:138101312-138101313	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs572203484	chr3:138101323-138101324	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs541318779	chr3:138101330-138101331	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs560691322	chr3:138101477-138101478	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34922658	chr3:138101507-138101508	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1199330	chr3:138101529-138101530	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549399480	chr3:138101546-138101547	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563022615	chr3:138101595-138101596	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532121719	chr3:138101618-138101619	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs551518760	chr3:138101629-138101630	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181386130	chr3:138101648-138101649	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534199794	chr3:138101655-138101656	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs139739692	chr3:138101730-138101731	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs556513439	chr3:138101755-138101756	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs1199329	chr3:138101788-138101789	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186577272	chr3:138101793-138101794	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556644404	chr3:138101802-138101803	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34140440	chr3:138101815-138101816	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs191800065	chr3:138101845-138101846	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558418155	chr3:138101858-138101859	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560631601	chr3:138101872-138101873	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540931908	chr3:138101895-138101896	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181746587	chr3:138101959-138101960	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149900772	chr3:138101960-138101961	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574418738	chr3:138101996-138101997	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186365587	chr3:138102013-138102014	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150067113	chr3:138102014-138102015	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1860 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138076000-138108200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:138078600-138100600	Weak transcription	NH-A	brain
3	chr3:138081600-138108200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:138083200-138100600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:138086800-138100600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:138087200-138100600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr3:138089200-138100800	Weak transcription	Fetal Lung	lung
8	chr3:138089400-138102400	Weak transcription	Spleen	Spleen
9	chr3:138090400-138119400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr3:138091400-138100800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:138094000-138104800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:138094600-138100600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:138097600-138100600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:138097600-138116000	Weak transcription	Aorta	Aorta
15	chr3:138097600-138116600	Weak transcription	Brain Germinal Matrix	brain
16	chr3:138098000-138100600	Weak transcription	Fetal Brain Female	brain
17	chr3:138098200-138104200	Enhancers	Fetal Heart	heart
18	chr3:138098400-138103800	Enhancers	Brain Substantia Nigra	brain
19	chr3:138098600-138102600	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr3:138099200-138104000	Enhancers	Right Ventricle	heart
21	chr3:138099600-138103200	Enhancers	Brain Hippocampus Middle	brain
22	chr3:138099600-138105200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr3:138099800-138101800	Enhancers	Rectal Smooth Muscle	rectum
24	chr3:138099800-138102000	Genic enhancers	HSMM	muscle
25	chr3:138099800-138103800	Enhancers	Adipose Nuclei	Adipose
26	chr3:138099800-138103800	Enhancers	Brain Anterior Caudate	brain
27	chr3:138099800-138103800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr3:138099800-138103800	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr3:138099800-138104000	Enhancers	Left Ventricle	heart
30	chr3:138099800-138104200	Enhancers	Placenta	Placenta
31	chr3:138099800-138104200	Enhancers	Right Atrium	heart
32	chr3:138100000-138100600	Enhancers	Stomach Smooth Muscle	stomach
33	chr3:138100000-138101600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr3:138100000-138101600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr3:138100000-138101800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr3:138100000-138102600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr3:138100000-138102600	Enhancers	Colon Smooth Muscle	Colon
38	chr3:138100000-138103600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr3:138100000-138103800	Enhancers	Brain Angular Gyrus	brain
40	chr3:138100000-138103800	Enhancers	Brain Cingulate Gyrus	brain
41	chr3:138100000-138104000	Genic enhancers	HSMMtube	muscle
42	chr3:138100200-138100800	Enhancers	Fetal Muscle Trunk	muscle
43	chr3:138100200-138100800	Genic enhancers	Fetal Muscle Leg	muscle
44	chr3:138100200-138101000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:138100200-138101400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr3:138100200-138101600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:138100200-138101600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr3:138100200-138101600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr3:138100200-138101600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr3:138100200-138101600	Enhancers	Rectal Mucosa Donor 29	rectum

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