Variant report

Variant	nsv877568
Chromosome Location	chr3:143621140-143992630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3090)
CpG islands
(count:1832)
Chromatin interactive
region (count:176)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:3090 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143693676-143695333	K562	blood:	n/a	n/a
2	ARID3A	chr3:143690276-143690865	K562	blood:	n/a	n/a
3	ARID3A	chr3:143690119-143690425	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:143692016-143692262	K562	blood:	n/a	n/a
5	ARID3A	chr3:143733861-143734419	K562	blood:	n/a	n/a
6	ARID3A	chr3:143880755-143881509	HepG2	liver:	n/a	chr3:143881380-143881396
7	ARID3A	chr3:143837779-143837958	HepG2	liver:	n/a	n/a
8	ATF1	chr3:143690072-143691003	K562	blood:	n/a	n/a
9	ATF1	chr3:143804936-143805091	K562	blood:	n/a	n/a
10	ATF1	chr3:143734003-143734287	K562	blood:	n/a	n/a
11	ATF1	chr3:143825901-143826204	K562	blood:	n/a	n/a
12	ATF1	chr3:143691998-143692250	K562	blood:	n/a	n/a
13	ATF2	chr3:143689546-143689945	GM12878	blood:	n/a	n/a
14	ATF2	chr3:143689913-143690495	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr3:143751294-143752090	GM12878	blood:	n/a	n/a
16	ATF2	chr3:143689986-143690694	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr3:143846788-143847440	GM12878	blood:	n/a	n/a
18	ATF2	chr3:143690518-143690969	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr3:143696616-143697247	GM12878	blood:	n/a	n/a
20	ATF2	chr3:143848494-143849137	GM12878	blood:	n/a	n/a
21	ATF2	chr3:143747447-143748199	GM12878	blood:	n/a	n/a
22	ATF2	chr3:143690239-143690706	GM12878	blood:	n/a	n/a
23	ATF2	chr3:143846465-143847491	GM12878	blood:	n/a	n/a
24	ATF2	chr3:143751298-143751934	GM12878	blood:	n/a	n/a
25	ATF2	chr3:143691190-143692375	GM12878	blood:	n/a	n/a
26	ATF2	chr3:143747393-143748103	GM12878	blood:	n/a	n/a
27	ATF2	chr3:143689985-143691159	GM12878	blood:	n/a	n/a
28	ATF2	chr3:143689642-143689972	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr3:143696796-143697225	GM12878	blood:	n/a	n/a
30	ATF2	chr3:143848478-143849143	GM12878	blood:	n/a	n/a
31	ATF3	chr3:143693632-143694035	K562	blood:	n/a	n/a
32	BACH1	chr3:143691359-143691614	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr3:143664823-143664828	K562	blood:	n/a	n/a
34	BACH1	chr3:143816071-143816361	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr3:143690053-143691021	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr3:143710544-143710680	K562	blood:	n/a	n/a
37	BACH1	chr3:143693163-143693272	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr3:143833588-143833943	K562	blood:	n/a	chr3:143833761-143833775
39	BACH1	chr3:143833582-143834019	H1-hESC	embryonic stem cell:	n/a	chr3:143833761-143833775
40	BACH1	chr3:143690304-143690487	K562	blood:	n/a	n/a
41	BACH1	chr3:143670241-143670516	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr3:143782248-143782473	K562	blood:	n/a	n/a
43	BACH1	chr3:143691840-143692192	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr3:143693737-143693998	K562	blood:	n/a	n/a
45	BATF	chr3:143751446-143751795	GM12878	blood:	n/a	n/a
46	BATF	chr3:143846881-143847436	GM12878	blood:	n/a	n/a
47	BATF	chr3:143777619-143777840	GM12878	blood:	n/a	n/a
48	BATF	chr3:143828841-143829119	GM12878	blood:	n/a	n/a
49	BATF	chr3:143777624-143777852	GM12878	blood:	n/a	n/a
50	BATF	chr3:143747542-143747965	GM12878	blood:	n/a	chr3:143747888-143747897

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143689810-143689860	HCM	heart:	n/a
2	chr3:143815849-143815899	HCM	heart:	n/a
3	chr3:143689810-143689860	HCM	heart:	n/a
4	chr3:143815849-143815899	HCM	heart:	n/a
5	chr3:143692146-143692196	HCM	heart:	n/a
6	chr3:143689810-143689860	PANC-1	pancreas:	n/a
7	chr3:143692056-143692106	PrEC	prostate:	n/a
8	chr3:143690246-143690296	NHDF-neo	bronchial:	n/a
9	chr3:143690145-143690195	HCT-116	colon:	n/a
10	chr3:143690246-143690296	HepG2	liver:	n/a
11	chr3:143692320-143692370	HRCEpiC	kidney:	n/a
12	chr3:143692087-143692137	BE2_C	brain:	n/a
13	chr3:143689972-143690022	AG09319	gingival:	n/a
14	chr3:143690208-143690258	BE2_C	brain:	n/a
15	chr3:143690741-143690791	HRPEpiC	eye:	n/a
16	chr3:143690246-143690296	K562	blood:	n/a
17	chr3:143695141-143695191	GM12892	blood:	n/a
18	chr3:143692785-143692835	HNPCEpiC	eye:	n/a
19	chr3:143690928-143690978	CMK	blood:	n/a
20	chr3:143692006-143692056	PANC-1	pancreas:	n/a
21	chr3:143691409-143691459	ECC-1	luminal epithelium:	n/a
22	chr3:143689584-143689634	K562	blood:	n/a
23	chr3:143689916-143689966	RPTEC	kidney:	n/a
24	chr3:143692134-143692184	GM12878	blood:	n/a
25	chr3:143815849-143815899	HIPEpiC	eye:	n/a
26	chr3:143690991-143691041	BE2_C	brain:	n/a
27	chr3:143692320-143692370	Hela-S3	cervix:	n/a
28	chr3:143690991-143691041	HCF	heart:	n/a
29	chr3:143690495-143690545	HAEpiC	amniotic membrane:	n/a
30	chr3:143703954-143704004	AG09319	gingival:	n/a
31	chr3:143689972-143690022	HAEpiC	amniotic membrane:	n/a
32	chr3:143690208-143690258	AG04449	skin:	fetal
33	chr3:143690404-143690454	Jurkat	blood:	n/a
34	chr3:143692146-143692196	CMK	blood:	n/a
35	chr3:143692255-143692305	HEK293	kidney:	embryo
36	chr3:143692255-143692305	SK-N-SH	brain:	n/a
37	chr3:143695141-143695191	ProgFib	skin:	n/a
38	chr3:143692255-143692305	HRCEpiC	kidney:	n/a
39	chr3:143815849-143815899	PrEC	prostate:	n/a
40	chr3:143692134-143692184	HIPEpiC	eye:	n/a
41	chr3:143692785-143692835	HUVEC	blood vessel:	n/a
42	chr3:143689584-143689634	HIPEpiC	eye:	n/a
43	chr3:143695141-143695191	AG04450	lung:	fetal
44	chr3:143690741-143690791	MCF-7	breast:	n/a
45	chr3:143847318-143847368	CMK	blood:	n/a
46	chr3:143692320-143692370	HCPEpiC	choroid plexus:	n/a
47	chr3:143691269-143691319	RPTEC	kidney:	n/a
48	chr3:143692255-143692305	PrEC	prostate:	n/a
49	chr3:143710453-143710503	HCT-116	colon:	n/a
50	chr3:143689810-143689860	LNCaP	prostate:	n/a

(count:176 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:143690019..143693356-chr3:143725620..143728125,4	K562	blood:
2	chr3:143672583..143675457-chr3:143688591..143691295,3	K562	blood:
3	chr3:143690019..143692645-chr3:143838592..143840602,2	MCF-7	breast:
4	chr3:143851188..143852094-chr3:143864087..143864848,2	MCF-7	breast:
5	chr3:143892267..143895225-chr3:144092173..144094543,2	MCF-7	breast:
6	chr12:49524816..49525687-chr3:143690429..143691195,2	Hela-S3	cervix:
7	chr3:143890771..143894320-chr3:143898037..143901332,4	MCF-7	breast:
8	chr3:143690286..143692409-chr3:143708074..143710291,2	K562	blood:
9	chr3:143694108..143696591-chr3:143721286..143722845,2	K562	blood:
10	chr3:143691448..143693867-chr3:143753525..143755680,2	K562	blood:
11	chr3:143970717..143972446-chr3:143972808..143975131,2	K562	blood:
12	chr3:143694211..143696611-chr3:143698183..143700521,4	K562	blood:
13	chr3:143882905..143885862-chr3:143887105..143889283,2	MCF-7	breast:
14	chr3:143693440..143695168-chr3:143824981..143826507,2	K562	blood:
15	chr3:143701901..143703424-chr3:143714628..143717411,2	K562	blood:
16	chr3:143689777..143690496-chr6:26055384..26056279,2	Hela-S3	cervix:
17	chr3:143695787..143698743-chr3:143748690..143750623,2	K562	blood:
18	chr3:143852522..143854486-chr3:143858842..143860873,2	K562	blood:
19	chr3:143804757..143807049-chr3:143809436..143811343,2	MCF-7	breast:
20	chr3:143677587..143679390-chr3:143686141..143687965,2	MCF-7	breast:
21	chr3:143797616..143799320-chr3:143802598..143805481,2	MCF-7	breast:
22	chr3:143717685..143719346-chr3:143782583..143784716,2	K562	blood:
23	chr3:143691612..143693749-chr3:143725620..143727478,2	K562	blood:
24	chr3:143705634..143708204-chr3:143731151..143734050,2	K562	blood:
25	chr3:143892804..143894519-chr3:143897127..143900073,2	K562	blood:
26	chr3:143604403..143605317-chr3:143669942..143670478,2	K562	blood:
27	chr3:143797616..143799320-chr3:143802598..143805481,2	MCF-7	breast:
28	chr3:143865202..143867000-chr3:143870211..143871810,2	K562	blood:
29	chr3:143701901..143703424-chr3:143714628..143717411,2	K562	blood:
30	chr3:143729064..143730884-chr3:143734825..143736583,2	MCF-7	breast:
31	chr3:143690837..143691539-chr4:113066463..113067171,2	Hela-S3	cervix:
32	chr3:143690072..143692415-chr3:143771127..143773744,2	MCF-7	breast:
33	chr3:143852522..143855348-chr3:143858842..143861138,3	K562	blood:
34	chr3:143862145..143864475-chr3:143867360..143869304,2	K562	blood:
35	chr12:16064190..16064741-chr3:143690280..143690998,2	Hela-S3	cervix:
36	chr3:143690118..143691701-chr3:143832544..143834145,2	K562	blood:
37	chr3:143970717..143972446-chr3:143972808..143975131,2	K562	blood:
38	chr3:143865202..143867000-chr3:143870211..143871810,2	K562	blood:
39	chr3:143619574..143622269-chr3:143688723..143691584,2	MCF-7	breast:
40	chr3:143648902..143651485-chr3:143654584..143656465,2	K562	blood:
41	chr3:143643732..143645627-chr3:143646287..143648927,2	MCF-7	breast:
42	chr19:57831383..57832246-chr3:143690551..143691404,2	NB4	blood:
43	chr3:143691690..143692193-chr3:143727265..143727917,2	MCF-7	breast:
44	chr3:143819810..143821704-chr3:143822907..143824829,2	K562	blood:
45	chr3:143705634..143708204-chr3:143731151..143734050,2	K562	blood:
46	chr3:143694586..143698442-chr3:143710768..143713586,3	K562	blood:
47	chr3:143690493..143693318-chr3:143755857..143758404,2	K562	blood:
48	chr3:143689026..143691160-chr3:143705975..143707584,2	MCF-7	breast:
49	chr3:143713688..143715373-chr3:143716970..143718917,3	K562	blood:
50	chr3:143804757..143807049-chr3:143809436..143811343,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST2-5	chr3:143753460-143753522	XLOC_002851
2	lnc-CHST2-5	chr3:143755567-143755742	XLOC_002851
3	lnc-C3orf58-1	chr3:143936262-143938475	NONHSAT092535

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	C3orf58	hsa-miR-155-5p	chr3:143710262-143710285
2	C3orf58	hsa-miR-148b-3p	chr3:143708801-143708808
3	C3orf58	hsa-miR-124-3p	chr3:143711129-143711148
4	C3orf58	hsa-miR-155-5p	chr3:143711059-143711081
5	C3orf58	hsa-miR-124-3p	chr3:143711141-143711147
6	C3orf58	hsa-miR-155-5p	chr3:143708824-143708847
7	C3orf58	hsa-miR-148b-3p	chr3:143708787-143708808

Variant related genes	Relation type
C3orf58	TF binding region
RNA5SP144	TF binding region
C3orf58	CpG island
RNA5SP144	CpG island
ENSG00000110700	chromatin interactions
ENSG00000174749	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000109046	chromatin interactions
ENSG00000178229	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000157593	chromatin interactions
ENSG00000196233	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000023697	chromatin interactions
ENSG00000185608	chromatin interactions
ENSG00000222778	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000181744	chromatin interactions
ENSG00000105771	chromatin interactions
ENSG00000138459	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000144848	chromatin interactions
ENSG00000269694	chromatin interactions
ENSG00000198931	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000178952	chromatin interactions
ENSG00000178188	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000100084	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000107485	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000181804	chromatin interactions
ENSG00000258017	chromatin interactions

Extended variants
information (count: 10289 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:10289 , 50 per page) page: 1 2 3 4 5 6 7 ... 206

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55884414	chr3:143621140-143621141	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565087588	chr3:143621146-143621147	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs113628533	chr3:143621189-143621190	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116501984	chr3:143621221-143621222	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs28550970	chr3:143621238-143621239	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551060326	chr3:143621259-143621260	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs116056209	chr3:143621308-143621309	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs60632557	chr3:143621311-143621312	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548491483	chr3:143621328-143621329	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs567192578	chr3:143621340-143621341	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs554526478	chr3:143621367-143621368	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184718733	chr3:143621411-143621412	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs58191086	chr3:143621434-143621435	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs78579743	chr3:143621460-143621461	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537435892	chr3:143621494-143621495	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145878351	chr3:143621500-143621501	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574192687	chr3:143621531-143621532	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7650329	chr3:143621544-143621545	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560049365	chr3:143621550-143621551	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547014530	chr3:143621560-143621561	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs77355988	chr3:143621583-143621584	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188686928	chr3:143621592-143621593	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565295610	chr3:143621593-143621594	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532584388	chr3:143621606-143621607	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368176112	chr3:143621632-143621633	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558218614	chr3:143621639-143621640	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs7628380	chr3:143621659-143621660	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs7640118	chr3:143621700-143621701	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs530125757	chr3:143621704-143621705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7628606	chr3:143621724-143621725	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs566903114	chr3:143621790-143621791	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534526652	chr3:143621797-143621798	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs552631353	chr3:143621823-143621824	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4396891	chr3:143621826-143621827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556205941	chr3:143621845-143621846	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141132094	chr3:143621877-143621878	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs191934338	chr3:143621916-143621917	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574205577	chr3:143621917-143621918	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7628788	chr3:143621935-143621936	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs150747906	chr3:143621938-143621939	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368765507	chr3:143621980-143621981	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138654795	chr3:143621997-143621998	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183743857	chr3:143621999-143622000	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188411961	chr3:143622000-143622001	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114059037	chr3:143622006-143622007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554231314	chr3:143622015-143622016	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139068448	chr3:143622069-143622070	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143521696	chr3:143622103-143622104	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562829501	chr3:143622111-143622112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572503902	chr3:143622113-143622114	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
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
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
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
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2299 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143618800-143621400	Enhancers	NHLF	lung
2	chr3:143619200-143621400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:143619200-143621400	Enhancers	HMEC	breast
4	chr3:143619400-143621600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:143619600-143621400	Enhancers	NHDF-Ad	bronchial
6	chr3:143628800-143629800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:143628800-143629800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr3:143628800-143629800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:143628800-143630000	Enhancers	HMEC	breast
10	chr3:143628800-143630000	Enhancers	NHEK	skin
11	chr3:143629800-143640400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:143637800-143647000	Enhancers	Primary B cells from peripheral blood	blood
13	chr3:143638000-143638400	Enhancers	Fetal Thymus	thymus
14	chr3:143638000-143639200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr3:143638200-143639000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr3:143638800-143639400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:143639000-143639400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:143639600-143640800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:143639800-143641000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr3:143639800-143643000	Enhancers	Primary B cells from cord blood	blood
21	chr3:143640200-143640400	Enhancers	GM12878-XiMat	blood
22	chr3:143640200-143640600	Enhancers	Primary hematopoietic stem cells	blood
23	chr3:143640200-143640800	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr3:143640200-143640800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr3:143640200-143640800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr3:143640400-143640600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr3:143640400-143640600	Weak transcription	GM12878-XiMat	blood
28	chr3:143640600-143641400	ZNF genes & repeats	GM12878-XiMat	blood
29	chr3:143640600-143643000	Weak transcription	Primary hematopoietic stem cells	blood
30	chr3:143640800-143642800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr3:143640800-143644800	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr3:143641000-143642600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr3:143641800-143643000	Weak transcription	GM12878-XiMat	blood
34	chr3:143642600-143643200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:143642800-143645600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr3:143643000-143643200	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr3:143643000-143643200	Enhancers	GM12878-XiMat	blood
38	chr3:143643000-143643600	Enhancers	Primary hematopoietic stem cells	blood
39	chr3:143643200-143643600	Enhancers	Primary B cells from cord blood	blood
40	chr3:143643200-143644000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:143643200-143644200	Flanking Active TSS	GM12878-XiMat	blood
42	chr3:143643600-143644000	Flanking Active TSS	Primary B cells from cord blood	blood
43	chr3:143643600-143644000	Active TSS	Primary hematopoietic stem cells	blood
44	chr3:143644000-143645400	Enhancers	Primary hematopoietic stem cells	blood
45	chr3:143644000-143645400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:143644000-143646000	Enhancers	Primary B cells from cord blood	blood
47	chr3:143644200-143644800	Enhancers	GM12878-XiMat	blood
48	chr3:143644800-143645400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr3:143644800-143645800	Weak transcription	GM12878-XiMat	blood
50	chr3:143645800-143646000	Enhancers	GM12878-XiMat	blood

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