Variant report

Variant	nsv1045906
Chromosome Location	chr15:56333180-56473614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:894)
CpG islands
(count:244)
Chromatin interactive
region (count:85)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56344799-56345413	K562	blood:	n/a	chr15:56345362-56345378 chr15:56345363-56345379
2	ARID3A	chr15:56335964-56336039	HepG2	liver:	n/a	n/a
3	ATF1	chr15:56334784-56334889	K562	blood:	n/a	n/a
4	ATF1	chr15:56334057-56334515	K562	blood:	n/a	n/a
5	ATF1	chr15:56344675-56345224	K562	blood:	n/a	n/a
6	ATF1	chr15:56453206-56453439	K562	blood:	n/a	n/a
7	ATF3	chr15:56332556-56333228	HCT-116	colon:	n/a	n/a
8	ATF3	chr15:56332652-56333227	HCT-116	colon:	n/a	n/a
9	BACH1	chr15:56344826-56345270	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:56453364-56453474	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr15:56336045-56336269	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:56332450-56333242	K562	blood:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
13	BHLHE40	chr15:56335509-56335704	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:56342093-56342208	K562	blood:	n/a	n/a
15	BHLHE40	chr15:56454112-56454339	K562	blood:	n/a	n/a
16	BHLHE40	chr15:56344734-56345243	K562	blood:	n/a	n/a
17	BHLHE40	chr15:56398112-56398409	GM12878	blood:	n/a	n/a
18	BRCA1	chr15:56344616-56345320	Hela-S3	cervix:	n/a	n/a
19	CCNT2	chr15:56363485-56363774	K562	blood:	n/a	n/a
20	CEBPB	chr15:56379424-56379757	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr15:56332502-56333248	HCT-116	colon:	n/a	chr15:56332904-56332915
22	CEBPB	chr15:56332556-56333287	A549	lung:	n/a	chr15:56332904-56332915
23	CEBPB	chr15:56380691-56380912	IMR90	lung:	n/a	chr15:56380793-56380806
24	CEBPB	chr15:56453175-56453518	K562	blood:	n/a	chr15:56453346-56453357
25	CEBPB	chr15:56380618-56380875	K562	blood:	n/a	chr15:56380793-56380806
26	CEBPB	chr15:56343923-56344265	A549	lung:	n/a	chr15:56344093-56344104
27	CEBPB	chr15:56351428-56351556	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr15:56410047-56410218	HepG2	liver:	n/a	chr15:56410109-56410120
29	CEBPB	chr15:56379455-56379746	A549	lung:	n/a	n/a
30	CEBPB	chr15:56331179-56333293	Hela-S3	cervix:	n/a	chr15:56332904-56332915 chr15:56331479-56331491
31	CEBPB	chr15:56379521-56379721	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:56453196-56453526	H1-hESC	embryonic stem cell:	n/a	chr15:56453346-56453357
33	CEBPB	chr15:56453264-56453399	K562	blood:	n/a	chr15:56453346-56453357
34	CEBPB	chr15:56332690-56333257	A549	lung:	n/a	chr15:56332904-56332915
35	CEBPB	chr15:56351210-56351696	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr15:56343836-56344412	Hela-S3	cervix:	n/a	chr15:56344093-56344104
37	CEBPB	chr15:56334144-56335345	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr15:56344614-56345304	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr15:56453185-56453525	Hela-S3	cervix:	n/a	chr15:56453346-56453357
40	CEBPB	chr15:56343972-56344272	HepG2	liver:	n/a	chr15:56344093-56344104
41	CEBPB	chr15:56441338-56441588	IMR90	lung:	n/a	n/a
42	CEBPB	chr15:56463512-56463724	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr15:56421457-56421593	K562	blood:	n/a	n/a
44	CEBPB	chr15:56332673-56333286	IMR90	lung:	n/a	chr15:56332904-56332915
45	CEBPB	chr15:56441356-56441374	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr15:56343937-56344229	IMR90	lung:	n/a	chr15:56344093-56344104
47	CEBPB	chr15:56414660-56414776	K562	blood:	n/a	n/a
48	CEBPB	chr15:56453212-56453518	A549	lung:	n/a	chr15:56453346-56453357
49	CEBPB	chr15:56453204-56453498	HepG2	liver:	n/a	chr15:56453346-56453357
50	CEBPB	chr15:56453172-56453536	IMR90	lung:	n/a	chr15:56453346-56453357

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56401513-56401563	HCT-116	colon:	n/a
2	chr15:56385430-56385480	U87	brain:	n/a
3	chr15:56438248-56438298	SK-N-MC	brain:	n/a
4	chr15:56342834-56342884	NB4	blood:	n/a
5	chr15:56401513-56401563	NH-A	brain:	n/a
6	chr15:56385430-56385480	ovcar-3	ovarian:	n/a
7	chr15:56438248-56438298	HIPEpiC	eye:	n/a
8	chr15:56438248-56438298	HMEC	breast:	n/a
9	chr15:56385430-56385480	SKMC	muscle:	n/a
10	chr15:56401513-56401563	BE2_C	brain:	n/a
11	chr15:56438248-56438298	HPAEpiC	pulmonary alveolar:	n/a
12	chr15:56438248-56438298	ovcar-3	ovarian:	n/a
13	chr15:56401513-56401563	NHDF-neo	bronchial:	n/a
14	chr15:56342834-56342884	BJ	skin:	n/a
15	chr15:56438248-56438298	HEK293	kidney:	embryo
16	chr15:56438248-56438298	HepG2	liver:	n/a
17	chr15:56438248-56438298	GM12878	blood:	n/a
18	chr15:56342834-56342884	HMEC	breast:	n/a
19	chr15:56438248-56438298	PrEC	prostate:	n/a
20	chr15:56385430-56385480	HCT-116	colon:	n/a
21	chr15:56401513-56401563	HepG2	liver:	n/a
22	chr15:56385430-56385480	Hela-S3	cervix:	n/a
23	chr15:56401513-56401563	ProgFib	skin:	n/a
24	chr15:56342834-56342884	MCF10A-Er-Src	breast:	n/a
25	chr15:56401513-56401563	AG09319	gingival:	n/a
26	chr15:56401513-56401563	Hepatocyte	liver:	n/a
27	chr15:56401513-56401563	Jurkat	blood:	n/a
28	chr15:56438248-56438298	HCT-116	colon:	n/a
29	chr15:56438248-56438298	Hepatocyte	liver:	n/a
30	chr15:56438248-56438298	BE2_C	brain:	n/a
31	chr15:56385430-56385480	MCF10A-Er-Src	breast:	n/a
32	chr15:56385430-56385480	NHDF-neo	bronchial:	n/a
33	chr15:56385430-56385480	HUVEC	blood vessel:	n/a
34	chr15:56385430-56385480	GM12891	blood:	n/a
35	chr15:56385430-56385480	HEEpiC	esophagus:	n/a
36	chr15:56342834-56342884	PANC-1	pancreas:	n/a
37	chr15:56401513-56401563	HRPEpiC	eye:	n/a
38	chr15:56385430-56385480	AG04450	lung:	fetal
39	chr15:56401513-56401563	ECC-1	luminal epithelium:	n/a
40	chr15:56438248-56438298	PANC-1	pancreas:	n/a
41	chr15:56438248-56438298	HL-60	blood:	n/a
42	chr15:56438248-56438298	HUVEC	blood vessel:	n/a
43	chr15:56385430-56385480	NHBE	bronchial:	n/a
44	chr15:56342834-56342884	H1-hESC	embryonic stem cell:	embryo
45	chr15:56438248-56438298	HRPEpiC	eye:	n/a
46	chr15:56438248-56438298	HNPCEpiC	eye:	n/a
47	chr15:56438248-56438298	NH-A	brain:	n/a
48	chr15:56385430-56385480	Caco-2	colon:	n/a
49	chr15:56401513-56401563	HNPCEpiC	eye:	n/a
50	chr15:56438248-56438298	NT2-D1	testis:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:56332693..56333405-chr15:56344692..56345448,2	MCF-7	breast:
2	chr15:56449170..56452087-chr15:56458652..56461237,3	K562	blood:
3	chr15:56467090..56469731-chr15:56488365..56490022,2	MCF-7	breast:
4	chr15:56389724..56392748-chr15:56393728..56397126,3	K562	blood:
5	chr15:56418167..56420878-chr15:56422690..56425672,3	K562	blood:
6	chr15:56381595..56383589-chr15:56533952..56536077,2	MCF-7	breast:
7	chr11:62554847..62555619-chr15:56384327..56384954,2	NB4	blood:
8	chr15:56452674..56455465-chr15:56458402..56460158,2	K562	blood:
9	chr15:56336255..56339253-chr15:56339399..56341903,2	K562	blood:
10	chr15:56454940..56456888-chr15:56470980..56473182,2	MCF-7	breast:
11	chr15:56281435..56283774-chr15:56390486..56392704,2	MCF-7	breast:
12	chr15:56385120..56387921-chr15:56395938..56398667,2	MCF-7	breast:
13	chr15:56369125..56370857-chr15:56537851..56540743,2	K562	blood:
14	chr15:56290352..56292488-chr15:56331467..56333363,2	MCF-7	breast:
15	chr15:56386726..56388923-chr15:56388990..56391326,2	MCF-7	breast:
16	chr15:56460981..56464277-chr15:56465842..56468866,3	K562	blood:
17	chr15:56393395..56396114-chr15:56404185..56407853,3	MCF-7	breast:
18	chr15:56286056..56286943-chr15:56344508..56345311,2	MCF-7	breast:
19	chr15:56284361..56286938-chr15:56465632..56467139,2	K562	blood:
20	chr15:56386726..56388923-chr15:56388990..56391326,2	MCF-7	breast:
21	chr15:56375041..56376639-chr15:56378973..56381059,2	MCF-7	breast:
22	chr15:56439893..56441422-chr15:56532922..56535832,2	MCF-7	breast:
23	chr15:56407805..56409350-chr15:56422499..56425257,2	K562	blood:
24	chr15:56418167..56420878-chr15:56422690..56425672,3	K562	blood:
25	chr15:56384379..56386985-chr15:56534620..56537262,4	MCF-7	breast:
26	chr15:56448755..56450713-chr15:56452777..56455848,3	K562	blood:
27	chr15:56321846..56324395-chr15:56332735..56334655,2	MCF-7	breast:
28	chr15:56460981..56464277-chr15:56465842..56468866,3	K562	blood:
29	chr15:56407805..56409350-chr15:56422499..56425257,2	K562	blood:
30	chr15:56404564..56406101-chr15:56409235..56411435,2	K562	blood:
31	chr15:56473450..56475107-chr15:56476965..56479266,2	MCF-7	breast:
32	chr15:56285336..56287267-chr15:56334658..56336784,2	K562	blood:
33	chr15:56284361..56286445-chr15:56418201..56421023,2	MCF-7	breast:
34	chr15:56284173..56286171-chr15:56338265..56340590,2	MCF-7	breast:
35	chr15:56284483..56288965-chr15:56332457..56336362,9	MCF-7	breast:
36	chr15:56206449..56208647-chr15:56387606..56390052,2	MCF-7	breast:
37	chr15:56404564..56406101-chr15:56409235..56411435,2	K562	blood:
38	chr15:56448755..56450713-chr15:56452777..56455848,3	K562	blood:
39	chr15:56344755..56346602-chr15:56535989..56538578,2	MCF-7	breast:
40	chr15:56450764..56452913-chr15:56454957..56457675,2	MCF-7	breast:
41	chr15:56332455..56334509-chr15:56340544..56343174,3	MCF-7	breast:
42	chr15:56389724..56392498-chr15:56393728..56396342,2	K562	blood:
43	chr15:56283406..56287093-chr15:56342307..56345229,4	MCF-7	breast:
44	chr15:56447230..56450204-chr15:56462832..56464767,2	K562	blood:
45	chr15:56283238..56284535-chr15:56344426..56345460,6	MCF-7	breast:
46	chr15:56452674..56455465-chr15:56458402..56460158,2	K562	blood:
47	chr15:56331376..56333572-chr15:56534686..56537481,2	MCF-7	breast:
48	chr15:56468018..56469682-chr15:56471943..56474273,2	K562	blood:
49	chr15:56454940..56456888-chr15:56470980..56473182,2	MCF-7	breast:
50	chr15:56453020..56453777-chr15:56537985..56538862,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFX7-2	chr15:56362416-56362488	l_1162_chr15:56293600-56416163_liver
2	lnc-RFX7-2	chr15:56359594-56359975	l_1162_chr15:56293600-56416163_liver
3	lnc-TEX9-2	chr15:56363619-56363837	NONHSAT044014
4	lnc-RFX7-2	chr15:56363458-56363839	l_1162_chr15:56293600-56416163_liver
5	lnc-RFX7-2	chr15:56416129-56416163	l_1162_chr15:56293600-56416163_liver

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	RFX7	hsa-miR-26b-5p	chr15:56383746-56383766
2	RFX7	hsa-miR-26b-5p	chr15:56384401-56384394
3	RFX7	hsa-miR-26b-5p	chr15:56384623-56384645
4	RFX7	hsa-miR-30b-5p	chr15:56383715-56383708
5	RFX7	hsa-miR-26b-5p	chr15:56384395-56384414
6	RFX7	hsa-miR-30b-5p	chr15:56383165-56383186
7	RFX7	hsa-miR-30b-5p	chr15:56383100-56383122
8	RFX7	hsa-miR-30b-5p	chr15:56383171-56383165
9	RFX7	hsa-miR-30b-5p	chr15:56383709-56383730

Variant related genes	Relation type
RFX7	TF binding region
CD24P2	TF binding region
RFX7	CpG island
CD24P2	CpG island
ENSG00000151575	chromatin interactions
ENSG00000069869	chromatin interactions
ENSG00000185475	chromatin interactions
ENSG00000181827	chromatin interactions
ENSG00000239703	chromatin interactions

Extended variants
information (count: 5440 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5440 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543737581	chr15:56333264-56333265	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs75714344	chr15:56333312-56333313	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs16976700	chr15:56333325-56333326	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs545127165	chr15:56333359-56333360	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs143086594	chr15:56333373-56333374	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs527845673	chr15:56333380-56333381	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs16976702	chr15:56333399-56333400	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374551017	chr15:56333409-56333410	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs561174143	chr15:56333516-56333517	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs73422779	chr15:56333528-56333529	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs550497051	chr15:56333533-56333534	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs188882698	chr15:56333558-56333559	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs12593506	chr15:56333649-56333650	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs559619699	chr15:56333734-56333735	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs59596096	chr15:56333735-56333736	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs576887335	chr15:56333749-56333750	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs11639252	chr15:56333768-56333769	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534733324	chr15:56333814-56333815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554792420	chr15:56333820-56333821	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs73422784	chr15:56333831-56333832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs146173099	chr15:56333850-56333851	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs193096878	chr15:56333858-56333859	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148405685	chr15:56333909-56333910	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs148505348	chr15:56333933-56333934	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs73422785	chr15:56333934-56333935	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs545018550	chr15:56333935-56333936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs559487067	chr15:56333964-56333965	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs77323784	chr15:56333972-56333973	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs141658124	chr15:56333991-56333992	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372226565	chr15:56334070-56334071	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375327961	chr15:56334103-56334104	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561694829	chr15:56334121-56334122	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182991581	chr15:56334152-56334153	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530271751	chr15:56334200-56334201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs148361604	chr15:56334210-56334211	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550577808	chr15:56334231-56334232	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530317479	chr15:56334269-56334270	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543715313	chr15:56334293-56334294	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs73422786	chr15:56334343-56334344	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs531982115	chr15:56334453-56334454	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs552178778	chr15:56334479-56334480	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187320789	chr15:56334510-56334511	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141520933	chr15:56334512-56334513	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528188835	chr15:56334519-56334520	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150548475	chr15:56334538-56334539	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs564072089	chr15:56334550-56334551	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs139564748	chr15:56334575-56334576	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs144447765	chr15:56334598-56334599	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs73422788	chr15:56334628-56334629	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs548511050	chr15:56334642-56334643	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2414 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56327600-56334800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr15:56329400-56334800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr15:56329800-56335000	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr15:56330200-56333400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr15:56330200-56335400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:56330400-56334000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr15:56330400-56336400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:56330600-56333400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr15:56330600-56333400	Enhancers	Placenta Amnion	Placenta Amnion
10	chr15:56330600-56333400	Enhancers	NHDF-Ad	bronchial
11	chr15:56330600-56333400	Enhancers	Osteobl	bone
12	chr15:56330600-56334000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr15:56330800-56334000	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr15:56330800-56334000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr15:56330800-56334600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr15:56330800-56336400	Enhancers	Fetal Intestine Large	intestine
17	chr15:56330800-56337400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:56331000-56334000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr15:56331000-56334200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr15:56331000-56336200	Enhancers	Fetal Intestine Small	intestine
21	chr15:56331400-56333400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr15:56331400-56334400	Enhancers	NHLF	lung
23	chr15:56331400-56335800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:56331400-56337800	Enhancers	HMEC	breast
25	chr15:56331600-56333400	Enhancers	K562	blood
26	chr15:56331600-56333600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:56331600-56334000	Weak transcription	Primary T cells from cord blood	blood
28	chr15:56331600-56335400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:56331800-56333400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr15:56332000-56333400	Enhancers	HSMM	muscle
31	chr15:56332000-56333400	Enhancers	HUVEC	blood vessel
32	chr15:56332000-56334200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr15:56332200-56333400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr15:56332200-56333400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:56332200-56333400	Enhancers	Stomach Mucosa	stomach
36	chr15:56332200-56333400	Enhancers	NH-A	brain
37	chr15:56332200-56336400	Enhancers	Placenta	Placenta
38	chr15:56332400-56333200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr15:56332400-56333200	Enhancers	Adipose Nuclei	Adipose
40	chr15:56332400-56333200	Enhancers	Duodenum Mucosa	Duodenum
41	chr15:56332400-56333400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:56332400-56333400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr15:56332400-56333400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr15:56332400-56333400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr15:56332400-56333400	Flanking Active TSS	Hela-S3	cervix
46	chr15:56332400-56333400	Enhancers	HSMMtube	muscle
47	chr15:56332400-56333600	Enhancers	Liver	Liver
48	chr15:56332400-56334800	Enhancers	HepG2	liver
49	chr15:56332600-56333200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr15:56332600-56333200	Enhancers	Duodenum Smooth Muscle	Duodenum

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