Variant report

Variant	nsv469547
Chromosome Location	chr15:34594557-34757807
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3669)
CpG islands
(count:3728)
Chromatin interactive
region (count:133)
LncRNA
region (count:9)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:3669 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34624072-34624459	K562	blood:	n/a	n/a
2	ARID3A	chr15:34630317-34630551	K562	blood:	n/a	n/a
3	ARID3A	chr15:34659662-34660316	K562	blood:	n/a	n/a
4	ARID3A	chr15:34731584-34731600	K562	blood:	n/a	n/a
5	ARID3A	chr15:34610679-34611244	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:34628988-34629112	K562	blood:	n/a	n/a
7	ARID3A	chr15:34650682-34650948	K562	blood:	n/a	n/a
8	ARID3A	chr15:34635077-34635629	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:34659927-34660209	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:34650075-34650188	K562	blood:	n/a	n/a
11	ARID3A	chr15:34630085-34630347	HepG2	liver:	n/a	n/a
12	ATF1	chr15:34626286-34626596	K562	blood:	n/a	n/a
13	ATF1	chr15:34624064-34624420	K562	blood:	n/a	n/a
14	ATF1	chr15:34635153-34635613	K562	blood:	n/a	n/a
15	ATF1	chr15:34633764-34633880	K562	blood:	n/a	n/a
16	ATF1	chr15:34609041-34609045	K562	blood:	n/a	n/a
17	ATF2	chr15:34635029-34635631	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr15:34619912-34620568	GM12878	blood:	n/a	n/a
19	ATF2	chr15:34659423-34660283	GM12878	blood:	n/a	n/a
20	ATF2	chr15:34634949-34635647	GM12878	blood:	n/a	n/a
21	ATF2	chr15:34635034-34635648	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr15:34610292-34610924	GM12878	blood:	n/a	n/a
23	ATF2	chr15:34635018-34635644	GM12878	blood:	n/a	n/a
24	ATF2	chr15:34662101-34662703	GM12878	blood:	n/a	n/a
25	ATF2	chr15:34628276-34629003	GM12878	blood:	n/a	n/a
26	ATF2	chr15:34619754-34620562	GM12878	blood:	n/a	n/a
27	ATF2	chr15:34627198-34628103	GM12878	blood:	n/a	n/a
28	ATF2	chr15:34626070-34626939	GM12878	blood:	n/a	n/a
29	ATF2	chr15:34626066-34626885	GM12878	blood:	n/a	n/a
30	ATF2	chr15:34662115-34662776	GM12878	blood:	n/a	n/a
31	ATF2	chr15:34627300-34627730	GM12878	blood:	n/a	n/a
32	ATF2	chr15:34628366-34630566	GM12878	blood:	n/a	n/a
33	ATF2	chr15:34625424-34626064	GM12878	blood:	n/a	n/a
34	ATF3	chr15:34635099-34635655	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF3	chr15:34635218-34635449	GM12878	blood:	n/a	n/a
36	ATF3	chr15:34629910-34630389	K562	blood:	n/a	chr15:34630060-34630080 chr15:34629995-34630004 chr15:34630294-34630303
37	ATF3	chr15:34610750-34611266	GM12878	blood:	n/a	chr15:34611025-34611034
38	ATF3	chr15:34635025-34635934	A549	lung:	n/a	n/a
39	ATF3	chr15:34610906-34611115	K562	blood:	n/a	chr15:34611025-34611034
40	ATF3	chr15:34635188-34635600	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF3	chr15:34610781-34611240	H1-hESC	embryonic stem cell:	n/a	chr15:34611025-34611034
42	ATF3	chr15:34635165-34635558	K562	blood:	n/a	n/a
43	ATF3	chr15:34635103-34635658	GM12878	blood:	n/a	n/a
44	BACH1	chr15:34611044-34611203	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr15:34629688-34630499	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr15:34729369-34729390	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr15:34659514-34660110	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr15:34597385-34597505	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr15:34659688-34659949	K562	blood:	n/a	n/a
50	BATF	chr15:34626261-34626514	GM12878	blood:	n/a	n/a

(count:3728 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34629953-34630003	HNPCEpiC	eye:	n/a
2	chr15:34659969-34660019	HL-60	blood:	n/a
3	chr15:34630395-34630445	NT2-D1	testis:	n/a
4	chr15:34635452-34635502	Hepatocyte	liver:	n/a
5	chr15:34635303-34635353	SAEC	small airway:	n/a
6	chr15:34726650-34726700	U87	brain:	n/a
7	chr15:34640893-34640943	NT2-D1	testis:	n/a
8	chr15:34629953-34630003	HNPCEpiC	eye:	n/a
9	chr15:34659969-34660019	HL-60	blood:	n/a
10	chr15:34630395-34630445	NT2-D1	testis:	n/a
11	chr15:34635452-34635502	Hepatocyte	liver:	n/a
12	chr15:34635303-34635353	SAEC	small airway:	n/a
13	chr15:34726650-34726700	U87	brain:	n/a
14	chr15:34640893-34640943	NT2-D1	testis:	n/a
15	chr15:34630047-34630097	HRE	kidney:	n/a
16	chr15:34629993-34630043	ovcar-3	ovarian:	n/a
17	chr15:34638511-34638561	HCPEpiC	choroid plexus:	n/a
18	chr15:34611009-34611059	ECC-1	luminal epithelium:	n/a
19	chr15:34628731-34628781	NT2-D1	testis:	n/a
20	chr15:34629056-34629106	BJ	skin:	n/a
21	chr15:34630356-34630406	Caco-2	colon:	n/a
22	chr15:34628815-34628865	HRE	kidney:	n/a
23	chr15:34634045-34634095	NB4	blood:	n/a
24	chr15:34611009-34611059	HMEC	breast:	n/a
25	chr15:34611069-34611119	Hepatocyte	liver:	n/a
26	chr15:34671426-34671476	SK-N-SH_RA	brain:	n/a
27	chr15:34611057-34611107	MCF10A-Er-Src	breast:	n/a
28	chr15:34658812-34658862	NT2-D1	testis:	n/a
29	chr15:34635227-34635277	NB4	blood:	n/a
30	chr15:34629995-34630045	AG10803	skin:	n/a
31	chr15:34630356-34630406	HEK293	kidney:	embryo
32	chr15:34629995-34630045	NB4	blood:	n/a
33	chr15:34630395-34630445	U87	brain:	n/a
34	chr15:34630011-34630061	Jurkat	blood:	n/a
35	chr15:34637567-34637617	SKMC	muscle:	n/a
36	chr15:34610829-34610879	NT2-D1	testis:	n/a
37	chr15:34635452-34635502	HUVEC	blood vessel:	n/a
38	chr15:34700272-34700322	GM12878	blood:	n/a
39	chr15:34612206-34612256	Caco-2	colon:	n/a
40	chr15:34659815-34659865	AG04450	lung:	fetal
41	chr15:34634045-34634095	ovcar-3	ovarian:	n/a
42	chr15:34635303-34635353	HNPCEpiC	eye:	n/a
43	chr15:34637638-34637688	MCF-7	breast:	n/a
44	chr15:34635227-34635277	PrEC	prostate:	n/a
45	chr15:34611057-34611107	MCF-7	breast:	n/a
46	chr15:34660076-34660126	NB4	blood:	n/a
47	chr15:34628731-34628781	SK-N-SH	brain:	n/a
48	chr15:34727209-34727259	BE2_C	brain:	n/a
49	chr15:34659687-34659737	HepG2	liver:	n/a
50	chr15:34635303-34635353	H1-hESC	embryonic stem cell:	embryo

(count:133 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:28558832..28559607-chr15:34634683..34635340,2	Hela-S3	cervix:
2	chr15:34633629..34635584-chr15:34657779..34659599,2	MCF-7	breast:
3	chr15:34604526..34606591-chr15:34629720..34631424,2	MCF-7	breast:
4	chr15:34635280..34637526-chr15:34658001..34660457,2	K562	blood:
5	chr15:34634571..34635945-chr15:34658808..34660439,12	MCF-7	breast:
6	chr15:34610196..34613869-chr15:34616298..34621917,4	K562	blood:
7	chr15:34608511..34610241-chr15:34630239..34631894,2	K562	blood:
8	chr15:34632759..34637829-chr15:34654252..34657716,5	K562	blood:
9	chr15:34626147..34627854-chr15:34654985..34656962,2	K562	blood:
10	chr15:34598914..34602759-chr15:34631261..34635438,4	K562	blood:
11	chr15:34500871..34503422-chr15:34659158..34662481,4	K562	blood:
12	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
13	chr15:34638937..34641770-chr15:34643644..34645209,2	K562	blood:
14	chr15:34658959..34659493-chr17:56756873..56757469,2	Hela-S3	cervix:
15	chr15:34633931..34636680-chr15:34728775..34730381,2	K562	blood:
16	chr15:34658931..34659843-chr17:42401742..42402293,2	HCT-116	colon:
17	chr15:34635057..34636788-chr15:34655744..34657443,2	MCF-7	breast:
18	chr15:34500928..34503711-chr15:34659510..34661352,2	MCF-7	breast:
19	chr15:34628783..34632143-chr15:34633761..34637127,4	MCF-7	breast:
20	chr15:34392784..34394847-chr15:34629052..34631553,2	K562	blood:
21	chr15:34642775..34644501-chr15:34648793..34650495,2	K562	blood:
22	chr15:34635280..34637526-chr15:34658001..34660457,2	K562	blood:
23	chr15:34615241..34617127-chr15:34618598..34620294,2	K562	blood:
24	chr15:34616765..34618642-chr15:34621899..34624086,2	K562	blood:
25	chr14:67878348..67879211-chr15:34659300..34659943,2	Hela-S3	cervix:
26	chr15:34632008..34636763-chr15:34655757..34660926,8	K562	blood:
27	chr15:34654804..34656714-chr15:34658910..34661703,3	K562	blood:
28	chr15:34630189..34630837-chr8:95835513..95836045,2	Hela-S3	cervix:
29	chr15:34546535..34549806-chr15:34599595..34603199,3	K562	blood:
30	chr15:34500616..34503501-chr15:34610779..34612770,2	K562	blood:
31	chr11:62420159..62420929-chr15:34659289..34659854,2	Hela-S3	cervix:
32	chr15:34613260..34615492-chr15:34628458..34631213,2	K562	blood:
33	chr15:34600219..34602527-chr15:34605319..34607496,2	K562	blood:
34	chr15:34659866..34661509-chr15:34661998..34663782,2	K562	blood:
35	chr15:34499795..34503886-chr15:34627014..34631557,6	K562	blood:
36	chr15:34612507..34614657-chr15:34617992..34620776,2	MCF-7	breast:
37	chr15:34597292..34600237-chr15:34600566..34603010,2	K562	blood:
38	chr15:34531119..34534573-chr15:34628473..34631118,3	MCF-7	breast:
39	chr15:34516899..34519877-chr15:34627913..34631706,5	K562	blood:
40	chr15:34626796..34628377-chr15:34649112..34652053,2	MCF-7	breast:
41	chr15:34642499..34645200-chr15:34648396..34650653,3	K562	blood:
42	chr15:34646339..34647917-chr15:34648014..34649516,2	K562	blood:
43	chr15:34638937..34641770-chr15:34643644..34645209,2	K562	blood:
44	chr15:34632776..34635331-chr15:34879472..34881728,2	K562	blood:
45	chr15:34729318..34730097-chr5:1799590..1800354,2	Hela-S3	cervix:
46	chr15:34633865..34636798-chr15:34637017..34639359,2	K562	blood:
47	chr15:34329481..34332420-chr15:34625067..34627371,2	K562	blood:
48	chr15:34635005..34635906-chr15:34659046..34660693,6	K562	blood:
49	chr15:34632759..34637829-chr15:34654252..34657716,5	K562	blood:
50	chr15:34623463..34625220-chr15:34629073..34631076,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPCAT4-1	chr15:34720816-34721126	NONHSAT041586
2	lnc-LPCAT4-1	chr15:34699777-34699936	NONHSAT041586
3	lnc-GOLGA8B-1	chr15:34752685-34752950	uc_384_-
4	lnc-C15orf55-4	chr15:34752685-34752950	uc_384_+
5	lnc-C15orf55-2	chr15:34607219-34607487	uc_383_+
6	lnc-LPCAT4-1	chr15:34698878-34699071	NONHSAT041586
7	lnc-NOP10-1	chr15:34607219-34607487	uc_383_-
8	lnc-C15orf55-1	chr15:34632408-34632569	NONHSAT041578
9	lnc-C15orf55-1	chr15:34628609-34630155	NONHSAT041578

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1233-3p	chr15:34674270-34674289	MIMAT0005588
hsa-miR-1233-5p	chr15:34674327-34674348	MIMAT0022943

No data

Variant related genes	Relation type
MIR1233-1	TF binding region
LPCAT4	TF binding region
ENSG00000261081	TF binding region
NUTM1	TF binding region
SLC12A6	TF binding region
ENSG00000260639	TF binding region
ENSG00000259904	TF binding region
GOLGA8A	TF binding region
ENSG00000207091	TF binding region
NOP10	TF binding region
ENSG00000266205	TF binding region
MIR1233-1	CpG island
LPCAT4	CpG island
ENSG00000261081	CpG island
NUTM1	CpG island
SLC12A6	CpG island
ENSG00000260639	CpG island
ENSG00000259904	CpG island
GOLGA8A	CpG island
ENSG00000207091	CpG island
NOP10	CpG island
ENSG00000266205	CpG island
ENSG00000259904	chromatin interactions
ENSG00000100558	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000136877	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000162545	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000134153	chromatin interactions
ENSG00000184507	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000259917	chromatin interactions
ENSG00000248668	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000182405	chromatin interactions
ENSG00000207091	chromatin interactions
ENSG00000083720	chromatin interactions
ENSG00000134152	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000013306	chromatin interactions
ENSG00000126698	chromatin interactions
ENSG00000164941	chromatin interactions
ENSG00000259468	chromatin interactions
ENSG00000185085	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000171421	chromatin interactions
ENSG00000169857	chromatin interactions

Extended variants
information (count: 5848 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:5848 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143602198	chr15:34594621-34594622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138071980	chr15:34594647-34594648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561167115	chr15:34594651-34594652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142546107	chr15:34594667-34594668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540271194	chr15:34594713-34594714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377129050	chr15:34594746-34594747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564809472	chr15:34594750-34594751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186672988	chr15:34594764-34594765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144704843	chr15:34594765-34594766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563070415	chr15:34594836-34594837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530235717	chr15:34594854-34594855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189908148	chr15:34594889-34594890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542569767	chr15:34594899-34594900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182180865	chr15:34594910-34594911	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141442208	chr15:34594914-34594915	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs552569566	chr15:34594921-34594922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192412343	chr15:34594933-34594934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538300942	chr15:34594936-34594937	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138606588	chr15:34594969-34594970	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs28705147	chr15:34594995-34594996	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs28755475	chr15:34594997-34594998	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs185374254	chr15:34595005-34595006	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111690467	chr15:34595012-34595013	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs544251844	chr15:34595037-34595038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188239781	chr15:34595059-34595060	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573206003	chr15:34595110-34595111	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs150720549	chr15:34595136-34595137	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192919059	chr15:34595137-34595138	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs76182175	chr15:34595158-34595159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113035167	chr15:34595159-34595160	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs62017480	chr15:34595161-34595162	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111542169	chr15:34595170-34595171	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs372102777	chr15:34595180-34595181	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34761920	chr15:34595181-34595182	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77106327	chr15:34595204-34595205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74716713	chr15:34595205-34595206	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs17236833	chr15:34595263-34595264	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577581005	chr15:34595378-34595379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs137855324	chr15:34595394-34595395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs75004397	chr15:34595398-34595399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147323116	chr15:34595436-34595437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545716261	chr15:34595456-34595457	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548419510	chr15:34595599-34595600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560392084	chr15:34595646-34595647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560599271	chr15:34595663-34595664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547640681	chr15:34595675-34595676	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552608996	chr15:34595690-34595691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs80226216	chr15:34595725-34595726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537853056	chr15:34595759-34595760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs8042422	chr15:34595822-34595823	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:69)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3956 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34551200-34608800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr15:34555200-34606600	Weak transcription	Thymus	Thymus
3	chr15:34577600-34608800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr15:34577600-34610200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr15:34577800-34608800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr15:34578200-34606800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr15:34579000-34603800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr15:34582200-34599000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:34582600-34609600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:34582600-34610200	Weak transcription	Fetal Lung	lung
11	chr15:34583400-34609600	Weak transcription	Adipose Nuclei	Adipose
12	chr15:34583800-34610600	Weak transcription	Pancreas	Pancrea
13	chr15:34585000-34609600	Weak transcription	Spleen	Spleen
14	chr15:34585000-34610600	Weak transcription	Lung	lung
15	chr15:34585200-34596400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr15:34585200-34598600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr15:34585200-34609600	Weak transcription	Fetal Stomach	stomach
18	chr15:34585200-34615600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr15:34585400-34602200	Weak transcription	Esophagus	oesophagus
20	chr15:34585400-34608600	Weak transcription	Liver	Liver
21	chr15:34585800-34604600	Weak transcription	Fetal Intestine Large	intestine
22	chr15:34585800-34610400	Weak transcription	Ovary	ovary
23	chr15:34586600-34609800	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr15:34587000-34610200	Weak transcription	Fetal Intestine Small	intestine
25	chr15:34587800-34604400	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr15:34589800-34597200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr15:34589800-34600400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr15:34589800-34610600	Weak transcription	Brain Cingulate Gyrus	brain
29	chr15:34590000-34598400	Weak transcription	Left Ventricle	heart
30	chr15:34590000-34609000	Weak transcription	Colon Smooth Muscle	Colon
31	chr15:34590000-34610400	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr15:34590000-34610600	Weak transcription	Small Intestine	intestine
33	chr15:34590200-34603800	Weak transcription	Primary B cells from peripheral blood	blood
34	chr15:34590400-34596800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr15:34590400-34599600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr15:34590400-34604200	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr15:34590800-34594600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr15:34591000-34595400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr15:34591400-34595800	Weak transcription	GM12878-XiMat	blood
40	chr15:34592000-34595200	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr15:34592000-34598600	Weak transcription	Aorta	Aorta
42	chr15:34592200-34600400	Weak transcription	Primary B cells from cord blood	blood
43	chr15:34592200-34608400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr15:34592600-34603800	Weak transcription	Primary T cells from cord blood	blood
45	chr15:34593000-34610600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr15:34593600-34605400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr15:34593800-34609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr15:34594000-34607000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:34594000-34609400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr15:34594000-34610600	Weak transcription	Gastric	stomach

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