Variant report

Variant	nsv569546
Chromosome Location	chr15:56274443-56337527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1597)
CpG islands
(count:796)
Chromatin interactive
region (count:78)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1597 , 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	chr15:56290869-56290907	K562	blood:	n/a	n/a
2	ARID3A	chr15:56285218-56285455	K562	blood:	n/a	n/a
3	ARID3A	chr15:56285729-56285953	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:56332578-56333150	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:56286628-56286918	K562	blood:	n/a	n/a
6	ARID3A	chr15:56332739-56333117	K562	blood:	n/a	n/a
7	ARID3A	chr15:56335964-56336039	HepG2	liver:	n/a	n/a
8	ATF1	chr15:56301135-56301199	K562	blood:	n/a	n/a
9	ATF1	chr15:56334784-56334889	K562	blood:	n/a	n/a
10	ATF1	chr15:56334057-56334515	K562	blood:	n/a	n/a
11	ATF1	chr15:56311295-56311472	K562	blood:	n/a	n/a
12	ATF1	chr15:56295967-56296197	K562	blood:	n/a	n/a
13	ATF1	chr15:56331861-56332106	K562	blood:	n/a	n/a
14	ATF1	chr15:56331028-56331089	K562	blood:	n/a	n/a
15	ATF1	chr15:56332674-56333153	K562	blood:	n/a	n/a
16	ATF1	chr15:56330262-56330473	K562	blood:	n/a	n/a
17	ATF1	chr15:56286965-56287213	K562	blood:	n/a	n/a
18	ATF3	chr15:56332652-56333227	HCT-116	colon:	n/a	n/a
19	ATF3	chr15:56295943-56296234	K562	blood:	n/a	chr15:56296138-56296151
20	ATF3	chr15:56332556-56333228	HCT-116	colon:	n/a	n/a
21	ATF3	chr15:56332580-56333175	A549	lung:	n/a	n/a
22	ATF3	chr15:56332545-56333126	HepG2	liver:	n/a	n/a
23	ATF3	chr15:56332737-56332952	K562	blood:	n/a	n/a
24	ATF3	chr15:56332688-56333008	HepG2	liver:	n/a	n/a
25	ATF3	chr15:56332633-56333036	K562	blood:	n/a	n/a
26	BACH1	chr15:56285350-56286282	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr15:56336045-56336269	GM12878	blood:	n/a	n/a
28	BDP1	chr15:56332391-56332686	Hela-S3	cervix:	n/a	n/a
29	BHLHE40	chr15:56285538-56285951	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:56335509-56335704	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:56332669-56333067	A549	lung:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
32	BHLHE40	chr15:56332707-56332960	HepG2	liver:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
33	BHLHE40	chr15:56330326-56330542	K562	blood:	n/a	n/a
34	BHLHE40	chr15:56332521-56333175	HepG2	liver:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
35	BHLHE40	chr15:56309879-56310348	K562	blood:	n/a	n/a
36	BHLHE40	chr15:56332639-56332959	HepG2	liver:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
37	BHLHE40	chr15:56310014-56310402	HepG2	liver:	n/a	n/a
38	BHLHE40	chr15:56298674-56298896	HepG2	liver:	n/a	n/a
39	BHLHE40	chr15:56332450-56333242	K562	blood:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
40	BHLHE40	chr15:56291015-56291031	K562	blood:	n/a	n/a
41	BHLHE40	chr15:56285172-56286542	K562	blood:	n/a	chr15:56285460-56285476
42	BHLHE40	chr15:56286927-56286969	K562	blood:	n/a	n/a
43	BHLHE40	chr15:56331823-56332101	K562	blood:	n/a	n/a
44	BRCA1	chr15:56320664-56320979	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr15:56285563-56285941	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr15:56285293-56285463	GM12878	blood:	n/a	n/a
47	BRCA1	chr15:56290670-56291397	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:56285288-56285308	H1-hESC	embryonic stem cell:	n/a	n/a
49	CBX3	chr15:56332260-56333177	HCT-116	colon:	n/a	n/a
50	CBX3	chr15:56306952-56307210	K562	blood:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56285261-56285311	HRCEpiC	kidney:	n/a
2	chr15:56286575-56286625	Jurkat	blood:	n/a
3	chr15:56284168-56284218	AG10803	skin:	n/a
4	chr15:56285261-56285311	HRCEpiC	kidney:	n/a
5	chr15:56286575-56286625	Jurkat	blood:	n/a
6	chr15:56284168-56284218	AG10803	skin:	n/a
7	chr15:56282277-56282327	NHBE	bronchial:	n/a
8	chr15:56285261-56285311	SK-N-SH_RA	brain:	n/a
9	chr15:56286336-56286386	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:56286067-56286117	SK-N-SH_RA	brain:	n/a
11	chr15:56286067-56286117	HNPCEpiC	eye:	n/a
12	chr15:56285484-56285534	Caco-2	colon:	n/a
13	chr15:56282277-56282327	HL-60	blood:	n/a
14	chr15:56286283-56286333	AoSMC	blood vessel:	n/a
15	chr15:56285761-56285811	HCF	heart:	n/a
16	chr15:56284168-56284218	PFSK-1	brain:	n/a
17	chr15:56290261-56290311	ECC-1	luminal epithelium:	n/a
18	chr15:56285484-56285534	SKMC	muscle:	n/a
19	chr15:56285761-56285811	MCF-7	breast:	n/a
20	chr15:56286067-56286117	PFSK-1	brain:	n/a
21	chr15:56290261-56290311	PrEC	prostate:	n/a
22	chr15:56285761-56285811	HCPEpiC	choroid plexus:	n/a
23	chr15:56286336-56286386	AG04449	skin:	fetal
24	chr15:56282277-56282327	CMK	blood:	n/a
25	chr15:56286575-56286625	HPAEpiC	pulmonary alveolar:	n/a
26	chr15:56290261-56290311	ProgFib	skin:	n/a
27	chr15:56286067-56286117	A549	lung:	n/a
28	chr15:56290261-56290311	MCF-7	breast:	n/a
29	chr15:56285484-56285534	GM12891	blood:	n/a
30	chr15:56286575-56286625	H1-hESC	embryonic stem cell:	embryo
31	chr15:56286336-56286386	ECC-1	luminal epithelium:	n/a
32	chr15:56284168-56284218	HEK293	kidney:	embryo
33	chr15:56285741-56285791	U87	brain:	n/a
34	chr15:56285484-56285534	HepG2	liver:	n/a
35	chr15:56285261-56285311	AG09319	gingival:	n/a
36	chr15:56286150-56286200	GM06990	blood:	n/a
37	chr15:56285484-56285534	HAEpiC	amniotic membrane:	n/a
38	chr15:56286150-56286200	HNPCEpiC	eye:	n/a
39	chr15:56285761-56285811	MCF10A-Er-Src	breast:	n/a
40	chr15:56285261-56285311	GM12878	blood:	n/a
41	chr15:56282277-56282327	HPAEpiC	pulmonary alveolar:	n/a
42	chr15:56284168-56284218	LNCaP	prostate:	n/a
43	chr15:56286150-56286200	HL-60	blood:	n/a
44	chr15:56286336-56286386	HCM	heart:	n/a
45	chr15:56284168-56284218	HUVEC	blood vessel:	n/a
46	chr15:56286575-56286625	HepG2	liver:	n/a
47	chr15:56286150-56286200	NT2-D1	testis:	n/a
48	chr15:56286150-56286200	LNCaP	prostate:	n/a
49	chr15:56282277-56282327	Hela-S3	cervix:	n/a
50	chr15:56285761-56285811	ECC-1	luminal epithelium:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:55737712..55738366-chr15:56285235..56286222,2	Hela-S3	cervix:
2	chr15:56326019..56328776-chr15:56329119..56330730,3	MCF-7	breast:
3	chr15:56336255..56339253-chr15:56339399..56341903,2	K562	blood:
4	chr1:100503143..100503837-chr15:56285483..56286241,2	Hela-S3	cervix:
5	chr15:56309948..56310461-chr15:56538175..56538871,2	MCF-7	breast:
6	chr15:56276877..56278529-chr15:56290959..56293005,2	MCF-7	breast:
7	chr15:56285854..56287620-chr15:56331269..56333297,2	K562	blood:
8	chr15:56288413..56291274-chr15:56330655..56333525,2	MCF-7	breast:
9	chr15:56328944..56331210-chr15:56334121..56335862,3	MCF-7	breast:
10	chr15:56272827..56275263-chr15:56276968..56278689,2	MCF-7	breast:
11	chr15:56285985..56288747-chr15:56326549..56330061,4	MCF-7	breast:
12	chr15:56285499..56287418-chr15:56534884..56536553,2	K562	blood:
13	chr15:56284455..56287261-chr15:56299264..56302045,2	MCF-7	breast:
14	chr15:56282892..56284804-chr15:56387312..56388901,2	MCF-7	breast:
15	chr1:145381291..145384278-chr15:56284107..56286728,2	MCF-7	breast:
16	chr15:56308090..56310952-chr15:56323916..56326374,2	MCF-7	breast:
17	chr15:56290352..56292488-chr15:56331467..56333363,2	MCF-7	breast:
18	chr1:233748980..233749780-chr15:56285541..56286277,2	Hela-S3	cervix:
19	chr15:56304158..56307081-chr15:56310322..56313297,2	K562	blood:
20	chr15:56284567..56286321-chr15:56327234..56329657,2	MCF-7	breast:
21	chr15:56283971..56286834-chr15:56291176..56293680,2	K562	blood:
22	chr15:56284455..56287261-chr15:56299264..56302045,2	MCF-7	breast:
23	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
24	chr15:56321602..56323899-chr15:56324883..56327290,2	K562	blood:
25	chr15:56328944..56331210-chr15:56334121..56335862,3	MCF-7	breast:
26	chr1:28994985..28995485-chr15:56285972..56286627,2	Hela-S3	cervix:
27	chr1:109234674..109235306-chr15:56285708..56286287,2	Hela-S3	cervix:
28	chr15:56275489..56278398-chr15:56279462..56282619,4	K562	blood:
29	chr15:56275489..56279024-chr15:56279462..56282619,5	K562	blood:
30	chr15:56279620..56282017-chr15:56535404..56538288,2	MCF-7	breast:
31	chr15:56281435..56283774-chr15:56390486..56392704,2	MCF-7	breast:
32	chr15:56290100..56291758-chr15:56342391..56345191,2	MCF-7	breast:
33	chr15:56308090..56310952-chr15:56323916..56326374,2	MCF-7	breast:
34	chr15:56284954..56286880-chr15:56299616..56301777,2	K562	blood:
35	chr15:56281891..56284127-chr15:56288031..56290159,2	K562	blood:
36	chr15:56285803..56286769-chr7:144532503..144533132,2	HCT-116	colon:
37	chr15:56040535..56042266-chr15:56323409..56324983,2	K562	blood:
38	chr15:56292596..56295463-chr15:56332389..56335036,2	MCF-7	breast:
39	chr15:56299007..56301700-chr15:56309609..56311858,2	MCF-7	breast:
40	chr15:56286068..56286594-chr15:56344895..56345645,2	MCF-7	breast:
41	chr15:56331395..56333344-chr15:56535817..56538241,2	MCF-7	breast:
42	chr15:56275489..56279024-chr15:56279462..56282619,5	K562	blood:
43	chr15:56326019..56328776-chr15:56329119..56330730,3	MCF-7	breast:
44	chr15:56326474..56328058-chr15:56328930..56331653,2	K562	blood:
45	chr15:56281891..56284127-chr15:56288031..56290159,2	K562	blood:
46	chr15:56332455..56334509-chr15:56340544..56343174,3	MCF-7	breast:
47	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
48	chr15:56326474..56328058-chr15:56328930..56331653,2	K562	blood:
49	chr15:56309924..56310815-chr15:56344688..56345628,4	MCF-7	breast:
50	chr15:56282101..56284524-chr15:56536077..56539290,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFX7-2	chr15:56293601-56293799	l_1162_chr15:56293600-56416163_liver
2	lnc-RFX7-3	chr15:56279929-56280199	NONHSAT044012
3	lnc-NEDD4-1	chr15:56321886-56322179	NONHSAT044013
4	lnc-RFX7-2	chr15:56305102-56305262	l_1162_chr15:56293600-56416163_liver
5	lnc-RFX7-2	chr15:56325626-56325839	l_1162_chr15:56293600-56416163_liver
6	lnc-RFX7-3	chr15:56285709-56285811	NONHSAT044012
7	lnc-RFX7-2	chr15:56321306-56321486	l_1162_chr15:56293600-56416163_liver

No data

Variant related genes	Relation type
RN7SL568P	TF binding region
NEDD4	TF binding region
CNOT6LP1	TF binding region
RN7SL568P	CpG island
NEDD4	CpG island
CNOT6LP1	CpG island
ENSG00000239703	chromatin interactions
ENSG00000176305	chromatin interactions
ENSG00000135750	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000181827	chromatin interactions
ENSG00000156875	chromatin interactions
ENSG00000069869	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000196511	chromatin interactions
ENSG00000134186	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000253958	chromatin interactions
ENSG00000163191	chromatin interactions
ENSG00000162419	chromatin interactions
ENSG00000230183	chromatin interactions
ENSG00000151575	chromatin interactions

Extended variants
information (count: 2247 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2247 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11632974	chr15:56274443-56274444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554192055	chr15:56274470-56274471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574185348	chr15:56274477-56274478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186086411	chr15:56274529-56274530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs80025455	chr15:56274533-56274534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12594988	chr15:56274549-56274550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546046687	chr15:56274569-56274570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559375576	chr15:56274575-56274576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545231042	chr15:56274606-56274607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541060742	chr15:56274622-56274623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190412443	chr15:56274662-56274663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530174837	chr15:56274695-56274696	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182921296	chr15:56274696-56274697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs71476761	chr15:56274748-56274749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs142364501	chr15:56274766-56274767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs71476762	chr15:56274771-56274772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs72543754	chr15:56274778-56274779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs8034692	chr15:56274779-56274780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs78063584	chr15:56274782-56274783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560538906	chr15:56274790-56274791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs73420363	chr15:56274794-56274795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567721696	chr15:56274804-56274805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs151295682	chr15:56274825-56274826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs369039492	chr15:56274828-56274829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556655676	chr15:56274846-56274847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372210470	chr15:56274890-56274891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576908717	chr15:56274907-56274908	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539237330	chr15:56274918-56274919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs560178127	chr15:56274931-56274932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117280067	chr15:56274991-56274992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573041218	chr15:56275038-56275039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140126503	chr15:56275052-56275053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561217938	chr15:56275106-56275107	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574906369	chr15:56275118-56275119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543900960	chr15:56275137-56275138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs531834801	chr15:56275165-56275166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563756177	chr15:56275212-56275213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532667146	chr15:56275217-56275218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527811197	chr15:56275225-56275226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376094634	chr15:56275230-56275231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559906374	chr15:56275253-56275254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187982091	chr15:56275259-56275260	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12911833	chr15:56275268-56275269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548493809	chr15:56275269-56275270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs147745854	chr15:56275273-56275274	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs531414352	chr15:56275274-56275275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536636291	chr15:56275276-56275277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549529582	chr15:56275284-56275285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190679904	chr15:56275285-56275286	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs551229793	chr15:56275294-56275295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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

Chromatin state (count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56229600-56282600	Weak transcription	NHLF	lung
2	chr15:56231400-56284200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr15:56236200-56276000	Weak transcription	HUVEC	blood vessel
4	chr15:56236800-56282800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:56243200-56276200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:56248200-56285200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:56251600-56281600	Weak transcription	Osteobl	bone
8	chr15:56253600-56282400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:56257600-56281600	Weak transcription	Fetal Intestine Large	intestine
10	chr15:56257600-56283600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:56257600-56283800	Weak transcription	Primary T cells from cord blood	blood
12	chr15:56262800-56276200	Weak transcription	NHEK	skin
13	chr15:56262800-56276400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:56262800-56276600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:56262800-56276600	Weak transcription	HMEC	breast
16	chr15:56263000-56275400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr15:56263800-56282400	Weak transcription	Fetal Intestine Small	intestine
18	chr15:56269400-56282400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr15:56270400-56281600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr15:56272600-56284200	Weak transcription	Lung	lung
21	chr15:56272800-56281600	Weak transcription	Psoas Muscle	Psoas
22	chr15:56273000-56281600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr15:56273000-56283000	Weak transcription	HSMMtube	muscle
24	chr15:56273600-56274800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr15:56273800-56274800	Enhancers	A549	lung
26	chr15:56273800-56277000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:56274000-56281600	Weak transcription	HSMM	muscle
28	chr15:56274200-56274600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr15:56274400-56283800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr15:56274400-56283800	Weak transcription	NH-A	brain
31	chr15:56274400-56284000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr15:56274600-56276200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:56274600-56278000	Weak transcription	Hela-S3	cervix
34	chr15:56274800-56282800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr15:56274800-56282800	Weak transcription	A549	lung
36	chr15:56275200-56276800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr15:56275400-56275600	Enhancers	Left Ventricle	heart
38	chr15:56275400-56276000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr15:56275400-56283000	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr15:56275600-56284000	Weak transcription	Aorta	Aorta
41	chr15:56275600-56284200	Weak transcription	Left Ventricle	heart
42	chr15:56276000-56276400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:56276000-56277600	Enhancers	HUVEC	blood vessel
44	chr15:56276200-56276600	Enhancers	Stomach Mucosa	stomach
45	chr15:56276200-56276800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr15:56276200-56277000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr15:56276200-56277400	Enhancers	NHEK	skin
48	chr15:56276400-56276600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr15:56276400-56276600	Enhancers	NHDF-Ad	bronchial
50	chr15:56276400-56277400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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