Variant report

Variant	esv1798487
Chromosome Location	chr15:59027139-59213678
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3513)
CpG islands
(count:2445)
Chromatin interactive
region (count:206)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3513 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59040631-59041032	K562	blood:	n/a	n/a
2	ARID3A	chr15:59086282-59086455	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:59063011-59063531	K562	blood:	n/a	n/a
4	ARID3A	chr15:59062801-59063620	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:59041643-59042081	K562	blood:	n/a	n/a
6	ARID3A	chr15:59134956-59135156	K562	blood:	n/a	n/a
7	ARID3A	chr15:59123034-59123175	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:59156691-59157389	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:59125888-59126267	K562	blood:	n/a	n/a
10	ARID3A	chr15:59041948-59042900	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:59127378-59127384	K562	blood:	n/a	n/a
12	ARID3A	chr15:59042958-59043022	K562	blood:	n/a	n/a
13	ARID3A	chr15:59098727-59098770	K562	blood:	n/a	chr15:59098731-59098747
14	ATF1	chr15:59097368-59097629	K562	blood:	n/a	n/a
15	ATF1	chr15:59062751-59063660	K562	blood:	n/a	chr15:59063467-59063481
16	ATF1	chr15:59041873-59042478	K562	blood:	n/a	n/a
17	ATF1	chr15:59210516-59210796	K562	blood:	n/a	n/a
18	ATF1	chr15:59071879-59072075	K562	blood:	n/a	n/a
19	ATF1	chr15:59158433-59158785	K562	blood:	n/a	n/a
20	ATF1	chr15:59125813-59126282	K562	blood:	n/a	n/a
21	ATF2	chr15:59062735-59063607	GM12878	blood:	n/a	chr15:59063467-59063481
22	ATF2	chr15:59158413-59158831	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr15:59042161-59042561	GM12878	blood:	n/a	n/a
24	ATF3	chr15:59063182-59063710	K562	blood:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
25	ATF3	chr15:59062924-59063709	A549	lung:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
26	ATF3	chr15:59041796-59042229	H1-hESC	embryonic stem cell:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
27	ATF3	chr15:59041856-59042237	H1-hESC	embryonic stem cell:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
28	ATF3	chr15:59041805-59042226	K562	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
29	ATF3	chr15:59041954-59042205	GM12878	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
30	ATF3	chr15:59041919-59042231	HepG2	liver:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
31	ATF3	chr15:59095848-59096053	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr15:59041797-59042286	GM12878	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
33	ATF3	chr15:59041880-59042188	K562	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
34	ATF3	chr15:59062871-59063734	A549	lung:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
35	BACH1	chr15:59062895-59063578	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr15:59156865-59157214	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr15:59041132-59041190	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr15:59134988-59135201	GM12878	blood:	n/a	n/a
39	BATF	chr15:59088090-59088336	GM12878	blood:	n/a	n/a
40	BATF	chr15:59134922-59135200	GM12878	blood:	n/a	n/a
41	BATF	chr15:59088024-59088402	GM12878	blood:	n/a	n/a
42	BCL3	chr15:59041625-59042621	A549	lung:	n/a	n/a
43	BCL3	chr15:59168519-59168937	A549	lung:	n/a	n/a
44	BCL3	chr15:59062776-59063544	A549	lung:	n/a	chr15:59063204-59063213 chr15:59063497-59063505
45	BCL3	chr15:59062699-59063768	A549	lung:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
46	BCL3	chr15:59167563-59168150	A549	lung:	n/a	n/a
47	BCL3	chr15:59158379-59158846	A549	lung:	n/a	n/a
48	BCLAF1	chr15:59062912-59063903	GM12878	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
49	BCLAF1	chr15:59062982-59063764	GM12878	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
50	BCLAF1	chr15:59062765-59063599	K562	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505

(count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59060978-59061028	HEEpiC	esophagus:	n/a
2	chr15:59063885-59063935	U87	brain:	n/a
3	chr15:59064161-59064211	SAEC	small airway:	n/a
4	chr15:59179584-59179634	ovcar-3	ovarian:	n/a
5	chr15:59063274-59063324	Hela-S3	cervix:	n/a
6	chr15:59060978-59061028	HEEpiC	esophagus:	n/a
7	chr15:59063885-59063935	U87	brain:	n/a
8	chr15:59064161-59064211	SAEC	small airway:	n/a
9	chr15:59179584-59179634	ovcar-3	ovarian:	n/a
10	chr15:59063274-59063324	Hela-S3	cervix:	n/a
11	chr15:59041175-59041225	ovcar-3	ovarian:	n/a
12	chr15:59042325-59042375	GM06990	blood:	n/a
13	chr15:59125919-59125969	HCPEpiC	choroid plexus:	n/a
14	chr15:59154450-59154500	HCPEpiC	choroid plexus:	n/a
15	chr15:59042684-59042734	BJ	skin:	n/a
16	chr15:59042242-59042292	ECC-1	luminal epithelium:	n/a
17	chr15:59063609-59063659	T-47D	breast:	n/a
18	chr15:59041175-59041225	NT2-D1	testis:	n/a
19	chr15:59063210-59063260	H1-hESC	embryonic stem cell:	embryo
20	chr15:59125919-59125969	GM06990	blood:	n/a
21	chr15:59041689-59041739	SK-N-SH_RA	brain:	n/a
22	chr15:59179550-59179600	HNPCEpiC	eye:	n/a
23	chr15:59063378-59063428	HL-60	blood:	n/a
24	chr15:59042352-59042402	PrEC	prostate:	n/a
25	chr15:59157075-59157125	HRPEpiC	eye:	n/a
26	chr15:59157857-59157907	HL-60	blood:	n/a
27	chr15:59063609-59063659	PrEC	prostate:	n/a
28	chr15:59179584-59179634	GM19239	blood:	n/a
29	chr15:59040869-59040919	HRE	kidney:	n/a
30	chr15:59041175-59041225	HUVEC	blood vessel:	n/a
31	chr15:59063210-59063260	K562	blood:	n/a
32	chr15:59160318-59160368	GM19239	blood:	n/a
33	chr15:59063113-59063163	GM12878	blood:	n/a
34	chr15:59063378-59063428	SAEC	small airway:	n/a
35	chr15:59156878-59156928	AG09309	skin:	n/a
36	chr15:59063274-59063324	NH-A	brain:	n/a
37	chr15:59171928-59171978	H1-hESC	embryonic stem cell:	embryo
38	chr15:59063885-59063935	HPAEpiC	pulmonary alveolar:	n/a
39	chr15:59157075-59157125	NH-A	brain:	n/a
40	chr15:59063261-59063311	NT2-D1	testis:	n/a
41	chr15:59179584-59179634	GM12892	blood:	n/a
42	chr15:59063885-59063935	HCM	heart:	n/a
43	chr15:59064161-59064211	PFSK-1	brain:	n/a
44	chr15:59179550-59179600	MCF-7	breast:	n/a
45	chr15:59041175-59041225	A549	lung:	n/a
46	chr15:59063195-59063245	Hepatocyte	liver:	n/a
47	chr15:59041689-59041739	H1-hESC	embryonic stem cell:	embryo
48	chr15:59179584-59179634	AG04449	skin:	fetal
49	chr15:59042352-59042402	PANC-1	pancreas:	n/a
50	chr15:59040869-59040919	T-47D	breast:	n/a

(count:206 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr15:59037438..59039932-chr15:59074278..59075927,2	K562	blood:
2	chr15:59030373..59033312-chr15:59035023..59037730,3	MCF-7	breast:
3	chr15:59046301..59048650-chr15:59061431..59063279,4	K562	blood:
4	chr15:58982751..58984795-chr15:59030172..59031707,2	K562	blood:
5	chr15:59204733..59207278-chr15:59208062..59211512,3	K562	blood:
6	chr15:59041392..59042094-chr16:56716160..56716780,2	Hela-S3	cervix:
7	chr15:59063628..59066119-chr15:59070101..59071953,2	MCF-7	breast:
8	chr15:59048564..59050956-chr15:59058721..59061333,2	K562	blood:
9	chr15:59204944..59209018-chr15:59223573..59227454,4	K562	blood:
10	chr15:59062764..59064503-chr15:59191462..59194303,2	K562	blood:
11	chr15:59062739..59063485-chr8:104427097..104427711,2	Hela-S3	cervix:
12	chr15:58519596..58520483-chr15:59049894..59051015,4	MCF-7	breast:
13	chr15:59040332..59042868-chr15:59224764..59227201,2	MCF-7	breast:
14	chr15:59158497..59160419-chr15:59185793..59188060,2	K562	blood:
15	chr15:59062962..59064061-chr17:73775541..73776117,3	Hela-S3	cervix:
16	chr15:59146076..59151361-chr15:59223071..59227542,5	MCF-7	breast:
17	chr15:59207257..59208801-chr15:59210562..59212811,2	K562	blood:
18	chr1:146556597..146557184-chr15:59063588..59064562,2	Hela-S3	cervix:
19	chr15:59023017..59026002-chr15:59026211..59028184,2	K562	blood:
20	chr10:60145015..60145625-chr15:59063219..59063805,2	Hela-S3	cervix:
21	chr15:59211354..59213234-chr15:59223328..59226412,3	MCF-7	breast:
22	chr15:59025699..59027960-chr15:59038496..59040906,2	K562	blood:
23	chr15:59038409..59043803-chr15:59043836..59048384,6	MCF-7	breast:
24	chr1:151881708..151882900-chr15:59041095..59042389,4	Hela-S3	cervix:
25	chr15:59062887..59063494-chr16:70557453..70557956,2	Hela-S3	cervix:
26	chr15:59038832..59043387-chr15:59060936..59065101,7	K562	blood:
27	chr15:59042046..59047020-chr15:59050998..59056418,7	K562	blood:
28	chr15:59040703..59045173-chr15:59068143..59071551,4	K562	blood:
29	chr15:59162668..59165557-chr15:59167625..59170277,3	K562	blood:
30	chr15:59041650..59042242-chr3:50336459..50337109,2	Hela-S3	cervix:
31	chr15:59046301..59048650-chr15:59061431..59063261,2	K562	blood:
32	chr15:59048564..59050956-chr15:59058721..59061333,2	K562	blood:
33	chr15:59041259..59043386-chr15:59054816..59056706,2	K562	blood:
34	chr15:59162668..59165557-chr15:59167625..59170277,3	K562	blood:
35	chr15:59171523..59173361-chr15:59197628..59200554,2	K562	blood:
36	chr15:59144722..59148208-chr15:59148286..59151538,5	K562	blood:
37	chr15:59167194..59169096-chr15:59170311..59172735,2	K562	blood:
38	chr15:59199885..59202097-chr15:59225544..59227395,2	K562	blood:
39	chr15:59171523..59173361-chr15:59197628..59200554,2	K562	blood:
40	chr15:59076693..59078946-chr15:59080915..59082801,2	K562	blood:
41	chr15:59200337..59203296-chr15:59205002..59207680,2	K562	blood:
42	chr15:59064062..59066974-chr15:59068078..59069600,2	MCF-7	breast:
43	chr15:59061712..59064488-chr15:59178344..59181230,2	K562	blood:
44	chr15:59061870..59064465-chr15:59224425..59227494,5	K562	blood:
45	chr15:59063370..59063986-chr5:34929328..34930251,2	Hela-S3	cervix:
46	chr15:59145262..59147109-chr15:59151611..59154178,2	K562	blood:
47	chr15:59086163..59088168-chr15:59090326..59092579,2	K562	blood:
48	chr15:59158497..59160419-chr15:59185793..59188060,2	K562	blood:
49	chr15:59185300..59188168-chr15:59204704..59206498,2	K562	blood:
50	chr15:59051351..59055079-chr15:59061641..59063693,4	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLTM-2	chr15:59211128-59211697	ENSG00000247934
2	lnc-ADAM10-1	chr15:59062586-59063173	ENSG00000245975.2
3	lnc-ADAM10-1	chr15:59062586-59063173	ENSG00000245975
4	lnc-ADAM10-3	chr15:59047824-59047963	NONHSAT044126
5	lnc-ADAM10-4	chr15:59052666-59052880	NONHSAT044127
6	lnc-RNF111-3	chr15:59148026-59149425	NONHSAT044131
7	lnc-ADAM10-1	chr15:59060273-59061078	ENSG00000245975
8	lnc-RNF111-3	chr15:59149733-59149750	NONHSAT044131
9	lnc-ADAM10-1	chr15:59060271-59061078	ENSG00000245975.2
10	lnc-RNF111-2	chr15:59152982-59154096	NONHSAT044134
11	lnc-RNF111-1	chr15:59109857-59109927	ENSG00000259402.1
12	lnc-ADAM10-8	chr15:59204762-59205000	NONHSAT044141
13	lnc-RNF111-1	chr15:59107471-59107925	ENSG00000259402.1
14	lnc-ADAM10-1	chr15:59062265-59063262	NONHSAT044129
15	lnc-FAM63B-3	chr15:59161858-59162333	NONHSAT044135
16	lnc-ADAM10-8	chr15:59193167-59193486	NONHSAT044141
17	lnc-ADAM10-3	chr15:59048272-59048446	NONHSAT044126

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM63B	hsa-miR-124-3p	chr15:59148311-59148330
2	SLTM	hsa-miR-186-5p	chr15:59172081-59172102

Variant related genes	Relation type
ENSG00000200318	TF binding region
ENSG00000242747	TF binding region
ENSG00000259173	TF binding region
ADAM10	TF binding region
ZNF444P1	TF binding region
RNF111	TF binding region
ENSG00000225798	TF binding region
ENSG00000259402	TF binding region
ENSG00000259353	TF binding region
FAM63B	TF binding region
ENSG00000245975	TF binding region
SLTM	TF binding region
ENSG00000200318	CpG island
ENSG00000242747	CpG island
ENSG00000259173	CpG island
ADAM10	CpG island
ZNF444P1	CpG island
RNF111	CpG island
ENSG00000225798	CpG island
ENSG00000259402	CpG island
ENSG00000259353	CpG island
FAM63B	CpG island
ENSG00000245975	CpG island
SLTM	CpG island
ENSG00000204261	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000259173	chromatin interactions
ENSG00000164934	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000164933	chromatin interactions
ENSG00000259353	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000243477	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000186792	chromatin interactions
ENSG00000170348	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000168724	chromatin interactions
ENSG00000108064	chromatin interactions
ENSG00000159147	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000204264	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000137845	chromatin interactions
ENSG00000124160	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000125457	chromatin interactions
ENSG00000173295	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000240065	chromatin interactions
ENSG00000159445	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000187193	chromatin interactions
ENSG00000236859	chromatin interactions
ENSG00000200318	chromatin interactions
ENSG00000157450	chromatin interactions
ENSG00000238279	chromatin interactions
ENSG00000259738	chromatin interactions
ENSG00000075624	chromatin interactions
UBE4A	miRNA target sites
PSAT1	miRNA target sites

Extended variants
information (count: 7353 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:7353 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16940712	chr15:59027139-59027140	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150787995	chr15:59027150-59027151	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs112056817	chr15:59027159-59027160	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs551972664	chr15:59027172-59027173	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs571783699	chr15:59027205-59027206	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs534268459	chr15:59027207-59027208	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs74017297	chr15:59027226-59027227	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567658151	chr15:59027262-59027263	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs536610342	chr15:59027270-59027271	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs556209769	chr15:59027405-59027406	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs149554686	chr15:59027424-59027425	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs183987157	chr15:59027432-59027433	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs538472730	chr15:59027450-59027451	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs558315981	chr15:59027455-59027456	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs527271299	chr15:59027461-59027462	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571835490	chr15:59027481-59027482	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs540723694	chr15:59027501-59027502	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs560589677	chr15:59027503-59027504	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs574359130	chr15:59027514-59027515	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs543357369	chr15:59027523-59027524	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs563058623	chr15:59027536-59027537	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs148430422	chr15:59027600-59027601	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs59946621	chr15:59027603-59027604	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs34111635	chr15:59027629-59027630	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs531997226	chr15:59027632-59027633	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs394845	chr15:59027671-59027672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs188883563	chr15:59027690-59027691	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs565478550	chr15:59027698-59027699	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527829599	chr15:59027700-59027701	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs533372447	chr15:59027762-59027763	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs74017298	chr15:59027766-59027767	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs567706889	chr15:59027798-59027799	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs144293463	chr15:59027829-59027830	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs577952307	chr15:59027833-59027834	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs560500292	chr15:59027940-59027941	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs550115293	chr15:59027992-59027993	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs371620351	chr15:59028003-59028004	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75418573	chr15:59028033-59028034	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs140067581	chr15:59028070-59028071	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs572021347	chr15:59028125-59028126	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs536097466	chr15:59028126-59028127	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs534470498	chr15:59028136-59028137	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs536126900	chr15:59028138-59028139	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs574444035	chr15:59028140-59028141	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs543063644	chr15:59028155-59028156	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs550189520	chr15:59028270-59028271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563277251	chr15:59028313-59028314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576690126	chr15:59028320-59028321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545709428	chr15:59028339-59028340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565540208	chr15:59028398-59028399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	19238632	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	19318576	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:5110 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58977200-59039200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr15:59008600-59028400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr15:59009600-59029600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr15:59009800-59035400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:59010800-59031200	Weak transcription	Dnd41	blood
6	chr15:59013200-59030200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr15:59013400-59029800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr15:59016800-59034200	Weak transcription	Brain Germinal Matrix	brain
9	chr15:59017200-59027400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr15:59017200-59034400	Weak transcription	Fetal Kidney	kidney
11	chr15:59017400-59029000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr15:59021800-59029000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:59021800-59029600	Weak transcription	Fetal Lung	lung
14	chr15:59022000-59029600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:59022200-59040200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr15:59022400-59029400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr15:59022600-59034800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr15:59022600-59038600	Weak transcription	Fetal Brain Female	brain
19	chr15:59022800-59029600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr15:59023000-59030400	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr15:59023600-59027200	Enhancers	NHEK	skin
22	chr15:59023600-59040000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr15:59023800-59027200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:59023800-59028600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr15:59024000-59038200	Weak transcription	Fetal Stomach	stomach
26	chr15:59024200-59034600	Weak transcription	Rectal Smooth Muscle	rectum
27	chr15:59024400-59027400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr15:59024400-59028400	Weak transcription	Primary B cells from cord blood	blood
29	chr15:59024400-59029600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr15:59024400-59029800	Weak transcription	Hela-S3	cervix
31	chr15:59024400-59029800	Weak transcription	HUVEC	blood vessel
32	chr15:59024400-59030000	Weak transcription	NHLF	lung
33	chr15:59024400-59030600	Weak transcription	Ovary	ovary
34	chr15:59024400-59032400	Weak transcription	Lung	lung
35	chr15:59024400-59035200	Weak transcription	Fetal Muscle Leg	muscle
36	chr15:59024600-59029000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr15:59024600-59029600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr15:59024600-59029800	Weak transcription	Duodenum Mucosa	Duodenum
39	chr15:59024600-59029800	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr15:59024600-59029800	Weak transcription	HSMM	muscle
41	chr15:59024600-59031800	Weak transcription	Primary B cells from peripheral blood	blood
42	chr15:59024600-59033200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr15:59024600-59034400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr15:59024800-59030000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr15:59025400-59028200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr15:59025400-59029600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr15:59025400-59029800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr15:59025400-59030200	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr15:59025400-59030200	Weak transcription	NH-A	brain
50	chr15:59025400-59030400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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