Variant report

Variant	esv1843037
Chromosome Location	chr15:59005922-59115159
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2334)
CpG islands
(count:1589)
Chromatin interactive
region (count:140)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2334 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59041948-59042900	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:59042958-59043022	K562	blood:	n/a	n/a
3	ARID3A	chr15:59062801-59063620	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:59040631-59041032	K562	blood:	n/a	n/a
5	ARID3A	chr15:59086282-59086455	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:59041643-59042081	K562	blood:	n/a	n/a
7	ARID3A	chr15:59098727-59098770	K562	blood:	n/a	chr15:59098731-59098747
8	ARID3A	chr15:59063011-59063531	K562	blood:	n/a	n/a
9	ATF1	chr15:59062751-59063660	K562	blood:	n/a	chr15:59063467-59063481
10	ATF1	chr15:59041873-59042478	K562	blood:	n/a	n/a
11	ATF1	chr15:59097368-59097629	K562	blood:	n/a	n/a
12	ATF1	chr15:59071879-59072075	K562	blood:	n/a	n/a
13	ATF2	chr15:59016522-59017071	GM12878	blood:	n/a	n/a
14	ATF2	chr15:59062735-59063607	GM12878	blood:	n/a	chr15:59063467-59063481
15	ATF2	chr15:59042161-59042561	GM12878	blood:	n/a	n/a
16	ATF3	chr15:59041880-59042188	K562	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
17	ATF3	chr15:59095848-59096053	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr15:59041796-59042229	H1-hESC	embryonic stem cell:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
19	ATF3	chr15:59041805-59042226	K562	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
20	ATF3	chr15:59041954-59042205	GM12878	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
21	ATF3	chr15:59063182-59063710	K562	blood:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
22	ATF3	chr15:59062871-59063734	A549	lung:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
23	ATF3	chr15:59041919-59042231	HepG2	liver:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
24	ATF3	chr15:59041856-59042237	H1-hESC	embryonic stem cell:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
25	ATF3	chr15:59041797-59042286	GM12878	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
26	ATF3	chr15:59062924-59063709	A549	lung:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
27	BACH1	chr15:59062895-59063578	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr15:59041132-59041190	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr15:59088090-59088336	GM12878	blood:	n/a	n/a
30	BATF	chr15:59088024-59088402	GM12878	blood:	n/a	n/a
31	BCL3	chr15:59062699-59063768	A549	lung:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
32	BCL3	chr15:59041625-59042621	A549	lung:	n/a	n/a
33	BCL3	chr15:59062776-59063544	A549	lung:	n/a	chr15:59063204-59063213 chr15:59063497-59063505
34	BCLAF1	chr15:59040498-59041050	GM12878	blood:	n/a	n/a
35	BCLAF1	chr15:59041667-59042538	GM12878	blood:	n/a	n/a
36	BCLAF1	chr15:59062982-59063764	GM12878	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
37	BCLAF1	chr15:59062912-59063903	GM12878	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
38	BCLAF1	chr15:59062765-59063599	K562	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
39	BHLHE40	chr15:59040333-59041128	GM12878	blood:	n/a	n/a
40	BHLHE40	chr15:59035031-59035275	HepG2	liver:	n/a	n/a
41	BHLHE40	chr15:59041799-59042374	HepG2	liver:	n/a	n/a
42	BHLHE40	chr15:59024969-59025132	K562	blood:	n/a	n/a
43	BHLHE40	chr15:59062863-59063903	K562	blood:	n/a	n/a
44	BHLHE40	chr15:59063034-59063636	GM12878	blood:	n/a	n/a
45	BHLHE40	chr15:59085998-59086375	HepG2	liver:	n/a	n/a
46	BHLHE40	chr15:59064126-59064545	K562	blood:	n/a	n/a
47	BHLHE40	chr15:59041995-59042213	A549	lung:	n/a	n/a
48	BHLHE40	chr15:59040938-59042760	K562	blood:	n/a	chr15:59041307-59041323 chr15:59042462-59042478
49	BHLHE40	chr15:59062813-59063860	HepG2	liver:	n/a	n/a
50	BHLHE40	chr15:59041633-59042646	GM12878	blood:	n/a	chr15:59042462-59042478

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59063261-59063311	H1-hESC	embryonic stem cell:	embryo
2	chr15:59063438-59063488	Jurkat	blood:	n/a
3	chr15:59063885-59063935	ovcar-3	ovarian:	n/a
4	chr15:59063261-59063311	H1-hESC	embryonic stem cell:	embryo
5	chr15:59063438-59063488	Jurkat	blood:	n/a
6	chr15:59063885-59063935	ovcar-3	ovarian:	n/a
7	chr15:59063176-59063226	HEEpiC	esophagus:	n/a
8	chr15:59063378-59063428	CMK	blood:	n/a
9	chr15:59040869-59040919	LNCaP	prostate:	n/a
10	chr15:59063176-59063226	NB4	blood:	n/a
11	chr15:59041175-59041225	HEK293	kidney:	embryo
12	chr15:59063699-59063749	HMEC	breast:	n/a
13	chr15:59060978-59061028	PFSK-1	brain:	n/a
14	chr15:59063274-59063324	HNPCEpiC	eye:	n/a
15	chr15:59063176-59063226	A549	lung:	n/a
16	chr15:59063261-59063311	GM19239	blood:	n/a
17	chr15:59042242-59042292	GM06990	blood:	n/a
18	chr15:59042352-59042402	HNPCEpiC	eye:	n/a
19	chr15:59041689-59041739	HCT-116	colon:	n/a
20	chr15:59041883-59041933	AG04450	lung:	fetal
21	chr15:59041175-59041225	GM19239	blood:	n/a
22	chr15:59042684-59042734	HCPEpiC	choroid plexus:	n/a
23	chr15:59042325-59042375	HRE	kidney:	n/a
24	chr15:59041175-59041225	GM12892	blood:	n/a
25	chr15:59063586-59063636	PrEC	prostate:	n/a
26	chr15:59063274-59063324	HRE	kidney:	n/a
27	chr15:59063438-59063488	BE2_C	brain:	n/a
28	chr15:59040869-59040919	NB4	blood:	n/a
29	chr15:59063586-59063636	GM19239	blood:	n/a
30	chr15:59063438-59063488	A549	lung:	n/a
31	chr15:59063272-59063322	NH-A	brain:	n/a
32	chr15:59063378-59063428	AG04450	lung:	fetal
33	chr15:59042684-59042734	NT2-D1	testis:	n/a
34	chr15:59063176-59063226	T-47D	breast:	n/a
35	chr15:59063438-59063488	HEEpiC	esophagus:	n/a
36	chr15:59063378-59063428	HCF	heart:	n/a
37	chr15:59042352-59042402	SAEC	small airway:	n/a
38	chr15:59041883-59041933	HEK293	kidney:	embryo
39	chr15:59063113-59063163	IMR90	lung:	fetal
40	chr15:59040869-59040919	A549	lung:	n/a
41	chr15:59040869-59040919	Caco-2	colon:	n/a
42	chr15:59063113-59063163	HMEC	breast:	n/a
43	chr15:59040869-59040919	GM06990	blood:	n/a
44	chr15:59024033-59024083	GM12892	blood:	n/a
45	chr15:59063885-59063935	HNPCEpiC	eye:	n/a
46	chr15:59042352-59042402	NB4	blood:	n/a
47	chr15:59042325-59042375	BJ	skin:	n/a
48	chr15:59063609-59063659	HRE	kidney:	n/a
49	chr15:59063438-59063488	MCF10A-Er-Src	breast:	n/a
50	chr15:59042282-59042332	HCPEpiC	choroid plexus:	n/a

(count:140 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:59041471..59042418-chr7:5569782..5570300,2	Hela-S3	cervix:
2	chr15:59007785..59010098-chr15:59010167..59012488,3	K562	blood:
3	chr15:59062926..59063673-chr6:32811899..32812879,2	Hela-S3	cervix:
4	chr15:59040418..59043088-chr15:59070016..59071551,2	K562	blood:
5	chr15:59076693..59078946-chr15:59080915..59082801,2	K562	blood:
6	chr15:59025413..59026960-chr15:59029067..59030744,2	K562	blood:
7	chr15:59021784..59023726-chr15:59040187..59042345,2	K562	blood:
8	chr15:59038007..59039912-chr15:59224020..59226642,2	K562	blood:
9	chr15:59075699..59078690-chr15:59123269..59125311,2	K562	blood:
10	chr15:59052627..59055079-chr15:59061662..59063562,2	K562	blood:
11	chr1:151881708..151882900-chr15:59041095..59042389,4	Hela-S3	cervix:
12	chr15:59038297..59040684-chr15:59062023..59064317,2	MCF-7	breast:
13	chr15:59109415..59111364-chr15:59224103..59226859,2	MCF-7	breast:
14	chr15:59057970..59061126-chr15:59061788..59064643,4	K562	blood:
15	chr15:59040971..59041536-chr6:31588491..31588996,2	Hela-S3	cervix:
16	chr15:59033413..59035094-chr15:59037580..59040574,2	MCF-7	breast:
17	chr15:59040077..59045685-chr15:59061303..59067063,14	K562	blood:
18	chr15:59023017..59026002-chr15:59026211..59028184,2	K562	blood:
19	chr15:59038486..59040541-chr15:59040847..59043052,2	MCF-7	breast:
20	chr15:59042171..59043978-chr15:59046627..59049380,3	K562	blood:
21	chr15:59061870..59064465-chr15:59224425..59227494,5	K562	blood:
22	chr15:59017485..59020377-chr15:59047037..59049380,2	MCF-7	breast:
23	chr15:59061712..59064488-chr15:59178344..59181230,2	K562	blood:
24	chr15:59037438..59039932-chr15:59074278..59075927,2	K562	blood:
25	chr15:59051351..59055079-chr15:59061641..59063693,4	K562	blood:
26	chr15:59046301..59048650-chr15:59061431..59063279,4	K562	blood:
27	chr15:59114714..59117798-chr15:59118942..59121518,3	K562	blood:
28	chr15:59026224..59028266-chr15:59062412..59064795,2	MCF-7	breast:
29	chr15:59063503..59065651-chr15:59082351..59084148,2	MCF-7	breast:
30	chr15:59040618..59043171-chr15:59061931..59064461,2	MCF-7	breast:
31	chr15:59069188..59071465-chr15:59071661..59073187,2	MCF-7	breast:
32	chr15:59033181..59035462-chr15:59039185..59042530,6	MCF-7	breast:
33	chr15:59086163..59088168-chr15:59090326..59092579,2	K562	blood:
34	chr15:59041223..59041976-chr20:44717836..44718630,2	Hela-S3	cervix:
35	chr15:59062813..59063449-chr8:8085838..8086625,2	Hela-S3	cervix:
36	chr15:59062739..59063485-chr8:104427097..104427711,2	Hela-S3	cervix:
37	chr15:59108477..59110665-chr15:59113171..59114867,2	K562	blood:
38	chr15:59049338..59052129-chr15:59052697..59054874,3	K562	blood:
39	chr15:59038832..59043387-chr15:59060936..59065101,7	K562	blood:
40	chr15:59025073..59028168-chr15:59040901..59043745,3	K562	blood:
41	chr15:58841936..58843699-chr15:59035411..59037859,2	MCF-7	breast:
42	chr15:59041435..59041987-chr21:34960400..34961391,2	Hela-S3	cervix:
43	chr1:149858036..149858746-chr15:59040718..59041595,2	Hela-S3	cervix:
44	chr1:153505831..153506827-chr15:59041415..59041985,2	Hela-S3	cervix:
45	chr15:58982751..58984795-chr15:59030172..59031707,2	K562	blood:
46	chr15:59040332..59042868-chr15:59224764..59227201,2	MCF-7	breast:
47	chr15:59021059..59023749-chr15:59034779..59037397,2	K562	blood:
48	chr15:59028939..59031990-chr15:59040702..59043851,4	K562	blood:
49	chr15:59006673..59008255-chr15:59014528..59016960,2	K562	blood:
50	chr15:59040077..59045685-chr15:59061303..59067063,14	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-4	chr15:59052666-59052880	NONHSAT044127
2	lnc-RNF111-1	chr15:59107471-59107925	ENSG00000259402.1
3	lnc-ADAM10-1	chr15:59062586-59063173	ENSG00000245975.2
4	lnc-ADAM10-3	chr15:59048272-59048446	NONHSAT044126
5	lnc-ADAM10-1	chr15:59060273-59061078	ENSG00000245975
6	lnc-ADAM10-1	chr15:59060271-59061078	ENSG00000245975.2
7	lnc-RNF111-1	chr15:59109857-59109927	ENSG00000259402.1
8	lnc-ADAM10-3	chr15:59047824-59047963	NONHSAT044126
9	lnc-ADAM10-1	chr15:59062586-59063173	ENSG00000245975
10	lnc-ADAM10-1	chr15:59062265-59063262	NONHSAT044129

No data

Variant related genes	Relation type
ENSG00000200318	TF binding region
ENSG00000259173	TF binding region
FAM63B	TF binding region
ENSG00000245975	TF binding region
ADAM10	TF binding region
ENSG00000259402	TF binding region
ENSG00000200318	CpG island
ENSG00000259173	CpG island
FAM63B	CpG island
ENSG00000245975	CpG island
ADAM10	CpG island
ENSG00000259402	CpG island
ENSG00000159147	chromatin interactions
ENSG00000259173	chromatin interactions
ENSG00000137845	chromatin interactions
ENSG00000236859	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000164934	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000199730	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000159445	chromatin interactions
ENSG00000243477	chromatin interactions
ENSG00000270986	chromatin interactions
ENSG00000125457	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000108064	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000186792	chromatin interactions
ENSG00000124160	chromatin interactions
ENSG00000240065	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000170348	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000187193	chromatin interactions
ENSG00000173295	chromatin interactions
ENSG00000168724	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000204264	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000204261	chromatin interactions
ENSG00000164933	chromatin interactions
ENSG00000200318	chromatin interactions
ENSG00000238279	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000103051	chromatin interactions
PSAT1	miRNA target sites
UBE4A	miRNA target sites

Extended variants
information (count: 4537 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4537 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8029805	chr15:59005922-59005923	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs8028872	chr15:59005926-59005927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530490544	chr15:59005962-59005963	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370884083	chr15:59005974-59005975	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs577540589	chr15:59006034-59006035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149817660	chr15:59006037-59006038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563879474	chr15:59006059-59006060	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184083404	chr15:59006077-59006078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563255843	chr15:59006114-59006115	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187338542	chr15:59006134-59006135	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145874636	chr15:59006156-59006157	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs71938417	chr15:59006171-59006172	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148582073	chr15:59006172-59006173	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548458242	chr15:59006174-59006175	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568562091	chr15:59006176-59006177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs537103335	chr15:59006180-59006181	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144232550	chr15:59006193-59006194	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551913589	chr15:59006194-59006195	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541354626	chr15:59006204-59006205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554900754	chr15:59006230-59006231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147770359	chr15:59006240-59006241	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373407333	chr15:59006251-59006252	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs8030378	chr15:59006259-59006260	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542025404	chr15:59006279-59006280	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs528436647	chr15:59006326-59006327	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146959615	chr15:59006328-59006329	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs575304533	chr15:59006329-59006330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543931448	chr15:59006357-59006358	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564150403	chr15:59006372-59006373	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150945174	chr15:59006377-59006378	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552934023	chr15:59006397-59006398	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560103446	chr15:59006398-59006399	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12907267	chr15:59006432-59006433	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528765567	chr15:59006456-59006457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs192124972	chr15:59006461-59006462	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs146534670	chr15:59006491-59006492	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372737840	chr15:59006495-59006496	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs71116591	chr15:59006523-59006524	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs199563986	chr15:59006526-59006527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543217020	chr15:59006549-59006550	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs377556163	chr15:59006555-59006556	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568520223	chr15:59006573-59006574	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531072312	chr15:59006620-59006621	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs550791352	chr15:59006631-59006632	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs140840300	chr15:59006683-59006684	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs112990788	chr15:59006685-59006686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552916702	chr15:59006763-59006764	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138666082	chr15:59006799-59006800	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535344836	chr15:59006824-59006825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555550344	chr15:59006833-59006834	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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

Chromatin state (count:3408 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58977200-59007800	Weak transcription	HepG2	liver
2	chr15:58977200-59039200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr15:58982600-59008000	Weak transcription	Fetal Brain Male	brain
4	chr15:58983200-59016600	Weak transcription	Small Intestine	intestine
5	chr15:58986600-59016600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr15:58987400-59012000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr15:58987600-59007800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr15:58989800-59016800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:58990000-59023400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr15:58991800-59012200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr15:58992000-59009000	Weak transcription	Placenta	Placenta
12	chr15:58992000-59010800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:58992000-59015800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr15:58992000-59023000	Weak transcription	Esophagus	oesophagus
15	chr15:58992000-59023800	Weak transcription	Aorta	Aorta
16	chr15:58992200-59008600	Weak transcription	Fetal Lung	lung
17	chr15:58992400-59011600	Weak transcription	HUVEC	blood vessel
18	chr15:58992400-59012000	Weak transcription	Brain Anterior Caudate	brain
19	chr15:58992600-59016600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr15:58992600-59021000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr15:58992800-59007200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr15:58992800-59008400	Weak transcription	A549	lung
23	chr15:58993200-59010200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr15:58993200-59010800	Weak transcription	K562	blood
25	chr15:58993400-59010600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr15:58994400-59012400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr15:58994400-59016400	Weak transcription	Adipose Nuclei	Adipose
28	chr15:58994800-59007600	Weak transcription	Dnd41	blood
29	chr15:58996000-59016600	Weak transcription	Colonic Mucosa	Colon
30	chr15:58996200-59016800	Weak transcription	Psoas Muscle	Psoas
31	chr15:58996400-59007600	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr15:58996600-59016600	Weak transcription	NHLF	lung
33	chr15:58996600-59016800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr15:58996800-59010800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr15:58998200-59009400	Weak transcription	Hela-S3	cervix
36	chr15:58998400-59016600	Weak transcription	Osteobl	bone
37	chr15:58998600-59016600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr15:58998600-59016800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr15:58999000-59013600	Weak transcription	Right Ventricle	heart
40	chr15:58999000-59023800	Weak transcription	Gastric	stomach
41	chr15:59000200-59008400	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr15:59000600-59012200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr15:59002400-59016200	Weak transcription	Left Ventricle	heart
44	chr15:59002600-59008600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr15:59003000-59007400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr15:59003000-59010000	Strong transcription	HSMM	muscle
47	chr15:59003400-59008800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr15:59003400-59016400	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr15:59003800-59006600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr15:59003800-59012400	Strong transcription	Fetal Thymus	thymus

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