Variant report

Variant	nsv1048114
Chromosome Location	chr15:50885156-50949798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:436)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:50885990-50886949	K562	blood:	n/a	n/a
2	ARID3A	chr15:50888476-50888556	K562	blood:	n/a	n/a
3	ARID3A	chr15:50914579-50914778	K562	blood:	n/a	n/a
4	ATF1	chr15:50916939-50917053	K562	blood:	n/a	n/a
5	ATF1	chr15:50886574-50886849	K562	blood:	n/a	n/a
6	ATF2	chr15:50946651-50947033	GM12878	blood:	n/a	n/a
7	BATF	chr15:50946645-50947003	GM12878	blood:	n/a	n/a
8	BATF	chr15:50946619-50946969	GM12878	blood:	n/a	n/a
9	CCNT2	chr15:50933565-50933899	K562	blood:	n/a	n/a
10	CCNT2	chr15:50886474-50886898	K562	blood:	n/a	n/a
11	CEBPB	chr15:50894829-50895045	A549	lung:	n/a	n/a
12	CEBPB	chr15:50889065-50889265	IMR90	lung:	n/a	n/a
13	CEBPB	chr15:50905825-50906178	HepG2	liver:	n/a	n/a
14	CEBPB	chr15:50894818-50895097	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:50916905-50917183	A549	lung:	n/a	n/a
16	CEBPB	chr15:50931794-50931833	K562	blood:	n/a	n/a
17	CEBPB	chr15:50929902-50930087	IMR90	lung:	n/a	chr15:50930024-50930035
18	CEBPB	chr15:50905849-50906159	IMR90	lung:	n/a	n/a
19	CEBPB	chr15:50905892-50906190	MCF-7	breast:	n/a	n/a
20	CEBPB	chr15:50905830-50906159	K562	blood:	n/a	n/a
21	CEBPB	chr15:50916859-50917181	K562	blood:	n/a	n/a
22	CEBPB	chr15:50905848-50906147	A549	lung:	n/a	n/a
23	CEBPB	chr15:50905719-50906245	MCF-7	breast:	n/a	n/a
24	CEBPB	chr15:50916902-50917200	IMR90	lung:	n/a	n/a
25	CEBPB	chr15:50931692-50932047	A549	lung:	n/a	n/a
26	CEBPB	chr15:50929899-50930169	HepG2	liver:	n/a	chr15:50930024-50930035
27	CEBPB	chr15:50889075-50889077	K562	blood:	n/a	n/a
28	CEBPB	chr15:50886533-50886784	K562	blood:	n/a	n/a
29	CEBPB	chr15:50916897-50917199	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:50905894-50906111	A549	lung:	n/a	n/a
31	CEBPB	chr15:50905827-50906151	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:50929889-50930144	A549	lung:	n/a	chr15:50930024-50930035
33	CEBPB	chr15:50905809-50906222	A549	lung:	n/a	n/a
34	CEBPD	chr15:50886481-50887012	K562	blood:	n/a	n/a
35	CEBPD	chr15:50933672-50934006	K562	blood:	n/a	n/a
36	CEBPD	chr15:50886419-50886927	K562	blood:	n/a	n/a
37	CTCF	chr15:50914640-50914790	GM12873	blood:	n/a	n/a
38	CTCF	chr15:50914576-50914901	GM12878	blood:	n/a	n/a
39	CTCF	chr15:50937040-50937190	GM12871	blood:	n/a	n/a
40	CTCF	chr15:50914660-50914810	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr15:50914660-50914810	HFF	foreskin:	n/a	n/a
42	CTCF	chr15:50915040-50915190	RPTEC	kidney:	n/a	n/a
43	CTCF	chr15:50914660-50914810	HMEC	breast:	n/a	n/a
44	CTCF	chr15:50914801-50914840	MCF-7	breast:	n/a	n/a
45	CTCF	chr15:50914640-50914790	HCFaa	heart:	n/a	n/a
46	CTCF	chr15:50915080-50915230	RPTEC	kidney:	n/a	n/a
47	CTCF	chr15:50914581-50914848	A549	lung:	n/a	n/a
48	CTCF	chr15:50914640-50914790	AG09319	gingival:	n/a	n/a
49	CTCF	chr15:50914620-50914770	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr15:50937111-50937256	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:50920452-50920502	NHDF-neo	bronchial:	n/a
2	chr15:50920452-50920502	NB4	blood:	n/a
3	chr15:50920452-50920502	SK-N-SH	brain:	n/a
4	chr15:50920452-50920502	HPAEpiC	pulmonary alveolar:	n/a
5	chr15:50920452-50920502	SKMC	muscle:	n/a
6	chr15:50920452-50920502	LNCaP	prostate:	n/a
7	chr15:50920452-50920502	RPTEC	kidney:	n/a
8	chr15:50920452-50920502	AoSMC	blood vessel:	n/a
9	chr15:50920452-50920502	HepG2	liver:	n/a
10	chr15:50920452-50920502	HL-60	blood:	n/a
11	chr15:50920452-50920502	HMEC	breast:	n/a
12	chr15:50920452-50920502	AG10803	skin:	n/a
13	chr15:50920452-50920502	K562	blood:	n/a
14	chr15:50920452-50920502	MCF10A-Er-Src	breast:	n/a
15	chr15:50920452-50920502	HIPEpiC	eye:	n/a
16	chr15:50920452-50920502	BE2_C	brain:	n/a
17	chr15:50920452-50920502	AG09319	gingival:	n/a
18	chr15:50920452-50920502	AG09309	skin:	n/a
19	chr15:50920452-50920502	GM12892	blood:	n/a
20	chr15:50920452-50920502	NH-A	brain:	n/a
21	chr15:50920452-50920502	Caco-2	colon:	n/a
22	chr15:50920452-50920502	HEEpiC	esophagus:	n/a
23	chr15:50920452-50920502	HRPEpiC	eye:	n/a
24	chr15:50920452-50920502	NHBE	bronchial:	n/a
25	chr15:50920452-50920502	HCPEpiC	choroid plexus:	n/a
26	chr15:50920452-50920502	Jurkat	blood:	n/a
27	chr15:50920452-50920502	GM19239	blood:	n/a
28	chr15:50920452-50920502	SK-N-SH_RA	brain:	n/a
29	chr15:50920452-50920502	MCF-7	breast:	n/a
30	chr15:50920452-50920502	HAEpiC	amniotic membrane:	n/a
31	chr15:50920452-50920502	HCT-116	colon:	n/a
32	chr15:50920452-50920502	CMK	blood:	n/a
33	chr15:50920452-50920502	AG04450	lung:	fetal
34	chr15:50920452-50920502	A549	lung:	n/a
35	chr15:50920452-50920502	BJ	skin:	n/a
36	chr15:50920452-50920502	HUVEC	blood vessel:	n/a
37	chr15:50920452-50920502	HRE	kidney:	n/a
38	chr15:50920452-50920502	HCF	heart:	n/a
39	chr15:50920452-50920502	T-47D	breast:	n/a
40	chr15:50920452-50920502	IMR90	lung:	fetal
41	chr15:50920452-50920502	Hela-S3	cervix:	n/a
42	chr15:50920452-50920502	NT2-D1	testis:	n/a
43	chr15:50920452-50920502	GM12878	blood:	n/a
44	chr15:50920452-50920502	HNPCEpiC	eye:	n/a
45	chr15:50920452-50920502	ovcar-3	ovarian:	n/a
46	chr15:50920452-50920502	Hepatocyte	liver:	n/a
47	chr15:50920452-50920502	ECC-1	luminal epithelium:	n/a
48	chr15:50920452-50920502	AG04449	skin:	fetal
49	chr15:50920452-50920502	SK-N-MC	brain:	n/a
50	chr15:50920452-50920502	U87	brain:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:50914710..50917387-chr15:50934928..50936647,2	MCF-7	breast:
2	chr15:50929757..50931631-chr15:50935588..50938584,2	MCF-7	breast:
3	chr15:50885914..50887497-chr15:50920391..50922756,2	K562	blood:
4	chr15:50644948..50647496-chr15:50903184..50905724,2	MCF-7	breast:
5	chr15:50646177..50648161-chr15:50884558..50887057,2	K562	blood:
6	chr15:50925249..50927102-chr15:51201168..51202804,2	MCF-7	breast:
7	chr15:50894679..50897378-chr15:50902879..50904659,2	MCF-7	breast:
8	chr15:50918354..50921026-chr15:51021586..51024072,2	MCF-7	breast:
9	chr15:50944212..50946075-chr15:50977425..50980194,3	K562	blood:
10	chr15:50891850..50893589-chr15:50903220..50904870,2	MCF-7	breast:
11	chr15:50916244..50918510-chr15:50943858..50945461,2	MCF-7	breast:
12	chr15:50916413..50918620-chr15:50919827..50924015,3	K562	blood:
13	chr15:50890587..50894134-chr15:50900500..50903052,3	MCF-7	breast:
14	chr15:50897808..50900573-chr15:50902086..50904020,3	K562	blood:
15	chr15:50914714..50916559-chr15:50917058..50919826,2	K562	blood:
16	chr15:50646177..50649955-chr15:50884558..50888661,4	K562	blood:
17	chr15:50645917..50650602-chr15:50893213..50896172,4	MCF-7	breast:
18	chr15:50914267..50915255-chr15:51177811..51178741,3	MCF-7	breast:
19	chr15:50917148..50919923-chr15:50927346..50929750,2	MCF-7	breast:
20	chr15:50551676..50553333-chr15:50885793..50888407,2	K562	blood:
21	chr15:50914576..50915250-chr15:51200327..51201089,2	MCF-7	breast:
22	chr15:50885914..50887497-chr15:50920391..50922756,2	K562	blood:
23	chr15:50646216..50648190-chr15:50918382..50920055,2	MCF-7	breast:
24	chr15:50878762..50881023-chr15:50884773..50886938,2	K562	blood:
25	chr15:50929757..50931631-chr15:50935588..50938584,2	MCF-7	breast:
26	chr15:50939543..50942459-chr15:50946221..50948158,2	K562	blood:
27	chr15:50882354..50884324-chr15:50884736..50886650,2	MCF-7	breast:
28	chr15:50889745..50892079-chr19:13048030..13049882,2	MCF-7	breast:
29	chr15:50933534..50935259-chr15:51198839..51201144,2	MCF-7	breast:
30	chr15:50909782..50912270-chr15:50977423..50980353,2	MCF-7	breast:
31	chr15:50932446..50935258-chr15:50953275..50954778,2	K562	blood:
32	chr15:50885676..50889608-chr15:50891608..50893462,3	K562	blood:
33	chr15:50714902..50717197-chr15:50911765..50913524,2	MCF-7	breast:
34	chr15:50897808..50900573-chr15:50902086..50904020,3	K562	blood:
35	chr15:50917148..50919923-chr15:50927346..50929750,2	MCF-7	breast:
36	chr15:50900703..50903174-chr15:51177027..51179659,2	K562	blood:
37	chr15:50865776..50869008-chr15:50882396..50886787,3	K562	blood:
38	chr15:50939543..50942459-chr15:50946221..50948158,2	K562	blood:
39	chr15:50889435..50893254-chr15:50893944..50897716,3	K562	blood:
40	chr15:50894679..50897378-chr15:50902879..50904659,2	MCF-7	breast:
41	chr15:50645350..50647759-chr15:50913615..50916284,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TRPM7	hsa-miR-10a-5p	chr15:50896505-50896530
2	TRPM7	hsa-miR-10a-5p	chr15:50896593-50896615

Variant related genes	Relation type
TRPM7	TF binding region
TRPM7	CpG island
ENSG00000179218	chromatin interactions
ENSG00000092439	chromatin interactions
ENSG00000081014	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000138592	chromatin interactions

Extended variants
information (count: 2718 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2718 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191116282	chr15:50885197-50885198	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs12904103	chr15:50885225-50885226	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs564053587	chr15:50885256-50885257	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs533904550	chr15:50885259-50885260	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs568184259	chr15:50885270-50885271	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs143376265	chr15:50885322-50885323	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs567691765	chr15:50885337-50885338	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs538522945	chr15:50885355-50885356	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs556936684	chr15:50885358-50885359	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs535157619	chr15:50885359-50885360	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs578214586	chr15:50885370-50885371	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs548774954	chr15:50885434-50885435	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs61403418	chr15:50885492-50885493	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs28460550	chr15:50885505-50885506	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs549983572	chr15:50885517-50885518	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs148379390	chr15:50885526-50885527	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs7172730	chr15:50885540-50885541	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572127404	chr15:50885544-50885545	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs563330458	chr15:50885601-50885602	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs570195878	chr15:50885633-50885634	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs560533385	chr15:50885652-50885653	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs141497458	chr15:50885668-50885669	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs146360972	chr15:50885714-50885715	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs182183096	chr15:50885718-50885719	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs537651050	chr15:50885762-50885763	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs139723375	chr15:50885765-50885766	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs374260570	chr15:50885782-50885783	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs368153984	chr15:50885844-50885845	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs186925744	chr15:50885859-50885860	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs370470588	chr15:50885866-50885867	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs199705543	chr15:50885871-50885872	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs201303254	chr15:50885874-50885875	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs34709007	chr15:50885906-50885907	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs367768346	chr15:50885924-50885925	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs527763327	chr15:50885932-50885933	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs558853834	chr15:50885957-50885958	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs371294148	chr15:50885973-50885974	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs567109	chr15:50885976-50885977	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs368592916	chr15:50885991-50885992	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs567654014	chr15:50886013-50886014	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs538287605	chr15:50886017-50886018	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs3759804	chr15:50886020-50886021	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs571987643	chr15:50886042-50886043	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs375244578	chr15:50886049-50886050	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs534715598	chr15:50886070-50886071	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs568527487	chr15:50886076-50886077	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs16963788	chr15:50886077-50886078	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs572589195	chr15:50886087-50886088	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs192894052	chr15:50886103-50886104	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs480280	chr15:50886199-50886200	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1801 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50846000-50950800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:50847000-50920600	Weak transcription	Aorta	Aorta
3	chr15:50848800-50894800	Strong transcription	Liver	Liver
4	chr15:50849000-50894600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:50850800-50892000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr15:50851800-50936400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr15:50852000-50897400	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr15:50852200-50890200	Weak transcription	Psoas Muscle	Psoas
9	chr15:50852200-50896800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr15:50852800-50887200	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr15:50852800-50888600	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr15:50852800-50893200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:50854600-50957400	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr15:50855600-50890200	Weak transcription	Fetal Brain Male	brain
15	chr15:50855600-50907200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:50855600-50919600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr15:50856400-50892600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:50857400-50922800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr15:50859400-50892000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr15:50859600-50888000	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr15:50859600-50916600	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr15:50860600-50888000	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr15:50860800-50891800	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr15:50861000-50893600	Strong transcription	Placenta	Placenta
25	chr15:50861600-50892200	Strong transcription	Dnd41	blood
26	chr15:50862800-50891000	Strong transcription	A549	lung
27	chr15:50864000-50907400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr15:50864200-50893800	Strong transcription	Osteobl	bone
29	chr15:50865800-50890000	Weak transcription	Brain Substantia Nigra	brain
30	chr15:50867400-50894800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr15:50867400-50908200	Weak transcription	Stomach Mucosa	stomach
32	chr15:50869200-50892400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr15:50869800-50893400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:50869800-50905400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:50869800-50922800	Weak transcription	Gastric	stomach
36	chr15:50869800-50967600	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr15:50870600-50886000	Weak transcription	NHEK	skin
38	chr15:50870800-50890200	Weak transcription	NHLF	lung
39	chr15:50871400-50891600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr15:50871600-50957600	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr15:50873600-50892200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr15:50874000-50887400	Strong transcription	HSMM	muscle
43	chr15:50874000-50892400	Strong transcription	Primary B cells from peripheral blood	blood
44	chr15:50874200-50889000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr15:50875600-50889200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr15:50875800-50892200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr15:50876200-50887200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:50876400-50897600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr15:50876600-50886800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr15:50876600-50891200	Strong transcription	Fetal Intestine Large	intestine

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