Variant report

Variant	nsv1049977
Chromosome Location	chr15:55502508-55555694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:948)
CpG islands
(count:184)
Chromatin interactive
region (count:125)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:55529100-55530323	K562	blood:	n/a	n/a
2	ARID3A	chr15:55527826-55528022	K562	blood:	n/a	n/a
3	ARID3A	chr15:55542686-55542931	K562	blood:	n/a	n/a
4	ARID3A	chr15:55526466-55527155	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:55547675-55547685	K562	blood:	n/a	n/a
6	ARID3A	chr15:55542492-55543043	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:55513290-55513722	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:55552870-55553285	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:55509833-55510139	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:55509887-55510127	K562	blood:	n/a	n/a
11	ARID3A	chr15:55550744-55550788	K562	blood:	n/a	n/a
12	ARID3A	chr15:55530654-55532559	K562	blood:	n/a	n/a
13	ATF1	chr15:55509853-55510124	K562	blood:	n/a	n/a
14	ATF1	chr15:55514846-55515135	K562	blood:	n/a	n/a
15	ATF1	chr15:55547268-55547416	K562	blood:	n/a	n/a
16	ATF1	chr15:55513452-55513853	K562	blood:	n/a	n/a
17	ATF1	chr15:55529617-55530115	K562	blood:	n/a	n/a
18	ATF1	chr15:55531712-55532710	K562	blood:	n/a	n/a
19	ATF1	chr15:55527854-55528080	K562	blood:	n/a	n/a
20	ATF2	chr15:55516813-55517609	GM12878	blood:	n/a	n/a
21	ATF2	chr15:55516942-55517584	GM12878	blood:	n/a	n/a
22	ATF2	chr15:55514723-55515204	GM12878	blood:	n/a	n/a
23	ATF2	chr15:55547721-55548440	GM12878	blood:	n/a	n/a
24	ATF2	chr15:55509734-55510174	GM12878	blood:	n/a	n/a
25	ATF2	chr15:55513407-55514139	GM12878	blood:	n/a	n/a
26	ATF2	chr15:55513439-55513945	GM12878	blood:	n/a	n/a
27	ATF3	chr15:55529616-55530176	K562	blood:	n/a	n/a
28	BACH1	chr15:55529278-55529911	K562	blood:	n/a	n/a
29	BACH1	chr15:55509968-55510092	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr15:55513633-55513927	GM12878	blood:	n/a	chr15:55513806-55513817
31	BATF	chr15:55548428-55548851	GM12878	blood:	n/a	n/a
32	BCL3	chr15:55513272-55513840	GM12878	blood:	n/a	n/a
33	BCLAF1	chr15:55509698-55510159	GM12878	blood:	n/a	n/a
34	BHLHE40	chr15:55527847-55528006	K562	blood:	n/a	n/a
35	BHLHE40	chr15:55549278-55549405	K562	blood:	n/a	n/a
36	BHLHE40	chr15:55531751-55532272	K562	blood:	n/a	n/a
37	BHLHE40	chr15:55542620-55542949	HepG2	liver:	n/a	n/a
38	BHLHE40	chr15:55513268-55513941	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:55541286-55541319	HepG2	liver:	n/a	n/a
40	BHLHE40	chr15:55529433-55530049	K562	blood:	n/a	n/a
41	BHLHE40	chr15:55517173-55517394	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:55513396-55514351	K562	blood:	n/a	n/a
43	BHLHE40	chr15:55530885-55530888	K562	blood:	n/a	n/a
44	BRCA1	chr15:55509913-55510107	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr15:55549124-55549509	K562	blood:	n/a	n/a
46	CCNT2	chr15:55529573-55530122	K562	blood:	n/a	n/a
47	CCNT2	chr15:55531717-55532277	K562	blood:	n/a	n/a
48	CEBPB	chr15:55509800-55510184	K562	blood:	n/a	n/a
49	CEBPB	chr15:55542632-55542902	HepG2	liver:	n/a	chr15:55542800-55542813 chr15:55542828-55542839 chr15:55542801-55542812
50	CEBPB	chr15:55542546-55543012	MCF-7	breast:	n/a	chr15:55542800-55542813 chr15:55542828-55542839 chr15:55542801-55542812

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55510003-55510053	HPAEpiC	pulmonary alveolar:	n/a
2	chr15:55510003-55510053	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:55510003-55510053	Hepatocyte	liver:	n/a
4	chr15:55513621-55513671	AG10803	skin:	n/a
5	chr15:55513621-55513671	AG09319	gingival:	n/a
6	chr15:55543264-55543314	Hepatocyte	liver:	n/a
7	chr15:55543264-55543314	HL-60	blood:	n/a
8	chr15:55510003-55510053	RPTEC	kidney:	n/a
9	chr15:55513621-55513671	T-47D	breast:	n/a
10	chr15:55543264-55543314	HIPEpiC	eye:	n/a
11	chr15:55510003-55510053	T-47D	breast:	n/a
12	chr15:55513621-55513671	HRPEpiC	eye:	n/a
13	chr15:55543264-55543314	AoSMC	blood vessel:	n/a
14	chr15:55543264-55543314	Hela-S3	cervix:	n/a
15	chr15:55510003-55510053	HCPEpiC	choroid plexus:	n/a
16	chr15:55513621-55513671	SK-N-SH	brain:	n/a
17	chr15:55543264-55543314	SK-N-MC	brain:	n/a
18	chr15:55510003-55510053	K562	blood:	n/a
19	chr15:55543264-55543314	HepG2	liver:	n/a
20	chr15:55510003-55510053	HRPEpiC	eye:	n/a
21	chr15:55510003-55510053	Hela-S3	cervix:	n/a
22	chr15:55513621-55513671	H1-hESC	embryonic stem cell:	embryo
23	chr15:55513621-55513671	A549	lung:	n/a
24	chr15:55543264-55543314	AG10803	skin:	n/a
25	chr15:55543264-55543314	A549	lung:	n/a
26	chr15:55513621-55513671	MCF10A-Er-Src	breast:	n/a
27	chr15:55510003-55510053	NT2-D1	testis:	n/a
28	chr15:55510003-55510053	HEEpiC	esophagus:	n/a
29	chr15:55543264-55543314	NHDF-neo	bronchial:	n/a
30	chr15:55543264-55543314	K562	blood:	n/a
31	chr15:55510003-55510053	HRE	kidney:	n/a
32	chr15:55510003-55510053	AG04449	skin:	fetal
33	chr15:55513621-55513671	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:55513621-55513671	AoSMC	blood vessel:	n/a
35	chr15:55513621-55513671	U87	brain:	n/a
36	chr15:55543264-55543314	HRE	kidney:	n/a
37	chr15:55510003-55510053	HCF	heart:	n/a
38	chr15:55543264-55543314	BJ	skin:	n/a
39	chr15:55543264-55543314	HAEpiC	amniotic membrane:	n/a
40	chr15:55543264-55543314	GM12891	blood:	n/a
41	chr15:55543264-55543314	H1-hESC	embryonic stem cell:	embryo
42	chr15:55513621-55513671	HCT-116	colon:	n/a
43	chr15:55543264-55543314	HCT-116	colon:	n/a
44	chr15:55510003-55510053	U87	brain:	n/a
45	chr15:55513621-55513671	HCF	heart:	n/a
46	chr15:55513621-55513671	HL-60	blood:	n/a
47	chr15:55510003-55510053	BE2_C	brain:	n/a
48	chr15:55543264-55543314	IMR90	lung:	fetal
49	chr15:55513621-55513671	CMK	blood:	n/a
50	chr15:55510003-55510053	NHDF-neo	bronchial:	n/a

(count:125 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:55528685..55531049-chr15:55537192..55539121,2	MCF-7	breast:
2	chr15:55487577..55489204-chr15:55541881..55543410,2	MCF-7	breast:
3	chr15:55529763..55532078-chr15:55535534..55537821,2	K562	blood:
4	chr15:55512853..55516000-chr15:55580346..55583057,3	K562	blood:
5	chr15:55520811..55529435-chr15:55529925..55534726,12	K562	blood:
6	chr15:55523127..55525294-chr15:55532956..55534638,2	MCF-7	breast:
7	chr15:55517285..55519190-chr15:55531855..55534772,2	K562	blood:
8	chr15:55536038..55538985-chr15:55542222..55544123,2	K562	blood:
9	chr15:55531824..55533387-chr15:55558858..55561281,2	K562	blood:
10	chr15:55542912..55546349-chr15:55547649..55552018,4	K562	blood:
11	chr15:55528450..55530631-chr15:55610596..55613298,2	K562	blood:
12	chr15:55508422..55515195-chr15:55580692..55586566,10	MCF-7	breast:
13	chr15:55488399..55490788-chr15:55526752..55530122,3	K562	blood:
14	chr15:55531291..55533361-chr15:55609048..55611784,2	K562	blood:
15	chr15:55523751..55526514-chr15:55535362..55537475,2	K562	blood:
16	chr15:55508852..55510864-chr15:55611127..55612962,2	MCF-7	breast:
17	chr15:55508435..55511802-chr15:55609851..55613340,4	K562	blood:
18	chr15:55520811..55529435-chr15:55529925..55534726,12	K562	blood:
19	chr15:55502637..55507829-chr15:55507957..55511534,4	MCF-7	breast:
20	chr15:55542912..55546349-chr15:55547649..55552018,4	K562	blood:
21	chr15:55550859..55553459-chr15:55571024..55573794,2	K562	blood:
22	chr15:55488419..55490351-chr15:55504345..55506910,2	K562	blood:
23	chr15:55536038..55538706-chr15:55541637..55544470,3	K562	blood:
24	chr15:55524517..55526709-chr15:55528227..55531220,3	MCF-7	breast:
25	chr15:55516237..55517775-chr15:55581619..55583951,2	K562	blood:
26	chr15:55509049..55510463-chr15:55582084..55583305,19	MCF-7	breast:
27	chr15:55532208..55534403-chr15:55539105..55541114,2	MCF-7	breast:
28	chr15:55509498..55510422-chr15:55731553..55732482,2	K562	blood:
29	chr15:55517285..55519190-chr15:55531855..55534772,2	K562	blood:
30	chr15:55509415..55510514-chr15:55582030..55583628,14	K562	blood:
31	chr15:55507731..55513408-chr15:55580265..55584053,9	MCF-7	breast:
32	chr15:55520021..55524159-chr15:55571941..55574919,3	K562	blood:
33	chr15:55529753..55531504-chr15:55533201..55534943,2	K562	blood:
34	chr15:55499151..55502246-chr15:55504126..55506184,4	K562	blood:
35	chr15:55536038..55538706-chr15:55541637..55544470,3	K562	blood:
36	chr15:55528122..55530871-chr15:55531948..55534527,2	MCF-7	breast:
37	chr15:55539059..55540962-chr15:55541694..55543566,2	K562	blood:
38	chr15:55546620..55548726-chr15:55579934..55582507,2	K562	blood:
39	chr15:55519854..55522805-chr15:55537341..55539230,2	MCF-7	breast:
40	chr15:55549763..55552169-chr15:55552285..55555168,2	K562	blood:
41	chr15:55514268..55516537-chr15:55573502..55575651,2	K562	blood:
42	chr15:55528685..55531049-chr15:55537192..55539121,2	MCF-7	breast:
43	chr15:55528122..55530871-chr15:55531948..55534527,2	MCF-7	breast:
44	chr15:55529177..55531366-chr15:55559639..55562184,2	K562	blood:
45	chr15:55488317..55491579-chr15:55501093..55504631,4	K562	blood:
46	chr15:55514943..55517401-chr15:55527045..55529673,2	K562	blood:
47	chr15:55529333..55531848-chr15:55546495..55549479,2	K562	blood:
48	chr15:55502637..55507829-chr15:55507957..55511534,4	MCF-7	breast:
49	chr15:55542658..55546534-chr15:55547557..55552018,8	K562	blood:
50	chr15:55525732..55527261-chr15:55579170..55581534,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSL24D1-2	chr15:55530316-55530689	NONHSAT043984

No data

Variant related genes	Relation type
RAB27A	TF binding region
RAB27A	CpG island
ENSG00000260916	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000137876	chromatin interactions
ENSG00000069974	chromatin interactions
ENSG00000225973	chromatin interactions
ENSG00000261652	chromatin interactions

Extended variants
information (count: 2277 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2277 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73409851	chr15:55502516-55502517	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542859441	chr15:55502519-55502520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543098402	chr15:55502600-55502601	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572160899	chr15:55502610-55502611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368320221	chr15:55502611-55502612	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7178980	chr15:55502624-55502625	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545795113	chr15:55502625-55502626	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372952364	chr15:55502626-55502627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563929568	chr15:55502644-55502645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73409853	chr15:55502681-55502682	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552776542	chr15:55502711-55502712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560003725	chr15:55502718-55502719	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528710734	chr15:55502744-55502745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548639474	chr15:55502754-55502755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568505964	chr15:55502760-55502761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs150122754	chr15:55502764-55502765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs138566221	chr15:55502765-55502766	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532336640	chr15:55502813-55502814	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545752802	chr15:55502829-55502830	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs564064309	chr15:55502849-55502850	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533006933	chr15:55502859-55502860	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs149302777	chr15:55502909-55502910	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs56328329	chr15:55502977-55502978	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs145519350	chr15:55503019-55503020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7179278	chr15:55503025-55503026	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529051492	chr15:55503041-55503042	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138122029	chr15:55503048-55503049	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs142711344	chr15:55503057-55503058	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115709833	chr15:55503087-55503088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs373367595	chr15:55503089-55503090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs28864456	chr15:55503092-55503093	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs370715157	chr15:55503099-55503100	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546501267	chr15:55503100-55503101	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374418062	chr15:55503104-55503105	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs201908828	chr15:55503119-55503120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs28889339	chr15:55503205-55503206	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs528680897	chr15:55503206-55503207	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs542095972	chr15:55503234-55503235	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186884304	chr15:55503246-55503247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs28784096	chr15:55503312-55503313	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs377244162	chr15:55503394-55503395	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533933569	chr15:55503426-55503427	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191836207	chr15:55503450-55503451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374754839	chr15:55503492-55503493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543774073	chr15:55503509-55503510	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553806527	chr15:55503535-55503536	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529529968	chr15:55503571-55503572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570530700	chr15:55503612-55503613	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs28499113	chr15:55503621-55503622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs28589609	chr15:55503630-55503631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:61)

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
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
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD

Chromatin state (count:1330 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55489600-55504000	Weak transcription	Spleen	Spleen
2	chr15:55489600-55513200	Weak transcription	Lung	lung
3	chr15:55489800-55503400	Weak transcription	Pancreas	Pancrea
4	chr15:55489800-55540200	Weak transcription	Esophagus	oesophagus
5	chr15:55490000-55509600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:55490000-55510000	Weak transcription	NHLF	lung
7	chr15:55490000-55513000	Weak transcription	Fetal Intestine Large	intestine
8	chr15:55490000-55513200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:55490000-55513200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr15:55490000-55513200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:55490000-55517200	Weak transcription	Aorta	Aorta
12	chr15:55490000-55529400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr15:55490000-55562800	Weak transcription	Ovary	ovary
14	chr15:55490200-55510000	Weak transcription	Fetal Kidney	kidney
15	chr15:55490200-55510200	Weak transcription	Fetal Lung	lung
16	chr15:55490200-55511400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:55490200-55511400	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr15:55490200-55511400	Weak transcription	Osteobl	bone
19	chr15:55490200-55513200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr15:55490200-55513800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr15:55490200-55514000	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr15:55490400-55510000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr15:55490400-55512600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:55490600-55510200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr15:55490800-55504200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr15:55491000-55513600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr15:55497800-55510000	Weak transcription	Primary B cells from cord blood	blood
28	chr15:55497800-55511200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:55497800-55513000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr15:55497800-55513000	Weak transcription	Hela-S3	cervix
31	chr15:55497800-55514000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr15:55497800-55518400	Weak transcription	Gastric	stomach
33	chr15:55498000-55505000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr15:55498000-55509400	Weak transcription	Stomach Mucosa	stomach
35	chr15:55498000-55509600	Weak transcription	Primary B cells from peripheral blood	blood
36	chr15:55498000-55509600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr15:55498000-55510000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr15:55498000-55510000	Weak transcription	Liver	Liver
39	chr15:55498000-55510200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr15:55498000-55510200	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr15:55498000-55510400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr15:55498000-55512800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr15:55498000-55512800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:55498000-55513200	Weak transcription	Primary T cells from cord blood	blood
45	chr15:55498000-55513400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr15:55498000-55514200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr15:55498200-55509600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr15:55498400-55505800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr15:55498400-55512400	Weak transcription	Fetal Stomach	stomach
50	chr15:55499800-55510200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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