Variant report

Variant	nsv878037
Chromosome Location	chr3:178825910-178871906
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1045)
CpG islands
(count:977)
Chromatin interactive
region (count:45)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:178864839-178866138	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:178867219-178867495	K562	blood:	n/a	n/a
3	ARID3A	chr3:178867811-178868081	K562	blood:	n/a	n/a
4	ARID3A	chr3:178864952-178866016	K562	blood:	n/a	n/a
5	ATF1	chr3:178864997-178866035	K562	blood:	n/a	n/a
6	ATF2	chr3:178866949-178867696	GM12878	blood:	n/a	n/a
7	ATF2	chr3:178866694-178867678	GM12878	blood:	n/a	n/a
8	ATF2	chr3:178864670-178866127	GM12878	blood:	n/a	n/a
9	ATF2	chr3:178865428-178866128	GM12878	blood:	n/a	n/a
10	ATF3	chr3:178865502-178866181	K562	blood:	n/a	chr3:178866086-178866095
11	BATF	chr3:178864759-178865278	GM12878	blood:	n/a	n/a
12	BATF	chr3:178867298-178867679	GM12878	blood:	n/a	n/a
13	BATF	chr3:178867235-178867566	GM12878	blood:	n/a	n/a
14	BATF	chr3:178865314-178865726	GM12878	blood:	n/a	chr3:178865391-178865401
15	BATF	chr3:178864715-178865017	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:178864707-178865046	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:178865380-178865648	GM12878	blood:	n/a	n/a
18	BCL11A	chr3:178864803-178865012	GM12878	blood:	n/a	n/a
19	BCL11A	chr3:178867293-178867560	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:178867280-178867680	GM12878	blood:	n/a	n/a
21	BCL3	chr3:178867251-178867610	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:178864685-178866128	GM12878	blood:	n/a	chr3:178865143-178865150 chr3:178866087-178866096
23	BCLAF1	chr3:178864656-178865854	GM12878	blood:	n/a	chr3:178865143-178865150
24	BCLAF1	chr3:178867041-178867566	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:178864802-178866711	K562	blood:	n/a	chr3:178866149-178866165 chr3:178866511-178866527 chr3:178866189-178866205 chr3:178865539-178865555 chr3:178866183-178866199 chr3:178866150-178866166 chr3:178866158-178866174 chr3:178866175-178866191
26	BHLHE40	chr3:178864765-178867970	GM12878	blood:	n/a	chr3:178866149-178866165 chr3:178866511-178866527 chr3:178866189-178866205 chr3:178865539-178865555 chr3:178866183-178866199 chr3:178866150-178866166 chr3:178866158-178866174 chr3:178866175-178866191
27	BHLHE40	chr3:178866945-178867903	K562	blood:	n/a	n/a
28	BRCA1	chr3:178869249-178869260	GM12878	blood:	n/a	n/a
29	BRCA1	chr3:178865245-178865274	GM12878	blood:	n/a	n/a
30	BRCA1	chr3:178864782-178866020	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr3:178826702-178827074	K562	blood:	n/a	n/a
32	CBX3	chr3:178865729-178866150	K562	blood:	n/a	n/a
33	CBX3	chr3:178864601-178866202	K562	blood:	n/a	chr3:178865161-178865172
34	CCNT2	chr3:178864906-178865305	K562	blood:	n/a	n/a
35	CCNT2	chr3:178865715-178867490	K562	blood:	n/a	chr3:178865972-178865981 chr3:178866086-178866095
36	CCNT2	chr3:178870479-178870697	K562	blood:	n/a	n/a
37	CEBPB	chr3:178864810-178866602	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:178865549-178865978	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:178865471-178866007	K562	blood:	n/a	n/a
40	CEBPB	chr3:178865531-178865909	K562	blood:	n/a	n/a
41	CEBPB	chr3:178865094-178865978	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:178860716-178860733	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr3:178865081-178865579	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:178865551-178865991	A549	lung:	n/a	n/a
45	CEBPB	chr3:178866646-178866693	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:178864825-178866068	GM12878	blood:	n/a	n/a
47	CEBPD	chr3:178864887-178865391	K562	blood:	n/a	n/a
48	CEBPD	chr3:178865539-178866622	K562	blood:	n/a	n/a
49	CEBPD	chr3:178865773-178866250	HepG2	liver:	n/a	n/a
50	CEBPD	chr3:178865487-178866159	K562	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:178865281-178865331	HL-60	blood:	n/a
2	chr3:178865281-178865331	HL-60	blood:	n/a
3	chr3:178866695-178866745	PrEC	prostate:	n/a
4	chr3:178869001-178869051	ProgFib	skin:	n/a
5	chr3:178866220-178866270	NHBE	bronchial:	n/a
6	chr3:178863507-178863557	HPAEpiC	pulmonary alveolar:	n/a
7	chr3:178865553-178865603	AG10803	skin:	n/a
8	chr3:178867004-178867054	HAEpiC	amniotic membrane:	n/a
9	chr3:178865678-178865728	HRE	kidney:	n/a
10	chr3:178864926-178864976	HMEC	breast:	n/a
11	chr3:178866004-178866054	AG09309	skin:	n/a
12	chr3:178863507-178863557	HAEpiC	amniotic membrane:	n/a
13	chr3:178864926-178864976	PANC-1	pancreas:	n/a
14	chr3:178866695-178866745	AG04450	lung:	fetal
15	chr3:178866004-178866054	HAEpiC	amniotic membrane:	n/a
16	chr3:178869001-178869051	HEEpiC	esophagus:	n/a
17	chr3:178865553-178865603	SKMC	muscle:	n/a
18	chr3:178867151-178867201	HAEpiC	amniotic membrane:	n/a
19	chr3:178865678-178865728	SK-N-MC	brain:	n/a
20	chr3:178866220-178866270	Jurkat	blood:	n/a
21	chr3:178865812-178865862	IMR90	lung:	fetal
22	chr3:178867151-178867201	AG10803	skin:	n/a
23	chr3:178867105-178867155	SAEC	small airway:	n/a
24	chr3:178864926-178864976	NH-A	brain:	n/a
25	chr3:178865812-178865862	AG09309	skin:	n/a
26	chr3:178865678-178865728	HCF	heart:	n/a
27	chr3:178866004-178866054	HepG2	liver:	n/a
28	chr3:178866220-178866270	HEEpiC	esophagus:	n/a
29	chr3:178864926-178864976	HCPEpiC	choroid plexus:	n/a
30	chr3:178831804-178831854	NT2-D1	testis:	n/a
31	chr3:178863507-178863557	GM19239	blood:	n/a
32	chr3:178866004-178866054	PANC-1	pancreas:	n/a
33	chr3:178866220-178866270	SK-N-SH_RA	brain:	n/a
34	chr3:178866695-178866745	GM06990	blood:	n/a
35	chr3:178865550-178865600	NT2-D1	testis:	n/a
36	chr3:178867004-178867054	HIPEpiC	eye:	n/a
37	chr3:178831804-178831854	HUVEC	blood vessel:	n/a
38	chr3:178867151-178867201	Hela-S3	cervix:	n/a
39	chr3:178866391-178866441	ovcar-3	ovarian:	n/a
40	chr3:178865550-178865600	U87	brain:	n/a
41	chr3:178866220-178866270	SK-N-SH	brain:	n/a
42	chr3:178866220-178866270	Hepatocyte	liver:	n/a
43	chr3:178863507-178863557	Caco-2	colon:	n/a
44	chr3:178866391-178866441	HCPEpiC	choroid plexus:	n/a
45	chr3:178831804-178831854	PrEC	prostate:	n/a
46	chr3:178865550-178865600	NH-A	brain:	n/a
47	chr3:178865678-178865728	GM12892	blood:	n/a
48	chr3:178866391-178866441	HCT-116	colon:	n/a
49	chr3:178867151-178867201	HMEC	breast:	n/a
50	chr3:178866695-178866745	BE2_C	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:52565783..52568292-chr3:178833471..178835400,2	MCF-7	breast:
2	chr3:178864344..178867597-chr3:179039214..179042429,8	K562	blood:
3	chr3:178785755..178789866-chr3:178859150..178861564,3	K562	blood:
4	chr3:178815966..178819405-chr3:178820702..178826616,6	MCF-7	breast:
5	chr3:178857450..178860291-chr3:178871002..178872705,2	K562	blood:
6	chr3:178860905..178862503-chr3:178864078..178865778,2	K562	blood:
7	chr3:178867742..178870161-chr3:178876132..178878163,2	MCF-7	breast:
8	chr3:178786925..178790579-chr3:178864297..178867679,5	K562	blood:
9	chr19:8386135..8386757-chr3:178865923..178866498,2	Hela-S3	cervix:
10	chr1:156561006..156561557-chr3:178866122..178866623,2	NB4	blood:
11	chr3:178781504..178783011-chr3:178869309..178871100,2	K562	blood:
12	chr3:178865885..178868102-chr3:178977747..178979601,3	MCF-7	breast:
13	chr3:178855332..178857552-chr3:178859935..178861757,2	K562	blood:
14	chr3:178864675..178865355-chr3:179033450..179034233,4	MCF-7	breast:
15	chr3:178866930..178870480-chr3:178976906..178979282,3	K562	blood:
16	chr3:178864944..178865541-chr3:179033491..179034021,2	MCF-7	breast:
17	chr20:46413088..46415020-chr3:178866381..178868022,2	MCF-7	breast:
18	chr3:178865393..178868343-chr3:179279324..179281019,2	K562	blood:
19	chr3:178753336..178756153-chr3:178870610..178872335,2	K562	blood:
20	chr3:178866029..178868505-chr3:179041655..179043720,2	K562	blood:
21	chr15:65595682..65597478-chr3:178866855..178869442,2	MCF-7	breast:
22	chr3:178869093..178870734-chr3:178895152..178896697,2	K562	blood:
23	chr3:178861208..178863528-chr3:178973600..178975107,2	K562	blood:
24	chr3:178860056..178863629-chr3:178865664..178868412,4	MCF-7	breast:
25	chr3:178863877..178866682-chr3:178977686..178979355,3	K562	blood:
26	chr3:178857450..178860291-chr3:178871002..178872705,2	K562	blood:
27	chr3:178860536..178862405-chr3:178864278..178865894,2	K562	blood:
28	chr3:178864291..178867045-chr3:179057738..179060531,2	MCF-7	breast:
29	chr3:178864492..178868931-chr3:179039553..179043493,6	MCF-7	breast:
30	chr14:75745109..75745980-chr3:178866032..178866667,2	Hela-S3	cervix:
31	chr3:178865407..178867483-chr3:179039203..179041371,3	K562	blood:
32	chr3:178842346..178844303-chr3:179040865..179042396,2	MCF-7	breast:
33	chr3:178865638..178866550-chr9:139257672..139258244,2	Hela-S3	cervix:
34	chr3:178733073..178733959-chr3:178864672..178865566,2	MCF-7	breast:
35	chr3:178787966..178791118-chr3:178865051..178866959,3	MCF-7	breast:
36	chr3:178865323..178865973-chr9:34178403..34179059,2	NB4	blood:
37	chr3:178864465..178866059-chr3:179064181..179066320,2	K562	blood:
38	chr3:178869977..178872315-chr3:178873899..178875807,3	K562	blood:
39	chr3:178863877..178868371-chr3:178977065..178980370,6	K562	blood:
40	chr3:178864911..178866513-chr3:178885186..178888175,2	MCF-7	breast:
41	chr3:178788447..178791036-chr3:178864497..178866649,2	MCF-7	breast:
42	chr3:178830287..178832658-chr3:179039963..179041863,2	MCF-7	breast:
43	chr3:178826731..178829120-chr3:178915234..178917162,2	MCF-7	breast:
44	chr3:178855332..178857552-chr3:178859935..178861757,2	K562	blood:
45	chr3:178865821..178866645-chr7:142960358..142960873,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZMAT3-1	chr3:178850557-178850659	XLOC_003337
2	lnc-ZMAT3-1	chr3:178865704-178865761	ENSG00000229102
3	lnc-ZMAT3-1	chr3:178850557-178850659	ENSG00000229102
4	lnc-ZMAT3-1	chr3:178865704-178865761	XLOC_003337

No data

Variant related genes	Relation type
PIK3CA	TF binding region
ENSG00000229102	TF binding region
PIK3CA	CpG island
ENSG00000229102	CpG island
ENSG00000201957	chromatin interactions
ENSG00000267855	chromatin interactions
ENSG00000121879	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000240429	chromatin interactions
ENSG00000229102	chromatin interactions
ENSG00000171121	chromatin interactions
ENSG00000260743	chromatin interactions
ENSG00000213221	chromatin interactions
ENSG00000233927	chromatin interactions
ENSG00000136518	chromatin interactions
ENSG00000170345	chromatin interactions
ENSG00000165006	chromatin interactions
ENSG00000197448	chromatin interactions
ENSG00000167774	chromatin interactions
ENSG00000196562	chromatin interactions
ENSG00000171109	chromatin interactions
ENSG00000121864	chromatin interactions
ENSG00000172667	chromatin interactions
ENSG00000163382	chromatin interactions

Extended variants
information (count: 928 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:928 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9831927	chr3:178825910-178825911	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556896380	chr3:178825930-178825931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573844155	chr3:178825936-178825937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542564930	chr3:178825939-178825940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559254152	chr3:178825942-178825943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572500801	chr3:178825969-178825970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554013314	chr3:178825972-178825973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544645119	chr3:178825973-178825974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564622860	chr3:178825994-178825995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141830971	chr3:178826036-178826037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150605281	chr3:178826044-178826045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139702264	chr3:178826093-178826094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144470205	chr3:178826128-178826129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540445291	chr3:178826157-178826158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549416964	chr3:178826242-178826243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566425968	chr3:178826245-178826246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147434436	chr3:178826288-178826289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551824825	chr3:178826342-178826343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7374077	chr3:178826358-178826359	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs187487254	chr3:178826365-178826366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557076304	chr3:178826398-178826399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191941739	chr3:178826447-178826448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567351879	chr3:178826486-178826487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536491906	chr3:178826508-178826509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563185712	chr3:178826535-178826536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544129369	chr3:178826553-178826554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552982772	chr3:178826633-178826634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367635356	chr3:178826710-178826711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145269678	chr3:178826770-178826771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560847702	chr3:178826772-178826773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113262358	chr3:178826806-178826807	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558152362	chr3:178826810-178826811	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574960846	chr3:178826813-178826814	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542583684	chr3:178826839-178826840	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563861184	chr3:178826841-178826842	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs59340081	chr3:178826842-178826843	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs184063728	chr3:178826899-178826900	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560076144	chr3:178826926-178826927	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188070194	chr3:178827017-178827018	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113602875	chr3:178827096-178827097	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371794980	chr3:178827104-178827105	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73050076	chr3:178827138-178827139	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192350988	chr3:178827163-178827164	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530985580	chr3:178827169-178827170	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184635296	chr3:178827196-178827197	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567787243	chr3:178827304-178827305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536043935	chr3:178827347-178827348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551899548	chr3:178827353-178827354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7372645	chr3:178827376-178827377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs566402335	chr3:178827454-178827455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Human papillomavirus	17975027	CNVD
Adenocarcinoma	18757405	CNVD
Lung cancer	18757405	CNVD
Squamous cell cancer	18757405	CNVD
small cell lung cancer	18757405	CNVD

Chromatin state (count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178825000-178827200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr3:178825400-178826400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr3:178825400-178826400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:178825400-178826400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:178825400-178826400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr3:178825400-178826400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:178825400-178826400	Enhancers	HUVEC	blood vessel
8	chr3:178825400-178826600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:178825400-178826600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr3:178825400-178826600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr3:178825400-178826600	Enhancers	HMEC	breast
12	chr3:178825400-178826600	Enhancers	HSMM	muscle
13	chr3:178825400-178826600	Enhancers	NHEK	skin
14	chr3:178825600-178826200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:178825600-178826400	Enhancers	HSMMtube	muscle
16	chr3:178825600-178826600	Enhancers	NH-A	brain
17	chr3:178825600-178826600	Enhancers	NHDF-Ad	bronchial
18	chr3:178825600-178826600	Enhancers	Osteobl	bone
19	chr3:178825800-178826400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr3:178826200-178826600	Enhancers	NHLF	lung
21	chr3:178826400-178826800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr3:178826400-178827400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr3:178826400-178829400	Weak transcription	HUVEC	blood vessel
24	chr3:178826600-178831600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr3:178826600-178833000	Weak transcription	Osteobl	bone
26	chr3:178826800-178827200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr3:178827200-178832800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr3:178827200-178832800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr3:178829400-178829800	Enhancers	HUVEC	blood vessel
30	chr3:178829800-178833000	Weak transcription	HUVEC	blood vessel
31	chr3:178830800-178831000	ZNF genes & repeats	Aorta	Aorta
32	chr3:178830800-178831000	Bivalent Enhancer	NHDF-Ad	bronchial
33	chr3:178830800-178833800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr3:178831600-178832200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr3:178831600-178832400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr3:178831600-178832400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr3:178832200-178834600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:178832400-178832800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr3:178832400-178833400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr3:178832600-178834400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr3:178832800-178833400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr3:178832800-178833800	Enhancers	Muscle Satellite Cultured Cells	--
43	chr3:178832800-178834000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr3:178832800-178834000	Enhancers	NHEK	skin
45	chr3:178833000-178833600	Enhancers	HMEC	breast
46	chr3:178833000-178833600	Enhancers	NH-A	brain
47	chr3:178833000-178834000	Enhancers	Osteobl	bone
48	chr3:178833000-178834200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:178833000-178834200	Enhancers	HUVEC	blood vessel
50	chr3:178833000-178834600	Enhancers	NHDF-Ad	bronchial

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