Variant report

Variant	nsv2855
Chromosome Location	chr1:151936470-151966381
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1978)
CpG islands
(count:428)
Chromatin interactive
region (count:148)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1978 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151947765-151948284	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:151945353-151945818	K562	blood:	n/a	n/a
3	ARID3A	chr1:151950294-151950461	K562	blood:	n/a	n/a
4	ARID3A	chr1:151948396-151948890	K562	blood:	n/a	n/a
5	ATF1	chr1:151945196-151945750	K562	blood:	n/a	n/a
6	ATF1	chr1:151960899-151961224	K562	blood:	n/a	n/a
7	ATF2	chr1:151956639-151957208	GM12878	blood:	n/a	n/a
8	ATF2	chr1:151956646-151957105	GM12878	blood:	n/a	n/a
9	ATF3	chr1:151960738-151961387	A549	lung:	n/a	n/a
10	ATF3	chr1:151964469-151965392	A549	lung:	n/a	n/a
11	ATF3	chr1:151960781-151961424	A549	lung:	n/a	n/a
12	ATF3	chr1:151945393-151945726	K562	blood:	n/a	n/a
13	ATF3	chr1:151964178-151965908	A549	lung:	n/a	n/a
14	ATF3	chr1:151945455-151945650	K562	blood:	n/a	n/a
15	ATF3	chr1:151960850-151961293	K562	blood:	n/a	n/a
16	ATF3	chr1:151961626-151962338	A549	lung:	n/a	n/a
17	BACH1	chr1:151964643-151966253	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:151944993-151945799	K562	blood:	n/a	n/a
19	BACH1	chr1:151944988-151945864	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr1:151956693-151957149	GM12878	blood:	n/a	chr1:151956914-151956925
21	BATF	chr1:151956789-151957095	GM12878	blood:	n/a	chr1:151956914-151956925
22	BCL11A	chr1:151956726-151957107	GM12878	blood:	n/a	n/a
23	BCL3	chr1:151952310-151954052	A549	lung:	n/a	chr1:151953096-151953104 chr1:151952661-151952670
24	BCL3	chr1:151947377-151948912	A549	lung:	n/a	n/a
25	BCL3	chr1:151964146-151966375	A549	lung:	n/a	chr1:151966339-151966352 chr1:151966156-151966165 chr1:151966351-151966364
26	BCL3	chr1:151945018-151946070	A549	lung:	n/a	n/a
27	BCL3	chr1:151960611-151962513	A549	lung:	n/a	chr1:151961086-151961095 chr1:151961087-151961096
28	BCL3	chr1:151960677-151963109	A549	lung:	n/a	chr1:151961086-151961095 chr1:151961087-151961096
29	BCL3	chr1:151951322-151952124	A549	lung:	n/a	n/a
30	BCL3	chr1:151950000-151951252	A549	lung:	n/a	n/a
31	BCL3	chr1:151956741-151957035	GM12878	blood:	n/a	n/a
32	BCL3	chr1:151962862-151966255	A549	lung:	n/a	chr1:151963188-151963197 chr1:151966156-151966165
33	BCL3	chr1:151952346-151953971	A549	lung:	n/a	chr1:151953096-151953104 chr1:151952661-151952670
34	BCL3	chr1:151948918-151949955	A549	lung:	n/a	n/a
35	BCL3	chr1:151948906-151949670	A549	lung:	n/a	n/a
36	BCLAF1	chr1:151956725-151957140	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:151945060-151945675	A549	lung:	n/a	n/a
38	BHLHE40	chr1:151944983-151945699	K562	blood:	n/a	n/a
39	BHLHE40	chr1:151956734-151957065	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:151960846-151961210	K562	blood:	n/a	n/a
41	BHLHE40	chr1:151965000-151965154	K562	blood:	n/a	n/a
42	BRCA1	chr1:151960457-151961432	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr1:151963268-151963641	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr1:151940455-151940777	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:151964430-151965989	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr1:151966232-151966262	HepG2	liver:	n/a	n/a
47	CBX3	chr1:151948377-151948887	K562	blood:	n/a	n/a
48	CBX3	chr1:151945032-151945877	HCT-116	colon:	n/a	n/a
49	CBX3	chr1:151945356-151945810	K562	blood:	n/a	n/a
50	CCNT2	chr1:151948525-151948868	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151965283-151965333	GM06990	blood:	n/a
2	chr1:151965283-151965333	GM06990	blood:	n/a
3	chr1:151965283-151965333	GM12878	blood:	n/a
4	chr1:151958685-151958735	BE2_C	brain:	n/a
5	chr1:151966207-151966257	AG04449	skin:	fetal
6	chr1:151965283-151965333	AoSMC	blood vessel:	n/a
7	chr1:151965283-151965333	Jurkat	blood:	n/a
8	chr1:151965283-151965333	NHDF-neo	bronchial:	n/a
9	chr1:151965283-151965333	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:151966207-151966257	SKMC	muscle:	n/a
11	chr1:151965283-151965333	U87	brain:	n/a
12	chr1:151965869-151965919	HCM	heart:	n/a
13	chr1:151965869-151965919	GM12891	blood:	n/a
14	chr1:151958685-151958735	GM12892	blood:	n/a
15	chr1:151965283-151965333	NH-A	brain:	n/a
16	chr1:151966104-151966154	HUVEC	blood vessel:	n/a
17	chr1:151965283-151965333	LNCaP	prostate:	n/a
18	chr1:151962816-151962866	IMR90	lung:	fetal
19	chr1:151966104-151966154	HCM	heart:	n/a
20	chr1:151965283-151965333	GM12892	blood:	n/a
21	chr1:151965283-151965333	NB4	blood:	n/a
22	chr1:151945663-151945713	T-47D	breast:	n/a
23	chr1:151966207-151966257	AoSMC	blood vessel:	n/a
24	chr1:151965283-151965333	BJ	skin:	n/a
25	chr1:151965869-151965919	HIPEpiC	eye:	n/a
26	chr1:151966207-151966257	HCT-116	colon:	n/a
27	chr1:151966104-151966154	BE2_C	brain:	n/a
28	chr1:151966207-151966257	HIPEpiC	eye:	n/a
29	chr1:151966104-151966154	PANC-1	pancreas:	n/a
30	chr1:151958685-151958735	A549	lung:	n/a
31	chr1:151945663-151945713	NH-A	brain:	n/a
32	chr1:151966207-151966257	NHBE	bronchial:	n/a
33	chr1:151962816-151962866	NHDF-neo	bronchial:	n/a
34	chr1:151966207-151966257	HL-60	blood:	n/a
35	chr1:151958685-151958735	GM06990	blood:	n/a
36	chr1:151966207-151966257	SK-N-MC	brain:	n/a
37	chr1:151965869-151965919	SKMC	muscle:	n/a
38	chr1:151965283-151965333	MCF10A-Er-Src	breast:	n/a
39	chr1:151965283-151965333	PANC-1	pancreas:	n/a
40	chr1:151966104-151966154	AG04449	skin:	fetal
41	chr1:151965283-151965333	K562	blood:	n/a
42	chr1:151965869-151965919	GM06990	blood:	n/a
43	chr1:151958685-151958735	AG09319	gingival:	n/a
44	chr1:151962816-151962866	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:151966104-151966154	SK-N-SH	brain:	n/a
46	chr1:151945663-151945713	MCF10A-Er-Src	breast:	n/a
47	chr1:151966207-151966257	NHDF-neo	bronchial:	n/a
48	chr1:151958685-151958735	Hela-S3	cervix:	n/a
49	chr1:151965869-151965919	ovcar-3	ovarian:	n/a
50	chr1:151958685-151958735	HCT-116	colon:	n/a

(count:148 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:151958341..151960703-chr1:152042436..152044270,2	MCF-7	breast:
2	chr1:151951145..151953064-chr1:151955721..151958103,2	K562	blood:
3	chr1:151965048..151965692-chr3:194304683..194305239,2	Hela-S3	cervix:
4	chr1:46152209..46153021-chr1:151964687..151965409,2	Hela-S3	cervix:
5	chr1:151905958..151908802-chr1:151940211..151943154,2	K562	blood:
6	chr1:110527017..110527837-chr1:151965192..151965963,2	Hela-S3	cervix:
7	chr1:151957747..151960576-chr1:152018452..152020674,2	MCF-7	breast:
8	chr1:151811099..151813697-chr1:151950500..151952589,2	MCF-7	breast:
9	chr1:151966036..151966766-chr19:571248..572063,2	Hela-S3	cervix:
10	chr1:151949201..151951606-chr1:152006321..152008860,3	MCF-7	breast:
11	chr1:151903606..151908213-chr1:151959560..151963672,4	MCF-7	breast:
12	chr1:151965198..151966038-chr19:17952815..17953701,2	Hela-S3	cervix:
13	chr1:151964523..151965166-chr16:30063994..30064886,2	Hela-S3	cervix:
14	chr1:151964397..151965397-chr11:67888029..67888810,2	Hela-S3	cervix:
15	chr1:151964899..151965569-chr12:46661445..46662251,2	Hela-S3	cervix:
16	chr1:151939365..151942240-chr1:151972408..151973945,2	K562	blood:
17	chr1:148241086..148242072-chr1:151964392..151964959,2	Hela-S3	cervix:
18	chr1:151918309..151920987-chr1:151938809..151942058,3	MCF-7	breast:
19	chr1:151955991..151958464-chr1:151959511..151962330,2	K562	blood:
20	chr1:151961486..151963073-chr4:87925886..87928690,2	MCF-7	breast:
21	chr1:151880619..151883226-chr1:151961289..151965303,4	K562	blood:
22	chr1:151880209..151887387-chr1:151961986..151968084,15	MCF-7	breast:
23	chr1:151951145..151953064-chr1:151955721..151958103,2	K562	blood:
24	chr1:151964883..151965535-chr17:48944301..48945101,2	Hela-S3	cervix:
25	chr1:151964881..151965549-chr11:93861551..93862232,2	Hela-S3	cervix:
26	chr1:151939119..151942240-chr1:151972408..151975216,4	K562	blood:
27	chr1:151917185..151918906-chr1:151960945..151963030,3	MCF-7	breast:
28	chr1:151937625..151940407-chr1:151960051..151962208,2	K562	blood:
29	chr1:151965186..151965687-chr18:11365448..11365948,2	Hela-S3	cervix:
30	chr1:151811113..151814780-chr1:151962857..151966577,5	MCF-7	breast:
31	chr1:151966344..151967208-chr17:48784695..48785497,2	Hela-S3	cervix:
32	chr1:151881917..151882541-chr1:151964402..151965113,2	Hela-S3	cervix:
33	chr1:151965176..151965807-chr6:26197923..26198879,2	Hela-S3	cervix:
34	chr1:151940215..151941175-chr1:151965901..151967410,8	MCF-7	breast:
35	chr1:151941333..151942883-chr17:57860165..57862402,2	MCF-7	breast:
36	chr1:151953443..151955255-chr1:151956966..151958733,2	K562	blood:
37	chr1:151906693..151908513-chr1:151954832..151956959,2	K562	blood:
38	chr1:151933684..151936159-chr1:151941486..151943210,2	MCF-7	breast:
39	chr1:151943551..151945492-chr1:151999086..152000598,2	K562	blood:
40	chr1:151939609..151941255-chr1:151968656..151969951,15	MCF-7	breast:
41	chr1:151881894..151884208-chr1:151935307..151938264,2	MCF-7	breast:
42	chr1:151940500..151941079-chr1:151961205..151961964,2	MCF-7	breast:
43	chr1:151965797..151966383-chr9:34048318..34048939,2	NB4	blood:
44	chr1:151964110..151964967-chr1:228645069..228645743,2	Hela-S3	cervix:
45	chr1:151964776..151965388-chr12:110939931..110940577,2	Hela-S3	cervix:
46	chr1:151965119..151965742-chr9:137000994..137001940,2	Hela-S3	cervix:
47	chr1:151429154..151431370-chr1:151947208..151949850,2	MCF-7	breast:
48	chr1:151861528..151864406-chr1:151963455..151965696,6	MCF-7	breast:
49	chr1:151943172..151945444-chr1:151966089..151968195,2	K562	blood:
50	chr1:151867153..151869066-chr1:151941093..151942676,2	MCF-7	breast:

No data

Variant related genes	Relation type
NBPF18P	TF binding region
S100A10	TF binding region
NBPF18P	CpG island
S100A10	CpG island
ENSG00000138069	chromatin interactions
ENSG00000064726	chromatin interactions
ENSG00000111845	chromatin interactions
ENSG00000196363	chromatin interactions
ENSG00000168710	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000101150	chromatin interactions
ENSG00000143365	chromatin interactions
ENSG00000234614	chromatin interactions
ENSG00000173113	chromatin interactions
ENSG00000201134	chromatin interactions
ENSG00000061794	chromatin interactions
ENSG00000149926	chromatin interactions
ENSG00000167658	chromatin interactions
ENSG00000223810	chromatin interactions
ENSG00000175567	chromatin interactions
ENSG00000152270	chromatin interactions
ENSG00000177352	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000181904	chromatin interactions
ENSG00000164091	chromatin interactions
ENSG00000127314	chromatin interactions
ENSG00000088298	chromatin interactions
ENSG00000249602	chromatin interactions
ENSG00000102908	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000197747	chromatin interactions
ENSG00000172493	chromatin interactions
ENSG00000118412	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000137434	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000172270	chromatin interactions
ENSG00000214087	chromatin interactions
ENSG00000011405	chromatin interactions
ENSG00000257261	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000151164	chromatin interactions
ENSG00000186615	chromatin interactions
ENSG00000229021	chromatin interactions
ENSG00000111371	chromatin interactions
ENSG00000126005	chromatin interactions
ENSG00000039523	chromatin interactions
ENSG00000115963	chromatin interactions
ENSG00000137073	chromatin interactions
ENSG00000051180	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000129084	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000105639	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000168237	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000154945	chromatin interactions
ENSG00000196950	chromatin interactions
ENSG00000225556	chromatin interactions
ENSG00000231770	chromatin interactions
ENSG00000229980	chromatin interactions
ENSG00000133250	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000163191	chromatin interactions
ENSG00000137807	chromatin interactions
ENSG00000267751	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000159445	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000159596	chromatin interactions
ENSG00000172432	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000259426	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000124688	chromatin interactions
ENSG00000099875	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000267637	chromatin interactions
ENSG00000159592	chromatin interactions
ENSG00000245849	chromatin interactions
ENSG00000126432	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000185359	chromatin interactions
ENSG00000110218	chromatin interactions

Extended variants
information (count: 1037 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6662611	chr1:151936485-151936486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562637596	chr1:151936502-151936503	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140137511	chr1:151936503-151936504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551143520	chr1:151936512-151936513	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571121373	chr1:151936529-151936530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10657503	chr1:151936550-151936551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371862494	chr1:151936551-151936552	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533816769	chr1:151936572-151936573	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs6662728	chr1:151936578-151936579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs150072100	chr1:151936607-151936608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs71710896	chr1:151936612-151936613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4997552	chr1:151936623-151936624	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs4997551	chr1:151936625-151936626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2337688	chr1:151936627-151936628	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2337689	chr1:151936629-151936630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs556242700	chr1:151936639-151936640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574919577	chr1:151936691-151936692	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs180706148	chr1:151936731-151936732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538773618	chr1:151936811-151936812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs558351751	chr1:151936874-151936875	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs185319351	chr1:151936928-151936929	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs190916046	chr1:151936990-151936991	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs554458611	chr1:151937080-151937081	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs183443578	chr1:151937154-151937155	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542588272	chr1:151937163-151937164	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs562574670	chr1:151937173-151937174	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs531656584	chr1:151937176-151937177	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs145539903	chr1:151937180-151937181	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113470673	chr1:151937232-151937233	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs75344361	chr1:151937397-151937398	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369723904	chr1:151937417-151937418	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs564690796	chr1:151937439-151937440	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs10675058	chr1:151937495-151937496	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs386635436	chr1:151937496-151937497	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs143665098	chr1:151937498-151937499	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs10675059	chr1:151937502-151937503	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs527489141	chr1:151937607-151937608	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs116176506	chr1:151937765-151937766	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs139642036	chr1:151937766-151937767	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs186539491	chr1:151937818-151937819	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs191481298	chr1:151937824-151937825	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs144282302	chr1:151937860-151937861	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs2932564	chr1:151937894-151937895	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs7554859	chr1:151937938-151937939	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs548369367	chr1:151937948-151937949	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs558691608	chr1:151937958-151937959	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs571710756	chr1:151938010-151938011	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534396286	chr1:151938018-151938019	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs6587635	chr1:151938055-151938056	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs6587636	chr1:151938080-151938081	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:123)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1632 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151930800-151940800	Weak transcription	NHDF-Ad	bronchial
2	chr1:151933600-151937200	Enhancers	HUVEC	blood vessel
3	chr1:151933600-151945000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:151934000-151940600	Weak transcription	Gastric	stomach
5	chr1:151934200-151936800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr1:151934200-151937000	Weak transcription	Stomach Mucosa	stomach
7	chr1:151934200-151940600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr1:151934200-151942600	Weak transcription	HSMM	muscle
9	chr1:151934400-151940200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:151934600-151936800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:151934600-151940600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:151934600-151953400	Weak transcription	Psoas Muscle	Psoas
13	chr1:151934800-151936800	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr1:151934800-151939600	Weak transcription	Fetal Intestine Small	intestine
15	chr1:151934800-151940200	Weak transcription	Fetal Intestine Large	intestine
16	chr1:151935200-151936600	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr1:151935200-151937000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr1:151935200-151940400	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:151935600-151937200	Enhancers	Adipose Nuclei	Adipose
20	chr1:151935800-151937000	Weak transcription	Fetal Muscle Leg	muscle
21	chr1:151935800-151937400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr1:151936000-151937000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:151936000-151945000	Weak transcription	HSMMtube	muscle
24	chr1:151936400-151936800	Weak transcription	NHEK	skin
25	chr1:151936400-151938800	Weak transcription	Hela-S3	cervix
26	chr1:151936600-151937000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr1:151936800-151937200	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr1:151936800-151937200	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr1:151936800-151937200	Enhancers	Spleen	Spleen
30	chr1:151936800-151937400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:151936800-151937800	Enhancers	NHEK	skin
32	chr1:151937000-151937200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:151937000-151937200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:151937000-151937200	Enhancers	Fetal Muscle Trunk	muscle
35	chr1:151937000-151937200	Enhancers	Fetal Muscle Leg	muscle
36	chr1:151937000-151937200	Enhancers	Left Ventricle	heart
37	chr1:151937000-151937200	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr1:151937000-151937200	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr1:151937000-151937400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:151937000-151937400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:151937000-151937400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:151937000-151937400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:151937000-151937400	Enhancers	Stomach Mucosa	stomach
44	chr1:151937200-151937400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr1:151937200-151938800	Weak transcription	HUVEC	blood vessel
46	chr1:151937200-151940200	Weak transcription	Adipose Nuclei	Adipose
47	chr1:151937200-151940200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr1:151937200-151940400	Weak transcription	Fetal Muscle Trunk	muscle
49	chr1:151937200-151940400	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr1:151937200-151940600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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