Variant report

Variant	esv3343743
Chromosome Location	chr1:161695553-161698101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:754)
CpG islands
(count:732)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:161697652-161697745	K562	blood:	n/a	n/a
2	ATF2	chr1:161696508-161697180	GM12878	blood:	n/a	n/a
3	ATF2	chr1:161697416-161697766	GM12878	blood:	n/a	n/a
4	ATF2	chr1:161697348-161697828	GM12878	blood:	n/a	n/a
5	BACH1	chr1:161697016-161697610	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:161695615-161696769	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:161697132-161697292	K562	blood:	n/a	n/a
8	BACH1	chr1:161696097-161696123	K562	blood:	n/a	n/a
9	BATF	chr1:161697444-161697722	GM12878	blood:	n/a	n/a
10	BCL3	chr1:161696620-161697171	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:161695962-161697186	GM12878	blood:	n/a	n/a
12	BCLAF1	chr1:161695548-161696333	GM12878	blood:	n/a	n/a
13	BCLAF1	chr1:161695565-161696820	K562	blood:	n/a	n/a
14	BCLAF1	chr1:161696353-161696875	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:161697335-161697827	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:161696702-161697167	A549	lung:	n/a	n/a
17	BHLHE40	chr1:161695665-161697806	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:161696883-161697216	HepG2	liver:	n/a	n/a
19	BHLHE40	chr1:161696037-161697726	K562	blood:	n/a	n/a
20	BRCA1	chr1:161696585-161696626	HepG2	liver:	n/a	n/a
21	BRCA1	chr1:161696978-161697508	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr1:161695717-161697392	K562	blood:	n/a	n/a
23	CCNT2	chr1:161695674-161697487	K562	blood:	n/a	n/a
24	CEBPB	chr1:161695770-161696076	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:161695863-161695924	K562	blood:	n/a	n/a
26	CEBPD	chr1:161696537-161696906	K562	blood:	n/a	n/a
27	CHD1	chr1:161696188-161697665	GM12878	blood:	n/a	n/a
28	CHD1	chr1:161696551-161696695	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr1:161695909-161697219	K562	blood:	n/a	n/a
30	CHD2	chr1:161695732-161695932	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr1:161696199-161696395	HepG2	liver:	n/a	n/a
32	CHD2	chr1:161696323-161697166	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr1:161696820-161697209	HepG2	liver:	n/a	n/a
34	CHD2	chr1:161695560-161697732	GM12878	blood:	n/a	n/a
35	CHD2	chr1:161696821-161697190	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr1:161696222-161696481	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr1:161696522-161697189	A549	lung:	n/a	n/a
38	CREB1	chr1:161696224-161697276	GM12878	blood:	n/a	n/a
39	CTCF	chr1:161695800-161695950	GM12872	blood:	n/a	n/a
40	CTCF	chr1:161695900-161696050	NHLF	lung:	n/a	n/a
41	CTCF	chr1:161695460-161695610	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:161697081-161697155	GM12878	blood:	n/a	n/a
43	CTCF	chr1:161695820-161695970	GM12869	blood:	n/a	n/a
44	CTCF	chr1:161695860-161696010	AG04450	lung:	n/a	n/a
45	CTCF	chr1:161695940-161696090	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:161695670-161695859	GM12892	blood:	n/a	n/a
47	CTCF	chr1:161695880-161696030	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr1:161696620-161696770	GM12868	blood:	n/a	n/a
49	CTCF	chr1:161695939-161696010	ProgFib	skin:	n/a	n/a
50	CTCF	chr1:161695816-161695832	GM10266	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161697574-161697624	PANC-1	pancreas:	n/a
2	chr1:161697083-161697133	HCPEpiC	choroid plexus:	n/a
3	chr1:161697052-161697102	SK-N-SH	brain:	n/a
4	chr1:161695678-161695728	H1-hESC	embryonic stem cell:	embryo
5	chr1:161696175-161696225	T-47D	breast:	n/a
6	chr1:161697281-161697331	HRPEpiC	eye:	n/a
7	chr1:161697052-161697102	NB4	blood:	n/a
8	chr1:161696302-161696352	HRPEpiC	eye:	n/a
9	chr1:161697574-161697624	PrEC	prostate:	n/a
10	chr1:161695659-161695709	HCF	heart:	n/a
11	chr1:161695659-161695709	K562	blood:	n/a
12	chr1:161695839-161695889	HCPEpiC	choroid plexus:	n/a
13	chr1:161696302-161696352	U87	brain:	n/a
14	chr1:161695839-161695889	GM06990	blood:	n/a
15	chr1:161696082-161696132	T-47D	breast:	n/a
16	chr1:161695678-161695728	HMEC	breast:	n/a
17	chr1:161697052-161697102	GM12892	blood:	n/a
18	chr1:161697052-161697102	HUVEC	blood vessel:	n/a
19	chr1:161697281-161697331	GM19239	blood:	n/a
20	chr1:161696175-161696225	HCT-116	colon:	n/a
21	chr1:161696082-161696132	HCT-116	colon:	n/a
22	chr1:161696175-161696225	AG09309	skin:	n/a
23	chr1:161697574-161697624	AG10803	skin:	n/a
24	chr1:161695961-161696011	K562	blood:	n/a
25	chr1:161695839-161695889	PANC-1	pancreas:	n/a
26	chr1:161695678-161695728	HEK293	kidney:	embryo
27	chr1:161697574-161697624	K562	blood:	n/a
28	chr1:161697083-161697133	Caco-2	colon:	n/a
29	chr1:161697281-161697331	LNCaP	prostate:	n/a
30	chr1:161696082-161696132	LNCaP	prostate:	n/a
31	chr1:161695839-161695889	T-47D	breast:	n/a
32	chr1:161697281-161697331	BJ	skin:	n/a
33	chr1:161695839-161695889	HMEC	breast:	n/a
34	chr1:161697052-161697102	NHDF-neo	bronchial:	n/a
35	chr1:161696302-161696352	H1-hESC	embryonic stem cell:	embryo
36	chr1:161697241-161697291	AG04449	skin:	fetal
37	chr1:161695659-161695709	AG10803	skin:	n/a
38	chr1:161697241-161697291	GM19239	blood:	n/a
39	chr1:161696175-161696225	Hela-S3	cervix:	n/a
40	chr1:161695961-161696011	PANC-1	pancreas:	n/a
41	chr1:161696302-161696352	AG10803	skin:	n/a
42	chr1:161695659-161695709	NHBE	bronchial:	n/a
43	chr1:161695659-161695709	MCF10A-Er-Src	breast:	n/a
44	chr1:161695678-161695728	HCF	heart:	n/a
45	chr1:161697083-161697133	HL-60	blood:	n/a
46	chr1:161696175-161696225	AG10803	skin:	n/a
47	chr1:161696082-161696132	HCPEpiC	choroid plexus:	n/a
48	chr1:161697083-161697133	AG09319	gingival:	n/a
49	chr1:161695839-161695889	ProgFib	skin:	n/a
50	chr1:161697574-161697624	AG09309	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:161651291..161653505-chr1:161696476..161699114,3	K562	blood:
2	chr1:161645664..161648632-chr1:161696817..161700044,3	K562	blood:
3	chr1:161697451..161700405-chr1:161734526..161737492,2	K562	blood:
4	chr1:161657417..161659539-chr1:161696325..161698709,3	K562	blood:
5	chr1:161696699..161697640-chr1:161719530..161720155,2	MCF-7	breast:
6	chr1:161640986..161643411-chr1:161696404..161699095,2	MCF-7	breast:
7	chr1:161696821..161698460-chr1:161718041..161719561,2	K562	blood:
8	chr1:161696482..161699035-chr1:161718061..161722028,6	K562	blood:
9	chr1:161696512..161697495-chr11:66610830..66611790,2	NB4	blood:
10	chr1:161695918..161698329-chr1:161735226..161737077,2	MCF-7	breast:
11	chr1:161591405..161593904-chr1:161697560..161699954,2	K562	blood:
12	chr1:161694367..161698874-chr1:161718174..161721030,6	MCF-7	breast:
13	chr1:161696651..161697360-chr16:2961887..2962457,2	NB4	blood:
14	chr1:161474965..161476524-chr1:161694397..161697249,2	K562	blood:
15	chr1:161648385..161650314-chr1:161696093..161698220,2	K562	blood:
16	chr1:161654373..161658306-chr1:161696464..161699587,3	MCF-7	breast:
17	chr1:161535342..161537175-chr1:161695826..161698506,2	MCF-7	breast:
18	chr1:161474965..161477021-chr1:161694558..161697249,2	K562	blood:
19	chr1:161696233..161698594-chr1:161718488..161721013,2	MCF-7	breast:
20	chr1:161695790..161697784-chr8:91655626..91657821,2	MCF-7	breast:
21	chr1:161683127..161685809-chr1:161696033..161698160,3	MCF-7	breast:
22	chr1:161696672..161698764-chr1:161719597..161721628,3	K562	blood:

No data

Variant related genes	Relation type
FCRLB	TF binding region
FCRLB	CpG island
ENSG00000143226	chromatin interactions
ENSG00000081721	chromatin interactions
ENSG00000226889	chromatin interactions
ENSG00000173653	chromatin interactions
ENSG00000059122	chromatin interactions
ENSG00000213075	chromatin interactions
ENSG00000118217	chromatin interactions
ENSG00000180694	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376524352	chr1:161695560-161695561	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs570646816	chr1:161695571-161695572	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs539222646	chr1:161695588-161695589	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs56368909	chr1:161695602-161695603	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs373956497	chr1:161695612-161695613	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141567912	chr1:161695623-161695624	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs576557871	chr1:161695632-161695633	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs7520519	chr1:161695639-161695640	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs35126350	chr1:161695666-161695667	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs555783403	chr1:161695678-161695679	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs376420928	chr1:161695713-161695714	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs139796104	chr1:161695723-161695724	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371919304	chr1:161695751-161695752	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546900428	chr1:161695775-161695776	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548692484	chr1:161695778-161695779	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200243110	chr1:161695786-161695787	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs3738330	chr1:161695837-161695838	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs372463922	chr1:161695853-161695854	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs375748940	chr1:161695886-161695887	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs377445918	chr1:161695899-161695900	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs568436929	chr1:161695903-161695904	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs376538728	chr1:161695942-161695943	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs536465503	chr1:161695943-161695944	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs138973877	chr1:161695949-161695950	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs560704170	chr1:161696005-161696006	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs533584562	chr1:161696006-161696007	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs1417582	chr1:161696088-161696089	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs562291750	chr1:161696107-161696108	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs372640903	chr1:161696136-161696137	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs5778228	chr1:161696150-161696151	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs531294203	chr1:161696173-161696174	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs182416412	chr1:161696203-161696204	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs561323347	chr1:161696260-161696261	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs559172201	chr1:161696318-161696319	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs527262696	chr1:161696349-161696350	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs573068237	chr1:161696369-161696370	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs114727710	chr1:161696381-161696382	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs375372824	chr1:161696389-161696390	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs117649845	chr1:161696390-161696391	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs539623074	chr1:161696464-161696465	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs549706716	chr1:161696466-161696467	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs371131821	chr1:161696489-161696490	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs374770887	chr1:161696495-161696496	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs570198587	chr1:161696509-161696510	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs202042884	chr1:161696531-161696532	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs555871257	chr1:161696586-161696587	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs200268538	chr1:161696648-161696649	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs200633919	chr1:161696663-161696664	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs112940407	chr1:161696669-161696670	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs369928909	chr1:161696683-161696684	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	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
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Acute lymphoblastic leukemia	19100363	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161689000-161695600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:161692200-161695600	Enhancers	K562	blood
3	chr1:161692400-161695600	Weak transcription	Gastric	stomach
4	chr1:161692600-161695600	Weak transcription	HSMMtube	muscle
5	chr1:161693800-161695600	Enhancers	NHDF-Ad	bronchial
6	chr1:161694600-161695600	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr1:161695000-161695600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:161695000-161695600	Enhancers	Colon Smooth Muscle	Colon
9	chr1:161695000-161695600	Enhancers	Esophagus	oesophagus
10	chr1:161695000-161696000	Enhancers	Spleen	Spleen
11	chr1:161695200-161695600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr1:161695200-161695600	Enhancers	Liver	Liver
13	chr1:161695200-161695600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
14	chr1:161695200-161695800	Flanking Active TSS	GM12878-XiMat	blood
15	chr1:161695400-161695600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:161695400-161695600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:161695400-161695600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:161695400-161695600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:161695400-161695600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:161695400-161695600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:161695400-161695600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr1:161695400-161695600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr1:161695400-161695600	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr1:161695400-161695600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr1:161695400-161695600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:161695400-161695600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:161695400-161695600	Enhancers	Adipose Nuclei	Adipose
28	chr1:161695400-161695600	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr1:161695400-161695600	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr1:161695400-161695600	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr1:161695400-161695600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr1:161695400-161695600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
33	chr1:161695400-161695600	Enhancers	Fetal Brain Male	brain
34	chr1:161695400-161695600	Flanking Active TSS	Fetal Brain Female	brain
35	chr1:161695400-161695600	Enhancers	Fetal Heart	heart
36	chr1:161695400-161695600	Bivalent/Poised TSS	Fetal Intestine Small	intestine
37	chr1:161695400-161695600	Active TSS	Fetal Lung	lung
38	chr1:161695400-161695600	Enhancers	Placenta	Placenta
39	chr1:161695400-161695600	Bivalent Enhancer	Fetal Stomach	stomach
40	chr1:161695400-161695600	Enhancers	Placenta Amnion	Placenta Amnion
41	chr1:161695400-161695600	Enhancers	Right Ventricle	heart
42	chr1:161695400-161695600	Active TSS	Stomach Smooth Muscle	stomach
43	chr1:161695400-161695600	Bivalent Enhancer	Dnd41	blood
44	chr1:161695400-161695600	Bivalent Enhancer	HepG2	liver
45	chr1:161695400-161695600	Enhancers	HMEC	breast
46	chr1:161695400-161695600	Enhancers	HUVEC	blood vessel
47	chr1:161695400-161695600	Enhancers	NHLF	lung
48	chr1:161695400-161695600	Flanking Active TSS	Osteobl	bone
49	chr1:161695400-161695800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
50	chr1:161695400-161695800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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