Variant report

Variant	esv3329004
Chromosome Location	chr5:145213984-145216532
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:489)
CpG islands
(count:854)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:145214933-145215166	K562	blood:	n/a	n/a
2	ARID3A	chr5:145214889-145215466	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:145214251-145214399	HepG2	liver:	n/a	n/a
4	ATF3	chr5:145214792-145215066	K562	blood:	n/a	n/a
5	BACH1	chr5:145214312-145215127	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr5:145214358-145215409	HepG2	liver:	n/a	chr5:145215122-145215138 chr5:145215123-145215139
7	BHLHE40	chr5:145216396-145216458	K562	blood:	n/a	n/a
8	BHLHE40	chr5:145214234-145215338	K562	blood:	n/a	chr5:145215122-145215138 chr5:145215123-145215139
9	BRCA1	chr5:145214863-145215232	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr5:145215201-145215211	HepG2	liver:	n/a	n/a
11	BRCA1	chr5:145214790-145214914	HepG2	liver:	n/a	n/a
12	BRCA1	chr5:145214990-145215120	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr5:145214042-145215516	K562	blood:	n/a	n/a
14	CBX3	chr5:145214808-145215160	K562	blood:	n/a	n/a
15	CCNT2	chr5:145214662-145215352	K562	blood:	n/a	n/a
16	CEBPB	chr5:145214808-145215050	K562	blood:	n/a	n/a
17	CEBPB	chr5:145214881-145215056	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr5:145214814-145215274	K562	blood:	n/a	n/a
19	CEBPB	chr5:145214771-145215443	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:145214865-145215052	A549	lung:	n/a	n/a
21	CEBPB	chr5:145214844-145215037	HepG2	liver:	n/a	n/a
22	CEBPD	chr5:145214673-145215359	HepG2	liver:	n/a	n/a
23	CHD2	chr5:145214987-145215211	H1-hESC	embryonic stem cell:	n/a	chr5:145215169-145215179
24	CHD2	chr5:145214769-145215301	HepG2	liver:	n/a	chr5:145215169-145215179
25	CHD2	chr5:145214580-145215289	Hela-S3	cervix:	n/a	chr5:145215169-145215179
26	CHD2	chr5:145214608-145215605	K562	blood:	n/a	chr5:145215169-145215179
27	CREB1	chr5:145214367-145215224	A549	lung:	n/a	n/a
28	CTCF	chr5:145214862-145215278	K562	blood:	n/a	chr5:145215112-145215130
29	CTCF	chr5:145215760-145215910	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr5:145214977-145215219	MCF-7	breast:	n/a	chr5:145215112-145215130
31	CTCF	chr5:145215072-145215182	HepG2	liver:	n/a	chr5:145215112-145215130
32	CTCF	chr5:145215020-145215170	HRPEpiC	eye:	n/a	chr5:145215112-145215130
33	CTCF	chr5:145214945-145215244	T-47D	breast:	n/a	chr5:145215112-145215130
34	CTCF	chr5:145215040-145215190	Hela-S3	cervix:	n/a	chr5:145215112-145215130
35	CTCF	chr5:145214960-145215110	RPTEC	kidney:	n/a	n/a
36	CTCF	chr5:145215800-145215950	A549	lung:	n/a	n/a
37	CTCF	chr5:145215030-145215196	Hela-S3	cervix:	n/a	chr5:145215112-145215130
38	CTCF	chr5:145215220-145215370	A549	lung:	n/a	n/a
39	CTCF	chr5:145214600-145214750	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr5:145215080-145215230	HUVEC	blood vessel:	n/a	chr5:145215112-145215130
41	CTCF	chr5:145215140-145215290	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr5:145215020-145215170	Hela-S3	cervix:	n/a	chr5:145215112-145215130
43	CTCF	chr5:145214939-145215252	K562	blood:	n/a	chr5:145215112-145215130
44	CTCF	chr5:145214980-145215130	HEK293	kidney:	n/a	chr5:145215112-145215130
45	CTCF	chr5:145214960-145215110	HCT-116	colon:	n/a	n/a
46	CTCF	chr5:145215140-145215290	GM12869	blood:	n/a	n/a
47	CTCF	chr5:145214847-145215315	A549	lung:	n/a	chr5:145215112-145215130
48	CTCF	chr5:145214847-145215317	K562	blood:	n/a	chr5:145215112-145215130
49	CTCF	chr5:145214925-145215242	A549	lung:	n/a	chr5:145215112-145215130
50	CTCF	chr5:145214737-145215319	K562	blood:	n/a	chr5:145215112-145215130

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:145215546-145215596	HRE	kidney:	n/a
2	chr5:145214981-145215031	CMK	blood:	n/a
3	chr5:145214971-145215021	GM12891	blood:	n/a
4	chr5:145214937-145214987	NHBE	bronchial:	n/a
5	chr5:145214993-145215043	A549	lung:	n/a
6	chr5:145215546-145215596	SAEC	small airway:	n/a
7	chr5:145214440-145214490	GM12892	blood:	n/a
8	chr5:145215784-145215834	HCPEpiC	choroid plexus:	n/a
9	chr5:145215169-145215219	SK-N-SH	brain:	n/a
10	chr5:145214744-145214794	Caco-2	colon:	n/a
11	chr5:145215125-145215175	LNCaP	prostate:	n/a
12	chr5:145215125-145215175	ECC-1	luminal epithelium:	n/a
13	chr5:145214979-145215029	Caco-2	colon:	n/a
14	chr5:145214981-145215031	NHBE	bronchial:	n/a
15	chr5:145215546-145215596	SK-N-SH	brain:	n/a
16	chr5:145214993-145215043	HMEC	breast:	n/a
17	chr5:145214981-145215031	AG09309	skin:	n/a
18	chr5:145214993-145215043	NHBE	bronchial:	n/a
19	chr5:145215784-145215834	SAEC	small airway:	n/a
20	chr5:145215125-145215175	Hela-S3	cervix:	n/a
21	chr5:145215055-145215105	RPTEC	kidney:	n/a
22	chr5:145215125-145215175	HUVEC	blood vessel:	n/a
23	chr5:145214971-145215021	AG09319	gingival:	n/a
24	chr5:145215784-145215834	HRCEpiC	kidney:	n/a
25	chr5:145214981-145215031	AoSMC	blood vessel:	n/a
26	chr5:145214440-145214490	T-47D	breast:	n/a
27	chr5:145215169-145215219	NH-A	brain:	n/a
28	chr5:145214769-145214819	AG04450	lung:	fetal
29	chr5:145215784-145215834	AG04449	skin:	fetal
30	chr5:145215055-145215105	HIPEpiC	eye:	n/a
31	chr5:145214971-145215021	GM19239	blood:	n/a
32	chr5:145215169-145215219	NHDF-neo	bronchial:	n/a
33	chr5:145214744-145214794	Hepatocyte	liver:	n/a
34	chr5:145214979-145215029	HCM	heart:	n/a
35	chr5:145214769-145214819	BE2_C	brain:	n/a
36	chr5:145214993-145215043	GM06990	blood:	n/a
37	chr5:145215629-145215679	HAEpiC	amniotic membrane:	n/a
38	chr5:145214769-145214819	HepG2	liver:	n/a
39	chr5:145214993-145215043	LNCaP	prostate:	n/a
40	chr5:145215169-145215219	ProgFib	skin:	n/a
41	chr5:145214769-145214819	Caco-2	colon:	n/a
42	chr5:145214971-145215021	IMR90	lung:	fetal
43	chr5:145214744-145214794	NH-A	brain:	n/a
44	chr5:145215546-145215596	NHBE	bronchial:	n/a
45	chr5:145214937-145214987	H1-hESC	embryonic stem cell:	embryo
46	chr5:145214769-145214819	SK-N-SH_RA	brain:	n/a
47	chr5:145215169-145215219	GM12891	blood:	n/a
48	chr5:145214769-145214819	HIPEpiC	eye:	n/a
49	chr5:145214937-145214987	HUVEC	blood vessel:	n/a
50	chr5:145214937-145214987	AG09309	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:145213194..145215106-chr5:145826697..145828661,2	K562	blood:
2	chr17:46125185..46125891-chr5:145214643..145215348,2	HCT-116	colon:
3	chr1:231555816..231556662-chr5:145214604..145215280,2	HCT-116	colon:
4	chr5:145215103..145216674-chr5:145218968..145221764,2	MCF-7	breast:
5	chr5:145213219..145215164-chr5:145314647..145317040,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRELID2-5	chr5:145214740-145214796	NONHSAT104387
2	lnc-PRELID2-5	chr5:145214215-145214495	NONHSAT104387

No data

Variant related genes	Relation type
PRELID2	TF binding region
PRELID2	CpG island
ENSG00000156463	chromatin interactions
ENSG00000082641	chromatin interactions
ENSG00000135766	chromatin interactions
ENSG00000113649	chromatin interactions
ENSG00000263412	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534402280	chr5:145214007-145214008	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs149045053	chr5:145214191-145214192	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs568898049	chr5:145214234-145214235	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs6896572	chr5:145214278-145214279	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs6876949	chr5:145214334-145214335	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6896600	chr5:145214339-145214340	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs569500527	chr5:145214386-145214387	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs113224360	chr5:145214405-145214406	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs35570934	chr5:145214407-145214408	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs6895551	chr5:145214427-145214428	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs74985941	chr5:145214443-145214444	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs183839535	chr5:145214462-145214463	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs527538529	chr5:145214471-145214472	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs538168597	chr5:145214521-145214522	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12658784	chr5:145214538-145214539	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs73306061	chr5:145214576-145214577	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557042868	chr5:145214601-145214602	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs573683200	chr5:145214647-145214648	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs569299133	chr5:145214664-145214665	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs531714746	chr5:145214682-145214683	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs112905738	chr5:145214695-145214696	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs370256767	chr5:145214710-145214711	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs374215370	chr5:145214716-145214717	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs377030040	chr5:145214729-145214730	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs371461902	chr5:145214764-145214765	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs373980375	chr5:145214775-145214776	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs375844133	chr5:145214791-145214792	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs368280361	chr5:145214793-145214794	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs145972329	chr5:145214800-145214801	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs553963912	chr5:145214808-145214809	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs567491631	chr5:145214861-145214862	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs535970940	chr5:145214873-145214874	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs534281389	chr5:145214885-145214886	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs73306063	chr5:145214889-145214890	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs544985334	chr5:145214903-145214904	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs558218580	chr5:145214951-145214952	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs572314191	chr5:145214958-145214959	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs373328844	chr5:145215010-145215011	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs188054263	chr5:145215012-145215013	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs561311736	chr5:145215035-145215036	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs376290746	chr5:145215037-145215038	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs192234574	chr5:145215070-145215071	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs574660832	chr5:145215114-145215115	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs183413269	chr5:145215130-145215131	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs370083459	chr5:145215175-145215176	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs149988108	chr5:145215187-145215188	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs35559855	chr5:145215188-145215189	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs531667716	chr5:145215215-145215216	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs551764292	chr5:145215217-145215218	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs111731923	chr5:145215265-145215266	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145172800-145214200	Weak transcription	Right Ventricle	heart
2	chr5:145183600-145214000	Weak transcription	Fetal Kidney	kidney
3	chr5:145196800-145214000	Weak transcription	Fetal Stomach	stomach
4	chr5:145201400-145214200	Weak transcription	Lung	lung
5	chr5:145207200-145214200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr5:145207400-145214000	Weak transcription	NHEK	skin
7	chr5:145209800-145214000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr5:145209800-145214200	Weak transcription	Small Intestine	intestine
9	chr5:145209800-145214200	Weak transcription	Hela-S3	cervix
10	chr5:145210400-145214000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr5:145210600-145214400	Weak transcription	Primary T cells from cord blood	blood
12	chr5:145210800-145214200	Weak transcription	Liver	Liver
13	chr5:145211000-145214200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:145211000-145214200	Weak transcription	Left Ventricle	heart
15	chr5:145211000-145214200	Weak transcription	Right Atrium	heart
16	chr5:145211000-145214400	Weak transcription	HSMMtube	muscle
17	chr5:145211200-145214000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr5:145211200-145214000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr5:145211200-145214000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:145211200-145214000	Weak transcription	NH-A	brain
21	chr5:145211400-145214000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr5:145212000-145214000	Enhancers	Fetal Lung	lung
23	chr5:145212400-145214200	Weak transcription	Gastric	stomach
24	chr5:145212600-145214000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr5:145212600-145214000	Flanking Active TSS	K562	blood
26	chr5:145212800-145214000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr5:145212800-145214000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr5:145212800-145215400	Active TSS	Colonic Mucosa	Colon
29	chr5:145212800-145216000	Active TSS	Rectal Smooth Muscle	rectum
30	chr5:145213000-145214000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr5:145213000-145215400	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr5:145213200-145214000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:145213200-145214200	Weak transcription	Aorta	Aorta
34	chr5:145213200-145215600	Active TSS	NHLF	lung
35	chr5:145213400-145214000	Weak transcription	Ovary	ovary
36	chr5:145213400-145214200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr5:145213400-145214200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:145213400-145214200	Enhancers	Brain Anterior Caudate	brain
39	chr5:145213400-145214200	Enhancers	Brain Cingulate Gyrus	brain
40	chr5:145213400-145214200	Enhancers	Colon Smooth Muscle	Colon
41	chr5:145213400-145214200	Enhancers	Fetal Brain Male	brain
42	chr5:145213400-145214200	Enhancers	Fetal Heart	heart
43	chr5:145213400-145214200	Weak transcription	Pancreas	Pancrea
44	chr5:145213400-145214200	Enhancers	Placenta Amnion	Placenta Amnion
45	chr5:145213400-145214200	Flanking Active TSS	HepG2	liver
46	chr5:145213400-145214800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:145213400-145215400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr5:145213400-145215400	Active TSS	Fetal Intestine Large	intestine
49	chr5:145213400-145215400	Active TSS	Fetal Intestine Small	intestine
50	chr5:145213600-145214000	Enhancers	Muscle Satellite Cultured Cells	--

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