Variant report

Variant	esv19715
Chromosome Location	chr1:228742638-228783674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1840)
CpG islands
(count:855)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1840 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:228783364-228783625	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:228743385-228743565	HepG2	liver:	n/a	n/a
3	ATF3	chr1:228783161-228783846	A549	lung:	n/a	n/a
4	ATF3	chr1:228743369-228743629	K562	blood:	n/a	n/a
5	BACH1	chr1:228782482-228782665	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr1:228756724-228756902	GM12878	blood:	n/a	chr1:228756756-228756769 chr1:228756760-228756769 chr1:228756837-228756850 chr1:228756750-228756763 chr1:228756749-228756762
7	BCL3	chr1:228782396-228784122	A549	lung:	n/a	chr1:228784016-228784025 chr1:228783302-228783315 chr1:228783943-228783956 chr1:228783147-228783156 chr1:228782764-228782773
8	BCL3	chr1:228771159-228771418	GM12878	blood:	n/a	n/a
9	BCL3	chr1:228757842-228758009	GM12878	blood:	n/a	n/a
10	BCL3	chr1:228757836-228758031	GM12878	blood:	n/a	n/a
11	BCL3	chr1:228782408-228783961	A549	lung:	n/a	chr1:228783302-228783315 chr1:228783943-228783956 chr1:228783147-228783156 chr1:228782764-228782773
12	BHLHE40	chr1:228782373-228782758	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:228771339-228771364	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:228747752-228747952	HepG2	liver:	n/a	chr1:228747812-228747828 chr1:228747817-228747833
15	BHLHE40	chr1:228745511-228745711	HepG2	liver:	n/a	chr1:228745571-228745587 chr1:228745576-228745592
16	BHLHE40	chr1:228782486-228782780	HepG2	liver:	n/a	n/a
17	BHLHE40	chr1:228782393-228782773	K562	blood:	n/a	n/a
18	BHLHE40	chr1:228771166-228771539	K562	blood:	n/a	n/a
19	BRCA1	chr1:228771344-228771359	GM12878	blood:	n/a	n/a
20	BRCA1	chr1:228782522-228782954	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:228783354-228784332	Hela-S3	cervix:	n/a	chr1:228783960-228783967
22	CBX3	chr1:228752250-228753181	K562	blood:	n/a	n/a
23	CBX3	chr1:228747705-228750045	K562	blood:	n/a	n/a
24	CBX3	chr1:228748818-228752205	K562	blood:	n/a	n/a
25	CBX3	chr1:228750132-228751007	K562	blood:	n/a	n/a
26	CBX3	chr1:228756716-228760610	K562	blood:	n/a	n/a
27	CBX3	chr1:228772523-228773375	K562	blood:	n/a	n/a
28	CBX3	chr1:228770156-228772097	K562	blood:	n/a	n/a
29	CBX3	chr1:228774747-228775535	K562	blood:	n/a	n/a
30	CBX3	chr1:228770193-228771056	K562	blood:	n/a	n/a
31	CBX3	chr1:228746295-228748726	K562	blood:	n/a	n/a
32	CBX3	chr1:228745450-228746485	K562	blood:	n/a	n/a
33	CBX3	chr1:228744029-228745432	K562	blood:	n/a	n/a
34	CBX3	chr1:228766705-228767765	K562	blood:	n/a	n/a
35	CBX3	chr1:228768957-228769762	K562	blood:	n/a	n/a
36	CBX3	chr1:228762327-228762990	K562	blood:	n/a	n/a
37	CBX3	chr1:228763642-228764366	K562	blood:	n/a	n/a
38	CBX3	chr1:228780121-228782451	K562	blood:	n/a	n/a
39	CBX3	chr1:228756779-228759666	K562	blood:	n/a	n/a
40	CBX3	chr1:228774646-228775517	K562	blood:	n/a	n/a
41	CBX3	chr1:228766654-228767753	K562	blood:	n/a	n/a
42	CBX3	chr1:228754548-228755287	K562	blood:	n/a	n/a
43	CBX3	chr1:228767896-228768693	K562	blood:	n/a	n/a
44	CBX3	chr1:228767906-228768647	K562	blood:	n/a	n/a
45	CBX3	chr1:228779133-228779900	K562	blood:	n/a	n/a
46	CBX3	chr1:228751049-228752148	K562	blood:	n/a	n/a
47	CBX3	chr1:228775560-228776734	K562	blood:	n/a	n/a
48	CBX3	chr1:228759936-228766629	K562	blood:	n/a	n/a
49	CBX3	chr1:228768708-228770057	K562	blood:	n/a	n/a
50	CBX3	chr1:228744333-228746248	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228773514-228773564	HRPEpiC	eye:	n/a
2	chr1:228773514-228773564	HRPEpiC	eye:	n/a
3	chr1:228783383-228783433	NH-A	brain:	n/a
4	chr1:228743131-228743181	HEK293	kidney:	embryo
5	chr1:228783274-228783324	AG09309	skin:	n/a
6	chr1:228773514-228773564	HCM	heart:	n/a
7	chr1:228756711-228756761	AG09319	gingival:	n/a
8	chr1:228782809-228782859	HRPEpiC	eye:	n/a
9	chr1:228743131-228743181	HepG2	liver:	n/a
10	chr1:228744111-228744161	T-47D	breast:	n/a
11	chr1:228773464-228773514	Hepatocyte	liver:	n/a
12	chr1:228756714-228756764	AG04449	skin:	fetal
13	chr1:228743235-228743285	HMEC	breast:	n/a
14	chr1:228742687-228742737	BE2_C	brain:	n/a
15	chr1:228782809-228782859	NT2-D1	testis:	n/a
16	chr1:228773464-228773514	CMK	blood:	n/a
17	chr1:228756714-228756764	HCT-116	colon:	n/a
18	chr1:228783383-228783433	NT2-D1	testis:	n/a
19	chr1:228756789-228756839	HCT-116	colon:	n/a
20	chr1:228743373-228743423	AG04450	lung:	fetal
21	chr1:228783274-228783324	Hepatocyte	liver:	n/a
22	chr1:228756789-228756839	LNCaP	prostate:	n/a
23	chr1:228773464-228773514	AG09319	gingival:	n/a
24	chr1:228742687-228742737	HCPEpiC	choroid plexus:	n/a
25	chr1:228783383-228783433	GM19239	blood:	n/a
26	chr1:228773464-228773514	HNPCEpiC	eye:	n/a
27	chr1:228744111-228744161	NHBE	bronchial:	n/a
28	chr1:228783274-228783324	H1-hESC	embryonic stem cell:	embryo
29	chr1:228743373-228743423	HEEpiC	esophagus:	n/a
30	chr1:228783274-228783324	LNCaP	prostate:	n/a
31	chr1:228773514-228773564	NT2-D1	testis:	n/a
32	chr1:228783545-228783595	GM12878	blood:	n/a
33	chr1:228742687-228742737	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:228773514-228773564	NHBE	bronchial:	n/a
35	chr1:228742687-228742737	GM19239	blood:	n/a
36	chr1:228756714-228756764	GM12892	blood:	n/a
37	chr1:228773514-228773564	ECC-1	luminal epithelium:	n/a
38	chr1:228742687-228742737	K562	blood:	n/a
39	chr1:228743131-228743181	HMEC	breast:	n/a
40	chr1:228773464-228773514	HCF	heart:	n/a
41	chr1:228783274-228783324	NT2-D1	testis:	n/a
42	chr1:228743131-228743181	LNCaP	prostate:	n/a
43	chr1:228743373-228743423	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:228756789-228756839	ECC-1	luminal epithelium:	n/a
45	chr1:228744111-228744161	HIPEpiC	eye:	n/a
46	chr1:228744111-228744161	HepG2	liver:	n/a
47	chr1:228743131-228743181	HL-60	blood:	n/a
48	chr1:228783383-228783433	HNPCEpiC	eye:	n/a
49	chr1:228742687-228742737	AG04449	skin:	fetal
50	chr1:228742687-228742737	PFSK-1	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228783048..228783985-chr16:3070059..3070679,2	HCT-116	colon:
2	chr1:228783070..228784014-chr12:123011279..123011841,2	Hela-S3	cervix:
3	chr1:228783138..228784040-chr9:140135254..140135781,2	HCT-116	colon:
4	chr1:17231506..17232339-chr1:228782832..228783652,2	Hela-S3	cervix:
5	chr1:228783073..228784051-chr7:5569241..5569745,2	Hela-S3	cervix:
6	chr1:169454738..169455424-chr1:228783655..228784433,2	Hela-S3	cervix:
7	chr1:228782241..228785119-chr1:228785249..228788137,2	K562	blood:

No data

Variant related genes	Relation type
RNA5S3	TF binding region
RNA5S17	TF binding region
RNA5S10	TF binding region
RNA5SP19	TF binding region
RNA5S6	TF binding region
DUSP5P1	TF binding region
RNA5S2	TF binding region
RNA5S12	TF binding region
RNA5S14	TF binding region
RNA5S16	TF binding region
RNA5S7	TF binding region
RNA5S1	TF binding region
RNA5S13	TF binding region
RNA5S5	TF binding region
RNA5S4	TF binding region
RNA5S15	TF binding region
ENSG00000206878	TF binding region
RNA5S8	TF binding region
RNA5S9	TF binding region
RNA5S11	TF binding region
RNA5S3	CpG island
RNA5S17	CpG island
RNA5S10	CpG island
RNA5SP19	CpG island
RNA5S6	CpG island
DUSP5P1	CpG island
RNA5S2	CpG island
RNA5S12	CpG island
RNA5S14	CpG island
RNA5S16	CpG island
RNA5S7	CpG island
RNA5S1	CpG island
RNA5S13	CpG island
RNA5S5	CpG island
RNA5S4	CpG island
RNA5S15	CpG island
ENSG00000206878	CpG island
RNA5S8	CpG island
RNA5S9	CpG island
RNA5S11	CpG island
ENSG00000184697	chromatin interactions
ENSG00000111011	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000183929	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000006327	chromatin interactions
ENSG00000213062	chromatin interactions
ENSG00000184445	chromatin interactions
ENSG00000117479	chromatin interactions

Extended variants
information (count: 628 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533611945	chr1:228742694-228742695	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
2	rs146917997	chr1:228742710-228742711	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
3	rs547210020	chr1:228742714-228742715	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
4	rs138216023	chr1:228742731-228742732	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
5	rs527915691	chr1:228742748-228742749	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs567198059	chr1:228742752-228742753	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs191758625	chr1:228742764-228742765	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs184081359	chr1:228742766-228742767	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs577012679	chr1:228742767-228742768	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs188481902	chr1:228742768-228742769	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs556455784	chr1:228742770-228742771	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs35202063	chr1:228742779-228742780	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs546498497	chr1:228742785-228742786	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs568019905	chr1:228742786-228742787	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs536750223	chr1:228742787-228742788	Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs557059750	chr1:228742819-228742820	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs570451262	chr1:228742821-228742822	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs74144513	chr1:228742825-228742826	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs145740982	chr1:228742848-228742849	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs66803435	chr1:228742864-228742865	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs58582992	chr1:228742865-228742866	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs10916346	chr1:228742867-228742868	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs57739836	chr1:228742879-228742880	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs566709421	chr1:228742887-228742888	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs572818322	chr1:228742912-228742913	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs541695574	chr1:228742928-228742929	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs61825664	chr1:228742930-228742931	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs76506307	chr1:228742947-228742948	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs138580517	chr1:228742975-228742976	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs149388241	chr1:228742981-228742982	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs575556724	chr1:228742982-228742983	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs544273389	chr1:228742986-228742987	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs564651573	chr1:228742996-228742997	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs533248458	chr1:228742997-228742998	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs540865271	chr1:228743000-228743001	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs180999381	chr1:228743012-228743013	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs144731316	chr1:228743026-228743027	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs549124944	chr1:228743051-228743052	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs138270838	chr1:228743058-228743059	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs185936516	chr1:228743060-228743061	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs530575112	chr1:228743086-228743087	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs550284200	chr1:228743088-228743089	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs570560163	chr1:228743127-228743128	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs539110981	chr1:228743129-228743130	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs190645029	chr1:228743141-228743142	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs566280656	chr1:228743150-228743151	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs142773872	chr1:228743151-228743152	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs370138941	chr1:228743163-228743164	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
49	rs79963770	chr1:228743177-228743178	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
50	rs575448463	chr1:228743194-228743195	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228742600-228742800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:228742600-228742800	Bivalent Enhancer	Fetal Brain Male	brain
3	chr1:228742600-228743000	Active TSS	Rectal Mucosa Donor 31	rectum
4	chr1:228742800-228743000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:228742800-228743200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr1:228742800-228743200	Bivalent Enhancer	Placenta	Placenta
7	chr1:228742800-228743400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
8	chr1:228742800-228743400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:228743000-228743200	Bivalent/Poised TSS	HepG2	liver
10	chr1:228743000-228743400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:228743000-228743600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
12	chr1:228743000-228744000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:228743200-228743600	Active TSS	HepG2	liver
14	chr1:228743200-228744000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:228743400-228743800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:228743800-228744000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:228756400-228756600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr1:228756400-228756800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
19	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
20	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:228756600-228756800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:228756600-228756800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
23	chr1:228756600-228756800	Enhancers	Primary T cells fromperipheralblood	blood
24	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
25	chr1:228756600-228756800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
27	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
28	chr1:228756600-228756800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:228756600-228756800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
32	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
33	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
34	chr1:228756600-228756800	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
36	chr1:228756600-228756800	Bivalent Enhancer	Fetal Intestine Small	intestine
37	chr1:228756600-228756800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
39	chr1:228756600-228756800	Bivalent Enhancer	Fetal Thymus	thymus
40	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Gastric	stomach
41	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Left Ventricle	heart
42	chr1:228756600-228756800	Bivalent/Poised TSS	Small Intestine	intestine
43	chr1:228756600-228756800	Flanking Bivalent TSS/Enh	Spleen	Spleen
44	chr1:228756600-228757000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:228756600-228757000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:228756600-228757000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:228756600-228757000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:228756600-228757000	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr1:228756600-228757000	Enhancers	Primary B cells from peripheral blood	blood
50	chr1:228756600-228757000	Active TSS	Primary T cells from cord blood	blood

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